Microstructure and viscoelasticity in thermotropic copolyesters: the influence of monomer concentration

This research investigates the influence of monomer composition on the thermal transitions, mi crostructure, and viscoelastic properties of thermotro pic liquid crystalline polymers (LCPs) based on 1, 4-hydroxy-benzoic acid (B) and 2,6-hydroxy-naphthoic acid (N). Compositions B–N of 1:1, 1:3, 3:1, and 2:1 mol% were studied. The solid-to-nematic transition T _s→n was greatly influenced by the monomer composition, ranging from 230 to 280 °C. However, the decomposition temperature T _dec was independent of composition, all the materials degrading at T _dec = 509 °C. Polarized optical microscopy showed a threaded texture in the nematic phase. Fiber X-ray diffraction showed aperiodic meridional maxima for all LCPs, the number of maxima depended on composition. B–N 3:1 and 1:3 mol% favor the orthorhombic crystallographic phase whereas the 1:1 and 2:1 mol% crystallized in a pseudohexagonal phase. Dynamic time sweeps showed that the nematic phases are stable at the temperatures studied. Strain sweeps showed the existence of a linear viscoelastic (LVE) regime. The LVE properties ranged from predominantly viscous (G^′ < G^″) for the 1:1 mol% composition to predominantly elastic (G^′ > G^″) and with a well-defined rubber-like regime for the 1:3 mol% composition, resembling the rheology of flexible polymer melts. The persistence length q appears to be the parameter driving the rheological behavior.

Angel Romo-UribeEmail: