Search Results (170)

Fenton oxidation can contribute to meeting effluent standards for COD in actual wastewater treatment plant effluents. However, Fenton oxidation is prone to produce iron sludge waste. The application of heterogeneous Fenton-like systems based on Fenton iron mud carbon in wastewater treatment plants is essential for Fenton iron mud reduction and recycling. In this study, a Fenton iron mud carbon catalyst/Ferrate salts/H₂O₂ (FSC/Fe(VI)/H₂O₂) system was developed to remove chemical oxygen demand (COD) from secondary effluents at the pilot scale. The results showed that the FSC/Fe(VI)/H₂O₂ system exhibited excellent COD removal performance with a removal rate of 57% under slightly neutral conditions in laboratory experiments. In addition, the effluent COD was stabilized below 40 mg·L⁻¹ for 65 days at the pilot scale. Fe(IV) and ¹O₂ were confirmed to be the main active species in the degradation process through electron paramagnetic resonance (EPR) and quenching experiments. C=O, O-C=O, N sites and Fe⁰ were responsible for the generation of Fe(IV) and ¹O₂ in the FSC/Fe(VI)/H₂O₂ system. Furthermore, the cost per ton of water treated by the pilot-scale FSC/Fe(VI)/H₂O₂ system was calculated to be only 0.6209 USD/t, further confirming the application potential of the FSC/Fe(VI)/H₂O₂ system. This study promotes the engineering application of heterogeneous Fenton-like systems for water treatment. Full article

In this study, the degradation of Nile Blue dye was investigated using homogeneous and heterogeneous photocatalytic methods based on the photo-Fenton reaction. More specifically, for homogeneous photocatalysis, the classical photo-Fenton (UV/Fe²⁺/H₂O₂) and modified photo-Fenton-like (UV/Fe²⁺/S₂O₈²⁻) systems were studied, while for heterogeneous photocatalysis, a commercial MOF catalyst, Basolite F300, and a natural ferrous mineral, geothite, were employed. Various parameters—including the concentrations of the oxidant and catalyst, UV radiation, and pH—were investigated to determine their influence on the reaction rate. In homogeneous systems, an increase in iron concentration led to an enhanced degradation rate of the target compound. Similarly, increasing the oxidant concentration accelerated the reaction rate up to an optimal level, beyond which radical scavenging effects were observed, reducing the overall efficiency. In contrast, heterogeneous systems exhibited negligible degradation in the absence of an oxidant; however, the addition of oxidants significantly improved the process efficiency. Among the tested processes, homogeneous techniques demonstrated a superior efficiency, with the conventional photo-Fenton process achieving complete mineralization within three hours. Kinetic analysis revealed pseudo-first-order behavior, with rate constants ranging from 0.012 to 0.688 min⁻¹ and correlation coefficients (R²) consistently above 0.90, confirming the reliability of the applied model under various experimental conditions. Nevertheless, heterogeneous techniques, despite their lower degradation rates, also achieved high removal efficiencies while offering the advantage of operating at a neutral pH without the need for acidification. Full article

This paper presents a study on the optimization of 2,4-Dichlorophenoxyacetic (2,4-D) acid removal from synthetic wastewater by batch Fenton-Ozonation. The aim of this study is to evaluate the potential of the catalytic system Fe-L27 coupled to ozonation in the presence and absence of H₂O₂ as an effective and affordable technique for the treatment of organic pollutants in water. Fenton-like catalysts for the removal of 2,4-D in aqueous solutions were elaborated using catalysts synthesized by the wet impregnation method. The ACs and prepared catalysts were characterized by nitrogen adsorption–desorption isotherms at 77 K, TGA, XPS, SEM, and TEM. Their efficiency as Fenton-like catalysts was studied. In a first step, a response surface modeling method was employed in order to find the optimal parameters of the Fenton process, and then the optimal O₃/H₂O₂ ratio was established at laboratory scale. Finally, the investigated advanced oxidation processes were carried out at pilot scale. The results show that Fenton-like catalysts obtained by the direct impregnation method enhance the degradation rate and mineralization of 2,4-D. Full article

