DOE-STD-6003-96, Safety of Magnetic Fusion Facilities: Guidance
Functional areas: Thermonuclear Experimental Reactor (ITER), Safety, Guidance, Fusion
This document provides guidance for the implementation of the requirements identified in DOE-STD-6002-96, Safety of Magnetic Fusion Facilities: Requirements. This guidance is intended for the managers, designers, operators, and other personnel with safety responsibilities for facilities designated as magnetic fusion facilities. While the requirements in DOE-STD-6002-96 are generally applicable to a wide range of fusion facilities, this Standard, DOE-STD-6003-96, is concerned mainly with the implementation of those requirements in large facilities such as the International Thermonuclear Experimental Reactor (ITER).
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Section 1
TS
NOT MEASUREMENT
SENSITIVE
DOE-STD-6003-96
May 1996
DOE STANDARD
SAFETY OF MAGNETIC FUSION
FACILITIES: GUIDANCE
U.S. Department of Energy AREA SAFT
Washington, D.C. 20585
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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Order No. DE96009494
DOE-STD-6003-96
TABLE OF CONTENTS
Page
FOREWORD......................................................................................................................... ix
DEFINITIONS ....................................................................................................................... xi
LIST OF ACRONYMS ......................................................................................................... xix
1. INTRODUCTION ............................................................................................................. 1
1.1 Purpose.................................................................................................................... 1
1.2 Background .............................................................................................................. 1
1.3 Implementation......................................................................................................... 2
1.4 Overview .................................................................................................................. 2
2. RADIATION AND HAZARDOUS MATERIAL .................................................................. 5
2.1 Dose Definitions....................................................................................................... 5
2.2 Public Exposures and Environmental Impacts......................................................... 6
2.2.1 Evaluation Guidelines for Exposures to the Public....................................... 7
2.2.2 Additional Guidance ..................................................................................... 8
2.2.3 Environment ................................................................................................. 8
2.3 Routine Worker Exposure ........................................................................................ 9
2.3.1 Radiation ...................................................................................................... 9
2.3.2 Hazardous Materials .................................................................................... 9
2.3.3 Common Industrial Hazards......................................................................... 10
2.3.4 Magnetic Fields ............................................................................................ 10
Section 2
2.4 Guidance for Meeting Regulatory Limits.................................................................. 11
2.4.1 Evaluation Guidelines................................................................................... 11
2.4.2 Exposure ...................................................................................................... 12
2.4.3 Meteorological Dispersion............................................................................ 12
2.5 Consequence Thresholds for PAGs and Emergency Response
Planning Guidelines ................................................................................................. 12
2.5.1 Radiological (No Ingestion) .......................................................................... 13
2.5.2 Radiological (Ingestion)................................................................................ 13
2.6 Models Used in Relating Exposures to Estimated Consequences .......................... 13
3. ENVIRONMENTAL AND PERMITTING REQUIREMENTS ............................................ 15
3.1 Federal Requirements.............................................................................................. 15
3.1.1 National Environmental Policy Act and Implementing
Guidelines, Regulations, and Orders ........................................................... 15
3.1.2 Federal Statutes and DOE Orders Relating to Environmental Quality......... 16
3.2 Federal and State Consultation, Permits, and Approvals......................................... 21
3.2.1 Federal Permits and Approvals.................................................................... 21
3.2.2 State and Local Permits and Approvals ....................................................... 23
3.3 Environmental Compliance Procedures and Scheduling......................................... 24
3.3.1 Environmental Documentation Guidelines ................................................... 24
3.3.2 Environmental Compliance Scheduling........................................................ 26
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4. PROGRAM MANAGEMENT FOR SAFETY .................................................................... 29
4.1 Design and Construction Management.................................................................... 29
4.2 Operations Management.......................................................................................... 30
4.3 Site Restoration Management ................................................................................. 30
4.4 Tools for Program Management Safety ................................................................... 30
4.4.1 Configuration Management .......................................................................... 30
4.4.2 Quality Assurance ........................................................................................ 32
4.4.3 Verification and Validation............................................................................ 33
4.4.4 Conduct of Operations ................................................................................. 34
4.4.5 Emergency Preparedness............................................................................ 35
4.4.6 Maintenance................................................................................................. 37
4.4.7 Training and Qualifications........................................................................... 39
4.4.8 Tritium Control, Accountability, and Physical Protection.............................. 41
Section 3
5. SAFETY ANALYSIS ........................................................................................................ 49
5.1 Facility Description................................................................................................... 51
5.1.1 General......................................................................................................... 51
5.1.2 Safety Structures, Systems, and Components ............................................ 52
5.2 Facility Mission/Processes ....................................................................................... 56
5.3 Hazards Analysis ..................................................................................................... 56
5.3.1 Inventory....................................................................................................... 56
5.3.2 Classification ................................................................................................ 57
5.4 Analysis of Off-Normal Conditions ........................................................................... 58
5.4.1 Event Scenario Identification and Classification .......................................... 59
5.4.2 Analysis Approach for the Safety Analysis Report ....................................... 62
5.4.3 Emergency Planning Basis Analysis............................................................ 63
5.5 Safety Analysis Report Process............................................................................... 64
5.5.1 Risk Assessment.......................................................................................... 65
5.5.2 Safety Analysis Report................................................................................. 66
5.6 Safety Envelope Configuration Control.................................................................... 68
5.7 Technical Safety Requirements ............................................................................... 69
5.7.1 Implementation of Technical Safety Requirements...................................... 70
5.7.2 Risk-Based Prioritization in Technical Safety Requirements ....................... 70
5.8 Startup and Restart of Fusion Facilities ................................................................... 71
5.8.1 Implementation of Startup and Restart Reviews.......................................... 71
5.8.2 Risk-Based Prioritization Implications for Startup and Restart Reviews ...... 72
5.9 Authorization Basis .................................................................................................. 72
6. FACILITY DESIGN GUIDANCE ...................................................................................... 73
6.1 Introduction and General Guidance ......................................................................... 73
6.1.1 Design Basis ................................................................................................ 73
6.1.2 Safety Functions and Structures, Systems, and Components ..................... 74
6.1.3 General Design Guidance............................................................................ 76
6.2 Systems Performing Safety Functions..................................................................... 86
6.2.1 Public Safety Function: Confinement Systems ............................................ 86
6.2.2 Worker Safety Function: Systems Controlling Operating Hazards............... 99
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Section 4
6.3 Systems Involved with Potential Safety Concerns................................................... 106
6.3.1 Afterheat Removal Systems......................................................................... 107
6.3.2 Rapid Plasma Shutdown System................................................................. 108
6.3.3 Control of Potential Energy Sources ............................................................ 108
6.3.4 Limiting Airborne and Liquid Releases to the Environment ......................... 115
6.4 Systems That Support Safety Functions.................................................................. 116
6.4.1 Instrument and Control Systems.................................................................. 116
6.4.2 Electrical Power Systems............................................................................. 119
6.4.3 Cooling Systems .......................................................................................... 122
6.4.4 Remote-Handling Systems........................................................................... 125
6.5 Impact of Facility Support and Experimental Systems on Safety Functions............ 134
6.5.1 Group 1 Systems.......................................................................................... 135
6.5.2 Group 2 Systems.......................................................................................... 136
7. SITE RESTORATION ...................................................................................................... 139
7.1 General .................................................................................................................... 139
7.2 Decommissioning, Decontamination, and Site Restoration in the Initial Design...... 139
7.3 Site Restoration........................................................................................................ 139
7.4 Waste Sent to Low-Level Waste Repository............................................................ 140
7.4.1 Requirements for Land Disposal of Radioactive Waste............................... 140
7.4.2 Methodology of 10 CFR 61 Extended to Fusion-Specific Isotopes.............. 143
7.4.3 Chemically Hazardous Materials Sent to a Hazardous Waste Site.............. 146
7.4.4 Mixed Waste Requirements ......................................................................... 147
7.5 Requirements on Low-Level Waste Repository ....................................................... 147
APPENDIX A CATEGORY 2 THRESHOLD QUANTITIES OF RADIONUCLIDES .......... 149
APPENDIX B IDENTIFICATION OF POTENTIAL HAZARDS, ENERGY SOURCES,
AND GENERIC ACCIDENTS FOR FUSION FACILITIES.......................... 165
B.1 Introduction.......................................................................................... 165
B.2 Hazards ............................................................................................... 165
B.2.1 Radiological Hazards............................................................... 165
B.2.2 Chemical Hazards ................................................................... 166
B.2.3 Industrial Hazards.................................................................... 166
B.3 Energy Sources................................................................................... 167
B.3.1 Plasma Energy ........................................................................ 167
B.3.2 Magnetic Energy...................................................................... 167
B.3.3 Decay Heat.............................................................................. 167
B.3.4 Chemical Energy ..................................................................... 168
B.3.5 Coolant Internal Energy........................................................... 168
Section 5
B.4 Potential Generic Accident Scenarios ................................................. 168
B.4.1 Loss-of-Coolant Event ............................................................. 169
B.4.2 Loss-of-Flow Event.................................................................. 169
B.4.3 Loss-of-Vacuum Event ............................................................ 170
B.4.4 Plasma Transients................................................................... 170
B.4.5 Magnet Transients................................................................... 170
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B.4.6 Loss of Cryogen....................................................................... 171
B.4.7 Tritium Plant Events................................................................. 171
B.4.8 Auxiliary System Accidents...................................................... 171
APPENDIX C REFERENCES AND SUPPLEMENTAL GUIDANCE ................................. 173
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LIST OF FIGURES
FIGURE Page
3.1 Phased schedule for environmental compliance activities ............................... 27
5.1 Flow logic of the safety analysis process ......................................................... 50
5.2 Event scenario/safety analysis process ........................................................... 60
LIST OF TABLES
TABLE Page
2.1 Evaluation guidelines for public protection from radiation ................................ 7
5.1 Safety system functional requirements ............................................................ 55
6.1 Suggested design codes for equipment ............................................................ 80
6.2 Group 1 systems .............................................................................................. 135
6.3 Group 2 systems .............................................................................................. 135
7.1 Surface contamination guidelines ..................................................................... 140
7.2 Classification boundaries as given in 10 CFR 61 ............................................. 142
7.3 Classification based on long-lived radionuclides .............................................. 143
7.4 Specific activity limits for shallow load burial of all radionuclides
with Z < 88 and half-lives >5 yr and <1012 yr ................................................... 144
A.1 Thresholds for radionuclides Category 2 .......................................................... 151
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DOE-STD-6003-96
FOREWORD
1. This DOE Standard is approved for use by all DOE Components and contractors. It was
developed by subject matter experts in the Fusion Safety Working Group under the general
direction of the Office of Fusion Energy Sciences. It has been reviewed by the Fusion Safety
Steering Committee with representation from DOE laboratories, contractors, and universities
involved with magnetic fusion research as well as the end user of fusion power, the electric
utility industry.
2. This Standard provides guidance to successfully achieve public and worker safety at mag-
netic fusion facilities. It is intended for use by managers, designers, operators, and other
personnel with safety responsibilities for such facilities. This Standard is concerned mainly
with large fusion facilities such as the International Thermonuclear Experimental Reactor.
Using a risk-based prioritization, the concepts presented here may also be applied to other
magnetic fusion facilities.
Section 6
3. Beneficial comments (recommendations, additions, deletions) and any pertinent data that
may be of use in improving this document should be addressed to:
Environment, Safety, and Health Program Manager
Office of Fusion Energy Sciences, ER-54
Office of Energy Research
U.S. Department of Energy
19901 Germantown Road
Germantown, Maryland 20874-1290
by using U.S. Department of Energy Standardization Document Improvement Proposal
Form (DOE F 1300.3) appearing at the end of this document or by letter.
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DOE-STD-6003-96
DEFINITIONS
Active—An adjective used to describe a feature or function of a component whose operation
depends on an external input such as an actuation, mechanical movement, or supply of power.
Administrative Controls—Provisions relating to organization and management, procedures,
recordkeeping, assessment, and reporting necessary to ensure the safe operation of a fusion
facility.
ALARA—As low as is reasonably achievable.
Anticipated Operational Occurrences—Operational processes deviating from normal opera-
tion that are expected to occur once or more during the operating life of the fusion facility.
Authorization Basis—Those aspects of the facility design basis and operational requirements
relied upon by the regulating authority to authorize operation. These aspects are considered to
be important to the safety of facility operations.
Blanket—The region surrounding the D-T plasma that absorbs the fusion neutrons, transform-
ing their energy into heat and breeding tritium to sustain the D-T fuel cycle.
Beyond-Design-Basis Event—An event of the same type as a design-basis event (e.g., fire,
earthquake, spill, explosion, etc.), but defined by parameters that exceed in severity the param-
eters defined for the design basis event.
Certification—Process by which management provides written endorsement of the satisfactory
achievement of qualification of an individual for a specialized operations position based upon its
criticality or safety impact and generally in response to a DOE Order or national consensus code
or standard.
Common Cause Failure—The failure of multiple devices or components to perform their func-
tions as a result of a single specific event or cause.
Comparable Industrial Facility—A facility in the industrial sector where workers are exposed
to hazards of a similar nature to those encountered in a fusion facility; for example, heavy lifting,
vacuum, cryogenics, high electrical potentials and/or currents, and radioactivity.
Confinement—A barrier that surrounds radioactive or hazardous materials designed to prevent
or mitigate the uncontrolled release of these materials to the environment.
Credible Events—Postulated events having estimated probabilities of occurrence >10–6 per
facility year. For natural phenomena, separate probability criteria based on site-specific informa-
tion and facility characteristics should be used.
Cryostat—A chamber, normally metallic, which surrounds the superconducting magnets of a
fusion facility to provide vacuum insulation from external heat loads.
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Decommissioning—The process of closing and securing a fusion facility so as to provide
adequate protection from radiation exposure and to isolate radioactive contamination from the
human environment.
Decontamination—The act of removing a chemical, biological, or radiological contaminant
from, or neutralizing its potential effect on, a person, object, or environment by washing, chemi-
cal action, mechanical cleaning, or other techniques.
Section 7
Design Basis—The set of requirements that bound the design of systems, structures, and
components within the facility.
Design Basis Events—Credible events considered in the facility safety analysis and in the
design of systems, structures, and components within the facility.
Disruption—A rapid loss of the plasma-stored thermal energy to the plasma-facing compo-
nents, introducing large thermal loads. Associated with this is a rapid decay of the plasma
current that can introduce large mechanical loads to structural components. Disruptions can
also generate high energy runaway electrons which impact the first wall.
Diversity—The existence of multiple components or systems to perform an identified function,
where such components or systems incorporate one or more attributes that are different from
each other.
Divertor—The component inside the vacuum vessel that diverts the plasma particles in the
outer shell of the plasma into a region where they strike a barrier, become neutralized, and are
pumped away.
Effluent—Material that is released into the environment.
Evaluation Guidelines—Dose/exposure values for radiation or hazardous materials that a
safety analysis evaluates against.
Experimental Equipment—Equipment or components installed in or around the facility for the
purpose of research and development, not including regular functioning parts of the fusion
facility itself (i.e., even when such regular functioning parts may be less than fully developed).
First Wall—Systems and components inside the vacuum vessel directly exposed to the plasma
ion and neutron fluxes; the first physical boundary that surrounds a plasma.
Fusion Facility—Any facility that utilizes or supports a magnetically confined plasma in which
fusion reactions take place. It includes the associated facility plant and equipment and any
experimental apparatus used at the facility.
Fusion Island—That part of the fusion facility on or inside the cryostat. Typically it includes the
cryostat, the magnetic coils, the vacuum vessel and attached pumps, the breeding blanket,
heating and fueling systems inside the cryostat, the divertor, and plasma diagnostics.
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Hazard—A source of danger (i.e., material, energy source, or operation) with the potential to
cause illness, injury, or death to personnel or damage to an operation or to the environment
(without regard for the likelihood or credibility of off-normal conditions or consequence
mitigation).
Hazard Analysis—The determination of material, system, process, and plant characteristics
that can produce undesirable consequences, followed by the assessment of hazardous situa-
tions associated with a process or activity.
Hazard Classification—Evaluation of the consequences of unmitigated releases to classify
facilities or operations into the following hazard categories:
– Hazard Category 1: The hazard analysis shows the potential for significant off-site
consequences.
– Hazard Category 2: The hazard analysis shows the potential for significant on-site
consequences.
– Hazard Category 3: The hazard analysis shows the potential for only significant localized
consequences.
Hazardous Material—Any solid, liquid, or gaseous material that is toxic, explosive, flammable,
corrosive, or otherwise physically or biologically threatening to health.
Inherent—An adjective to describe a design feature or function that operates without the appli-
cation of a separate input such as an activation signal. An example of an inherent design feature
is a fail-safe valve that closes automatically on loss of power.
Section 8
ITER—International Thermonuclear Experimental Reactor.
Maintenance—The organized activity, both administrative and technical, directed toward keep-
ing structures, systems, and components in good operating condition, including both preventive
and corrective aspects.
Maintenance Personnel—Persons responsible for performing maintenance and repair of
mechanical and electrical equipment.
Managers—Persons whose assigned responsibilities include ensuring that a fusion facility is
safely and reliably operated and that supporting operating and administrative activities are
properly controlled.
May—Permission; neither a requirement nor a recommendation.
Mitigative Feature—Any structure, system, or component that serves to mitigate the conse-
quences of a release of hazardous materials in an off-normal event scenario.
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Monitoring—Continuous or periodic measurement and/or observation of parameters or deter-
mination of the status of a system or component. Sampling may be involved as a preliminary
step to measurement.
Normal Conditions—Conditions associated with the routine operation of the facility.
Normal Operations—Activities at a facility performed within specific normal operational limits
and conditions, including startup, operation, shutdown, maintenance, and testing. Normal
operations do not include anticipated operational occurrences.
Off-Normal Conditions—Conditions beyond anticipated operational occurrences that include
all credible events.
Operations—Activities at a fusion facility performed within specific operational limits and condi-
tions, including startup, operation, shutdown, maintenance, and testing.
Operations and Facility Support Personnel—Those individuals who perform technical func-
tions (such as engineering evaluations, program reviews, technical problem resolution, or data
analyses, within their area of expertise) or safety, quality assurance, radiation protection, emer-
gency services, and training functions.
Operators—Persons responsible for manipulating fusion facility controls, monitoring facility
parameters, and operating facility equipment.
Certified Operators—Operators who require certification as determined by facility
management.
Qualified Operators—Operators who require qualification as determined by facility
management.
Passive—An adjective that describes a function that requires no operation or movement of
component parts.
Physical Separation—Isolation by geometry (distance, orientation, etc.), by appropriate
barriers, or a combination thereof.
Plasma—The fourth state of matter; basically an ionized gaseous system composed of an elec-
trically equivalent number of electrons and positive ions.
Plasma Beta—The ratio of plasma pressure (proportional to the product of density and
temperature) to the confining magnetic field pressure (proportional to magnetic field strength
squared). As the beta limit is approached, the plasma is more likely to experience a disruption.
Potential Safety Concern—A feature and/or process determined to be capable of challenging
a public safety function and to which a risk-informed decision-making process is applied during
design.
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Poloidal Field Coils—Coils providing the magnetic field that encircles the plasma axis in
toroidal devices.
