Inorganic arsenic in drinking water from groundwater sources is one of the potential causes of arsenic-contaminated environments, and it is highly toxic to human health even at low concentrations. The purpose of this study was to develop a magnetic adsorbent capable of removing arsenic from water. Fe₃O₄-monolithic resorcinol-formaldehyde carbon xerogels are a type of porous material that forms when resorcinol and formaldehyde (RF) react to form a polymer network, which is then cross-linked with magnetite. Sonication-assisted direct and indirect methods were investigated for loading Fe₃O₄ and achieving optimal mixing and dispersion of Fe₃O₄ in the RF solution. Variations of the molar ratios of the catalyst (R/C = 50, 100, 150, and 200), water (R/W = 0.04 and 0.05), and Fe₃O₄ (M/R = 0.01, 0.03, 0.05, 0.1, 0.15, and 0.2), and thermal treatment were applied to evaluate their textural properties and adsorption capacities. Magnetic carbon xerogel monoliths (MXRF600) using indirect sonication were pyrolyzed at 600 °C for 6 h with a nitrogen gas flow in the tube furnace. Nanoporous carbon xerogels with a high surface area (292 m²/g) and magnetic properties were obtained. The maximum monolayer adsorption capacity of As(III) and As(V) was 694.3 µg/g and 1720.3 µg/g, respectively. The incorporation of magnetite in the xerogel structure was physical, without participation in the polycondensation reaction, as confirmed by XRD, FTIR, and SEM analysis. Therefore, Fe₃O₄-monolithic resorcinol-formaldehyde carbon xerogels were developed as a potential adsorbent for the effective removal of arsenic with low and high ranges of As(III) and As(V) concentrations from groundwater.

Arsenic contamination of groundwater is still a global problem due to the toxicity at low dose on human health confirmed by epidemiological studies. Magnetic xerogel monoliths (MXs) were synthesized by the sol-gel polymerization using resorcinol, formaldehyde, alkaline catalyst and magnetite. The varying molar ratios of magnetite and resorcinol (M/R) in the gel were evaluated for As(V) removal from groundwater. The surface chemistry, structure and morphology of MXs related to arsenic adsorption were characterized by X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy and point of zero charge. Batch adsorption experiments were carried out to investigate the effects of Fe contents, initial pH and adsorbent dose on As(V) removal performance. The MXs with molar ratio of M/R at 0.15 gave the maximum As(V) adsorption capacity and removal with values of 62.8 µg/g and 86.7%, respectively. The adsorption data were well described by the Elovich equation of the kinetic model and the Freundlich isotherm. The thermodynamic studies demonstrated that the adsorption process was endothermic and spontaneous in nature. MXs showed to be a good alternative for As(V) removal from groundwater and achieving the efficient desorption, and thus fulfilled the Mexican standard for drinking water.

This paper presents a novel family of jarosites with the molecular formula MFe₃(SO₄)₂(OH)₆·xH₂O; M = Na, K, NH₄ that have high efficiency in the adsorption of As(V) and Pb(II) dissolved in water. The jarosites have been prepared by conventional heating at temperatures close to 95 °C for 3 h. The synthesis method was improved and optimized to reduce the time and energy consumption. The improved conventional heating method allowed for the synthesis of Na− and K−jarosites with a yield of up to 97.8 wt.% at 105 and 150 °C, respectively, in 3 h. The Na−, K−, and NH₄−jarosites were synthesized at 150 °C in 5 min via a microwave-assisted method, which yielded jarosite crystalline agglomerates with more uniform topography, shape, and size than the conventional method. Both methods allowed the selective synthesis of jarosites. Chemical decomposition of jarosites suspended in water occurred at a pH less than 2 and higher than 10 and temperatures up to 150 °C. In the solid state, the jarosites were thermally stable at least to 300 °C. The Na−jarosite presented a maximum adsorption capacity (Q_max) of 65.6 mg g⁻¹ for As(V) and 94 mg g⁻¹ for Pb(II). The jarosites are considered promising bifunctional adsorbents for the remediation of contaminated water due to their improved synthesis method, stability, and high adsorption capacity for ions of different natures.

Arsenic contamination demands innovative, sustainable remediation. This study presents a fuzzy approach for synthesizing a magnetic biochar nanocomposite from pecan shell agricultural waste for efficient arsenic removal. Using a Multi-Input Fuzzy Rules Emulated Network (MiFREN), a systematic investigation of the synthesis process revealed that precursor type (biochar), Fe:precursor ratio (1:1), and iron salt type were the most significant parameters governing material crystallinity and adsorption performance, while particle size and N₂ atmosphere had a minimal effect. The MiFREN-identified optimal material, the magnetic biochar composite (FS7), achieved > 90% arsenic removal, outperforming the least efficient sample by 50.61%. Kinetic analysis confirmed chemisorption on a heterogeneous surface (q_e = 12.74 mg/g). Regeneration studies using 0.1 M NaOH demonstrated high stability, with FS7 retaining > 70% removal capacity over six cycles. Desorption occurs via ion exchange and electrostatic repulsion, with post-use analysis confirming structural integrity and resistance to oxidation. Application to real groundwater from the La Laguna region proved highly effective; FS7 maintained selectivity despite competing ions like ${Na}^{+}$, ${Cl}^{-},$ and ${SO}_4^{2-}$. By integrating AI-driven optimization with reusability and real contaminated water, this research establishes a scalable framework for transforming agricultural waste into a high-performance adsorbent, supporting global Clean Water and Sanitation goals.

This study developed iron-oxide-functionalized carbon xerogels for enhanced arsenic adsorption to mitigate global water contamination. The composites were synthesized by integrating magnetite nanoparticles (15–20 nm) into a resorcinol–formaldehyde matrix via sol–gel polycondensation, followed by controlled pyrolysis. Key parameters—magnetite/resorcinol ratios (0.03–0.07), carbonization conditions (temperature, heating rate, duration), and H₂O₂-induced surface modification—were optimized to maximize adsorption performance. Characterization (SEM/EDX, XRD, FTIR, BET, TEM) confirmed uniform magnetite dispersion (~5 wt%) and revealed that pyrolysis at 850 °C enhanced porosity (378.8 m²/g surface area) and refined surface chemistry. Adsorption kinetics followed Elovich (R² = 0.9396) and Power Function (R² = 0.9443) models, indicating chemisorption dominance. Response Surface Methodology optimized desorption parameters using a Central Composite Design with three factors and two center points with repetition. A kinetic study of As(V) desorption from carbon xerogels was conducted, yielding optimal conditions: 1.0 M KOH, 160 rpm agitation, and 90 min contact time. The adsorbent retained >88% regeneration efficiency over four cycles, demonstrating robust reusability. Synergistic effects of magnetite incorporation, tailored pyrolysis, and H₂O₂ modification significantly improved arsenic selectivity and capacity in complex matrices, while enabling magnetic recovery.