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Received September 25, 2012
Accepted November 23, 2012
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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Low-temperature CO oxidation over water tolerant Pt catalyst supported on Al-modified CeO2

Department of Chemical Engineering, Chungbuk National University, Cheongju, Chungbuk 361-763, Korea 1Green Chemistry Division, Korea Research Institute of Chemical Technology, Yuseong, Daejeon 305-600, Korea 2R&D Center, Heesung Catalysts Corp., 507-1Da, Jungwang-Dong, Shiheung-City, Gyeonggi-do 429-450, Korea
chshin@chungbuk.ac.kr
Korean Journal of Chemical Engineering, March 2013, 30(3), 598-604(7), 10.1007/s11814-012-0207-9
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Abstract

A series of xAl-(1-x)Ce oxides (x=0-0.20) were prepared as supports by the coprecipitation method. 1 wt% Pt was impregnated on the Al-modified Ce oxide supports, which were tested as catalysts for CO oxidation in the absence and presence of H2O vapor. The prepared catalysts were characterized by X-ray diffraction (XRD), N2 sorption, CO temperature-programmed reduction (CO-TPR), 27Al magic-angle spinning (MAS) NMR, and CO-chemisorption analyses._x000D_ Upon comparison of the catalytic results obtained from the 1 wt% Pt/xAl-(1-x)Ce oxide catalysts, the Pt/0.10Al-0.90Ce oxide catalyst was found to exhibit the highest catalytic activity. When water vapor was present in the feed stream, the catalytic activity increased remarkably, and T90% shifted to a temperature ca. 30 ℃ lower compared to that in dry conditions due to the promotion effect by the water-gas shift reaction. The catalytic activity could be correlated with the Pt dispersion and the amount of surface or lattice oxygen.

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