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Effect of ionic strength on adsorption of As(Ⅲ) and As(V) on variable charge soils

查看全文 作  者:XU [1]Renkou;WANG [1,3]Yong;TIWARI [2]Diwakar;WANG [1]Houyan 高影响力作者 机构地区:[1]State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanfing 210008, China;[2]Department of Chemistry, Mizoram University, Tanhril Campus, Aizawl 796009, India;[3]Graduate University of Chinese Academy of Sciences, Beifing 100049, China高影响力机构 出  处:《Journal of Environmental Sciences》索引2009年第21卷第7期,共6页高影响力期刊 基  金:supported by the Knowledge Innovation Program Foundation of the Chinese Academy of Sciences (No. KZCX2-YW-409);the National Natural Science Foundation of China (No. 20577054) 摘  要:The study was to investigate the adsorption behavior of arsenite (As(III)) and arsenate (As(V)) on two variable charge soils, i.e., Haplic Acrisol and Rhodic Ferralsol at dierent ionic strengths and pH with batch methods. Results indicated that the amount of As(III) adsorbed by these two soils increased with increasing solution pH, whereas it decreased with increasing ionic strength under the acidic condition. This suggested that As(III) was mainly adsorbed on soil positive charge sites through electrostatic attraction under the acidic condition. Moreover, intersects of As(V) adsorption-pH curves at dierent ionic strengths (a characteristic pH) are obtained for both soils. It was noted that above this pH, the adsorption of As(V) was increased with increasing ionic strength, whereas below it the reverse trend was true. Precisely the intersect pH was 3.6 for Haplic Acrisol and 4.5 for Rhodic Ferralsol, which was near the values of PZSE (soil point of zero salt eect) of these soils. The eects of ionic strength and pH on arsenate adsorption by these soils were interpreted by the adsorption model. The results of zeta potential suggested that the potential in adsorption plane becomes less negative with increasing ionic strength above soil PZSE and decreases with increasing ionic strength below soil PZSE. These results further supported the hypothesis of the adsorption model that the potential in the adsorption plane changes with ionic strength with an opposite trend to surface charge of the soils. Therefore, the change of the potential in the adsorption plane was mainly responsible for the change of arsenate adsorption induced by ionic strength on variable charge soils. 关 键 词:可变电荷土壤 离子强度 吸附
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