P. Gao et al., RHEOLOGY OF LOW NEMATIC TRANSITION-TEMPERATURE THERMOTROPIC LIQUID-CRYSTALLINE COPOLYESTER HBA HQ/SA/, Polymer engineering and science, 36(22), 1996, pp. 2771-2780
The rheology of a liquid crystalline copolyester of hydroxybenzoic aci
d, hydroqui none, and sebacic acid (HBA/HQ/SA copolyester) was studied
on both a rotational and a capillary rheometer. DSC studies show that
the copolyester has a crystal-mesophasic and a broad mesophasic-isotr
opic transition at 170 degrees C and 220 degrees C. Optical texture ob
servations show the mesophase is characterized by line defect textures
, which are characteristic of a nematic structure. At 220 degrees C, b
oth isotropic and nematic phases coexist with the latter being the maj
or. As temperature reaches 250 degrees C, a clear dominance of isotrop
ic phase is observed. At this temperature, the nematic phase of irregu
lar shapes randomly disperses within the isotropic matrix. Subsequent
rheological studies were thus conducted in crystal/nematic biphase, si
ngle nematic phase, nematic/isotropic biphase, and the near single iso
tropic phase. Dynamic strain sweep measurements show that a linear vis
coelastic region exists at all temperatures tested. The maximum strain
amplitude for the linear viscoelastic region is found to be highly st
ructure dependent; it is >100% in the nematic phase, similar to 20% in
the biphases, and only about 5% in the isotropic phase. The concurren
ce of curves obtained at different temperatures in a Cole-Cole plot of
G' vs. G '' indicates similar structures in the nematic phase and bip
hases. Measurements of steady shear viscosity using a rotational rheom
eter and a roundhole capillary rheometer show that in the nematic phas
e the copolyester behaves as a shear thinning fluid for a wide shear r
ate range of 1 similar to 10,000 s(-1), in which the power law index I
s about 0.6 similar to 0.8, and the viscosity is <10 Pa.s at shear rat
es >1 s(-1).