27.120.30 - Fissile materials and nuclear fuel technology
ICS 27.120.30 Details
Fissile materials and nuclear fuel technology
Spaltbare Materialien
Matériaux fissiles et technologie du combustible nucléaire
Cepljivi materiali in jedrska gorivna tehnologija
General Information
Frequently Asked Questions
ICS 27.120.30 is a classification code in the International Classification for Standards (ICS) system. It covers "Fissile materials and nuclear fuel technology". The ICS is a hierarchical classification system used to organize international, regional, and national standards, facilitating the search and identification of standards across different fields.
There are 772 standards classified under ICS 27.120.30 (Fissile materials and nuclear fuel technology). These standards are published by international and regional standardization bodies including ISO, IEC, CEN, CENELEC, and ETSI.
The International Classification for Standards (ICS) is a hierarchical classification system maintained by ISO to organize standards and related documents. It uses a three-level structure with field (2 digits), group (3 digits), and sub-group (2 digits) codes. The ICS helps users find standards by subject area and enables statistical analysis of standards development activities.
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This document specifies a method which covers the determination of Gd2O3 content in UO2 fuel pellets, by X-ray fluorescence spectrometry.
Either wave dispersion X-ray fluorescence (WD-XRF) or energy dispersion X-ray fluorescence (ED-XRF) is applicable, however, this document states a method by using WD-XRF using Gd Lα-line.
This method has been tested for mass fractions of from 2 % to 10 % Gd2O3.
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This document specifies a method which covers the determination of Gd2O3 content in UO2 fuel pellets, by X-ray fluorescence spectrometry.
Either wave dispersion X-ray fluorescence (WD-XRF) or energy dispersion X-ray fluorescence (ED-XRF) is applicable, however, this document states a method by using WD-XRF using Gd Lα-line.
This method has been tested for mass fractions of from 2 % to 10 % Gd2O3.
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This document describes an analytical method for the determination of uranium in samples from pure product materials such as U metal, UO2, UO3, uranyl nitrate hexahydrate, uranium hexafluoride and U3O8 from the nuclear fuel cycle. This procedure is sufficiently accurate and precise to be used for nuclear materials accountability. This method can be used directly for the analysis of most uranium and uranium oxide nuclear reactor fuels, either irradiated or un-irradiated, and of uranium nitrate product solutions. Fission products equivalent to up to 10 % burn-up of heavy atoms do not interfere, and other elements which could cause interference are not normally present in sufficient quantity to affect the result significantly. The method recommends that an aliquot of sample is weighed and that a mass titration is used, in order to obtain improved precision and accuracy. This does not preclude the use of alternative techniques which could give equivalent performance. The use of automatic device(s) in the performance of some critical steps of the method has some advantages, mainly in the case of routine analysis.
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This document is applied to fuel fabrication. It describes the ceramographic procedure used to prepare sintered (U,Pu)O2 pellets for qualitative and quantitative examination of the (U,Pu)O2 pellet microstructure.
The examinations are performed
a) before any treatment or any etching, and
b) after thermal treatment or after chemical or ion etching.
They allow
— observation of any cracks, intra- and intergranular pores or inclusions, and
— measurement of the grain size, porosity and plutonium homogeneity distribution.
The mean grain diameter is measured by one of the classic methods: counting (intercept method), comparison with standard grids or typical images, etc.[2]. The measurement of individual grain sizes requires uniform development of the microstructure over the entire specimen.
The plutonium cluster and pore distribution and localization are generally analysed by automatic image analysis systems. The plutonium distribution is usually revealed by chemical etching or by alpha autoradiography. A scanning electron microscope (SEM) or a microprobe can also be used. In this case an additional preparation can be needed depending on the equipment used. This preparation is not in the scope of this standard.
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This document is applied to fuel fabrication. It describes the ceramographic procedure used to prepare sintered (U,Pu)O2 pellets for qualitative and quantitative examination of the (U,Pu)O2 pellet microstructure.
The examinations are performed
a) before any treatment or any etching, and
b) after thermal treatment or after chemical or ion etching.
They allow
— observation of any cracks, intra- and intergranular pores or inclusions, and
— measurement of the grain size, porosity and plutonium homogeneity distribution.
The mean grain diameter is measured by one of the classic methods: counting (intercept method), comparison with standard grids or typical images, etc.[2]. The measurement of individual grain sizes requires uniform development of the microstructure over the entire specimen.
The plutonium cluster and pore distribution and localization are generally analysed by automatic image analysis systems. The plutonium distribution is usually revealed by chemical etching or by alpha autoradiography. A scanning electron microscope (SEM) or a microprobe can also be used. In this case an additional preparation can be needed depending on the equipment used. This preparation is not in the scope of this standard.
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This document is applied to fuel fabrication. It describes the ceramographic procedure used to prepare sintered (U,Pu)O2 pellets for qualitative and quantitative examination of the (U,Pu)O2 pellet microstructure. The examinations are performed a) before any treatment or any etching, and b) after thermal treatment or after chemical or ion etching. They allow - observation of any cracks, intra- and intergranular pores or inclusions, and - measurement of the grain size, porosity and plutonium homogeneity distribution. The mean grain diameter is measured by one of the classic methods: counting (intercept method), comparison with standard grids or typical images, etc.[2]. The measurement of individual grain sizes requires uniform development of the microstructure over the entire specimen. The plutonium cluster and pore distribution and localization are generally analysed by automatic image analysis systems. The plutonium distribution is usually revealed by chemical etching or by alpha autoradiography. A scanning electron microscope (SEM) or a microprobe can also be used. In this case an additional preparation can be needed depending on the equipment used. This preparation is not in the scope of this standard.
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This document specifies an analytical method for determining the neptunium concentration by spectrophotometry, with spectrophotometer implemented in hot cell or glove box allowing the analysis of high activity solutions, with a standard uncertainty, with coverage factor k = 1 of about 5 %, in nitric acid solutions after the dissolution of nuclear reactor irradiated fuels, at different steps of the process in a nuclear fuel reprocessing plant or in other nuclear facilities. The method is applicable to sample from the process containing a concentration of neptunium between 10 mg·l-1 and 400 mg·l-1 and uranium concentrations of up to 300 g·l-1.
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This document specifies a method which applies to the preparation and validation of the standard materials generally called “large size spikes” with an uncertainty suitable for international nuclear safeguards used for measuring the content of plutonium and/or uranium by isotope dilution mass spectrometry. This measurement methodology can be applied to input solutions of irradiated Magnox and light water reactor fuels (boiling water reactor or pressurized water reactor); in final products at spent-fuel reprocessing plants; in feed and products of mixed oxide of plutonium and uranium (MOX); and in uranium fuel fabrication.
