Search Results (392)

Phenolic compounds constitute the predominant group of recalcitrant organic contaminants in coal chemical wastewater. In this study, humic acid and urea were used as carbon and nitrogen sources to prepare nitrogen-doped carbon material (labeled as NC-800) through a two-step calcination process. Using this catalyst (NC-800) to activate PMS for phenol degradation achieved 100% phenol removal across a wide pH range (1–9). The removal rate remained at 99.62% even with high concentrations of inorganic anions or natural organic matter, breaking through the limitations of traditional Fenton-like reactions in terms of acid–base environment and anion influence. The quenching experiment and electron spin resonance (ESR) spectroscopy results indicated that the N-C/PMS system generated three active species hydroxyl radicals (•OH), superoxide radicals (O₂^•−), and singlet oxygen (¹O₂) through the active sites in electron-rich regions such as graphite nitrogen, pyrrole nitrogen, and C=O. An electrochemical test revealed that the system formed a metastable NC-800-PMS* complex during the reaction, indicating the existence of a non-radical pathway of electron transfer. The combination of free radicals (•OH, O₂^•−) and non-free radicals (¹O₂, electron transfer) facilitated the rapid degradation of phenol, providing a theoretical basis for phenol degradation. Full article

Introducing hierarchical structure into zeolites or synthesizing two-dimensional (2D) zeolite nanosheets have drawn much attention in catalysis and separation process due to the improvement in zeolites’ diffusion properties. In this study, Fe incorporated on the MFI zeolite framework (Fe-MFI) with the nanosheet morphology and unique hierarchical pore structure was successfully synthesized and applied for the adsorption and degradation of Rhodamine B (RhB) in a Fenton-like reaction in the presence of H₂O₂. The synthesis involved a seed-directed hydrothermal method in the presence of NH₄F and a subsequent NaOH treatment made the synthesized hierarchical Fe-MFI nanosheets (Fe-20-10) characterized by abundant highly dispersed framework Fe³⁺ species. As a result of these features, the Fe-20-10 showed excellent ability of adsorption and degradation efficiency of RhB, and enhanced durability due to negligible leaching of framework Fe³⁺ species. Moreover, the hydroxyl radicals were determined as the main the reactive oxygen species of RhB degradation, and a possible adsorption–degradation pathway was proposed. This work offers guidance for developing high-performance Fenton-like degradation catalysts. Full article

Developing a robust Fenton-like catalyst through a feasible method is a significant challenge and is crucial for sustainability in wastewater treatment. Herein, we report a novel dual-phase H₂O₂ activation for ^•OH generation via both heterogeneous surface-mediated reactions and homogeneous radical propagation pathways. Mechanistic investigations revealed that the surface Fe²⁺/Fe³⁺ redox cycle was the primary driver of catalysis at pH 5. Notably, the catalyst produced fewer secondary pollutants than Fenton reactions and was effective in treating pollutants with high concentrations. The oxidative performance of the PAS-ISe was comparable to that of commercial FeSO₄·7H₂O in terms of chemical oxygen demand (COD) removal efficiency and reaction kinetics. Besides, the utility of the catalyst was 2-75-fold greater than that of state-of-the-art Fenton or photo-Fenton-like catalysts. A detailed techno-economic analysis confirmed the feasibility of this strategy and significant cost advantages over existing heterogeneous catalyst synthesis methods. This study concurrently proposes a low-cost approach to valorizing hazardous sludge and effectively treating industrial wastewater, which may support circular economic principles. Full article

Recently, researchers have been focused on the recycling as well as transforming of bio-waste streams into a valuable resource. Banana peels are promising for such application, due to their wide availability. In this context, the integration of banana peel-derived biochar with environmentally benign magnetite has significantly broadened its potential applications as a solar photocatalyst compared to the conventional photocatalysts. The materials are mixed in varied proportions of Ban-Char500-Mag@-(0:1), Ban-Char500@Mag-(1:1) and Ban-Char500@Mag-(2:1) and characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM) augmented with dispersive X-ray spectroscopy (EDX). Such modification is leading to an improvement in its application as a solar photocatalyst using the photochemical solar collector facility. The study discusses the factors controlling acetaminophen removal from aqueous effluent within 30 min of solar illumination time. Furthermore, the highlighted optimum parameters are pH 3.0, using 10 mg/L of the Ban-Char500@Mag-(1:1) catalyst and 100 mg/L of the hydrogen peroxide as a Fenton combination system for removing a complete acetaminophen from wastewater (100% oxidation). Also, the temperature influence in the oxidation system is studied and the high temperature is unfavorable, which verifies that the reaction is exothermic in nature. The catalyst is signified as a sustainable (recoverable, recyclable and reusable) substance, and showed a 72% removal even though it was in the six cyclic uses. Further, the kinetic study is assessed, and the experimental results revealed the oxidation process is following the first-order kinetic reaction. Also, the kinetic–thermodynamic parameters of activation are investigated and it is confirmed that the oxidation is exothermic and non-spontaneous in nature. Full article

