Abstract
the molecular motion in polymers is restricted to specific groups or structural rearrangements responsible for secondary relaxations. Numerous studies of subglass processes have been reported by utilizing mainly dynamic mechanical (MS) and dielectric (DS) spectroscopic techniques. There is a consensus about the Arrhenius temperature dependence of the characteristic relaxation rates, the inherent broad distribution, as well as the short correlation length of the underlying thermal fluctuations. Therefore, the observed agreement between MS, DS, and light scattering results for one polymeric glass system
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