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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Ethanol steam reforming over Rh/CexZr1-xO2 catalysts: Impact of the CO-CO2-CH4 interconversion reactions on the H-2 production
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Ethanol steam reforming over Rh/CexZr1-xO2 catalysts: Impact of the CO-CO2-CH4 interconversion reactions on the H-2 production

机译:Rh / CexZr1-xO2催化剂上的乙醇蒸汽重整:CO-CO2-CH4相互转化反应对H-2产生的影响

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CexZr1-xO2 mixed oxide-supported 1 wt.%Rh catalysts were prepared by wet impregnation using Rh nitrate as a precursor and calcined at 900 degrees C. They were characterized by BET surface area, XRD, CO2 chemisorption and H-2 chemisorption at -85 degrees C and tested in the ethanol steam reforming at 600 degrees C under atmospheric pressure, with water to ethanol molar ratio equal to 4, without carrier gas. The best performances, i.e. the highest hydrogen yield and the lowest coke deposition, were obtained over Rh/Ce0.5Zr0.5O2, i.e. 3.63 mol H-2/mol(ethanol). This catalyst was subsequently evaluated under various reaction conditions. Whatever the temperature and the water to ethanol ratio, the ethanol steam reforming yielded a large amount of methane, which tends to reduce the H2 production. To elucidate the origin of the methane production, CO/CO2/CH4 interconversion reactions were studied. It was shown that such catalyst favours the formation of methane via CO hydrogenation. The direct hydrogenation of CO2 was not observed. In parallel, the catalyst was active in the reverse water gas shift (RWGS) reaction between CO2 and H2, leading CO and H2O. (C) 2007 Elsevier B.V. All rights reserved.
机译:以硝酸铑为前体,通过湿法浸渍法制备了CexZr1-xO2混合氧化物负载的1 wt。%Rh催化剂,并在900摄氏度下煅烧。它们的特征在于BET表面积,XRD,CO2化学吸附和H-2在-的化学吸附85摄氏度,并在大气压下于600摄氏度的乙醇蒸汽重整中进行测试,水与乙醇的摩尔比等于4,无载气。在Rh / Ce0.5Zr0.5O2上获得了最好的性能,即最高的氢气产率和最低的焦炭沉积,即3.63 mol H-2 / mol(乙醇)。随后在各种反应条件下评估该催化剂。无论温度和水与乙醇的比例如何,乙醇蒸汽重整都会产生大量的甲烷,这往往会降低H2的产生。为了阐明甲烷产生的起源,研究了CO / CO2 / CH4相互转化反应。结果表明,这种催化剂有利于通过CO加氢形成甲烷。没有观察到CO 2的直接氢化。同时,该催化剂在CO2和H2之间的逆水煤气变换(RWGS)反应中具有活性,导致CO和H2O提前。 (C)2007 Elsevier B.V.保留所有权利。

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