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The Nature of Active Copper Species in Cu/SiO2 Catalysts for Hydrogenation of Methyl Acetate to Ethanol (PPT)

机译:Cu / SiO2催化剂中活性铜物种的性质乙酸甲酯氢化乙醇甲酯(PPT)

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1. We successfully prepared a series of Cu/SiO2 catalysts with remarkable differences on state of Cu species and exclued the other factors' influence. 2. The conversion of MA grew linearly associated with the Cu (0) surface area increasement under a certain value. However, with more Cu (0) active sites, the samples catalytic activity increaed with enrichment of Cu (I) surface area. 3. These relationships strongly proved there was a synergy of active copper species on the hydrogenation of MA and indicated that when there is insufficient of Cu (0) species, the catalytic activity of hydrogenation determined by the activity of H2, whereas, it would be decided by the adsorption of methoxy and acyl species as the amount of surface Cu (0) achieved to a certain degree. 4. The calculated results showed the MA could be adsorbed by (Cu)_x~(δ+)/SiO2 but not activated by Cu (111). And the H2 is much easilier dissociated on Cu (111) than on (Cu)_x~(δ+)+/SiO2. These calculatedresults are agreed with the experiments data.
机译:1.我们成功地制备了一系列Cu / SiO2催化剂,具有显着差异的Cu物种,并排除了其他因素的影响。 2. MA的转换在一定值下与Cu(0)表面积升高线性相关。然而,通过更多的Cu(0)活性位点,样品催化活性增强了Cu(I)表面积的富集。这些关系强烈证明,在MA的氢化方面存在活性铜物种的协同作用,并表明当没有足够的Cu(0)种时,通过H 2的活性确定氢化的催化活性,而这将是通过在一定程度上达到的表面Cu(0)的量,通过对甲氧基和酰基物质的吸附来决定。 4.计算结果显示MA可以被(Cu)_〜(δ+)/ siO 2吸附,但不被Cu(111)激活。并且H 2在Cu(111)上易于on(Cu)_〜(δ+)+ / siO 2。这些算法与实验数据同意。

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