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Photocatalytic properties of rutile TiO2 acicular particles in aqueous 4-chlorophenol solution

Published online by Cambridge University Press:  31 January 2011

Sun-Jae Kim
Affiliation:
Sejong Advanced Institute of Nano Technologies, Sejong University, Seoul 143–747, Korea
Jong-Kuk Lee
Affiliation:
Department of Materials Engineering, Chosun University, KwangJu 501–759, Korea
Eun Gu Lee
Affiliation:
Department of Materials Engineering, Chosun University, KwangJu 501–759, Korea
Hee-Gyoun Lee
Affiliation:
IGC-SuperPower, 450 Duane Avenue, Schenectady, New York 12304
Seon-Jin Kim
Affiliation:
Division of Materials Science and Engineering, Hanyang University, Seoul 133–791, Korea
Kyoung Sub Lee
Affiliation:
Division of Materials Science and Engineering, Hanyang University, Seoul 133–791, Korea
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Abstract

The photocatalytic properties of TiO2 rutile powder with acicular primary particles were characterized using the photocatalytic reaction in aqueous 4-chlorophenol (4CP) solution and compared to those of TiO2 anatase with almost the same surface area of approximately 200 m2g. The characteristics of commercial P-25 TiO2 powders with the surface area of approximately 55 m2/g were also compared to rutile and anatase powders. The rutile phase powders surpassed both anatase and P-25 ones in decomposition rate for 4CP. The excellent photo-oxidative ability of the powder was dependent on the specific powder-preparation method, which led to a direct crystallization in aqueous solution, regardless of the crystalline structures of the powders.

Type
Articles
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1.Kim, S.J., Park, S.D., Jeon, C.J., Cho, Y.H., Rhee, C.K., Kim, W.W, and Lee, E.G., J. Sol-Gel Sci. Technol. 22, 63 (2001).CrossRefGoogle Scholar
2.Kim, S.J., Park, S.D., Jeong, Y.H., and Park, S., J. Am. Ceram. Soc. 82, 927 (1999).CrossRefGoogle Scholar
3.Kasuga, T., Hiramatsu, M., Hoson, A., Sekino, T., and Niihara, K., Adv. Mater. 11, 1307 (1999).3.0.CO;2-H>CrossRefGoogle Scholar
4.Seo, D-S., Lee, J-K., and Kim, H.K., J. Korean Ceram. Soc. 37, 700 (2001).Google Scholar
5.Chen, D. and Ray, A.K., Appl. Catal., B 23, 143 (1999).CrossRefGoogle Scholar
6.Li, X., Cubbage, J.W., Tetzlaff, T.A., and Jenks, W.S., J. Org. Chem. 63, 8509 (1999).CrossRefGoogle Scholar
7.Rodriguez, J., Gomez, M., Lindquist, S-E., Granqvist, C.G., Thin Solid Films 360, 250 (2000).CrossRefGoogle Scholar
8.Pandiyan, T., Rivas, O. Martinez, Martinez, J. Orozco, Amezcua, G. Burillo, and Carrillo, M.A. Martinez, J. Photochem. Photobiol., A 146, 149 (2002).Google Scholar