Search Results (2,397)

Industrial wastewater containing refractory organic compounds, heavy metals, and emerging contaminants poses a significant challenge to conventional treatment methods due to their high chemical stability and toxicity. This review systematically summarizes recent advances in Fenton-based advanced oxidation processes (AOPs) for industrial wastewater treatment, with a particular focus on the paradigm shift from homogeneous to heterogeneous catalytic systems. Homogeneous Fenton processes, which rely on Fe²⁺/H₂O₂ reactions, exhibit rapid reaction kinetics but are severely limited by a narrow operational pH range (2–4) and the generation of substantial iron sludge. In contrast, heterogeneous Fenton systems employing immobilized or supported catalysts—such as iron-loaded zeolites, metal–organic frameworks, and carbon-based composites—broaden the applicable pH range to near-neutral conditions (4–8), enable catalyst recovery and reuse over multiple cycles, and enhance process sustainability by reducing iron leaching and sludge production. Integration with external energy inputs—such as photo, electricity, or ultrasound—can further promote radical generation and mass transfer, improving degradation efficiency while reducing chemical consumption. Practical applications in treating wastewater from textile, pharmaceutical, and electroplating industries have demonstrated effective contaminant removal and enhanced biodegradability. However, most current research remains at the laboratory scale, with long-term catalyst stability, operational costs, and scalability representing major barriers to large-scale implementation. Future research should focus on developing stable and regenerable catalysts, advancing pilot-scale studies of integrated systems, and conducting long-term evaluations under real wastewater conditions to promote the development of efficient, low-carbon, and sustainable solutions for industrial wastewater treatment. Full article

The proposed work assesses the potential of Paulownia leaf-derived materials as sustainable adsorbents for the efficient removal of Pb(II) from aqueous solutions. Raw Paulownia leaf biomass (PL), biochar obtained by pyrolysis at 400 °C (BC), and (3-aminopropyltriethoxysilane)-functionalized oxidized biochar (APTES-OBC) were prepared. Their physicochemical properties were characterized using SEM/EDS and FTIR, and their Pb(II) adsorption performances were comprehensively investigated through pH-dependent, adsorbent dosage, kinetic, isotherm, thermodynamic, and ion-exchange studies and compared. The obtained results showed that APTES functionalization significantly improved Pb(II) adsorption performance, with adsorption capacities following the order APTES-OBC (291.86 mg/g) > BC (121.82 mg/g) > PL (104.29 mg/g). The Sips isotherm best described Pb(II) adsorption on the carbonized adsorbents, indicating heterogeneous adsorption, whereas the Redlich-Peterson isotherm model showed the best agreement with Pb(II) adsorption on the PL. The adsorption kinetics were most accurately represented by the pseudo-second-order model, indicating that chemisorption-related interactions played a dominant role during Pb(II) uptake. Diffusion studies revealed a three-stage adsorption mechanism. Ion-exchange experiments confirmed the release of Ca²⁺, K⁺, Mg²⁺, and Na⁺ ions, indicating that ion exchange contributes to the Pb(II) adsorption mechanism. However, the lower release of these ions from APTES-OBC, despite its superior adsorption capacity, indicates that Pb(II) removal is predominantly governed by surface complexation and coordination with amino-functionalized silane groups following APTES functionalization. Overall, the findings highlight a sustainable approach for the valorization of Paulownia leaf waste into efficient and environmentally safe adsorbents for heavy metal elimination from water systems. Full article

