Water-plasma-activated g-C3N4 for enhanced photodegradation of bisphenol A synergized with persulfate oxidation

被引:14
|
作者
Xu, Jian [1 ]
Li, Xinran [1 ]
Zheng, Yanxia [1 ]
Yu, Xuelian [1 ]
Zhou, Jing [2 ]
An, Xiaoqiang [3 ]
机构
[1] China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
[2] Jilin Jianzhu Univ, Key Lab Songliao Aquat Environm, Minist Educ, Changchun, Peoples R China
[3] Tsinghua Univ, Ctr Water & Ecol, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
关键词
g-C3N4; Water-plasma; Nitrogen vacancies; Persulfate activation; Bisphenol A; COBALT-DOPED G-C3N4; PEROXYMONOSULFATE PMS; DEGRADATION; CARBON; TIO2; VACANCIES; GRAPHENE; KINETICS; CATALYST;
D O I
10.1016/j.apsusc.2022.153163
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
Herein, a facile water-plasma strategy is employed to modify the surface structure of graphite-carbon nitride (g-C3N4) to enhance its photocatalytic performance for persulfate activation. High energy electrons and highly active free radicals from water-plasma discharge not only induce nitrogen vacancies, but also generate hydrophilic groups on g-C3N4 surface, which can effectively modulate the energy levels, facilitate the interaction of water with catalyst, and meanwhile promote the separation and transfer of photogenerated charge carriers. When used for bisphenol A (BPA) degradation, water-plasma-activated g-C3N4 exhibits 4.5-fold enhancement of reaction rate compared to that of pristine g-C3N4. This work offers deep insights into in-situ defect engineering of g-C3N4 as Fenton-like catalyst.
引用
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页数:7
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