丁烯在ZnO-SiO2上的异构化

T. Sumiyoshi, K. Tanabe, H. Hattori
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引用次数: 5

摘要

研究了正丁烯在不同摩尔比的ZnO-SiO2二元氧化物上的异构化反应,探讨了活性位点的性质和反应机理。ZnO与SiO2混合后,表面出现酸性位点和碱性位点。通过对吸附吡啶的红外光谱分析,确定其酸位为路易斯酸。酸性的CO2分子对异构化反应没有阻滞作用,而碱性分子如吡啶和氨对异构化反应有阻滞作用。氘化催化剂上形成的产物含有少量的D原子。共异构化结果表明,反应涉及分子内氢转移,反应的慢步是C-H键的裂解。因此,丁烯异构化反应发生在路易斯酸位点,并由氢化物离子的抽离引发,这是反应速率的决定步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isomerization of Butene over ZnO-SiO2
Isomerization of n-butenes was investigated over binary oxides ZnO-SiO2 having different mole ratios and the nature of active sites and the mechanism of the reaction were examined.On mixing of ZnO and SiO2, there appeared acidic sites and basic sites on the surface. The type of the acid sites was of Lewis acid which was determined by IR study of adsorbed pyridine.The isomerization was not retarded by acidic molecule of CO2 but by basic molecules such as pyridine and ammonia. The products formed over the deuterated catalyst contained a small amount of D atoms. The results of co-isomerization indicate that the reaction involves intramolecular hydrogen transfer and that the slow step is C-H bond cleavage. Therefore, it is concluded that the isomerization of butenes takes place on Lewis acid sites and is initiated by the abstraction of hydride ion which is the rate determining step.
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