“…Arrhenius-like, with values 0.64 ± 0.01 eV for b relaxation and 0.38 ± 0.02 eV for g relaxation that are in agreement with values given in the literature [43]. Their magnitudes, which were determined as a temperature invariant D 3T, were 52 ± 12 K and 15.5 ± 6.3 K and the a parameters were 0.39 ± 0.02 for b and 0.38 ± 0.02 for g relaxation, respectively.…”
“…Arrhenius-like, with values 0.64 ± 0.01 eV for b relaxation and 0.38 ± 0.02 eV for g relaxation that are in agreement with values given in the literature [43]. Their magnitudes, which were determined as a temperature invariant D 3T, were 52 ± 12 K and 15.5 ± 6.3 K and the a parameters were 0.39 ± 0.02 for b and 0.38 ± 0.02 for g relaxation, respectively.…”
“…In a recent study on the Brill transition in transcrystalline nylon 66 we pointed out that the explanation for the effect of the crystalline structure on this first order transition must be based on the existence of reciprocal interactions between the crystalline and amorphous phases [14], which corresponded to the finding that structural changes within the crystalline domains in the lamellae (as in the Brill transition) are accompanied by changes in the packing of the amorphous chain segments outside the lamellae [15]. According to the scientific literature, nylon 66 exhibits three loss peaks, labeled α, β and γ (see e.g., [16][17][18]), representing different processes in the amorphous phase. Perhaps the only reference to an additional peak (shoulder) was made by Takayanagi in his study of nylon 6 [19].…”
Abstract.A prominent α′ process in specifically treated nylon 66 and microcomposite samples is identified by dynamic mechanical analysis and proposed to be an amorphous phase counterpart of the Brill transition identified by synchrotron wide-angle X-ray diffraction (WAXD). It is suggested that this α′ process, which marks a critical free volume change and an onset of segmental chain movement in the amorphous phase, precedes and prompts the Brill transition in the crystalline phase.
“…This relaxation is assigned to more co-operative motions of CH 2 sequences involving water molecules H-bonded to the free NH groups [8,13,1518,[22][23][24][25][26].…”
Section: Dielectric Spectroscopy Of 'As Received' Samplesmentioning
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