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Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine

The synthesis of a palladium-containing iodovanadinite derivative, hypothetically “PdPb(9)(VO(4))(6)I(2)”, was attempted using PdI(2) as a source of iodine in searching for a novel waste form for radioiodine. Stoichiometric amounts of Pb(3)(VO(4))(2) and PdI(2) were batched and reacted at elevated t...

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Autores principales: Johnstone, E. V., Bailey, D. J., Lawson, S., Stennett, M. C., Corkhill, C. L., Kim, M., Heo, J., Matsumura, D., Hyatt, N. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055183/
https://www.ncbi.nlm.nih.gov/pubmed/35517431
http://dx.doi.org/10.1039/d0ra04114a
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author Johnstone, E. V.
Bailey, D. J.
Lawson, S.
Stennett, M. C.
Corkhill, C. L.
Kim, M.
Heo, J.
Matsumura, D.
Hyatt, N. C.
author_facet Johnstone, E. V.
Bailey, D. J.
Lawson, S.
Stennett, M. C.
Corkhill, C. L.
Kim, M.
Heo, J.
Matsumura, D.
Hyatt, N. C.
author_sort Johnstone, E. V.
collection PubMed
description The synthesis of a palladium-containing iodovanadinite derivative, hypothetically “PdPb(9)(VO(4))(6)I(2)”, was attempted using PdI(2) as a source of iodine in searching for a novel waste form for radioiodine. Stoichiometric amounts of Pb(3)(VO(4))(2) and PdI(2) were batched and reacted at elevated temperatures in sealed vessels. Batched material was also subjected to high-energy ball-milling (HEBM) in order to reduce reaction time and the potential for iodine volatilization during subsequent reaction at 200–500 °C. The resulting products were characterized using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray analysis, IR spectroscopy, thermal analysis and Pd K XANES. Results showed that PdI(2) can function as a sacrificial iodine source for the formation of iodovanadinite, prototypically Pb(10)(VO(4))(6)I(2), however, the incorporation of Pd into this phase was not definitively observed. The sacrificial reaction mechanism involved the decomposition of PdI(2) to Pd metal and nascent I(2), with the latter incorporated into the iodovanadinite Pb(10)(VO(4))(6)I(2) phase. In comparison to processing using standard solid state reaction techniques, the use of HEBM prior to high temperature reaction generates a more homogeneous end-product with better iodine retention for this system. Overall, the key novelty and importance of this work is in demonstrating a method for direct immobilisation of undissolved PdI(2) from nuclear fuel reprocessing, in a composite wasteform in which I-129 is immobilised within a durable iodovandinite ceramic, encapsulating Pd metal.
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spelling pubmed-90551832022-05-04 Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine Johnstone, E. V. Bailey, D. J. Lawson, S. Stennett, M. C. Corkhill, C. L. Kim, M. Heo, J. Matsumura, D. Hyatt, N. C. RSC Adv Chemistry The synthesis of a palladium-containing iodovanadinite derivative, hypothetically “PdPb(9)(VO(4))(6)I(2)”, was attempted using PdI(2) as a source of iodine in searching for a novel waste form for radioiodine. Stoichiometric amounts of Pb(3)(VO(4))(2) and PdI(2) were batched and reacted at elevated temperatures in sealed vessels. Batched material was also subjected to high-energy ball-milling (HEBM) in order to reduce reaction time and the potential for iodine volatilization during subsequent reaction at 200–500 °C. The resulting products were characterized using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray analysis, IR spectroscopy, thermal analysis and Pd K XANES. Results showed that PdI(2) can function as a sacrificial iodine source for the formation of iodovanadinite, prototypically Pb(10)(VO(4))(6)I(2), however, the incorporation of Pd into this phase was not definitively observed. The sacrificial reaction mechanism involved the decomposition of PdI(2) to Pd metal and nascent I(2), with the latter incorporated into the iodovanadinite Pb(10)(VO(4))(6)I(2) phase. In comparison to processing using standard solid state reaction techniques, the use of HEBM prior to high temperature reaction generates a more homogeneous end-product with better iodine retention for this system. Overall, the key novelty and importance of this work is in demonstrating a method for direct immobilisation of undissolved PdI(2) from nuclear fuel reprocessing, in a composite wasteform in which I-129 is immobilised within a durable iodovandinite ceramic, encapsulating Pd metal. The Royal Society of Chemistry 2020-07-02 /pmc/articles/PMC9055183/ /pubmed/35517431 http://dx.doi.org/10.1039/d0ra04114a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Johnstone, E. V.
Bailey, D. J.
Lawson, S.
Stennett, M. C.
Corkhill, C. L.
Kim, M.
Heo, J.
Matsumura, D.
Hyatt, N. C.
Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title_full Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title_fullStr Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title_full_unstemmed Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title_short Synthesis and characterization of iodovanadinite using PdI(2,) an iodine source for the immobilisation of radioiodine
title_sort synthesis and characterization of iodovanadinite using pdi(2,) an iodine source for the immobilisation of radioiodine
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055183/
https://www.ncbi.nlm.nih.gov/pubmed/35517431
http://dx.doi.org/10.1039/d0ra04114a
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