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In this study we evaluated the arsenate adsorption capacity of red muds (RM), wastes tailing from the alumina production, at different pH values (4, 7, and 10). RM samples were artificially enriched in batch tests with solutions containing increasing concentrations of As(V). The pH of the solution significantly affected the adsorption, which increased with the decrease of pH. Moreover a sequential extraction procedure [H(2)O; (NH(4))(2)SO(4); NH(4)H(2)PO(4); NH(4)(+)-oxalate; NH(4)(+)-oxalate+ascorbic acid] was applied to RM samples exchanged with arsenate. Using this approach it was shown that low concentrations of arsenate sorbed in RM were present as water soluble and exchangeable fractions, while NH(4)(+)-oxalate and NH(4)(+)-oxalate+ascorbic acid extracted most of the adsorbed arsenate from RM at different pH values. Besides, FT-IR spectroscopy was used to better understand the nature of RM surface configuration after As(V) sorption. In the FT-IR spectra the presence of As(V) species was highlighted by a well resolved band at 865 cm(-1). The intensity and broadness of this band increased at the decreasing of pH. This band could be related to nu(As-O) vibration of an inner-sphere Al-O-As complex and/or due to As-O bonds of the adsorbed As(V) species on Fe oxides of RM samples.
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http://dx.doi.org/10.1016/j.jhazmat.2009.09.145 | DOI Listing |
J Hazard Mater
November 2024
Environmental Geochemistry Laboratory, Department of Earth and Environmental Sciences, Indian Institute of Science Education and Research (IISER) Bhopal, Bhopal Bypass Road, Bhauri 462066, Madhya Pradesh, India; Environmental Geochemistry, Bayreuth Center for Ecology and Environmental Research (BayCEER), University of Bayreuth, 95440 Bayreuth, Germany. Electronic address:
Understanding processes regulating thioarsenate (HAsSO; n = 1 - 3; x = 1 - 3) mobility is essential to predicting the fate of arsenic (As) in aquatic environments under anoxic conditions. Under such conditions, natural organic matter (NOM) is known to effectively sorb arsenite and arsenate due to metal cation-bridged ternary complexation with the NOM. However, the extent and mechanism of thioarsenate sorption onto NOM via similar complexation has not been investigated.
View Article and Find Full Text PDFEnviron Sci Technol Lett
November 2024
School of Earth Sciences, University of Bristol, Bristol BS8 1RJ, United Kingdom.
Arsenic is a global pollutant. Recent studies found that Fe(II) can oxidize As(III), but the extent of oxidation with mixed-valent iron minerals and the mechanisms involved are unknown. In this study, we investigated whether As(III) can be oxidized under reducing conditions using green rust sulfate (GR-SO), an Fe mineral containing both Fe(II) and Fe(III).
View Article and Find Full Text PDFBiochem Biophys Res Commun
December 2024
Microbial Adapdation and Chromatin Remodelling Laboratory, Department of Biological Sciences and Bioengineering, Indian Institute of Technology Kanpur, India; Environmental Microbiology Laboratory, Center for Environmental Science and Engineering, Indian Institute of Technology Kanpur, India; Kotak School of Sustainability, Indian Institute of Technology Kanpur, India. Electronic address:
Arsenic (As) poisoning in aquifers is a serious problem worldwide, especially in the middle-Gangetic Plain (MGP) of India. Microbially-mediated As speciation in such aquifers is governed by the arsenate-reductase enzyme, ArsC, encoded by the arsC gene of As-metabolizing bacteria. In this study, ArsC1 (119 aa) and ArsC2 (141 aa) of a highly resistant strain to arsenic, Citrobacter youngae IITK SM2 (CyIITKSM2), isolated from a mixed-oxic MGP groundwater were biochemically characterized.
View Article and Find Full Text PDFJ Agric Food Chem
November 2024
Environmental Geochemistry, Bayreuth Center for Ecology and Environmental Research (BayCEER), University of Bayreuth, Bayreuth 95440, Germany.
Sulfate fertilization has been proposed to limit arsenic (As) mobility in paddy soils and accumulation in rice grains. However, As and sulfur (S) have complex biogeochemical interactions. Besides the desired precipitation of sulfides that sorb or incorporate As, S can enhance As biotic methylation and abiotic thiolation.
View Article and Find Full Text PDFIntegr Environ Assess Manag
November 2024
DeSimone Consulting Engineers, New York, New York, USA.
Monosodium methanearsonate (MSMA), the sodium salt of monomethylarsonic acid (MMA), is used as a selective, broad-spectrum contact herbicide to control weeds in cotton and a variety of turf. In water, MSMA dissociates into ions of sodium (Na) and of MMA, which is the herbicide's active component. Certain soil microorganisms can methylate MMA to dimethylarsinic acid (DMA) other microorganisms can demethylate MMA to inorganic arsenic (iAs).
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