The nature and origin of molecular motions in macromolecular polar and nonp
olar polymers which can affect the operation of electrets, are dependent on
their morphology including crystallinity. A qualitative theory of polymer
chain dynamics is provided by the reptation model in which a polymer chain
moves in a snake-like motion parallel to its own contour. Molecular motions
in amorphous polymers are more well defined than those in crystalline poly
mers. In contrast to mechanical relaxation theories, the dielectric relaxat
ion models are quite empirical, except in the Debye case. In addition to di
polar rotations, space charge relaxations can appear in all amorphous and s
emicrystalline polymers, and can be detected mostly by electrical studies.
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