Journal
CHEMICAL ENGINEERING SCIENCE
Volume 247, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ces.2021.117079
Keywords
Kinetic and thermodynamic; Mechanism model; Levulinic acid; Ethyl levulinate; Esterification
Categories
Funding
- Ministry of Higher Education (MOHE), Malaysia [Q.J130000.2546.19H95, Q.J130000.2651.16J62, R.J130000.7113.04E78]
- Universiti Teknologi Malaysia (UTM) [Q.J130000.2546.19H95, Q.J130000.2651.16J62, R.J130000.7113.04E78]
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This study investigated the reaction analysis over a new ionic liquid-furfural carbon catalyst, deriving mathematical equations to determine the kinetic-thermodynamic parameters and proposing a suitable reaction mechanism. Results showed that the reaction is endothermic, non-spontaneous, and forms an ordered system at the transition state. The proposed mechanism includes nucleophilic substitution and Eley-Rideal mechanism.
The ethyl levulinate is one of promising platform chemical from biomass and commonly involved the esterification reaction of levulinic acid. The reactions are extensively focussed on the catalytic performance by various catalysts and presented limited work on the kinetic, thermodynamic and mechanism study for heterogeneous catalyst reaction. To fill this gap, the reaction analysis over a new ionic liquid-furfural carbon catalyst has been investigated in this work. The mathematical equations were derived to determine the kinetic-thermodynamic parameters, and proposed suitable mechanism for the reaction. Pseudo-first order model presents high correlation coefficient and accuracy with the reaction rate constant of 0.0037-0.0127 min(-1) and E-a = 17.3 kJ/mol. The reaction is endothermic and non spontaneous with ordered system at transition state. The proposed combined nucleophilic substitution and Eley-Rideal mechanism is comprised of S(N)2 steps and heterogeneous catalytic reaction. The results provide insights on the reaction for future designing and scaling-up the esterification process. (C) 2021 Elsevier Ltd. All rights reserved.
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