Zhang Xiang, Gu Xiaogang, Lu Shuguang, Brusseau Mark L, Xu Minhui, Fu Xiaori, Qiu Zhaofu, Sui Qian
State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237, China.
Soil, Water and Environmental Science Department, School of Earth and Environmental Sciences, The University of Arizona, 429 Shantz Building, Tucson, AZ 85721, United States.
Chem Eng J. 2017 Oct 1;325:188-198. doi: 10.1016/j.cej.2017.05.004. Epub 2017 May 10.
The enhancement effect of an environmentally friendly reducing agent, ascorbic acid (AA), on trichloroethene (TCE) degradation by Fe(III)-activated calcium peroxide (CP) was evaluated. The addition of AA accelerated the transformation of Fe(III) to Fe(II), and the complexation of Fe(III)/Fe(II) with AA and its products alleviated the precipitation of dissolved iron. These impacts enhanced the generation of reactive oxygen species (ROSs). Investigation of ROSs using chemical probe tests, electron paramagnetic resonance (EPR) tests, and radical scavenger tests strongly confirm large production of hydroxyl radicals (HO•) that is responsible for TCE degradation. The generation of Cl from the degraded TCE was complete in the enhanced CP/Fe(III)/AA system. The investigation of solution matrix effects showed that the TCE degradation rate decreases with the increase in solution pH, while Cl, SO and NO anions have minor impact. Conversely, HCO significantly inhibited TCE degradation due to pH elevation and HO• scavenging. The results of experiments performed using actual groundwater indicated that an increase in reagent doses are required for effective TCE removal. In summary, the potential effectiveness of the CP/Fe(III)/AA oxidation system for remediation of TCE contaminated groundwater has been demonstrated. Additional research is needed to develop the system for practical implementation.
评估了一种环境友好型还原剂抗坏血酸(AA)对Fe(III)活化过氧化钙(CP)降解三氯乙烯(TCE)的增强作用。AA的添加加速了Fe(III)向Fe(II)的转化,并且Fe(III)/Fe(II)与AA及其产物的络合减轻了溶解态铁的沉淀。这些影响增强了活性氧(ROS)的生成。使用化学探针测试、电子顺磁共振(EPR)测试和自由基清除剂测试对ROS进行研究有力地证实了负责TCE降解的羟基自由基(HO•)大量生成。在增强后的CP/Fe(III)/AA体系中,降解TCE产生的Cl完全生成。溶液基质效应研究表明,TCE降解速率随溶液pH升高而降低,而Cl、SO和NO阴离子影响较小。相反,HCO由于pH升高和HO•清除而显著抑制TCE降解。使用实际地下水进行的实验结果表明,有效去除TCE需要增加试剂剂量。总之,已证明CP/Fe(III)/AA氧化体系在修复受TCE污染地下水方面具有潜在有效性。需要开展更多研究以开发该体系用于实际应用。