CO在过量H2中优于CeO2/CuO催化剂的优先氧化:煅烧温度的影响

Zhiming Gao , Ming Zhou , Hao Deng , Yong Yue
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引用次数: 12

摘要

与经典构型CuO/CeO2催化剂不同,采用浸渍法制备了反构型CeO2/CuO催化剂(Ce/Cu原子比= 10/100)。选择了5种煅烧温度,考察了CeO2与CuO载体的相互作用。结果表明,随着煅烧温度从500℃升高到900℃,CeO2颗粒在载体上发生烧结,部分Ce4+离子扩散到CuO晶体中,形成固溶体。TPR测量表明界面络合物Ce-O-Cu的形成。在700℃下煅烧的催化剂在过量H2流中优先氧化CO的活性最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preferential oxidation of CO in excess H2 over CeO2/CuO catalyst: Effect of calcination temperature

Different from the classical configuration CuO/CeO2 catalyst, the inverse configuration CeO2/CuO catalyst (atomic ratio of Ce/Cu = 10/100) was prepared by impregnation method. Five calcination temperatures were selected to investigate the interaction between CeO2 and CuO support. It is found that as calcination temperature increased from 500 to 900°C, sintering of CeO2 particles on the support occurred together with the diffusion of a portion of Ce4+ ions into CuO crystals, forming solid solution. Formation of interface complex Ce-O-Cu was suggested by TPR measurements. The catalyst calcined at 700°C gives the highest activity for preferential oxidation of CO in excess H2 stream.

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来源期刊
Journal of Natural Gas Chemistry
Journal of Natural Gas Chemistry 化学-工程:化工
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