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This document specifies an analytical method for the electrochemical measurement of pure plutonium nitrate solutions of nuclear grade, with an expanded uncertainty not exceeding ±0,2 % at the confidence level of 0,95 for a single determination (coverage factor, k = 2). The method is applicable for aqueous solutions containing plutonium at more than 0,5 g/l and test samples containing plutonium between 4 mg and 15 mg. Application of this technique to solutions containing plutonium at less than 0,5 g/l and test samples containing plutonium at less than 4 mg requires experimental demonstration by the user that applicable data quality objectives will be met.
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This document specifies an analytical method for the electrochemical measurement of pure plutonium nitrate solutions of nuclear grade, with an expanded uncertainty not exceeding ±0,2 % at the confidence level of 0,95 for a single determination (coverage factor, k = 2). The method is applicable for aqueous solutions containing plutonium at more than 0,5 g/l and test samples containing plutonium between 4 mg and 15 mg. Application of this technique to solutions containing plutonium at less than 0,5 g/l and test samples containing plutonium at less than 4 mg requires experimental demonstration by the user that applicable data quality objectives will be met.
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This document specifies an analytical method for the electrochemical measurement of pure plutonium nitrate solutions of nuclear grade, with an expanded uncertainty not exceeding ±0,2 % at the confidence level of 0,95 for a single determination (coverage factor, k = 2). The method is applicable for aqueous solutions containing plutonium at more than 0,5 g/l and test samples containing plutonium between 4 mg and 15 mg. Application of this technique to solutions containing plutonium at less than 0,5 g/l and test samples containing plutonium at less than 4 mg requires experimental demonstration by the user that applicable data quality objectives will be met.
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This document specifies a method which covers the determination of Gd2O3 content in UO2 fuel pellets, by X-ray fluorescence spectrometry. Either wave dispersion X-ray fluorescence (WD-XRF) or energy dispersion X-ray fluorescence (ED-XRF) is applicable, however, this document states a method by using WD-XRF using Gd Lα-line. This method has been tested for mass fractions of from 2 % to 10 % Gd2O3.
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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.
SCOPE
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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SCOPE
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.
5.6 Typical uranium analyses are conducted using sample loadings between 50 nanograms and 800 nanograms. For uranium isotope ratios the total evapo...
SCOPE
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.
SCOPE
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.
5.5 Spot Check an...
SCOPE
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.
1.3.2 For measurement of plutonium in gloveboxes, installed measurement equipment may provide sufficient efficiency for performing counting using neutron coincidence techniques in reasonable counting times.
1.4 The measurement of nuclear material holdup in process equipment requires a scientific knowledge of radiation sources and detectors, radiation transport, modeling methods, calibration, facility operations, and uncertainty analysis. It is subject to the constraints of the facility, management, budget, and schedule, plus health and safety requirements, as well as the laws of physics. This guide does not purport to instruct the NDA practitioner on these principles.
1.5 The measurement process includes...
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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.
SCOPE
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.
SCOPE
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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This document is applicable to the determination of gadolinium as Gd2O3 in powder blends and sintered
pellets of Gd2O3 + UO2 and ((U, Gd) O2) from mass fraction 10 g/kg to 100 g/kg (i.e. 1 % to 10 %), using
a suitable ICP-AES instrument.
This methodology is capable of demonstrating compliance with agreed upon fuel specifications and
associated data quality objectives provided the user has performed qualification measurements
under their established measurement control program to demonstrate that measurement uncertainty
requirements will be met with the desired level of confidence at the specification
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This document specifies a method for the determination of uranium concentrations in nitric acid or TBP-DILUANT (for example TBP-kerosene) solutions coming from the nuclear fuel cycle.
The method is applicable
— for process control of solutions, free of suspension, which contain between 10 g/l to 300 g/l uranium,
and
— for high accuracy purposes (Safeguards) to nitric acid solutions, free of suspension, which contain
between 100 g/l and 220 g/l uranium.
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This document specifies a method for the determination of uranium concentrations in nitric acid or TBP-DILUANT (for example TBP-kerosene) solutions coming from the nuclear fuel cycle.
The method is applicable
— for process control of solutions, free of suspension, which contain between 10 g/l to 300 g/l uranium,
and
— for high accuracy purposes (Safeguards) to nitric acid solutions, free of suspension, which contain
between 100 g/l and 220 g/l uranium.
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This document is applicable to the determination of gadolinium as Gd2O3 in powder blends and sintered
pellets of Gd2O3 + UO2 and ((U, Gd) O2) from mass fraction 10 g/kg to 100 g/kg (i.e. 1 % to 10 %), using
a suitable ICP-AES instrument.
This methodology is capable of demonstrating compliance with agreed upon fuel specifications and
associated data quality objectives provided the user has performed qualification measurements
under their established measurement control program to demonstrate that measurement uncertainty
requirements will be met with the desired level of confidence at the specification
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SIGNIFICANCE AND USE
3.1 This practice uses one monitor (cobalt) with a nearly 1/v absorption cross-section curve and a second monitor (silver) with a large resonance peak so that its resonance integral is large compared to its thermal cross section. The pertinent data for these two reactions are given in Table 1. The equations are based on the Westcott formalism ((2, 3) and Practice E261) and determine a Westcott 2200 m/s neutron fluence rate nv0 and the Westcott epithermal index parameter . References (4-6) contain a general discussion of the two-reaction test method. In this practice, the absolute activities of both cobalt and silver monitors are determined. This differs from the test method in the references wherein only one absolute activity is determined. (A) The numbers in parentheses following given values are the uncertainty in the last digit(s) of the value; 0.729 (8) means 0.729 ± 0.008, 70.8(1) means 70.8 ± 0.1.(B) The decay constant, λ, is defined as ln(2) / t1/2 with units of sec–1, where t1/2 is the nuclide half-life in seconds.(C) Calculated using Eq 10.(D) In Fig. 1, Θ = 4ErkT/AΓ2 = 0.2 corresponds to the value for 109Ag for T = 293 K, ∑r = N0σr,max,T=0Kσr,max,T=0K = 31138.03 barn at 5.19 eV (13). The value of σr,max,T=0K = 31138.03 barns is calculated using the Breit-Wigner single-level resonance formula where the 109Ag atomic mass is A = 108.9047558 amu (14), the ENDF/B-VIII.0 (MAT = 4731) (13) resonance parameters are: resonance total width Γ = 0.1427333 eV, formation neutron width Γn = 0.0127333 eV, and radiative/decay width Γγ = 0.13 eV, with a resonance spin J=1, and the statistical spin factor where s1 = 1/2 and s2 = 1/2 are the spins of the two particles (neutron and 109Ag ground state (15)) forming resonance.
