Low-temperature CO oxidation over water tolerant Pt catalyst supported on Al-modified CeO2

被引:8
|
作者
Park, Jung-Hyun [1 ]
Cho, Jun Hee [1 ]
Kang, Sung Eun [1 ]
Cho, Kyung Ho [2 ]
Lee, Tae Woo [3 ]
Han, Hyun Sik [3 ]
Shin, Chae-Ho [1 ]
机构
[1] Chungbuk Natl Univ, Dept Chem Engn, Chonju 361763, Chungbuk, South Korea
[2] Korea Res Inst Chem Technol, Green Chem Div, Taejon 305600, South Korea
[3] Heesung Catalysts Corp, R&D Ctr, Shiheung City 429450, Gyeonggi Do, South Korea
关键词
Platinum; Al Modified CeO2; CO Oxidation; CO-TPR; Al-27 MAS NMR; GAS SHIFT REACTION; FUEL-CELL APPLICATIONS; CARBON-MONOXIDE; PERFORMANCE; METHANOL; OXIDES; NMR; DEPOSITION; AL-27; H-2;
D O I
10.1007/s11814-012-0207-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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), N-2 sorption, CO temperature-programmed reduction (CO-TPR), Al-27 magic-angle spinning (MAS) NMR, and CO-chemisorption analyses. 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 T-90% shifted to a temperature ca. 30 degrees C 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.
引用
收藏
页码:598 / 604
页数:7
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