Js. He et al., FACTORS INFLUENCING MICROSTRUCTURE FORMATION IN POLYBLENDS CONTAININGLIQUID-CRYSTALLINE POLYMERS, Polymer engineering and science, 35(21), 1995, pp. 1695-1704
Four isotropic polymers, poly(butylene terephthalate) (PBT), polycarbo
nate (PC), polyethersulfone (PES) and polysulfone (PSU), were blended
by extrusion with a thermotropic liquid crystalline polymer (LCP) at d
ifferent temperatures. The morphology of extrudates was observed by me
ans of scanning electron microscopy and the intrinsic aspect ratio of
LCP fibrils and particles separated from matrix resin was measured wit
h an image analysis. Special attention was paid to the LCP fibrillatio
n in these four matrices in a wide temperature range from 270 to 360 d
egrees C and the internal relations among the effects of processing pa
rameters, such as viscosity ratio, extrusion temperature, and LCP conc
entration. The results show that the viscosity ratio of the dispersed
LCP phase to the continuous phase is a decisive factor determining the
formation of LCP fibrils, but its effect closely relates with the LCP
content. In the range of viscosity ratios investigated, 0.004 to 6.9,
and lower LCP content of 10%, significant fibrillation took place onl
y at viscosity ratios below 0.01. It is predicted that the upper Limit
of the viscosity ratio for LCP fibrillation will increase with increa
sing LCP content. A comparison of the morphologies of LCP/PES blends w
ith different LCP concentrations reveals that the LCP phase becomes co
ntinuous at a concentration of less than 50%, and high LCP content doe
s not always favor the formation of long and uniform LCP fibrils. The
extrusion temperature has a marked effect on the size of the minor LCP
domains. For fibril forming systems, the percentage of LCP fibrils wi
th larger aspect ratios increases with increasing extrusion temperatur
es. All these results are explained by the combined role of deformatio
n and coalescence of the LCP dispersed phase in the blend.