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

机译:厌氧条件下土壤中六氯环己烷(HCH)异构体的还原脱氯。

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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.
机译:在来自荷兰两个地点的许多受污染的土壤样品中,测试了产甲烷条件下β-六氯环己烷的生物厌氧还原性脱氯。来自严重污染地区的土壤显示出β-六氯环己烷迅速脱氯为苯和氯苯,而乳酸为电子给体。来自相邻的轻微污染地点的土壤在4个月内未显示出β-六氯环己烷的大量脱氯。选择污染严重的样品以优化脱氯。分别或同时添加的所有测试六氯环己烷异构体(α-,β-,γ-和δ-)均在该土壤样品中脱氯。在30摄氏度的温度下观察到最快的脱氯反应。用乙酸盐,丙酸酯,乳酸盐,甲醇,H2,酵母提取物和垃圾渗滤液作为电子给体观察到β-六氯环己烷的脱氯。在装有选定重度污染土壤样品的土壤渗滤柱中,进水口中存在10 mM硫酸盐导致β-六氯环己烷同时脱氯并减少硫酸盐含量。当向色谱柱中加入10 mM硝酸盐而不是硫酸盐时,脱氯立即停止。除去进水中的硝酸盐后,脱氯活性在约1个月内恢复。同样在单独的色谱柱中,从实验开始就添加硝酸盐并未导致β-六氯环己烷的脱氯。讨论了这些实验对污染土壤的原位生物修复的意义。

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