ASTM C967-87(1996)
(Specification)Standard Specification for Uranium Ore Concentrate
Standard Specification for Uranium Ore Concentrate
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1.1 This specification covers uranium ore concentrate containing a minimum of 65 weight% uranium.
1.2 This specification does not include requirements for health and safety. Observance of this standard does not relieve the user of the obligation to be aware of and conform to all applicable international, national, state, and local regulations pertaining to possessing, shipping, or using source nuclear material (see 2.2).
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
General Information
Relations
Standards Content (Sample)
NOTICE: This standard has either been superseded and replaced by a new version or
withdrawn. Contact ASTM International (www.astm.org) for the latest information.
Designation: C 967 – 87 (Reapproved 1996)
AMERICAN SOCIETY FOR TESTING AND MATERIALS
100 Barr Harbor Dr., West Conshohocken, PA 19428
Reprinted from the Annual Book of ASTM Standards. Copyright ASTM
Standard Specification for
Uranium Ore Concentrate
This standard is issued under the fixed designation C 967; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
INTRODUCTION
This specification is intended to provide the nuclear industry with a general standard for uranium
ore concentrate. Material conforming to this specification will generally meet the requirements for
conversion to uranium hexafluoride. However, the converter may relax or supplement this specifica-
tion upon mutual agreement with the customer.
1. Scope 2.3 ANSI Standard:
ANSI/ASME NQA-1 Quality Assurance Requirements for
1.1 This specification covers uranium ore concentrate con-
Nuclear Facilities
taining a minimum of 65 weight % uranium.
1.2 This specification does not include requirements for
3. Terminology Definitions
health and safety. Observance of this specification does not
3.1 Except as otherwise defined herein, definitions of terms
relieve the user of the obligation to be aware of and conform to
are as given in Terminology C 859.
all applicable international, national, state, and local regula-
tions pertaining to possessing, shipping, or using source
4. Chemical Composition
nuclear material (see 2.2).
4.1 Uranium Content—The uranium content, as received,
1.3 The values stated in SI units are to be regarded as the
shall be a minimum of 65 weight %.
standard. The values given in parentheses are for information
4.2 Isotopic Content—The isotopic content shall be that of
only.
naturally occurring uranium (0.7105 to 0.7115 % U).
4.3 Insoluble Uranium—The uranium insoluble in nitric
2. Referenced Documents
acid shall be a maximum of 0.10 weight % on a uranium basis.
2.1 ASTM Standards:
4.4 Extractable Organic—The extractable organic shall be a
C 859 Terminology Relating to Nuclear Materials
maximum of 0.10 weight % on an as-received basis of an
C 1022 Test Methods for Chemical and Atomic Absorption
undried sample.
Analysis of Uranium-Ore Concentrate
4.5 Impurity Content—The impurity content shall be less
C 1075 Practices for Sampling Uranium-Ore Concentrate
than the maximum limits specified in Table 1.
2.2 U.S. Government Documents:
Nuclear Materials Licensing Code of Federal Regulations
5. Physical Properties
(latest edition) Title 10, Chapter 1, Nuclear Regulatory
5.1 Particle Size—All of a representative sample (Section
Commission
6) shall pass through a sieve with an aperature of 6.35 mm ( ⁄4
Nuclear Materials Licensing Code of Federal Regulations,
in.).
Title 49, Transportation Chapter 1, Materials Transporta-
5.2 Ability to Flow—Concentrate shall be sufficiently free-
tion Bureau
flowing to permit sampling.
Nuclear Materials Licensing Code of Federal Regulations,
5.3 Foreign Matter—Concentrate shall be free of all mate-
Energy Part 50 (10CFR 50) Licensing of Domestic Pro-
rials and objects that: (a) are not produced as a constituent of
duction and Utilization Facilities
concentrates in the milling of uranium ore, or, (b) would or
could be detrimental to the sampling of concentrates or to the
1 equipment used in such sampling.
This specification is under the jurisdiction of ASTM Committee C-26 on
Nuclear Fuel Cycle and is the direct responsibility of Subcommittee C26.02 on Fuel
6. Sampling
and Fertile Material Specifications.
