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首页> 外文期刊>American Chemical Society, Division of Fuel Chemistry, Preprints >KINETICS OF CATALYTIC STAGES FOR METHANE AROMATIZATION OVER Mo/HMCM-22 CATALYST
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KINETICS OF CATALYTIC STAGES FOR METHANE AROMATIZATION OVER Mo/HMCM-22 CATALYST

机译:Mo / HMCM-22催化剂上甲烷芳构化反应的动力学

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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 methaneatural 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:世界经济的飞速发展和国际油价的上涨促使能源多样化。用于生产清洁燃料和化学中间体的气液分离(GTL)工艺正变得越来越重要,目前受到广泛关注。与煤炭和生物质相比,天然气是GTL工艺的有利原料[1]。除了费-托合成甲醇和二甲醚外,非氧化甲烷芳构化还提供了一种有趣的可能途径,可将甲烷/天然气直接转化为液体[2]。由于其吸热性,甲烷的非催化直接热解需要超过1400 K的温度,因此,甲烷完全分解为碳和氢变得不可避免[3]。甲烷的氧化芳构化在热力学上是可行的(放热过程),在998 K时,甲烷转化率为20%时C2的选择性达到60%[4]。

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