Literature DB >> 32367496

Lipase-catalyzed synthesis of propyl-phenyl acetate: a kinetic and thermodynamic study.

Prerana D Tomke1, Virendra K Rathod2.   

Abstract

This study focuses on the synthesis of propyl-phenyl acetate via esterification reaction in the presence of immobilized Candida antartica lipase-B (CAL-B). In this work, the effect of relevant factors (kinetics and thermodynamic) on total percent conversion and process optimization was studied. The reaction was performed in heptane medium with 1:2 molar ratio of benzoic acid: n-propanol with 0.6% (w/v) biocatalyst loading at 40 °C to attain a maximum conversion of 96.1% within 40 min of reaction time. Effect of increase in temperature on ∆G values indicates that lipase is more promising at moderate temperature (40 °C). A second-order kinetic model was proposed to evaluate apparent kinetic constants that indicate a good agreement between the experimental and theoretical data (0.94 ≤ R2 ≤ 0.99) with high initial reaction rate (113.5 mM/min). Finally, the catalyst CAL-B was successfully reused eight times without any significant decrease in relative activity.

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Keywords:  Esterification; Immobilized lipase (CAL-B); Kinetic study; Propyl-phenyl acetate; Thermodynamic

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Year:  2020        PMID: 32367496     DOI: 10.1007/s00449-020-02358-w

Source DB:  PubMed          Journal:  Bioprocess Biosyst Eng        ISSN: 1615-7591            Impact factor:   3.210


  1 in total

1.  The effect of enzyme loading, alcohol/acid ratio and temperature on the enzymatic esterification of levulinic acid with methanol for methyl levulinate production: a kinetic study.

Authors:  Miaojia Song; Xiaohui Di; Yu Zhang; Yongming Sun; Zhongming Wang; Zhenhong Yuan; Ying Guo
Journal:  RSC Adv       Date:  2021-04-22       Impact factor: 3.361

  1 in total

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