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Treatment of 14-dioxane and trichloroethene co-contamination by an activated binary persulfate-peroxide oxidation process

机译:活化的过硫酸盐-过氧化物二元氧化工艺处理14-二恶烷和三氯乙烯共污染

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摘要

The efficacy of a binary oxidant system, hydrogen peroxide (H2O2) and persulfate, was investigated for treatment of 1,4-dioxane (dioxane) and trichloroethene (TCE) co-contamination. Batch experiments were conducted to examine the catalytic efficiency of Fe2+ and NaOH based activation, oxidant decomposition rates, contaminant degradation effectiveness, and competitive degradation effects. For NaOH-activation, the oxidant decomposition rate was moderate and sustained during the entire test period of 96 hours. However, dioxane degradation was limited (~33%). Conversely, the oxidants were depleted within 24 hours for the Fe2+-activated system, and dioxane degradation was complete within 4 hours. The activation and radical generation processes were different between Fe2+ and NaOH activation. Both dioxane and TCE underwent complete degradation in the co-contaminant experiment. The results of this study indicate that the Fe2+-catalyzed binary hydrogen peroxide-persulfate oxidant system is effective for oxidation of the tested contaminants separately and as co-contaminants.
机译:研究了二元氧化剂系统过氧化氢(H2O2)和过硫酸盐对1,4-二恶烷(dioxane)和三氯乙烯(TCE)共污染的处理效果。进行了分批实验,研究了Fe 2 + 和NaOH的活化效率,氧化剂的分解速率,污染物的降解效率和竞争性降解效果。对于NaOH活化,氧化剂的分解速率适中,并且在整个96小时的测试过程中均保持不变。但是,二恶烷的降解受到限制(〜33%)。相反,对于Fe 2 + 活化体系,氧化剂在24小时内被耗尽,二恶烷的降解在4小时内完成。 Fe 2 + 和NaOH的活化和自由基生成过程不同。在共污染实验中,二恶烷和TCE都经历了完全降解。这项研究的结果表明,Fe 2 + 催化的二元过氧化氢-过硫酸盐氧化剂体系能够有效地分别氧化被测污染物并作为共污染物。

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