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首页> 外文期刊>Journal of soil & sediments >Ferrous ions accelerate sulfide-induced abiotic dechlorination of DDT in waterlogged paddy soil and in soil solution
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Ferrous ions accelerate sulfide-induced abiotic dechlorination of DDT in waterlogged paddy soil and in soil solution

机译:亚铁离子加速淹水稻田和土壤溶液中滴滴涕的硫化物诱导的非生物脱氯

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摘要

Purpose Abiotic dechlorination of organochlorine pollutants seems to occur more efficiently in nature than previously thought. Ferrous (Fe~(2+)) and sulfide (S~(2-)) ions have been shown to be effective dechlorinating reagents. However, little is known about the interactions between Fe~(2+) and S~(2-) during dechlorination of l,l,l-trichoro-2,2-bis(p-chlorophenyl)-ethane (DDT) in soil, in spite of the fact that these ions co-exist in waterlogged soils. Materials and methods An anaerobic soil incubation experiment was run for 192 h to investigate S~(2-) (1.0, 10 mM)-induced abiotic dechlorination of p,p'-DDT in waterlogged soil (soil/water= 1/20). In addition, the influence of Fe~(2+) (3.0 mM) on S~(2-) (0.5, 5.0 mM)-induced abiotic dechlorination of p,p'-DDT (2 μg m l~(-1)) was evaluated in soil solution and in distilled deionized water to identify the dechlorination mechanism under anaerobic incubation conditions for 6 h due to the complexity of soil, based on the determination of residual p,p -DDT in media by gas chromatograph (GC)-ECD and the identification of metabolites of p,p'-DDT by GC-MSD. Results and discussion S~(2-)-induced dechlorination of p,p'-DDT exhibited rapid and slow phases in three media (waterlogged soil, soil solution, and distilled deionized water). The addition of Fe~(2+) significantly accelerated S~(2-) induced dechlorination, reduced the remaining concentrations of p.p'-DDT at the turning point and the end point for the dechlorination reaction, and shortened the time to reach equilibrium in two aqueous media. In all, 93% and 48% of p,p'-DDTwas dechlorinated in soils supplied with 1.0 and 10 mM S~(2-) respectively. The underlying mechanism can be attributed to the coupling effect of Fe~(2+) and S~(2-) on dechlorination of DDT since the rates of dechlorination of p,p'-DDT treated by 0.5 and 5.0 mM S~(2-) over 6 h were significantly greater with Fe~(2+) addition than without Fe~(2+) addition in aqueous phase media. The metabolites of p,p'-DDT found in the three media were identified as p,p'-DDD, p,p'-DDE, and p,p'-DDMU, with or without the addition of Fe~(2+). Conclusions Combined Fe~(2+)/S~(2~)-induced dechlorination of DDT could be important for in situ remediation of DDT-contaminated soil/sediment given that Fe~(2+) and S~(2-)often co-exist in anaerobic conditions.
机译:目的在自然界中,有机氯污染物的非生物脱氯似乎比以前认为的更有效。已证明亚铁离子(Fe〜(2+))和硫化物(S〜(2-))是有效的脱氯剂。然而,关于土壤中的1,l,l-三甲基-2,2-双(对氯苯基)乙烷(DDT)脱氯过程中Fe〜(2+)与S〜(2-)之间的相互作用的了解甚少。尽管这些离子在浸水的土壤中共存。材料和方法厌氧土壤培养实验进行了192小时,以研究S〜(2-)(1.0,10 mM)对淹水土壤中p,p'-DDT的非生物脱氯作用(土壤/水= 1/20) 。此外,Fe〜(2+)(3.0 mM)对S〜(2-)(0.5,5.0 mM)诱导的p,p'-DDT(2μgml〜(-1))非生物脱氯的影响在土壤溶液和蒸馏去离子水中进行了评估,以鉴定由于土壤的复杂性而在厌氧培养条件下持续6 h的脱氯机理,方法是通过气相色谱(EC)-ECD测定介质中的残留p,p -DDT并通过GC-MSD鉴定p,p'-DDT的代谢产物。结果与讨论S〜(2-)诱导的p,p'-DDT脱氯在三种介质(涝渍土壤,土壤溶液和蒸馏去离子水)中显示出快速相和慢相。 Fe〜(2+)的添加显着促进了S〜(2-)诱导的脱氯,降低了脱氯反应的转折点和终点的p.p'-DDT残留浓度,并缩短了到达反应的时间。在两种水性介质中达到平衡。在提供1.0和10 mM S〜(2-)的土壤中,总共有93%和48%的p,p'-DDT被脱氯。潜在的机理可以归因于Fe〜(2+)和S〜(2-)对DDT脱氯的耦合作用,因为p,p'-DDT的脱氯速率分别为0.5和5.0 mM S〜(2 -)在水相介质中添加Fe〜(2+)超过6 h明显大于未添加Fe〜(2+)。在三种介质中发现的p,p'-DDT的代谢物被鉴定为p,p'-DDD,p,p'-DDE和p,p'-DDMU,添加或不添加Fe〜(2+ )。结论Fe〜(2 +)/ S〜(2〜)联合滴滴涕脱氯对DDT污染土壤/沉积物的原位修复很重要,因为Fe〜(2+)和S〜(2-)经常存在。在厌氧条件下共存。

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  • 来源
    《Journal of soil & sediments》 |2011年第7期|p.1209-1220|共12页
  • 作者单位

    College of Resources and Environment,Graduate University of Chinese Academy of Sciences,Beijing 100049, People's Republic of China;

    rnCollege of Resources and Environment,Graduate University of Chinese Academy of Sciences,Beijing 100049, People's Republic of China;

    rnCollege of Resources and Environment,Graduate University of Chinese Academy of Sciences,Beijing 100049, People's Republic of China;

    rnResearch Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing 100085, People's Republic of China;

    rnCollege of Resources and Environment,Graduate University of Chinese Academy of Sciences,Beijing 100049, People's Republic of China;

    rnInstitute of environmental resources and soil fertilizer,Zhejiang academy of agricultural Sciences,Hangzhou 310021, People's Republic of China;

    rnResearch Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing 100085, People's Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    abiotic dechlorination; ferrous iron; organochlorine; sulfide;

    机译:非生物脱氯;亚铁有机氯硫化物;

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