Polymer, Vol.41, No.19, 7175-7192, 2000
The influence of molecular weight and thermal history on the thermal, rheological, and mechanical properties of metallocene-catalyzed linear polyethylenes
Several linear polyethylene homopolymers of varied molecular weight (13 less than or equal to M-w less than or equal to 839 kg/mol) were synthesized with a metallocene catalyst and characterized. The synthetic approach resulted in relatively narrow molecular weight distributions (2.3 < (M) over bar(w)/(M) over bar(n) < 3.6) as measured by size exclusion chromatography. The melt rheological data, \eta*(omega)\ were modeled by the Carreau-Yasuda equation. The as-polymerized polymer fluffs were compression molded into films of quenched and slowly cooled thermal treatments, This resulted in a rauge of sample densities between 0.9302 and 0.9800 g/cm(3), due to variations in the crystal content. The thermal, morphological, and mechanical behaviors were examined for the dependencies on both molecular weight and thermal treatment. The small-strain tensile deformation properties, Young's modulus, yield stress, and yield strain, were directly related to percent crystallinity, independent of molecular weight. However, increasing molecular weight led to a suppression of the peak in the stress-strain curves at the yield point. The large-strain deformation properties, toughness and strain at break, were influenced by the competing effects of percent crystallinity and molecular weight, The slit-smeared long spacings increased with molecular weight. There was a progression from ridged and planar lamellae to curved C and S-shaped lamellae with increasing molecular weight. Thermal treatment had a large influence on the shape of the mechanical alpha-relaxation, while the crystal content affected the magnitudes of the mechanical gamma and beta-relaxations. (C) 2000 Elsevier Science Ltd. All rights reserved.
Keywords:MELT-CRYSTALLIZED POLYETHYLENE;RANDOM COPOLYMERS;RELAXATIONPROCESSES;VISCOELASTIC PROPERTIES;TENSILE PROPERTIES;ALPHA-RELAXATION;POLYMER MELTS;SHEAR-FLOW;MORPHOLOGY;ETHYLENE