A novel electrochemically enhanced homogeneous PMS-heterogeneous CoFe2O4 synergistic catalysis for the efficient removal of levofloxacin

被引:119
作者
Zhang, Qianyu [1 ]
Sun, Xiaoqin [1 ]
Dang, Yuan [1 ]
Zhu, Jun-Jie [1 ,2 ]
Zhao, Yuan [3 ]
Xu, Xiaoxiang [4 ]
Zhou, Yuanzhen [1 ]
机构
[1] Xian Univ Architecture & Technol, Sch Chem & Chem Engn, Xian 710055, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210023, Peoples R China
[3] Jiangnan Univ, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China
[4] Tongji Univ, Sch Chem Sci & Engn, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
CoFe2O4; Electrochemistry; PMS activation; LVF degradation; Homogeneous-heterogeneous catalysis; FENTON-LIKE REACTION; ORANGE II; PEROXYMONOSULFATE ACTIVATION; CUFE2O4; NANOPARTICLES; FE-CO/SBA-15; CATALYST; NITRATE REDUCTION; MAGNETIC COFE2O4; DEGRADATION; OXIDATION; MECHANISM;
D O I
10.1016/j.jhazmat.2021.127651
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel electrochemically enhanced homogeneous-heterogeneous catalytic system was constructed by placing the prepared heterogeneous catalyst (CoFe2O4/NF) in parallel between the anode and the cathode for peroxymonosulfate (PMS) activation to remove levofloxacin (LVF) in this work. Over 90% of LVF could be effectively removed by the constructed system after 40 min's degradation. And the electrical energy consumption was only 2.51 kWh/m(3), which was lower than 54.5% of the traditional electrochemical advanced oxidation process. Besides, the system broadened the response range of pH and overcame the inhibitory effect of alkaline conditions on degradation. These activities were mainly due to the high generation ability of free radical (SO4-, center dot OH and O-2(-)) and non-radical (O-1(2)). And the SO4- was found to be the main radical for LW degradation. The high SO4- generation ability was demonstrated to be resulted from the dual effects of synergy of CoFe2O4/PMS and enhancement of electrochemistry in EC/CoFe2O4/PMS system. In detail, electrochemistry could effectively Promote the continuous circulation of Co2+/Co3+ and Fe2+/Fe3+ redox cycles on the surface of CoFe2O4 to enhance the activation of PMS, thereby generating SO4-. This work can provide a promising and cost-effective approach to construct highly efficient organic pollutant degradation system.
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页数:12
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