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Intensification and Optimization of FAME Synthesis via Acid-Catalyzed Esterification Using Central Composite Design (CCD)

[Image: see text] The acid-catalyzed pre-treatment esterification process is required for low-cost feedstock with high free fatty acids (FFAs) to avoid the saponification that occurs during alkali-catalyzed transesterification for the production of fatty acid alkyl esters (FAAE). Reverse hydrolysis...

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Detalles Bibliográficos
Autores principales: Saeed, Alaaddin M. M., Sharma, Shivika, Hassan, Saeikh Zaffar, Ghaleb, Atef M., Cao, Gui-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373212/
https://www.ncbi.nlm.nih.gov/pubmed/37521596
http://dx.doi.org/10.1021/acsomega.3c02434
Descripción
Sumario:[Image: see text] The acid-catalyzed pre-treatment esterification process is required for low-cost feedstock with high free fatty acids (FFAs) to avoid the saponification that occurs during alkali-catalyzed transesterification for the production of fatty acid alkyl esters (FAAE). Reverse hydrolysis in acid-catalyzed esterification causes a decrease in fatty acid methyl ester (FAME) yield. Therefore, the esterification process must be intensified. This study aims to develop and optimize a low-temperature intensification process to enhance biodiesel yield and reduce energy consumption. Three intensification systems were studied: co-solvent technique, co-solvent coupled with adsorption of water using molecular sieves, and entrainer-based continuous removal of water. The process variables of esterification reaction in co-solvents without the adsorption system were optimized by using central composite design (CCD). The study showed that the co-solvent without the adsorption system was effective in intensifying the FFA conversion (X(FFA)) at low temperatures, compared to the other two systems, due to the dilution effect at high co-solvent/entrainer amount required for sufficient vapors in the adsorption system. Optimized process variables have achieved 95% X(FFA) within 75 min at 55 °C, 20 mL/100 g of oil DEE, 9 MR, 3 wt % H(2)SO(4), and 320–350 RPM in a co-solvent without the adsorption system.