Antibiotic resistance has been recognized as a global threat to human health. Therefore, it is urgent to develop effective strategies to address the contamination of water environments caused by antibiotics. In this study, Fe/Mn bimetallic-modified biochar (FMBC) was synthesized through a one-pot oxidation/reduction-hydrothermal co-precipitation method, demonstrating an exceptional photocatalytic-Fenton degradation performance for oxytetracycline (OTC). Characterization techniques including FTIR, SEM, XRD, VSM, and N₂ adsorption–desorption analysis confirmed that the Fe/Mn bimetals were successfully loaded onto the surface of biochar in the form of Fe₃O₄ and MnFe₂O₄ mixed crystals and exhibited favorable paramagnetic properties that facilitate magnetic recovery. A key innovation is the utilization of biochar’s inherent phenol/quinone structures as reactive sites and electron transfer mediators, which synergistically interact with the loaded bimetallic oxides to significantly enhance the generation of highly reactive ·OH radicals, thereby boosting catalytic activity. Even after five recycling cycles, the material exhibited minimal changes in degradation efficiency and bimetallic crystal structure, indicating its notable stability and reusability. The photocatalytic degradation experiment conducted in a Fenton-like reaction system demonstrates that, under the conditions of pH 4.0, a H₂O₂ concentration of 5.16 mmol/L, a catalyst dosage of 0.20 g/L, and an OTC concentration of 100 mg/L, the optimal degradation efficiency of 98.3% can be achieved. Additionally, the pseudo-first-order kinetic rate constant was determined to be 4.88 min⁻¹. Furthermore, this study elucidated the detailed degradation mechanisms, pathways, and the influence of various ions, providing valuable theoretical insights and technical support for the degradation of antibiotics in real wastewater. Full article

Sludge-derived biochar (SDB) synthesized by the pyrolysis of sludge is gaining enormous interest as a sustainable solution to wastewater treatment and sludge disposal. Despite the proliferation of general biochar reviews, a focused synthesis on SDB-specific advances, particularly covering the recent surge in multifunctional wastewater treatment applications (2020–2025), receives little emphasis. In particular, a critical analysis of recent trends, application challenges, and future research directions for SDB is still limited. Unlike broader biochar reviews, this mini-review highlights the comparative advantages and limitations of SDB, identifies emerging integration strategies (e.g., bio-electrochemical systems, catalytic membranes), and outlines future research priorities toward enhancing the durability and environmental safety of SDB applications. Specifically, this review summarized the advances from 2020 to 2025, focusing exclusively on functional modifications, and practical applications of SDB across diverse wastewater treatment technologies involved in adsorption, catalytic oxidation, membrane integration, electrochemical processes and bio-treatment systems. Quantitative comparisons of adsorption capacities (e.g., >99% Cd2+ removal, >150 mg/g tetracycline adsorption) and catalytic degradation efficiencies are provided to illustrate recent improvements. The potential of SDB in evaluating traditional and emerging contaminant degradation among the Fenton-like, persulfate, and peracetic acid activation systems was emphasized. Integration with membrane technologies reduces fouling, while electrochemical applications, including microbial fuel cells, yield higher power densities. To improve the functionality of SDB-based systems in targeting contamination removal, modification strategies, i.e., thermal activation, heteroatom doping (N, S, P), and metal loading, played crucial roles. Emerging trends highlight hybrid systems and persistent free radicals for non-radical pathways. Despite progress, critical challenges persist in scalability, long-term stability, lifecycle assessments, and scale-up implementation. The targeted synthesis of this review offers valuable insights to guide the development and practical deployment of SDB in sustainable wastewater management. Full article

Rainwater needs to be recognized as a natural water source for domestic use, but finding viable processes to remove its contaminants is essential. The aim of this work was to compare the UV/H₂O₂ and UV/Fenton-like processes for the oxidation of 3,5-dihydroxybenzoic acid (3,5-DHBA) in rainwater. The reactions were assessed using ultraviolet-visible (UV-Vis) and molecular fluorescence spectroscopies, and the results showed the formation of new and similar chromophoric compounds in both processes, which were subsequently degraded. At environmentally relevant concentrations of chemical oxidants, namely H₂O₂ at 10⁻⁴ M, the chromophoric organic compounds in solution were degraded within 24 h by the UV/H₂O₂ process and within 4 h by the UV/Fenton-like process. However, when the concentration of H₂O₂ was increased by one order of magnitude for the UV/H₂O₂ process (from 10⁻⁴ M to 10⁻³ M), oxidation rates were similar and nearly complete after 4 h for both UV/H₂O₂ and UV/Fenton-like processes. These findings highlight that the presence of more oxidizing agents in the oxidation system improves the synergistic effect, leading to a greater contribution of the free radical oxidation pathway, particularly through hydroxyl radicals. Thus, by increasing the concentration of H₂O₂ in the UV/H₂O₂ process to 10⁻³ M, it was possible to achieve a similar level of oxidation (close to 100% after 4 h, as indicated by a decrease in fluorescence intensity) as the UV/Fenton-like process at environmentally relevant concentrations (10⁻⁴ M), but using fewer chemical reactants, since UV/H₂O₂ process does not require Fe(III) as catalyst and oxidant. Therefore, the UV/H₂O₂ process can be considered a simpler and cleaner process for removing organic contaminants from rainwater. Full article

