MODELING OXYANION ADSORPTION ON FERRALIC SOIL, PART 2: CHROMATE, SELENATE, MOLYBDATE, AND ARSENATE ADSORPTION

被引:13
|
作者
Perez, Claudio [1 ,2 ]
Antelo, Juan [3 ]
Fiol, Sarah [1 ]
Arce, Florencio [1 ]
机构
[1] Univ Santiago de Compostela, Dept Phys Chem, Santiago De Compostela, Spain
[2] Univ Nacl Autonoma Mexico, Insituto Geol, Environm Biogeochem Grp, Mexico City, DF, Mexico
[3] Univ Santiago de Compostela, Dept Soil Sci & Agr Chem, Santiago De Compostela, Spain
关键词
Oxyanion; Adsorption; Speciation; Charge distribution model; Soil contamination; X-RAY-ABSORPTION; CHARGE-DISTRIBUTION; SURFACE COMPLEXATION; ANION ADSORPTION; IONIC-STRENGTH; PHOSPHATE; GOETHITE; SORPTION; MECHANISMS; SPECIATION;
D O I
10.1002/etc.2581
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
High levels of oxyanions are found in the soil environment, often as a result of human activity. At high concentrations, oxyanions can be harmful to both humans and wildlife. Information about the interactions between oxyanions and natural samples is essential for understanding the bioavailability, toxicity, and transport of these compounds in the environment. In the present study, the authors investigated the reactivity of different oxyanions (AsO4, MoO4, SeO4, and CrO4) at different pH values in 2 horizons of a ferralic soil. By combining available microscopic data on iron oxides with the macroscopic data obtained, the authors were able to use the charge distribution model to accurately describe the adsorption of these 4 oxyanions and thus to determine the surface speciation. The charge distribution model was previously calibrated and evaluated using phosphate adsorption/desorption data. The adsorption behavior on ferralic soil is controlled mainly by the natural iron oxides present, and it is qualitatively analogous to that exhibited by synthetic iron oxides. The highest adsorption was found for arsenate ions, whereas the lowest was found for selenate, with chromate and molybdate ions showing an intermediate behavior. Environ Toxicol Chem 2014;33:2217-2224. (c) 2014 SETAC
引用
收藏
页码:2217 / 2224
页数:8
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