Waste aluminum dust generated from aluminum refining and machining processes contains high fractions of Al₂O₃ and SiO₂, making it a potential secondary aluminosilicate resource for zeolite synthesis. In this study, waste aluminum dust was converted into functional zeolite materials through dry fusion purification, NaOH-assisted hydrothermal synthesis, acid purification, Si/Al ratio control, and cation-exchange modification. The raw dust was subjected to dry fusion at 1600 °C under an Ar atmosphere to remove metallic impurities and obtain an aluminosilicate precursor. Na-type zeolite was then synthesized using 50 wt.% NaOH solution at 90 °C for 24 h. The as-synthesized Na-type zeolite exhibited an estimated chemical purity of 97.501 wt.% based on measured residual impurities, with Mg, Ca, K, and Ti remaining as major impurities. HCl leaching at 0.25 M for 24 h increased the estimated chemical purity based on measured residual impurities to 98.469 wt.% while retaining the major zeolitic diffraction features. The Si/Al ratio was further controlled using water glass, and the maximum Si/Al ratio of 1.77 was obtained at a Na-type zeolite-to-water-glass mass ratio of 1:2 after reaction at 90 °C for 6 h. The purified and composition-controlled zeolite was subsequently modified with Mg²⁺ and K⁺ ions to prepare Mg-modified and K-modified zeolites. Under fixed batch conditions using a relatively high zeolite dosage and a single initial concentration, Mg-modified zeolite reduced Pb, Hg, Cr(VI), and Cd concentrations from 100 ppm to 0.004, 0.00059, 0.018, and 0.004 ppm, respectively, while K-modified zeolite reduced the total hardness of synthetic hard water from 308.3 to 40.13 ppm as CaCO₃. These results should be interpreted as preliminary batch-performance results under the tested conditions rather than as maximum adsorption capacities or a complete adsorption-mechanism evaluation. Overall, this study demonstrates the feasibility of valorizing waste aluminum dust into purified and cation-modified zeolite materials for potential water-treatment applications. Further adsorption isotherm, kinetic, dosage-dependent, BET surface area, pore-volume, pore-size distribution, and quantitative phase analyses are required to evaluate adsorption capacity, adsorption mechanism, true zeolite phase purity, and framework–performance relationships. Full article

This study advances sustainable wastewater management by investigating the efficacy of untreated pine cone powder (PCP), an abundant and renewable forest byproduct, for Fe^II removal from aqueous solutions. The surface morphology and composition of PCP was characterized by performing SEM-EDX, FTIR, point of zero charge, and total specific surface area analysis. Investigation of experimental factors revealed that equilibrium adsorption capacity increases with higher pH and temperature but decreases with elevated initial Fe^II concentration and ionic strength. The experimental kinetic and equilibrium data were best fitted to the pseudo first-order and Freundlich models, respectively. Thermodynamic analysis further indicated that the adsorption process was spontaneous and endothermic in nature, accompanied by an increase of randomness at the solid–liquid interface. Low activation and Temkin bonding energies suggest that physical adsorption is the dominant removal mechanism. With a maximum Langmuir adsorption capacity of 12.7 mg g⁻¹, PCP represents a promising eco-friendly adsorbent for the removal of Fe^II. By transitioning from conventional, high-footprint water treatments to such low-impact, eco-friendly alternatives, this research supports the circular valorization of biomass as a viable solution for the sustainable mitigation of industrial heavy metal pollution. Full article

This review provides a comparative critical synthesis of biochar and enhanced rock weathering (ERW), identifies key trends and gaps in soil carbon research, and outlines pathways for improving carbon sequestration and monitoring in soil systems. From a global perspective, materials and agricultural studies were read to examine the properties of these amendments and their effects in cropland and forest soils. The main research question guiding this literature review was as follows: What are common trends in published biochar and ERW studies? Major themes were derived from the stated question and structure the Discussion. The Web of Science provided access to relevant literature for both biochar and ERW, and a total of 38 articles (biochar: 17; ERW: 21) were read and covered in this paper. The findings conveyed the growing number of Chinese studies on these amendments to resolve climate-related soil quality affecting crop yields and potential for carbon sequestration, namely carbon dioxide removal or CDR—which sequesters CO₂ that is already in the atmosphere. Studies commonly used application rates of <5% for biochar and 5 or 50 t/ha for ERW, with (wood) biochar commonly processed at temperatures of 500–550 °C. Finer powders were known to be more effective due to their increased surface area, although there were emissions trade-offs to consider for climate change mitigation. There were options for using glacial rock flour (GRF) as an alternative. For ERW, the type of minerals matters, with basaltic amendments being most investigated and minerals like zeolite, for example, having quick responses and potential to filter out heavy metals. Depth of analysis was an issue in the studies, especially affecting ERW work—which needs to adopt greater depths (>60 cm) and both soil organic carbon (SOC) and soil inorganic carbon (SIC) or total carbon need address, particularly for ERW since studies only provided selective coverage. Biochar studies tended to focus more on crop yields and were not as concerned as ERW studies in CDR. Many studies agreed that these are promising products that need to be economically compared before being applied at a large scale. More field studies are needed to test biochar, while limitations imposed by soil pH (acidification affecting dissolution and nutrient availability) and climate need consideration for ERW—especially since it works best in warm, humid climates. The application rate and duration are important variables to also consider for ERW, and both SOC and SIC dynamics are subsystem components requiring consideration. Ultimately, studies call for field trials executed in the long term at greater depth and in different climates and representing different soil types. Full article

