Oxidative degradation of organic pollutants utilizing molecular oxygen and visible light over a supported catalyst of Fe(bpy)32+ in water

被引:96
作者
Li, J
Ma, WH
Huang, YP
Tao, X
Zhao, JC [1 ]
Xu, YM
机构
[1] Chinese Acad Sci, Ctr Mol Sci, Inst Chem, Lab Photochem, Beijing 100080, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
dioxygen activation; iron complex; photodegradation; pollutant;
D O I
10.1016/j.apcatb.2003.09.003
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
This article explores a supported catalyst of Fe(bpy)(3)(2+) on a cationic exchange resin (Amberlite IRA 200) as a photocatalyst for the degradation of organic pollutants by activating molecular oxygen under visible irradiation (lambda > 420 nm) in water. Different from Fe(bpy)(3)(2+) which is not photoactive in solution, the supported catalyst exhibits a very efficient photoactivity for the degradation of N,N-dimethylaniline and the cationic dyes of Rhodamine B (RhB) and Malachite Green (MG) in an aerated aqueous medium. TOC removal yield was 75, 60 and 58%, respectively, after 700 min of visible light irradiation. The photocatalytic activity of the supported Fe(bpy)(3)(2+) remained unchanged after 22 cycles of over 100 h. The photocatalyst was characterized by UV-Vis diffuse reflectance, and X-ray photoelectron spectroscopies (XPS). EPR studies suggest that the active superoxide species {Fe(bpy)(3)(3+) O-2(.-)} are involved in the light-activated reaction. A reaction mechanism is proposed in the text. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 24
页数:8
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