Postulated Initiating Events (PIE)—Identified happenings or conditions that lead to anticipated
operational occurrences, off-normal conditions, and their consequential failure effects.
Section 9
Potential Safety Concern—A feature and/or process determined to be capable of challenging
a public safety function and to which a risk-informed decision-making process is applied during
design.
Preventive Feature—Any structure, system, or component that serves to prevent the release of
hazardous material in an off-normal event scenario.
Public—All individuals outside the fusion facility site boundary.
Public Safety Function—Essential characteristics or performance needed to ensure the safety
and the protection of the public and the environment during operations, anticipated operational
occurrences, and off-normal conditions.
Qualification—Process by which factors, such as education, experience, and any special
requirements (e.g., medical examination) are evaluated in addition to training to assure that an
individual can competently perform a specialized job function to an anticipated level of
proficiency.
Qualified—The ability to perform a specific job function based upon completion of a training,
qualification, or certification program developed for the job function. Trained personnel are
qualified to perform their job function based upon completion of training. Qualified and certified
personnel are qualified to perform their job function based upon completion of a specific
program. As used in this document, the term “qualified” personnel has two meanings, based
upon context:
Qualified personnel are those personnel who have successfully completed either training,
qualification, or certification requirements appropriate to their job function.
Qualified personnel are those personnel who have successfully completed a formal qualifi-
cation program appropriate to their job function.
Quality Assurance—Those planned and systematic actions necessary to provide adequate
confidence that an item or service will satisfy specified requirements for intended service.
Redundancy—Provision of more than the minimum number of similar elements or systems, so
that loss of any one does not result in the loss of the required function.
Risk—The quantitative or qualitative expression of possible loss that considers both the prob-
ability that an event will occur and the consequence of that event.
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Risk-Informed Prioritization Approach—A reasoned approach where the degree to which
requirements or recommendations are applied and resources expended is commensurate with
the risks involved and the facility programmatic importance. Minor hazards require implementa-
tion at a lower level than higher risk hazards to workers, the public, and the environment.
Runaway Electrons—Those electrons in a plasma that gain energy from an applied electric
field faster than they lose energy from collisions; such high-energy electrons can damage
plasma-facing components.
Safety Analysis—A documented process: (1) to provide systematic identification of hazards
within a given facility; (2) to describe and analyze the adequacy of the measures taken to elimi-
nate, control, or mitigate identified hazards; and (3) to analyze and evaluate potential off-normal
events and their associated risks.
Safety Analysis Report (SAR)—A report that documents the adequacy of safety analysis to
ensure that a fusion facility can be constructed, operated, maintained, shut down, and decom-
missioned safely and in compliance with applicable laws and regulations.
Section 10
Safety Basis—The combination of information relating to the control of hazards at a fusion
facility (including design, engineering analyses, and administrative controls) upon which is
based the conclusion that activities at the facility can be conducted safely.
Safety-Class Structures, Systems, and Components (safety-class SSCs)—Systems,
structures, or components whose failure could adversely affect the environment or safety and
health of the public as identified by safety analyses. The phrase “adversely affect” means that
Evaluation Guidelines are exceeded. Safety-class SSCs are systems, structures, or components
whose preventive or mitigative function is necessary to keep radioactive and hazardous material
exposure to the public below the off-site Evaluation Guidelines.
Safety Limits—Limits on process variables associated with those physical barriers, generally
passive, that are necessary for the intended facility functions and that are found to be required
to guard against the uncontrolled release of radioactivity and other hazardous materials.
Safety-Significant Structures, Systems, and Components (safety-significant SSCs)—
Structures, systems, and components not designated as safety-class SSCs but whose preven-
tive or mitigative function is a major contributor to defense-in-depth (i.e., prevention of uncon-
trolled releases to the public) and/or worker safety as determined from hazard analysis. Gener-
ally, safety-significant SSC designations based on worker safety are limited to those SSCs
whose failure could result in an acute worker fatality or serious injury to workers.
Safety Structures, Systems, and Components (safety SSCs)—The set of safety-class
structures, systems, and components, and safety-significant structures, systems, and compo-
nents for a given fusion facility.
Shall—A firm requirement that must be met to be in compliance with this Standard.
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Shall Consider—The need for and applicability of stated features or attributes must be evalu-
ated and the results of the evaluation documented.
Should—A desirable option or recommendation, departure from which is permissible.
Site boundary—A well-marked boundary of the property over which the owner and operator
can exercise strict control without the aid of outside authorities.
Standard Industrial Hazards—Hazards that are routinely encountered in general industry and
construction and for which national consensus codes and/or standards (e.g., OSHA, transporta-
tion safety) exist to guide safe design and operation without the need for special analysis to
define safe design and/or operational parameters.
Supervisors—Persons who are responsible for the quantity and quality of work and who direct
the actions of the operators or other personnel.
Technicians—Persons responsible for performing specific maintenance or analytical laboratory
work.
Technical Safety Requirement—Those requirements that define the bounding conditions for
safe operation, the bases thereof, and the management or administrative controls required to
ensure the safe operation of a facility.
Tokamak—The mainline magnetic fusion confinement configuration that employs discrete
toroidal coils surrounding a torus-shaped vacuum vessel with poloidal field coils either captured
by or external to the toroidal field coils. A large current induced in the plasma provides part of
the magnetic field required for plasma confinement.
Section 11
Toroidal Field Coils—The coils surrounding the vacuum vessel that provide the major confin-
ing magnetic field for the plasma.
Unreviewed Safety Question—A formalized uncertainty brought about by a proposed change,
test, or experiment or the identification of analytic inadequacy when (a) the probability of occur-
rence or the consequences of an accident or malfunction of equipment important to safety pre-
viously evaluated by safety analyses could be increased; (b) the possibility for an accident or
malfunction of a different type than any evaluated previously by safety analyses could be
created; or (c) any margin of safety, as defined in the basis for any Technical Safety Require-
ment, could be reduced.
Vertical Displacement Event—A sudden loss of plasma position control. For highly shaped
tokamak plasmas, active vertical position control is required to maintain the vertical position.
Loss of the position control is known as a Vertical Displacement Event (VDE). If the main
plasma contacts the plasma-facing components, the currents in the plasma can rapidly dis-
appear, leading to a disruption.
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Workers—Persons performing work at the facility or on the site of the facility.
Worker Safety Function—Essential characteristics or performance needed to assure the pro-
tection of workers during normal operations, anticipated operational occurrences, and off-normal
conditions.
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LIST OF ACRONYMS
AC Administrative Control
ac alternating current
ACGIH American Conference of Governmental Industrial Hygienists
AEA Atomic Energy Act
AIRFA American Indian Religious Freedom Act
ALARA as low as reasonably achievable
ANSI American National Standards Institute
ASME American Society of Mechanical Engineers
BDBA beyond-design-basis accident
CAA Clean Air Act
CAP-88 Clean Air Act Assessment Package-1988
CCTV closed-circuit television
CED committed effective dose
CEQ Council on Environmental Quality
CERCLA Comprehensive Environmental Response, Compensation, and Liability Act
D-D deuterium-deuterium
D-T deuterium-tritium
DBA design-basis accident
dc direct current
DOE Department of Energy
DOT Department of Transportation
EA Environmental Assessment
EAL Emergency Action Level
ED effective dose
EG Evaluation Guideline
EIS Environmental Impact Statement
EIS/ROD environmental impact statement/record of decision
EMM electromechanical manipulator
EMS Emergency Management System
EOC Emergency Operations Center
EPA Environmental Protection Agency
FAA Federal Aviation Administration
FWS Fish and Wildlife Service
HEPA high-efficiency particulate air
HVAC heating, ventilating, and air conditioning
I&C instrumentation and control
ICRP International Commission on Radiological Protection
IEEE Institute of Electrical and Electronic Engineers
IPCEA Insulated Power Cable Engineers Association
ITER International Thermonuclear Experimental Reactor
JET Joint European Torus
LCE loss-of-coolant event
LCOs Limiting Conditions for Operations
LCS Limiting Control Setting
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Section 12
LFE loss-of-flow event
LLW low-level waste
LVE loss-of-vacuum event
MACCS MELCOR Accident Consequence Code System
MAP Mitigation Action Plan
MC&A Materials Control and Accountability
MEI most exposed individual
MG motor generator
MSM master slave manipulator
NAAQS National Ambient Air Quality Standards
NCRP National Council on Radiation Protection and Measurements
NDE nondestructive examination
NEPA National Environmental Policy Act
NESHAPS National Emission Standards for Hazardous Air Pollutants
NFPA National Fire Protection Association
NIOSH National Institute of Occupational Safety and Health
NPDES National Pollutant Discharge Elimination System
NRC Nuclear Regulatory Commission
NSPS New Source Performance Standards
OSHA Occupational Safety and Health Act
PAG Protective Action Guideline
PF poloidal field
PFC plasma-facing component
PIE postulated initiating event
PRA probabilistic risk assessment
PSD Prevention of Significant Deterioration
PTC permit to construct
PVTC pressure/volume/temperature/composition
QA quality assurance
QAP Quality Assurance Plan
QC quality control
RCRA Resource Conservation and Recovery Act
RF radio frequency
SA specific activity
SAR safety analysis report
SARA Superfund Amendments and Reauthorization Act
SHIPO State Historic Preservation Office
SIP State Implementation Plan
SL safety limit
SR Surveillance Requirement
SSCs structures, systems, and components
TF toroidal field
TFTR Tokamak Fusion Test Reactor
TSCA Toxic Substances Control Act
TSD treatment, storage, and disposal
TSR Technical Safety Requirement
xx
DOE-STD-6003-96
UHMWPE Ultra-high molecular weight polyethylene
UPS uninterruptable power supply
USQ Unreviewed Safety Question
V&V verified and validated
VDE vertical displacement event
xxi
DOE-STD-6003-96
xxii
Intentionally Left Blank
DOE-STD-6003-96
1. INTRODUCTION
1.1 Purpose
This document provides guidance for the implementation of the requirements identified
in DOE-STD-6002-96, Safety of Magnetic Fusion Facilities: Requirements. This guidance is
intended for the managers, designers, operators, and other personnel with safety responsibili-
ties for facilities designated as magnetic fusion facilities. While the requirements in DOE-STD-
6002-96 are generally applicable to a wide range of fusion facilities, this Standard, DOE-STD-
6003-96, is concerned mainly with the implementation of those requirements in large facilities
such as the International Thermonuclear Experimental Reactor (ITER). Using a risk-based
prioritization, the concepts presented here may also be applied to other magnetic fusion
facilities. This Standard is oriented toward regulation in the Department of Energy (DOE)
environment as opposed to regulation by other regulatory agencies. As the need for guidance
involving other types of fusion facilities or other regulatory environments emerges, additional
guidance volumes should be prepared. The concepts, processes, and recommendations set
forth here are for guidance only. They will contribute to safety at magnetic fusion facilities.
1.2 Background
When the development of fusion facilities began changing from comparatively small-scale
experiments in physics to large facilities with megawatt-power levels and significant activation
concerns, a need to develop safety requirements and associated guidance for fusion became
apparent. Fusion systems are sufficiently different from other nuclear facilities that the require-
ments and regulations governing existing nuclear facilities are not fully appropriate for the regu-
lation of magnetic fusion facilities.
Section 13
Efforts were begun to develop a group of documents that would be appropriate for safety
regulation in magnetic fusion facilities. The documents that resulted from that process consist
of a requirements document, DOE-STD-6002-96, Safety of Magnetic Fusion Facilities: Require-
ments, which attempts to assemble in one place those requirements needed for safety, and this
guidance document, which sets forth information that will assist fusion developers in meeting
those requirements.
The intent in this guidance document is to provide a fairly complete, though not exhaus-
tive, set of instructions that if followed will contribute to the achievement of safety. There has
been a conscious effort to include either directly or by reference those items that are germane
to safety so that the manager, designer, or operator will be able to clearly identify actions that
should be taken to meet the requirements using risk-based prioritization.
The guidance provided here represents the collective wisdom of a broad and diverse
group with experience in nuclear facility safety as well as with fusion. The concepts presented
are included not only because they have been applied successfully to other kinds of facilities,
but because they were deemed to make sense for fusion.
1
DOE-STD-6003-96
A conscious attempt has been made to exclude from this document concepts and advice
not directly related to safety. In this sense, this document is not intended to be exhaustive. Of
the many sound design or management practices that make good sense for a project, the ones
included here are those that are directly safety-related.
The intent here has been to identify concerns, practices, or procedures that will contribute
to safety. Often, these are only summarized, not detailed here. Where appropriate guidance is
available from other sources such as DOE Orders or other Standards, those sources are refer-
enced here.
This Standard was written in the reference frame of the Orders, Standards, and other
documents that were in force at the time of writing. It was recognized that the DOE directives
system was under major revision and that some of the references included here may be out of
date at the time this Standard is implemented. Therefore, the user is encouraged to use the
most current version of documents referred to here or their replacements.
1.3 Implementation
The requirements in DOE-STD-6002-96 and the guidance in this Standard should be
implemented using a risk-based prioritization approach. The degree to which they are applied
should be commensurate with the risk involved. Fusion facilities that involve only minor hazards
will require implementation at a lower level than will facilities such as ITER where activation and
tritium inventories will be concerns.
1.4 Overview
The responsibility for safety at fusion facilities, as all other facilities, lies with those having
charge of the program or project. Safety is a requirement during all phases of the facility life
cycle. It must be incorporated into the design, implemented during operations, and integrated
into facility removal and site restoration. Success in the latter two phases often hinges on the
success with which safety foresight and planning have been included in the design. To assist
managers, designers, operators, and removal staffs in achieving safety, there are a number of
tools (i.e., considerations, practices, processes, or other vehicles) that if implemented will con-
tribute substantially to the overall safety of the facility. Those deemed most appropriate for
fusion facilities are described in subsequent sections of this Standard.
Section 14
Chapter 2 of this volume provides guidance on radiation and hazardous materials
management to ensure that safety objectives are met. A primary consideration in any nuclear
facility, including fusion facilities, is the management of radioactivity and hazardous materials.
Protection from radiation and hazardous materials at all times is a primary concern for worker
safety. The design and operating protocols of the facility should incorporate features that will
limit exposures to radioactivity or hazardous materials in off-normal events as well as under
normal operating conditions. Guidance on how to provide that protection is presented in
Chapter 2.
2
DOE-STD-6003-96
Environmental considerations are summarized in Chapter 3. References to requirements
in the environmental area are listed here with annotations because such a listing is not readily
available from other sources.
Program management considerations to achieve safety are addressed in Chapter 4. As
indicated previously, the ultimate responsibility for safety lies with management. Integration of
safety in the design, operation, and site restoration all involve the implementation of safety-
related processes and a safety culture. In Chapter 4 the most significant of the tools available
for achievement of safety are discussed: configuration management, quality assurance, conduct
of operations, emergency planning, and tritium accountability.
A major area of involvement for safety professionals with management is in the prepara-
tion of safety analysis to evaluate the extent to which a given facility or design meets safety
goals. Chapter 5 of this Standard includes guidance on how to establish the facility hazard
classification; identify safety-related structures, systems, and components; develop technical
safety requirements; and deal with unresolved safety questions. A key concept in safety analy-
sis is the design basis and the associated requirements for approving facility operation. The
analysis process described in Chapter 5 makes use of that concept and indicates how various
off-normal event scenarios should be dealt with in the analysis.
Chapter 6 is the most comprehensive of the chapters. It addresses design requirements
and considerations for safety in design of fusion facilities. It begins with general design guidance
that applies to all systems; then systems performing safety functions are described with design
considerations to achieve those functions. Guidance is also provided for systems with potential
safety concerns. These systems are not required to operate to achieve safety, but their failure
may influence the levels of defense-in-depth available to the facility. Safety design guidance for
supporting systems (those systems that support those systems providing safety functions) is
also presented. The chapter concludes with guidance on safety in experimental systems and
facility support.
The final chapter in this Standard, Chapter 7, is concerned with facility removal and site
restoration. It provides guidance for returning the site of the fusion facility to its original condition
at the end of its useful life. Safety in this phase of the life cycle will be strongly influenced by
planning and design features that have been incorporated from the outset of the project.
Section 15
Appendices in this Standard provide additional supporting information. Appendix A is a list
of isotopes for radiological considerations specific to fusion facilities. Appendix B is an overview
of hazards typically associated with magnetic fusion facilities. Appendix C supplements this vol-
ume with a listing of available orders, standards, and other documents appropriate to manage-
ment of projects within DOE and lists specific references cited in the text.
3
DOE-STD-6003-96
Intentionally Left Blank
4
DOE-STD-6003-96
2. RADIATION AND HAZARDOUS MATERIAL
The neutron flux in a fusion facility will result in activation of the first wall and structure,
resulting in the production of radioactive materials. The level of activation is a function of power
level, fuel cycle [deuterium-deuterium (D-D) vs deuterium-tritium (D-T)], and materials choice.
Fusion experiments and power plants presently envisioned will also use strong magnetic fields,
radio-frequency heating, and some potentially hazardous materials such as beryllium and
vanadium. This section summarizes general guidance regarding radiological, magnetic field,
and hazardous material concerns expected to be present at fusion facilities.
Chemically hazardous materials are sometimes specified in the design of a fusion power
core because of their mechanical or nuclear properties. The most prominent of these materials
are beryllium, used as a first wall coating and as a neutron multiplier, and vanadium, used as a
first wall and blanket structure material.
2.1 Dose Definitions
The effective dose E has associated with it the same probability of the occurrence of
cancer and genetic effects whether received by the whole body via uniform irradiation or by
partial or individual organ irradiation. Although an assumption of uniformity may be a sufficient
approximation in many external irradiation cases, in others more precise evaluation of individual
tissue doses will be necessary. With external irradiation, differences may arise with depth in the
body and with orientation of the body in the generally nonuniform radiation field. When irradia-
tion is from radionuclides deposited in various tissues and organs, nonuniform or partial body
exposures usually occur. Tissues also vary in their sensitivity to radiation. The effective dose E
is a concept similar to the effective dose equivalent HE used by ICRP Publication 26 (ICRP
1977) and NCRP Report No. 91 (NCRP 1987). However, they are conceptually different. The
effective dose E is intended to provide a means for handling nonuniform irradiation situations, as
did the earlier dose equivalent.
The effective dose E is the sum of the weighted equivalent doses for all irradiated tissues
or organs. The tissue weighting factor wT takes into account the relative detriment to each organ
and tissue including the different mortality and morbidity risks from cancer, the risk of severe
hereditary effects for all generations, and the length of life lost due to these effects. The risks for
all stochastic effects will be the same whether the whole body is irradiated uniformly or
nonuniformly if
E = wTHT
T
∑ , (1)
where wT is the tissue weighting factor representing the proportionate detriment (stochastic)
tissue T when the whole body is irradiated uniformly, and HT is the equivalent dose received by
tissue T. For further explanation see NCRP Report No. 116 (NCRP 1993).
Doses mean the 50-yr committed effective dose (CED) unless otherwise stated. The
exposure times and exposure pathways to be included in the calculation of CED should be
Section 16
5
DOE-STD-6003-96
appropriate for the fusion isotopes involved, the accident scenario, and the public mitigative
actions (if any) being considered.