Ferrous oxalate dihydrate (α-FOD) was synthesized from Ecuadorian black sands for phenol removal from aqueous solutions. Visible light-driven photodegradation kinetics were studied by varying the initial pollutant concentration, solution pH, and α-FOD dosage and by adding peroxydisulfate (PDS), including quenching tests. A representative model of phenol photodegradation was obtained by the Langmuir–Hinshelwood mechanism over a large range of concentrations (apparent kinetic constant, k = 0.524 h⁻¹). Almost complete removal was reached within 1 h under dark + 9 h under visible irradiation. The degradation rate was slightly affected by pH in the range of 3 to 9, with a significant improvement at pH 11 (k = 1.41-fold higher). The optimal α-FOD dosage was ~0.5 g/L. Two regimes were observed when using PDS: first, a heterogeneous Fenton-like process during the first few minutes after PDS addition; second, pure photocatalysis to completely remove the phenol. When comparing the two systems, without and with PDS, the half-life time for pure photocatalysis was 2.5 h (after the lamp was switched on). When adding PDS (1.0 mM), the half-life time was reduced to a few minutes (5 min after PDS addition, phenol removal was 66%). The photocatalyst presented remarkable degradation efficiency up to five repeated cycles. Full article

Four different-sized carbon microspheres, CS, obtained by a facile hydrothermal method, are applied as a hard template for the preparation of a series of macroporous LaFeO₃. The average particle size of the CS obtained is between 0.350 and 0.700 µm. The macroporous LaFeO₃ are tested in a Fenton-like activation of peroxymonosulfate, PMS, for oxidation of tetracycline hydrochloride, TCH, in model water solution under visible-light irradiation. The effect of parameters such as type of irradiation, temperature of the reaction, and type of the water matrixes was tested. The oxidation of the pollutant TCH is evaluated by total organic carbon and organic nitrogen measurements. The results showed the superior catalytic activity of macroporous LaFeO₃ in comparison to pure LaFeO₃. Rate constants between 0.036 and 0.184 min⁻¹ at 25 °C were obtained. The activation energy for the process with the most active macroporous LaFeO₃ was 33.88 kJ/mol, a value lower than for the catalytic process with PMS only, proving the positive role of the macroporous LaFeO₃ for TCH degradation. Radical scavenger measurements showed that singlet oxygen, produced during the catalytic degradation process, was responsible for the performance of macroporous LaFeO₃/PMS/visible light for TCH degradation. The catalysts proved to be efficient and recyclable. Full article

Metal-doped carbon dots (CDs) have become one of the most popular catalytic materials for Fenton-like reactions, mainly due to their low production cost, minimal toxicity, and high catalytic efficiency. Theses reactions not only provide an efficient decontamination method for the degradation of organic pollutants in wastewater but also demonstrate a wide range of sensing applications. Metal doping introduces new catalytically active centres, which increase the binding selectivity to the reactants and offer an additional advantage of improved catalytic degradation and sensing activity. The metal-doped CDs optimise the electronic structure of pristine CDs, thereby enhancing their catalytic properties and reaction rates. These enhancements make them an attractive option for water treatment and sensor design. The objective of this review is to provide a comprehensive overview of the current research progress in the utilisation of metal-doped CDs as Fenton-like reaction catalysts for the degradation of pollutants and sensing applications. This review examines the advantages of metal-doped carbon dots in terms of catalytic efficiency, selectivity, and application scope and discusses the potential challenges and future research directions. The aim is to promote further the sustainable application and green development of CD technology in environmental governance and analytical chemistry. Full article

