Publication | Open Access
Nuclear forensic analysis of uranium oxide powders interdicted in Victoria, Australia
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2015
Year
EngineeringNuclear DataRadioactive ContaminationForensic ChemistryChemistryAnalytical ChemistryNuclear MaterialsUranium SamplesElemental CharacterizationDepleted Uranium PowderNuclear SecurityNuclear EngineeringRadioactive Waste DisposalEnvironmental RadiochemistryNuclear CeramicUranium Oxide PowdersNatural SciencesRadioanalytical ChemistryPolice InvestigationNuclear ExperimentsNuclear Forensic Analysis
Abstract Nuclear forensic analysis was conducted on two uranium samples confiscated during a police investigation in Victoria, Australia. The first sample, designated NSR-F-270409-1, was a depleted uranium powder of moderate purity (∼ 1000 μg/g total elemental impurities). The chemical form of the uranium was a compound similar to K 2 (UO 2 ) 3 O 4 · 4H 2 O. While aliquoting NSR-F-270409-1 for analysis, the body and head of a Tineid moth was discovered in the sample. The second sample, designated NSR-F-270409-2, was also a depleted uranium powder. It was of reasonably high purity (∼ 380 μg/g total elemental impurities). The chemical form of the uranium was primarily UO 3 · 2H 2 O, with minor phases of U 3 O 8 and UO 2 . While aliquoting NSR-F-270409-2 for analysis, a metal staple of unknown origin was discovered in the sample. The presence of 236 U and 232 U in both samples indicates that the uranium feed stocks for these samples experienced a neutron flux at some point in their history. The reactor burn-up calculated from the isotopic composition of the uranium is consistent with that of spent fuel from natural uranium (NU) fueled Pu production. These nuclear forensic conclusions allow us to categorically exclude Australia as the origin of the material and greatly reduce the number of candidate sources.