Acute dose is defined for specific organs depending on what short-term exposure is the
best predictor of acute health effects. For example, the acute lung dose is typically the 1-yr
CED, and the bone marrow acute dose is typically considered as the 7-day CED or 100% of the
7-day CED plus 50% of the 8–30th day CED. Thus, for the same exposure time periods, the
acute dose is always less than (or equal to for very short half-lives) the 50-yr CED.
Early dose is the 50-yr CED from the first 7 days of exposure following the onset of an
accident, specifically the inhalation and cloudshine doses during plume passage, inhalation from
resuspended/re-emitted isotopes during the first 7 days, and the groundshine dose from the first
7 days. This dose measure is appropriate when contemplating the need for short-term public
mitigative actions. The early dose is generally calculated for the most exposed individual (MEI)
of the public, assumed to reside at the site boundary or (for release elevated above ground
level) where the plume reaches the ground.
Two-hour (prompt) dose is the 50-yr CED resulting from the first 2 hours of exposure fol-
lowing the onset of an accident, as in DOE 6430.1A. This dose measure implicitly assumes
evacuation within 2 hours.
Chronic dose is the 50-yr CED from 50-yr exposure after an event, specifically from
inhalation of resuspended or re-emitted isotopes, groundshine, and ingestion of radionuclides.
This dose measure is appropriate when contemplating whether long-term public mitigative
actions are needed and, if so, when and for how long. When calculated for an individual, the
chronic dose should include reasonable assumptions about the fraction of time an individual
resides at the site boundary and the fraction of food produced at that location. Because of the
long time scales, the chronic dose is more appropriately calculated for the “average” resident of
the surrounding area.
The factor χ is the instantaneous concentration of a radioactive or hazardous material (in
becquerels per cubic meter or grams per cubic meter) at a given location distant from the point
where the material is released into the environment. The factor Q is the amount of material
released, expressed in grams or becquerels; ′ Q is the rate of material release emission from a
continuous point source. The ratios χ/Q and χ ′ Q are determined by the atmospheric condi-
tions, the distance between the source and distant location atmospheric transport, and the time
since release. For further explanation, see Slade (AEC 1968).
2.2 Public Exposures and Environmental Impacts
A significant part of 10 CFR 20 is directed toward protecting the public, the environment,
and workers from the risks of exposure to radiation. Part of 40 CFR 61 is also concerned with
protecting the public from chronic exposure to radiation. In addition, exposures to workers, the
public, and the environment must be kept “as low as reasonably achievable” (ALARA).
“Reasonably achievable” levels are typically a fraction of those allowed by 10 CFR 20 and
40 CFR 61.
6
DOE-STD-6003-96
Section 17
For comparison with the evaluation guidelines, only plume passage dose is evaluated.
Plume passage dose includes the following pathways: (1) direct cloudshine and (2) 50-yr CED
from inhalation for the duration of plume passage. These pathways are considered an immedi-
ate threat. Other slow-developing pathways are not included because they are a measure of the
effectiveness of public health measures (e.g., interdiction) rather than the severity of the acci-
dent itself. If dose is evaluated on public access roads that are not controllable by the licensee,
the time of exposure to the plume should be based on realistic vehicle passage time estimates.
2.2.1 Evaluation Guidelines for Exposures to the Public
The following goals and requirements have been established in DOE-STD-6002-96 for
exposures to the general public during normal and anticipated operational occurrences and for
off-normal conditions and accidents. The origin of each of the limits follows Table 2.1.
Evaluation guidelines for public exposures to nonradiological materials should be in
accordance with federal, state, and local regulatory and permit requirements.
TABLE 2.1. Evaluation guidelines for public protection from radiation
Fusion radiological
release requirement
Regulatory limit
(evaluation guidelines)
Normal and anticipated
operational occurrences
100 µSv/yr
[10 mrem/yr]a
1 mSv/yr
[100 mrem/yr]b
Off-normal conditions (per
event)
10 mSv
[1 rem]c
(no public evacuation)
250 mSv
[25 rem]d
aThis value, which is a limit for the MEI, is consistent with the limit on the emissions of radionuclides to
the ambient air for DOE facilities as stated in 40 CFR 61.92. In meeting this limit, a facility would be well
below the exposure limit mandated by the Nuclear Regulatory Commission (NRC) safety goals for
nuclear facilities (51 FR 30028) and the DOE safety goals. Both of these goals, which consider the
average exposure to the population within 10 miles of a facility, state that the risk to the population
resulting from nuclear operations should not exceed 0.1% of the sum of all cancer fatality risks resulting
from all other causes. The radiological cancer risk coefficient is about 0.4%/0.1 Sv for long-term
exposures (BEIR-V, p. 6), and the annual cancer fatality risk due to all causes is about 200/100,000
people. If we conservatively assume that the site-boundary to average exposure ratio is 2, then the
routine exposure limit should be
(0.1%) (200 per year/100,000 people) (0.1 Sv/0.4%) (2) = 0.1 mSv/yr = 10 mrem/yr.
bThis value is based on the 10 CFR 20.1301 dose limits on individual members of the public.
cThis requirement is based on the limit in the Protective Action Guideline (PAG) (EPA 1991) at which
public sheltering and evacuation should be undertaken.
dThis is the required limit for exposure due to an accident. This value is based on the design basis
acceptance criteria for nuclear reactor siting in 10 CFR 100.
7
DOE-STD-6003-96
2.2.2 Additional Guidance
10 CFR 100 defines requirements for siting of nuclear reactor facilities. These guide-
lines have also been applied to nonreactor nuclear facilities (DOE 6430.1A). According to
10 CFR 100.11, the maximum calculated dose to an off-site individual from exposure that
results from internal and external sources of radiation must not exceed 250-mSv (25-rem),
50-yr CED to the whole body. If multiple organs receive doses during the same exposure, the
ED shall not exceed 250 mSv (25 rem). The exposure duration should be consistent with the
requirement for no public evacuation. DOE 6430.1A recommends using meteorological condi-
tions that result in unfavorable dispersion (e.g., the higher of the 0.5% χ/Q for each sector of the
site and the 5% direction independent χ/Q for the site). In the absence of site-specific meteor-
ology, conservative assumptions (Class F, 1.0-m/s wind speed) should be used for design
assessments. Further guidance is contained in Sections 2.4.3 and 5.4.3.
Section 18
DOE Order 6430.1A notes that these values are guidelines and do not constitute accept-
able limits on the doses to the public in the event of an accident. These guidelines are used by
DOE to evaluate the facility design in combination with the site characterization with respect to
the risk to the public from low-probability accidents. Accidents to be evaluated for comparison to
these dose guidelines include events with a probability of occurrence >10–6/yr. When the doses
are calculated, the degraded performance of engineered safety features and administrative
controls should be assumed unless they can be shown to be capable of performing their safety
function.
The radionuclides of concern in a fusion facility cover a wide range of characteristics.
Tritium is generally the most mobile. Tritium is hazardous if it is taken into the body via inges-
tion, inhalation, or absorption through the skin. Because of the relatively low energy of the beta
particle, 18-keV maximum energy, it does not present a significant hazard outside the body.
Other radionuclides are the products of neutron activation. These radionuclides, usually imbed-
ded in a metal, have much higher energies and undergo γ-decay. Typical radionuclides are
Fe-55, Co-58, Co-60, Mn-54, Mn-56, Ni-59, and Ni-63. Alloying elements and impurities further
increase the range of activation products.
2.2.3 Environment
Radiation protection standards have been developed expressly for the protection of
humans. It has been generally accepted that by protecting humans we are protecting the
environment. Recently, the ICRP stated (ICRP 1991):
The Commission believes that the standard of environmental control needed to protect
man to the degree currently thought desirable will ensure that other species are not put at risk.
Occasionally, individual members of non-human species might be harmed, but not to the extent
of endangering whole species or creating imbalance between species.
Additional guidance on other areas of environmental protection is provided in Chapter 3.
8
DOE-STD-6003-96
The Environmental Protection Agency (EPA) has set limits on the emissions of beryllium
into the environment from industries that process beryllium ores, metal, oxide, alloys, or waste.
40 CFR 61 limits the amount of beryllium emitted to 10 g in a 24-h period or to an amount that
would result in atmospheric levels of 0.01-µg beryllium/m3 of air, averaged over a 30-day
period. EPA’s Office of Water Regulations and Standards limits the concentration of beryllium in
water to between 0.68 and 68 ng beryllium/L for protection of human health.
2.3 Routine Worker Exposure
2.3.1 Radiation
In a fusion facility, occupational exposure to radiation can result from gamma radiation,
neutron fluxes, tritium ingestion or inhalation, and the mobilization of activation products. The
exposures from all these sources are combined into an effective dose (ED) that accounts for the
energy, half-life, and biological mobility of each of the radionuclides.
Under 10 CFR 20 and 10 CFR 835, the radiological workers at commercial and DOE
facilities are limited to an annual ED (internal and external) exposure of 50 mSv (5 rem). Expo-
sures to organs, tissues, or extremities are limited to 500 mSv (50 rem). Lower limits apply to
declared pregnant women, minors (less than 18 years old) and students, visitors, and the public.
Under DOE requirements, permission of the Cognizant Secretarial Officer is required for all
occupational doses in excess of 2 rem. Higher exposures are tolerated for emergency
situations, such as saving a human life, recovering a deceased victim, and protecting health and
property.
Section 19
The goal for doses due to normal and anticipated operational occurrences is 10 mSv/yr
(1 rem/yr). In all cases the dose to workers must be as low as reasonably achievable. This value
is based on ICRP 26 and NCRP 116 recommendations.
Doses should be kept “as low as reasonably achievable” (ALARA). In the design of facili-
ties the design objective for controlling personnel exposure from external sources of radiation in
areas of continuous occupational occupancy (2000 hours per year) shall be to maintain expo-
sure level below an average of 0.5 mrem (5 microsieverts) per hour and as far below this aver-
age as is reasonably achievable. The design objectives for exposure rates for potential expo-
sure to a radiological worker where occupancy differs from the above shall be ALARA and shall
not exceed 20 percent of the applicable standards of 10 CFR 835.202 (10 CFR 835).
2.3.2 Hazardous Materials
There may be a number of hazardous materials in a fusion facility such as metallic dust,
diborane, inert gases, and organic compounds. Other regulations are concerned with exposures
to these hazardous materials and other industrial hazards. In this guidance emphasis is given to
beryllium and vanadium because these materials are more relevant to fusion facilities. Exposure
limits should be taken from National Institute of Occupational Safety and Health (NIOSH) recom-
mendations (NIOSH 1994), Occupational Safety and Health Act (OSHA) regulations
(29 CFR 1910), and industrial standards.
9
DOE-STD-6003-96
2.3.2.1 Beryllium
Beryllium and beryllium compounds can pose potential health risks to humans. They may
be used as plasma-facing components in ITER. This section summarizes the current U.S. regu-
lations about allowable emission to the environment and permissible occupational exposure to
workers.
OSHA regulations limit permissible exposures to a time-weighted average of
0.002 mg/m3 for the beryllium concentration in workroom air. For short-term exposure (i.e.,
30 min), the exposure limit is 0.025 mg/m3. The NIOSH recommends an exposure guideline of
0.0005 mg/m3 in workroom air during an 8-h shift. There are also limits on acceptable beryllium
ambient air concentrations and drinking water quality standards for a number of states in the
United States (DHHS 1993). This Standard recommends the adoption of the NIOSH exposure
guidelines for beryllium in a fusion facility.
2.3.2.2 Vanadium Oxides
Since absorption of vanadium is chiefly by the respiratory tract, mechanical enclosure of
many vanadium-using operations is required. If this is impractical, the worker must be provided
with an air-fed unit to ensure complete respiratory protection from vanadium pentoxide (Finkel
1983). NIOSH 15-min time-weighted average exposure limits for vanadium compounds in air
are 0.05 mg vanadium/m3. For metallic vanadium, ferrovanadium dust, and vanadium carbide,
the NIOSH exposure limits are 1.0 mg V/m3 (3 mg V/m3 for short-term exposures) (NIOSH
1994). OSHA exposure limits are 0.5 mg V2O5 /m3 for vanadium dust, 0.1 mg V2O5 /m3 for
vanadium fume, and 1 mg/m3 for ferrovanadium dust (29 CFR 1910). This Standard recom-
mends the adoption of the NIOSH exposure guidelines for vanadium in a fusion facility.
2.3.3 Common Industrial Hazards
As with any large industrial facility, a fusion power plant facility will contain other hazards,
such as flammable materials, rotating machinery, and nonbreathable gases. These hazards are
not unique to fusion power and will therefore be regulated according to existing OSHA criteria
(29 CFR 1910, 1926) or commonly accepted industrial safety practices.
Section 20
2.3.4 Magnetic Fields
The magnetic confinement fusion facilities addressed in this Standard may have magnetic
fields of considerable strength extending throughout areas of the facilities and possibly beyond
interior rooms. These fields may be steady state, or they may vary in time and/or space. In
general, the magnetic field at the site boundary will be very low, usually less than the earth’s
magnetic field (~50 µT).
The recommended limits for occupational exposures to steady-state and low-frequency
magnetic fields are those established by the American Conference of Governmental Industrial
Hygienists (ACGIH). At present, the ACGIH states:
10
DOE-STD-6003-96
Routine occupational exposure should not exceed
BTLV = C
f
, (2)
where
BTLV = the threshold limit value for the magnetic field in millitesla (mT)
C = a constant equal to 60 mT-Hz
f = the field frequency in Hertz (Hz).
At frequencies below 1 Hz, the threshold limit value is 60 mT. The magnetic field
strengths in these limits are root-mean-square (rms) values.
For workers wearing cardiac pacemakers, the threshold limit value may not protect
against electromagnetic interference with pacemaker function. The threshold limit for pace-
maker wearers should be reduced by a safety factor of 10.
In the future, this Standard will adopt modifications of the ACGIH threshold limit value for
magnetic fields.
2.4 Guidance for Meeting Regulatory Limits
This section provides guidance for calculational procedures to meet the regulatory limits
given in DOE-STD-6002-96. Guidance on the types of off-normal analyses required to meet
these regulatory limits is provided in Section 5.4 of this Standard.
2.4.1 Evaluation Guidelines
Evaluation Guidelines (EGs) are accident impact criteria established for the purpose of
evaluating the acceptability of facility safety design. For radionuclide releases, criteria are given
for ED and are termed “dose values.” It is important to note that these criteria do not necessarily
constitute acceptable limits for human health impacts in the event of an accident. Rather, they
are used to evaluate the level of safety associated with the design of the facility with respect to
the risk from low-probability accidents. EGs are typically established using a risk-based frame-
work. Higher dose values are associated with lower frequency to provide balance in the design
with appropriate focus at both the high- and low-probability ends of the accident frequency
scale. Dose values are given for normal operation and anticipated operational occurrences.
A second set of dose values is given for off-normal conditions. Events with an estimated fre-
quency of <10–6/yr are considered hypothetical, and comparison to an EG is not required. The
method is comparable to that established in DOE Standard 3009, Preparation Guide for U.S.
Department of Energy Nonreactor Nuclear Facility Safety Analysis Reports. EGs are provided
for off-site (public) locations.
11
DOE-STD-6003-96
2.4.2 Exposure
Off-site doses are evaluated for the most exposed individual (MEI). This is a hypothetical
individual located at the closest point on the site boundary (or at off-site distance of maximum
air concentration for elevated releases).
2.4.3 Meteorological Dispersion
Section 21
Site-specific 5% weather conditions (i.e., stability class and wind speed more unfavorable
than 95% of the expected weather) without regard to wind direction, defined by at least 1 yr of
weather data, should be used for diffusive transport to downwind receptors. Alternatively, site-
specific climatological studies using actual measurements of diffusion/dilution characteristics
under representative meteorological conditions can be used as a basis for determining site-
specific dilution factors (χ/Qs) (see NOAA 1989 for example). These weather conditions should
be determined using the anticipated release height of the accident cloud (e.g., ground level or
elevated). For evaporating chemicals, a range of stability class/wind speed combinations should
be examined due to the chemical-specific effects of these parameters on source emission rates
and downwind dispersion. A dense gas model may need to be used for evaluation of impacts at
near-field receptor distances if the chemical/air mixture density at the source exceeds the ambi-
ent air density by 50%. Dense gas effects are usually insignificant at far-field receptor distances.
2.5 Consequence Thresholds for PAGs and Emergency Response Planning Guidelines
As stated in DOE-STD-6002-96, the Fusion Radiological Release Requirement for off-
normal events at fusion facilities is that no events result in a public exposure greater than
10 mSv (1 rem). If the projected early dose to the surrounding population can be shown to be
less than 10 mSv, then no public protective action planning would be necessary.
In determining whether a given event at a fusion facility will require protective action, best
estimate meteorology and system operation are assumed. All estimates of the site-specific
transport coefficients (χ/Q) are based on at least 1 yr of meteorological data. Best-estimate
meteorology can be used to determine public exposures in three ways:
a. Use the annual average windspeed and the highest-frequency stability conditions in
determining the χ/Q at the site boundary.
b. Calculate the hourly χ/Q for meteorological conditions throughout the year. Select the
50 percentile χ/Q to determine off-site transport.
c. Using meteorological data for at least 1 yr, use a Monte Carlo technique to select
random starting times for the off-normal event. Average the public exposure due to
each of the transients to obtain the best-estimate off-site doses.
Because of differences among the mean, median, and mode of the χ/Q distributions
through the year, the preferred method is “c” above. Further guidance in the application of best
estimate off-site dose calculation can be found in NUREG-0654/FEMA-REP-1.
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DOE-STD-6003-96
2.5.1 Radiological (No Ingestion)
Guidance for sheltering, evacuation, and food interdiction is given in the EPA “Manual of
Protective Action Guides and Protective Actions for Nuclear Incidents” (EPA 1991). A nuclear
incident is divided into three phases: early, intermediate, and late. During the early phases shel-
tering or evacuation is the appropriate measure to consider. The PAGs are criteria based upon
the potentially avoided dose, which determine whether action must be taken.
a. Evacuation (or, for some situations, sheltering) should normally be initiated to avoid a
10-mSv (1-rem) dose to a standard man for ”early” pathways inhalation (CED) and
external gamma ED (cloudshine/immersion and ground surface).
Section 22
b. For radionuclides with long effective half-times in the body, use 50-mSv (5-rem)
CED + ED as the action criterion. For committed effective dose equivalent to the skin,
use 500 mSv (50 rem) for the action criterion.
2.5.2 Radiological (Ingestion)
During the intermediate and late phases of the incident, controls on the ingestion of con-
taminated food and water are appropriate (FDA 1982). The avoided doses at which such inter-
diction is appropriate are shown below:
a. “Preventative PAG”—5 mSv (0.5 rem) to “whole body, bone marrow, or any other
organ.” This is the level at which protective actions having minimal impact should be
taken.
b. “Emergency PAG”—50 mSv (5 rem) to “whole body, bone marrow, or any other
organ.” This is the level at which food should be isolated for condemnation or other
disposition.
2.6 Models Used in Relating Exposures to Estimated Consequences
The following code systems are examples of tools that have been accepted for use in a
regulatory context for relating releases, exposures, and estimated consequences. This list is not
all inclusive, and other codes of greater capability might be developed in the future.
