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

被引:3
|
作者
Saeed, Alaaddin M. M. [3 ]
Sharma, Shivika [1 ]
Hassan, Saeikh Zaffar [1 ]
Ghaleb, Atef M. M. [2 ]
Cao, Gui-Ping [3 ]
机构
[1] Aligarh Muslim Univ, Zakir Husain Coll Engn & Technol, Fac Engn & Technol, Dept Petr Studies, Aligarh 202002, India
[2] Alfaisal Univ, Coll Engn, Dept Ind Engn, Riyadh 11533, Saudi Arabia
[3] East China Univ Sci & Technol, State Key Lab Chem Engn, UNILAB, Shanghai 200237, Peoples R China
来源
ACS OMEGA | 2023年 / 8卷 / 29期
关键词
BIODIESEL PRODUCTION; OLEIC-ACID; REACTIVE DISTILLATION; MICROWAVE IRRADIATION; WATER REMOVAL; FATTY-ACIDS; OIL; TRANSESTERIFICATION; SOLUBILITY; SYSTEMS;
D O I
10.1021/acsomega.3c02434
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The acid-catalyzed pre-treatment esterification processis requiredfor low-cost feedstock with high free fatty acids (FFAs) to avoidthe saponification that occurs during alkali-catalyzed transesterificationfor the production of fatty acid alkyl esters (FAAE). Reverse hydrolysisin acid-catalyzed esterification causes a decrease in fatty acid methylester (FAME) yield. Therefore, the esterification process must beintensified. This study aims to develop and optimize a low-temperatureintensification process to enhance biodiesel yield and reduce energyconsumption. Three intensification systems were studied: co-solventtechnique, co-solvent coupled with adsorption of water using molecularsieves, and entrainer-based continuous removal of water. The processvariables of esterification reaction in co-solvents without the adsorptionsystem were optimized by using central composite design (CCD). Thestudy showed that the co-solvent without the adsorption system waseffective 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 requiredfor sufficient vapors in the adsorption system. Optimized processvariables have achieved 95% X (FFA) within75 min at 55 & DEG;C, 20 mL/100 g of oil DEE, 9 MR, 3 wt % H2SO4, and 320-350 RPM in a co-solvent without theadsorption system.
引用
收藏
页码:26206 / 26217
页数:12
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