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Oxidative steam reforming of ethanol over Rh catalyst supported on Ce1-xLaxOy (x=0.3) solid solution prepared by urea co-precipitation method

机译:尿素共沉淀法制备的负载于Ce1-xLaxOy(x = 0.3)固溶体上的Rh催化剂上的乙醇氧化蒸汽重整

摘要

A Ce1-xLaxOy solid solution (CL) is prepared by a co-precipitation method using urea as a precipitant, with varying urea/metal molar ratio (N). The supported rhodium catalysts are then prepared by an impregnation method for use in hydrogen production from oxidative steam reforming (OSR) of ethanol. X-ray diffraction and Raman spectra results confirm the formation of CL, and the crystal structures of these catalysts are not very sensitive to the urea/metal molar ratios (N = 5-15). However, the surface area and reducibility of the Rh/CL-N catalysts decrease monotonically with increasing N. During the OSR process, a similar tendency is also observed for ethanol conversion and hydrogen selectivity. Among the catalysts tested, Rh/CL-5 shows the best catalytic performance, achieving >97% ethanol conversion at 300 degrees C with H-2 yield rate of 210 mu mol g-cat(-1) s(-1). At 450 degrees C, its hydrogen selectivity reaches 117%, with no observable change after 72 h aging. (C) 2013 Elsevier B.V. All rights reserved.
机译:通过共沉淀法,使用尿素作为沉淀剂,通过改变尿素/金属摩尔比(N),制备Ce1-xLaxOy固溶体(CL)。然后通过浸渍方法制备负载的铑催化剂,以用于由乙醇的氧化蒸汽重整(OSR)生产氢气。 X射线衍射和拉曼光谱结果证实了CL的形成,并且这些催化剂的晶体结构对脲/金属摩尔比(N = 5-15)不是很敏感。然而,Rh / CL-N催化剂的表面积和还原性随N的增加而单调降低。在OSR过程中,乙醇转化率和氢选择性也观察到类似趋势。在所测试的催化剂中,Rh / CL-5表现出最佳的催化性能,在300摄氏度下H>产率为210μmol g-cat(-1)s(-1)时,乙醇转化率> 97%。在450摄氏度下,其氢选择性达到117%,老化72小时后没有观察到变化。 (C)2013 Elsevier B.V.保留所有权利。

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