Fp. La Mantia et al., On the mechanism of compatibilization of polyolefin/liquid crystalline polymer blends with graft copolymers, J APPL POLY, 77(14), 2000, pp. 3027-3034
The compatibilization mechanism of some compatibilizers for blends of polyo
lefins with a liquid crystalline polymer (LCP) was studied. Polyethylene (P
E) and polypropylene (PP) were blended with a semirigid LCP (SBH) in a batc
h mixer, either with and without compatibilizers. The latter were two comme
rcially available samples of functionalized polyolefins, that is, a PE-g-MA
(HDM) and a PP-g-AA (Polybond 1001) copolymer and some purposely synthesiz
ed PE-g-LCP and PP-g-LCP copolymers. Microtomed films of the binary and the
ternary blends were annealed at 240 degrees C on the hot stage of a polari
zing microscope and the changes undergone by their morphology were recorded
as a function of time. The results indicate that the compatibilizers lower
the interfacial tension, thereby providing an improvement of the minor pha
se dispersion. In addition to this, the rate of the coalescence caused by t
he high-temperature treatment is appreciably reduced in the systems compati
bilized with the PE-SBH and PP-SBH graft copolymers. Among the commercial c
ompatibilizers, only Polybond 1001 displayed an effect comparable to that o
f the above copolymers. HDM improved the morphology of the as-prepared PE b
lends, but failed to grant sufficient morphological stabilization against a
nnealing-induced coarsening. The results are discussed with reference to th
e chemical structure of the different compatibilizers. (C) 2000 John Wiley
& Sons, Inc.