The miscibility, phase behavior and cure kinetics of the reactive blen
ds of an alcohol-soluble nylon with an epoxy resin, i.e. diglycidyl et
her of bisphenol A (DGEBA), were studied by differential scanning calo
rimetry (d.s.c.) and Fourier transform infra-red spectroscopy (FTi.r.)
. Differential scanning calorimetry (d.s.c.) studies showed that all t
he uncured nylon/DGEBA blends were crystallizable and exhibited two gl
ass transition temperatures (T(g)s). The lower T, is independent of co
mposition and is due to the glass transition of DGEBA phase. The highe
r T-g varies with composition and is attributable to the glass transit
ion of the nylon-rich phase. Nylon is partially miscible with DGEBA, a
nd the extent of miscibility is dependent on the blend composition. Ny
lon and DGEBA in all the uncured blends can react with each other abov
e 200 degrees C. The curing reaction of nylon with DGEBA is dependent
on the blend composition. The nucleophilic attack on oxirane ring by a
mide nitrogen of nylon is dominant curing reaction in low DGEBA compos
itions, and another type of curing reaction with relatively large acti
vation energy and frequency factor also occurred which becomes dominan
t when the DGEBA content reaches 63 wt% or more. FTi.r. studies reveal
ed there does exist two types of reactions during curing of nylon with
DGEBA. All the cured nylon/DGEBA blends show a composition-independen
t T-g, which is the glass transition of cured nylon-DGEBA network. All
other blends are uncrystallizable after curing except for the 90/10 a
nd 80/20 nylon/DGEBA blends. The curing greatly destroyed the crystall
inity of the blends. (C) 1998 Elsevier Science Ltd. All rights reserve
d.