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Mobilization of soil-borne arsenic by three common organic acids: Dosage and time effects

Version 2 2024-06-05, 05:56
Version 1 2020-08-10, 17:04
journal contribution
posted on 2024-06-05, 05:56 authored by OO Onireti, Chu Xia LinChu Xia Lin
A batch experiment was conducted to investigate the mobilization of soil-borne arsenic by three common low-molecular-weight organic acids with a focus on dosage and time effects. The results show that oxalic acid behaved differently from citric acid and malic acid in terms of mobilizing As that was bound to iron compounds. At an equivalent molar concentration, reactions between oxalic acid and soil-borne Fe were kinetically more favourable, as compared to those between either citric acid or malic acid and the soil-borne Fe. It was found that reductive dissolution of soil-borne Fe played a more important role in liberating As, as compared to non-reductive reactions. Prior to the 7th day of the experiment, As mobility increased with increasing dose of oxalic acid while there was no significant difference (P > 0.05) in mobilized As among the treatments with different doses of citric acid or malic acid. The dosage effect on soil-borne As mobilization in the citric acid and malic acid treatments became clear only after the 7th day of the experiment. Soluble Ca present in the soils could cause re-immobilization of As by competing with solution-borne Fe for available organic ligands to form practically insoluble organic compounds of calcium (i.e. calcium oxalate). This resulted in transformation of highly soluble organic complexes of iron (i.e. iron oxalate complexes) into slightly soluble organic compounds of iron (i.e. iron oxalate) or free ferric ion, which then reacted with the solution-borne arsenate ions to form practically insoluble iron arsenates in the latter part of the experiment.

History

Journal

Chemosphere

Volume

147

Pagination

352-360

Location

Amsterdam, The Netherlands

ISSN

0045-6535

eISSN

1879-1298

Language

eng

Publication classification

C1.1 Refereed article in a scholarly journal

Copyright notice

2015, Elsevier Ltd.

Publisher

Elsevier

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