Photocatalytic membrane reactor for degradation of acid red B wastewater

被引:58
作者
Jiang, Huabing [1 ]
Zhang, Guoliang [1 ]
Huang, Tao [1 ]
Chen, Jinyuan [1 ]
Wang, Qidong [2 ]
Meng, Qin [3 ]
机构
[1] Zhejiang Univ Technol, Coll Biol & Environm Engn, Hangzhou 310014, Zhejiang, Peoples R China
[2] Tsinghua Univ, Dept Environm Sci & Engn, Beijing 100084, Peoples R China
[3] Zhejiang Univ, Coll Mat & Chem Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Acid red B; Titanium dioxide; Photocatalysis; Membrane; Reactor; TITANIUM-DIOXIDE; KINETICS; MICROFILTRATION; PERFORMANCE; SEPARATION; OXIDATION; TIO2; DYES;
D O I
10.1016/j.cej.2009.04.011
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nano-titanium dioxide (TiO2) photocatalyst was prepared by acid-sol method using tetrabutyl titanate and ethanol, which appeared to be anatase by XRD analysis. The wastewater containing azo dye acid red B was then subjected to photocatalytic degradation with photocatalyst TiO2 and UV as light source in a slurry photocatalytic membrane reactor, which included a double layer cylindrical photocatalytic reaction zone and a plate frame membrane separation part. Two kinds of ultrafiltration (UF) membranes PVDF700 and PAN700 were applied and the combined process with photocatalysis was operated by a continuous re-circulating mode during treatment. At first, the adsorption characteristic of the titanium dioxide catalyst under different pH values was analyzed and the optimal operation condition of the photocatalytic process was achieved by changing TiO2 dose and initial concentration of the dye. Then the performance of photocatalyst separation process by ultrafiltration (UF) was investigated. It was found that the degradation of acid red B was followed by first-order kinetics and the efficiency of photocatalysis can be evaluated by the initial reaction rate. Finally, the conglomeration and hydrophilizion phenomena by TiO2 in the coupling system and its effect to different ultrafiltration membranes were analyzed. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:571 / 577
页数:7
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