Heavy metals (HMs) such as copper (Cu), lead (Pb), cadmium (Cd), chromium (Cr) and zinc (Zn) from industrial activities are discharged into nearby water resources after treatment. In the present study, the potential of utilizing chemically activated carbon derived from water hyacinths as a sustainable and low-cost adsorbent for heavy metal removal from industrial wastewater from the Nakawa industrial area, Uganda was investigated. The measured physicochemical parameters of wastewater (temperature, pH, electrical conductivity, total dissolved solids, turbidity, dissolved oxygen, chlorides and total hardness) varied significantly among the three sampled sites (p < 0.05), except for pH. Similarly, the concentration of the HMs in the samples (0.54 ± 0.04 mg L⁻¹ for Cr to 93.54 ± 0.07 mg L⁻¹ for Pb) varied significantly between sites (p < 0.05), exceeding the maximum permissible limits of Cd, Pb, Cr, Cu and Zn specified in the National Environment Standards for Discharge of Effluent into Water or Land. The water hyacinth biomass was activated using eggshell powder and phosphoric acid, followed by thermal treatment. Characterization using Fourier-transform infrared spectroscopy and scanning electron microscopy confirmed that there was improvement in its surface functionality and porosity post activation. Batch adsorption experiments indicated that optimal removal of the HMs was achieved at pH 4–5, contact time of 90 min, and 1.0 g of adsorbent. Maximum adsorption capacities of Pb, Cd, Cu, Cr and Zn were in the range of 1.04–8.36 mg g⁻¹. Under the optimized conditions, the eggshell-activated carbon derived from water hyacinths had removal efficiencies of 91.2 ± 9.1% (range: 71.3–100%). Adsorption occurred through both monolayer and multilayer coverage, as indicated by the experimental data which fitted well to the Freundlich isotherm (Cd²⁺, Pb²⁺, Zn²⁺ and Cu²⁺ ions) and Langmuir isotherm model (Cr³⁺ ions). These results support the potential of water hyacinth-derived activated carbon as an ecofriendly alternative for treating low concentrations of these HMs in industrial wastewater. Full article

With increasing global concerns about industrial wastewater treatment and the need for sustainable practices, this study explores the potential of softwood sawdust as an eco-friendly, cost-effective adsorbent for removing heavy metal ions, specifically zinc (Zn²⁺) and lead (Pb²⁺), from synthetic model solutions. Factors affecting adsorption include adsorbent particle size, pH, adsorbent dosage, and contact time. A remarkable removal efficiency of 98.2% for Zn²⁺ and 98.1% for Pb²⁺ under optimal adsorption conditions of −106 µm average particle size at 8 pH and 0.3 g of adsorbent dosage using 50 (mg/L) initial concentrations for 60 min at ambient temperature. Characterization of the adsorbent used by XRD, FTIR, SEM, and BET analysis confirmed the structural integrity and surface properties of wood sawdust. It is clear that there is a gradual decline in adsorption capacity over multiple reuse cycles due to the depletion of active functional groups. The results confirm wood sawdust’s effectiveness as a locally available, low-cost, and biodegradable option for treating wastewater, eliminating metal ions, supporting environmental conservation, and aligning with sustainability goals. Full article

Wastewater containing heavy metals and dyes poses serious environmental risks. This study developed a multifunctional composite by coating polyurethane foam (PUF) with milled activated carbon (mAC) and a zirconium-based metal–organic framework (Zr-MOF) for the simultaneous removal of hexavalent chromium (Cr(VI)) and Congo red (CR). The composite was synthesized using a hydrothermal method to grow Zr-MOF on the surface. The SEM analysis confirmed the successful incorporation of mAC and surface modification with Zr-MOF, which resulted in increased surface roughness and porous morphology. XRD and FTIR confirmed the presence of organic ligands connected to the metal structure and the functional groups of each component in composite materials. The optimum conditions for Zr-MOF/mAC/PUF adsorption (nearly 100% removal) in the binary Cr(VI)/CR solution (50 mg/L each) were 25 °C, pH 9, and 150 rpm for 24 h. The Zr-MOF/mAC/PUF was hydrophilic with a swelling ratio of 2.64 g/g. The thermodynamic investigation of Zr-MOF/mAC/PUF resulted in 141.6218 kJ/mol for Cr(VI) and 166.111 kJ/mol for CR of ΔH° (rapid adsorption), negative ΔG° (spontaneous adsorption), a high positive value of ΔS° (disorder structure) and low activation energy (approximately 2.5 to 2.8 kJ/mol). After analyzing the isotherm and reaction kinetics, the possible mechanism could be endothermic physicochemical adsorption and pseudo-second-order kinetic behavior, with electrostatic attraction and diffusion control. The study of 6-times-reused Zr-MOF/mAC/PUF adsorption identified as a decrease of 7.55 percentage point without changing notable morphology and functional groups, based on SEM and FTIR. Full article

