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Kinetic study of uranium residue dissolution in ammonium carbonate media

The purpose of this study was to determine the kinetics of the dissolution of a uranium residue in ammonium carbonate media. The residue is generated in the production of medical isotopes. The effects of parameters, such as varying peroxide and carbonate concentrations, dissolution time as well as t...

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Autores principales: Kweto, B., Groot, D. R., Stassen, E., Suthiram, J., Zeevaart, J. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514662/
https://www.ncbi.nlm.nih.gov/pubmed/26224977
http://dx.doi.org/10.1007/s10967-014-3396-3
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author Kweto, B.
Groot, D. R.
Stassen, E.
Suthiram, J.
Zeevaart, J. R.
author_facet Kweto, B.
Groot, D. R.
Stassen, E.
Suthiram, J.
Zeevaart, J. R.
author_sort Kweto, B.
collection PubMed
description The purpose of this study was to determine the kinetics of the dissolution of a uranium residue in ammonium carbonate media. The residue is generated in the production of medical isotopes. The effects of parameters, such as varying peroxide and carbonate concentrations, dissolution time as well as temperature on the extraction rate have been separately studied. Results indicate complete dissolution of the residue at 60 °C, after 30 min, in ammonium carbonate solution enriched with hydrogen peroxide. The yield and rate of uranium extraction were found to increase as a function of both temperature, in the range of 25–60 °C, and hydrogen peroxide concentration. The extraction process was governed by chemical reaction as the activation energy was found to be 45.5 kJ/mol. The order of reaction with respect to uranium concentration was found to be approximately first order.
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spelling pubmed-45146622015-07-27 Kinetic study of uranium residue dissolution in ammonium carbonate media Kweto, B. Groot, D. R. Stassen, E. Suthiram, J. Zeevaart, J. R. J Radioanal Nucl Chem Article The purpose of this study was to determine the kinetics of the dissolution of a uranium residue in ammonium carbonate media. The residue is generated in the production of medical isotopes. The effects of parameters, such as varying peroxide and carbonate concentrations, dissolution time as well as temperature on the extraction rate have been separately studied. Results indicate complete dissolution of the residue at 60 °C, after 30 min, in ammonium carbonate solution enriched with hydrogen peroxide. The yield and rate of uranium extraction were found to increase as a function of both temperature, in the range of 25–60 °C, and hydrogen peroxide concentration. The extraction process was governed by chemical reaction as the activation energy was found to be 45.5 kJ/mol. The order of reaction with respect to uranium concentration was found to be approximately first order. Springer Netherlands 2014-08-24 2014 /pmc/articles/PMC4514662/ /pubmed/26224977 http://dx.doi.org/10.1007/s10967-014-3396-3 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Kweto, B.
Groot, D. R.
Stassen, E.
Suthiram, J.
Zeevaart, J. R.
Kinetic study of uranium residue dissolution in ammonium carbonate media
title Kinetic study of uranium residue dissolution in ammonium carbonate media
title_full Kinetic study of uranium residue dissolution in ammonium carbonate media
title_fullStr Kinetic study of uranium residue dissolution in ammonium carbonate media
title_full_unstemmed Kinetic study of uranium residue dissolution in ammonium carbonate media
title_short Kinetic study of uranium residue dissolution in ammonium carbonate media
title_sort kinetic study of uranium residue dissolution in ammonium carbonate media
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514662/
https://www.ncbi.nlm.nih.gov/pubmed/26224977
http://dx.doi.org/10.1007/s10967-014-3396-3
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