Ultrasound-assisted lipase catalyzed synthesis of propyl caprate: Process optimization, kinetic, and thermodynamic evaluation

被引:6
作者
Parikh, Dhara T. [1 ]
Lanjekar, Kavita J. [1 ]
Rathod, Virendra K. [1 ]
机构
[1] Inst Chem Technol, Dept Chem Engn, Matunga E Mumbai 400019, Maharashtra, India
关键词
Lipase; Ultrasound-assisted esterification; Kinetics; Ordered bi-bi mechanism; Thermodynamics; ENZYMATIC-SYNTHESIS; GLYCEROL CARBONATE; CINNAMYL ACETATE; COOKING OIL; NOVOZYM; 435; SOLVENT; TRANSESTERIFICATION; ESTERS; ESTERIFICATION; ACID;
D O I
10.1016/j.cep.2021.108633
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The present work evaluates the influence of ultrasound on lipase-catalyzed esterification for the synthesis of propyl caprate in a solvent-free system. The optimum conditions were found as molar ratio of capric acid: 1-propyl alcohol 1:3, catalyst loading 1% (w/w), molecular sieves loading 5% (w/w), temperature 60 degrees C, agitation speed 100 rpm, sonication frequency 22 kHz, duty cycle 80% (10 min) and ultrasound power 100 W yielding 86.86% conversion of capric acid. Compared to conventional agitation, ultrasound technology significantly improved process productivity to around 3% more acid conversion for each batch with 50% less requirement of catalyst amount and 5 fold less reaction time with enhanced enzyme recycling up to 9 cycles and stability. The activation energy requirement was lower (6.22 kcal/mol) with ultrasound than the conventional approach (9.028 kcal/mol). Furthermore, the esterification process was observed to be endothermic and spontaneous, with enthalpy (Delta H), entropy (Delta S), and the Gibbs free energy change (Delta G) values of 83.66 kJ/mol, 250.23 J/mol/K, and -2.74 kJ/mol, respectively. An ordered bi-bi mechanism involving the dead-end complex formation with lipase and inhibition of the reaction by capric acid was presented. Ultrasound application was found to be an influential tool to enhance the performance of biocatalyst in this esterification reaction.
引用
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页数:12
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