DOE-HDBK-1141-2008, Radiological Assessor Training
Functional areas: Radiological Assessor, Training
This handbook describes a Radiological Assessor Training program. It includes standards and policies as well as recommendations for material development and program administration. It is intended for use by DOE and DOE contractors for the development of facilityspecific radiological assessor training. This material is intended for assessment of occupational radiation protection programs.
Project Number TRNG-0060
Version history and related documents
Supersedes
Earlier documents this one replaced.
- DOE-HDBK-1141-2001 Module 1-3Radiological Assessor Training - Student's Guide Module 1-3 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 4-7Radiological Assessor Training - Student's Guide Module 4-7 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 8-12Radiological Assessor Training - Student's Guide Module 8-12 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 1-3Radiological Assessor Training Instructor's Guide Module 1-3 (Aug 20, 2008)
- DOE_HDBK-1141-2001Radiological Assessor Training - Foreword (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 4-7Radiological Assessor Training - Instructor's Guide Module 4-7 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 8-10Radiological Assessor Training - Instructor's Guide Module 8-10 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Module 13-20Radiological Assessor Training - Instructor's Guide Module 13-20 (Aug 20, 2008)
- DOE-HDBK-1141-2001 Chg Notice 1Radiological Assessor Training (Aug 20, 2008)
Related documents
Document text
Text extracted from the attached file. Refer to the original document for the authoritative version.
Section 1
DOE-HDBK-1141-2008
August 2008
DOE HANDBOOK
Radiological Assessor Training
U.S. Department of Energy AREA TRNG
Washington, D.C. 20585
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
NOT MEASUREMENT
SENSITIVE
This document is available on the Department of Energy
Technical Standards Program Web site at
http://tis.eh.doe.gov/techs\
Foreword
This Handbook describes an implementation process for training as recommended in
Implementation Guide G441.1-1B, Radiation Protection Programs, March 2007, and as outlined
in DOE- STD- 1098-99, CN1, March 2005, DOE Radiological Control (the Radiological Control
Standard - RCS). The Handbook is meant to assist those individuals within the Department of
Energy, Managing and Operating contractors, and Managing and Integrating contractors
identified as having responsibility for implementing training required by Title 10 Code of Federal
Regulations Part 835 Occupational Radiation Protection (10 CFR 835) and training
recommended by the RCS. This training is intended for auditors and assessors to assist in
meeting the training requirements of 10 CFR 835 for the conduct of audits and assessments of
occupational radiation protection programs. While this Handbook addresses many
requirements of 10 CFR 835 Subpart B, it must be supplemented with facility-specific
information to achieve full compliance.
This Handbook contains recommended training materials consistent with other DOE radiological
safety training materials. The training material consists of the following five parts:
Program Management Guide - This part contains detailed information on how to use the
Handbook material.
Instructor’s Guide - This part contains lesson plans for instructor use, including notation of
key points for inclusion of facility-specific information.
Overheads - This part contains overheads instructor use corresponding to the Instructor's
Guide.
Student’s Guide - This part contains student handout material and also should be
augmented by facility-specific information.
Handouts - This part contains several student handouts that provide supporting information
for various modules.
This training material is targeted for individuals with a basic knowledge of radiological protection
concepts and provides material on how to conduct a radiological assessment.
This Handbook was produced in Microsoft Word and has been formatted for printing on a HP
4M (or higher) LaserJet printer. Overheads were produced in Powerpoint. Copies of this
Handbook may be obtained from either the DOE Radiation Safety Training Home Page Internet
site (http://www.hss.energy.gov/healthsafety/wshp/radiation/RST/rstmater.htm) or the Technical
Standards Internet site (http://www.hss.energy.gov/nuclearsafety/techstds).
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U.S. Department of Energy
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Table of Contents
Page
Introduction ................................................................................................................................... 1
Purpose and Scope .................................................................. 1
Section 2
Compliance with 10 CFR 835-Subpart B ................................. 1
Goal of Training Program ......................................................... 2
Organizational Relationships and Reporting Structure ............ 2
Training Program Descriptions................................................................................................... 3
Overview of Training Program.................................................. 3
Prerequisites ............................................................................. 3
Proficiency Requirements......................................................... 4
Retraining.................................................................................. 5
Instructor Training and Qualifications....................................... 5
Training Program Material Development ................................................................................... 6
Training Material Presentation.................................................. 6
Training Certificates .................................................................. 7
Training Aids, References ........................................................ 7
Training Program Standards and Policies................................................................................. 8
Lectures, Seminars, Training Exercises, etc............................ 8
Delinquent Training/Failure ...................................................... 8
Exceptions and Waivers ........................................................... 8
Administration............................................................................................................................... 9
Training Records....................................................................... 9
Training Program Development/Change Requests ................. 9
Audits (internal and external).................................................... 9
Evaluating Training Program Effectiveness ........................... 10
References and Supporting Documents.................................................................................. 11
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Introduction
Purpose and Scope This handbook describes a Radiological Assessor
Training program. It includes standards and policies as
well as recommendations for material development and
program administration. It is intended for use by DOE
and DOE contractors for the development of facility-
specific radiological assessor training. This material is
intended for assessment of occupational radiation
protection programs. This material does not address
environmental radiation protection programs.
Compliance with 10 CFR
835-Subpart B
The DOE training materials for Radiological Assessor
Training reflect the requirements identified in 10 CFR
835-Subpart B, Management and Administrative
Requirements, and recommendations identified in the
DOE Implementation Guide G441.1-1B, Radiation
Protection Programs Guide, and in DOE-STD-1098-99,
DOE Radiological Control Standard. When implemented
in its entirety and supplemented as noted with
appropriate facility-specific information, this handbook
provides an acceptable method to meet the requirements
of 10 CFR 835-Subpart B for training of individuals
Section 3
(auditors and assessors) responsible for developing and
implementing measures necessary for ensuring
compliance with 10 CFR 835 (10 CFR 835.103).
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However, it is incumbent on management of each facility
to review the content of this handbook against the
radiological hazards present to ensure that the training
content is appropriate to each individual’s prior training,
work assignments, and degree of exposure to potential
radiological hazards.
Training described in this handbook does not eliminate
the need for additional training on facility-specific
hazards. Notations throughout the program documents
indicate the need for facility-specific information. If the
noted section is not applicable to the facility, no
information need be presented. The site Radiological
Control Manager or designee should concur in facility-
generated radiological training material.
Goal of Training
Program
The goal of the training program is to provide a sufficient
level of knowledge and skills in radiological assessment
fundamentals commensurate with the assigned duties and
potential radiological hazards encountered at DOE
facilities using or possessing radioactive materials and/or
radiation-producing devices.
Organizational
Relationships and
Reporting Structure
The DOE Office of Health, Safety and Security’s Office of
Worker Safety and Health Policy (HS-11) is responsible
for approving and maintaining the training materials.
The establishment of a comprehensive and effective
contractor site radiological control training program is the
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responsibility of line management and their subordinates.
The training function may be performed by a separate
training organization, but the responsibility for quality and
effectiveness rests with line management.
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Training Program Descriptions
Overview of Training
Program
Radiological Assessor Training may be provided to
individuals (auditors and assessors) responsible for
developing and implementing measures necessary for
ensuring compliance with 10 CFR 835 at a DOE site or
facility. The terminal objective is that, upon completion of
this training, individuals with appropriate education and
experience may conduct audits, assessments, appraisals
and surveillances of occupational radiation protection
programs at a DOE site or facility in accordance with 10
CFR 835.103 and in meeting other quality assurance
requirements.
Prerequisites
The material is targeted for individuals with a baseline
knowledge of radiological protection concepts and
provides material on how to conduct a radiological
assessment. DOE has developed training materials for
radiation protection concepts as part of the Department’s
Technical Qualification Program. Students participating in
the Radiological Assessors Training should be able to
demonstrate competence of radiation protection concepts
equivalent to the DOE Technical Qualification Program
Topic Area Radiation Protection. The student Manual for
the Radiation Protection Topic Area provides a good
review of the competency topical expectations.
DOE has also provided guidance on qualifications of
radiological assessors in DOE STD-1107-97 Knowledge,
Skills, and Abilities for Key Radiation Protection Positions
Section 4
at DOE Facilities. Students should be capable of meeting
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Proficiency
Requirements
this standard prior to conducting independent technical
evaluations/assessments of radiation protection programs
(i.e. evaluations beyond simple surveillances of radiation
protection program implementation).
In accordance with 10 CFR 835-Subpart B, each
individual shall have appropriate education, training and
skills to discharge their responsibilities for ensuring
compliance with 10 CFR 835. Refer to DOE Order
5480.20A, Personnel Selection, Qualification, and
Training Requirements for DOE Nuclear Facilities, for
qualification requirements for technical staff (this category
frequently includes radiological assessors).
An examination or performance demonstration is
recommended.
Retraining Sites are encouraged to develop periodic training and
retraining for radiological assessors and auditors.
Retraining should focus on lessons learned and site
specific events as necessary.
Materials developed in support of training should be
documented in accordance with 10 CFR 835.704,
Administrative Records.
Instructor Training and
Qualifications
All classroom instruction should be provided by instructors
qualified in accordance with the contractor’s site instructor
qualification program. Training staff (contractor and
subcontractor, if used) should possess both technical
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knowledge and experience, and the developmental and
instructional skills required to fulfill their assigned duties.
1.Training staff responsible for program management,
supervision, and development should have and maintain
the education, experience, and technical qualifications
required for their jobs.
2.Instructors should have the technical qualifications,
including adequate theory, practical knowledge, and
experience, for the subject matter that they are assigned
to teach.
3.Methods should be in place at each contractor site to
ensure that individual instructors meet and maintain
position qualification requirements.
4.Subject matter experts without instructor qualification
may provide training in their area of expertise. However, if
these subject matter experts are to be permanent
instructors, they should be trained as instructors in the
next practical training cycle.
DOE Order 5480.20A, Personnel Selection, Qualification,
and Training Requirements for DOE Nuclear Facilities,
discusses qualification requirements for instructors.
DOE has also provided guidance on qualifications of
radiological instructors in DOE STD-1107-97 Knowledge,
Skills, and Abilities for Key Radiation Protection Positions
at DOE Facilities.
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Training Program Material Development
Training Material
Presentation
Training materials consist of lesson plans, overheads,
student guides, and handouts. To ensure appropriate
training, facility-specific materials must be added to the
materials when necessary to adequately train individuals
for facility-specific radiological hazards.
For example, facility-specific modules may be added to
cover such topical areas as: reactors, breeder reactors,
spent fuel storage, radwaste burial, radwaste storage,
high level waste storage, tank farms, reprocessing plants,
and vitrification plants.
Section 5
Conversely, modules with no applicability to a facility or
site may be omitted (e.g., a tritium facility may want to
omit modules on uranium and plutonium).
It is estimated that this material could be presented in 44
hours. The Table of Contents in the Instructor's Guide
provides a recommended breakdown of time per module.
Training Certificates A training certificate that identifies the individual’s
current training status may be provided to qualified
personnel. Each facility is responsible for determining
the training status of employees. Facilities have the
option of utilizing a certificate as proof of training.
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Training Aids,
References
Facility-specific training aids should be developed at the
facility to suit individual training styles. Each facility may
add information, activities, and/or view graphs to
enhance the program.
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Training Program Standards and Policies
Lectures, Seminars,
Training Exercises, etc.
Delinquent
Training/Failure
Radiological assessor training is designed to be delivered
in a classroom setting. An alternate delivery method may
be implemented with computer-based training (CBT)
equipment or web-based training (WBT) equipment. The
presentation of training should include DOE developed
materials and facility-specific information.
Employees who are delinquent on initial training or
retraining should lose their status of being qualified
assessors or auditors until successful completion of the
delinquent training requirement.
Exceptions and Waivers
Successful completion of the Radiological Assessor
Training at one DOE site may be recognized by other
DOE sites. However, the determination as to the
adequacy of training as required by 10 CFR 835-Subpart
B is the responsibility of the facility in which the individual
will be conducting assessments.
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Administration
Training Records Training records and course documentation shall meet
the requirements of 10 CFR 835.704 Administrative
Records.
Training Program
Development/Change
Requests
All requests for program changes and revisions that are
generic in nature may be submitted using DOE F 1300.3
Document Improvement Proposal. A copy of DOE F
1300.3 and instructions are included at the end of this
document.
Audits (internal and
external)
Internal verification of training effectiveness may be
accomplished through senior instructor or supervisor
observation of practical applications and discussions of
course material. Results should be documented and
maintained by the organization responsible for
Radiological Control Training.
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Evaluating Training
Program Effectiveness
Verification of the effectiveness of Radiological Assessor
Training should be accomplished by surveying a limited
subset of former students in the workplace. This
evaluation should include observation of practical
applications and discussion of the course material.
DOE/HSS has issued guidelines for evaluating the
effectiveness of radiological training through the DOE
Operations Offices and DOE Field Offices. These
guidelines are available from the DOE Radiation Safety
Training Home Page. (See the Foreword of this
Section 6
document.)
For additional guidance, refer to DOE STD 1070-94,
Guide for Evaluation of Nuclear Facility Training
Programs. The guidelines contained in these documents
are relevant for the establishment and implementation of
post-training evaluation programs.
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References and Supporting Documents
U.S. Department of Energy, DOE Order 5480.20 change 1, Personnel Selection,
Qualification, and Training Requirements for DOE Nuclear Facilities, July 2001.
U.S. Department of Energy, DOE STD-1098-99, Radiological Control, Reaffirmed
December 2004.
U.S. Department of Energy, DOE STD-1107-97, Knowledge, Skills, and Abilities for
Key Radiation Protection Positions at DOE Facilities, January 1997.
U.S. Department of Energy, 10 CFR 835, Occupational Radiation Protection, June
2007.
Part 2 of 5
Radiological Assessor Training
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Instructor's Guide
Office of Health, Safety and Security
U.S. Department of Energy
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Instructor's Guide
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Table of Contents
Regulatory Documents * (2).............................................................................Module1-1
10 CFR Part 835, Background and Focus (3)..................................................Module 2-1
Overview of the DOE Radiological Control Manual (3) ....................................Module 3-1
Elements of a Radiological Control Program (2) ..............................................Module 4-1
Technical Safety Requirements (2)..................................................................Module 5-1
Radiological Aspects of Uranium (2)................................................................Module 6-1
Radiological Aspects of Tritium (2) ..................................................................Module 7-1
Radiological Aspects of Plutonium (2) .............................................................Module 8-1
Radiological Work Permits (2)..........................................................................Module 9-1
Contamination Containment and Temporary Control Measures (1)...............Module 10-1
Radiological Work Site Mockup Demonstration (2)........................................Module 11-1
Radiation-Generating Devices (2)..................................................................Module 12-1
Radiological Aspects of Accelerators (2) .......................................................Module 13-1
Assessment Techniques (3) ..........................................................................Module 14-1
Planning and Conducting Assessments (3) ...................................................Module 15-1
Case Studies (2) ............................................................................................Module 16-1
Review and Critique of Findings and Improved Writing of Findings (2)..........Module 17-1
Compliance-Based Versus Performance-Based Evaluations (1)...................Module 18-1
Field Exercise Guidelines (4) .........................................................................Module 19-1
Course Summary (2 - with exam) ..................................................................Module 20-1
* (#) - Estimated time in hours
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Section 7
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Module 1 - 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Regulatory Documents
Objectives:
Upon completion of this training, the participant will be able to:
1. Identify the hierarchy of regulatory documents.
2. Define the purpose of 10 CFR Part 835.
3. Define the purpose of the DOE Radiological Control Standard.
4. Define the terms “shall” and “should” as used in the above documents.
5. Describe the role of the Defense Nuclear Facilities Safety Board (DNFSB) at
DOE sites and facilities.
Training Aids:
Overhead Transparencies (OTs): OT 1.1 – OT 1.17 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, 10 CFR Part 820, Procedural Rules for DOE Nuclear
Activities, 2007.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
2007.
U.S. Department of Energy, Radiological Control, DOE STD-1098-99,
Reaffirmed December 2004.
U.S. Department of Energy, Department of Energy Radiological Health and Safety
Policy, DOE P 441.1, April 1996.
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Module 1 - 2
I. Introduction
II. DOE radiological health and safety
A. Policy (some key points in summary)
• Establish and maintain a system of
regulatory policy and guidance.
• Ensure appropriate training is developed and
delivered and the technical competence of
the DOE workforce.
• Establish and maintain, from the lowest to
the highest levels, line management
involvement and accountability for
Departmental radiological performance.
• Ensure radiological measurements,
analyses, worker monitoring results, and
estimates of public exposures are accurate
and appropriately made.
• Conduct radiological operations in a manner
that controls the spread of radioactive
materials and reduces exposure to the work
force and the general public and utilizes a
process that seeks exposure level as low as
reasonably achievable (ALARA).
• Incorporate dose reduction, contamination
reduction, and waste minimization features
into the design of new facilities and
significant modifications to existing facilities
in the earliest planning stages.
• Conduct oversight to ensure Departmental
requirements are being complied with and
appropriate radiological work practices are
being implemented.
Show OT 1.1 and OT 1.2.
State objectives.
Discuss that this is from DOE P
441.1
Show OT 1.3.
Show OT 1.4.
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B. History
DOE has provided numerous written standards
for on-site radiological protection, the most
recent regulation being 10 CFR Part 835,
Occupational Radiation Protection, Amended
June 2007. This regulation was preceded by:
• DOE Notice 5480.6 of June 17, 1992,
Radiological Control, which specified that the
DOE Radiological Control Manual (DOE/EH-
0256T) would supersede DOE Order
5480.11.
• DOE Order 5480.11, Radiation Protection for
Occupational Workers. The purpose was to
establish radiation protection standards and
program requirements for DOE and DOE
contractors for the protection of workers from
ionizing radiation.
The establishment of DOE radiological
Section 8
protection standards did not start with these
documents. A chronology of dose limits of DOE
and its predecessor agencies, the Atomic
Energy Commission (1946-1975) and the
Energy Research and Development
Administration (1975-1977), demonstrate a
lowering of whole body dose limits over the last
50 years.
In the establishment of these dose limits, DOE
has followed recommendations of national and
international radiological protection groups,
notably the International Commission on
Radiological Protection (ICRP) and the National
Council on Radiation Protection and
Measurements (NCRP).
Show OT 1.5.
Discuss that there are different
limit which will be discussed later
(e.g., whole body, lens of the eye,
and skin).
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Module 1 - 4
C. Hierarchy of requirements
Currently within DOE there are two parallel
hierarchies of requirements:
• Rules and/or regulations (these terms are
used interchangeably in this training)
• DOE Orders
III. Rules and regulations
In response to the enforcement authority in the
Price-Anderson Amendments Act (PAAA) of 1988,
DOE is converting its contractual requirement in
orders to enforceable rules to enhance contractor
accountability for safety.
A. DOE enforcement of rules under PAAA
10 CFR Part 820 (effective on September 16,
1993) sets forth the procedures to implement the
provisions of the PAAA. Part 820 requires
contractors to comply with DOE Nuclear Safety
Requirements.
PAAA demands a “large stick” to enhance
contractor accountability for safety. Rules
provide authority for the assessment of civil and
criminal penalties and thus provide the large
stick.
Show OT 1.6.
Obj. 1
Identify the hierarchy of regulatory
documents.
Show OT 1.7.
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Module 1 - 5
B. Penalties under Part 820
1. Civil penalties
DOE may assess civil penalties against any
person subject to Part 820, for violations of:
• Codified rules in the CFR
• Compliance orders
• Any program or plan required by a rule or
compliance order
Note: Certain nonprofit educational
institutions and other listed institutions are
exempt from assessment of civil penalties.
2. Criminal penalties
If a person subject to the Atomic Energy Act
of 1954, as amended, or Nuclear Safety
Requirements, has by action or omission
knowingly and willfully violated, caused to be
violated, attempted to violate, or conspired to
violate any section of the Atomic Energy Act
of 1954, as amended, or applicable DOE
Nuclear Safety Requirements, the person
shall be subject to criminal sanctions.
3. The “carrot and stick” approach
DOE may provide monetary incentives in its
management and operating (M&O) contracts
for actions consistent with or exceeding
requirements, and to penalize actions and
activities that were not in compliance with
requirements.
Noncompliance with the Radiation Protection
Program can subject a contractor to PAAA
enforcement. There are provisions to
mitigate penalties for self-identifying and
reporting violations.
Discuss site-specific monetary
incentives.
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Module 1 - 6
C. DOE Nuclear Safety Requirements
DOE Nuclear Safety Requirements are the set of
enforceable rules, regulations, or orders relating
to nuclear safety that have been adopted by
DOE (or by another agency if DOE specifically
identifies it).
Section 9
Compliance orders are issued by the Secretary.
They identify a situation that violates, potentially
violates, or otherwise is inconsistent with the:
• Atomic Energy Act of 1954, as amended
• Nuclear statutes
• Nuclear Safety Requirements
Compliance orders:
• Mandate a remedy or other action
• States the reason for the remedy or other
action
D. 10 CFR Part 835
On December 14, 1993, DOE published a final
rule in the Federal Register (58 FR 65458) Title
10 Code of Federal Regulations Part 835,
Occupational Radiation Protection (10 CFR
835). On November 4, 1998 an amendment to
10 CFR 835 was published in the Federal
Register (63 FR 59663). On June 8, 2007 an
amendment to 10 CFR 835 was published in the
Federal Register (72 FR 31904).
The purpose of 10 CFR 835 is the codification of
radiological protection requirements. It contains
“shall” statements, which are legally binding. It
also contains:
• Prescriptive language
Show OT 1.8.
Obj. 2
Define the purpose of
10 CFR Part 835.
Define prescriptive language.
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Module 1 - 7
• Added emphasis on ALARA
• Requirements for a Radiation Protection
Program (RPP)
• Federal law
• Criminal and civil penalties for violations
E. Radiation Protection Program (10 CFR Part 835)
Each site, under Part 835, must submit a written
Radiation Protection Program (RPP).
The RPP requires careful consideration because
noncompliance may subject a contractor to
PAAA enforcement
F. Guidance documents for 10 CFR Part 835
Two types of regulatory guidance documents
have been developed:
• Guidance for implementing the provisions of
10 CFR Part 835.
• Guidance providing technical positions.
The above are available through the DOE HS-11
website at:
http://www.hss.energy.gov/healthsafety/wshp/radiation/
Unlike the requirements specifically set forth in
10 CFR Part 835, the provisions in guidance
documents are not mandatory. They are
intended solely to describe the rationale for, and
the objectives of, regulatory requirements and/or
to identify acceptable methods for implementing
regulatory requirements.
Show OT 1.9.
Show OT 1.10.
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Instructor's Guide
Module 1 - 8
Failure to follow a guidance document does not
in itself indicate noncompliance with a specific
requirement of the rule. A finding of
noncompliance is found for a failure to satisfy
the regulatory requirement.
Following a guidance document in the
prescribed manner will ordinarily create a
presumption of compliance with a related
regulatory requirement.
1. Technical guidance
Technical guidance describes and
disseminates technical methods and
techniques for fulfilling implementation and,
in turn, the requirements in 10 CFR Part 835.
Examples of this guidance are DOE
Technical Standards and DOE Radiological
Control Technical Positions (RCTPs).
2. Implementation guides (IGs)
Implementation guidance is intended to
identify and make available to DOE
contractors basic program elements and
acceptable methods for implementing
specific provisions of the final rule. Thirteen
implementation guides have been condensed
into one G441.1-1B, March 7, 2007.
G. Relationship between 10 CFR Part 835 and
10 CFR Part 20
10 CFR Part 20 is the occupational radiological
regulation issued by the Nuclear Regulatory
Commission (NRC).
The question of consistency among federal
Section 10
agencies in their occupational radiological
protection regulations became a major point of
discussion during the rule making process.
Refer students to website for
RCTPs:
Insert appropriate URL
Review RCTPs and discuss as
applicable to the site.
Refer students to website for IGs:
Insert appropriate URL
Show OT 1.11.
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Module 1 - 9
While agreeing with the goal of consistency,
DOE believes that it must promulgate its own
regulations because of the unique nature and
diversity of radiological activities within the DOE
complex. The final rule allows DOE to establish
more rigorous requirements in areas of particular
concern. Overall 10 CFR Part 835 has many
similarities as 10 CFR Part 20.
IV. DOE STD Radiological Control and Orders
A. Radiological Control
In January 1992, a memorandum was sent to the
heads of DOE elements involved in managing
radiological programs. In the memorandum, the
Secretary directed a series of initiatives to
enhance the conduct of radiological operations
within the Department of Energy. Also in this
memo, the Assistant Secretary of Environment,
Safety and Health was directed to develop a
comprehensive and definitive radiological control
manual. The DOE Radiological Control Manual
was developed to meet that directive and was
approved by the Secretary and promulgated with
DOE Notice 5480.6, Radiological Control, in July
1992.
After the issuance of 10 CFR 835 as a final rule
in December 1993, DOE Notice N441.1,
Radiological Protection for DOE Activities, was
issued on 9-30-95. This cancelled the notice
which made the Radiological Control Manual a
requirements document. However, the notice
stated that "cancelled orders that are
incorporated by reference in a contract shall
remain in effect until the contract is modified to
delete the reference.
N441.1 also retained some of the radiation
protection requirements from the Radiological
Control Manual that were not included in 10 CFR
835.
Show OT 1.12.
Obj. 3
Define the purpose of the DOE
Radiological Control Standard.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor's Guide
Module 1 - 10
In July, 1999, the Radiological Control Manual
was replaced by the standard, DOE-STD-1098-
99, Radiological Control. Many DOE sites
contractually must still adhere to the provisions
of either the Radiological Control Manual or the
Radiological Control Standard. Subsequent to
the 1998 amendment to 10 CFR 835, the
effective date of N441.1 has passed.
The DOE Radiological Control Standard is not
regulatory in nature. It is a guidance document
that describes DOE’s policy and expectations for
an excellent radiological control program.
1. Implementation
If a site fully implements a provision of the
DOE Radiological Control Standard, the user
will have most likely complied with any
related statutory, regulatory, or contractual
requirements. Users are cautioned that they
must review the source document (10 CFR
835) to ensure compliance.
2. Enforceability
When incorporated into contracts, the
provisions of the DOE Radiological Control
Standard or Manual are binding
requirements.
If portions of the Site-Specific Radiological
Control Manual are incorporated in the RPP
under Part 835 and approved by DOE, they
are also binding.
B. The Site-Specific Radiological Control Manual
• The DOE Radiological Control Standard
states that a Site-Specific Radiological
Control Manual should be written and
followed.
Section 11
.
Radiological Assessor Training
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C. Relationship between 10 CFR Part 835 and the
DOE Radiological Control Standard
1. Compliance
• The Office of Enforcement and
Investigation (HS-40) will enforce 10 CFR
Part 835. It can assess fines and
penalties.
• The Program Offices will audit for both
compliance with 10 CFR 835 and
contractual agreements including the DOE
Radiological Control Standard or Manual,
Orders, etc. Results of these audits can
affect the contractor’s award fee.
2. What if there are conflicts?
10 CFR Part 835 takes precedence over
requirements of the DOE Radiological
Control Standard and orders. It is unlikely
that there will be a conflicting requirement
between the two documents, although one
document may have a requirement that is not
addressed in the other.
Show OT 1.13.
What is the relationship between
Part 835 and the DOE
Radiological Control Standard
regarding compliance issues?
Show OT 1.14.
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Instructor's Guide
Module 1 - 12
It is planned that all requirements for nuclear
safety will be incorporated into rules.
3. “Shall” and “should” statements
• 10 CFR Part 835 contains “shall”
statements. “Shall” statements in Part
835 are legally binding.
Processes for exemption relief from Part
835 are set forth in Subpart E to Part 820.
If relief is requested from provisions of
Part 835, the exemption must be
considered and granted, if appropriate, by
the Chief Health, Safety and Security
Officer (HS-1).
• The use of “should” in the DOE
Radiological Control Standard recognizes
that there may be site- or facility-specific
attributes that warrant special treatment.
It also recognizes that literal compliance
with the elements and requirements of the
provision may not achieve the desired
level of radiological control performance.
Obj. 4
Define the terms “shall” and
“should” as used in the above
documents.
Refer students to website for
exemption decisions:
http://tis.eh.doe.gov/whs/rhmwp/e
xemption.html
Review exemption decisions and
discuss as applicable to the site.
Radiological Assessor Training
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Module 1 - 13
D. DOE Standards
DOE has developed several technical standards
for occupational radiation protection. Depending
on the site-specific application, some standards
are required to be followed. For example, sites
which need to monitor individual external
exposures to ionizing radiation need to follow the
DOE Laboratory Accreditation Program
(DOELAP) standards. Other standards may be
incorporated by reference in the site RPP.
Other standards provide technical guidance on
specific applications, but adherence to the
standard may not be required.
Prior to conducting an assessment, the site
requirements documents must be reviewed to
determine applicable requirements.
Show OT 1.15.
Refer students to website for
technical standards:
Insert appropriate URL
Radiation protection standards are
also on:
Insert appropriate URL
Review standards and discuss as
applicable to the site.
Radiological Assessor Training
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Instructor's Guide
Module 1 - 14
V. Defense Nuclear Facilities Safety Board
A. Establishment
The Atomic Energy Act of 1954 was amended by
adding Chapter 21, Defense Nuclear Facilities
Safety Board (DNFSB). This amendment
established an independent board in the
executive branch to provide oversight of some
DOE operations at DOE facilities and sites.
Section 12
B. Members
The DNFSB consists of five members appointed
by the President with consent of the Senate.
The Board shall:
• Review and evaluate standards
• Investigate any event or practice at a DOE
defense nuclear facility that the Board
determines has adversely affected or may
adversely affect public health and safety.
The Board may:
• Establish reporting requirements for the
Secretary of Energy
By evaluating how well DOE meets its
objectives, the DNFSB helps DOE achieve and
maintain excellence in radiological protection.
C. Secretary of Energy
The Secretary of Energy shall fully cooperate
with the Board.
Obj. 7
Describe the role of the Defense
Nuclear Facilities Safety Board
(DNFSB) at DOE sites and
facilities.
Show OT 1.16.
Radiological Assessor Training
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Instructor's Guide
Module 1 - 15
D. DNFSB Recommendations
DNFSB provides DOE with recommendations for
improving safety at DOE defense nuclear
facilities. Examples include:
DNFSB Recommendation 91-6 dealt with
radiological protection concerns throughout
the DOE defense nuclear facilities complex,
and identified several actions to be taken by
the Department to improve radiological
protection performance.
DNFSB Recommendation 92-7 dealt with
training and qualification at DOE sites and
facilities.
DNFSB Recommendation 98-1 dealt with
resolution of internal audit findings.
DNFSB Recommendation 99-1 dealt with
safe storage of fissionable materials.
Implementation of DOE and site commitments
made in response to DNFSB recommendations
are areas to review during an assessment.
Show OT 1.17.
Summarize lesson.
Review objectives.
Ask for questions.
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Radiological Assessor Training
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Instructor’s Guide
Module 2 - 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: 10 CFR Part 835, Background
and Focus
Objectives:
Upon completion of this training, the participant will be able to:
1. Describe the contents of 10 CFR Part 835.
2. Identify the site requirements of 10 CFR Part 835.
Training Aids:
Overhead Transparencies (OTs): OT 2.1 – OT 2.32 (may be supplemented or
substituted with updated or
site-specific information)
Handout - “Dosimetric Quantities in 10 CFR Part 835”
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
Handout - “Dosimetric Quantities in 10 CFR Part 835”
10 CFR 835
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 2
References:
U.S. Department of Energy, 10 CFR Part 820, Procedural Rules for DOE Nuclear
Facilities, 2007.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
2007.
U.S. Department of Energy, Order 5400.5, Radiation Protection of the Public and
the Environment, 1990.
U.S. Department of Energy, DOE STD-1107-97 Knowledge, Skills, and Abilities for
Key Radiation Protection Positions at DOE Facilities, Reaffirmed June 2005.
U.S. Department of Energy, DOE G 441.1-1B, Radiation Protection Programs
Guide, March 2007.
U.S. Department of Energy, DOE O 231.1-1A, Change 2, Environment, Safety
and Health Reporting, 2004.
U.S. Department of Energy, DOE M 231.1-1A, Change 2, Environment, Safety and
Health Reporting Manual, 2004.
Radiological Assessor Training
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Instructor’s Guide
Section 13
Module 2 - 1
I. Introduction
This module provides an overview of many of the
provisions of 10 CFR 835. For completeness,
individuals should always reference back to 10 CFR
835 for the complete text.
II. Outline of 10 CFR Part 835
Part 835 is the codification of radiological protection
requirements. Part 835 contains 14 subparts and
five appendices. The outline consists of the
following subparts:
A — General Provisions
B — Management and Administrative
Requirements
C — Standards for Internal and External Exposure
D — Reserved
E — Monitoring of Individuals and Areas
F — Entry Control Program
G — Posting and Labeling
H — Records
I — Reports to Individuals
J — Radiation Safety Training
K — Design and Control
L — Radioactive Contamination Control
M — Sealed Radioactive Source Control
N — Emergency Exposure Situations
Under 10 CFR Part 835, each site must submit a
Radiation Protection Program (RPP).
Part 835 helps to ensure that DOE facilities are
operated in a manner such that occupational
radiological exposure to workers is maintained
within acceptable limits and as low as is reasonably
achievable (ALARA).
Show OT 2.1.
Emphasize that this lesson is an
overview of major areas of
10 CFR Part 835. Not every provision is
addressed in this module 10 CFR 835
should be reviewed in its entirety to
ensure compliance.
Provide copies of 10 CFR 835 for
reference.
State objectives.
Show OT 2.2.
Obj. 1
Describe the contents of
10 CFR Part 835.
Show OT 2.3.
Obj. 2
Identify the site requirements of 10
CFR Part 835.
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Instructor’s Guide
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A. Subpart A - General Provisions
Subpart A contains the scope of the rule. The
rule in this part establishes radiological
protection standards, limits, and program
requirements for protecting individuals from
ionizing radiation resulting from the conduct of
DOE activities.
It also includes activities excluded from the
provisions of the rule. Activities that are
excluded include the following (summarized):
• Activities regulated through a license by the
Nuclear Regulatory Commission (NRC) or a
state under an agreement with the NRC.
• Activities conducted under the authority of the
Director, Naval Nuclear Propulsion Program.
• Specified activities conducted under the
Nuclear Explosives and Weapons Surety
Program.
• Radioactive material transportation.
• DOE activities in other countries with
acceptable radiation protection program.
• Background radiation.
Occupational doses received as a result of
excluded activities and radioactive material
transportation, as listed above, shall be
considered when determining compliance with
the occupational dose limits (835.202 and
835.207), and with the limits for the embryo/fetus
(835.206).
Subpart A also addresses:
• Definitions
• Radiological units (Curie, rad, roentgen, rem,
and multiples)
Show OT 2.4.
Discuss radioactive material
transportation definition.
Show OT 2.5.
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B. Subpart B - Management and Administrative
Requirements
The RPP shall:
• Include formal plans and measures for
applying the ALARA process to occupational
exposures.
• Specify the existing and/or anticipated
operational task.
• Address, but not be limited to, each
requirement in Part 835.
• Include plans, schedules, and other
measures for achieving compliance.
DOE may direct or make modifications to an
Section 14
RPP. An initial RPP or update shall be
considered approved 180 days after its
submission unless rejected by DOE at an earlier
date.
Internal Audits (10 CFR 835.102)
Internal audits of the radiation protection
program, including examination of program
content and implementation, shall be conducted
through a process that ensures that all functional
elements are reviewed no less frequently than
every 36 months. This training material and
DOE G 441.1-1B, Radiation Protection Programs
Guide, provide guidance on DOE's expectations.
Show OT 2.6.
Discuss again DOE's series of
Implementation Guides and their
purpose.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 4
Education, Training and Skills (10 CFR 835.103)
Individuals responsible for developing and
implementing measures necessary for ensuring
compliance with the requirements of this part
shall have the appropriate education, training,
and skills to discharge these responsibilities.
DOE STD-1107-97, Reaffirmed June 2005,
Knowledge, Skills, and Abilities for Key Radiation
Protection Positions at DOE Facilities, provides
guidance on DOE's expectations.
Written Procedures (10 CFR 835.104)
Written procedures are required, as necessary,
to ensure compliance with 835, commensurate
with radiological hazards and education, training
and skills of exposed individuals.
C. Subpart C - Standards for Internal and External
Exposure
This subpart addresses limits for:
• General employees (occupational)
• Embryos/fetus of declared pregnant worker
(i.e., A woman who has voluntarily declared
to her employer, in writing, her pregnancy for
the purpose of being subject to the
occupational dose limits to the embryo/fetus.
This declaration may be revoked, in writing,
at any time by the declared pregnant worker.)
• Occupationally exposed minors
• General public in a controlled area
It also addresses:
• Planned special exposures
• Nonuniform exposures of the skin
• Concentrations of radioactive material in air
Show OT 2.7.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 5
1. Summary of dose limits
10 CFR Part 835 employs the rem unit for
several different physical quantities. For
information about these quantities refer
participants to page 1 of handouts, “Dosimetric
Quantities in 10 CFR Part 835.”
Show OT 2.8 and OT 2.9.
Exposed Individual Annual Limit
General Employee: Whole Body (internal and external) (TED) 5.0 rem
General Employee: Lens of Eye (ED) 15.0 rem
General Employee: Extremity (below elbow and knees) and skin (SED) 50.0 rem
General Employee: Any Organ or Tissue (other than lens of eye) (DED + CED) 50.0 rem
Declared Pregnant Worker: Embryo/Fetus (gestation period) (ED) 0.5 rem
Occupationally Exposed Minors (under age 18): (TED) 0.1 rem *
Members of the Public in Controlled Areas: (TED) 0.1 rem
• And 10% of other general employee limits.
2. Planned special exposures (PSEs)
It is acknowledged that unusual conditions
can arise in which higher-than-normal doses
can be justified. In these well-planned, well-
controlled, and highly infrequent and unusual
conditions operating management would be
permitted to allow specified individual doses
exceeding the occupational limit, such as 5
rem per year.
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Instructor’s Guide
Module 2 - 6
The term "unusual conditions" is made clear
by specifying that alternatives which would
preclude exposures higher than the
prescribed dose limits must be either
unavailable or impractical.
Section 15
10 CFR 835.204 specifies requirements for
annual and lifetime dose from PSEs. It also
specifies requirements for determining
previous individual exposures prior to
allowing a PSE.
Every PSE must be approved in advance by
DOE and requires the informed consent of
the employee involved.
3. Concentration of radioactive material in air
Appendices A and C contain the derived air
concentration (DAC) values used in the
control of occupational exposure to airborne
radioactive material.
DACs are listed in appendices A and C of 10
CFR 835. For intakes (appendix A), they are
the airborne concentration that equals the
annual limit on intake (ALI) divided by the
volume of air breathed by an average worker
for a working year of 2000 hours (assuming a
breathing volume of 2400 m3).
The ALI is the smaller value of intake of a
given radionuclide in a year by a
standardized man that would result in a CED
of 5 rems or a HT,50 of 50 rems to any
individual organ or tissue.
Show OT 2.10.
Show OT 2.11.
Define DAC in terms of dose
equivalent.
Radiological Assessor Training
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Instructor’s Guide
Module 2 - 7
Appendix C contains DACs for controlling
external dose from being immersed in a cloud
of airborne radioactive material.
Estimation of internal dose shall be based on
bioassay data rather than air concentration
values unless bioassay data are:
• Unavailable (e.g., radon or very short lived
radioisotopes)
• Less accurate than internal dose
estimates based on representative air
concentration values
• Inadequate
E. Subpart D - Reserved
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E. Subpart E - Monitoring of Individuals and Areas
This subpart addresses:
• General requirements
• Instrumentation
• Individual monitoring - external
• Individual monitoring - internal
• Air monitoring
• Receipt of packages containing radioactive
material
1. General requirements (10 CFR 835.401)
Monitoring of individuals and areas shall
be performed to:
• Demonstrate compliance with Part
835.
• Document radiological conditions.
• Detect changes in the radiological
conditions.
• Detect the gradual buildup of
radioactive material.
• Verify the effectiveness of engineering
and process controls in containing
radioactive material and reducing
radiation exposure.
• Identify and control potential sources
of individual exposure to radiation
and/or radioactive material.
Show OT 2.12.
Radiological Assessor Training
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Instructor’s Guide
Module 2 - 9
2. Instrumentation
Instruments and equipment used for
monitoring and contamination control shall
be:
• Periodically maintained and calibrated
on an established frequency.
• Appropriate for the type(s), levels, and
energies of the radiation(s)
encountered.
• Appropriate for existing environmental
conditions.
• Routinely tested for operability.
3. Individual monitoring - external (10 CFR
835.402)
For the purpose of monitoring individual
exposure to external radiation, personnel
dosimetry shall be provided to and used
by:
• Radiological Workers likely to receive:
– An effective dose to the whole body
of 0.1 rem (100 mrem) or more in a
year
– A shallow equivalent dose to the
skin or to any extremity of 5 rem or
more in a year
– A lens of the eye equivalent dose
of 1.5 rem or more in a year
• Declared Pregnant Workers who are
likely to receive from external sources
an equivalent dose to the embryo/fetus
in excess of 10 percent of the
applicable limit.
Section 16
Show OT 2.13.
Show OT 2.14.
Radiological Assessor Training
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Instructor’s Guide
Module 2 - 10
• Members of the public in a controlled
area and occupationally exposed
minors likely to receive, in one year,
from external sources, a dose in
excess of 50 percent of the applicable
limits.
• Individuals entering a High or Very
High Radiation Area.
DOE Laboratory Accreditation for
Personnel Dosimetry is required for
external dose monitoring programs
implemented to demonstrate compliance
with 10 CFR 835.
4. Individual monitoring - internal (10 CFR
835.402)
Internal dose evaluation programs
(including routine bioassay programs)
shall be conducted for:
• Radiological Workers who, under
typical conditions, are likely to receive
0.1 rem or more committed effective
dose from all occupational radionuclide
intakes in a year.
• Declared Pregnant Workers likely to
receive an intake or intakes resulting in
an equivalent dose to the embryo/fetus
in excess of 10 percent of the limit.
• Members of the public in a controlled
area and occupationally exposed
minors who are likely to receive a
committed effective dose in excess of
50 percent of the limit from all intakes
in a year.
Show OT 2.15.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 11
DOE Laboratory Accreditation for
Radiobioassay is required for internal dose
monitoring programs implemented to
demonstrate compliance with 10 CFR 835.
5. Air monitoring (10 CFR 835.403)
Measurements of radioactivity concentrations
in the ambient air of the workplace shall be
performed as follows:
• Air sampling shall be performed in
occupied areas where an individual is
likely to receive an exposure of 40 DAC-
hrs or more in a year (i.e. an annual
intake of 2 percent or more of the specific
ALI value) for the mixture of isotopes.
• Samples shall be taken as necessary to
characterize the levels or concentration of
airborne radioactive material when
respirators are worn for radiation
protection purposes.
• Real-time air monitoring shall be
performed when there is a need to alert
potentially exposed individuals to
unexpected increases in airborne
radioactivity levels such that immediate
action is necessary in order to minimize or
stop inhalation exposures.
Compliance due date 1-1-02.
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Instructor’s Guide
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6. Receipt of Packages Containing Radioactive
Material (10 CFR 835.405)
Establishes requirements to monitor certain
types of packages and sets a time limit of not
later than 8 hours after the beginning of the
working day following receipt of the package.
F. Subpart F - Entry Control Program (10 CFR
835.501)
Subpart F addresses entry into:
• Radiological Areas
• High Radiation Areas
• Very High Radiation Areas
1. Radiological Areas
The degree of control shall be commensurate
with existing and potential radiological
hazards within the area.
Show OT 2.16.
Show OT 2.17.
Discuss different types of
radiological areas.
Radiological Assessor Training
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Instructor’s Guide
Module 2 - 13
One or more of the following methods
shall be used to ensure control:
• Signs and barricades
• Control devices on entrances
• Conspicuous visual and/or audible
alarms
• Locked entrance ways
• Administrative controls
“No control(s) shall be installed at any
radiological area exit that would prevent
rapid evacuation of personnel under
emergency conditions.”
Section 17
2. High Radiation Areas
A High Radiation Area is an area where
radiation levels exist such that an
individual could exceed a deep equivalent
dose to the whole body of 0.1 rem in any
one hour at 30 centimeters from the
source or from any surface that the
radiation penetrates.
If an individual receives a deep equivalent
dose exceeding 1.0 rem in an hour (at 30
cm), a High Radiation Area shall have one
or more of the following:
• A control device that prevents entry to
the area when high radiation levels
exist or that, upon entry, causes the
radiation level to be reduced below
that level that defines a High Radiation
Area.
• A device that functions automatically to
prevent use or operation of the
radiation source or field while
individuals are in the area.
Show OT 2.18.
Show OT 2.19.
Show OT 2.20.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 14
• A control device that energizes a
conspicuous visible or audible alarm
signal so that the individual entering
the High Radiation Area and the
supervisor of the activity are made
aware of the entry.
• Entryways that are locked. During
periods when access to the area is
required, positive control over each
entry is maintained.
• Continuous direct or electronic
surveillance that is capable of
preventing unauthorized entry.
• A control device generating audible
and visual alarm signals to alert
personnel in the area before use or
operation of the radiation source and
in sufficient time to permit evacuation
of the area or activation of a secondary
control device that will prevent use or
operation of the source.
3. Very High Radiation Areas
A Very High Radiation Area is an area in
which an individual could receive a dose
in excess of 500 rad in one hour at 1
meter from the radiation source or from
any surface that the radiation penetrates.
In addition to the requirements for a High
Radiation Area, additional measures shall
be implemented to ensure individuals are
not able to gain unauthorized access to
Very High Radiation Areas.
“No control(s) shall be established in a
High or Very High Radiation Area that
would prevent rapid evacuation of
personnel.”
Show OT 2.21.
Show OT 2.22.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 15
G. Subpart G - Posting and Labeling
Subpart G addresses the general requirements
for signs:
• Yellow background
• Black or magenta radiation symbol
• Clear and conspicuous signs
In addition, Subpart G addresses specific posting
requirements for:
• Controlled Areas
• Radiation Areas
• High Radiation Areas
• Very High Radiation Areas
• Airborne Radioactivity Areas
• Contamination Areas
• High Contamination Areas
• Radioactive Material Areas
This subpart also addresses exceptions to
posting and labeling.
H. Subpart H - Records
Subpart H addresses requirements for records
documenting compliance with Part 835 and with
the Radiation Protection Program.
Records that are specifically required include
those necessary to demonstrate compliance with
the ALARA provisions of the rule.
Show OT 2.23.
Discuss posting and labeling
exceptions.
Show OT 2.24.
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10 CFR 835 also requires that certain records be
maintained, including records of:
• Individual monitoring
• Sealed source inventory and control
• Results of surveys for the release of material
and equipment
Section 18
• Results of specified monitoring for radiation
and radioactive material
• Maintenance and calibration of radiation
monitoring instruments
• Internal audits
Each individual’s training as a general employee
and as a Radiological Worker must be recorded.
Where appropriate, demonstration and
documentation of proficiency is required.
Refer to 10 CFR 835 Subpart H for a complete
listing of required records.
DOE M 231.1-2, Change 2, Environment, Safety
and Health Reporting Manual specifies radiation
protection reporting requirements that may be
applicable to the site or facility being assessed.
I. Subpart I - Reports to Individuals (10 CFR
835.801)
Subpart I addresses reports to individuals and
their accessibility to reports, including:
Discuss applicability of O 231.1 to
the site or facility.
Show OT 2.25.
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Instructor’s Guide
Module 2 - 17
On an annual basis, each DOE or DOE
contractor-operated site or facility must provide
each individual monitored for occupational
exposure a radiation dose report of his/her
occupational exposure at that site or facility.
Upon the request from an individual terminating
employment, records of exposure shall be
provided to that individual as soon as the data
are available, but not later than 90 days after
termination. A written estimate of the radiation
dose received by that employee based on
available information shall be provided at the
time of termination, if requested.
J. Subpart J - Radiation Safety Training
This subpart addresses radiation safety training.
The tailored approach to training requirements
are based on:
• Unescorted access to or receiving
occupational dose in controlled areas (e.g.,
General Employees)
• Unescorted access to radiological areas or
unescorted assignment as Radiological
Workers
Requirements of Part 835 include:
• Verification by examination for certain training
(e.g., Radiological Worker Training)
• Intervals of training not to exceed twenty four
months
• List of topics which must be included in
training
• Provisions for limited use of escorts in lieu of
training
Show OT 2.26.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 18
K. Subpart K - Design and Control
Subpart K addresses added emphasis on facility
and equipment design and administrative
controls to maintain radiological exposures
ALARA.
1. Facility design and modifications (10 CFR
835.1001)
During the design of new facilities or
modification of old facilities, the following
objectives shall be adopted:
• Optimal methods shall be used to assure
ALARA
• Maintain exposure levels below an
average of 0.5 mrem/hr
• Avoid release of radioactivity to the
workplace atmosphere
• The design or modification of a facility and
the selection of materials shall include
features that facilitate operations,
maintenance, decontamination, and
decommissioning
Show OT 2.27.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 19
2. Workplace controls (10 CFR 835.1003)
During routine operations, the combination of
physical design features and administrative
control shall provide that:
• The anticipated occupational dose to
general employees shall not exceed the
limits
• The ALARA process is utilized for
personnel exposures to ionizing radiation
L. Subpart L - Radioactive Contamination Control
1. Control of material and equipment
This section addresses the requirements for
Section 19
release of materials and equipment from
radiological areas to controlled areas.
Releases to uncontrolled areas are
addressed in DOE O 5400.5. Some of the
provisions:
• Specifies conditions for material and
equipment in contamination areas (CAs),
high contamination areas (HCAs), and
airborne radioactivity areas (ARAs) to be
released to a controlled area
• Addresses movement of material and
equipment with removable surface
contamination, on-site from one
radiological area for immediate placement
in another radiological area
• Specifies conditions for material and
equipment with fixed contamination to be
released for use in controlled areas
outside of radiological areas
Show OT 2.28.
Show OT 2.29.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 20
Control of Areas (10 CFR 835.1102) addresses
• Prevention of inadvertent transfer or
removal of contamination to locations
outside radiological areas under
normal conditions
• Where contamination levels exceed
values in Appendix D, the area is
controlled commensurate with hazards
• Areas with fixed contamination
exceeding radioactivity values may be
located outside radiological areas,
provided certain controls, conditions,
or provisions are met
• Personnel monitoring for
contamination upon exiting CAs,
HCAs, or ARAs
• Use of protective clothing in CAs and
HCAs
M. Subpart M - Sealed Radioactive Source Control
Sealed radioactive sources shall be used,
handled and stored in a manner commensurate
with the hazard.
Specifies values (Appendix E) for sources which
must be inventoried and leak tested at intervals
not to exceed six months.
N. Subpart N - Emergency Exposure Situations
This subpart addresses:
• Employees who have exceeded dose limits
as result of authorized emergency exposure
• Nuclear accident dosimetry
Show OT 2.30.
Show OT 2.31.
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 21
Individuals whose occupational
exposures have exceeded any limits as a
result of an authorized emergency
exposure may be permitted to return to
work provided that certain conditions are
met.
Nuclear accident dosimetry
Nuclear accident dosimetry involves
installations possessing sufficient
quantities of fissile material to constitute a
critical mass, and shall include;
• Method to conduct initial screening of
personnel involved
• Method and equipment for analysis of
biological materials
• A system of fixed nuclear accident
dosimeter units
• Personal nuclear accident dosimeters
Show OT 2.32.
Summarize lesson.
Review objectives.
Ask for questions.
T
T
Radiological Assessor Training
DOE-HDBK-1141- 2008
Instructor’s Guide
Module 2 - 22
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Radiological Assessor Training
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Instructor’s Guide
Module 3 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Overview of the DOE Radiological
Control Standard
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe the managerial responsibilities in the DOE Radiological Control
Standard.
2. Describe the contents of the DOE Radiological Control Standard.
Training Aids:
Overhead Transparencies (OTs): OT 3.1 – OT 3.12 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
Section 20
U.S. Department of Energy, O 440.1B, Worker Protection Program for DOE
(Including the National Nuclear Security Agency) Federal Employees, May 2007.
Module 2 Page 0
I. Introduction
II. DOE Radiological Control Standard
The DOE Radiological Control Standard is written
for line management. It is designed to assist line
managers in fulfilling their duties and responsibilities
for implementing an occupational radiation
protection program.
It is also designed to assist site/facility workers in
having the information they need to be responsible
for their own radiological exposures and to help
ensure that the controls are in place to eliminate
any releases, unplanned exposures or uptake, and
to apply ALARA principles. The emphasis is on
teamwork and support from line management.
The Radiological Control Standard may be
considered as an occupational radiation protection
good practices document. Individual sites may
have contractual commitments to implement
sections of the standard.
III. Chapter 1, Excellence in Radiological Control
This chapter defines the roles of DOE and the
contractors in achieving the goal of radiological
control excellence. It consists of the following five
sections:
• DOE Radiological Control Standard
• Leadership in Radiological Control
• Improving Radiological Control Performance
• Contractor Radiological Control Organization
• DOE Management
Show OT 3.1.
State objectives.
Obj. 1
Describe the managerial
responsibilities in the DOE
Radiological Control Standard.
Discuss site commitments to
follow the Radiological Control
Standard or Manual.
Emphasize the need to review
site requirements documents
prior to conducting an
assessment.
Show OT 3.2.
Obj. 2
Describe the contents of the
DOE Radiological Control
Standard.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 1
A. DOE Radiological Control Standard
The contractor is responsible for implementing
an occupational radiation protection program.
To assist this effort, they may develop a Site
Radiological Control Standard Implementation
Plan. The Site-Specific Radiological Control
Standard, which is developed from the
Implementation Plan, does not require DOE
approval.
B. Leadership in Radiological Control
Commitment of senior management to
radiological control is defined in this section of
the Standard.
The responsibilities and accountability of each
individual for ALARA and radiological excellence
is emphasized.
Worker responsibilities and the concepts of
conduct of radiological operations are clearly
defined.
C. Improving Radiological Control Performance
The use of critiques as a management tool,
rather than as a method to “fix blame” or “shoot
the messenger,” and the importance of real root
cause identification are emphasized. Over 20
radiological performance indicators are identified
that are tools designed to assist managers in
focusing their priorities and attention on
radiological control performance.
D. Contractor Radiological Control Organization
This section discusses the contractor’s
radiological control organization and the
qualifications of the Radiological Control
Manager.
Show OT 3.3.
Show OT 3.4.
Show OT 3.5.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 2
E. DOE Management
This section discusses the roles and
responsibilities of DOE management for
providing guidance and performance evaluation
of radiological control programs.
Section 21
IV. Chapter 2, Radiological Standards
This chapter deals with administrative control dose
limits, contamination control and control levels, and
posting.
A. Administrative Control Levels (ACLs) and Dose
Limits
Lifetime control levels and dose limits for
Radiological Workers, members of the public,
embryos/fetuses, and special control levels are
discussed in this section.
For most facilities an ACL of 500 millirem or less
will be challenging for Radiological Workers.
Individual occupational doses, in rem, should be
kept below the individual's age in years.
B. Contamination Control and Control Levels
In this section, personnel contamination control,
removable and fixed contamination control
levels, and airborne radioactivity control levels
are given.
