Blending of biodegradable polymers in combination with low-price organic fillers has proven to be a suitable approach to produce cost-effective composites in order to address pollution issues and develop products with superior mechanical properties. In the present research work PBAT/PHB/Babassu composites with 25, 50, and 75% of each polymer and 20% of Babassu were produced by melting extrusion. Their thermal, mechanical, and morphological behavior was investigated by differential scanning calorimetry (DSC), tensile testing, and scanning electron microscopy (SEM). Blending PBAT with PHB inhibited the crystallization of both polymers whereas adding Babassu did not significantly change their melting behaviour. Incorporation of Babassu reduced the tensile strength of its respective blends between 4.8 and 32.3%, and elongation at break between 26.0 and 66.3%. PBAT as highly ductile and low crystalline polymer may be seen as a crystallization tool control for PHB as well as a plasticizer to PBAT/PHB blends and PBAT/PHB/Babassu composites. As PBAT content increases: (i) elongation at break increases and (ii) surface fracture becomes more refined indicating the presence of more energy dissipation mechanisms. As PBAT/PHB/Babassu composites are biodegradable, environmental friendly, and cost effective, products based on these compounds have a great potential since their mechanical properties such as ductility, stiffness, and tensile strength are still suitable for several applications even at lower temperatures (−40 °C).

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Epoxidized soybean oil (ESO) compounds were cured with methyl tetrahydrophthalic anhydride (MTHPA) as hardener and 2,4,6-tris (dimethylaminomethyl) phenol (DEH 35) as catalyst. To figure out MTHPA and DEH 35's influence during curing and degradation, ESO/MTHPA/DEH 35 compounds were investigated using Fourier-Transform Infrared Spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetry (TG).FTIR spectra of uncured resin showed the secondary interactions among ESO's carbonyl groups with MTHPA and DEH 35's hydroxyls and amines. Curing progress was followed tracking the evolution of reactive groups, that is, epoxy and carbonyl bands and corroborated with released heat of DSC scans. ESO 87:5 and ESO 87:10 compounds cured using higher heating rates presented higher released enthalpy suggesting denser reticulation, and they also displayed lower activation energy E a ð Þ for curing, which was evaluated using the Friedman model. Increasing the hardener and catalysts contents promoted higher thermal stability and lower degradation rates, while higher E a for degradation was verified.