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Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study

The most advanced methodology for the pyroprocessing of spent nuclear fuel is the electrorefining of uranium metal in LiCl–KCl eutectic, in which uranium is solubilized as U(III). The production of U(III) in LiCl–KCl eutectic by the chlorination of uranium metal using BiCl(3) has been performed for...

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Autores principales: Lambert, Hugues, Kerry, Timothy, Sharrad, Clint A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061103/
https://www.ncbi.nlm.nih.gov/pubmed/30100650
http://dx.doi.org/10.1007/s10967-018-5953-7
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author Lambert, Hugues
Kerry, Timothy
Sharrad, Clint A.
author_facet Lambert, Hugues
Kerry, Timothy
Sharrad, Clint A.
author_sort Lambert, Hugues
collection PubMed
description The most advanced methodology for the pyroprocessing of spent nuclear fuel is the electrorefining of uranium metal in LiCl–KCl eutectic, in which uranium is solubilized as U(III). The production of U(III) in LiCl–KCl eutectic by the chlorination of uranium metal using BiCl(3) has been performed for research purposes. In this work, this reaction was studied in-situ by visual observation, electronic absorption spectroscopy and electrochemistry at 450 °C. The most likely mechanism has been determined to involve the initial direct oxidation of uranium metal by Bi(III) to U(IV). The dissolved U(IV) then reacts with unreacted uranium metal to form U(III).
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spelling pubmed-60611032018-08-09 Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study Lambert, Hugues Kerry, Timothy Sharrad, Clint A. J Radioanal Nucl Chem Article The most advanced methodology for the pyroprocessing of spent nuclear fuel is the electrorefining of uranium metal in LiCl–KCl eutectic, in which uranium is solubilized as U(III). The production of U(III) in LiCl–KCl eutectic by the chlorination of uranium metal using BiCl(3) has been performed for research purposes. In this work, this reaction was studied in-situ by visual observation, electronic absorption spectroscopy and electrochemistry at 450 °C. The most likely mechanism has been determined to involve the initial direct oxidation of uranium metal by Bi(III) to U(IV). The dissolved U(IV) then reacts with unreacted uranium metal to form U(III). Springer International Publishing 2018-06-28 2018 /pmc/articles/PMC6061103/ /pubmed/30100650 http://dx.doi.org/10.1007/s10967-018-5953-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Lambert, Hugues
Kerry, Timothy
Sharrad, Clint A.
Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title_full Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title_fullStr Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title_full_unstemmed Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title_short Preparation of uranium(III) in a molten chloride salt: a redox mechanistic study
title_sort preparation of uranium(iii) in a molten chloride salt: a redox mechanistic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061103/
https://www.ncbi.nlm.nih.gov/pubmed/30100650
http://dx.doi.org/10.1007/s10967-018-5953-7
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