3.2 The advantages of this approach are the elimination of four difficulties associated with the use of cadmium: (1) the perturbation of the field by the cadmium; (2) the inexact cadmium cut-off energy; (3) the low melting temperature of cadmium; a...
SCOPE
1.1 This practice covers a suitable means of obtaining the thermal neutron fluence rate, or fluence, in nuclear reactor environments where the use of cadmium, as a thermal neutron shield as described in Test Method E262, is undesirable for reasons such as potential spectrum perturbations or due to temperatures above the melting point of cadmium.
1.2 The reaction 59Co(n,γ )60Co results in a well-defined gamma emitter having a half-life of 5.2711 years2 (8)3 (1).4 The reaction 109Ag(n,γ)110mAg results in a nuclide with a well-known, complex decay scheme with a half-life of 249.78 (2) days (1). Both cobalt and silver are available either in very pure form or alloyed with other metals such as aluminum. A reference source of cobalt in aluminum alloy to serve as a neutron fluence rate monitor wire standard is available from the National Institute of Standards and Technology (NIST) as Standard Reference Material (SRM) 953.5 The competing activities from neutron activation of other isotopes are eliminated, for the most part, by waiting for the short-lived products to die out before counting. With suitable techniques, thermal neutron fluence rate in the range from 108 cm−2·s−1 to 3 × 1015 cm−2·s−1 can be measured. Two calculational practices are described in Section 9 for the determination of neutron fluence rates. The practice described in 9.3 may be used in all cases. This practice describes a means of measuring a Westcott neutron fluence rate in 9.2 (Note 1) by activation of cobalt- and silver-foil monitors (see Terminology E170). For the Wescott Neutron Fluence Convention method to be applicable, the measurement location must be well moderated and be well represented by a Maxwellian low-energy distribution and an (1/E) epithermal distribution. These conditions are usually only met in positions surrounded by hydrogenous moderator without nearby strongly multiplying or absorbing materials.
Note 1: Westcott fluence rate ...
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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.
SCOPE
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.
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 Technic...
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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.
SCOPE
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
5.1 Refer to Guide E844 for the selection, irradiation, and quality control of neutron dosimeters.
5.2 Refer to Practice E261 for a general discussion of the determination of fast-neutron fluence rate with threshold detectors.
5.3 Pure aluminum in the form of foil or wire is readily available and easily handled. 27Al has an abundance of 100 % (1).3
5.4 24Na has a half-life of 14.958 (2)4 h (2) and emits gamma rays with energies of 1.368630 (5) and 2.754049 (13) MeV (2).
5.5 Fig. 1 shows a plot of the International Reactor Dosimetry and Fusion File (IRDFF-II) cross section (3, 4) versus neutron energy for the fast-neutron reaction 27Al(n,α) 24Na (3) along with a comparison to the current experimental database (5, 6). While the RRDF-2008 and IRDFF-1.05 cross sections extend from threshold up to 60 MeV, due to considerations of the available validation data, the energy region over which this standard recommends use of this cross section for reactor dosimetry applications only extends from threshold at ~4.25 MeV up to 20 MeV. This figure is for illustrative purposes and is used to indicate the range of response of the 27Al(n,α) reaction. Refer to Guide E1018 for recommended sources for the tabulated dosimetry cross sections.
FIG. 1 27Al(n,α)24Na Cross Section, from IRDFF-II Library, with EXFOR Experimental Data
5.6 Two competing activities, 28Al (2.25 (2) minute half-life) and 27Mg (9.458 (12) minute half-life), are formed in the reactions 27Al(n,γ)28Al and 27Al(n,p)27Mg, respectively, but these can be eliminated by waiting 2 h before counting.
SCOPE
1.1 This test method covers procedures measuring reaction rates by the activation reaction 27Al(n,α)24Na.
1.2 This activation reaction is useful for measuring neutrons with energies above approximately 6.5 MeV and for irradiation times up to about two days (for longer irradiations, or when there are significant variations in reactor power during the irradiation, see Practice E261).
1.3 With suitable techniques, fission-neutron fluence rates above 106 cm−2·s−1 can be determined.
1.4 Detailed procedures for other fast neutron detectors are referenced in Practice E261.
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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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.
SCOPE
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.
1.3 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI unit...
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SIGNIFICANCE AND USE
4.1 Materials handling equipment operability and long-term integrity are concerns that originate during the design and fabrication sequences. Such concerns are most efficiently addressed during one or the other of these stages. Equipment operability and integrity can be compromised during handling and installation sequences. For this reason, the subject equipment should be handled and installed under closely controlled and supervised conditions.
4.2 This guide is intended as a supplement to other standards (Section 2, Referenced Documents), and to federal and state regulations, codes, and criteria applicable to the design of equipment intended for this use.
4.3 This guide is intended to be generic and to apply to a wide range of types and configurations of materials handling equipment.
4.4 The term materials handling equipment is used herein in a generic sense. It includes manipulators, cranes, carts or bogies, and special equipment for handling tools and material in hot cells.
4.5 This service imposes stringent requirements on the quality and the integrity of the equipment, as follows:
4.5.1 Boots and similar protective covers should not restrict movement of the equipment, should be properly sealed to the equipment and should withstand the radiation, cell atmosphere, dust, cell temperatures, chemical exposures, and cleaning and decontamination reagents, and also resist snags and tearing.
4.5.2 Materials handling equipment should be capable of withstanding rigorous chemical cleaning and decontamination procedures.
4.5.3 Materials handling equipment should be designed and fabricated to remain dimensionally stable throughout its life cycle.
4.5.4 Attention to fabrication tolerances is necessary to allow the proper fit-up between components for the proper installation and mounting of materials handling equipment in hot cells, for example, when parts or components are being replaced. Fabrication tolerances should be controlled to provide sufficie...
SCOPE
1.1 Intent:
1.1.1 This guide covers materials handling equipment used in hot cells (shielded cells) for the processing and handling of nuclear and radioactive materials. The intent of this guide is to aid in the selection and design of materials handling equipment for hot cells in order to minimize equipment failures and maximize the equipment utility.
1.1.2 It is intended that this guide record the principles and caveats that experience has shown to be essential to the design, fabrication, installation, maintenance, repair, replacement, and decontamination and decommissioning of materials handling equipment capable of meeting the stringent demands of operating, dependably and safely, in a hot cell environment where operator visibility is limited due to the radiation exposure hazards.