Due to its efficiency, advanced oxidation processes (AOP), such as photo-Fenton, have become an alternative for removing emerging contaminants like paracetamol. The objective of this work was to perform a life cycle assessment (LCA) according to ISO 14040/44 for a heterogeneous photo-Fenton process catalyzed by Cu/Fe-pillared clays (PILC) for the removal of paracetamol from water. The study covered catalyst synthesis and four treatment scenarios, with inventories built from experimental data and ecoinvent datasets; treatment time was 120 min per functional unit. Environmental impacts for catalyst synthesis were quantified with ReCiPe 2016 (midpoint), while toxicity-related impacts of the degradation stage were assessed with USEtox™ (human carcinogenic toxicity, human non-carcinogenic toxicity, and freshwater ecotoxicity). Catalyst synthesis dominated most midpoint categories, the global warming potential for 1 g of Cu/Fe-PILC was 10.98 kg CO₂ eq. Toxicity results for S4 (photo-Fenton Cu/Fe PILC) showed very low values: 9.73 × 10⁻¹² CTUh for human carcinogenic and 1.29 × 10⁻¹³ CTUh for human non-carcinogenic. Freshwater ecotoxicity ranged from 5.70 × 10⁻⁴ PAF·m³·day at pH 2.7 (≥60 min) to 1.67 × 10⁻⁴ PAF·m³·day at pH 5.8 (120 min). Overall, optimizing pH and reaction time, are key levers to improve the environmental profile of AOP employing Cu/Fe-PILC catalysts. Full article

Per- and polyfluoroalkyl substances (PFAS) are a diverse group of synthetic fluorinated compounds widely used in industrial and consumer products due to their exceptional thermal stability and hydrophobicity. However, these same properties contribute to their environmental persistence, bioaccumulation, and potential adverse health effects, including hepatotoxicity, immunotoxicity, endocrine disruption, and increased cancer risk. Traditional water treatment technologies, such as coagulation, sedimentation, biological degradation, and even advanced membrane processes, have demonstrated limited efficacy in removing PFAS, as they primarily separate or concentrate these compounds rather than degrade them. In response to these limitations, photoassisted processes have emerged as promising alternatives capable of degrading PFAS into less harmful products. These strategies include direct photolysis using UV or VUV irradiation, heterogeneous photocatalysis with materials such as TiO₂ and novel semiconductors, light-activated persulfate oxidation generating sulfate radicals, and photo-Fenton reactions producing highly reactive hydroxyl radicals. Such approaches leverage the generation of reactive species under irradiation to cleave the strong carbon–fluorine bonds characteristic of PFAS. This review provides a comprehensive overview of emerging photoassisted technologies for PFAS removal from water, detailing their fundamental principles, degradation pathways, recent advancements in material development, and integration with hybrid treatment processes. Moreover, it discusses current challenges related to energy efficiency, catalyst deactivation, incomplete mineralization, and scalability, outlining future perspectives for their practical application in sustainable water treatment systems to mitigate PFAS pollution effectively. Full article

In this work, the removal of Cu(II) ions from an aqueous effluent was studied using an Mg/Fe layered double hydroxide (LDH) as the adsorbent. The material was synthesized and characterized before and after the adsorption process to identify structural and morphological changes induced by copper uptake. Techniques such as X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), ultraviolet-visible spectroscopy (UV-Vis), Raman spectroscopy, and nitrogen physisorption (BET) were employed to confirm the interaction between the metal ions and the LDH surface. The LDH-Mg/Fe exhibited a high maximum adsorption capacity of 526 mg/g, and the adsorption kinetics followed a pseudo-second-order model, achieving over 90% removal of Cu(II) within 2.5 h. The Cu(II)-loaded material was subsequently evaluated as a sustainable catalyst in two applications: (i) an organic synthesis via “click” chemistry, reaching yields of up to 85%, and (ii) the decoloration of Congo Red via a Fenton-like process, achieving a decoloration efficiency of at least 84%. These dual uses demonstrate the potential of Cu(II)-loaded LDH as a cost-effective and environmentally friendly approach to simultaneous pollutant removal and catalytic valorization. Full article