Current edition approved May 29, 1987. Published July 1987. Originally
6.1 The lot size and
...
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SIGNIFICANCE AND USE
5.1 Specific gamma-ray emitting radionuclides in UF6 are identified and quantified using a high-resolution gamma-ray energy analysis system, which includes a high-resolution germanium detector. This test method shall be used to meet the health and safety specifications of C787, C788, and C996 regarding applicable fission products in reprocessed uranium solutions. This test method may also be used to provide information to parties such as conversion facilities on the level of uranium decay products in such materials. Pa-231 is a specific uranium decay product that may be present in uranium ore concentrate and is amenable to analysis by gamma spectrometry.
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1.1 This test method covers the measurement of gamma energy emitted from fission products in uranium hexafluoride (UF6) and uranyl nitrate solution. This test method may also be used to measure the concentration of some uranium decay products. It is intended to provide a method for demonstrating compliance with UF6 Specifications C787 and C996, uranyl nitrate Specification C788, and uranium ore concentrate Specification C967.
1.2 The lower limit of detection is estimated at 5000 MeV Bq/kg (MeV kg-1/s-1) of uranium and is the square root of the sum of the squares of the individual reporting limits of the nuclides to be measured. The limit of detection was determined on a pure, aged natural uranium (ANU) solution. The value is dependent upon the detector efficiency and background that can be achieved.
1.3 The fission product nuclides to be measured are 106Ru/106Rh, 103Ru, 137Cs, 144Ce, 144Pr, 141Ce, 95Zr, 95Nb, and 125Sb. Among the uranium decay product nuclides that may be measured is 231Pa. Other gamma energy-emitting fission and uranium decay nuclides present in the spectrum at detectable levels should be identified and quantified as required by the data quality objectives.
1.4 The values stated in SI units are to be regarded as standard. Additionally, the non-SI units of kiloelectron volts and megaelectron volts are to be regarded as standard. No other units of measurement are included in this standard.
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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1.1 This terminology standard covers terms, definitions, descriptions of terms, nomenclature, and explanations of acronyms and symbols specifically associated with standards under the jurisdiction of Committee C26 on Nuclear Fuel Cycle. The content of this terminology standard may also be applicable to documents not under the jurisdiction of Committee C26, in which case this terminology standard may be referenced in those documents.
1.2 While subcommittees within Committee C26 are free to only provide terms and definitions within individual standards, each subcommittee may request the addition of utilized terms and definitions to this terminology standard if it believes that such serves the broader interest of Committee C26 and the nuclear fuel cycle profession. Therefore, terms and definitions proposed for inclusion in Terminology C859 need not be used in more than one committee standard before being considered.
1.3 In general, technical terms that are defined in common dictionaries would not also be defined in this terminology standard unless there is a need to emphasize a specific definition in making appropriate use of a Committee C26 standard.
1.4 Subcommittee C26.10 (Nondestructive Assay) also has a terminology standard applicable to its standards: Terminology C1673.
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
5.1 The total evaporation method is used to measure the isotopic composition of uranium, plutonium, and americium materials, and may be used to measure the elemental concentrations of these elements when employing the IDMS technique.
5.2 Uranium and plutonium compounds are used as nuclear reactor fuels. In order to be suitable for use as a nuclear fuel the starting material must meet certain criteria, such as found in Specifications C757, C833, C753, C776, C787, C967, C996, or as specified by the purchaser. The uranium concentration, plutonium concentration, or both, and isotope abundances are measured by TIMS following this method.
5.3 Americium-241 is the decay product of 241Pu isotope. The abundance of the 241Am isotope together with the abundance of the 241Pu parent isotope can be used to estimate radio-chronometric age of the Pu material for nuclear forensic applications Ref (6). The americium concentration and isotope abundances are measured by TIMS following this method.
5.4 The total evaporation method allows for a wide range of sample loading with no significant change in precision or accuracy. The method is also suitable for trace-level loadings with some loss of precision and accuracy. The total evaporation method and modern instrumentation allow for the measurement of minor isotopes using ion counting detectors, while the major isotope(s) is(are) simultaneously measured using Faraday cup detectors.
