The structure and physical properties of in situ composites based on semiflexible thermotropic liquid crystalline copolyesteramide and poly(butylene terephthalate)
Rky. Li et al., The structure and physical properties of in situ composites based on semiflexible thermotropic liquid crystalline copolyesteramide and poly(butylene terephthalate), J POL SC PP, 38(3), 2000, pp. 403-414
Liquid crystalline polymer-poly(butylene terephthalate) (LCP/PBT) blends we
re prepared by melt mixing. The LCP employed was a thermotropic copolyester
amide based on 30 mol % of p-amino benzoic acid (ABA) and 70 mol % of poly(
ethylene terephthalate) (PET). The thermal, dynamic mechanical and rheologi
cal properties, morphology, and crystal structure of LCP/PBT blends were st
udied. The results showed that the semiflexible ABA30/PET LCP is miscible i
n the melt state with PET, and they are partial miscible in the solid state
. Differential scanning calorimetric measurements showed that the introduct
ion of the semiflexible LCP into LCP/PBT blends retards the crystallization
rate of PBT. However, the LCP dispersed phase acted as the sites for the n
ucleation of spherulites and enhance the degree of crystallinity of PET. Ho
t-stage optical microscopy examination revealed that the LCP microfibers wi
th random orientation are dispersed in the PET matrix of compression molded
LCP/PBT blends. Under the application of a shearing force, the LCP domains
in the PET matrix tended to deform into microfibers, and to orient themsel
ves along the flow direction. The formation of microfibers resulted in an i
ncrease of the storage modulus. The torque measurements indicated that the
melting viscosity of the LCP/PBT blends is much lower than that of the pure
PET. Finally, the wide-angle X-ray diffraction patterns indicated that PET
shows no structural change with the incorporation of LCP, but the apparent
crystal sizes of several diffraction planes change significantly. (C) 2000
John Wiley & Sons, Inc.