镓促进的H-ZSM-5催化剂上乙烷的芳构化反应

Philippe Schulz, Manfred Baerns *
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引用次数: 49

摘要

在不同Si/Al比(15、25、34、50、75和95)和镓含量(1.5 ~ 6 wt -%)的镓促进H-ZSM-5催化剂上,乙烷部分转化为芳烃。温度在823 ~ 973 K之间变化;乙烷分压为80kpa。在873 K(乙烷转化率28.2%,W/F= 19.2 g h mol - 1)条件下,镓(3.1 wt.-%)/ zsm5 (Si/Al = 15)催化剂的最大芳烃选择性为57%。催化剂的制备方法(初湿浸渍或离子交换)对催化剂的活性和选择性没有影响。动力学测量表明,乙烷被沸石外表面的Ga203和H-ZSM-5催化剂的酸中心脱氢生成乙烯;在随后的步骤中,乙烯在沸石的通道中被低聚和环化。芳香烃是进一步脱氢后形成的。主要是苯、甲苯和二甲苯。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aromatization of ethane over gallium-promoted H-ZSM-5 catalysts

Ethane was partly converted to aromatics over gallium-promoted H-ZSM-5 catalysts having different Si/Al ratios (15,25,34,50,75 and 95) and gallium contents ranging from 1.5 to 6 wt.-%. Temperatures varied between 823 and 973 K; the ethane partial pressure was 80 kPa. A maximum aromatics selectivity of 57% was obtained for a gallium (3.1 wt.-% )/ZSM 5 (Si/Al = 15) catalyst at 873 K (ethane conversion: 28.2%;W/F= 19.2 g h mol−1). The method of catalyst preparation (incipient wetness impregnation or ion exchange) had no influence on catalyst activity and selectivity. Kinetic measurements indicated that ethane is dehydrogenated by both Ga203 at the outside surface of the zeolite and by the acid centres of the H-ZSM-5 catalysts to ethylene; in a subsequent step the ethylene is oligomerized and cyclized in the channels of the zeolite. Aromatic hydrocarbons are formed after further dehydrogenation. Mainly benzene, toluene and xylenes were obtained.

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