Photooxidation‐induced conformational changes and degradation behaviors of poly(butylene succinate) and poly(butylene succinate‐co‐adipate)

Author:

Padermshoke Adchara1,An Yingjun1,Kajiwara Tomoko1,Masunaga Hiroyasu2,Kobayashi Yutaka3,Ito Hiroshi34,Sasaki Sono567,Noguchi Hiroshi8,Kusuno Atsushi8,Takahara Atsushi1ORCID

Affiliation:

1. Research Center for Negative Emission Technologies Kyushu University Fukuoka Japan

2. Japan Synchrotron Radiation Research Institute Sayo‐gun Hyogo Japan

3. Research Center for GREEN Materials and Advanced Processing Yamagata University Yamagata Japan

4. Graduate School of Organic Materials Science Yamagata University Yamagata Japan

5. Department of Biobased Materials Science, Graduate School of Science and Technology Kyoto Institute of Technology Kyoto Japan

6. Faculty of Fiber Science and Engineering Kyoto Institute of Technology Kyoto Japan

7. RIKEN RSC‐Rigaku Collaboration Center RIKEN SPring‐8 Center Sayo‐gun Hyogo Japan

8. Science & Innovation Center Mitsubishi Chemical Corporation Kanagawa Japan

Abstract

AbstractTwo biodegradable polyesters, poly(butylene succinate) (PBS) and poly(butylene succinate‐co‐adipate) (PBSA), were artificially aged in a UV irradiation test chamber, and their photodegradation behaviors investigated. The attenuated total reflection (ATR) infrared (IR) spectra of the initial and UV‐aged samples revealed conformational changes in the tetramethylene sequences of the photoaged PBS and PBSA. The one‐dimensional wide‐angle X‐ray scattering (WAXS) profiles showed that the (110) d‐spacing of the α‐form crystal progressively decreased during UV aging, suggesting that the crystalline polymer chains became arranged more closely along the fiber axis. Accordingly, we conclude that PBS and PBSA transform from their TGTGT to nearly TTTTT conformations upon photoaging. The observed WAXS, small‐angle X‐ray scattering, and IR spectral data suggest that photodegradation preferentially occurs in the amorphous phase of each polymer. The less crystallizable butylene adipate co‐unit enhances the degradability of PBSA, with prolonged photooxidation leading to partial degradation of the crystalline region of the copolymer. This finding is consistent with and may be linked to the higher biodegradability of PBSA compared to PBS.

Funder

New Energy and Industrial Technology Development Organization

Publisher

Wiley

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