The mechanical properties and the low temperature specific heat have been measured in a class of polymer electrolytes based on complexes of poly(ethylene) oxide (PEO) and sodium metal salts. These blends are semicrystalline polymers whose degree of crystallinity is affected by the salt concentration: increasing the salt molar fraction tends to produce a single crystalline phase. The "fragility" of the amorphous phase has been obtained by modelling the mechanical αa relaxation. Increasing crystallinity increase the non-exponentiality of the αa relaxation and decreases both the fragility and the excess specific heat over that predicted by the Debye theory. These effects proves that the additional low-energy vibrations causing the low temperature excess specific heat are mainly introduced by the amorphous phase with no correlation with the degree of fragility.
Fragility and low temperature excess specific heat in polymer electrolytes
CARINI, Giuseppe;D'ANGELO, Giovanna;TRIPODO, Gaspare;
1998-01-01
Abstract
The mechanical properties and the low temperature specific heat have been measured in a class of polymer electrolytes based on complexes of poly(ethylene) oxide (PEO) and sodium metal salts. These blends are semicrystalline polymers whose degree of crystallinity is affected by the salt concentration: increasing the salt molar fraction tends to produce a single crystalline phase. The "fragility" of the amorphous phase has been obtained by modelling the mechanical αa relaxation. Increasing crystallinity increase the non-exponentiality of the αa relaxation and decreases both the fragility and the excess specific heat over that predicted by the Debye theory. These effects proves that the additional low-energy vibrations causing the low temperature excess specific heat are mainly introduced by the amorphous phase with no correlation with the degree of fragility.Pubblicazioni consigliate
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