In the context of circular economy, waste generated by fruit processing can be used to produce new materials with a wide range of uses. This study presents a method to synthesize biochar from peach kernel or grape pit waste. The adsorbents were tested in the removal of hexavalent chromium from synthetic wastewater with Cr6+ concentrations specific to plating processes. Characterization by BET, SEM, FTIR, and TG-DTG confirmed the formation of porous structures, and a well-functionalized surface. The effects of contact time, initial Cr6+ concentration, and adsorbent dose were investigated in static conditions. Both materials are efficient in hexavalent chromium removal, with sorption equilibrium achieved within 180 min. Kinetic studies indicated that the removal process follows a pseudo-second-order model. Equilibrium studies showed that optimal sorption occurred at pH = 6, with sorption capacities of 78.54 mg/g for biochar from peach kernels and 67.57 mg/g for biochar from grape pits. Hexavalent chromium followed a Sips adsorption isotherm for both biochars. Following the reusability study, it can be concluded that biochar from peach kernels maintains removal efficiency higher than 75% after four cycles.
Phosphates are key pollutants involved in the eutrophication of water bodies, creating the need for efficient and low-cost strategies for their removal in order to meet environmental quality standards. This study presents a comparative thermodynamic evaluation of phosphate ion adsorption from aqueous solutions using two sustainable and readily available materials: autoclaved aerated concrete (AAC) and pumice stone (PS). Batch experiments were conducted under acidic (pH 3) and alkaline (pH 9) conditions to determine equilibrium adsorption capacities, and kinetic experiments were carried out for the best-performing adsorbent. Adsorption data were fitted to the Langmuir and the Freundlich isotherm models, while kinetic data were evaluated using pseudo-first-order and pseudo-second-order models. The Freundlich model showed the best correlation (R2 = 0.90 − 0.97), indicating the heterogeneous nature of the adsorbent surfaces, whereas the Langmuir parameters suggested monolayer adsorption, with maximum capacities of 1006.69 mg/kg for PS and 859.20 mg/kg for AAC at pH 3. Kinetic results confirmed a pseudo-second-order behavior, indicating chemisorption as the main mechanism and the rate-limiting step in the adsorption process. To the best of our knowledge, this is the first study to compare the thermodynamic performance of AAC and PS for phosphate removal under identical experimental conditions. The findings demonstrate the potential of both materials as efficient, low-cost, and thermodynamically favorable adsorbents. Furthermore, the use of AAC, an industrial by-product, and PS, a naturally abundant volcanic material, supports resource recovery and waste valorization, aligning with the principles of the circular economy and sustainable water management.