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Carbon isotope fractionation during dechlorination of 1,2,3,4-tetrachlorodibenzo-p-dioxin by a Dehalococcoides-containing culture

机译:含Dehaloccocoides的培养物对1,2,3,4-四氯二苯并-对-二恶英进行脱氯过程中的碳同位素分馏

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摘要

Carbon isotope fractionation was observed during dechlorination of 1,2,3.4-tetrachlorodibenzo-p-dioxin (1,2,3,4-TeCDD) by a mixed culture containing Dehalococcoides ethenogenes strain 195. Fractionation was examined when 1,2,3,4-TeCDD was added as the only chlorinated compound and when 1,2,3,4-TeCDD was added with a known growth substrate, tetrachloroethene (PCE). The 1,2,3,4-TeCDD was dechlorinat-ed to 1,2,4-trichlorodibenzo-p-dioxin (1,2,4-TrCDD) which was enriched in ~(13)C relative to 1,2,3,4-TeCDD with isotope separation factors, ε_c. of 1.3±0.2‰ and 1.7±0.4‰ (average ±95% confidence interval (CI)) in cultures with and without PCE, respectively. The 1,2,4-TrCDD was further dechlorinated to 1,3-dichlorodibenzo-p-dioxin (1,3-DCDD) which was depleted in ~(13)C relative to 1,2,4-TrCDD with ε_c of -2.4 ± 0.4‰ and -2.9 ± 0.8‰ (average ± 95% CI) in cultures with and without PCE, respectively. This demonstrates carbon isotope fractionation during sequential reductive dechlorination of PCDDs, where isotope fractionation during dechlorination of the intermediate was substantial and a ~(13)C depleted lightly chlorinated PCDD congener was ultimately formed during dechlorination of more highly chlorinated PCDD congeners. Despite reproducible, statistically significant differences between isotope compositions of the parent, 1,2,3,4-TeCDD and daughter, 1,2,4-TrCDD and 1,3-DCDD congeners in triplicate bottles of both treatments, fractionation factors for 1,2,3,4-TeCDD could not be determined for all replicates by regression analysis of the plot of the Rayleigh equation. It is possible that dissolution of 1,2,3,4-TeCDD imposed a kinetic limitation on dechlorination, thus masking isotope fractionation during its dechlorination.
机译:通过含有脱卤代球菌埃德森菌菌株195的混合培养物在1,2,3.4-四氯二苯并-对-二恶英(1,2,3,4-TeCDD)脱氯过程中观察到碳同位素分级分离。在1,2,3,添加4-TeCDD作为唯一的氯化化合物,当添加1,2,3,4-TeCDD和已知的生长底物四氯乙烯(PCE)时。将1,2,3,4-TeCDD脱氯为1,2,4-三氯二苯并-对-二恶英(1,2,4-TrCDD),相对于1,2,N〜(13)C富集,具有同位素分离因子ε_c的3,4-TeCDD。在有和没有PCE的培养物中,其分别为1.3±0.2‰和1.7±0.4‰(平均±95%置信区间(CI))。将1,2,4-TrCDD进一步脱氯为1,3-二氯二苯并-对-二恶英(1,3-DCDD),相对于1,2,4-TrCDD在ε_c为-的情况下,在〜(13)C中将其耗尽。在有和没有PCE的培养物中,分别为2.4±0.4‰和-2.9±0.8‰(平均±95%CI)。这证明了PCDDs的顺序还原脱氯过程中的碳同位素分馏,其中中间体脱氯过程中的同位素分馏是重要的,并且在高度氯化的PCDD同类物的脱氯过程中最终形成了〜(13)C耗尽的轻度氯化的PCDD同类物。尽管母体1,2,3,4-TeCDD和子代1,2,4-TrCDD和1,3-DCDD同系物的同位素组成在两种处理的三次重复瓶中的可重现,统计学上显着差异,但分馏因子为1通过瑞利方程图的回归分析无法确定所有重复的,2,3,4-TeCDD。 1,2,3,4-TeCDD的溶解可能会对脱氯反应造成动力学限制,从而掩盖了其脱氯过程中的同位素分级分离。

著录项

  • 来源
    《Chemosphere》 |2010年第10期|p.1113-1119|共7页
  • 作者单位

    Department of Environmental Sciences, Rutgers University, New Brunswick, NJ 08901, USA;

    rnDepartment of Isotope Biogeochemistry, UFZ-Helmholtz Centre for Environmental Research, Leipzig-Halle, Leipzig D-04318, Germany,European Commission, DC RTD unit E.2 - Biotechnologies,Square de Meeus 8 (SDME 08/046) B-1049 Brussels, Belgium;

    rnDepartment of Isotope Biogeochemistry, UFZ-Helmholtz Centre for Environmental Research, Leipzig-Halle, Leipzig D-04318, Germany;

    rnDepartment of Isotope Biogeochemistry, UFZ-Helmholtz Centre for Environmental Research, Leipzig-Halle, Leipzig D-04318, Germany;

    rnDepartment of Environmental Sciences, Rutgers University, New Brunswick, NJ 08901, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    dechlorination; dioxin; dehalococcoides; compound specific isotope analysis;

    机译:脱氯二恶英脱卤球菌;化合物特异性同位素分析;

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