文献类型：期刊文献

英文题名：Insights into the performance, mechanism, and ecotoxicity of levofloxacin degradation in CoFe2O4 catalytic peroxymonosulfate process

作者：Liu, Lili[1];Zhan, Rui[1];Zhang, Meng[1,2];Li, Jianan[1];Wang, Zhiping[3];Mi, Haosheng[1];Zhang, Yunxiao[1]

机构：[1]East China Univ Sci & Technol, Sch Resource & Environm Engn, State Environm Protect Key Lab Environm Risk Asse, Shanghai 200237, Peoples R China;[2]Chinese Acad Sci, Inst Geochem, State Key Lab Environm Geochem, Guiyang 550081, Peoples R China;[3]Shanghai Jiao Tong Univ, Sch Environm Sci & Technol, Shanghai 200240, Peoples R China

年份：2022

卷号：10

期号：3

外文期刊名：JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING

收录：;EI(收录号：20221011758796);WOS:【SCI-EXPANDED(收录号:WOS:000790512300001)】；

基金：Acknowledgments This work was supported by National Natural Science Foundation of China (Grant No. 41771513, 41907110) , China Postdoctoral Science Foundation (Grant No. 2020M671029) , and National Key Research and Development Program of China (Grant No. 2018YFC1901000) .

语种：英文

外文关键词：Levofloxacin; CoFe2O4; Peroxymonosulfate; Reaction mechanisms; Ecotoxicity assessment

摘要：The catalysis effectiveness and influence factors of CoFe2O4 nanoparticles were investigated with peroxymonosulfate (PMS) as oxidant. Meanwhile, the degradation mechanism of levofloxacin (LVF) and the toxicity of its degradation products were analyzed. Efficient LVF degradation (95.4%) could be achieved within 30 min in CoFe2O4/PMS system with the optimum reaction conditions. The removal efficiency of LVF was decreased from 94.66% to 27.38% as the concentration of HCO3- increased from 0 to 20 mM, while increased to nearly 100% with 5 mM H2PO4- addition. The inhibition effect of Cl on LVF removal decreased as the concentration of Cl- increased, and the addition of humic acid did not affect the final removal efficiency of LVF significantly. According to the results of degradation experiments and XPS analysis, both Co(II)/ Co(III) and Fe(II)/ Fe(III) redox pairs were involved in PMS catalysis, and Co(II)/ Co(III) played a dominant role. SO4 center dot- was the dominant free radical in CoFe2O4/PMS system for LVF degradation, and five possible degradation pathways were proposed based on the eleven degradation products. Compared with LVF, more toxic degradation products were generated in degradation pathways of decarboxylation and conversion of quinolone moieties, due to the coexisting of SO4 center dot- and HO center dot. Meanwhile, the luminescence inhibition ratio of the reaction solution (23.5%) was still higher than the original LVF solution (21.4%) by the end of the experiment. Therefore, the degradation pathways that generate toxic products should be avoided or detoxification by the complete mineralization of LVF, which needs further research via the targeted optimization of CoFe2O4/PMS system.