首页> 外文学位 >Surfactant-enhanced anaerobic degradation of 1,1,1-trichloro-2,2-bis-(p-chlorophenyl)-ethane (DDT).
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Surfactant-enhanced anaerobic degradation of 1,1,1-trichloro-2,2-bis-(p-chlorophenyl)-ethane (DDT).

机译:表面活性剂增强的1,1,1-三氯-2,2-双-(对氯苯基)-乙烷(DDT)厌氧降解。

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摘要

The pesticide DDT is a persistent contaminant in soils and sediments. Although it has long been known to be biodegradable under anaerobic conditions, little is known about the specific factors that cause it to be recalcitrant in anaerobic environmental systems or about the microorganisms responsible for its degradation.; The addition of the nonionic surfactant Brij 30 was evaluated as a means of enhancing solubilization, potential bioavailability and biodegradability of DDT and its metabolite DDD. Experiments were performed with both a DDT-contaminated soil and in soil-free liquid suspension. Detailed analyses of electron donors and potential electron acceptors were performed to provide insights into modes of microbial metabolism under these conditions.; In sealed anaerobic microcosms containing aged contaminated soil and liquid medium with surfactant, DDT was degraded at significantly greater rates and extents than in microcosms without surfactant. Concentrations of the dechlorination product DDD increased but did not accumulate stoichiometrically with DDT disappearance. The presence of added carbon source did not significantly increase the ultimate extent of DDT degradation. Decreases in surfactant concentration over time suggested use of surfactant as either a carbon source or as an electron donor in the dechlorination process. Subsequent experiments were conducted with surfactant in the absence of soil to characterize the mode of DDT degradation and the role of the surfactant.; In soil-free microcosms using butyrate or hydrogen as potential electron donors, surfactant was observed to significantly increase the extent of DDT degradation but with little accumulation of DDD. Significant release of chloride was observed (approximately 3 mumol chloride per mumol DDT degraded) in microcosms amended with butyrate. Microcosms with both hydrogen and butyrate added as electron donors exhibited the greatest extent of DDT degradation with virtually no accumulation of DDD, while microcosms with hydrogen alone exhibited substantially less degradative activity. Protein yields correlated with both sulfate reduction and DDT degradation in surfactant-amended microcosms, suggesting that DDT degradation may be mediated by anaerobic sulfate-reducing organisms. Headspace hydrogen threshold concentrations in several of these microcosms were consistent with those typically observed in cultures dominated by sulfate-reducing organisms.; In addition, Brij 30 surfactant has been implicated as an electron donor in these systems. The hydrophobic moiety of this surfactant appears to be degraded under sulfate-reducing conditions and the electrons donated appear to be used predominately for growth and dechlorination in cultures amended with butyrate only. These findings strongly suggest that surfactant can play a role in enhanced bioremediation, not only as a means to enhance bioavailability, but as an agent to promote microbial dechlorination.
机译:农药滴滴涕是土壤和沉积物中的持久性污染物。尽管人们早就知道它在厌氧条件下是可生物降解的,但对于导致其在厌氧环境系统中难降解的具体因素或引起其降解的微生物知之甚少。评价了添加非离子表面活性剂Brij 30的方法,以增强DDT及其代谢产物DDD的增溶性,潜在的生物利用度和生物降解性。实验是在DDT污染的土壤和无土壤液体悬浮液中进行的。对电子供体和潜在的电子受体进行了详细的分析,以洞察在这些条件下的微生物代谢模式。在含有老化的污染土壤和带有表面活性剂的液体介质的密封厌氧微生物世界中,DDT的降解速率和程度明显高于不含表面活性剂的微生物世界。脱氯产物DDD的浓度增加,但没有化学计量地随着DDT的消失而积累。添加碳源的存在并没有显着增加DDT降解的最终程度。表面活性剂浓度随时间降低建议在脱氯过程中将表面活性剂用作碳源或电子给体。随后的实验是在没有土壤的情况下用表面活性剂进行的,以表征DDT降解的方式和表面活性剂的作用。在使用丁酸酯或氢作为潜在电子供体的无土壤微观世界中,观察到表面活性剂显着增加了DDT的降解程度,但DDD很少积累。在用丁酸酯修正的微观世界中,观察到了氯化物的显着释放(每降解的每摩尔DDT大约3摩尔氯化物)。既有氢又有丁酸盐作为电子供体的缩微膜显示出最大程度的DDT降解,几乎没有DDD的积累,而仅含氢的缩微膜显示出明显的降解活性。在表面活性剂修饰的微观世界中,蛋白质产量与硫酸盐还原和DDT降解都相关,这表明DDT降解可能是由厌氧硫酸盐还原生物介导的。这些微观世界中的顶空氢阈值浓度与硫酸盐还原生物为主的培养物中通常观察到的浓度一致。另外,Brij 30表面活性剂已被暗示在这些系统中作为电子给体。该表面活性剂的疏水部分似乎在硫酸盐还原条件下被降解,并且所提供的电子似乎主要用于仅用丁酸酯修饰的培养物中的生长和脱氯。这些发现强烈表明,表面活性剂不仅可以作为提高生物利用度的手段,而且可以作为促进微生物脱氯的剂,在增强生物修复中发挥作用。

著录项

  • 作者

    Walters, Glenn W.;

  • 作者单位

    The University of North Carolina at Chapel Hill.;

  • 授予单位 The University of North Carolina at Chapel Hill.;
  • 学科 Biology Microbiology.; Environmental Sciences.; Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 145 p.
  • 总页数 145
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 微生物学;环境科学基础理论;环境污染及其防治;
  • 关键词

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