Biodegradable blends of urea plasticized thermoplastic starch (UTPS) and poly(ε-caprolactone) (PCL) were prepared in a co-rotating twin screw extruder. The UTPS and PCL content varied in a range of 25wt%. The materials were characterized by capillary rheometry, scanning electron microscopy (SEM), termogravimetry (TGA), differential scanning calorimetry (DSC) and tensile tests. Capillary rheometry showed better interaction between UTPS and PCL at 110°C than at 130°C. SEM showed immiscibility of all blends and good dispersion of UTPS in PCL matrix up to 50wt%. However, a co-continuous morphology was found for UTPS/PCL 75/25. Thermal analysis showed that introducing PCL in UTPS, increased T due to higher thermal stability of PCL, and blends presented an intermediate behavior of neat polymers. The presence of PCL in blends improved significantly the mechanical properties of neat UTPS. Because they are totally biodegradable, these blends can be vehicles for controlled or slow release of nutrients to the soil while degraded.

Bionanocomposite films of poly(E-caprolactone) (PCL) and poly(butilene succinate-co-adipate) (PBSA) blends with cellulose nanocrystals (CNW) grafted with PCL chains (CNW-g-PCL) were prepared by solution casting and their thermal properties and crystallinity were studied. The CNW surface was modified with PCL chains by grafting "from" approaches, in an effort to improve their compatibility with the polymer blends. The grafting efficiency was evidenced by FTIR and TGA analysis. The acicular morphology of CNW-g-PCL was characterized by SEM. The TGA results showed an increase in the thermal stability of the CNW grafted with PCL chains. The PCL/PBSA blends showed higher thermal stability in comparison with the neat polymers and PCL/PBSA/CNW-g-PCL bionanocomposites. DSC results showed the CNW-g-PCL act as a nucleating agent in the bionanocomposites. Additionally, a better interaction of the CNW-g-PCL in the blends of 30/70 composition in comparison with the blends of 50/50 composition was characterized. The results obtained for aforementioned films prepared by solution casting encourage the production of such bionanocomposites by melt compounding (extrusion), aiming the achievement of new bionanocomposites materials with improved thermal and mechanical properties.

This paper reports on a study of highly filled composites of polypropylene (PP) and 75% by weight sugarcane bagasse fiber with and without alkali treatment and with and without coupling agent (SEBS-g-MA). Composites were prepared using a Rheomix600 mixer connected to a HAAKE torque rheometer. The thermal and mechanical behavior of these composites were investigated by thermogravimetry (TGA), differential Scanning Calorimetry (DSC), flexural tests, impact tests and scanning electron microscopy. Scanning electron microscopy (SEM) images taken from sugarcane bagasse fibers showed enhancements in the fiber's surface topography after the surface treatment process. The FTIR, TGA and SEM results for the fibers showed that the alkali treatment modified the fiber surface as well as the chemical composition. The impact test results showed a good potential of SEBS-g-MA as coupling agent and impact modifier in highly filled composites, increasing by more than 100% the impact strength of the composite as compared to those without the coupling agent. Scanning electron microscopy showed that addition of coupling agent improved the interfacial adhesion between the fibers and polypropylene.