Dielectric, mechanical, and NMR retardation (correlation) spectra for relaxations in linear polyethylene were calculated in normalized form and intercompared. For each of the two local‐mode relaxations in the γ region, called γ 1 and γ 2 , these spectra are found to be in excellent agreement. For the α region, the spectra for two mechanical processes, called α 1 and α 2 , two NMR processes, called α′ and α, and one dielectric process α were calculated. Excellent agreement is found between the spectra for the dielectric α and NMR α′ processes and also spectra for the mechanical α 2 and NMR α processes, due to molecular motion in the interior of crystals. However, the spectrum for the mechanical α 1 process is different from that for the dielectric α and NMR α′ processes, though the activation energy for the first process is almost the same as for the other two. This behavior is interpreted on the assumption that the dielectric α and NMR α′ processes are caused by molecular motion in lamellar surface layers while the mechanical α 1 process is due to grain‐boundary slip with viscous resistance of the surface layers in the boundaries. The shapes of the spectra, including the spectrum for the β process, are not affected by diluent.
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Kakizaki et al. (1985) studied this question.
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