Electrokinetic remediation of metals and organics from historically contaminated soil

被引:4
|
作者
Maini, G
Sharman, AK
Knowles, CJ
Sunderland, G
Jackman, SA
机构
[1] NERC, Ctr Ecol & Hydrol, Oxford OX1 3SR, England
[2] EA Technol Ltd, Chester CH1 6ES, Cheshire, England
[3] Univ Oxford, Oxford Ctr Environm Biotechnol, Dept Engn Sci, Oxford OX1 3PJ, England
[4] Viridian EHC Ltd, Whitstable CT5 3QT, Kent, England
关键词
electrokinetics; remediation; metals; PAHs; BTEX compounds;
D O I
10.1002/1097-4660(200008)75:8<657::AID-JCTB263>3.0.CO;2-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The electrokinetic remediation of an historically contaminated soil is described. The soil was contaminated with a range of metals including lead, zinc, manganese, copper and arsenic, polycyclic aromatic hydrocarbons (PAHs) and benzene, toluene, ethylbenzene and xylene (BTEX). A small-scale experiment (973.2g dry weight soil), utilising a planar electrode configuration, investigated the potential for moving metals and organics. After 23 days treatment at a current density of 3.72A /m(-2), 44% of calcium and 29% of manganese were removed from the soil at the cathode. Of the other contaminating metals, zinc and lead moved towards the cathode, but with no significant removal from the soil. Movement of PAHs was also observed, with a 94% reduction in concentration in the third of the soil closest to the anode after 23 days. A larger scale experiment (46.7kg dry weight soil) utilised a hexagonal array of tubular anodes surrounding a central tubular cathode. Treatment for 112 days led to acidification of the soil to pH 2.59 closest to the anode in a direct line between the anode and cathode. Soil not directly in line between the electrodes was not acidified significantly. Movement of metal ions was observed, in line with the electrodes, with concentrations of lead and arsenic increasing to 162% and 171% of starting concentrations closest to the anode, respectively, and those of zinc, copper and manganese decreasing to 42%, 68% and 57%, respectively. At positions not directly in line with the electrodes, no significant metal movements were observed. Overall, there was no significant removal of contaminating metals from the soil. PAHs and BTEX compounds were moved by electroosmosis towards the cathode, with soil concentrations of PAHs reduced from 720 mgkg(-1) to 4.7 mgkg(-1) after 22 days. PAHS (28mg) and benzene (9660mg) were recovered in granular activated carbon (GAC) columns. (C) 2000 Society of Chemical Industry.
引用
收藏
页码:657 / 664
页数:8
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