Membrane technology is widely used in various aspects of wastewater treatment; however, single membrane technology has a series of disadvantages, such as high selectivity, poor recycling performance, and susceptibility to contamination. In this study, a treatment method combining an advanced oxidation process and membrane separation technology was proposed, and a geopolymer-based Fenton-like catalytic tubular membrane (GFM) was prepared by using H₂O₂ as a blowing agent by the direct foaming method. It was shown that the optimum conditions for the preparation of the membrane were a water glass modulus of 1.8 M, the addition of foaming agent of 1 mL, and a thickness of the membrane of 6.5 mm, with a flux of 6942 L·m⁻²·h⁻¹. Due to the characteristics of the tubular membrane, the possibility of adding hydrogen peroxide directly inside the membrane allows an optimal Fenton-like removal, which is better than outside the membrane, thus reducing the consumption of hydrogen peroxide. The tubular membrane has a multi-stage porous structure, high flux, and a high specific surface area (68.74 m²/g). The GFM/H₂O₂ Fenton-like system formed is capable of almost completely degrading all kinds of synthetic dyes under various stringent conditions, and the XRD, FTIR, and TG analyses and cycling tests showed that the GFM has excellent stability and a significant advantage in terms of reusability. Full article

To degrade high-concentration and toxic organic effluents, we developed Fe-Cu active sites loaded on biomass-source carbon aerogel (CA) to produce a low-cost and high-efficiency magnetic Fenton-like catalyst for the catalytic oxidative decomposition of organic pollutants. It exhibits excellent performance in catalytic Fenton-like reactions for RhB removal at an ultrahigh initial concentration of up to 1000 ppm. To be specific, Fe₃O₄ and Cu nanoparticles are generated in situ on a mesoporous CA support, denoted as an Fe₃O₄-Cu/CA catalyst. Experimentally, factors including initial dye concentration, catalyst dosage, H₂O₂ dosage, pH, and temperature, which significantly influence the oxidative degradation rate of RhB, are carefully studied. The RhB (1000 ppm) degradation ratio reaches 93.7% within 60 min under low catalyst and H₂O₂ dosage. The catalyst also shows slight metal leaching (almost 1.4% of total Fe and 4.0% of total Cu leached after a complete degradation of 25 μmol RhB under conditions of 15 mg catalyst dosage, 20 mL RhB solution (600 ppm), and 200 μL 30 wt% H₂O₂ dosage, at pH of 2.5, at 40 °C), good catalytic activity for degrading organic pollutants, excellent reusability, and good catalytic stability (the degradation ratio is nearly 82.95% in the 8th cycle reaction). The synergistic effect between Fe and Cu species plays a vital role in promoting the redox cycle of Fe(III)/Fe(II) and enhancing the generation of ·OH. It is suitable for ultrahigh-concentration organic pollutant degradation in practical wastewater treatment applications. Full article

In the present study, cellulose and lignin with different weight ratios were mixed and pyrolyzed to prepare biochars for organic dye pollutant removal in water via Fenton-like catalysis. The results indicated that a higher cellulose content in a biomass precursor could result in a lower biochar yield with a lower carbon content in the biochar. Moreover, with the increase in cellulose content, the resulting biochar had a higher graphitization degree with higher levels of crystallinity, as well as a richer porosity. When using Rhodamine B (RhB) as the dye probe, the biochar derived from a higher cellulose/lignin ratio precursor exhibited better adsorptive performance. It was further found that the biochar could act as a Fenton-like catalyst to activate peroxydisulfate (PDS) and accelerate RhB removal via a degradation route, in which single oxygen (¹O₂) was identified as the active species. Therefore, the biochar/PDS catalytic system exhibited prominent RhB removal stability in various water matrices with a wide pH application range. This study develops a new approach to prepare biomass-derived biochar with high organic removal capacity via Fenton-like catalysis assisted with adsorption synergy. Full article

