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.

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.

Sustainability can be defined as the ability of meet presents needs without compromise the ability of future generations to find their own needs. In this matter, scientists have been warning about natural resource scarcity, and now several researchers are aiming their efforts to develop sustainable technologies. Here, we focus on finding novel uses to biochar, a carbon rich material made from biomass that is usually applied on soil amendment. To expand its applications, biochars were activated using two different methods: a physical activation using CO₂; and a chemical one using KOH. We investigate here the dielectric properties of composites made with both activated biochars from white birch, where composites were made using silicone rubber matrix. It was also investigated the influence of composites made with biochar in powder and in flakes. All samples were characterized over the X-band frequency range. Composites made with powder presented a linear permittivity over the frequency range, while composites made with flakes presented oscillations on different frequencies. These oscillations are related to the composite surface, which induces reflection effects because of flakes arrangement in the top surface. Such effects widen opportunities to engineer new materials to be explored as radar-absorbing materials.

In this manuscript, the electromagnetic wave absorption properties of sustainable porous carbon composites were evaluated over the X-band frequency range (8.2 - 12.4 GHz). The porous carbon material was made from the byproduct of cellulose production and was used as additive on the development of radar absorbing material (RAM) composites. These porous carbon materials have different characteristics, such as porosity size (180 µm < Ø₁ < 250 µm and 425 µm < Ø₂ < 500 µm) and particle size (ϕ₁ < 250 µm and 250 µm < ϕ₂ < 425 µm). Composite materials were also studied as frequency selective surface (FSS) structures. It was shown how complex permittivity and reflection loss (RL) can be manipulated over the frequency range using FSS structure. While regular RAM presented RL of 19 dB at ~11.8 GHz, FSS structure presented a RL of 19 dB shifted to 12.4 GHz regarding the same carbon porous material (with particles between 250 and 425 µm and porosity between 180 and 250 µm). It was demonstrated here the potential use of sustainable porous carbon as RAM, and how FSS structure can be used to tune the frequency of the RL maximum peak.