DOE-HDBK-1122-99 Module 2.07, Fundamentals Academic Training Instructor's Guide Phase I; Module 2.07, Respiratory Protection
Functional areas: Radiological Training, Technician Training, Instructor's Guide, Respiratory Protection, Radiological Control
Internal dosimetry controls require the use of engineering controls to prevent the internal deposition of radioactive and
non-radiological contaminants. However, when engineering and administrative controls are not available or feasible,
respiratory protection may be necessary. The RCT should know and apply the considerations used in determining the
respiratory protection equipment that is most appropriate for the job. Inappropriate use of or the use of the wrong
respiratory protection equipment may result in undesirable health effects.
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Section 1
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Module 2.07 Respiratory Protection Instructor’s Guide
2.07-1
Course Title: Radiological Control Technician
Module Title: Respiratory Protection
Module Number: 2.07
Objectives:
2.07.01 Explain the purpose of respiratory protection standards and regulations.
2.07.02 Identify the OSHA, ANSI, and DOE respiratory protection program
requirements.
2.07.03 Identify the standards which regulate respiratory protection.
2.07.04 Describe the advantages and disadvantages (limitations) of each of the
following respirators:
a. Air purifying, particulate removing filter respirators
b. Air purifying, Chemical Cartridge and Canister respirators for
Gases and Vapors
c. Full-face, supplied-air respirators
d. Self-contained breathing apparatus (SCBA)
e. Combination atmosphere supplying respirators
2.07.05 Define the term protection factor (PF).
2.07.06 State the difference between a qualitative and quantitative fit test.
2.07.07 State the recommended physical functions the subject must perform during
a respirator fit test.
2.07.08 State how the term protection factor (PF) is applied to the selection of
respiratory protection equipment.
2.07.09 State the general considerations and considerations for the nature of the
hazard when selecting the proper respiratory protection equipment.
� 2.07.10 Identify the types of respiratory equipment available for use at your site.
2.07.11 Identify the quality specification breathing air must meet.
References:
1. "Basic Radiation Protection Technology", Gollnick, D., Pacific Radiation
corporation, Altadena, 2nd edition.
2. "Guide to Sampling Airborne Radioactive Materials in a Nuclear Facility"
3. "Radiation Protection", General Physics Corporation, 1989.
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4. "Introduction Health Physics", Second Edition, Cember, H., Pergamon Press,
London, 1983.
5. "Limits for Inhalation of Radon Daughters by Workers", ICRP Publication 32.
6. "Limits for Intakes of Radionuclides by Workers", ICRP Publication 30.
7. "Operational Health Physics Training Course", Moe, H.J., et. al., Argonne
National Laboratory, Argonne, 88-26.
8. "Radiation Detection and Measurement", Knoll, G., John Wiley and Sons, New
York, 1979.
9. 10 CFR 835, "Occupational Radiation Protection", 1998.
10. "Practices of Respiratory Protection", ANSI Z88.2, 1992.
11. "Manual of Respiratory Protection Against Airborne Radioactive
Material",NUREG-0041, 1976.
12. Respiratory Protection, Federal OSHA, 29 CFR 1910, 134.
13. OSHA 29 CFR 1910. 134
14. ANSI Z88.2-1992
15. CGA G7.1-1989
Instructional Aids:
1. Overhead projector and screen
2. Chalkboard
3. Markerboard
4. Lessons learned
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I. MODULE INTRODUCTION
A. Self Introduction
1. Name
2. Phone number
3. Background
4. Emergency procedure review
B. Motivation
Internal dosimetry controls require the use of engineering
controls to prevent the internal deposition of radioactive and
non-radiological contaminants. However, when engineering
and administrative controls are not available or feasible,
respiratory protection may be necessary. The RCT should
know and apply the considerations used in determining the
respiratory protection equipment that is most appropriate for
the job. Inappropriate use of or the use of the wrong
respiratory protection equipment may result in undesirable
health effects.
C. Lesson Overview
Section 2
1. Requirements and regulations
2. Types of equipment
3. Protection factors
4. Fit testing
5. Selection of respirators
6. Site respiratory equipment
7. Supplied air quality testing
8. Sorbents and protection against radioiodines
9. Communications
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D. Introduction of Objectives O.H.: Objectives
II. MODULE OUTLINE
A. REQUIREMENTS AND REGULATIONS
1. DOE Requirements
The DOE Order 440.1 mandates the requirements for a
respiratory protection program contained in ANSI Z88.2
and 29 CFR 1910.134.
