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Tytuł artykułu

Degradation of nanoclay-filled polylactide composites

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Nanoclay-filled polylactide (PLA 3051D) composite materials were tested in this study and their capacity for degradation was investigated. Activated and lyophilized smectite clay was used. The filler, its morphology, and grain size distribution were characterized by the use of transmission electron microscopy, scanning electron microscopy, and the dynamic light scattering technique. Samples of pure polylactide and polylactide filled with 3% wt., 5% wt., and 10% wt. of nanoclay in subsequent series were obtained by injection molding. The optimum amount of the filler in the nanocomposites was evalu-ated based on an assessment of mechanical properties as well as capacity to degrade. The 3% wt. mass fraction of nanofiller in the polylactide matrix was found to be the most effective in enhancement of both tensile strength (RM) and Young’s Modulus (E). It was also reported that polylactide nanocomposites filled with 3% wt. of smectite clay were characterized by the highest decrease in molecular mass of the matrix polymer after degradation tests (6 weeks incubation in water at 80°C). The observed decrease in degradation time and the overall changes distinguished in the nanocomposite structure suggest the poten-tial for application of the material in the packaging industry.
Rocznik
Strony
91--99
Opis fizyczny
Bibliogr. 21 poz., rys., tab.
Twórcy
  • AGH – University of Science and Technology, Faculty of Materials Science and Ceramics, Mickiewicza 30, 30-059 Cracow, Poland
  • AGH – University of Science and Technology, Faculty of Energy and Fuels, Mickiewicza 30, 30-059 Cra-cow, Poland
autor
  • AGH – University of Science and Technology, Faculty of Energy and Fuels, Mickiewicza 30, 30-059 Cra-cow, Poland
autor
  • AGH – University of Science and Technology, Faculty of Materials Science and Ceramics, Mickiewicza 30, 30-059 Cracow, Poland
autor
  • AGH – University of Science and Technology, Faculty of Materials Science and Ceramics, Mickiewicza 30, 30-059 Cracow, Poland,
autor
  • J. Haber Institute of Catalysis and Surface Chemistry PAS, Niezapominajek 8, 30-239 Cracow, Poland and Institute of Physical Chemistry PAS, Kasprzaka 44/52, 01-224 Warsaw, Poland
  • AGH – University of Science and Technology, Faculty of Materials Science and Ceramics, Mickiewicza 30, 30-059 Cracow, Poland
Bibliografia
  • 1. ALEXANDRE M., DUBOIS P., 2000. Polymer layered silicate nanocomposite: preparation, properties and use of new class of materials. Materials Science Engineering, 28 (1–2), 1–63.
  • 2. APPENDINI P., HOTCHKISS J.H., 2002. Review of antimicrobial food packaging. Innovative Food Science and Emerging Technologies 3, 113–126.
  • 3. AURAS R., HARTE B., SELKE S., 2004. An overview of polylactides as packaging materials, Macro-mol. Biosci. 4 (9), 835–839.
  • 4. AVELLA M., De VLIEGER J.J., ERRICO M.E., FISCHER S., VACCA P., VOLPE M.G., 2005. Biode-gradable starch/clay nanocomposite films for food packaging applications. Food Chemistry 93, 467–474.
  • 5. DRUMRIGHT R.E., GRUBER P.R., HENTON D.E., 2000. Polylactic acid technology. Advances Mate-rials 12 (23), 1841–1846.
  • 6. FUKUSHIMA K., TABUANI D., ABBATE C., ARENA M., FERRERI L., 2010. Effect of sepiolite on the biodegradation of poly(lactic acid) and polycaprolactone. Polymer Degradation and Stability 95, 2049–2056.
  • 7. FUKUSHIMA K., TABUANI D., CAMINO G., 2009. Nanocomposites of PLA and PCL based on mont-morillonite and sepiolite. Materials Science Engineering C 29, 1433–1441.
  • 8. LUNT J., 1998. Large-scale production, properties and commercial applications of polylactic acid poly-mers. Polymer Degradability Stability 59, 145–152.
  • 9. MATUSIK J., STODOLAK E., BAHRANOWSKI K., 2011. Synthesis of polylactide/clay composites using structurally different kaolines and kaolinite nanotubes. Applied Clay Science 51, 102–109
  • 10. MURARIU M., DECHIEF A., BONNAUD L., PAINT Y., GALLOS A., FONTAINE G., BOURBIGOT S., DUBOIS P., 2010. The production and properties of polylactide composites filled with expanded graphite. Polymer Degradation and Stability 95, 889–900.
  • 11. NAKAMURA T., HITOMI S., WATANABE S., SHIMIZU Y., JAMSHIDI K., HYON S.H., IKADA Y., 1989. Bioabsorption of polylactides with different molecular properties. J. Biomed. Mater. Res. 23, 1115.
  • 12. PADUA G.W., WANG Q.,2012. Nanotechnology research methods for foods and bioproducts. Wiley-Blackwell.
  • 13. PFAENDNER R., 2010. Nanocomposite: Industrial opportunity or challenge. Polymer Degradation and Stability 95, 369–373.
  • 14. PLATT D., editor., 2006. Biodegradable polymers – market reports. Shawbury, Shrewsbury, Shropshire: UK: Smithers Rapra Limited.
  • 15. SINHA RAY S., BOUSMINA M., 2005. Biodegradable polymers and their layered silicate nanocompo-sites: in greening the 21st century materials world. Prog. Materials Science 50 8, 962–1079.
  • 16. SINHA RAY S., OKAMOTO K., OKAMOTO M., 2003. Structure-property relationship in biodegrada-ble poly(butylenes succinate)/layered silicate nanocomposites. Macromolecules 36, 2355–2367.
  • 17. SOLARSKI S., FERREIRA M., DEVAUX E., 2008. Ageing of polylactide and polylactide nanocompo-site filaments. Polymer Degradation and Stability 93, 707–713.
  • 18. SORRENTINO A., GORRASI G., VITTORIA V., 2007. Potential perspectives of bio-nanocomposites for food packaging applications. Trends in Food Science and Technology 18, 84–95.
  • 19. TSUJI H., 2002, Polylactides, in Biopolymers, Wiley-VCH, chap. 5.
  • 20. TSUJI H., IKARASHI K., 2004. In vitro hydrolysis of poly(L-lactide) crystalline residues as extended-chain crystallites. Effects of pH and enzyme. Polymer Degradation Stability 85, 647–656.
  • 21. TSUJI H., MIZUNO A., IKADA Y., 1998. Blends of aliphatic polyesters III. Biodegradation of solution-cast blends from poly(L-lactide) and poly(caprolactone). Journal Applied Polymer Science 70, 11, 2259–2268.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-0d3bc8b8-7359-4970-b0b8-2bce2d3b654e
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