Structure-Property Relationships of Copolymers Obtained by Ring-Opening Polymerization of Glycolide and E-Caprolactone. Part 1. Synthesis and Characterization - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Biomacromolecules Année : 2005

Structure-Property Relationships of Copolymers Obtained by Ring-Opening Polymerization of Glycolide and E-Caprolactone. Part 1. Synthesis and Characterization

Résumé

A series of copolymers with various compositions were synthesized by bulk ring opening polymerisation of glycolide and e-caprolactone, using stannous (II) octoate or zirconium (IV) acetylacetonate as initiator. Reaction time and temperature were varied so as to induce different chain microstructures. The resulting copolymers were characterized by 1H NMR, SEC, DSC and X-ray diffraction. The average lengths of glycolyl (LG) and caproyl sequences (LC), the degree of randomness (R) were calculated and compared to the values of completely random chains. The concentration of CGC sequences was also obtained which resulted from the transesterification reactions. Data showed that stannous (II) octoate leads to less transesterification than zirconium (IV) acetylacetonate, and lower temperature leads to less transesterification than higher temperature. The copolymers exhibited a more or less blocky chain structure because of the reactivity difference between glycolide and e-caprolactone. The crystalline structure and thermal properties depend on both the composition and the chain microstructure. PGA- and PCL-type crystallites were obtained for copolymers with intermediate compositions.

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hal-00416946 , version 1 (15-09-2009)

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Suming Li. Structure-Property Relationships of Copolymers Obtained by Ring-Opening Polymerization of Glycolide and E-Caprolactone. Part 1. Synthesis and Characterization. Biomacromolecules, 2005, 6 (1), pp.483-488. ⟨10.1021/bm0494592⟩. ⟨hal-00416946⟩
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