The rheological characterization of two commercial thermotropic liquid
crystalline polymers based on poly(ethylene terephthalate) (PET) and
para-hydroxybenzoic acid (PHB) is carried out. The thermal transitions
determined by DMTA are explained by the random character of these cop
olyesters, in comparison with nonrandom copolyesters synthesized by Ja
ckson and Kuhfuss. The evolution of the dynamic viscoelastic functions
with time in the nematic state is concave in shape for the 20%PET/80%
PHB copolymer, a result that leads us to treat this system as a suspen
sion of solid spheres (unmolten crystals) where the volume fraction of
crystals increases with time according to an Avrami equation. The res
ponse of 40%PET/60%PHB copolymer is similar to a chemical or physical
gelation and the hypothesis that the polydomain structure gives rise t
o a network is considered. Continuous flow, time-independent viscosity
results reveal the existence of a three-region flow curve for 40%PET/
60%PHB copolymer, but a Newtonian zone followed by a shear thinning re
gion for 20%PET/80%PHB sample. At high temperatures the isotropization
of the samples leads to a very strong decrease of the activation ener
gy of flow, which becomes zero for 40%PET/60%PHB. (C) 1998 John Wiley
& Sons, Inc.