三氯化铝催化有机硅单体副产共沸物歧化反应密度泛函理论研究

doi:10.11949/j.issn.0438-1157.20141522

化工学报 ›› 2015, Vol. 66 ›› Issue (5): 1730-1737.DOI: 10.11949/j.issn.0438-1157.20141522

• 催化、动力学与反应器 • 上一篇下一篇

三氯化铝催化有机硅单体副产共沸物歧化反应密度泛函理论研究

谭军, 欧阳玉霞, 孙萍, 刘辉, 陈洁, 韦晓燕

嘉兴学院生物与化学工程学院, 浙江嘉兴 314001

收稿日期:2014-10-10 修回日期:2015-01-20 出版日期:2015-05-05 发布日期:2015-05-05
通讯作者: 谭军
基金资助:
嘉兴市科技计划项目(2012AY1025,2014AY11019);国家自然科学基金项目(20906038);浙江省自然科学基金项目(Y4090135)。

Density functional theory study on disproportionation reaction of methylchlorosilane azeotrope byproducts catalyzed by AlCl₃

TAN Jun, OUYANG Yuxia, SUN Ping, LIU Hui, CHEN Jie, WEI Xiaoyan

School of Biological and Chemical Engineering, Jiaxing University, Jiaxing 314001, Zhejiang, China

Received:2014-10-10 Revised:2015-01-20 Online:2015-05-05 Published:2015-05-05
Supported by:
supported by the Science and Technology Project Foundation of Jiaxing City (2012AY1025, 2014AY11019), the National Natural Science Foundation of China (20906038) and the Natural Science Foundation of Zhejiang Province (Y4090135).

摘要/Abstract

摘要： AlCl₃催化(CH₃)₃SiCl和SiCl₄的歧化反应体系中可能存在(CH₃)₃SiCl与SiCl₄生成(CH₃)₂SiCl₂与CH₃SiCl₃(反应1),(CH₃)₂SiCl₂与SiCl₄生成CH₃SiCl₃(反应2)和(CH₃)₃SiCl与CH₃SiCl₃生成(CH₃)₂SiCl₂(反应3)等反应。本文采用密度泛函理论对这3种反应进行了研究。结果发现在AlCl₃ 催化剂上,可能发生CH₃AlCl₂中间体生成的分步反应和反应物共吸附反应,对两种情况下3种反应的反应路径均进行了计算,发现3种反应均偏向于以双分子共吸附机理进行。3种反应的能垒排序是反应2 >反应1 >反应3。同时,热力学数据分析发现,在543.15～593.15 K之间,温度变化对反应2的摩尔Gibbs反应能变基本无影响,但在593.15 K时,反应1和反应3的Gibbs自由能变显著减小。这些计算结果显示,如果适当调控反应温度,就能够在保证反应1和3进行的同时,抑制反应2的进行,从而实现歧化产物组成的调控,有利于(CH₃)₂SiCl₂的生成。

关键词: 三甲基氯硅烷, 四氯化硅, 三氯化铝, 歧化反应, 密度泛函理论

Abstract: The disproportionation reaction between (CH₃)₃SiCl and SiCl₄ catalyzed by AlCl₃ involves three reactions; the reaction between (CH₃)₃SiCl and SiCl₄ to form (CH₃)₂SiCl₂and CH₃SiCl₃(R1), the reaction between (CH₃)₂SiCl₂and SiCl₄to form CH₃SiCl₃(R2) and the reaction between (CH₃)₃SiCl and CH₃SiCl₃ to form (CH₃)₂SiCl₂(R3). Density functional theory was used to study these reactions. The possible catalytic mechanisms of AlCl₃ were stepwise reaction pathway of forming intermediate CH₃AlCl₂ and co-adsorption pathway of two reactants on AlCl₃. The co-adsorption mechanism was more likely for these three reactions. The energy barrier ranking of these reactions was R2 >R1 >R3. By analyzing the thermodynamics data of these reactions, the effect of temperature on the Gibbs reaction energy of R2 was almost negligible within a temperature range of 543.15 K to 593.15 K. However, the Gibbs reaction energy of R1 and R3 significantly decreased at 593.15 K. These studies indicated that through appropriate temperature regulation, the reactions of R1 and R3 could be the dominant reactions while R2 would be effectively suppressed, influencing product distribution and facilitating formation of (CH₃)₂SiCl₂.

Key words: trimethylchlorosilane, tetrachlorosilane, aluminium trichloride, disproportionation reaction, density functional theory

中图分类号:

O641
O647

谭军, 欧阳玉霞, 孙萍, 刘辉, 陈洁, 韦晓燕. 三氯化铝催化有机硅单体副产共沸物歧化反应密度泛函理论研究[J]. 化工学报, 2015, 66(5): 1730-1737.

TAN Jun, OUYANG Yuxia, SUN Ping, LIU Hui, CHEN Jie, WEI Xiaoyan. Density functional theory study on disproportionation reaction of methylchlorosilane azeotrope byproducts catalyzed by AlCl₃[J]. CIESC Journal, 2015, 66(5): 1730-1737.

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三氯化铝催化有机硅单体副产共沸物歧化反应密度泛函理论研究

Density functional theory study on disproportionation reaction of methylchlorosilane azeotrope byproducts catalyzed by AlCl₃

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三氯化铝催化有机硅单体副产共沸物歧化反应密度泛函理论研究

Density functional theory study on disproportionation reaction of methylchlorosilane azeotrope byproducts catalyzed by AlCl3

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Density functional theory study on disproportionation reaction of methylchlorosilane azeotrope byproducts catalyzed by AlCl₃