A multistep (semi)-continuous biocatalytic setup for the production of polycaprolactone.
Journal
Reaction chemistry & engineering
ISSN: 2058-9883
Titre abrégé: React Chem Eng
Pays: England
ID NLM: 101673784
Informations de publication
Date de publication:
29 Feb 2024
29 Feb 2024
Historique:
received:
12
10
2023
accepted:
12
12
2023
medline:
4
3
2024
pubmed:
4
3
2024
entrez:
4
3
2024
Statut:
epublish
Résumé
Biocatalysis has gained increasing importance as an eco-friendly alternative for the production of bulk and fine chemicals. Within this paradigm, Baeyer Villiger monoxygenases (BVMOs) serve as enzymatic catalysts that provide a safe and sustainable route to the conventional synthesis of lactones, such as caprolactone, which is employed for the production of polycaprolactone (PCL), a biocompatible polymer for medicinal applications. In this work, we present a three-step, semi-continuous production of PCL using an entirely biocatalytic process, highlighting the merits of continuous manufacturing for enhancing biocatalysis. First, caprolactone is produced in batch from cyclohexanol using a coenzymatic cascade involving an alcohol dehydrogenase (ADH) and BVMO. Different process parameters and aeration modes were explored to optimize the cascade's productivity. Secondly, the continuous extraction of caprolactone into an organic solvent, needed for the polymerization step, was optimized. 3D-printed mixers were applied to enhance the mass transfer between the organic and the aqueous phases. Lastly, we investigated the ring-opening polymerization of caprolactone to PCL catalyzed by
Identifiants
pubmed: 38433980
doi: 10.1039/d3re00536d
pii: d3re00536d
pmc: PMC10903532
doi:
Types de publication
Journal Article
Langues
eng
Pagination
713-727Informations de copyright
This journal is © The Royal Society of Chemistry.
Déclaration de conflit d'intérêts
There are no conflicts to declare.