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.

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.

Fire-resistant elastic materials made from tannin, a natural polyphenol extracted from tree barks, and having the appearance and the consistence of rubber are described. They can be produced in any dimension and with any shape based on a quite simple protocol, only consisting in mixing tannin, water and ethylene glycol, in the presence of a low amount of p-toluene sulphonic acid. After curing at 85 °C in an oven and subsequent drying, black elastic blocks are recovered whose mechanical properties can be easily adjusted from the proportions of the ingredients, especially with the amount of ethylene glycol acting as plasticiser. As a result, materials from extra-soft to hard can be obtained. Their retardant performance towards fire is demonstrated, a well-known feature of phenolic compounds here observed for the first time with an elastic material. Physicochemical analyses are performed and explain the chemistry behind the performances of these new biosourced materials.

Energy storage is currently one of the most significant technological challenges globally, and supercapacitor is a prominent candidate over batteries due to its ability for fast charging and long lifetime. Supercapacitors typically use porous carbon as electrodes, because of both the high conductivity and surface area of the material. However, the state-of-the-art porous carbon described in the literature uses toxic chemicals and complex procedures that enhance costs and pollute the environment. Thus, a more sustainable procedure to produce porous carbon is highly desirable. In this context, xerogel-like carbons were prepared by a new, cheap, simple route to polymerization reactions of tannin-formaldehyde in a bio-oil by-product. Using bio-oil in its natural pH allowed a cost reduction and avoided using new reactants to change the reactional medium. Textural properties and electrochemical performances were improved by fast activating the material per 20 min. The non-activated carbon xerogel presented a capacitance of 92 F/g, while the activated one had 132 F/g, given that 77% of the components used are eco-friendly. These results demonstrate that renewable materials may find applications as carbon electrodes for supercapacitors. Overhauling the synthesis route with a different pH or replacing formaldehyde may enhance performance or provide a 100% sustainable carbon electrode.