Noble metal catalysts for the preferential oxidation of carbon monoxide in the presence of hydrogen (PROX)

被引:240
作者
Mariño, F
Descorme, C
Duprez, D
机构
[1] Univ Poitiers, CNRS, UMR 6503, LACCO, F-86022 Poitiers, France
[2] Univ Buenos Aires, FIUBA, DIQ, Lab Proc Catalit, RA-1428 Buenos Aires, DF, Argentina
[3] Inst Rech Catalyse, CNRS, F-69626 Villeurbanne, France
关键词
preferential oxidation of CO; PROX; hydrogen purification; noble metals; platinum; iridium; palladium; supported catalysts; acido-basicity; redox; oxygen mobility; fuel cells; WGSR;
D O I
10.1016/j.apcatb.2004.06.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oxide-supported noble metal catalysts were tested in the preferential oxidation of carbon monoxide (PROX) reaction in the temperature range between 50 and 300degreesC. Both the influence of the noble metal nature (Pt, Ir, Pd), the support physical and chemical properties (redox, acidity, basicity) and the reaction conditions (oxygen stoichiometry) on the catalyst activity and selectivity was evaluated. Platinum and iridium were shown to be the most active and selective catalysts in the whole temperature range compared with palladium. Furthermore, noble metals supported over ceria-based oxides were shown to be active and selective, especially at low temperature. Additionally, it was observed that the higher the molar fraction in ceria in the oxide, the higher the activity and the selectivity in the PROX reaction. Ceria, with the highest oxygen mobility at the oxide surface, was shown to be the best support. Accordingly, on simple oxides (CeO2, SiO2-Al2O3, Al2O3, SiO2, La2O3 and MgO), the induced mobility of the oxygen atoms at the surface of the support determined elsewhere, well correlated with the basicity of the support, was shown to be one key parameter for the performances of the catalysts in the PROX reaction. Finally, the formation of water (hydrogen oxidation) at high temperature and high oxygen excess was shown to be responsible for the increasing activity of the catalysts in the conversion Of CO to CO2 via the water gas shift reaction (WGSR). (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 66
页数:8
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