UV-H2O2对高碱度地下水中1,4-二恶烷和VOCs的破坏作用

Issam Najm, Karl Linden, Bryan Liu, Joseph Liles, Steve Winners
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摘要

采用紫外-过氧化氢(UV-H2O2)高级氧化工艺(AOP)对3个高碱度(CaCO3为281 mg/L)地下水样品中1,4-二氧六环(47 μg/L)和三氯乙烯(TCE)、四氯乙烯(PCE)、1,1-二氯乙烯(1,1- dce)三种不同浓度的挥发性有机化合物(VOCs)进行了实验评价。紫外剂量范围为0 ~ 5500 mJ/cm2, H2O2浓度范围为0 ~ 16 mg/L。结果表明,碳酸氢盐和碳酸盐碱度在很大程度上支配了羟基自由基的消耗,从而影响了1,4-二恶烷的破坏速率。在UV-H2O2处理之前,去除高氯酸盐、氯酸盐和硝酸盐对1,4-二恶烷的破坏没有明显的影响,而去除TOC则使1,4-二恶烷的破坏率提高了约25%。根据H2O2浓度和紫外线剂量的组合,1,4-二恶烷的破坏范围从可忽略到大于99%。
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Destruction of 1,4-Dioxane and VOCs with UV-H2O2 in a high alkalinity groundwater

Bench-scale testing was conducted to evaluate the application of an Ultraviolet-hydrogen peroxide (UV-H2O2) advanced oxidation process (AOP) for the destruction of 1,4-Dioxane (47 μg/L) and varying concentrations of three volatile organic chemicals (VOCs), including trichloroethylene (TCE), tetrachloroethylene (PCE), and 1,1-dichloroethylene (1,1-DCE), from three samples of groundwater containing high alkalinity (281 mg/L as CaCO3). The UV doses applied ranged from zero to 5500 mJ/cm2 while the H2O2 concentrations ranged from 0 to 16 mg/L. The results showed that the bicarbonate and carbonate alkalinity greatly dominated the hydroxyl radical consumption and thus the 1,4-Dioxane destruction rate. The removal of perchlorate, chlorate, and nitrate prior to UV-H2O2 treatment had no discernable effect on 1,4-Dioxane destruction, while the removal of TOC increased the rate of 1,4-Dioxane destruction by approximately 25%. Depending on the combination of H2O2 concentration and UV dose, 1,4-Dioxane destruction ranged from negligible to greater than 99%.

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