C. Posting
Posting requirements are presented in this
section and include several non-regulatory areas
including: Radiological Buffer Areas,
Underground Radioactive Material Areas, and
Soil Contamination Areas.
Show OT 3.6.
Discuss site specific ACLs and
other limits.
Discuss non-regulatory posting
used at the site.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 3
V. Chapter 3, Conduct of Radiological Work
The planning of radiological work, work preparation
(e.g., Radiological Work Permits), and the
requirements for the entry to and exit from the
various types of controlled areas are contained in
this chapter. Also covered are: radiological work
performance, the aspects of radiological work in
different operations with radiation-generating
equipment, and construction and restoration
projects.
A. Planning Radiological Work
This section emphasizes that the conduct of
radiological work is a line responsibility. Worker
responsibility, along with systematic planning,
provides the necessary information for safe
radiological work. Of fundamental importance is
the requirement to plan work with an emphasis
on ALARA principles.
B. Work Preparation
In this section, the Radiological Work Permit
(RWP) is discussed. This chapter states that the
RWP is the key to any particular radiological
operation, and preplanning is essential.
C. Entry and Exit Requirements
The minimum requirements for entry into and
exit from defined radiological areas and other
non-regulatory areas are discussed in this
section.
Show OT 3.7.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 4
D. Radiological Work Controls
This section discusses radiological work as a
team effort involving the Radiological Workers,
their supervisors, and Radiological Control
personnel. The DOE Radiological Control
Standard discusses stop-radiological work
authority for Radiological Control Technicians
(RCTs), their supervisors, line supervision, and
workers through their supervisors because of:
• Inadequate radiological controls
• Radiological controls not being implemented
• A radiological control hold point not being
satisfied
DOE O 440.1B, May 2007, Worker Protection
Program for DOE (Including National Nuclear
Security Administration)Federal Employees
specifies that individuals have the authority to
stop work due to hazardous conditions.
This stop work authority is not limited to just
radiological hazards. Workers may "stop work
when they discover employee exposures to
imminent danger conditions or other serious
hazards." Contractors are required to have
procedures addressing stop work authority.
E. Evaluation of Performance
Section 22
Evaluation of performance, critiques, post job
reviews, and lessons learned are discussed in
this section.
Discuss that, per O 440.1A, stop
work authority is not limited to
radiological hazards.
Show OT 3.8.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 5
F. Special Applications
This section examines the special aspects for
the control of radiological work when working
with the following:
• Plutonium
• Uranium
• Tritium
• Accelerators
• Radiation Generating Devices
G. Radiological Design Criteria
This section addresses design objectives for
design of new facilities and modification of
existing facilities.
VI. Chapter 4, Radioactive Materials
The requirements for labeling, storage, control,
release, and transportation of radioactive materials,
and the control of radioactive sources, are
discussed in this chapter. This chapter also deals
with the management of solid and liquid radioactive
wastes, and airborne radioactivity. Support activities
such as personnel protective clothing and
equipment, laundry, decontamination and vacuum
cleaners, and portable air-handling equipment are
also discussed.
VII. Chapter 5, Radiological Health Support Operations
This chapter discusses the requirements for
external dosimetry, internal dosimetry, a respiratory
protection program, the handling of contaminated
personnel, radiological monitoring and surveys, and
instrumentation and calibration.
Show OT 3.9.
Show OT 3.10.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 6
VIII. Chapter 6, Training and Qualification
The requirements that ensure personnel have the
training and qualifications needed to safely work in
and around radiological areas and to maintain their
own doses and those of others (ALARA) are
discussed in this chapter.
A. General Radiological Training
Within these sections, training and qualification
standards are discussed for:
• General Employees
• Radiological Workers I and II
• Radiological Control Technicians and
Supervisors
B. Other Radiological Training
This section addresses training and qualification
for:
• Managers/supervisors
• ALARA training for:
– Engineers
– Schedulers
– Procedure writers
• Radiological control personnel
– Dosimetry technicians
– Instrument technicians
– Medical personnel
– Records clerk
– Whole body counter technicians
– Laboratory personnel
• Radiographers
• Radiation-generating device operators
• Emergency response personnel
Show OT 3.11.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 7
C. Training for Special Applications
This section addresses training for the following
facilities:
• Plutonium
• Uranium
• Tritium
• Accelerators
IV. Chapter 7, Radiological Records
The requirements for employee and visitor records,
radiological control procedures (policies,
procedures, Radiological Work Permits (RWPs),
ALARA, and quality assurance records), radiological
surveys, instrumentation and calibration records,
records management, and radiological reporting are
presented in this section.
Show OT 3.12.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 3 - 8
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Elements of a Radiological Control
Program
Section 23
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify factors that influence the scope and magnitude of a Radiological
Control Program at any nuclear facility.
2. Identify typical elements of a Radiological Control Program.
Training Aids:
Overhead Transparencies (OTs): OT 4.1 – OT 4.5 (may be supplemented or
substituted with updated or
site-specific information)
Handouts - “List of Radiological Control Program Elements”
“Elements of a Radiological Control Program”
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, 10 CFR Part 820, Procedural Rules for DOE Nuclear
Facilities, 2007.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
2007.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 2
I. Introduction
II. Radiological Control Program
A. Overall program
The Radiological Control Program consists of
the commitments, policies, and procedures that
are administered by a site or facility to meet the
EH Health and Safety Policy.
The Radiation Protection Program required by
10 CFR Part 835 is an element of the overall
Radiological Control Program.
The Radiological Control Program should
address the following:
• Requirements
• Responsibilities
• Programs/procedures
• Assessments
B. Size of the program
Radiological Control Programs vary in size.
There are several factors that may affect the
magnitude of a Radiological Control Program.
The specific mission, types and quantities of
radioactive material, and the radiation-
generating devices that will be used at the site
are just a few.
Show OT 4.1.
State objectives.
Show OT 4.2.
Obj. 1
Identify factors that influence the
scope and magnitude of a
Radiological Control Program at any
nuclear facility.
• What to do?
• Who does it?
• How is it done?
• Is it being done, and how well?
Ask participants what factors may
affect program size–list on flip
chart.
Encourage participants to write
responses in their Student’s Guide.
Responses should include the
following:
• The specific facility mission
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 3
III. Elements of a radiological control program
A. Requirements
• The radiation-generating
devices at the site
• The types and quantities of
radioactive materials in use at
the site
• The physical and chemical
forms of the radioactive
materials in use at the site
• The physical location of the
site in relation to the
population centers
• The size of the work force
• The age of the facility
• The original facility design
criteria
Ask participants how a site would
determine what had to be
included in their program.
Encourage participants to write
responses in their student’s
guide.
Responses should include:
• Hazard assessment/
characterization
• Requirements/ commitments
– Contract
– RPP (10 CFR Part 835)
– Other federal regulations
– State regulations
– Site RadCon Manual
Implementation Plan
– Orders
– Other
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 4
B. Responsibilities
C. Programs/procedures
Ask participants how a site
should address and document
these responsibilities.
Responses should include:
• Organization and
administration
– Upper management
commitment
• Personnel training and
qualification
Section 24
Ask participants what type of
subprograms should be included
or what areas should be
addressed in the responsibilities.
Responses should include:
• Work controls (engineered,
administrative, personal
protective equipment)
• Posting and labeling
• Entry controls
• Radioactive materials controls
• Criticality controls
• Radiation-generating devices
• Contamination controls
• Respiratory protection
• ALARA
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 5
D. Assessments
• Dosimetry
– External
– Internal
• Instrumentation and alarms
• Monitoring
– Workplace
– Environmental
– Air
• Radioactive waste
management
• Transportation and receipt of
radioactive material
• Emergency response
• Reporting
• Records
Ask participants what types of
subprograms should be
established to monitor and
improve program performance.
Responses should include:
• Internal audits and
investigations
• Trend analysis
• Performance indicators
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 6
IV. List of Radiological Control Program Elements
• Organization and administration
• Personnel training and qualification
• Quality assurance
• ALARA
• Radiological Work Control
– Procedures
– Radiological Work Permits
• Posting and labeling
• Radioactive material control
– Source control
– Release of materials
– Receipt and transportation
• Radiation-generating devices
– Sealed source
– X-ray machines
• Entry control
• Contamination control
• Instrumentation/alarms
• Monitoring
– Workplace
– Effluent
– Environmental
Show OT 4.3.
Obj. 2
Identify typical elements of a
Radiological Control Program.
Refer participants to
page 4 of handouts, “List of
Radiological Control Program
Elements,” which has different
element names, but similar
functions.
Show OT 4.4.
Show OT 4.5.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 7
• Dosimetry
– External
– Internal
- Program management (e.g., staffing,
technical basis, procedures, quality
assurance)
- Individual monitoring (e.g., air monitoring,
contamination monitoring, bioassay)
- Internal dose evaluation
• Respiratory protection
• Facility specific features
– Uranium
– Plutonium
– Tritium
– Accelerators
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance indicators
Refer participants to page 10 of
handouts, “Elements of a
Radiological Control Program.”
These provide a more detailed
listing/breakdown of elements.
As time allows, review selected
elements.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 4 – 8
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Technical Safety Requirements
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe the purpose of DOE Order 5480.22 and its relationship to 10 CFR
830.205.
2. Describe the purpose of Technical Safety Requirements (TSRs) in regard to
facility operations/activities.
3. Identify the source(s) of information required to develop reasonable and
appropriate TSRs.
4. Describe the responsibilities for the development and use of TSRs.
5. List the criteria for identifying problems in meeting TSRs.
Section 25
6. List areas in TSRs which could be reviewed as part of a radiological
assessment.
Training Aids:
Overhead Transparencies (OTs): OT 5.1 – OT 5.13 (may be supplemented or
Substituted with updated or
Site-specific information)
Handouts - “Typical Safety Analysis Report (SAR) Contents”
“Technical Safety Requirement (TSR) Format and Content”
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 2
References:
U.S. Department of Energy, 10 CFR 830, Nuclear Safety Management, 2000.
U.S. Department of Energy, Operation Procedure Identifying, Reporting, and
Tracking Nuclear Safety Noncompliances, June 1998.
I. Introduction
II. Purpose of 10 CFR 830.205
On October 10, 2000 an Interim final rule was
published in the Federal Register for 10 CFR 830,
"Nuclear Safety Management". The Interim Final Rule
was effective December 11, 2000, and codifies
requirements for TSRs in 10 CFR 830.205. The new
rule required contractors to develop and submit TSRs
to DOE for approval by April 10, 2003.
TSRs are a critical element in the overall DOE safety
program.
A. Definitions (Paragraph 6)
• Technical Safety Requirements are those
requirements that define the conditions, safe
boundaries, and the management or
administrative controls necessary to ensure the
safe operation of nuclear facilities and to reduce
the potential risk to the public and facility
workers from uncontrolled releases of
radioactive materials or from radiation exposure
due to inadvertent criticality. Technical Safety
Requirements consist of safety limits, operating
limits, surveillance requirements, administrative
controls, use and application instructions, and
the bases thereof.
• A controlled document is content maintained
uniformly among the copies by an Administrative
Control System (paragraph 6, Item e).
Show OT 5.1 and OT 5.2.
State objectives.
Obj. 1
Describe the purpose of DOE
Order 5480.22 and its relationship
to 10 CFR 830.205.
This material may need to be
updated to reflect final
implementation guidance for 10
CFR 830 when it is finalized.
Show OT 5.3.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 3
Basis: Summary statements of the reasons for
the operating limits and associated surveillance
requirements. It shows how the numerical
value, condition, or the surveillance fulfills the
purpose from the safety documentation.
B. Policy (Paragraph 7)
It is the policy of the Department that nuclear
facilities operate Cognizant Secretarial Officer
(CSO)-approved Technical Safety
Requirements, which prescribe the bounds for
safe operation of these facilities in order to
protect the health and safety of the public and
reduce risk to workers.
The TSRs constitute a contract between the
operating contractor and DOE management of
the methods that will be utilized or constraints to
be applied to minimize the potential risk of
operating the proposed facility or conducting the
proposed activity.
NOTE: TSRs apply to actions by specific facility
personnel and their commitments to responsible
DOE managers.
The Technical Safety Requirements document is
to be a controlled document.
TSRs are not based upon maintaining worker
doses below some acceptable level following an
uncontrolled release of hazardous material or
inadvertent criticality; rather, the risk to workers
is reduced through controls that reduce the
likelihood and potential impact of such events.
Section 26
Show OT 5.4.
Obj. 2
Describe the purpose of
Technical Safety Requirements
(TSRs) in regard to facility
operations/activities.
Show OT 5.5.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 4
C. Source for bases (justification) of TSRs
In the development of limits, set-points, staffing
requirements, and other parameters for input
into the individual TSRs, the facility/operation-
specific Safety Analysis Report (SAR),
particularly the accident analyses contained
therein, is normally the primary basis.
The limitations that are included in the TSRs
should be derived from the facility-specific safety
analysis, which considers all credible accidents.
This includes the most significant possible
releases of radioactive and hazardous materials,
criticality scenarios, and the accidental releases
expected during the life of the facility.
Careful and thorough examination of these
accident analyses will provide values for defining
the operational limits necessary to ensure that
facility operations do not occur outside the
bounds assumed in the analyses. Such an
examination will also identify parameters and
operating conditions that should be limited in
order to reduce, provide warning of, and mitigate
the uncontrolled releases of hazardous materials
and to prevent inadvertent criticality.
Examples of requirements expected to be
developed include:
• Operating limits for principal process
parameters
• Technical and administrative conditions that
must be met
• Availability of safety equipment and systems
• Critical functions of instrumentation and
controls
Obj. 3
Identify the source(s) of information
required to develop reasonable and
appropriate TSRs.
Show OT 5.6.
SAR text of interest
• Principal Safety Criteria
• Accident Analysis
• Deviation of TSRs
Show OT 5.7.
Show OT 5.8.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 5
Operations within the boundaries of the resulting
requirements will provide reasonable assurance
that the nuclear facility will not:
• Threaten the health and safety of the public
• Pose an undue risk to workers from the
uncontrolled releases of radioactive or other
hazardous materials and inadvertent
criticality
For facilities that do not have an approved SAR,
the technical input into the TSRs must be
derived from existing documents/analyses that
specifically demonstrate the limiting conditions
that the facility is expected to experience during
normal operations and potential accident
conditions.
In order to serve as the basis for the TSRs,
these studies must systematically evaluate:
• All potential off-normal conditions that could
occur during the life of the facility
• What could be considered design basis
accidents
D. Responsibilities for TSRs
• Prepare → Contractor
• Review → DOE Field Office
• Approve → CSO
Refer participants to page 24 of
handouts, “Typical Safety
Analysis Report (SAR)
Contents.”
Show OT 5.9.
Show OT 5.10.
Obj. 4
Describe the responsibilities for
the development and use of
TSRs.
Refer participants to page 26 of
handouts, “Technical Safety
Requirement (TSR) Format and
Content.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 6
E. Identification of violations
Violations of a TSR occur as the result of four
circumstances:
• Exceeding a Safety Limit (SL)
Section 27
• Failing to take the necessary actions within
the required time limit following:
– Exceeding a Limit Control Setting (LCS)
– Failing to meet Limiting Conditions for
Operations (LCO)
– Failing to successfully meet a
Surveillance Requirement (SR)
• Failing to perform a surveillance within the
required time limit
• Failing to comply with an Administrative
Control (AC) requirement
As stated previously, compliance with TSRs is
required by 10 CFR 830.205, violations may be
enforceable under PAAA.
F. Reporting Requirements (DOE Order
231.1A,Change 1
A, Chg 1) Occurrence Reporting and Processing of
Operations Information, June 2004
• Categorization
– Operational Emergency
– Significance Category 1 - 4
• Notification
• Follow-up notification
• Occurrence Report preparation
TSR ACs may impose additional facility- or
operations-specific reporting requirements,
which must also be carefully and fully followed.
Show OT 5.11.
Note that the violation relates to failure
to comply with an Action Statement.
The actions required to be taken when
LCSs are exceeded, or when operations
outside an LCO occur, are intended to
provide compensatory protection for the
same safety concerns for which the limit
was established. Thus, exceeding the
limit by itself is not considered a
violation but is a reportable event as an
Off-Normal Occurrence.
Obj. 5
List the criteria for identifying problems
in meeting TSRs.
Show OT 5.12.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 7
Violations of TSRs may need to be reported as
part of the Noncompliance Tracking System
(NTS). For guidance on NTS reports, refer to
Operation Procedure Identifying, Reporting, and
Tracking Nuclear Safety Noncompliances, June
1998, prepared by the DOE Office of
Enforcement (HS - 40).
G. Ancillary guidance
The TSR document shall be kept current at all
times so that it reflects the facility as it exists and
is analyzed in the SAR. The TSR must be
approved prior to changes in the facility or facility
practices.
TSRs should be written in a clear and concise
manner, in language that is understandable by
those in the facility operating organization. The
TSR should not contain excessive details that
belong more appropriately in the SAR.
The scope and content of TSRs are to be limited
to only the most critical nuclear safety areas.
This serves to make TSR Documents more
useful for controlling facility safety.
H. Radiological Assessment of TSR Compliance
TSRs typically specify requirements for several
areas that may be reviewed as part of a
radiological assessment. These areas include:
Area monitors:
Criticality monitors
Area Radiation Monitors
Air Monitors (i.e., real time air monitors,
fixed head air samplers)
TSRs are the primary source of
the more important safety
requirements that are imposed
upon any facility
operations/activities. The bases
for the TSRs can be found in
the Safety Analysis Report,
principally in the chapters on
Safety Criteria and Accident
Analysis.
Obj. 6 List areas in TSRs which
could be reviewed as part of a
radiological assessment
Show OT 5.13.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 8
Surveillance requirements for area monitors
HEPA ventilation systems and their surveillances
Shift Staffing
Facility staff qualification, training and
retraining
Audits and reviews
Summarize lesson.
Review objectives.
Ask for questions.
Section 28
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 5 – 9
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Aspects of Uranium
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify the radiological properties of uranium.
2. Describe the toxicological properties and behavior of uranium.
3. Identify appropriate instrumentation, measurement techniques, and special
radiological survey methods for uranium.
4. Describe personnel protection requirements, external dose control techniques,
and internal dose control techniques.
5. Describe special controls and considerations required for uranium operations.
Training Aids:
Overhead Transparencies (OTs): OT 6.1 – OT 6.11 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 2
References:
ICRP Publication 30, Limits for Intakes of Radionuclides by Workers, 1979.
U.S. Department of Energy, DOE-STD-1136-2000, Guide of Good Practices for
Occupational Radiological Protection in Uranium Facilities, 2004.
U.S. Department of Energy, DOE-STD-1121-98, Internal Dosimetry, Reaffirmation
May 2003.
U.S. Department of Energy, DOE-HDBK-1113-98, Radiological Safety Training for
Uranium Facilities, Reaffirmation May 2005.
U.S. Department of Energy, DOE-STD-1098-99 Chg 1, Radiological Control,
March 2005.
U.S. Environmental Protection Agency, Federal Guidance Report No. 11, Limiting
Values of Radionuclide Intake and Air Concentration, and Dose Conversion
Factors for Inhalation, Submersion, and Ingestion, EPA-520/1-88-020, 1988.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 3
I. Introduction
The guidance in DOE-STD-1136-2000, Guide of
Good Practices for Occupational Radiological
Protection in Uranium Facilities, 2004 should be
reviewed in detail prior to conducting an
assessment of uranium facilities. The following is a
brief overview of the radiological aspects of
uranium.
II. Radiological aspects of uranium
A. Radiological properties of uranium
Fifteen radioisotopes exist, but the three of most
concern to the uranium industry are:
Uranium-238:
99.7% abundant in natural uranium;
half-life = 4.5 billion yrs,
specific activity = 3.3 E-7 Ci/g
Uranium-235:
0.72% abundant;
half-life = 710 million yrs,
specific activity = 2.1 E-6 Ci/g
Uranium-234:
0.006% abundant;
half-life = 247 thousand yrs,
specific activity = 6.2 E-3 Ci/g
Enriched uranium has a higher content of
Uranium-235 than found in nature. Typical
enrichment values are:
• 2%-3% Uranium-235: power reactor grade
fuel
• >90% Uranium-235: weapons grade material
Show OT 6.1 and OT 6.2.
State objectives.
Show OT 6.3.
Obj. 1
Identify the radiological properties
of uranium.
Review DOE-STD-1136-2000,
Guide of Good Practices for
Occupational Radiological
Protection in Uranium Facilities,
2004.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 4
Specialized reactor fuel may have enrichments
other than those listed above.
The uranium byproduct of enrichment is reduced
in Uranium-235 content and is called depleted
uranium. Its typical composition is as follows:
Section 29
• 99.75% Uranium-238
• 0.20% Uranium-235
• 0.0007% Uranium-234
As a result of the differences in specific
activities, Uranium-234 may account for a
significant fraction, or even the majority, of the
radioactivity for enriched uranium.
For example, for 3% enriched uranium (i.e., 3%
Uranium-235), the Uranium-234 (with an
abundance of 0.03%) would have approximately
6 times the activity as Uranium-238 and
approximately 30 times the activity as
Uranium-235.
Uranium-238 and Uranium-234 are part of the
uranium decay series, while Uranium-235 is part
of the actinium series. Therefore, following
chemical separation, decay products will
continue to grow in. The most significant of
these are Thorium-234 and Protactinium-234m
from the uranium series and Thorium-231 from
the actinium series.
Other small amounts of radioactive material may
be present as the result of reprocessing
uranium. These include Neptunium, Plutonium,
Technetium-99, and other radioisotopes of
uranium, including Uranium-232 and
Uranium-236.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 5
B. Radioisotopes
The primary radioisotopes of uranium are all
long-lived alpha-emitters. The specific activity
(Ci/g) of uranium increases as enrichment
increases; therefore, enriched uranium is a more
serious radiation hazard.
In most uranium facilities, the inhalation hazard
from alpha particles released in the respiratory
tract is the predominant radiological hazard
associated with the alpha emitting uranium
isotopes. In addition, uranium decay products
are primarily beta-emitters. For external
exposure, the major concern is the high-energy
beta particle from Protactinium-234m (2.29
MeV). As a result of beta radiation, the typical
contact dose with a block of uranium is
approximately 200 mrad/hr.
Trace contaminants such as Technetium-99 and
Uranium-232 may result in additional external
radiation dose when present.
As a result of the alpha-neutron reaction, casks
of enriched uranium hexafluoride may also emit
neutrons. Typical dose rates are on the order of
a few mrem/hr.
Show OT 6.4.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 6
C. Criticality
Uranium-235 and Uranium-233 are both fissile
materials; therefore, facilities handling enriched
uranium and/or Uranium-233 have the potential
for criticality accidents, generating large
amounts of neutron and gamma radiation.
D. Toxicological properties of uranium
Uranium is a heavy metal poison and is toxic in
much the same way lead or mercury is. For
soluble compounds of low enrichments (< 5%
Uranium-235), the toxic properties of uranium
override the radiological hazards. The kidney is
the primary organ of concern.
For insoluble compounds of any enrichment or
all compounds of highly enriched uranium, the
radiological hazards are limiting.
III. Detection, measurement, and survey techniques
A. Monitoring program
A radiation protection monitoring program in a
uranium facility must ensure the detection of
typical ionizing radiations over wide energy
ranges.
To detect alpha radiation from the uranium
isotopes surveys using photon-sensitive portable
and fixed alpha detectors such, as zinc sulfide or
gas proportional counters, should be used.
Appropriate beta detection instrumentation
should be available to measure decay products
such as Protactinium-234m. If Technetium-99 is
suspected, special low-energy beta particle
detection equipment should be available.
Section 30
Obj. 2
Describe the toxicological
properties and behavior of
uranium.
See Table 2-13 of
DOE-STD-1136-2000
Show OT 6.5.
Obj. 3
Identify appropriate
instrumentation, measurement
techniques, and special
radiological survey methods for
uranium.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 7
If large quantities of uranium hexafluoride are
present, appropriate neutron survey instruments
should be available to measure the neutron
radiation.
If the facility contains enriched uranium and/or
Uranium-233, appropriate criticality safety alarm
systems shall be in place and appropriate
neutron and gamma survey instruments
available.
Continuous air monitors (CAMs), sample
extraction lines that go to CAMs, and continuous
radiation dose monitors should be placed
outside glove boxes and fume hoods.
B. Survey Techniques
Monitoring practices include, but are not limited
to, the following:
• Contamination surveys of the workplace
• Release surveys
• External exposure surveys
• Airborne contamination surveys
• Routine surveillance by a Radiological
Control Technician
All work areas must be monitored for
contamination levels on a regularly scheduled
basis. The frequency of such surveys will
depend on the potential for dispensability of the
radioactive material. During these routine
surveys, all work enclosures, work surfaces,
floors, and equipment within the workplace
should be surveyed.
Show OT 6.6.
C. Workplace characterization
At the time a program is established,
measurements of external dose should be made
Show OT 6.7.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 8
at all locations where it occurs to delineate the
levels involved (workplace characterization).
Additional measurements should be made at the
same frequency as the contamination surveys to
identify the buildup of uranium in HEPA filters
and glove boxes.
Airborne contamination surveys should be
performed for:
• Prompt detection of airborne contamination
for worker protection
• Personnel dose assessment
• Monitoring of trends within the workplace
• Special studies
IV. Personnel protection requirements
Workers in uranium facilities need to be
appropriately trained on the hazards. DOE has
developed DOE-HDBK-1113-98, Radiological
Safety Training for Uranium Facilities,
Reaffirmation
May 2005. This handbook provides DOE's
guidance on expectations for training of uranium
workers.
A. Personnel air sampling
The use of personnel air sampling programs
should be considered in monitoring individual
Radiological Workers.
B. Protective clothing
As a minimum, personnel who perform
operations in controlled areas should wear
coveralls – protective clothing is required in
contamination areas, not controlled areas. No
personal outer clothing should be permitted
under coveralls. For inspections or visits, lab
Show OT 6.8.
Obj. 4
Describe personnel protection
requirements, external dose
control techniques, and internal
dose control techniques.
Review DOE-HDBK-1113-98,
Radiological Safety Training for
Uranium Facilities, 1998.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 9
coats, gloves, and shoe covers may be
permissible.
Protective clothing should be removed at the
Section 31
step-off pad, and personnel monitoring for
contamination shall be performed. If this is not
practical, strict control of the movement of
personnel shall be maintained from the step-off
pad to a location where protective clothing can
be removed. Personnel wearing protective
clothing shall not be allowed to mingle with
individuals wearing personal street clothing.
Protective clothing shall not be allowed in
uncontrolled areas such as offices, lunchrooms,
or control rooms.
C. Respiratory protection
Respiratory protection should be readily
available. Respiratory protective equipment
should be used for all bag-out operations, bag
and glove changes, and any situation involving a
potential or actual breach of confinement.
V. External dose control
A. Beta radiation
Beta radiation is usually the dominant external
radiation hazard in work with unshielded forms
of uranium. The primary concern is
Protactinium-234m, though other radionuclides
may be present. Particular care should be taken
in operations such as melting and casting, where
decay products could be separated and
concentrated. Appropriate measurements
should be made of the material and appropriate
extremity dosimetry worn by workers handling
the material.
Show OT 6.9.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 10
B. Gamma radiation
Gamma radiation is normally not the controlling
factor at uranium facilities. However, gamma
fields can exist in areas where large quantities of
uranium are stored. Appropriate actions
including time, distance, and shielding
considerations should be taken to maintain
radiation doses ALARA.
C. Neutron radiation
Neutron radiation from enriched uranium fluoride
compounds should also be considered in
determining potential external radiation hazards.
VI. Internal dose control
Intakes
In most uranium facilities, the primary
radiological hazard is the potential for internal
intakes of uranium. This hazard must be
controlled by appropriate facility and equipment
design, contamination control procedures, and
protective clothing.
Inhalation is the primary route of concern.
Uranium transported from the lungs is deposited
in the bone (22%), kidney (12%), or other
tissues (12%), or excreted (54%), according to
International Commission on Radiological
Protection (ICRP) Publication 30.
Control must be verified by a bioassay program.
Urinalysis is the most common technique, but
fecal analysis and in vivo monitoring may also
be appropriate.
Show OT 6.10.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 11
DOE-STD-1121-98, Internal Dosimetry,
Reaffirmation May 2003, provides technical
guidance on internal dosimetry programs,
including evaluation of occupational internal
doses from exposure to radon and thoron. This
standard should be reviewed prior to conducting
assessments of internal dosimetry programs.
VII.Special controls and considerations at uranium
operations
A. Criticality alarm systems (gamma or neutron)
shall be provided in each area where an
accidental criticality is possible. Site
requirements documents relating to criticality
alarms should be reviewed prior to the
assessment, if applicable. These
requirements may include: ANSI/ANS 8.1,
Nuclear Criticality Safety in Operations with
Fissionable Materials Outside Reactors;
ANSI/ANS 8.3 Criticality Accident Alarm
Systems; ANSI/ANS 8.7, Nuclear Criticality
Safety in the Storage of Fissile Materials;
ANSI/ANS 8.15, Nuclear Criticality Control of
Special Actinide Elements; and ANSI/ANS
8.19, ANS Administrative Procedures for
Nuclear Criticality.
Section 32
B. All DOE facilities that possess sufficient
quantities and kinds of fissile material to
constitute a potentially critical mass shall
provide nuclear accident dosimetry (fixed and
personal). The number of dosimeters
needed and their placement will depend on
the nature of the operation, structural design
of the facility, and accessibility of areas to
personnel. An analysis of the dosimeters
and their placement should be conducted
and documented.
Review DOE-STD-1121-98,
Internal Dosimetry.
Reaffirmation May 2003
Show OT 6.11.
Obj. 5
Describe special controls and
considerations required for
uranium operations.
Reference 10 CFR 835.1304.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 6 – 12
C. Uranium metal in finely divided form is
pyrophoric; therefore, any grinding or milling
operations must be carefully conducted to avoid
fires.
Uranium hexafluoride is commonly found in
many uranium operations. This material is a
solid at room temperatures but volatilizes readily
at elevated temperatures. As a gas, it is
extremely hazardous, forming hydrofluoric acid
when it comes in contact with water. Operations
involving uranium hexafluoride must be
conducted very carefully to prevent release of
the gas.
D. External radiation hazards from uranium are
primarily associated with decay products;
therefore, operations in which the decay
products can separate and concentrate must be
monitored carefully. For example, crucibles
used to melt depleted uranium and casks used
to ship uranium hexafluoride are sometimes
more radioactive after they are emptied than
when they are full. The reason is that the decay
products are left in the emptying process and
are no longer self-shielded by the uranium.
Summarize lesson.
Review objectives.
Answer questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Aspects of Tritium
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe the radiological properties of tritium.
2. Identify personnel protection requirements and dose control techniques.
3. Identify the biological effects of internally deposited tritium.
4. Describe appropriate instrumentation, measurement techniques, and special
radiological survey methods for tritium.
5. Identify special controls and considerations required for the use of tritium.
Training Aids:
Overhead Transparencies (OTs): OT 7.1 – OT 7.14 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 2
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1121-98, Internal Dosimetry, Reaffirmation
May 2003.
U.S. Department of Energy, DOE-HDBK-1129-99, DOE Handbook Tritium
Handling and Safe Storage, Reaffirmation 2007.
U.S. Department of Energy, DOE-HDBK-1105-96, Radiological Training for Tritium
Facilities, Reaffirmation 2002.
U.S. Department of Energy, DOE-HDBK-1079-94, Primer on Tritium Safe
Handling Practices, 1994.
U.S. Department of Energy, Radiological Control Technical Position, RCTP 01 -
02, Acceptable Approaches for Developing Air Concentration Values for
Controlling Exposures to Special Tritium Compounds, 2001.
Section 33
U.S. Environmental Protection Agency, Federal Guidance Report No. 11, Limiting
Values of Radionuclide Intake and Air Concentration, and Dose Conversion
Factors for Inhalation, Submersion, and Ingestion, EPA-520/1-88-020, 1988.
ICRP Publication 30, Limits for Intakes of Radionuclides by Workers, 1979.
ICRP Publication 66, Human Respiratory Tract Model for Radiological Protection,
1994.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 3
I. Introduction
II. Radiological aspects of tritium
A. There are three primary sources of tritium.
These are:
1. Environmental sources - Reactions between
cosmic rays and the upper atmosphere
14N + 1n � 3H + 12C
2H + 2H � 3H + 1H
2. By-product of power reactors
• Ternary fission - A fission event resulting
in fission fragments, one of which is
tritium. Occurrence typically has a 0.1%
yield.
B-10 (n, 2 alpha) 3H
Li-7 (n, n alpha) 3H
3. DOE production of tritium (Hanford,
Savannah River reactors) is by the following
reaction:
6Li + 1n � 3H + alpha
Show OT 7.1 and OT 7.2.
State objectives.
Show OT 7.3.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 4
B. Chemical and radiological properties of tritium
1. Chemical forms
• Elemental tritium (tritium gas, HT, DT, T2)
• Tritiated water (tritium oxide, HTO, DTO,
T2O)
• Special tritium compounds (STCs):
created by intentional combination of
tritium with the desired materials or by
inadvertent contamination of a material
that has been subjected to the presence of
tritium for a period of time.
These are classified in a number of ways,
depending on their host material (metal or
organic), rate of tritium release (stable or
unstable), and physical form (particulate or
non-particulate). They include:
- Organically bound tritium (OBT); the
main types of OBT encountered in the
DOE complex are solvents, oils, and
solid particulates (e.g., plastics, nylon,
and organic dust forms).
- Particulates; stable or insoluble forms
are referred to as stable tritiated
particulates (STPs).
Show OT 7.4.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 5
2. Radiological properties
• 3H � 3He + beta minus and anti-neutrino
• Emax = 18.6 keV, Eavg = 5.69 keV
• Half-life = 12.32 years
• Specific activity = 9619 Ci/gram
• ALIwater = 3000 MBq = 8 E4 µCi
(inhalation and ingestion)
• DACwater = 0.8 MBq/m3 = 2 E-5 µCi/cm3
• DACelemental = 2 E4 MBq/m3 = 0.5 µCi/cm3
• f1 = 1
• Committed dose equivalent per unit
intake = 1.73 E-11 Sv/Bq =
6.4 E-2 mrem/µCi
• DACelemental/DACwater = 25,000
In addition, DOE has issued guidance on
radiological protection for special tritiated
compounds in Radiological Control Technical
Position, RCTP 0 1 - 02, Acceptable Approaches
for Developing Air Concentration Values for
Controlling Exposures to Special Tritium
Compounds. DOE has also issued RCTP 06-01,
Acceptable Approaches for Developing Sealed
Radioactive Sources and Posting and Labeling
Requirements for Special Tritium Compounds
(STCs).
DOE has also developed a technical standard,
Radiological Control Programs for Special
Tritium Compounds,
DOE- HDBK-1184-2004, Change Notice 1 May
2006.
Obj. 1
Describe the radiological
properties of tritium.
Show OT 7.5.
Section 34
Review Radiological Control
Technical Position, RCTP 01 -
02, Acceptable Approaches for
Developing Air Concentration
Values for Controlling Exposures
to Special Tritium Compounds.
Rev Review Radiological Control
Programs for Special Tritium
Compounds,
DOE- HDBK-1184-2004
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 6
C. Potential exposure pathways of tritium
Dose pathways and biological effects
• Inhalation
– Elemental tritium (tritium gas) - Limiting
condition is exposure to the lung
– Approximately 0.005% of HT inhaled is
converted to HTO prior to exhalation
– Nearly 100% of inhaled HTO is
incorporated into body fluids/tissues.
• Ingestion
– Tritiated water
• Assumed to be instantaneous
• Biological half-life is normally ten
days, but may be reduced by a
factor or two-three with increased
fluid intake
• Skin absorption of HTO through intact skin
≈50% of that inhaled.
For different modes of entry of STCs:
– STPs behave with the characteristics
of the particle to which they are
attached.
- Soluble OBT distributes throughout the
body causing a whole body dose.
Insoluble OBT can be taken into the
body by inhalation when in particulate
form. Airborne droplets of insoluble
components of oils may be treated as
stable particulates.
Show OT 7.6.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 7
D. General sources of tritium releases
1. Gaseous releases - ventilation exhaust
systems
2. Liquid wastes
• Aqueous
• Organic (e.g., oils)
3. Solid wastes
• Contaminated wastes
• Treatment residues
E. Exposure controls for tritium
The personnel protection requirements for tritium
include:
• Airborne contamination controls
• Surface contamination controls
1. Airborne controls
• Differential room pressure zones
• Dilution ventilation
• Room-air detritiation systems
• Local exhaust ventilation
Show OT 7.7.
Show OT 7.8.
Obj. 2
Identify personnel protection
requirements and dose control
techniques.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 8
2. Contamination controls
• Good housekeeping
• Good work practices
3. Personnel protective equipment
• Air supplied respirators
• Protective clothing
F. Metabolism of tritium
The tritium beta lacks sufficient energy to
penetrate the dead cell layer in skin. Therefore,
it is of little consequence as an external hazard.
The beta particles can produce Bremsstrahlung
radiation when they interact with matter,
although the tritium Bremsstrahlung is extremely
low energy. It is remotely possible that the
Bremsstrahlung exposure could become
significant around materials with very high
specific activities and little or no shielding.
Tritium can deliver a radiation dose if it gets
inside the body. Modes of entry include:
• Inhalation
• Ingestion
• Absorption
1. Inhalation
Tritium gas (HT) is only slightly incorporated
into the body when inhaled. Approximately
0.005% of HT inhaled is converted to tritiated
water prior to being exhaled. Depending
upon the rate at which HT converts to HTO in
vivo, it is possible that some dissolved HT
may be excreted in urine.
Obj. 3
Identify the biological effects of
internally deposited tritium.
Show OT 7.9.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 9
Section 35
Tritiated water (HTO) is much more
radiologically hazardous than tritium gas.
Inhaled HTO enters the body through the lung
fluids with 100% efficiency, and mixes rapidly
with body water. Nearly 100% of tritiated water
(HTO) inhaled is incorporated into body fluids
and tissues.
2. Ingestion
Ingested HTO is assumed to be completely and
instantaneously absorbed from the
gastrointestinal tract and mixes rapidly with the
body fluids so that following ingestion, the
concentration in sweat, sputum, urine, blood,
perspiration and expired water vapor is the
same.
3. Absorption
There is negligible skin absorption for tritium
gas. Some HT can be absorbed through the
skin from contact with surface contamination.
This uptake is probably in the form of HTO,
resulting from the oxidation of HT. Some tritium
may be retained in the skin in the form of
organics, presumably resulting from exchange
reactions with HT on or in the skin.
HTO can be readily absorbed through the skin.
It will be uniformly distributed in all biological
fluids within one to two hours.
Most exposures are to HTO, which rapidly
enters the body water via absorption through
the lungs and/or skin. A small amount of HT
can dissolve in lung fluids, convert to HTO, and
enter the body fluids. Exposures to HTO are
approximately 10,000 to 25,000 times more
hazardous than exposure to HT. HTO has an
effective half-life in the body in the range of 4 to
18 days, with a mean effective half-life of about
9 or 10 days.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 10
Most tritium leaves the body either in urine or
through evaporation from the lungs and skin. The
dose commitment from an uptake of one curie of
HTO is approximately 63 rem.
For the above 3 discussed modes of entry: STPs
and insoluble components of tritiated oils behave
with the characteristics of the particle to which they
are attached.
For dose calculations for STPs, ICRP Publication
66 uses absorption types; slow, medium, and fast
(S, M, F). These are used in place of the lung
retention classes (day, week, and year; D, W, Y)
used in ICRP Publication 30. Depending on the
absorption type of the compound, the dose per
intake will be different than HTO.
For example: The air concentration value (which
could be used in assessing dose per intake) for
Type S STP is 10 times more restrictive than HTO,
while the air concentration value for Type F STP is
5 times less restrictive than HTO.
Soluble OBTs act somewhat similar to HTO,
however a larger percentage of nuclear
transformations occur in the stomach. The dose
per intake is approximately twice that of HTO.
Skin absorption is also a valid intake pathway for
tritiated oil components and solvent OBT.
G. Methods of tritium containment
1. Primary - Process equipment and piping
2. Secondary
• Glove boxes
• Temporary vented enclosures
Review Types S, M, F
Show OT 7.10.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 11
3. Tertiary - Room and associated ventilation systems
• Effluent recovery systems
• Emergency containment systems
H. Airborne tritium controls
1. Differential room pressure zones - The air
ventilation system plays a key role in controlling
the spread of contamination. In addition to
providing the necessary humidity and
temperature control for a building, differential
pressure zones should be established within a
building to ensure that the air flows from areas
with lower hazardous contamination potential to
areas with more hazardous contamination
potential.
Section 36
2. Dilution ventilation - Dilution ventilation is the
once-through flow technique of exchanging
outside air for inside air for comfort and basic
contamination control.
3. Room-air detritiation systems - Such a system
uses tritium monitors located in the room
exhaust to activate (close) fast acting dampers.
The dampers then route the exhaust through a
special oxidation/drying system and return the
air to the room.
3. Local exhaust ventilation - The primary
advantage of local exhaust ventilation
techniques is the removal of airborne tritium,
regardless of its evolution rate or chemical or
physical form. In addition, these techniques
use relatively low flow rates compared to
normal ventilation requirements.
Show OT 7.11.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 12
I. Measurement techniques for tritium
1. Air monitoring - Fixed and portable ionization
chambers most widely used.
2. Differential monitoring - Separate monitoring
of HT and HTO components through the use
of bubblers in conjunction with desiccants or
catalysts.
3. Discrete sampling - Samples collected with a
bubbler or “cold finger” type sampler, then
later analyzed by liquid scintillation counting
techniques.
4. Process monitoring
• Stack, room, hood, glove box
• Mass spectroscopy, gas chromatography,
calorimetry
5. Surface monitoring
• Difficult to measure directly due to low-
energy emission
• May have some success with thin window
GM (pancake style probe), thin window
sodium iodine, or gas flow proportional
counters
• Smears taken for loose contamination,
and measured by dissolution and analysis
by liquid scintillation counting techniques
6. Liquid Monitoring - Liquid scintillation
counting techniques
Show OT 7.12.
Obj. 4
Describe appropriate instrumentation,
measurement techniques, and special
radiological survey methods for tritium.
Flow-through ionization chambers
Typical example - TRITON radioactive
gas monitors
Explain how the ionization chamber
works.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 13
J. Bioassay program for tritium workers
An adequate bioassay program for tritium
workers would test for chronic and acute
exposure.
1. Chronic exposure - Periodic urinanalysis for
tritium (daily to biweekly identified in Tritium
Good Practices Manual)
2. Acute exposure
• Wait one to two hours.
• Void bladder.
• Collect sample as soon as possible
thereafter.
• Continue to collect daily to determine
individual half-life.
Dose from exposure to STCs may need to be
assessed based on air monitoring results, see
RCTP 99-02.
DOE-STD-1121-99, Internal Dosimetry, 1999,
provides guidance on internal dosimetry
programs including monitoring and assessing
dose from tritium.
K. Tritium effluent recovery systems
1. Purpose - Reduce tritium available for
release
2. Method - Tritium gas converted to HTO and
ultimately a stable waste form
Show OT 7.13.
Obj. 5
Identify special controls and
considerations required for the use of
tritium.
Review DOE-STD-1121-99, Internal
Dosimetry, 1999, for tritium applications.
Show OT 7.14.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 7 – 14
L. Inventory control and accountability for tritium
1. Nuclear materials, including tritium, need to
be controlled and have material
accountability.
2. Appendix D to the Tritium Good Practices
Manual discusses inventory control and
defines it to consist of:
Section 37
• Measurements
• Measurement controls
• Determination of holdup in systems
• Development of predictors
• Establishment of accounting practices
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Aspects of
Plutonium
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify the radiological properties of plutonium.
2. Identify the biological effects of plutonium.
3. Identify special controls and considerations required for plutonium operations.
4. Describe appropriate instruments, measurement techniques, and special
radiological survey methods for plutonium.
5. Describe personnel protection requirements and dose control techniques for
plutonium.
Training Aids:
Overhead Transparencies (OTs): OT 8.1 – OT 8.12 (may be supplemented or
substituted with updated
or site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 2
References:
American National Standards Institute, ANSI/ANS, Criticality Accident Alarm
Systems, 1986.
American National Standards Institute, ANSI/ANS 8.1, Nuclear Criticality Safety in
Operations with Fissionable Materials Outside Reactors, 1983.
American National Standards Institute, ANSI/ANS 8.19, ANS Administrative
Procedures for Nuclear, 1984.
ICRP Publication 30 Part 4, Limits for Intakes of Radionuclides by Workers: an
Addendum, 1988.
U.S. Department of Energy, DOE-STD-1128-98, Guide of Good Practices for
Occupational Radiological Protection in Plutonium Facilities, Change Notice 2,
December 2006.
U.S. Department of Energy, DOE-STD-1121-98, Internal Dosimetry, Reaffirmation
May 2003.
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Change
Notice 1, March 2005
U.S. Department of Energy, Radiological Control Technical Position 2001-01,
Questions and Answers Concerning Acceptable Approaches to Implementing
Bioassay Program Requirements, January 2001.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 3
I. Introduction
The guidance in DOE-STD-1128-98, Guide of Good
Practices for Occupational Radiological Protection in
Plutonium Facilities, Change Notice 2 December
2006 should be reviewed in detail prior to conducting
an assessment of plutonium facilities. The following
is a brief overview of the radiological aspects of
plutonium.
II. Background
Plutonium was first synthesized in the winter of 1940-
41 by a team of scientists at the University of
California. Its potential use in weapons was quickly
identified, and much of the effort of the Manhattan
Project was in the production of sizable quantities of
plutonium. Other uses for plutonium include use as:
• Reactor fuel
• Heat sources in thermoelectric generators to
power satellites
• Components in portable neutron sources
Plutonium is a silvery-white metal that readily
oxidizes to a dull gray color. It can be found in a
variety of physical and chemical forms. Several of
the chemical forms (including the pure metal) are
pyrophoric, so care must be exercised in handling the
material. Because of the pyrophoric nature of
plutonium and its alloys, the preferred form for
storing, shipping, and handling is as plutonium oxide.
III. Radiological properties of plutonium
Section 38
A. Isotopes
There are 15 isotopes of plutonium, all
radioactive, beginning with Plutonium-232 and
ending with Plutonium-246. The radioisotopes of
primary interest are Plutonium-238, Plutonium-
239, and Plutonium-240, all of which are primarily
alpha-emitters.
Show OT 8.1 and OT 8.2.
State objectives.
Review DOE-STD-1128-98,
Guide of Good Practices for
Occupational Radiological
Protection in Plutonium Facilities
Change Notice 2 December
2006.
Pyrophoric = able to ignite
spontaneously
Obj. 1
Identify the radiological
Properties of plutonium.
Show OT 8.3.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 4
1. Plutonium-238 (half-life = 87.7 yrs) is most
commonly used as a heat source in
thermoelectric generators. Because of its heat
production, care must be taken in handling
gram or larger quantities, as it could melt
plastic or ignite other materials.
2. Plutonium-239 (half-life = 24,000 yrs) is the
primary component of plutonium reactor fuel
(>85%) and weapons grade plutonium (>90%),
with Plutonium-240 (half-life = 6,560 yrs)
constituting most of the remainder in both
cases.
3. Plutonium radioisotopes emit relatively few
high-energy gamma rays, so kilogram
quantities can often be processed without
serious gamma dose problems. However,
small amounts of some radioisotopes or decay
products can increase external dose. For
example, Plutonium-241 decays by beta
emission to Americium-241, which emits a 60-
keV gamma ray. This can be a significant
source of dose to hands in glove boxes.
4. Neutron dose rates from spontaneous fission
and from alpha-neutron reactions with light
elements may be significant (e.g., 1 kg of
Pu-F4 (Pu-238) would have a contact neutron
dose equivalent rate of 4800 rem/hr).
B. Biological effects of internally deposited plutonium
The primary hazards from the most common
chemical form of plutonium (PuO2) are inhalation
and ingestion. This chemical form is relatively
insoluble. Therefore, uptake through the gastroin-
testinal (GI) system following an ingestion is
small.
Inhaled plutonium can remain in the lungs for a
considerable time before being removed through
the lymph system.
Show OT 8.4.
Obj. 2
Identify the biological effects of
plutonium.
.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 5
Plutonium is difficult to remove from the body.
The primary method is through the administration
of chelating agents as soon after the intake as
possible. Trained medical personnel are needed
to administer chelating agents.
The plutonium that enters the systemic system is
mostly translocated to the liver and the bone (as
is discussed in the following section).
Accordingly, development of cancer in these
organs and in the lungs are of particular interest in
evaluating long-term effects from intakes of
plutonium.
C. Survey techniques
A radiation protection program in a plutonium
facility shall ensure the detection of all types of
radiation (i.e., alpha, beta, gamma, x-ray, and
neutron) over large energy ranges. Alpha-
sensitive instruments are necessary for most
contamination control surveys.
Continuous air monitors (CAMs), sample
extraction lines that go to CAMs, and continuous
radiation dose monitors should be placed outside
the glove boxes and hoods.
Neutron surveys become important when
Section 39
processing tens of grams of Plutonium-238 or
hundreds of grams of mixed isotopes of
plutonium, particularly compounds (i.e., PuO2,
PuF4). The neutron survey is important in
instances where photon shields, such as leaded
glass, are used. Such shields normally stop all of
the charged particles, most of the low-energy
photons, and essentially none of the neutrons.
Under these circumstances, neutron radiation is
likely to be the major contributor to whole body
dose.
Exposure rate surveys are normally conducted
with photon-sensitive instruments with known
energy responses for photons with energies
≥ 10 keV.
Show OT 8.5.
Obj. 3
Identify special controls and
considerations required for
plutonium operations.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 6
Monitoring practices include, but are not limited
to, the following:
• Contamination surveys of the workplace
• Release surveys
• External exposure rate surveys
• Airborne radioactivity surveys (both real time
(CAMs) and historical (fixed air head))
• Routine surveillance by a Radiological Control
Technician
All workplaces shall be monitored for
contamination levels on a regularly scheduled
basis. The frequency of such surveys will depend
on the potential for dispensability of the
radioactive material. As a minimum, all gloves,
work surfaces, floors, and equipment within the
workplace should be surveyed.
Airborne radioactivity surveys should be
performed for:
• Prompt detection of airborne contaminants for
worker protection
• Personnel dose assessment
• Monitoring of trends within the workplace
• Special studies
Intakes
In most plutonium facilities, the primary
radiological hazard is the potential for internal
intakes of plutonium. This hazard must be
controlled by appropriate facility and equipment
design, contamination control procedures, and
protective clothing/equipment.
Show OT 8.6.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 7
Plutonium transferred from the initial entry site is
assumed to be translocated to the liver (45%) and
the bone (45). Retention half-life in the liver is 20
yrs and in the bone is 50 yrs, according to
International Commission on Radiological
Protection (ICRP) Publication 30.
Control must be verified by a bioassay program.
Urinalysis is the most common technique, but
fecal analysis and in vivo monitoring may also be
appropriate.
DOE-STD-1121-98, Internal Dosimetry,
Reaffirmation May 2003 provides technical
guidance on internal dosimetry programs,
including enhanced workplace monitoring for
instances where there is a technology shortfall,
such as for plutonium. This standard should be
reviewed prior to conducting assessments of
internal dosimetry programs.
The standard also discusses appropriate
evaluation of bioassay results.
D. Monitoring instruments
DOE-STD-1128-98, Guide of Good Practices for
Occupational Radiological Protection in Plutonium
Facilities, Change Notice 2 December 2006 has
additional guidance on monitoring
instrumentation.
Facilities that deal with unencapsulated plutonium
should have continuously operating effluent
monitors to determine whether or not plutonium is
being released to the environment.
Per ICRP Publication 48, studies
have indicated an average
partitioning of plutonium between
liver and bone of 30% and 50%.
However, due to high individual
variability, use of the 45% liver
and 45% bone partitioning is still
recommended.
Section 40
Review DOE-STD-1121-98,
Internal Dosimetry, Reaffirmation
May 2003.
Discuss technology shortfall -
routine bioassay cannot reliably
detect exposures of 100 millirem.
Show OT 8.7.
Obj. 4
Describe appropriate
instruments, measurement
techniques, and special
radiological survey methods for
plutonium.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 8
Criticality alarm systems (gamma or neutron)
should be provided in each area where an
accidental criticality is possible.
E. Sources of external dose
External dose control for plutonium is primarily
concerned with photon dose rates from handling
plutonium in a glove box and from the neutron
dose rate from some mixtures of plutonium.
While significant high-energy penetrating photons
are not commonly associated with plutonium, low-
energy photons (x- and gamma-rays) can create
significant dose rate problems to extremities. This
is particularly a concern when large amounts of
Plutonium-238, Plutonium-241, or Americium-241
(from the decay of Plutonium-241) are present.
Neutrons can also represent a potentially
significant dose due to spontaneous fission
(alpha, neutron) reactions or neutron induced
fission. The neutron dose is largely determined
by the radioisotope and other materials near the
source.
F. Control of external dose
External dose control is accomplished with
traditional dose reduction techniques:
• Time (minimize)
• Distance (maximize)
• Shielding (use as needed)
Other work practices, including good
housekeeping and specialized tool and equipment
design, can reduce external dose, as well.
Show OT 8.8.
Show OT 8.9.
Long-handled tongs, for example.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 9
G. Techniques for internal dose control
The confinement system is a series of physical
barriers that, together with a ventilation system,
minimizes the potential for release of radioactive
material into work areas and the environment
under normal and abnormal conditions, thereby
minimizing internal dose.
Generally, three confinement systems are used to
achieve the confinement system objectives at
plutonium handling facilities. They consist of the
following:
• Primary confinement is provided by piping,
tanks, glove boxes, encapsulating material,
and the like, and any off-gas system that
controls effluent from within the primary
confinement. It provides confinement of the
area immediately surrounding the hazardous
material.
• Secondary confinement is provided by the
walls, floor, roof, and associated ventilation
exhaust systems of the cell or enclosure
surrounding the process material or
equipment. Except in the case of glove box
operations, the area inside this barrier is
usually unoccupied; it provides protection for
operating personnel.
• Tertiary confinement is provided by the walls,
floor, roof, and associated ventilation exhaust
system of the facility. It provides a final barrier
against release of hazardous material to the
environment.
Show OT 8.10.
The term “containment” is also
used for “confinement.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 10
Different devices may be used to confine and
control radioactive material. The selection of the
appropriate device will depend on the quantity of
material, its form, and the operations to be
performed.
Fume hoods may be used for some operations
Section 41
with plutonium, depending on the quantity and
dispersability of the material. In general,
plutonium fume hood operations shall be limited
to wet chemistry processes and less than 100 mg
of plutonium.
Higher levels of plutonium are generally handled
in glove boxes. Care should be taken in the
design of the glove box to ensure confinement of
the material and any fire.
Ventilation may also be employed to confine
plutonium, although it usually is used in
conjunction with other measures.
H. Personnel protection
Workers in plutonium facilities need to be
appropriately trained on the hazards. DOE has
developed Radiological Safety Training for
Plutonium Facilities, DOE-HDBK-1145-2001,
Reaffirmation January 2007. This document
provides DOE's guidance on expectations for
training of plutonium workers.
