TY - JOUR
T1 - Epoxy vitrimer materials by lipase-catalyzed network formation and exchange reactions
AU - Bakkali-Hassani, Camille
AU - Edera, Paolo
AU - Langenbach, Jakob
AU - Poutrel, Quentin Arthur
AU - Norvez, Sophie
AU - Gresil, Matthieu
AU - Tournilhac, François
N1 - Funding Information:
This work was funded by the European Union’s Horizon 2020 FET Open Project Self-Healing Soft Robotics SHERO [Grant No. 828818]. P.E. thanks CNRS for financial support. Anton Paar France SAS is thanked for loan of the MCR702 rheometer. Michel Cloître is gratefully acknowledged for helpful discussions.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/3/21
Y1 - 2023/3/21
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85148865470
U2 - 10.1021/acsmacrolett.2c00715
DO - 10.1021/acsmacrolett.2c00715
M3 - Article
AN - SCOPUS:85148865470
SN - 2161-1653
VL - 12
SP - 338
EP - 343
JO - ACS Macro Letters
JF - ACS Macro Letters
IS - 3
ER -