Poly(lactic acid) (PLA) and polypropylene (PP) were comparatively investigated as matrices for injection-moulded composites containing small (1-3 wt%) amounts of short sisal fibre. The morphology, thermal and dynamic mechanical properties, as well as degradation characteristics were investigated. The scanning electron microscopy (SEM) micrographs of the composites show more intimate contact and better interaction between the fibres and PLA, compared to PP. This improved interaction was confirmed by the Fourier-transform infrared (FTIR) spectroscopy results which showed the presence of hydrogen bonding interaction between PLA and the fibres. The thermal stability (as determined through thermogravimetric analysis [TGA]) of both polymers increased with increasing fibre content, with a more significant improvement in the case of PP. The differential scanning calorimetry (DSC) results showed a significant influence of the fibres on the cold crystallization and melting behaviour of PLA, even at the low fibre contents of 1-3%. The influence of the fibres on the melting characteristics of the PP was negligible, but it had a significant influence on the nonisothermal crystallization temperature range. Both the storage and loss moduli of the PLA decreased with increasing fibre content below the glass transition of PLA, but the influence on the loss modulus was more significant. The dynamic mechanical analysis (DMA) results clearly show cold crystallization of PLA around 110 C, and the presence of fibres gave rise to higher modulus values between the cold crystallization and melting of the PLA. The presence of fibres also had an influence on the dynamic mechanical properties of PP. This article further describes basic biodegradation observations for the investigated samples.
The morphology and thermal stability of melt-mixed poly(lactic acid) (PLA)/poly(hydroxybutyrate-co-valerate) (PHBV) blends and nanocomposites with small amounts of TiO 2 nanoparticles were investigated. PLA/PHBV at 50/50 w/w formed a cocontinuous structure, and most of the TiO 2 nanoparticles were well dispersed in the PLA phase and on the interface between PLA and PHBV, with a small number of large agglomerates in the PHBV phase. Thermogravimetric analysis (TGA) and TGA-Fouriertransform infrared spectroscopy was used to study the thermal stability and degradation behavior of the two polymers, their blends, and nanocomposites. The thermal stability of PHBV was improved through blending with PLA, whereas that of the PLA was reduced through blending with PHBV, and the presence of TiO 2 nanoparticles seemingly improved the thermal stability of both polymers in the blend. However, the degradation kinetics results revealed that the nanoparticles could catalyze the degradation process and/or retard the volatilization of the degradation products, depending on their localization and their interaction with the polymer in question.
Nanocomposites of polycarbonate (PC) reinforced with nanosized silica particles were prepared by a melt mixing technique in an internal mixer. Two kinds of commercial hydrophilic fumed silicas differing in their specific surface area were added in amounts up to 5% by volume, and their reinforcing action was compared to that of organically modified silica, loaded in the same amounts. Particle–matrix interactions were investigated by means of rheological and dynamic-mechanical thermal analysis, demonstrating the important role played by the organic modifi- cation in the interactions with the polymer matrix, and showing an optimal nano- particle loading around 2 vol%. The scratch resistance of the nanocomposites obtained from hydrophilic silicas was investigated, and a remarkable enhancement in the indenter’s penetration resistance was observed for all the compositions with respect to pristine PC. The same behaviour was observed for the Shore D hardness and for the impact resistance of the nanocomposites that also significantly improved with the maximum load shifting from a minimum value of 521 N for pristine PC up to values grater than 1330 N for the nanocomposites, demonstrating the activation of effective mechanisms of energy dissipation due to the presence of the nanofillers
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