It is known that the self-ordering ability is a characteristic trait of polymers forming a liquid-crystal phase. The processes of self-orientation of mesomorphic polymers in the liquid state are due to factors such as concentration of the solution or the temperature of the melt. In solid polymers the same role may be played by the temperature and the level of deformation (in a loaded specimen). It was shown in (1) that when some critical deformation is attained, it leads to the formation of structures with high thermal stability in polyamides (PA) obtained from a lyotropic solution, and in thermotropic polyester. Improved thermal stability manifests itself during extension, a consequence of which is also increased rigidity of the material and its self-reinforcement in the mechanical field. In our present work we obtained results enabling us to characterize processes of spontaneous deformation of aromatic PA both along the axis of orientation and transversely. The cause of deformation is the effect of a thermal field, and weak mechanical fields are used solely for fixing the specimen in a certain position; there the small loads applied to high-modulus materials barely bring about their deformation. In our work we chose infrared (IR) spectroscopy as directmore » method of investigating structural changes in spontaneous deformation. In distinction to x-ray structure analysis IR spectroscopy yields more complete information on the orientation of the crystalline as well as of the amorphous phase of polymers, and also on the molecular mobility.« less
Read full abstract