2. OSHA REGULATIONS - 29 CFR 1910.134
Purpose: Specify the minimal acceptable program which
must contain or address the following:
Objective 2.07.01
a. Written procedures
b. Respirator selection
c. The user shall be instructed and trained in proper use
of respirators
d. Respirators shall be cleaned and disinfected after
each use
e. Respirators stored in a clean, sanitary location
f. Respirators inspected routinely and replaced when
necessary
g. Appropriate surveillance of work area conditions and
degree of employee exposure or stress
h. Regular evaluation of program
i. Persons should be physically able to use equipment
as certified by a physician
j. Approved respirators shall be used when they are
available
3. ANSI Z88.2 - 1992: Further specifies the minimal
acceptable program
Objective 2.07.02
Objective 2.07.03
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a. Individual exposures limited by both inhalation and
skin absorption
b. Air sampling and bioassays
c. Engineering controls are primary method
d. When an individual is exposed to greater than the
specified DAC or other exposure limits.
e. Respiratory protection equipment must be
NIOSH/MSHA certified
f. If allowance for use of respiratory protection
equipment is made,
1) Protection factor must be greater than ratio of
peak exposure concentration and associated DAC
2) Average concentration inhaled must be less than
associated DAC
3) If exposure is later found to be greater than
estimated, corrected value shall be used.
If less than estimated,
the corrected value may
be used
4) Surveys and bioassays conducted as appropriate
to evaluate actual exposures.
5) Written procedures must be established.
6) Determination by a qualified health care
professional of a user's physical capability
7) A written policy statement must be issued
a) Engineering controls
b) Routine, non-routine and emergency use
c) Periods of use
8) Each user must be advised upon failure of
equipment, physical stress or deterioration of
operating conditions.
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9) Equipment is appropriate for environment and
special equipment, such as communication
devices issued when needed.
10) Emergency use equipment must be specifically
certified as such by NIOSH/MSHA.
B. TYPES OF EQUIPMENT
Objective 2.07.04
1. Air purifying, particulate-removing filter respirators
a. Description "dust," "mist" or
"fume" respirators
1) Filtering action removes particulate
2) Operate in negative pressure (NP) mode
3) Exception is a special type of powered air
purifying respirator that is designed to never be
negative pressure.
b. Limitations
1) Do not provide oxygen NEVER to be worn in
oxygen-deficient
atmospheres
2) No protection against gases or vapors
3) Should not be used for abrasive blasting
operations
Section 3
4) Battery operated respirators are limited by battery
life.
5) High humidity may increase breathing resistance
as paper elements become water saturated.
6) Not to be used in IDLH atmospheres
2. Air Purifying, Chemical Cartridge and Canister
Respirators for Gases and Vapors
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a. Description - use cartridges or canisters containing
chemicals to remove specific vapors and gases.
The difference between
a cartridge and a
canister is the volume
of the sorbent.
Canisters have longer
capacity and are used in
gas masks.
b. Limitations
1) Do not provide oxygen NEVER to be worn in
oxygen deficient
atmospheres
2) Unless approved by DOE, no credit for
protection against radioactive gases and vapors
3) High humidity shortens life of the sorbent
material and increases breathing resistance.
4) Not to be used in IDLH atmospheres
3. Atmosphere Supplying Respirators - Supplied Air
a. Description
1) Use central source of breathing air delivered to
wearer through a line or hose.
2) Either tight-fitting facepiece or loose-fitting
hood/suit
3) Demand device - during inhalation there may be
negative pressure in the mask.
4) Pressure demand device - positive air pressure
inside mask is maintained at all times.
5) Continuous-flow air line - is designed to create
positive pressure in facepiece.
b. Limitations
1) Not used in IDLH atmospheres (not for emergency
escape or rescue)
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2) Trailing air supply hose severely limits mobility.
3) Length of hose, number of potential users and
pressure of the supply system are interdependent.
No more than five sections of hose with a
maximum length of 250 feet.
4) Control of air quality is essential.
5) "Bubble suits" must be tested for exact
conditions of use.
c. Special considerations
1) Where air line respirator is a suit, requires a
standby rescue person with SCBA
2) Follow all manufacturers instruction and written
facility/site procedures
3) If all hoses and fittings are same then a single
pressure gauge is appropriate.
4) For situations where each user has different hose
lengths, different number of connection or
different air pressure requirements then a
separate pressure gauge should be used.
4. Atmosphere Supplying Respirators - Self-Contained
Breathing Apparatus (SCBA)
a. Description
1) Allows the user to carry a respirable breathing
supply
Air supply may last 3
minutes to four hours
2) There are two groups of SCBAs closed circuit
and open circuit
a) Closed circuit SCBAs - "rebreathing" device Designed primarily for
1-4 hours use in toxic
atmospheres
b) Open circuit SCBA exhausts the exhaled air
to the atmosphere
Service life is shorter
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c) Two types of open circuit SCBA are
available, "demand" or "pressure demand."
