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Microbial Mineralization of Dichloroethene and Vinyl Chloride under Hypoxic Conditions

机译:低氧条件下二氯乙烯和氯乙烯的微生物矿化

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摘要

Mineralization of l4C-radiolabled vinyl chloride ([1,2-~(14)C] VC) and cw-dichloroethene ([1,2-~(14)C] cw-DCE) under hypoxic (initial dissolved oxygen (DO) concentrations about 0.1 mg/L) and nominally anoxic (DO minimum detection limit = 0.01 mg/L) was examined in chloroethene-exposed sediments from two groundwater and two surface water sites. The results show significant VC and dichloroethene (DCE) mineralization under hypoxic conditions. All the sample treatments exhibited pseudo-first-order kinetics for DCE and VC mineralization over an extended range of substrate concentrations. First-order rates for VC mineralization were approximately 1 to 2 orders of magnitude higher in hypoxic groundwater sediment treatments and at least three times higher in hypoxic surface water sediment treatments than in the respective anoxic treatments. For VC, oxygen-linked processes accounted for 65 to 85% of mineralization at DO concentrations below 0.1 mg/L, and ~(14)CO_2 was the only degradation product observed in VC treatments under hypoxic conditions. Because the lower detection limit for DO concentrations measured in the field is typically 0.1 to 0.5 mg/L, these results indicate that oxygen-linked VC and DCE biodegradation can be significant under field conditions that appear anoxic. Furthermore, because rates of VC mineralization exceeded rates of DCE mineralization under hypoxic conditions, DCE accumulation without concomitant accumulation of VC may not be evidence of a DCE degradative "stall" in chloroethene plumes. Significantly, mineralization of VC above the level that could reasonably be attributed to residual DO contamination was also observed in several nominally anoxic (DO minimum detection limit = 0.01 mg/L) microcosm treatments.
机译:缺氧(初始溶解氧(DO))下14C辐射的氯乙烯([1,2-〜(14)C] VC)和cw-二氯乙烯([1,2-〜(14)C] cw-DCE)的矿化在两个地下水和两个地表水站点暴露于氯乙烯的沉积物中检测了浓度约为0.1 mg / L)和名义上缺氧(DO最低检测限= 0.01 mg / L)。结果表明在低氧条件下有明显的VC和二氯乙烯(DCE)矿化。所有样品处理均在扩展的底物浓度范围内显示出DCE和VC矿化的拟一级动力学。缺氧地下水沉积物处理中VC矿化的一级速率比缺氧处理高约1至2个数量级,低氧地表水沉积物处理中至少高三倍。对于VC,在DO浓度低于0.1 mg / L时,与氧相关的过程占矿化程度的65%至85%,〜(14)CO_2是在低氧条件下VC处理中观察到的唯一降解产物。由于现场测得的溶解氧浓度的下限通常为0.1至0.5 mg / L,因此这些结果表明,在出现缺氧的现场条件下,与氧相关的VC和DCE的生物降解作用可能很大。此外,由于在缺氧条件下VC的矿化速率超过了DCE的矿化速率,因此没有伴随VC积累的DCE积累可能不是氯乙烯羽流中DCE降解“失速”的证据。值得注意的是,在几种名义上的缺氧(DO最低检出限= 0.01 mg / L)微观世界的处理中,也观察到VC的矿化程度超过合理地归因于残留DO污染的水平。

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  • 来源
    《Ground Water Monitoring & Remediation》 |2011年第4期|p.39-49|共11页
  • 作者单位

    U.S. Geological Survey, South Carolina Water Science Center, Columbia;

    U.S. Geological Survey, South Carolina Water Science Center,Columbia, SC 29210;

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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:34:04

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