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Plutonium(IV) Sorption during Ferrihydrite Nanoparticle Formation
[Image: see text] Understanding interactions between iron (oxyhydr)oxide nanoparticles and plutonium is essential to underpin technology to treat radioactive effluents, in cleanup of land contaminated with radionuclides, and to ensure the safe disposal of radioactive wastes. These interactions inclu...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011701/ https://www.ncbi.nlm.nih.gov/pubmed/32064412 http://dx.doi.org/10.1021/acsearthspacechem.9b00105 |
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author | Smith, Kurt F. Morris, Katherine Law, Gareth T. W. Winstanley, Ellen H. Livens, Francis R. Weatherill, Joshua S. Abrahamsen-Mills, Liam G. Bryan, Nicholas D. Mosselmans, J. Frederick W. Cibin, Giannantonio Parry, Stephen Blackham, Richard Law, Kathleen A. Shaw, Samuel |
author_facet | Smith, Kurt F. Morris, Katherine Law, Gareth T. W. Winstanley, Ellen H. Livens, Francis R. Weatherill, Joshua S. Abrahamsen-Mills, Liam G. Bryan, Nicholas D. Mosselmans, J. Frederick W. Cibin, Giannantonio Parry, Stephen Blackham, Richard Law, Kathleen A. Shaw, Samuel |
author_sort | Smith, Kurt F. |
collection | PubMed |
description | [Image: see text] Understanding interactions between iron (oxyhydr)oxide nanoparticles and plutonium is essential to underpin technology to treat radioactive effluents, in cleanup of land contaminated with radionuclides, and to ensure the safe disposal of radioactive wastes. These interactions include a range of adsorption, precipitation, and incorporation processes. Here, we explore the mechanisms of plutonium sequestration during ferrihydrite precipitation from an acidic solution. The initial 1 M HNO(3) solution with Fe(III)((aq)) and (242)Pu(IV)((aq)) underwent controlled hydrolysis via the addition of NaOH to pH 9. The majority of Fe(III)((aq)) and Pu(IV)((aq)) was removed from solution between pH 2 and 3 during ferrihydrite formation. Analysis of Pu–ferrihydrite by extended X-ray absorption fine structure (EXAFS) spectroscopy showed that Pu(IV) formed an inner-sphere tetradentate complex on the ferrihydrite surface, with minor amounts of PuO(2) present. Best fits to the EXAFS data collected from Pu–ferrihydrite samples aged for 2 and 6 months showed no statistically significant change in the Pu(IV)–Fe oxyhydroxide surface complex despite the ferrihydrite undergoing extensive recrystallization to hematite. This suggests the Pu remains strongly sorbed to the iron (oxyhydr)oxide surface and could be retained over extended time periods. |
format | Online Article Text |
id | pubmed-7011701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70117012020-02-12 Plutonium(IV) Sorption during Ferrihydrite Nanoparticle Formation Smith, Kurt F. Morris, Katherine Law, Gareth T. W. Winstanley, Ellen H. Livens, Francis R. Weatherill, Joshua S. Abrahamsen-Mills, Liam G. Bryan, Nicholas D. Mosselmans, J. Frederick W. Cibin, Giannantonio Parry, Stephen Blackham, Richard Law, Kathleen A. Shaw, Samuel ACS Earth Space Chem [Image: see text] Understanding interactions between iron (oxyhydr)oxide nanoparticles and plutonium is essential to underpin technology to treat radioactive effluents, in cleanup of land contaminated with radionuclides, and to ensure the safe disposal of radioactive wastes. These interactions include a range of adsorption, precipitation, and incorporation processes. Here, we explore the mechanisms of plutonium sequestration during ferrihydrite precipitation from an acidic solution. The initial 1 M HNO(3) solution with Fe(III)((aq)) and (242)Pu(IV)((aq)) underwent controlled hydrolysis via the addition of NaOH to pH 9. The majority of Fe(III)((aq)) and Pu(IV)((aq)) was removed from solution between pH 2 and 3 during ferrihydrite formation. Analysis of Pu–ferrihydrite by extended X-ray absorption fine structure (EXAFS) spectroscopy showed that Pu(IV) formed an inner-sphere tetradentate complex on the ferrihydrite surface, with minor amounts of PuO(2) present. Best fits to the EXAFS data collected from Pu–ferrihydrite samples aged for 2 and 6 months showed no statistically significant change in the Pu(IV)–Fe oxyhydroxide surface complex despite the ferrihydrite undergoing extensive recrystallization to hematite. This suggests the Pu remains strongly sorbed to the iron (oxyhydr)oxide surface and could be retained over extended time periods. American Chemical Society 2019-09-16 2019-11-21 /pmc/articles/PMC7011701/ /pubmed/32064412 http://dx.doi.org/10.1021/acsearthspacechem.9b00105 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Smith, Kurt F. Morris, Katherine Law, Gareth T. W. Winstanley, Ellen H. Livens, Francis R. Weatherill, Joshua S. Abrahamsen-Mills, Liam G. Bryan, Nicholas D. Mosselmans, J. Frederick W. Cibin, Giannantonio Parry, Stephen Blackham, Richard Law, Kathleen A. Shaw, Samuel Plutonium(IV) Sorption during Ferrihydrite Nanoparticle Formation |
title | Plutonium(IV) Sorption during Ferrihydrite Nanoparticle
Formation |
title_full | Plutonium(IV) Sorption during Ferrihydrite Nanoparticle
Formation |
title_fullStr | Plutonium(IV) Sorption during Ferrihydrite Nanoparticle
Formation |
title_full_unstemmed | Plutonium(IV) Sorption during Ferrihydrite Nanoparticle
Formation |
title_short | Plutonium(IV) Sorption during Ferrihydrite Nanoparticle
Formation |
title_sort | plutonium(iv) sorption during ferrihydrite nanoparticle
formation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011701/ https://www.ncbi.nlm.nih.gov/pubmed/32064412 http://dx.doi.org/10.1021/acsearthspacechem.9b00105 |
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