GENII (Napier 1988) is a coupled system of computer codes used to estimate potential
radiation doses to individuals or populations from both routine and accidental releases of
radionuclides to air or water and residual contamination from spills or decontamination
operations.
The MACCS (MELCOR Accident Consequence Code System) (Chanin 1990) code sys-
tem calculates impacts of severe accidents at nuclear reactors on the surrounding environment.
Principle phenomena considered include atmospheric transport dose mitigation actions, dose
accumulation, and health effects. The MACCS code has been expanded to include isotopes of
interest in fusion facilities.
13
DOE-STD-6003-96
The RSAC (Wenzel 1993) code calculates the consequences of the release of radio-
nuclides to the atmosphere. A user can generate a radioactive inventory, decay and ingrow the
inventory during transport through process facilities and the environment, model the downwind
dispersion of the activity, and calculate doses to downwind individuals. Doses are calculated
through the inhalation, immersion, ground surface, and ingestion pathways.
The CAP-88 (Clean Air Act Assessment Package-1988) (Parks 1992) computer model is
a set of computer programs, data bases, and associated utility programs for estimation of dose
and risk from routine radionuclide emissions to air. CAP-88 must be used to show compliance
with 40 CFR 61.93(a) unless the EPA approves an alternate.
The CAP-88-PC software package allows users to perform full-featured dose and risk
assessments in a personal computer environment for the purpose of demonstrating compliance
with 40 CFR 61.93(a) for routine radionuclide releases to the air. CAP-88-PC provides the
CAP-88 methodology for assessments of both collective populations and MEIs. The complete
set of dose and risk factors used in CAP-88 is provided. CAP-88-PC used a modified Gaussian
plume equation to estimate the average dispersion of radionuclides released from up to six
sources. The sources may be either elevated stacks, such as a smokestack, or uniform area
sources, such as a pile of uranium mill tailings. Plume rise can be calculated assuming either a
momentum or buoyancy-driven plume. Assessments are done for a circular grid of distances
and directions for a radius of 80 km (50 miles) around the facility.
14
Section 23
DOE-STD-6003-96
3. ENVIRONMENTAL AND PERMITTING REQUIREMENTS
This chapter is a compilation of environmental and permitting requirements potentially
applicable to magnetic fusion facilities. It is not intended nor should it be interpreted to be the
definitive listing of all environmental laws and regulations to which a new fusion facility would be
subject. The information is provided to facilitate planning for preparing the environmental and
permitting documentation that may be required. Ongoing rulemaking may influence the applica-
bility and completeness of the environmental and permitting requirements that must be satisfied
for specific fusion facilities. In addition, state and local regulations may impose additional
requirements and more stringent standards on those facilities. Requirements in this chapter are
only repeated here from original sources for user convenience and do not constitute new
requirements.
3.1 Federal Requirements
3.1.1 National Environmental Policy Act and Implementing Guidelines, Regulations, and
Orders
National Environmental Policy Act (NEPA) of 1969 (42 USC 4321 et seq.; 40 CFR 1500–
1508) establishes national policies and goals for the protection of the environment. Section 102
requires Federal agencies to incorporate environmental considerations into their planning and
decision-making processes using a systematic interdisciplinary approach. The Council on
Environmental Quality (CEQ) regulations implementing NEPA (40 CFR 1500–1508) contain
action-forcing provisions to ensure that Federal agencies consider environmental information
before making decisions on proposed actions. The NEPA process includes decision points at
which the significance of environmental effects is considered, project alternatives are identified,
and any appropriate mitigation measures are identified and adapted. Title 10 CFR 1021 estab-
lishes DOE’s policy of complying fully with NEPA, and DOE Order 451.1 describes the roles of
the various DOE offices in implementing the Act.
The NEPA review process consists of evaluating the potential environmental effects of a
Federal undertaking, establishing possible alternatives to the proposed action, and determining
the level of NEPA documentation required to proceed with the action. Three levels of NEPA
documentation include determination of categorical exclusion, preparation of an environmental
assessment/finding of no significant impact (EA/FONSI), and preparation of an environmental
impact statement/record of decision (EIS/ROD). For major Federal actions with the potential for
significant environmental impacts, an EIS is typically required.
The National Environmental Policy Act Compliance Program (10 CFR 1021, DOE Order
451.1) establishes procedures to implement NEPA, including the level of review necessary
under NEPA. This Order promotes smooth generation, review, and release of documents pur-
suant to NEPA and provides for the cooperation between various elements of DOE. Further
guidance on preparing EAs and EISs is provided in DOE’s NEPA “Greenbook” (DOE, 1993b).
Executive Order 12114, “Environmental Effects Abroad of Major Federal Actions”
(44 FR 1957), establishes procedural and other actions to be taken by Federal agencies to
15
DOE-STD-6003-96
Section 24
further the purposes of NEPA with respect to the environment outside the United States, its
territories, and possessions. Final DOE guidelines for implementing the Order were published in
the Federal Register in 1981 (46 FR 1009). Therein, the categories of actions and the manda-
tory environmental review requirements are identified. Major Federal actions that could poten-
tially affect the global environment or resources require some level of environmental review and
documentation, depending on the nature of the action and the environments potentially
impacted.
3.1.2 Federal Statutes and DOE Orders Relating to Environmental Quality
3.1.2.1 Federal Statutes
The Atomic Energy Act (AEA) of 1954, as amended [42 USC 2011, et seq.; 10 CFR 20,
39, 60, 61, 71, 100, 762, 835, 960, 962 and 40 CFR 190–192], authorizes the conduct of atomic
energy activities and governs the design, location, and operation of facilities (including Federal
facilities) involved with nuclear materials. DOE facilities are not required by the AEA to be
permitted or licensed but are required to comply with the act and its amendments.
The Pollution Prevention Act of 1990 declares a national policy to prevent pollution at the
source and to recycle pollution in an environmentally safe manner. The Act provides that the fol-
lowing hierarchical sequence of steps be taken in dealing with pollution: (1) pollution should be
prevented or reduced at the source whenever possible; (2) polluting materials should be recy-
cled in an environmentally safe manner whenever feasible; (3) polluting materials should be
treated in an environmentally safe manner; (4) disposal or other release to the environment is to
be employed only as a last resort and conducted in an environmentally safe manner.
The Clean Air Act, as amended [42 USC 7401 et seq. (40 CFR 50–80)], provides require-
ments to protect and enhance the quality of the nation’s air resources and to promote public
health and welfare. The act establishes National Ambient Air Quality Standards (NAAQS), Pre-
vention of Significant Deterioration (PSD) regulations, National Emission Standards for Haz-
ardous Air Pollutants (NESHAPS), and New Source Performance Standards (NSPS). The EPA
can delegate permitting and regulatory authority to a state. Delegation under the Clean Air Act
can take forms other than a State Implementation Plan (SIP).
The Water Pollution Control Act, amended by the Clean Water Act of 1977 (33 USC 1251
et seq.; 40 CFR 110, 116, 117, 121, 122, 124, 129, 230, 401, 403; 33 CFR 289, 320, 323, 327,
and 330), pertains to restoration and maintenance of the chemical, physical, and biological
integrity of the nation’s waters. Using minimum technology-based guidelines set by the Envi-
ronmental Protection Agency (EPA), states will issue National Pollutant Discharge Elimination
System (NPDES) permits to discharge wastes into U.S. waters; a NPDES permit is required for
discharges to waters of the United States. Fusion facilities must comply with applicable U.S.
Army Corps of Engineers dredge and fill regulations. Impacts to wetlands greater than 10 acres
require a permit from the U.S. Army Corps of Engineers. In addition, some states have more
stringent requirements pertaining to wetlands. It is recommended that an expert on water quality
be consulted for establishing the water quality requirements for the site in question.
16
DOE-STD-6003-96
Section 25
The Safe Drinking Water Act, as amended [42 USC 300(f–j) et seq.; 40 CFR 140–149],
establishes uniform Federal standards for drinking water quality. The EPA has the authority to
delegate enforcement of these standards to the states. This act sets two types of standards for
drinking water, primary and secondary. Primary standards are mandatory and apply to sub-
stances that may have adverse affects on health. Secondary standards are advisory and affect
color, smell, taste, or other physical characteristics of drinking water. This act also pertains to
groundwater aquifers, banning underground injection of certain materials in or near groundwater
recharge areas.
The Solid Waste Disposal Act, as amended by the Resource Conservation and Recovery
Act (RCRA) (42 USC 6901 et seq., 40 CFR 240–282 and 124), established a comprehensive
program for regulating and managing solid waste (Subtitle D), hazardous waste, including
radioactive mixed waste (Subtitle C), and underground storage tanks (Subtitle I), and for pro-
moting the use of recycled and recovered materials (Subtitle F).
The Toxic Substances Control Act (TSCA) (15 USC 2601 et seq.; 40 CFR 700–799) pro-
vides the regulatory vehicle for controlling exposure and use of raw industrial chemicals that fall
outside the jurisdiction of other environmental laws. TSCA assures that chemicals are evaluated
before use to ensure they pose no unnecessary risk to health or the environment. Fusion facility
personnel shall review proposed chemical use to assure that appropriate alternatives have been
evaluated. The management of PCBs is also regulated under TSCA. There are specific require-
ments for facilities that maintain transformers and other equipment containing PCB dielectric
fluid.
The Federal Facility Compliance Act waives sovereign immunity for fines and penalties
for RCRA violations at Federal facilities. However, the effective date of the waiver has been
delayed for mixed waste storage prohibition violations, as long as the Federal facility is in com-
pliance with all other applicable requirements of RCRA. During this period, DOE is required to
prepare plans for developing the required treatment capacity for mixed wastes stored or gener-
ated at each facility. Each plan must be approved by the host state or the EPA after consultation
with other affected states, and a consent order must be issued by the regulator requiring com-
pliance with the plan. The Federal Facility Compliance Act further provides that the DOE will not
be subject to fines and penalties for land disposal restriction storage prohibition violations for
mixed waste as long as it is in compliance with such an approved plan and consent order and
meets all other applicable regulations.
The Comprehensive Environmental Response, Compensation, and Liability Act
(CERCLA), as amended (42 USC §9601 ET SEQ.), provides a statutory framework for the
cleanup of waste sites containing hazardous substances and—as amended by the Superfund
Amendments and Reauthorization Act—provides an emergency response program in the event
of a release (or threat of a release) of a hazardous substance to the environment. Using the
Hazard Ranking System, Federal and private sites are ranked and may be included on the
National Priorities List. The Comprehensive Environmental Response, Compensation, and Lia-
bility Act, as amended, requires such Federal facilities having such sites to undertake investiga-
tions and remediation as necessary. The Act also includes requirements for reporting releases
of certain hazardous substances in excess of specified amounts to State and Federal agencies.
Section 26
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DOE-STD-6003-96
The Emergency Planning and Community Right-To-Know Act of 1986 (42 USC 10227;
40 CFR 350–372) was enacted as Title III of the Superfund Amendments and Reauthorization
Act (SARA). This act establishes requirements for emergency planning, spill reporting, haz-
ardous chemical inventory reporting, and toxic chemical release reporting. The act also provides
for the establishment of state and local emergency planning committees to prepare plans to
respond to potential chemical emergencies. A facility emergency coordinator must be desig-
nated, and a list or copies of Material Safety Data Sheets for hazardous substances at the site
must be submitted to the Local Emergency Planning Committee, the State Emergency
Response Commission, and the local fire department.
Reporting Requirements. An annual hazardous chemical inventory report
shall be submitted to the Local Emergency Planning Committee, the State Emer-
gency Response Commission, and local fire department. A Toxic Chemical
Release Form for specified toxic chemicals shall also be submitted annually. In
the event of a hazardous substance release, appropriate notifications of Federal,
state, and local authorities shall be made.
The Hazardous Materials Transportation Act (49 USC 180 et seq.; 49 CFR 171–178)
establishes requirements for the transportation of hazardous materials by road, air, and rail.
Packaging, labeling, marking, and shipping requirements are specified for quantities and forms
of substances that are designated as hazardous. Hazardous materials, including radioactive
materials and wastes, must be shipped from the fusion facility site in accordance with the appli-
cable U.S. Department of Transportation packaging, labeling, marking, and placarding
requirements.
Floodplain/Wetlands Executive Orders (EO 11988 & EO 11990; 10 CFR 1022) protect
wetlands and minimize adverse effects of development in floodplains. The proposed site for the
fusion facility must be evaluated to determine if it contains wetlands or floodplains. If floodplains/
wetlands do occur at the proposed site, a notice must be published in the Federal Register and
Federal, state, and local agencies notified of a proposed floodplain/wetlands assessment. This
assessment shall identify alternate measures to minimize harmful impacts to floodplains or wet-
lands due to activities. A statement of finding must be published for public record.
The Farmland Protection Policy Act (7 USC 4201 et seq.; 7 CFR 658) seeks to minimize
the extent to which Federal programs contribute to the unnecessary and irreversible conversion
of farmland to nonagricultural uses and assure that Federal programs are administered in a
manner that will be compatible with state and local government and private programs and
policies to protect farmland. The Soil Conservation Service must be requested to determine
whether the site or any part of the site is farmland by using site assessment criteria and the rela-
tive value of the site. If the evaluation results in a high score for the site, alternatives shall be
considered that could lessen adverse effects on the site as farmland.
The Archaeological Resources Protection Act of 1979 (16 USC 47000 et seq.; 43 CFR 7;
36 CFR 296) requires that a determination be made of the measures that shall be taken if
archaeological resources present on Federal land may be damaged during project-related activi-
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DOE-STD-6003-96
Section 27
ties. Archaeological resources are defined as any material remains of past human life or activi-
ties of archaeological interest.
The National Historic Preservation Act of 1966, as amended (16 USC 470 et seq.;
36 CFR 60 and 800; Historic Sites, Buildings and Antiquities Act; 16 USC 461 et seq.), endeav-
ors to preserve, maintain, and enrich irreplaceable cultural, educational, inspirational, and eco-
nomic history. A determination must be made if the project area contains any site, structure, or
object identified in, or eligible to be included, in the National Register of Historic Places and
determine if the proposed project will affect the site, structure, or object adversely. If the effect
would be adverse, the Advisory Council on Historic Preservation must be consulted to deter-
mine what actions should be taken.
The American Antiquities Act (16 USC 432 et seq.; 25 CFR 261; 36 CFR 296; and
43 CFR 3-7) protects historic and prehistoric ruins, monuments, and objects of antiquity on
lands owned and/or controlled by the Federal government. Additionally, the act stipulates that
the Federal government is to provide leadership in the preservation, restoration, and mainte-
nance of the historical cultural environment of the nation.
The American Indian Religious Freedom Act (AIRFA) (42 USC 1996; 36 CFR 296 and
43 CFR 7) protects and preserves for Native Americans their inherent right of freedom to
believe, express, and exercise their traditional religious rights guaranteed by the First Amend-
ment of the U.S. Constitution. This includes access to sites; use and possession of sacred
objects; and freedom to worship through ceremonial and traditional rites. A determination must
be made whether the project site is in an area related to Native American religious rites or is a
sacred site.
The Migratory Bird Treaty Act (16 USC 703 et seq.; 50 CFR 10) prohibits the killing, cap-
turing, transporting, etc., of migratory birds, their nests, and eggs, and any part of such bird,
nest, and egg.
The Fish and Wildlife Coordination Act (16 USC 661 et seq.) mandates that wildlife con-
servation receive equal consideration and coordination with other features of water resource
programs through planning, development, maintenance, and coordination of wildlife conserva-
tion and rehabilitation.
The Bald and Golden Eagles Protection Act (16 USC 668–668d; 50 CFR Parts 13 and
22) prohibits the killing, capturing, and transporting of any bald and golden eagles, living or
dead, their nests, and eggs, and any part of such a bird, nest, and egg.
The National Wildlife Refuge Systems Administration Act of 1966 (16 USC 668OD–
668EE; 50 CFR 25, 27, 28 and 29) establishes the National Wildlife Refuge System by consoli-
dating fish and wildlife conservation under the Fish and Wildlife Service (FWS). This will include
fish and wildlife in danger of extinction; wildlife ranges, game ranges, wildlife management
areas; or waterfowl production areas.
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DOE-STD-6003-96
The Endangered Species Act of 1973 (16 USC 1531 et seq.; 50 CFR 17, 222, 226, 227,
402, 424, 450, 451, 452, and 453) prohibits Federal agencies from taking any action that would
jeopardize the continued existence of any threatened or endangered species or result in the
destruction or adverse modification of critical habitat unless an exemption has been obtained.
Section 28
Objects Affecting Navigable Airspace (49 USC 1501; 14 CFR 77) requires that all persons
give adequate public notice of the construction or alteration, or the proposed construction or
alteration, of any structure that would be a hazard to air navigation, and regulates structures that
could obstruct air navigation. The Federal Aviation Administration (FAA) has the following pro-
cedures that must be followed: Notice of Proposed Construction, Construction Permit, and a
Notice of Progress of Construction or Alteration.
The Rivers and Harbors Appropriations Act of 1899 (33 USC 401–413, 06; 33 USC
33 CFR 209, 320, 325, 326, 329, and 330), the Bridge Act of 1949, and Construction and
Operation of Bridges Act of 1946 (33 USC 525; 33 CFR 114–115) prevent alteration or modifi-
cation of the course, location, current condition, or capacity of any navigable water in the United
States without a permit. “U.S. navigable waters” have been defined in a loose manner by regula-
tors. Dry lake beds, arroyos, and ditches have all been considered navigable waters. Bridge
construction is also regulated under this act. The U.S. Army Corps of Engineers has established
an integrated permitting process that allows a single permit application to be used for compli-
ance with regulated activities. A permit must be obtained from the U.S. Army Corps of
Engineers for any activity regulated under this act.
The Noise Control Act of 1972, as amended [42 USC 4901–4918 (EO 12088)] directs all
Federal agencies to carry out programs within their jurisdictions in a manner that furthers a
national policy of promoting an environment free from noise that jeopardizes health and welfare.
If the noise levels and/or emissions from a fusion facility would jeopardize the health or welfare
of the public in the area surrounding the site, a plan to minimize noise emissions must be pre-
pared. The plan may require a change in design parameters.
3.1.2.2 DOE Orders and Guidance
DOE Orders are internal department documents that set policy and specify procedures for
implementing that policy. They may apply to specific sites and facilities or to all areas of DOE
operations. In some cases, DOE Orders may mandate compliance with existing Federal, state,
and local regulations. Because specific DOE Orders may change or new Orders are issued, a
review of the latest DOE Orders should be conducted.
The General Environmental Protection Program (DOE Order 5400.1) establishes environ-
mental protection requirements, authorities, and responsibilities for DOE operations for ensuring
compliance with applicable federal, state, and local environmental protection laws and regula-
tions, executive orders, and internal DOE policies. This Order implements DOE policy, which
mandates that all operations be conducted in an environmentally safe and sound manner,
including protection of the public and the environment. DOE Order 5400.1 requires that DOE
operations be conducted in compliance with the letter and spirit of applicable environmental
statutes, regulations, and standards. This includes sound environmental management of current
20
DOE-STD-6003-96
activities, the correction of existing problems, the minimization of risks to the environment or
public health, and anticipating and addressing potential environmental problems before they
threaten the quality of the environment or public welfare. DOE Order 5400.1 describes the envi-
ronmental monitoring required to demonstrate compliance with environmental laws and
regulations.
