Search Results (238)

This review summarizes recent applications of carbon-based materials as catalysts in the ozonation of wastewater contaminated with persistent organic pollutants. Methods available for production of commonly used inexpensive carbonaceous materials such as biochar and hydrochar are presented. Differences between production methods of active carbon and biochar or hydrochar are discussed. Interestingly, biochar, in a role of rather simple and cheap charcoal, is catalytically active and increases the rate of oxidative degradation of nonbiodegradable aqueous contaminants such as drugs or textile dyestuffs. This review documents that even the addition of biochar to the ozonized wastewater increases the rate of removal of persistent organic pollutants. Cheap bio-based carbonaceous materials such as biochar work as adsorbent of dissolved pollutants and catalysts for ozone-based degradation of organic compounds via the formation of reactive oxygen species (ROS). Low-molecular-weight degradation products produced by ozonation of pharmaceuticals and textile dyes are presented. The combination of air-based ozone generation, together with application of biochar, represents a sustainable AOP-based wastewater treatment method. Full article

Environmental pollution from ozone and wastewaters containing dyes from various industries is an important problem for humanity. In this study, novel composite catalysts based on manganese carbonate ore from the Obrochishte deposit, Bulgaria, were used successfully in two environmentally relevant catalytic processes—the ozone decomposition and photocatalytic decolourization of Malachite Green (MG) dye under UV illumination. Manganese carbonate ore/NiO, manganese oxides, and silver-containing composites were synthesized via co-precipitation, followed by calcination at 500 °C or hydrothermal treatment at 160 °C, and then thermal treatment. The phase and elemental composition, structure, morphology, and textural characteristics of the obtained composites were investigated using powder X-ray diffraction analysis, wavelength-dispersive X-ray fluorescence, Fourier-transform infrared spectroscopy, scanning electron microscopy, nitrogen adsorption–desorption isotherms, and the BET method. The materials exhibit a mesoporous structure. The results established that the thermally treated MnCO₃ ore/NiO, manganese oxides, and Ag-containing composites demonstrate a higher catalytic efficiency for the removal of ozone (85%, 93%, and 99%) in comparison with hydrothermally treated analogues—79%, 66%, and 98%, respectively. The thermally treated manganese carbonate ore/silver-containing composite exhibits the highest photocatalytic ability (83% degree of decolourization of MG dye) compared to the other investigated catalysts. Full article

Activated carbon has shown good catalytic performance in water treatment, but its wide application is limited by its high price. Activated coke exhibits functional groups and is low-cost. However, there is limited research on activated coke as a catalyst. In our previous study, powdered activated coke (PAC) exhibited good catalytic performance in NH₃-N treatment with ozonation. Increasing nitrogen selectivity is the key to harmless degradation of NH₃-N, which has received little attention. In this paper, manganese-loaded powdered coke (Mn–PAC) was prepared, aiming to further improve the nitrogen selectivity. Under the same conditions, the PAC/O₃ system achieved 92.16% NH₃-N removal and 49.46% nitrogen selectivity, while the Mn–PAC/O₃ system achieved almost 100% NH₃-N removal and 79.31% N₂ selectivity. When Mn–PAC was reused for the sixth time, the system achieved about 70% and 46% NH₃-N removal and N₂ selectivity, both of which were about 10% higher than those of PAC. Complex redox and synergistic interactions existed in the Mn–PAC/O₃ system. The Mn–PAC surface contains reactive sites such as C=C, C=O, π–π bonds, ArOH, and various MnO_x. These components collectively facilitate ozone decomposition into ·OH, ·O₂⁻, and ¹O₂. The ¹O₂ may play a significant role in converting NH₃-N to N₂. Full article

