1985
DOI: 10.1016/0032-3861(85)90192-2
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Relaxation processes in crystalline polymers: experimental behaviour — a review

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Cited by 617 publications
(420 citation statements)
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References 94 publications
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“…This view is supported by the value of the apparent activation energy of the plastic flow contribution, approx. 30 kcal/mol, which is identical to the value of the activation energy of the dielectrical e-relaxation [30]. This interpretation is in accordance with the results and conclusions of Wilding and Ward in the case of meh-spun/drawn HDPE fibers [6,7].…”
Section: Irreversible Deformation (Plastic Flow)supporting
confidence: 88%
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“…This view is supported by the value of the apparent activation energy of the plastic flow contribution, approx. 30 kcal/mol, which is identical to the value of the activation energy of the dielectrical e-relaxation [30]. This interpretation is in accordance with the results and conclusions of Wilding and Ward in the case of meh-spun/drawn HDPE fibers [6,7].…”
Section: Irreversible Deformation (Plastic Flow)supporting
confidence: 88%
“…Diffusion of these small defects throughout the crystal lattice results in a 180 ~ rotational-C/2 translational (screw-jump) motion of the crystalline stem [24][25][26][27][28][29]. This screw-jump mechanism is generally accepted as being the molecular origin of the dielectrical e-transition in polyethylene [24][25][26][27][28][29][30][31].…”
Section: Irreversible Deformation (Plastic Flow)mentioning
confidence: 99%
“…For amorphous polymers, a non-symmetric distribution of times is expected for the α relaxation, associated with macromolecular segmental motion, at temperatures immediately above the glass transition. But for semi-crystalline polymers and more generally for heterogeneous systems, published data by Boyd [55], Laredo [56], Cebe [57], Noda [58], Ryabov [59], Janik [60], Feldman [61], Ortiz-Serna [29][30] etc., show that symmetrical distributions are observed for the α relaxation processes. However, the temperature dependence of a for the β process differs from that observed for the glass rubber relaxation since it decreases with temperature.…”
Section: Dielectric Measurementsmentioning
confidence: 99%
“…It is then caused in the PVDF main chains by cooperative micro-Brownian motions within their amorphous regions [35,36]. The process at about 10 0 Hz is ascribed to the molecular motions within the crystalline fraction of the PVDF material and it is named as α C relaxation [37][38][39][40]. The presence in all the specimens of this relaxation associated with motions within crystallites confirms that the primary polymorph developed is the non-polar α-phase since it practically disappears when β crystals are majority [41].…”
Section: Electric Propertiesmentioning
confidence: 99%