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在磁铁矿催化芬顿类反应中三氯乙烯降解过程中的稳定碳同位素分馏。

Stable carbon isotope fractionation during trichloroethene degradation in magnetite-catalyzed Fenton-like reaction.

机构信息

School of Environmental Studies, China University of Geosciences, Wuhan 430074, China.

出版信息

J Contam Hydrol. 2013 Feb;145:37-43. doi: 10.1016/j.jconhyd.2012.11.007. Epub 2012 Dec 20.

DOI:10.1016/j.jconhyd.2012.11.007
PMID:23286906
Abstract

Mineral-catalyzed Fenton-like oxidation of chlorinated ethylenes is an attractive technique for in situ soil and groundwater remediation. Stable carbon isotope enrichment factors associated with magnetite-catalyzed Fenton-like oxidation of trichloroethylene (TCE) have been determined, to study the possibility of applying stable carbon isotope analysis as a technique to assess the efficacy of remediation implemented by Fenton-like oxidation. The carbon enrichment factors (ε values) ranged from -2.7‰ to -3.6‰ with a mean value of -3.3±0.3‰, and only small differences were observed for different initial reactive conditions. The ε values were robust and reproducible, and were relatively insensitive to a number of environmental factors such as ratios of reactants and PCE co-contamination, which can reduce the uncertainty associated with application of isotope enrichment factors for quantification of in situ remediation by Fenton-like reaction. ε values for Fenton-like oxidation of TCE were intermediate in those previously reported for aerobic biological processes (ε=-1.1 to -20.7‰). Thus, field-derived ε values that are more negative than those for Fenton-like oxidation, may indicate the occurrence of aerobic biodegradation at contaminated sites undergoing in situ remediation with Fenton-like reaction. However, stable carbon isotope analysis is unable to determine whether there is the occurrence of biodegradation processes if field-derived ε values are less negative than those for Fenton-like oxidation.

摘要

矿物催化类芬顿氧化法是一种用于原位土壤和地下水修复的有吸引力的技术。已经确定了与磁铁矿催化类芬顿氧化三氯乙烯(TCE)相关的稳定碳同位素富集因子,以研究稳定碳同位素分析作为评估类芬顿氧化修复效果的技术的可能性。碳富集因子(ε 值)的范围为-2.7‰至-3.6‰,平均值为-3.3±0.3‰,不同初始反应条件下仅观察到微小差异。ε 值是稳健且可重复的,并且对许多环境因素相对不敏感,例如反应物的比例和 PCE 共污染,这可以降低应用同位素富集因子对通过类芬顿反应进行原位修复进行定量的不确定性。与先前报道的好氧生物过程(ε=-1.1 至-20.7‰)相比,TCE 的类芬顿氧化的ε 值处于中间位置。因此,如果现场衍生的 ε 值比类芬顿氧化的 ε 值更负,则可能表明在使用类芬顿反应进行原位修复的污染场地中发生了好氧生物降解。然而,如果现场衍生的 ε 值小于类芬顿氧化的 ε 值,则稳定碳同位素分析无法确定是否存在生物降解过程。

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