Vinasses are a residual liquid generated after the production of beverages, such as mezcal and tequila, from agave (Agave L.), sugarcane (Saccharum officinarum L.) or sugar beet (Beta vulgaris L.). These effluents have specific characteristics such as an acidic pH (from 3.9 to 5.1), a high chemical oxygen demand (50,000–95,000 mg L−1) and biological oxygen demand content (18,900–78,300 mg L−1), a high total solids content (79,000 and 37,500 mg L−1), high total volatile solids 79,000 and 82,222 mg L−1, and K+ (10–345 g L−1) content. Vinasses are most commonly discarded onto soil. Irrigation of soil with vinasses, however, may induce physical, chemical and biochemical changes and affect crop yields. Emission of greenhouse gases (GHG), such as carbon dioxide, nitrous oxide and methane, might increase from soils irrigated with vinasses. An estimation of GHG emission from soil irrigated with vinasses is given and discussed in this review.

An L-glutathione-functionalized silica adsorbent was applied in this study to remove malathion from aqueous media. This adsorbent has demonstrated an improved adsorption efficiency of malathion. The maximum uptake achieved was 130 mg g⁻¹ at pH 8. Equilibrium was reached after about 90 min. A pseudo-second-order model best described the adsorption kinetics. The adsorption isotherms were best simulated by the Freundlich model. The functional groups are thermally stable up to about 150 °C. The elemental analysis results indicated high glutathione ligand densities. The results of this study show that the environmentally friendly L-glutathione functionalized silica is a promising candidate for the removal of malathion from water at the industrial level.

Research on using biochar as an adsorbent of contaminants in aqueous matrices has gained significant relevance in recent years due to the surface chemistry and porous structure of biochar, which facilitate the retention of a wide range of pollutants. This study explores the adsorption performance of a novel biochar produced from agave bagasse—a readily available agro-industrial waste in Mexico—through low-temperature pyrolysis. The biochar was evaluated for its capacity to remove conventional water quality parameters (chemical oxygen demand (COD), nitrates (NO₃⁻), total nitrogen (TN), total phosphorus (TP), ammonium (NH₄⁺), turbidity, apparent color, and true color) from water samples collected from the polluted Bustillos Lagoon in Chihuahua, Mexico. Additionally, the removal of emerging pharmaceutical contaminants, specifically acetaminophen (Act) and diclofenac (Dfc), was assessed in synthetic aqueous solutions. Potentiometric titration analyses revealed a significant contribution of surface acidity in the adsorption of pharmaceutical derivatives, highlighting the relevance of functional groups retained during low-temperature pyrolysis. The biochar derived from agave bagasse (BBAF1) was tested in a fixed-bed column system and compared with two commercial activated carbons (CACCF2 and CVCF3). The BBAF1 biochar achieved average removal efficiencies ranging from 50% to 90% for all conventional parameters. In contrast, those of ACT and DFC were between 0.43 and 0.67 mg g⁻¹ (59–85%) and 0.34 and 0.62 mg g⁻¹ (37–79%), respectively, demonstrating their potential as an adsorbent material for improving water quality. This work supports the development of circular economic strategies by valorizing agricultural residues while offering an effective solution to environmental pollution challenges.

The development of oxidation-resistant and regenerable materials remains a major challenge for mercury removal from contaminated waters and industrial effluents. In this study, a zwitterionic mesoporous silica gel functionalized with L-cysteine (SG-3PS-Cys) was synthesized, where the thiol group is covalently anchored to the silica framework, preventing oxidative degradation while preserving –NH₃⁺ and –COO⁻ groups for Hg(II) coordination. Spectroscopic analyses (FTIR, XPS, and ¹³C NMR) confirmed the formation of a stable, thiol-free binding environment in which mercury interacts through carboxylate oxygen atoms, electrostatically stabilized by neighboring ammonium groups. The material exhibited a high surface area (134 m² g⁻¹) and uniform mesoporosity (9.8 nm), achieving a maximum Hg(II) uptake of 82.7 mg g⁻¹ at pH 3 with rapid kinetics and cooperative S-type isotherms. The adsorbent retained 72% of its capacity after five regeneration cycles and maintained 38.7% selectivity toward Hg(II) in multicomponent solutions. DFT-based surface energy distribution analysis supported the zwitterionic coordination mechanism, revealing energetically homogeneous and high-affinity binding domains. Beyond its chemical stability, the material introduces a sustainable route for mercury remediation, linking surface energy, electrostatic effects, and porosity to achieve durable performance under acidic and complex aqueous conditions. These findings provide a mechanistic and design framework for the next generation of non-thiol adsorbents capable of selective and reusable Hg(II) removal in environmentally relevant scenarios.

Reframing solid–solution interactions beyond classical site-density descriptions requires an interpretation integrating surface energetics, polarizability, and vibrational response. In this work, an energetic framework is developed to rationalize the interaction of As(V) with CNTsG0.5, a PAMAM-functionalized carbon nanotube hybrid selected after comparative evaluation of generation-dependent energetic responses. CNTs were synthesized by chemical vapor deposition, partially oxidized to introduce oxygenated anchoring groups, and covalently grafted with PAMAM, producing a chemically integrated solid phase with tunable dipole density and conformational flexibility. Comparative analysis identified CNTsG0.5 as the most suitable configuration, exhibiting a balanced distribution of accessible high- and low-energy regions enabling polarization-driven interactions with As(V). Time- and concentration-dependent responses were analyzed to resolve energetic accessibility and polarization strength. Results reveal rapid establishment of electronic coupling together with an energetically heterogeneous response associated with domains of distinct interaction strength. Spectroscopic evidence (FTIR, Raman, and XPS) confirms that As(V) interaction induces localized electronic rearrangements involving amide, amine, and oxygenated functionalities, consistent with charge redistribution and vibrational coupling at the CNT–PAMAM hybrid interface. DFT-derived surface-energy distributions, f(E), obtained from N₂ physisorption, correlate with these spectroscopic signatures. The combined experimental strategy provides design principles for hybrid solids governed by cooperative electronic response and surface-energy matching.