By using the method proposed in the previous papers, the detailed fine structure in amorphous region of nylon 66 film and filament is disclosed from their dynamic loss tangent (tan δ) -temperature (T) curve. In annealing process, the elastic modulus fraction f
e decreases and heterogeneity index of amorphous region n
t increases monotonously with an increase in annealing temperature T
a for the unoriented film. In the annealing process of wet state, the f
e related to α
2 absorption, observed at 30°C (for 110 Hz), decreases more abruptly than that of α
1 absorption observed at 120°C (for 110 Hz). On the contrary, in the annealing process of dry state, the f
e related to α
1 decreases more abruptly than α
2. With an increase in stretching ratio, the f
e of the stretched film and filament decrease and their n
t increase monotonously. These tendencies of f
e and n
t during annealing and stretching are not limited to nylon 66, but have a general characters for another fiber-forming polymers, such as polyacrylonitrile, polyethyleneterephthalate, polypropylene and polyvinylalcohol.
Both f
e and n
t-T
a curves of the stretched film show minimum when the film is annealed in dry state for a fixed time of period and n
t increases nonotonously with T
a when the film is annealed in wet state. The complicated T
a dependence of f
e and n
t can be explained in termsof disorientation of oriented polymeric chains in the annealing process.
A new peak in tan δ-T curve is observed at ca. 90°C (for 110 Hz) for the samples annealed in dry state at T
a=200°C. This peak is closely connected to the amorphous state produced during the annealing process. Several peaks are observed in the main dispersion region oftan δ-T curve, corresponding to the annealing in dry or wet state and adsorption of water and these can reasonably be resolved by the theory in the view of heterogenieties of the packing states of polymeric chains in amorphous region.
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