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Liquid phase propylene epoxidation with H 2 O 2 on TS ‐1/ SiO 2 catalyst in a fixed‐bed reactor: experiments and deactivation kinetics
Author(s) -
Feng Wenping,
Wang Yaquan,
Wu Guoqiang,
Lin Yi,
Xu Juan,
Shi Hainan,
Zhang Teng,
Wang Shuhai,
Wu Xiaoxue,
Yao Pengxu
Publication year - 2015
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/jctb.4462
Subject(s) - catalysis , hydrogen peroxide , methanol , chemistry , activation energy , kinetics , chemical kinetics , reaction rate , order of reaction , inorganic chemistry , peroxide , sorption , reaction rate constant , nuclear chemistry , organic chemistry , adsorption , physics , quantum mechanics
BACKGROUND The epoxidation of propylene with H 2 O 2 in liquid phase catalyzed by a TS ‐1/ SiO 2 catalyst in a fixed‐bed reactor has been studied. The effects of reaction temperature (313–328 K), methanol concentrations (55–70 wt%) and hydrogen peroxide concentrations (9–15 wt%) on the reaction are investigated. The fresh, deactivated and regenerated catalysts were characterized with XRD , FT‐IR , UV –vis, N 2 sorption and TG to study the reasons for catalyst deactivation. In addition, the kinetics of catalyst deactivation was studied by fitting the experimental data. RESULTS The rate of decrease of H 2 O 2 conversion decreases with increasing reaction temperature and methanol concentration, but increases with increasing hydrogen peroxide concentration. The reason for catalyst deactivation is that the bulky organic matter covers the active centers. The study on deactivation kinetics shows that the deactivation reaction order is 2, and an expression for H 2 O 2 conversion as a function of reaction time is obtained. CONCLUSION The operating conditions such as reaction temperature, methanol concentration and hydrogen peroxide concentration remarkably affect the reaction. The kinetic parameters including deactivation reaction order and activation energy are developed by fitting the experimental data based on the Wojciechowski model. © 2014 Society of Chemical Industry