Drastically enhanced visible-light photocatalytic degradation of colorless aromatic pollutants over TiO2 via a charge-transfer-complex path: A correlation between chemical structure and degradation rate of the pollutants

被引:91
作者
Wang, Nan [1 ]
Zhu, Lihua [1 ]
Huang, Yingping [2 ]
She, Yuanbin [3 ]
Yu, Yanmin [3 ]
Tang, Heqing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Coll Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] China Three Gorges Univ, Chem & Life Sci Coll, Yichang 443002, Peoples R China
[3] Beijing Univ Technol, Coll Environm & Energy Engn, Beijing 100124, Peoples R China
基金
美国国家科学基金会;
关键词
Titanium dioxide; Charge-transfer; Surface complex; Visible-light irradiation; Degradation; TRANSITION-METAL IONS; AQUEOUS SUSPENSION; PHENOLIC-COMPOUNDS; DOPED TIO2; PHOTODEGRADATION; 4-CHLOROPHENOL; PHOTOOXIDATION; TRANSFORMATION; IRRADIATION; ADSORPTION;
D O I
10.1016/j.jcat.2009.06.006
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
Photocatalytic degradation of colorless aniline and phenolic pollutants was investigated over TiO2 under visible-light irradiation, which was confirmed to proceed via a charge-transfer-complex (CTC)-mediated pathway. The correlation between the chemical structure and the degradation rate of these pollutants was established experimentally and theoretically. It was found that an electron-donating substituent in benzene ring, which raises the highest occupied molecular orbital and lowers the ionization potential of the organic compound, is favorable to the CTC-mediated photodegradation of the pollutant, but an electron-withdrawing substituent has a reversed effect. The addition of sacrificial electron acceptors was adopted to enhance the degradation and mineralization of the aromatic pollutants. The increased degradation rate by 3 to 10 times suggests that the CTC-mediated photocatalytic technique has promising applications in the removal of colorless organic pollutants in the presence of sacrificial electron acceptors. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:199 / 206
页数:8
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