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Np(V) Retention at the Illite du Puy Surface

[Image: see text] In this study, Np(V) retention on Illite du Puy (IdP) was investigated since it is essential for understanding the migration behavior of Np in argillaceous environments. The presence of structural Fe(III) and Fe(II) in IdP was confirmed by Fe K-edge X-ray absorption near-edge struc...

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Autores principales: Schacherl, Bianca, Joseph, Claudia, Beck, Aaron, Lavrova, Polina, Schnurr, Andreas, Dardenne, Kathy, Geyer, Frank, Cherkezova-Zheleva, Zara, Göttlicher, Jörg, Geckeis, Horst, Vitova, Tonya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10399294/
https://www.ncbi.nlm.nih.gov/pubmed/37460108
http://dx.doi.org/10.1021/acs.est.2c09356
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author Schacherl, Bianca
Joseph, Claudia
Beck, Aaron
Lavrova, Polina
Schnurr, Andreas
Dardenne, Kathy
Geyer, Frank
Cherkezova-Zheleva, Zara
Göttlicher, Jörg
Geckeis, Horst
Vitova, Tonya
author_facet Schacherl, Bianca
Joseph, Claudia
Beck, Aaron
Lavrova, Polina
Schnurr, Andreas
Dardenne, Kathy
Geyer, Frank
Cherkezova-Zheleva, Zara
Göttlicher, Jörg
Geckeis, Horst
Vitova, Tonya
author_sort Schacherl, Bianca
collection PubMed
description [Image: see text] In this study, Np(V) retention on Illite du Puy (IdP) was investigated since it is essential for understanding the migration behavior of Np in argillaceous environments. The presence of structural Fe(III) and Fe(II) in IdP was confirmed by Fe K-edge X-ray absorption near-edge structure (XANES) and (57)Fe Mössbauer spectroscopy. In batch sorption experiments, a higher Np sorption affinity to IdP was found than to Wyoming smectite or iron-free synthetic montmorillonite. An increase of the relative Np(IV) ratio sorbed onto IdP with decreasing pH was observed by solvent extraction (up to (24 ± 2)% at pH 5, c(0)(Np) = 10(–6) mol/L). Furthermore, up to (33 ± 5)% Np(IV) could be detected in IdP diffusion samples at pH 5. Respective Np M(5)-edge high-energy resolution (HR-) XANES spectra suggested the presence of Np(IV/V) mixtures and weakened axial bond covalency of the NpO(2)(+) species sorbed onto IdP. Np L(3)-edge extended X-ray absorption fine structure (EXAFS) analysis showed that significant fractions of Np were coordinated to Fe—O entities at pH 9. This highlights the potential role of Fe(II/III) clay edge sites as a strong Np(V) surface complex partner and points to the partial reduction of sorbed Np(V) to Np(IV) via structural Fe(II).
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spelling pubmed-103992942023-08-04 Np(V) Retention at the Illite du Puy Surface Schacherl, Bianca Joseph, Claudia Beck, Aaron Lavrova, Polina Schnurr, Andreas Dardenne, Kathy Geyer, Frank Cherkezova-Zheleva, Zara Göttlicher, Jörg Geckeis, Horst Vitova, Tonya Environ Sci Technol [Image: see text] In this study, Np(V) retention on Illite du Puy (IdP) was investigated since it is essential for understanding the migration behavior of Np in argillaceous environments. The presence of structural Fe(III) and Fe(II) in IdP was confirmed by Fe K-edge X-ray absorption near-edge structure (XANES) and (57)Fe Mössbauer spectroscopy. In batch sorption experiments, a higher Np sorption affinity to IdP was found than to Wyoming smectite or iron-free synthetic montmorillonite. An increase of the relative Np(IV) ratio sorbed onto IdP with decreasing pH was observed by solvent extraction (up to (24 ± 2)% at pH 5, c(0)(Np) = 10(–6) mol/L). Furthermore, up to (33 ± 5)% Np(IV) could be detected in IdP diffusion samples at pH 5. Respective Np M(5)-edge high-energy resolution (HR-) XANES spectra suggested the presence of Np(IV/V) mixtures and weakened axial bond covalency of the NpO(2)(+) species sorbed onto IdP. Np L(3)-edge extended X-ray absorption fine structure (EXAFS) analysis showed that significant fractions of Np were coordinated to Fe—O entities at pH 9. This highlights the potential role of Fe(II/III) clay edge sites as a strong Np(V) surface complex partner and points to the partial reduction of sorbed Np(V) to Np(IV) via structural Fe(II). American Chemical Society 2023-07-17 /pmc/articles/PMC10399294/ /pubmed/37460108 http://dx.doi.org/10.1021/acs.est.2c09356 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Schacherl, Bianca
Joseph, Claudia
Beck, Aaron
Lavrova, Polina
Schnurr, Andreas
Dardenne, Kathy
Geyer, Frank
Cherkezova-Zheleva, Zara
Göttlicher, Jörg
Geckeis, Horst
Vitova, Tonya
Np(V) Retention at the Illite du Puy Surface
title Np(V) Retention at the Illite du Puy Surface
title_full Np(V) Retention at the Illite du Puy Surface
title_fullStr Np(V) Retention at the Illite du Puy Surface
title_full_unstemmed Np(V) Retention at the Illite du Puy Surface
title_short Np(V) Retention at the Illite du Puy Surface
title_sort np(v) retention at the illite du puy surface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10399294/
https://www.ncbi.nlm.nih.gov/pubmed/37460108
http://dx.doi.org/10.1021/acs.est.2c09356
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