Preparation of Al/TiO2 nanometer photo-catalyst film and the effect of H2O addition on photo-catalytic performance for benzene removal

被引:38
作者
Lee, BY [1 ]
Park, SH [1 ]
Kang, MS [1 ]
Lee, SC [1 ]
Choung, SJ [1 ]
机构
[1] Kyung Hee Univ, Ind Liaison Res Inst, Sch Environm Appl Chem, Dept Chem Engn, Yongin 449701, Gyeonggi, South Korea
关键词
Al/TiO2; thermal stability; benzene removal; H2O addition; PHOTOCATALYTIC DEGRADATION; TIO2; 4-CHLOROPHENOL; OXIDATION; WATER;
D O I
10.1016/S0926-860X(03)00542-8
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
The nanometer particles of Tio(2) and Al/TiO2 (1.0, 5.0, and 10.0 wt.%) were obtained by a sol-gel method. The TiO2 and Al/TiO2 particles were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), DLS, TG-DSC, and UV-Vis spectroscopy. The TiO2 and Al/TiO2 Particles exhibited a uniform anatase structure with particle size below 100-150 nm. Obtained Al/TiO2 particles absorbed wavelengths above 270 nm. The absorption band was shifted to longer wavelength (red shift). In addition, the surface area of 10.0 wt.% Al/TiO2 was very large (290 m(2)/g), compared with that of pure TiO2 (50-70 m(2)/g). From XRD results, we suggested that a new structure connected by Al-O-Ti framework was generated. In particular. for Al/TiO2, the anatase structure was stable after thermal treatment at 800 degreesC, while pure TiO2 was easily transferred to the rutile type after thermal treatment above 700 degreesC. On the other hand, the conversion of benzene was higher in pure TiO2 than in Al/TiO2 without H2O addition during reaction; however, the conversion surprisingly enhanced about 40% over 10.0 wt.% Al/TiO2 catalyst with 10 mol-wt.% H2O addition in a continuous photo-reaction system. In addition, no photo-catalytic deactivation was found over 10.0 wt.% Al/TiO2 until 10h, when 10 mol-wt.% H2O was added during the benzene decomposition reaction. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:371 / 380
页数:10
相关论文
共 29 条
[1]   Activity of cadmium sulfide photocatalysts for hydrogen production from water: Role of support [J].
Arora, MK ;
Sahu, N ;
Upadhyay, SN ;
Sinha, ASK .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1999, 38 (07) :2659-2665
[2]   Photocatalytically assisted hydrolysis of chlorinated methanes under anaerobic conditions [J].
Calza, P ;
Minero, C ;
Pelizzetti, E .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (08) :2198-2203
[3]   Preparation and photocatalytic properties of a novel kind of loaded photocatalyst of TiO2/SiO2/γ-Fe2O3 [J].
Chen, F ;
Zhao, JC .
CATALYSIS LETTERS, 1999, 58 (04) :245-247
[4]   PREPARATION AND UTILIZATION OF ORGANICALLY MODIFIED SILICA-TITANIA PHOTOCATALYSTS FOR DECONTAMINATION OF AQUATIC ENVIRONMENTS [J].
DAGAN, G ;
SAMPATH, S ;
LEV, O .
CHEMISTRY OF MATERIALS, 1995, 7 (03) :446-453
[5]   Novel silica gel supported TiO2 photocatalyst synthesized by CVD method [J].
Ding, Z ;
Hu, XJ ;
Lu, GQ ;
Yue, PL ;
Greenfield, PF .
LANGMUIR, 2000, 16 (15) :6216-6222
[6]  
FORMENTI M, 1978, CATALYSIS, V2, P87
[7]  
HERMANN SH, 1999, J MATER RES, V14, P4551
[8]   Heterogeneous photocatalysis: fundamentals and applications to the removal of various types of aqueous pollutants [J].
Herrmann, JM .
CATALYSIS TODAY, 1999, 53 (01) :115-129
[9]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[10]   Synthesis of Fe/TiO2 photocatalyst with nanometer size by solvothermal method and the effect of H2O addition on structural stability and photodecomposition of methanol [J].
Kang, M .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2003, 197 (1-2) :173-183