Photocatalytic degradation of trichloroethylene in water using TiO2 pellets

被引:134
作者
Yamazaki, S
Matsunaga, S
Hori, K
机构
[1] Yamaguchi Univ, Dept Chem, Fac Sci, Yamaguchi 7538512, Japan
[2] Yamaguchi Univ, Fac Engn, Dept Chem Engn & Appl Chem, Ube, Yamaguchi 7558611, Japan
关键词
trichloroethylene; titanium dioxide; peroxodisulfate; photocatalyst;
D O I
10.1016/S0043-1354(00)00347-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A recirculating system of aqueous trichloroethylene (TCE) solutions through the packed bed reactor with TiO(2) pellets has been developed in order to mineralize TCE without difficulties for filtration and recovery of catalyst. The TiO(2) pellets prepared by sol-gel method have photocatalytic activity similar to commercially available PC-101 and PC-102 in the powder form and to ST-B11 pellets. in batch experiments with TiO(2) powders, Degussa P-25 is the most active photocatalyst, which indicates that specific surface area is not an important factor controlling the photocatalytic activity in aqueous solutions. The degradation rates of TCE in the recirculating system with TiO(2) pellets decreased in the presence of H(2)O(2), while were remarkably accelerated by adding S(2)O(8)(2-). The presence of S(2)O(8)(2-) ions more than 0.01 mod dm (-3) completely suppressed hole-electron recombination and mineralized 50 ppm TCE with the 2h irradiation. In a reactor without TiO(2) photocatalysts, TCE was photodegraded by SO; radicals which produced by photodissociation of S(2)O(8)(2-). The degradation rates increased with increase of the initial S(2)O(8)(2-) concentration. However, ICE was not mineralized but converted to intermediates which were slowly degraded to Cl(-) by continuing the irradiation. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1022 / 1028
页数:7
相关论文
共 26 条
[1]  
ALEKABI H, 1993, TR MET ENV, V3, P321
[2]  
ANDERSON MA, 1993, TR MET ENV, V3, P405
[3]  
BAHNEMANN D, 1994, AQUATIC AND SURFACE PHOTOCHEMISTRY, P261
[4]  
BLAKE DM, 1999, BIOGRAPHY WORK HETER
[5]   Photocatalytic oxidation of chlorinated hydrocarbons in water [J].
Crittenden, JC ;
Liu, JB ;
Hand, DW ;
Perram, DL .
WATER RESEARCH, 1997, 31 (03) :429-438
[6]  
DAVIES MJ, 1984, J CHEM SOC PERK T 2, P503, DOI 10.1039/p29840000503
[7]   KINETICS OF THE GAS-SOLID HETEROGENEOUS PHOTOCATALYTIC OXIDATION OF TRICHLOROETHYLENE BY NEAR UV ILLUMINATED TITANIUM-DIOXIDE [J].
DIBBLE, LA ;
RAUPP, GB .
CATALYSIS LETTERS, 1990, 4 (4-6) :345-354
[8]   Gas-phase photooxidation of trichloroethylene on TiO2 and ZnO:: Influence of trichloroethylene pressure, oxygen pressure, and the photocatalyst surface on the product distribution [J].
Driessen, MD ;
Goodman, AL ;
Miller, TM ;
Zaharias, GA ;
Grassian, VH .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (03) :549-556
[9]   Mechanism of photooxidation of trichloroethylene on TiO2: Detection of intermediates by infrared spectroscopy [J].
Fan, JF ;
Yates, JT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (19) :4686-4692
[10]   CHLORINATED BY-PRODUCTS FROM THE TIO2-MEDIATED PHOTODEGRADATION OF TRICHLOROETHYLENE AND TETRACHLOROETHYLENE IN WATER [J].
GLAZE, WH ;
KENNEKE, JF ;
FERRY, JL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (01) :177-184