The use of personal air sampling programs should
be considered to monitor individual workers for
exposure to airborne plutonium. Section 4.4.4 of
DOE-STD-1121-98, Internal Dosimetry,
Reaffirmation May 2003 discusses use of
breathing zone or personal air monitoring when
there is a technology shortfall (i.e., the derived
investigation level is less than the minimum
detectable activity). Technology shortfalls are
common for routine plutonium bioassay programs.
Show OT 8.11.
Obj. 5
Describe personnel protection
requirements and dose control
techniques for plutonium.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 8 – 11
In addition, DOE has issued guidance on use of
air monitoring results when there is a technology
shortfall in Radiological Control Technical Position
(RCTP) 2001-01, Questions and Answers
Concerning Acceptable Approaches to
Implementing Bioassay Program Requirements.
In part, RCTP 2001-01 states that, when there is
a technology shortfall for bioassay and air
monitoring results indicate exposures greater than
100 millirem in a year are likely, one should
assess dose based on the air monitoring results.
As a minimum, personnel who perform operations
in controlled areas should wear coveralls and
shoe covers. For inspections or visits, lab coats
and shoe covers may be permissible. When
contaminated wet areas are to be entered, water-
repellent (plastic or rubber) clothing shall be worn.
No personal outer clothing should be permitted
under coveralls.
Hands should be protected by a minimum of two
barriers; for example, at least one pair of
surgeon’s gloves and one pair of rubber gloves
should be worn.
Protective clothing should be removed at the step-
off pad, and personnel monitoring for
contamination shall be performed.
Respiratory protection equipment shall be readily
available. Respiratory protection equipment
should be used for all bag-out operations, bag
and glove changes, and any situation involving a
potential or actual breach of confinement.
Protection, in the form of air-purifying or
atmosphere-supplying respirators, shall be used
whenever concentrations of radionuclides in the
air are likely to exceed the applicable DACs.
I. Inventory control and accountability requirements
Real-time or near real-time accountability systems
should be incorporated if possible.
Review Radiological Control
Technical Position 2001-01,
Questions and Answers Concerning
Acceptable Approaches to
Implementing Bioassay Program
Requirements
DAC = Derived Air Concentration, a
10 CFR 835 limit for airborne
radioactivity.
Show OT 8.12.
Radiological Assessor Training
DOE-HDBK-1141-2008
Section 42
Instructor’s Guide
Module 8 – 12
J. Criticality safety considerations
Criticality alarm systems (gamma or neutron) shall
be provided in each area where an accidental
criticality is possible.
Criticality safety requirements may include:
ANSI/ANS 8.3-1986, Criticality Accident Alarm
Systems; ANSI/ANS 8.1-1983, Nuclear Criticality
Safety in Operations with Fissionable Materials
Outside Reactors; and ANSI/ANS 8.19-1984,
ANS Administrative Procedures for Nuclear
Criticality.
It is important to review site requirements
documents prior to conducting the assessment.
All DOE facilities that possess sufficient quantities
and kinds of fissile material to potentially
constitute a critical mass shall provide nuclear
accident dosimetry.
Reference 10 CFR 835.1304.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Work Permits
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify types of job hazards that are not addressed by Radiological Work
Permits (RWPs).
2. Describe the two basic types of RWPs.
3. Determine the types of jobs that may and may not be worked under the
controls imposed by RWPs.
4. Identify typical time limits for the two basic types of RWPs.
5. List essential elements of an effective RWP.
6. List RWP program elements that may be included in a radiological
assessment.
Training Aids:
Overhead Transparencies (OTs): OT 9.1 – OT 9.11 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Change
Notice 1, March 2005.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
Amended June 2007.
U.S. Department of Energy, Order 440.1-1A, Worker Protection Program for DOE
(Including the National Nuclear Security Administration) Federal Employees Guide
for Use with DOE O 440.1B March 2007.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 2
I. Introduction
10 CFR Part 835.501(d) requires written
authorizations to control entry and perform work in
radiological areas, commensurate with the
radiological hazards. DOE-STD-1098-99,
Radiological Control, Reaffirmed December 2004,
Chapter 3, Part 2, provides guidance on DOE's
expectations for such written authorizations.
These written authorizations may take a variety of
forms tailored to the work processes involved.
Often, the form will be that of a Radiological Work
Permit (RWP), discussed in detail below.
II. Radiological Work Permits (RWPs)
A. Purpose
The RWP is designed to document the
radiological conditions and associated controls
in a work area. The RWP should be integrated
with other work authorizations that address
safety and health issues, such as those for
industrial safety and hygiene, welding, and
confined space entry.
Articles 311 and 312 of DOE-STD-1098-99
provide guidance on preparing work control
procedures consistent with the principles of
Integrated Safety Management. This
includes use of multidiciplinary teams to
prepare work control procedures for tasks
involving significant types of hazards and
referring to U.S. Department of Energy,
Order 440.1-1A, Worker Protection Program
for DOE (Including the National Nuclear
Security Administration) Federal Employees
Guide for Use with DOE O 440.1B March
2007.
Section 43
B. Typical RWP process
1. Requester submits an RWP request form.
Show OT 9.1 and OT 9.2.
State objectives.
Review Chp 3, Part 2 of DOE-
STD-1098-99, Radiological
Control, Reaffirmed December
2004.
Obj. 1
Identify types of job hazards that
are not addressed by
Radiological Work Permits
(RWPs).
Show OT 9.3.
The process may be different at
your site or facility.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 3
2. Radiological Control Supervisor accepts
form, collects additional job information as
necessary, and assures that completion of
appropriate radiological surveys to be
performed in the work area.
3. Radiological Control Technicians, or other
appropriately trained and authorized
personnel, perform surveys, analyze
samples, and report results.
4. RWP controls are established based on the
results of the surveys.
5. Radiological Control personnel, in
consultation with relevant technical staff,
complete, distribute and implement the RWP.
6. Radiological Workers and Radiological
Control personnel review completed RWP,
prior to start of job, during pre-job briefs,
and/or ALARA reviews.
7. Radiological Worker/Supervisor advises
Radiological Control personnel when job is
complete (so RWP can be terminated).
8. Radiological Control personnel maintain
surveys and RWP documentation.
C. Types of RWPs
There are two basic types of Radiological Work
Permits:
• Job-specific RWP
• General RWP
The job-specific permit is used for jobs which
present a greater potential for significant
radiation dose, airborne radioactivity, or spread
of contamination, and which involve “hands on”
work.
Show OT 9.4.
Show OT 9.5.
Obj. 2
Describe the two basic types of
RWPs.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 4
Examples of jobs that would likely require job-
specific RWPs include those where work is:
• Performed with detailed, specific, written
work procedures, approved in advance by
Radiological Control personnel
Obj. 3
Determine the types of jobs that
may and may not be worked
under the controls imposed by
RWPs.
• “Hands-on” work performed infrequently on
radiological systems (e.g., valve replacement
in process buildings)
• Performed in areas in which the radiological
conditions have no history of remaining
stable
The general RWP typically is used for jobs with
less potential for health physics concerns and for
routine, repetitive jobs that do not involve “hands
on” work.
Examples of jobs that may be worked under a
general RWP include:
• Routine tours, inspections, inventories, valve
lineups, equipment tagouts, surveys, and
equipment operation.
• Work routinely performed on nonradiological
systems (e.g., fire protection systems in shut-
down process buildings).
• Routine operations involving radioactive
material for which the radiological conditions
have a history of remaining stable.
Keep in mind that there may be a need for other
(nonradiological) permits or authorizations to
safely perform these jobs. For example permits
may be needed to address nonradiological
hazards, such as: electrical, confined space,
asbestos, hazardous materials, respiratory
protection, fire, heavy equipment and
scaffolding.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 5
D. Time limits
The job-specific RWP usually remains in effect
only for the duration of the job (typically less
than 30 days).
Section 44
The general RWP typically is approved for a
period of time of one year or less.
Show OT 9.6.
Obj. 4
Identify typical time limits for the
two basic types of RWPs.
E. Elements of an RWP include:
• Description of work (detailed)
• Radiological conditions (contamination,
airborne, radiation levels) in the work area
• Dosimetry (TLD badge, self-reading
dosimetry, special dosimetry) requirements
• Requirements for a pre-job briefing, if
necessary
• Radiological Control Technician coverage
(start of job, continuous, intermittent)
• Training requirements to work in the area
• Protective clothing requirements
• Respiratory protection equipment
requirements
• Stay time requirements
• Radiological conditions that may limit work or
void the RWP
• Special dose reduction (ALARA) or
contamination reducing measures to be
considered
Show OT 9.7.
Obj. 5
List essential elements of an
effective RWP.
“Valve work” is not a detailed
work description.
Briefings are needed most for
elevated radiation or
contamination levels: workers in
High Contamination Areas need
briefings more than workers in
Contamination Areas.
Show OT 9.8.
Discuss stay time, accidents,
and alarms.
Discuss staff rotation, alarming
dosimetry, planning, and
shielding.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 6
• Special personnel contamination monitoring
requirements
• Work document number (if used)
• Unique RWP identification number
• Date of permit issue and expiration date
• Signatures of Radiological Worker and
supervisor (attesting to their understanding of
RWP requirements and agreement to follow)
and Radiological Control staff
Show OT 9.9.
If time allows, show examples of
contemporary RWPs,
highlighting required information
and radiological controls.
F. RWP Elements for Radiological Assessment
The following are RWP program elements
which may be reviewed as part of a
radiological assessment:
• RWPs appropriately required for activities
and areas
• Completeness of information on RWPs
• Adequacy of radiological surveys to
support RWP
• Worker adherence to RWP requirements
• RWP appropriately reviewed and
approved
• Adequacy of worker monitoring (TLDs,
bioassay, air monitoring RCT coverage)
specified on RWP
• ALARA considerations included in RWP
• RWP program implemented in accordance
with written procedures
Obj. 6
List RWP program elements that
may be included in a radiological
assessment.
Show OT 9.10.
Show OT 9.11.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 9 – 7
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Contamination Containment and
Temporary Control Measures
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe what temporary engineered radiological controls can be used to
reduce or eliminate contamination spread.
2. Describe why engineered and administrative controls are needed.
Training Aids:
Overhead Transparencies (OTs): OT 10.1 – OT 10.5 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
Section 45
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
Amended June 2007.
U.S. Department of Energy, DOE-STD-1121-98, Internal Dosimetry, Reaffirmation
May 2003.
U.S. Department of Energy, Radiological Control Technical Position 2001-01,
Questions and Answers Concerning Acceptable Approaches to Implementing
Bioassay Program Requirements, 2001.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 2
I. Introduction
10 CFR Part 835, Occupational Radiation
Protection, specifies contamination control
requirements in Subpart L. Chapters 3 and 4 of
DOE-STD-1098-99, Radiological Control,
Reaffirmed December 2004 provides guidance on
meeting the requirements and additional
information for implementing an effective
contamination control program. All of these
documents should be reviewed prior to conducting
an assessment.
II. Contamination containment and temporary control
measures
Minimization of internal dose
The minimization and control of internal dose
should be conducted in accordance with the
following hierarchy of controls:
1. Engineered controls, including containment
of radioactive material at the source
wherever applicable, should be the primary
method of minimizing airborne radioactivity
and internal dose to workers.
Engineered controls are devices such as
glove boxes, glove bags, portable filtration
units, and containment tents. They should
be used to prevent worker inhalation of
radionuclides.
Portable and fixed/permanent shielding
using dense materials (lead) or portable
plastic interlocking fluid filled containers are
also engineered features, used to minimize
external radiation dose.
Show OT 10.1.
State objectives.
Review
10 CFR Part 835, Occupational
Radiation Protection
DOE-STD-1098-99, Radiological
Control, Reaffirmed December 2004
Show OT 10.2.
Obj. 1
Describe what temporary
engineered radiological controls
can be used to reduce or eliminate
contamination spread.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 3
The use of these devices reduces the spread
of contamination, cleanup time, and
decontamination costs. These measures
help maintain doses ALARA. In addition,
they can reduce the need for respirators and
the impact on work in nearby areas.
Engineered controls should be used in
accordance with technical instructions,
proper training, and effective administrative
controls
Site-specific manuals should contain generic
instructions on the design, controls, training,
and use of engineered controls.
2. Administrative controls, including access
restrictions and the use of specific work
practices designed to minimize airborne
contamination, should be used as the
secondary method to minimize worker
internal dose.
Obj. 2
Describe why engineered and
administrative controls are
needed.
Show OT 10.3.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 4
3. Only when engineered and administrative
controls have been applied and the potential
for airborne radioactivity still exists, should
personnel protective equipment, including
use of respiratory protection, be considered.
Chapter 3 of DOE-STD-1098-99 discusses:
Access controls for Contamination Areas
Controlling the spread of contamination
Monitoring for contamination.
Appendix 3 C, Contamination Control
Practices, includes recommended selection
of protective clothing, and a recommended
sequence for donning and doffing.
Section 46
Use of respiratory protection should be
considered under the following conditions:
• Entry into posted Airborne Radioactivity
Areas
• During breach of contaminated systems
or components
• Work in areas or on equipment with
removable contamination levels greater
than 100 times the values in Table 2-2 of
DOE-STD-1098-99
• During work on contaminated or activated
surfaces with the potential to generate
airborne radioactivity
The selection of respiratory protection
equipment should include consideration of
worker safety, comfort, and efficiency. The
use of positive pressure respiratory
protection devices is recommended wherever
practicable to alleviate fatigue and increase
comfort.
Show OT 10.4.
Air-supplied respirators, for
example
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 5
Respirators can provide adequate protection
for workers in an airborne radioactivity
environment, but engineered controls may be
more practical. By using engineered controls
instead of respirators, the worker is not
subjected to the stresses created by wearing
a respirator. It is more difficult to breath and
communicate when wearing a respirator.
Vision is impaired, and the respirator is not
comfortable. Productivity can therefore be
improved by using engineered features
instead of respirators.
To minimize intakes of radioactive material
by personnel, smoking, eating, or chewing
shall not be permitted in Contamination, High
Contamination, Airborne Radioactivity Areas,
or Radiological Buffer Areas established for
contamination control purposes.
Contamination should be contained at its
source. The principle is to prevent
contamination spread from occurring. The
most effective methods based on sound
ALARA principles should be used. All
controls should be documented and clearly
controlled by RWPs.
Respirators may be appropriate for simple,
straightforward jobs.
In specific situations the use of respiratory
protection may be contraindicated due to
physical limitations or the potential for
significantly increased external dose.
Show OT 10.5.
Example: Work in high radiation
fields and airborne radioactivity.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 10 – 6
In such situations, written authorization
should be obtained from the line organization
manager and the Radiological Control
Manager prior to incurring internal dose.
Specific justification of the need to accept the
dose, including a description of measures
taken to mitigate the intake of airborne
radioactivity, should be documented as part
of the radiological work documentation.
The use of personal air sampling programs
should be considered to monitor individual
workers for exposure to airborne radioactive
material, especially when the use of
respiratory protection is contraindicated. This
is particularly important when there is a
bioassay program technology shortfall (i.e.,
the derived investigation level is less than the
minimum detectable activity). Section 4.4.4
of DOE-STD-1121-98, Internal Dosimetry,
discusses use of breathing zone or personal
air monitoring.
In addition, DOE has issued guidance on use
of air monitoring results when there is a
technology shortfall in Radiological Control
Technical Position (RCTP) 2001-01,
Questions and Answers Concerning
Acceptable Approaches to Implementing
Bioassay Program Requirements.
Section 47
In part, RCTP 2001-01 states that, when
there is a technology shortfall for bioassay
and air monitoring results indicate exposures
greater than 100 millirem in a year are likely,
one should assess dose based on the air
monitoring results.
Review Radiological Control
Technical Position 2001-01,
Questions and Answers
Concerning Acceptable
Approaches to Implementing
Bioassay Program Requirements
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Work Site Mockup
Demonstration
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify poor radiological work practices, in and around a mock radiological
work site.
2. Inspect a typical contamination containment (glove bag).
3. Develop field assessment notes to support findings (hands-on exercise).
Training Aids:
Overhead Transparencies (OTs): OT 11.1 (may be supplemented or
substituted with updated or
site-specific information)
Materials needed for this exercise are listed on the following pages.
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control,
Reaffirmation December 2004.
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
The exercise is a mock-up demonstration that is performed
by the instructors to give the participants an opportunity to
assess and identify poor radiological work practices.
The participants should be instructed to identify and make
notes of the poor radiological practices during the
demonstration. After the demonstration, ask the
participants to:
• Identify poor radiological practices
• Make recommendations for improvement
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 2
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
(continued)
Description of Mock-up Demonstration Area
The area is intended to simulate an actual, posted area
where radiological work is performed.
White plastic PVC pipes and junctions are used to create a
support structure for a heavyweight clear plastic
contamination containment (glove bag). The glove bag
measures approximately 2 ft wide x 2 ft high x 3 ft long.
The glove bag has four glove ports, which allow the
installation of four sets of heavy rubber gloves for
Radiological Workers #1 and #2. The bag is suspended
from the PVC pipes by “bungee” cords.
Inside the glove bag is a valve, with two shutoff valves
installed on both sides. The valves are installed on PVC
pipe, which penetrates the glove bag. The penetrations are
taped, to ensure a good seal.
Normally a polyethylene (poly) bottle would be connected
to the glove bag, to collect any liquid released inside the
bag. In this exercise, the poly bottle is intentionally not
installed.
Radiological rope barrier and standard signs (which
intentionally contain improper wording or incorrect color
combinations) surround the posted area, which measures
about 15 ft x 15 ft square. One exit, with step-off pad, is
provided, through which the actors enter the area.
Directly beneath the glove bag is a simulated area of high
radiation called a “hot spot,” with a standard label filled-in
to indicate the dose rate. A yellow lead blanket is provided
to cover (shield) the “hot spot.”
Section 48
The simulated job, which is controlled by a Radiological
Work Permit (RWP), is valve removal by Radiological
Workers #1 and #2, supported by a Radiological Control
(DOE RadCon) Technician, a Quality Inspector, and a
DOE Representative.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 3
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
(continued)
Supplies and Equipment for Mock Exercise
This item is needed: To:
rubber mallet install and dismantle PVC pipe support
standard screwdriver tighten glove hose clamps
pipe wrench tighten valve connections
"hot spot" blank labels enter field information on dose rates
"bogus'" radiological
signs (RADIATION
AREA signs with
incorrect wording and/or
colors)
simulate erroneous posting of radiological
area
step-off pad simulate radiological area exit
razor knife cut glove penetrations into bag
yellow tape seal valve-to-glove bag surfaces
yellow lead blanket shield "hot spots"
yellow poly bottle stage in background, outside radiological
area
stanchions ("rad rope") simulate radiological area boundaries
office trash can serve as a "prop"
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 4
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
(continued)
Setup for Mock Exercise
Complete the following tasks prior to the implementation of
the mock-up exercise:
q Install PVC containment supports, pipe with valve and
glove bag.
q Place a tear in one finger of a glove attached to a glove
bag (large enough to stick a finger through).
q Open both isolation (green-handled) valves.
q Prepare a "hot spot" label and write "500 mrem/hr" on
the label.
q Stick label onto mock hot spot and place yellow lead
blanket over it.
q String yellow and magenta poly rope through stanchions
to establish mock radiological area.
q Place defective signs (wrong color or wording) onto the
rope; for example, “Radiation Zone.”
q Place poly bottle in background (5 ft behind containment
supports).
q Place a yellow plastic waste bag just outside the
radiological area.
q Prepare RWP for this job showing High Radiation Area,
Radiological Buffer Area, thermoluminescent
dosimeters (TLDs) and pocket dosimeters, continuous
Radiological Control Technician coverage, and pre-job
briefing required (instructor reviews with the class
members in an earlier session).
q Brief players before mock exercise (see Module 11 of
Instructor’s Guide).
q Dress players (include “maternity padding” for DOE
Representative).
q Paint simulated cut on right hand of Worker 2.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
(continued)
Setup for Mock Exercise
Complete the following tasks prior to the implementation of
the mock-up exercise:
Q
Q
CO oO O O O O OO
Install PVC containment supports, pipe with valve and
glove bag.
Place a tear in one finger of a glove attached to a glove
bag (large enough to stick a finger through).
Open both isolation (green-handled) valves.
Prepare a "hot spot" label and write "500 mrem/hr" on
the label.
Stick label onto mock hot spot and place yellow lead
blanket over it.
String yellow and magenta poly rope through stanchions
to establish mock radiological area.
Place defective signs (wrong color or wording) onto the
rope; for example, “Radiation Zone.”
Place poly bottle in background (5 ft behind containment
supports).
Section 49
Place a yellow plastic waste bag just outside the
radiological area.
Prepare RWP for this job showing High Radiation Area,
Radiological Buffer Area, thermoluminescent
dosimeters (TLDs) and pocket dosimeters, continuous
Radiological Control Technician coverage, and pre-job
briefing required (instructor reviews with the class
members in an earlier session).
Brief players before mock exercise (see Module 11 of
Instructor's Guide).
Dress players (include “maternity padding” for DOE
Representative).
Paint simulated cut on right hand of Worker 2.
Module 11 —4
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 5
I. Introduction
II. Mockup demonstration
Show OT 11.1.
State objectives.
Refer to previous pages for
instructions on setting up for the
mockup demonstration.
A. Storyboard
Ask participants to observe the
demonstration and watch for poor
radiological work practices.
Encourage participants to write
down poor work practices in their
student’s guide for discussion after
demonstration.
Player(s) Action Dialogue
Workers #1 and #2
Approach posted
radiological area.
Worker #2
Chews gum and rubs
the open cut on his
hand.
Worker #1
Worker #2
Asks Worker #2:
Replies:
"Do you have the
RWP?"
"I thought you had it."
Worker #2
Asks Worker #1:
"Where is that
RadCon Technician?"
Worker #1
Replies:
"I haven't seen him."
Worker #1
Pulls out his pocket
dosimeter, raps it on the
pipe, and reads it.
Asks Worker #2:
"Where is your
dosimeter?"
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 6
Player(s) Action Dialogue
Worker #2
Replies:
"I'll just use your
reading."
Worker #1
Asks Worker #2:
"Are you ready to get
started?"
Worker #2
Replies:
Takes a sip from his soft
drink and places the cup
on the floor.
"In a minute..."
Workers #1 and #2
Enter radiological area.
Engage in small talk:
what happened over
the weekend, hunting,
children.
Worker #2
Sticks used chewing
gum to pipe support.
Notices green isolation
valves are open.
Calls out to Worker #1:
“Hey, these valves are
open.”
Worker #1
Replies to Worker #2:
“So, close them.”
Worker #2
Closes only one valve.
Comments to Worker
#1:
“I wish we had been
trained to work on this
valve. It sure would
be easier if we knew
what we were doing
and had received a
pre-job briefing.”
Worker #1
Replies:
Sticks finger through a
hole in a torn glove bag.
“No big deal, we can
wing it.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 7
Player(s) Action Dialogue
Worker #1
Works a short minute.
Asks Worker 2:
“Have you seen the
replacement valve?”
Worker #2
Points to the valve
outside the area and
replies:
Leaves the area to get
the replacement valve.
“It’s over there, I’ll get
it.”
Worker #1
Loiters in area, close to
“hot spot.”
RadCon Technician
Enters the scene and
walks around the area,
but does not provide
much assistance to the
workers.
Demonstrate his
contamination survey
instrument (with a
pancake probe).
DOE Representative
and Quality Inspector
Enter the area and
engage in small talk with
Worker #1.
Worker #1
Resumes work.
DOE Representative
Relocates lead blanket,
then sits over “hot spot.”
Worker #2
Returns with
replacement valve and
knocks over his soft
drink.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 8
Player(s) Action Dialogue
Worker #1
Worker #2
Worker #1
Worker #2
Section 50
Continues working.
Shakes hands because
they have become wet.
Complains:
Turns to Worker #2 and
replies:
Shuts the valve off.
“Hey, there is rusty
water in this glove
bag.”
“Well, shut the valve.”
Worker #1
Opens the glove bag's
zipper and places the
replacement valve in the
bottom of the glove bag.
Quality Inspector
Worker #2
Quality Inspector
Complains:
Reaches into his pocket
and offers the Quality
Inspector a stick of gum.
Replies:
Takes the gum.
“My mouth is sure
dry.”
“Would you like a stick
of gum.”
“Sure, thanks.”
Quality Inspector
Moves the poly bottle
into area and sits on it.
Quality Inspector
Worker #2
Quality Inspector
Reaches into area to
“help” Workers #1 and
#2 with the job.
Asks the Quality
Inspector:
Replies:
“How many of these
jobs have you done?”
“None, I’m new.
Matter of fact, I’m
scheduled for GERT
next Tuesday.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 9
Player(s) Action Dialogue
Worker #1 and
Worker #2
Worker #1
Remove the defective
valve. Look around for
the bag to place the
valve in.
Complains:
“Where’s the bag to
put this thing in?”
RadCon Technician
Leaves the controlled
area. Returns with the
yellow bag and prepares
to receive the defective
valve from Workers #1
and #2.
Worker #2
Fumbles about and
misses the yellow bag,
dropping the valve on
the floor.
“OOPS”
RadCon Technician
Picks up the valve and
puts it into the plastic
bag, laying it on the
floor. He leaves the
area without monitoring
Quality Inspector
Worker #1
Quality Inspector
Drops his pen into the
area of the spill.
Picks up the pen and
hands it to the Quality
Inspector.
Accepts the pen and
does not request it to be
monitored or
decontaminated.
Quality Inspector and
DOE Representative
Leave the area.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 10
Player(s) Action Dialogue
Worker #1
Worker #2
Worker #2
Asks Worker #2:
Replies:
Places lead blanket over
the spill.
“What should we do
about the spill?”
“It’s almost breaktime.
RadCon will take care
of it later.”
Worker #1
Picks up bagged valve
and throws it into a
nearby trash can.
Workers #1 and #2
Leave the area.
B. Deliberate errors from mock exercise
• Workers #1 and #2 are dressed differently for the
same job
• Protective clothing worn by Worker #1 is not taped
at wrists, ankles
• Bearded Worker #1 wearing respirator
• Half-face respirator used (type not recommended
for radioactive materials)
• Wrong (yellow) canisters installed in mask
• Worker #2 chews gum
• No RWP copy at work site
• No RadCon Technician present (RWP calls for
continuous coverage)
• Worker #1 abuses pocket dosimeter
• Worker #2 has no pocket dosimeter
• Quality Inspector, RadCon Technician, and DOE
Representative have no TLD badges
• Worker #2 drinks soft drink in area
• Green isolation valves not closed prior to beginning
work
• No pre-job briefing (based on dialogue)
• No training for this job (based on dialogue)
• Torn glove (glove bag not inspected for integrity
prior to job start)
• No corrective action to torn glove
Ask participants to identify errors
observed during the
demonstration. Encourage
participants to write down the
errors in their student’s guide,
then discuss each of the errors.
0
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 11
• Replacement valve not taken into area
• Worker #1 loiters in high radiation area while #2
Section 51
gets replacement valve
• RadCon Technician not actively involved in job
assistance
• RadCon Technician does not have proper survey
instrument for measuring radiation levels
• DOE Representative moves lead blanket without
replacing it to original position
• DOE Representative (pregnant) sits over
unshielded hot spot
• Worker #2 has open cut on hand
• Worker #2 creates liquid spill (knocks over soft
drink)
• Inappropriate response to spill (covers with lead
blanket, no notice to RadCon)
• Quality Inspector is given gum in area and chews it
• Poly bottle not installed for glove bag
• Quality Inspector is in area without having received
General Employee Radiological Training (GERT)
• No yellow plastic bag in area to receive old valve
dropped onto floor
• Worker #2 drops old valve onto floor (creating
another spill)
• RadCon Technician does no monitoring after valve
dropped onto floor
• Quality Inspector drops pen into contamination and
there is no monitoring or decontamination of the
pen
• Worker #1 puts used, contaminated valve into
ordinary trash can
NOTE: Participants will detect other errors that are not
listed.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 11 – 12
This page intentionally left blank.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiation-Generating Devices
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify radiation-generating devices.
2. Describe the basic components of an x-ray machine.
3. Identify the most common use of x-rays.
4. Identify the potential hazards associated with x-rays.
5. Identify the most common use of sealed gamma ray sources and the potential
hazards.
6. Identify the most common use of beta and neutron sources and the potential
hazards.
Training Aids:
Overhead Transparencies (OTs): OT 12.1 – OT 12.11 (may be supplemented or
substituted with updated
or site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 2
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
Amended June 2007.
ANSI N43.2-1989a, Radiation Safety for X-ray Diffraction and Fluorescence
Analysis Equipment, 1989.
ANSI N43.3-1993, Installations Using Non-Medical X-ray and Sealed Gamma Ray
Sources Energies up to 10 MeV, 1993.
U.S. Nuclear Regulatory Commission, 10 CFR Part 34, Licenses for Radiography
and Radiation Safety Requirements for Radiographic Operations, 1992.
Update to DOE G 441.1-1B, Radiation Protection Programs for Use with Title 10,
Code of Federal Regulations, Part 835, Occupational Radiation Protection.
Section 7.0 Radiation Generating Devices.
Section 15.0 Sealed Radioactive Source Accountability and Control.
U.S. Department of Energy, DOE HDBK-1109-97, Radiological Safety Training for
Radiation-Producing (X-Ray) Devices, Reaffirmation January 2007.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 3
I. Introduction
Section 52
Update to DOE G 441.1-1B, Radiation Protection
Programs for Use with Title 10, Code of Federal
Regulations, Part 835, Occupational Radiation
Protection. Section 7.0 Radiation Generating
Devices, includes provisions for exposure to ionizing
radiation from DOE activities. Included in the 10
CFR 835 definition of a radiological worker is
"operation of radiation producing devices". 10 CFR
835 also specifies requirements for sealed
radioactive sources.
II. DOE Guidance
Update to DOE G 441.1-1B, Radiation Protection
Programs for Use with Title 10, Code of Federal
Regulations, Part 835, Occupational Radiation
Protection. Section 7.0 Radiation Generating Devices,
provides guidance on DOE's expectations for
controlling exposure from radiation generating
devices (RGD). The IG includes a definition of a
RGD as "a collective term for devices which produce
ionizing radiation including, certain sealed
radioactive sources, small particle accelerators used
for single purpose applications which produce
ionizing radiation (e.g., radiography), and electron
generating devices that produce x-rays incidentally."
For sealed radioactive sources, refer to DOE
Update to DOE G 441.1-1B, Radiation Protection
Programs for Use with Title 10, Code of Federal
Regulations, Part 835, Occupational Radiation
Protection, Section 15.0 Sealed Radioactive Source
Accountability and Control.
Article 365 of DOE-STD-1098-99, Radiological
Control, Reaffirmed December 2004 provides
additional guidance, including the use of ANSI
N43.3, ANSI N43.2, and 10 CFR Part 34 for
meeting its requirements covering RGDs.
DOE HDBK-1109-97, Radiological Safety Training
for Radiation-Producing (X-Ray) Devices, provides
guidance on DOE's expectations for radiation safety
training for individuals using RGDs.
Show OT 12.1 and OT 12.2.
State objectives.
Review 10 CFR 835 radiological
worker definition.
Show OT 12.3.
Review Update to DOE G
441.1-1B, Radiation
Protection Programs for Use
with Title 10, Code of Federal
Regulations, Part 835,
Occupational Radiation
Protection, Section 7.0
Radiation Generating
Devices.
Show OT 12.4.
Obj. 1
Identify radiation
generating devices.
Update to DOE G 441.1-1B,
Radiation Protection
Programs for Use with Title
10, Code of Federal
Regulations, Part 835,
Occupational Radiation
Protection, Section 15.0
Sealed Radioactive Source
Accountability and Control.
Review DOE-STD-1098-99,
Radiological Control, Reaffirmed
December 2004
(Article 365).
Review DOE HDBK-1109-97,
Radiological Safety Training for
Radiation-Producing (X-Ray)
Devices
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 4
III. X-ray machines
A. Components
X-ray devices have been in existence for about
100 years. Although there are many different
designs of x-ray machines, they all have the
same basic components. These include a
source of electrons, an electrical potential
difference to accelerate the electrons, and an
anode, or target for the accelerated electrons to
strike.
Usually, the source of electrons in an x-ray
machine is a thin wire filament from which
electrons are emitted when it is heated by a
large electrical current. Controlling the current
through the filament, then, becomes a way to
control the number of electrons available for
acceleration.
The electrical potential difference between the
Section 53
cathode (filament) and the anode (or target) is
the force that accelerates the electrons. The
larger the potential difference, the more kinetic
energy the electrons will acquire. The potential
difference is measured in units of kilovolts (kV).
The energy of the electrons is measured in units
of kilo electron volts (keV), with one electron volt
being the amount of energy required to move
one electron through a potential difference of
one volt.
The accelerated electrons then strike the anode
(or target). The target may consist of various
materials, depending on the purpose and design
of the x-ray tube. X-ray production is most
efficient in high atomic number targets, like
tungsten.
Show OT 12.5.
Obj. 2
Describe the basic components of
an x-ray machine.
The number of electrons moving
across the x-ray tube, or the tube
current, is adjusted on the x-ray
machine control panel with the
milliAmpere (mA) control. In
some x-ray machines, the mA
may be fixed, and not adjustable
by the operator.
Electrons interact in the target by
one of the following mechanisms:
• Excitation
• Ionization
• Bremsstrahlung
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 5
When electrons strike and excite target atoms,
the kinetic energy of the electrons is deposited in
the target as heat. When electrons ionize target
atoms, characteristic x-rays will be emitted as
electrons from outer shells fill vacancies created
by ejected electrons.
B. X-ray energy spectrum
The energy of the x-ray photons coming out of
the x-ray machine is of interest to the users of
the machine. The typical energy spectrum from
an x-ray machine consists of the characteristic x-
rays from the target, which have discrete
energies, and the bremsstrahlung photons which
have a whole range of energies, the maximum
energy depending on the potential difference
across the tube. For a typical x-ray machine, the
bremsstrahlung photons far outnumber the
characteristic x-rays.
When the accelerated electrons
simply decelerate (brake) as they
come near the large, positively
charged nucleus of a target atom, the
change in energy resulting from the
deceleration is emitted as a
bremsstrahlung photon. If the
accelerated electron loses all of its
energy and essentially comes to rest,
then the energy of the bremsstrahlung
photon will be equal to the initial
kinetic energy of the electron.
Show OT 12.6.
Bremsstrahlung is German for
“braking radiation.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 6
C. Design features
The cathode and anode of the x-ray tube are
enclosed in an evacuated glass tube or
envelope. The vacuum is necessary to ensure
that the accelerated electrons will interact in the
target, and not with gas molecules.
The x-rays are produced in all directions in the
target. However, only x-rays directed toward the
exit port, or window, will comprise the useful
beam.
Several devices are used to control the size of
the useful x-ray beam. A lead diaphragm is a
sheet of lead with a hole in it. It is placed near
the exit port, and restricts the size of the useful
beam by absorbing x-rays that don't pass
through the hole. The size of the beam is not
adjustable with this type of device unless
another diaphragm with a different-size opening
is used.
Section 54
For some operations, the size of the useful
beam must be adjusted by the operator. An
adjustable collimator is essentially a set of
movable lead sheets. Two sheets restrict the
width of the beam, and two sheets restrict the
length of the beam. The operator can then
adjust the size of the beam to any desired
combination of length and width.
Often, the lowest energy x-rays are not desired
in the beam. The low energy x-rays can be
filtered out by placing absorbing material (called
filters) in the path of the beam. Aluminum or
copper is commonly used, depending on the
energy of the machine. The addition of filters
increases the average energy of the beam, since
the lower energy x-rays are removed from the
beam when they are absorbed by the filters.
The anode is usually encased in
copper, which serves to dissipate the
heat. In many x-ray machines, the
anode rotates at a high speed, which
increases the area of bombardment
and therefore is also useful in
dissipating heat.
The x-ray tube housing is an
insulated metal casing around the
glass envelope that provides both
electrical and radiation shielding.
The housing will intercept most of
the x-rays produced in the target that
are not part of the useful beam.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 7
D. Common uses and hazards
X-ray machines are most commonly used for
radiography, or the examination or inspection of
the structure of materials by non-destructive
means.
X-ray machines used in medicine are fairly
standardized in appearance, and in the way they
are installed. That is not true of x-ray machines
used for industrial applications. X-ray machines
may be fixed installations, mobile units, or
completely enclosed cabinet systems. The
cabinet x-ray systems are commonly used for
security applications (e.g., baggage inspection
units).
The major hazard from x-ray machines is the
external dose hazard to machine operators and
other people in the vicinity. No one should ever
be exposed to the primary (or useful) beam.
Exposure to leakage radiation (from the housing)
and scatter radiation should be reduced by
appropriate controls.
IV. Analytical x-ray machines
A. Fluorescence analysis
Characteristic x-rays that result from ionization of
atoms can be used to identify atoms, since the
characteristic x-rays will have energies that are
unique to that element. This forms the basis for
x-ray fluorescence spectroscopy. A sample to
be analyzed is irradiated by a beam of high-
intensity x-rays. The x-rays ionize atoms in the
sample, which emit characteristic x-rays when
the electron shell vacancies created by
ionization are filled.
Obj. 3
Identify the most common use of x-rays.
The energy of the x-rays required will
depend on the density, thickness, and
atomic number of the objects or structures
to be imaged, or examined. Dense, thick,
high atomic number objects or structures
require more energetic x-rays.
Show OT 12.7.
Obj. 4
Identify the potential hazard associated
with x-rays.
Show OT 12.8.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 8
The characteristic x-rays can be analyzed by
determining their energy, or by determining their
wavelength. Either way, the result leads to
information about the elemental composition of
the sample.
These instruments are usually completely
enclosed. Access doors are provided for
changing samples, and the doors are equipped
with interlocks to prevent access to the x-ray
beam.
Section 55
The hazard is primarily an external dose hazard
to scattered radiation from the components and
the sample, and is typically fairly low.
B. X-ray diffraction
When x-rays are scattered by a crystalline solid,
they are scattered from the different atoms, but
only in certain directions. This technique is used
for crystal structure research.
The primary beam and the diffracted beams are
very small and well collimated. In some types of
diffraction equipment, the sample cannot be
enclosed in a structure. The primary beam is
controlled by a shutter that opens and closes.
The major hazard associated with diffraction
units is intense, localized exposure from the
primary beam to the hands or eyes that can
occur during sample changing or beam
alignment procedures with the shutter
inadvertently open. The primary beam is very
small, but may have an intensity of up to 40,000
R/min. At this exposure rate, even short
exposures of the hands and fingers could result
in severe injury, and potential loss of fingers.
Collimated = focused
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 9
V. Sealed gamma ray sources
Sealed gamma ray sources are used for a variety of
applications in industry. Gamma ray sources are
the most common sealed source encountered,
although others are used and are discussed later.
Radiography is probably the most common use, and
may be performed with the gamma rays from sealed
sources of Cobalt-60, Cesium-137, or Iridium-192.
Other uses of sealed gamma ray sources are
thickness gauges (e.g., to determine the thickness
of sheet metal), level gauges (e.g., to determine a
fluid level in a container), and density gauges (e.g.,
to measure the geologic formation porosity during
oil and mineral logging).
The hazard from these sources is primarily an
external dose hazard. The most common cause of
overexposure incidents with gamma radiography
sources results from radiographers failing to
perform radiation surveys to verify that the gamma
source is back in the shielded position. Also, if
mechanical damage to the source encapsulation
occurs, radioactive material contamination will be a
hazard as well.
VI. Other sealed sources
Sealed sources of beta particles may be used as
thickness gauges (e.g., measurement of dust on
filter paper, or gauging thickness of thinner plastics).
Show OT 12.9.
Obj. 5
Identify the most common use of
sealed gamma ray sources and the
potential hazards.
Show OT 12.10.
Obj. 6
Identify the most common use of
beta and neutron sources and the
potential hazards.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 10
Neutron sources have a variety of applications and
are commonly used in moisture gauges (e.g.,
determining moisture content in raw materials such
as gravel, wood chips, etc.). The fast neutrons
emitted by the source are moderated by the
hydrogen atoms in the material being measured,
and can then be detected with a neutron detector.
Of course, the more moisture contained in the
material, the more hydrogen atoms will be present.
Neutron sources are also used to some extent for
radiography of very dense materials like lead or
steel, which otherwise would require very high
energy photons to radiograph.
Californium-252 emits neutrons after undergoing
spontaneous fission, and therefore serves as a
neutron source. Neutrons can also be produced
fairly easily by nuclear reactions in certain materials
such as beryllium.
Section 56
The primary hazard from beta and neutron sources
is from the external radiation fields they generate.
These sources would only become an internal
hazard should the source rupture or leak and
radioactive material subsequently is inhaled or
ingested. An additional hazard of neutron activation
exists around neutron sources.
10 CFR 835 Subpart M "Sealed Radioactive Source
Control" establishes requirements for accountable
sealed radioactive sources. Requirements include
provisions for (at intervals not to exceed 6 months):
inventory
posting
leak testing
Fast neutrons moderated (slowed
down) to slow neutrons, which are
detected.
When an alpha-emitting material is
combined with beryllium, the
alpha/beryllium reaction results in
the formation of Carbon-12 and a
neutron. Some common sources of
this type are combinations of
Americium-241 and Beryllium (AmBe
sources) and Plutonium-239 and
Beryllium (PuBe sources). Another
nuclear reaction that can produce
neutrons is the photo-neutron
reaction. For this reaction to occur,
a gamma-emitting material is
combined with beryllium, resulting in
the production of neutrons. An
example of this type of neutron
source is the combination of
Antimony-124 and Beryllium (SbBe
source).
Neutron activation can produce
gamma-emitters (external dose
concern).
Review definition of accountable
sealed radioactive source.
Discuss 10 CFR 835.3(e) provision
to allow 30 day grace period for
certain time intervals.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 11
VII. Other radiation-generating devices
Other radiation-generating devices (RGDs) that may
be encountered are small particle accelerators (<10
MeV) used for radiography, ion implantation, or the
production of incidental photons or particles
(neutron generators).
Some RGDs produce radiation incidental to their
primary purpose. Examples of devices that produce
radiation incidentally are electron beam welders,
electron microscopes, and pulse generators.
VIII. Categorizing RGD installations
The ANSI standards referenced earlier categorize
RGD installations into the following categories for
radiation safety purposes.
A. Exempt shielded installations
The RGD and all objects exposed to the source
of radiation shall be within a permanent
enclosure that, under all circumstances of use,
possesses sufficient inherent shielding and
prevents inadvertent entry to any part of the
body. The exposure at any accessible region 5
cm from the outside surface of the enclosure
shall not exceed 0.5 mrem in any one hour.
Show OT 12.11.
Each category is discussed briefly.
The ANSI standards and other
referenced documents should be
consulted for complete information
and requirements for each category.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 12 – 12
B. Shielded installation
The RGD and all objects exposed to the source
are within a permanent enclosure from which
persons are excluded during the irradiation.
Some of the requirements for shielded
installations include mandatory interlocks,
audible and visual warning devices, a "crash"
button, and posting of warning signs.
Skyshine is the term used to describe radiation
emerging more or less vertically from a shielded
enclosure, which then scatters from air
molecules to produce radiation at some distance
from the source.
C. Unattended installation
The RGD is installed in a single-purpose
Section 57
shielded enclosure, and the design shall ensure
that individuals are not exposed to doses
exceeding 100 mrem in a year.
D. Open installation
Open installations must be conspicuously
posted, and have a conspicuously defined
perimeter. The perimeter must delimit the area
in which the exposure can exceed 5 mrem in
any one hour. The operational staff shall
provide constant surveillance. Other
requirements include use of survey meters,
personnel dosimetry, and temporary shielding.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Radiological Aspects of
Accelerators
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Identify the general characteristics of accelerators.
2. Identify the types of particles accelerated.
3. Identify the two basic types of accelerators.
4. Identify uses for accelerators.
5. Define prompt radiation.
6. Identify prompt radiation sources.
7. Define radioactivation.
8. Explain how contaminated material differs from activated material with regard
to radiological concerns.
9. Identify activation sources.
10. Identify engineered and administrative controls at accelerator facilities.
11. Identify the special radiological concern and recommended instrument for each
type of accelerator radiation survey.
Training Aids:
Overhead Transparencies (OTs): OT 13.1 – OT 13.12 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 2
References:
Stanford Linear Accelerator Center, Health Physics Manual of Good
Practices for Accelerator Facilities, SLAC-327, 1988.
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
Amended June 2007.
DOE G 441.1-1B, Radiation Protection Programs for Use with Title 10, Code of
Federal Regulations, Part 835, Occupational Radiation Protection, Section 7.0
Radiation Generating Devices.
U.S. Department of Energy, DOE HDBK-1108-2002, Radiological Safety Training
for Accelerator Facilities, Reaffirmed January 2007.
U.S. Department of Energy, DOE O420.2B, Safety of Accelerator Facilities, July
2004.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 3
I. Introduction
10 CFR Part 835, Occupational Radiation Protection,
includes provisions for exposure to ionizing radiation
from DOE activities, which includes exposures from
accelerator operations.
II. DOE Guidance
DOE G 441.1-1B, Radiation Protection Programs for
Use with Title 10, Code of Federal Regulations, Part
835, Occupational Radiation Protection, Section 7.0
Radiation Generating Devices provides guidance on
DOE's expectations for controlling exposure from
accelerators.
Article 364 of DOE-STD-1098-99, Radiological
Control, Reaffirmation December 2004 provides
similar guidance, and includes guidance to use the
Health Physics Manual of Good Practices for
Accelerator Facilities, SLAC-327, in meeting
occupational radiation protection requirements for
accelerators.
Section 58
DOE HDBK-1108-2002, Radiological Safety Training
for Accelerator Facilities, Reaffirmation January 2007
provides guidance on DOE's expectations for
radiation safety training for individuals using
accelerators.
Show OT 13.1, OT 13.2, and OT
13.3.
State objectives.
Review DOE G441.1-1B,
Review DOE O 420.2B, Safety of
Accelerator Facilities.
Review DOE-STD-1098-99,
Radiological Control
(Article 364).
Review Health Physics Manual of
Good Practices for Accelerator
Facilities, SLAC-327.
Review DOE HDBK-1108-2002,
Reaffirmation January 2007
Radiological Safety Training for
Accelerator Facilities.
III. General characteristics of accelerators
Accelerators are devices that increase the speed
and thus the energy of charged particles.
A. Accelerator energy
Accelerators are normally rated by the maximum
energy to which the particles are accelerated.
The energy imparted to the charged particles is
determined by the potential difference measured
in volts (V) in the electrical field. At all but the
Obj. 1
Identify the general
characteristics of accelerators.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 4
smallest accelerators, the acceleration is
accomplished by directing the charged particles
repeatedly through regions containing
radiofrequency electromagnetic fields.
One electron volt (eV) is the energy gained by an
electron accelerated through an electric potential
of 1 volt.
An electron accelerated across a gap by means
of a 10,000 volt, or 10 kilovolt (kV), potential
difference is said to have gained 10 kilo electron
volts (10 keV) of energy after crossing the gap.
Other energy units commonly encountered at
accelerators are: MeV (1 million, or 106 electron
volts), GeV (1 billion, or 109 electron volts), and
TeV (1 trillion, or 1012 electron volts). These units
of energy are commonly used not only for
electrons, but for all charged particles.
B. Types of particles accelerated
Particles accelerated include:
• Electrons
• Protons
• Nuclei of various elements
Show OT 13.4.
Obj. 2
Identify the types of particles
accelerated.
C. Types of accelerators
The accelerated charged particle may move in
either a linear (straight line) or in a circular
(curved) path as the result of moving
perpendicular to a magnetic field; these are the
two basic types of accelerators.
1. Linear accelerators
Straight-line accelerators suffer from the
disadvantage that the finite length of flight
path limits the particle energies that can be
Show OT 13.5.
Obj. 3
Identify the two basic types of
accelerators.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 5
achieved.
Linear accelerators include:
• Van de Graaffs
• Cockcrott-Waltons
2. Circular-path accelerators
In circular-path accelerators, magnets guide
the particle along a spiral path, allowing a
single electric field to apply many cycles of
acceleration.
Circular-path accelerators include:
• Cyclotrons
• Betatrons
• Synchrotrons
Until the 1980's, all accelerators used for both
physics research and in practical applications,
such as in medicine and in materials science
operated in a so-called "fixed target" mode. In
this mode the accelerated energetic particles are
delivered to a target made of some material at
rest in the laboratory.
Since that time, research facilities have been
Section 59
constructed in which counter-circulating
accelerated beams of particles collide with each
other, rather than with targets at rest in the
laboratory. The use of accelerated particles in
this "colliding beam" mode has been done to take
advantage of the fact that the total energy of the
colliding particles, including both their kinetic
energies and the energy included in their masses
at rest, becomes available in the collision
process. This condition is not true for fixed target
collisions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 6
Such colliders are not nearly as numerous as
other types of accelerators, but represent
important research facilities in which basic
physics research is conducted.
D. Purpose and uses
Accelerators were originally designed to study the
structure of matter. Accelerators today are used
not only for basic research purposes, but for
many other applications as well. Examples
include:
• Production of radioisotopes
• Generation of bremsstrahlung for radiography
• Induction of fusion
• Pumping for lasers
• Detoxification of hazardous waste
• Production of synchrotron radiation
Show OT 13.6.
Obj. 4
Identify uses for accelerators.
E. Facility size/complexity
Small accelerators/facilities usually mean simpler
controls, less staff to coordinate, smaller areas to
monitor, and fewer points of access to control.
However, small accelerators (lower energy) can
produce very intense levels of radiation.
As the size and complexity of the installation
increases, so does the importance of clear and
concise communication channels and a detailed
formality of operations.
IV. Radiological concerns
A. Prompt radiation
Show OT 13.7.
Obj. 5
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 7
Prompt radiation results from the accelerator
beam or the interaction of the beam with matter
only while the accelerator is operating. Prompt
radiation components include:
1. Primary beam
The primary beam consists of accelerated
charged particles prior to any interactions that
may decrease the beam’s energy or intensity.
It is the most intense form of radiation present
at an accelerator facility and is made
inaccessible to personnel through engineered
and administrative controls.
2. Secondary beam
The secondary beam is produced by
interaction of the primary beam with matter
such as targets or beamline components.
The secondary beam may consist of:
Define prompt radiation.
Obj. 6
Identify prompt radiation sources.
• Electromagnetic radiation
• Neutrons
• Charged particles
3. Skyshine
Skyshine is the term used to describe
radiation emerging more or less vertically
from a shielded enclosure, which then
scatters from air molecules to produce
radiation at some distance from the source.
4. Electromagnetic radiation (photons)
Prompt photons may include those produced
by:
• Bremsstrahlung: Photons emitted through
the deceleration of charged particles in the
beam
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 8
• Electromagnetic cascades: Multiple
photons emitted through initial high-energy
interactions
• Synchrotron radiation: Photons emitted as
charged particles are accelerated in a
curved path (a dramatically more
significant effect for electrons than it is for
protons having the same kinetic energy)
Section 60
• Thermal neutron capture: Photons can be
emitted as a result of nuclear reactions in
which materials present in the accelerator
enclosure absorb thermalized neutrons
produced by the accelerated beams.
5. Neutrons
Neutrons can be produced through nuclear
interactions of the primary and secondary
beams with matter. They can also be
produced by interaction of high energy
photons with matter (photonuclear reaction).
Neutron radiation is a concern within any area
where the beam can interact with physical
objects.
6. Muons
Muons are particles that are physically similar
to electrons, but are about 200 times heavier.
Energies in excess of 212 MeV are required
to produce muons by means of pair
production at electron accelerators. At proton
and ion accelerators, muons cannot readily be
produced at energies below about 140 MeV
since charged pions or kaons, which decay
into muons, must first be produced. Due to
the short ranges of low energy muons in
matter, they are not normally of concern for
accelerators of less than 500 MeV kinetic
energy.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 9
Muons travel mainly in the direction of the
beam that produced them, with very little
deviation from the beam path. They are a
concern directly downstream of targets and
beam dumps.
B. Residual radioactivity (radioactivation)
Radioactivation is the process by which materials
become radioactive. It is commonly referred to
as “induced radioactivity” or simply “activation.”
Generally energies above 10 MeV are needed to
activate materials.
Activated materials will continue to emit radiation
after shutoff of the beam. The length of time
depends on the half-life and quantity of the
activated element.
1. Contaminated materials versus activated
materials
Contaminated materials are considered to be
items with removable surface contamination.
Activated materials are considered to be
volume contamination, meaning the
radioactive materials are dispersed
throughout the items.
Show OT 13.8.
Obj. 7
Define radioactivation.
Obj. 8
Explain how contaminated
material differs from activated
material with regard to
radiological concerns.
Activated materials normally do not present a
potential loose contamination hazard except
during activities such as:
• Grinding
• Burning
• Machining
• Handling filters of coolant water
Activated materials are normally controlled
based on the residual external radiation dose
rate.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 10
2. Activated materials
Materials that may become radioactive
include:
• Any material within the accelerator
enclosure
• Beamline components
• Air
• Liquids
Accelerators used to produce radioisotopes
present special problems because of the
variety of target materials used, and because
the parameters of machine and target are
deliberately optimized to produce radioactive
materials.
Obj. 9
Identify activation sources.
• Beamline components
Items that intercept a portion of the beam are
most likely to be activated. Among those
items which have the highest probability for
activation are:
– Targets
– Beam dumps or stops
– Collimators and scrapers
– Septa and other magnets
– Cavities and beamline
• Air
Air and other gases in the accelerator
enclosure may be activated. Typically, the
activation products are short-lived gaseous
radionuclides of the elements in the air.
Examples are Oxygen-15 from Oxygen-16.
Section 61
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 11
The two major concerns of air activation
products are:
– Worker (delays entry)
– Environmental (releases from enclosures)
• Liquids
Tritium is frequently produced in water used to
cool the target and/or experimental
equipment. As this water supply is usually a
closed system, the concentration of the tritium
in the water will slowly increase.
Other activated liquids may include:
– Oil in vacuum pumps
– Cryogenic fluids
C. Ancillary sources
Accelerators employ devices to either impart
energy to particles, or redirect them during the
acceleration process. The following devices may
emit ionizing radiation while they are operating.
1. Klystrons
Klystrons provide power to accelerate
charged particles. They emit x-rays during
operation.
2. Radiofrequency (RF) cavities
These devices accelerate charged particles
using electromagnetic fields. Trace gases
within the RF cavity cause photons to be
emitted by the accelerated particles.
3. Electrostatic separators/septa
These devices split a particle beam into two
beams using static electric fields. The high
voltages associated with these devices cause
electrons to accelerate in the vacuum within
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 12
the beamline. They emit x- or gamma rays.
V. Radiological and other controls
Controls are used at accelerator facilities to protect
personnel from exposure to ionizing radiation and
other hazards, which include:
• Electrical
• Mechanical
• Cryogenic
• Nonionizing radiation
The design of an effective safety program
incorporates a combination of engineered and
administrative controls.
A. Engineered controls
Engineered controls are the primary controls at
an accelerator facility.
1. Active engineered controls
Active engineered controls include devices
that sense changing conditions and can
trigger a safety action. Examples may
include:
• Status lights
• Alarms
• Interlocks
• Scram buttons
2. Passive engineered controls
Once installed, passive engineered controls
are used to prevent personnel entry or reduce
Show OT 13.9.
