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Modelling of C/Cl isotopic behaviour during chloroethene biotic reductive dechlorination: Capabilities and limitations of simplified and comprehensive models

机译:氯乙烯生物还原性脱氯过程中C / Cl同位素行为的建模:简化和全面模型的能力和局限性

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摘要

Predicting the fate of chloroethenes in groundwater is essential when evaluating remediation strategies. Such predictions are expected to be more accurate when incorporating isotopic parameters. Although secondary chlorine isotope effects have been observed during reductive dechlorination of chloroethenes, development of modelling frameworks and simulation has thus far been limited. We have developed a novel mathematical framework to simulate the C/Cl isotopic fractionation during reductive dechlorination of chloroethenes. This framework differs from the existing state of the art by incorporating secondary isotopic effects and considering both C and Cl isotopes simultaneously. A comprehensive general model (GM), which is expected to be the closest representation of reality thus far investigated, was implemented. A less computationally intensive simplified model (SM), with the potential for use in modelling of complex reactive transport scenarios, was subsequently validated based on its comparison to GM. The approach of GM considers all isotopocules (i.e. molecules differing in number and position of heavy and light isotopes) of each chloroethene as individual species, of which each is degraded at a different rate. Both models GM and SM simulated plausible C/Cl isotopic compositions of tetrachloroethene (PCE), trichloroethene (TCE) and cis-1,2-dichloroethene (cDCE) during sequential dechlorination when using experimentally relevant kinetic and isotopic parameters. The only major difference occurred in the case where different secondary isotopic effects occur at the different non-reacting positions when PCE is dechlorinated down to cDCE. This observed discrepancy stems from the unequal Cl isotope distribution in TCE that arises due to the occurrence of differential secondary Cl isotopic effects during transformation of PCE to TCE. Additionally, these models are shown to accurately reproduce experimental data obtained during reductive dechlorination by bacterial enrichments harbouring Sulfurospirillum spp. where secondary isotope effects are known to have occurred. These findings underscore a promising future for the development of reactive transport models that incorporate isotopic parameters.
机译:在评估补救策略时,预测地下水中氯乙烯的命运至关重要。当结合同位素参数时,预计此类预测会更加准确。尽管在氯乙烯的还原性脱氯过程中观察到了次级氯同位素的作用,但迄今为止,建模框架和模拟的开发受到了限制。我们已经开发了一种新颖的数学框架,可以模拟氯乙烯的还原脱氯过程中的C / Cl同位素分馏。该框架与现有技术不同,它包含了次级同位素效应并同时考虑了C和Cl同位素。已实施了一个综合通用模型(GM),该模型有望成为迄今为止研究的最接近的现实表示形式。随后,根据与通用模型的比较,验证了一种计算量较小的简化模型(SM),该模型具有用于复杂反应运输情景建模的潜力。 GM的方法将每种氯乙烯的所有同位素(即重和轻同位素的数量和位置不同的分子)都视为单独的物种,它们各自以不同的速率降解。当使用实验相关的动力学和同位素参数时,模型GM和SM都模拟了在连续脱氯过程中四氯乙烯(PCE),三氯乙烯(TCE)和顺式1,2-二氯乙烯(cDCE)的可能的C / Cl同位素组成。唯一的主要区别是在PCE脱氯至cDCE时,在不同的非反应位置发生了不同的次级同位素效应。这种观察到的差异源于TCE中Cl同位素分布不均,这是由于PCE向TCE转化过程中次生Cl同位素效应的发生而引起的。此外,显示这些模型可以准确地复制在还原脱氯过程中通过含有硫螺旋藻菌种的细菌富集获得的实验数据。已知发生二次同位素效应的地方。这些发现强调了开发结合同位素参数的反应性传输模型的有希望的未来。

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