Hierarchical assembly of highly efficient visible-light-driven Ag/g-C3N4/kaolinite composite photocatalyst for the degradation of ibuprofen

被引:54
|
作者
Sun, Zhiming [1 ]
Zhang, Xiangwei [1 ]
Dong, Xiongbo [1 ]
Liu, Xiaorui [1 ]
Tan, Ye [1 ]
Yuan, Fang [1 ]
Zheng, Shuilin [1 ]
Li, Chunquan [1 ]
机构
[1] China Univ Min & Technol Beijing, Sch Chem & Environm Engn, Beijing 100083, Peoples R China
基金
北京市自然科学基金;
关键词
Photocatalyst; Ag nanoparticles; g-C3N4; Kaolinite; Ibuprofen; Visible-light-driven; THERMALLY ACTIVATED PERSULFATE; ENHANCED DEGRADATION; FACILE SYNTHESIS; WATER; PPCPS; KAOLINITE; REMOVAL; AG; PEROXYMONOSULFATE; PERFORMANCE;
D O I
10.1016/j.jmat.2020.04.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel Ag/g-C3N4/kaolinite composite photocatalyst was fabricated for the first time through a two-step assembly strategy by employing in situ calcination and a photodeposition process. The synthesized Ag/gC(3)N(4)/kaolinite composite reached a higher degradation rate of ibuprofen (IBP) with a reaction rate constant of 0.0113 min(-1) at an Ag content of 7% under visible-light irradiation, which was approximately 1.87 times that of the Ag/g-C3N4 composite. Based on the physicochemical properties, the enhanced photocatalytic activity was attributed to the stronger adsorption property, wider photoresponse range and more efficient separation and transfer of electron-hole pairs. Furthermore, the incorporation of monodispersed Ag nanoparticles onto the g-C3N4/kaolinite sheets provided more reactive sites for the IBP degradation. In addition, according to the EPR study and trapping experiments, it was demonstrated that holes (h(+)) should be the key reactive species. A possible pathway of IBP degradation was also proposed based on the detected intermediates. Overall, the results of this work may facilitate the design of a novel visible-light-driven photocatalyst with a high efficiency that is derived from a natural mineral for environmental remediation. (C) 2020 The Chinese Ceramic Society. Production and hosting by Elsevier B.V.
引用
收藏
页码:582 / 592
页数:11
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