Adsorbed species on TiO2 associated with the photocatalytic oxidation of trichloroethylene under UV

被引:17
作者
Joung, Soon-Kil [1 ]
Amemiya, Takashi [1 ]
Murabayashi, Masayuki [1 ]
Itoh, Kiminori [1 ]
机构
[1] Yokohama Natl Univ, Grad Sch Environm & Informat Sci, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
关键词
adsorbed species; DCAC; phosgene; TCE; TiO2; photocatalyst; surface;
D O I
10.1016/j.jphotochem.2006.04.040
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
Fourier Transform Infrared (FIF-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS) were used to investigate the species adsorbed on TiO2 related to photocatalytic activity. Dichloroacetyl chloride (DCAC), which is generated during the photocatalytic oxidation of trichloroethylene (TCE), was the only species adsorbed on TiO2. Two types of DCAC were adsorbed - one at low concentration and another at high concentration. While adsorbed phosgene produced from DCAC was adsorbed strongly to TiO2, the adsorption of DCAC was relatively weak. The surface structures of the adsorbed DCAC at low and high concentrations on TiO2 were carboxylate compounds on single Ti-O bonds. The surface structures of carboxylate compounds were resolved to those of adsorbed phosgene, bidentate carbonate compounds, on the two Ti-O bonds during photocatalytic oxidation under UV irradiation. The adsorbed DCAC on TiO2 reduces the photooxidation rate of TCE, and the CHCl2 stretching vibration of adsorbed DCAC was considered to be the inactive species. The adsorbed DCAC and dichloroacetic acid (DCAA) were converted to adsorbed phosgene by photocatalytic oxidation on TiO2. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 281
页数:9
相关论文
共 31 条
[1]   Photocatalytic oxidation of trichloroethylene in humidified atmosphere [J].
Amama, PB ;
Itoh, K ;
Murabayashi, M .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2001, 176 (1-2) :165-172
[2]   ESCA AND SIMS STUDIES OF PLASMA TREATMENTS OF INTRAOCULAR LENSES [J].
BRINEN, JS ;
GREENHOUSE, S ;
PINATTI, L .
SURFACE AND INTERFACE ANALYSIS, 1991, 17 (02) :63-70
[3]   Comparative studies of phenol and salicylic acid photocatalytic degradation: influence of adsorbed oxygen [J].
Chhor, K ;
Bocquet, JF ;
Colbeau-Justin, C .
MATERIALS CHEMISTRY AND PHYSICS, 2004, 86 (01) :123-131
[4]   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
[5]   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
[6]   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
[7]   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
[8]  
HOLDEN W, 1993, TR MET ENV, V3, P393
[9]   GAS-PHASE CHLORINE-PHOTOSENSITIZED OXIDATION OF TRICHLOROETHYLENE [J].
HUYBRECHTS, G ;
MEYERS, L .
TRANSACTIONS OF THE FARADAY SOCIETY, 1966, 62 (524P) :2191-+
[10]   In situ solid-state NMR observations of photocatalytic surface chemistry: Degradation of trichloroethylene [J].
Hwang, SJ ;
Petucci, C ;
Raftery, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (33) :7877-7878