4.6 Article

Photodegradation of Poly(lactic acid) Stereocomplex by UV-Irradiation

期刊

JOURNAL OF POLYMERS AND THE ENVIRONMENT
卷 20, 期 3, 页码 706-712

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10924-012-0424-7

关键词

Polylactide; Stereocomplex; Photodegradation; UV-irradiation; Biodegradable polyesters

资金

  1. Japan Society for the Promotion of Science (JSPS) [16500291]
  2. Grants-in-Aid for Scientific Research [16500291] Funding Source: KAKEN

向作者/读者索取更多资源

Neat poly(l-lactic acid) (PLLA) and poly(d-lactic acid) (PDLA) films and PLLA/PDLA blend films were prepared by solution casting, and their photodegradation by UV-irradiation was investigated using wide-angle X-ray scattering (WAXS), gel permeation chromatography, differential scanning calorimetry, tensile testing, and polarized optical microscopy. The PLLA/PDLA blend film was more photodegradation-resistant than the neat PLLA and PDLA films when photodegradation was monitored by molecular weight, melting temperature, and WAXS crystalline peak positions. This indicates that the chains in both amorphous and crystalline regions of the PLLA/PDLA blend film were photo-cleavage-resistant compared to those of the neat PLLA and PDLA films. The changes in melting temperature and WAXS crystalline peak positions before and after photodegradation respectively indicated the increased crystalline lattice disorder and the decreased crystalline lattice sizes of the neat PLLA and PDLA films, whereas these changes were insignificant for the blend films. Photodegradation caused no significant change in tensile properties, with the exception of significant decreases in the tensile strength and elongation at break of PLLA/PDLA blend film. However, the tensile strength and elongation at break of the PLLA/PDLA blend film retained higher values compared to those of the neat PLLA and PDLA films during photodegradation. In spite of the slower photodegradation of the PLLA/PDLA blend film traced by M (n), T (m), and WAXS crystalline peak positions than that of neat PLLA and PDLA films, the rapid decrease in tensile strength and elongation at break of the former than that of the latter should be due to the highly-ordered structural difference between them, i.e., the three dimensional dry gel of the former and the spherulites of the latter.

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