This article systematically reviews the structural characteristics of layered double hydroxides and biochar (LDHs/biochar) composites, summarizes the features and optimization strategies of preparation methods such as coprecipitation, hydrothermal synthesis, ball milling, and calcination–reconstruction, analyzes their adsorption performance and mechanisms in controlling various water pollutants including organic contaminants, heavy metals, and nutrients, and provides insights into future research trends and practical applications, aiming to offer references for improving material performance and promoting practical use. The existing research results show that LDHs/biochar composites exhibit good application potential for various pollutants, such as dyes, antibiotics, heavy metal ions, and phosphates. The coprecipitation method is simple and easy to operate, and the LDHs/biochar composites prepared by this method exhibit favorable adsorption performance, with potential for industrial-scale production. The mechanisms of pollutant removal by LDHs/biochar composites primarily include electrostatic attraction, ion exchange, hydrogen bonding, complexation, and π–π electron interactions. Both the biomass type and the LDH type influence the adsorption performance of the composites. Therefore, designing LDHs/biochar composites based on pollutant characteristics and adsorption mechanisms is key to achieving effective pollution control. Currently, research on target pollutant-oriented material design and material regeneration remains underdeveloped and requires further breakthroughs. Full article

Agricultural and food-processing residues, as well as fruit by-products, represent widely available but still underutilised resources. Although numerous laboratory-scale studies have demonstrated their ability to remove heavy metals from contaminated water, their practical implementation remains limited by incomplete understanding of long-term stability, regeneration efficiency, and end-of-life environmental safety. This review critically evaluates the current state of biosorbent research, with particular emphasis on the full life cycle of these materials, including adsorption performance, regeneration strategies, repeated-use potential, and post-exhaustion management. While focusing primarily on agricultural residues, the review also integrates key findings from alternative materials such as algae, microbial biomass, and industrial sludge to provide a comprehensive evaluation. Particular attention is given to the distinction between desorption and regeneration, metal recovery from desorption streams, and the associated environmental burden of secondary waste generation. In addition to commonly proposed valorisation routes, such as incorporation into construction materials, thermal conversion, and reuse in energy or catalytic applications, the review highlights that most end-of-life pathways remain partial solutions rather than true closed-loop systems. In many cases, only a small fraction of spent biosorbents can be effectively incorporated into secondary products, while remaining residues still require further treatment or disposal. The lack of standardised criteria for defining biosorbent exhaustion and performance thresholds further limits comparability across studies and hinders scale-up. Overall, current evidence suggests that biosorbent-based wastewater treatment should be considered a promising but still partially circular system, where full material closure has not yet been achieved. Addressing these gaps is essential for advancing toward more robust and environmentally sustainable implementation and for improving the circularity of biosorbent-based wastewater treatment systems. Full article

The contamination of aquatic environments by cadmium and other toxic heavy metals represents a major environmental concern requiring efficient and operationally sustainable remediation strategies. In this work, iron oxide materials were synthesized through a microwave-assisted hydrothermal method and evaluated for Cd(II) removal from aqueous systems. Different precursor compositions and organic additives were initially screened in order to identify the most suitable adsorbent formulation. The selected Fe-Tart material was characterized by FTIR, SEM-EDS, and XRD analyses, revealing hydroxylated and poorly crystalline iron oxide structures with heterogeneous surface organization. Batch adsorption experiments were performed under controlled conditions to investigate the influence of pH and equilibrium adsorption behavior, while adsorption data were analyzed using Langmuir and Freundlich isotherm models. Cd(II) uptake showed strong pH dependence, with adsorption progressively increasing from acidic to near-neutral conditions and reaching approximately 80% removal at pH 7–8. The Langmuir model provided the best fitting results (R² = 0.988), suggesting preferential occupation of energetically comparable surface sites with a maximum adsorption capacity of 6.51 mg g⁻¹. The adsorption behavior was interpreted within a pH-dependent surface complexation framework involving hydroxylated iron oxide surfaces. Although the adsorption capacity remained lower than that reported for some highly engineered adsorbents, the results indicate that microwave-assisted synthesis may provide a relatively simple and rapid route for preparing iron oxide-based materials potentially applicable to water remediation systems. Full article

