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Coupling Bioflocculation of Dehalococcoides to High-Dechlorination Rates for Ex situ and In situ Bioremediation.

机译:脱卤球菌的生物絮凝与高脱氯率的异位和原位生物修复偶联。

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摘要

Bioremediation of trichloroethene (TCE) using Dehalococcoides mccartyi-containing microbial cultures is a recognized and successful remediation technology. Our work with an upflow anaerobic sludge blanket (UASB) reactor has shown that high-performance, fast-rate dechlorination of TCE can be achieved by promoting bioflocculation of Dehalococcoides mccartyi -containing cultures. The bioreactor achieved high maximum conversion rates of 1.63 +/- 0.012 mmol Cl- Lculture-1 h-1 at an HRT of 3.6 hours and >97% dechlorination of TCE to ethene while continuously fed 2 mM TCE. The UASB generated bioflocs from a microbially heterogeneous dechlorinating culture and produced Dehalococcoides mccartyi densities of 1.73x10-13 cells Lculture -1 indicating that bioflocculation of Dehalococcoides mccartyi -containing cultures can lead to high density inocula and high-performance, fast-rate bioaugmentation culture for in situ treatment. The successful operation of our pilot scale bioreactor led to the assessment of the technology as an onsite ex-situ treatment system. The bioreactor was then fed TCE-contaminated groundwater from the Motorola Inc. 52nd Street Plant Superfund site in Phoenix, AZ augmented with the lactate and methanol. The bioreactor maintained >99% dechlorination of TCE to ethene during continuous operation at an HRT of 3.2 hours. Microbial community analysis under both experimental conditions reveals shifts in the community structure although maintaining high rate dechlorination. High density dechlorinating cultures containing bioflocs can provide new ways to 1) produce dense bioaugmentation cultures, 2) perform ex-situ bioremediation of TCE, and 3) increase our understanding of Dehalococcoides mccartyi critical microbial interactions that can be exploited at contaminated sites in order to improve long-term bioremediation schemes.
机译:使用含有麦卡迪氏脱球菌的微生物培养物对三氯乙烯(TCE)进行生物修复是一种公认​​的成功修复技术。我们在上流式厌氧污泥床(UASB)反应器上的工作表明,通过促进含Dehalococcoides mccartyi的培养物的生物絮凝,可以实现TCE的高性能,快速脱氯。该生物反应器在3.6小时的HRT时实现了1.63 +/- 0.012 mmol的Cl-Lculture-1 h-1的高最大转化率,并且在连续进料2 mM TCE的情况下,TCE脱氯> 97%。 UASB从微生物异质脱氯培养物中产生了生物絮凝物,并产生了1.73x10-13细胞Lculture -1的Dehalococcoides mccartyi密度,表明含Dehalococcoides mccartyi的培养物的生物絮凝可以导致高密度接种和高性能,快速的生物强化培养原位治疗。我们的中试规模生物反应器的成功运行导致对该技术作为现场异位处理系统的评估。然后从亚利桑那州凤凰城的Motorola Inc. 52nd Street Plant Superfund站点向生物反应器供入受TCE污染的地下水,并补充了乳酸和甲醇。在HRT为3.2小时的连续运行过程中,生物反应器将TCE脱氯保持在99%以上。在两种实验条件下的微生物群落分析显示,尽管保持了高速率的脱氯,但群落结构发生了变化。包含生物絮凝剂的高密度脱氯培养物可提供以下新方法:1)产生致密的生物强化培养物; 2)对TCE进行异位生物修复; 3)增进我们对麦加氏脱球菌的关键微生物相互作用的理解,以便在受污染的场地利用微生物改善长期生物修复方案。

著录项

  • 作者

    Fajardo-Williams, Devyn.;

  • 作者单位

    Arizona State University.;

  • 授予单位 Arizona State University.;
  • 学科 Environmental engineering.;Civil engineering.;Microbiology.;Hydrologic sciences.
  • 学位 M.S.
  • 年度 2015
  • 页码 39 p.
  • 总页数 39
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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