Search Results (2,822)

The valorization of phosphogypsum (PG), a byproduct of phosphoric acid production, along with waste glass (WG) and silica fume (SF) into value-added materials has attracted growing attention in recent years. The present study aims to synthesize three types of porous geopolymers (GD, GDP, and GDG) using Tunisian clay and locally available mineral wastes, and to investigate their potential as low-cost adsorbents for the removal of methylene blue (MB) dye from aqueous solutions. The physicochemical characteristics of the raw precursors and the resulting porous geopolymers were analyzed using various techniques, including FTIR, XRD, BET, and SEM. Variations in Si/Al, Na/Al, and Ca/Al ratios play a critical role in the geopolymer structure. The high Ca/Al ratio in GDP (porous geopolymer from calcined clay and phosphogypsum) promotes the formation of C-A-S-H, leading to increased macroporosity, which favors adsorption capacity despite the presence of a more heterogeneous morphology. The results indicated that the maximum adsorption capacity (Qmax) for MB dye was obtained for the GDP sample, reaching 68 mg/g. Adsorption experiments revealed the successful removal of MB dye by geopolymers, with the Langmuir isotherm and pseudo-second-order kinetic models adequately describing the adsorption process. The MB uptake by geopolymers was facilitated by weak physicochemical interactions, including electrostatic attraction, hydrogen bonding, and π–π interactions. This study proposes a simple and effective alkali activation strategy that combines different industrial wastes within a single geopolymer system, resulting in improved porosity and adsorption efficiency. Overall, the findings highlight the potential of these waste-derived geopolymers as promising and sustainable adsorbents for wastewater treatment applications. Full article

The P(IA-HBP-AA-AM)/MMT composite was successfully synthesized via in situ polymerization and characterized using FTIR, XRD, TGA, and other techniques. The material was then applied as an adsorbent for the removal of heavy metals from simulated mining-contaminated water (prepared based on the typical ionic composition of real mining wastewater). Static adsorption experiments revealed that P(IA-HBP-AA-AM)/MMT composite could efficiently remove Pb(II) from contaminated water, and the adsorption behavior was well described by the pseudo-second-order kinetic model and the Langmuir isotherm model. Thermodynamic analysis indicated that the adsorption of Pb(II) onto the P(IA-HBP-AA-AM)/MMT composite was an endothermic and spontaneous process. At pH = 4.5 and T = 45 °C, the maximum adsorption capacity obtained from model fitting was 249.38 mg/g. The material exhibited strong selectivity for Pb(II), even in the presence of competing metal ions such as Cd(II), Zn(II), Al(III), Fe(III), K(I), and Na(I). Moreover, after five adsorption–desorption cycles, it still retained approximately 90% of its Pb(II) removal efficiency. Furthermore, dynamic adsorption experiments showed that the saturation adsorption capacity of Pb(II) reached 178.7 mg/g, with a column utilization efficiency of approximately 41%. These findings demonstrate the promising potential of P(IA-HBP-AA-AM)/MMT composite for the removal of Pb(II) from mining-contaminated water. Full article

Wastewater from street food activities is a major pollution source. In this study, sewage sludge (SS) from a treatment plant in Thailand was converted into a porous adsorbent via NaOH activation and calcination (SS-B-C600), while SS-C600 was used as a control. Characterization revealed that both samples were composed of SiO₂ with minor kaolinite. FTIR confirmed Si–O–Si vibrations in both samples, while SS-B-C600 showed enhanced –OH (Si–OH) groups, indicating improved surface hydroxylation. Activation significantly enhanced the adsorption performance for methylene blue (MB) in laboratory-scale experiments. The equilibrium data were best fitted by the Langmuir isotherm model, indicating monolayer adsorption, with maximum capacities of 3.11 mg/g (SS-C600) and 7.56 mg/g (SS-B-C600). The kinetic results were well described by the pseudo-second-order model, suggesting that the adsorption mechanism is governed by a combination of porosity and surface interactions through physisorption. DFT calculations revealed that intermolecular hydrogen bonds between MB and aluminosilicate play a key role in the formation of the complex, while the calculated interaction energy (ΔE = −304.27 kJ/mol) further confirmed the presence of strong intermolecular interactions. Moreover, SS-B-C600 showed stable performance over three reuse cycles, highlighting its potential as a cost-effective and sustainable adsorbent. Full article

