Composites of poly(L-lactide) with hemp fibers: Morphology and thermal and mechanical properties

✍ Scribed by Robert Masirek; Zbigniew Kulinski; Donatella Chionna; Ewa Piorkowska; Mariano Pracella

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 791 KB
• Volume: 105
• Category: Article
• ISSN: 0021-8995
• DOI: 10.1002/app.26090

✦ Synopsis

Abstract

Composites of poly(L‐lactide) (PLA) with hemp fibers (Cannabis sativa), prepared by batch mixing and plasticized with poly(ethylene glycol) (PEG; weight‐average molecular weight = 600 g/mol), were examined by polarized optical microscopy, scanning electron microscopy, wide‐angle X‐ray scattering, differential scanning calorimetry, thermogravimetric analysis, and mechanical tests. The properties of both fully amorphous and semicrystalline samples of PLA/hemp and PLA–PEG/hemp composites were analyzed as a function of the fiber amount. The cold‐crystallization kinetics of PLA in amorphous composites were investigated under isothermal conditions within the range of 70–130°C. For PLA/hemp samples, the bulk crystallization rate displayed a maximum near 110°C, whereas for plasticized samples, a higher and almost constant crystallization rate was observed over the entire temperature range, independently of the hemp amount. The kinetics were then analyzed on the basis of the Avrami model. The effect of fibers on the growth morphology of PLA spherulites, as well as the influence of the plasticizer on the melting behavior of PLA crystals and their reorganization during heating, was also examined. The thermogravimetric analysis of the composites, carried out in both nitrogen and air, showed that the degradation process of fiber‐filled systems started earlier than that of plain PLA, independently of the presence of the plasticizer. Mechanical tests showed that the modulus of elasticity of the composites markedly increased with the hemp content, reaching 5.2 GPa in the case of crystallized PLA reinforced with 20 wt % hemp, whereas the elongation and stress at break decreased with an increasing amount of fiber for all examined systems. Plasticization with PEG did not improve the tensile properties of the composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 105: 255–268, 2007