SynopsisRandom polyesteramides with different chemical compositions and block polyesteramides have been prepared by a two-step polycondensation method from adipoyl dichloride, 1,lO-decandiol, and 1,6-diaminohexane. A sample of alternating microstructure has been synthesized by melt polycondensation of 1,lO-decandiol and preformed bisesteramides. The thermal and viscoelastic behavior has been investigated and related to the chemical composition and chain microstructure. The random copolymers exhibit one transition in the crystalline phase, whereas two transitions are shown by the block copolymers. The viscoelastic behavior suggests that in the amorphous component a partial microsegregation of phase occurs, generating an intermediate structure between a monophasic and a biphasic amorphous system.
Quenched films of isotactic polypropylene were drawn at 110°C up to draw ratio λ = 18. The axial elastic modulus was measured as function of λ up to the highest achieved λ. The sorption and diffusion of CH2Cl2 at 25°C in the undrawn and drawn samples were studied. Exclusively transparent samples were used for the measurement of the density and transport properties. This reduces the maximum usable draw ratio to 15. The drawing process is inhomogeneous with neck propagation. In the neck the draw ratio increases by about 6. As a consequence of the increasing fraction of taut tie molecules the axial elastic modulus increases faster than the draw ratio. The transport parameters D, S, and λ indicate that the original lamellar morphology is completely transformed into the microfibrillar structure.
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