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Selectivity determinants for dual function catalysts: applied to methanol selective oxidation on iron molybdate

机译:双功能催化剂的选择性决定因素:应用于钼酸铁对甲醇的选择性氧化

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摘要

Evolution of the IRAS spectrum with temperature after adsorbing methanol at room temperature. The bands at 2930 and 2820 cm− 1 are due to the methoxy species C–H stretches, while that at 2870 is due to the formate.\udHere, we report a simple, quantitative model to describe the behaviour of bi-cationic oxide catalysts, in terms of selectivity variation as a function of increased loading of one cation into a sample of the other. We consider its application to a particular catalytic system, namely the selective oxidation of methanol, which proceeds with three main C1 products, namely CO2, CO, and H2CO. The product selectivity varies in this order as Mo is added in increasing amounts to an iron oxide catalyst, and the product selectivity is determined by the distribution of dual sites and single sites of each species.
机译:在室温下吸附甲醇后,IRAS光谱随温度的变化。在2930和2820 cm− 1处的谱带归因于甲氧基物质CH的延伸,而在2870870cm-1处的谱带归因于甲酸盐。\ ud此处,我们报告了一种简单的定量模型来描述双阳离子氧化物催化剂的行为就选择性变化而言,它是一种阳离子向另一种样品中增加的负载量的函数。我们考虑将其应用于特定的催化系统,即甲醇的选择性氧化,该过程会伴随着三种主要的C1产物,即CO2,CO和H2CO进行。当将Mo越来越多地添加到氧化铁催化剂中时,产物的选择性以此顺序变化,并且产物的选择性由每种物质的双位和单位的分布决定。

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