Effects of surface fluorination of TiO2 on photocatalytic oxidation of gaseous acetaldehyde

被引:141
作者
Kim, Hwajin [1 ]
Choi, Wonyong [1 ]
机构
[1] Pohang Univ Sci & Technol, Sch Environm Sci & Engn, Pohang 790784, South Korea
关键词
photocatalysis; surface fluorinated TiO2; acetaldehyde degradation; photocatalytic oxidation kinetics; air purification;
D O I
10.1016/j.apcatb.2006.06.011
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
Surface fluorinated TiO2 (F-TiO2) shows interesting photocatalytic behaviors that are distinguished from bare TiO2 in many ways. The effects of surface fluorination of TiO2 on the photocatalytic oxidation (PCO) of acetaldehyde under the ambient air conditions were investigated in this study. Both bare TiO2 and F-TiO2 films were compared for the adsorption and degradation of acetaldehyde. The surface fluorination of TiO2 markedly inhibited the adsorption of acetaldehyde and the total amount of CH3CHO adsorbed on F-TiO2 was as low as 30% of that on bare TiO2, However, the PCO rate constant for CO, production was highly enhanced with F-TiO2 on the contrary. The total amount of CH3CHO adsorbed on the photocatalyst films could be quantitatively converted into CO2. The first-order rate constant for the photocatalytic generation Of CO2 increased by 2.5 times upon the surface fluorination of TiO2. The effects of surface fluorination on the dark adsorption of acetaldehyde and the PCO kinetics were compared and discussed in detail. The present study demonstrates that the enhanced PCO activity with F-TiO2 is also observed at the F-TiO2/ air interface while the similar phenomenon was previously observed at the F-TiO2/water interface. The enhanced PCO activities of F-TiO2 might be apparently masked by the hindered adsorption of substrates on F-TiO, but the PCO kinetics on F-TiO2 is indeed much faster than that on bare TiO2. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 132
页数:6
相关论文
共 26 条
[1]   Different inactivation Behaviors of MS-2 phage and Escherichia coli in TiO2 photocatalytic disinfection [J].
Cho, M ;
Chung, HM ;
Choi, WY ;
Yoon, JY .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (01) :270-275
[2]   Investigation on TiO2-coated optical fibers for gas-phase photocatalytic oxidation of acetone [J].
Choi, W ;
Ko, JY ;
Park, H ;
Chung, JS .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 31 (03) :209-220
[3]   Heterogeneous photocatalytic oxidation of benzene, toluene, cyclohexene and cyclohexane in humidified air:: comparison of decomposition behavior on photoirradiated TiO2 catalyst [J].
Einaga, H ;
Futamura, S ;
Ibusuki, T .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 38 (03) :215-225
[4]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[5]   Highly enhanced photocatalytic oxidation of CO on titania deposited with Pt nanoparticles: kinetics and mechanism [J].
Hwang, S ;
Lee, MC ;
Choi, W .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 46 (01) :49-63
[6]   Visible-light-induced photocatalytic degradation of 4-chlorophenol and phenolic compounds in aqueous suspension of pure titania: Demonstrating the existence of a surface-complex-mediated path [J].
Kim, S ;
Choi, W .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (11) :5143-5149
[7]   Simultaneous and synergistic conversion of dyes and heavy metal ions in aqueous TiO2 suspensions under visible-light illumination [J].
Kyung, H ;
Lee, J ;
Choi, WY .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (07) :2376-2382
[8]   Halide acid pretreatments of photocatalysts for oxidation of aromatic air contaminants: rate enhancement, rate inhibition, and a thermodynamic rationale [J].
Lewandowski, M ;
Ollis, DF .
JOURNAL OF CATALYSIS, 2003, 217 (01) :38-46
[9]   Preparation and characterisation of novel thick sol-gel titania film photocatalysts [J].
Mills, A ;
Elliott, N ;
Hill, G ;
Fallis, D ;
Durrant, JR ;
Willis, RL .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2003, 2 (05) :591-596
[10]   Photocatalytic transformation of organic compounds in the presence of inorganic anions. 1. Hydroxyl-mediated and direct electron-transfer reactions of phenol on a titanium dioxide-fluoride system [J].
Minero, C ;
Mariella, G ;
Maurino, V ;
Pelizzetti, E .
LANGMUIR, 2000, 16 (06) :2632-2641