Fourier transform infrared spectroscopy (FTIR) was used to follow the
curing of the diglycidylether of bisphenol A (DGEBA) typical epoxide r
esin by poly( styrene-alt-maleic anhydride) (AMS), the reaction being
accelerated by triethylamine (TEA) in the presence of methanol. The st
udy was done in an isothermal mode for four temperatures: 85, 82, 80,
and 75 degrees C. We followed: for each temperature, the variation of
the area of the epoxy band (916 cm(-1)) versus time. After 200 min of
reaction, the degree of conversion of epoxy is 0.5 at 85 degrees C. A
postcure at 100 degrees C during 96 h allows one to reach a total conv
ersion of epoxy. The reaction mechanism involves three steps to form t
he tridimensional network. (C) 1998 John Wiley & Sons, Inc. J Appl Pol
ym Sci 69: 1167-1178, 1998.