Zhong Hua, Tian Yaling, Yang Qi, Brusseau Mark L, Yang Lei, Zeng Guangming
College of Environmental Science and Engineering, Hunan University, Changsha 410082, China.
School of Water Resources and Hydropower Engineering, Wuhan University, Wuhan 430070, China.
Chem Eng J. 2017 Jan 1;307:399-407. doi: 10.1016/j.cej.2016.08.069. Epub 2016 Aug 16.
In this study, batch and column experiments were conducted to evaluate the feasibility of using persulfate oxidation to treat groundwater contaminated by landfill leachate (CGW). In batch experiments, persulfate was compared with HO, and permanganate for oxidation of organic compounds in CGW. It was also compared with the potential of biodegradation for contaminant removal from CGW. Persulfate was observed to be superior to HO and permanganate for degradation of total organic carbon (TOC) in the CGW. Conversely, biodegradation caused only partial removal of TOC in CGW. In contrast, persulfate caused complete degradation of the TOC in the CGW or aged CGW, showing no selectivity limitation to the contaminants. Magnetite (FeO) enhanced degradation of leachate compounds in both CGW and aged CGW with limited increase in persulfate consumption and sulfate production. Under dynamic flow condition in 1-D column experiments, both biodegradation and persulfate oxidation of TOC were enhanced by FeO. The enhancement, however, was significantly greater for persulfate oxidation. In both batch and column experiments, FeO by itself caused minimal consumption of persulfate and production of sulfate, indicating that magnetite is a good persulfate activator for treating CGW in heterogeneous systems The results of the study show that the persulfate-based in-situ chemical oxidation (ISCO) method has great potential to treat the groundwater contaminated by landfill leachate.
在本研究中,进行了批量实验和柱实验,以评估使用过硫酸盐氧化法处理受垃圾渗滤液污染的地下水(CGW)的可行性。在批量实验中,将过硫酸盐与羟基自由基(HO)和高锰酸盐用于CGW中有机化合物的氧化进行了比较。还将其与从CGW中去除污染物的生物降解潜力进行了比较。观察到过硫酸盐在降解CGW中的总有机碳(TOC)方面优于HO和高锰酸盐。相反,生物降解仅导致CGW中TOC的部分去除。相比之下,过硫酸盐导致CGW或老化CGW中TOC的完全降解,对污染物没有选择性限制。磁铁矿(Fe₃O₄)在CGW和老化CGW中均增强了渗滤液化合物的降解,而过硫酸盐消耗和硫酸盐生成的增加有限。在一维柱实验的动态流动条件下,Fe₃O₄增强了TOC的生物降解和过硫酸盐氧化。然而,过硫酸盐氧化的增强作用明显更大。在批量实验和柱实验中,Fe₃O₄本身导致过硫酸盐的消耗和硫酸盐的生成极少,表明磁铁矿是在非均相系统中处理CGW的良好过硫酸盐活化剂。研究结果表明,基于过硫酸盐的原位化学氧化(ISCO)方法在处理受垃圾渗滤液污染的地下水方面具有巨大潜力。