THERMAL-CONDUCTIVITY AND THERMAL EXPANSIVITY OF THERMOTROPIC LIQUID-CRYSTALLINE POLYMERS

The thermal conductivity and thermal expansivity of a thermotropic liquid crystalline copolyesteramide with draw ratio lambda from 1.3 to 15 have been measured parallel and perpendicular to the draw direction from 120 to 430 K. The sharp rise in the axial thermal conductivity K-parallel to and the drastic drop in the axial expansivity alpha(parallel to) at low lambda, and the saturation of these two quantities at lambda > 4 arise from the corresponding increase in the degree of chain orientation revealed by wide-angle x-ray diffraction. In the transverse direction, the thermal conductivity and expansivity exhibit the opposite trends but the changes are relatively small. The draw ratio dependences of the thermal conductivity and expansivity agree reasonably with the predictions of the aggregate model. At high orientation, K-parallel to of the copolyesteramide is slightly higher than that of polypropylene but one order of magnitude lower than that of polyethylene. In common with other highly oriented polymers such as the lyotropic liquid crystalline polymer, Kevlar 49, and flexible chain polymer, polyethylene, alpha(p)arallel to of the copolyesteramide is negative, with a room temperature value differing from those of Kevlar 49 and polyethylene by less than 50%. Both the axial and transverse expansivity show transitions at about 390 and 270 K, which are associated with large-scale segmental motions of the chains and local motions of the naphthalene units, respectively. (C) 1995 John Wiley & Sons, Inc.