Lu Xiaoxia, Li Guanghe, Zhang Xu, Zhang Weihua
Dept. of Environmental Science and Engineering, Tsinghua University, Beijing 100084.
Huan Jing Ke Xue. 2002 Jul;23(4):37-41.
Based on column experiments, the oxidative degradations of some chlorinated hydrocarbons under three less-reduced redox conditions were investigated. The results showed that in the presence of nitrate and manganese oxide, 1,2-dechloroethane (1,2-DCA) and vinyl chloride (VC) could be oxidized. The transformation rates of 1,2-DCA under denitrification and manganese reduction were 1.18/h and 0.54/h, respectively, while those of VC were 0.29/h and 0.15/h, respectively. In the presence of iron, degradation of VC was not clear. In addition, the degradation of 1,2-DCA was inhibited. For other chlorinated hydrocarbons, such as 1,1,1-trichloroethane, trichloroethene, cis-dichloroethene and trans-dichloroethene, no degradation occurred under the three studied redox conditions. Monochlorobenzene exhibited relative high removal in the columns, however, due to its high soil adsorption potential, it was not known yet whether microbial activities were involved.
基于柱实验,研究了三种弱还原氧化还原条件下一些氯代烃的氧化降解情况。结果表明,在硝酸盐和氧化锰存在的情况下,1,2 - 二氯乙烷(1,2 - DCA)和氯乙烯(VC)可以被氧化。在反硝化和锰还原条件下,1,2 - DCA的转化速率分别为1.18/h和0.54/h,而VC的转化速率分别为0.29/h和0.15/h。在铁存在的情况下,VC的降解不明显。此外,1,2 - DCA的降解受到抑制。对于其他氯代烃,如1,1,1 - 三氯乙烷、三氯乙烯、顺式二氯乙烯和反式二氯乙烯,在三种研究的氧化还原条件下均未发生降解。氯苯在柱中表现出较高的去除率,然而,由于其对土壤的高吸附潜力,尚不清楚是否涉及微生物活动。