Electrodialytic versus acid extraction of heavy metals from soil washing residue

被引:18
|
作者
Jensen, Pernille E. [1 ]
Ottosen, Lisbeth M. [1 ]
Allard, Bert [2 ]
机构
[1] Tech Univ Denmark, Dept Civil Engn, DK-2800 Lyngby, Denmark
[2] MTM Res Ctr, S-70182 Orebro, Sweden
关键词
Electrodialysis; Soil washing; Heavy metals; Remediation; Electrokinetics; CONTAMINATED SOIL; ELECTROKINETIC REMEDIATION; DESORPTION-KINETICS; CLAYEY SOILS; REMOVAL; CU; PB; CR; SPECIATION; CR(III);
D O I
10.1016/j.electacta.2012.07.002
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The feasibility of electrodialytic remediation (EDR) for treatment of suspended sludge after soil washing is in focus in the present paper. Five industrially contaminated soils were treated in laboratory scale remediation experiments, and the toxic elements of the investigation were: As, Cd, Cu, Cr, Ni, Zn and Pb. The results showed that all investigated elements could be removed from all soils to some extent by EDR. For all anthropogenic contaminants, higher extraction can be obtained under the influence of the direct current during EDR than by washing. During EDR most elements were transferred primarily to the cathode, where Cu and Pb precipitated at the cathode, while Cd, Cr, Ni and Zn primarily, or solely (for Ni), were dissolved in the catholyte, showing how cationic species dominated the chemistry of these elements. Despite the differences between the soils, the remediation results were explained well by the hydrolytic chemistry of the elements, with a difference between the soils. The only element transported primarily towards the anode, was arsenic suggesting that As(V) is the dominating species, and showing that As(III) is oxidized during the remediation process. In contrast the kinetic stability of Cr(III) hinders oxidation of this element, and leaves this as the least removable of the seven. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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