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This investigation focuses on the preparation of bio‐based composites from recycled poly (ethylene terephthalate) (PET) and sisal fibers (3 cm, 15 wt %), via thermopressing process. Plasticizers derived from renewable raw materials are used, namely, glycerol, tributyl citrate (TBC) and castor oil (CO), to decrease the melting point of the recycled PET (Tm ∼ 265°C), which is sufficiently high to initiate the thermal decomposition of the lignocellulosic fiber. All used materials are characterized by thermogravimetric analysis and differential scanning calorimetry, and the composites are also characterized via dynamic mechanical thermal analysis. The storage modulus (30°C) and the tan δ peak values of CT [PET/sisal/TBC] indicate that TBC also acts as a compatibilizing agent at the interface fiber/PET, as well as a plasticizer. To compare different processing methods, rheometry/thermopressing and compression molding are used to prepare the recycled PET/sisal/glycerol/CO composites. These two different methods of processing show no significant influence on the thermal properties of these composites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40386.

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Cellulose nanocrystals (CNC) were prepared from curauá fibers via acid hydrolysis, and used as reinforcing phase for high‐density biopolyethylene (HDBPE) or green polyethylene. Castor oil (CO), epoxidized soybean oil (ESO) and epoxidized linseed oil (ELO) were chosen as compatibilizers for this study. Nanocomposites reinforced with CNC (3, 6, and 9 wt %) were processed by extrusion, using CO (3, 6, and 9 wt %) to evaluate its action as CNC dispersing agent in the HDBPE matrix. From the results obtained for these films, the CNC and oil contents were set at 3 wt%. In addition to CO, ELO, and ESO were also used, and besides processing by extrusion, extrusion/hot‐pressing process was also considered, in order to compare the two processing techniques. The nanocomposites were characterized by microscopic, thermal, mechanical, and rheological analyses. The presence of oil leads to less opaque films and improved dispersion. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 1010–1019

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