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Received February 25, 2008
Accepted August 9, 2008
- 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 CuO-CeO2-Al2O3 catalyst with mesopore structure for water gas shift reaction
Jun-Keun Kim
Younghun Kim
Joo-Won Park
Jong-Soo Bae
Do-Young Yoon
Jae-Goo Lee1
Jae-Ho Kim1
Choon Han†
Department of Chemical Engineering, Kwangwoon University, Seoul 139-701, Korea 1Climate Change Technology Research Division, Korea Institute of Energy Research, Daejeon 305-343, Korea
chan@kw.ac.kr
Korean Journal of Chemical Engineering, January 2009, 26(1), 32-35(4), 10.1007/s11814-009-0006-0
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Abstract
The water gas shift (WGS) reaction has been investigated widely in fuel cell technologies due to the potential for high fuel efficiency and lower emissions during the production of pure hydrogen. Industrially, the WGS reaction occurs in one of the following two ways: (a) high-temperature in the range of 310-450 ℃ with Fe-Cr catalyst, (b) lowtemperature in the range of 210-250 ℃ with Cu-ZnO-Al2O3. In this study, a mesoporous catalyst was prepared, with a large surface area and uniformity in both pore size and distribution, by using a one-pot synthesis method. The prepared CuO-CeO2-Al2O3 brought high CO conversion (82%), and was suitable for WGS reaction at low temperature (250 ℃).
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Gorte RJ, Zhao S, Catal. Today, 104(1), 18 (2005)
Kim Y, Kim P, Kim C, Yi J, J. Mater. Chem., 13, 2353 (2003)
Kim Y, Kim C, Kim P, Yi J, J. Non-Cryst. Solids, 351, 550 (2005)
Sobczak I, Goscianska J, Ziolek M, Grams J, Verrier C, Bazin P, Marie O, Daturi M, Catal. Today, 114(2-3), 281 (2006)
Kim P, Joo JB, Kim H, Kim W, Kim Y, Song IK, Yi J, Catal. Lett., 104(3-4), 181 (2005)
Neuville DR, Cormier L, Montouillout V, Massiot D, J. Non-Cryst. Solids, 353, 180 (2007)
Bore MT, Pham HN, Ward TL, Datye AK, Chem. Commun., 22, 2620 (2004)