Study of the Interaction of Ethanol with the Bronsted and Lewis Acid Sites on Metal Oxide Surfaces Using the DV-X.ALPHA. Method.

Yuji Shinohara, H. Satozono, T. Nakajima, Satoshi Suzuki, S. Mishima
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引用次数: 12

Abstract

The interactions of ethanol with a Bronsted acid site (a hydroxy group) and with a Lewis acid site (a metal ion) on surfaces of seven metal oxides (SiO2-Al2O3, SiO2, TiO2, ZnO, MgO, MnO and CdO) have been investigated using the DV-Xα method. The oxides were selected from a series of catalysts, whose selectivities for the dehydration and the dehydrogenation of ethanol had been experimentally determined by P. Sabatier and A. Mailhe.By comparing the results of the DV-Xα calculations from several models of ethanol interacting with the Bronsted or Lewis acid sites with the experimental selectivities, it was concluded that a proton shift from the Bronsted site to the ethanol oxygen occurs when ethanol strongly interacts with the site and that this shift changed the electronic state of ethanol for the dehydration to be favorable. These results indicate that the dehydration of ethanol on oxide catalysts proceeds by the E1 mechanism.
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用dv - x - alpha研究乙醇与金属氧化物表面Bronsted和Lewis酸位的相互作用。方法。
采用DV-Xα方法研究了乙醇与7种金属氧化物(SiO2- al2o3, SiO2, TiO2, ZnO, MgO, MnO和CdO)表面的Bronsted酸位(羟基)和Lewis酸位(金属离子)的相互作用。由P. Sabatier和a . Mailhe从一系列催化剂中选择了氧化物,并通过实验测定了它们对乙醇脱水和脱氢的选择性。通过将几种乙醇与Bronsted或Lewis酸位相互作用模型的DV-Xα计算结果与实验选择性进行比较,得出结论:当乙醇与Bronsted或Lewis酸位发生强相互作用时,质子从Bronsted位转移到乙醇氧上,这种转移改变了乙醇的电子态,有利于脱水。这些结果表明,乙醇在氧化物催化剂上的脱水是通过E1机制进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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