The development of heterostructures incorporating photocatalysts optimized for visible-light activity represents a major breakthrough in the field of environmental remediation research, offering innovative and sustainable solutions for environmental purification. This study explores the photocatalytic capabilities of a SnFe₂O₄/g-C₃N₄ heterojunction nanocomposite, successfully synthesized from graphitic carbon nitride (g-C₃N₄) and tin ferrate (SnFe₂O₄) and applied to the degradation of the cationic dye brilliant cresyl blue (BCB) in an aqueous solution. These two components are particularly attractive due to their low cost and ease of fabrication. Various characterization techniques, including XRD, FTIR, SEM, and TEM, were used to confirm the successful integration of SnFe₂O₄ and g-C₃N₄ phases in the synthesized catalysts. The photocatalytic and photo-Fenton-like activity of the heterojunction composites was evaluated by the degradation of brilliant cresyl blue under visible LED illumination. Compared to the pure components SnFe₂O₄ and g-C₃N₄, the SnFe₂O₄/g-C₃N₄ nanocomposite demonstrated a superior photocatalytic performance. Furthermore, the photo-Fenton-like performance of the composites is much higher than the photocatalytic performances. The significant improvement in photo-Fenton activity is attributed to the synergistic effect between SnFe₂O₄ and g-C₃N₄, as well as the efficient separation of photoexcited electron/hole pairs. The recyclability of the SnFe₂O₄/g-C₃N₄ composite toward BCB photo-Fenton like degradation was also shown. This study aimed to assess the modeling and optimization of photo-Fenton-like removal BCB using the SnFe₂O₄/g-C₃N₄ nanomaterial. The main parameters (photocatalyst dose, initial dye concentration, H₂O₂ volume, and reaction time) affecting this system were modeled by two approaches: a response surface methodology (RSM) based on a Box–Behnken design and artificial neural network (ANN). A comparison was made between the predictive accuracy of RSM for brilliant cresyl blue (BCB) removal and that of the artificial neural network (ANN) approach. Both methodologies provided satisfactory and comparable predictions, achieving R² values of 0.97 for RSM and 0.99 for ANN. Full article

The increasing presence of persistent pollutants in industrial wastewater underscores the shortcomings of conventional treatment methods, prompting the adoption of advanced oxidation processes (AOPs) for sustainable water remediation. This review examines the development of AOPs, focusing on their ability to produce hydroxyl radicals and reactive oxygen species (ROS) to mineralize complex pollutants. Homogeneous systems such as Fenton’s reagent show high degradation efficiency. However, challenges like pH sensitivity, catalyst recovery issues, sludge generation, and energy-intensive operations limit their scalability. Heterogeneous catalysts, such as TiO₂-based photocatalysts and Fe₃O₄ composites, offer improved pH adaptability, visible-light activation, and recyclability. Emerging innovations like ultraviolet light emitting diode (UV-LED)-driven systems, plasma-assisted oxidation, and artificial intelligence (AI)-enhanced hybrid reactors demonstrate progress in energy efficiency and process optimization. Nevertheless, key challenges remain, including secondary byproduct formation, mass transfer constraints, and economic feasibility for large-scale applications. Integrating AOPs with membrane filtration or biological treatments enhances treatment synergy, while advances in materials science and computational modeling refine catalyst design and reaction mechanisms. Addressing barriers in energy use, catalyst durability, and practical adaptability requires multidisciplinary collaboration. This review highlights AOPs as pivotal solutions for water security amid growing environmental pollution, urging targeted research to bridge gaps between laboratory success and real-world implementation. Full article

Herein, a heterogeneous Fenton-like catalyst was designed by immobilizing iron oxide (FeS) and nickel sulfide (NiS) on the surface of β-cyclodextrin (β-CD), creating a NiS/FeS@β-CD composite for degrading triphenylmethane cresol red dye. Varied instruments were used to study the physical and chemical characteristics of the NiS/FeS@β-CD catalyst. The appropriate catalytic conditions of the Fenton-like degradation of cresol red by NiS/FeS@β-CD were identified, clarifying that the higher degradation % fulfilled 99.86% with an adsorption % of 27.44% at a cresol red concentration = 50 mg/L, NiS/FeS@β-CD dose = 0.01 g, pH = 3, processing temperature = 30 °C, H₂O₂ concentration = 100 mg/L, and H₂O₂ volume = 1 mL. The kinetic assessments depicted the preference of the second order to represent the Fenton-like degradation of cresol red by NiS/FeS@β-CD. The mechanistic proposition of the adsorption/Fenton-like degradation of cresol red was understood using a quenching test and XPS analysis. Finally, to confirm the durability of NiS/FeS@β-CD, a reusability test was proceeded on the catalyst for five adsorption/Fenton-like degradation runs, with identifying the leaching concentrations of nickel and iron from the catalyst by ICP-OES after each run. Full article