Fourier transform infrared study of the performance of nanostructured TiO2 particles for the photocatalytic oxidation of gaseous toluene

被引:338
作者
Maira, AJ
Coronado, JM
Augugliaro, V
Yeung, KL
Conesa, JC
Soria, J
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Madrid 29049, Spain
[2] Univ Palermo, Dipartimento Ingn Chim Proc & Mat, I-90128 Palermo, Italy
[3] Hong Kong Univ Sci & Technol, Dept Chem Engn, Kowloon, Hong Kong, Peoples R China
关键词
photocatalysis; nanoparticles; titanium dioxide; toluene; volatile organic compounds; FTIR; hydrothermal treatment;
D O I
10.1006/jcat.2001.3301
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
Thermal and hydrothermal treatments have been applied to an amorphous TiO2 precursor for obtaining nanosized TiO2 particles (P11t and P11h, respectively) of different photocatalytic properties. The activity of these catalysts has been tested by performing the toluene oxidation in gas phase in a continuous photoreactor. A Fourier transform infrared (FTIR) investigation of the catalysts under conditions prevailing during the test photoreaction has also been carried out. The photoreactivity results showed that CO2 was the main oxidation product and benzaldehyde a stable intermediate. Anatase P11t photoactivity was similar to that observed for commercial photocatalysts, while anatase P11h presented a marked improvement. The FTIR study on these samples indicate that P11h has a higher number of hydrogen-bonded hydroxyl groups that are more stable under RT outgassing than P11t. The higher photoactivity of P11h is attributed to the participation of these hydrogen-bonded hydroxyls in the toluene conversion to CO2. FTIR spectra also suggest that benzaldehyde, the minor oxidation product, originates from toluene adsorbed on isolated hydroxyls. Benzaldehyde is more strongly adsorbed on P11h than on P11t; the presence of water vapor in the reacting mixture, however, facilitates its desorption and/or photooxidation. (C) 2001 Academic Press.
引用
收藏
页码:413 / 420
页数:8
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