This paper studies the formation process of a composite material based on an organic substance, biochar from sunflower husks, and an inorganic substance, nickel (II)-copper (II) ferrites of the composition Cu_xNi_1−xFe₂O₄ (x = 0.0; 0.5; 1.0). The obtained materials were characterized by X-ray phase analysis, scanning electron microscopy, and FTIR spectroscopy. It is shown that when replacing copper (II) cations with nickel (II) cations, the average parameters and volume of the unit cell gradually decrease, and the cation–anion distances in both the tetrahedral and octahedral spinel grids also decrease with regularity. The oxide materials were found to form a film on the surface of biochar, repeating its porous structure. The obtained materials exhibit high catalytic activity in the methyl orange decomposition reaction under the action of hydrogen peroxide in an acidic medium; the degradation of methyl orange in an aqueous solution occurs 30 min after the start of the reaction. This result may be associated with the formation of the Fenton system during the oxidation–reduction process. A significant increase in the reaction rate in the system containing mixed nickel–copper ferrite as a catalyst may be associated with the formation of a more defective structure due to the Jahn–Teller effect manifestation, which creates additional active centers on the catalyst surface. Full article

Despite the immense potential in environmental remediation, the translation of magnetic nanomaterials (MNMs) from laboratory innovations to practical, field-scale applications remains hindered by significant technical and environmental challenges. This is particularly evident in soil environments—which are inherently more complex than aquatic systems and have received comparatively less research attention. Beginning with an outline of the fundamental properties that make iron-based MNMs effective as adsorbents and catalysts for heavy metals and organic pollutants, this review systematically examines their core contaminant removal mechanisms. These include adsorption, catalytic degradation (e.g., via Fenton-like reactions), and magnetic recovery. However, the practical implementation of MNMs is constrained by several key limitations, such as particle agglomeration, oxidative instability, and reduced efficacy in multi-pollutant systems. More critically, major uncertainties persist regarding their long-term environmental fate and biocompatibility. In light of these challenges, we propose that future efforts should prioritize the rational design of stable, selective, and intelligent MNMs through advanced surface engineering and interdisciplinary collaboration. Full article

The selective oxidation of methane to methanol under mild conditions remains a significant challenge due to its stable C-H bond and the propensity for overoxidation of products. Herein, we investigated the Fe- and Cu-modified ZSM-5 catalysts using H₂O₂ as an oxidant for the selective oxidation of methane. It was found that the Fe/Cu ratio had a great impact on methanol yield. The Fe₃Cu₁ displayed the highest methanol yield of 29.7 mmol g_cat⁻¹ h⁻¹ with a selectivity of 80.9% at 70 °C. Further analysis revealed that Fe₃Cu₁ showed the highest Fe³⁺ and Cu⁺ contents. The optimal dual valence cycle not only facilitates the efficient utilization of H₂O₂, promoting the activation of methane to •CH₃ at the Fe site, but also suppresses the deep oxidation caused by the Fenton-like effect of Fe/H₂O₂, thus maintaining the high yield and high selectivity of methanol. Full article

Large amounts of spent, radioactive, ion-exchange resins have been generated worldwide, and their production is expected to grow due to a renaissance of nuclear power. Such waste is being stored at individual plant sites around the world, awaiting a reliable disposal route to overcome the downsides of the state-of-the-art management approaches. In this work, a first-of-its-kind pre-disposal strategy is proposed, based on the integration of a heterogeneous Fenton-like treatment with conditioning in an alkali-activated matrix. In particular, the circular economy is pursued by repurposing two industrial by-products, coal fly ash and steel slag, both as catalysts of the Fenton treatment and precursors of the conditioning matrix. The obtained waste forms have been preliminarily tested for leaching and compressive strength according to the Italian waste acceptance criteria for disposal. The proposed technology, tested at laboratory scale up to 100 g of virgin cationic resin, has proven successful in decomposing the waste and synthesizing waste forms with an overall volume increase of only 30%, thereby achieving a remarkable result compared to state-of-the-art technologies. Full article

