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厌氧条件下土壤中六氯环己烷(HCH)异构体的还原脱氯作用。

Reductive dechlorination of hexachlorocyclohexane (HCH) isomers in soil under anaerobic conditions.

作者信息

Middeldorp Peter J M, van Doesburg Wim, Schraa Gosse, Stams Alfons J M

机构信息

TNO Environment, Energy and Process innovation, PO Box 342, 7300 AH Apeldoorn, The Netherlands.

出版信息

Biodegradation. 2005 Jun;16(3):283-90. doi: 10.1007/s10532-004-1573-8.

Abstract

The biological anaerobic reductive dechlorination of beta-hexachlorocyclohexane under methanogenic conditions was tested in a number of contaminated soil samples from two locations in the Netherlands. Soils from a heavily polluted location showed rapid dechlorination of beta-hexachlorocyclohexane to benzene and chlorobenzene with lactate as electron donor. Soils from an adjacent slightly polluted location did not show substantial dechlorination of beta-hexachlorocyclohexane within 4 months. A heavily polluted sample was selected to optimise the dechlorination. All tested hexachlorocyclohexane isomers (alpha-, beta-, gamma-, and delta-), either added separately or simultaneously, were dechlorinated in this soil sample. The most rapid dechlorination was observed at a temperature of 30 degrees C. Dechlorination of beta-hexachlorocyclohexane was observed with acetate, propionate, lactate, methanol, H2, yeast extract and landfill leachate as electron donors. In a soil percolation column, packed with a selected heavily polluted soil sample, the presence of 10 mM sulphate in the influent led to simultaneous dechlorination of beta-hexachlorocyclohexane and sulphate reduction. When the column was fed with 10 mM nitrate instead of sulphate, dechlorination ceased immediately. After omitting nitrate from the influent, dechlorination activity recovered in about 1 month. Also in a separate column, the addition of nitrate from the start of the experiment did not result in dechlorination of beta-HCH. The significance of these experiments for in situ bioremediation of polluted soils is discussed.

摘要

在荷兰两个地点采集的多个受污染土壤样本中,测试了在产甲烷条件下β-六氯环己烷的生物厌氧还原脱氯情况。来自污染严重地点的土壤以乳酸作为电子供体时,β-六氯环己烷能快速脱氯生成苯和氯苯。来自相邻轻度污染地点的土壤在4个月内未表现出β-六氯环己烷的大量脱氯。选择了一个污染严重的样本以优化脱氯过程。在该土壤样本中,所有测试的六氯环己烷异构体(α-、β-、γ-和δ-),无论是单独添加还是同时添加,均发生了脱氯。在30摄氏度时观察到脱氯速度最快。以乙酸盐、丙酸盐、乳酸、甲醇、氢气、酵母提取物和垃圾渗滤液作为电子供体时,均观察到了β-六氯环己烷的脱氯现象。在一个填充有选定的重度污染土壤样本的土壤渗滤柱中,进水含有10 mM硫酸盐时,导致β-六氯环己烷同时脱氯和硫酸盐还原。当向该柱中加入10 mM硝酸盐而非硫酸盐时,脱氯立即停止。从进水去除硝酸盐后,脱氯活性在约1个月内恢复。同样在一个单独的柱中,从实验开始就添加硝酸盐并未导致β-六氯环己烷脱氯。讨论了这些实验对污染土壤原位生物修复的意义。

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