Using Ethanol for Continuous Biodiesel Production with Trace Catalyst and CO₂ Co-Solvent
Abstract
The continuous biodiesel production process under sub- and supercritical conditions using a trace amount of potassium hydroxide (KOH) as a catalyst has been studied. CO2 was added as a co-solvent to reduce the reaction time and increase biodiesel yield. The proposed procedure enables simultaneous transesterification and esterification of triglycerides and free fatty acid (FFA), respectively. The shorter reaction time and milder reaction conditions may reduce energy consumption due to the simplification of the separation and purification steps. The process variables, including reaction temperature, ethanol to oil molar ratio, catalyst amount, and process pressure, were systematically optimized. The highest biodiesel yield (98.12%) was obtained after a 25-min reaction time using only 0.11% wt. of KOH and a 20:1 ethanol to oil ratio. The process optimum temperature and pressure were 240 °C and 120 bar, respectively. The proposed kinetic model suggested a first-order reaction with an activation energy of 15.7 kJ·mol-1 and a reaction rate constant of 0.0398/min-1. The thermodynamic parameters such as Gibbs free energy, enthalpy, and entropy were calculated as 144.82 kJ·mol-1, 11.4 kJ·mol-1, −0.26 kJ·mol-1 and at 240 °C, respectively.
Recommended Citation
A. A. Hassan et al., "Using Ethanol for Continuous Biodiesel Production with Trace Catalyst and CO₂ Co-Solvent," Fuel Processing Technology, vol. 203, Elsevier B.V., Jun 2020.
The definitive version is available at https://doi.org/10.1016/j.fuproc.2020.106377
Department(s)
Chemical and Biochemical Engineering
Research Center/Lab(s)
Center for Research in Energy and Environment (CREE)
Second Research Center/Lab
Center for High Performance Computing Research
Keywords and Phrases
Biodiesel; CO2 Co-Solvent; Kinetic Model; Supercritical Ethanol
International Standard Serial Number (ISSN)
0378-3820
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2020 Elsevier B.V., All rights reserved.
Publication Date
01 Jun 2020
Comments
The authors gratefully acknowledge the financial support of the Wayne and Gayle Laufer Foundation for this work.