Characteristics and Photocatalytic Activity of TiO2 Films Immobilized on Ceramic, Glass and Stainless Steel

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To study the effects of substrate materials on the photocatalytic activity, TiO2 films were immobilized on the inner wall surface of ceramic, glass and stainless steel tubes by sol-gel method. X-ray diffraction (XRD) results indicated that the crystal form of TiO2 were all anatase type with theoretical particle size of 15 nm. According to the X-ray photoelectron spectroscopy (XPS) results, appearance of the element Na was observed which would decrease the photocatalytic activity. Scanning electron microscope (SEM) photos showed that the film coating on the ceramic and glass were even and uniform with thickness of about 300 nm and practical particle size of 20 nm to 100 nm. However, the film coating on stainless steel was hackly which would lead to diffraction of lights. The degradation rate constants of methylene blue (MB) with initial concentration of 5 mg.L-1 were 0.049 min-1、0.029 min-1 and 0.023 min-1 with films coating on ceramic, stainless steel and glass tubes respectively. Degraded with TiO2 film coating on ceramic tube, the according rate constants of phenol were 0.37, 0.14, 0.04 and 0.02 min-1 for initial concentration of 2, 10, 50 and 100 mg.L-1 respectively.

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413-417

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February 2013

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] A. A. Ismail: Microporous and Mesoporous Materials 149(2011), 69-75.

Google Scholar

[2] C. Ma, W. Dong, L. Fang, et al: Thin Solid Films 520(2012), 5727-5732.

Google Scholar

[3] M. Kazemi, M.R. Mohammadizadeh: Chem. Eng. Res. Design. 90(2012), 1473-1479.

Google Scholar

[4] R.Q. Cabrera, E.R. Latimer, A. Kafizas, et al: J. Photochemistry & Photobiology, A: Chemistry 239(2012), 60-64.

Google Scholar

[5] İ. Tatlıdil, E. Bacaksız, C.K. Buruk, et al.: J. Alloys and Compounds 517( 2012), 80-86.

Google Scholar

[6] M. Pelaez, P. Falaras, A.G. Kontos, et al.: Applied Catalysis B, Environmental 121-122(2012), 30.

Google Scholar

[7] I. Stambolova, М. Shipochka, V. Blaskov, et al: J. Photochemistry & Photobiology, B: Biology 117(2012), 19-26.

DOI: 10.1016/j.jphotobiol.2012.08.006

Google Scholar

[8] W.H. Ching, L. Michael, Y.C.L. Dennis: Solar Energy 77(2004), 129.

Google Scholar

[9] S.B. Kim, S.C. Hong: Applied Catalysis B: Environmental 35(2002), 305.

Google Scholar

[10] L. Zhang, K. Tatsuo, S. Noriaki, et al: Separation and Purification Technology 31(2003), 105.

Google Scholar

[11] J. Shang, W. Li, Y. Zhu: J. Molecular Catalysis A: Chemical 202(2003), 187.

Google Scholar

[12] M. Langlet, A. Kim, M. Audier, et al: Thin Solid Films 429(2003), 13.

Google Scholar

[13] T. Watanabe, A. Nakajima, R. Wang, et al: Thin Solid Films 351(1999), 260.

Google Scholar

[14] E. Aubry, J. Lambert, V. Demange, et al: Surface & Coatings Technology 206(2012), 4999.

Google Scholar

[15] A. Panniello, M.L. Curri, D. Diso, et al: Applied Catalysis B, Environmental 121 (2012), 190.

Google Scholar

[16] C.G. Kuo, C.Y. Hsu, S.S. Wang, et al: Applied Surface Science 258(2012), 6952.

Google Scholar

[17] S. Zhang, L. Chen, H. Liu, et al: Chemical Engineering Journal 200-202(2012), 300.

Google Scholar

[18] Z. Yang, S. Gao, H. Li, et al: J. Colloid and Interface Science 375(2012), 172.

Google Scholar

[19] A. Fernandez, G. Lassaletta, V. M. Jimenez, et al: Applied Catalysis B: Environmental 7(1995), 49.

Google Scholar

[20] C. He, Y. Yu, X. Hu, et al: Applied Surface Science 200(2002), 239.

Google Scholar

[21] I. Yumi, I. Hideaki, K. Takuya, et al: Chemosphere 53(2003), 1193.

Google Scholar

[22] J. Yu, X. Zhao, Q. Zhao: Thin Solid Films 379(2000), 7.

Google Scholar