Section 29
The Waste Minimization Crosscut Plan (SEN-37-92, March 13, 1992) was implemented
by the DOE Secretary of Energy in accordance with the Pollution Prevention Act of 1990. This
plan identifies key objectives and strategies for the Department’s achievement of excellence in
waste minimization.
The Environmental, Safety, and Health Appraisal Program (DOE Order 5482.1B) estab-
lishes the program to evaluate the protection of the environment and the health, and safety of
the public. This Order also establishes criteria for a safe and healthful work place for employees
of the DOE and the DOE contractors.
The Environmental Protection, Safety, and Health Protection Information Reporting
Requirements (DOE Order 5484.1) establish the requirements and procedures for the reporting
of information having environmental protection, safety, or health protection significance for DOE
Operations. The Order identifies accidents and incidents and provides instruction in the areas of
format and content of accident/incident investigation reports.
3.2 Federal and State Consultation, Permits, and Approvals
3.2.1 Federal Permits and Approvals
National Emission Standards for Hazardous Air Pollutants (NESHAPS) (40 CFR Part 61)
regulate substances that potentially will be emitted by fusion facilities, such as beryllium and
radionuclides. If the fusion facility will result in a predicted effective dose (ED) to a maximally
exposed member of the public equal to or greater than 1% of the standard for radionuclides [i.e.,
0.001 mSv/yr (0.1 mrem/yr)], a NESHAPS permit to construct (PTC) application must be
submitted prior to the initiation of construction to obtain the approval of the Regional
Administrator of the EPA. The EPA will provide notification of approval or intention to deny
approval of construction within 60 days after receipt of a complete application. After construction
of the fusion facility, the EPA must be notified of the anticipated date of initial start-up of the
source at least 30 days prior to that date and the actual date of initial start-up of the source
within 15 days after that date.
A Prevention of Significant Deterioration (PSD) of Air Quality review is required if the
emission rate of any criteria air pollutant (carbon monoxide, hydrocarbons, nitrogen oxides, total
suspended particulates, photochemical oxidants, sulfur oxides, and lead) from routine opera-
tions of a stationary source is greater than 250 tons/yr. If necessary, a new PSD permit applica-
tion or a modification to an existing permit must be submitted to the appropriate state agency
before construction of a fusion facility.
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DOE-STD-6003-96
According to the National Pollutant Discharge Elimination System (NPDES), states will
issue NPDES permits to discharge wastes into waters of the United States using minimum
technology-based guidelines set by the EPA. An NPDES permit for all discharges to waters of
the United States must be obtained. Fusion facilities shall comply with applicable U.S. Army
Corps of Engineers dredge and fill regulations. Impacts to wetlands greater than 10 acres will
require an additional permit from the U.S. Army Corps of Engineers.
Safe Drinking Water Act. If future fusion facilities affect existing or require new drinking
water systems, a permit to conduct monitoring must be obtained as required.
The Resource Conservation and Recovery Act (RCRA) was established to regulate solid
and hazardous wastes.
Section 30
a. Solid Waste. Subtitle D requires each state to prepare a solid waste management
plan to prohibit new open dumps and require upgrading or closing of all existing
dumps. Federal guidelines for solid waste collection, transport, separation, recovery,
and disposal practices have been promulgated.
b. Hazardous Waste. Under the land disposal restrictions (40 CFR 268) the generator of
hazardous waste must assure a system of manifesting, reporting, standards, and
permits to achieve control of hazardous waste from generation to final disposition.
These requirements apply to generators and transporters of hazardous waste and
owners and operators of hazardous waste treatment, storage, and disposal (TSD)
facilities. Reuse, reclamation, and recycling of hazardous waste is also subject to the
regulatory program.
Under the land disposal restrictions (40 CFR 268) waste generators must assure that the
waste is treated prior to ultimate disposal to the land. Specific requirements have been estab-
lished by the EPA, usually requiring treatment to a particular contaminant concentration, but
occasionally requiring a specific treatment method.
There are also extensive regulations for the various processes or techniques by which
hazardous wastes may be managed. These detailed standards include requirements for the
proper management of containers, tank systems, surface impoundments, waste piles, land
treatment, landfills, incinerators, and miscellaneous units (those not covered by the specifically
identified techniques). State regulations may be more extensive than the Federal system and
must be reviewed for applicability.
The operation of the fusion facilities may require preparation of a new RCRA Part A or
Part B permit application, a change in existing interim status, or a modification to an existing
permit, depending on site location.
1. Underground storage tanks. All new underground storage tanks must be permitted
prior to installation. Any person proposing to install a tank must file a notification prior
to installation and prior to operation. The underground tank rules in RCRA Subtitle I
22
DOE-STD-6003-96
cover any substance defined as hazardous under CERCLA (Superfund) and includes
underground tanks containing petroleum products.
2. Federal procurement guidelines. The EPA has established and published Federal
guidelines for several materials: building installation products containing recovered
materials; cement and concrete containing fly ash; paper and paper products contain-
ing recovered material; lubricating oils containing re-refined oil; and retreaded tires.
Particular attention should be paid to the cement and concrete guideline as it may
apply to the construction phase of the program. Major procurement actions for ser-
vices and materials for the fusion facilities should include specifications for the use of
recycled and recovered materials.
The Fish and Wildlife Coordination Act and National Wildlife Refuge Systems Administra-
tion Act Permit Requirements include consultation with the FWS concerning project activities
that (1) may conflict with the protection and conservation purposes set by the National Wildlife
Refuge System (a permit may also be required); (2) may impact birds, especially migratory birds
on the site; and (3) may modify, control, or impound, due to construction activities, a body of
water greater than or equal to 10 acres. The State Administrator of wildlife resources must also
be consulted for (2) and (3).
Section 31
In the Bald and Golden Eagles Protection Act, a Federal Fish and Wildlife License Permit
is required if upon investigation of the proposed site, a golden eagle’s nest is found and must be
disturbed. A Federal Fish and Wildlife License Permit Application shall be submitted to the
Assistant Regional Director for Law Enforcement of the district in which the site is located. If a
permit is granted, the Director of Law Enforcement of the district in which the site is located shall
be notified in writing at least 10 days, but no more than 30 days, before any golden eagle nest is
taken. Any mitigation measures determined by the Director shall be complied with and a report
of activities conducted under the permit shall be submitted to the Director within 10 days follow-
ing the permit’s expiration.
The Archaeological Resources Protection and National Historic Preservation Acts require
consultation with the Advisory Council on Historic Preservation if a proposed project will impact
a site with historic/prehistoric ruins, monument, or object of antiquity, or a site on the National
Register of Historic Places.
The AIRFA provides the following guidance. If a project site falls into the category of a
Native American religious or sacred site, consultation is required with Native American leaders
to determine if the proposed action would infringe on constitutional rights or impact Native
American traditional religions.
3.2.2 State and Local Permits and Approvals
Specific state and local permitting and approval requirements may vary by location; how-
ever, general guidance is provided in the following sections.
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3.2.2.1 Air
Most states have been granted the authority by EPA to implement some, if not all, of the
requirements of the Clean Air Act.
a. Permit to Construct (PTC). Applications for a PTC and an Operating Permit for the
proposed facility should be submitted to the state 15 to 18 months prior to commence-
ment of construction. Generally (although this may vary from state to state), the state
will notify the applicant within 30 days whether the application for PTC or operating
permit is complete and within 60 days will issue a proposed approval, proposed con-
ditional approval, or proposed denial, with an opportunity for public comments to
follow.
b. NESHAP Analysis. A NESHAP analysis is generally submitted to the state along with
the PTC application. State review of the PTC application does not occur until the EPA
approves the NESHAP document. Data collection (ambient air and engineering data)
for the analysis typically takes 1 yr, and preparation of the analysis about 6 months.
3.2.2.2 Archaeological Finds
If archaeological resources are determined to be endangered by a project-related activity,
application for a permit from the jurisdictional land manager to remove or excavate an archaeo-
logical site must be submitted. Activities are coordinated with the State Historic Preservation
Office (SHIPO). The DOE must be qualified to do the permitted removal or excavation. Archaeo-
logical resources excavated or removed remain the property of the United States. The remains
and the copies of records and data must be archived by a suitable institution.
3.2.2.3 Other State Requirements
Other state requirements will likely include water quality standards and wastewater treat-
ment requirements, solid and hazardous waste requirements, and special provisions for wildlife.
These vary by state and will have to be developed when specific fusion facility sites are
selected.
Section 32
3.3 Environmental Compliance Procedures and Scheduling
3.3.1 Environmental Documentation Guidelines
3.3.1.1 NEPA Compliance Plan
Specific environmental mitigation commitments identified in fusion facility NEPA docu-
ments are incorporated into the design and operation of the facility through an approved Mitiga-
tion Action Plan (MAP). The MAP describes how mitigation of adverse environmental conse-
quences will be implemented and monitored to assure effectiveness. The implementation of the
MAP will be the responsibility of the design, construction and operating organizations. The plan
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a. details Program Manager quarterly reporting requirements,
b. documents progress in implementation of mitigation measures required by the MAP,
c. determines whether the measures are adequately reducing or eliminating adverse
environmental impacts,
d. establishes procedures that prepare NEPA review and approval prior to implementa-
tion for unforeseen activities not addressed in the fusion facility EIS, and
e. is updated as required to accommodate changes to the MAP from unforeseen
activities.
3.3.1.2 Environmental Compliance Plan
Each fusion facility will develop an Environmental Compliance Plan that describes the
method by which a particular fusion facility complies with applicable environmental regulatory
requirements. This includes addressing Federal, state, and local environmental statutes. While
this guidance document provides a compilation of environmental requirements potentially appli-
cable to fusion facilities, the Environmental Compliance Plan provides guidance on how the
program managers can meet those requirements.
The Plan describes the program’s understanding of environmental requirements for the
preconstruction and construction phases of the fusion facility. The Plan is updated periodically to
reflect results of periodic consultation with the appropriate Federal and state agencies and
affected Indian tribes.
The Environmental Compliance Plan consists of five separate sections: Permits Require-
ments, Monitoring Requirements (Chapter IV of DOE Order 5400.1), Pollution Prevention
Requirements, Training Requirements, and Site Unique Requirements.
3.3.1.3 OSHA Compliance Plan
The Occupational Safety and Health Administration (OSHA) has instituted a series of
requirements that establish a level of safety and safety assurance. These requirements, those
promulgated by state and local regulators, and internal DOE requirements published in DOE
Orders must be followed. The OSHA program encompasses the protection of workers, the
public, and property from the hazards associated with the construction, operation and mainte-
nance, and decommissioning of a facility.
The program incorporates four separate disciplines: industrial safety, industrial hygiene,
fire protection, and radiation protection. Additionally, the program requires that emergency pro-
cedures are in place to mitigate the impact of accidents that threaten the health and safety of
the facility occupants, personnel in the immediate areas surrounding the facility, or the public.
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3.3.2 Environmental Compliance Scheduling
Environmental review planning is an integral part of “phased compliance,” that is, a com-
prehensive, integrated environmental compliance strategy (DOE Order 4700.1); a sample
schedule is shown in Fig. 3.1. The strategy is characterized by
a. conducting the environmental evaluations and consultative environmental reviews
during the conceptual or preliminary design phase,
Section 33
b. completing the NEPA documentation process prior to commencement of full detailed
design, and
c. submitting permit applications and coordinating permit reviews with the detailed
design phase.
Delayed compliance can result when inadequate attention is given to environmental
requirements early in the design phase. In many instances, the permitting authority will not
begin review of permit applications until at least a draft NEPA document has been circulated.
Delay of the NEPA document, therefore, can delay start of construction and make the NEPA
document and other environmental review processes critical path items.
26
FIGURE 3.1. Phased schedule for environmental compliance activities.
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4. PROGRAM MANAGEMENT FOR SAFETY
Appropriate management practices and controls should be integrated into the fusion pro-
ject life cycle to ensure safety. This integration function is key to ensuring that safety is “built-in”
to the fusion facility life cycle process rather than an “add-on,” which is typically expensive and
less effective. Related to this goal is the concept of making safety achievement a function of line
management with criteria and hardware related to safety incorporated at the lowest practical
level of the work breakdown structure. This section provides guidance on management-related
areas needed to integrate safety into the fusion facility life cycle. Program management includes
controlling the configuration of the facility and the documentation of that configuration so that
operation within the authorized safety envelope can be demonstrated. In addition, this section
presents tools (processes, systems, and controls) that can be used by program management to
implement safety effectively. As used in this section, the facility life cycle includes design and
construction, operations, and site restoration. Different organizations may be responsible for the
various life cycle phases of the facility. Each organization must be aware of the need of the
other organization and incorporate these needs in a safe and controlled manner.
4.1 Design and Construction Management
From project inception appropriate controls should be integrated into project execution to
ensure that intended safety features are incorporated into the fusion facility. Safety should be
integrated into project activities, including initial mission and performance criteria definition,
design, and construction. A specific responsibility of project management is to ensure that this
integration of safety with other project activities or disciplines takes place and to hold project line
management accountable for each aspect of their assigned systems, including safety perfor-
mance. The basic facility mission requirements, including protection of the facility workers and
the public as well as minimization of the impact to the environment, should be established
before design commences. For example, the no-public-evacuation requirement in DOE-STD-
6002-96 should be a strong driver in fusion device size (power) and materials selection to
ensure that the potentially releasable in-vessel tritium and hazardous material inventories are
consistent with the no-evacuation requirement for the chosen site.
Section 34
Safety assessment (Chapter 5) and design (Chapter 6) are complementary activities that
should be performed iteratively throughout the design process to ensure that safety require-
ments are adequately incorporated into the design. Achievement of safety criteria and goals at
an individual system level should be a documented part of conceptual, preliminary, and final
design and should be evaluated as part of the formal design review process. Additionally, a sys-
tems integration approach should be used to evaluate interactions between individual systems
including common-mode failures to ensure that safety goals are met globally.
The project manager’s responsibilities include developing systems, processes, and orga-
nizational structures that will facilitate safety during design and construction. The project man-
ager should consider an organizational structure that will allow the safety and design profes-
sionals to work as a team and that will make line management responsible for both safety and
performance requirements for each system. Furthermore, there will be cases where safety
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requirements will conflict with other design requirements for the facility. The project manage-
ment system should have a process that will allow potential cost/safety/performance trade-offs
to be made in a structured rational manner.
4.2 Operations Management
Operations management should ensure that the operations organization is knowledgeable
of the safety envelope and authorization basis and the need to maintain the facility configuration
and operation within these constraints. Proposed changes to facility configuration and operation
should be reviewed against the safety envelope and authorization basis and approved prior to
implementation. The operations manager may call upon safety professionals for analytical
support, but the responsibility and authority for safe operations remains with the line man-
agement of the facility. The operations manager should establish a policy under which clear
lines of responsibility for normal operations and off-normal conditions are established. Chapter 5
of this volume provides the details of the authorization basis and technical safety requirements.
4.3 Site Restoration Management
Site restoration involves the dismantling of the fusion facility and the packaging of
radioactive hazardous materials prior to shipment to a repository or recycling center. Manage-
ment of the fusion facility during the site restoration phase requires maintaining configuration
control while the condition of the facility is rapidly evolving. The safety analyses may have to be
updated as safety and confinement systems are removed from service. Documentation of the
condition of components and their hazardous inventories as they are packaged is necessary.
Removal of hazardous materials from the site may allow some relaxation of controls as the on-
site inventory is reduced.
4.4 Tools for Program Management Safety
The following sections describe tools that can be used during the design, operations, and
site restoration of a fusion facility. These tools include configuration management, quality assur-
ance (QA), verification and validation, conduct of operations, emergency preparedness, mainte-
nance, training and qualification, tritium control, accountability and physical protection. These
tools, if used effectively, will help assure the safety of the fusion facility.
4.4.1 Configuration Management
Section 35
Configuration management is a tool that is designed to determine and control baselines
and ensure that each system/component properly interfaces physically and functionally. The
role of safety in configuration management is to ensure that the original product and each
approved change to the product do not jeopardize the safety of the product. Configuration man-
agement actions are called for in Department of Energy (DOE) Order 4700.1, Project Manage-
ment Plan.
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4.4.1.1 Configuration Management Process Application
Configuration management should be consistent with the quality, size, scope, and com-
plexity of the project involved (graded approach). The configuration management process
should be tailored to the specific project and to particular products. The selection of equipment
and other items for formal configuration management is determined by the need to control its
inherent characteristics or to control its interface with other systems. Configuration control
applies to hardware, software, and documentation associated with the facility.
A permanent copy of the controlled identification documents should be maintained
throughout the life cycle, beginning with the initial baseline documentation and including pro-
posed and approved changes from those baselines.
Configuration control must be exercised on a basis appropriate to the level of importance
and to the stage in the life cycle. Affected project activities, such as engineering, logistic sup-
port, QA, safety, maintenance, and procurement need to be involved in evaluating proposed
changes in the configuration of an item throughout its life cycle. This would normally be
accomplished through a Configuration Control Board.
4.4.1.2 Change Control
Changes affecting the configuration of an item are to be limited to those that are neces-
sary or offer significant benefits. Changes are required to correct deficiencies; incorporate
approved changes in experimental, operational or logistic support characteristics; or effect sub-
stantial life cycle cost savings.
Each change must be evaluated for Unreviewed Safety Questions (USQ). The process of
reviewing for USQs is described in Chapter 5.
Data required for effective evaluation of changes must be made available to those indi-
viduals responsible for change decisions. Every proposed configuration change should be eval-
uated on the basis of change criteria, including not making the proposed change. The evalua-
tion should take into consideration each aspect of the change on the products or systems with
which it interfaces. Such aspects may include safety, design, performance, cost, schedule,
operational effectiveness, logistics support, transportability, and training.
As changes are authorized, appropriate updates to safety envelopes, authorization basis
and operating procedures must occur. This approach assures that operations personnel know
the plant configuration and its operating limits.
4.4.1.3 Record Keeping and Reporting
Configuration records and reports include identification of the following:
a. technical documentation (drawings, calculations, specifications, etc.) comprising the
approved configuration identification;
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b. proposed changes to configuration, the status of such changes, and the individual
responsible for change decisions;
c. approved changes to configuration, including the specific number or kind of items to
which the changes apply, and the activity responsible for implementation.
Section 36
Only the minimum information necessary to manage configuration effectively and eco-
nomically will be recorded and reported.
4.4.2 Quality Assurance
A quality assurance (QA) process shall be considered in the design, selection of materi-
als, specifications, fabrication, construction, installation, operating procedures, maintenance,
and testing of fusion facilities. The requirements of 10 CFR 830.120 shall be used for develop-
ment of this program.
A Quality Assurance Plan (QAP) is developed by applying the QA criteria specified in
Sections 4.4.2.1–4.4.2.3 using a graded approach. The QAP discusses how these criteria are
satisfied. Appropriate standards are used, wherever applicable, to develop and implement the
QAP.
