In the present study poly (butylene sebacate-co-terephthalate)s having different compositions were synthesized with a high yield and a random distribution by thermal transesterification of poly (butylene sebacate) and poly (butylene terephthalate) homopolymers. The copolymer with the highest comonomer ratio was the least crystalline sample, although the melting peaks corresponding to both, sebacate and terephthalate-rich phases were still observable in calorimetric heating runs. This copolymer was associated with interesting thermal and mechanical properties, as the maximum melting point was higher than 100 °C and the storage modulus was also high (i.e. 1.1 × 109 N/m2 and 1.7 108 N/m2 were determined just before and after the main glass transition temperature of -12 °C).\ud \ud As all studied samples were thermally stable up to temperatures clearly higher than the fusion temperature, they could be easily processed. Increasing the terephthalate content of the copolymers resulted in higher hydrophobicity, which had a minor influence on cell adhesion and proliferation of both fibroblast-like and epithelial-like cells. Hydrolytic and enzymatic degradability were assessed and the effect of composition and crystallinity on the degradation rate was investigated. Molecular weight measurements during exposure to a hydrolytic media indicated a first order kinetic mechanism during the initial stages of degradation before reaching a limiting molecular size, which was indicative of solubilization. The most amorphous sample appears as a highly promising biodegradable material since it showed a significant weight loss during exposure to all selected degradation media, but also exhibited good performance and properties that were comparable to those characteristic of polyethylenePeer ReviewedPostprint (author's final draft

Random poly(ethylene-co-1,4-cyclohexylenedimethylene terephthalate) and poly(ethylene-co-1,4-cyclohexylenedimethylene terephthalate)/organoclay nanocomposites were synthesized via in situ polymerization of terephthalic acid, ethylene glycol, 1,4-cyclohexane dimethanol, and aminosilane-modified Cloisite30B. An amorphous copolyester was produced with incorporating 30 mol% of 1,4-cyclohexane dimethanol in glycol part. Samples were characterized using Fourier transform spectroscopy, nuclear magnetic resonance, ¹³C-NMR and ¹H-NMR, X-ray diffraction, transmission electron microscopy, differential scanning calorimetry, thermal gravimetric analysis, and dynamic mechanical thermal analysis. Intrinsic viscosities of samples were in the 0.51–0.55 dL/g range. A commercial organoclay was modified prior to add into the reactor. ¹H-NMR and ¹³C-NMR spectra were applied to determine cis: trans isomer ratio of 1,4-cyclohexane dimethanol in polymer chains, Molar ratio of 1,4-cyclohexane dimethanol: ethylene glycol in polymer chains, degree of randomness, mean length of sequences, M_n, and Mark–Houwinks equation parameters. X-ray diffraction results of nanocomposites, including 0.5 and 1 wt% of organoclay, showed no peak in small angles, hence, modified organoclay presented exfoliated structure in polymer matrix. Differential scanning calorimetry analyses revealed that all samples were amorphous. Oxygen, nitrogen, and carbon dioxide diffusion rates in samples were investigated. Nanocomposite, including 3 wt% of organoclay, has about 60% less permeability in comparison to neat copolyester.