The present manuscript describes the use of natural fibers as natural and sustainable reinforcement agents for advanced bio-based composite materials for strategic sectors, for example, the construction sector. The characterization carried out shows the potential of both natural hemp and linseed fibers, as well as their composites, which can be used as insulation materials because their thermal conductivity properties can be compared with those observed in typical construction materials such as pine wood. Nevertheless, linseed composites show better mechanical performance and hemp has higher fire resistance. It has been demonstrated that these natural fibers share similar properties; on the other hand, each of them should be used for a specific purpose. The work also evaluates the use of bio matrixes in composites, demonstrating their feasibility and how they impact the final material’s properties. The proposed bio-resin enhances fire resistance and decreases the water absorption capacity of the natural fibers, enabling the use of composites as a final product in the construction sector. Therefore, it has been demonstrated that it is possible to manufacture a biocomposite with non-woven natural fibers. In fact, for properties such as thermal conductivity, it is capable of competing with current materials. Proving that biomaterials are a suitable solution for developing sustainable products, fulfilling the requirements of the end-user applications, as it has been demonstrated in this research with the non-woven fibers for the non-structural components.

The expansion of the use of polymeric membranes in gas separation requires the development of membranes based on new polymers with improved properties and their assessment under real operating conditions. In particular, the fabrication of ultrathin films of high performance polymers that can be used as the selective layer in composite membranes will allow large reductions in the amount of the expensive polymer used and, hence, the cost of membrane fabrication. In this contribution, two polymers of intrinsic microporosity (PIMs) with very different chain configurations (two-dimensional, 2D, chains or conventional contorted three-dimensional, 3D, conformation) have been compared in their ability to form ultrathin films, showing the relevance of polymer design to obtain compact and defect-free films. Monolayers of the 2D polymer PIM-TMN-Trip can be efficiently deposited onto poly[1-(trimethylsilyl)-1-propyne] (PTMSP) to obtain composite membranes with a CO2/N2 selectivity similar to that of the corresponding thick membranes of the same PIM using only a small fraction of the selective polymer (less than 0.1%).

The growing quantities of plastic waste have raised environmental concerns, with almost a quarter of disposed plastics being sent to landfill. This has motivated research efforts into various recycling technologies to ease dependence on fossil resources, increasing circularity. Irradiation of various kinds, such as electron beam, beta and gamma rays, has been studied in the past as a way of revamping end-of-life polymer properties. The present work focuses on the effects of gamma radiation on the processability of new and recycled polymers, which is intimately linked with their rheological properties. In this study, both virgin and recycled polymers were irradiated under different radiation doses and the effects of the radiation on their viscosity assessed and compared. Results were analyzed making use of different theoretical relationships, and the causes of the changes in rheology were investigated by means of various characterization techniques, such as GPC, FTIR, EPR and DSC. Finally, the rheological curves of all samples were fitted to the Ostwald–de Waele relationship and the dependence of its parameters on the absorbed dose fitted to a function.

In order to reduce the negative impact on the environment of the current composite materials, renewable sources have been used as raw materials. One of the most promising approaches is the substitution of the reinforcement material by natural fibers, which are usually obtained from more sustainable resources (agro-waste). However, these materials have still some limitations and drawbacks for their use in high performance applications, one of the reasons being a poor interaction between fiber and matrix. Recent studies show the possibility of improving their mechanical properties by means of the application of a third material to increase interaction between fiber and matrix. In this paper the use of humins (a by-product of the production of furandicarboxylic acid) has been proved to be an efficient bio-binder for natural fibers and epoxy resin. Bio-composites containing different loadings of humins for large parts for ground transportation applications have been produced by liquid resin infusion, validating the aforementioned approach. The results obtained have demonstrated the feasibility of the strategy of using humins for improving the mechanical properties of bio-composites, accelerating the potential for their market acceptance.

In the pursuit of environmental sustainability, reduced emissions, and alignment with circular economy principles, bio-epoxy resin nanocomposites have emerged as a promising alternative to traditional petroleum-based resins. This study investigates the development of novel bio-epoxy nanocomposites incorporating iron-oxide nanoparticles (Fe₂O₃, MnP) as multifunctional fillers at loadings of 0.5 wt.% and 3.0 wt.%. MnP nanoparticles were synthesized and subsequently functionalized with citric acid (MnP-CA) to enhance their surface properties. Comprehensive characterization of MnP and MnP-CA was performed using X-ray diffraction (XRD) to determine the crystalline structure, attenuated total reflection Fourier-transform infrared spectroscopy (ATR-FTIR), thermogravimetric analysis (TGA), and zeta potential measurements to confirm surface functionalization. The bio-epoxy resins matrix (bio-EP), optimized for compatibility with MnP and MnP-CA, was thoroughly analyzed in terms of chemical structure, thermal stability, curing behavior, dynamic–mechanical properties, and surface characteristics. Non-isothermal differential scanning calorimetry (DSC) was employed to evaluate the curing kinetics of both the neat (bio-EP) and the MnP/MnP-CA-reinforced composites, offering insights into the influence of nanoparticle functionalization on the resin system. Surface zeta potential measurements further elucidated the effect of filler content on the surface charge and hydrophilicity. Magnetic characterization revealed superparamagnetic behavior in all MnP- and MnP-CA-reinforced (bio-EP) composites. This research provides a foundational framework for the design of green bio-epoxy nanocomposites, demonstrating their potential as environmentally friendly materials and representing an emerging class of sustainable alternatives. The results underscore the viability of bio-epoxy systems as a transformative solution for advancing sustainable resin technologies across eco-conscious industries.