Show OT 13.10.
Obj. 10
Identify engineered and
administrative controls at
accelerator facilities.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 13
radiation dose and require no further action to
perform their intended function. Passive
engineered controls may include:
• Barriers
• Shielding
B. Administrative controls
Administrative controls require human interaction
in order to be effective.
Key administrative controls include:
• Signs/postings
• Search and secure (sweep) procedures
• Controlled access procedures
• Configuration control procedures
• Radiological Work Permits (RWPs)
VI. Monitoring
Monitoring for radiation at accelerators can be
complicated. Special techniques and
instrumentation may be necessary due to the
existence of:
• Mixed radiation fields (photons, protons,
neutrons)
• Pulsed beams
• Very high-energy radiation
• High dose rates
Show OT 13.11.
Show OT 13.12.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 14
A. Prompt radiation
Measurements of prompt radiation fields are
required for occupational and environmental
monitoring and for accident dosimetry and
calibration of dosimeters, as well as for research
purposes. In selecting measurement techniques
and instruments, it is important to consider the
purpose of the measurement and the radiation
field’s parameters.
Section 62
1. Mixed radiation fields
The complexity of the radiation field and the
radiation measurements increase with the
energy of the accelerator.
2. Pulsed radiation
Prompt pulsed radiation must be measured
with specialized survey instruments. Ion
chambers are typically used and are
recommended.
3. Neutrons
Neutron monitoring is complicated and must
be conducted by highly trained individuals
with specialized instruments.
B. Environmental monitoring
Environmental sampling/monitoring may include:
• Prompt radiation (neutrons, skyshine, muons)
• Sampling exhausted air from beam housings
• Surface/groundwater (on and off site)
• Monitoring of radiation levels at site boundary
(from storage areas)
Obj. 11
Identify the special radiological
concern and recommended
instrument for each type of
accelerator radiation survey.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 15
C. Personnel monitoring
Simple dosimeters, such as those used in
personal dosimetry and simple survey
instruments, should be calibrated when possible
in radiation fields that are similar to those in
which they will be used. To interpret
measurements made with these instruments, one
must know as much as possible about the
radiation field that is being measured.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 13 – 16
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 - 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Assessment Techniques
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe the difference between structured and unstructured assessments.
2. Describe the difference between vertical and horizontal reviews.
3. List the documents needed in order to perform a radiological assessment.
4. Define the term assessment.
5. Describe how to evaluate a contractor assessment program.
6. Describe the desired characteristics of performance goals.
7. List five performance indicators used in assessing Radiation Protection
Program effectiveness.
Training Aids:
Overhead Transparencies (OTs): OT 14.1 – OT 14.13 (may be supplemented or
Substituted with updated
or site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 - 2
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, 1999.
U.S. Department of Energy, 10 CFR Part 835, Occupational Radiation Protection,
1998.
U.S. Department of Energy, DOE G441.1-1, Management and Administration of
Radiation Protection Programs Guide, 1999.
U.S. Department of Energy, Order 232.1A, Occurrence Reporting and Processing
of Operations Information, 1997.
U.S. Department of Energy, DOE-EM-STD-5505-96; DOE Limited Standard
Operations Assessments, 1996.
DOE-STD-1070-94; DOE Standard Guidelines for Evaluation of Nuclear Facility
Training Programs, Reaffirmed 1999.
Radiological Assessors Training (for Auditors and Inspectors)
Applied Radiological Control
Instructor’s Guide
Module14–1
I. Introduction
Self assessment is part of an effective worker health
Section 63
and safety program. As such, there are many
requirements related to conducting self
assessments and maintaining quality assurance
programs, such as those required under 10 CFR
830.120 ,or as part of an effective Integrated Safety
Management program. This module focuses on the
radiation protection required assessments and
audits.
10 CFR Part 835, Occupational Radiation
Protection, requires, in 10 CFR 835.102, that
internal audits of the Radiation Protection Program
be conducted at least every 36 months. The audits
shall include all radiation protection functional
elements.
Section 4.1.4 of DOE G441.1-1, Management and
Administration of Radiation Protection Programs
Guide, provides guidance on meeting the 10 CFR
835 requirement for audits. Section 4.2 of the
Guide includes a listing of radiation protection
functional elements and associated DOE guidance
documents.
Article 134 of DOE-STD-1098-99, Radiological
Control, provides additional guidance on
radiological control assessments.
Show OT 14.1 and OT 14.2.
State objectives.
Review DOE G441.1-1,
Management and Administration of
Radiation Protection Programs
Guide.
Review Article 134 of DOE-STD-
1098-99, Radiological Control.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -2
II. Types of assessments
It can be extremely damaging if we, as overseers,
facility representatives, and assessors, violate the
high standards of performance and rules that we
are to assess. It is important to understand that we
are constantly being monitored and that we must
set the example with regard to radiological
protection.
The methods used to gather or capture information
can detract from the effectiveness of the
assessment process.
Assessment techniques can be enhanced through
training and practice. These techniques will
improve the ability to see, observe, and better
understand.
There are two types of assessments: unstructured
and structured. “Unstructured” reviews means “not
looking for one specific area or thing.” “Minimum
preparation” method is accomplished through going
with workers on routines. These could be described
as general assessments.
It is very important to understand
that we are dealing with people
and that we have some of the
same human tendencies that they
do.
Follow all health physics rules.
Good interpersonal skills are
essential.
Show OT 14.3.
Obj. 1
Describe the difference between
structured and unstructured
assessments.
The more preparation put into the assessment, the
more effective it is, no matter what type of
assessment is conducted.
The second type of assessment is “structured,”
which involves looking specifically at one issue and
reviewing it from every angle.
Two traditional methods within the structured
inspection are the vertical and horizontal review.
Vertical review is the assessment of a narrow
subject area in great detail, for example, assessing
the Radiological Control Organization from top to
bottom.
Horizontal review is the assessment of a broad
Obj. 2
Describe the difference between
vertical and horizontal reviews.
Show OT 14.4.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -3
range of related subjects in generally less detail, for
example, assessment of radiological protection
across all organizations at a nuclear facility.
III. Assessment guidance
A. Documents
IMPORTANT: Put the burden of producing
Section 64
documents on the site. If the site personnel
state that it is not appropriate that they comply,
they must provide DOE with written support for
that position.
The DOE and site basic documents an assessor
should have for radiological compliance include
(determine the extent of applicability and site
commitments to adhere to the documents):
• 10 CFR Part 835
• Site Radiation Protection Program
• DOE-STD-1098-99, Radiological Control
• Other applicable federal regulations
• Applicable DOE orders
Ask why the documents are
needed.
Obj. 3
List the documents needed in
order to perform a radiological
assessment.
Show OT 14.5.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -4
• State regulations
• DOE Implementation Guides
• Site DOE contract
• Site commitments (corrective actions,
DNFSB recommendation responses)
• Site reports (deficiency, occurrence)
• Site-Specific RadCon Manual
• Approved exemptions
• Peer group/industry group
standards/recommendations
– DOE standards
– ANSI standards
– NRC Regulatory Guides
B. Compliance issues
1. Compliance is only the tip of the iceberg.
2. What are the issues?
• What happened?
• Why did it happen?
• Will corrective action prevent recurrence?
• How can we ensure it will not happen
again?
Show OT 14.6.
What can you use to support the
findings?
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -5
3. Determine the degree of consequence of
noncompliance effects and ramifications of
noncompliance.
4. Procedural compliance is only part of the
overall commitment to excellence in
radiological control.
• Acknowledge good practices
The DOE radiological control policy is that
“continuing improvement is essential to
excellence in radiological control.”
• Encourage what is good.
5. Need to distinguish between requirements
("shall" statements) and recommendations
("should" statements).
C. Compliance orders
Compliance orders are issued by the Secretary.
They identify a situation that violates, potentially
violates, or otherwise is inconsistent with the:
• Atomic Energy Act of 1954 as amended
• Nuclear statutes
• Nuclear Safety Requirements
Compliance orders mandate a remedy or other
action, and state the reason for the remedy or
other action.
What is site management doing to
encourage excellence in
radiological protection?
Differentiate between
requirements and good practices.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -6
Examine orders and responses to orders for:
• Timelines
• Accuracy
• Completeness (Was the problem solved?)
IV. Assessing radiological performance
A. Internal audits, inspections, reviews,
investigations, and self-assessments comprise
“assessments” and are part of the numerous
checks and balances needed in an effective
Radiation Protection Program.
Internal audits of the Radiation Protection
Program shall be conducted such that over a
three-year period, all functional elements are
assessed for program performance, applicability,
content, and implementation. These should be
performed by individuals who are organizationally
independent from the organization responsible for
developing and implementing the Radiation
Protection Program.
B. DOE-EM-STD-5505-96; DOE Limited Standard
Operations Assessments, contains very good
methodology for performing assessments.
Section 65
There are three major components of an effective
assessment program: management assessments,
operational assessments, and quality assurance
assessments. For each of these, functional areas
are identified that represent specific areas of
managerial or technical activity. Within each
functional area, performance objectives are
defined that represent essential characteristics or
conditions of an effective safety program. The
criteria associated with each performance
objective are intended to serve as guidelines for
the assessments.
Show OT 14.7.
Obj. 4
Define the term assessment.
Reference 10 CFR 835.102.
Show OT 14.8.
Obj. 5
Describe how to evaluate a
contractor assessment.
Review DOE-EM-STD-5505-96;
DOE Limited Standard
Operations Assessments.
Provide an example of a
fundamental area and associated
performance objectives and
criteria.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -7
Both management and operational assessments
are operationally focused and performance-
oriented. They deal with the safety culture of the
facility, how safely it is being operated, and the
condition of its documentation and equipment.
The design of the facility and its process
systems is presumed, for purposes of the
management and operational assessments, to
permit safe operation. This is based on the
presumption of an appropriate selection and
application of design standards by the architect-
engineer and the operating contractor, and of
appropriate independent reviews by DOE or its
predecessor agencies of the design, the
construction activities, and the Safety Analysis
Report.
The criteria listed do not address every activity
that might be relevant to a performance
objective. Therefore, meeting all criteria does
not necessarily ensure that the performance
objective is fully met. Conversely, a specific
facility might achieve the performance objective
without meeting all criteria.
In part, because of the various ways in which the
performance objectives can be met, effective
assessments emphasize the performance
objectives rather than the criteria. The methods
for determining whether a criterion is met are not
given. Consequently, considerable expertise
and judgment are required to be exercised in
conducting the assessments.
Although the quality assurance assessments
have a broad perspective, covering the overall
quality assurance program of the facility, they
are relevant to assessing radiological protection
performance.
DOE-STD-1070-94; DOE Standard Guidelines
for Evaluation of Nuclear Facility Training
Programs, provides guidance on evaluating
training programs at nuclear facilities.
Review DOE-STD-1070-94; DOE
Standard Guidelines for Evaluation
of Nuclear Facility Training
Programs.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -8
C. Radiation Protection Program deficiencies
Managers should encourage the positive view
that identifying even minor deficiencies
represents an opportunity for further
improvement.
Radiological work practices should be
continually scrutinized and questioned so that
opportunities for improvement can be identified,
assessed, and incorporated into the Radiation
Protection Program.
The number of deficiencies, alone, does not
measure the overall quality of the Radiation
Protection Program.
D. Critiques
One assessment method is the critique. An
honest review and establishment of facts, which
are in chronological order, is necessary to arrive
at the truth.
Section 66
This is a formal process established to obtain
pertinent facts following an unusual radiological
situation or at the satisfactory conclusion of a
new or unusual operation involving radiological
controls.
The process should be used to quickly establish
facts in chronological order so that the
underlying reasons or causes for the success or
failure are well understood. Work force
participation should be encouraged. Critiques
are a management tool and should not be used
to “fix blame” or “shoot the messenger.” This
process complements the Occurrence Reporting
and Processing of DOE Order 232.1A.
Show OT 14.9.
The type of deficiency must also
be considered. For example, sites
with a more aggressive program to
identify deficiencies would tend to
have more.
Show OT 14.10.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -9
In developing corrective action plans, managers
should address basic underlying reasons for the
identified deficiencies or concerns, not just the
specific symptoms identified by the reviewer.
E. Radiation Protection Assessment Program
To accurately assess the performance of the
Radiation Protection Program, an assessment
program should be formalized, created, and
implemented.
Elements of a Radiation Protection Assessment
Program
Hold open discussion on
elements of a Radiation
Protection monitoring and
assessment program. List
responses on the flip chart.
Encourage participants to write
responses in their Student’s
Guide. Responses should
include:
• Problem areas
• Reportable occurrences
• Critiques
• Performance indicators
• Goals
Stress why these responses are
important to the effectiveness of
the program.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -10
F. Radiation Protection Program Performance
The contractor senior site executive should
establish, approve, and maintain a radiological
performance goals program. The performance
goals should be measurable, achievable,
auditable, challenging, and meaningful in
promoting improvement. Chapter1, part 3 of
DOE-STD-1098-99, Radiological Control,
provides guidance on appropriate radiological
goals.
Goals need to be developed primarily by those
responsible for performing the work. Forming a
Radiological Awareness Committee that
includes the active participation of the work
force is encouraged.
Radiological performance goals should be
reviewed at least annually and revised as
appropriate. Normally, more stringent goals
should be set annually to reflect the improved
radiological performance at the facility.
Occasionally, the goals may be made less
stringent to accommodate changes in work load
or mission.
G. Performance indicators
To evaluate performance, one needs to be able
to measure change. This means dimensions
must be identified. One must be able to track,
trend, post, paint, count, look at, and assign
numbers. What gets measured, gets done.
Show OT 14.11.
Obj. 6
Describe the desired characteristics
of performance goals.
Show OT 14.12.
Review chapter 1, part 3 of DOE-STD-
1098-99, Radiological Control.
Obj. 7
List five performance indicators used
in assessing Radiation Protection
Program effectiveness.
Show OT 14.13.
Ask participants for performance
indicators. Hold open discussion.
List responses on the flip chart.
Encourage participants to write
responses in their Student’s Guide.
Refer to Table 1-1 of DOE-STD-
1098-99, Radiological Control.
Section 67
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -11
Responses should include:
1. Exposure control
• Collective dose
• Average worker dose
• Maximum dose to
worker
• Number of unplanned
doses greater than the
administrative control
level
• Number of dose
assessments for lost or
damaged dosimeters
• Maximum neutron dose
to a worker
2. Personnel contamination
• Number of skin and
personal clothing
contaminations
• Number of contaminated
wounds
• Number of facial
contaminations
3. Control of internal exposure
• Number of positive
bioassays
• Number of airborne
events
• Number of alarms on
airborne monitors (actual
and false)
• Number of Airborne
Radioactivity Areas
• Area of Airborne
Radioactivity Areas in
square feet
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 14 -12
4. Control of Contamination
Areas
• Number of
Contamination and High
Contamination Areas
• Area of Contamination
Areas in square feet
• Area of High
Contamination Areas in
square feet
• Number of spills
5. Minimization of radioactive
waste
• Volume and activity of
radioactive waste in
cubic feet and curies,
respectively
• Cubic feet of waste not
subject to volume
reduction by
incineration, compaction,
or other means
6. Control of radioactive
discharges
• Volume and activity of
radioactive discharges in
cubic feet and curies,
respectively
• Number of unplanned or
accidental releases
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Planning and Conducting
Assessments
Objectives:
Upon completion of this lesson, the participant will be able to:
1. List 10 of the 19 elements of a Radiation Protection Program.
2. Identify five deficiencies in a Radiation Protection Program that point to the
need for an assessment.
3. Describe the preparations needed to conduct a Radiation Protection Program
assessment.
4. Describe how to conduct a Radiation Protection Program assessment.
5. Describe two qualifying conditions for a follow-up assessment.
6. Describe what actions should be taken when assessments indicate marginal
radiological control performance.
Training Aids:
Overhead Transparencies (OTs): OT 15.1 – OT 15.24 (may be supplemented or
substituted with updated
or site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE G441.1-1B, Management and Administration of
Radiation Protection Programs Guide, 2007.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -2
I. Introduction
II. Assessments
A. Reasons for conducting assessments include the
following:
• Determine regulatory compliance.
• Formally document Radiation Protection
Program strengths and weaknesses.
• Investigate a specific incident.
• Document conditions that need a follow-up
assessment.
B. Basic elements of a Radiation Protection
Program
• Organization and administration
• Personnel training and qualification
• Quality assurance
• ALARA
• Radiological work control
– Procedures
– RWPs
• Posting and labeling
• Radioactive material control
– Source control
– Release of materials
– Receipt and transportation
Show OT 15.1 and OT 15.2.
State objectives.
Section 68
Ask for reasons for conducting an
assessment. List responses on
flip chart.
Ensure that responses include
four reasons listed in lesson plan.
Show OT 15.3.
Obj. 1
List 10 of the 19 elements of a
Radiation Protection Program.
Explain the essential functions of
each element in contributing to
an effective program.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -3
• Radiation-generating devices
– Sealed source
– X-ray machines
• Entry control
• Contamination control
• Instrumentation and alarms
• Monitoring
– Workplace
– Effluent
– Environmental
• Dosimetry
– External
– Internal (bioassay)
• Respiratory protection
• Facility-specific features
– Uranium
– Plutonium
– Tritium
– Accelerators
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance indicators
C. Indications that an assessment is needed
• Exceeding administrative dose control levels
or regulatory limits
• Loss of control of radioactive material
Show OT 15.4.
Show OT 15.5.
Show OT 15.6.
Obj. 2
Identify five deficiencies in a
Radiation Protection Program that
point to the need for an
assessment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -4
• Unmonitored/excessive release of
radioactive material to the environment
• Excessive numbers of skin contamination
incidents
• Uptakes of radioactive material by
employees
• Excessive numbers of radiological incidents
• Inadequate training
• Ineffective work control systems
• Incomplete or inaccurate radiological surveys
• Incomplete or inaccurate records
III. Preparing for the assessment
To adequately prepare for the assessment:
• Review operating history
• Examine previous assessment reports
• Collect input from person(s) assessed
• Determine applicability of industry issues
• Review policies and procedures
• Assemble regulations and guidance documents
• Prepare an assessment plan
Show OT 15.7.
Show OT 15.8.
Obj. 3
Describe the preparations needed
to conduct a Radiation Protection
Program assessment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -5
A. Operating history
Review the operating history. The following
documents can be extremely helpful in preparing
for the assessment:
• Occurrence reports
• Radiological deficiency reports
• Violations/citations
• Facility design changes
B. Previous assessments
Examine previous assessment reports.
Documents that could be helpful are:
• DNFSB Recommendations
• Self-assessments
• Corporate quality assurance reports
• External audits
C. Input from person(s) to be assessed
• Management
• Radiological Control Manager
• Radiological Control Organization’s
“customers”
D. Industry issues
• Emerging technical issues
• Application of best industry standards to site
program
Show OT 15.9.
Show OT 15.10.
Show OT 15.11.
Show OT 15.12.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -6
E. Policies and procedures
• Operating procedures
• Radiological control policies
F. Regulations and guidance documents
• Federal
• State
• Site
• Industry or peer group
G. Assessment plan
• Identify elements to be assessed.
• Generate specific questions and/or standards
against which to measure performance.
• Develop record sheet for assessment
responses, data, and field notes.
• Allocate time for each assessment activity.
• Intentionally leave unscheduled time.
Section 69
IV. Conducting the assessment
A. General guidance
Remember the assessment is a positive activity,
designed to help those being appraised. Follow
the plan, but be flexible.
Include nothing in the assessment findings that
is not based on fact, requirement, or
commitment. If in doubt, leave it out (but raise it,
informally as a matter deserving a closer look).
Show OT 15.13.
Show OT 15.14.
Show OT 15.15.
Have a backup plan for slack
time. Preparation time should
equal or exceed time spent
conducting the assessment.
Obj. 4
Describe how to conduct a
Radiation Protection Program
assessment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -7
Share the findings with the point(s) of contact
each day. There should be no surprises at the
daily Radiological Control Manager debriefing or
at the final debriefing.
B. Announced versus unannounced assessments
1. Announced assessments are scheduled
through a pre-assessment memorandum. The
following information should be addressed:
• Assessment objectives
• Assessor(s)
• Assessment duration
• Request for a site point of contact
• Any special needs
• Recommended time and place for pre-
and post-assessment conferences
2. Unannounced assessments
• Used to determine “real” program
performance
• Back-shift, off-hours tours may reveal
relaxation in program standards
• Vary the assessment schedule
Note: Contact the Radiological Control
Manager and line management immediately
if there is a serious problem.
Show OT 15.16.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -8
3. Available methods for conducting an
assessment include:
• Document reviews
• Personnel interviews
• Field observations
4. Recommended assessment approach (in
order)
• Review upper-tier procedures describing
the Radiation Protection Program.
• Conduct a short (one hour or less) tour of
the site/facility.
• Interview Radiological Control
Organization staff and “customers.”
• Conduct detailed and follow-up tours,
interviews, and document reviews.
5. Perform document reviews of:
• Operating procedures
• Records for:
– Dosimetry
– Work control Radiological Work Permit
– Surveys (contamination, radiation
level, air, special)
– Occurrence, deficiency reports, and
critiques
– Regulatory reports
– Radioactive effluent reports
– Training and qualification
– Instrument calibration and response
testing
• Special studies
Show OT 15.17.
Show OT 15.18.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -9
6. Site/facility tour
• Tour the site/facility, preferably with an
experienced individual from the site.
• Make notes of housekeeping and facility
condition. Items to look for include:
– Leaks, spills
– Dirt, rust, and clutter
– Poor equipment maintenance
– Radiological control posting
– Radiological Control Technician and
Radiological Worker interface
– Employee morale
7. Conduct interviews with the following:
• Radiological Control Manager
• Radiological Control Supervisor(s)
• Radiological Control Technical Leads
• Qualified Radiological Control Technicians
• Radiological Control Organization’s
“Customers”
• DOE Site Representatives
• Facility Manager
The following are the details:
• Radiological Control Manager
– Knowledge of current radiological
control regulations, industry standards
– Identification of program deficiencies
and priorities
– Obstacles to improving program
performance
Section 70
Show OT 15.19.
Show OT 15.20.
Attempt to determine the
information for each of the
positions interviewed.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -10
• Radiological Control Supervisor(s)
– Level of support given Radiation
Protection Program and Radiological
Control Manager
– Identification of program deficiencies
and priorities
– Obstacles to improving program
performance
Note: Compare responses to those from
Radiological Control Manager.
• Radiological Control staff members
responsible for major technical functional
areas.
Examples of these functional areas
include:
– Organization and administration
– Personnel training and qualification
– Quality assurance
– ALARA
– Radiological work control
+ Procedures
+ RWPs
– Posting and labeling
– Radioactive material control
+ Source control
+ Release of materials
+ Receipt and transportation
– Radiation-generating devices
+ Sealed source
+ X-ray machines
– Entry control
– Contamination control
– Instrumentation alarms
– Monitoring
+ Workplace
+ Effluent
+ Environmental
– Dosimetry
+ External
+ Internal (bioassay)
– Respiratory protection
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -11
– Facility-specific features
+ Uranium
+ Plutonium
+ Tritium
+ Accelerators
– Radioactive waste management
– Emergency response
– Records
– Assessments/performance indicators
Document their responses to incidents in
their technical area.
Discuss impediments to improving their
programs.
• Qualified Radiological Control Technicians
– The depth and breadth of knowledge of
radiation protection
– Technical issues unique to the
site/facility
– Effectiveness of the working
relationship between Radiological
Control Technicians and their
“customers”
• Radiation Protection Program “customers”
– Knowledge of fundamental radiation
protection concepts and good
Radiological Worker practices
– Working relationship with the
Radiological Control Technicians
– Obvious or hidden problems
– Poor communications
– Division of work problems
– Overall, how the Radiological Control
Organization is regarded (“policeman”
vs. team member)
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -12
• DOE Representatives
– If the Radiological Control Organization
staff solicits his/her input on technical
decisions affecting Radiation Protection
Program performance
– If the relationship is one of mutual
respect or adversarial in nature
• Facility Manager
– Whether the Facility Manager has
made a written commitment and is
striving to achieve excellence in the
Radiation Protection Program
– His/her perspective on how the
Radiation Protection Program should
be improved, and the necessary
priorities
8. Observe Radiological Workers/Radiological
Control Technicians in the workplace
• Recommendations for observing work
include:
– Dress as the individuals being
observed are dressed.
– Work the same hours they work.
– Stand away from the immediate work
area, but close enough to watch the
work proceed.
– Resist the urge to get involved in the
work.
– Be professional and courteous, but not
familiar.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -13
• Key areas to watch for include:
– Procedure violations
– Failure to follow RWP requirements for:
+ Dosimetry
+ Protective clothing
+ Respiratory protection
+ Radiological Control Technician
coverage
+ Surveys
+ Special instructions
Section 71
– Poor Radiological Worker practices:
+ Reaching across radiological
boundaries
+ Scratching body with gloved hand
+ Inadequate frisking
+ Loitering in a high radiation field
– Lack of organization or formality in the
work process
– Poor housekeeping, disorderly work
area
– Wasted time and effort due to
ineffective work planning
– Communication problems
– Poor relationships between
Radiological Workers and Radiological
Control Technicians
C. Post-assessment actions
At the post-assessment conference, summarize
the findings identified during the assessment.
This is an opportunity for additional questions
about the findings. Any requests for corrective
actions, dates, or a need for follow-up
assessments can be identified at this time.
Thank everyone for cooperation and support
during the assessment.
1. Publish assessment findings.
Show OT 15.21.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -14
2. Receive site responses, which should include
the following:
• Action items
• Responsible individuals/groups
• Action item due dates
3. Accept/reject/modify responses.
4. Develop corrective action tracking list.
5. Publish a periodic action item status report.
6. Maintain a separate file of open action items.
7. Personally verify the closure of action items.
8. Evaluate the adequacy of actions taken to
close open findings:
• Has root cause been correctly identified
and corrected?
• Are follow-up assessments needed?
D. Follow-up assessments
1. Qualifying conditions
• Widespread problem
– Problem occurs at several locations in
the same facility or several facilities at
the same site.
– Problem identified by the assessment
is only part of a larger, more generic
deficiency.
• Recurring problem: earlier efforts to
resolve the problem have been ineffective.
Show OT 15.22.
Show OT 15.23.
Obj. 5
Describe two qualifying
conditions for a follow-up
assessment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -15
2. Actions
• Widespread problem
– Take a longer sample to confirm/refute
a widespread problem
– Look for related problems in the same
work unit.
• Recurring problem
– Scrutinize root cause analysis.
– Try a different approach to solving the
problem.
– Solicit outside help. Perhaps others
have “lessons learned”.
3. Incorporate follow-up assessment information
into corrective action tracking system.
V. Marginal radiological performance
When radiological control performance is less than
adequate, strengthen line management’s
commitment to radiological control by notifying the
Radiological Control Organization to obtain their
support in improving radiological support.
In cases where the work force does not have the
required level of sensitivity for radiological work
practices, additional management attention is
needed to assure the proper outcome. Line
management should be held accountable for
implementation of the Radiation Protection Program.
Show OT 15.24.
Obj. 5
Describe what actions should be
taken when assessments
indicate marginal radiological
control performance.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 15 -16
Initial actions should include:
• More direct line supervision in the work space
• Curtailment of work schedules
• Addition of extra radiological control personnel
• Conduct of additional training
Take action, then reevaluate
conditions. If necessary, repeat
and/or revise actions until
deficiency is resolved.
Section 72
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Case Studies
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Describe causes of radiological incidents.
2. Identify primary cause and contributing causes of radiological incidents.
3. Describe effective corrective actions.
Training Aids:
Overhead Transparencies (OTs): OT 16.1 – OT 16.7 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
References:
Investigation Report KY/E-112, C-337-A Contamination Incident at the Paducah
Gaseous Diffusion Plant, 1991.
Martin Marietta Energy Systems, Occurrence Report, ORO–MMES-
PGDPOPERD-1991-1045, 1991.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 2
I. Introduction
II. Case studies guidance
Point to remember: If each root cause is not
adequately treated/corrected by a corrective action,
recurrence of the event or some variation of it is
likely.
Review a reconstruction of events from the available
data.
A proper investigation report or occurrence report
reconstructs the events as they occurred.
Show OT 16.1.
State objectives.
The radiological incident about
which the case study is
developed concerned a loss of
control of radioactive
contamination at the Paducah
Gaseous Diffusion Plant in
August of 1991. This event was
worsened by the fact that some
contamination was carried
offsite to employees’ homes and
personal possessions.
As a group, discuss the known
facts and whether there is
enough information to
reconstruct the event.
Determine whether the
“performance of the workers” or
the “systems in place” led to the
event. This discussion will lead
to how the systems support the
workers and the workers
support the systems.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 3
III. Description of occurrence (edited from investigation
report)
A. Incident
The layout of the buildings and equipment at this
site are included.
Two employees at the Paducah Gaseous Diffusion
Plant (PGDP) received skin and clothing
contamination from Thorium-234 (234Th) and
Protactinium 234m (234mPa) while disconnecting a
used uranium hexafluoride (UF6) cylinder at the
C-337-A building, UF6 Feed Vaporization Facility, on
August 23, 1991.
B. Scenario of events
Starting at shift change, 12 employees, one of them
a Health Physics Technician, found contamination
on shoes and clothing. The incident was initially
identified during routine monitoring of the C-337-A
facility by a Health Physics Technician at 0900 (two
hours after the shift change). Efforts were initiated
by Health Physics to survey the area, identify the
source, and control the spread of contamination.
Surveys indicated widespread contamination in both
radiological and nonradiological areas of C-337
(adjacent to C-337-A) and C-337-A.
At some unspecified time, a critique was conducted
by the Assistant Shift Superintendent and all
personnel involved in the accident were interviewed.
All personnel who had been in the facility on the day
Section 73
shift were contacted and surveyed. One individual
was found to have contaminated shoes and skin
contamination on the elbow and was taken to a
change house in C-337 for decontamination. Later
this employee’s personal clothing was also found to
be contaminated, and through further investigation it
was learned that this contamination occurred in the
change house.
A thorough survey was conducted in the change
Discuss underlying reference
materials to support a program
of radiological questions which
would preclude occurrence of
such an event.
Obj. 1
Describe causes of radiological
incidents.
Obj. 2
Identify primary cause and
contributing causes of
radiological incidents.
Obj. 3
Describe effective corrective
actions.
Show OT 16.2.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 4
house, and it was discovered that, in addition to a
few articles in the change house itself, two locks and
lockers used by Employee No. 1 (who performed the
pigtail changes on the previous shift) were
contaminated. This employee returned to work at
1830 on August 23, 1991. Surveys of the locker
contents indicated contamination on company-
issued clothing worn the previous shift. The
employee was also found to have skin
contamination of 6500 dpm/100 cm2 on the arm,
4500 dpm/100 cm2 on the knee, and 2750 dpm/100
cm2 on each ankle.
A survey of the employee’s coworker’s (Employee
No. 2) locker revealed contaminated items (both
company-issued and personal). Personal surveys
conducted when Employee No. 2 returned to work
showed the presence of skin contamination of 4500
dpm/100 cm2 on hair, 5000 dpm/100 cm2 on neck,
and 40,000 and 15,000 dpm/100 cm2 on wrists.
Later (2130 hours on August 23 for Employee No. 2,
and 1900 hours on August 24 for Employee No. 1)
surveys were conducted at the employees’ homes.
Monitoring of one employee’s home found one
T-shirt and one pillowcase slightly contaminated. A
pair of shoes at the other employee’s home was
found slightly contaminated. This employee’s (No.
2) coveralls had already been sent to the laundry,
since it was not recognized they were contaminated.
After laundering, significant contamination was still
present (up to levels of 250,000 dpm/100 cm2 at
ankles, and lower levels at other places). A survey
of the laundry equipment did not indicate any
contamination.
Based on statements from the involved employees,
they utilized the required personal protective
clothing and equipment for the job at the time. The
autoclave area is designated as a Contamination
Zone. Anti-contamination clothing designated for
cylinder changes at the time of the incident
consisted of company-issued coveralls (blues),
gloves, and shoe scuffs. Operational procedures
require the use of a respirator when disconnecting
pigtails. Surveys conducted as part of this
Show OT 16.3.
Show OT 16.4.
Show OT 16.5.
Some area designations have
changed since 1991 (e.g.,
Contamination Zone).
“Anti-contamination clothing” is
another term for “protective
clothing.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 5
investigation did not show any contamination on the
employees’ respirators or respirator cartridges.
The actual incident began between the hours of
0130 and 0415 on August 23, 1991, at the PGDP
C-337-A Feed Vaporization Facility.
The operators routinely assigned to C-337-A for the
Section 74
period of 1900 hours on August 22, 1991, through
0700 hours on August 23, 1991, were not available
due to the illness of one and an alternate work
assignment of the other at another facility (C-360).
Two operators who are not routinely assigned to the
area were then assigned to cover C-337-A. One
operator (No. 2) was qualified for operation of the
facility while the other (No. 1) was in training for
qualification. (This is in compliance with facility
Operational Safety Requirements.) Supervisor
interaction was minimal, with only one brief visit
around the middle of the shift.
The operations in process at the time of the incident
were the routine disconnection and removal of
emptied UF6 feed cylinders and subsequent
replacement with full cylinders. This operation
consists of disconnecting a short length of
connecting pipe between the cylinder and the
system piping that leads to the diffusion process
equipment. This pipe is called a pigtail; it has
threaded connections and gaskets on each end.
Since pigtails are routinely reused, each cylinder
change requires replacement of gaskets on pigtails
to minimize the possibility of UF6 releases during
heating and feeding of the UF6 into the diffusion
process. At times these gaskets can be difficult to
remove from the pigtail. A special tool is available to
assist in the removal of these gaskets; however,
difficulty can still be encountered. The pigtails used
that night had been used for several feeding cycles,
as is normally the case. The exact number of cycles
could not be determined.
Show OT 16.6.
Show OT 16.7.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 6
There are levels of 234Th and 234mPa that occur
naturally from the decay of 238U present in the
cylinder pigtail, pigtail gaskets, and cylinder valves.
Approximately one curie each of those two
radioisotopes builds up in a cylinder within a few
months. These materials are less volatile than UF6,
so they remain as solids at the autoclave
temperature, but some small amounts are entrained
in the UF leaving the cylinder and small quantities
are deposited in the cylinder valve and pigtail as the
UF passes through it. These materials are present
as removable surface contamination in these
components, as well as being present in quantity in
the cylinder heels (the material remaining in the
cylinder after feeding). No containment of the ends
of the pigtail during the gasket removal process was
required by procedure. Additionally, the facility-
specific training program does not address the
specific contamination hazard the cylinder/pigtail
change represents.
The operators changed four cylinders on the shift.
The cylinder number, autoclave used, and
approximate time of change (from logs and recorder
data) are shown below:
Refer participants to
the last page of this module.
Cylinder Number Autoclave Number Approximate Time
K-438 3 West 0130 08/23/91
K-505 5 West 0320 08/23/91
K-472 1 West 0500 08/23/91*
AC-1090 4 West 0500 08/23/91
*Time is very approximate. Operator statements place the change late in shift.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 7
Section 75
There was a portable fan temporarily positioned to
cool employees just north of the 5 West autoclave
control panel, inside the Contamination Zone. The
fan had only been in place a few weeks. It was
operating during the shift in question. Apparently no
one had questioned the use of this fan in the area
prior to the event. Circumstantial evidence places
one operator exiting from either the 4 West or 5
West autoclave in the path of this fan while trying to
remove a pigtail gasket. The area of highest surface
contamination was spread along a line from the fan
(located by 5 West autoclave), past the 4 West
autoclave to the 3 West autoclave control panel in
the direction that the fan blows.
Self-monitoring performed by the employees upon
exiting the Contamination Zone where the job was
performed was inadequate, in that the employees
did not recognize the contamination present on their
skin and/or clothing. The employees performed
their other duties during the remainder of the shift,
thereby spreading this contamination to both
radiological and nonradiological areas. This spread
of contamination to nonradiological areas through
failure to recognize personal contamination at exit
monitoring stations caused other personnel to
become contaminated when the shift change at
0700 on August 23, 1991, brought new personnel
into these areas.
Based on the interview with Employee No. 1, the
employee traveled to C-337 around 0400 for a
break. Upon exiting the vaporizer Contamination
Zone and going to the C-337-A Operation’s
Monitoring Room, the Bicron frisker was indicating
high but not alarming due to high ambient
background radiation levels. The employee reset
the monitor and remonitored. The employee
indicated that the reading was elevated, but was not
alarmed this time. The employee stated this was
normal since the background in that area is often
high.
Show OT 16.6.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 8
At approximately 0600 on August 23, 1991, both
operators left C-337-A bound for the C-337 change
houses and the C-337 Area Control Room for shift
turnover. Both operators stated they used Bicron
friskers to check for contamination prior to entering
the nonradiological (green) pathway in C-337.
Training previously received by each operator for
each type of frisking equipment was documented.
Employee No. 1 noted that the Berthold hand-and-
foot monitor previously used was “not operating
properly,” so the employee used the Bicron frisker.
Neither operator noted any contamination.
Employee No. 2 monitored hands and feet only,
based on subsequent interviews, which indicated
that the employee did not know that a whole-body
frisk was required when exiting a radiological area.
Based on statements from both employees, they
showered, changed into personal clothing,
completed the shift turnover activities, and exited the
building after monitoring hands and feet at the
building exit, as required.
Since some personnel exit monitoring data is
regularly recorded, this data was reviewed. The
operators passed between the C-337-A Operation’s
Monitoring Room and the C-337 Area Control Room
several times during the shift and should have
performed a whole-body frisk for contamination each
time. Data for Employee No. 2 was not available, as
the employee used a Bicron frisker. (These
instruments do not have the added feature of storing
monitoring data for later review.) Data for employee
No. 1 shows 0414 hours on August 23, 1991, as the
first time a monitor station evaluated this operator as
contaminated. This station would normally be used
when passing from C-337-A to the C-337
nonradiological walkway when going to the
maintenance shops and change houses (restrooms,
lockers, and showers).
Section 76
Show OT 16.2.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 9
This same employee was also known to be
contaminated at the C-337 building exit on two
separate monitors (twice on one, once on the other)
when leaving after the shift change approximately
0700 on August 23, 1991. The employee stated that
the first monitor alarmed, but that the second
monitor did not indicate the contamination.
No monitoring data was found for the second
employee, since he did not utilize equipment
capable of storing this information.
Personal egress monitoring data from the facility
was also reviewed, and individuals from prior shifts
were contacted and monitored. An operator who
was in the C-337-A area extensively from 0700 to
1830 hours on August 22, 1991, had a new pair of
company-issued shoes, which were found to be free
of contamination. This operator had left the C-337-A
facility at 1830 hours on August 22, 1991.
Additionally, routine surveys on August 19, 1991, did
not indicate a similar contamination problem. Since
no significant contamination problems were
identified prior to 1900 hours on August 22, 1991,
the investigation focused on the activities from 1900
hours on August 22, 1991, to 0700 hours on August
23, 1991.
Urinalysis, as well as in vivo internal dosimetry
assessments, was performed on these employees
and did not indicate any evidence of internal
contamination. Personnel whole-body external
radiation dosimeters worn by both employees,
although externally contaminated, did not indicate
that abnormal doses to ionizing radiation were
received.
Skin dose calculations showed less than 0.10 rem
for Employee No. 2 and 1.50 rem for Employee
No. 1, compared to an annual limit of 50 rem.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 10
It was noted that in the occurrence report of
Reference 2, there had been 26 similar occurrence
reports (in 1991) at the facility.
IV. Compensatory measures
Following the detection of contamination, several
actions were taken by facility management in order
to determine the source and type of contamination,
the personnel and areas which may have been
contaminated, and actions which could be taken to
minimize additional spread of contamination. The
following list of significant actions were
accomplished after the event:
1. A critique of the incident was conducted,
interviewing all individuals involved.
2. All nonradiological areas were decontaminated,
and contamination levels within the radiological
areas were reduced.
3. Personal protective equipment requirements in
C-337-A were upgraded to require full anti-
contamination protective clothing within the
Contamination Area.
4. A full-time Health Physics Technician was
stationed at C-337-A and required to monitor all
personnel and equipment leaving the radiological
area.
5. The two operators involved in the incident were
sent to the Fernald, Ohio (DOE), facility for in
vivo (whole-body) monitoring.
6. The fan was removed from the facility.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 11
7. In vitro urine bioassay samples were obtained
from the individuals involved in the incident, as
well as other individuals who were either
contaminated on previous shifts or involved in
surveying and decontaminating the area.
8. Dosimeters were collected and monitored to
assist in determination of radiation dose.
Section 77
9. A walkdown of all plant boundary control stations
was performed by senior management to
determine location of substandard boundary
control stations.
10. Efforts were initiated to determine other possible
sources of Th234 and Pa234m at other plant
locations.
11. Actions were initiated to reduce the potential for
the spread of contamination from the UF6
cylinder pigtails during disconnection, gasket
replacement, and reconnection activities.
12. Surveillance was established by line
management of exit monitoring stations.
13. An investigation for an organizational finding was
initiated.
14. A news release was issued.
15. A plant announcement was made and a plant
bulletin was issued to emphasize the
seriousness of the situation and the need for
proper monitoring.
16. Complete locker room surveys were performed
by Health Physics Technicians.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 12
17. Meetings with union membership were
conducted by union leadership to emphasize the
importance of monitoring.
18. A letter, jointly signed by PGDP management
and union leadership, was issued to all PGDP
employees.
19. A DOE visit from Headquarters (HQ) Health and
Safety personnel was conducted. They
concluded that the breadth and scope of the
organization finding investigation was
appropriate.
20. The Portsmouth Gaseous Diffusion Plant was
notified of the incident for possible application at
its site.
21. Operators involved in the incident were not
allowed to work in radiological areas until
Radiation Worker retraining had been completed.
22. All fact sheets were put into “operator-required
reading” files.
23. Development of a training film to review
monitoring requirements and techniques was
initiated. Upon completion, review of this film will
be mandatory for all employees.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 13
Analysis - Contamination Levels on Gaskets and Pigtails
Sample Number
Nuclide Analyzed
Concentration
(dpm)
C-337-A Gaskets (2 gaskets combined for one
sample)
234
Th and
234m
Pa
U activity
11,000,000 Beta*
156,000 Alpha
C-310 Burp Station Gasket (1 gasket)
234
Th and
234m
Pa
U activity
163,000 Beta
140,000 Alpha
C-310 Product Withdrawal Gasket (1 gasket)
234
Th and
234m
Pa
U activity
40,000 Beta
1,900 Alpha
C-315 Tails Withdrawal Gasket (2 gaskets)
234
Th and
234m
Pa
U activity
117,000 Beta
20,600 Alpha
C-360 Sampling and Transfer Facility Gasket
(3 gaskets)
234
Th and
234m
Pa
U activity
1,500,000 Beta
78,000 Alpha
SP-8757, Pigtails coupling, feed header end
of pigtail
234
Th and
234m
Pa
U activity
see Note 1 Beta*
see Note 1 Alpha
SP-8758, Pigtail coupling, cylinder end of
pigtail
234
Th and
234m
Pa
U activity
see Note 1 Beta
see Note 1 Alpha
SP-8759, Material knocked loose from SP-
8757
234
Th and
234m
Pa
U activity
2,300,000 Beta
27,000 Alpha
SP-8760, Material knocked loose from SP-
8758
234
Th and
234m
Pa
U activity
2,300,000 Beta
75,000 Alpha
*Each radionuclide contributes 50 percent to this total activity.
Note 1: Beta/gamma levels were too high to be accurately counted on the spectrometer due to
detector dead time (saturation).
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 16 – 14
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Radiological Assessor Training
Section 78
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Review and Critique of Findings
and Improved Writing of Findings
Objectives:
Upon completion of this lesson, the participant will be able to:
1. List the three finding categories and describe how to separate surface
issues from underlying substantial issues.
2. List three of the five priority groupings for assessment findings.
3. Identify the three steps needed to write an appropriate finding.
4. List three suggestions for effective presentation of findings and concerns.
Training Aids:
Overhead Transparencies (OTs): OT 17.1 – OT 17.4 (may be supplemented or
substituted with updated
or site-specific information)
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 2
I. Introduction
II. Writing assessment findings
A. Organization of findings
There may be considered to be three categories
of assessment findings in order of increasing
severity:
• Surface findings (Type I) are usually
indicators of underlying issues that may be
more significant. Note that a common
problem is treating or correcting only the
surface issue while ignoring the underlying
problem—this results in problem recurrence.
• Substantial findings (Type II) are typically
issues that are underlying and more
significant. Note that correcting the
underlying problem results in solving the
problem.
• Organizational findings (Type III) deal with
programmatic or global issues. Note that
correcting these is very difficult if they involve
system, organizational, or institutional
problems.
Show OT 17.1.
State objectives.
Obj. 1
List the three finding categories
and describe how to separate
surface issues from underlying
substantial issues.
Show OT 17.2.
Example - One Radiological
Worker is seen leaving
Contamination Area without
frisking properly.
Example - Lack of monitoring
training or adequate monitoring
instrumentation.
Example - Culture is such that
frisking is not routinely performed,
nor protective clothing worn.
Now, remembering that there are
three levels of findings, we must
analyze the long list of findings
compiled during the field exercise
and establish what is really
important in the “big picture.”
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 3
First, group like, related, or similar findings
into a broader issue.
Then, review the overall list of groupings for
priority. The bases are:
1. Imminent danger
• Life Safety Code
• Personnel Safety
• Facility Safety
• Criticality
• Confined Space
• Traps
2. Not imminent, but potential danger
• Environmental monitoring, e.g.,
inadequate stack monitors
3. Violations of regulations, laws, orders
4. Areas where adverse public opinion may
reside
5. Performance and effectiveness issues
• Usually a large number of findings fall
into this category, which captures
effectiveness and quality issues.
Finally, establish what is most important and
what should be brought to the attention of the
senior DOE and contractor management.
Obj. 2
List three of the five priority
groupings for assessment
findings.
Show 17.3.
Place the findings on dry erase
board, list the groups (concerns)
that constitute the basis for a
concern or overall finding.
Section 79
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 4
B. Writing of findings
When it has been established what issues will
be brought to site management, review
techniques for writing about the findings:
There is an established style or method often
used in industry for writing findings. It consists
of the following three steps:
1. List the requirement
2. State what was observed (different from
requirement)
3. State the concern
III. Presentation of Findings
After findings are prepared in written form, it is
important that they be presented properly. Skills for
presenting findings are directly related to the
techniques used for writing findings.
Some rules to keep in mind when presenting
findings are listed below.
• Identify the assessment team leader and
members, and their organizational affiliation.
• Explain the reason for the assessment.
• NEVER, NEVER read the findings in a close-out.
Most senior management can read as well as
the presenter.
• Present the most significant findings first.
Obj. 3
Identify the three steps needed
to write a finding properly.
There are cases where a strict
format does not work.
Show OT 17.4.
Obj. 4
List three suggestions for
effective presentation of findings
and concerns.
Procedural requirement,
recurrent problem area, industry
issue, management request.
In case time is limited or
diminished.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 5
• Be prepared to present additional information to
support the finding. In most cases, there is
much more material in the file than is
appropriate to be included in the write-up. Be
prepared to use that material to support the
finding.
• In some cases, this is the time to cover material
in the report that was not written for public
consumption.
• It may be appropriate to discuss other material
such as related findings from previous reports or
audits.
• Maintain proper perspective by including both
positive and negative findings.
• Start with the positive findings, then make a
clear, shift to the negative findings or concerns.
• Explain the concerns/findings enough so that
senior management will understand the issue.
• Thank the site contact person and most senior
manager(s) for help and hospitality extended
during the assessment.
Identify follow-up issues and
generic findings.
Indicate the severity, ramification
of the finding.
Pause periodically and ask if
there are questions.
Summarize lesson
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 17 – 6
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Compliance-Based Versus
Performance-Based Evaluations
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Define compliance-based audits.
2. Define performance-based assessments.
3. Describe the four key elements of the assessment process.
4. Describe the advantage of planning for an assessment.
5. Identify the preferred type of checklist.
Training Aids:
Overhead Transparencies (OTs): OT 18.1 – OT 18.3 (may be supplemented or
substituted with updated or
site-specific information)
Equipment Needs:
Overhead projector
Screen
Student Materials:
Student’s Guide
References:
Section 80
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 2
I. Introduction
II. Compliance-based versus performance-based
evaluations
A. Compliance-based audits
A compliance-based audit is a comparison of the
requirements laws, rules, orders, guidance,
policies, procedures, and other documentation
with site practices to confirm implementation of
the specific requirements. For example,
determining whether bioassay samples were
collected in accordance with site procedure
requirements.
B. Performance-based assessments
Assessment is fundamental to the operation of a
satisfactory Radiation Protection Program.
A performance-based assessment is a review of
how the actual performance of the task is
accomplished and assessing whether the intent
of the requirement is being met. For example,
determining whether bioassay samples were
being analyzed for the appropriate isotopes
given the workplace environment.
Show OT 18.1.
State objectives.
Show OT 18.2.
Obj. 1
Define compliance-based audits.
Obj. 2
Define performance-based
assessments.
We should be monitoring and
assessing as opposed to auditing,
appraising, and inspecting.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 3
III. Assessment process
The assessment process is one of the evaluation
methods used to determine the status and
effectiveness of an overall management system.
With this perspective, the assessment process
should be planned and scheduled to accomplish the
following:
• Evaluate the effectiveness of program
implementation in order to meet compliance
requirements
• Provide input for assessment process
improvement.
The assessment process consists of four phases:
1. Planning
2. Performance
3. Reporting
4. Response evaluation, follow-up, and close-out
A. Planning
Planning is the key to a successful assessment.
It is possible to go immediately to the field to
observe, work with, and find out how things are
being done. That is one element and approach
to the process, but there is a greater advantage
to be made with proper planning and
preparation.
Show OT 18.3.
Obj. 3
Describe the four key elements of
the assessment process.
Obj. 4
Discuss the advantage of
planning for an assessment.
Benefits:
• You are not just observing the
field, but comparing how things
are done with how the program
states they are to be done.
• You will know what to expect,
and where and when to look for
it.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 4
The most successful assessments start with a
checklist. The checklist development is critical
to the success of the assessment and serves as
a commonly accepted method for documenting
what was looked at and what the results were. It
also serves as a guide to the person performing
the assessment and provides objective evidence
that an assessment was performed.
In performing the assessment, several types of
checklists can be used. The preferred style of a
checklist is the question-and-answer variety.
With this kind of checklist, the assessor has to
write-in an evaluation of the answer to each
question and any qualifying remarks. The
question-and-answer format is more difficult to
review, but provides more information with which
to judge the performance level of a system
element.
B. Performance
The elements of conducting an effective
Section 81
Radiation Protection Program assessment are:
• Overall plan (annual)
• Establish weekly, daily, breakdown
• Actually write a plan (modify later)
• Preparations-obtain material
• Use protocol for entry, conduct, exit
• Keep contact informed/no surprises
• You will understand justifiable
differences for things you see.
The site maybe doing some
unorthodox things for very good
reasons.
Obj. 5
Identify the preferred type of
checklist.
See also Module 15, Planning
and Conducting Assessments.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 5
C. Report
Documentation of the findings and observations
(note taking) in the field will involve some
combination of the following:
• Record book
• 3 x 5 cards
• Actual times, logistics
• What, when, who, why, where, how
• Documents reviewed
• Interviews
Then comes the time to start to put the report
together, whether a weekly report or the
inspection report of some other type. The
following are suggested:
• Distill as information is gathered, while
memory fresh
• Start draft report early
D. Post-assessment actions
• Evaluate assessment responses
• Establish corrective actions and due dates
• Track the status of open action items
• Perform follow-up assessments as necessary
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 18 – 6
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 19 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Field Exercise Guidelines
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Demonstrate applied field assessment techniques.
2. Present a finding to the class after return from the field.
Training Aids:
Overhead Transparencies (OTs): OT 19.1 – OT 19.4 (may be supplemented or
substituted with updated
or site-specific information)
Handout - “Field Exercise Guidelines for Participants”
Equipment Needs:
Overhead projector
Screen
Flip chart
Markers
Masking tape
Student Materials:
Student’s Guide
References:
U.S. Department of Energy, DOE-STD-1098-99, Radiological Control, Reaffirmed
December 2004.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 19 – 2
I. Introduction
II. Field exercise guidelines
A. Briefing for field exercise
The field instructors have prepared to take their
participants to the field. They have visited the
facility and areas for review, and have compiled
information for their participants to use in
preparation for the field exercise.
B. Preparations to go to field
A tendency exists to identify surface issues and
seek correction of the many items found while
walking through the facility. It is vital that
personnel who assess be able to sort the issues
noted and categorize them so effective use of
resources can be made. In other words,
identification of symptoms leads to contractors
working on the symptoms and not on the
underlying, substantive problems.
It can be extremely damaging if we (as overseers,
facility representatives, auditors, or assessors)
violate the high standards of performance and
rules that are being assessed.
Personal safety and facility safety are first and
foremost.
Show OT 19.1.
State objectives.
This afternoon, we are going to
start the preparations for going to a
facility where we will be assessing
radiological operations. This
training should enhance our
assessment skills.
Section 82
Good assessment techniques can
be taught and learned through
classroom discussions, but nothing
brings it all together like the
application of techniques under the
tutelage of an experienced field
instructor. This is your opportunity
to apply the material and practice
the methods learned during the
field exercise portion of the course.
Show OT 19.2.
It is important to understand that
we are constantly being
monitored ourselves and that we
must set the example.
Please follow all radiation
protection rules and regulations.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 19 – 3
C. Findings
Each person will make a presentation to the
group. The team leaders will introduce the
group, tell where you went, and introduce each
presenter. Each person should take no more
that one and one-half minutes for the
presentation of a finding. Some of the “cats and
dogs,” or other findings and observations, will be
covered at the end of the individual findings.
The Lead Field Instructor will monitor the overall
presentation and comment as appropriate.
We hope to see presentations in this form:
1. List the requirement.
2. State what was observed.
3. State the concern.
Show OT 19.3.
Review the requirement for each
person to prepare one finding or
concern to be shared with the
class
(one-and-one-half minute time limit
per finding).
Show OT 19.4.
Refer participants to page 49 of
handouts, “Field Exercise
Guidelines for Participants.” Allow
sufficient time for participants to
read and ask questions.
Obj. 1
Demonstrate applied field
assessment techniques.
Obj. 2
Present a finding to the class after
return from the field.
Summarize lesson.
Review objectives.
Ask for questions.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 19 – 4
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Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 20 – 1
DEPARTMENT OF ENERGY LESSON PLAN
Course Material Topic: Course Summary
Objectives:
Upon completion of this lesson, the participant will be able to:
1. Demonstrate an understanding of the knowledge required to perform basic
assessments of occupational radiation protection programs and activities at
DOE nuclear sites and facilities.
Equipment Needs:
Overhead projector
Screen
Student Materials:
Final examination - as applicable.
Radiological Assessor Training
DOE-HDBK-1141-2008
Instructor’s Guide
Module 20 – 2
I. Summary
(Insert individualized summary.)
Review course highlights.
Ask for questions.
As applicable:
Administer examination.
Upon completion of examination
by participants, review exam.
Collect all exams.
