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

机译:用于在氢气存在下优先氧化一氧化碳的贵金属催化剂(PROX)

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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.
机译:在50至300摄氏度的温度范围内,在一氧化碳(PROX)反应的优先氧化中测试了氧化物负载的贵金属催化剂。评估了贵金属性质(Pt,Ir,Pd),载体物理和化学性质(氧化还原,酸度,碱度)和反应条件(氧化学计量)对催化剂活性和选择性的影响。与钯相比,铂和铱在整个温度范围内被证明是最具活性和选择性的催化剂。此外,负载在二氧化铈基氧化物上的贵金属显示出活性和选择性,尤其是在低温下。另外,观察到氧化物中二氧化铈中的摩尔分数越高,PROX反应中的活性和选择性越高。氧化铈在氧化物表面的氧迁移率最高,被证明是最好的载体。因此,在简单的氧化物(CeO2,SiO2-Al2O3,Al2O3,SiO2,La2O3和MgO)上,在其他地方确定的与载体的碱度密切相关的载体表面氧原子的诱导迁移率显示为PROX反应中催化剂性能的一个关键参数。最后,在高温和过量氧气的情况下,水的形成(氢氧化)被证明是通过水煤气变换反应(WGSR)将CO转化为CO2的催化剂活性增加的原因。 (C)2004 Elsevier B.V.保留所有权利。

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