Modelado de la biodegradación en biorreactores de lodos de hidrocarburos totales del petróleo intemperizados en suelos y sedimentos (Biodegradation modeling of sludge bioreactors of total petroleum hydrocarbons weathering in soil and sediments)
The growing interest in research and development of eco-friendlier materials makes attractive the use of bio-based and biodegradable polymers such as polylactic acid (PLA). However, the higher cost of PLA compared to conventional polymers limits its applications. Moreover, raw materials for rotational molding must be in a powder form, which further increases their cost. So, the main objective of this study was to use agave fibers to produce lower-cost PLA based rotomolded biocomposites (BC) without compromising its bio-sourced origin and to compare with a standard rotomolding resin: linear medium density polyethylene (LMDPE). To improve the fiber-matrix interface, a chemical surface treatment of the fibers with glycidyl methacrylate grafted polylactic acid (GMA-g-PLA) in solution was evaluated. The results showed that a better biocomposites’ morphology was obtained, especially with the fibers treated twice. The surface treatment was also shown to substantially improve the flexural and tensile properties of treated fiber biocomposites at higher fiber content (25% wt.) compared to those with untreated fiber. The surface treatment also led to a substantial reduction of the biocomposites porosity and water absorption. Overall, the samples were shown to have better mechanical properties than neat LMDPE while being eco-friendlier due to their bio-nature.
In this work, three different nanoclays (1.44P, 1.34MN, and Cloisite 15A) were used to reinforce an injection grade poly(lactic acid) (PLA). The nanocomposites (NCs) were prepared using three different nanoclay concentration levels (1, 3, and 5 wt%) in a twin-screw extruder. To evaluate their mechanical performance (static and dynamic tests) and thermal properties, the respective samples were obtained by injection molding. Results showed that the three nanoclays significantly increased the tensile and flexural modulus of the injection grade PLA. The 1.34MN NCs also showed improvement in the tensile strength. An increment in flexural strength was obtained with 1.34MN and 1.44P nanoclays, while with nanoclay 15A, the flexural strength decreased. Additionally, the use of 5 wt% of 1.44P nanoclay allowed an increase in impact strength while using 1.34MN and 15A nanoclays, the impact strength was similar to the one observed for pure PLA. In general, mechanodynamic analysis results showed that storage modulus increased with nanoclay content; while thermogravimetric analysis indicated that none of the nanoclays has a significant effect over the degradation temperature of pure PLA. Differential scanning calorimetry results showed that the crystallinity of PLA is enhanced with nanoclay inclusion. For 1.34MN NCs, X-ray diffraction observations exposed that the mineral clay relative intensity peaks disappeared indicating nanoclay exfoliation, which contributes to the increase in tensile and flexural strength in the NCs. Nevertheless for 1.44P and 15A nanoclays, an increase in the interlayer distance (intercalation) was detected.
Sugarcane straw (SCS) is a common agro-industrial waste that is usually incinerated or discarded in fields after harvesting, increasing the importance of developing added-value applications for this residue. In this study, sustainable biocomposites were produced, and the effect of sugarcane straw as a filler/reinforcement of commercial biopolymers was evaluated. Biocomposites were prepared using polylactic acid (PLA), polyhydroxybutyrate (PHB), polyhydroxybutyrate-co-hydroxyvalerate (PHBV), or green polyethylene (Green-PE) with different fiber contents (20, 30, and 40 wt.%). Dry-blending followed by compression molding was used for the biocomposites preparation. The results showed that PLA, PHB, and PHBV biocomposites retained the same impact strength as the neat matrices, even with 40 wt.% of sugarcane straw. The flexural and tensile modulus of PLA, PHB, and PHBV biocomposites increased with 20% of SCS, whereas, in Green-PE biocomposites, these properties increased at all fiber contents. Since any compatibilizer was used, both the flexural and tensile strength decreased with the addition of SCS. However, even with the highest content of SCS, the tensile and flexural strength values were around 20 MPa, making these materials competitive for specific industrial applications.
This study focused on the effect of the processing method on the thermal, mechanical, and biodegradation properties of polylactic acid/polyhydroxybutyrate (PLA/PHB) blends and their wood biocomposites. The blending techniques were dry‐blending or twin‐screw extrusion, both followed by compression molding. PLA/PHB blends were prepared using 15 and 25% wt. of PHB and biocomposites with 20 and 30% wt. of wood particles. Moreover, a compatibilizer was used during the extrusion process to achieve better matrix‐fiber adhesion. The results showed that the crystallinity of PLA significantly increased with PHB and wood, especially after twin‐screw extrusion. The best results in tensile, flexural, and impact strength were obtained with the extruded and compatibilized PLA/PHB blends, with values higher than the neat biopolymers. The compatibilized biocomposite with 15% wt. PHB, and 20% wt. wood particles showed higher tensile, flexural, and impact properties than PLA. The biodegradation test showed that all samples were disintegrated (above 40%) after 40 days in compost medium, observing slight decreases in the biodegradation rate when PHB or wood particles were added. Even when the lower mechanical properties were obtained with the dry‐blending technique, they are still competitive for different applications, providing the possibility to produce blends and biocomposites, avoiding the extrusion process that requires more energy consumption and longer processing times.
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