Abstract
Novel re-mendable polyurethanes were prepared by the Diels-Alder cycloaddition reaction of urethane bismaleimides to bisfuryl monomers. The urethane bismaleimides were synthesized by an addition reaction of 4-maleimidophenylisocyanate to macrodiols, such as polycaprolactone diol (Mn − 1250 and 2000), PEA-2000 and PBA-2000. The bisfuryl monomers were obtained by the reaction of 2-furfuryl alcohol with hexamethylene diisocyanate or by open-ring reaction of the oxirane ring from diglycidyl bisphenol A with furfuryl amine.
Notes
a Endothermal peak temperature.
b Onset polymerization temperature.
c Exothermal peak temperature.
d Temperature of completion of the polymerization reaction.
a Glass transition temperature determined from the first maximum of loss modulus by DMA measurements.
b Initial decomposition temperature.
c Temperatures for 5 and 10% weight loss.
d Glass transition temperature from DSC measurement.