Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/27786
Title: Heterogeneous catalysed esterification of propionic acid with n-amyl alcohol over a microporous cation-exchange resin dowex 50wx4
Authors: İzci, Alime
Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.
Erdem, Beyhan
AAI-1238-2021
14023997200
Keywords: Propionic acid
Heterogeneous catalysis
n-Amyl Alcohol, Dowex 50Wx4
Liquid-phase esterification
Acetic-acid
Kinetics
Methanol
Isobutanol
Chemistry
Activation energy
Batch reactors
Catalysis
Catalysts
Equilibrium constants
Esters
Ion exchange resins
Microporosity
Molecules
Positive ions
Reaction rates
Saturated fatty acids
Volatile fatty acids
Amyl alcohol
Apparent activation energy
Cation exchange resins
Dowex 50Wx4
Equilibrium conversion
Experimental conditions
Reaction temperature
Water concentrations
Propionic acid
Issue Date: 2010
Publisher: Walter De Gruyter GMBH
Citation: Erdem, B. ve İzci, A. (2010). "Heterogeneous catalysed esterification of propionic acid with n-amyl alcohol over a microporous cation-exchange resin dowex 50wx4". Zeitschrift fur Physikalische Chemie, 224(5), 781-793.
Abstract: Kinetics of heterogeneous catalysed esterification of propionic acid with n-amyl alcohol was studied with a microporous cation-exchange resin catalyst. Dowex 50Wx4, in a stirred batch reactor to synthesise amyl propionate. Effects of various parameters such as speed of agitation, catalyst loading, and reaction temperature on reaction rate were investigated. The equilibrium conversion of propionic acid increased with in catalyst loading and reaction temperature. Stirrer speed had virtually no effect on the reaction rate under the experimental conditions. The apparent activation energy was found to be 43.167 kJmol(-1) for the formation of amyl propionate and the equilibrium constant, which is independent of temperature ranging from 318 to 348 K. was found to be 4.05. It was also observed that the initial reaction rate decreased with water concentrations and increased with that of acid and increased with that of alcohol linearly. The reaction was found to occur between an adsorbed acid molecule and a molecule of alcohol in the bulk and it was concluded that the reaction mechanism can be represented by Eley-Rideal model.
URI: https://doi.org/10.1524/zpch.2010.5498
https://www.degruyter.com/document/doi/10.1524/zpch.2010.5498/html
http://hdl.handle.net/11452/27786
ISSN: 0942-9352
Appears in Collections:Scopus
Web of Science

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