The increasing accumulation of mine waste and the associated release of toxic elements represent a major environmental challenge, particularly in regions impacted by Pb–Zn mining activities. In this context, this study aims to investigate the valorization of mine waste from Lakhouat, an abandoned Pb–Zn site in Northern Tunisia, as a sustainable additive in metakaolin-based geopolymers. This approach contributes to circular economy strategies by transforming hazardous waste into value-added materials for environmental and construction applications. Geopolymer formulations were synthesized by incorporating mine waste at different proportions (0, 5, 10, 20, and 30 wt.%) with metakaolin, while maintaining constant SiO₂/Al₂O₃ and Na₂O/Al₂O₃ molar ratios. The materials were prepared through alkali activation using sodium silicate and sodium hydroxide, followed by curing. Comprehensive characterization was carried out using X-ray fluorescence (XRF), X-ray diffraction (XRD), and scanning electron microscopy (SEM). In addition, adsorption experiments using methylene blue (MB) were conducted to evaluate the environmental performance of the synthesized geopolymers. The results revealed that the mine waste contains high concentrations of potentially toxic elements (up to 2.23 wt.% Pb and 8.2 wt.% Zn), highlighting the need for effective stabilization. Microstructural analysis confirmed the formation of predominantly amorphous geopolymer matrices with varying degrees of reaction depending on MW content. The highest compressive strengths (25–30 MPa) were achieved for formulations containing 5–10 wt.% MW after 28 days of curing. Furthermore, the geopolymers demonstrated efficient methylene blue removal, following pseudo-second-order kinetics and fitting the Langmuir isotherm model, with enhanced adsorption performance observed at higher MW contents. These findings indicate that MW-based geopolymers are promising materials for mine waste valorization and methylene blue removal. However, standardized leaching tests are required to confirm the long-term immobilization of Pb, Zn, Cd, As, and other potentially toxic elements within the geopolymer matrix. The study highlights their potential as sustainable, low-impact materials, supporting waste valorization and contributing to the development of environmentally resilient systems within a circular economy framework. Full article

Wastewater containing such inorganic contaminants, especially phosphate and nitrate ions, has to be treated thoroughly before disposal into natural environments. This is a precautionary measure to avoid adverse effects on public health, which are exacerbated when these two pollutants are present in an aqueous system. The present research investigated how the adsorption process is influenced by factors such as the effect of ion composition, contact time, temperature and competitive adsorption behavior in multi-anion systems using Ternary Biopolymer–Bentonite Beads. This study used five isotherms and four kinetic models to investigate phosphate ions removal on prepared natural Clay-Bio-polymer composite beads. The results indicate that the pseudo-second-order (PSO) kinetic model provides the most accurate description of the adsorption process. Moreover, the correlation coefficients (R²) obtained for both the Langmuir and Freundlich isotherm models are nearly equal to 1, confirming their strong reliability in fitting the experimental data. The strong fit of both the Langmuir and Freundlich models indicates that the adsorption process exhibits mixed behavior, with both monolayer adsorption on relatively homogeneous sites and multilayer adsorption on heterogeneous sites. This mixed-behavior system is typical of composite adsorbents with diverse surface properties. The Redlich-Peterson model, a hybrid of Langmuir and Freundlich, showed the best overall correlation (R² = 0.990 for H₂PO₄⁻ and 0.998 for NO₃⁻). The applicability of the Sips and Toth isotherm models, which account for both uniform and non-uniform adsorption behaviors, validated the experimental results. In the competitive binary system, the maximum adsorption capacities achieved by the composite were 121.844 mg/g for H₂PO₄⁻ and 27.979 mg/g for NO₃⁻. The results indicate strong competition between H₂PO₄⁻ and NO₃⁻ ions for the available active sites, reflecting an antagonistic adsorption. A positive value of ∆H° verifies that the adsorption process is endothermic and primarily physical, consistent with the experimental observations. The negative ∆G° values demonstrate that the adsorption occurs spontaneously, whereas the positive ∆S° indicates an increase in randomness at the solid–liquid interface during the uptake of phosphate ions. Full article