4.4.2.1 Management
A written QAP must be developed, implemented, and maintained. The QAP will describe
the organizational structure, functional responsibilities, levels of authority, and interfaces for
those managing, performing, and assessing the work, as well as management processes,
including planning, scheduling, and resource considerations (cf. Sections 4.1–4.4).
Personnel must be trained and qualified to ensure that they are capable of performing
their assigned work. Continuing training is provided to ensure that job proficiency is maintained
(cf. Section 4.4.7).
Processes to detect and prevent quality problems must be established and implemented.
Items, services, and processes that do not meet established requirements are identified, con-
trolled, and corrected according to the importance of the problem and the work affected. Correc-
tion includes identifying the causes of problems and working to prevent recurrence. Item charac-
teristics, process implementation, and other quality-related information are reviewed, and the
data are analyzed to identify items, services, and processes needing improvement.
Documents must be prepared, reviewed, approved, issued, used, and revised to pre-
scribe processes, specify requirements, or establish design. Records are specified, prepared,
reviewed, approved, and maintained (cf. Section 4.4.1).
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4.4.2.2 Performance
Work will be performed to established technical standards and administrative controls
using approved instructions, procedures, or other appropriate means. Items are identified and
controlled to ensure their proper use and maintained to prevent their damage, loss, or deteriora-
tion. Equipment used for process monitoring or data collection is calibrated and maintained
(cf. Section 4.4.1).
Items and processes must be designed using sound engineering/scientific principles and
appropriate standards. Design work, including changes, incorporates applicable requirements
and design bases. Design interfaces are identified and controlled. The adequacy of design pro-
ducts is verified or validated by individuals or groups other than those who performed the work.
Verification and validation work must be completed before approval and implementation of the
design (cf. Chapter 6).
Procured items and services must meet established requirements and perform as speci-
fied. Prospective suppliers are evaluated and selected on the basis of specified criteria. Pro-
cesses to ensure that approved suppliers continue to provide acceptable items and services
must be established and implemented (cf. Section 4.4.1).
Inspection and testing of specified items, services, and processes must be conducted
using established acceptance and performance criteria. Equipment used for inspections and
tests must be calibrated and maintained (cf. Section 4.4.1).
Section 37
4.4.2.3 Assessment
Managers must assess their management processes and identify and correct problems
that hinder the organization from achieving its objectives.
Independent assessments are planned and conducted to measure item and service
quality, to measure the adequacy of work performance, and to promote improvement. The group
performing independent assessments must have sufficient authority and freedom from the line
to carry out its responsibilities. Persons conducting independent assessments must be
technically qualified and knowledgeable in the areas assessed.
4.4.3 Verification and Validation
Computer codes used to perform design and safety analysis for fusion facilities may be
required to be verified and validated (V&V). Verification and validation will be performed using a
graded approach that is based on the importance and complexity of the system/component.
V&V actions are not specifically defined in DOE Orders.
The QA plan documents the functional requirements for each piece of software, the
acceptance criteria to be used in the V&V process, the approach to be taken to verification and
validation, and the software configuration control strategy that will be used. The results of the
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V&V process should be documented. Documentation should be prepared to manage the config-
uration control of the software itself.
Many of the standards and requirements used to verify and validate computer codes were
developed for commercial nuclear power plants. Guidance information is embodied in ASME
NQA-1 and ASME NQA-2 standards, as well as several American National Standards Institute
(ANSI)/Institute of Electrical and Electronic Engineers (IEEE) Standards (ANSI/IEEE STD 730,
828, 829, 830, 983, and 1012).
Verification is defined as the process of determining whether the software is coded cor-
rectly and conforms to the specified software requirements. Full verification would require a line-
by-line check of the entire computer code to ensure correctness. However, other less stringent
methods are considered applicable, such as developing a series of calculational cases or input
decks that test much of the logic in the code to ensure that the code performs as stated in the
users' manual. As a general rule, design and safety analysis should be verified because it is
good engineering practice.
Validation is defined as the process of evaluating software to ensure compliance with
software requirements and physical applicability to the process being modeled on the hardware
being used. Validation is generally more involved than verification. Validation of a code consists
of comparing its output with known analytical solutions for problems similar, yet perhaps simpler,
than the problem at hand. Validation also includes benchmarking the code against relevant
experimental data, thus ensuring that the analysis reasonably captures the correct physics and
chemistry. Validation can also include comparison with an existing, already validated, computer
code.
The number and type of benchmarking problems needed to validate a computer code are
functions of the complexity of the phenomena being modeled, the codes range of applicability,
and the data that are or could be available. For a complicated computer code, verification could
require that individual models and submodels in the code be V&V using separate-effects data
and that integral validation of the code also be performed. These issues are functions of the
specific technical areas and need to be considered in the respective V&V processes.
Section 38
Due to the current experimental nature of fusion devices, it may not be possible to com-
pletely verify and validate a code. In such cases, other options should be explored to assure
safety of the facility. These options may include but are not limited to the use of test coupons to
be evaluated after specific periods of operation and qualification of materials/equipment using
deuterium-deuterium operations before using tritium as a fuel.
4.4.4 Conduct of Operations
Experience has shown that the better operating facilities have well-defined, effectively
administered policies and programs to govern the activities of the operating organization, includ-
ing the areas described by these guidelines. The guidance is based upon well-developed indus-
trial operations practices. They are written to be flexible, so that they encompass the range of
facilities and operations.
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Each fusion facility should develop a conduct of operations program in accordance with
DOE Order 5480.19, Conduct of Operations, using a graded approach. Specifics for each of the
sections can be found in the references for this chapter.
Fusion facilities should have a policy that assures operations are managed, organized,
and conducted in a manner to assure an acceptable level of safety and operators have proce-
dures in place to control the conduct of their operations.
The following areas should be addressed by the conduct of operations program: Opera-
tions Organization and Administration; Shift Routines and Operating Practices; Control Area
Activities; Communications; Control of On-Shift Training; Investigation of Abnormal Events;
Notifications; Control of Equipment and System Status; Lockouts and Tagouts; Independent
Verification; Logkeeping; Operations Turnover; Operations Aspects of Facility Chemistry and
Unique Processes; Required Reading; Timely Orders to Operators; Operations Procedures;
Operator Aid Postings; Equipment and Pipe Labeling.
4.4.5 Emergency Preparedness
Fusion facilities should develop an emergency management program, using a graded
approach, consistent with the determined level of risk at the facility. The requirements for
emergency preparedness at DOE facilities are specified in DOE Order 151.1, Comprehensive
Emergency Management. Appendix C provides a listing of guidance documents that may be
useful in developing the site-specific emergency management program.
The Emergency Management System (EMS) should include a graded approach to
emergency management concepts such as planning, preparedness, and response. “Planning”
includes the development and preparation of emergency plans and procedures and the identifi-
cation of necessary personnel and resources to provide an effective response. “Preparedness”
includes the training of personnel, acquisition and maintenance of resources, and exercising of
the plans, procedures, personnel, and resources essential for emergency response. “Response”
represents the implementation of planning and preparedness during an emergency and involves
the effective decisions, actions, and application of resources that must be accomplished to miti-
gate consequences and recover from an emergency.
4.4.5.1 Operational Emergency Event Classes
Section 39
Operational emergencies involving hazardous materials (radiological and nonradiological)
should be classified as one of the operational emergency classes (e.g., Alert, Site Area Emer-
gency, or General Emergency). Emergency Action Levels (EALs), the specific criteria used to
recognize and categorize events, should be developed for the spectrum of potential operational
emergencies consistent with the hazards assessment. The need for some emergency levels will
be eliminated for radiological emergencies if the site boundary dose limit specified as a fusion
radiological release requirement in DOE-STD-6002-96 is met.
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4.4.5.2 Emergency Plans and Procedures
An emergency plan and procedures should be developed for the facility. The plan is a
documented “concept of operation” that describes the essential elements that have been con-
sidered and the provisions that have been made to mitigate emergency situations. The plan
should incorporate information about the emergency response roles of supporting organizations
and agencies and should be consistent with a graded approach to managing an incident. Pro-
grams should contain emergency implementing procedures [e.g., EALs, event categorization,
notification, and Emergency Operations Center (EOC) operation] as well as other procedures
currently in use (e.g., equipment operation, radiological monitoring, and maintenance) that
would be utilized in, or associated with, emergency response activities.
Procedures must maintain consistency with the general graded approach and nomencla-
ture of emergency planning and preparedness elements within Federal and State agencies, pri-
vate industry, tribal, and local authorities.
4.4.5.3 Hazards Assessment
Hazards assessments provide the technical basis for emergency management programs.
The extent of emergency planning and preparedness required for a particular facility directly
corresponds to the type and scope of hazards present and the potential consequences of off-
normal events. A hazards assessment includes identification of any hazards and targets unique
to a facility, analyses of potential events, and evaluation of potential event consequences. The
Final Safety Analysis Report (see Chapter 5) provides for potential off-normal events at the
facility.
Methodology, models, and evaluation techniques used in the hazards assessment should
be documented. The assessment should include a determination of the size of the Emergency
Planning Zones where applicable, that is, the area surrounding the facility for which special
planning and preparedness efforts are required to ensure that prompt and effective protective
actions can be taken to minimize the risk to workers, the general public, and the environment.
Other hazards assessments are documented in Material Safety Data Sheets; Safety
Assessments; Spill Prevention, Control, and Countermeasure Plans; Pre-Fire Plans; Environ-
mental Assessments and Impact Statements (EAs and EISs); Emergency Response Planning
Guidelines; Severe Accident Analyses; and the Emergency and Hazardous Chemical Inventory
Forms and Toxic Chemical Release Forms, prepared pursuant to the requirements of the
Emergency Planning and Community Right-to-Know Act (SARA Title III).
4.4.5.4 Emergency Response Organization
An emergency response organization should have overall responsibility for the initial and
ongoing response to, and mitigation of, an emergency, and must perform, but not be limited to,
the following functions:
Section 40
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DOE-STD-6003-96
a. Provide for prompt initial notification of emergency response personnel and response
organizations, including appropriate off-site elements and for continuing effective
communication among the response organizations throughout an emergency.
b. Event categorization, determination of the emergency class, notification, provision of
protective action recommendations, management and decision making, control of
on-site emergency activities, consequence assessment, medical support, public
information, activation and coordination of on-site response resources, security,
communications, administrative support, recovery operations, and coordination and
liaison with off-site support and response organizations.
4.4.5.5 Emergency Facilities Equipment and Personnel Preparedness
An EOC should be established. The staffing, operation, and response activities pertaining
to the EOC should be predetermined and documented. Primary and backup means of commu-
nications should be available in the EOC.
Training must be provided to affected workers regarding operational emergencies and be
available to off-site emergency response organizations. Training should be provided annually to
workers who may have to take protective actions (e.g., assembly, evacuation) in the event of an
emergency. Training should be in place for the instruction and qualification of personnel com-
prising the facility emergency response organization.
A coordinated program of drills and exercises should be an integral part of the emergency
management program. Drills should be used to develop and maintain personnel skills, expertise,
and response capability. Drills should be of sufficient scope and frequency to ensure adequate
response capability. A full participation exercise should be conducted annually in accordance
with established plans and implementing procedures. Off-site response organizations should be
invited to participate in site-wide exercises at least every 3 years. A critique process should be
conducted for each exercise to provide accomplishments and shortcomings discovered during
the exercise.
4.4.6 Maintenance
Safe operation of a fusion facility is directly dependent on the scope, depth, and quality of
the facilities maintenance program. Formal maintenance programs lead to increased effective-
ness and safety benefits.
Maintenance at fusion facilities is the aggregate of those planned and systematic actions
required to prevent the degradation or failure of, and to promptly restore the intended function of
structures, systems, and components (SSCs). This applies to each part of the plant that could
significantly impact safe operation. The basis for this is the fundamental principle of defense
in-depth. Primary emphasis should be on the success of the maintenance program to prevent
the degradation or failure of, and to promptly restore the intended function of, those SSCs.
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DOE-STD-6003-96
Fusion facilities present unique situations for maintenance programs. As an example, a
program to control magnetic tools and materials around the tokamak is necessary to prevent
unexpected missiles during machine operations (due to magnetic fields). In addition, remote
maintenance will be used on some components. These actions add a complexity to the program
that must be controlled to assure safety.
Requirements for maintenance for DOE facilities are specified in DOE Order 430.1, Life
Cycle Asset Management. The reference section for Chapter 4 provides a listing of guidance
documents that may be helpful in developing the site specific maintenance program.
Section 41
4.4.6.1 Maintenance Policy, Goals and Objectives, and Procedures
Effective implementation and control of maintenance should be achieved by establishing
written standards for the scope, objectives, and conduct of maintenance; by defining responsi-
bilities; and by periodically observing and assessing performance commensurate with impor-
tance to safety.
The policies, goals, and objectives should address planning to establish a proactive main-
tenance program as opposed to reactive maintenance and to ensure that the maintenance activ-
ities for SSCs are consistent with their importance and function.
Goals for maintenance should be established in those areas that have the potential for
significant impact on plant safety. The goals should be directed toward improving or sustaining
equipment reliability and performance by effective maintenance in areas key to plant safety and
risk.
Procedures should be established and utilized as necessary for the conduct of mainte-
nance activities commensurate with the activities importance to safety. The maintenance proce-
dures should provide systematic guidance to the craftsman; should be technically correct, com-
plete, and up-to date; and should be presented utilizing sound human factors principles.
Radiological exposure control during maintenance activities should be considered in
developing procedures and work orders and in planning and scheduling maintenance. Health
physics personnel should be involved in the planning and execution of appropriate maintenance
work to ensure that personnel are not unnecessarily exposed and as-low-as-reasonably-
achievable (ALARA) goals are met.
4.4.6.2 Plant Maintenance Organization
The management of maintenance should include a defined maintenance organization
with specific lines of authority, responsibility, and accountability. The management of mainte-
nance requires effective written and oral communication between the maintenance department
and other supporting groups such as operations, health physics, and engineering. Criteria for
selecting personnel with acceptable qualifications to perform their assignments are necessary
for effective staffing. The personnel qualification and training requirements should be specified.
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4.4.6.3 Types of Maintenance
The maintenance program should include surveillance to obtain in-service performance
and operational data; predictive maintenance to analyze data collected from surveillance; pre-
ventive maintenance based on manufacturer’s recommendations, operating experience, good
engineering practice (including aging concerns), and predictive maintenance feedback; and cor-
rective maintenance, as necessary. The maintenance program should ensure that recommen-
dations and information from industry and individual vendors are reviewed and considered for
incorporation into appropriate areas of the program.
4.4.6.4 Work Control Process
Section 42
The work control process should be based on procedures that provide for the identifica-
tion of deficiencies, planning and preparation for work, setting appropriate conditions for work,
work procedures, supervisory authority, documentation of completed work, postmaintenance
testing, return-to-service procedures, and review of completed work packages. The work control
process begins with the identification of deficiencies or the need for planned or predictive main-
tenance and the generation of a maintenance request. Planning and scheduling activities should
then be performed. The work package should specify the appropriate plant conditions for the
work; define the required isolation or tagouts and component deenergization; incorporate appro-
priate QA, quality control (QC) functions, and ALARA considerations; and require appropriate
supervisory authorization prior to starting work. The work package should contain postmainte-
nance testing requirements and clearances or return-to-service procedures, provide for docu-
mentation of completed work, and provide for a review of the completed package. The post-
maintenance testing program should establish specific performance acceptance criteria that
ensure a high level of confidence in the ability of the component to perform its design function
when returned to service.
Process indicators, which provide information regarding the effectiveness of execution
of the elements of the maintenance program, should be monitored to provide insight regarding
potential problem areas in the conduct of maintenance activities. Examples are postmainte-
nance test results, periodic surveillance test results, ratio of preventive to corrective mainte-
nance, maintenance work order backlog, time to restore component function after failure dis-
cover, and frequency of rework.
4.4.7 Training and Qualifications
The responsibilities and authority for training and certification must be specific, and
appropriate plans and procedures must be developed and implemented. Each fusion facility
should be responsible for the following:
a. Develop and implement a training and qualification program using a graded approach
based upon the hazards of the facility.
b. Prepare, approve, and implement a training plan that sets forth the staffing, training,
and qualification requirements.
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DOE-STD-6003-96
c. Establish an organization that is responsible for the training and qualification of facility
personnel. The duties, responsibilities, qualifications, and authority of training organi-
zation personnel should be documented and clearly defined.
d. Establish training and qualification criteria for contracted personnel used in facility
organizations.
Training and qualification requirements for DOE nuclear facilities are specified in DOE
Order 5480.20, Personnel Selection, Qualification, Training, and Staffing Requirements at DOE
Reactor and Non-Reactor Nuclear Facilities. The reference section for Chapter 4 provides a
listing of guidance documents that may be useful in developing the site-specific training and
qualification programs.
4.4.7.1 Facility Training Plan
The facility training plan is the document that provides the overall description of facility
staffing, training, qualification, and certification programs. This plan should be prepared to
address the following:
a. initial and continuing training programs, including maintenance of training;
b. training and qualification programs for personnel who require formal qualification and
certification; and
Section 43
c. examination program requirements for qualification and certification.
The facility training plan should be supplemented, as needed, with written procedures that
address, as a minimum: examination and operational evaluation development, approval, secu-
rity, administration, and maintenance; administration of medical requirements; and record
keeping requirements.
4.4.7.2 Personnel Selection and Staffing
Each facility should establish a process for the selection and assignment of personnel.
The personnel selection process should include an evaluation of their education, experience,
previous training, and existing job skills and capabilities. It is the responsibility of management
to assure that personnel assigned to a specific job function have the requisite background
and/or receive sufficient qualification training for the job.
The following categories of facility staff are identified as requiring training, qualification, or
certification to perform job functions:
a. operators and their supervisors,
b. experimenters,
40
DOE-STD-6003-96
c. technicians—training,
d. maintenance personnel—training,
e. supervisors and managers—training,
f. operations and facility support functions.
Specific requirements for certifying, qualifying, and training personnel are specified in the
Order and general guidance documentation.
4.4.7.3 Records
The program and procedures should specify the records used to document the training,
qualification, and certification granted. Records should be documented and include the following
types of information:
a. records of education and experience, including resumes;
b. results of medical examinations (when required);
c. records of training completed, such as attendance sheets or computer summaries;
d. results of examinations, including written examinations and operational evaluations
(when required); and
e. approvals and effective dates, if applicable.
4.4.8 Tritium Control, Accountability, and Physical Protection
The purposes of requirements placed on tritium control, accountability, and physical pro-
tection at fusion facilities are to
a. meet legal requirements for environmental releases, waste disposal, and transporta-
tion of tritium;
b. prevent the diversion of the material for unauthorized use;
c. gain knowledge of the process efficiency, that is, how much tritium is produced and
used in processes under investigation;
d. meet the requirements of the DOE Orders for DOE fusion facilities;
e. assure operational safety of the facilities by providing knowledge of the location and
form of tritium;
41
DOE-STD-6003-96
f. prevent unwanted buildup of tritium within a facility; and
g. protect and control tritium commensurate with its monetary value.
It is difficult to determine the distribution and precise inventory of tritium in a fusion facility.
