首页> 外文期刊>Environmental toxicology and chemistry >DEHYDROCHLORINATION OF 1,1,1-TRICHLOROETHANE AND PENTACHLOROETHANE BY MICROBIALLY REDUCED FERRUGINOUS SMECTITE
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DEHYDROCHLORINATION OF 1,1,1-TRICHLOROETHANE AND PENTACHLOROETHANE BY MICROBIALLY REDUCED FERRUGINOUS SMECTITE

机译:微生物还原铁矾土对1,1,1-三氟乙烷和五氯乙烷的加氢脱氯

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Reduction of structural Fe(Ⅲ) in smectite clay minerals has been identified as a means to promote dechlorination of polychlorinated ethanes, but its environmental significance has yet to be fully assessed because Fe reduction has normally been achieved by agents uncommon in the environment (e.g., dithionite). This study reports the dehydrochlorination of pentachloroethane and 1,1,1 -Irichloroethane in the presence of ferruginous smectite reduced by two cultures of microorganisms, Shewanella oneidensis strain MR-1 (MR-R) and an enrichment culture from rice paddy soils (PS-R), in aqueous suspension under anoxic conditions. Microbially reduced ferruginous smectite facilitated dehydrochlorination of 1,1,1-trichloroethane to 1,1-dichloroethene with up to 60% conversion within 3 h of incubation time. In contrast, no formation of 1,1-dichloroethene was observed after incubation of 1,1,1-trichloroethane with chemically reduced ferruginous smectite for 24 h. Microbially reduced ferruginous smectite by MR-R and PS-R promoted the dehydrochlorination of pentachloroethane to tetrachloroethene by 80 and 15%, respectively, after 3 h of incubation time. The conversion of pentachloroethane to tetrachloroethene in the presence of chemically reduced ferruginous smectite after 24 h was 65%. These results indicate that structural Fe(Ⅱ) in clay minerals has the potential to be an important reductant controlling the fate of organic chemicals in contaminated sediments.
机译:绿土粘土矿物中结构性Fe(Ⅲ)的还原已被认为是促进多氯乙烷脱氯的一种方法,但其环境意义尚未得到充分评估,因为铁的还原通常是在环境中不常见的试剂实现的(例如,连二亚硫酸盐)。这项研究报告说,在两种微生物培养物米氏希瓦氏菌(Shewanella oneidensis)菌株MR-1(MR-R)和稻田土壤(PS-PS)的富集培养减少的铁质蒙脱石存在下,五氯乙烷和1,1,1-异氯乙烷的脱氯化氢作用。 R),在缺氧条件下的水悬浮液中。微生物还原的铁质蒙脱石可在孵育3小时内促进1,1,1-三氯乙烷脱氯化氢为1,1-二氯乙烯,转化率高达60%。相反,将1,1,1-三氯乙烷与化学还原的铁质蒙脱石一起孵育24小时后,未观察到1,1-二氯乙烯的形成。孵育3小时后,通过MR-R和PS-R微生物还原铁质蒙脱石分别促进了五氯乙烷脱氯化氢为四氯乙烯的80%和15%。在化学还原的铁质蒙脱石存在下,经过24小时后,五氯乙烷向四氯乙烯的转化率为65%。这些结果表明,粘土矿物中的结构性Fe(Ⅱ)有可能成为控制受污染沉积物中有机化学物质命运的重要还原剂。

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