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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.
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 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.
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