• Demand SCBA - air flows into facepiece
only on demand of the wearer.
When the person
inhales note: demand-
type SCBA does not
provide any higher
degree of protection
against airborne
contaminants than air-
purifying respirator
with same facepiece,
but it does provide
protection against
oxygen deficiency.
• Pressure demand - maintains positive
pressure in facepiece at all times
regardless of "demand" of user.
Recommended for
emergency use, escape
and rescue.
b. Combination atmosphere supplying respirators
Section 4
1) Combination Pressure Demand Breathing
Apparatus provides respiratory protection for
personnel who must work in atmospheres that are
IDLH.
Equipped with small air
cylinder in case
primary air supply
(hose line) is
interrupted.
2) Dual-purpose Breathing Apparatus combines all
capabilities of SCBA and a supplied air respirator
in one unit.
c. Limitations of the pressure and demand SCBA
1) Air supply is limited
2) Bulky and heavy
3) Demand type not for fire fighting 10CFR20 Appendix R
Section H
d. Special considerations of the pressure demand SCBA
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1) Only pressure-demand type SCBA should be
selected for emergency use, rescue and reentry
into contaminated area.
Section 5.5 of NUREG
0041
2) Performance of SCBAs in high temperature
environments, such as fires may lead to rapid
deterioration of components.
B. PROTECTION FACTORS Objective 2.07.05
1. Overall protection afforded by a given respirator design
is defined in terms of its protection factor (PF).
2. An assigned PF is defined as the level of protection that
would be expected from a class or type of respirator to a
properly fitted and trained user.
3. Application of PFs
4. Z88.2 Protection Factors
Table 1 - “Assigned Protection Factors”
C. FIT TESTING Objective 2.07.06
1. Definitions
a. Qualitative fit test:
Test to determine if there is any mask leakage,
usually using irritant smoke.
b. Quantitative fit test:
Test to determine quantity of mask leakage and
assign a "fit factor," an oil or dust particles are the
typical challenge atmospheres used.
2. Qualitative fit tests are sometimes performed in lieu of
quantitative fit tests.
a. Can use challenge atmospheres such as Isoamyl
Acetate (banana oil) or irritant smoke (e.g. stannic
chloride or titanium tetrachloride).
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b. A qualitative fit test uses the same series of exercises
as quantitative fit testing.
Irritant smoke tests are
most effective
c. An abbreviated qualitative “fit check” may be used
prior to entry into a contaminated area.
3. At least a qualitative test must be formed - a negative
pressure type is typical.
4. Additional factors to be considered
a. Use of communication devices
b. Sorbent canisters with respirators
5. Respirator face pieces and cartridges must be periodically
tested.
a. Test a portion of particulate cartridges upon
procurement.
Minimum requirement
- each site may be more
restrictive
b. Test all particulate cartridges prior to re-use.
c. Respirator facepieces are tested annually using:
1) Test head mannequin Penetration value of
less than or equal to
0.003% is acceptable
2) Challenge atmosphere with a light scattering
photometer
6. Fit testing of individual is normally quantitative Objective 2.07.07
a. Involves measurement of a challenge atmosphere
both inside and outside respiratory facepiece
b. A "fit factor" is determined by dividing concentration
of challenge atmosphere outside respirator by
concentration inside facepiece.
Note: DOP has been
discontinued as a
challenge atmosphere
since it is a potential
carcinogen
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c. An oil mist may be used as a challenge atmosphere.
d. Apparatus uses photometry as system for measuring
challenge and breathing zone atmospheres.
e. Subject generally performs the following functions
during fit testing:
Section 5
Highlight significance
of functions as related
to job performance
1) Normal breathing
2) Deep breathing
3) Moving head from side to side
4) Moving head up and down
5) Frown
6) Talking
7) Running in place
8) Normal breathing
D. SELECTION OF RESPIRATORS
1. Most critical factor: the protection factor for respirator
device to be used needs to be greater than ratio of work
area concentration to associated DAC.
Objective 2.07.08
10 CFR 835
2. Only approved respirators shall be selected. ANSI Z88.2, 1980
3. General considerations. The selection of a proper
respirator for any given situation shall require
consideration of the following factors:
Objective 2.07.09
a. The nature of the hazard
b. The characteristics of the hazardous operation or
process
c. The location of the hazardous area with respect to a
safe area having respirable air.
