Poly(butylene succinate/diglycolate) random copolymers (P(BSxBDGy)) of various compositions were synthesized and characterized from the molecular, thermal, structural and mechanical point of view. All the polymers showed a good thermal stability and at room temperature they appeared as semicrystalline materials. The main effect of copolymerization was a lowering in the crystallinity and a decrease of T m respect to homopolymers. The dependence of T m on composition for copolymers with high butylene succinate unit content was well described by Baur's equation. WAXD measurements indicated that two different crystalline phases are present, depending on composition: copolymers with high BS unit content are characterized by PBS crystal phase, whereas those rich in BDG co-units crystallized in PBDG lattice. Amorphous samples showed a monotonic increment of T g as the content of BDG units is increased and this can be explained on the basis of interchain interactions, due to the high electronegativity of ether-oxygen atoms. A Fox-type equation was found to fit the T g data of completely amorphous samples, permitting the extrapolation of pure PBS T g value for the completely amorphous polymer. © 2012 Elsevier Ltd. All rights reserved.

Novel eco-friendly random copolyesters of poly(butylene succinate) containing ether-linkages

Gigli M.;
2012

Abstract

Poly(butylene succinate/diglycolate) random copolymers (P(BSxBDGy)) of various compositions were synthesized and characterized from the molecular, thermal, structural and mechanical point of view. All the polymers showed a good thermal stability and at room temperature they appeared as semicrystalline materials. The main effect of copolymerization was a lowering in the crystallinity and a decrease of T m respect to homopolymers. The dependence of T m on composition for copolymers with high butylene succinate unit content was well described by Baur's equation. WAXD measurements indicated that two different crystalline phases are present, depending on composition: copolymers with high BS unit content are characterized by PBS crystal phase, whereas those rich in BDG co-units crystallized in PBDG lattice. Amorphous samples showed a monotonic increment of T g as the content of BDG units is increased and this can be explained on the basis of interchain interactions, due to the high electronegativity of ether-oxygen atoms. A Fox-type equation was found to fit the T g data of completely amorphous samples, permitting the extrapolation of pure PBS T g value for the completely amorphous polymer. © 2012 Elsevier Ltd. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3718046
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