5.5 The new generation of miniaturized ion counters allow extremely small samples, in the picogram range, to be measured via the total evaporation method. The method may be employed for measuring environmental or safeguards inspection samples containing nanogram quantities of uranium or plutonium. Very small loadings require special sample handling and careful evaluation of measurement uncertainties.
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1.1 This method describes the determination of the isotopic composition, or the concentration, or both, of uranium, plutonium, and americium as nitrate solutions by the total evaporation method using a thermal ionization mass spectrometer (TIMS) instrument. Purified uranium, plutonium, or americium nitrate solutions are deposited onto a metal filament and placed in the mass spectrometer. Under computer control, ion currents are generated by heating of the filament(s). The ion currents are continually measured until the whole deposited solution sample is exhausted. The measured ion currents are integrated over the course of the measurement and normalized to a reference isotope ion current to yield isotope ratios.
1.2 In principle, the total evaporation method should yield isotope ratios that do not require mass bias correction. In practice, samples may require this bias correction. Compared to the conventional TIMS method described in Test Method C1625, the total evaporation method is approximately two times faster, improves precision of the isotope ratio measurements by a factor of two to four, and utilizes smaller sample sizes. Compared to the C1625 method, the total evaporation method provides “major” isotope ratios 235U/238U, 240Pu/239Pu, and 241Am/243Am with improved accuracy.
1.3 The total evaporation method is prone to biases in the “minor” isotope ratios (233U/238U, 234U/238U, and 236U/238U ratios for uranium materials and 238Pu/239Pu, 241Pu/239Pu, 242Pu/239Pu, and 244Pu/239Pu ratios for plutonium materials) due to peak tailing from adjacent major isotopes. The magnitude of the absolute bias is dependent on measurement and instrumental characteristics. The relative bias, however, depends on the relative isotopic abundances of the sample. The use of an electron multiplier equipped with an energy filter may eliminate or diminish peak tailing effects. Measurement of the abundance sensitivity of the instrument m...
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SIGNIFICANCE AND USE
5.1 This test method can be used on plutonium matrices in nitrate solutions.
5.2 This test method has been validated for all elements listed in Test Methods C757 except sulfur (S) and tantalum (Ta).
5.3 This test method has been validated for all of the cation elements measured in Table 1. Phosphorus (P) requires a vacuum or an inert gas purged optical path instrument.
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1.1 This test method covers the determination of 25 elements in plutonium (Pu) materials. The Pu is dissolved in acid, the Pu matrix is separated from the target impurities by an ion exchange separation, and the concentrations of the impurities are determined by inductively coupled plasma-atomic emission spectroscopy (ICP-AES).
1.2 This test method is specific for the determination of impurities in 8 M HNO3 solutions. Impurities in other plutonium materials, including plutonium oxide samples, may be determined if they are appropriately dissolved (see Practice C1168) and converted to 8 M HNO3 solutions.
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions that are provided for information only and are not considered standard. Additionally, the non-SI units of molarity and centimeters of mercury are to be regarded as standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Some specific hazards statements are given in Section 9 on Hazards.
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
5.1 This guide assists in satisfying requirements in such areas as safeguards, SNM inventory control, nuclear criticality safety, waste disposal, and decontamination and decommissioning (D&D). This guide can apply to the measurement of holdup in process equipment or discrete items whose neutron production properties may be measured or estimated. These methods may meet target accuracy for items with complex distributions of SNM in the presence of moderators, absorbers, and neutron poisons; however, the results are subject to larger measurement uncertainties than measurements of less complex items.
5.2 Quantitative Measurements—These measurements result in quantification of the mass of SNM in the holdup. They include all the corrections and descriptive information, such as isotopic composition, that are available.
5.2.1 High-quality results require detailed knowledge of radiation sources and detectors, radiation transport, calibration, facility operations, and error analysis. Consultation with qualified NDA personnel is recommended (Guide C1490).
5.2.2 Holdup estimates for a single piece of process equipment or piping often include some compilation of multiple measurements. The holdup estimate must appropriately combine the results of each individual measurement. In addition, uncertainty estimates for each individual measurement must be made and appropriately combined.