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d. The period of time for which respirator protection
may be provided
e. The activity of workers in the hazardous area
f. The physical characteristics, functional capabilities,
and limitations of respirators of various types.
g. The respirator-protection factors and respirator fit
h. Requirement of facility/site written procedures
4. Nature of Hazard. The following factors concerning the
nature of the hazard requiring the use of respirators shall
be considered in respirator selection:
a. Type of hazard
• Oxygen deficiency
• Contaminant
b. Physical properties
c. Chemical properties
d. Physiological effects on the body
e. Actual concentration of a toxic material or airborne
radioactivity level both average and peak
f. Whether the hazard is an immediately-dangerous-to-
life-or-health (IDLH) concentration
g. Warning properties
5. Recognition and evaluation of the respiratory hazard
(oxygen deficiency or contaminant(s)) shall be an
essential part of selecting a respirator except in
emergency or rescue operations. Initial monitoring of the
respiratory hazard shall be carried out to obtain data
needed for the selection of proper respiratory protection.
The data should include:
a. Identification of the type of respiratory hazard
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1) Oxygen deficiency
2) Specific contaminant(s)
b. Nature of contaminant(s)
1) Particulate matter
2) Vapor(s) or gas(es)
c. Concentration of respiratory hazard
6. The following factors concerning the hazardous
operation or process shall be taken into account in
selecting the proper respirator:
a. Operation or process characteristics both as-built and
modified
b. Work-area characteristics
c. Materials, including raw materials, end products, and
byproducts (actual and potential)
d. Worker activities
E. SITE RESPIRATORY EQUIPMENT Objective 2.07.10
(Insert site specific material here)
F. SUPPLIED AIR QUALITY TESTING
1. Referenced in 29 CFR 1910.134 Objective 2.07.11
a. Compressed breathing air shall meet at least quality
specification for Grade D breathing air.
b. Breathing air specifications are listed in Compressed
Gas Association G 7.1-1989.
2. No explicit limit for water vapor but is contaminant
3. Acceptable analytical procedures for measuring the
respirable air components
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4. Frequency of performing air quality tests is
recommended by ANSI Z88.2-1992
Section 6
a. For bottled air systems received from a supplier that
does not fill cylinders with any other gasses, the tests
should check 10% of the cylinders from each lot for
ppm CO and odor. In addition, if the supplier fills
cylinders with gas other than air, analyze all
cylinders for percent oxygen.
b. For facilities which generate respirable air, the
sampling should be performed:
1) Prior to each lot fill
2) Once during the lot fill
3) Once upon completion of the lot fill
c. For compressed air supply systems sampling
frequency is best performed prior to each use of a
specific manifold system.
In cases of heavy usage
then a daily check of
the system may be
more appropriate.
5. Separate breathing air supply and distribution system is
the ideal source or worker-supplied air
G. SORBENTS AND PROTECTION AGAINST
RADIOIODINES
1. The regulations specifically prohibit the use of PFs for
canister sorbents as protection against radioiodine
atmospheres
The efficiency of the charcoal canister is dependent upon:
a. chemical form of the radioiodine,
b. humidity of the atmosphere,
c. and breathing rate of the user.
2. Approval may be obtained to use PF's for sorbent
cartridges.
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3. Examples of limiting conditions of use (user must follow
manufactures instructions and DOE approval criteria):
a. Total challenge in the work place (radioactive iodine,
non-radioactive iodine or the halogenated
compounds) may not exceed 1 ppm.
b. Temperature in the work area may not exceed 100
�F.
c. Respirator wearers must have demonstrated a fit
factor greater than 100 for half mask, 1000 for full
face piece.
d. Service life is 8 hours maximum. This is calculated
from the time the canister is unsealed and includes
periods of non-use.
e. Canisters will not be used in the presence of organic
solvents, vapors, or chemicals.
f. Canisters must be stored in sealed humidity-barrier
packaging in a cool, dry environment.
H. COMMUNICATIONS
1. Conventional respirators distort the human voice to some
extent.
2. Special attachments are often needed to ensure adequate
communications
a. Speaking diaphragm
b. Various methods of electronically transmitting and
amplifying speech through the respirator.
c. Any communication device that is an integral part of
respirator must be part of NIOSH/MSHA approval.
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III. SUMMARY
A. Review major topics
1. Requirements and regulations
2. Types of equipment
3. Protection factors
4. Fit testing
5. Selection of respirators
6. Site respiratory equipment
7. Supplied air quality testing
8. Sorbents and protection against radioiodines
9. Communications
2. Review learning objectives
IV. EVALUATION
Evaluation should consist of a written examination comprised of
multiple choice, fill-in the blank, matching and/or short answer
questions. 80% should be the minimum passing criteria for
examinations.
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Module Number: 2.07