Visible light photocatalytic mineralization of bisphenol A by carbon and oxygen dual-doped graphitic carbon nitride

被引:35
作者
Gu, Jiayu [1 ]
Chen, Huan [1 ]
Jiang, Fang [1 ]
Wang, Xin [2 ]
机构
[1] Nanjing Univ Sci & Technol, Key Lab Jiangsu Prov Chem Pollut Control & Resour, Sch Environm & Biol Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Nanjing Univ Sci & Technol, Key Lab Soft Chem & Funct Mat, Minist Educ, Nanjing 210094, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Graphitic carbon nitride; Visible-light photocatalytic; BPA mineralization; Carbon-oxygen dual-doping; METHYLENE-BLUE; HYDROGEN-BONDS; DEGRADATION; WATER; REDUCTION; CHARGE; TIO2; PHOTOREACTIVITY; DECOMPOSITION; IRRADIATION;
D O I
10.1016/j.jcis.2019.01.023
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 facile thermal polymerization was applied to synthesize carbon and oxygen dual-doped graphitic carbon nitride (MACN) with controllable electronic band structure using malonic acid and urea as precursors. The C and O atoms substituted the sp(2) N atom in graphitic carbon nitride (CN). The 1MACN (1 represented that the weight ratio of malonic acid to urea is 1% during the synthesis) with optimal band structure could decompose 15 ppm bisphenol A (BPA) within 150 min, and the mineralization rate reached to 52%. The superior photocatalytic performance of 1MACN was mainly ascribed to electronic band structure together with optical properties. On the one hand, the formation of delocalized big it bonds favored the electrons transfer after the introducing of carbon atoms. On the other hand, a positive charge density existed on the C atoms because of high electronegativity of contiguous O (3.44) that substituted N compared with C (2.55), which could attribute to high activity of MACN catalyst. The study will contribute to the further improvement of visible-light photocatalytic BPA degradation and mineralization. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:97 / 106
页数:10
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