To enhance the formation of hydroxyl radicals (•OH) when polishing single crystal silicon carbide (SiC), this study proposes a catalytic-assisted polishing approach based on a Fe₃O₄/ZnO/graphite hybrid system. Firstly, methyl orange degradation experiments were conducted using Fe₃O₄/ZnO/graphite hybrid catalysts. Secondly, a resin-based abrasive tool embedded with the Fe₃O₄/ZnO/graphite hybrid was developed. Subsequently, polishing experiments under dry, water, and hydrogen peroxide conditions were performed based on the abrasive tool. The corresponding surface roughness (Sa) were 26.51 nm, 12.955 nm and 4.593 nm, separately. The material removal rate were 0.733 mg/h (1.586 μm/h), 2.800 mg/h (6.057 μm/h) and 4.733 mg/h (10.239 μm/h), respectively. The results demonstrate that the Fe₃O₄/ZnO/graphite hybrid synergistically enhanced •OH generation through Fenton reactions and tribocatalysis of ZnO. Therefore, the increased •OH productivity contributes to SiC oxidation and SiO₂ removal, improving both polishing efficiency and surface finish. The catalytic-assisted polishing provides a novel approach for the high-efficiency ultra-precision machining for SiC. Full article

The rapid industrial development in recent years has led to severe pollution of aquatic environments. It is necessary to develop green and highly efficient treatment technologies for addressing environmental pollution and realizing carbon peaking and carbon neutrality goals. This study aims to explore the effect of magnetic fields on chemical oxygen demand (COD) degradation by Fenton reaction. The experimental results demonstrated the following: (1) Magnetic fields convert macromolecular organic compounds into low-molecular-weight organic compounds, promoting the attack of radicals on organic pollutants. (2) The magnetic Fenton process achieved COD removal efficiency of 60.0%. (magnetic field intensity: 1.5 T, magnetization duration: 5 min, pH = 5.0, Fe²⁺ = 2.0 mmol/L, H₂O₂ = 2.0 mmol/L, reaction time: 40 min). (3) The magnetic Fenton process consumes less acidic reagent. Notably, it achieves a 33.3% reduction in both catalyst and oxidant usage under the same COD removal efficiency. This study verifies the feasibility of applying the method in real sewage treatment plants, demonstrating promising application prospects. Full article

This study reports the hydrothermal synthesis, characterization, and Fenton-like catalytic performance of CeO₂–CoFe₂O₄ nanocomposites for degrading Congo Red (CR) dye and the oxytetracycline (OTC) antibiotic. A series of Ce-doped cobalt ferrite samples was prepared using a hydrothermal reaction. Additionally, the 50Ce-CFO sample was further activated with H₂O₂ treatment. XRD, FTIR, and SEM analyses confirmed the formation of a spinel phase alongside segregated CeO₂, which acts as a grain-growth inhibitor. The increased Ce content promotes particle amorphization. FTIR showed changes in the intensity of the M–O stretching band, indicating Ce-induced bond polarization in the spinel lattice. In H₂O₂ decomposition tests, the 50Ce-CFO catalyst fully decomposes H₂O₂ in 160 min, while the activated sample completes it in 125 min. Fenton-like degradation of CR and OTC by untreated and activated 50Ce-CFO sample followed pseudo-first-order kinetics. Catalyst stability was confirmed using post-reaction XRD, FTIR, and SEM analyses. Incorporation of CeO₂ into CoFe₂O₄ refines the crystallite size, increases the BET surface area, and enhances adsorption capacity, while the Ce⁴⁺/Ce³⁺ redox couple promotes reactive oxygen species generation. Owing to this dual structural and catalytic role, the CeO₂-CoFe₂O₄ composites exhibit significantly improved Fenton-like catalytic activity, enabling the efficient degradation of organic pollutants. Full article

Water contamination by emerging pollutants poses a significant environmental challenge, demanding innovative treatment technologies beyond conventional methods. Advanced oxidation processes (AOPs) utilizing niobium-based catalysts, particularly niobium oxide (Nb₂O₅) and its modified forms, are prominent due to their high chemical stability, effective reactive oxygen species (ROS) generation, and versatility. This review systematically examines recent advancements in Nb₂O₅-based catalysts across various AOPs, including heterogeneous photocatalysis, electrocatalysis, and Fenton-like reactions, highlighting their mechanisms, material modifications, and performance. Following PRISMA and InOrdinatio guidelines, 381 papers were selected for this synthesis. The main findings indicate that niobium incorporation enhances pollutant degradation by extending light absorption, reducing electron–hole recombination, and increasing ROS generation. Structural modifications such as crystalline phase tuning, defect engineering, and the formation of heterostructures further amplify catalytic efficiency and stability. These catalysts demonstrate considerable potential for water treatment, effectively degrading a broad range of persistent contaminants such as dyes, pharmaceuticals, pesticides, and personal care products. This review underscores the environmental benefits and practical relevance of Nb₂O₅-based systems, identifying critical areas for future research to advance sustainable water remediation technologies. Full article