Robust biocatalyst for the green continuous flow synthesis of esters from biomass-derived furfuryl alcohol and C8–C18 carboxylic acids

Abstract

A sustainable method suitable for industrial-scale continuous flow synthesis of esters from biomass-derived furfuryl alcohol (FA) and C8–C18 carboxylic acids was developed. Under optimized reaction conditions, lipase from Aspergillus oryzae immobilized on an octyl-silane MgO·SiO2 material demonstrated high activity. A conversion of 88.7–90.2% for FA with 100% selectivity to esters using a FA : fatty acid molar ratio of 1 : 3 and cyclohexane as the solvent at 25 °C in 45 min was achieved in a batch system. The biocatalyst retained its high activity for at least 10 consecutive reaction cycles. Successful upgradation from a batch to continuous flow reactor led to an increased FA conversion of up to 96.8%, with a reagent flow rate of 0.070 mL min−1 and a residence time of 10.5 minutes. The biocatalyst maintained excellent performance for 30 h. The developed method, considered within the framework of green chemistry metrics, ensures a balance between the high activity, stability, recyclability, and biodegradability of the catalyst. This work proposes as a generic approach to green chemistry dedicated to support the biocatalytic continuous flow synthesis of value-added chemicals.

Graphical abstract: Robust biocatalyst for the green continuous flow synthesis of esters from biomass-derived furfuryl alcohol and C8–C18 carboxylic acids

Supplementary files

Article information

Article type
Paper
Submitted
02 Aug 2024
Accepted
19 Aug 2024
First published
26 Aug 2024

Green Chem., 2024, Advance Article

Robust biocatalyst for the green continuous flow synthesis of esters from biomass-derived furfuryl alcohol and C8–C18 carboxylic acids

A. Wolny, D. Więcławik, J. Zdarta, S. Jurczyk, T. Jesionowski and A. Chrobok, Green Chem., 2024, Advance Article , DOI: 10.1039/D4GC03821E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements