Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
Supramolecular rubbers incorporating a large number of physical cross-links through cooperative hydrogen bonds display high self-healing properties but limited solvent and creep resistance due to the lack of chemical cross-links. Increasing both chemical cross-links and H-bonding is therefore desirable but limited by the functionality of monomers. The present work thus devises a convergent chemical platform permitting to increase the number of chemical cross-links without changing the concentration of hydrogen-bonding groups. Starting from a single reactive prepolymer, functionalized with a defined number of hydrogen-bonding groups, a series of networks presenting different ratios of diepoxide and tetraepoxide were prepared. The curing process (controlled by 2-MI catalyst), thermomechanical behavior, and tensile properties recovery of the cured materials were investigated. Gelation state was quantified and compared to theoretical predictions. The introduction of tetrafunctional epoxide in the presence of 2-MI gave rise to gelled materials characterized by higher rigidity and strength and significantly improved creep resistance. Self-healing was observed for all materials, with 50% to 100% complete recovery in a day depending on tetraepoxide content.
Dario Floreano, Alexander Scott Keller