OT 1.1
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Regulatory Documents
Objectives:
• Identify the hierarchy of regulatory
documents.
• Define the purpose of 10 CFR Part 835.
• Define the purpose of the DOE Radiological
Control Standard.
OT 1.2
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Regulatory Documents
(cont.)
Objectives:
• Define the terms "shall" and "should" as
used in the above documents.
• Describe the role of the Defense Nuclear
Facilities Safety Board (DNFSB) at DOE
sites and facilities.
OT 1.3
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DOE Radiological Health
and Safety Policy
• Establish and maintain a system of
regulatory policy and guidance.
• Ensure appropriate training and the
technical competence of the DOE
workforce.
• Establish and maintain line management
involvement and accountability.
Section 83
OT 1.4
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DOE Radiological Health
and Safety Policy (cont.)
• Ensure accurate and appropriately made
measurements.
• Conduct radiological operations that
control the spread of radioactive materials
and are ALARA.
• Incorporate measures to minimize
contamination.
• Conduct oversight to ensure compliance.
OT 1.5
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Written Standards
• 10 CFR Part 835
• DOE Radiological Control
Standard
OT 1.6
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Hierarchy of Requirements
Two parallel hierarchies:
• Rules and/or
regulations
• DOE Orders
OT 1.7
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Rules and Regulations
• Price-Anderson Amendments Act (PAAA)
of 1988
• 10 CFR Part 820 of 1993:
– Civil penalties
– Criminal penalties
• DOE Nuclear Safety Requirements
OT 1.8
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10 CFR Part 835
• Purpose: Codification of radiation
protection requirements
• Prescriptive language
• Emphasis on ALARA
• Radiation Protection Program
requirements
• Federal law
• Criminal and civil penalties for violations
OT 1.9
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Radiation Protection
Program
• Required by 10 CFR Part 835
• Noncompliance may lead to PAAA
enforcement
OT 1.10
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0
Guidance Documents
(10 CFR Part 835)
Two types:
• Implementation guides
• Technical positions
OT 1.11
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10 CFR 835 vs. 10 CFR 20
10 CFR Part 835:
• DOE sites
and facilities
• Unique
activities
10 CFR Part 20:
• NRC
OT 1.12
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2
DOE Radiological Control
Standard
• Originally promulgated as the Radiological Control
Manual with DOE Notice 5480.6 (July 1992)
• Purpose: provides guidance for comprehensive
radiological control program - not a regulation
• Notice which made the Radiological Control Manual a
requirement was cancelled by N441.1 (Sept 1995):
– May still be be contractual requirement
– Updated on July 1999 by DOE STD-1098-99
Radiological Control
OT 1.13
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3
10 CFR 835 vs. DOE
Radiological Control Standard
10 CFR Part 835:
• EH-10 enforces
• “Shall”
statements
(mandatory
requirements)
• Program Offices
audit
DOE Radiological
Control Standard:
• Program Offices
audit contractual
agreements
• Mostly “should”
statements
(recognizes site-
or facility-specific
attributes)
OT 1.14
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Conflicts
10 CFR 835 requirements take precedence over
DOE Radiological Control Standard
Unlikely the two will conflict, one may have a
requirement that is not in other
OT 1.15
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5
DOE Standards
• Some DOE Standards are
requirements for certain sites:
for example, DOELAP
• Others provide guidance
• As part of assessment, need to
review site requirements
documents
OT 1.16
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6
Defense Nuclear Facilities
Safety Board
• Five-member board:
– Reviews and evaluates standards
– Investigates any event or practice at
DOE nuclear facilities that the Board
determines has (or may) adversely
affect public health and safety
– May establish reporting requirements
for the Secretary of Energy
Section 84
OT 1.17
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DNFSB Recommendations
91-6:
• Radiological protection performance
92-7:
• Enhance radiological qualification
98-1:
• Resolution of audit findings
99-1:
• Safe storage of fissionable material
OT 2.1
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10 CFR Part 835,
Background and Focus
Objectives:
• Describe the contents of 10 CFR Part 835.
• Identify the site requirements of 10 CFR
Part 835.
OT 2.2
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10 CFR Part 835
A — General Provisions
B — Management and Administrative
Requirements
C — Standards for Internal and External
Exposure
D — Reserved
E — Monitoring of Individuals and Areas
F — Entry Control Program
G — Posting and Labeling
OT 2.3
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10 CFR Part 835 (cont.)
H — Records
I — Reports to Individuals
J — Radiation Safety Training
K — Design and Control
L — Radioactive Contamination Control
M — Sealed Radioactive Source Control
N — Emergency Exposure Situations
OT 2.4
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Exclusions from 10 CFR
Part 835
• Activities regulated by the NRC
• Activities under authority of the Director, Naval Nuclear
Propulsion Program
• Specified activities conducted under the Nuclear
Explosives and Weapons Surety Program
• Radioactive material transportation
• DOE activities in certain foreign countries
• Background radiation
• Radioactive material on or within material, equipment
and real property which is approved for release when
the radiological conditions of the material, equipment
and real property have been documented to comply with
the criteria for release set forth in a DOE authorized
limit which has been approved by a Secretarial Officer in
consultation with the Chief Health, Safety and Security
Officer.
OT 2.5
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Exclusions from 10 CFR
Part 835 (Cont.)
Occupational doses received as a result of
excluded activities and radioactive material
transportation, as listed above, shall be
considered when determining compliance
with the occupational dose limits (835.202
and 835.207), and with the limits for the
embryo/fetus (835.206).
OT 2.6
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Included in the RPP
• Formal plans and measures for applying
ALARA to occupational exposures
• Existing and anticipated operational tasks
• Each requirement in Part 835
• Plans, schedules, and other compliance
measures
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Standards for Internal and
External Exposure
Addresses limits for:
• General employees (occupational)
• Embryos/fetus
• Occupationally exposed minors
• Members of public in controlled area
• Planned special exposures
• Nonuniform exposures of the skin
• Concentrations of radioactive material in
air
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Summary of Dose Limits
Exposed Individual
General Whole Body (internal and
Employee: external)
“ “ Lens of Eye
“ “ Extremity (below elbow and
knees) and skin
Annual Limit
5.0 rem
15.0 rem
50.0 rem
OT 2.9
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.9
Summary of Dose Limits
(cont.)
Exposed Individual
General Employee: Any Organ or Tissue
(other than lens of eye)
Declared Pregnant Worker: Embryo/Fetus
(gestation period)
Section 85
Occupationally exposed minors: (also have limit of 10% of
other General Employee limits)
Members of the Public in Controlled Areas:
Annual Limit
50.0 rem
0.5 rem
0.1 rem
0.1 rem
OT 2.10
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8
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.1
0
Planned Special Exposures
• Advance approval of DOE
• Informed employee consent
OT 2.11
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.1
1
DACs
DACs are listed in appendices A and C of
10 CFR 835.
For intakes, they are the airborne
concentration that equals the annual limit on
intake (ALI) divided by the volume of air
breathed by an average worker for a
working year of 2000 hours (assuming a
breathing volume of 2400 m3).
OT 2.12
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.1
2
Monitoring of Individuals
and Areas
• Demonstrate compliance with Part 835
• Document radiological conditions
• Detect changes in conditions
• Detect the gradual buildup of radioactive
material
• Verify effectiveness of engineering and
process controls
• Identify and control potential radiation
sources and/or radioactive material
OT 2.13
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.1
3
Instrumentation
• Periodically maintained and calibrated
• Reviewed for appropriateness:
– Types, levels, and energies of radiation
– Environmental conditions
• Routinely tested for operability
OT 2.14
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.1
4
Individual Monitoring –
External
Dosimetry provided to and used by:
• Radiological Workers
• Declared Pregnant Workers
• Occupationally exposed minors and
members of the public in controlled area
• Persons entering High or Very High
Radiation Areas
OT 2.15
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.1
5
Individual Monitoring –
Internal
Conducted for:
• Radiological Workers
• Declared Pregnant Workers
• Occupationally exposed minors and
members of the public in a controlled area
OT 2.16
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.1
6
Receipt of Packages of
Packages Containing
Radioactive Material
Applicable to certain types of packages:
• Requires monitoring
• Specifies time limit for monitoring; within 8
hours after start of next working day
OT 2.17
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.1
7
Entry Control Program
• Radiological Areas
• High Radiation Areas
• Very High Radiation Areas
OT 2.18
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.1
8
Methods to Ensure Control
• Signs and barricades
• Control devices on entrances
• Alarms
• Locked entrances
• Administrative controls
OT 2.19
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.1
9
Radiological Area Egress
–No control(s) shall be installed at
any radiological area exit that
would prevent rapid evacuation of
personnel under emergency
conditions.
OT 2.20
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0
High Radiation Areas
• Where an individual could exceed a deep dose
equivalent of 0.1 rem in one hour, measured
30 cm from the source or from any surface
that the radiation penetrates
• If individual could receive a dose > 1.0 rem in
an hour require one or more of the following:
– Control devices
– Alarms
– Surveillance to prevent entry
– Locks
OT 2.21
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.2
1
Very High Radiation Areas
• Dose in excess of 500 rad in one hour at 1
meter from source or from any surface
that the radiation penetrates
Section 86
OT 2.22
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.2
2
Very High Radiation Areas
(Cont.)
– In addition to the requirements for a High
Radiation Area, additional measures shall
be implemented to ensure individuals are
not able to gain unauthorized access to
Very High Radiation Areas.
– “No control(s) shall be established in a
High or Very High Radiation Area that
would prevent rapid evacuation of
personnel.”
OT 2.23
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8
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.2
3
Signs
• Yellow background
• Black or magenta radiation symbol
• Clear and conspicuous signs
OT 2.24
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.2
4
Records Requirements
Include:
• Demonstrate compliance with 10 CFR 835
• Individual monitoring
• Sealed source inventory and control
• Results of surveys:
– Release of material and equipment
– Radiation and radioactive material in the
workplace
• Maintenance and calibration of instruments
• Internal audits
• Radiation safety training
OT 2.25
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.2
5
Reports to Individuals
Include:
• Annual report of dose
• Employment termination record of exposure
OT 2.26
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.2
6
Radiation Safety Training
• Based on:
– Area access
– Receiving occupational dose
– Assignment as Radiological Worker
• Requirements:
– Examination for certain level (e.g., Radiological
Worker Training)
– Training intervals of twenty four months or less
– Specifies topics
– Provision for allowing use of escorts
OT 2.27
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.2
7
Design and Control
• Facility design and modifications:
– Optimization methods shall be used
– Maintain dose rates below 0.5
mrem/hour
– Avoid release of airborne radioactivity
– Facilitate operations, maintenance,
decontamination, and
decommissioning
OT 2.28
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8
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.2
8
Workplace Controls
• Physical design features and administrative
controls shall provide:
– Occupational dose to general employees
not exceed the limits
– ALARA process is utilized
OT 2.29
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.2
9
Radioactive Contamination
Control
• To controlled areas (Part 835)
• To uncontrolled areas (DOE O 5400.5)
• Monitor contamination level
• Provisions to release to controlled area
items with fixed contamination
• Requires personnel monitoring
• Requires protective clothing
OT 2.30
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.3
0
Sealed Radioactive Source
Control
• Sealed radioactive sources shall be used,
handled and stored in a manner
commensurate with the hazard.
OT 2.31
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.3
1
Emergency Exposure
Situations
Addresses:
• Employees who have exceeded dose limits
as a result of an authorized emergency
exposure
• Nuclear accident dosimetry
OT 2.32
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.3
2
Nuclear Accident
Dosimetry
• Required for installations possessing
potential critical mass
• Method to conduct initial screening
• Method and equipment to analyze
biological materials
• A system of fixed nuclear accident
dosimeters
• Personal nuclear accident dosimeters
OT 3.1
O
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3
.1
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8
Overview of the DOE
Radiological Control
Standard
Objectives:
Section 87
• Describe the managerial responsibilities in
the DOE Radiological Control Standard.
• Describe the contents of the DOE
Radiological Control Standard.
OT 3.2
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.2
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8
Excellence in
Radiological Control
(Chapter 1)
• DOE Radiological Control Standard
• Leadership in Radiological Control
• Improving Radiological Control
Performance
• Contractor Radiological Control
Organization
• DOE Management
OT 3.3
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3
.3
D
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8
Leadership in
Radiological Control
• Commitment of senior management
• ALARA accountability
• Conduct of radiological operations
OT 3.4
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.4
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8
Improving Radiological
Performance
• Critiques used as a management tool
• Root cause identification
• Over 20 radiological performance
indicators:
– Tools to focus priorities on radiological
control performance
OT 3.5
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.5
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8
Contractor Radiological
Control Organization
• Requirements for the contractor
• Qualifications of the Radiological Control
Manager
OT 3.6
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.6
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8
Radiological Standards
(Chapter 2)
• Administrative Control Levels and Dose
Limits
• Contamination Control and Control
Levels
• Posting
OT 3.7
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.7
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Conduct of
Radiological Work
(Chapter 3)
• Planning Radiological Work
• Work Preparation
• Entry and Exit Requirements
• Radiological Work Controls
OT 3.8
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.8
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Conduct of
Radiological Work
(Chapter 3) (cont.)
• Evaluation of Performance
• Special Applications
• Radiological Design Criteria
• Design of New Facilities
• Modification of Existing Facilities
OT 3.9
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.9
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8
Radioactive Materials
(Chapter 4)
• Identification, Storage, and Control
• Release and Transportation
• Source Controls
• Waste Management
– Solids
– Liquids
• Airborne Management
OT 3.10
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0
D
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8
Radiological Health
Support Operations
(Chapter 5)
• External Dosimetry
• Internal Dosimetry
• Respiratory Protection Program
• Handling Radiologically Contaminated
Personnel
• Radiological Monitoring and Surveys
• Instrumentation and Calibration
OT 3.11
O
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.1
1
D
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8
Training and Qualification
(Chapter 6)
• General Employee Radiological Training
• Radiological Worker Training
• Radiological Control
Technician/Supervisor Qualification
• Other Radiological Training
• Training for Special Applications
OT 3.12
O
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.1
2
D
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8
Radiological Records
(Chapter 7)
Requirements for:
• Employee Records
• Visitor records
• Radiological Control Procedures
• Radiological Surveys
• Instrumentation and Calibration Records
• Radiological Reporting
OT 4.1
O
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.1
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8
Elements of a Radiological
Control Program
Objectives:
• Identify factors that influence the scope
and magnitude of a Radiological Control
Program at any nuclear facility.
• Identify typical elements of a
Radiological Control Program.
OT 4.2
O
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.2
D
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8
Radiological Control
Program
• Requirements
Section 88
• Responsibilities
• Programs/procedures
• Assessments
OT 4.3
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.3
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8
Radiological Control
Program Elements
• Organization and administration
• Personnel training and qualifications
• Quality assurance
• ALARA
• Radiological work control
• Posting and labeling
OT 4.4
O
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.4
D
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8
Radiological Control
Program Elements (cont.)
• Radioactive material control
• Radiation-generating devices
• Entry control
• Contamination control
• Instrumentation/alarms
• Monitoring
OT 4.5
O
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.5
D
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8
Radiological Control
Program Elements (cont.)
• Dosimetry
• Respiratory protection
• Facility-specific features
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance indicators
OT 5.1
O
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5
.1
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8
Technical Safety
Requirements
Objectives:
• Describe the purpose of DOE Order 5480.22 and
its relationship to 10 CFR 830.205.
• Describe the purpose of Technical Safety
Requirements (TSRs) in regard to facility
operations/activities.
• Identify the source(s) of information required to
develop reasonable and appropriate TSRs.
OT 5.2
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.2
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8
Technical Safety
Requirements (cont.)
Objectives:
• Describe the responsibilities for the
development and use of TSRs.
• List the criteria for identifying problems in
meeting TSRs.
• List areas in TSRs which could be reviewed
as part of a radiological assessment.
OT 5.3
O
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.3
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8
Technical Safety
Requirements
• Definition
• TSRs consist of:
– Safety limits
– Operating limits
– Surveillance requirements
– Administrative controls
– Use and application instructions
– Bases for above items
OT 5.4
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.4
D
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8
Basis
Summary statements of the reasons for the
operating limits and associated surveillance
requirements. It shows how the numerical
value, condition, or the surveillance fulfills the
purpose from the safety documentation.
OT 5.5
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.5
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8
TSRs
• Contract between operating contractor and
DOE management
• Minimize potential risk
• Controlled document
• Reduce likelihood and potential impact of
events
OT 5.6
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.6
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8
Facility-Specific
Safety Analysis
Considers all credible accidents including:
• Most significant possible releases
• Criticality scenarios
• Expected accidental releases during life of
facility
OT 5.7
O
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5
.7
D
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8
Accident Analysis
Provides:
• Values for defining operational limits
• Parameters and operating conditions that
should be limited
OT 5.8
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.8
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8
Requirements Expected to
Be Developed
• Operating limits
• Technical and administrative conditions
• Availability of safety equipment and
systems
• Critical functions of instrumentation and
controls
OT 5.9
O
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.9
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8
Analyses
• In order to serve as the basis for the TSRs,
studies must systematically evaluate:
– All potential off-normal conditions that
could occur during the life of the facility
– What could be considered design basis
accidents
Section 89
OT 5.10
O
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.1
0
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8
Responsibilities for TSRs
• Preparation Contractor
• Review DOE Field Office
• Approval CSO
OT 5.11
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.1
1
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0
8
Violations of a TSR
Four circumstances:
• Exceeding Safety Limit
• Failure to take necessary actions within time
allotted
• Failure to perform surveillance within
required time
• Failure to comply with Administrative
Control requirement
OT 5.12
O
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5
.1
2
D
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8
Reporting Requirements
• Categorization
– Operational Emergency
– Significance Category 1 - 4
• Notification
• Follow-up notification
• Occurrence Report preparation
• Noncompliance Tracking System
OT 5.13
O
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.1
3
D
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8
Area monitors
• Criticality monitors
• Area Radiation Monitors
• Air Monitors (i.e., real time air monitors,
fixed head air samplers)
OT 6.1
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8
O
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6
.1
Radiological Aspects
of Uranium
Objectives:
• Identify the radiological properties of
uranium.
• Describe the toxicological properties and
behavior of uranium.
• Identify appropriate instrumentation,
measurement techniques, and special
radiological survey methods for uranium.
OT 6.2
D
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8
O
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6
.2
Radiological Aspects
of Uranium (cont.)
Objectives:
• Describe personnel protection requirements,
external dose control techniques, and internal
dose control techniques.
• Describe special controls and considerations
required for uranium operations.
OT 6.3
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8
O
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6
.3
Radiological Properties
Uranium can:
• Occur naturally
• Be man-made
• Become enriched for reactor fuel or
weapons
• Be depleted
OT 6.4
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8
O
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6
.4
Radioisotopes
• Alpha and beta emitters
• Emit neutrons
• Fissile material
OT 6.5
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O
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6
.5
Detection and
Measurement
• Health physics program ensures detection
• Exposure rate surveys using photon-
sensitive instruments
• Beta detectors (decay products)
• Neutron surveys
• Continuous air monitors
OT 6.6
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.6
Survey Techniques
• Monitoring practices:
– Contamination surveys of the workplace
– Release surveys
– External exposure surveys
– Airborne contamination surveys
– Routine surveillance by a RCT
• Regularly scheduled monitoring (all work areas)
OT 6.7
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.7
Workplace
Characterization
• Airborne contamination surveys:
– Prompt detection
– Personnel dose assessment
– Monitoring of trends
– Special studies
OT 6.8
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.8
Personnel Protection
• Personnel air sampling
• Protective clothing
• Respiratory protection
OT 6.9
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6
.9
External Dose Control
• Beta radiation
• Gamma radiation:
– Time
– Distance
– Shielding
• Neutron radiation
OT 6.10
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0
Internal Dose Control
Hazard must be controlled by:
• Appropriate facility and equipment design
• Contamination control procedures
• Protective clothing
• Control verified by:
– Bioassay program
OT 6.11
D
O
Section 90
E
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.1
1
Special Controls
• Criticality safety:
– Alarm systems
– Nuclear accident dosimetry
– Fire prevention
• Hydrofluoric acid
• Separation/concentration of decay products
OT 7.1
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.1
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Radiological Aspects of
Tritium
Objectives:
• Describe the radiological properties of
tritium.
• Identify personnel protection requirements
and dose control techniques.
• Identify the biological effects of internally
deposited tritium.
OT 7.2
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.2
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8
Radiological Aspects of
Tritium (cont.)
Objectives:
• Describe appropriate instrumentation,
measurement techniques, and special
radiological survey methods for tritium.
• Identify special controls and considerations
required for the use of tritium.
OT 7.3
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.3
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Radiological Aspects of
Tritium
• Primary sources:
– Environmental
– By-product of power reactors
– DOE production
OT 7.4
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.4
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Chemical Forms
• Elemental tritium
• Tritiated water
• Organically bound tritium
(OBT)
• Stable metal tritides (SMT)
OT 7.5
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.5
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Radiological Properties of
Tritium
• Radiological properties:
– Beta particle emitter
– Weak beta particle energy (18 keV max)
– 12.3 yr half-life
– High specific activity (9619 Ci/g)
OT 7.6
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.6
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8
Dose Pathways
• Inhalation
• Ingestion
• Skin absorption
OT 7.7
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.7
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General Sources of
Release
• Gaseous releases (ventilation exhaust
systems)
• Liquid wastes
• Solid wastes
OT 7.8
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.8
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8
Dose Controls
• Airborne controls
• Contamination controls
• Personnel protection equipment
OT 7.9
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.9
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Modes of Entry
• Inhalation
• Ingestion
• Absorption
OT 7.10
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0
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8
Containment
• Primary
• Secondary
• Tertiary
OT 7.11
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1
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8
Airborne Controls
• Differential room pressure zones
• Dilution ventilation
• Room-air detritiation systems
• Local exhaust ventilation
OT 7.12
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2
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Measurement Techniques
• Air monitoring
• Differential monitoring
• Discrete sampling
• Process monitoring
• Surface monitoring
• Liquid monitoring
OT 7.13
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.1
3
D
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8
Special Controls
(Bioassay)
• Chronic exposure:
– Periodic urinalysis
• Acute exposure:
– Wait one to two hours.
– Void bladder.
– Collect sample as soon as
possible.
– Collect daily.
OT 7.14
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4
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8
Special Controls (cont.)
• Dose assessment for SMTs and OBT may
need to be based on air monitoring
• Tritium effluent recovery system:
– Reduces tritium available for release
– Tritium gas converted to tritiated water
– Inventory control and accountability:
– Tritium = nuclear material
OT 8.1
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.1
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Radiological Aspects
of Plutonium
Objectives:
• Identify the radiological properties of
plutonium.
Section 91
• Identify the biological effects of plutonium.
• Identify special controls and considerations
required for plutonium operations.
OT 8.2
O
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.2
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8
Radiological Aspects of
Plutonium (cont.)
Objectives:
• Describe appropriate instruments,
measurement techniques, and special
radiological survey methods for plutonium.
• Describe personnel protection requirements
and dose control techniques for plutonium.
OT 8.3
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.3
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Radiological Properties of
Plutonium
• 15 isotopes, all radioactive
• Pu-238 (heat source)
• Pu-239 (reactor fuel, weapons)
• Pu-240 (reactor fuel, weapons)
• Alpha-emitters:
– Some associated gamma radiation
OT 8.4
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.4
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Biological Effects of
Plutonium
• Exposure pathways:
– Inhalation
– Ingestion
• Retention in body
• Removal (chelating agents)
• Long-term concerns:
– Lung cancer
– Leukemia
OT 8.5
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Survey
Techniques
• Health physics program for detection of
all types of radiation
• Alpha-sensitive instruments
• Continuous air monitors
• Neutron surveys
• Exposure rate surveys
OT 8.6
O
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.6
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Survey
Techniques (cont.)
Monitoring practices:
• Regularly scheduled contamination
surveys
• Release surveys
• External exposure rate surveys
• Airborne radioactivity surveys
• Routine surveillance by Radiological
Control Technician
OT 8.7
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.7
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Monitoring Instruments
• Meet site specific requirements
• Effluent monitors
• Criticality alarms
OT 8.8
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.8
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8
Sources of External Dose
• High-energy gamma photons
• Low-energy photons:
– Extremity dose
– From large amounts of Pu-238, Pu-241,
Am-241
• Neutrons
OT 8.9
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.9
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8
External Dose Control
• Time
• Distance
• Shielding
• Other work practices:
– Good housekeeping
– Specially designed
tools and equipment
OT 8.10
O
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.1
0
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8
Internal Dose Control
• Confinement systems:
– Primary
– Secondary
– Tertiary
• Confinement devices:
– Fume hoods
– Glove boxes
– Ventilation
OT 8.11
O
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1
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8
Personnel Protection
• Training
• Air sampling
• Protective clothing
• Respiratory protection equipment
OT 8.12
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2
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Special Controls
• Inventory and accountability
• Criticality safety:
– Alarm systems
– Nuclear accident dosimetry
OT 9.1
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Radiological Work
Permits
Objectives:
• Identify types of job hazards that are not
addressed by Radiological Work Permits
(RWPs).
• Describe the two basic types of RWPs.
• Determine the types of jobs that may and
may not be worked under the controls
imposed by RWPs.
OT 9.2
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Radiological Work
Permits (cont.)
Objectives:
• Identify typical time limits for the two basic
types of RWPs.
• List essential elements of an effective RWP.
• List RWP program elements which may be
included in a radiological assessment.
OT 9.3
O
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Section 92
K
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8
RWP Process
• Requester submits RWP request
form.
• Radiological Control Supervisor
accepts form, assures completion of
surveys of work area.
• Trained personnel perform surveys.
• RWP controls established.
• RWP form completed and posted.
OT 9.4
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RWP
Process (cont.)
• Radiological Control and work group review
RWP:
– Pre-job briefings
– ALARA reviews
• Radiological Control terminates RWP when
job is finished or RWP expires.
• Radiological Control maintains survey and
RWP documentation.
OT 9.5
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Types of RWPS
• Job-specific RWP:
– Potential for significant radiation dose,
airborne radioactivity, or spread of
contamination
– “Hands on” work with potential health
physics concerns
• General RWP:
– “Hands on” and other work with less
potential for health physics concerns
OT 9.6
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RWP Time Limits
• Job-specific RWP:
– Duration of job
– Usually ≤≤≤≤ 30 days
• General RWP:
– Standing use (tours, rounds)
– Usually ≤≤≤≤ 1 year
– Often renewed on calendar year basis
OT 9.7
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Elements of an RWP
• Description of work (detailed)
• Radiological conditions
• Dosimetry requirements
• Pre-job briefing requirements
• Radiological Control Technician
coverage requirements
• Training requirements
OT 9.8
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Elements of an RWP (cont.)
• Protective clothing requirements
• Respiratory protection requirements
• Stay time requirements
• Conditions limiting work or voiding RWP
• ALARA measures
• Contamination monitoring requirements
• Work document number
OT 9.9
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Elements of an RWP (cont.)
• Unique RWP number
• Permit issue and expiration date
• Signatures:
– Read and understand RWP
– Agree to follow controls
OT 9.10
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RWP Elements for
Radiological Assessment
• RWPs appropriately required for activities
and areas
• Completeness of information on RWPs
• Adequacy of radiological surveys to support
RWP
• Worker adherence to RWP requirements
OT 9.11
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RWP Elements for
Radiological Assessment
(cont.)
• RWP appropriately reviewed and approved
• Adequacy of worker monitoring (TLDs,
bioassay, air monitoring RCT coverage)
specified on RWP
• ALARA considerations included in RWP
• RWP program implemented in accordance
with written procedures
OT 10.1
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Contamination Containment
and Temporary Control
Measures
Objectives:
• Describe what temporary engineered
radiological controls can be used to reduce
or eliminate contamination spread.
• Describe why engineered and administrative
controls are needed.
OT 10.2
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Engineered Controls
• Glove boxes
• Glove bags
• Portable filtration units
• Containment tents
• Portable shielding
OT 10.3
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Administrative Controls
• Access restrictions
• Work practices
OT 10.4
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.4
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Use of Respiratory
Protection
Section 93
• Airborne Radioactivity Areas
• Breach of contaminated systems
• High removable contamination
• Work may generate airborne
radioactivity
OT 10.5
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Special Conditions
• Use of respiratory protection
contraindicated:
– Physical limitations
– Increased dose from respirator use
– Written authorization required
»Prior to incurring internal dose
»Specific justification of dose
acceptance
OT 11.1
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.1
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Radiological Work Site
Mockup Demonstration
Objectives:
• Identify poor radiological work practices, in
and around a mock radiological work site.
• Inspect a typical contamination containment
(glove bag).
• Develop field assessment notes to support
findings (hands-on exercise).
OT 12.1
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Radiation-Generating
Devices
Objectives:
• Identify radiation-generating devices.
• Describe the basic components of an x-ray
machine.
• Identify the most common use of x-rays.
• Identify the potential hazards associated
with x-rays.
OT 12.2
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Radiation-Generating
Devices (cont.)
Objectives:
• Identify the most common use of sealed
gamma ray sources and the potential
hazards.
• Identify the most common use of beta and
neutron sources and the potential hazards.
OT 12.3
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.3
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Radiation-Generating
Devices (cont.)
To meet the intent of the 10 CFR 835 use:
• DOE G 441.1- 5
• ANSI N43.3
• ANSI N43.2
• 10 CFR Part 34
OT 12.4
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Radiation-Generating
Devices (cont.)
Include:
• Devices producing ionizing radiation
• Sealed sources emitting ionizing radiation
• Small particle accelerators
• Electron-generating devices
OT 12.5
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X-Ray Machine Design
Basic components include:
• A source of electrons
• An electrical potential difference to
accelerate the electrons
• An anode or target to strike
• An evacuated tube for all the above
components
OT 12.6
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.6
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X-ray Energy Spectrum
• Characteristic x-rays
– Discrete energies
• Bremsstrahlung photons
– Produced with range of
energies
OT 12.7
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.7
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X-ray Machines
Radiography:
• Medical applications:
– Standardized appearance and installation
• Industrial applications:
– Fixed installation
– Mobile units
– Enclosed cabinet system
OT 12.8
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.8
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Analytical X-ray Machines
• Fluorescence analysis
• X-ray diffraction
OT 12.9
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Sealed Gamma Ray
Sources
Uses:
• Radiography
• Thickness gauges
• Level gauges
• Density gauges
OT 12.10
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.1
0
D
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8
Other Sealed Sources
• Beta particles (thickness gauges)
• Neutrons:
– Moisture gauges
– Radiography of dense materials
OT 12.11
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1
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Radiation-Generating
Device Installations
ANSI Categories:
• Exempt shielded
• Shielded
• Unattended
• Open
OT 13.1
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Radiological Aspects
of Accelerators
Section 94
Objectives:
• Identify the general characteristics of
accelerators.
• Identify the types of particles
accelerated.
• Identify the two basic types of accelerators.
• Identify uses for accelerators.
• Define prompt radiation.
• Identify prompt radiation sources.
OT 13.2
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Radiological Aspects
of Accelerators (cont.)
Objectives:
• Define radioactivation.
• Explain how contaminated material differs
from activated material with regard to
radiological concerns.
• Identify activation sources.
OT 13.3
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Radiological Aspects
of Accelerators (cont.)
Objectives:
• Identify engineered and administrative
controls at accelerator facilities.
• Identify the special radiological concern and
recommended instrument for each type of
accelerator radiation survey.
OT 13.4
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Accelerated Particles
• Electrons
• Protons
• Nuclei of various elements
OT 13.5
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Types of Accelerators
• Linear accelerators:
– Van de Graaff
– Cockcrott-Waltons
• Circular-path accelerators:
– Cyclotrons
– Betatrons
– Synchrotrons
• Colliders
OT 13.6
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Uses for Accelerators
• Basic research
• Production of radioisotopes
• Generation of bremsstrahlung for
radiography
• Induction of fusion
• Pumping for lasers
• Detoxification of hazardous waste
• Production of synchrotron radiation
OT 13.7
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Radiological Concerns
• Prompt radiation:
– Primary beam
– Secondary beam
– Skyshine
– Electromagnetic radiation
– Neutrons
– Muons
OT 13.8
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Radiological Concerns
(cont.)
• Residual radioactivity:
– Contaminated materials
– Activated materials
• Ancillary sources
OT 13.9
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Controls
• Engineered controls
• Administrative controls
OT 13.10
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Engineered Controls
• Passive:
– Barriers
– Shielding
• Active:
– Status lights
– Alarms
– Interlocks
– Scram buttons
OT 13.11
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Administrative Controls
• Signs/postings
• Search and secure procedures
• Controlled access procedures
• Configuration control
procedures
• Radiological Work Permits
(RWPs)
OT 13.12
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Monitoring
• May be complicated (unique conditions)
• Prompt radiation fields
• Environmental
• Personnel
OT 14.1
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.1
Assessment Techniques
Objectives:
• Describe the difference between
structured and unstructured
assessments.
• Describe the difference between vertical and
horizontal reviews.
• List the documents needed in order to
perform a radiological assessment.
OT 14.2
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Assessment Techniques
(cont.)
Objectives:
• Define the term assessment.
• Describe how to evaluate a contractor
assessment program using DOE’s Technical
Safety Appraisal approach.
• Describe the desired characteristics of
performance goals.
Section 95
• List five performance indicators used in
assessing Radiation Protection Program
effectiveness.
OT 14.3
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Assessment Types
• Unstructured
• Structured techniques:
– Vertical review
– Horizontal review
OT 14.4
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Vertical versus Horizontal
Reviews
• Vertical:
– Narrow scope
– Detailed assessment
• Horizontal:
– Broad scope
– Less detailed assessment
OT 14.5
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Documents Needed for
Assessment
• 10 CFR Part 835
• Site Radiation Protection
Program
• DOE-STD-1098-98 Radiological
Control
• Other federal regulations
• Applicable DOE orders
• State regulations
• DOE Implementation Guides
OT 14.6
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Documents Needed for an
Assessment (cont.)
• Site DOE contract
• Site commitments
• Site reports (deficiency, occurrence)
• Site-Specific RadCon Manual
• Approved exemptions
• Peer/industry group standards/recommendations
OT 14.7
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Assessing Radiological
Performance
• Assessments include:
– Internal audits
– Inspections
– Reviews
– Investigations
– Self-assessments
OT 14.8
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Assessment Approach
• Assessments:
– Management
– Operational
– Quality assurance
• Functional areas:
– Performance objectives
– Criteria for each performance objective
OT 14.9
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.9
Radiation Protection
Deficiencies
• Managers should regard them as
opportunities.
• Work practices should be continually
scrutinized.
• Number of deficiencies does not
measure overall quality.
OT 14.10
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Critiques
• Formal process to obtain pertinent facts
• Follow radiological incident
• Quickly establish facts in chronological
order
• Focus on “lessons learned,” not on blame
• Complement the Occurrence Reporting and
Processing of DOE Order 232.1A
OT 14.11
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Radiation Protection
Program Performance
Goals should be:
• Established, approved, and maintained by
contractor senior site executive
• Measurable
• Achievable
• Auditable
• Challenging
• Meaningful in promoting improvement
OT 14.12
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2
Radiation Protection
Program Performance (cont.)
• Developed by those performing work
• Reviewed at least annually
• Revised as appropriate
OT 14.13
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Performance Indicators
• Evaluate Radiation Protection Program
performance.
• “What gets measured, gets done.”
OT 15.1
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Planning and Conducting
Assessments
Objectives:
• List 10 of the 19 elements of a Radiation
Protection Program.
• Identify five deficiencies in a Radiation
Protection Program that point to the need
for an assessment.
• Describe the preparations needed to
conduct a Radiation Protection Program
assessment.
OT 15.2
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Planning and Conducting
Assessments (cont.)
Objectives:
• Describe how to conduct a Radiation
Protection Program assessment.
Section 96
• Describe two qualifying conditions for a
follow-up assessment.
• Describe what actions should be taken
when assessments indicate marginal
radiological control performance.
OT 15.3
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Elements of a Radiation
Protection Program
• Organization and administration
• Personnel training and
qualification
• Quality assurance
• ALARA
• Radiological work control
• Posting and labeling
• Radioactive material control
OT 15.4
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Elements of a Radiation
Protection Program (cont.)
• Radiation-generating devices
• Entry control
• Contamination control
• Instrumentation and alarms
• Monitoring
• Dosimetry
• Respiratory protection
OT 15.5
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Elements of a Radiation
Protection Program (cont.)
• Facility-specific features
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance
indicators
OT 15.6
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Indicators: Assessment Is
Needed
• Exceeding administrative dose levels
or regulatory limits
• Loss of radioactive material control
• Unmonitored/excessive release to
environment
• Excessive number of skin
contamination incidents
• Uptakes of radioactive material
• Excessive number of radiological
incidents
OT 15.7
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Indicators: Assessment Is
Needed (cont.)
• Inadequate training
• Ineffective work control systems
• Incomplete or inaccurate:
– Radiological surveys
– Records
OT 15.8
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Assessment Preparation
• Review operating history
• Examine previous assessment reports
• Collect input from person(s) assessed
• Determine applicability of industry issues
• Review policies and procedures
• Assemble regulations and guidance
documents
• Prepare an assessment plan
OT 15.9
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Operating History
• Occurrence reports
• Radiological deficiency reports
• Violations/citations
• Facility design changes
OT 15.10
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Previous Assessments
• DNFSB Recommendations
• Self-assessments
• Corporate quality assurance
• External audit group
OT 15.11
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Input from Person(s) to be
Assessed
• Management
• Radiological Control Manager
• Radiological Control Organization’s
"customers"
OT 15.12
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Industry Issues
• Emerging technical issues
• Application of best industry
standards
OT 15.13
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Policies and Procedures
• Operating procedures
• Radiological control policies
OT 15.14
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Regulations and Guidance
Documents
• Federal
• State
• Site
• Industry/peer group
OT 15.15
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Assessment Plan
• Identify elements to assess.
• Generate specific questions.
• Develop record sheet.
• Allocate time (backup plan).
• Leave unscheduled time.
OT 15.16
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Types of Assessments
• Announced
• Unannounced
OT 15.17
Section 97
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Assessment Methods
• Document reviews
• Personnel interviews
• Field observations
OT 15.18
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Recommended Approach
• Review upper-tier procedures
• Conduct short site tour
• Interview key persons
• Conduct follow-up actions
OT 15.19
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Key Interviews
• Radiological Control Manager
• Radiological Control Supervisors
• Radiological Control Technical Leads
• Radiological Control Technicians
OT 15.20
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Key Interviews (cont.)
• Radiological Control Organization’s
“customers”
• DOE Representatives
• Facility Manager
OT 15.21
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Post-Assessment
Actions
• Publish findings
• Receive responses
• Accept/reject/modify responses
• Develop action tracking list
• Publish status report
OT 15.22
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Post-Assessment
Actions (cont.)
• Maintain file of open action items.
• Verify closure of action items.
• Evaluate adequacy of actions taken:
– Root cause identified?
– Follow-up assessments needed?
OT 15.23
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Follow-up Assessments
Qualifying conditions:
• Widespread problem
• Recurring problem
OT 15.24
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Marginal Radiological
Performance
Initial actions should include:
• More direct line supervision in the work
space
• Curtailment of work schedules
• Addition of extra radiological control
personnel
• Conduct of additional training
OT 16.1
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Case Studies
Objectives:
• Describe causes of radiological incidents.
• Identify primary cause and contributing
causes of radiological incidents.
• Describe effective corrective actions.
OT 16.2
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Operations
Monitoring
Room
C-337 A Feed Facility
N
Truck Alley
C-337 Ground Floor
Area
Control
Room
Men
x
x
x
x x
x
Boundary
Control Station
Nonradiological
Walkway
x
Locker Room
Shower Facilities
Women
Legend
x
OT 16.3
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6,500 Pre
< 1,000 Post
2,750 Pre
<1,000 Post
4,500 Pre
< 1,000 Post
2,750 Pre
<1,000 Post
Pre and Post Decontamination Skin Contamination
( dpm per probe area; beta/gamma)
Employee No. 1
OT 16.4
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4,500 Pre
Less than
1,000 Post
5,000 Pre
Less than
1,000 Post
Units dpm Probe
beta/gamma
Hair found to
be uniformly
contaminated
2,500 dpm
below where
cap would sit
40,000 Pre
Less than
1,000 Post
15,000 Pre
Less than
1,000 Post
Skin Contamination of Employee No. 2
OT 16.5
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Units dpm Probe
beta/gamma
10,000
7,000
5,000
10,000
20,000
250,000
8,000
12,000
25,000
Coveralls - Operator 2
(after one washcycle)
10,000
10,000
20,000
130,000 160,000
21,000
5,000
12,000
7,000
Contamination on Employee No. 2 Coveralls
80,000
OT 16.6
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Autoclave
Autoclave
Autoclave
Autoclave Autoclave
Autoclave
Autoclave
Section 98
Autoclave
Autoclave
Autoclave
Contamination Zone
N
Clear
Walkway
Radiological Regulated
x
x
x
x
x
Office
Roll Up
Door
Operations
Monitoring
Room
Break
Room
Truck Alley
Maintenance
Shop
Monitoring Station
Scale
C-337-A Feed Facility
OT 16.7
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x
x
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1
Cylinder Valve
UF6
CylinderTo Feed
Header
Teflon Gaskets
Pigtail
OT 17.1
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Review and Critique of
Findings and Improved
Writing of Findings
Objectives:
• List the three finding categories and
describe how to separate surface issues
from underlying substantial issues.
• List three of the five priority groupings for
assessment findings.
• Identify the three steps needed to write an
appropriate finding.
• List three suggestions for effective
presentation of findings and concerns.
OT 17.2
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Finding Categories
• Surface:
– Minor issues
– Easy to correct
• Substantial:
– More significant issues
– Ease in correcting varies
• Organizational:
– Programmatic issues
– Difficult to correct
OT 17.3
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Priority Groupings
In decreasing order of priority:
• Imminent danger
• Not imminent, but potential danger
• Violations of regulations, laws, and
orders
• Adverse public opinion
• Performance and effectiveness
issues
OT 17.4
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Writing Findings
• List requirement
• State observation
• State concern
OT 18.1
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Compliance-Based Versus
Performance-Based
Evaluations
Objectives:
• Define compliance-based audits.
• Define performance-based assessments.
• Describe the four key elements of the
assessment process.
• Describe the advantage of planning for an
assessment.
• Identify the preferred type of checklist.
OT 18.2
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Bases
• Compliance-based audits
• Performance-based assessments
OT 18.3
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Assessment Process
• Planning
• Performance
• Reporting
• Post-assessment actions:
– Response evaluation
– Followup
– Closeout
OT 19.1
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Field Exercise Guidelines
Objectives:
• Demonstrate applied field assessment
techniques.
• Present a finding to the class after return
from the field.
OT 19.2
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Assessor Conduct
• Set a good example
• Remember safety:
– Personal
– Facility
– Radiological
OT 19.3
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After Return from the Field
• Write up 1 finding (prescribed format):
– Observe 1½-2 minute time limit
– Coordinate with group members
• Present to class tomorrow morning
• Site personnel should be invited to exit
briefing
OT 19.4
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Presentation Findings
• List the requirement
• State what was observed
• State the concern
Part 4 of 5
Radiological Assessor Training
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Office of Health, Safety and Security
U.S. Department of Energy
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Radiological Assessor Training
Section 99
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Table of Contents
Regulatory Documents .....................................................................................Module1-1
10 CFR Part 835, Background and Focus .......................................................Module 2-1
Overview of the DOE Radiological Control Manual..........................................Module 3-1
Elements of a Radiological Control Program ...................................................Module 4-1
Technical Safety Requirements .......................................................................Module 5-1
Radiological Aspects of Uranium .....................................................................Module 6-1
Radiological Aspects of Tritium........................................................................Module 7-1
Radiological Aspects of Plutonium...................................................................Module 8-1
Radiological Work Permits...............................................................................Module 9-1
Contamination Containment and Temporary Control Measures ....................Module 10-1
Radiological Work Site Mockup Demonstration .............................................Module 11-1
Radiation-Generating Devices .......................................................................Module 12-1
Radiological Aspects of Accelerators.............................................................Module 13-1
Assessment Techniques................................................................................Module 14-1
Planning and Conducting Assessments.........................................................Module 15-1
Case Studies .................................................................................................Module 16-1
Review and Critique of Findings and Improved Writing of Findings...............Module 17-1
Compliance-Based Versus Performance-Based Evaluations ........................Module 18-1
Field Exercise Guidelines ..............................................................................Module 19-1
Course Summary...........................................................................................Module 20-1
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Radiological Assessor Training
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Student's Guide
Module 1 - 1
I. Introduction
II. DOE radiological health and safety
A. Policy (some key points in summary)
• Establish and maintain a system of
regulatory policy and guidance.
• Ensure appropriate training is developed and
delivered and the technical competence of
the DOE workforce.
• Establish and maintain, from the lowest to
the highest levels, line management
involvement and accountability for
Departmental radiological performance.
• Ensure radiological measurements,
analyses, worker monitoring results, and
estimates of public exposures are accurate
and appropriately made.
• Conduct radiological operations in a manner
that controls the spread of radioactive
materials and reduces exposure to the work
force and the general public and utilizes a
process that seeks exposure level as low as
reasonably achievable (ALARA).
• Incorporate dose reduction, contamination
reduction, and waste minimization features
into the design of new facilities and
significant modifications to existing facilities
in the earliest planning stages.
Section 100
• Conduct oversight to ensure Departmental
requirements are being complied with and
appropriate radiological work practices are
being implemented.
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Student's Guide
Module 1 - 2
B. History
DOE has provided numerous written standards
for on-site radiological protection, the most
recent regulation being 10 CFR Part 835,
Occupational Radiation Protection, Amended
June 2007. This regulation was preceded by:
• DOE Notice 5480.6 of June 17, 1992,
Radiological Control, which specified that the
DOE Radiological Control Manual (DOE/EH-
0256T) would supersede DOE Order
5480.11.
• DOE Order 5480.11, Radiation Protection for
Occupational Workers (effective December,
1988). The purpose was to establish
radiation protection standards and program
requirements for DOE and DOE contractors
for the protection of workers from ionizing
radiation.
The establishment of DOE radiological
protection standards did not start with these
documents. A chronology of dose limits of DOE
and its predecessor agencies, the Atomic
Energy Commission (1946-1975) and the
Energy Research and Development
Administration (1975-1977), demonstrate a
lowering of whole body dose limits over the last
50 years.
In the establishment of these dose limits, DOE
has followed recommendations of national and
international radiological protection groups,
notably the International Commission on
Radiological Protection (ICRP) and the National
Council on Radiation Protection and
Measurements (NCRP).
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C. Hierarchy of requirements
Currently within DOE there are two parallel
hierarchies of requirements:
• Rules and/or regulations (these terms are
used interchangeably in this training)
• DOE Orders
III. Rules and regulations
In response to the enforcement authority in the
Price-Anderson Amendments Act (PAAA) of 1988,
DOE is converting its contractual requirement in
orders to enforceable rules to enhance contractor
accountability for safety.
A. DOE enforcement of rules under PAAA
10 CFR Part 820 (effective on September 16,
1993, Amended June 2007) sets forth the
procedures to implement the provisions of the
PAAA. Part 820 requires contractors to comply
with DOE Nuclear Safety Requirements.
PAAA demands a “large stick” to enhance
contractor accountability for safety. Rules
provide authority for the assessment of civil and
criminal penalties and thus provide the large
stick.
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Module 1 - 4
B. Penalties under Part 820
1. Civil penalties
DOE may assess civil penalties against any
person subject to Part 820, for violations of:
• Codified rules in the CFR
• Compliance orders
• Any program or plan required by a rule or
compliance order
Note: Certain nonprofit educational
institutions and other listed institutions are
exempt from assessment of civil penalties.
2. Criminal penalties
If a person subject to the Atomic Energy Act
of 1954, as amended, or Nuclear Safety
Requirements, has by action or omission
knowingly and willfully violated, caused to be
violated, attempted to violate, or conspired to
violate any section of the Atomic Energy Act
of 1954, as amended, or applicable DOE
Nuclear Safety Requirements, the person
shall be subject to criminal sanctions.
3. The “carrot and stick” approach
Section 101
DOE may provide monetary incentives in its
management and operating (M&O) contracts
for actions consistent with or exceeding
requirements, and to penalize actions and
activities that were not in compliance with
requirements.
Noncompliance with the Radiation Protection
Program can subject a contractor to PAAA
enforcement. There are provisions to
mitigate penalties for self identifying and
reporting violations.
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Module 1 - 5
C. DOE Nuclear Safety Requirements
DOE Nuclear Safety Requirements are the set of
enforceable rules, regulations, or orders relating
to nuclear safety that have been adopted by
DOE (or by another agency if DOE specifically
identifies it).
Compliance orders are issued by the Secretary.
They identify a situation that violates, potentially
violates, or otherwise is inconsistent with the:
• Atomic Energy Act of 1954, as amended
• Nuclear statutes
• Nuclear Safety Requirements
Compliance orders:
• Mandate a remedy or other action
• States the reason for the remedy or other
action
D. 10 CFR Part 835
On December 14, 1993, DOE published a final
rule in the Federal Register (58 FR 65458) Title
10 Code of Federal Regulations Part 835,
Occupational Radiation Protection (10 CFR
835). On November 4, 1998 an amendment to
10 CFR 835 was published in the Federal
Register (63 FR 59663).
The purpose of 10 CFR 835 is the codification of
radiological protection requirements. It contains
“shall” statements, which are legally binding. It
also contains:
• Prescriptive language
Radiological Assessor Training
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Module 1 - 6
• Added emphasis on ALARA
• Requirements for a Radiation Protection
Program (RPP)
• Federal law
• Criminal and civil penalties for violations
E. Radiation Protection Program (10 CFR Part 835)
Each site, under Part 835, must submit a written
Radiation Protection Program (RPP).
The RPP requires careful consideration because
noncompliance may subject a contractor to
PAAA enforcement
F. Guidance documents for 10 CFR Part 835
Two types of regulatory guidance documents
have been developed:
• Guidance for implementing the provisions of
10 CFR Part 835.
• Guidance providing technical positions.
The above are available through the DOE HS-11
website at:
Insert appropriate URL
Unlike the requirements specifically set forth in
10 CFR Part 835, the provisions in guidance
documents are not mandatory. They are
intended solely to describe the rationale for, and
the objectives of, regulatory requirements and/or
to identify acceptable methods for implementing
regulatory requirements.
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Module 1 - 7
Failure to follow a guidance document does not
in itself indicate noncompliance with a specific
requirement of the rule. A finding of
noncompliance is found for a failure to satisfy
the regulatory requirement.
Following a guidance document in the
prescribed manner will ordinarily create a
presumption of compliance with a related
regulatory requirement.
1. Technical guidance
Technical guidance describes and
disseminates technical methods and
techniques for fulfilling implementation and,
in turn, the requirements in
10 CFR Part 835. Examples of these
guidance are DOE Technical Standards and
DOE Radiological Control Technical
Positions (RCTPs).
2. Implementation guides (IGs)
Section 102
Implementation guidance is intended to
identify and make available to DOE
contractors basic program elements and
acceptable methods for implementing
specific provisions of the final rule. Thirteen
implementation guides have been developed
for 10 CFR Part 835.
G. Relationship between 10 CFR Part 835 and
10 CFR Part 20
10 CFR Part 20 is the occupational radiological
regulation issued by the Nuclear Regulatory
Commission (NRC).
The question of consistency among federal
agencies in their occupational radiological
protection regulations became a major point of
discussion during the rule making process.
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Student's Guide
Module 1 - 8
While agreeing with the goal of consistency,
DOE believes that it must promulgate its own
regulations because of the unique nature and
diversity of radiological activities within the DOE
complex. The final rule allows DOE to establish
more rigorous requirements in areas of particular
concern. Overall 10 CFR Part 835 has many
similarities as 10 CFR Part 20.
IV. DOE STD Radiological Control and Orders
A. Radiological Control
In January 1992, a memorandum was sent to the
heads of DOE elements involved in managing
radiological programs. In the memorandum, the
Secretary directed a series of initiatives to
enhance the conduct of radiological operations
within the Department of Energy. Also in this
memo, the Assistant Secretary of Environment,
Safety and Health was directed to develop a
comprehensive and definitive radiological control
manual. The DOE Radiological Control Manual
was developed to meet that directive and was
approved by the Secretary and promulgated with
DOE Notice 5480.6, Radiological Control, in July
1992.
After the issuance of 10 CFR 835 as a final rule
in December 1993, DOE Notice N441.1,
Radiological Protection for DOE Activities, was
issued on 9-30-95. This cancelled the notice
which made the Radiological Control Manual a
requirements document. However, the notice
stated that "cancelled orders that are
incorporated by reference in a contract shall
remain in effect until the contract is modified to
delete the reference.
N441.1 also retained some of the radiation
protection requirements from the Radiological
Control Manual that were not included in 10 CFR
835.
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Student's Guide
Module 1 - 9
In July, 1999, the Radiological Control Manual
was replaced by the standard, DOE-STD-1098-
99, Radiological Control. Many DOE sites
contractually must still adhere to the provisions
of either the Radiological Control Manual or the
Radiological Control Standard. Subsequent to
the 1998 amendment to 10 CFR 835, the
effective date of N441.1 has passed.
The DOE Radiological Control Standard is not
regulatory in nature. It is a guidance document
that describes DOE’s policy and expectations for
an excellent radiological control program.
1. Implementation
If a site fully implements a provision of the
DOE Radiological Control Standard, the user
will have most likely complied with any
related statutory, regulatory, or contractual
requirements. Users are cautioned that they
must review the source document (10 CFR
835) to ensure compliance.
2. Enforceability
When incorporated into contracts, the
provisions of the DOE Radiological Control
Standard are binding requirements.
If portions of the Site-Specific Radiological
Control Standard are incorporated in the RPP
under Part 835 and approved by DOE, they
are also binding.
Section 103
B. The Site-Specific Radiological Control Standard
• The DOE Radiological Control Standard
states that a Site-Specific Radiological
Control Standard should be written and
followed.
.
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C. Relationship between 10 CFR Part 835 and the
DOE Radiological Control Standard
1. Compliance
• The Office of Enforcement (HS - 40) will
enforce 10 CFR Part 835. It can assess
fines and penalties.
• The Program Offices will audit for both
compliance with 10 CFR 835 and
contractual agreements including the DOE
Radiological Control Standard, Orders, etc.
Results of these audits can affect the
contractor’s award fee.
2. What if there are conflicts?
10 CFR Part 835 takes precedence over
requirements of the DOE Radiological
Control Standard and orders. It is unlikely
that there will be a conflicting requirement
between the two documents, although one
document may have a requirement that is not
addressed in the other.
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Module 1 - 11
It is planned that all requirements for nuclear
safety will be incorporated into rules.
3. “Shall” and “should” statements
• 10 CFR Part 835 contains “shall”
statements. “Shall” statements in Part
835 are legally binding.
Processes for exemption relief from Part
835 are set forth in Subpart E to Part 820.
If relief is requested from provisions of
Part 835, the exemption must be
considered and granted, if appropriate, by
the Chief Health, Safety and Security
Officer (HS - 1).
• The use of “should” in the DOE
Radiological Control Standard recognizes
that there may be site- or facility-specific
attributes that warrant special treatment.
It also recognizes that literal compliance
with the elements and requirements of the
provision may not achieve the desired
level of radiological control performance.
