Granular activated carbons were obtained from grape seeds by pyrolysis at 600°C and subsequent physical activation with CO₂ (750–900°C, 1–3 h, 25–74% burn-off). The carbon and ash content increased during the activation, reaching values of 79.0% and 11.4%, respectively. Essentially microporous materials with BET surface areas between 380 and 714 m²/g were obtained. The performance of the activated carbon in the adsorption of diuron in aqueous phase was studied within the 15–45°C temperature range. Equilibrium data showed that the maximum uptake increased with temperature from 120 to 470 µmol/g, also evidencing some dependence of the adsorption mechanism on temperature. Data were fitted to five isotherm models [Langmuir, Freundlich, Dubinin–Radushkevich, BET, and GAB (Guggenheim, Anderson, and de Boer)]. Kinetic data were analyzed using first- and second-order rate equations and intraparticle diffusion model. The second-order rate constant values obtained (2.8–13.5 × 10⁻³ g/µmol min) showed that the hollow core morphology of the material favors the adsorption kinetics.

Aqueous-phase reforming has been revealed as a novel, interesting and efficient process for the treatment of wastewater containing organic pollutants. However, due to the relatively severe operating conditions (above 15 bar and 200 °C), this process could become economically competitive if any solution for energy or material valorization is implemented. Most research has been devoted to direct the process to H₂ production as an alternative to reach economic sustainability, but the results obtained were not competitive in the current market of hydrogen and syngas. In this work, a preliminary simulation study (using Aspen HYSYS software) of the process heat balance in different conditions was implemented to induce a heat integration that would allow the auto-sustainability of the process, even generating in some cases an excess of energy that could constitute an opportunity for a positive economic balance. The results showed that this approach would only be possible by maximizing the methane production to the detriment of hydrogen production.

Nitrogen-doped porous carbons were prepared using a chitosan biopolymer as both a carbon and nitrogen precursor and metallic salts (CaCl₂ and ZnCl₂-KCl) as a templating agent with the aim of evaluating their performance as catalyst supports. Mixtures of chitosan and templating salts were prepared by simple grinding subjected to pyrolysis and finally washed with water to remove the salts. The resulting materials were characterized, showing that homogeneous nitrogen doping of carbon was achieved (7–9% wt.) thanks to the presence of a nitrogen species in the chitosan structure. A lamellar morphology was developed with carbon sheets randomly distributed and folded on themselves, creating slit-shaped pores. Substantial porosity was observed in both the micropore and mesopore range with a higher surface area and microporosity in the case of the materials prepared by ZnCl₂-KCl templating and a larger size of mesopores in the case of ZnCl₂. Catalysts with well-dispersed Pd nanoparticles (around 10 nm in diameter size) were synthesized using the chitosan-based carbons obtained both by salt templating and direct chitosan pyrolysis and tested in the aqueous phase hydrodechlorination of 4-chlorophenol. The fast and total removal of 4-chlorophenol was observed in the case of catalysts based on carbons obtained by templating with CaCl₂ and ZnCl₂-KCl in spite of the low metal content of the catalysts (0.25% Pd, wt.).