Fenton试剂用于水系统和土壤浆料中TCE的降解

Katherine R. Weeks, C. Bruell, N. Mohanty
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引用次数: 34

摘要

芬顿的反应由铁催化的过氧化氢(H2O2)组成,产生羟基自由基(·OH),一种强氧化剂。·OH可与H2O2和铁发生反应,并能破坏多种有机污染物。在本实验室研究中,以三氯乙烯(TCE)为目标污染物,在水和土浆体系中观察了Fenton反应,目的是最大化TCE降解,同时最小化H2O2降解。芬顿反应触发了一个复杂的反应矩阵,涉及到·OH、H2O2、铁、TCE和土壤有机物。在有机碳(fOC)含量高的土壤浆料中,铁倾向于吸附土壤有机物和/或颗粒。在水体系中,H2O2:Fe2+:TCE能够及时降解TCE、降低成本和降低H2O2降解的最佳配比为300mg /L: 25mg /L: 60mg /L(摩尔比为19:1:1),而fOC高达约1%且土水比为1:5(重量比)的土壤浆料需要大约10倍的H2O2,最佳配比为3000mg /L: 5mg /L: 60mg /L(摩尔比为190:0.2:1)。在fOC较高的土壤浆料中,由于土壤有机质的竞争,TCE的降解率下降,土壤有机质似乎充当了·OH的汇。在fOC较高的土壤浆料中,H2O2降解率趋于增加,这很可能是由于土壤有机物对·OH的需求增加、有效铁的增加和其他氧化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of Fenton's Reagent for the Degradation of TCE in Aqueous Systems and Soil Slurries
Fenton's reaction is comprised of hydrogen peroxide (H2O2) catalyzed by iron, producing the hydroxyl radical (·OH), a strong oxidant. ·OH in turn may react with H2O2 and iron and is capable of destroying a wide range of organic contaminants. In this laboratory study, Fenton's reaction was observed in aqueous and soil slurry systems using trichloroethylene (TCE) as the target contaminant, with the goal of maximizing TCE degradation while minimizing H2O2 degradation. Fenton's reaction triggers a complex matrix of reactions involving ·OH, H2O2, iron, TCE, and soil organics. In soil slurries with a high fraction of organic carbon (fOC), iron tends to sorb to soil organics and/or particles. In aqueous systems the optimal ratio of H2O2:Fe2+:TCE to degrade TCE in a timely fashion, minimize costs, and minimize H2O2 degradation is 300 mg/L: 25 mg/L: 60 mg/L (19:1:1 molar ratio), while soil slurries with a fOC up to approximately 1% and a soil:water ratio of 1:5 (weight ratio) require about ten times the amount of H2O2, the optimal ratio being 3000 mg/L: 5 mg/L: 60 mg/L (190:0.2:1 molar ratio). TCE degradation rates were observed to decrease in soil slurries with higher fOC because of competition by soil organic matter, which appears to act as a sink for ·OH. H2O2 degradation rates tended to increase in soil slurries with higher fOC, most likely due to increased demand for ·OH by soil organics, increased available iron and other oxidation processes.
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