Tannins are one of the most natural, non-toxic, and highly reactive aromatic biomolecules classified as polyphenols. The reactive phenolic compounds present in their chemical structure can be an alternative precursor for the preparation of several polymeric materials for applications in distinct industries: adhesives and coatings, leather tanning, wood protection, wine manufacture, animal feed industries, and recently also in the production of new porous materials (i.e., foams and gels). Among these new polymeric materials synthesized with tannins, organic and carbon gels have shown remarkable textural and physicochemical properties. Thus, this review presents and discusses the available studies on organic and carbon gels produced from tannin feedstock and how their properties are related to the different operating conditions, hence causing their cross-linking reaction mechanisms. Moreover, the steps during tannin gels preparation, such as the gelation and curing processes (under normal or hydrothermal conditions), solvent extraction, and gel drying approaches (i.e., supercritical, subcritical, and freeze-drying) as well as the methods available for their carbonization (i.e., pyrolysis and activation) are presented and discussed. Findings from organic and carbon tannin gels features demonstrate that their physicochemical and textural properties can vary greatly depending on the synthesis parameters, drying conditions, and carbonization methods. Research is still ongoing on the improvement of tannin gels synthesis and properties, but the review evaluates the application of these highly porous materials in multidisciplinary areas of science and engineering, including thermal insulation, contaminant sorption in drinking water and wastewater, and electrochemistry. Finally, the substitution of phenolic materials (i.e., phenol and resorcinol) by tannin in the production of gels could be beneficial to both the bioeconomy and the environment due to its low-cost, bio-based, non-toxic, and non-carcinogenic characteristics.

Thermal treatments such as torrefaction and fast pyrolysis are commonly employed methods to produce biofuels with high-energetic properties. In this study, wood chips were heat-treated at different temperatures of torrefaction (315 °C) and fast pyrolysis (400 and 454 °C) to form energetic pellets. Three softwoods, jack pine (JP), balsam fir (BF), and black spruce (BS), were evaluated. Pellets are produced using 20% moisture content and 15% pyrolytic lignin as a binder. Untreated- and treated-wood residues were characterized by surface chemistry, elemental analysis, and chemical composition, whereas all pellets were characterized in terms of density, high heat value (HHV), and durability. Results showed that both thermal treatments caused significant changes in the physicochemical structure of wood residues. Using temperatures higher than 315 °C leads to the disappearance of hydroxyl groups, a decrease in oxygen and hydrogen contents, and an increase in carbon content. Regardless of the treatment temperature, pellets made from heat-treated JP had the best durability (93%). In contrast, the calorific values of wood-treated pellets reached up to 31 MJ/kg, compared to untreated-wood pellets (19 MJ/kg). Thus, the densification of the thermal-treated wood residues represents a potential approach for producing biofuels with high energetic value.

In this study, activated biochar was produced using pilot-scale technologies of fast pyrolysis and activation to create desirable morphology, surface chemistry, and adsorptive properties for application in supercapacitors. First, residues from white birch were converted into biochar by fast pyrolysis (~ 450 °C). Then, physical (using CO₂) or chemical (using KOH) activation was carried out in a homemade pilot-scale furnace at 900 °C. These synthesized materials presented distinct porosity structures: micro-/mesoporous (CO₂ material) and highly microporous (KOH material), reaching surface areas of up to 1700 m² g⁻¹. Electrochemical results showed that KOH-activated biochar had higher specific electrical capacitance in both acidic and neutral electrolytes with a maximum specific capacitance value of 350 and 118 F g⁻¹ at 1 A g⁻¹, respectively; while, for CO₂-activated biochar, the maximum obtained values were 204 and 14 F g⁻¹. The greater proportion of oxygenated and nitrogenated functional groups on the surface of the KOH activated biochar, along with its high surface area (with wider porosity), improved its performance as a supercapacitor electrode. Specifically, the low proportion of ultramicropores was determinant for its better electrochemical behavior, especially in the neutral electrolyte. Indeed, these results are similar to those found in the literature on the electrical capacitance of carbonaceous materials synthesized in a small-scale furnace. Thus, the chemical-activated biochar made from wood residues in pilot-scale furnaces is a promising material for use as electrodes for supercapacitors.