This study investigated the impact of cobalt/nickel-silicate loadings on graphitic carbon nitride at 10% and 20% doses, designated (CoNiSi-10) and (CoNiSi-20), for the removal of ciprofloxacin (CPF), a hazardous, bioaccumulative antibiotic. The synthesized composites were characterized in detail using SEM, EDX, TEM, N₂ adsorption–desorption, XRD, and FTIR techniques. The CoNiSi-10 and CoNiSi-20 exhibited CPF q_t values of 64 and 107 mg g⁻¹, respectively, which were consistent with the surface area results. Adsorption kinetics indicated that CPF uptake on CoNiSi-10 and CoNiSi-20 fitted the Lagergren model, with the liquid-film and intraparticle-diffusion mechanisms co-governing CPF sorption. The isotherm investigations indicated CPF adsorption on CoNiSi-10 and CoNiSi-20 aligned with the Langmuir model, suggesting a homogeneous surface, while the Dubinin-Radushkevich results primarily indicated physisorption-based CPF removal. The thermodynamic analyses supported the physisorption outcome and indicated that CPF sorption onto CoNiSi-10 and CoNiSi-20 was endothermic. A five-cycle reusability test yielded average efficiencies of 94% and 96% for CoNiSi-10 and CoNiSi-20, respectively, and an after-sorption analysis indicated their stability and robustness. The ease of synthesis and excellent sorption performance may nominate CoNiSi-10 and CoNiSi-20 as promising adsorbents for treating pharmaceutically contaminated wastewater. Full article

The adsorption of aromatic hydrocarbons from liquid paraffin is essential because of their harmful nature, long-lasting presence, and detrimental effects on the quality of the product. In this study, we investigated the adsorption of naphthalene from liquid paraffin by using a nanoclay-based adsorbent prepared from boron enrichment process waste. The characterization of the prepared adsorbent was carried out by using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS) and N₂ adsorption–desorption techniques, which confirmed the development of a layered nanostructure containing boron that possesses a porous and high-surface-area format appropriate for the adsorption. The hydrothermal treatment significantly increased the BET surface area from 35.42 to 112.15 m²/g, indicating the successful formation of a porous nanostructure. The kinetic and isotherm parameters of the adsorption process were calculated from experimental data. The adsorption of naphthalene followed pseudo-second-order kinetics and the isotherm fit well to the Langmuir model. Adsorption experiments revealed that the optimum adsorption performance was achieved at pH 4.0, and equilibrium was reached within 90 min. The adsorption kinetics were best described by the pseudo-second-order model (R² > 0.99), while the equilibrium data showed excellent agreement with the Langmuir isotherm model (R² = 0.995), suggesting monolayer adsorption. The maximum adsorption capacity of BNC was determined as 365.20 mg/g, which was more than twice that of the raw BEW (247.59 mg/g). Thermodynamic analysis indicated that the adsorption process was spontaneous at lower temperatures and exothermic, with a ΔH° value of −15.42 kJ/mol for BNC. The results suggest that the adsorption occurs through a multi-step process, beginning with external film diffusion, followed by pore diffusion and surface interaction. Based on the kinetic, isotherm, and spectroscopic data, a supramolecular adsorption mechanism is suggested, which encompasses π-π interactions, van der Waals forces, and surface complexation between naphthalene and the nanoclay structure. These results indicate that boron enrichment process waste-derived nanoclay is a sustainable, economical, and efficient adsorbent for removing naphthalene from liquid paraffin. Full article