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D. DOE Standards
DOE has developed several technical standards
for occupational radiation protection. Depending
on the site specific application, some standards
are required to be followed. For example, sites
which need to monitor individual external
exposures to ionizing radiation need to follow the
DOE Laboratory Accreditation Program
(DOELAP) standards. Other standards may be
incorporated by reference in the site RPP.
Other standards provide technical guidance on
specific applications, but adherence to the
standard may not be required.
Prior to conducting an assessment, the site
requirements documents must be reviewed to
determine applicable requirements.
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Module 1 - 13
V. Defense Nuclear Facilities Safety Board
A. Establishment
The Atomic Energy Act of 1954 was amended by
adding Chapter 21, Defense Nuclear Facilities
Safety Board (DNFSB). This amendment
established an independent board in the
executive branch to provide oversight of some
DOE operations at DOE facilities and sites.
B. Members
The DNFSB consists of five members appointed
by the President with consent of the Senate.
The Board shall:
• Review and evaluate standards
• Investigate any event or practice at a DOE
defense nuclear facility that the Board
determines has adversely affected or may
adversely affect public health and safety.
The Board may:
• Establish reporting requirements for the
Secretary of Energy
By evaluating how well DOE meets its
Section 104
objectives, the DNFSB helps DOE achieve and
maintain excellence in radiological protection.
C. Secretary of Energy
The Secretary of Energy shall fully cooperate
with the Board.
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Module 1 - 14
D. DNFSB Recommendations
DNFSB provides DOE with recommendations for
improving safety at DOE defense nuclear
facilities. Examples include:
DNFSB Recommendation 91-6 dealt with
radiological protection concerns throughout
the DOE defense nuclear facilities complex,
and identified several actions to be taken by
the Department to improve radiological
protection performance.
DNFSB Recommendation 92-7 dealt with
training and qualification at DOE sites and
facilities.
DNFSB Recommendation 98-1 dealt with
resolution of internal audit findings.
DNFSB Recommendation 99-1 dealt with
safe storage of fissionable materials.
Implementation of DOE and site commitments
made in response to DNFSB recommendations
are areas to review during an assessment.
Radiological Assessor Training
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Student's Guide
Module 2 - 1
I. Introduction
This module provides an overview of many of the
provisions of 10 CFR 835. For completeness,
individuals should always reference back to 10 CFR
835 for the complete text.
II. Outline of 10 CFR Part 835
Part 835 is the codification of radiological protection
requirements. Part 835 contains 14 subparts and
five appendices. The outline consists of the
following subparts:
A — General Provisions
B — Management and Administrative
Requirements
C — Standards for Internal and External Exposure
D — Reserved
E — Monitoring of Individuals and Areas
F — Entry Control Program
G — Posting and Labeling
H — Records
I — Reports to Individuals
J — Radiation Safety Training
K — Design and Control
L — Radioactive Contamination Control
M — Sealed Radioactive Source Control
N — Emergency Exposure Situations
Under 10 CFR Part 835, each site must submit a
Radiation Protection Program (RPP).
Part 835 helps to ensure that DOE facilities are
operated in a manner such that occupational
radiological exposure to workers is maintained
within acceptable limits and as low as is reasonably
achievable (ALARA).
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A. Subpart A - General Provisions
Subpart A contains the scope of the rule. The
rule in this part establishes radiological
protection standards, limits, and program
requirements for protecting individuals from
ionizing radiation resulting from the conduct of
DOE activities.
It also includes activities excluded from the
provisions of the rule. Activities that are
excluded include the following (summarized):
• Activities regulated through a license by the
Nuclear Regulatory Commission (NRC) or a
state under an agreement with the NRC.
• Activities conducted under the authority of the
Director, Naval Nuclear Propulsion Program.
• Specified activities conducted under the
Nuclear Explosives and Weapons Surety
Program.
• Radioactive material transportation.
• DOE activities in other countries with
acceptable radiation protection program.
• Background radiation.
Occupational doses received as a result of
excluded activities and radioactive material
transportation, as listed above, shall be
considered when determining compliance with
the occupational dose limits (835.202 and
835.207), and with the limits for the embryo/fetus
(835.206).
Subpart A also addresses:
Section 105
• Definitions
• Radiological units (Curie, rad, roentgen, rem,
and multiples)
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B. Subpart B - Management and Administrative
Requirements
The RPP shall:
• Include formal plans and measures for
applying the ALARA process to occupational
exposures.
• Specify the existing and/or anticipated
operational task.
• Address, but not be limited to, each
requirement in Part 835.
• Include plans, schedules, and other
measures for achieving compliance.
DOE may direct or make modifications to an
RPP. An initial RPP or update shall be
considered approved 180 days after its
submission unless rejected by DOE at an earlier
date.
Compliance with 835.402(d) for radiobioassay
program accreditation shall be achieved no later
than January 1, 2002.
Internal Audits (10 CFR 835.102)
Internal audits of the radiation protection
program, including examination of program
content and implementation, shall be conducted
through a process that ensures that all functional
elements are reviewed no less frequently than
every 36 months. This training material and
DOE G 441.1, Management and Administration
of Radiation Protection Programs Guide, provide
guidance on DOE's expectations.
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Education, Training and Skills (10 CFR 835.103)
Individuals responsible for developing and
implementing measures necessary for ensuring
compliance with the requirements of this part
shall have the appropriate education, training,
and skills to discharge these responsibilities.
DOE STD-1107-97 Knowledge, Skills, and
Abilities for Key Radiation Protection Positions at
DOE Facilities, provides guidance on DOE's
expectations.
Written Procedures (10 CFR 835.104)
Written procedures are required, as necessary,
to ensure compliance with 835, commensurate
with radiological hazards and education, training
and skills of exposed individuals.
C. Subpart C - Standards for Internal and External
Exposure
This subpart addresses limits for:
• General employees (occupational)
• Embryos/fetus of declared pregnant worker
(i.e., A woman who has voluntarily declared
to her employer, in writing, her pregnancy for
the purpose of being subject to the
occupational dose limits to the embryo/fetus.
This declaration may be revoked, in writing,
at any time by the declared pregnant worker.)
• Occupationally exposed minors
• General public in a controlled area
It also addresses:
• Planned special exposures
• Nonuniform exposures of the skin
Radiological Assessor Training
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Module 2 - 5
• Concentrations of radioactive material in air
1. Summary of dose limits
10 CFR Part 835 employs the rem unit for
several different physical quantities. For
information about these quantities refer
participants to page 1 of handouts, “Dosimetric
Quantities in 10 CFR Part 835.”
Exposed Individual Annual Limit
General Employee: Whole Body (internal and external) (TED) 5.0 rem
General Employee: Lens of Eye 15.0 rem
General Employee: Extremity (below elbow and knees) and skin 50.0 rem
General Employee: Any Organ or Tissue (other than lens of eye) (DED + CED) 50.0 rem
Declared Pregnant Worker: Embryo/Fetus (gestation period) 0.5 rem
Occupationally Exposed Minors (under age 18): (TED) 0.1 rem *
Members of the Public in Controlled Areas: (TED) 0.1 rem
• And 10% of other general employee limits.
Section 106
2. Planned special exposures (PSEs)
It is acknowledged that unusual conditions
can arise in which higher-than-normal doses
can be justified. In these well-planned, well-
controlled, and highly infrequent and unusual
conditions operating management would be
permitted to allow specified individual doses
exceeding the occupational limit, such as 5
rem per year.
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The term "unusual conditions" is made clear
by specifying that alternatives which would
preclude exposures higher than the
prescribed dose limits must be either
unavailable or impractical.
10 CFR 835.204 specifies requirements for
annual and lifetime dose from PSEs. It also
specifies requirements for determining
previous individual exposures prior to
allowing a PSE.
Every PSE must be approved in advance by
DOE and requires the informed consent of
the employee involved.
3. Concentration of radioactive material in air
Appendices A and C contain the derived air
concentration (DAC) values used in the
control of occupational exposure to airborne
radioactive material.
DACs are listed in appendices A and C of 10
CFR 835. For intakes (appendix A), they are
the airborne concentration that equals the
annual limit on intake (ALI) divided by the
volume of air breathed by an average worker
for a working year of 2000 hours (assuming a
breathing volume of 2400 m3).
The ALI is the smaller value of intake of a
given radionuclide in a year by a
standardized man that would result in a
CEDE of 5 rems or a CDE of 50 rems to any
individual organ or tissue.
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Appendix C contains DACs for controlling
external dose from being immersed in a cloud
of airborne radioactive material.
Estimation of internal dose shall be based on
bioassay data rather than air concentration
values unless bioassay data are:
• Unavailable (e.g., radon or very short lived
radioisotopes)
• Less accurate than internal dose
estimates based on representative air
concentration values
• Inadequate
E. Subpart D - Reserved
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E. Subpart E - Monitoring of Individuals and Areas
This subpart addresses:
• General requirements
• Instrumentation
• Individual monitoring - external
• Individual monitoring - internal
• Air monitoring
• Receipt of packages containing radioactive
material
1. General requirements (10 CFR 835.401)
Monitoring of individuals and areas shall
be performed to:
• Demonstrate compliance with Part
835.
• Document radiological conditions.
• Detect changes in the radiological
conditions.
• Detect the gradual buildup of
radioactive material.
• Verify the effectiveness of engineering
and process controls in containing
radioactive material and reducing
radiation exposure.
• Identify and control potential sources
of individual exposure to radiation
and/or radioactive material.
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2. Instrumentation
Instruments and equipment used for
monitoring and contamination control shall
be:
• Periodically maintained and calibrated
on an established frequency.
• Appropriate for the type(s), levels, and
energies of the radiation(s)
encountered.
• Appropriate for existing environmental
conditions.
• Routinely tested for operability.
3. Individual monitoring - external (10 CFR
835.402)
Section 107
For the purpose of monitoring individual
exposure to external radiation, personnel
dosimetry shall be provided to and used
by:
• Radiological Workers likely to receive:
– An effective dose equivalent to the
whole body of 0.1 rem (100 mrem)
or more in a year
– A shallow dose equivalent to the
skin or to any extremity of 5 rem or
more in a year
– A lens of the eye dose equivalent
of 1.5 rem or more in a year
• Declared Pregnant Workers who are
likely to receive from external sources
a dose equivalent to the embryo/fetus
in excess of 10 percent of the
applicable limit.
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• Members of the public in a controlled
area and occupationally exposed
minors likely to receive, in one year,
from external sources, a dose in
excess of 50 percent of the applicable
limits.
• Individuals entering a High or Very
High Radiation Area.
DOE Laboratory Accreditation for
Personnel Dosimetry is required for
external dose monitoring programs
implemented to demonstrate compliance
with 10 CFR 835.
4. Individual monitoring - internal (10 CFR
835.402)
Internal dose evaluation programs
(including routine bioassay programs)
shall be conducted for:
• Radiological Workers who, under
typical conditions, are likely to receive
0.1 rem or more committed effective
dose equivalent from all occupational
radionuclide intakes in a year.
• Declared Pregnant Workers likely to
receive an intake or intakes resulting in
a dose equivalent to the embryo/fetus
in excess of 10 percent of the limit.
• Members of the public in a controlled
area and occupationally exposed
minors who are likely to receive a
committed effective dose equivalent in
excess of 50 percent of the limit from
all intakes in a year.
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DOE Laboratory Accreditation for
Radiobioassay is required for internal dose
monitoring programs implemented to
demonstrate compliance with 10 CFR 835.
5. Air monitoring (10 CFR 835.403)
Measurements of radioactivity concentrations
in the ambient air of the workplace shall be
performed as follows:
• Air sampling shall be performed in
occupied areas where an individual is
likely to receive an exposure of 40 DAC-
hrs or more in a year (i.e. an annual
intake of 2 percent or more of the specific
ALI value) for the mixture of isotopes.
• Samples shall be taken as necessary to
characterize the levels or concentration of
airborne radioactive material when
respirators are worn for radiation
protection purposes.
• Real-time air monitoring shall be
performed when there is a need to alert
potentially exposed individuals to
unexpected increases in airborne
radioactivity levels such that immediate
action is necessary in order to minimize or
stop inhalation exposures.
6. Receipt of Packages Containing Radioactive
Material (10 CFR 835.405)
Establishes requirements to monitor certain
types of packages and sets a time limit of not
later than 8 hours after the beginning of the
working day following receipt of the package.
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F. Subpart F - Entry Control Program (10 CFR
835.501)
Subpart F addresses entry into:
• Radiological Areas
• High Radiation Areas
• Very High Radiation Areas
1. Radiological Areas
The degree of control shall be commensurate
with existing and potential radiological
hazards within the area.
Section 108
One or more of the following methods
shall be used to ensure control:
• Signs and barricades
• Control devices on entrances
• Conspicuous visual and/or audible
alarms
• Locked entrance ways
• Administrative controls
“No control(s) shall be installed at any
radiological area exit that would prevent
rapid evacuation of personnel under
emergency conditions.”
2. High Radiation Areas
A High Radiation Area is an area where
radiation levels exist such that an
individual could exceed a deep dose
equivalent to the whole body of 0.1 rem in
any one hour at 30 centimeters from the
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source or from any surface that the
radiation penetrates.
If an individual receive a deep dose
equivalent exceeding 1.0 rem in an hour
(at 30 cm), a High Radiation Area shall
have one or more of the following:
• A control device that prevents entry to
the area when high radiation levels
exist or that, upon entry, causes the
radiation level to be reduced below
that level that defines a High Radiation
Area.
• A device that functions automatically to
prevent use or operation of the
radiation source or field while
individuals are in the area.
• A control device that energizes a
conspicuous visible or audible alarm
signal so that the individual entering
the High Radiation Area and the
supervisor of the activity are made
aware of the entry.
• Entryways that are locked. During
periods when access to the area is
required, positive control over each
entry is maintained.
• Continuous direct or electronic
surveillance that is capable of
preventing unauthorized entry.
• A control device generating audible
and visual alarm signals to alert
personnel in the area before use or
operation of the radiation source and
in sufficient time to permit evacuation
of the are or activation of a secondary
control device that will prevent use or
operation of the source.
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3. Very High Radiation Areas
A Very High Radiation Area is an area in
which an individual could receive a dose
in excess of 500 rad in one hour at 1
meter from the radiation source or from
any surface that the radiation penetrates.
In addition to the requirements for a High
Radiation Area, additional measures shall
be implemented to ensure individuals are
not able to gain unauthorized access to
Very High Radiation Areas.
“No control(s) shall be established in a
High or Very High Radiation Area that
would prevent rapid evacuation of
personnel.”
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G. Subpart G - Posting and Labeling
Subpart G addresses the general requirements
for signs:
• Yellow background
• Black or magenta radiation symbol
• Clear and conspicuous signs
In addition, Subpart G addresses specific posting
requirements for:
• Controlled Areas
• Radiation Areas
• High Radiation Areas
• Very High Radiation Areas
• Airborne Radioactivity Areas
• Contamination Areas
• High Contamination Areas
• Radioactive Material Areas
This subpart also addresses exceptions to
posting and labeling.
H. Subpart H - Records
Subpart H addresses requirements for records
documenting compliance with Part 835 and with
the Radiation Protection Program.
Records that are specifically required include
those necessary to demonstrate compliance with
the ALARA provisions of the rule.
Section 109
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10 CFR 835 also requires that certain records be
maintained, including records of:
• Individual monitoring
• Sealed source inventory and control
• Results of surveys for the release of material
and equipment
• Results of specified monitoring for radiation
and radioactive material
• Maintenance and calibration of radiation
monitoring instruments
• Internal audits
Each individual’s training as a general employee
and as a Radiological Worker must be recorded.
Where appropriate, demonstration and
documentation of proficiency is required.
Refer to 10 CFR 835 Subpart H for a complete
listing of required records.
DOE G 441.1-1B, Occupational Radiation
Protection Record-Keeping and Reporting Guide,
provides additional guidance on record-keeping
requirements, including reference to DOE O
231.1A, Change 1, Environment, Safety and
Health Reporting, and DOE M 231.1-1A, Change
2, Environment, Safety and Health Reporting
Manual. This order and manual specify radiation
protection reporting requirements that may be
applicable to the site or facility being assessed.
I. Subpart I - Reports to Individuals (10 CFR
835.801)
Subpart I addresses reports to individuals and
their accessibility to reports, including:
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On an annual basis, each DOE or DOE
contractor-operated site or facility must provide
each individual monitored for occupational
exposure a radiation dose report of his/her
occupational exposure at that site or facility.
Upon the request from an individual terminating
employment, records of exposure shall be
provided to that individual as soon as the data
are available, but not later than 90 days after
termination. A written estimate of the radiation
dose received by that employee based on
available information shall be provided at the
time of termination, if requested.
J. Subpart J - Radiation Safety Training
This subpart addresses radiation safety training.
The tailored approach to training requirements
are based on:
• Unescorted access to or receiving
occupational dose in controlled areas (e.g.,
General Employees)
• Unescorted access to radiological areas or
unescorted assignment as Radiological
Workers
Requirements of Part 835 include:
• Verification by examination for certain training
(e.g., Radiological Worker Training)
• Intervals of training not to exceed twenty four
months
• List of topics which must be included in
training
• Provisions for limited use of escorts in lieu of
training
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DOE G 441.1-1B, Radiation Protection Program
Guide, provides additional guidance on DOE's
expectations on radiation safety training.
K. Subpart K - Design and Control
Subpart K addresses added emphasis on facility
and equipment design and administrative
controls to maintain radiological exposures
ALARA.
1. Facility design and modifications (10 CFR
835.1001)
During the design of new facilities or
modification of old facilities, the following
objectives shall be adopted:
• Optimal methods shall be used to assure
ALARA
• Maintain exposure levels below an
average of 0.5 mrem/hr
• Avoid release of radioactivity to the
workplace atmosphere
• The design or modification of a facility and
the selection of materials shall include
features that facilitate operations,
maintenance, decontamination, and
decommissioning
Section 110
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2. Workplace controls (10 CFR 835.1003)
During routine operations, the combination of
physical design features and administrative
control shall provide that:
• The anticipated occupational dose to
general employees shall not exceed the
limits
• The ALARA process is utilized for
personnel exposures to ionizing radiation
L. Subpart L - Radioactive Contamination Control
1. Control of material and equipment
This section addresses the requirements for
release of materials and equipment from
radiological areas to controlled areas.
Releases to uncontrolled areas are addressed
in DOE O 5400.5. Some of the provisions:
• Specifies conditions for material and
equipment in contamination areas (CAs),
high contamination areas (HCAs), and
airborne radioactivity areas (ARAs) to be
released to a controlled area
• Addresses movement of material and
equipment with removable surface
contamination, on-site from one
radiological area for immediate placement
in another radiological area
• Specifies conditions for material and
equipment with fixed contamination to be
released for use in controlled areas
outside of radiological areas
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Control of Areas (10 CFR 835.1102) addresses
• Prevention of inadvertent transfer or
removal of contamination to locations
outside radiological areas under
normal conditions
• Where contamination levels exceed
values in Appendix D, the area is
controlled commensurate with hazards
• Areas with fixed contamination
exceeding radioactivity values may be
located outside radiological areas,
provided certain controls, conditions,
or provisions are met
• Personnel monitoring for
contamination upon exiting CAs,
HCAs, or ARAs
• Use of protective clothing in CAs and
HCAs
M. Subpart M - Sealed Radioactive Source Control
Sealed radioactive sources shall be used,
handled and stored in a manner commensurate
with the hazard.
Specifies values (Appendix E) for sources which
must be inventoried and leak tested at intervals
not to exceed six months.
N. Subpart N - Emergency Exposure Situations
This subpart addresses:
• Employees who have exceeded dose limits
as result of authorized emergency exposure
• Nuclear accident dosimetry
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Individuals whose occupational
exposures have exceeded any limits as a
result of an authorized emergency
exposure may be permitted to return to
work provided that certain conditions are
met.
Nuclear accident dosimetry
Nuclear accident dosimetry involves
installations possessing sufficient
quantities of fissile material to constitute a
critical mass, and shall include;
• Method to conduct initial screening of
personnel involved
• Method and equipment for analysis of
biological materials
• A system of fixed nuclear accident
dosimeter units
• Personal nuclear accident dosimeters
T
T
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I. Introduction
II. DOE Radiological Control Standard
The DOE Radiological Control Standard is written
for line management. It is designed to assist line
managers in fulfilling their duties and responsibilities
for implementing an occupational radiation
protection program.
Section 111
It is also designed to assist site/facility workers in
having the information they need to be responsible
for their own radiological exposures and to help
ensure that the controls are in place to eliminate
any releases, unplanned exposures or uptake, and
to apply ALARA principles. The emphasis is on
teamwork and support from line management.
The Radiological Control Standard may be
considered as an occupational radiation protection
good practices document. Individual sites may
have contractual commitments to implement
sections of the standard.
III. Chapter 1, Excellence in Radiological Control
This chapter defines the roles of DOE and the
contractors in achieving the goal of radiological
control excellence. It consists of the following five
sections:
• DOE Radiological Control Standard
• Leadership in Radiological Control
• Improving Radiological Control Performance
• Contractor Radiological Control Organization
• DOE Management
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A. DOE Radiological Control Standard
The contractor is responsible for implementing
an occupational radiation protection program.
To assist this effort, they may develop a Site
Radiological Control Standard Implementation
Plan. The Site-Specific Radiological Control
Standard, which is developed from the
Implementation Plan, does not require DOE
approval.
B. Leadership in Radiological Control
Commitment of senior management to
radiological control is defined in this section of
the Standard.
The responsibilities and accountability of each
individual for ALARA and radiological excellence
is emphasized.
Worker responsibilities and the concepts of
conduct of radiological operations are clearly
defined.
C. Improving Radiological Control Performance
The use of critiques as a management tool,
rather than as a method to “fix blame” or “shoot
the messenger,” and the importance of real root
cause identification are emphasized. Over 20
radiological performance indicators are identified
that are tools designed to assist managers in
focusing their priorities and attention on
radiological control performance.
D. Contractor Radiological Control Organization
This section discusses the contractor’s
radiological control organization and the
qualifications of the Radiological Control
Manager.
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E. DOE Management
This section discusses the roles and
responsibilities of DOE management for
providing guidance and performance evaluation
of radiological control programs.
IV. Chapter 2, Radiological Standards
This chapter deals with administrative control dose
limits, contamination control and control levels, and
posting.
A. Administrative Control Levels (ACLs) and Dose
Limits
Lifetime control levels and dose limits for
Radiological Workers, members of the public,
embryos/fetuses, and special control levels are
discussed in this section.
For most facilities an ACL of 500 millirem or less
will be challenging for Radiological Workers.
Individual occupational doses, in rem, should be
kept below the individual's age in years.
B. Contamination Control and Control Levels
In this section, personnel contamination control,
removable and fixed contamination control
levels, and airborne radioactivity control levels
are given.
C. Posting
Posting requirements are presented in this
Section 112
section and include several non-regulatory areas
including: Radiological Buffer Areas,
Underground Radioactive Material Areas, and
Soil Contamination Areas.
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V. Chapter 3, Conduct of Radiological Work
The planning of radiological work, work preparation
(e.g., Radiological Work Permits), and the
requirements for the entry to and exit from the
various types of controlled areas are contained in
this chapter. Also covered are: radiological work
performance, the aspects of radiological work in
different operations with radiation-generating
equipment, and construction and restoration
projects.
A. Planning Radiological Work
This section emphasizes that the conduct of
radiological work is a line responsibility. Worker
responsibility, along with systematic planning,
provides the necessary information for safe
radiological work. Of fundamental importance is
the requirement to plan work with an emphasis
on ALARA principles.
B. Work Preparation
In this section, the Radiological Work Permit
(RWP) is discussed. This chapter states that the
RWP is the key to any particular radiological
operation, and preplanning is essential.
C. Entry and Exit Requirements
The minimum requirements for entry into and
exit from defined radiological areas and other
non-regulatory areas are discussed in this
section.
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D. Radiological Work Controls
This section discusses radiological work as a
team effort involving the Radiological Workers,
their supervisors, and Radiological Control
personnel. The DOE Radiological Control
Standard discusses stop-radiological work
authority for Radiological Control Technicians
(RCTs), their supervisors, line supervision, and
workers through their supervisors because of:
• Inadequate radiological controls
• Radiological controls not being implemented
• A radiological control hold point not being
satisfied
DOE O 440.1B, Worker Protection Program for
DOE (Including the National Nuclear Safety
Administration) Federal Employees, May, 2007,
specifies that individuals have the authority to
stop work due to hazardous conditions.
This stop work authority is not limited to just
radiological hazards. Workers may "stop work
when they discover employee exposures to
imminent danger conditions or other serious
hazards." Contractors are required to have
procedures addressing stop work authority.
E. Evaluation of Performance
Evaluation of performance, critiques, post job
reviews, and lessons learned are discussed in
this section.
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F. Special Applications
This section examines the special aspects for
the control of radiological work when working
with the following:
• Plutonium
• Uranium
• Tritium
• Accelerators
• Radiation Generating Devices
G. Radiological Design Criteria
This section addresses design objectives for
design of new facilities and modification of
existing facilities.
VI. Chapter 4, Radioactive Materials
The requirements for labeling, storage, control,
release, and transportation of radioactive materials,
and the control of radioactive sources, are
discussed in this chapter. This chapter also deals
with the management of solid and liquid radioactive
wastes, and airborne radioactivity. Support activities
such as personnel protective clothing and
equipment, laundry, decontamination and vacuum
cleaners, and portable air-handling equipment are
also discussed.
Section 113
VII. Chapter 5, Radiological Health Support Operations
This chapter discusses the requirements for
external dosimetry, internal dosimetry, a respiratory
protection program, the handling of contaminated
personnel, radiological monitoring and surveys, and
instrumentation and calibration.
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VIII. Chapter 6, Training and Qualification
The requirements that ensure personnel have the
training and qualifications needed to safely work in
and around radiological areas and to maintain their
own doses and those of others (ALARA) are
discussed in this chapter.
A. General Radiological Training
Within these sections, training and qualification
standards are discussed for:
• General Employees
• Radiological Workers I and II
• Radiological Control Technicians and
Supervisors
B. Other Radiological Training
This section addresses training and qualification
for:
• Managers/supervisors
• ALARA training for:
– Engineers
– Schedulers
– Procedure writers
• Radiological control personnel
– Dosimetry technicians
– Instrument technicians
– Medical personnel
– Records clerk
– Whole body counter technicians
– Laboratory personnel
• Radiographers
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• Radiation-generating device operators
• Emergency response personnel
C. Training for Special Applications
This section addresses training for the following
facilities:
• Plutonium
• Uranium
• Tritium
• Accelerators
IV. Chapter 7, Radiological Records
The requirements for employee and visitor records,
radiological control procedures (policies,
procedures, Radiological Work Permits (RWPs),
ALARA, and quality assurance records), radiological
surveys, instrumentation and calibration records,
records management, and radiological reporting are
presented in this section.
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I. Introduction
II. Radiological Control Program
A. Overall program
The Radiological Control Program consists of
the commitments, policies, and procedures that
are administered by a site or facility to meet the
EH Health and Safety Policy.
The Radiation Protection Program required by
10 CFR Part 835 is an element of the overall
Radiological Control Program.
The Radiological Control Program should
address the following:
• Requirements
• Responsibilities
• Programs/procedures
• Assessments
B. Size of the program
Radiological Control Programs vary in size.
There are several factors that may affect the
magnitude of a Radiological Control Program.
The specific mission, types and quantities of
radioactive material, and the radiation-
generating devices that will be used at the site
are just a few.
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III. Elements of a radiological control program
A. Requirements
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B. Responsibilities
C. Programs/procedures
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D. Assessments
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IV. List of Radiological Control Program Elements
• Organization and administration
• Personnel training and qualification
• Quality assurance
• ALARA
• Radiological Work Control
– Procedures
– Radiological Work Permits
Section 114
• Posting and labeling
• Radioactive material control
– Source control
– Release of materials
– Receipt and transportation
• Radiation-generating devices
– Sealed source
– X-ray machines
• Entry control
• Contamination control
• Instrumentation/alarms
• Monitoring
– Workplace
– Effluent
– Environmental
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• Dosimetry
– External
– Internal
- Program management (e.g., staffing,
technical basis, procedures, quality
assurance)
- Individual monitoring (e.g., air monitoring,
contamination monitoring, bioassay)
- Internal dose evaluation
• Respiratory protection
• Facility specific features
– Uranium
– Plutonium
– Tritium
– Accelerators
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance indicators
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I. Introduction
II. Purpose of DOE Order 5480.22
The intended purpose of DOE Order 5480.22,
Technical Safety Requirements, is “to clearly state
the requirements to have Technical Safety
Requirements (TSRs) prepared for DOE nuclear
facilities and to delineate the criteria, content,
scope, format, approval process, and reporting
requirements of these documents and revisions
thereof.”
On October 10, 2000 an Interim final rule was
published in the Federal Register for 10 CFR 830,
"Nuclear Safety Management". The Interim Final
Rule was effective December 11, 2000, and codifies
requirements for TSRs in 10 CFR 830.205. The
new rule requires contractors to develop and submit
TSRs to DOE for approval by April 10, 2003. In the
interim, contractors are required to meet existing
safety bases, including TSRs.
TSRs are a critical element in the overall DOE
safety program.
A. Definitions (Paragraph 6)
• Technical Safety Requirements are those
requirements that define the conditions, safe
boundaries, and the management or
administrative controls necessary to ensure
the safe operation of nuclear facilities and to
reduce the potential risk to the public and
facility workers from uncontrolled releases of
radioactive materials or from radiation
exposure due to inadvertent criticality.
Technical Safety Requirements consist of
safety limits, operating limits, surveillance
requirements, administrative controls, use and
application instructions, and the bases
thereof.
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• A controlled document is content maintained
uniformly among the copies by an
Administrative Control System (paragraph 6,
Item e).
Basis: Summary statements of the reasons for
the operating limits and associated surveillance
requirements. It shows how the numerical
value, condition, or the surveillance fulfills the
purpose from the safety documentation.
B. Policy (Paragraph 7)
It is the policy of the Department that nuclear
facilities operate Cognizant Secretarial Officer
(CSO)-approved Technical Safety
Requirements, which prescribe the bounds for
safe operation of these facilities in order to
protect the health and safety of the public and
reduce risk to workers.
The TSRs constitute a contract between the
operating contractor and DOE management of
the methods that will be utilized or constraints to
be applied to minimize the potential risk of
operating the proposed facility or conducting the
proposed activity.
NOTE: TSRs apply to actions by specific facility
personnel and their commitments to responsible
DOE managers.
Section 115
The Technical Safety Requirements document is
to be a controlled document.
TSRs are not based upon maintaining worker
doses below some acceptable level following an
uncontrolled release of hazardous material or
inadvertent criticality; rather, the risk to workers
is reduced through controls that reduce the
likelihood and potential impact of such events.
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C. Source for bases (justification) of TSRs
In the development of limits, set-points, staffing
requirements, and other parameters for input
into the individual TSRs, the facility/operation-
specific Documented Safety Analysis ,
particularly the accident analyses contained
therein, is normally the primary basis.
The limitations that are included in the TSRs
should be derived from the facility-specific safety
analysis, which considers all credible accidents.
This includes the most significant possible
releases of radioactive and hazardous materials,
criticality scenarios, and the accidental releases
expected during the life of the facility.
Careful and thorough examination of these
accident analyses will provide values for defining
the operational limits necessary to ensure that
facility operations do not occur outside the
bounds assumed in the analyses. Such an
examination will also identify parameters and
operating conditions that should be limited in
order to reduce, provide warning of, and mitigate
the uncontrolled releases of hazardous materials
and to prevent inadvertent criticality.
Examples of requirements expected to be
developed include:
• Operating limits for principal process
parameters
• Technical and administrative conditions that
must be met
• Availability of safety equipment and systems
• Critical functions of instrumentation and
controls
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Operations within the boundaries of the resulting
requirements will provide reasonable assurance
that the nuclear facility will not:
• Threaten the health and safety of the public
• Pose an undue risk to workers from the
uncontrolled releases of radioactive or other
hazardous materials and inadvertent
criticality
For facilities that do not have an approved DSA,
the technical input into the TSRs must be
derived from existing documents/analyses that
specifically demonstrate the limiting conditions
that the facility is expected to experience during
normal operations and potential accident
conditions.
In order to serve as the basis for the TSRs,
these studies must systematically evaluate:
• All potential off-normal conditions that could
occur during the life of the facility
• What could be considered design basis
accidents
D. Responsibilities for TSRs
• Prepare → Contractor
• Review → DOE Field Office
• Approve → CSO
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E. Identification of violations
Violations of a TSR occur as the result of four
circumstances:
• Exceeding a Safety Limit (SL)
• Failing to take the necessary actions within
the required time limit following:
– Exceeding a Limit Control Setting (LCS)
– Failing to meet Limiting Conditions for
Operations (LCO)
– Failing to successfully meet a
Surveillance Requirement (SR)
• Failing to perform a surveillance within the
required time limit
• Failing to comply with an Administrative
Control (AC) requirement
As stated previously, compliance with TSRs is
Section 116
required by 10 CFR 820.205, violations may be
enforceable under PAAA.
F. Reporting Requirements (DOE Order 231.1A
Change 1) Occurrence Reporting and
Processing of Operations Information
• Categorization
– Operational Emergency
– Significance Category (1 – 4)
• Notification
• Follow-up notification
• Occurrence Report preparation
TSR ACs may impose additional facility- or
operations-specific reporting requirements,
which must also be carefully and fully followed.
Radiological Assessor Training
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Violations of TSRs may need to be reported as
part of the Noncompliance Tracking System
(NTS). For guidance on NTS reports, refer to
Operation Procedure Identifying, Reporting, and
Tracking Nuclear Safety Noncompliances, June
1998, prepared by the DOE Office of
Enforcement (HS-40).
G. Ancillary guidance
The TSR document shall be kept current at all
times so that it reflects the facility as it exists and
is analyzed in the SAR. The TSR must be
approved prior to changes in the facility or
facility practices.
TSRs should be written in a clear and concise
manner, in language that is understandable by
those in the facility operating organization. The
TSR should not contain excessive details that
belong more appropriately in the SAR.
The scope and content of TSRs are to be limited
to only the most critical nuclear safety areas.
This serves to make TSR Documents more
useful for controlling facility safety.
H. Radiological Assessment of TSR Compliance
TSRs typically specify requirements for several
areas that may be reviewed as part of a
radiological assessment. These areas include:
Area monitors:
Criticality monitors
Area Radiation Monitors
Air Monitors (i.e., real time air monitors,
fixed head air samplers)
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Surveillance requirements for area monitors
HEPA ventilation systems and their
surveillances
Shift Staffing
Facility staff qualification, training and
retraining
Audits and reviews
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I. Introduction
The guidance in DOE-STD-1136-2004, Guide of
Good Practices for Occupational Radiological
Protection in Uranium Facilities, 2004, should be
reviewed in detail prior to conducting an
assessment of uranium facilities. The following is a
brief overview of the radiological aspects of
uranium.
II. Radiological aspects of uranium
A. Radiological properties of uranium
Fifteen radioisotopes exist, but the three of most
concern to the uranium industry are:
Uranium-238:
99.7% abundant in natural uranium;
half-life = 4.5 billion yrs,
specific activity = 3.3 E-7 Ci/g
Uranium-235:
0.72% abundant;
half-life = 710 million yrs,
specific activity = 2.1 E-6 Ci/g
Uranium-234:
0.006% abundant;
half-life = 247 thousand yrs,
specific activity = 6.2 E-3 Ci/g
Enriched uranium has a higher content of
Uranium-235 than found in nature. Typical
enrichment values are:
• 2%-3% Uranium-235: power reactor grade
fuel
• >90% Uranium-235: weapons grade material
Radiological Assessor Training
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Module 6 - 2
Specialized reactor fuel may have enrichments
other than those listed above.
The uranium byproduct of enrichment is reduced
in Uranium-235 content and is called depleted
uranium. Its typical composition is as follows:
Section 117
• 99.75% Uranium-238
• 0.20% Uranium-235
• 0.0007% Uranium-234
As a result of the differences in specific
activities, Uranium-234 may account for a
significant fraction, or even the majority, of the
radioactivity for enriched uranium.
For example, for 3% enriched uranium (i.e., 3%
Uranium-235), the Uranium-234 (with an
abundance of 0.03%) would have approximately
6 times the activity as Uranium-238 and
approximately 30 times the activity as
Uranium-235.
Uranium-238 and Uranium-234 are part of the
uranium decay series, while Uranium-235 is part
of the actinium series. Therefore, following
chemical separation, decay products will
continue to grow in. The most significant of
these are Thorium-234 and Protactinium-234m
from the uranium series and Thorium-231 from
the actinium series.
Other small amounts of radioactive material may
be present as the result of reprocessing
uranium. These include Neptunium, Plutonium,
Technetium-99, and other radioisotopes of
uranium, including Uranium-232 and
Uranium-236.
Radiological Assessor Training
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B. Radioisotopes
The primary radioisotopes of uranium are all
long-lived alpha-emitters. The specific activity
(Ci/g) of uranium increases as enrichment
increases; therefore, enriched uranium is a more
serious radiation hazard.
In most uranium facilities, the inhalation hazard
from alpha particles released in the respiratory
tract is the predominant radiological hazard
associated with the alpha emitting uranium
isotopes. In addition, uranium decay products
are primarily beta-emitters. For external
exposure, the major concern is the high energy
beta particle from Protactinium-234m (2.29
MeV). As a result of beta radiation, the typical
contact dose with a block of uranium is
approximately 200 mrad/hr.
Trace contaminants such as Technetium-99 and
Uranium-232 may result in additional external
radiation dose when present.
As a result of the alpha-neutron reaction, casks
of enriched uranium hexafluoride may also emit
neutrons. Typical dose rates are on the order of
a few mrem/hr.
Radiological Assessor Training
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C. Criticality
Uranium-235 and Uranium-233 are both fissile
materials; therefore, facilities handling enriched
uranium and/or Uranium-233 have the potential
for criticality accidents, generating large
amounts of neutron and gamma radiation.
D. Toxicological properties of uranium
Uranium is a heavy metal poison and is toxic in
much the same way lead or mercury is. For
soluble compounds of low enrichments (< 5%
Uranium-235), the toxic properties of uranium
override the radiological hazards. The kidney is
the primary organ of concern.
For insoluble compounds of any enrichment or
all compounds of highly enriched uranium, the
radiological hazards are limiting.
III. Detection, measurement, and survey techniques
A. Monitoring program
A radiation protection monitoring program in a
uranium facility must ensure the detection of
typical ionizing radiations over wide energy
ranges.
To detect alpha radiation from the uranium
isotopes, exposure rate surveys using photon-
sensitive portable and fixed alpha detectors
such, as zinc sulfide or gas proportional
counters, should be used.
Appropriate beta detection instrumentation
should be available to measure decay products
such as Protactinium-234m. If Technetium-99 is
suspected, special low-energy beta particle
detection equipment should be available.
Section 118
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If large quantities of uranium hexafluoride are
present, appropriate neutron survey instruments
should be available to measure the neutron
radiation.
If the facility contains enriched uranium and/or
Uranium-233, appropriate criticality safety alarm
systems shall be in place and appropriate
neutron and gamma survey instruments
available.
Continuous air monitors (CAMs), sample
extraction lines that go to CAMs, and continuous
radiation dose monitors should be placed
outside glove boxes and fume hoods.
B. Survey Techniques
Monitoring practices include, but are not limited
to, the following:
• Contamination surveys of the workplace
• Release surveys
• External exposure surveys
• Airborne contamination surveys
• Routine surveillance by a Radiological
Control Technician
All work areas must be monitored for
contamination levels on a regularly scheduled
basis. The frequency of such surveys will
depend on the potential for dispensability of the
radioactive material. During these routine
surveys, all work enclosures, work surfaces,
floors, and equipment within the workplace
should be surveyed.
Radiological Assessor Training
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C. Workplace characterization
At the time a program is established,
measurements of external dose should be made
at all locations where it occurs to delineate the
levels involved (workplace characterization).
Additional measurements should be made at the
same frequency as the contamination surveys to
identify the buildup of uranium in HEPA filters
and glove boxes.
Airborne contamination surveys should be
performed for:
• Prompt detection of airborne contamination
for worker protection
• Personnel dose assessment
• Monitoring of trends within the workplace
• Special studies
IV. Personnel protection requirements
Workers in uranium facilities need to be
appropriately trained on the hazards. DOE has
developed DOE-HDBK-1113-98, Radiological
Safety Training for Uranium Facilities, 1998.
This handbook provides DOE's guidance on
expectations for training of uranium workers.
A. Personnel air sampling
The use of personnel air sampling programs
should be considered in monitoring individual
Radiological Workers.
B. Protective clothing
As a minimum, personnel who perform
operations in controlled areas should wear
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 6 - 7
coveralls, gloves, and shoe covers. No personal
outer clothing should be permitted under
coveralls. For inspections or visits, lab coats,
gloves, and shoe covers may be permissible.
Protective clothing should be removed at the
step-off pad, and personnel monitoring for
contamination shall be performed. If this is not
practical, strict control of the movement of
personnel shall be maintained from the step-off
pad to a location where protective clothing can
be removed. Personnel wearing protective
clothing shall not be allowed to mingle with
individuals wearing personal street clothing.
Protective clothing shall not be allowed in
uncontrolled areas such as offices, lunchrooms,
or control rooms.
C. Respiratory protection
Respiratory protection should be readily
available. Respiratory protective equipment
should be used for all bag-out operations, bag
and glove changes, and any situation involving a
potential or actual breach of confinement.
V. External dose control
Section 119
A. Beta radiation
Beta radiation is usually the dominant external
radiation hazard in work with unshielded forms
of uranium. The primary concern is
Protactinium-234m, though other radionuclides
may be present. Particular care should be taken
in operations such as melting and casting, where
decay products could be separated and
concentrated. Appropriate measurements
should be made of the material and appropriate
extremity dosimetry worn by workers handling
the material.
Radiological Assessor Training
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B. Gamma radiation
Gamma radiation is normally not the controlling
factor at uranium facilities. However, significant
gamma fields can exist in areas where large
quantities of uranium are stored. Appropriate
actions including time, distance, and shielding
considerations should be taken to maintain
radiation doses ALARA.
C. Neutron radiation
Neutron radiation from enriched uranium fluoride
compounds should also be considered in
determining potential external radiation hazards.
VI. Internal dose control
Intakes
In most uranium facilities, the primary radiological
hazard is the potential for internal intakes of
uranium. This hazard must be controlled by
appropriate facility and equipment design,
contamination control procedures, and protective
clothing.
Inhalation is the primary route of concern.
Uranium transported from the lungs is deposited
in the bone (22%), kidney (12%), or other tissues
(12%), or excreted (54%), according to
International Commission on Radiological
Protection (ICRP) Publication 30.
Control must be verified by a bioassay program.
Urinalysis is the most common technique, but
fecal analysis and in vivo monitoring may also be
appropriate.
Radiological Assessor Training
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DOE-STD-1121-98, Internal Dosimetry,
Reaffirmed May 2003, provides technical
guidance on internal dosimetry programs,
including evaluation of occupational internal
doses from exposure to radon and thoron. This
standard should be reviewed prior to conducting
assessments of internal dosimetry programs.
VII. Special controls and considerations at uranium
operations
A. Criticality alarm systems (gamma or neutron)
shall be provided in each area where an
accidental criticality is possible. Site
requirements documents relating to criticality
alarms should be reviewed prior to the
assessment, if applicable. These
requirements may include: ANSI/ANS 8.1,
Nuclear Criticality Safety in Operations with
Fissionable Materials Outside Reactors;
ANSI/ANS 8.3 Criticality Accident Alarm
Systems; ANSI/ANS 8.7, Nuclear Criticality
Safety in the Storage of Fissile Materials;
ANSI/ANS 8.15, Nuclear Criticality Control of
Special Actinide Elements; and ANSI/ANS
8.19, ANS Administrative Procedures for
Nuclear Criticality.
B. All DOE facilities that possess sufficient
quantities and kinds of fissile material to
constitute a potentially critical mass shall
provide nuclear accident dosimetry (fixed and
personal). The number of dosimeters needed
and their placement will depend on the nature
of the operation, structural design of the
facility, and accessibility of areas to
personnel. An analysis of the dosimeters and
their placement should be conducted and
documented.
Radiological Assessor Training
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C. Uranium metal in finely divided form is
pyrophoric; therefore, any grinding or milling
operations must be carefully conducted to avoid
fires.
Section 120
Uranium hexafluoride is commonly found in many
uranium operations. This material is a solid at
room temperatures but volatilizes readily at
elevated temperatures. As a gas, it is extremely
hazardous, forming hydrofluoric acid when it
comes in contact with water. Operations
involving uranium hexafluoride must be
conducted very carefully to prevent release of the
gas.
D. External radiation hazards from uranium are
primarily associated with decay products;
therefore, operations in which the decay products
can separate and concentrate must be monitored
carefully. For example, crucibles used to melt
depleted uranium and casks used to ship
uranium hexafluoride are sometimes more
radioactive after they are emptied than when they
are full. The reason is that the decay products
are left in the emptying process and are no longer
self-shielded by the uranium.
Radiological Assessor Training
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I. Introduction
II. Radiological aspects of tritium
A. There are three primary sources of tritium.
These are:
1. Environmental sources - Reactions between
cosmic rays and the upper atmosphere
14N + 1n � 3H + 12C
2H + 2H � 3H + 1H
2. By-product of power reactors
• Ternary fission - A fission event resulting
in fission fragments, one of which is
tritium. Occurrence typically has a 0.1%
yield.
B-10 (n, 2 alpha) 3H
Li-7 (n, n alpha) 3H
3. DOE production of tritium (Hanford,
Savannah River reactors) is by the following
reaction:
6Li + 1n � 3H + alpha
Radiological Assessor Training
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Student's Guide
Module 7 - 2
B. Chemical and radiological properties of tritium
1. Chemical forms
• Elemental tritium (tritium gas, HT, DT, T2)
• Tritiated water (tritium oxide, HTO, DTO,
T2O)
• Special tritium compounds (STCs):
created by intentional combination of
tritium with the desired materials or by
inadvertent contamination of a material
that has been subjected to the presence of
tritium for a period of time.
These are classified in a number of ways,
depending on their host material (metal or
organic), rate of tritium release (stable or
unstable), and physical form (particulate or
non-particulate). They include:
- Organically bound tritium (OBT); the
main types of OBT encountered in the
DOE complex are solvents, oils, and
solid particulates (e.g., plastics, nylon,
and organic dust forms).
- Particulates; stable or insoluble forms
are referred to as stable tritiated
particulates (STPs).
Radiological Assessor Training
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2. Radiological properties
• 3H � 3He + beta minus and anti-neutrino
• Emax = 18.6 keV, Eavg = 5.69 keV
• Half-life = 12.32 years
• Specific activity = 9619 Ci/gram
• ALIwater = 3000 MBq = 8 E4 µCi
(inhalation and ingestion)
• DACwater = 0.8 MBq/m3 = 2 E-5 µCi/cm3
• DACelemental = 2 E4 MBq/m3 = 0.5 µCi/cm3
• f1 = 1
• Committed equivalent dose per unit
intake = 1.73 E-11 Sv/Bq =
6.4 E-2 mrem/µCi
• DACelemental/DACwater = 25,000
In addition, DOE has issued guidance on
radiological protection for special tritiated
compounds in Radiological Control Technical
Position, RCTP 99 - 02, Acceptable Approach for
Developing Air Concentration Values for
Controlling Exposures to Tritiated Particulate
Aerosols and Organically-Bound Tritium. DOE
has also issued RCTP 06-01, Acceptable
Approaches for Developing Sealed Radioactive
Sources and Posting and Labeling Requirements
for Special Tritium Compounds (STCs).
Section 121
DOE has also developed a technical standard,
Radiological Control Programs for Special
Tritium Compounds, DOE-HDBK-1184-2004,
Change Notice 1 May 2006.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 7 - 4
C. Potential exposure pathways of tritium
Dose pathways and biological effects
• Inhalation
– Elemental tritium (tritium gas) - Limiting
condition is exposure to the lung
– Approximately 0.005% of HT inhaled is
converted to HTO prior to exhalation
– Nearly 100% of inhaled HTO is
incorporated into body fluids/tissues.
• Ingestion
– Tritiated water
• Assumed to be instantaneous
• Biological half-life is normally ten
days, but may be reduced by a
factor or two-three with increased
fluid intake
• Skin absorption of HTO through intact skin
≈50% of that inhaled.
For different modes of entry of STCs:
– STPs behave with the characteristics
of the particle to which they are
attached.
- Soluble OBT distributes throughout the
body causing a whole body dose.
Insoluble OBT can be taken into the
body by inhalation when in particulate
form. Airborne droplets of insoluble
components of oils may be treated as
stable particulates.
Radiological Assessor Training
DOE-HDBK-1141-2008
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D. General sources of tritium releases
1. Gaseous releases - ventilation exhaust
systems
2. Liquid wastes
• Aqueous
• Organic (e.g., oils)
3. Solid wastes
• Contaminated wastes
• Treatment residues
E. Exposure controls for tritium
The personnel protection requirements for tritium
include:
• Airborne contamination controls
• Surface contamination controls
1. Airborne controls
• Differential room pressure zones
• Dilution ventilation
• Room-air detritiation systems
• Local exhaust ventilation
Radiological Assessor Training
DOE-HDBK-1141-2008
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Module 7 - 6
2. Contamination controls
• Good housekeeping
• Good work practices
3. Personnel protective equipment
• Air supplied respirators
• Protective clothing
F. Metabolism of tritium
The tritium beta lacks sufficient energy to
penetrate the dead cell layer in skin. Therefore,
it is of little consequence as an external hazard.
The beta particles can produce Bremsstrahlung
radiation when they interact with matter,
although the tritium Bremsstrahlung is extremely
low energy. It is remotely possible that the
Bremsstrahlung exposure could become
significant around materials with very high
specific activities and little or no shielding.
Tritium can deliver a radiation dose if it gets
inside the body. Modes of entry include:
• Inhalation
• Ingestion
• Absorption
1. Inhalation
Tritium gas (HT) is only slightly incorporated
into the body when inhaled. Approximately
0.005% of HT inhaled is converted to tritiated
water prior to being exhaled. Depending
upon the rate at which HT converts to HTO in
vivo, it is possible that some dissolved HT
may be excreted in urine.
Radiological Assessor Training
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Module 7 - 7
Tritiated water (HTO) is much more
radiologically hazardous than tritium gas.
Inhaled HTO enters the body through the lung
fluids with 100% efficiency, and mixes rapidly
with body water. Nearly 100% of tritiated water
(HTO) inhaled is incorporated into body fluids
and tissues.
2. Ingestion
Ingested HTO is assumed to be completely and
instantaneously absorbed from the
gastrointestinal tract and mixes rapidly with the
body fluids so that following ingestion, the
concentration in sweat, sputum, urine, blood,
perspiration and expired water vapor is the
same.
Section 122
3. Absorption
There is negligible skin absorption for tritium
gas. Some HT can be absorbed through the
skin from contact with surface contamination.
This uptake is probably in the form of HTO,
resulting from the oxidation of HT. Some tritium
may be retained in the skin in the form of
organics, presumably resulting from exchange
reactions with HT on or in the skin.
HTO can be readily absorbed through the skin.
It will be uniformly distributed in all biological
fluids within one to two hours.
Most exposures are to HTO, which rapidly
enters the body water via absorption through
the lungs and/or skin. A small amount of HT
can dissolve in lung fluids, convert to HTO, and
enter the body fluids. Exposures to HTO are
approximately 10,000 to 25,000 times more
hazardous than exposure to HT. HTO has an
effective half-life in the body in the range of 4 to
18 days, with a mean effective half-life of about
9 or 10 days.
Radiological Assessor Training
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Module 7 - 8
Most tritium leaves the body either in urine or
through evaporation from the lungs and skin. The
dose commitment from an uptake of one curie of
HTO is approximately 63 rem.
For the above 3 discussed modes of entry: STPs
and insoluble components of tritiated oils behave
with the characteristics of the particle to which they
are attached.
For dose calculations for STPs, ICRP Publication
66 uses absorption types; slow, medium, and fast
(S, M, F). These are used in place of the lung
retention classes (day, week, and year; D, W, Y)
used in ICRP Publication 30. Depending on the
absorption type of the compound, the dose per
intake will be different than HTO.
For example: The air concentration value (which
could be used in assessing dose per intake) for
Type S STP is 10 times more restrictive than HTO,
while the air concentration value for Type F STP is
5 times less restrictive than HTO.
Soluble OBTs act somewhat similar to HTO,
however a larger percentage of nuclear
transformations occur in the stomach. The dose
per intake is approximately twice that of HTO.
Skin absorption is also a valid intake pathway for
tritiated oil components and solvent OBT.
G. Methods of tritium containment
1. Primary - Process equipment and piping
2. Secondary
• Glove boxes
• Temporary vented enclosures
Radiological Assessor Training
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Module 7 - 9
3. Tertiary - Room and associated ventilation systems
• Effluent recovery systems
• Emergency containment systems
H. Airborne tritium controls
1. Differential room pressure zones - The air
ventilation system plays a key role in controlling
the spread of contamination. In addition to
providing the necessary humidity and
temperature control for a building, differential
pressure zones should be established within a
building to ensure that the air flows from areas
with lower hazardous contamination potential to
areas with more hazardous contamination
potential.
2. Dilution ventilation - Dilution ventilation is the
once-through flow technique of exchanging
outside air for inside air for comfort and basic
contamination control.
3. Room-air detritiation systems - Such a system
uses tritium monitors located in the room
exhaust to activate (close) fast acting dampers.
The dampers then route the exhaust through a
special oxidation/drying system and return the
air to the room.
Section 123
3. Local exhaust ventilation - The primary
advantage of local exhaust ventilation
techniques is the removal of airborne tritium,
regardless of its evolution rate or chemical or
physical form. In addition, these techniques
use relatively low flow rates compared to
normal ventilation requirements.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 7 - 10
I. Measurement techniques for tritium
1. Air monitoring - Fixed and portable ionization
chambers most widely used.
2. Differential monitoring - Separate monitoring
of HT and HTO components through the use
of bubblers in conjunction with desiccants or
catalysts.
3. Discrete sampling - Samples collected with a
bubbler or “cold finger” type sampler, then
later analyzed by liquid scintillation counting
techniques.
4. Process monitoring
• Stack, room, hood, glove box
• Mass spectroscopy, gas chromatography,
calorimetry
5. Surface monitoring
• Difficult to measure directly due to low-
energy emission
• May have some success with thin window
GM (pancake style probe), thin window
sodium iodine, or gas flow proportional
counters
• Smears taken for loose contamination,
and measured by dissolution and analysis
by liquid scintillation counting techniques
6. Liquid Monitoring - Liquid scintillation
counting techniques
Radiological Assessor Training
DOE-HDBK-1141-2008
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Module 7 - 11
J. Bioassay program for tritium workers
An adequate bioassay program for tritium
workers would test for chronic and acute
exposure.
1. Chronic exposure - Periodic urinanalysis for
tritium (daily to biweekly identified in Tritium
Good Practices Manual)
2. Acute exposure
• Wait one to two hours.
• Void bladder.
• Collect sample as soon as possible
thereafter.
• Continue to collect daily to determine
individual half-life.
