Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/27287
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dc.contributor.authorSmith, Euanen
dc.contributor.authorNaidu, Ravendraen
dc.contributor.authorAlston, Angus MacCallumen
dc.date.issued2002en
dc.identifier.citationJournal of Environmental Quality, 2002; 31(2):557-563en
dc.identifier.issn0047-2425en
dc.identifier.urihttp://hdl.handle.net/2440/27287-
dc.description.abstractReceived for publication November 30, 1999. There are more than 10000 arsenic (As) contaminated sites in Australia. The ability of soils at these contaminated sites to sorb As is highly variable and appreciable amounts of As have been recorded in the subsurface soils. The potential risk of surface and ground water contamination by As at these sites is a major environmental concern. Factors that influence adsorption capacity of soils influence the bioavailability and subsequent mobility of As in soils. In the present study we investigated the effect of PO³⁻4 and Na⁺ and Ca²⁺ on the sorption of AsV and AsIII by an Oxisol, a Vertisol, and two Alfisols. The presence of P (0.16 mmol L⁻¹) greatly decreased AsV sorption by soils containing low amounts of Fe oxides (<100 mmol kg⁻¹), indicating competitive adsorption between P and AsV for sorption sites. In contrast, the presence of a similar amount of P had little effect on the amount of AsV adsorbed by soils with high Fe content (>800 mmol kg⁻¹). However, AsV sorption substantially decreased from 0.63 to 0.37 mmol kg⁻¹ as P concentration was increased from 0.16 to 3.2 mmol L⁻¹ in selected soils. This suggests increased competition between P and AsV for soil sorption sites, through either the higher affinity or the effect of mass action of the increasing concentration of P in solution. A similar effect of P on AsIII sorption was observed in the low sorbing Alfisol and high affinity Oxisol. However, the amount of AsIII sorbed by the Oxisol was much greater than the Alfisol for all treatments. The presence of Ca²⁺ increased the amount of AsV sorbed compared with that of Na+ and was manifested through changes in the surface charge characteristics of the soils. A similar trend in AsIII sorption was recorded with changes in index cation, although the effect was not as marked as recorded for AsV.en
dc.description.statementofresponsibilityE. Smith, R. Naidu and A. M. Alstonen
dc.language.isoenen
dc.publisherAmerican Society of Agronomyen
dc.rights© 2002 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of Americaen
dc.source.urihttps://dl-sciencesocieties-org.proxy.library.adelaide.edu.au/publications/jeq/articles/31/2/557en
dc.titleChemistry of inorganic arsenic in soils: II. Effect of phosphorus, sodium, and calcium on arsenic sorptionen
dc.typeJournal articleen
dc.contributor.schoolSchool of Earth and Environmental Sciences : Soil and Land Systemsen
dc.identifier.doi10.2134/jeq2002.5570en
Appears in Collections:Soil and Land Systems publications

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