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FTIR investigations indicated hydrogen bonding interaction between the hydroxyl groups of MCDEA-cured ER and the carbonyl groups of PCL in the cured system, which is an important driving force for the miscibility of the cured ER/PCL blends.
Fracture energy G1c of the cured system was highly improved.
The dielectric analysis technique was used to characterize an epoxy cured system consisting of a diglycidyl ether of bisphenol A (DGEBA, n=0) and 1,2 diaminecyclohexane (DCH).
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The PVI grafting was also examined by use of ultraviolet cured systems involving photosensitizers.
Exfoliation state has been investigated using small angle X-ray scattering (SAXS) in cured systems and during curing reaction.
The input parameters were generated from kinetics simulation, which outputs the structure information for the cured systems.
The α- and β-relaxation temperatures of the cured systems were determined using dynamic mechanical thermal analysis.
Measurements on fully cured systems at different temperatures confirmed that CRL only was observed when the system was in the glassy state.
The morphology of the cured systems after removal of ESO was examined using scanning electron microscopy, and the composition of epoxy precursors/solvent for phase inversion was determined.
The developed method would hold great promise in further molecular simulations for structure and properties of epoxy resin or other cured systems.
Bonding strength of all the cured systems had a maximum peak during curing, due to the increase in the internal stress which occurred during the curing shrinkage of the epoxy resins.
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