Forensic Signatures of Nuclear Materials Processing

Date

2018-11-15 14:13

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Cranfield University

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Poster

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Citation

Thompson, Nathan (2018). Forensic Signatures of Nuclear Materials Processing. Cranfield Online Research Data (CORD). Poster. https://doi.org/10.17862/cranfield.rd.7346708.v1

Abstract

Poster presented at the 2018 Defence and Security Doctoral Symposium.The field of nuclear forensics has been noted of relevance in the effort to tackle illicit trafficking of nuclear material. Forensic signatures can be considered a ‘fingerprint’ of the material, obtained by analytical methods such as X-Ray diffraction spectroscopy (XRD) and scanning electron microscopy (SEM). The forensic signatures obtained from characterising nuclear material may help to determine the origin and processing conditions of the sample. The aim of this project is to investigate how the physical and chemical characteristics of UO3 powder produced from aqueous reprocessing are affected by the processing route, conditions and impurities present. This will be used to develop a library of characteristic forensic signatures to aid in the discrimination of material from different sources.To date, work in this project has included the investigation of forensic signatures of studtite calcination products, whereby calcination products up to 1050 ˚C were characterised. Further investigations are being carried out into using X-Ray absorption spectroscopy (XAS) as a means of characterising amorphous UO3 phases produced by calcination. Additionally, an investigation into the effect of a fractional factorial matrix of processing variables on UO3signatusignatures (from studtite intermediate) is being conducted. Note from author: In this presentation, the thermal decomposition of synthetic studtite is examined for its potential nuclear forensic signatures. The morphologies of the finished particles are presented for discussion.

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Keywords

'Uranium', 'Decomposition', 'Signatures', 'DSDS18 poster', 'DSDS18', 'Nuclear Chemistry', 'Forensic Chemistry'

Rights

CC BY-NC 4.0

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