Phenolic resins bearing varying concentrations of phenyl maleimide function
s were synthesized by copolymerizing phenol with N-(4-hydroxyphenyl)maleimi
de (HPM) and formaldehyde in the presence of an acid catalyst. The resins u
nderwent a two-stage curing, through condensation of methylol groups and ad
dition polymerization of maleimide groups. The cure characterization of the
resin by dynamic mechanical analysis confirmed the two-stage cure and the
dominance of maleimide polymerization over methylol condensation in the net
work buildup process. The kinetics of both cure reactions, studied by the R
ogers method, substantiated the earlier proposed cure mechanism for each st
age. Although the initial decomposition temperature of the cured resin was
not significantly improved, enhancing the crosslink density through HPM imp
roved thermal stability of the material in a higher temperature regime. The
anaerobic char yield also increased proportional to the maleimide content.
Isothermal pyrolysis and analysis of the char confirmed that pyrolysis occ
urs by loss of hydrocarbon and nitrogenous products. The resins serve as ef
fective matrices in silica- and glass fabric-reinforced composites whose me
chanical properties are optimum for moderately crosslinked resins, in which
failure occurs through a combination of fiber debonding and resin fracture
. (C) 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1664-1674, 2001.