Dose from exposure to STCs may need to be
assessed based on air monitoring results, see
RCTP 99-02.
DOE-STD-1121-99, Internal Dosimetry, 1999,
provides guidance on internal dosimetry
programs including monitoring and assessing
dose from tritium.
K. Tritium effluent recovery systems
1. Purpose - Reduce tritium available for
release
2. Method - Tritium gas converted to HTO and
ultimately a stable waste form
.
Radiological Assessor Training
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L. Inventory control and accountability for tritium
1. Nuclear materials, including tritium, need to
be controlled and have material
accountability.
2. Appendix D to the Tritium Good Practices
Manual discusses inventory control and
defines it to consist of:
• Measurements
• Measurement controls
• Determination of holdup in systems
• Development of predictors
• Establishment of accounting practices
I. Introduction
The guidance in DOE-STD-1128-98, Guide of Good
Practices for Occupational Radiological Protection in
Plutonium Facilities, Change Notice 2 December
2006 should be reviewed in detail prior to conducting
an assessment of plutonium facilities. The following
is a brief overview of the radiological aspects of
plutonium.
II. Background
Plutonium was first synthesized in the winter of 1940-
41 by a team of scientists at the University of
California. Its potential use in weapons was quickly
identified, and much of the effort of the Manhattan
Project was in the production of sizable quantities of
plutonium. Other uses for plutonium include use as:
• Reactor fuel
• Heat sources in thermoelectric generators to
power satellites
Section 124
• Components in portable neutron sources
Plutonium is a silvery-white metal that readily
oxidizes to a dull gray color. It can be found in a
variety of physical and chemical forms. Several of
the chemical forms (including the pure metal) are
pyrophoric, so care must be exercised in handling the
material. Because of the pyrophoric nature of
plutonium and its alloys, the preferred form for
storing, shipping, and handling is as plutonium oxide.
III. Radiological properties of plutonium
A. Isotopes
There are 15 isotopes of plutonium, all
radioactive, beginning with Plutonium-232 and
ending with Plutonium-246. The radioisotopes of
primary interest are Plutonium-238, Plutonium-
239, and Plutonium-240, all of which are primarily
alpha-emitters.
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1. Plutonium-238 (half-life = 87.7 yrs) is most
commonly used as a heat source in
thermoelectric generators. Because of its heat
production, care must be taken in handling
gram or larger quantities, as it could melt
plastic or ignite other materials.
2. Plutonium-239 (half-life = 24,000 yrs) is the
primary component of plutonium reactor fuel
(>85%) and weapons grade plutonium (>90%),
with Plutonium-240 (half-life = 6,560 yrs)
constituting most of the remainder in both
cases.
3. Plutonium radioisotopes emit relatively few
high-energy gamma rays, so kilogram
quantities can often be processed without
serious gamma dose problems. However,
small amounts of some radioisotopes or decay
products can increase external dose. For
example, Plutonium-241 decays by beta
emission to Americium-241, which emits a 60-
keV gamma ray. This can be a significant
source of dose to hands in glove boxes. Large
amounts of Americium-241 can produce high
dose-rates due to higher energy gamma rays.
4. Neutron dose rates from spontaneous fission
and from alpha-neutron reactions with light
elements may be significant (e.g., 1 kg of
Pu-F4 (Pu-238) would have a contact neutron
dose equivalent rate of 4800 rem/hr).
B. Biological effects of internally deposited plutonium
The primary hazards from the most common
chemical form of plutonium (PuO2) are inhalation
and ingestion. This chemical form is relatively
insoluble. Therefore, uptake through the gastroin-
testinal (GI) system following an ingestion is
small.
Inhaled plutonium can remain in the lungs for a
considerable time before being removed through
the lymph system.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 8 - 2
Plutonium is difficult to remove from the body.
The primary method is through the administration
of chelating agents as soon after the intake as
possible. Trained medical personnel are needed
to administer chelating agents.
The plutonium that enters the systemic system is
mostly translocated to the liver and the bone (as
is discussed in the following section).
Accordingly, development of cancer in these
organs and in the lungs are of particular interest in
evaluating long-term effects from intakes of
plutonium.
C. Survey techniques
A radiation protection program in a plutonium
facility shall ensure the detection of all types of
radiation (i.e., alpha, beta, gamma, x-ray, and
neutron) over large energy ranges. Alpha-
sensitive instruments are necessary for most
contamination control surveys.
Continuous air monitors (CAMs), sample
extraction lines that go to CAMs, and continuous
radiation dose monitors should be placed outside
the glove boxes and hoods.
Section 125
Neutron surveys become important when
processing tens of grams of Plutonium-238 or
hundreds of grams of mixed isotopes of
plutonium, particularly compounds (i.e., PuO2,
PuF4). The neutron survey is important in
instances where photon shields, such as leaded
glass, are used. Such shields normally stop all of
the charged particles, most of the low-energy
photons, and essentially none of the neutrons.
Under these circumstances, neutron radiation is
likely to be the major contributor to whole body
dose.
Exposure rate surveys are normally conducted
with photon-sensitive instruments with known
Radiological Assessor Training
DOE-HDBK-1141-2008
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Module 8 - 3
energy responses for photons with energies
≥ 10 keV.
Monitoring practices include, but are not limited
to, the following:
• Contamination surveys of the workplace
• Release surveys
• External exposure rate surveys
• Airborne radioactivity surveys (both real time
(CAMs) and historical (fixed air head))
• Routine surveillance by a Radiological Control
Technician
All workplaces shall be monitored for
contamination levels on a regularly scheduled
basis. The frequency of such surveys will depend
on the potential for dispensability of the
radioactive material. As a minimum, all gloves,
work surfaces, floors, and equipment within the
workplace should be surveyed.
Airborne radioactivity surveys should be
performed for:
• Prompt detection of airborne contaminants for
worker protection
• Personnel dose assessment
• Monitoring of trends within the workplace
• Special studies
Intakes
In most plutonium facilities, the primary
radiological hazard is the potential for internal
intakes of plutonium. This hazard must be
controlled by appropriate facility and equipment
Radiological Assessor Training
DOE-HDBK-1141-2008
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Module 8 - 4
design, contamination control procedures, and
protective clothing/equipment.
Plutonium transferred from the initial entry site is
assumed to be translocated to the liver (45%) and
the bone (45). Retention half-life in the liver is 20
yrs and in the bone is 50 yrs, according to
International Commission on Radiological
Protection (ICRP) Publication 30.
Control must be verified by a bioassay program.
Urinalysis is the most common technique, but
fecal analysis and in vivo monitoring may also be
appropriate.
U.S. Department of Energy, DOE-STD-1121-98,
Internal Dosimetry, Reaffirmation May 2003. provides
technical guidance on internal dosimetry programs,
including enhanced workplace monitoring for
instances where there is a technology shortfall, such as
for plutonium. This standard should be reviewed
prior to conducting assessments of internal dosimetry
programs.
The standard also discusses appropriate
evaluation of bioassay results.
D. Monitoring instruments
DOE-STD-1128-98, Change Notice 2 December
2006 has additional guidance on monitoring
instrumentation.
Facilities that deal with unencapsulated plutonium
should have continuously operating effluent
monitors to determine whether or not plutonium is
being released to the environment.
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Criticality alarm systems (gamma or neutron)
should be provided in each area where an
accidental criticality is possible.
E. Sources of external dose
External dose control for plutonium is primarily
concerned with photon dose rates from handling
plutonium in a glove box and from the neutron
dose rate from some mixtures of plutonium.
Section 126
While significant high-energy penetrating photons
are not commonly associated with plutonium, low-
energy photons (x- and gamma-rays) can create
significant dose rate problems to extremities. This
is particularly a concern when large amounts of
Plutonium-238, Plutonium-241, or Americium-241
(from the decay of Plutonium-241) are present.
Neutrons can also represent a potentially
significant dose due to spontaneous fission
(alpha, neutron) reactions or neutron induced
fission. The neutron dose is largely determined
by the radioisotope and other materials near the
source.
F. Control of external dose
External dose control is accomplished with
traditional dose reduction techniques:
• Time (minimize)
• Distance (maximize)
• Shielding (use as needed)
Other work practices, including good
housekeeping and specialized tool and equipment
design, can reduce external dose, as well.
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G. Techniques for internal dose control
The confinement system is a series of physical
barriers that, together with a ventilation system,
minimizes the potential for release of radioactive
material into work areas and the environment
under normal and abnormal conditions, thereby
minimizing internal dose.
Generally, three confinement systems are used to
achieve the confinement system objectives at
plutonium handling facilities. They consist of the
following:
• Primary confinement is provided by piping,
tanks, glove boxes, encapsulating material,
and the like, and any off-gas system that
controls effluent from within the primary
confinement. It provides confinement of the
area immediately surrounding the hazardous
material.
• Secondary confinement is provided by the
walls, floor, roof, and associated ventilation
exhaust systems of the cell or enclosure
surrounding the process material or
equipment. Except in the case of glove box
operations, the area inside this barrier is
usually unoccupied; it provides protection for
operating personnel.
• Tertiary confinement is provided by the walls,
floor, roof, and associated ventilation exhaust
system of the facility. It provides a final barrier
against release of hazardous material to the
environment.
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Different devices may be used to confine and
control radioactive material. The selection of the
appropriate device will depend on the quantity of
material, its form, and the operations to be
performed.
Fume hoods may be used for some operations
with plutonium, depending on the quantity and
dispersability of the material. In general,
plutonium fume hood operations shall be limited
to wet chemistry processes and less than 100 mg
of plutonium.
Higher levels of plutonium are generally handled
in glove boxes. Care should be taken in the
design of the glove box to ensure confinement of
the material and any fire.
Ventilation may also be employed to confine
plutonium, although it usually is used in
conjunction with other measures.
H. Personnel protection
Workers in plutonium facilities need to be
appropriately trained on the hazards. DOE has
developed Radiological Safety Training for
Plutonium Facilities, DOE-HDBK-1145-2001.
This document provides DOE's guidance on
expectations for training of plutonium workers.
The use of personal air sampling programs should
Section 127
be considered to monitor individual workers for
exposure to airborne plutonium. Section 4.4.4 of
DOE-STD-1121-98, Reaffirmed May 2003,Internal
Dosimetry, discusses use of breathing zone or
personal air monitoring when there is a
technology shortfall (i.e., the derived investigation
level is less than the minimum detectable activity).
Technology shortfalls are common for routine
plutonium bioassay programs.
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In addition, DOE has issued guidance on use of
air monitoring results when there is a technology
shortfall in Radiological Control Technical Position
(RCTP) 2001-01, Questions and Answers
Concerning Acceptable Approaches to
Implementing Bioassay Program Requirements.
In part, RCTP 2001-01 states that, when there is
a technology shortfall for bioassay and air
monitoring results indicate exposures greater than
100 millirem in a year are likely, one should
assess dose based on the air monitoring results.
As a minimum, personnel who perform operations
in controlled areas should wear coveralls and
shoe covers. For inspections or visits, lab coats
and shoe covers may be permissible. When
contaminated wet areas are to be entered, water-
repellent (plastic or rubber) clothing shall be worn.
No personal outer clothing should be permitted
under coveralls.
Hands should be protected by a minimum of two
barriers; for example, at least one pair of
surgeon’s gloves and one pair of rubber gloves
should be worn.
Protective clothing should be removed at the step-
off pad, and personnel monitoring for
contamination shall be performed.
Respiratory protection equipment shall be readily
available. Respiratory protection equipment
should be used for all bag-out operations, bag
and glove changes, and any situation involving a
potential or actual breach of confinement.
Protection, in the form of air-purifying or
atmosphere-supplying respirators, shall be used
whenever concentrations of radionuclides in the
air are likely to exceed the applicable DACs.
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Module 8 - 9
I. Inventory control and accountability requirements
Real-time or near real-time accountability systems
should be incorporated if possible.
J. Criticality safety considerations
Criticality alarm systems (gamma or neutron) shall
be provided in each area where an accidental
criticality is possible.
Criticality safety requirements may include:
ANSI/ANS 8.3-1986, Criticality Accident Alarm
Systems; ANSI/ANS 8.1-1983, Nuclear Criticality
Safety in Operations with Fissionable Materials
Outside Reactors; and ANSI/ANS 8.19-1984,
ANS Administrative Procedures for Nuclear
Criticality.
It is important to review site requirements
documents prior to conducting the assessment.
All DOE facilities that possess sufficient quantities
and kinds of fissile material to potentially
constitute a critical mass shall provide nuclear
accident dosimetry.
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Student's Guide
Module 9 - 1
I. Introduction
10 CFR Part 835.501(d) requires written
authorizations to control entry and perform work in
radiological areas, commensurate with the
radiological hazards. DOE-STD-1098-99,
Radiological Control, July 1999, Chapter 3, Part 2,
provides guidance on DOE's expectations for such
written authorizations.
Section 128
These written authorizations may take a variety of
forms tailored to the work processes involved.
Often, the form will be that of a Radiological Work
Permit (RWP), discussed in detail below.
II. Radiological Work Permits (RWPs)
A. Purpose
The RWP is designed to document the
radiological conditions and associated controls
in a work area. The RWP should be integrated
with other work authorizations that address
safety and health issues, such as those for
industrial safety and hygiene, welding, and
confined space entry.
Articles 311 and 312 of DOE-STD-1098-99
provide guidance on preparing work control
procedures consistent with the principles of
Integrated Safety Management. This includes
use of multidiciplinary teams to prepare work
control procedures for tasks involving significant
types of hazards and referring to DOE Order
440.1B, Worker Protection Program for DOE
(Including National Nuclear Security
Administration) Federal Employees.
B. Typical RWP process
1. Requester submits an RWP request form.
2. Radiological Control Supervisor accepts
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Module 9 - 2
form, collects additional job information as
necessary, and assures that completion of
appropriate radiological surveys to be
performed in the work area.
3. Radiological Control Technicians, or other
appropriately trained and authorized
personnel, perform surveys, analyze
samples, and report results.
4. RWP controls are established based on the
results of the surveys.
5. Radiological Control personnel, in
consultation with relevant technical staff,
complete, distribute and implement the RWP.
6. Radiological Workers and Radiological
Control personnel review completed RWP,
prior to start of job, during pre-job briefs,
and/or ALARA reviews.
5. Radiological Worker/Supervisor advises
Radiological Control personnel when job is
complete (so RWP can be terminated).
8. Radiological Control personnel maintain
surveys and RWP documentation.
C. Types of RWPs
There are two basic types of Radiological Work
Permits:
• Job-specific RWP
• General RWP
The job-specific permit is used for jobs which
present a greater potential for significant
radiation dose, airborne radioactivity, or spread
of contamination, and which involve “hands on”
work.
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Examples of jobs that would likely require job-
specific RWPs include those where work is:
• Performed with detailed, specific, written
work procedures, approved in advance by
Radiological Control personnel
• “Hands-on” work performed infrequently on
radiological systems (e.g., valve replacement
in process buildings)
• Performed in areas in which the radiological
conditions have no history of remaining
stable
The general RWP typically is used for jobs with
less potential for health physics concerns and for
routine, repetitive jobs that do not involve “hands
on” work.
Examples of jobs that may be worked under a
general RWP include:
• Routine tours, inspections, inventories, valve
lineups, equipment tagouts, surveys, and
equipment operation.
• Work routinely performed on nonradiological
systems (e.g., fire protection systems in shut-
down process buildings).
• Routine operations involving radioactive
material for which the radiological conditions
have a history of remaining stable.
Keep in mind that there may be a need for other
Section 129
(nonradiological) permits or authorizations to
safely perform these jobs. For example permits
may be needed to address nonradiological
hazards, such as: electrical, confined space,
asbestos, hazardous materials, respiratory
protection, fire, heavy equipment and
scaffolding.
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D. Time limits
The job-specific RWP usually remains in effect
only for the duration of the job (typically less
than 30 days).
The general RWP typically is approved for a
period of time of one year or less.
E. Elements of an RWP include:
• Description of work (detailed)
• Radiological conditions (contamination,
airborne, radiation levels) in the work area
• Dosimetry (TLD badge, self-reading
dosimetry, special dosimetry) requirements
• Requirements for a pre-job briefing, if
necessary
• Radiological Control Technician coverage
(start of job, continuous, intermittent)
• Training requirements to work in the area
• Protective clothing requirements
• Respiratory protection equipment
requirements
• Stay time requirements
• Radiological conditions that may limit work or
void the RWP
• Special dose reduction (ALARA) or
contamination reducing measures to be
considered
• Special personnel contamination monitoring
requirements
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• Work document number (if used)
• Unique RWP identification number
• Date of permit issue and expiration date
• Signatures of Radiological Worker and
supervisor (attesting to their understanding of
RWP requirements and agreement to follow)
and Radiological Control staff
F. RWP Elements for Radiological Assessment
The following are RWP program elements
which may be reviewed as part of a
radiological assessment:
• RWPs appropriately required for activities
and areas
• Completeness of information on RWPs
• Adequacy of radiological surveys to
support RWP
• Worker adherence to RWP requirements
• RWP appropriately reviewed and
approved
• Adequacy of worker monitoring (TLDs,
bioassay, air monitoring RCT coverage)
specified on RWP
• ALARA considerations included in RWP
• RWP program implemented in accordance
with written procedures
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Module 10 - 1
I. Introduction
10 CFR Part 835, Occupational Radiation
Protection, Amended June 2007, specifies
contamination control requirements in Subpart L.
Chapters 3 and 4 of DOE-STD-1098-99,
Radiological Control, Reaffirmed December 2004
also provide guidance on meeting the requirements
and additional information for implementing an
effective contamination control program. All of
these documents should be reviewed prior to
conducting an assessment.
II. Contamination containment and temporary control
measures
Minimization of internal dose
The minimization and control of internal dose
should be conducted in accordance with the
following hierarchy of controls:
1. Engineered controls, including containment
of radioactive material at the source
wherever applicable, should be the primary
method of minimizing airborne radioactivity
and internal dose to workers.
Engineered controls are devices such as
glove boxes, glove bags, portable filtration
units, and containment tents. They should
be used to prevent worker inhalation of
radionuclides.
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Section 130
Student's Guide
Module 10 - 2
The use of these devices reduces the spread
of contamination, cleanup time, and
decontamination costs. These measures
help maintain doses ALARA. In addition,
they can reduce the need for respirators and
the impact on work in nearby areas.
Engineered controls should be used in
accordance with technical instructions,
proper training, and effective administrative
controls
Site-specific manuals should contain generic
instructions on the design, controls, training,
and use of engineered controls.
2. Administrative controls, including access
restrictions and the use of specific work
practices designed to minimize airborne
contamination, should be used as the
secondary method to minimize worker
internal dose.
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3. Only when engineered and administrative
controls have been applied and the potential
for airborne radioactivity still exists, should
personnel protective equipment, including
use of respiratory protection, be considered.
Chapter 3 of DOE-STD-1098-99 discusses:
Access controls for Contamination Areas
Controlling the spread of contamination
Monitoring for contamination.
Appendix 3 C, Contamination Control
Practices, includes recommended selection
of protective clothing, and a recommended
sequence for donning and doffing.
Use of respiratory protection should be
considered under the following conditions:
• Entry into posted Airborne Radioactivity
Areas
• During breach of contaminated systems
or components
• Work in areas or on equipment with
removable contamination levels greater
than 100 times the values in Table 2-2 of
DOE-STD-1098-99
• During work on contaminated or activated
surfaces with the potential to generate
airborne radioactivity
The selection of respiratory protection
equipment should include consideration of
worker safety, comfort, and efficiency. The
use of positive pressure respiratory
protection devices is recommended wherever
practicable to alleviate fatigue and increase
comfort.
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Module 10 - 4
Respirators can provide adequate protection
for workers in an airborne radioactivity
environment, but engineered controls may be
more practical. By using engineered controls
instead of respirators, the worker is not
subjected to the stresses created by wearing
a respirator. It is more difficult to breath and
communicate when wearing a respirator.
Vision is impaired, and the respirator is not
comfortable. Productivity can therefore be
improved by using engineered features
instead of respirators.
To minimize intakes of radioactive material
by personnel, smoking, eating, or chewing
shall not be permitted in Contamination, High
Contamination, Airborne Radioactivity Areas,
or Radiological Buffer Areas established for
contamination control purposes.
Contamination should be contained at its
source. The principle is to prevent
contamination spread from occurring. The
most effective methods based on sound
ALARA principles should be used. All
controls should be documented and clearly
controlled by RWPs.
Respirators may be appropriate for simple,
straightforward jobs.
In specific situations the use of respiratory
protection may be contraindicated due to
physical limitations or the potential for
significantly increased external dose.
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Section 131
In such situations, written authorization
should be obtained from the line organization
manager and the Radiological Control
Manager prior to incurring internal dose.
Specific justification of the need to accept the
dose, including a description of measures
taken to mitigate the intake of airborne
radioactivity, should be documented as part
of the radiological work documentation.
The use of personal air sampling programs
should be considered to monitor individual
workers for exposure to airborne radioactive
material, especially when the use of
respiratory protection is contraindicated. This
is particularly important when there is a
bioassay program technology shortfall (i.e.,
the derived investigation level is less than the
minimum detectable activity). Section 4.4.4
of DOE-STD-1121-98, Internal Dosimetry,
discusses use of breathing zone or personal
air monitoring.
In addition, DOE has issued guidance on use
of air monitoring results when there is a
technology shortfall in Radiological Control
Technical Position (RCTP) 2001-01,
Questions and Answers Concerning
Acceptable Approaches to Implementing
Bioassay Program Requirements.
In part, RCTP 2001-01 states that, when
there is a technology shortfall for bioassay
and air monitoring results indicate exposures
greater than 100 millirem in a year are likely,
one should assess dose based on the air
monitoring results.
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Student's Guide
Module 11 - 1
Radiological Work Site
Mockup Demonstration
Checklist for Module 11
The exercise is a mock-up demonstration that is performed
by the instructors to give the participants an opportunity to
assess and identify poor radiological work practices.
You will be instructed to identify and make notes of the
poor radiological practices during the demonstration.
Observe the demonstration and watch for poor radiological
work practices. Write down poor work practices in your
student’s guide for discussion after demonstration. After
the demonstration:
• Identify poor radiological practices
• Make recommendations for improvement
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Module 11 - 2
Notes
Radiological Assessor Training
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Student's Guide
Module 12 - 1
I. Introduction
10 CFR Part 835, Occupational Radiation
Protection, includes provisions for exposure to
ionizing radiation from DOE activities. Included in
the 10 CFR 835 definition of a radiological worker is
"operation of radiation producing devices". 10 CFR
835 also specifies requirements for sealed
radioactive sources.
II. DOE Guidance
Article 365 of DOE-STD-1098-99, Radiological
Control, provides additional guidance, including the
use of ANSI N43.3, ANSI N43.2, and 10 CFR Part
34 for meeting its requirements covering RGDs.
DOE HDBK-1109-97, Radiological Safety Training
for Radiation-Producing (X-Ray) Devices,
Reaffirmed January 2007, provides guidance on
DOE's expectations for radiation safety training for
individuals using RGDs.
Radiological Assessor Training
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Student's Guide
Module 12 - 2
III. X-ray machines
A. Components
X-ray devices have been in existence for about
100 years. Although there are many different
designs of x-ray machines, they all have the
same basic components. These include a
source of electrons, an electrical potential
difference to accelerate the electrons, and an
anode, or target for the accelerated electrons to
strike.
Section 132
Usually, the source of electrons in an x-ray
machine is a thin wire filament from which
electrons are emitted when it is heated by a
large electrical current. Controlling the current
through the filament, then, becomes a way to
control the number of electrons available for
acceleration.
The electrical potential difference between the
cathode (filament) and the anode (or target) is
the force that accelerates the electrons. The
larger the potential difference, the more kinetic
energy the electrons will acquire. The potential
difference is measured in units of kilovolts (kV).
The energy of the electrons is measured in units
of kilo electron volts (keV), with one electron volt
being the amount of energy required to move
one electron through a potential difference of
one volt.
The accelerated electrons then strike the anode
(or target). The target may consist of various
materials, depending on the purpose and design
of the x-ray tube. X-ray production is most
efficient in high atomic number targets, like
tungsten.
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Module 12 - 3
When electrons strike and excite target atoms,
the kinetic energy of the electrons is deposited in
the target as heat. When electrons ionize target
atoms, characteristic x-rays will be emitted as
electrons from outer shells fill vacancies created
by ejected electrons.
B. X-ray energy spectrum
The energy of the x-ray photons coming out of
the x-ray machine is of interest to the users of
the machine. The typical energy spectrum from
an x-ray machine consists of the characteristic x-
rays from the target, which have discrete
energies, and the bremsstrahlung photons which
have a whole range of energies, the maximum
energy depending on the potential difference
across the tube. For a typical x-ray machine, the
bremsstrahlung photons far outnumber the
characteristic x-rays.
C. Design features
The cathode and anode of the x-ray tube are
enclosed in an evacuated glass tube or
envelope. The vacuum is necessary to ensure
that the accelerated electrons will interact in the
target, and not with gas molecules.
The x-rays are produced in all directions in the
target. However, only x-rays directed toward the
exit port, or window, will comprise the useful
beam.
Several devices are used to control the size of
the useful x-ray beam. A lead diaphragm is a
sheet of lead with a hole in it. It is placed near
the exit port, and restricts the size of the useful
beam by absorbing x-rays that don't pass
through the hole. The size of the beam is not
adjustable with this type of device unless
another diaphragm with a different-size opening
is used.
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Module 12 - 4
For some operations, the size of the useful
beam must be adjusted by the operator. An
adjustable collimator is essentially a set of
movable lead sheets. Two sheets restrict the
width of the beam, and two sheets restrict the
length of the beam. The operator can then
adjust the size of the beam to any desired
combination of length and width.
Often, the lowest energy x-rays are not desired
in the beam. The low energy x-rays can be
filtered out by placing absorbing material (called
filters) in the path of the beam. Aluminum or
copper is commonly used, depending on the
energy of the machine. The addition of filters
increases the average energy of the beam, since
the lower energy x-rays are removed from the
beam when they are absorbed by the filters.
Section 133
D. Common uses and hazards
X-ray machines are most commonly used for
radiography, or the examination or inspection of
the structure of materials by non-destructive
means.
X-ray machines used in medicine are fairly
standardized in appearance, and in the way they
are installed. That is not true of x-ray machines
used for industrial applications. X-ray machines
may be fixed installations, mobile units, or
completely enclosed cabinet systems. The
cabinet x-ray systems are commonly used for
security applications (e.g., baggage inspection
units).
The major hazard from x-ray machines is the
external dose hazard to machine operators and
other people in the vicinity. No one should ever
be exposed to the primary (or useful) beam.
Exposure to leakage radiation (from the housing)
and scatter radiation should be reduced by
appropriate controls.
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IV. Analytical x-ray machines
A. Fluorescence analysis
Characteristic x-rays that result from ionization of
atoms can be used to identify atoms, since the
characteristic x-rays will have energies that are
unique to that element. This forms the basis for
x-ray fluorescence spectroscopy. A sample to
be analyzed is irradiated by a beam of high-
intensity x-rays. The x-rays ionize atoms in the
sample, which emit characteristic x-rays when
the electron shell vacancies created by
ionization are filled.
The characteristic x-rays can be analyzed by
determining their energy, or by determining their
wavelength. Either way, the result leads to
information about the elemental composition of
the sample.
These instruments are usually completely
enclosed. Access doors are provided for
changing samples, and the doors are equipped
with interlocks to prevent access to the x-ray
beam.
The hazard is primarily an external dose hazard
to scattered radiation from the components and
the sample, and is typically fairly low.
B. X-ray diffraction
When x-rays are scattered by a crystalline solid,
they are scattered from the different atoms, but
only in certain directions. This technique is used
for crystal structure research.
The primary beam and the diffracted beams are
very small and well collimated. In some types of
diffraction equipment, the sample cannot be
enclosed in a structure. The primary beam is
controlled by a shutter that opens and closes.
The major hazard associated with diffraction
units is intense, localized exposure from the
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primary beam to the hands or eyes that can
occur during sample changing or beam
alignment procedures with the shutter
inadvertently open. The primary beam is very
small, but may have an intensity of up to 40,000
R/min. At this exposure rate, even short
exposures of the hands and fingers could result
in severe injury, and potential loss of fingers.
.
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V. Other radiation-generating devices
Other radiation-generating devices (RGDs) that may
be encountered are small particle accelerators (<10
MeV) used for radiography, ion implantation, or the
production of incidental photons or particles
(neutron generators).
Some RGDs produce radiation incidental to their
primary purpose. Examples of devices that produce
radiation incidentally are electron beam welders,
electron microscopes, and pulse generators.
Section 134
VI. Categorizing RGD installations
The ANSI standards referenced earlier categorize
RGD installations into the following categories for
radiation safety purposes.
A. Exempt shielded installations
The RGD and all objects exposed to the source
of radiation shall be within a permanent
enclosure that, under all circumstances of use,
possesses sufficient inherent shielding and
prevents inadvertent entry to any part of the
body. The exposure at any accessible region 5
cm from the outside surface of the enclosure
shall not exceed 0.5 mrem in any one hour.
B. Shielded installation
The RGD and all objects exposed to the source
are within a permanent enclosure from which
persons are excluded during the irradiation.
Some of the requirements for shielded
installations include mandatory interlocks,
audible and visual warning devices, a "crash"
button, and posting of warning signs.
Skyshine is the term used to describe radiation
emerging more or less vertically from a shielded
enclosure, which then scatters from air
molecules to produce radiation at some distance
from the source.
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C. Unattended installation
The RGD is installed in a single-purpose
shielded enclosure, and the design shall ensure
that individuals are not exposed to doses
exceeding 100 mrem in a year.
D. Open installation
Open installations must be conspicuously
posted, and have a conspicuously defined
perimeter. The perimeter must delimit the area
in which the exposure can exceed 5 mrem in
any one hour. The operational staff shall
provide constant surveillance. Other
requirements include use of survey meters,
personnel dosimetry, and temporary shielding.
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I. Introduction
10 CFR Part 835, Occupational Radiation Protection,
includes provisions for exposure to ionizing radiation
from DOE activities, which includes exposures from
accelerator operations.
II. DOE Guidance
Article 364 of DOE-STD-1098-99, Radiological
Control, provides similar guidance, and includes
guidance to use the Health Physics Manual of Good
Practices for Accelerator Facilities, SLAC-327, in
meeting occupational radiation protection
requirements for accelerators.
DOE HDBK-1108-97, Radiological Safety Training
for Accelerator Facilities, provides guidance on
DOE's expectations for radiation safety training for
individuals using accelerators.
III. General characteristics of accelerators
Accelerators are devices that increase the speed
and thus the energy of charged particles.
A. Accelerator energy
Accelerators are normally rated by the maximum
energy to which the particles are accelerated.
The energy imparted to the charged particles is
determined by the potential difference measured
in volts (V) in the electrical field. At all but the
smallest accelerators, the acceleration is
accomplished by directing the charged particles
repeatedly through regions containing
radiofrequency electromagnetic fields.
One electron volt (eV) is the energy gained by an
electron accelerated through an electric potential
of 1 volt.
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An electron accelerated across a gap by means
of a 10,000 volt, or 10 kilovolt (kV), potential
difference is said to have gained 10 kilo electron
volts (10 keV) of energy after crossing the gap.
Section 135
Other energy units commonly encountered at
accelerators are: MeV (1 million, or 106 electron
volts), GeV (1 billion, or 109 electron volts), and
TeV (1 trillion, or 1012 electron volts). These units
of energy are commonly used not only for
electrons, but for all charged particles.
B. Types of particles accelerated
Particles accelerated include:
• Electrons
• Protons
• Nuclei of various elements
C. Types of accelerators
The accelerated charged particle may move in
either a linear (straight line) or in a circular
(curved) path as the result of moving
perpendicular to a magnetic field; these are the
two basic types of accelerators.
1. Linear accelerators
Straight-line accelerators suffer from the
disadvantage that the finite length of flight
path limits the particle energies that can be
achieved.
Linear accelerators include:
• Van de Graaffs
• Cockcrott-Waltons
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2. Circular-path accelerators
In circular-path accelerators, magnets guide
the particle along a spiral path, allowing a
single electric field to apply many cycles of
acceleration.
Circular-path accelerators include:
• Cyclotrons
• Betatrons
• Synchrotrons
Until the 1980's, all accelerators used for both
physics research and in practical applications,
such as in medicine and in materials science
operated in a so-called "fixed target" mode. In
this mode the accelerated energetic particles are
delivered to a target made of some material at
rest in the laboratory.
Since that time, research facilities have been
constructed in which counter-circulating
accelerated beams of particles collide with each
other, rather than with targets at rest in the
laboratory. The use of accelerated particles in
this "colliding beam" mode has been done to take
advantage of the fact that the total energy of the
colliding particles, including both their kinetic
energies and the energy included in their masses
at rest, becomes available in the collision
process. This condition is not true for fixed target
collisions.
Such colliders are not nearly as numerous as
other types of accelerators, but represent
important research facilities in which basic
physics research is conducted.
D. Purpose and uses
Accelerators were originally designed to study the
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structure of matter. Accelerators today are used
not only for basic research purposes, but for
many other applications as well. Examples
include:
• Production of radioisotopes
• Generation of bremsstrahlung for radiography
• Induction of fusion
• Pumping for lasers
• Detoxification of hazardous waste
• Production of synchrotron radiation
E. Facility size/complexity
Small accelerators/facilities usually mean simpler
controls, less staff to coordinate, smaller areas to
monitor, and fewer points of access to control.
However, small accelerators (lower energy) can
produce very intense levels of radiation.
As the size and complexity of the installation
increases, so does the importance of clear and
concise communication channels and a detailed
formality of operations.
IV. Radiological concerns
A. Prompt radiation
Prompt radiation results from the accelerator
beam or the interaction of the beam with matter
only while the accelerator is operating. Prompt
radiation components include:
1. Primary beam
The primary beam consists of accelerated
Section 136
charged particles prior to any interactions that
may decrease the beam’s energy or intensity.
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It is the most intense form of radiation present
at an accelerator facility and is made
inaccessible to personnel through engineered
and administrative controls.
2. Secondary beam
The secondary beam is produced by
interaction of the primary beam with matter
such as targets or beamline components.
The secondary beam may consist of:
• Electromagnetic radiation
• Neutrons
• Charged particles
3. Skyshine
Skyshine is the term used to describe
radiation emerging more or less vertically
from a shielded enclosure, which then
scatters from air molecules to produce
radiation at some distance from the source.
4. Electromagnetic radiation (photons)
Prompt photons may include those produced
by:
• Bremsstrahlung: Photons emitted through
the deceleration of charged particles in the
beam
• Electromagnetic cascades: Multiple
photons emitted through initial high-energy
interactions
• Synchrotron radiation: Photons emitted as
charged particles are accelerated in a
curved path (a dramatically more
significant effect for electrons than it is for
protons having the same kinetic energy)
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• Thermal neutron capture: Photons can be
emitted as a result of nuclear reactions in
which materials present in the accelerator
enclosure absorb thermalized neutrons
produced by the accelerated beams.
5. Neutrons
Neutrons can be produced through nuclear
interactions of the primary and secondary
beams with matter. They can also be
produced by interaction of high energy
photons with matter (photonuclear reaction).
Neutron radiation is a concern within any area
where the beam can interact with physical
objects.
6. Muons
Muons are particles that are physically similar
to electrons, but are about 200 times heavier.
Energies in excess of 212 MeV are required
to produce muons by means of pair
production at electron accelerators. At proton
and ion accelerators, muons cannot readily be
produced at energies below about 140 MeV
since charged pions or kaons, which decay
into muons, must first be produced. Due to
the short ranges of low energy muons in
matter, they are not normally of concern for
accelerators of less than 500 MeV kinetic
energy.
Muons travel mainly in the direction of the
beam that produced them, with very little
deviation from the beam path. They are a
concern directly downstream of targets and
beam dumps.
B. Residual radioactivity (radioactivation)
Radioactivation is the process by which materials
become radioactive. It is commonly referred to
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as “induced radioactivity” or simply “activation.”
Generally energies above 10 MeV are needed to
activate materials.
Activated materials will continue to emit radiation
after shutoff of the beam. The length of time
depends on the half-life and quantity of the
activated element.
1. Contaminated materials versus activated
materials
Contaminated materials are considered to be
items with removable surface contamination.
Activated materials are considered to be
volume contamination, meaning the
radioactive materials are dispersed
throughout the items.
Activated materials normally do not present a
potential loose contamination hazard except
during activities such as:
Section 137
• Grinding
• Burning
• Machining
• Handling filters of coolant water
Activated materials are normally controlled
based on the residual external radiation dose
rate.
2. Activated materials
Materials that may become radioactive
include:
• Any material within the accelerator
enclosure
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• Beamline components
• Air
• Liquids
Accelerators used to produce radioisotopes
present special problems because of the
variety of target materials used, and because
the parameters of machine and target are
deliberately optimized to produce radioactive
materials.
• Beamline components
Items that intercept a portion of the beam are
most likely to be activated. Among those
items which have the highest probability for
activation are:
– Targets
– Beam dumps or stops
– Collimators and scrapers
– Septa and other magnets
– Cavities and beamline
• Air
Air and other gases in the accelerator
enclosure may be activated. Typically, the
activation products are short-lived gaseous
radionuclides of the elements in the air.
Examples are Oxygen-15 from Oxygen-16.
The two major concerns of air activation
products are:
– Worker (delays entry)
– Environmental (releases from enclosures)
• Liquids
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Tritium is frequently produced in water used to
cool the target and/or experimental
equipment. As this water supply is usually a
closed system, the concentration of the tritium
in the water will slowly increase.
Other activated liquids may include:
– Oil in vacuum pumps
– Cryogenic fluids
C. Ancillary sources
Accelerators employ devices to either impart
energy to particles, or redirect them during the
acceleration process. The following devices may
emit ionizing radiation while they are operating.
1. Klystrons
Klystrons provide power to accelerate
charged particles. They emit x-rays during
operation.
2. Radiofrequency (RF) cavities
These devices accelerate charged particles
using electromagnetic fields. Trace gases
within the RF cavity cause photons to be
emitted by the accelerated particles.
3. Electrostatic separators/septa
These devices split a particle beam into two
beams using static electric fields. The high
voltages associated with these devices cause
electrons to accelerate in the vacuum within
the beamline. They emit x- or gamma rays.
V. Radiological and other controls
Controls are used at accelerator facilities to protect
personnel from exposure to ionizing radiation and
other hazards, which include:
• Electrical
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• Mechanical
• Cryogenic
• Nonionizing radiation
The design of an effective safety program
incorporates a combination of engineered and
administrative controls.
A. Engineered controls
Engineered controls are the primary controls at
an accelerator facility.
1. Active engineered controls
Active engineered controls include devices
that sense changing conditions and can
trigger a safety action. Examples may
include:
• Status lights
• Alarms
• Interlocks
• Scram buttons
2. Passive engineered controls
Once installed, passive engineered controls
are used to prevent personnel entry or reduce
radiation dose and require no further action to
perform their intended function. Passive
engineered controls may include:
• Barriers
• Shielding
.
Section 138
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B. Administrative controls
Administrative controls require human interaction
in order to be effective.
Key administrative controls include:
• Signs/postings
• Search and secure (sweep) procedures
• Controlled access procedures
• Configuration control procedures
• Radiological Work Permits (RWPs)
VI. Monitoring
Monitoring for radiation at accelerators can be
complicated. Special techniques and
instrumentation may be necessary due to the
existence of:
• Mixed radiation fields (photons, protons,
neutrons)
• Pulsed beams
• Very high-energy radiation
• High dose rates
A. Prompt radiation
Measurements of prompt radiation fields are
required for occupational and environmental
monitoring and for accident dosimetry and
calibration of dosimeters, as well as for research
purposes. In selecting measurement techniques
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and instruments, it is important to consider the
purpose of the measurement and the radiation
field’s parameters.
1. Mixed radiation fields
The complexity of the radiation field and the
radiation measurements increase with the
energy of the accelerator.
2. Pulsed radiation
Prompt pulsed radiation must be measured
with specialized survey instruments. Ion
chambers are typically used and are
recommended.
3. Neutrons
Neutron monitoring is complicated and must
be conducted by highly trained individuals
with specialized instruments.
B. Environmental monitoring
Environmental sampling/monitoring may include:
• Prompt radiation (neutrons, skyshine, muons)
• Sampling exhausted air from beam housings
• Surface/groundwater (on and off site)
• Monitoring of radiation levels at site boundary
(from storage areas)
C. Personnel monitoring
Simple dosimeters, such as those used in
personal dosimetry and simple survey
instruments, should be calibrated when possible
in radiation fields that are similar to those in
which they will be used. To interpret
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measurements made with these instruments, one
must know as much as possible about the
radiation field that is being measured.
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Module 14 - 1
I. Introduction
Self assessment is part of an effective worker health
and safety program. As such, there are many
requirements related to conducting self
assessments and maintaining quality assurance
programs, such as those required under 10 CFR
830.120 ,or as part of an effective Integrated Safety
Management program. This module focuses on the
radiation protection required assessments and
audits.
10 CFR Part 835, Occupational Radiation
Protection, requires, in 10 CFR 835.102, that
internal audits of the Radiation Protection Program
be conducted at least every 36 months. The audits
shall include all radiation protection functional
elements.
DOE G441.1-1B, Radiation Protection Programs
Guide, provides guidance on meeting the 10 CFR
835 requirement for audits. Section 4.2 of the
Guide includes a listing of radiation protection
functional elements and associated DOE guidance
documents.
Article 134 of DOE-STD-1098-99, Radiological
Control, provides additional guidance on
radiological control assessments.
Section 139
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II. Types of assessments
It can be extremely damaging if we, as overseers,
facility representatives, and assessors, violate the
high standards of performance and rules that we
are to assess. It is important to understand that we
are constantly being monitored and that we must
set the example with regard to radiological
protection.
The methods used to gather or capture information
can detract from the effectiveness of the
assessment process.
Assessment techniques can be enhanced through
training and practice. These techniques will
improve the ability to see, observe, and better
understand.
There are two types of assessments: unstructured
and structured. “Unstructured” reviews means “not
looking for one specific area or thing.” “Minimum
preparation” method is accomplished through going
with workers on routines. These could be described
as general assessments.
The more preparation put into the assessment, the
more effective it is, no matter what type of
assessment is conducted.
The second type of assessment is “structured,”
which involves looking specifically at one issue and
reviewing it from every angle.
Two traditional methods within the structured
inspection are the vertical and horizontal review.
Vertical review is the assessment of a narrow
subject area in great detail, for example, assessing
the Radiological Control Organization from top to
bottom.
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Horizontal review is the assessment of a broad
range of related subjects in generally less detail, for
example, assessment of radiological protection
across all organizations at a nuclear facility.
III. Assessment guidance
A. Documents
IMPORTANT: Put the burden of producing
documents on the site. If the site personnel
state that it is not appropriate that they comply,
they must provide DOE with written support for
that position.
The DOE and site basic documents an assessor
should have for radiological compliance include
(determine the extent of applicability and site
commitments to adhere to the documents):
• 10 CFR Part 835
• Site Radiation Protection Program
• DOE-STD-1098-99, Radiological Control
• Other applicable federal regulations
• Applicable DOE orders
• State regulations
• DOE Implementation Guides
• Site DOE contract
• Site commitments (corrective actions,
DNFSB recommendation responses)
• Site reports (deficiency, occurrence)
• Site-Specific RadCon Manual
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• Approved exemptions
• Peer group/industry group
standards/recommendations
– DOE standards
– ANSI standards
– NRC Regulatory Guides
B. Compliance issues
1. Compliance is only the tip of the iceberg.
2. What are the issues?
• What happened?
• Why did it happen?
• Will corrective action prevent recurrence?
• How can we ensure it will not happen
again?
3. Determine the degree of consequence of
noncompliance effects and ramifications of
noncompliance.
4. Procedural compliance is only part of the
overall commitment to excellence in
radiological control.
• Acknowledge good practices
The DOE radiological control policy is that
“continuing improvement is essential to
excellence in radiological control.”
• Encourage what is good.
5. Need to distinguish between requirements
("shall" statements) and recommendations
("should" statements).
Section 140
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C. Compliance orders
Compliance orders are issued by the Secretary.
They identify a situation that violates, potentially
violates, or otherwise is inconsistent with the:
• Atomic Energy Act of 1954 as amended
• Nuclear statutes
• Nuclear Safety Requirements
Compliance orders mandate a remedy or other
action, and state the reason for the remedy or
other action.
Examine orders and responses to orders for:
• Timelines
• Accuracy
• Completeness (Was the problem solved?)
IV. Assessing radiological performance
A. Internal audits, inspections, reviews,
investigations, and self-assessments comprise
“assessments” and are part of the numerous
checks and balances needed in an effective
Radiation Protection Program.
Internal audits of the Radiation Protection
Program shall be conducted such that over a
three-year period, all functional elements are
assessed for program performance, applicability,
content, and implementation. These should be
performed by individuals who are organizationally
independent from the organization responsible for
developing and implementing the Radiation
Protection Program.
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B. DOE-EM-STD-5505-96; DOE Limited Standard
Operations Assessments, contains very good
methodology for performing assessments.
There are three major components of an effective
assessment program: management assessments,
operational assessments, and quality assurance
assessments. For each of these, functional areas
are identified that represent specific areas of
managerial or technical activity. Within each
functional area, performance objectives are
defined that represent essential characteristics or
conditions of an effective safety program. The
criteria associated with each performance
objective are intended to serve as guidelines for
the assessments.
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Both management and operational assessments
are operationally focused and performance-
oriented. They deal with the safety culture of the
facility, how safely it is being operated, and the
condition of its documentation and equipment.
The design of the facility and its process
systems is presumed, for purposes of the
management and operational assessments, to
permit safe operation. This is based on the
presumption of an appropriate selection and
application of design standards by the architect-
engineer and the operating contractor, and of
appropriate independent reviews by DOE or its
predecessor agencies of the design, the
construction activities, and the Safety Analysis
Report.
The criteria listed do not address every activity
that might be relevant to a performance
objective. Therefore, meeting all criteria does
not necessarily ensure that the performance
objective is fully met. Conversely, a specific
facility might achieve the performance objective
without meeting all criteria.
In part, because of the various ways in which the
performance objectives can be met, effective
assessments emphasize the performance
objectives rather than the criteria. The methods
for determining whether a criterion is met are not
given. Consequently, considerable expertise
and judgment are required to be exercised in
conducting the assessments.
Although the quality assurance assessments
Section 141
have a broad perspective, covering the overall
quality assurance program of the facility, they
are relevant to assessing radiological protection
performance.
DOE-STD-1070-94, Reaffirmed April 1999,
Guidelines for Evaluation of Nuclear Facility
Training Programs, provides guidance on
evaluating training programs at nuclear facilities.
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C. Radiation Protection Program deficiencies
Managers should encourage the positive view
that identifying even minor deficiencies
represents an opportunity for further
improvement.
Radiological work practices should be
continually scrutinized and questioned so that
opportunities for improvement can be identified,
assessed, and incorporated into the Radiation
Protection Program.
The number of deficiencies, alone, does not
measure the overall quality of the Radiation
Protection Program.
D. Critiques
One assessment method is the critique. An
honest review and establishment of facts, which
are in chronological order, is necessary to arrive
at the truth.
This is a formal process established to obtain
pertinent facts following an unusual radiological
situation or at the satisfactory conclusion of a
new or unusual operation involving radiological
controls.
The process should be used to quickly establish
facts in chronological order so that the
underlying reasons or causes for the success or
failure are well understood. Work force
participation should be encouraged. Critiques
are a management tool and should not be used
to “fix blame” or “shoot the messenger.” This
process complements the Occurrence Reporting
and Processing of DOE Order 231.1-2.
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In developing corrective action plans, managers
should address basic underlying reasons for the
identified deficiencies or concerns, not just the
specific symptoms identified by the reviewer.
E. Radiation Protection Assessment Program
To accurately assess the performance of the
Radiation Protection Program, an assessment
program should be formalized, created, and
implemented.
Elements of a Radiation Protection Assessment
Program
F. Radiation Protection Program Performance
The contractor senior site executive should
establish, approve, and maintain a radiological
performance goals program. The performance
goals should be measurable, achievable,
auditable, challenging, and meaningful in
promoting improvement. Chapter1, part 3 of
DOE-STD-1098-99, Radiological Control,
provides guidance on appropriate radiological
goals.
Goals need to be developed primarily by those
responsible for performing the work. Forming a
Radiological Awareness Committee that
includes the active participation of the work force
is encouraged.
Radiological performance goals should be
reviewed at least annually and revised as
appropriate. Normally, more stringent goals
should be set annually to reflect the improved
radiological performance at the facility.
Occasionally, the goals may be made less
stringent to accommodate changes in work load
or mission.
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G. Performance indicators
To evaluate performance, one needs to be able
to measure change. This means dimensions
must be identified. One must be able to track,
trend, post, paint, count, look at, and assign
numbers. What gets measured, gets done.
Section 142
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I. Introduction
II. Assessments
A. Reasons for conducting assessments include the
following:
• Determine regulatory compliance.
• Formally document Radiation Protection
Program strengths and weaknesses.
• Investigate a specific incident.
• Document conditions that need a follow-up
assessment.
B. Basic elements of a Radiation Protection
Program
• Organization and administration
• Personnel training and qualification
• Quality assurance
• ALARA
• Radiological work control
– Procedures
– RWPs
• Posting and labeling
• Radioactive material control
– Source control
– Release of materials
– Receipt and transportation
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• Radiation-generating devices
– Sealed source
– X-ray machines
• Entry control
• Contamination control
• Instrumentation and alarms
• Monitoring
– Workplace
– Effluent
– Environmental
• Dosimetry
– External
– Internal (bioassay)
• Respiratory protection
• Facility-specific features
– Uranium
– Plutonium
– Tritium
– Accelerators
• Radioactive waste management
• Emergency response
• Records
• Assessments/performance indicators
C. Indications that an assessment is needed
• Exceeding administrative dose control levels
or regulatory limits
• Loss of control of radioactive material
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• Unmonitored/excessive release of
radioactive material to the environment
• Excessive numbers of skin contamination
incidents
• Uptakes of radioactive material by
employees
• Excessive numbers of radiological incidents
• Inadequate training
• Ineffective work control systems
• Incomplete or inaccurate radiological surveys
• Incomplete or inaccurate records
III. Preparing for the assessment
To adequately prepare for the assessment:
• Review operating history
• Examine previous assessment reports
• Collect input from person(s) assessed
• Determine applicability of industry issues
• Review policies and procedures
• Assemble regulations and guidance documents
• Prepare an assessment plan
Radiological Assessor Training
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Student's Guide
Module 15 - 4
A. Operating history
Review the operating history. The following
documents can be extremely helpful in preparing
for the assessment:
• Occurrence reports
• Radiological deficiency reports
• Violations/citations
• Facility design changes
B. Previous assessments
Examine previous assessment reports.
Documents that could be helpful are:
• DNFSB Recommendations
• Self-assessments
• Corporate quality assurance reports
• External audits
C. Input from person(s) to be assessed
• Management
• Radiological Control Manager
• Radiological Control Organization’s
“customers”
D. Industry issues
• Emerging technical issues
• Application of best industry standards to site
program
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Module 15 - 5
E. Policies and procedures
• Operating procedures
• Radiological control policies
F. Regulations and guidance documents
• Federal
• State
• Site
• Industry or peer group
G. Assessment plan
• Identify elements to be assessed.
• Generate specific questions and/or standards
against which to measure performance.
• Develop record sheet for assessment
responses, data, and field notes.
• Allocate time for each assessment activity.
• Intentionally leave unscheduled time.
Section 143
IV. Conducting the assessment
A. General guidance
Remember the assessment is a positive activity,
designed to help those being appraised. Follow
the plan, but be flexible.
Include nothing in the assessment findings that
is not based on fact, requirement, or
commitment. If in doubt, leave it out (but raise it,
informally as a matter deserving a closer look).
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Share the findings with the point(s) of contact
each day. There should be no surprises at the
daily Radiological Control Manager debriefing or
at the final debriefing.
B. Announced versus unannounced assessments
1. Announced assessments are scheduled
through a pre-assessment memorandum. The
following information should be addressed:
• Assessment objectives
• Assessor(s)
• Assessment duration
• Request for a site point of contact
• Any special needs
• Recommended time and place for pre-
and post-assessment conferences
2. Unannounced assessments
• Used to determine “real” program
performance
• Back-shift, off-hours tours may reveal
relaxation in program standards
• Vary the assessment schedule
Note: Contact the Radiological Control
Manager and line management immediately
if there is a serious problem.
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3. Available methods for conducting an
assessment include:
• Document reviews
• Personnel interviews
• Field observations
4. Recommended assessment approach (in
order)
• Review upper-tier procedures describing
the Radiation Protection Program.
• Conduct a short (one hour or less) tour of
the site/facility.
• Interview Radiological Control
Organization staff and “customers.”
• Conduct detailed and follow-up tours,
interviews, and document reviews.
5. Perform document reviews of:
• Operating procedures
• Records for:
– Dosimetry
– Work control Radiological Work Permit
– Surveys (contamination, radiation
level, air, special)
– Occurrence, deficiency reports, and
critiques
– Regulatory reports
– Radioactive effluent reports
– Training and qualification
– Instrument calibration and response
testing
• Special studies
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Module 15 - 8
6. Site/facility tour
• Tour the site/facility, preferably with an
experienced individual from the site.
• Make notes of housekeeping and facility
condition. Items to look for include:
– Leaks, spills
– Dirt, rust, and clutter
– Poor equipment maintenance
– Radiological control posting
– Radiological Control Technician and
Radiological Worker interface
– Employee morale
7. Conduct interviews with the following:
• Radiological Control Manager
• Radiological Control Supervisor(s)
• Radiological Control Technical Leads
• Qualified Radiological Control Technicians
• Radiological Control Organization’s
“Customers”
• DOE Site Representatives
• Facility Manager
The following are the details:
• Radiological Control Manager
– Knowledge of current radiological
control regulations, industry standards
– Identification of program deficiencies
and priorities
– Obstacles to improving program
performance
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• Radiological Control Supervisor(s)
– Level of support given Radiation
Protection Program and Radiological
Control Manager
– Identification of program deficiencies
and priorities
– Obstacles to improving program
performance
Section 144
Note: Compare responses to those from
Radiological Control Manager.
• Radiological Control staff members
responsible for major technical functional
areas.
Examples of these functional areas
include:
– Organization and administration
– Personnel training and qualification
– Quality assurance
– ALARA
– Radiological work control
+ Procedures
+ RWPs
– Posting and labeling
– Radioactive material control
+ Source control
+ Release of materials
+ Receipt and transportation
– Radiation-generating devices
+ Sealed source
+ X-ray machines
– Entry control
– Contamination control
– Instrumentation alarms
– Monitoring
+ Workplace
+ Effluent
+ Environmental
– Dosimetry
+ External
+ Internal (bioassay)
– Respiratory protection
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– Facility-specific features
+ Uranium
+ Plutonium
+ Tritium
+ Accelerators
– Radioactive waste management
– Emergency response
– Records
– Assessments/performance indicators
Document their responses to incidents in
their technical area.
Discuss impediments to improving their
programs.
