Theoretical investigation of double-bond isomerization of 1-hexene to trans-2-hexene on H-ZSM-5 zeolite

被引：7

作者：

Li, Yan-Feng ^{[1
]}

He, Peng ^{[1
]}

Zhu, Ji-Qin ^{[1
]}

Liu, Hui ^{[1
]}

Shao, Qian ^{[2
]}

Tian, Hui-Ping ^{[2
]}

机构：

[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China

[2] SINOPEC, Res Inst Petr Proc, Beijing 100083, Peoples R China

来源：

JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM | 2010年 / 940卷 / 1-3期

关键词：

Hexene; ZSM-5; Double-bond isomerization; Alkoxy intermediate; Density functional theory; DENSITY-FUNCTIONAL THEORY; IR; OLEFINS; HYDROCARBONS; ADSORPTION; CATALYSIS; HYDROGENATION; ENTHALPIES; SIMULATION; MECHANISM;

D O I：

10.1016/j.theochem.2009.10.034

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The double-bond isomerization of 1-hexene to trans-2-hexene on the surface of ZSM-5 zeolite has been investigated by using density functional theory with a 3T cluster model simulating the Bronsted active site of the zeolite. Upon a basis of the calculated results, we found that the double-bond isomerization proceeds via the formation of alkoxy intermediates, in which case, 1-hexene is first adsorbed on the acidic site of the zeolite surface, yielding a stable alkoxy intermediate, and then, the alkoxy intermediate is decomposed, giving rise to the adsorbed trans-2-hexene on the zeolite surface. The calculated apparent activation energy for this isomerization reaction is 10.47 kcal/mol, which is in agreement with those reported activation barrier values, either obtained experimentally or theoretically in the literature. The results can well explain the formation of the carbenium ions and the energetic aspects during the course of double-bond isomerization. (C) 2009 Elsevier B.V. All rights reserved.

引用

页码：135 / 139

页数：5

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