Usually, measurement before injection into the plasma chamber and after removal from the
plasma chamber is possible (referred to as inventory by difference). However, tritium production
in the machine is also possible. Therefore, the actual amount of tritium remaining in the machine
is difficult to determine (this can affect the safety analysis, because there is usually an upper
bound on the amount of tritium allowed in the vessel). Sampling tiles or protective surfaces
maybe a way of determining the tritium levels; however, those samples may or may not be
representative of the tritium levels throughout the vacuum vessel.
Section 44
It is therefore critical that the designers of the facility determine appropriate means to
reliably measure tritium in the fusion facility. This should be done early in the design process to
minimize tritium holdup, allow for pumping and purging systems to evacuate the tritium, and
specify appropriate instrumentation for measurement. These actions will assure safety of the
facility, reduce the risk of a release and improve worker safety. Methods for measurement of
tritium are specified in later paragraphs.
Tritium is the predominant nuclear material used at fusion facilities. It is of interest
because of safety concerns, its monetary value, and possible unauthorized diversion for other
applications. Although public exposures and environmental releases are expected to be small
and well below regulatory limits from a fusion facility, tritium is a radioactive material, and the
public will need to be assured that safety has not been compromised.
Other nuclear material that must be controlled and accounted for at fusion facilities
includes depleted uranium (U-238) and deuterium. Depleted uranium is used for storage of
tritium, fission chambers, and various radioactive check- and calibration-sources. Deuterium in
quantities greater than 100 g is also controlled at DOE facilities (DOE Order 5633.3B and
5660.1B). The control and accountability of these materials is relatively straightforward and does
not present significant problems for operating facilities. The scope and extent of the
accountability program for these materials should be based on the monetary value of the
material and should include inventories and some measurements.
4.4.8.1 Requirements
The requirements placed on the control and accountability of tritium fall into three cate-
gories. Those required by the U.S. law, those required by DOE Orders, and those required by
“good practices.” It is also important to note that requirements are not consistent throughout the
international community.
a. Legal requirements. The legal requirements on tritium measurement are as follows:
1. Environmental facility emissions, which include air emissions and releases to the
ground water or at facilities outfalls, are regulated. These include federal and state
42
DOE-STD-6003-96
requirements in the following laws: Clean Water Act for water quality standards
and effluent limitations, and Federal Clean Air Act, which set ambient air quality
standards.
EPA regulates the type and quantity of facility emission. EPA specifies the mea-
surement techniques for air emissions and must approve any requests for devia-
tions. EPA sets the limits for exposure to the public and the notification required
when certain quantities of radioactive materials are emitted. State laws usually
regulate the facility outfalls. State requirements are not uniform across the
country.
2. Department of Transportation (DOT) requirements specify packaging requirements
that are dependent on the form and quantity of tritium. DOT must also approve
packaging containers when the radioactive material is transported on public
highways.
3. Waste storage requirements are in place when mixed hazardous waste may be
involved. The EPA administers the Resource Conservation and Recovery Act
(RCRA). In many cases this authority has been delegated to the state.
4. Waste disposal requirements are generally state specific.
Section 45
5. 10 CFR 830 Nuclear Safety Rules and 10 CFR 835 Occupational Radiation
Protection apply to the radiological activities in a fusion facility. Because these
requirements are part of the U.S. law, they must be followed by each facility that
handles tritium or radioactive materials as applicable.
The details of the state requirements will not be discussed in this section because
they vary widely.
b. DOE Orders. DOE Orders are requirements placed on DOE facilities that define
operations and the methods of conducting business. DOE 5633.3B, “Control and
Accountability of Nuclear Materials” specified the minimum requirements and pro-
cedures based on the amount of tritium and the form of the tritium in a facility.
Important requirements from this order follow:
1. Tritium is protected, controlled, and accounted for as Category III or IV Special
Nuclear Material. The level of protection and control depends upon the form and
quantity of the tritium. The reportable transaction quantity is 0.01 g (~100 Ci).
2. Each facility must have a Materials Control and Accountability (MC&A) Plan. The
scope and content requirements for the plan are determined by the manager of
the DOE operations office.
3. DOE Order 5633.3B requires that tritium be inventoried biennially. Where feasible,
inventory values should be based on measured values.
43
DOE-STD-6003-96
4. Inventory requirements are placed on the shipper and receivers of controlled
material and methods to control and resolve inventory differences.
5. Access controls, depending on the tritium form, must be established.
Each fusion facility must establish an independent organization to provide oversight of the
nuclear materials control and accountability. The physical protection requirements are specified
in DOE Order 5632.1C, “Protection and Control of Safeguards and Security Interests,” and DOE
5332.1C-1, “Manual for Protection and Control of Safeguards and Security Interests.” The
current DOE requirements are dependent on the quantity and form. These include control of
tritium by personnel with a U.S. DOE L clearance and controlled locks, alarms, and access
during nonworking hours. A higher level may be required if there are sabotage risks or classified
information interests at the facility.
Other Orders specify waste requirements, environmental monitoring, and personnel pro-
tection. These are not discussed in this section. The DOE Order requirements are in general not
legal requirements. The facility can negotiate with DOE to determine the most cost-effective
manner of implementing the requirements and still maintain facility safety and material
accountability.
4.4.8.2 Nuclear Material Locations at a Fusion Facility
Typical locations, inputs, and outputs, and measurement points for tritium at a fusion facil-
ity are identified below.
a. Inputs to tritium are shipments into the facility and production of tritium at the facility.
b. Locations of tritium within a facility are “in-process,” in-system holdup, in-waste sys-
tems, and in-storage.
c. The exit streams of tritium from a facility include shipments of tritium from the facility
and waste streams (tritium stack emissions, water releases, solid waste and acciden-
tal tritium releases).
d. Measurement locations include input tritium shipments to the facility, exit shipments
from the facility, in-process measurements, in-storage measurements, waste stream
measurements, personnel exposure measurements, workplace measurements, and
stack emission measurements.
Section 46
4.4.8.3 Tritium Measurements Method
Two primary categories of tritium measurements are made at fusion facilities. One cate-
gory is for determining the quantity and location of tritium within the facility. These measure-
ments are generally of large quantities of tritium in high concentrations. The second category is
for environmental or safety determinations. These are generally lower concentrations and small
quantities.
44
DOE-STD-6003-96
This section will discuss methods for both categories. The measurements techniques for
tritium can be grouped in the three general areas: composition measurements, thermal mea-
surements, and tritium concentration measurements.
Composition measurements determine the actual concentration determination for each
atomic/molecular species. This method can be used for gases only. Thermal methods
(calorimetry) rely on the radioactive heat of decay of tritium. For 1 g of tritium ~0.333 W is gen-
erated by decay. The temperature increase or heat generation is measured. Calorimetry can be
used for tritium in any form: solid, liquid, or gas. The only radioactive material present must be
tritium because other radioactive materials will contribute to the thermal properties of the
sample. The final method determined the total tritium concentration by the measurement of the
products or the effects of the products of the radioactive decay. The beta particle can cause
scintillation effects or ionization effects. These effects can be measured and the concentration of
tritium determined. The following methods are used or proposed to be used for measurement of
tritium: Pressure/Volume/Temperature/Composition (PVTC), using either a mass spectrometer
or laser RAMAN spectrometer for the composition measurement; Beta scintillation counter; Self-
assaying tritium storage beds; Scintillation Counting; and Ion Chamber.
Most of the techniques discussed here are batch samples, however some techniques can
be used for “on-line/real time” measurements.
a. Composition Measurements. PVTC measurement is used for measurement of
gaseous samples only. A representative sample of the gas is taken. The gas that is to
be measured must be mixed well. The volume, pressure, and temperature must be
measured accurately. The temperature is difficult to measure accurately because of
temperature gradients caused by the heat of decay of tritium. The composition of the
gas in the sample is then measured using a mass spectrometer or a laser RAMAN
spectrometer.
The mass spectrometer will measure all gas species. A high-resolution mass spec-
trometer is required to distinguish between different molecules with the same mass
number. For example HT and D2 have the same mass number, but must be sepa-
rated to determine the tritium concentration. All species that can contain tritium must
be measured. This includes, water as HTO, methane as C(H,D,T)4, ammonia as
N(H,D,T)3, etc. The sum of all the species containing tritium can then be determined.
If the approximate gas composition is unknown, the use of the mass spectrometer
may be difficult.
The laser RAMAN spectrometer is a relatively new system that can be used to mea-
sure molecular concentrations in a gas mixture. The sample is placed in a cell with
optical windows. The laser excites the rotational or vibrational atomic levels in the gas
molecules. The light emitted as the excited levels decay back to the ground state is
detected using a photodetector system. The measurement is absolute in that the fre-
quency spectrum of each molecule is unique. The intensity is proportional to the
amount of gas present. The disadvantages of the RAMAN method are that the amount
of inert gases cannot be determined. Common inert gases at a fusion facility are the
Section 47
45
DOE-STD-6003-96
isotopes of helium. Both of these techniques can be used for real-time measurements.
For the mass spectrometer system a sample is bled to a high vacuum system for mea-
surement. The RAMAN system is easily adopted to real-time measurements. The gas
stream at atmospheric pressure is passed through an optical cell. The spectrum for a
mixture hydrogen isotopes can be determined in ~1 min. The total accuracy of these
measurements is ~3 to 5%. The mass spectrometer technique has been the standard
method that DOE facilities have used for the determination of the tritium inventory. It is
a proven system although it requires an expensive spectrometer ($200K) and accurate
determination of the temperature, pressure, and volume. The RAMAN system has not
been accepted. Experiments are currently being performed to demonstrate that this will
be an acceptable technique.
b. Thermal Methods. The primary method to inventory large quantities of tritium in the
liquid or solid form is to use a calorimeter. The sample is placed in a thermally iso-
lated container. The power required to maintain the temperature of the container is
then a measure of the amount of tritium in the sample. Containers can accept sam-
ples that vary from several inches in diameter up to a 55-gal drum. The lower limit
of accuracy can be as low as 100 Ci. Calorimeters are expensive ($200K+). They
require high-tech electronics. They are the primary methods used to measure tritium
in waste such as HTO on molecular sieve. They have not been used to measure
process tritium except in a very specific application. For example, solid tritium storage
beds that can be disconnected and moved have been placed in a calorimeter
designed to accept the bed. New methods are being developed to allow for the deter-
mination of the amount of tritium stored on a solid storage bed, When tritium is stored
on a uranium bed the temperature increase of the bed can be used to determine the
amount of tritium stored on the bed. When tritium is stored on a material such as
LaAlNi, usually gas is passed through the secondary containment to maintain the
temperature. The temperature rise of the gas as it passes through the bed can then
be used to determine the amount of tritium. Both of these methods are being pro-
posed for tritium accountability. Their acceptance is now based on a case-by-case
system, and they are not used widely. Development of these methods will be impor-
tant for the operation of fusion facilities. They offer potential savings in time and effort
to account for the tritium in a facility.
c. Tritium Concentration Measurement. A Beta scintillation counter has been used for
tritium measurement if only the total tritium composition is required. In this instrument,
the gas is passed over a crystal that will scintillate with the beta from the tritium decay.
A photomultiplier tube is used to detect the light. The tritium concentration can then be
determined from the signal from the photomultiplier tube. This method is commonly
used for gas inventory requirements. Liquid scintillation is commonly used to
determine small concentrations of tritium. The tritium liquid or compounds containing
tritium are placed in a scintillation liquid. The liquid is then placed in a counter that
determines the amount of tritium by the light emitted from the sample. Ion chambers
are commonly used to determine environmental tritium releases and to monitor the
atmosphere for personnel safety. Process ion chambers are used for determining
tritium concentrations in secondary containment. Specially designed ion chambers
Section 48
46
DOE-STD-6003-96
can be used to determine high concentrations of tritium. Ion chambers will measure
any radioactive material that can cause ion pairs. They are also susceptible to con-
tamination from materials that adsorb on surfaces and can only be used for gas.
4.4.8.4 Facility Measurement Recommendations
a. Measurement of tritium input/output to facility. The primary method used historically
for the measurements of the tritium shipment has been the PVTC measurement with
the composition determined by either a mass spectrometer or beta scintillation
counter. A calorimeter can be used for the measurement of tritium absorbed on solid
storage beds that are designed to be used as primary shipping containers and also
be placed in the calorimeter.
b. In-process tritium measurements. The measurement of tritium within a facility has
usually been by PVTC. This requires a shutdown of the process and transferring of all
the gas to a volume for sampling and measurement. This is usually a substantial dis-
ruption of the process and will take a significant time. Tritium that is “held up” in pro-
cess cannot be directly measured. This includes tritium in walls of the system, tritium
in process components such as a molecular sieve, and tritium contained within the
waste disposal system. It must be estimated by difference measurements. Real-time
measurements of tritium amounts are done when tritium is moved around the facility
or process. These are usually done by PVTC measurements. The laser RAMAN
system offered advantages for the measurement of composition as tritium flows from
location to location. The use of self-assaying storage beds will greatly reduce the time
required to determine the tritium in storage.
c. Tritium in waste streams. The characterization of tritium contained in waste streams is
important, and one of the more difficult measurements to make. Ionization chamber
measurements, calorimetry, and difference measurements are used to determine the
tritium levels.
d. Stack emission measurements. Stack emissions are determined by ion chambers.
The primary method used by facilities for the reporting to the EPA is based on a pas-
sive monitoring system. A small fraction of the air stream exhausted from a facility is
passed through a system to remove the tritium. Both liquids such as glycol and solids
such as molecular sieve are used to absorb HTO. These system can distinguish
between HTO and HT by passing the sample through a catalyst that will convert HT
to HTO. The second collection system then collects the HT as HTO.
47
DOE-STD-6003-96
Intentionally Left Blank
48
DOE-STD-6003-96
5. SAFETY ANALYSIS
This chapter of the Standard describes the safety analysis requirements applicable to
fusion facilities and provides guidance for the implementation of these requirements and criteria
for determining that the requirements have been met.
Safety analyses are performed to show that the risks associated with operation of a facil-
ity have been identified, quantified, and managed. Management of risk can be accomplished
(1) by demonstrating that the risk is within the bounds of an approved safety envelope, (2) by
showing that the risk consequences are mitigated to meet the established evaluation guidelines,
and (3) by having the risks themselves eliminated or reduced by demonstrable controls.
Section 49
The completion of a safety analysis requires information on the facility, the site character-
istics important for evaluating facility safety, and the principal equipment and processes required
to fulfill the facility mission. From this baseline descriptive information, hazards can be identified.
Facility risk descriptions are then developed from the hazard inventories, system functional pro-
cess descriptions, and a listing of off-normal conditions postulated to result from both internal
and external causes. The entire analysis process is documented in a Safety Analysis Report
(SAR) and in Technical Safety Requirements (TSRs); the guidance for these is addressed in
later subsections.
The safety analysis has many purposes. In addition to establishing the safety of the facil-
ity, the safety analysis is used to develop TSRs and to determine readiness for construction and
operational authorization. The graphical illustration of the functional relationship of the major
items included in the safety analysis process is shown in Fig. 5.1.
As discussed in Section 1.3, a risk-based prioritization approach is to be taken in the
implementation of safety analysis requirements as well as in the implementation of the other ele-
ments of this Standard. Actions taken to ensure compliance with requirements are a function of
the several factors cited in the definition of risk-based prioritization. The factors most relevant to
fusion safety analysis considerations are risk and magnitude of hazard. The other factors
included in the risk-based approach are mission and facility life cycle. As such, the importance
of these factors is discussed where appropriate in the applicable sections of this chapter.
The project has the responsibility for the development of specific criteria for the applica-
tion of a risk-based prioritization approach to the system specific criteria. Concurrence with the
specifics of the risk-based approach taken by a facility should be obtained from the regulator
prior to its implementation. The identification of relevant criteria will flow from the nature and
purpose of the system itself.
49
DOE-STD-6003-96
FIGURE 5.1. Flow logic of the safety analysis process.
50
DOE-STD-6003-96
5.1 Facility Description
5.1.1 General
Safety analyses inherently contain a description of the facility being analyzed that is suffi-
cient to convey an understanding of the nature and magnitude of the physical plant and systems
involved in the implementation of the facility mission. The description should be sufficient to
allow the reader to understand how the hazardous materials, systems, components, and pro-
cesses that are discussed later relate to the system as a whole and to understand the role and
relevance of the safety systems in the facility. The facility description should also include those
site characteristics that constitute or contribute to facility hazards. The site information should be
sufficient to provide a basis of understanding of the hazards and the mechanisms by which
radiological or hazardous material could have consequences to the public, environment, or
workers.
Useful guidance on the content of a facility description portion of a safety analyses is
available in Department of Energy (DOE) Order 5480.23, attachment 1, page 24 (DOE 1992b):
Section 50
Safety analyses should contain descriptions of the facility and the principal
equipment and processes provided to fulfill the mission of the facility and should
delineate the plans, provisions, and requirements for their operation, mainte-
nance, and surveillance. Information on the design of principal structures, com-
ponents, and systems should be furnished in sufficient detail to support the
identification of hazards, principal safety criteria, selection of engineered safety
features, and the analysis of off-normal conditions. This information should
include the following, using drawings as necessary:
a. A listing of the safety structures, systems, components, equipment, and
processes discussed in this section of the report;
b. Detailed descriptions of structures or containers used to confine radioac-
tive materials or hazardous chemicals;
c. Detailed descriptions of safety-significant mechanical, electrical, and fluid
systems (i.e. decay heat removal methods...) including functions, design
bases, and relevant design features;
d. Detailed descriptions of chemical process systems, including information
on design configuration, dimensions, materials of construction, pressure
and temperature limits, corrosion allowances, and any other operating
limits, and;
e. A functional description of process and operational support systems,
including instrumentation and control systems...
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DOE-STD-6003-96
The facility description information must be an integral part of the safety analysis, but it is
possible to accomplish this by providing the information in nonsafety analysis sections of facility
documentation or even in totally separate documents, either of which would then be referenced
in the specific safety analysis discussions. The configuration control requirements applicable to
SARs would also apply to information referenced in the SARs but contained in other documents.
(See configuration control requirements of Chapter 4.)
5.1.2 Safety Structures, Systems, and Components
Safety structures, systems, and components (SSCs) implement the safety functions
associated with a facility. The two categories of safety functions associated with fusion facilities
are (1) public safety functions or essential characteristics needed to ensure the safety of the
facility and protection of the public and environment during operations and during and following
off-normal conditions; and (2) worker safety functions that ensure the health and safety of the
workers.
The public safety function for fusion is the confinement of radioactive and hazardous
material under normal and off-normal conditions. Potential public safety concerns related to
confinement include (1) ensuring afterheat removal, (2) providing rapid plasma shutdown,
(3) controlling of coolant internal energy, (4) controlling of chemical energy sources,
(5) controlling of magnetic energy, and (6) limiting air and water discharges from the facility.
Worker safety functions are related to worker hazards and routine releases. The issues
associated with the worker safety function that should be evaluated are (1) limiting occupational
exposure to radiation, (2) limiting the exposure to electromagnetic fields, and (3) controlling
other industrial hazards and hazardous materials.
