Epoxy vitrimer materials by lipase-catalyzed network formation and exchange reactions

Camille Bakkali-Hassani, Paolo Edera, Jakob Langenbach, Quentin Arthur Poutrel, Sophie Norvez, Matthieu Gresil, François Tournilhac

Research output: Contribution to journalArticleResearchpeer-review

Abstract

The preparation and reprocessing of an epoxy vitrimer material is performed in a fully biocatalyzed process wherein network formation and exchange reactions are promoted by a lipase enzyme. Binary phase diagrams are introduced to select suitable diacid/diepoxide monomer compositions overcoming the limitations (phase separation/sedimentation) imposed by curing temperature inferior than 100 °C, to protect the enzyme. The ability of lipase TL, embedded in the chemical network, to catalyze efficiently exchange reactions (transesterification) is demonstrated by combining multiple stress relaxation experiments at 70-100 °C and complete recovery of mechanical strength after several reprocessing assays (up to 3 times). Complete stress relaxation ability disappears after heating at 150 °C, due to enzyme denaturation. Transesterification vitrimers thus designed are complementary to those involving classical catalysis (e.g., using the organocatalyst triazabicyclodecene) for which complete stress relaxation is possible only at high temperature.

Original languageEnglish
Pages (from-to)338-343
Number of pages6
JournalACS Macro Letters
Volume12
Issue number3
DOIs
Publication statusPublished - 21 Mar 2023

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