用户名: 密码: 验证码:
Role of Reactive Oxygen Species for 1,1,1-Trichloroethane Degradation in a Thermally Activated Persulfate System
详细信息    查看全文
文摘
A thermally activated persulfate (PS) system was applied to degrade 1,1,1-trichloroethane (TCA) in aqueous solution. The generation of reactive oxygen species (ROS) in the system and their roles in TCA degradation were investigated. The experimental results showed that TCA (0.15 mM) could be completely oxidized in 1 h at 50 掳C with a PS concentration of 30 mM. TCA degradation and PS decomposition well fitted a pseudo-first-order kinetic model. In addition, the chemical probe method was developed to identify the ROS. The results showed that SO4鈥⑩€?/sup>, HO鈥?/sup>, and O2鈥⑩€?/sup> were all generated in the system and the generation intensities could be strengthened with the increase of PS concentration. The tests for PS persistence in solution indicated that oxidative species were intensified during the initial 2 h, suggesting more SO4鈥⑩€?/sup> and HO鈥?/sup> were generated, whereas after 12 h SO4鈥⑩€?/sup> and HO鈥?/sup> intensities were slightly reduced. In contrast, O2鈥⑩€?/sup> generated in the system was maintained at a stable level after reaction but at a slightly lower intensity simply due to quenching by PS or other species. Radical scavenger tests showed that HO鈥?/sup> was the predominant radical species responsible for TCA degradation, and this was also confirmed by electron paramagnetic resonance (EPR) spectrum analysis in the system. Finally, two different pathways, dechlorination and C鈥揅 bond breakage, were proposed as the main TCA degradation mechanism. In conclusion, a thermally activated PS process is a highly promising technique for TCA degradation, and the potential to degrade highly oxidized organic contaminants greatly increases its application in in situ chemical oxidation (ISCO) remediation in contaminated sites.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700