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Visible-light-driven activation of peroxymonosulfate for accelerating ciprofloxacin degradation using CeO2/Co3O4 p-n heterojunction photocatalysts
被引:186
|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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