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KINETICS OF CATALYTIC STAGES FOR METHANE AROMATIZATION OVER Mo/HMCM-22 CATALYST

机译:Mo / HMCM-22催化剂甲烷芳族化催化阶段的动力学

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摘要

Rapid development of the world economy and increase of the international oil price urge to diversify energy sources. Gas-To-Liquids (GTL) processes for the production of clean fuels and chemical intermediates are becoming increasingly important and, at present, receive extensive attention. Compared to coal and biomass, natural gas is the favorable feedstock for GTL processes [1]. In addition to Fischer-Tropsch, methanol and dimethyl ether syntheses, non-oxidative methane aromatization presents an interesting possible route for direct conversion of methane/natural gas to liquids [2]. Due to its endothermic nature, the non-catalytic direct pyrolysis of methane requires temperatures exceeding 1400 K and, hence, the total dissociation of methane into carbon and hydrogen becomes unavoidable [3]. Oxidative aromatization of methane is thermodynamically feasible (exothermic process) with C2 selectivity amounting to 60% at 20% methane conversion, at 998 K [4].
机译:世界经济的快速发展和国际油价增加促使能源多样化。用于生产清洁燃料和化学中间体的燃气液(GTL)工艺变得越来越重要,目前受到广泛的关注。与煤和生物质相比,天然气是GTL工艺的有利原料[1]。除了离豆荚,甲醇和二甲醚合成之外,非氧化甲烷芳族化呈一种有趣的可能途径,用于将甲烷/天然气直接转化为液体[2]。由于其吸热性质,甲烷的非催化直接热解因此需要超过1400k的温度,因此,甲烷将甲烷与碳和氢的总解离变为不可避免的[3]。甲烷的氧化芳族化是热动力学可行的(放热过程),C2选择性在20%甲烷转化下的60%,在998k [4]。

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