The overuse of fossil-based resources to produce thermoplastic materials and rubbers is dramatically affecting the environment, reflected in its clearest way as global warming. As a way of reducing this, multiple efforts are being undertaken including the use of more sustainable alternatives, for instance, those of natural origin as the main feedstock alternative, therefore having a lower carbon footprint. Contributing to this goal, the synthesis of bio-based rubbers based on β-myrcene and trans-β-farnesene was addressed in this work. Polymyrcene (PM) and polyfarnesene (PF) were synthesized via coordination polymerization using a neodymium-based catalytic system, and their properties were compared to the conventional polybutadiene (PB) and polyisoprene (PI) also obtained via coordination polymerization. Moreover, different average molecular weights were also tested to elucidate the influence over the materials’ properties. The crosslinking of the rubbers was carried out via conventional and efficient vulcanization routes, comparing the final properties of the crosslinking network of bio-based PM and PF with the conventional fossil-based PB and PI. Though the mechanical properties of the crosslinked rubbers improved as a function of molecular weight, the chemical structure of PM and PF (with 2 and 3 unsaturated double bonds, respectively) produced a crosslinking network with lower mechanical properties than those obtained by PB and PI (with 1 unsaturated double bond). The current work contributes to the understanding of improvements (in terms of crosslinking parameters) that are required to produce competitive rubber with good sustainability/performance balance.

Composites based on low-density polyethylene (LDPE) were prepared withAgavefiber powder (AFP) that was coated by plasma polymerization process using ethylene gas. Treated and pristine AFP were analyzed by infrared spectroscopy, scanning electron microscopy, and contact water angle for the assessment of surface properties. The polymer composites were prepared by melt mixing using 0, 5, 10, and 20 wt% of AFP and their mechanical and thermal properties were measured. Dispersion evaluation in water confirmed that the AFP treated changed from hydrophilic to hydrophobic behavior and it was also corroborated with water contact angle tests. The addition of treated and untreated AFP (200 mesh) at 20 wt% promotes an increase of Young’s modulus of the composites of up to 60% and 32%, respectively, in relation to the neat matrix. Also, an increase of crystallinity of LDPE was observed by the addition of treated and untreated AFP; however no significant effect on the crystallization temperature was observed in LDPE containing AFP.