吉林大学学报(地球科学版) ›› 2018, Vol. 48 ›› Issue (4): 1212-1220.doi: 10.13278/j.cnki.jjuese.20170240
张凤君1, 刘哲华1, 苏小四2, 吕聪1, 刘佳露1
Zhang Fengjun1, Liu Zhehua1, Su Xiaosi2, Lü Cong1, Liu Jialu1
摘要: 为了探究高级氧化技术对土壤中有机氯代烃的氧化降解作用,为ISCO(in situ chemical oxidation)技术体系提供重要的理论依据和数据支撑,考察了热活化过硫酸盐(persulfate,PS)氧化降解不同类型土壤(砂类土壤、黏土类土壤)中挥发性氯代烃污染物(三氯乙烯(TCE)、三氯乙烷(TCA)、顺式-1,2-二氯乙烯(cis-1,2-DCE)、1,2-二氯乙烷(1,2-DCA))的效能;同时,通过硫酸盐与土壤相互作用过程研究,探究了不同土壤介质中有机质和无机组分在过硫酸盐消耗中所占比例。结果表明:在50℃时,热活化过硫酸盐可有效降解土壤中1,2-DCA、cis-1,2-DCE、TCA和TCE,砂类土壤介质中4种氯代烃降解效果依次为25%、89%、5%和61%,黏土类土壤介质中4种氯代烃降解效果依次为35%、86%、8%和63%;4种氯代烃的降解效果从高到低顺序依次为cis-1,2-DCE、TCE、1,2-DCA、TCA,砂类土壤中的氯代烃总体降解效果优于黏土类土壤中氯代烃的降解效果。另外,土壤中过硫酸盐氧化降解氯代烃反应研究发现,砂类和黏土类土壤介质组分中有机质消耗率分别为81.3%和72.6%,铁元素消耗率分别为80.5%和38.6%,表明土壤介质组分与过硫酸盐发生了氧化还原反应,从而导致过硫酸盐自身的大量消耗。由此可知,土壤介质中的有机质、铁元素等矿物质均参与过硫酸盐的消耗过程,且土壤有机质、铁元素与氯代烃之间在消耗过硫酸盐反应上存在竞争关系,土壤组分过多地消耗了过硫酸盐,导致了氯代烃的氧化降解效率较低。因此,针对实际有机氯代烃污染场地,采用过硫酸盐氧化技术进行修复时,过硫酸盐的实际投加量要远高于化学计量值,需充分考虑到土壤组分对过硫酸盐自身的消耗作用。
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