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土壤对氯乙烯的非生物还原脱氯作用。

Abiotic reductive dechlorination of chlorinated ethylenes by soil.

作者信息

Lee Woojin, Batchelor Bill

机构信息

Environment and Process Technology Division, Korea Institute of Science and Technology, P.O. Box 131, Cheongryang, Seoul 130-650, South Korea.

出版信息

Chemosphere. 2004 May;55(5):705-13. doi: 10.1016/j.chemosphere.2003.11.033.

Abstract

Abiotic reductive dechlorination of chlorinated ethylenes by soil in anaerobic environments was characterized to improve knowledge of the behavior of chlorinated ethylenes in natural systems, including systems modified to promote attenuation of contaminants. Target organics in the soil suspension reached sorption equilibrium in 2 days and the sorption isotherm of target organics was properly described by the linear sorption model. A modified Langmuir-Hinshelwood model was developed to describe the kinetics of reductive dechlorination of target organics by soil. The rate constants for the reductive dechlorination of chlorinated ethylenes at the reactive surfaces of reduced soils were found in the range between 0.055 (+/- 8.9%) and 2.60 (+/- 3.2%) day(-1). The main transformation products in reduced soil suspensions were C2 hydrocarbons. No chlorinated intermediates were observed at concentrations above detection limits. Five cycles of reduction of the soil followed by oxidation of the soil with trichloroethylene (TCE) did not affect the removal of TCE. The removal was affected by the reductants used and increased in the order: Fe(II) < dithionite < Fe(II) + dithionite.

摘要

对厌氧环境中土壤对氯乙烯的非生物还原脱氯作用进行了表征,以增进对氯乙烯在自然系统(包括为促进污染物衰减而改良的系统)中行为的了解。土壤悬浮液中的目标有机物在2天内达到吸附平衡,目标有机物的吸附等温线可用线性吸附模型恰当描述。开发了一种修正的朗缪尔 - 欣谢尔伍德模型来描述土壤对目标有机物的还原脱氯动力学。在还原土壤的反应表面上,氯乙烯还原脱氯的速率常数在0.055(±8.9%)至2.60(±3.2%)天⁻¹范围内。还原土壤悬浮液中的主要转化产物是C₂烃。未观察到浓度高于检测限的氯代中间体。用三氯乙烯(TCE)对土壤进行五次还原 - 氧化循环,并未影响TCE的去除。去除效果受所用还原剂的影响,其顺序为:Fe(II) <连二亚硫酸盐<Fe(II) + 连二亚硫酸盐。

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