The wet recovery of spent lithium iron phosphate (LFP) batteries is severely hindered by the low efficiency of copper removal. Here, a new process has been developed using a copper-removing chelating resin with pyridine nitrogen, carboxyl, and hydroxyl groups for the selective separation of copper ions. This copper chelating resin achieved a copper removal efficiency of 96.99% and reduced the residual copper content to below 10 milligrams per liter, significantly outperforming the traditional iron powder method. The adsorption process is highly sensitive to pH, with the highest efficiency at pH 1.75. A concentration of 2.0 moles per liter of H₂SO₄ can achieve a desorption rate of approximately 95%. The adsorption process follows the Langmuir isothermal equation and the pseudo-second-order kinetic model, corresponding to single-layer chelated chemical adsorption. Mechanism studies have confirmed that the synergistic coordination effect of the multifunctional groups helps in the efficient capture of copper ions. This copper chelating resin exhibits excellent stability, reversibility, and reusability, providing a promising method for efficient copper removal and recovery in the wet metallurgical recycling of LFP. Full article

The pressing issues of organic pollutants contamination of aquatic ecosystems challenges current research. Herein, we prepared three melamine-based POFs, to remove organic dyes from water. Melamine was polymerized with 1,4-dibromobutane (POF-1,4), terephthalaldehyde (POF-TerA) and trimesic acid (POF-TriA), obtaining POFs of different structural order degree and aromaticity. POFs were characterized using FT-IR spectroscopy, thermal gravimetric analysis, BET, powder X-ray diffraction and scanning electron microscopy. They were employed to remove cationic (Rhodamine B, RhB and Methylene Blue, MB) and anionic dyes (Methyl Orange, MO and Eosin Yellow, EY), using UV-vis investigation. The adsorption process was studied from the kinetic and thermodynamic points of view and reusing the best adsorbent was also considered. Data collected evidence that adsorption capacity depends on the POF structure, with maximum adsorption capacity, according to Langmuir isotherm model, of 329 mg/g for POF-1,4/MO and 472 mg/g for POF-TerA/RhB. Interactions involved in the adsorption were also elucidated. Comparison with reported data demonstrates that our materials show comparable performance to some previously reported systems. Furthermore, POF-TriA, is effective for dye mixtures and reusable three times without performance loss, after washing with methanol, avoiding harsh acidic/basic treatments. Results obtained systematically relate the adsorption efficiency to structural features of melamine-based POFs, representing useful support in designing such materials to remove selected classes of contaminants. Full article

This study investigates the potential of several sustainable agricultural by-products—including olive stones, cork, and almond shells, which are locally available in Alentejo, Portugal—as low-cost adsorbents for the removal of methylene blue (MB) from synthetic wastewater. The biomass residues were evaluated both in their raw form and after conversion into activated carbons (ACs) through chemical activation with KOH at 973 K. The produced ACs exhibited well-developed surface areas (760–1103.5 m² g⁻¹) and porous structures (0.31–0.51 cm³ g⁻¹). The adsorbents were characterised in terms of their chemical and textural properties. Raw biomass materials presented acidic surface groups, whereas the ACs presented neutral or basic groups. Batch adsorption experiments were conducted to assess the effects of adsorbent particle size, solution pH, initial MB concentration, stirring speed, contact time, and temperature on dye removal efficiency. Among all tested materials, the ACs achieved superior MB adsorption capacities, ranging from 244.2 to 317.6 mg g⁻¹, compared to the untreated biomass adsorbents, which showed capacities between 34.1 and 46.4 mg g⁻¹. The adsorption data were best described by the Langmuir isotherm model, while the kinetic data closely followed the pseudo-second-order (PSO) model. Thermodynamic analysis revealed that MB adsorption was spontaneous and endothermic; however, the relatively low enthalpy values indicated that physical interactions contributed significantly, particularly in the case of the raw biomass adsorbents. This suggests that the PSO model may also be applicable when physical adsorption is the dominant mechanism. This work demonstrates the novel use of cork, olive stone, and almond shell biomasses and their derived ACs as sustainable adsorbents, highlighting an integrated approach that simultaneously promotes efficient wastewater treatment, waste valorisation, and circular economy-driven socio-economic development. Full article

