Perez, JPH, Tobler, DJ, Thomas, AN et al. (4 more authors) (2019) Adsorption and Reduction of Arsenate during the Fe²+- Induced Transformation of Ferrihydrite. ACS Earth and Space Chemistry, 3 (6). pp. 884-894. ISSN 2472-3452
Abstract
Iron (oxyhydr)oxides play an important role in controlling the mobility and toxicity of arsenic (As) in contaminated soils and groundwaters. Dynamic changes in subsurface geochemical conditions can impact As sequestration and remobilization since the fate of As is highly dependent on the dominant iron mineral phases present and, specifically, the pathways through which these form or transform. To assess the fate of arsenate [As(V)] in subsurface settings, we have investigated the Fe²+-induced transformation of As(V)-bearing ferrihydrite (As(V)-FH) to more crystalline phases under environmentally relevant anoxic subsurface conditions. Specifically, we examined the influence of varying Fe²+(aq)/Fe(III)solid ratios (0.5, 1, 2) on the behavior and speciation of mineral-bound As species during the transformation of As(V)-FH to crystalline iron-bearing phases at circumneutral pH conditions. At all Fe²+(aq)/Fe(III)solid ratios, goethite (GT), green rust sulfate (GRSO4), and lepidocrocite (LP) formed within the first 2 h of reaction. At low ratios (0.5 to 1), initially formed GRSO4 and/or LP dissolved as the reaction progressed, and only GT and some unreacted FH remained after 24 h. At Fe²+(aq)/Fe(III)solid ratio of 2, GRSO4 remained stable throughout the 24 h of reaction, alongside GT and unreacted As(V)-FH. Despite the fact that majority of the starting As(V)-FH transformed to other phases, the initially adsorbed As was not released into solution during the transformation reactions, and ∼99.9% of it remained mineral-bound. Nevertheless, the initial As(V) became partially reduced to As(III), most likely because of the surface-associated Fe²+-GT redox couple. The extent of As(V) reduction increased from ∼34% to ∼40%, as the Fe²+(aq)/Fe(III)solid ratio increased from 0.5 to 2. Overall, our results provide important insights into transformation pathways of iron (oxyhydr)oxide minerals in As contaminated, anoxic soils and sediments and demonstrate the impact that such transformations can have on As mobility and also importantly oxidation state and, hence, toxicity in these environments.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | (c) 2019, American Chemical Society. This is an author produced version of a paper published in ACS Earth and Space Chemistry. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemical & Process Engineering (Leeds) The University of Leeds > Faculty of Environment (Leeds) > School of Earth and Environment (Leeds) > Earth Surface Science Institute (ESSI) (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 26 Jun 2019 15:52 |
Last Modified: | 25 Apr 2020 00:38 |
Status: | Published |
Publisher: | American Chemical Society |
Identification Number: | 10.1021/acsearthspacechem.9b00031 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:147716 |