Changes of the Molecular Mobility of Poly(ε-caprolactone) upon Drawing, Studied by Dielectric Relaxation Spectroscopy
Xiao Yan Yang (China Lucky Group Corporation)
Shao Shuai Liu (China Lucky Group Corporation)
A.V. Korobko (Dutch Polymer Institute)
Stephen J. Picken (TU Delft - ChemE/Advanced Soft Matter, Dutch Polymer Institute)
Nicolaas A.M. Besseling (Dutch Polymer Institute, TU Delft - OLD ChemE/Organic Materials and Interfaces)
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Abstract
Dielectric relaxation spectroscopy (DRS) of poly(ε-caprolactone) with different draw ratios showed that the mobility of polymer chains in the amorphous part decreases as the draw ratio increases. The activation energy of the α process, which corresponds to the dynamic glass transition, increases upon drawing. The enlarged gap between the activation energies of the α process and the β process results in a change of continuity at the crossover between the high temperature a process and the α and β processes. At low drawing ratios the a process connects with the β process, while at the highest drawing ratio in our measurements, the a process is continuous with the α process. This is consistent with X-ray diffraction results that indicate that upon drawing the polymer chains in the amorphous part align and densify upon drawing. As the draw ratio increases, the α relaxation broadens and decreases its intensity, indicating an increasing heterogeneity. We observed slope changes in the α traces, when the temperature decreases below that at which τα ≈ 1 s. This may indicate the glass transition from the ‘rubbery’ state to the non-equilibrium glassy state.
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