The development of bicontinuous morphologies in 10 wt% polysulfone (PSu)-ep
oxy (DGEBA)/anhydride (MTHPA) blends, was followed by optical and scanning
electron microscopy. Blends cured at 80 degrees C revealed the formation of
large epoxy-rich domains surrounded by a PSu-rich matrix, soon after the c
loud point. Advancing the cure led to an increase in the volume fraction an
d the coalescence of epoxy-rich domains. A bicontinuous primary morpholcgy
was thus generated. A secondary phase separation was observed in both prima
ry phases from the very beginning of the phase-separation process. While sp
inodal demixing was clearly the mechanism by which the primary morphology w
as generated, nucleation-growth could be responsible of the secondary phase
separation. Postcure steps produced a change in the composition of phases
as revealed by DMA, and in the secondary morphology as observed by SEM. A p
ostcure at 120 degrees C led to a single T-g at 115 degrees C with a small
shoulder at higher temperatures. A postcure at 200 degrees C led to a T-g a
t 108 degrees C for the epoxy-rich phase and a T-g at 137 degrees C for the
PSu-rich phase. The partial purification of the thermoplastic phase produc
ed a significant enhancement of toughness. K-IC was increased from 0.65 MPa
m(1/2) for the neat thermoset to 1.10 MPa m(1/2) for the blend postcured a
t 200 degrees C. (C) 1999 Elsevier Science Ltd. All rights reserved.