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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 March 30, 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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Degradation of Chlorophenol by Photocatalysts with Various Transition Metals

Dept. of Environ. Eng., Pukyong National University, Busan 608-737, Korea
leejk@pknu.ac.kr
Korean Journal of Chemical Engineering, May 2005, 22(3), 382-386(5), 10.1007/BF02719415
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Abstract

In this research, the photocatalytic degradation of 4-chlorophenol (4-CP) in TiO2 aqueous suspension was studied. TiO2 photocatalysts were prepared by sol-gel method. The dominant anatase-structure on TiO2 particles was observed after calcining the TiO2 gel at 500 ℃ for 1 hr. Photocatalysts with various transition metals (Fe, Cu, Nd, Pd and Pt) loading were tested to evaluate the effect of transition metal impurities on photodegradation. The photocatalytic degradation in most cases follows first-order kinetics. The maximum photodegradation efficiency was obtained with TiO2 dosage of 0.4 g/L, retention time of 1 min and air flow rate of 2,500 cc/min. The photodegradation efficiency with Pt-TiO2 or Pd-TiO2 is higher than pure TiO2 powder. The optimal content value of Pt and Pd is 2 wt%. However, the photodegradation efficiency with Fe(1.0 wt%)-TiO2 and Cu(1.0 wt%)-TiO2 is lower than pure TiO2 powder.

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