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As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria
Iron oxides/oxyhydroxides, namely maghemite, iron oxide-silica composite, akaganeite, and ferrihydrite, are studied for As(V) and As(III) removal from water in the pH range 2–8. All sorbents were characterized for their structural, morphological, textural, and surface charge properties. The same exp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840107/ https://www.ncbi.nlm.nih.gov/pubmed/35159671 http://dx.doi.org/10.3390/nano12030326 |
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author | Sanna Angotzi, Marco Mameli, Valentina Fantasia, Alessandra Cara, Claudio Secci, Fausto Enzo, Stefano Gerina, Marianna Cannas, Carla |
author_facet | Sanna Angotzi, Marco Mameli, Valentina Fantasia, Alessandra Cara, Claudio Secci, Fausto Enzo, Stefano Gerina, Marianna Cannas, Carla |
author_sort | Sanna Angotzi, Marco |
collection | PubMed |
description | Iron oxides/oxyhydroxides, namely maghemite, iron oxide-silica composite, akaganeite, and ferrihydrite, are studied for As(V) and As(III) removal from water in the pH range 2–8. All sorbents were characterized for their structural, morphological, textural, and surface charge properties. The same experimental conditions for the batch tests permitted a direct comparison among the sorbents, particularly between the oxyhydroxides, known to be among the most promising As-removers but hardly compared in the literature. The tests revealed akaganeite to perform better in the whole pH range for As(V) (max 89 mg g(−1) at pH(0) 3) but to be also efficient toward As(III) (max 91 mg g(−1) at pH(0) 3–8), for which the best sorbent was ferrihydrite (max 144 mg g(−1) at pH(0) 8). Moreover, the study of the sorbents’ surface chemistry under contact with arsenic and arsenic-free solutions allowed the understanding of its role in the arsenic uptake through electrophoretic light scattering and pH measurements. Indeed, the sorbent’s ability to modify the starting pH was a crucial step in determining the removal of performances. The As(V) initial concentration, contact time, ionic strength, and presence of competitors were also studied for akaganeite, the most promising remover, at pH(0) 3 and 8 to deepen the uptake mechanism. |
format | Online Article Text |
id | pubmed-8840107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88401072022-02-13 As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria Sanna Angotzi, Marco Mameli, Valentina Fantasia, Alessandra Cara, Claudio Secci, Fausto Enzo, Stefano Gerina, Marianna Cannas, Carla Nanomaterials (Basel) Article Iron oxides/oxyhydroxides, namely maghemite, iron oxide-silica composite, akaganeite, and ferrihydrite, are studied for As(V) and As(III) removal from water in the pH range 2–8. All sorbents were characterized for their structural, morphological, textural, and surface charge properties. The same experimental conditions for the batch tests permitted a direct comparison among the sorbents, particularly between the oxyhydroxides, known to be among the most promising As-removers but hardly compared in the literature. The tests revealed akaganeite to perform better in the whole pH range for As(V) (max 89 mg g(−1) at pH(0) 3) but to be also efficient toward As(III) (max 91 mg g(−1) at pH(0) 3–8), for which the best sorbent was ferrihydrite (max 144 mg g(−1) at pH(0) 8). Moreover, the study of the sorbents’ surface chemistry under contact with arsenic and arsenic-free solutions allowed the understanding of its role in the arsenic uptake through electrophoretic light scattering and pH measurements. Indeed, the sorbent’s ability to modify the starting pH was a crucial step in determining the removal of performances. The As(V) initial concentration, contact time, ionic strength, and presence of competitors were also studied for akaganeite, the most promising remover, at pH(0) 3 and 8 to deepen the uptake mechanism. MDPI 2022-01-20 /pmc/articles/PMC8840107/ /pubmed/35159671 http://dx.doi.org/10.3390/nano12030326 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sanna Angotzi, Marco Mameli, Valentina Fantasia, Alessandra Cara, Claudio Secci, Fausto Enzo, Stefano Gerina, Marianna Cannas, Carla As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title | As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title_full | As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title_fullStr | As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title_full_unstemmed | As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title_short | As((III, V)) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria |
title_sort | as((iii, v)) uptake from nanostructured iron oxides and oxyhydroxides: the complex interplay between sorbent surface chemistry and arsenic equilibria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840107/ https://www.ncbi.nlm.nih.gov/pubmed/35159671 http://dx.doi.org/10.3390/nano12030326 |
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