负载型镍和铂催化剂上环己烷和环己烯的脱氢反应

Khaliq Ahmed , Hasan M. Chowdhury
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引用次数: 18

摘要

比较了实验室制备的两种镍催化剂和一种商用铂催化剂在环己烷和环己烯脱氢制苯过程中的活性。在300°C时,15%镍铝催化剂与商用铂催化剂相比具有优势;在200-340°C的较低温度和较高温度范围内,铂催化剂更有效。20%镍的催化剂在研究范围内的所有温度下都比较不利。结果表明,吸附苯的取向不仅与镍催化剂中金属的分散有关,还与温度有关。在环己烯脱氢过程中,有一小部分发生歧化,歧化的程度与催化剂和温度有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dehydrogenation of cyclohexane and cyclohexene over supported nickel and platinum catalysts

The activities of two nickel catalysts prepared in our laboratory and of a commercial platinum catalyst were compared for benzene formation by dehydrogenation of cyclohexane and cyclohexene. A 15% nickel on alumina catalyst compares favourably with the commercial platinum catalyst at 300 °C; at lower as well as higher temperatures in the range 200–340 °C, the platinum catalyst is more effective. A 20% nickel catalyst compares unfavourably at all temperatures in the range studied. Results indicate that the orientation of adsorbed benzene depends on the dispersion of metal in the nickel catalyst and also on the temperature. During dehydrogenation of cyclohexene a small fraction was disproportionating, the extent of which was found to depend on the catalyst and the temperature.

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