5.3 Scan—Radiation scanning, typically gamma, may be used to provide a qualitative description of the extent, location, and the relative quantity of holdup. It can be used to plan or supplement the quantitative neutron measurements. Other indicators (for example, visual) may also indicate a need for a holdup measurement.
5.4 Nuclide Mapping—To appropriately interpret the neutron data, the specific neutron yield is needed. Isotopic measurements to determine the relative isotopic composition of the holdup at specific locations may be required, depending on the facility.
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1.1 This guide describes passive neutron measurement methods used to nondestructively estimate the amount of neutron-emitting special nuclear material compounds remaining as holdup in nuclear facilities. Holdup occurs in all facilities in which nuclear material is processed. Material may exist, for example, in process equipment, in exhaust ventilation systems, and in building walls and floors.
1.1.1 The most frequent uses of passive neutron holdup techniques are for the measurement of uranium or plutonium deposits in processing facilities.
1.2 This guide includes information useful for management, planning, selection of equipment, consideration of interferences, measurement program definition, and the utilization of resources.
1.3 Counting modes include both singles (totals) or gross counting and neutron coincidence techniques.
1.3.1 Neutron holdup measurements of uranium are typically performed on neutrons emitted during (α, n) reactions and spontaneous fission using singles (totals) or gross counting. While the method does not preclude measurement using coincidence or multiplicity counting for uranium, measurement efficiency is generally not sufficient to permit assays in reasonable counting times.
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SIGNIFICANCE AND USE
5.1 Plutonium and uranium mixtures are used as nuclear reactor fuels. For use as a nuclear reactor fuel, the material must meet certain criteria for combined uranium and plutonium content, effective fissile content, and impurity content as described in Specifications C757 and C833. After dissolution using one of the procedures described in this practice, the material is assayed for plutonium and uranium to determine if the content is correct as specified by the purchaser.
5.2 Unique plutonium materials, such as alloys, compounds, and scrap metals, are typically dissolved with various acid mixtures or by fusion with various fluxes. Many plutonium salts are soluble in hydrochloric acid. One or more of the procedures included in this practice may be effective for some of these materials; however their applicability to a particular plutonium material shall be verified by the user.
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1.1 This practice is a compilation of dissolution techniques for plutonium materials that are applicable to the test methods used for characterizing these materials. Dissolution treatments for the major plutonium materials assayed for plutonium or analyzed for other components are listed. Aliquots of the dissolved materials are dispensed on a mass basis when one of the analyses must be of high precision, such as plutonium assay; otherwise they are dispensed on a volume basis.
1.2 Procedures in this practice are intended for the dissolution of plutonium metal, plutonium oxide, and uranium-plutonium mixed oxides. Aliquots of dissolved materials are analyzed using test methods, such as those developed by Subcommittee C26.05 on Methods of Test, to demonstrate compliance with applicable requirements. These may include product specifications such as Specifications C757 and C833.
1.3 One or more of the procedures in this practice may be applicable to unique plutonium materials, such as alloys, compounds, and scrap materials. The user must determine the applicability of this practice to such materials.
1.4 The treatments, in order of presentation, are as follows:
Procedure Number
Procedure Title
Section
1
Dissolution of Plutonium Metal with Hydrochloric Acid at Room Temperature
9
2
Dissolution of Plutonium Metal with Hydrochloric Acid and Heating
10
3
Dissolution of Plutonium Metal with Sulfuric Acid
11
4
Dissolution of Plutonium Oxide and Uranium-Plutonium Mixed
Oxide by the Sealed-Reflux Technique
12
5
Dissolution of Plutonium Oxide and Uranium-Plutonium Mixed Oxides by Sodium Bisulfate Fusion
13
6
Dissolution of Uranium-Plutonium Mixed Oxides and Low-Fired Plutonium Oxide in Beakers
14
7
Open-Vessel (with Reflux Condenser) Dissolution of Plutonium Oxide Powder
15
8
Open-Vessel (with Reflux Condenser) Dissolution of Mixed Oxide Powder
16
9
Closed-Vessel Hot Block Dissolution of Plutonium Oxide Powder
17
10
Open-Vessel (with Reflux Condenser) Dissolution of Mixed Oxide Pellets
18
1.5 The values stated in SI units are to be regarded as standard. The non-SI unit of molarity (M) is also to be regarded as standard. Values in parentheses (non-SI units), where provided, are for information only and are not considered standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
5.1 This test method allows the determination of 241Am in a plutonium solution without separation of the americium from the plutonium. It is generally applicable to any solution containing 241Am.
