Kinetics and network structure of thermally cured vinyl ester resins

Bisphenol-A diglycidyl ether dimethacrylate was blended with styrene at varying concentrations and this model v inyl ester resin (VER) was compared with two commercial VERs. The VERs were characterized using gravimetry, FTIR spectroscopy, NMR spectroscopy, differential scanning calorimetry (DSC) and DMTA. NMR spectroscopy differentiated between a novolac epoxy-based multimethacrylate oligomer and the two bisphenol-A epoxy-based dimethacrylate oligomers. Reaction kinetics were studied using scanning and isothermal DSC and isothermal FTIR spectroscopy using benzoyl peroxide as the thermal initiator, The presence of oxygen was found to inhibit significantly the polymerization, Increased initiator concentration raised the rate of isothermal polymerization, but did not affect the final conversion while increased styrene concentration reduced the polymerization rate constant and increased the total conversion. This was interpreted in terms of the variations in the termination rate and the stability of the styryl radical on the cure rate and the effect of vitrification on the extent of cure. From measurements of the dynamic mechanical properties as a function of temperature, the breadth of the glass transition tan delta curve and the magnitude of the rubbery modulus was found to increase while the tan delta maximum decreased with increased crosslink density. The T-g, as measured by DSC, and the temperature of the tan delta maximum, as measured by DMTA, were not significantly affected by the styrene content in the resin per se. but were dependent on the combined effects of composition and crosslink density of the network. (C) 2002 Elsevier Science Ltd. All rights reserved.