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Low temperature CO2 hydrogenation to alcohols and hydrocarbons over Mo2C supported metal catalysts

机译:Mo2C负载的金属催化剂上的低温CO2加氢生成醇和烃

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A series of M/Mo2C (M = Cu, Pd, Co and Fe) were synthesized and evaluated for CO2 hydrogenation at 135-200 degrees C in liquid 1,4-dioxane solvent. The Mo2C served as both a support and a co-catalyst for CO2 hydrogenation, exhibiting turnover frequencies of 0.6 x 10(-4) and 20 x 10(-4) s(-1) at 135 and 200 degrees C, respectively. Methanol was the major product at 135 degrees C, while CH3OH, C2H5OH, and C2+ hydrocarbons were produced at 200 degrees C. The addition of Cu and Pd onto the high surface area Mo2C enhanced the production of CH3OH, while Co and Fe enhanced the production of C2+ hydrocarbons. Results for CO2, CO, and CH3OH hydrogenation experiments suggested that CO2 was the primary source for CH3OH while CO was the intermediate to hydrocarbons during CO2 hydrogenation. Characterization of the spent M/Mo2C catalysts revealed very little change in the surface and bulk chemistries and structures, indicating their stability in the liquid environment. (C) 2016 Elsevier Inc. All rights reserved.
机译:合成了一系列M / Mo2C(M = Cu,Pd,Co和Fe),并在液态1,4-二恶烷溶剂中在135-200摄氏度下评估了CO2加氢。 Mo2C既用作CO2加氢的载体,又用作助催化剂,在135和200摄氏度时分别显示0.6 x 10(-4)和20 x 10(-4)s(-1)的转换频率。甲醇是135摄氏度下的主要产物,而CH3OH,C2H5OH和C2 +碳氢化合物是在200摄氏度下产生的。在高表面积Mo2C中添加Cu和Pd可以提高CH3OH的产量,而Co和Fe可以提高产量。 C2 +碳氢化合物。 CO2,CO和CH3OH加氢实验的结果表明,CO2是CH3OH的主要来源,而CO是CO2加氢过程中碳氢化合物的中间体。废M / Mo2C催化剂的表征表明,表面和本体化学与结构变化很小,表明它们在液体环境中的稳定性。 (C)2016 Elsevier Inc.保留所有权利。

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