• Qualified Radiological Control Technicians
– The depth and breadth of knowledge of
radiation protection
– Technical issues unique to the
site/facility
– Effectiveness of the working
relationship between Radiological
Control Technicians and their
“customers”
• Radiation Protection Program “customers”
– Knowledge of fundamental radiation
protection concepts and good
Radiological Worker practices
– Working relationship with the
Radiological Control Technicians
– Obvious or hidden problems
– Poor communications
– Division of work problems
– Overall, how the Radiological Control
Organization is regarded (“policeman”
vs. team member)
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• DOE Representatives
– If the Radiological Control Organization
staff solicits his/her input on technical
decisions affecting Radiation Protection
Program performance
– If the relationship is one of mutual
respect or adversarial in nature
• Facility Manager
– Whether the Facility Manager has
made a written commitment and is
striving to achieve excellence in the
Radiation Protection Program
– His/her perspective on how the
Radiation Protection Program should
be improved, and the necessary
priorities
8. Observe Radiological Workers/Radiological
Control Technicians in the workplace
• Recommendations for observing work
include:
– Dress as the individuals being
observed are dressed.
– Work the same hours they work.
– Stand away from the immediate work
area, but close enough to watch the
work proceed.
– Resist the urge to get involved in the
work.
– Be professional and courteous, but not
familiar.
• Key areas to watch for include:
– Procedure violations
– Failure to follow RWP requirements for:
+ Dosimetry
+ Protective clothing
+ Respiratory protection
+ Radiological Control Technician
coverage
+ Surveys
+ Special instructions
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– Poor Radiological Worker practices:
+ Reaching across radiological
boundaries
+ Scratching body with gloved hand
+ Inadequate frisking
+ Loitering in a high radiation field
– Lack of organization or formality in the
work process
– Poor housekeeping, disorderly work
area
– Wasted time and effort due to
ineffective work planning
– Communication problems
– Poor relationships between
Section 145
Radiological Workers and Radiological
Control Technicians
C. Post-assessment actions
At the post-assessment conference, summarize
the findings identified during the assessment.
This is an opportunity for additional questions
about the findings. Any requests for corrective
actions, dates, or a need for follow-up
assessments can be identified at this time.
Thank everyone for cooperation and support
during the assessment.
1. Publish assessment findings.
2. Receive site responses, which should include
the following:
• Action items
• Responsible individuals/groups
• Action item due dates
3. Accept/reject/modify responses.
4. Develop corrective action tracking list.
5. Publish a periodic action item status report.
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Module 15 - 13
6. Maintain a separate file of open action items.
7. Personally verify the closure of action items.
8. Evaluate the adequacy of actions taken to
close open findings:
• Has root cause been correctly identified
and corrected?
• Are follow-up assessments needed?
D. Follow-up assessments
1. Qualifying conditions
• Widespread problem
– Problem occurs at several locations in
the same facility or several facilities at
the same site.
– Problem identified by the assessment
is only part of a larger, more generic
deficiency.
• Recurring problem: earlier efforts to
resolve the problem have been ineffective.
2. Actions
• Widespread problem
– Take a longer sample to confirm/refute
a widespread problem
– Look for related problems in the same
work unit.
• Recurring problem
– Scrutinize root cause analysis.
– Try a different approach to solving the
problem.
– Solicit outside help. Perhaps others
have “lessons learned”.
3. Incorporate follow-up assessment information
into corrective action tracking system.
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V. Marginal radiological performance
When radiological control performance is less than
adequate, strengthen line management’s
commitment to radiological control by notifying the
Radiological Control Organization to obtain their
support in improving radiological support.
In cases where the work force does not have the
required level of sensitivity for radiological work
practices, additional management attention is
needed to assure the proper outcome. Line
management should be held accountable for
implementation of the Radiation Protection Program.
Initial actions should include:
• More direct line supervision in the work space
• Curtailment of work schedules
• Addition of extra radiological control personnel
• Conduct of additional training
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 16 - 1
I. Introduction
II. Case studies guidance
Point to remember: If each root cause is not
adequately treated/corrected by a corrective action,
recurrence of the event or some variation of it is
likely.
Review a reconstruction of events from the available
data.
A proper investigation report or occurrence report
reconstructs the events as they occurred.
Radiological Assessor Training
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Module 16 - 2
III. Description of occurrence (edited from investigation
report)
A. Incident
The layout of the buildings and equipment at this
site are included.
Section 146
Two employees at the Paducah Gaseous Diffusion
Plant (PGDP) received skin and clothing
contamination from Thorium-234 (234Th) and
Protactinium 234m (234mPa) while disconnecting a
used uranium hexafluoride (UF6) cylinder at the
C-337-A building, UF6 Feed Vaporization Facility, on
August 23, 1991.
B. Scenario of events
Starting at shift change, 12 employees, one of them
a Health Physics Technician, found contamination
on shoes and clothing. The incident was initially
identified during routine monitoring of the C-337-A
facility by a Health Physics Technician at 0900 (two
hours after the shift change). Efforts were initiated
by Health Physics to survey the area, identify the
source, and control the spread of contamination.
Surveys indicated widespread contamination in both
radiological and nonradiological areas of C-337
(adjacent to C-337-A) and C-337-A.
At some unspecified time, a critique was conducted
by the Assistant Shift Superintendent and all
personnel involved in the accident were interviewed.
All personnel who had been in the facility on the day
shift were contacted and surveyed. One individual
was found to have contaminated shoes and skin
contamination on the elbow and was taken to a
change house in C-337 for decontamination. Later
this employee’s personal clothing was also found to
be contaminated, and through further investigation it
was learned that this contamination occurred in the
change house. A thorough survey was conducted in
the change house, and it was discovered that, in
addition to a few articles in the change house itself,
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 16 - 3
two locks and lockers used by Employee No. 1 (who
performed the pigtail changes on the previous shift)
were contaminated. This employee returned to work
at 1830 on August 23, 1991. Surveys of the locker
contents indicated contamination on company-
issued clothing worn the previous shift. The
employee was also found to have skin
contamination of 6500 dpm/100 cm2 on the arm,
4500 dpm/100 cm2 on the knee, and 2750 dpm/100
cm2 on each ankle.
A survey of the employee’s coworker’s (Employee
No. 2) locker revealed contaminated items (both
company-issued and personal). Personal surveys
conducted when Employee No. 2 returned to work
showed the presence of skin contamination of 4500
dpm/100 cm2 on hair, 5000 dpm/100 cm2 on neck,
and 40,000 and 15,000 dpm/100 cm2 on wrists.
Later (2130 hours on August 23 for Employee No. 2,
and 1900 hours on August 24 for Employee No. 1)
surveys were conducted at the employees’ homes.
Monitoring of one employee’s home found one
T-shirt and one pillowcase slightly contaminated. A
pair of shoes at the other employee’s home was
found slightly contaminated. This employee’s (No.
2) coveralls had already been sent to the laundry,
since it was not recognized they were contaminated.
After laundering, significant contamination was still
present (up to levels of 250,000 dpm/100 cm2 at
ankles, and lower levels at other places). A survey
of the laundry equipment did not indicate any
contamination.
Based on statements from the involved employees,
they utilized the required personal protective
clothing and equipment for the job at the time. The
autoclave area is designated as a Contamination
Zone. Anti-contamination clothing designated for
cylinder changes at the time of the incident
consisted of company-issued coveralls (blues),
gloves, and shoe scuffs. Operational procedures
require the use of a respirator when disconnecting
pigtails. Surveys conducted as part of this
investigation did not show any contamination on the
Section 147
Radiological Assessor Training
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Student's Guide
Module 16 - 4
employees’ respirators or respirator cartridges.
The actual incident began between the hours of
0130 and 0415 on August 23, 1991, at the PGDP
C-337-A Feed Vaporization Facility.
The operators routinely assigned to C-337-A for the
period of 1900 hours on August 22, 1991, through
0700 hours on August 23, 1991, were not available
due to the illness of one and an alternate work
assignment of the other at another facility (C-360).
Two operators who are not routinely assigned to the
area were then assigned to cover C-337-A. One
operator (No. 2) was qualified for operation of the
facility while the other (No. 1) was in training for
qualification. (This is in compliance with facility
Operational Safety Requirements.) Supervisor
interaction was minimal, with only one brief visit
around the middle of the shift.
The operations in process at the time of the incident
were the routine disconnection and removal of
emptied UF6 feed cylinders and subsequent
replacement with full cylinders. This operation
consists of disconnecting a short length of
connecting pipe between the cylinder and the
system piping that leads to the diffusion process
equipment. This pipe is called a pigtail; it has
threaded connections and gaskets on each end.
Since pigtails are routinely reused, each cylinder
change requires replacement of gaskets on pigtails
to minimize the possibility of UF6 releases during
heating and feeding of the UF6 into the diffusion
process. At times these gaskets can be difficult to
remove from the pigtail. A special tool is available to
assist in the removal of these gaskets; however,
difficulty can still be encountered. The pigtails used
that night had been used for several feeding cycles,
as is normally the case. The exact number of cycles
could not be determined.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 16 - 5
There are levels of 234Th and 234mPa that occur
naturally from the decay of 238U present in the
cylinder pigtail, pigtail gaskets, and cylinder valves.
Approximately one curie each of those two
radioisotopes builds up in a cylinder within a few
months. These materials are less volatile than UF6,
so they remain as solids at the autoclave
temperature, but some small amounts are entrained
in the UF leaving the cylinder and small quantities
are deposited in the cylinder valve and pigtail as the
UF passes through it. These materials are present
as removable surface contamination in these
components, as well as being present in quantity in
the cylinder heels (the material remaining in the
cylinder after feeding). No containment of the ends
of the pigtail during the gasket removal process was
required by procedure. Additionally, the facility-
specific training program does not address the
specific contamination hazard the cylinder/pigtail
change represents.
The operators changed four cylinders on the shift.
The cylinder number, autoclave used, and
approximate time of change (from logs and recorder
data) are shown below:
Cylinder Number Autoclave Number Approximate Time
K-438 3 West 0130 08/23/91
K-505 5 West 0320 08/23/91
K-472 1 West 0500 08/23/91*
AC-1090 4 West 0500 08/23/91
*Time is very approximate. Operator statements place the change late in shift.
Radiological Assessor Training
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Module 16 - 6
Section 148
There was a portable fan temporarily positioned to
cool employees just north of the 5 West autoclave
control panel, inside the Contamination Zone. The
fan had only been in place a few weeks. It was
operating during the shift in question. Apparently no
one had questioned the use of this fan in the area
prior to the event. Circumstantial evidence places
one operator exiting from either the 4 West or 5
West autoclave in the path of this fan while trying to
remove a pigtail gasket. The area of highest surface
contamination was spread along a line from the fan
(located by 5 West autoclave), past the 4 West
autoclave to the 3 West autoclave control panel in
the direction that the fan blows.
Self-monitoring performed by the employees upon
exiting the Contamination Zone where the job was
performed was inadequate, in that the employees
did not recognize the contamination present on their
skin and/or clothing. The employees performed
their other duties during the remainder of the shift,
thereby spreading this contamination to both
radiological and nonradiological areas. This spread
of contamination to nonradiological areas through
failure to recognize personal contamination at exit
monitoring stations caused other personnel to
become contaminated when the shift change at
0700 on August 23, 1991, brought new personnel
into these areas.
Based on the interview with Employee No. 1, the
employee traveled to C-337 around 0400 for a
break. Upon exiting the vaporizer Contamination
Zone and going to the C-337-A Operation’s
Monitoring Room, the Bicron frisker was indicating
high but not alarming due to high ambient
background radiation levels. The employee reset
the monitor and remonitored. The employee
indicated that the reading was elevated, but was not
alarmed this time. The employee stated this was
normal since the background in that area is often
high.
Radiological Assessor Training
DOE-HDBK-1141-2008
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Module 16 - 7
At approximately 0600 on August 23, 1991, both
operators left C-337-A bound for the C-337 change
houses and the C-337 Area Control Room for shift
turnover. Both operators stated they used Bicron
friskers to check for contamination prior to entering
the nonradiological (green) pathway in C-337.
Training previously received by each operator for
each type of frisking equipment was documented.
Employee No. 1 noted that the Berthold hand-and-
foot monitor previously used was “not operating
properly,” so the employee used the Bicron frisker.
Neither operator noted any contamination.
Employee No. 2 monitored hands and feet only,
based on subsequent interviews, which indicated
that the employee did not know that a whole-body
frisk was required when exiting a radiological area.
Based on statements from both employees, they
showered, changed into personal clothing,
completed the shift turnover activities, and exited the
building after monitoring hands and feet at the
building exit, as required.
Since some personnel exit monitoring data is
regularly recorded, this data was reviewed. The
operators passed between the C-337-A Operation’s
Monitoring Room and the C-337 Area Control Room
several times during the shift and should have
performed a whole-body frisk for contamination each
time. Data for Employee No. 2 was not available, as
the employee used a Bicron frisker. (These
instruments do not have the added feature of storing
monitoring data for later review.) Data for employee
No. 1 shows 0414 hours on August 23, 1991, as the
first time a monitor station evaluated this operator as
contaminated. This station would normally be used
when passing from C-337-A to the C-337
nonradiological walkway when going to the
maintenance shops and change houses (restrooms,
lockers, and showers).
Section 149
Radiological Assessor Training
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Student's Guide
Module 16 - 8
This same employee was also known to be
contaminated at the C-337 building exit on two
separate monitors (twice on one, once on the other)
when leaving after the shift change approximately
0700 on August 23, 1991. The employee stated that
the first monitor alarmed, but that the second
monitor did not indicate the contamination.
No monitoring data was found for the second
employee, since he did not utilize equipment
capable of storing this information.
Personal egress monitoring data from the facility
was also reviewed, and individuals from prior shifts
were contacted and monitored. An operator who
was in the C-337-A area extensively from 0700 to
1830 hours on August 22, 1991, had a new pair of
company-issued shoes, which were found to be free
of contamination. This operator had left the C-337-A
facility at 1830 hours on August 22, 1991.
Additionally, routine surveys on August 19, 1991, did
not indicate a similar contamination problem. Since
no significant contamination problems were
identified prior to 1900 hours on August 22, 1991,
the investigation focused on the activities from 1900
hours on August 22, 1991, to 0700 hours on August
23, 1991.
Urinalysis, as well as in vivo internal dosimetry
assessments, was performed on these employees
and did not indicate any evidence of internal
contamination. Personnel whole-body external
radiation dosimeters worn by both employees,
although externally contaminated, did not indicate
that abnormal doses to ionizing radiation were
received.
Skin dose calculations showed less than 0.10 rem
for Employee No. 2 and 1.50 rem for Employee
No. 1, compared to an annual limit of 50 rem.
Radiological Assessor Training
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Module 16 - 9
It was noted that in the occurrence report of
Reference 2, there had been 26 similar occurrence
reports (in 1991) at the facility.
IV. Compensatory measures
Following the detection of contamination, several
actions were taken by facility management in order
to determine the source and type of contamination,
the personnel and areas which may have been
contaminated, and actions which could be taken to
minimize additional spread of contamination. The
following list of significant actions were
accomplished after the event:
1. A critique of the incident was conducted,
interviewing all individuals involved.
2. All nonradiological areas were decontaminated,
and contamination levels within the radiological
areas were reduced.
3. Personal protective equipment requirements in
C-337-A were upgraded to require full anti-
contamination protective clothing within the
Contamination Area.
4. A full-time Health Physics Technician was
stationed at C-337-A and required to monitor all
personnel and equipment leaving the radiological
area.
5. The two operators involved in the incident were
sent to the Fernald, Ohio (DOE), facility for in
vivo (whole-body) monitoring.
6. The fan was removed from the facility.
Radiological Assessor Training
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Module 16 - 10
7. In vitro urine bioassay samples were obtained
from the individuals involved in the incident, as
well as other individuals who were either
contaminated on previous shifts or involved in
surveying and decontaminating the area.
8. Dosimeters were collected and monitored to
assist in determination of radiation dose.
9. A walkdown of all plant boundary control stations
Section 150
was performed by senior management to
determine location of substandard boundary
control stations.
10. Efforts were initiated to determine other possible
sources of Th234 and Pa234m at other plant
locations.
11. Actions were initiated to reduce the potential for
the spread of contamination from the UF6
cylinder pigtails during disconnection, gasket
replacement, and reconnection activities.
12. Surveillance was established by line
management of exit monitoring stations.
13. An investigation for an organizational finding was
initiated.
14. A news release was issued.
15. A plant announcement was made and a plant
bulletin was issued to emphasize the
seriousness of the situation and the need for
proper monitoring.
16. Complete locker room surveys were performed
by Health Physics Technicians.
Radiological Assessor Training
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Module 16 - 11
17. Meetings with union membership were
conducted by union leadership to emphasize the
importance of monitoring.
18. A letter, jointly signed by PGDP management
and union leadership, was issued to all PGDP
employees.
19. A DOE visit from Headquarters (HQ) Health and
Safety personnel was conducted. They
concluded that the breadth and scope of the
organization finding investigation was
appropriate.
20. The Portsmouth Gaseous Diffusion Plant was
notified of the incident for possible application at
its site.
21. Operators involved in the incident were not
allowed to work in radiological areas until
Radiation Worker retraining had been completed.
22. All fact sheets were put into “operator-required
reading” files.
23. Development of a training film to review
monitoring requirements and techniques was
initiated. Upon completion, review of this film will
be mandatory for all employees.
Radiological Assessor Training
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Module 16 - 12
Analysis - Contamination Levels on Gaskets and Pigtails
Sample Number
Nuclide Analyzed
Concentration
(dpm)
C-337-A Gaskets (2 gaskets combined for one
sample)
234
Th and
234m
Pa
U activity
11,000,000 Beta*
156,000 Alpha
C-310 Burp Station Gasket (1 gasket)
234
Th and
234m
Pa
U activity
163,000 Beta
140,000 Alpha
C-310 Product Withdrawal Gasket (1 gasket)
234
Th and
234m
Pa
U activity
40,000 Beta
1,900 Alpha
C-315 Tails Withdrawal Gasket (2 gaskets)
234
Th and
234m
Pa
U activity
117,000 Beta
20,600 Alpha
C-360 Sampling and Transfer Facility Gasket
(3 gaskets)
234
Th and
234m
Pa
U activity
1,500,000 Beta
78,000 Alpha
SP-8757, Pigtails coupling, feed header end
of pigtail
234
Th and
234m
Pa
U activity
see Note 1 Beta*
see Note 1 Alpha
SP-8758, Pigtail coupling, cylinder end of
pigtail
234
Th and
234m
Pa
U activity
see Note 1 Beta
see Note 1 Alpha
SP-8759, Material knocked loose from SP-
8757
234
Th and
234m
Pa
U activity
2,300,000 Beta
27,000 Alpha
SP-8760, Material knocked loose from SP-
8758
234
Th and
234m
Pa
U activity
2,300,000 Beta
75,000 Alpha
*Each radionuclide contributes 50 percent to this total activity.
Note 1: Beta/gamma levels were too high to be accurately counted on the spectrometer due to
detector dead time (saturation).
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 17 - 1
I. Introduction
II. Writing assessment findings
A. Organization of findings
There may be considered to be three categories
of assessment findings in order of increasing
severity:
Section 151
• Surface findings (Type I) are usually
indicators of underlying issues that may be
more significant. Note that a common
problem is treating or correcting only the
surface issue while ignoring the underlying
problem—this results in problem recurrence.
• Substantial findings (Type II) are typically
issues that are underlying and more
significant. Note that correcting the
underlying problem results in solving the
problem.
• Organizational findings (Type III) deal with
programmatic or global issues. Note that
correcting these is very difficult if they involve
system, organizational, or institutional
problems.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 17 - 2
First, group like, related, or similar findings
into a broader issue.
Then, review the overall list of groupings for
priority. The bases are:
1. Imminent danger
• Life Safety Code
• Personnel Safety
• Facility Safety
• Criticality
• Confined Space
• Traps
2. Not imminent, but potential danger
• Environmental monitoring, e.g.,
inadequate stack monitors
3. Violations of regulations, laws, orders
4. Areas where adverse public opinion may
reside
5. Performance and effectiveness issues
• Usually a large number of findings fall
into this category, which captures
effectiveness and quality issues.
Finally, establish what is most important and
what should be brought to the attention of the
senior DOE and contractor management.
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DOE-HDBK-1141-2008
Student's Guide
Module 17 - 3
B. Writing of findings
When it has been established what issues will
be brought to site management, review
techniques for writing about the findings:
There is an established style or method often
used in industry for writing findings. It consists
of the following three steps:
1. List the requirement
2. State what was observed (different from
requirement)
3. State the concern
III. Presentation of Findings
After findings are prepared in written form, it is
important that they be presented properly. Skills for
presenting findings are directly related to the
techniques used for writing findings.
Some rules to keep in mind when presenting
findings are listed below.
• Identify the assessment team leader and
members, and their organizational affiliation.
• Explain the reason for the assessment.
• NEVER, NEVER read the findings in a close-out.
Most senior management can read as well as
the presenter.
• Present the most significant findings first.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 17 - 4
• Be prepared to present additional information to
support the finding. In most cases, there is
much more material in the file than is
appropriate to be included in the write-up. Be
prepared to use that material to support the
finding.
• In some cases, this is the time to cover material
in the report that was not written for public
consumption.
• It may be appropriate to discuss other material
such as related findings from previous reports or
audits.
• Maintain proper perspective by including both
positive and negative findings.
• Start with the positive findings, then make a
clear, shift to the negative findings or concerns.
• Explain the concerns/findings enough so that
senior management will understand the issue.
• Thank the site contact person and most senior
manager(s) for help and hospitality extended
during the assessment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Section 152
Student's Guide
Module 18 - 1
I. Introduction
II. Compliance-based versus performance-based
evaluations
A. Compliance-based audits
A compliance-based audit is a comparison of the
requirements laws, rules, orders, guidance,
policies, procedures, and other documentation
with site practices to confirm implementation of
the specific requirements. For example,
determining whether bioassay samples were
collected in accordance with site procedure
requirements.
B. Performance-based assessments
Assessment is fundamental to the operation of a
satisfactory Radiation Protection Program.
A performance-based assessment is a review of
how the actual performance of the task is
accomplished and assessing whether the intent
of the requirement is being met. For example,
determining whether bioassay samples were
being analyzed for the appropriate isotopes
given the workplace environment.
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 18 - 2
III. Assessment process
The assessment process is one of the evaluation
methods used to determine the status and
effectiveness of an overall management system.
With this perspective, the assessment process
should be planned and scheduled to accomplish the
following:
• Evaluate the effectiveness of program
implementation in order to meet compliance
requirements
• Provide input for assessment process
improvement.
The assessment process consists of four phases:
1. Planning
2. Performance
3. Reporting
4. Response evaluation, follow-up, and close-out
A. Planning
Planning is the key to a successful assessment.
It is possible to go immediately to the field to
observe, work with, and find out how things are
being done. That is one element and approach
to the process, but there is a greater advantage
to be made with proper planning and
preparation.
The most successful assessments start with a
checklist. The checklist development is critical
to the success of the assessment and serves as
a commonly accepted method for documenting
what was looked at and what the results were. It
also serves as a guide to the person performing
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 18 - 3
the assessment and provides objective evidence
that an assessment was performed.
In performing the assessment, several types of
checklists can be used. The preferred style of a
checklist is the question-and-answer variety.
With this kind of checklist, the assessor has to
write-in an evaluation of the answer to each
question and any qualifying remarks. The
question-and-answer format is more difficult to
review, but provides more information with which
to judge the performance level of a system
element.
B. Performance
The elements of conducting an effective
Radiation Protection Program assessment are:
• Overall plan (annual)
• Establish weekly, daily, breakdown
• Actually write a plan (modify later)
• Preparations-obtain material
• Use protocol for entry, conduct, exit
• Keep contact informed/no surprises
C. Report
Documentation of the findings and observations
(note taking) in the field will involve some
combination of the following:
• Record book
• 3 x 5 cards
• Actual times, logistics
• What, when, who, why, where, how
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 18 - 4
• Documents reviewed
• Interviews
Then comes the time to start to put the report
together, whether a weekly report or the
inspection report of some other type. The
following are suggested:
Section 153
• Distill as information is gathered, while
memory fresh
• Start draft report early
D. Post-assessment actions
• Evaluate assessment responses
• Establish corrective actions and due dates
• Track the status of open action items
• Perform follow-up assessments as necessary
Radiological Assessor Training
DOE-HDBK-1141-2008
Student's Guide
Module 19 - 1
I. Introduction
II. Field exercise guidelines
A. Briefing for field exercise
The field instructors have prepared to take their
participants to the field. They have visited the
facility and areas for review, and have compiled
information for their participants to use in
preparation for the field exercise.
B. Preparations to go to field
A tendency exists to identify surface issues and
seek correction of the many items found while
walking through the facility. It is vital that
personnel who assess be able to sort the issues
noted and categorize them so effective use of
resources can be made. In other words,
identification of symptoms leads to contractors
working on the symptoms and not on the
underlying, substantive problems.
It can be extremely damaging if we (as overseers,
facility representatives, auditors, or assessors)
violate the high standards of performance and
rules that are being assessed.
Personal safety and facility safety are first and
foremost.
C. Findings
Each person will make a presentation to the
group. The team leaders will introduce the group,
tell where you went, and introduce each
presenter. Each person should take no more that
one and one-half minutes for the presentation of
a finding. Some of the “cats and dogs,” or other
findings and observations, will be covered at the
end of the individual findings.
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Student's Guide
Module 19 - 2
The Lead Field Instructor will monitor the overall
presentation and comment as appropriate.
We hope to see presentations in this form:
1. List the requirement.
2. State what was observed.
3. State the concern.
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Student's Guide
Module 20 - 1
I. Summary
(Insert individualized summary.)
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CONCLUDING MATERIAL
Review Activity: Preparing Activity:
DOE Field Offices DOE-HS-11
NNSA
HSS ID Project Number:
EM SR TRNG-0015
NE OH
SC RL
GC
IA
RW
NN
National Laboratories Operations Offices
BNL AL
LLNL NV
LANL OAK
PNL OR
Sandia CH
ANL
New Brunswick
ORNL
SRNL
Site Offices
Amarillo Site Office
Kirtland Site Office
Princeton Site Office
Fernald Site Office
Kansas City Site Office
Miamisburg Site Office
Y-12 Site Office
Part 5 of 5
Radiological Assessor Training
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Handouts
Office of Health, Safety and Security
U.S. Department of Energy
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Table of Contents Page
Dosimetric Quantities in 10 CFR Part 835 ......................................................................................3
Radiological Control Program Elements .........................................................................................5
Section 154
Elements of a Radiological Control Program ................................................................................11
Typical Safety Analysis Report (SAR) Contents...........................................................................25
Technical Safety Requirement (TSR) Format and Content ...........................................................27
Field Exercise Guidelines for Participants.....................................................................................33
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Dosimetric Quantities in 10 CFR Part 835
Term
Definition
Absorbed dose (D)
The average energy imparted by ionizing radiation to
the matter in a volume element divided by the mass of
the matter in the volume. The absorbed dose is
expressed in units of rad (or gray) (1 rad = 0.01 gray).
Equivalent dose (HT)
HT = DT,R x wR The product of absorbed dose (DT,R)
in rad (or gray) in tissue and a radiation weighting
factor (wR ). Equivalent dose is expressed in units of
rem (or sievert) (1 rem = 0.01 sievert).
Deep equivalent dose
The equivalent dose derived from external radiation at a
depth of 1 cm in tissue.
Lens of the eye equivalent dose
The external exposure of the lens of the eye taken as
the equivalent dose at a tissue depth of 0.3 cm.
Shallow equivalent dose
The equivalent dose derived from external radiation at a
depth of 0.007 cm in tissue.
Committed equivalent dose (HT,50)
The equivalent dose calculated to be received by a
tissue or organ over a 50 year period after the intake of
a radionuclide into the body (HT,50). Committed
equivalent dose is expressed in units of rem (or
sievert).
Committed effective dose (E50)
The sum of the committed equivalent doses to various
tissues in the body (HT,50), each multiplied by the
appropriate tissue weighting factor (wT)--that is, E50 =
sum of wTHT,50. Committed effective dose is expressed
in units of rem (or sievert).
Effective dose (E)
The summation of the products of the equivalent dose
received by specified tissues of the body (HT) and the
appropriate weighting factor (wT)--that is, HE = sum of
wTHT. It includes the dose from radiation sources
internal and/or external to the body. For purposes of
compliance with this part, equivalent dose to the whole
body may be used as effective dose for external
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4
exposures. The effective dose is expressed in units of
rem (or sievert).
Total effective dose (TED)
The sum of the effective doses (for external
exposures) and the committed effective dose (for
internal exposures).
Radiological Assessor Training
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Handouts
5
Radiological Control Program Elements
Management oversight
• Management commitment and policy
• Management responsibilities
• Resource and budget development
• Directives, procedures, and manuals
• ALARA and other safety committees
• Emergency response organization
• Control of experimental activities
Radiological control organization
• Organizational independence
• Responsibilities, authorities, and functions
• Staffing levels
Training
• General requirements
• General employee training
• Radiological Worker training
• Radiological control staff qualification
• Operations personnel
• Manager and supervisor
• Respiratory protection
• Medical personnel
Section 155
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6
Radiological Control Program Elements (cont.)
• Visitors
• Emergency response personnel
• Occupational Safety and Health Administration (OSHA) training
Reviews, audits, and evaluations
• Management overview practices
• Review of incidents
• Internal audits
• Quality assurance program
• Safety analyses and assessments
Oversight of radiological design criteria
• General requirements
• Structural and facility design
• Ventilation systems
• Instrumentation and equipment
• Special tools and enclosures
• Containment systems
Radiological work practices and administrative controls
• ALARA concepts and controls
• Establishment of dose limits
• Emergency plans and procedures
Radiological Assessor Training
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7
Radiological Control Program Elements (cont.)
• Contamination control work practices
• Planning work
• Posting and access control
• Protective clothing and laundry
• Respiratory protection
• Radiation procedures
• Emergency response actions
Radioactive materials control
• Feed, process, and output materials
• Collection and control of radioactive samples
• Radwaste management
• Contamination materials and equipment
• Sealed radiation sources/calibration sources
• Packaging and labeling for transportation
Dosimetry programs
• General requirements
• External dosimetry
• Internal dosimetry
• Nuclear accident dosimetry
• Quality control
Radiological Assessor Training
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Handouts
8
Radiological Control Program Elements (cont.)
Instrumentation and alarms
• General requirements
• Air monitoring and sampling systems
• Effluent monitoring and sampling systems
• Fixed and portable monitoring systems
• Nuclear accident monitoring systems
• Warning and alarm systems
X-ray and source radiography
• General requirements
• Radiological safety
• Testing, operations, and calibration
• Emergency response
• Transporting and receiving sources
Workplace surveys and monitoring
• General requirements
• Dose rate surveys
• Contamination surveys (personnel, airborne, surface)
• Documentation
Radiological Assessor Training
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9
Radiological Control Program Elements (cont.)
Reporting
• Occurrences
• Operational events and emergency notifications
• Reports on employees’ exposure
• OSHA complaints involving radioactive material
Radionuclide-specific guidance
• Uranium
• Plutonium
• Tritium
• Fission products
Radiation-producing machines
• X-ray machines
• Accelerators
• Radiography equipment
Emergency response
• Contamination of workplace
• Contamination of individuals
• Radiation overexposures
• Criticality accidents
Radiological Assessor Training
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10
Radiological Control Program Elements (cont.)
• Environmental releases
• Loss of radioactive material
Records
• Identification of required records
• Records management program
• Record media
• Record storage criteria
• Computerization of records
Conduct of operations
• Features and controls depend on specifics:
– Site
– Job
– Radionuclide
Data and trend analysis
• Features and controls depend on specifics:
– Site
– Job
– Radionuclide
Radiological Assessor Training
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11
Elements of a Radiological Control Program
Section 156
The following pages list typical elements of a Radiological Control Program. The
listing of these elements is intended to describe the magnitude of a complete
protection program. These elements were derived from several sources.
The list is a generic compilation of program elements and is not intended to
describe the program at any specific facility. Effective Radiological Control
Programs will vary from site to site and facility to facility based on many factors.
These factors include:
• The specific facility mission
• The types and quantities of radioactive materials in use at the site
• The physical and chemical forms of radioactive materials in use at the
site
• The physical location of the site in relation to the population centers
• The size of the work force
• The age of the facility
• The original facility design criteria
Some of the elements of a Radiological Control Program are dependent on the
specific radionuclides present at a site. For example, internal dosimetry methods
are specifically dependent on the type of radionuclide being tested for.
The purpose of this list is to allow the user to compare a specific program with
the elements identified here. It is up to the user to integrate the appropriate
elements into his/her own site’s programs.
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Elements of a Radiological Control Program (cont.)
Management oversight of the Radiological Control Program
• Management commitment and policy
• Management responsibilities, authorities, and functions
• Resource and budget development
• Policy communications, directives, procedures, and manuals
• ALARA and other radiological safety committees
• Emergency response organization and responsibilities
• Control of experimental activities involving radioactive materials
Radiological control organization
• Organizational independence and reporting level includes:
– Organizational charts
– Reporting chain of the Radiological Control Organization
– Methods to maintain independence from the operating level
– Radiological Control Organization’s interfaces with the operating
organizations
– Specification of corporate personnel to augment the plant’s emergency
staff
– Augmentation by contractor personnel
• Responsibilities, authorities, and functions
• Authorized staffing levels
Training
• General requirements
• General employee training
Radiological Assessor Training
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13
Elements of a Radiological Control Program (cont.)
• Radiological control staff qualification and training requirements and
methods for the following categories of workers:
– Health Physics Technicians
– Support technicians (bioassay, dosimetry, count room, calibration)
– Supervisors
– Managers
– Technical support staff
• Radiological Worker training requirements and methods for the following
categories of workers:
– Reactor and nonreactor nuclear facility operators
– Maintenance personnel
– Construction personnel
– Supervisors of radiological workers
– Exempt personnel and contractor personnel
• Additional radiological training for the following operations personnel:
– Reactor operators
– Nonreactor nuclear facility operators
– Instrument and electronics technicians
– Fissile material handlers
• Manager and supervisor training requirements
• Respiratory protection training
• Medical personnel training for radiological protection
• Visitor training requirements
• Emergency radiological response training
Section 157
• OSHA training and instruction
Reviews, audits, and evaluations
• Management overview practices for the following:
– Triennial management review of procedures
– Peer review of procedures
– Management appraisals
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Elements of a Radiological Control Program (cont.)
• Review of incidents, exposure data, and industry information
• Internal audits
– Internal audits
– Functional appraisals
– Operational readiness reviews
– Inspection of construction and operating activities
• Quality assurance program
• Safety analysis and assessment reviews
Radiological control organization’s oversight of radiological design criteria
• General requirements
• Structural, surface, and facility design
– Compartmentalization
– Layout to regulate flow of material and personnel
– Permanent and temporary shielding
– Control of traffic patterns
– Radiological zoning
– Drainage basins
– Design location of change rooms and shower facilities
– Decontamination facilities
• Ventilation system design, air cleanup systems, and other design
elements, including:
– Exhaust systems
– Piping systems for radioactive liquids
– Ducts
– Conduits
– High Efficiency Particulate Air (HEPA) Filters
– Valves
– Pumps
Radiological Assessor Training
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Elements of a Radiological Control Program (cont.)
• Instrumentation and equipment design or selection for the following:
– Computer systems
– Process control instrumentation
– Alarms and warning systems
– Auxiliary lighting
– Communication systems
• Design of special tools and enclosures including:
– Glove boxes
– Hoods
– Tents
– Robotics
– Remote manipulators
– Portable temporary ventilation systems
• Containment systems
Radiological safety work practices and administrative controls
• General ALARA concepts and controls, including:
– Overall concept of keeping exposures ALARA
– Setting and reestablishing person-rem goals
– General methods of achieving ALARA goals
– Basic principles of time, distance, and shielding
– Documenting and maintaining trend analyses of historical exposure
data, job-specific dose estimates, and experiences
• Establishment and control of individual and collective dose limits,
including:
– Regulatory limits to workers
– Administrative limits to workers
– Derived air concentrations
– Limits of radionuclides in drinking water in controlled areas and
external sources
– Limits for annual effective dose equivalent for fetuses (for consistency
with instructor’s guide), students, and those under 18 years of age
– Limits and policies for controlling exposure to pregnant women
– Documentation of planned special exposures exceeding annual
effective dose limits in unusual situations (nonemergency)
– Limits for emergency rescue and recovery operations
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Elements of a Radiological Control Program (cont.)
• Emergency plans and procedures
– Guidance on the periodic conduct of emergency drills
– Basic requirements for the availability and accessibility of emergency
equipment and supplies
– Lifesaving procedures
• Radiation and contamination control work practices
– Adherence to procedures, Radiological Work Permits, status boards,
and special job plans
– Designating low-dose waiting areas
– Location of drinking water fountains
– Eating, smoking, and drinking in controlled areas
– Assigning health protection inspectors for radiological job coverage
– Personnel decontamination methods
– Miscellaneous work performance methods, preparation of work areas,
Section 158
cutting of systems and components, and venting and draining methods
– Radiological maintenance exposure reduction methods
– Practices to avoid skin contamination (other than protective clothing)
– Log for shift and daily activities
• Planning, preparing, and scheduling work
– Developing exposure estimates based on previous history on time and
dose rate estimates
– Using accurate exposure estimates
– Controlling the number of personnel used to perform work
– Determining the stay time of workers
– Providing adequate equipment, tools, and procedures at the task site
– Establishing a collective exposure level
– Establishing facility-specific radiological exposure goals for each job
estimated to exceed a preestablished exposure action level, maximum
individual radiological exposure, and person-rem received in repetitive
jobs that result in a significant accumulation of exposure
– Conducting pre- and post- job briefings
– Using mock-up equipment and performing dry runs
– Establishing a plan to document pertinent information for an ultimate
decontamination and decommissioning activity
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Elements of a Radiological Control Program (cont.)
• Radiological posting and access control
– Identification of entrances to radiological areas and establishment of
entrance requirements for each type of area
– Placement and use of step-off pads
– Radiation level marking on tags and status boards
– Consistency of measurements used when marking radiation levels
– Specification of airborne contamination limits
– Tagging, roping, and barricading radiological areas
– Posting and maintaining radiation symbols and status boards
– Using interlock and air lock functions
– Posting types and policies for use
– Meaning of alarm signals and actions to be taken
• Protective clothing and laundry
– Conditions under which protective clothing is worn
– Types of protective clothing
– Donning protective clothing (proper dressing out)
– Removal of protective clothing
– Proper disposal of protective clothing
– Use of change rooms and clothing bins
– Storage, laundering, monitoring, and reuse of protective clothing
– Proper segregation of contaminated clothing
– Laundry facilities, responsibilities, and procedures
• Respiratory protection program
– Respirator protection factors
– Application of types of respirators
– Physical limitations for a proper seal (e.g., eyeglasses, beards)
– Storage and use of respiratory equipment
• Policy and methods for the development of radiological safety and
operating procedures
• Emergency response actions
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Elements of a Radiological Control Program (cont.)
Radioactive materials control
• Feed, process, and output materials
• Practices for the collection and control of radioactive samples
– Types of samples to be collected
– Analyses performed on each sample
– Sampling and analysis schedule
– Sample collection points (access, shielding, ventilating)
– Liquid and gaseous samples
– Routine grab samples
– Remote systems to collect containment and dry well samples
– Chain-of-custody records for each sample
• Radioactive waste and waste management
– Segregation of uncontaminated waste from contaminated waste
– Waste processing systems (including operational envelope for
decontamination factors, radionuclide concentrations, and equipment
specifications)
– Disposal methods, burial grounds
– Waste-handling capabilities for decontamination solutions,
Section 159
contaminated oil and organics
– Release rates, compliance with technical specification limits, total
activity release, total volume release
– Sanitary waste segregation
– Drainage from personnel decontamination and safety shower water
runoff
– Labeling of waste containers, such as 55-gallon drums
– Record keeping
• Contaminated materials and equipment
– Tagging of tools and materials
– Vacuum cleaners in contaminated areas or potentially contaminated
areas
• Sealed radiation sources/calibration sources
– Inventory practices
– Leak testing
– Record keeping
• Packaging and labeling for transportation of radioactive material
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Elements of a Radiological Control Program (cont.)
Dosimetry program
• General requirements
– Components of a dosimetry program
– Monitoring the dosimetry program
– Maintenance of exposure records
• External dosimetry
– Selection and testing of the proper dosimetry device DOE Laboratory
Accreditation Program
– Control and use of:
+ Thermoluminescent dosimeters (TLDs)
+ Pocket dosimeters, self-reading dosimeters
+ Personnel alarm dosimeters
+ Nuclear track emulsions
+ Track etch
+ Whole-body dosimetry
+ Extremity dosimetry
+ Neutron dosimetry
– Actions for lost dosimetry, unexpected results, or other abnormal
situations
• Internal dosimetry
– Selection of the proper internal dosimetry methods
– Policies and methods for:
+ Whole-body counting
+ Thyroid counting
+ Lung counting
+ Urinalysis
+ Fecal analysis
+ Blood activity
+ Nasal swipes
+ Use of air monitoring results
– Determination of dose based on internal dosimetry results
• Nuclear accident dosimetry
• Quality control for dosimetry
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Elements of a Radiological Control Program (cont.)
Radiological safety instrumentation and alarms
• General requirements
– Acquisition
– Receipt and testing
– Implementation
– Maintenance and functional checks
– Calibration and calibration facility requirements
– Audible and visual indicator alarms
– Documentation and record keeping requirements
• Air monitoring and sampling systems
– Policies and use for:
+ Continuous air monitors
+ High-volume air samplers
+ Low-volume air samplers
+ Halogen-absorbing cartridge or filter
+ Silver zeolite cartridge or filter
+ Impingers
+ Personnel label samplers
+ Kanne chambers and other tritium monitors
+ Leak detectors
+ Breathing zone sampling equipment
– System design and performance to national consensus standards
– Airflow studies and source characterization
– The use and control of filtering media
– Source-term characteristics
– Proper placement and operation of equipment
– Documentation and record keeping requirements
• Effluent monitoring and sampling systems for:
– Stack monitors
– Off-gas monitors
– Exhaust fans
– Filter compartments
– Filter flappers
– Dampers
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Elements of a Radiological Control Program (cont.)
• Fixed and portable dose rate and contamination monitoring instruments
– Policies and controls for the use of radiation detectors
+ Photon, neutron, beta, alpha monitors
+ Proportional and scintillation counters
+ Count rate meters
+ Ion chambers
+ Geiger-Mueller tubes and counters
+ Hand and shoe counters, pancake monitors
+ Portal monitors
+ Chest counters
+ Area radiation monitors
+ Small dimension probes for wound monitors
Section 160
– Testing
– Calibration schedule and standards
– Functional checks
– Maintenance
– Storage
– Inventory
– Documentation and record keeping
• Nuclear accident monitoring systems
– Nuclear incident monitors
– Criticality monitors
– Emergency radiological instrumentation systems for criticality incidents
• Warning and alarm systems
– Periodic testing of the alarms
– Alarm use in practice drills
– Alarm panels and indicators
– Type and placement for each facility/area
– Calibration
– Audible and visual indicators
– System backup in the event of loss of power
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Elements of a Radiological Control Program (cont.)
X-ray and source radiography
• General requirements
• Radiological safety
• Testing, operations, and calibration
• Emergency response
• Transporting and receiving radiography sources
Workplace surveys and monitoring
• General requirements
– Survey frequencies (continuous monitoring, follow-up surveys)
– Survey of routine and nonroutine activities
– Monitoring conditions
– Points at which monitoring will be required
– Survey and monitoring techniques and methods
– Implementation of a comprehensive routine surveillance program for
radiation, contamination, and airborne surveys
• Schedules, policies, and control of dose rate surveys (routine, nonroutine,
emergency)
• Schedules, policies, and practices for contamination surveys (personnel,
airborne, and surface)
– Monitoring workers during and following work
– Surveys of gloves
– Techniques for self-monitoring upon exit
– Accessibility of exit monitoring equipment, surveys for loose surface
contamination
– Accuracy of detection (amount and source identification)
– Personnel air sampling (breathing zones)
– Procedures to follow when contamination is detected
– Participation of health physics staff in developing, implementing, and
auditing the survey and self-monitoring program
– Smearable radioactive contamination
– Surveys of injured personnel
• Documentation and record keeping requirements
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Elements of a Radiological Control Program (cont.)
Reporting
• Unusual occurrences
• Operational events and emergency notifications
• Reports on employee exposures
• Occupational safety and health complaints involving radioactive material
Development of radionuclide-specific guidance for:
• Uranium
• Plutonium
• Tritium
• Fission products
Radiation-producing machines
• X-ray machines
• Accelerators
• Radiography equipment
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Elements of a Radiological Control Program (cont.)
Radiological accidents and emergency response
• Contamination of workplace
• Contamination of individuals
• Radiological overexposures
• Criticality accidents
• Environmental release
• Loss of radioactive material
Records maintenance requirements
• Identification of required records
• Records management program
• Record media
• Record storage criteria
• Computerization of records
Conduct of operations as it relates to radiological protection
Data and trend analysis
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Typical Safety Analysis Report (SAR) Contents
Introduction
Site Characteristics
Principal Safety Criteria (Success Criteria)
Process/Operations Descriptions
Waste Processing and Handling
Buildings, Structures, and Support Systems
Section 161
Safety- and Nonsafety-Class Components (including engineered safety features)
Comparison with Criteria (including backfitting)
Special Safety Interest
Hazard Analysis and Classification
Assessment of Normal Operations
Analysis of Abnormal Conditions and Accidents
Derivation of Technical Safety Requirements
Management and Institutional Safety Provisions
Facility Safety Programs
Conduct of Operations
Maintenance Management
Testing and In-Service Surveillance
Procedures
Employee Selection and Training
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Typical Safety Analysis Report (SAR) Contents (cont.)
Human Factors–Machine Interface
Emergency Preparedness
Provisions for Decontamination and Decommissioning
Quality Assurance
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Technical Safety Requirement (TSR) Format and Content
Format/sections (hierarchy of requirements)
1. Use and Applications
2. Safety Limits
3. Operational Limits
4. Surveillance Requirements
5. Administrative Controls
6. Appendices
1. Use and application
This section should contain basic information and instructions for using
and applying the individual TSRs. Use and application include the
following elements:
a. Definitions (Specifically defined terms are
to appear in uppercase type throughout the TSR document.)
b. Operational Modes
c. Logical Connections
d. Completion Times
e. Frequency Notations
2. Safety Limits (SLs)
SLs should describe as precisely as possible the parameter being limited
and state the limit in measurable units.
a. Applicability
Each SL is to have a mode applicability statement.
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Technical Safety Requirement (TSR) Format and Content (cont.)
b. Actions
Action statements are to completely describe the actions to be taken in
the event that the SL is not met.
c. Selection of SLs
SLs are those limits which, if exceeded, could directly cause the failure
of one or more of the barriers that prevent the uncontrolled release of
radioactive or other hazardous materials.
Combined Section 3/4
Within the TSR document, Section 3 delineates the Operational Limits,
and Section 4 describes the Surveillance Requirements. There is usually
a one-to-one correlation between the operational limits and the
surveillance related to each. Thus, for convenience, each limit is typically
presented at the same place as its related surveillance, and the
combined information is designated Section 3/4.
This combined section should contain the Limiting Control Settings and
the Limiting Conditions for Operation, as well as mode applicability
information, Action Statements, and Surveillance Requirements, for each
requirement.
3. Operational Limits (OLs)
The initial conditions of the safety (accident) analyses upon which the
authorization to operate is based are the least conservative limits of
acceptable operation. These initial condition values must be adjusted for
both instrument error and the expected instrument drift between
surveillances, and an allowance should be made for calculational
uncertainties prior to being used as limits in the TSRs.
The most conservative value for each parameter contained in the safety
analyses makes up the envelope within which the facility must operate in
order to ensure that the SAR analyses found safe operations. Provided
the facility is operated within these SAR initial condition limits, the SAR
results accurately demonstrate that the consequences of
accidents/transients/incidents are acceptable.
Section 162
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Technical Safety Requirement (TSR) Format and Content (cont.)
a. Limiting Control Settings (LCSs)
LCSs should describe, as precisely as possible, the parameter being
controlled and its limits, or the limiting setting of the device to control it.
b. Limiting Conditions for Operation (LCOs)
The LCO statement describes, as precisely as possible, the lowest
functional capability or performance level or equipment required for
continued safe operation of the facility.
Other elements to be address under OLs include:
c. Applicability (mode applicability)
d. Action (Action Statement in the event the LCS or LCO is not met)
e. Surveillance Requirements
f. LCSs of instruments that monitor process variables at nonreactor
nuclear facilities (NNFs) are the settings that either initiate protective
devices themselves or sound an alarm to alert personnel to take action
in order to protect barriers that prevent the uncontrolled release of
radioactive materials.
g. Selection of LCOs (for NNFs) should be written only for systems and
equipment that meet one (or more) of the following descriptions:
• Installed instrumentation that is used to detect and indicate in the
control room or other control location an inadvertent criticality or a
significant degradation of the physical barriers that prevent the
uncontrolled release of radioactive materials
• Structures, systems, and components that are relied upon in the
SAR to function or actuate to prevent or mitigate accidents, or
transients that either involve the assumed failure of, or present a
challenge to, the integrity of a physical barrier that prevents the
uncontrolled release of radioactive materials
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Technical Safety Requirement (TSR) Format and Content (cont.)
• Process variables that are initial conditions for those design basis
accidents or transient analyses which involve the assumed failure
of, or present a challenge to, the integrity of a radioactive material
barrier.
• Systems and equipment that are used for handling fissile material
The term unusual conditions is made clear in the final rule by
specifying that alternatives which would preclude exposures higher
than the prescribed dose limits must be either unavailable or
impractical.
h. Special test exceptions may be allowed under controlled conditions.
4. Surveillance Requirements (SRs)
SR Statements consist of short descriptions of each requirement and its
frequency of performance. A frequency of performance is mandatory.
These statements should be as brief as possible, but should identify
those requirements needed to ensure compliance with the LCS or LCO.
Each Surveillance Requirement should begin with a verb. Consistency in
the use of terms and sentence structure between requirements is
important.
5. Administrative controls (ACs)
This section should impose administrative requirements necessary to
control operation of the facility such that it meets the TSRs. These
include:
• Contractor Responsibility
• Contractor Organization
• Procedures
• Programs
• Minimum Operations Shift Complement
• Operating Support
• Staff Qualifications and Training
• OPERABILITY Definition and Implementation
• TSR Basis Control
• Reviews and Audits
• Reporting Requirements
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Technical Safety Requirement (TSR) Format and Content (cont.)
Section 163
6. Appendices
• The Bases Appendix shall provide brief summary statements of the
reasons for the SLs, OLs, and associated SRs. The bases shall show
the numeric values, the conditions, the surveillances, and the Action
Statements that fulfill the purpose derived from the safety
documentation. The primary purpose for describing the basis of each
requirement is to ensure that any future changes to the requirement
will not affect its original intent or purpose.
• The purpose of the Design Features Appendix is to describe in detail
those features not covered elsewhere in the TSRs which, if altered or
modified, would have a significant effect on safety. Three areas should
be addressed: vital passive components, configuration and physical
arrangement, and materials.
Numbering System within the TSR Document
Safety Limits
SLs should begin with 2.1 and continue with 2.2, 2.3, etc.
Operational Limits
OLs begin with 3.1 and continue with 3.2, 3.3, etc. Any subdivision of
OLs should be numbered with an additional number added to the
number of the LSC, i.e., 3.2.2, 3.2.3, etc. OLs should be grouped by
principal system or function, and each OL within a group should be
numbered sequentially. LCSs are normally the first requirement within
a group.
For NNFs, a standardized grouping of requirements may be difficult
because of the diversity of facility types. However, many will have the
following subdivisions:
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Technical Safety Requirement (TSR) Format and Content (cont.)
• Applicability
• Criticality, Radioactivity, and Hazardous
• Confinement/Ventilation
• Fire Detection and Suppression
• Emergency Power
• Chemical Systems
• Instrumentation
• Experimental Facilities
Surveillance Requirements
SRs should be designated with numbers beginning with 4. The second
number should correspond to the same grouping scheme utilized for
the LCS or the LCO, and the third number in the sequence indicates
the LCS or the LCO that this surveillance supports. Hence, the SR will
have numbers the same as the corresponding LCS or LCO, except for
the first number, which will be a “4” instead of a “3.”
Bases (Bases Appendix)
Bases are numbered in accordance with the SL, LCS, or LCO that they
support.
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Field Exercise Guidelines for Participants
You are to apply performance-based assessment techniques in the field. It is
important that the exercise be flexible and broad. Therefore, you should be given
the “controlled” freedom to move about in the facility. Sufficient personnel should
be available for interaction and to answer any questions.
• After being issued security and dosimetry badges, you will observe a practice
radiological control assessment performed by your field instructor.
• Following lunch, you will have the opportunity to conduct the assessment
under the observation of your field instructor. He/she will give you “on the
spot” guidance and help you individually at times.
• The aim of this field exercise is to demonstrate recommended methods and
techniques of conducting radiological control assessments in the field by
giving you some practice.
• You will spend several hours in a facility. The emphasis shall be on
assessing proper radiological protection practices, policies, and procedures.
• You are to practice assessing by selecting an item or area and delving into it.
Section 164
It is important to practice the identification of surface issues (Type I), but more
important to deal with the underlying issues (Types II and III).
• You will be performing a review of an issue, procedure, program (like
ALARA), or system walk-down. You may observe a routine evolution, a test,
or some maintenance job.
• Be alert to any routines, tests, or maintenance taking place during your facility
visit. These give the best opportunity to see how the people do their jobs.
• Be alert to waste minimization and prevention. Always question material use
and the discharge of materials to waste streams or the environment.
• Be alert to leaks or discharges of any kind.
• Work at looking at the big picture for issues such as minimization of controlled
areas and control of work, personnel, and dose.
• During the evening, you will be writing one item as a concern or finding to
present at the debrief on Friday morning. Therefore, you need to support the
finding with what requirement exists and why your concern or finding is valid.
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Field Exercise Guidelines for Participants (cont.)
• In the morning debrief, you will present your finding or issue for practice.
• It is important that you coordinate with the other members of your group so
you present different findings/observations.
• You will have one and one-half minutes or so to present your finding.
• You should present your finding in this format:
1. This is the requirement.
2. Contrary to the requirement, this is what was noted.
3. Therefore, I/we have the following concern/finding.
• Don’t count on the people to whom you are presenting your finding to
recognize what is wrong; you must justify it in enough detail that there is no
doubt (make your case).
• Your field instructor will take care of thanks to the facility personnel during the
debrief. (It takes too much time if each person does it.)
• Your instructor will collect your completed written finding at the completion of the class
debrief.
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CONCLUDING MATERIAL
Review Activity: Preparing Activity:
DOE Field Offices DOE-HS-11
HS ID Project Number:
EM SR TRNG-0060
NE OH
SC RL
GC
IA
RW
NN
National Laboratories Operations Offices
BNL AL
LLNL NV
LANL OAK
PNL OR
Sandia CH
ANL
New Brunswick
ORNL
SRNL
Site Offices
Amarillo Site Office
Kirtland Site Office
Princeton Site Office
Fernald Site Office
Kansas City Site Office
Miamisburg Site Office
Y-12 Site Office