Several ethylene homopolymers and ethene/α-olefin-copolymers with crystallinities ranging between 85 and 12% were characterized by dynamic-mechanical measurements. The occurring relaxations were correlated to the crystallinity of the polymeric materials and to morphology. The α-relaxation, being attributed to interlamellar shear, was found to be around 60 oC with activation energies of about 120 kJ/mol in samples with more than 42% crystallinity. The β-transition shows a much greater variety among the different samples characterized. Its relaxation temperatures
vary between .40 and 10 oC with activation energies between 200 and 400 kJ/mol. The α- and β-relaxation of several quenched samples with crystallinities between 63 and 42% were found to overlap, thus producing bimodal maxima and different activation energies from the Arrhenius plots. A separation of these overlapping relaxations was only possible by measuring the relaxations over a frequency range of more than three orders of magnitude.
In other words, the material behaves thermorheologically complex, as several processes with different activation energies overlap each other. Thus, no master curve can be constructed, but instead a discussion about the relaxation time dependent activation energy would have to be conducted [30,33]. However, this complicated method does not have to be conducted, as E'' is a clearly separable peak, whose activation energy can, therefore, be determined with relative ease from the peak temperature.
This value was adopted, as it is approximately the mean of the crystallinity of the neighboring samples.
Piel C, Polymerizations of Ethene and Ethene-co-alpha-Olefin: Investigations on Short- and Long-Chain Branching and Structure Property Relationships. Department of Technical and Macromolecular Chemistry, Vol. Ph. D. Hamburg: University of Hamburg, 2005