Visible-light-driven activation of peroxymonosulfate for accelerating ciprofloxacin degradation using CeO2/Co3O4 p-n heterojunction photocatalysts

被引:197
作者
Shen, Chun-Hui [1 ,2 ]
Wen, Xiao-Ju [1 ]
Fei, Zheng-Hao [1 ]
Liu, Zong-Tang [1 ]
Mu, Qi-Ming [1 ]
机构
[1] Yancheng Teachers Univ, Sch Chem & Environm Engn, Yancheng 224051, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Coll Chem Engn, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Co3O4/CeO2; PMS; Ciprofloxacin; Photocatalytic; RADICAL GENERATION; BISPHENOL-A; MECHANISM; EFFICIENT; PATHWAYS; CATALYST; CARBON; ACID; NANOCOMPOSITES; NANOPARTICLES;
D O I
10.1016/j.cej.2019.123612
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The development of simple and effective approaches for the synthesis of bimetallic oxide heterojunction photocatalyst which are used to activate peroxymonosulfate (PMS) under visible-light-driven is highly feasible but remains a great challenge. In this work, the Co3O4/CeO2 composite was prepared by a facile chemical reaction, followed by annealing in a muffle furnace and then applied to activate PMS for ciprofloxacin (CIP) degradation. Various characterizations confirmed the formation of p-n heterojunction between Co3O4 and CeO2. Meanwhile, the 5 wt% Co3O4/CeO2/PMS composite showed highest degradation rate of CIP (87.8%) under visible light irradiation. The obtained Co3O4/CeO2/PMS system still exhibited a good catalytic performance in presence of different anion. Besides, the active radical h(+), center dot OH, center dot O-2(-), and SO4-center dot are involved in CIP degradation. The excellent degradation performance can be interpreted as the synergistic effect between Co3O4/CeO2 heterojunction photocatalyst and PMS activation. Moreover, the energy band structure and valence band deviation of Co3O4/CeO2 p-n heterogeneous junction were confirmed. This work would give a reference for combining the photocatalyst and activation of PMS under visible light for further removal of pollutants.
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页数:13
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