5.2 The 241Am in solid plutonium materials may be determined when these materials are dissolved (see Practice C1168).
5.3 When the plutonium solution contains unacceptable levels of fission products or other materials, this method may be used following a tri-n-octylphosphine oxide (TOPO) extraction, ion exchange or other similar separation techniques (see Test Methods C758 and C759).
5.4 This test method is less subject to interferences from plutonium than alpha counting since the energy of the gamma ray used for the analysis is better resolved from other gamma rays than the alpha particle energies used for alpha counting.
5.5 The minimal sample preparation reduces the amount of sample handling and exposure to the analyst.
5.6 This test method is applicable only to homogeneous solutions. This test method is not suitable for solutions containing solids.
5.7 Solutions containing 241Am at concentrations as little as 1 × 10−5 g/L may be analyzed using this method. The lower limit depends on the detector used and the counting geometry. Solutions containing high concentrations may be analyzed following an appropriate dilution.
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1.1 This test method covers the quantitative determination of 241Am by gamma-ray spectrometry in plutonium nitrate solution samples that do not contain significant amounts of radioactive fission products or other high specific activity gamma-ray emitters.
1.2 This test method can be used to determine the 241Am in samples of plutonium metal, oxide and other solid forms, when the solid is appropriately sampled and dissolved.
1.3 The values stated in SI units are to be regarded as standard. Additionally, the non-SI units of electron volts, kiloelectron volts, and liters are to be regarded as standard. No other units of measurement are included in this standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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ABSTRACT
This specification covers finished sintered and ground (uranium-plutonium) dioxide pellets for use in thermal reactors. It applies to uranium-plutonium dioxide pellets containing plutonium additions up to 15 % weight. The diversity of manufacturing methods shall be recognized by which uranium-plutonium dioxide pellets are produced and the many special requirements for chemical and physical characterization that may be imposed by the operating conditions to which the pellets will be subjected in specific reactor systems. The following are different chemical requirements that shall be determined: uranium content, plutonium content, impurity content, stoichiometry, moisture content, gas content, and americium-241 content. Nuclear requirements such as isotopic content, plutonium equivalent at a given date, equivalent boron content, and reactivity shall also be determined. Physical properties of the pellets like dimensions, density, grain size, pore morphology, plutonium-oxide homogeneity, plutonium-oxide particle size, plutonium-oxide particle distribution, integrity, and surface cracks shall be determined as well. The surfaces of finished pellets shall be visually free of loose chips, oil, macroscopic inclusions, and foreign materials. An estimate of the fuel pellet irradiation stability shall be obtained unless adequate allowance for such effects are factored into the fuel rod design. The estimate of the stability shall consist of either conformance to the thermal stability test as specified in the or by adequate correlation of manufacturing process or microstructure to in-reactor behavior, or both.
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1.1 This specification covers finished sintered and ground (U, Pu)O2 pellets for use in light water reactors. It applies to (U, Pu)O2 pellets containing a plutonium mass fraction up to 15 % (that is, mass of Pu divided by the sum of masses U, Pu, and Am yielding 0.15 or less).
1.2 Pellets produced under this specification are available in four grades.
1.2.1 Grade R—240Pu / (Pu + Am) isotope mass fraction is at least 19 %.
1.2.2 Grade F—240Pu / (Pu + Am) isotope mass fraction is at least 7 % and less than 19 %.
1.2.3 Grade N1—240Pu / (Pu + Am) isotope mass fraction is less than 7 %.
1.2.4 Grade N2—240Pu /239Pu isotope mass fraction does not exceed 0.10 (10 %).
1.3 There is no discussion of or provision for preventing criticality incidents, nor are health and safety requirements, the avoidance of hazards, or shipping precautions and controls discussed. Observance of this specification does not relieve the user of the obligation to be aware of and conform to all applicable international, federal, state, and local regulations pertaining to possessing, processing, shipping, or using source or special nuclear material. Examples of U.S. government documents are Code of Federal Regulations Title 10, Part 50—Domestic Licensing of Production and Utilization Facilities; Code of Federal Regulations Title 10, Part 71—Packaging and Transportation of Radioactive Material; and Code of Federal Regulations Title 49, Part 173—General Requirements for Shipments and Packaging.