This study examined the removal of toxic heavy metals Pb²⁺ and As⁵⁺ from wastewaters by applying a waste nut biomass for adsorption. The waste material was steam-activated and further modified with zinc nitrate tetrahydrate to improve its affinity for arsenate. The adsorption performance was evaluated across a range of contact times, sorbent dosages, initial metal concentrations, and pH levels, for both single-metal and mixed-metal systems. When the raw material was modified by Zn, the maximum uptake of As⁵⁺ reached a value of 51 mg/g, at a sorbent dosage of 2 g/L. In binary metal solutions, the biochar exhibited maximum capacities of 25.5 mg/g for Pb²⁺ and 48.5 mg/g for As⁵⁺, indicating minimal competition between the two ions for adsorption sites on the biochar surface. Full article

This study investigates the feasibility of utilizing locally sourced Nicotiana tabacum biomass from Adıyaman, Türkiye, as a cost-effective biosorbent for the removal of copper and chemical oxygen demand (COD) from industrial wastewater originating from the Adıyaman Organized Industrial Zone. Batch adsorption experiments were conducted to systematically investigate the influence of solution pH, contact time, and initial metal concentration on adsorption performance. The untreated wastewater exhibited elevated pollution levels, with mean chemical oxygen demand and copper concentrations of 925 ± 391 mg/L and 2.54 ± 0.97 mg/L, respectively. Four tobacco-derived biosorbents (Çelikhan, Ova, Bulam, and Çağlan) were evaluated under optimized experimental conditions (pH ≈ 8.3, 60 min contact time, and a biosorbent dosage of 2.2 g/L). The Çelikhan biosorbent exhibited the highest copper removal efficiency (approximately 83%), whereas chemical oxygen demand removal ranged between 28% and 34%. The adsorption kinetics were well described by the pseudo-second-order model, with coefficients of determination ranging from 0.987 to 1.000. Isotherm analysis further indicated favorable adsorption behavior, with a maximum Langmuir adsorption capacity of 1.867 mg/g. Fourier transform infrared (FT-IR) spectroscopy confirmed the involvement of hydroxyl, carbonyl, and ester functional groups in metal binding. These findings highlight tobacco biomass as a sustainable and cost-effective biosorbent for industrial wastewater treatment. This study presents the first comprehensive evaluation of locally sourced Adıyaman tobacco biomass as a biosorbent for the removal of copper and organic pollutants from real industrial wastewater, integrating kinetic, isotherm, and FT-IR analyses to elucidate the underlying adsorption mechanisms. Full article

Lead (Pb²⁺) and cadmium (Cd²⁺) are among the most hazardous heavy metal pollutants in wastewater owing to their high toxicity, environmental persistence, and detrimental impacts on human health and aquatic ecosystems. In this study, a novel ternary magnetic composite, SnFe₂O₄/activated carbon/polypyrrole (SnFe₂O₄/AC/PPy), was effectively synthesized and tested as an effective adsorbent in the removal of Pb²⁺ and Cd²⁺ from aqueous water. The composite was prepared by depositing spinel SnFe₂O₄ nanoparticles on activated carbon, followed by in situ polymerization of polypyrrole to enhance surface functionality and adsorption affinity. The successful fabrication of the porous SnFe₂O₄/AC/PPy hybrid composite was confirmed through FTIR, XRD, SEM–EDS, BET, XPS, and VSM characterization. The composite demonstrated a relatively high surface area (352.3 m²/g) and adequate magnetic responsiveness (12.33 emu/g), ensuring facile magnetic separation following wastewater treatment. Batch adsorption experiments showed great removal efficiency of 95.02 and 92.48% for Pb²⁺ and Cd²⁺ ions, respectively, at optimum conditions. The adsorption equilibrium data followed the Langmuir isotherm model with maximum adsorption capacities of 187.07 mg/g for Pb²⁺ and 96.45 mg/g for Cd²⁺ ions, which were attributed to monolayer adsorption on homogenous active sites. The kinetic and isothermal model indicated that the adsorption process was controlled by the combination of physical and chemical interactions. Thermodynamic parameters showed negative Gibbs free energy and enthalpy changes (ΔH° = −49.74 kJ/mol for Pb²⁺ and −38.82 kJ/mol for Cd²⁺ ions), confirming the spontaneous and exothermic nature of adsorption. Furthermore, the increasingly negative ΔG° values at lower temperatures indicated that the adsorption was thermodynamically more favorable under cooler conditions. According to the regeneration studies, the composite maintained a high removal efficiency after five consecutive cycles. In general, SnFe₂O₄/AC/PPy composite has good potential as a stable, reusable, and high-performance adsorbent to treat heavy metal wastewater. Full article