Reactive blending of polypropylene (PP) and amorphous polyamide (aPA)
was carried out using a gram-scale mixer. Maleic anhydride-grafted PP
was used as a reactive PP. Time resolved light scattering analysis sho
wed that, compared with non reactive systems, the reactive one yielded
finer particles of sub-mu m, via a faster size-reduction process, and
exhibited better stability of dispersed particles for static annealin
g, suggesting the emulsifying effect of in situ formed PP-aPA graft co
polymer. Both ellipsometry and transmission electron microscopy showed
that the interface established in the reactive system was very thick
(similar to 40 nm); it was several times the coil size of the componen
t polymer. The thick interface is assumed to be a layer of accumulated
micelles of the in situ formed graft copolymer. In the thick interfac
e, instead of cross-hatched lamellar crystallites, long lamellar cryst
als were found to develop. (C) 1997 Elsevier Science Ltd.