化学
环境化学
氯胺化
水处理
溴酸盐
氯胺
水质
矿化(土壤科学)
氯
环境工程
环境科学
无机化学
有机化学
生物
溴化物
氮气
生态学
作者
Yixuan Yu,Yao Li,Mindong Bai,Zhixin Ji,Ji Li,Xiaodian Huang
标识
DOI:10.1016/j.cej.2018.10.196
摘要
The accumulation of antibiotics in river watersheds and lakes could induce the spread of antibiotic-resistance genes in drinking water, causing damage to human health. An OH equipment, that produces OH by strong ionization discharge combined with water jet cavitation effect, was installed in a drinking water treatment system of 12,000 m3 per day in Xiang’an water plant, Xiamen of China. The NFX as a model antibiotic was mixed into a branched pipe at a flow rate of 1.0 m3 h−1 for OH mineralization. As a result, the OH after coagulation sedimentation at 1.0 mg L−1 and after sand filtration at 0.5 mg L−1 degraded NFX to not detected within only 20 s. Moreover, the OH mineralizes the NFX into CO2 and H2O by breaking the CF bond, and opening the piperizine, nalidixic, and benzene rings, while NaClO only opens the piperizine ring and adversely forms chlorinated intermediates. By OH disinfection at 0.5 mg L−1 in the main pipe of 500 m3 h−1, all algae blooms were inactivated; the tests of 106 drinking water quality indicators satisfied the Chinese Standards; any disinfection by-products, such as bromate and trihalomethanes (THMs) were not be detected. By NaClO disinfection, the total THMs increased to 190 μg L−1, which is 2.4 times higher than the limit regulated by Environmental Protection Agency (80 μg L−1). To prevent the spread of antibiotic-resistance genes in humans, OH advanced oxidation based on strong ionization discharge could be apply to mineralize antibiotics during practical drinking water treatment.
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