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Unexpectedly efficient ion desorption of graphene-based materials

Ion desorption is extremely challenging for adsorbents with superior performance, and widely used conventional desorption methods involve high acid or base concentrations and large consumption of reagents. Here, we experimentally demonstrate the rapid and efficient desorption of ions on magnetite-gr...

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Autores principales: Xia, Xinming, Zhou, Feng, Xu, Jing, Wang, Zhongteng, Lan, Jian, Fan, Yan, Wang, Zhikun, Liu, Wei, Chen, Junlang, Feng, Shangshen, Tu, Yusong, Yang, Yizhou, Chen, Liang, Fang, Haiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700706/
https://www.ncbi.nlm.nih.gov/pubmed/36434112
http://dx.doi.org/10.1038/s41467-022-35077-9
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author Xia, Xinming
Zhou, Feng
Xu, Jing
Wang, Zhongteng
Lan, Jian
Fan, Yan
Wang, Zhikun
Liu, Wei
Chen, Junlang
Feng, Shangshen
Tu, Yusong
Yang, Yizhou
Chen, Liang
Fang, Haiping
author_facet Xia, Xinming
Zhou, Feng
Xu, Jing
Wang, Zhongteng
Lan, Jian
Fan, Yan
Wang, Zhikun
Liu, Wei
Chen, Junlang
Feng, Shangshen
Tu, Yusong
Yang, Yizhou
Chen, Liang
Fang, Haiping
author_sort Xia, Xinming
collection PubMed
description Ion desorption is extremely challenging for adsorbents with superior performance, and widely used conventional desorption methods involve high acid or base concentrations and large consumption of reagents. Here, we experimentally demonstrate the rapid and efficient desorption of ions on magnetite-graphene oxide (M-GO) by adding low amounts of Al(3+). The corresponding concentration of Al(3+) used is reduced by at least a factor 250 compared to conventional desorption method. The desorption rate reaches ~97.0% for the typical radioactive and bivalent ions Co(2+), Mn(2+), and Sr(2+) within ~1 min. We achieve effective enrichment of radioactive (60)Co and reduce the volume of concentrated (60)Co solution by approximately 10 times compared to the initial solution. The M-GO can be recycled and reused easily without compromising its adsorption efficiency and magnetic performance, based on the unique hydration anionic species of Al(3+) under alkaline conditions. Density functional theory calculations show that the interaction of graphene with Al(3+) is stronger than with divalent ions, and that the adsorption probability of Al(3+) is superior than that of Co(2+), Mn(2+), and Sr(2+) ions. This suggests that the proposed method could be used to enrich a wider range of ions in the fields of energy, biology, environmental technology, and materials science.
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spelling pubmed-97007062022-11-27 Unexpectedly efficient ion desorption of graphene-based materials Xia, Xinming Zhou, Feng Xu, Jing Wang, Zhongteng Lan, Jian Fan, Yan Wang, Zhikun Liu, Wei Chen, Junlang Feng, Shangshen Tu, Yusong Yang, Yizhou Chen, Liang Fang, Haiping Nat Commun Article Ion desorption is extremely challenging for adsorbents with superior performance, and widely used conventional desorption methods involve high acid or base concentrations and large consumption of reagents. Here, we experimentally demonstrate the rapid and efficient desorption of ions on magnetite-graphene oxide (M-GO) by adding low amounts of Al(3+). The corresponding concentration of Al(3+) used is reduced by at least a factor 250 compared to conventional desorption method. The desorption rate reaches ~97.0% for the typical radioactive and bivalent ions Co(2+), Mn(2+), and Sr(2+) within ~1 min. We achieve effective enrichment of radioactive (60)Co and reduce the volume of concentrated (60)Co solution by approximately 10 times compared to the initial solution. The M-GO can be recycled and reused easily without compromising its adsorption efficiency and magnetic performance, based on the unique hydration anionic species of Al(3+) under alkaline conditions. Density functional theory calculations show that the interaction of graphene with Al(3+) is stronger than with divalent ions, and that the adsorption probability of Al(3+) is superior than that of Co(2+), Mn(2+), and Sr(2+) ions. This suggests that the proposed method could be used to enrich a wider range of ions in the fields of energy, biology, environmental technology, and materials science. Nature Publishing Group UK 2022-11-25 /pmc/articles/PMC9700706/ /pubmed/36434112 http://dx.doi.org/10.1038/s41467-022-35077-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xia, Xinming
Zhou, Feng
Xu, Jing
Wang, Zhongteng
Lan, Jian
Fan, Yan
Wang, Zhikun
Liu, Wei
Chen, Junlang
Feng, Shangshen
Tu, Yusong
Yang, Yizhou
Chen, Liang
Fang, Haiping
Unexpectedly efficient ion desorption of graphene-based materials
title Unexpectedly efficient ion desorption of graphene-based materials
title_full Unexpectedly efficient ion desorption of graphene-based materials
title_fullStr Unexpectedly efficient ion desorption of graphene-based materials
title_full_unstemmed Unexpectedly efficient ion desorption of graphene-based materials
title_short Unexpectedly efficient ion desorption of graphene-based materials
title_sort unexpectedly efficient ion desorption of graphene-based materials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700706/
https://www.ncbi.nlm.nih.gov/pubmed/36434112
http://dx.doi.org/10.1038/s41467-022-35077-9
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