1.1.3 This guide may apply to materials handling equipment in other radioactive remotely operated facilities such as suited entry repair areas and canyons, but does not apply to materials handling equipment used in commercial power reactors.
1.1.4 This guide covers mechanical master-slave manipulators and electro-mechanical manipulators, but does not cover electro-hydraulic manipulators.
1.2 Applicability:
1.2.1 This guide is intended to be applicable to equipment used under one or more of the following conditions:
1.2.1.1 The materials handled or processed constitute a significant radiation hazard to man or to the environment.
1.2.1.2 The equipment will generally be used over a long-term life cycle (for example, in excess of two years), but equipment intended for use over a shorter life cycle is not excluded.
1.2.1.3 The equipment can neither be accessed directly for purposes of operation or maintenance, nor can the equipment be viewed directly, for example, without shielded viewing windows, periscopes, or a video monitoring system.
1.3 User Caveats:
1.3.1 This standard is not a substitute for applied engin...
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SIGNIFICANCE AND USE
5.1 Uranium hexafluoride is normally produced and handled in large (typically 1 to 14-ton) quantities and must, therefore, be characterized by reference to representative samples (see ISO 7195). The samples are used to determine compliance with the applicable commercial specification C787. The quantities involved, physical properties, chemical reactivity, and hazardous nature of UF6 are such that for representative sampling, specially designed equipment must be used and operated in accordance with the most carefully controlled and stringent procedures. This practice can be used by UF6 converters to review the effectiveness of existing procedures or as a guide to the design of equipment and procedures for future use.
5.2 The intention of this practice is to avoid liquid UF6 sampling once the cylinder has been filled. For safety reasons, manipulation of large quantities of liquid UF6 should be avoided when possible.
5.3 It is emphasized that this practice is not meant to address conventional or nuclear criticality safety issues.
SCOPE
1.1 This practice covers methods for withdrawing representative sample(s) of uranium hexafluoride (UF6) during a transfer occurring in the gas phase. Such transfer in the gas phase can take place during the filling of a cylinder during a continuous production process, for example the distillation column in a conversion facility. Such sample(s) may be used for determining compliance with the applicable commercial specification, for example Specification C787.
1.2 Since UF6 sampling is taken during the filling process, this practice does not address any special additional arrangements that may be agreed upon between the buyer and the seller when the sampled bulk material is being added to residues already present in a container (“heels recycle”). Such arrangements will be based on QA procedures such as traceability of cylinder origin (to prevent for example contamination with irradiated material).
1.3 If the receiving cylinder is purged after filling and sampling, special verifications must be performed by the user to verify the representativity of the sample(s). It is then expected that the results found on volatile impurities with gas phase sampling may be conservative.
1.4 This practice is only applicable when the transfer occurs in the gas phase. When the transfer is performed in the liquid phase, Practice C1052 should apply. This practice does not apply to gas sampling after the cylinder has been filled since the sample taken will not be representative of the cylinder.
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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SIGNIFICANCE AND USE
5.1 Factors governing selection of a method for the determination of plutonium include available quantity of sample, sample purity, desired level of reliability, and equipment.
5.1.1 This test method determines 5 mg to 20 mg of plutonium with prior dissolution using Practice C1168.
5.1.2 This test method calculates plutonium mass fraction in solutions and solids using an electrical calibration based upon Ohm’s Law and the Faraday Constant.
5.1.3 Chemical standards are used for quality control. When prior chemical separation of plutonium is necessary to remove interferences, the quality control standards should be included with each chemical separation batch (9).
5.2 Fitness for Purpose of Safeguards and Nuclear Safety Application—Methods intended for use in safeguards and nuclear safety applications shall meet the requirements specified by Guide C1068 for use in such applications.
SCOPE
1.1 This test method describes the determination of dissolved plutonium from unirradiated nuclear-grade (that is, high-purity) materials by controlled-potential coulometry. Controlled-potential coulometry may be performed in a choice of supporting electrolytes, such as 0.9 mol/L (0.9 M) HNO3, 1 mol/L (1 M) HClO4, 1 mol/L (1 M) HCl, 5 mol/L (5 M) HCl, and 0.5 mol/L (0.5 M) H2SO4. Limitations on the use of selected supporting electrolytes are discussed in Section 6. Optimum quantities of plutonium for this procedure are 5 mg to 20 mg.
1.2 Plutonium-bearing materials are radioactive and toxic. Adequate laboratory facilities, such as gloved boxes, fume hoods, controlled ventilation, etc., along with safe techniques must be used in handling specimens containing these materials.
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
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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SIGNIFICANCE AND USE
5.1 Certified reference materials (CRMs) prepared from nuclear materials are well characterized, traceable, and sufficiently homogenous and stable for their intended use. Usually they are certified using the most unbiased and precise measurement methods available, often with more than one laboratory being used on a national or international level. CRMs are at the top of the metrological hierarchy of reference materials. A graphical representation of a typical national nuclear measurement system is shown in Fig. 3.
FIG. 3 Typical National Nuclear Measurement System
5.2 Working reference materials (WRMs) need to have quality characteristics that are similar to CRMs, although the rigor used to achieve those characteristics is not usually as stringent as for CRMs. Similarly, production of WRMs should be in accordance with applicable requirements of ISO 17034. Where possible, CRMs are typically used to calibrate the methods used for establishing reference values assigned to WRMs, thus providing traceability to CRMs as required by ISO/IEC 17025. A WRM is normally prepared for a specific application.
5.3 Because of the importance of having highly reliable measurement data from nuclear material analysis, particularly for material control and accountability purposes, CRMs are used for calibration when available. However, CRMs prepared from nuclear materials are not always available for specific applications. Thus, there may be a need for a laboratory to prepare nuclear material WRMs to meet specific needs; for example, to match the matrix in process samples. In such cases, a WRM can be tailored to meet specific needs of a process or laboratory. Also, CRM supply may be too limited for use in the quantities needed for long-term, routine use. When properly prepared, WRMs will serve equally well as CRMs for most applications, and using WRMs will help preserve supplies of CRMs.
5.4 Difficulties may be encountered in the preparation of RMs from nuclear materials becaus...
SCOPE
1.1 This guide covers the preparation and characterization of working reference materials (WRM) that are produced by a laboratory for its own use in the analysis of nuclear fuel cycle materials. Guidance is provided for proper planning, preparation, packaging, and storage; requirements for characterization; homogeneity and stability considerations; and value assignment. When traceability to SI is desired for a WRM, it will be achieved by a defined, statistically sound characterization process that is traceable to a certified value on a certified reference materials. While the guidance provided is generic for nuclear fuel cycle materials, detailed examples for some materials are provided in the appendixes.
