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A mechanistic basis for the effects of Mn loading on C2+ oxygenates synthesis directly from syngas over Rh-MnOx/SiO2 catalysts

机译:Mn负载对Rh-MnOx / SiO2催化剂上合成气直接由合成气合成C2 +含氧化合物影响的机理基础

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Kinetics of the synthesis of C2+ oxygenates directly from syngas was investigated over a series of Rh-MnOx/SiO2 catalysts (atomic ratio of Mn/Rh=0, 0.5 and 5.0). It was evidenced that the activation energies for C2+ oxygenates changed little when introducing MnOx while the apparent activation energies for hydrocarbons, especially methane, increased remarkably. Kinetic parameters indicate that the formation of hydrocarbons can be suppressed in the presence of MnOx. In the meantime, the reaction orders with respect to different products were also altered with the variation of MnOx, loadings. In accordance with in situ DRIFTS, we found that two new active sites on Rh surfaces resulting from the Rh-MnOx interaction might be responsible for the enhancement of reaction rates and the selectivity to C2+ oxygenates. However, the over-loading of MnOx leads to a decrease in the number of active sites. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在一系列Rh-MnOx / SiO2催化剂(Mn / Rh的原子比= 0、0.5和5.0)上研究了直接从合成气合成C2 +含氧化合物的动力学。有证据表明,引入MnOx时,C2 +含氧化合物的活化能几乎没有变化,而碳氢化合物(尤其是甲烷)的表观活化能显着增加。动力学参数表明,在MnOx存在下可以抑制烃的形成。同时,随着MnOx,负载量的变化,针对不同产物的反应顺序也发生了变化。根据原位DRIFTS,我们发现由Rh-MnOx相互作用导致的Rh表面上的两个新活性位点可能是反应速率提高和对C2 +含氧化合物选择性的原因。但是,MnOx的超载导致活性位点数量的减少。 (C)2015 Elsevier Ltd.保留所有权利。

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