The global demand for wood as a building material is steadily growing, while the availability of this natural resource is diminishing. This situation has led to the development of alternative materials. Of the various synthetic materials that have been explored and advocated, polymer composites claim a major participation as building materials. There has been a growing interest in utilizing natural fibres as reinforcement in polymer composite for making low cost construction materials in recent years. Natural fibres are prospective reinforcing materials and their use until now has been more traditional than technical. They have long served many useful purposes but the application of the material technology for the utilization of natural fibres as reinforcement in polymer matrix took place in comparatively recent years. Economic and other related factors in many developing countries where natural fibres are abundant, demand that scientists and engineers apply appropriate technology to utilize these natural fibres as effectively and economically as possible to produce good quality fibre reinforced polymer composites for housing and other needs. Among the various natural fibres, sisal is of particular interest in that its composites have high impact strength besides having moderate tensile and flexural properties compared to other lignocellulosic fibres. The present paper surveys the research work published in the field of sisal fibre reinforced polymer composites with special reference to the structure and properties of sisal fibre, processing techniques, and the physical and mechanical properties of the composites.

Compression molded biodegradable films based on poly(butylene succinate) (PBS) and poly(butylene adipate-co-terephthalate) (PBAT) at varying weights were prepared, and their relevant properties for packaging applications are here reported. The melt rheology of the blends was first studied, and the binary PBS/PBAT blends exhibited marked shear thinning and complex thermoreological behavior, due to the formation of a co-continuous morphology in the 50 wt% blend. The films were characterized by infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), mechanical tensile tests, scanning electron microscopy (SEM), and oxygen and water vapor permeability. PBS crystallization was inhibited in the blends with higher contents of PBAT, and FTIR and SEM analysis suggested that limited interactions occur between the two polymer phases. The films showed increasing stiffness as the PBS percentage increased; further, a sharp decrease in elongation at break was noticed for the films containing percentages of PBS greater than 25 wt%. Gas permeability decreased with increasing PBS content, indicating that the barrier properties of PBS can be tuned by blending with PBAT. The results obtained point out that the blend containing 25 wt% PBS is a good compromise between elastic modulus (135 MPa) and deformation at break (390%) values. Overall, PBS/PBAT blends represent an alternative for packaging films, as they combine biodegradability, good barrier properties and reasonable mechanical behavior.

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).

The aim of this work was to produce filaments of PLA/PBAT and NPK fertilizer adsorbed on organophilized bentonite intended for application in the prototyping of biodegradable agricultural artifacts in 3D printing, using the Fused Deposition Modeling (FDM) technique. This is the first time that we have reported this composite for a 3D printing approach. Systems containing PLA/PBAT, organobentonite and NPK were initially processed in an internal mixer and later extruded as filaments in a single-screw extruder. The prototypes were printed by FDM. Structural, morphological and thermal properties, as well as NPK releasing, were investigated. The results suggest that exfoliated and/or intercalated nanocomposites were obtained by the organoclay addition to the PLA/PBAT blend. The morphological analysis revealed a good surface quality of the impressions. Systems containing organobentonite released approximately 22% less fertilizer in 24 h compared to the systems without organobentonite. This difference is due to the higher concentration of nanoparticles that generate more barriers to the diffusion of NPK. The release data for these systems had a better fit to the kinetic model of Korsmeyer-Peppas. Thus, studied filaments have the potential to retard the release of fertilizer and are suitable for further development of structures for agricultural applications by FDM.

As propriedades tênseis de compósitos de matriz poliéster, reforçados por fibras curtas de sisal foram determinadas em função do comprimento, teor e orientação das fibras. Os resultados mostram que, para os compósitos investigados, a resistência à tração aumentou com o comprimento das fibras (5 – 45 mm), atingiu um plateau (45 – 55 mm) e então decresceu (55 – 75 mm) enquanto os valores de módulo e de alongamento na ruptura não dependiam do comprimento das fibras. A resistência à tração dos compósitos aumentou com o teor de fibras até 50% em peso e, a partir daí, tendeu a decrescer. A resistência à tração de compósitos reforçados por fibras orientadas e testados longitudinalmente ao reforço foi 10 vezes maior do que a sua resistência transversal e 3 vezes maior do que a resistência de compósitos reforçados por fibras dispostas ao acaso.