1.2 This guide does not apply to the production and characterization of certified reference materials (CRM). Refer to ISO 17034 and ISO Guide 35 for guidance on reference material production, characterization, certification, sale, and distribution requirements.
1.3 The information provided by this guide is found in the following sections:
Section
Perform WRM Planning
6
Prepare and Process Materials
7
Packaging and Storage of Materials
8
Perform Homogeneity Study
9
Perform Stability Studies
10
Characterize Materials
11
Perform Uncertainty Analysis
12
Produce Documentation
13
Carry Out WRM Utilization and Monitoring
14
1.4 The values stated in SI units are to be regarded as standard. The non-SI units of molar, M, and normal, N, are also regarded as standard. Any non-SI units of measurement shown in parentheses are for information only.
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...
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SIGNIFICANCE AND USE
5.1 This test method is used to ascertain whether or not materials meet specifications for plutonium concentration or plutonium mass fraction.
5.1.1 The materials (nuclear grade plutonium nitrate solutions, plutonium metal, plutonium oxide powder, and mixed oxide and carbide powders and pellets) to which this test method applies are subject to nuclear safeguards regulations governing their possession and use. However, adherence to this test method does not automatically guarantee regulatory acceptance of the resulting safeguards measurements. It remains the sole responsibility of the user of this test method to ensure that its application to safeguards has the approval of the proper regulatory authorities.
5.1.2 When used in conjunction with appropriate certified reference materials (CRMs), this test method can demonstrate traceability to the international measurements system (SI).
5.2 Fitness for Purpose of Safeguards and Nuclear Safety Application—Methods intended for use in safeguards and nuclear safety applications shall meet the requirements specified by Guide C1068 for use in such applications.
5.3 A chemical calibration of the coulometer is necessary for accurate results.
FIG. 1 Example of a Cell Design Used at Los Alamos National Laboratory (LANL)
SCOPE
1.1 This test method covers the determination of milligram quantities of plutonium in unirradiated uranium-plutonium mixed oxide having a U/Pu ratio range of 0.1 to 10. This test method is also applicable to plutonium metal, plutonium oxide, uranium-plutonium mixed carbide, various plutonium compounds including fluoride and chloride salts, and plutonium solutions.
1.2 The recommended amount of plutonium for each aliquant in the coulometric analysis is 5 mg to 10 mg. Precision worsens for lower amounts of plutonium, and elapsed time of electrolysis becomes impractical for higher amounts of plutonium.
1.3 The quantity values stated in SI units are to be regarded as standard. The quantity values with non-SI units are given in parentheses for information only.
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. Specific precautionary statements are given in Section 9.
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 Measurement results from this test method assists in demonstrating regulatory compliance in such areas as safeguards SNM inventory control, criticality control, waste disposal, and decontamination and decommissioning (D&D). This test method can apply to the measurement of holdup in process equipment or discrete items whose gamma-ray absorption properties may be measured or estimated. This method may be adequate to accurately measure items with complex distributions of radioactive and attenuating material, however, the results are subject to larger measurement uncertainties than measurements of less complex distributions of radioactive material.
5.2 Scan—A scan is used to provide a qualitative indication of the extent, location, and the relative quantity of holdup. It can be used to plan or supplement the quantitative measurements.
5.3 Nuclide Mapping—Nuclide mapping measures the relative isotopic composition of the holdup at specific locations. It can also be used to detect the presence of radionuclides that emit radiation which could interfere with the assay. Nuclide mapping is best performed using a high resolution detector (such as HPGe) for best nuclide and interference detection. If the holdup is not isotopically homogeneous at the measurement location, that measured isotopic composition will not be a reliable estimate of the bulk isotopic composition.
5.4 Quantitative Measurements—These measurements result in quantification of the mass of the measured nuclides in the holdup. They include all the corrections, such as attenuation, and descriptive information, such as isotopic composition, that are available
5.4.1 High quality results require detailed knowledge of radiation sources and detectors, transmission of radiation, calibration, facility operations and error analysis. Judicious use of subject matter experts is required (Guide C1490).
5.5 Holdup Monitoring—Periodic re-measurement of holdup at a defined point using the same technique and a...
SCOPE
1.1 This test method describes gamma-ray methods used to nondestructively measure the quantity of 235U or 239Pu present as holdup in nuclear facilities. Holdup may occur in any facility where nuclear material is processed, in process equipment, in exhaust ventilation systems and in building walls and floors.
1.2 This test method includes information useful for management, planning, selection of equipment, consideration of interferences, measurement program definition, and the utilization of resources (1, 2, 3, 4) .2
1.3 The measurement of nuclear material hold up in process equipment requires a scientific knowledge of radiation sources and detectors, transmission of radiation, calibration, facility operations and uncertainty analysis. It is subject to the constraints of the facility, management, budget, and schedule; plus health and safety requirements. The measurement process includes defining measurement uncertainties and is sensitive to the form and distribution of the material, various backgrounds, and interferences. The work includes investigation of material distributions within a facility, which could include potentially large holdup surface areas. Nuclear material held up in pipes, ductwork, gloveboxes, and heavy equipment, is usually distributed in a diffuse and irregular manner. It is difficult to define the measurement geometry, to identify the form of the material, and to measure it without interference from adjacent sources of radiation.
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...
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SIGNIFICANCE AND USE
4.1 The materials covered that must meet ASTM specifications are uranium metal and uranium oxide.
4.2 Uranium materials are used as nuclear reactor fuel. For this use, these materials must meet certain criteria for uranium content, uranium-235 enrichment, and impurity content, as described in Specifications C753 and C776. The material is assayed for uranium to determine whether the content is as specified.
4.3 Uranium alloys, refractory uranium materials, and uranium containing scrap and ash are unique uranium materials for which the user must determine the applicability of this practice. In general, these unique uranium materials are dissolved with various acid mixtures or by fusion with various fluxes.
SCOPE
1.1 This practice covers dissolution treatments for uranium materials that are applicable to the test methods used for characterizing these materials for uranium elemental, isotopic, and impurities determinations. Dissolution treatments for the major uranium materials assayed for uranium or analyzed for other components are listed.