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.5 The following safety hazards caveat pertains only to the technical requirements portion, Section 4, of this specification: This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
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SIGNIFICANCE AND USE
5.1 Uranium hexafluoride is a basic material used to produce nuclear reactor fuel. To be suitable for this purpose, the material must meet criteria for isotopic composition. This test method is designed to determine whether the material meets the requirements described in Specifications C787 and C996.
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1.1 This test method is applicable to the isotopic analysis of uranium hexafluoride (UF6) with 235U concentrations less than or equal to 5 % and 234U, 236U concentrations of 0.0002 to 0.1 %.
1.2 This test method may be applicable to the analysis of the entire range of 235U isotopic compositions providing that adequate Certified Reference Materials (CRMs or traceable standards) are available.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
4.1 The purpose of this guide is to provide information that will help to ensure that nuclear fuel dissolution facilities are conceived, designed, fabricated, constructed, and installed in an economic and efficient manner. This guide will help facilities meet the intended performance functions, eliminate or minimize the possibility of nuclear criticality and provide for the protection of both the operator personnel and the public at large under normal and abnormal (emergency) operating conditions as well as under credible failure or accident conditions.
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1.1 It is the intent of this guide to set forth criteria and procedures for the design, fabrication and installation of nuclear fuel dissolution facilities. This guide applies to and encompasses all processing steps or operations beyond the fuel shearing operation (not covered), up to and including the dissolving accountability vessel.
1.2 Applicability and Exclusions:
1.2.1 Operations—This guide does not cover the operation of nuclear fuel dissolution facilities. Some operating considerations are noted to the extent that these impact upon or influence design.
1.2.1.1 Dissolution Procedures—Fuel compositions, fuel element geometry, and fuel manufacturing methods are subject to continuous change in response to the demands of new reactor designs and requirements. These changes preclude the inclusion of design considerations for dissolvers suitable for the processing of all possible fuel types. This guide will only address equipment associated with dissolution cycles for those fuels that have been used most extensively in reactors as of the time of issue (or revision) of this guide. (See Appendix X1.)
1.2.2 Processes—This guide covers the design, fabrication and installation of nuclear fuel dissolution facilities for fuels of the type currently used in Pressurized Water Reactors (PWR). Boiling Water Reactors (BWR), Pressurized Heavy Water Reactors (PHWR) and Heavy Water Reactors (HWR) and the fuel dissolution processing technologies discussed herein. However, much of the information and criteria presented may be applicable to the equipment for other dissolution processes such as for enriched uranium-aluminum fuels from typical research reactors, as well as for dissolution processes for some thorium and plutonium-containing fuels and others. The guide does not address equipment design for the dissolution of high burn-up or mixed oxide fuels.
1.2.2.1 This guide does not address special dissolution processes that may require substantially different equipment or pose different hazards than those associated with the fuel types noted above. Examples of precluded cases are electrolytic dissolution and sodium-bonded fuels processing. The guide does not address the design and fabrication of continuous dissolvers.
1.2.3 Ancillary or auxiliary facilities (for example, steam, cooling water, electrical services) are not covered. Cold chemical feed considerations are addressed briefly.
1.2.4 Dissolution Pretreatment—Fuel pretreatment steps incidental to the preparation of spent fuel assemblies for dissolution reprocessing are not covered by this guide. This exclusion applies to thermal treatment steps such as “Voloxidation” to drive off gases prior to dissolution, to mechanical decladding operations or process steps associated with fuel elements disassembly and removal of end fittings, to chopping and shearing operations, and to any other pretreatment operations judged essential to an efficient nuclear fuels dissolution step.
1.2.5 Fundamentals—This guide does not address specific chemical, physical or mechanical technology, fluid mechanics, stress analysis or other engineering fundamentals that are also applied in the creation of a safe design for nuclear fuel dissolution facilities.
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