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Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism

Hexavalent chromium contamination of groundwater is a worldwide problem caused by anthropogenic and natural processes. We report the rate of Cr(VI) removal by two humic acids (extracted from Miocene age lignite and younger peat soil) in aqueous suspensions across a pH range likely to be encountered...

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Autores principales: Aldmour, Suha T., Burke, Ian T., Bray, Andrew W., Baker, Daniel L., Ross, Andrew B., Gill, Fiona L., Cibin, Giannantonio, Ries, Michael E., Stewart, Douglas I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394447/
https://www.ncbi.nlm.nih.gov/pubmed/30565111
http://dx.doi.org/10.1007/s11356-018-3902-1
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author Aldmour, Suha T.
Burke, Ian T.
Bray, Andrew W.
Baker, Daniel L.
Ross, Andrew B.
Gill, Fiona L.
Cibin, Giannantonio
Ries, Michael E.
Stewart, Douglas I.
author_facet Aldmour, Suha T.
Burke, Ian T.
Bray, Andrew W.
Baker, Daniel L.
Ross, Andrew B.
Gill, Fiona L.
Cibin, Giannantonio
Ries, Michael E.
Stewart, Douglas I.
author_sort Aldmour, Suha T.
collection PubMed
description Hexavalent chromium contamination of groundwater is a worldwide problem caused by anthropogenic and natural processes. We report the rate of Cr(VI) removal by two humic acids (extracted from Miocene age lignite and younger peat soil) in aqueous suspensions across a pH range likely to be encountered in terrestrial environments. Cr(VI) was reduced to Cr(III) in a first-order reaction with respect Cr(VI) concentration, but exhibited a partial order (~ 0.5) with respect to [H+]. This reaction was more rapid with the peat humic acid, where Cr(VI) reduction was observed at all pH values investigated (3.7 ≤ pH ≤ 10.5). (13)C NMR and pyrolysis GC-MS spectroscopy indicate that the reaction results in loss of substituted phenolic moieties and hydroxyl groups from the humic acids. X-ray absorption spectroscopy indicated that at all pH values the resulting Cr(III) was associated with the partially degraded humic acid in an inner-sphere adsorption complex. The reaction mechanism is likely to be controlled by ester formation between Cr(VI) and phenolic/hydroxyl moieties, as this initial step is rapid in acidic systems but far less favourable in alkaline conditions. Our findings highlight the potential of humic acid to reduce and remove Cr(VI) from solution in a range of environmental conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11356-018-3902-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-63944472019-03-15 Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism Aldmour, Suha T. Burke, Ian T. Bray, Andrew W. Baker, Daniel L. Ross, Andrew B. Gill, Fiona L. Cibin, Giannantonio Ries, Michael E. Stewart, Douglas I. Environ Sci Pollut Res Int Research Article Hexavalent chromium contamination of groundwater is a worldwide problem caused by anthropogenic and natural processes. We report the rate of Cr(VI) removal by two humic acids (extracted from Miocene age lignite and younger peat soil) in aqueous suspensions across a pH range likely to be encountered in terrestrial environments. Cr(VI) was reduced to Cr(III) in a first-order reaction with respect Cr(VI) concentration, but exhibited a partial order (~ 0.5) with respect to [H+]. This reaction was more rapid with the peat humic acid, where Cr(VI) reduction was observed at all pH values investigated (3.7 ≤ pH ≤ 10.5). (13)C NMR and pyrolysis GC-MS spectroscopy indicate that the reaction results in loss of substituted phenolic moieties and hydroxyl groups from the humic acids. X-ray absorption spectroscopy indicated that at all pH values the resulting Cr(III) was associated with the partially degraded humic acid in an inner-sphere adsorption complex. The reaction mechanism is likely to be controlled by ester formation between Cr(VI) and phenolic/hydroxyl moieties, as this initial step is rapid in acidic systems but far less favourable in alkaline conditions. Our findings highlight the potential of humic acid to reduce and remove Cr(VI) from solution in a range of environmental conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11356-018-3902-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-12-18 2019 /pmc/articles/PMC6394447/ /pubmed/30565111 http://dx.doi.org/10.1007/s11356-018-3902-1 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research Article
Aldmour, Suha T.
Burke, Ian T.
Bray, Andrew W.
Baker, Daniel L.
Ross, Andrew B.
Gill, Fiona L.
Cibin, Giannantonio
Ries, Michael E.
Stewart, Douglas I.
Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title_full Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title_fullStr Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title_full_unstemmed Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title_short Abiotic reduction of Cr(VI) by humic acids derived from peat and lignite: kinetics and removal mechanism
title_sort abiotic reduction of cr(vi) by humic acids derived from peat and lignite: kinetics and removal mechanism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394447/
https://www.ncbi.nlm.nih.gov/pubmed/30565111
http://dx.doi.org/10.1007/s11356-018-3902-1
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