Abstract
The kinetics of reaction of ternary blends based on Bisphenol A diglycidyl ether, Bisphenol A and sulfanilamide curing agent was investigated using FTIR, HPLC, SEC following two different synthesis paths. Four the same initial composition prepolymers differing by the cross-link point distribution and the chain length between cross-links have been synthesized and their solid state behavior has been studied. For the formulation DGEBA: SAA: BA = 4.0: 1.25: 1.5 mol (catalyst—0.005 e.e.w. DGEBA), though the schedules have different kinetics, finally the prepolymers with equal conversion of epoxy groups and mass-average molar mass were obtained by both schedules. The dynamic mechanical spectroscopy performed in the glass transition region displays the evolution of the viscoelastic characteristics as a function of cross-link density. For similar formulations networks obtained by schedule 1 have higher values of Tg and ö than networks obtained by schedule 2, perhaps due to a higher real cross-link density.