Arsenate immobilization associated with microbial oxidation of ferrous ion in complex acid sulfate water

Article

Ma, Yingqun and Lin, Chuxia. 2012. "Arsenate immobilization associated with microbial oxidation of ferrous ion in complex acid sulfate water ." Journal of Hazardous Materials. 217-218, pp. 238-245. https://doi.org/10.1016/j.jhazmat.2012.03.021
Article Title

Arsenate immobilization associated with microbial oxidation of ferrous ion in complex acid sulfate water

ERA Journal ID4682
Article CategoryArticle
AuthorsMa, Yingqun (Author) and Lin, Chuxia (Author)
Journal TitleJournal of Hazardous Materials
Journal Citation217-218, pp. 238-245
Number of Pages8
Year2012
PublisherElsevier
Place of PublicationAmsterdam, Netherlands
ISSN0304-3894
1873-3336
Digital Object Identifier (DOI)https://doi.org/10.1016/j.jhazmat.2012.03.021
Web Address (URL)http://www.sciencedirect.com/science/article/pii/S0304389412002890
Abstract

Chemical, XRD, SEM, RS, FTIR and XPS techniques were used to investigate arsenate immobilization associated with microbial Fe2+ oxidation in a complex acid sulfate water system consisting of a modified 9 K solution (pH 2.0) plus As, Cu, Cd, Pb, Zn and Mn. At a 1:12.5:70 molar ratio of As:Fe:S, schweretmannite formation was impeded. This was in contrast with the predominant presence of schwertmannite
when the heavy metals were absent, suggesting that a schwertmannite binding model is not valid for explaining arsenate immobilization in the complex system. In this study, arsenate was initially immobilized through co-precipitation with non-Fe metals and phosphate. Subsequently when sufficient Fe3+ was produced from Fe2+ oxidation, formation of a mixed iron, arsenate and phosphate phase predominated.
The last stage involved surface complexation of arsenate species. Pb appeared to play an insignificant role in arsenate immobilization due to its strong affinity for sulfate to form anglesite. Phosphate strongly competed with arsenate for the available binding sites. However, As exhibited an increased capacity to compete with P and S for available binding sites from the co-precipitation to surface complexation stage.
Adsorbed As tended to be in HAsO4 2− form. The scavenged arsenate species was relatively stable after 2464-h aging.

Keywordsarsenic; acid sulfate water; ochreous precipitate; co-precipitation; absorption
ANZSRC Field of Research 2020370799. Hydrology not elsewhere classified
370901. Geomorphology and earth surface processes
410499. Environmental management not elsewhere classified
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Byline AffiliationsSouth China Agricultural University, China
Australian Centre for Sustainable Catchments
Institution of OriginUniversity of Southern Queensland
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