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In this work, renewable composites were prepared by the association of a thermosetting resin synthesized via free-radical polymerization, using a mixture of tung oil, n-butyl methacrylate, and divinylbenzene, with silica-rich fillers, namely an algae biomass with high silica content, and a well-sorted sand. Furthermore, to investigate if the interaction between the non-polar resin and polar reinforcements could be improved, enhancing the materials’ mechanical properties, itaconic anhydride, a bio-derived molecule obtained from itaconic acid, was introduced to the resin composition. Thermogravimetric analysis (TGA) suggested that the thermal stability of the composites was overall not changed with the addition of itaconic anhydride. The mechanical properties of the sand composites, however, did improve, as the storage modulus at room temperature, measured by dynamic mechanical analysis (DMA), almost doubled in the presence of itaconic anhydride. The glass transition temperatures of the materials increased by approximately 30 °C when sand was used as a reinforcement. Water absorption experiments validated an increase in the polarity of the unreinforced resin by the addition of itaconic anhydride to its formulation. The composites, however, did not exhibit a significant difference in polarity in the presence of itaconic anhydride. Finally, scanning electron microscopy (SEM), equipped with energy dispersive spectroscopy (EDS), demonstrated better matrix–filler adhesion in the presence of itaconic anhydride for high-silica algae composites. 

Climate change, biomass utilization, and bioenergy recovery are among the biggest current global concerns. Wood is considered an environmentally benign material. Nevertheless, it must be processed for desired applications. Upon thermal treatment ranging from 180 °C to 280 °C, under low oxygen concentrations, wood becomes a material with improved dimensional stability, resistance to fungal attacks, grindability, hydrophobicity, and storage stability. Several strategies for wood treatment have been investigated over the course of the past decades, including the use of steam, nitrogen, smoke, vacuum, water, and hot oil. The goal of this work is to investigate the influence of pressure and atmosphere on the torrefaction of poplar. Through a systematic analysis of poplar wood samples treated under reduced pressures and different atmospheres, while keeping the same heating profile, it was possible to establish that changes observed for mass loss, color change, wood composition (via TGA/DTG analysis), functional groups (via FTIR), elemental analysis, and X-ray diffractograms relate directly to known reaction pathways occurring during torrefaction. Changes observed under reduced pressures have been associated with the relative concentration of oxygen in the reaction atmosphere and to the reduced diffusion times experienced by reactive by-products during the treatment. Conversely, extended diffusion times resulted in more significant changes for reactions carried out under N2, water vapor, and air.