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Biodegradable poly(ethylene succinate) blends and copolymers containing minor amounts of poly(butylene succinate)

Authors

  • Hsin-Ying Lu,

    1. Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan, Republic of China
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  • Ming Chen,

    Corresponding author
    1. Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan, Republic of China
    • Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan, Republic of China
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  • Chi He Chen,

    1. Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan, Republic of China
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  • Jin-Shan Lu,

    1. Department of Materials and Optoelectronic Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan, Republic of China
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  • Kim-Chi Hoang,

    1. Department of Chemical and Material Engineering, Ta-Hwa Institute of Technology, Hsinchu 30743, Taiwan, Republic of China
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  • Min Tseng

    1. Bioresource Collection and Research Center, Food Industry Research and Development Institute, Hsinchu 300, Taiwan, Republic of China
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Abstract

Poly(ethylene succinate) (PES), poly(butylene succinate) (PBS), and PES-rich copolyesters were synthesized using an effective catalyst, titanium tetraisopropoxide. PES was blended with minor amounts of PBS for the comparison. The compositions of the copolyesters and the blends were determined from NMR spectra. Their thermal properties were studied using a differential scanning calorimeter (DSC), a temperature modulated DSC (TMDSC), and a thermogravimetric analyzer. No significant difference exists among the thermal stabilities of these polyesters and blends. For the blends, the reversible curves of TMDSC showed a distinct glass-rubber transition temperature (Tg), however, the variation of the Tg values with the blend compositions was small. Isothermal crystallization kinetics and the melting behavior after crystallization were examined using DSC. Wide-angle X-ray diffractograms (WAXD) were obtained for the isothermally crystallized specimens. The results of DSC and WAXD indicate that the blends have a higher degree of crystallinity and a higher melting temperature than those of the corresponding copolymers. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

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