Synergistic effect of mesoporous graphitic carbon nitride and peroxydisulfate in visible light-induced degradation of atenolol: A combined experimental and theoretical study

被引:24
作者
Cui, Minshu [1 ,2 ]
Cui, Kangping [1 ,2 ]
Liu, Xinglong [1 ,2 ]
Shi, Jianpeng [1 ,2 ]
Chen, Xing [3 ]
Chen, Yihan [1 ,2 ]
机构
[1] Hefei Univ Technol, Sch Resources & Environm Engn, Hefei 230009, Peoples R China
[2] Hefei Univ Technol, Key Lab Nanominerals & Pollut Control Higher Educ, Hefei 230009, Peoples R China
[3] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Peoples R China
基金
国家重点研发计划;
关键词
Photocatalysis; Density functional theory; Mesoporous graphitic carbon nitride; Peroxydisulfate; Atenolol; WASTE-WATER TREATMENT; PHOTOCATALYTIC DEGRADATION; BISPHENOL-A; ORGANIC POLLUTANTS; ADVANCED OXIDATION; ELECTRON-TRANSFER; DOPED G-C3N4; PEROXYMONOSULFATE; PERSULFATE; MECHANISM;
D O I
10.1016/j.cej.2020.127979
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The visible light sensitive metal-free mesoporous graphitic carbon nitride (mpg-CN) was fabricated for photodegradation of atenolol (ATN), a widely used drug for cardiovascular diseases. Peroxydisulfate (PDS) as an electron acceptor as well as a radical origin was introduced to enhance the catalytic performance, and retaining the nature of metal-free and mesoporous of mpg-CN. The photo-induced holes, SO4?- and O2?- were identified as the active species. Integrated with density functional theory (DFT) calculations and photoelectrochemical experiments, the interaction among PDS, catalyst, and ATN is unveiled. PDS can obtain an electron from the catalyst, hence to improve the separation of electron-hole pairs and activates itself. ATN has stable chemical adsorption states on catalyst surface. Then the electron-deficient catalysts can acquire electrons from ATN. In addition, primary degradation sites of ATN and following possible degradation pathways were explored with DFT calculations and mass spectrometry analysis.
引用
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页数:12
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