The non isothermal crystallization behavior of two model blends of immiscib
le polymers (an isotactic polypropylene and a polyamide-6) was examined by
a quenching procedure within a range of cooling rates from 0.1 to above 100
0 degrees C/s in order to emulate the solidification conditions arising dur
ing polymer processing. The final structure of the blend was analyzed by de
nsity and WAXD and the transition from stable to metastable phases in the b
lends and the pure homopolymers was compared examining their dependence on
cooling rate. this shows that crystallization in the blends is always faste
r since the transitions move to larger cooling rates. Observation of morpho
logical details suggests that this can be due to enhanced nucleation at the
interface. The density variation in the case of the polyamide-6 rich blend
is larger than expected from an additive volume contribution which maya be
ascribed to development of microvoids at the interface. In the case of the
isotactic polypropylene rich blend the additive volume contribution is con
sistent wit experimental observations.