1.2 The treatments, in order of presentation, are as follows:
Procedure Title
Section
Dissolution of Uranium Metal and Oxide with Nitric Acid
8.1
Dissolution of Uranium Oxides with Nitric Acid and Residue
Treatment
8.2
Dissolution of Uranium-Aluminum Alloys in Hydrochloric Acid
with Residue Treatment
8.3
Dissolution of Uranium Scrap and Ash by Leaching with Nitric
Acid and Treatment of Residue by Carbonate Fusion
8.4
Dissolution of Refractory Uranium-Containing Material by
Carbonate Fusion
8.5
Dissolution of Uranium—Aluminum Alloys
Uranium Scrap and Ash, and Refractory
Uranium-Containing Materials by
Microwave Treatment
8.6
1.3 The values stated in SI units 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. Specific hazards statements are given in Section 7.
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 Uranium material is used as a fuel in certain types of nuclear reactors. To be suitable for use as nuclear fuel, the starting material shall meet certain specifications such as those described in Specifications C753, C776, C787, C833, C967, C996, and C1008, or as specified by the purchaser. The isotope amount ratios of uranium material can be measured by mass spectrometry following this test method to ensure that they meet the specification.
5.2 The MTE method can be used for a wide range of sample sizes even in samples containing as low as 20 µg of uranium. If the uranium sample is in the form of uranium hexafluoride, it has to be converted into a uranium nitrate solution for measurement by the MTE method. The concentration of the loading solution for MTE has to be in the range of 1 mg/g to 6 mg/g to allow a sample loading of 2 µg to 6 µg of uranium. A minimum loading of 3 µg uranium per filament is strongly recommended. This is needed to have a sufficient and stable ion signal especially for the two minor isotopes (234U and 236U) thus enabling the internal calibration of SEM versus the Faraday cups using the 234U ion beam signal during the measurement.
5.3 Until now, the instrument capabilities for the MTE method have only been implemented on the TRITON™ TIMS instrument.5 Therefore, all recommendations for measurement parameters in this test method are specified for the TRITON instrument. The manufacturers of other TIMS instruments (for example, IsotopX and Nu Instruments) have indicated plans to implement the modifications needed in their instruments to use the MTE method.
5.4 The MTE method described here can also be extended to measurement of elements other than uranium. Note that the MTE method has already been implemented for plutonium and calcium.
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1.1 This test method describes the determination of the isotope amount ratios of uranium material as nitrate solutions by the modified total evaporation (MTE) method using a thermal ionization mass spectrometer (TIMS) instrument.
1.2 The analytical performance in the determination of the 235U/238U major isotope amount ratio by MTE is similar to the (“classical”) total evaporation (TE) method as described in C1672. However, in the MTE method, the evaporation process is interrupted on a regular basis to allow measurements and subsequent corrections for background from peak tailing, perform internal calibration of a secondary electron multiplier (SEM) detector versus the Faraday cups, peak centering, and ion source refocusing. Performing these calibrations and corrections on a regular basis during the measurement, improves precision, and significantly reduces uncertainties for the minor isotope amount ratios 234U/238U and 236U/238U as compared to the TE method.
1.3 In principle, the MTE method may yield major isotope amount ratios without the need for mass fractionation correction. However, depending on the measurement conditions, small variations are observed between sample turrets. Therefore, a small correction based on measurements of a certified reference material is recommended to improve consistency. The uncertainty around the mass fractionation correction factor usually includes unity.
1.4 Units—The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered 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 issu...
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SIGNIFICANCE AND USE
4.1 Factors governing selection of a method for the determination of uranium include available quantity of sample, sample purity, desired level of reliability, and equipment availability.
4.2 This test method is suitable for samples between 20 mg to 300 mg of uranium, is applicable to fast breeder reactor (FBR)-mixed oxides having a uranium to plutonium ratio of 2.5 and greater, is tolerant towards most metallic impurity elements usually specified for FBR-mixed oxide fuel, and uses no special equipment.
4.3 The ruggedness of the titration method has been studied for both the volumetric (6) and the weight (7) titration of uranium with dichromate.
SCOPE
1.1 This test method covers unirradiated uranium-plutonium mixed oxide having a uranium to plutonium ratio of 2.5 and greater. The presence of larger amounts of plutonium (Pu) that give lower uranium to plutonium ratios may give low analysis results for uranium (U) (1)2, if the amount of plutonium together with the uranium is sufficient to slow the reduction step and prevent complete reduction of the uranium in the allotted time. Use of this test method for lower uranium to plutonium ratios may be possible, especially when 20 mg to 50 mg quantities of uranium are being titrated rather than the 100 mg to 300 mg in the study cited in Ref (1). Confirmation of that information should be obtained before this test method is used for ratios of uranium to plutonium less than 2.5.
1.2 The amount of uranium determined in the data presented in Section 12 was 20 mg to 50 mg. However, this test method, as stated, contains iron in excess of that needed to reduce the combined quantities of uranium and plutonium in a solution containing 300 mg of uranium with uranium to plutonium ratios greater than or equal to 2.5. Solutions containing up to 300 mg uranium with uranium to plutonium ratios greater than or equal to 2.5 have been analyzed (1) using the reagent volumes and conditions as described in Section 10.
1.3 The values stated in SI units 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. For specific hazard statements, see Section 8.
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
4.1 The process of selection, training and qualification of personnel involved with NDA measurements is one of the quality assurance elements for an overall quality NDA measurement program.
4.2 This guide describes an approach to selection, qualification, and training of personnel that is to be used in conjunction with other NDA Quality Assurance (QA) program elements. The selection, qualification and training processes can vary and this guide provides one such approach.
4.3 The qualification activities described in this guide assume that NDA personnel are already proficient in general facility operations and safety procedures. The training and activities that developed this proficiency are not covered in this guide.
4.4 This guide describes a basic approach and principles for the qualification of NDA professionals and technical specialists and operators. A different approach may be adopted by the management organization based on its particular organization and facility specifics. However, if a variation of the approach of this guide is applied, the resulting selection, training, and qualification programs must meet the requirements of the facility quality assurance program and should provide all the applicable functions of Section 5.
4.5 This guide may be used as an aid in the preparation of a Training Implementation Plan (TIP) for the Transuranic Waste Characterization Program (TWCP).
4.6 This guide describes education and expertise guidance for NDA auditors due to the importance and complexity of proper oversight of NDA activities.
SCOPE
1.1 This guide contains good practices for the selection, training, qualification, and professional development of personnel performing analysis, calibration, physical measurements, or data review using nondestructive assay equipment, methods, results, or techniques. The guide also covers NDA personnel involved with NDA equipment setup, selection, diagnosis, troubleshooting, or repair. General guidelines for the selection, training, and qualification of NDA auditors are included as well, but at a lower level of detail due to the variability of the personnel’s responsibilities performing this functions. Selection, training, and qualification programs based on this guide are intended to provide assurance that NDA personnel are suitably qualified and experienced personnel (SQEP) to perform their jobs competently. This guide presents a series of options but does not recommend a specific course of action.
