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10 CFR 20.1204 - Determination of internal exposure.

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§ 20.1204
Determination of internal exposure.
(a) For purposes of assessing dose used to determine compliance with occupational dose equivalent limits, the licensee shall, when required under § 20.1502, take suitable and timely measurements of—
(1) Concentrations of radioactive materials in air in work areas; or
(2) Quantities of radionuclides in the body; or
(3) Quantities of radionuclides excreted from the body; or
(4) Combinations of these measurements.
(b) Unless respiratory protective equipment is used, as provided in § 20.1703, or the assessment of intake is based on bioassays, the licensee shall assume that an individual inhales radioactive material at the airborne concentration in which the individual is present.
(c) When specific information on the physical and biochemical properties of the radionuclides taken into the body or the behavior or the material in an individual is known, the licensee may—
(1) Use that information to calculate the committed effective dose equivalent, and, if used, the licensee shall document that information in the individual's record; and
(2) Upon prior approval of the Commission, adjust the DAC or ALI values to reflect the actual physical and chemical characteristics of airborne radioactive material (e.g., aerosol size distribution or density); and
(3) Separately assess the contribution of fractional intakes of Class D, W, or Y compounds of a given radionuclide (see appendix B to part 20) to the committed effective dose equivalent.
(d) If the licensee chooses to assess intakes of Class Y material using the measurements given in § 20.1204(a)(2) or (3), the licensee may delay the recording and reporting of the assessments for periods up to 7 months, unless otherwise required by §§ 20.2202 or 20.2203, in order to permit the licensee to make additional measurements basic to the assessments.
(e) If the identity and concentration of each radionuclide in a mixture are known, the fraction of the DAC applicable to the mixture for use in calculating DAC-hours must be either—
(1) The sum of the ratios of the concentration to the appropriate DAC value (e.g., D, W, Y) from appendix B to part 20 for each radio-nuclide in the mixture; or
(2) The ratio of the total concentration for all radionuclides in the mixture to the most restrictive DAC value for any radionuclide in the mixture.
(f) If the identity of each radionuclide in a mixture is known, but the concentration of one or more of the radionuclides in the mixture is not known, the DAC for the mixture must be the most restrictive DAC of any radionuclide in the mixture.
(g) When a mixture of radionuclides in air exists, licensees may disregard certain radionuclides in the mixture if—
(1) The licensee uses the total activity of the mixture in demonstrating compliance with the dose limits in § 20.1201 and in complying with the monitoring requirements in § 20.1502(b), and
(2) The concentration of any radionuclide disregarded is less than 10 percent of its DAC, and
(3) The sum of these percentages for all of the radionuclides disregarded in the mixture does not exceed 30 percent.
(h) (1) In order to calculate the committed effective dose equivalent, the licensee may assume that the inhalation of one ALI, or an exposure of 2,000 DAC-hours, results in a committed effective dose equivalent of 5 rems (0.05 Sv) for radionuclides that have their ALIs or DACs based on the committed effective dose equivalent.
(2) When the ALI (and the associated DAC) is determined by the nonstochastic organ dose limit of 50 rems (0.5 Sv), the intake of radionuclides that would result in a committed effective dose equivalent of 5 rems (0.05 Sv) (the stochastic ALI) is listed in parentheses in table 1 of appendix B to part 20. In this case, the licensee may, as a simplifying assumption, use the stochastic ALIs to determine committed effective dose equivalent. However, if the licensee uses the stochastic ALIs, the licensee must also demonstrate that the limit in § 20.1201(a)(1)(ii) is met.
[56 FR 23396, May 21, 1991, as amended at 60 FR 20185, Apr. 25, 1995]

Title 10 published on 2012-01-01

The following are only the Rules published in the Federal Register after the published date of Title 10.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

  • 2013-03-19; vol. 78 # 53 - Tuesday, March 19, 2013
    1. 78 FR 16922 - Physical Protection of Byproduct Material
      GPO FDSys XML | Text
      NUCLEAR REGULATORY COMMISSION
      Final rule.
      Effective Date: This final rule is effective on May 20, 2013. Compliance Date: Compliance with this final rule is required on March 19, 2014.
      10 CFR Parts 20, 30, 32, 33, 34, 35, 36, 37, 39, 51, 71, and 73

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


United States Code
U.S.C. : Title 42 - THE PUBLIC HEALTH AND WELFARE

§ 2014 - Definitions

§ 2021 - Cooperation with States

§ 2021b - Definitions

§ 2073 - Domestic distribution of special nuclear material

§ 2093 - Domestic distribution of source material

§ 2095 - Reports

§ 2111 - Domestic distribution

§ 2133 - Commercial licenses

§ 2134 - Medical, industrial, and commercial licenses

§ 2201 - General duties of Commission

§ 2232 - License applications

§ 2236 - Revocation of licenses

§ 2297f - Gaseous diffusion facilities

§ 5841 - Establishment and transfers

§ 5842 - Licensing and related regulatory functions respecting selected Administration facilities

§ 5846 - Compliance with safety regulations

USC : Title 44 - PUBLIC PRINTING AND DOCUMENTS

§ 3504 note - Authority and functions of Director

Title 10 published on 2012-01-01

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 10 CFR 20 after this date.

  • 2013-03-19; vol. 78 # 53 - Tuesday, March 19, 2013
    1. 78 FR 16922 - Physical Protection of Byproduct Material
      GPO FDSys XML | Text
      NUCLEAR REGULATORY COMMISSION
      Final rule.
      Effective Date: This final rule is effective on May 20, 2013. Compliance Date: Compliance with this final rule is required on March 19, 2014.
      10 CFR Parts 20, 30, 32, 33, 34, 35, 36, 37, 39, 51, 71, and 73