Thermal properties of poly(butylene isophthalate) and its copolyesters with poly(butylene adipate)
β Scribed by Maria Cristina Righetti; Maria Pizzoli; Andrea Munari
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 403 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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β¦ Synopsis
Abstract
The thermal properties of uniformly random poly(butylene adipate/isophthalate) copolyesters of various composition and different molecular weight were investigated by means of differential scanning calorimetry. All copolymers were partially crystalline, and the main effect of copolymerization was a lowering in the amount of crystallinity and a decrease of melting temperature with respect to pure homopolymers. The heat of fusion of 100% crystalline poly(butylene isophthalate), estimated by different methods, was found to fall within the range 22β25 kJ Β· mol^β1^. Completely amorphous samples, obtained by rapid quenching from the melt, showed a monotonic decrease of the glass transition temperature T~g~ and a monotonic increase of the heat capacity increment Ξ__C__~p~ with increasing butylene adipate content in the copolymers. The T~g~βcomposition dependence was found to be well fitted by the Couchman equation with no excess enthalpy correction.
π SIMILAR VOLUMES
The viscoelastic properties of random poly(butylene adipate/isophthalate) copolymers of various molecular weights and compositions were investigated by dynamic testing in the molten state. For all samples the storage and loss components of the dynamic shear modulus, G( v) and GΠ( v), were measured a
Characterization of poly(butylene adipate-co-succinate) (PBAS)/poly(butylene terephthalate) (PBT) copolyesters resulting from the intermolecular ester-exchange reaction between molten PBAS and PBT have been analyzed using 1 H-NMR spectroscopy, differential scanning calorimetry, wide-angle X-ray diff
The melting behavior and the isothermal crystallization kinetics of poly(buty1ene adipate), poly(buty1ene isophthalate) and their random copolymers were investigated by means of differential scanning calorimetry. Multiple endotherms, commonly observed on the melting polyesters, were found to be iinf