Hydrology and Atmospheric Sciences Department, School of Earth and Environmental Sciences, University of Arizona, 429 Shantz Building, Tucson, AZ, 85721, USA.
Beijing Key Laboratory of Water Resources and Environmental Engineering, China University of Geosciences, Beijing, 100083, People's Republic of China.
Environ Sci Pollut Res Int. 2018 Nov;25(32):32088-32095. doi: 10.1007/s11356-018-3153-1. Epub 2018 Sep 14.
The efficacy of a binary oxidant system, hydrogen peroxide (HO) 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 Fe 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 h. However, dioxane degradation was limited (~ 33%). Conversely, the oxidants were depleted within 24 h for the Fe-activated system, and dioxane degradation was complete within 4 h. The activation and radical generation processes were different between Fe and NaOH activation. Both dioxane and TCE underwent complete degradation in the co-contaminant experiment. The results of this study indicate that the Fe-catalyzed binary hydrogen peroxide-persulfate oxidant system is effective for oxidation of the tested contaminants separately and as co-contaminants.
研究了二元氧化剂体系过氧化氢(HO)和过硫酸盐对 1,4-二恶烷(二恶烷)和三氯乙烯(TCE)共存污染的处理效果。进行了批实验以考察基于 Fe 和 NaOH 的催化效率、氧化剂分解速率、污染物降解效果和竞争降解效果。对于 NaOH 活化,在 96 小时的整个测试期间,氧化剂分解速率适中且持续。然而,二恶烷的降解受到限制(约 33%)。相比之下,Fe 活化体系中的氧化剂在 24 小时内耗尽,并且二恶烷在 4 小时内完全降解。Fe 和 NaOH 活化的激活和自由基生成过程不同。在共存污染物实验中,二恶烷和 TCE 都完全降解。本研究结果表明,Fe 催化的二元过氧化氢-过硫酸盐氧化剂体系对测试污染物的单独和共存污染物的氧化有效。