FIBRES & TEXTILES IN EASTERN EUROPE, cilt.13, sa.4, ss.15-21, 2005 (SCI-Expanded)
Six commercially available high-strength, high-modulus polyethylene fibres have been studied with the aim of developing a deeper understanding of their structure-property relationships. Structural studies have been carried out on the measurement of crystallite size and orientation parameters using a wide range of techniques including optical microscopy, thermal analysis and wide-angle X-ray diffraction techniques, together with polarised IR spectroscopy. Birefringence, melting temperatures, melting enthalpies and crystallinity values are found to increase with increasing tensile strength and modulus as a direct result of the increased chain alignment induced during the fibre-drawing stages. Careful examination of the results show that improving the chain alignment encourages the alignment and lateral perfection of unoriented non-crystalline chains. Analysis of wide-angle X-ray diffraction, polarised IR spectroscopy and thermal analysis confirms the presence of a three-phase structure consisting of polymorphic crystalline (i.e. orthorhombic and monoclinic), highly oriented non-crystalline (i.e. paracrystalline) and unoriented non-crystalline (i.e. amorphous) structures, as opposed to the classical two-phase (crystalline and amorphous) structures. Analysis of polarised IR data shows the existence of a polymorphic structure consisting of highly oriented orthorhombic and monoclinic crystallites, together with highly oriented non-crystalline structure containing pseudo-hexagonally packed chains. Analysis of second order orientation parameter