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实验室中模拟厌氧填埋条件下 VCCs 和 CFCs 的生物降解。

Biological degradation of VCCs and CFCs under simulated anaerobic landfill conditions in laboratory test digesters.

机构信息

Department of Waste Management, Technical University of Hamburg-Harburg, Helmholtzstrasse 27, D-68723, Schwetzingen, Germany.

出版信息

Environ Sci Pollut Res Int. 1997;4(4):209-16. doi: 10.1007/BF02986348.

Abstract

The biological degradation of volatile halogenated hydrocarbons (chlorocarbons (VCCs) and chlorofluorocarbons (CFCs)) was investigated under simulated conditions of landfills in laboratory test digesters. Fully halogenated VCCs (tetrachloroethylene, 1,1,1-trichloroethane, tetrachloromethane and dichloromethane) and CFCs (trichlorofluoromethane (R11), dichlorodifluoromethane (R12) and 1,1,2-trichlorotrifluoroethane (R113)) were degraded under anaerobic conditions in addition to the methanogenic bacteria in municipal solid waste (MSW) and organic wastes. These substances showed different degradation reactions in the simulated acid and methanephases of MSW landfills. It is assumed that R11 and R113 could be decomposed completely under methanogenic conditions. Dichlorofluoromethane (R21) was observed as the reductive degradation product of R11 and was further degraded during the methanephase, but hardly at all under acid conditions. Chlorodifluoromerhane (R22) as a degradation product of R12 was not degraded, even not in the methanephase. In the acidphase, R11 was the only CFC to be dechlorinated, although only in small quantities. The degradation products of tetrachloroethylene differed under the various environmental conditions. In the acidphase, 1,1-dichloroethylene was detected as the only dichloroethylene, whereas in particular cis-1,2-dichloroethylene but also trans-1,2-dichloroethylene, 1,1-dichloroethylene and vinyl chloride could be detected as metabolites in the methanephase. Dichloromethane and chloroethane, as metabolites of 1,1,1-trichloroethane, could hardly be degraded at all in the acidphase. The degradation of VCCs and CFCs is largely independent of the substrate used. The investigations have demonstrated that the measured biodegradation rates (0.3-15 mg/m(3) (material vol)./h) cannot be improved considerably since they are limited by the inhibiting effect of the substances and their degradation products.

摘要

在实验室试验消化器中模拟垃圾填埋场条件下,研究了挥发性卤代烃(氯代烃 (VCC) 和氯氟碳化合物 (CFC))的生物降解。在厌氧条件下,除了城市固体废物 (MSW) 和有机废物中的产甲烷菌外,还降解了全卤代 VCC(四氯乙烯、1,1,1-三氯乙烷、四氯化碳和二氯甲烷)和 CFC(三氯氟甲烷 (R11)、二氯二氟甲烷 (R12) 和 1,1,2-三氯三氟乙烷 (R113))。这些物质在 MSW 填埋场的模拟酸性和产甲烷相中表现出不同的降解反应。据推测,R11 和 R113 可以在产甲烷条件下完全分解。二氯二氟甲烷 (R21) 被观察为 R11 的还原降解产物,并在产甲烷相中进一步降解,但在酸性条件下几乎不降解。R12 的降解产物二氯氟甲烷 (R22) 甚至在产甲烷相中也未降解。在酸性相中,只有 R11 是唯一被脱氯的 CFC,尽管脱氯量很小。四氯乙烯的降解产物在各种环境条件下有所不同。在酸性相中,仅检测到 1,1-二氯乙烯作为唯一的二氯乙烯,而在产甲烷相中特别可以检测到顺式-1,2-二氯乙烯和反式-1,2-二氯乙烯、1,1-二氯乙烯和氯乙烯作为代谢产物。二氯甲烷和氯乙烷作为 1,1,1-三氯乙烷的代谢产物,在酸性相中几乎完全无法降解。VCC 和 CFC 的降解在很大程度上与所用的基质无关。研究表明,由于受物质及其降解产物的抑制作用限制,所测量的生物降解速率(0.3-15mg/m3(物质体积)/h)无法显著提高。

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