首页> 外文OA文献 >Reductive dechlorination of chlorinated aliphatic hydrocarbons by Fe(ii) in degradative solidification/stabilization
【2h】

Reductive dechlorination of chlorinated aliphatic hydrocarbons by Fe(ii) in degradative solidification/stabilization

机译:Fe(ii)在降解性固化/稳定化反应中对氯化脂肪族烃的还原脱氯作用

摘要

This dissertation examines the applicability of the iron-based degradative solidification/stabilization (DS/S-Fe(II)) to various chlorinated aliphatic hydrocarbons (CAHs) that are common chemicals of concern at contaminated sites. The research focuses on the transformation of 1,1,1-trichloroethane (1,1,1-TCA), 1,1,2,2-tetrachloro-ethane (1,1,2,2-TetCA) and 1,2-dichloroehtane (1,2-DCA) by Fe(II) in cement slurries. It also investigates the degradation of 1,1,1-TCA by a mixture of Fe(II), cement and three iron-bearing phyllosilicates. Transformation of 1,1,1-TCA and 1,1,2,2-TetCA by Fe(II) in 10% cement slurries was characterized using batch reactors. Dechlorination kinetics of 1,1,1-TCA and TCE* (TCE that was produced by transformation of 1,1,2,2-TetCA) was strongly dependent on Fe(II) dose, pH and initial target organic concentration. Degradation of target organics in DS/S-Fe(II) process was generally described by a pseudo-first-order rate law. However, saturation relationships between the rate constants and Fe(II) dose or between the initial degradation rates and target organic concentration were observed. These behaviors were properly described by a modified Langmuir-Hinshelwood kinetic model. This supports the working hypothesis of this research that reductive dechlorination of chlorinated ethanes occurs on the surface of active solids formed in mixtures of Fe(II) and cement. Transformation products for 1,1,1-TCA and 1,1,2,2-TetCA in mixtures of Fe(II) and cement were identified. The major product of the degradation of 1,1,1-TCA was 1,1-DCA, which indicates that the reaction followed a hydrogenolysis pathway. However, a small amount of ethane was also observed. TCE* was rapidly produced by degradation of 1,1,2,2-TetCA and is expected to undergo ????-elimination to produce acetylene. Dechlorination of 1,1,1-TCA in suspension of Fe(II), cement and three soil minerals (biotite, vermiculite, montmorillonite) was characterized using batch reactors. A first-order rate model was generally used to describe the dechlorination kinetics of 1,1,1-TCA in this heterogeneous system. The rate constants for 1,1,1-TCA in mixtures of Fe(II), cement and soil minerals were influenced by soil mineral types, Fe(II) dose and the mass ratio of cement to soil mineral. It was demonstrated that structural Fe(II) and surface-bound Fe(II) in the soil minerals affect dechlorination kinetics and the effects vary with mineral types. Furthermore, it suggests that the reductant formed from Fe(II) and cement hydration components is also effective in systems that include soil minerals.
机译:本文研究了铁基降解固化/稳定化(DS / S-Fe(II))在各种受污染场所常见的化学氯化物脂族烃(CAHs)中的适用性。研究重点在于1,1,1-三氯乙烷(1,1,1-TCA),1,1,2,2-四氯乙烷(1,1,2,2-TetCA)和1,2的转化水泥浆中的Fe(II)生成的-dichloroehtane(1,2-DCA)。它还研究了Fe(II),水泥和三种含铁页硅酸盐的混合物对1,1,1-TCA的降解作用。使用分批反应器表征了Fe(II)在10%水泥浆中对1,1,1-TCA和1,1,2,2-TetCA的转化。 1,1,1-TCA和TCE *(通过1,1,2,2-TetCA转化产生的TCE)的脱氯动力学在很大程度上取决于Fe(II)剂量,pH和初始目标有机浓度。 DS / S-Fe(II)过程中目标有机物的降解通常由拟一级速率定律描述。但是,观察到速率常数与Fe(II)剂量之间或初始降解速率与目标有机物浓度之间的饱和关系。通过修改的Langmuir-Hinshelwood动力学模型正确描述了这些行为。这支持了这项研究的工作假设,即在由Fe(II)和水泥的混合物形成的活性固体表面上发生氯化乙烷的还原脱氯反应。确定了Fe(II)和水泥混合物中1,1,1-TCA和1,1,2,2-TetCA的转化产物。 1,1,1-TCA降解的主要产物是1,1-DCA,这表明该反应遵循氢解途径。但是,也观察到少量的乙烷。通过1,1,2,2-TetCA的降解迅速产生了TCE *,并预期经过α-消除以产生乙炔。使用间歇反应器表征了Fe(II),水泥和三种土壤矿物质(黑云母,ver石,蒙脱石)悬浮液中1,1,1-TCA的脱氯作用。一阶速率模型通常用于描述该异构系统中1,1,1-TCA的脱氯动力学。 Fe(II),水泥和土壤矿物混合物中1,1,1-TCA的速率常数受土壤矿物类型,Fe(II)剂量和水泥与土壤矿物的质量比的影响。结果表明,土壤矿物中的结构Fe(II)和表面结合的Fe(II)影响脱氯动力学,并且其影响随矿物类型而变化。此外,这表明由Fe(II)和水泥水合组分形成的还原剂在包括土壤矿物质的系统中也有效。

著录项

  • 作者

    Jung Bahng Mi;

  • 作者单位
  • 年度 2007
  • 总页数
  • 原文格式 PDF
  • 正文语种 en_US
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号