Dendritic hyperbranched polymers (HBPs) show outstanding performance as tou
gheners in epoxy resins. The critical strain energy release rate, G(Ic), of
a DGEBF resin is increased by a factor of 6 from 120 J/m(2) to 720 J/m(2)
using only a 5% modifier weight content. This does not lead to a decrease i
n resin stiffness or glass transition temperature and the favourable proces
sability of epoxy resins is fully maintained without requiring the use of s
olvents. Toughness properties are induced by a finely-dispersed particulate
structure which is obtained by a controlled phase separation process durin
g resin curing. A strong mechanical phase interaction is ensured by chemica
l bonding through reactive epoxy groups grafted onto the HBP. By tailoring
the HBP's epoxy functionality and polarity to control reactivity, phase sep
aration, final morphology and phase interactions, this toughening system is
potentially applicable to a variety of thermoset resins. With this in view
, the influence of the chemical architecture of the HBP modifiers on phase
separation, processability, properties and toughening mechanisms is investi
gated. (C) 1999 Elsevier Science Ltd. All rights reserved.