For the removal of hexavalent chromium [Cr(VI)] from drinking water, a hybrid biosorbent designated chitosan–natural diatomaceous earth (CNDE) was developed and thoroughly characterized. The material couples the ion-exchange and chelating capacity of chitosan—applied at an 85% degree of deacetylation—with the high-surface-area mineral framework of natural diatomaceous earth, onto which the polymer was deposited as a conformal coating. Surface morphology and internal microstructure were examined by scanning and transmission electron microscopy (SEM/TEM), while elemental composition across the hybrid matrix was resolved by energy-dispersive X-ray spectroscopy (EDX). Fourier transform infrared (FTIR) spectroscopy was employed to identify the surface functional groups responsible for chromate binding, and streaming current measurements established the pH of zero charge (pH_pzc), which governs the electrostatic environment at the sorbent–solution interface. Specific surface area was quantified by the Brunauer–Emmett–Teller (BET) method, and the balance of surface acidic and basic sites was determined through titrimetric analysis of total acidity and alkalinity. Thermogravimetric analysis (TGA) was conducted to assess thermal stability. Batch equilibrium isotherm experiments were performed to evaluate Cr(VI) uptake from model drinking water prepared using dilute potassium dichromate solutions adjusted to target pH levels. The effects of solution pH and competing anions (chloride and sulfate) were also investigated. Kinetic studies were conducted to determine the rate of Cr(VI) adsorption, and residual metal concentrations were measured using inductively coupled plasma mass spectrometry (ICP-MS). Results indicated that CNDE containing 30% chitosan (CNDE30) achieved effective Cr(VI) removal at pH 5. Adsorption was strongly pH-dependent, decreasing as pH increased from 5 to 8. Equilibrium data were well described by both Langmuir and Freundlich isotherm models, while kinetic data followed a pseudo-second-order model. The presence of chloride ions (15 mg/L) reduced adsorption capacity by approximately one-third, whereas sulfate at the same concentration significantly inhibited Cr(VI) removal. Overall, the isotherm results suggest that CNDE30 is a promising material for Cr(VI) removal from drinking water. Its cost-effectiveness, ease of synthesis, and potential for reuse make it particularly attractive for small-scale and decentralized water treatment applications. Full article

The release of persistent azo dyes into aquatic systems remains a critical environmental and toxicological concern due to their high chemical stability, resistance to biodegradation, and potential to generate carcinogenic aromatic amines. This study evaluates the adsorption of Amberlite XAD-4 (X4), a hydrophobic polystyrene–divinylbenzene resin, for the removal of the toxic azo dye Direct Red 23 (DR 23) from aqueous solutions. Batch experiments were performed to assess the influence of contact time and initial dye concentration, supported by kinetic and equilibrium modeling. Adsorption proceeded through a multistage mechanism involving thin-layer diffusion, intraparticle diffusion, and final equilibrium, which was reached after 48 h. The pseudo-second-order kinetic model (PSO) with R² = 0.9648 best described the adsorption behavior. Equilibrium data was fitted by the Langmuir isotherm (R² = 0.9990), yielding a maximum adsorption capacity of 56.8 mg g⁻¹, consistent with the experimentally observed saturation plateau. FTIR spectra revealed characteristic shifts in aromatic, –N=N– (≈1500 cm⁻¹), and –SO₃²⁻ (1180–1040 cm⁻¹) bands, which, corroborating the data provided by SEM/EDX analysis, completes the adsorption of DR 23 on the X4 matrix. TG/DSC analysis showed modifications in thermal behavior after adsorption without compromising resin stability, supporting strong dye–resin interactions. Overall, the integrated kinetic, isotherm, spectroscopic, and thermal analyses demonstrate that X4 is stable and an adsorbent with desorption capability using chemical agents, highlighting its potential for mitigating the environmental and toxicological risks associated with azo dye contamination in wastewater. Full article

