Influence of adsorption on the photodegradation of various dyes using surface bond-conjugated TiO2/SiO2 photocatalyst

被引:6
作者
Hu, C [1 ]
Wang, YZ [1 ]
Tang, HX [1 ]
机构
[1] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
anionic dye; adsorption; cationic dye; NH4+; photodegradation; TiO2/SiO2/water interface;
D O I
10.1016/S0926-3373(01)00236-3
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
The adsorption and photodegradation have been investigated in illuminated surface bond-conjugated TiO2/SiO2 suspension for five commercial dyes, including cationic dyes, cationic blue X-GRL (CBX) and cationic pink FG (FG), and anionic reactive brilliant red K-2G (K-2G), reactive yellow KD-3G (KD-3G), and acid red B (ARB). Two adsorption modes are proposed. In the TiO2/SiO2 system, CBX and FG (FG) adsorbed on the catalyst surface by a penta-heterocycle N group, whereas, the other three anionic dyes adsorbed on the catalyst surface by a sulfonate group. The mode of adsorption of substrates to the TiO2/SiO2 particle surface is relevant factor to the formation of NH4+. The nitrogen of azo group was transformed to NH4+ ions and N-2 gas, and the penta-heterocycle and benzene-ring- su bsti Lute N groups in CBX and FG were transformed predominantly to NH4+ ions. The triazine ring and its substitute groups are much stable in the period of 8 h irradiation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:95 / 105
页数:11
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