This standard guide does not address the qualifications per se of an NDA Manager. However, it is expected that the NDA Manager is familiar with NDA techniques, and can make informed decisions on the acceptability of the assay results. If an NDA Manager does not have adequate technical qualifications in the NDA field, they are recommended to undergo training to gain familiarity in this area.
An NDA Manager with no relevant NDA experience should have access to a Senior NDA Professional who will give guidance for all technical decisions such as applicability and limitation of methods, reasonableness of results, needed upgrades and advantageous development investments.
1.2 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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This document describes an analytical method for the determination of uranium in samples from pure product materials such as U metal, UO2, UO3, U3O8, uranyl nitrate hexahydrate and uranium hexafluoride from the nuclear fuel cycle. This procedure is sufficiently accurate and precise to be used for nuclear materials accountability. This method can be used directly for the analysis of most uranium and uranium oxide nuclear reactor fuels, either irradiated or un-irradiated, and of uranium nitrate product solutions. Fission products equivalent to up to 10 % burn-up of heavy atoms do not interfere, and other elements which could cause interference are not normally present in sufficient quantity to affect the result significantly. The method recommends that an aliquot of sample is weighed and that a mass titration is used, in order to obtain improved precision and accuracy. This does not preclude the use of alternative techniques which could give equivalent performance. The use of automatic device(s) in the performance of some critical steps of the method has some advantages, mainly in the case of routine analysis. This method does not generate a toxic mixed waste as does the potassium dichromate titration in ISO 7097-1.
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SIGNIFICANCE AND USE
4.1 The test methods in this standard are designed to show whether a given material meets the specifications prescribed in Specification C967.
4.2 Because of the variability of matrices of uranium-ore concentrate and the limited availability of suitable reference or calibration materials, the precision and bias of these test methods should be established by each individual laboratory that will use them. The precision and bias statements given for each test method are those reported by various laboratories and can be used as a guideline.
4.3 Instrumental test methods such as X-ray fluorescence and emission spectroscopy can be used for the determination of some impurities where such equipment is available.
SCOPE
1.1 These test methods cover procedures for the chemical and atomic absorption analysis of uranium-ore concentrates to determine compliance with the requirements prescribed in Specification C967.
1.2 The analytical procedures appear in the following order:
Sections
Uranium by Ferrous Sulfate Reduction—Potassium Dichromate
Titrimetry
9
Nitric Acid-Insoluble Uranium
10 to 18
Extractable Organic Material
19 to 26
Determination of Arsenic
27
Carbonate by CO2 Gravimetry
28 to 34
Fluoride by Ion-Selective Electrode
35 to 42
Halides by Volhard Titration
43 to 50
Phosphorus by Spectrophotometry
52 to 60
Determination of Silicon
61
Determination of Thorium
62
Calcium, Iron, Magnesium, Molybdenum, Titanium, and Vana-
dium by Atomic Absorption Spectrophotometry
63 to 72
Potassium and Sodium by Atomic Absorption
Spectrophotometry
73 to 82
Boron by Spectrophotometry
83 to 92
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.
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. A specific precautionary statement is given in Section 7.
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 provides the chemical and physical properties and requirements for nuclear-grade aluminum oxide powder intended for fabrication into shapes for nuclear applications. The materials shall conform to physical requirements as to particle size distribution, and specific surface area, and chemical requirements as to loss-on-ignition, and total and elemental concentrations of all impurities. Impurities may include silicaon, iron-chromium-nickel, magnesium, sodium, calcium, hafnium, fluorine, fluorine-chlorine-iodine-bromine, gadolinium, samarium, europium, and dysprosium.
SCOPE
1.1 This specification provides the chemical and physical requirements for nuclear-grade aluminum oxide powder intended for fabrication into shapes for nuclear applications. Two specific uses for which this powder is intended are Al2O3 pellets and Al2O3 − B4C composite pellets for use as thermal insulator or burnable neutron absorbers, respectively.
1.2 The material described herein shall be particulate in nature.
1.3 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
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
5.1 Factors governing selection of a method for the determination of uranium include available quantity of sample, homogeneity of material sampled, sample purity, desired level of reliability, and facility available equipment.
5.2 This uranium assay method is referenced in the Test Methods for Chemical, Mass Spectrometric, and Spectrochemical Analysis of Nuclear-Grade Uranium Dioxide Powders and Pellets (Test Methods C696) and in the Test Methods for Chemical, Mass Spectrometric, and Spectrochemical, Nuclear, and Radiochemical Analysis of Nuclear-Grade Uranyl Nitrate Solutions (Test Methods C799). This uranium assay method may also be used for uranium hexafluoride and uranium ore concentrate. This test method determines 20 mg to 200 mg of uranium; is applicable to product, fuel, and scrap material after the material is dissolved; is tolerant towards most metallic impurity elements usually specified in product and fuel; and uses no special equipment.
5.3 The ruggedness of the titration method has been studied for both the volumetric (6) and the weight (7) titration of uranium with dichromate.
5.4 Fitness for Purpose of Safeguards and Nuclear Safety Application—Methods intended for use in safeguards and nuclear safety applications shall meet the requirements specified by Guide C1068 for use in such applications.
5.4.1 When used in conjunction with the appropriate certified reference materials (SRM6 or CRM), this procedure can demonstrate traceability to the national measurement base. However, use of the test method does not automatically guarantee regulatory acceptance of the resulting safeguards measurements. It remains the sole responsibility of the user of this test method to assure that its application to safeguards has the approval of the proper regulatory authorities.
SCOPE
1.1 This test method, commonly referred to as the Modified Davies and Gray technique, covers the titration of uranium in product, fuel, and scrap materials after the material is dissolved. The test method is versatile and has been ruggedness tested. With appropriate sample preparation, this test method can give precise and unbiased uranium assays over a wide variety of material types (1, 2).2 Details of the titration procedure in the presence of plutonium with appropriate modifications are given in Test Method C1204.
1.2 Uranium levels titrated are usually 20 mg to 50 mg, but up to 200 mg uranium can be titrated using the reagent volumes stated in this test method.
1.3 The values stated in SI units 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. For specific safeguard and safety precaution statements, see Section 5.
