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Reaction kinetics and mechanism for hydration of cyclohexene over ion-exchange resin and H-ZSM-5

机译:环己烯在离子交换树脂和H-ZSM-5上的水合反应动力学及机理

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摘要

The kinetics of liquid-phase cyclohexene hydration over ion-exchange resin and H-ZSM-5 were, respectively, investigated in a batch autoclave reactor. In order to identify the reaction mechanism involved in the heterogeneous cyclohexene hydration, a pseudo-homogeneous (PH) model and three heterogeneous models based on the Langmuir-Hinshelwood-Hougen-Watson (LHHW) mechanism and Eley-Rideal (ER) mechanism were established to correlate the kinetic data. The results indicated that the heterogeneous models exhibited a more satisfactory agreement with the experimental data than the PH model. According to the kinetic studies and spectroscopic analysis, it is proposed that cyclohexene hydration catalyzed by H-ZSM-5 belongs to the ER mechanism, which accounts that the reaction is between adsorbed water and bulk cyclohexene, while it belongs to the LHHW mechanism over the ion-exchange resin. Nevertheless, the activation energies are similar for the two catalysts, which implies similar controlling steps are encountered in the reaction.
机译:在间歇高压釜反应器中分别研究了离子交换树脂和H-ZSM-5上液相环己烯水合的动力学。为了确定异质环己烯水合反应的反应机理,建立了基于Langmuir-Hinshelwood-Hougen-Watson(LHHW)机理和Eley-Rideal(ER)机理的假均相(PH)模型和三种异质模型。以关联动力学数据。结果表明,与PH模型相比,异质模型与实验数据的一致性更好。根据动力学研究和光谱分析,提出H-ZSM-5催化的环己水合属于ER机理,认为反应是吸附水与本体环己烯之间的反应,而属于LHHW机理。离子交换树脂。然而,两种催化剂的活化能相似,这意味着在反应中会遇到相似的控制步骤。

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