Preparation of Novel TiO2-Silica Filter Photocatalyst Derived from Titanium Alkoxy-Diolate Precursor

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Commercially available TiO2 (Degussa, P-25) is well-known as a highly active photocatalyst. However, in order to work as a photocatalyst, TiO2 must be dispersed onto a substrate without any binders but this still remains very difficult. We thus attempted to develop a novel TiO2 system with high photocatalytic activity. TiO2 anchored silica fibers (TAS) were prepared by chemical vapor deposition using titanium (IV) ethoxide and 1,3-butanediol. The content of TiO2 in TAS was varied from 0.5 to 5 mass%. It was observed that the surface of TAS was covered with anatase TiO2 particles 5-10 nm in diameter. TAS shows higher activity at a lower loading amount compared to P-25. Measurement of the acetaldehyde decomposition rate constant of P-25 and TAS carrying 2 mass% of titanium oxide under ultraviolet irradiation showed a value for TAS that was 1.4 times that of P-25. TAS showed a solid acidity amount higher than the P-25 in NH3-TPD measurements. It was considered that some Si species from the silica fibers migrated into the TiO2 layer by calcination, increasing the solid acidity of TAS. As a result, the adsorption of acetaldehyde increased, and the photocatalyst activity improved.

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191-194

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June 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] A. Hasegawa, S. Yanagiya, T. Kudo, T. Akazawa, N. Kakuta, J. Ceram. Soc. Jpn. 115 (2007) 59-64.

Google Scholar

[2] T. Kudo, Y. Nakamura, A. Ruike, A. Hasegawa, Topics in Catalysis 35 (2005) 225-229.

Google Scholar

[3] L. Saadouna, J. A. Ayllón, J. Jiménez-Becerrilb, J. Peral, X. Domènechb, R. Rodríguez-Clemente, Applied Catal. B: Environmental 21 (1999) 269-277.

Google Scholar

[4] A. Hasegawa, T. Yamagishi, T. Akazawa, N. Kakuta, J. Soc. Inorg. Mat. Jpn. 16 (2009) 37-43.

Google Scholar

[5] Y. Arai, K. Tanaka, A. L. Khlaifat, J. Mol. Catal. A: Chem. 243 (2006) 85–88.

Google Scholar

[6] M. S. Vohra, K. Tanaka, Environ. Sci. Technol. 35 (2001) 411-415.

Google Scholar