In this study, a functional surface coating composed of Fe-Mn binary oxide (FM) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, PP) was applied to a PVDF membrane (PP-FM-PVDF) for efficient arsenate (As(V)) removal. PP acts as a dispersant and hydrophilic modifier, ensuring uniform FM distribution and reducing the water contact angle to 50.1°. The PP-FM-PVDF membrane achieves a maximum As(V) adsorption capacity of 30.43 mg/g, outperforming pristine and singly modified membranes. The batch adsorption data fit the Langmuir isotherm (R² = 0.999) and pseudo-second-order kinetic model (R² = 0.99), indicating monolayer chemisorption. The coating increases the specific surface area to 27.33 m²/g and the tensile strength to 6.41 MPa. Dynamic filtration shows that 2.70 L (2149.7 L/m²) of 100 μg/L As(V) solution can be treated before the permeate concentration exceeds the WHO guideline of 10 μg/L. After alkaline regeneration (pH 11), 62.9% of the initial capacity is retained. Complementary surface-sensitive analyses (zeta potential, XPS, and EXAFS) reveal that arsenate adsorption occurs primarily through ligand exchange between arsenate oxyanions and Fe/Mn surface hydroxyl groups on the coating, forming inner-sphere bidentate complexes (Fe–O–As and Mn–O–As), while electrostatic interactions play a secondary, pH-dependent role. This surface engineering strategy—synergistically integrating a conductive hydrophilic polymer with a metal oxide as a functional coating on PVDF—offers a reusable, high-performance platform for arsenate remediation, underscoring the critical role of interface design in environmental membrane applications. Full article

Mercury contamination in water poses severe environmental and health risks, requiring efficient and sustainable removal strategies. In this study, rice husk (RH), rice husk-derived materials, including rice ash (RHA), and Mobil Composition of Matter No. 41 (MCM-41) were evaluated as adsorbents for Hg(II) removal in aqueous systems. Among the tested materials, MCM-41 exhibited superior adsorption performance, achieving up to 98% Hg(II) removal under optimal conditions (pH 6.8, 3 g L⁻¹ of adsorbent, and a pollutant concentration of 0.90 mg L⁻¹). Adsorption followed a pseudo-second-order kinetic model and was best described by the Langmuir isotherm, indicating monolayer adsorption. The maximum adsorption capacity reached 0.80 mg g⁻¹. Thermodynamic analysis revealed that the process was spontaneous and exothermic, primarily governed by coordination interactions and hydrogen bonding with surface silanol groups. The adsorbent’s applicability was further assessed in distilled water, synthetic industrial wastewater, and river water. Although high removal efficiencies were maintained, a decrease was observed in complex matrices due to competition from coexisting ions. Reusability tests demonstrated that MCM-41 retained its performance over four adsorption cycles. Environmental safety was evaluated through ecotoxicological and microbiological assays. Daphnia magna exhibited high sensitivity to Hg(II) (EC₅₀ values of 0.0220 mg L⁻¹ at 24 h and 0.0158 mg L⁻¹ at 48 h), while treated samples showed improved germination indices of Lactuca sativa, particularly in distilled and river water. However, residual toxicity persisted in industrial wastewater matrices. Overall, rice husk-derived MCM-41 is a promising and sustainable adsorbent for Hg(II) removal, though further optimization is needed to mitigate residual toxicity in complex water matrices. Full article

This study presents experimental adsorption–desorption data of CH₄ and CO₂ on shale samples from the Cesar-Ranchería Basin, Colombia, a region with limited characterization of gas–rock interactions under reservoir-relevant conditions. The work addresses the behavior of early-mature shales, contributing to the understanding of gas retention mechanisms in tropical basins. Adsorption–desorption isotherms were obtained using a high-pressure manometric system at 50 °C and 80 °C, with pressures up to 3 MPa, and were fitted using the Langmuir model. The results show a consistently higher adsorption capacity for CO₂ compared to CH₄ across all conditions, along with a clear decrease in adsorption capacity with increasing temperature, confirming the exothermic nature of the process. No hysteresis was observed, indicating fully reversible adsorption dominated by physisorption mechanisms. The integration of adsorption data with mineralogical, BET surface area, and geochemical characterization provides insight into the factors controlling gas retention in early-mature shales. The results highlight the combined influence of surface area, organic matter, and clay mineralogy on adsorption performance, and demonstrate that CO₂ exhibits a stronger affinity for the shale matrix under all tested conditions. These findings contribute experimental evidence of gas adsorption behavior in an underexplored basin and provide a reference framework for evaluating gas storage potential in similar geological settings. Full article