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 the properties and requirements for pellets of stabilized cubic hafnium oxide used in nuclear reactors. Hafnium oxide should consist of a stabilizing agent, the recommended of which is yttrium oxide, though others such as calcium oxide and magnesium oxide may also be used as agreed upon by the buyer and seller. The material shall meet specified values of the following requirements: physical dimensions; density; mechanical properties; phase stabilization; impurity concentration limits; moisture concentration limit; visual appearance; end and circumferential chips; cracks; and fissures and other defects.
SCOPE
1.1 This specification applies to pellets of stabilized cubic hafnium oxide used in nuclear reactors.
1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
1.3 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 Refer to Guide E844 for the selection, irradiation, and quality control of neutron dosimeters.
5.2 Refer to Practice E261 for a general discussion of the determination of fast-neutron fluence rate with threshold detectors.
5.3 Titanium has good physical strength, is easily fabricated, has excellent corrosion resistance, has a melting temperature of 1668 °C, and can be obtained with satisfactory purity.
5.4 46Sc has a half-life of 83.787 (16)4 days (2). The 46Sc decay emits a 0.889271 (2) MeV gamma 99.98374 (35) % of the time and a second gamma with an energy of 1.120537 (3) MeV 99.97 (2) % of the time.
5.5 The recommended “representative isotopic abundances” for natural titanium (3) are:
8.25 (3) % 46Ti
7.44 (2) % 47Ti
73.72 (2) % 48Ti
5.41 (2) % 49Ti
5.18 (2) % 50Ti
5.6 The radioactive products of the neutron reactions 47Ti(n,p)47Sc (τ1/2 = 3.3485 (9) d) (2) and 48Ti(n,p)48Sc (τ1/2 = 43.67 h), (3) might interfere with the analysis of 46Sc.
5.7 Contaminant activities (for example, 65Zn and 182Ta) might interfere with the analysis of 46Sc. See 7.1.2 and 7.1.3 for more details on the 182Ta and 65Zn interference.
5.8 46Ti and 46Sc have cross sections for thermal neutrons of 0.59 ± 0.18 and 8.0 ± 1.0 barns, respectively (4); therefore, when an irradiation exceeds a thermal-neutron fluence greater than about 2 × 1021 cm–2, provisions should be made to either use a thermal-neutron shield to prevent burn-up of 46Sc or measure the thermal-neutron fluence rate and calculate the burn-up.
5.9 Fig. 1 shows a plot of the International Reactor Dosimetry and Fusion File, IRDFF-II cross section (5) versus neutron energy for the fast-neutron reactions of titanium which produce 46Sc (that is, natTi(n,X)46Sc). Included in the plot is the 46Ti(n,p) reaction and the 47Ti(n,np:d) contributions to the 46Sc production, normalized per natTi atom with the individual isotopic contributions weighted using the natural abundances (3). This figure ...
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1.1 This test method covers procedures for measuring reaction rates by the activation reaction natTi(n,X)46Sc. The “X” designation represents any combination of light particles associated with the production of the residual 46Sc product. Within the applicable neutron energy range for fission reactor applications, this reaction is a properly normalized combination of three different reaction channels: 46Ti(n,p)46Sc; 47Ti(n, np)46Sc; and 47Ti(n,d)46Sc.
Note 1: The 47Ti(n,np)46Sc reaction, ENDF-6 format file/reaction identifier MF=3, MT=28, is distinguished from the 47Ti(n,d)46Sc reaction, ENDF-6 format file/reaction identifier MF=3/MT=104, even though it leads to the same residual product (1).2 The combined reaction, in the IRDFF-II library, has the file/reaction identifier MF=10/MT=5.
Note 2: The cross section for the combined 47Ti(n,np:d) reaction is relatively small for energies less than 12 MeV and, in fission reactor spectra, the production of the residual 46Sc is not easily distinguished from that due to the 46Ti(n,p) reaction.
1.2 The reaction is useful for measuring neutrons with energies above approximately 4.4 MeV and for irradiation times, under uniform power, up to about 250 days (for longer irradiations, or for varying power levels, see Practice E261).
1.3 With suitable techniques, fission-neutron fluence rates above 109 cm–2·s–1 can be determined. However, in the presence of a high thermal-neutron fluence rate, 46Sc depletion should be investigated.
1.4 Detailed procedures for other fast-neutron detectors are referenced in Practice E261.
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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 an...
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ABSTRACT
This specification covers sintered uranium dioxide pellets containing 235U for use in nuclear reactors. Chemical requirements include uranium content, impurity content, stoichiometry, and moisture content. Maximum concentration limits are specified for impurity elements such as: aluminum, carbon, calcium+magnesium, chlorine, chromium, cobalt, fluorine, hydrogen, iron, nickel, nitrogen, silicon, and thorium. Chemical analyses shall be performed. Nuclear requirements include isotopic content and equivalent boron content. The following are physical characteristics of the material: dimensions, pellet density, grain size and pore morphology, pellet integrity –
SCOPE
1.1 This specification is for finished sintered UO2 pellets. It applies to UO2 pellets containing uranium (U) of any 235U concentration for use in nuclear reactors.
1.2 This specification recognizes the presence of reprocessed U in the fuel cycle and consequently defines isotopic limits for UO2 pellets made from commercial grade UO2. Such commercial grade UO2 is defined so that, regarding fuel design and manufacture, the product is essentially equivalent to that made from unirradiated U. UO2 falling outside these limits cannot necessarily be regarded as equivalent and may thus need special provisions at the fuel fabrication plant or in the fuel design.
1.3 This specification does not include (a) provisions for preventing criticality accidents, (b) requirements for health and safety, (c) avoidance of hazards, or (d) shipping precautions and controls. Observance of this specification does not relieve the user of the obligation to be aware of and conform to all federal, state, and local regulations pertaining to possessing, shipping, processing, or using source or special nuclear material. Examples of U.S. Government documents are Code of Federal Regulations (Latest Edition), Title 10, Part 50, Title 10, Part 70, Title 10, Part 71, and Title 49, Part 173.
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 precautionary 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 or 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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SCOPE
1.1 This specification applies to pellets of aluminum oxide that may be ultimately used in a reactor core, for example, as filler or spacers within fuel, burnable poison, or control rods. In order to distinguish between the subject pellets and “burnable poison” pellets, it is established that the subject pellets are not intended to be used as neutron-absorbing material.
1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.
1.3 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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SCOPE
1.1 This specification defines the physical and chemical requirements for zirconium oxide powder intended for fabrication into shapes, either entirely or partially of zirconia, for use in a nuclear reactor core.
1.2 The material described herein shall be particulate in nature.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
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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