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In this article, the properties of a polylactide and starch composite (PLA/starch) and an acrylic acid grafted polylactide and starch composite (PLA-g-AA/starch) were compared. The composite containing PLA-g-AA was found to have much better dispersion and homogeneity of starch in the polymer matrix than the composite containing PLA, indicating better compatibility between the two phases. Better mechanical and thermal properties of the PLA-g-AA/starch composite, notably an increase in tensile strength and elongation at breakpoint, evidenced its superiority to the PLA/starch composite. Furthermore, the lower viscosity of PLA-g-AA/starch makes it easier to process than PLA/starch. Weight loss on exposure to a soil environment over a period of three months showed that the starch in the composites was almost completely biodegradable, even at a high degree of substitution (60 wt.-% starch). After three months in soil, a reduction in the mechanical properties of the blends was observed, especially in those with higher starch contents.

Differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD) and dynamic mechanical analysis (DMA) properties of poly(lactic acid)/ poly(butylene adipate-co-terephthalate) (PLA/PBAT) specimens suggest that only small amounts of poor PLA and/ or PBAT crystals are present in their corresponding melt crystallized specimens. In fact, the percentage crystallinity, peak melting temperature and onset re-crystallization temperature values of PLA/PBAT specimens reduce gradually as their PBAT contents increase. However, the glass transition temperatures of PLA molecules found by DSC and DMA analysis reduce to the minimum value as the PBAT contents of PLA x PBAT y specimens reach 2.5 wt %. Further morphological and DMA analysis of PLA/PBAT specimens reveal that PBAT molecules are miscible with PLA molecules at PBAT contents equal to or less than 2.5 wt %, since no distinguished phase-separated PBAT droplets and tan d transitions were found on fracture surfaces and tan d curves of PLA/PBAT specimens, respectively. In contrast to PLA, the PBAT specimen exhibits highly deformable properties. After blending proper amounts of PBAT in PLA, the inherent brittle deformation behavior of PLA was successfully improved. Possible reasons accounting for these interesting crystallization, compatible and tensile properties of PLA/PBAT specimens are proposed.

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ABSTRACT:In this study, tetra isopropyl ortho titanate (TTIP) and polycaprolactone (PCL) were chosen as the ceramic precursor and the continuous phase, respectively, for the preparation of novel nanocomposites by using an in situ sol-gel process. In addition, acrylic acid grafted polycaprolactone (PCL-g-AA) was investigated as an alternative to PCL. The hybrids (PCL/TiO 2 and PCL-g-AA/TiO 2 ) were characterized via Fourier transform infrared (FTIR) spectroscopy, dynamic mechanical thermal analysis (DMA), X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), and Instron mechanical testing. It was found that the carboxylic acid groups of acrylic acid acted as coordination sites for the titania phase to form chemical bonds, thus improving the properties of the acrylic acid grafted composite compared with its acrylicacid-free counterpart. The TiO 2 content also determined the strength of interfacial bonding between the polymer chains and the ceramic phase, as shown by changes in glass transition temperature (T g ) with TiO 2 content. The maximum values of tensile strength and T g were obtained with the PCL-g-AA/TiO 2 composite at 10 wt % TiO 2 . At TiO 2 contents above this, excess particles led to segregation between the organic and inorganic phases.

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