It is recommended that the SSCs required to implement the public safety function should
employ the requirements imposed on systems defined as being safety-class SSCs in DOE 1994
(DOE STD-3009-94). The specific definition of a safety-class system is as follows:
Section 51
Systems, structures, or components including primary environmental moni-
tors and portions of process systems, whose failure could adversely affect the
environment, or safety and health of the public as identified in the safety analysis.
The safety-class SSCs are associated with the public safety function of confinement that
protects the public and the environment from exceeding the radiological evaluation guidelines in
DOE-STD-6002.
It is recommended that the SSCs that address potential safety concerns or are required
to protect the worker safety functions should employ the requirements imposed on systems
defined as being designated as safety-significant SSCs in DOE 1994 (DOE STD-3009-94). The
specific definition of a safety-significant system is as follows:
Structures, systems, and components not designated as safety-class
SSCs but whose preventive or mitigative function is a major contributor to
52
DOE-STD-6003-96
defense in depth (i.e., prevention of uncontrolled material releases) and/or worker
safety as determined from hazard analysis.
The safety-significant SSCs have the goals of (1) ensuring the availability of the public
safety functions via defense-in-depth and (2) supporting the health and safety of workers during
routine operations. The safety-significant SSCs would not be required to mitigate the conse-
quences of off-normal events to meet the evaluation guidelines for the public or the environ-
ment. This function is the responsibility of the safety-class SSCs. However, because the SSCs
that address the potential safety concern related to confinement will reduce potential threats to
confinement through either accident prevention or mitigation, they are considered to contribute
to defense-in-depth and thus are designated as safety-significant.
The categorization of a safety-class SSC is a two-step process. The first step is to identify
early in the design the SSCs whose failure would result in exceeding evaluation guidelines. This
should be by a “top down” functional hazards analysis. The second step is to verify in the final
stages of design that the safety-class SSCs are actually needed to be functional, as indicated by
the safety analysis process. If the SSCs are verified as being needed in the safety analysis
process, then the equipment would be designated as safety-class SSCs. These components
also must perform the required safety functions. This design approach would be as follows:
a. identify all potential hazards associated with the facility,
b. identify all SSCs needed to control those hazards,
c. identify the safety-class SSCs necessary to ensure that evaluation guidelines are not
exceeded, and
d. verify, through detailed safety analysis, the need for the systems in item (c) to meet
the evaluation guidelines provided in DOE-STD-6002.
The safety-class SSCs should be designed such that a minimum number of active or
passive mitigative systems identified from and credited within the safety analysis are available to
ensure that the evaluation guidelines are not exceeded. Reliable SSCs are required to be
employed to satisfy the requirements of safety-class items. Use of defense-in-depth principles
such as redundancy, simplicity in design, independence, fail safe, fault tolerant, and multiple
(diverse) methods for increasing the reliability and reducing the consequence to acceptable
levels is permitted and encouraged. In most cases, the use of passive methods of accomplish-
ing the safety function is preferred over using active systems.
Section 52
The next step in the process would be to perform the required system safety analysis.
The safety analysis results would verify the adequacy of the safety-class SSCs to mitigate the
release of hazardous material to meet the evaluation guidelines specified in DOE-STD-6002.
Thus, the results of this evaluation determine which of the SSCs would be required to satisfy the
public safety function. It may result in multiple SSCs being required to satisfy the safety system
requirements for a particular off-normal condition scenario. In most cases, the SSCs identified in
the hazards assessment review would be the same as those verified by the safety analysis as
53
DOE-STD-6003-96
being SSCs required to implement safety. In addition, the safety analysis would verify the ade-
quacy of safety-significant SSCs in addressing the potential safety concerns. Worker protection
and potential safety concerns associated with the public safety function are identified in
DOE-STD-6002.
Descriptions of each SSC that is providing safety functions are required in the SAR. A basic
descriptive model of the facility and its equipment must be provided in which the required SSCs
are addressed in detail commensurate with their preventive or mitigative role in meeting off-
normal condition evaluation guidelines. For example, consider a facility that cannot meet
evaluation guidelines, as discussed in DOE-STD-6002, unless credit is taken for system A.
Besides being noted in the general facility description, system A together with associated codes
and standards would be described in the section on safety-class SSCs. This system would typi-
cally be associated with a specific TSR (discussed in Section 5.7) and would be described in
detail commensurate with its importance to the safety basis. However, only the characteristics of
the SSC that are necessary to perform the safety function are classified as part of the safety
system. For example, if a valve in a system is only required to provide an external pressure
boundary, then only the pressure boundary function would be classified as a safety system
characteristic and all other functions, such as the valve operability, response time, etc. would
not be included in the safety system definition.
Conversely, if the consequences of all hazardous releases or off-normal conditions exam-
ined meet the evaluation guidelines without relying on the safety-class function of process
system B, then system B would not be considered to be a safety system performing a safety
function. Detailed identification of its functional basis and construction is not necessary because
it is not a significant contributor to the overall facility safety basis. There would also be no need
to discuss administrative provisions (e.g., initial testing, maintenance) required to ensure the
operability of system B, nor would there be a need for a specific TSR (e.g., Safety Limit, Limiting
Condition For Operation, etc.) covering system B. If a system is designated as safety-significant,
industry recognized codes and standards are to be applied and minimal, if any, TSRs are to be
specified for the operation of the system components (see Section 5.7).
Section 53
A risk-based prioritization approach can be used to develop requirements for the safety-
class and safety-significant SSCs. One of the dominant factors governing risk-based prioritiza-
tion is the severity of the off-normal condition consequences associated with the facility and the
number and type of the SSCs needed to prevent evaluation guidelines from being exceeded. If,
for example, the defense-in-depth principles are satisfied by providing other SSCs to mitigate
the consequences, then added inspections and other quality pedigree requirements of the first
system would not be as important as if the original SSCs were the only means of accomplishing
the safety function. If the consequences of the off-normal condition exceed the evaluation guide-
lines by a large margin and there is no other system that will mitigate or prevent the release for
the off-normal condition, then special precautions should be taken in the design and in develop-
ing the inspection program to ensure that the system will be available to function when called
upon. This may involve special inspections, alternate design approaches, or other actions that
would significantly enhance system reliability. The rigor of compliance with the design and
inspection requirements could be relaxed for systems that have multiple backups for preventing
off-normal conditions or mitigating the off-normal condition consequences.
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DOE-STD-6003-96
The design of the SSCs that perform the safety-class and safety-significant safety func-
tions should meet the appropriate requirements established in Table 5.1.
TABLE 5.1. Safety system functional requirements
Requirement Safety-Class Safety Function Safety-Significant Safety Function
System design Reliable methods of accomplishing the required
safety function should be provided. Some of the
design techniques that would ensure system
reliability would include redundancy, diversity,
simplicity in design, independence, fail safe, fault
tolerant. Each method should be analyzed to identify
potential failure mechanisms from performing the
safety function in the system and to minimize those
failures in the design. For further guidance on
providing reliable system designs, see
Section 6.7.3.1.
Nonredundant systems are normally used to
perform the worker safety function. The safety
system should be analyzed to preclude failures
mechanisms that could disrupt the system
function. Multiple systems may be employed, at
the discretion of the facility developer, to ensure
that the system functions are performed.
Codes and
Standards
Nationally accepted design codes should be used in
the design (see Chapter 6). The applicability,
adequacy, and sufficiency of the codes and
standards used should be evaluated. These codes
and standards should be supplemented or modified
as necessary to ensure system performance in
keeping with the importance of the safety functions
to be performed.
The codes and standards used for these systems
should be those which have been validated
through satisfactory performance in commercial
application.
Reliability
Safety system should be demonstrated to have a
high reliability. One of the ways to demonstrate this
is by providing multiple, redundant, diverse
systems/barriers to accomplish the safety function.
The safety system should be equivalent to that
associated with commercial industrial safety
practices.
Section 54
Quality The SSCs should require an appropriate level of
quality for the design and construction to ensure the
system function is performed. Quality assurance in
accordance with the requirements of 10 CFR
830.120 should be implemented.
The systems required should be designed
in accordance with industrial quality requirements.
Testability/
surveillance
The SSCs should be tested/surveyed periodically to
determine that the function can be provided.
Acceptance criteria should be established to
evaluate the test results that demonstrate when the
system is performing its intended function. The test
frequency should be established to ensure that the
system demand and reliability requirements are
achieved.
The SSCs should be tested/surveyed periodically
to determine that the function can be provided.
Natural
phenomena
The SSCs should be designed to withstand
appropriate natural phenomena and continue to
provide the required safety function. Design for
natural phenomena should be in accordance with
facility performance goals per DOE Order 420.1
(DOE 1995a).
Design for natural phenomena should be in
accordance with facility performance goals per
DOE Order 420.1 (DOE 1995a).
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5.2 Facility Mission/Processes
Descriptive information on the overall mission is required as part of the SAR. It is also a
major factor in the development of the risk-based prioritization approach being implemented
throughout each aspect of facility safety design.
Information on the facility processes is used primarily in the hazards analysis phase of
the safety analysis. Facility process information and facility description information are used to
develop the inventory of facility hazards. Facility risks can then be established by identifying the
accessibility of each hazard.
The first criterion for determining the sufficiency of mission and process information in the
safety documentation is whether there is enough to support closure of the safety analysis. That
is, are there undocumented aspects of the facility mission or its processes that would in any way
affect the conclusions of the safety analysis with respect to the particular component, system,
and so on. The conclusion should be that there are not; should there be any situation that pro-
duces an answer to the contrary, then the mission/process descriptive information is deficient.
A second criterion for the sufficiency of mission information is whether there is enough to
implement a risk-based prioritization approach throughout the safety design activity. The previ-
ously described design and analysis activities would normally provide the necessary information
to satisfy the requirement.
5.3 Hazards Analysis
The hazards analysis performed for a given facility provides a measure of the risk poten-
tial for operation of that facility. The results of the hazards analysis will dictate the level of detail
required for the safety analysis that must be performed for approval to operate. The following
steps must be performed in the development of the hazards analysis:
a. Identify the potential energy sources, the initiating events, and inventories of radioac-
tive and hazardous material that could be present in the facility both during routine
operations and shutdown conditions, based on the classification methodology devel-
oped in such documents as DOE-STD-1027-92 (DOE 1992d).
b. Classify the facility into categories according to the its hazard potential using an
approach that does not account for safety system mitigation.
Section 55
The categories with the higher hazard potential for a facility require a more detailed safety
analysis to demonstrate that the facility can be operated safely.
5.3.1 Inventory
The inventory of the radioactive and hazardous material is one of the determining factors
in the hazards analysis classification of a facility. A set of radioactive inventory limits has been
developed for use in the classification of fusion facilities into various hazard categories
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described in the following section. Because the radionuclide inventory limits contained in
DOE-STD-1027 are primarily associated with the fission process, the radionuclide list has been
expanded to include additional isotopes that could be present in fusion facilities. The expanded
limits for Category 2 fusion facilities are provided in Appendix A to this Standard.
The radioactive and hazardous material inventories can be segmented provided it can be
shown that the potential consequences associated with the hazardous material are limited to the
segmented amount rather than the inventory present in the more than one segment or the entire
facility. Based on the guidance presented in DOE 1992d, inventory segmentation is allowed if
the hazardous material in one segment could not interact with the inventory in other segments to
result in larger potential consequences than from any of the individual segments. For example,
independence of the heating, ventilating, and air conditioning (HVAC) and piping must exist to
demonstrate independence for facility segmentation purposes. This independence must be
demonstrated and places the “burden of proof” on the analyst.
5.3.2 Classification
The classification of fusion facilities should follow the guidance provided in DOE-STD-
1027-92 (DOE 1992d). This guide provides for three facilities hazard categories summarized as
follows:
a. Hazard Category 1—Hazard analysis shows the potential for significant off-site con-
sequences. Fusion facilities in this category would be designated by the cognizant
DOE official.
b. Hazard Category 2—Hazard analysis shows the potential for significant on-site con-
sequences. Examples include facilities with the sufficient quantities of hazardous
radioactive materials that meet or exceed the inventory values contained in the guid-
ance document used for classifying facilities (DOE 1992d).
c. Hazard Category 3—Hazard analysis shows the potential for significant localized con-
sequences at a facility. Examples include facilities with quantities of hazardous radio-
active materials that meet or exceed the inventory values contained in the guidance
document used for classifying facilities.
In addition to these three categories, there is an additional category for all of the facilities
that have less hazard potential than the least of the previous three categories. This category is
defined as follows:
d. Below Hazard Category 3—Hazard analysis shows the potential consequences to be
below the guidelines of the requirements described in DOE-STD-1027-92, as modified
by this Standard. An example of this is those facilities that have inventories of radio-
active material less than those specified for Category 3 facilities for hazard catego-
rization. Thus, these facilities would be classified as non-nuclear facilities. It should be
noted that many of the smaller fusion facilities could fall into this category.
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5.4 Analysis of Off-Normal Conditions
Section 56
The requirements of this Standard indicate that the safety of fusion facilities should
be analyzed to demonstrate that the facility meets the evaluation guidelines discussed in
DOE-STD-6002. This section provides guidance on the type of analysis of off-normal conditions
required for use in meeting the evaluation guidelines and the fusion requirements related to no
off-site evacuation. The types of analyses used to demonstrate compliance with these require-
ments are different and need discussion in this section.
The level of analysis of off-normal conditions for fusion facilities should be based on the
risk to the public, the environment, and the worker. Facilities with minimal risk will only require
that a scoping conservative analysis be performed to satisfy the safety analysis requirements.
However, a facility with a large potential safety risk to the public, the workers, or the environ-
ment (Category 1 and 2 facilities) will require a more detailed analysis of off-normal conditions to
satisfy the safety analysis requirements for such facilities as given in this section.
It is important that the safety analysis address the institutional and human factors safety
issues. Experience has confirmed that the risk associated with operating nuclear facilities is a
combination of the institutional approach to safety, human factors safety, and safety in design.
As used here, the institutional approach to safety includes
a. management and organization of facility operations;
b. the safety culture sustained by management;
c. performance objectives and the measurement of operational performance;
d. management oversight and assessment;
e. feedback of operational experience;
f. management controls of operations, surveillance, and maintenance;
g. related management efforts to achieve and sustain safe operations.
Human factors safety, as used here, refers to
a. the allocation of control functions to personnel vs automatic devices;
b. staffing and qualification of operating crews;
c. personnel training;
d. the preparation, validation, and use of written procedures to guide operations,
surveillance, and maintenance;
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DOE-STD-6003-96
e. the design of human-machine interface to build on strengths and protect against the
susceptibility of human error in operating crews.
Safety in design includes
a. identifying the potential off-normal conditions and incorporating systems performing
safety functions in the facility design to reduce the overall risk from those conditions;
b. designing reliable safety features using appropriate codes and standards that will
ensure the availability of the safety when required;
c. categorizing the facilities to their appropriate risk potential because the level of safety
features that are required for a given facility will be a direct function of the significant
risks present in a facility;
d. using defense-in-depth concepts in the design to ensure the safety of the public,
worker, and the environment;
e. incorporating the as-low-as-reasonably-achievable (ALARA) principles in the facility
design to reduce the risk potential to the workers during normal and off-normal
conditions.
The specific features associated with the design of a facility are discussed in detail in
Chapter 6.
5.4.1 Event Scenario Identification and Classification
Figure 5.2 is a flow chart that can be used to understand the steps required in the analy-
sis process. First, a list of postulated initiating events should be developed. Based on the
generic hazard and accident scenario identification (presented in Appendix B), these initiating
events could include the following:
Section 57
a. loss of coolant (e.g., water and cryogen);
b. loss of flow;
c. magnet transients (arcing, quench, coil displacement, and magnet missile);
d. transient overpower;
e. plasma disruptions [including vertical displacement events (VDEs) and runaway
electrons];
f. loss of vacuum;
g. initiating events in the tritium plant;
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FIGURE 5.2. Event scenario/safety analysis process.
60
DOE-STD-6003-96
h. initiating events in auxiliary systems [e.g., neutral beams, radio frequency (RF),
pumping, and fueling];
i. initiating events in balance of plant systems (e.g., loss of off-site power);
j. operator errors; and
k. external events.
The initiating events should consider all aspects of fusion facility operation, including
plasma operation, bakeout and conditioning, and maintenance. Because fusion facilities operate
in modes that are different from other facilities (e.g., bakeout and conditioning, in pulsed mode
for some machines), these potential plant states should be examined carefully. In the develop-
ment of these postulated initiating events, completeness is somewhat problematic. Practical
completeness can then best be achieved by collective review of the results by safety analysts
and designers who understand the facility.
From these postulated initiating events, event scenarios should be developed that exam-
ine the response of the fusion facility to these initiating events, accounting for potential failure of
other systems (e.g., confinement). The use of event trees or event sequence diagrams may be
useful here. The event scenarios should span a wide range of expected frequencies, including
those events expected to occur once or more during the operating life of the facility [i.e., an
anticipated operational occurrence (f > ~10–2/yr); those events not expected to occur, but may
occur, during the life of the plant (10–2/yr > f > 10–4/yr); those events that would not be expected
to occur during the life of the plant but which form the limiting events needed in the design basis
(10–4/yr > f > 10–6/yr); and events beyond the design basis (f < ~10–6/yr)].
Once the events have been developed, they should be categorized into three types based
on their estimated frequency: anticipated operational occurrence, off-normal conditions, and
beyond-design-basis events. The off-normal conditions type includes both the anticipated
operational occurrences and events expected to occur once or more during the lifetime of the
facility. Based on these events, bounding or limiting events of each kind (e.g., loss of flow, loss
of coolant, and loss of vacuum) should then be selected for detailed quantitative analysis.
Two types of analysis methodologies should be used for the safety assessment for the
fusion facilities: a deterministic, conservative approach and a best-estimate, realistic approach.
Each type of analysis methodology is required for a different portion of the required safety
assessment. The deterministic, conservative approach is to be used in the design-basis assess-
ment for the SAR to ensure that a bounding estimate of the facility safety is determined. The
best-estimate, realistic approach is to be used for analysis of beyond-design-basis events for
the SAR and in the determination of the emergency planning assessment. However, a conser-
vative risk-based approach can be used in place of the deterministic conservative approach
since either approach would satisfy the intent of performing a conservative safety assessment.
These are discussed in the next two sections.
Section 58
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5.4.2 Analysis Approach for the Safety Analysis Report
Because there is no previously identified design basis for large fusion facilities like the
International Thermonuclear Experimental Reactor (ITER), a subset of the event scenarios
identified in Section 5.4.1 needs be selected to form the design basis and to undergo detailed
quantitative analysis as part of the SAR. There is varying information that can be used to
develop an appropriate criteria to be used in this selection. DOE Order 420.1 (DOE 1995a) and
DOE-STD-3009 (DOE 1994) indicate that events down to ~10–6/yr should be considered. Many
advanced fission plants are also considering similar criteria. It is recommended that for fusion
facilities, internally initiated event sequences down to ~10–6/yr be used. For external events,
guidance given in DOE Order 420.1 (DOE 1995a) should be consulted.
Two different types of calculations should be performed: best estimate and conservative.
Conservative calculations should be performed for those events identified as part of the design
basis. As part of the calculation, all key assumptions need to be stated and the level of conser-
vatism noted (e.g., 110% nominal power). The results of these conservative calculations are