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Rapid Cross-Linking of Epoxy Thermosets Induced by Solvate Ionic Liquids

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posted on 2024-08-06, 12:06 authored by Nishar HameedNishar Hameed, Daniel J. Eyckens, Benjamin M. Long, Nisa SalimNisa Salim, Jaworski Capricho, Linden Servinis, Mandy De Souza, Magenta D. Perus, Russell J. Varley, Luke C. Henderson
The high-volume manufacture of fiber-reinforced composites faces a huge challenge because long resin curing times put a low ceiling on the total output of parts produced per year. To translate the benefits from using epoxy in large-volume production platforms, cure cycle times of less than 1 min must be achieved. In this work, we report solvate ionic liquids (SILs) as simple and efficient rapid curing catalytic additives in epoxy systems. Ultrafast curing was observed at low levels of 1-5% of SIL in epoxy resin, and the cure rate is enhanced up to 26-fold without compromising the mechanical and thermal properties. Further investigations revealed that enhancement in the cure rate is dependent on the type of SILs employed, influenced by the metal center, the ligands around the metal, and the identity of the counter anion. The relative Lewis acidity of each of the active complexes was calculated, and the rapid cure effect was attributed to the activation of the epoxide moietyviathe Lewis acidic nature of the SIL. Making epoxy thermosets rapidly processable enables enormous benefits, finding applications in a whole variety of transformation methods that exist for traditional glass and metals.

Funding

Polymers with controllable networks

Australian Research Council

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PDF (Accepted manuscript)

ISSN

2637-6105

Journal title

ACS Applied Polymer Materials

Volume

2

Issue

7

Pagination

6 pp

Publisher

American Chemical Society (ACS)

Copyright statement

Copyright © 2020 the authors. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Polymer Materials, copyright © 2020 American Chemical Society, after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsapm.0c00257.

Language

eng

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