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In relation to this article, we declare that there is no conflict of interest.
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Received December 21, 2004
Accepted April 4, 2005
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Preparation of Nanosized TiO2 Particles via Ultrasonic Irradiation and Their Photocatalytic Activity on the Decomposition of 4-Nitrophenol

Division of Applied Chemical Engineering, Pukyong National University, 100 Yongdang-dong, Nam-gu, Busan 608-739, Korea
sshong@pknu.ac.kr
Korean Journal of Chemical Engineering, July 2005, 22(4), 547-551(5), 10.1007/BF02706640
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Abstract

TiO2 nanoparticles were prepared by hydrolysis of TTIP (titanium tetraisopropoxide) using an ultrasonication technique coupled with a sol-gel method. The physical properties of nanosized TiO2 were investigated. The photocatalytic degradation of 4-nitrophenol was studied by using a batch reactor in the presence of UV light. The crystallite size of the anatase phase is increased with an increase of REtOH ratio (EtOH/H2O molar ratio). The particles’ crystallite size prepared with and without ultrasonic irradiation is marginally different. Those particles prepared with ultrasonic irradiation show a higher activity on the photocatalytic decomposition of 4-nitrophenol compared to those prepared without ultrasonic irradiation. The photocatalytic activity decreases with an increase of REtOH ratio. In addition, the photocatalytic activity shows the highest value on the titania particle calcined at 500 ℃.

References

Alivisatos AP, MRS Bull., 23 (1995)
Augugliaro V, Palmisano L, Schiavello M, Sclafani A, Appl. Catal., 69, 323 (1991) 
Awate SV, Waghmode SB, Patil KR, Agashe MS, Joshi PN, Korean J. Chem. Eng., 18(2), 257 (2001)
Cao X, Koltypin Y, Prozorov R, Kataby G, Gedanken A, J. Mater. Chem., 7, 2447 (1997) 
Cullity BD, Elements of X-Ray Diffraction, 2nd edn., p. 102, Addison-Wesley, Reading, MA (1978)
Fujishima A, Hashimoto K, Watanabe T, TiO2 Photocatalysis, p. 124, Inc., Tokyo (1999)
Hong SS, Lee MS, Lee GD, React. Kinet. Catal. Lett., 80, 145 (2003) 
Hong SS, Ju CS, Lim CG, Ahn BH, Lim KT, Lee GD, J. Ind. Eng. Chem., 7(2), 99 (2001) 
Hyeon TH, Fang MM, Suslick KS, J. Am. Chem. Soc., 118(23), 5492 (1996) 
Jung KY, Park SB, Appl. Catal. B: Environ., 25(4), 249 (2000) 
Jung SC, Imaishi N, Korean J. Chem. Eng., 18(6), 867 (2001)
Lim KT, Hwang HS, Lee MS, Lee GD, Hong SS, Johnston KP, Chem. Commun., 14, 1528 (2002) 
Suryanyana C, Froes FH, Metall. Trans., 23A, 1071 (1992)
Turchi CS, Ollis DF, J. Catal., 122, 178 (1990) 
Ward DA, Ho EI, Ind. Eng. Chem. Res., 34(2), 421 (1995) 
Wold A, Chem. Mater., 5, 280 (1993) 
Yang J, Mei S, Ferreira JMF, Mater. Sci. & Eng. C, 15, 183 (2001) 
Yu JG, Yu JC, Ho WK, Leung MKP, Cheng B, Zhang GK, Zhao XJ, Appl. Catal. A: Gen., 255(2), 309 (2003) 

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