Catalytic ozonation has been widely utilized in environmental applications, such as the removal of pharmaceutical active compounds (PHACs) from wastewater, due to its outstanding catalytic efficiency. To further enhance its performance and expand its practical application, ozone-based hybrid processes have been investigated, including ultraviolet radiation/ozonation, hydrogen peroxide/ozonation, ultrasonication/ozonation, and biological treatment/ozonation. Ozone degrades pollutants via two primary pathways: direct oxidation (via molecular ozone) and indirect oxidation (via reactive intermediates). Enhancing ozone decomposition into various reactive oxygen species (ROS), predominantly hydroxyl radicals, can significantly augment the degradation efficiency of pollutants. The surface adsorption and electron transfer processes of catalysts can promote ozone activation and decomposition into ROS to achieve the efficient degradation and mineralization of pollutants. Among catalysts, Mn-based catalysts have been extensively studied in past research. They have demonstrated exceptional performance when combined with other metals, such as Mn/Ce, Mn/Fe, and Mn/Co, etc., due to synergistic effects arising from bimetallic interactions. The inherent characteristics of catalyst supports may also influence the generation process of ROS. Choosing an appropriate support is conducive to promoting the uniform distribution of catalytic active sites on the catalyst surface and avoiding the agglomeration of metal particles, and it is also beneficial for the recovery and reuse of the catalyst. Furthermore, coupling catalytic ozonation processes with techniques like high-gravity technology, jet reactor systems, and micro–nano-bubbles can improve the utilization efficiency of ozone by exploiting gas cavitation effects. In this paper, we summarize the research progress in the degradation of PHACs using catalytic ozonation and discuss strategies for improving the mass transfer efficiency of ozone in water. Finally, the challenges and opportunities associated with applying catalytic ozonation in practical applications are also discussed. Full article

For effective water purification, the combination of membrane separation and catalytic degradation technologies not only permits continuous pollutant degradation but also successfully reduces membrane fouling. In recent years, catalytic membranes (CMs) have garnered a lot of interest in the water treatment industry. The main benefits of CMs are methodically explained in this review, emphasizing the synergistic effect of membrane separation and catalysis. These benefits include stable catalyst loading achieved through membrane structure manipulation, nanoconfinement, and effective degradation of organic pollutants. The application of catalytic membranes in water treatment is then thoroughly summarized, and they are separated into five main groups based on their unique catalytic reaction mechanisms: ozone catalytic membranes, photocatalytic membranes, electrocatalytic membranes, Fenton-type catalytic membranes, and persulfate catalytic membranes. The mechanisms and performance characteristics of each kind of CM are looked at in greater detail. Finally, research directions and future prospects for water treatment using catalytic membranes are proposed. This review provides recommendations for future research and development to ensure the effective use of catalytic membranes in water treatment, in addition to providing a thorough examination of the advancements made in their application in the treatment of various wastewaters. Full article

Naproxen (NPX), a nonsteroidal anti-inflammatory drug, is considered an emerging contaminant due to its persistence and potential environmental risks. In this study, NPX degradation was investigated through ozonation using nickel–iron foam (NiFeF) and NiO-modified NiFeF (NiO/NiFeF). The effect of the foam size was investigated using three configurations: S1 (1 cm × 2.5 cm), S2 (2 cm × 2.5 cm), and S3 (2 cm × 5 cm). Complete NPX removal was achieved in all systems, with degradation times of 4 min for ozonation alone, 2 min for NiFeF-S1, and 1 min for NiO/NiFeF-S2 and NiO/NiFeF-S3. The NiO/NiFeF catalyst was synthesized via ultrasonic spray pyrolysis, resulting in a porous structure with abundant active sites. Compared with conventional ozonation, NiO/NiFeF-S1 improved the total organic carbon (TOC) removal rate by 6.2-fold and maintained 87.5% of its activity after five reuse cycles, demonstrating excellent stability. High-resolution mass spectrometry revealed that catalytic ozonation generated fewer by-products (22 vs. 27 for ozonation alone) and promoted more selective pathways, including demethylation, ring-opening oxidation, and partial mineralization to CO₂ and H₂O. This enhanced performance is attributed to the synergy between NiO and NiFeF, which facilitates reactive oxygen species generation and electron transfer. These results demonstrate the potential of NiO/NiFeF as an efficient and stable catalyst for pharmaceutical removal from water. Full article

Nitrogen oxides (NO_x), one of the major air pollutants, not only are key substances in forming acid rain and photochemical smog, but can also enter the stratosphere and damage the ozone layer to some extent. The selective catalytic reduction (NH₃-SCR) technology has been widely utilized in industrial flue gas treatment for its efficient removal of NO_x. In recent years, nitrogen-doped carbon materials (NC) have emerged as a novel type of environmentally friendly catalyst, showing outstanding performance in the low-temperature NH₃-SCR reaction. This paper reviews the application advancements of nitrogen-doped carbon materials in the NH₃-SCR reaction, with a focus on the catalytic mechanisms, modification strategies, and stability issues. This paper analyzes multiple improvement ideas, such as regulating metal types and distributions to achieve synergy effects, optimizing carrier loading, and designing morphology structures, and discusses how these measures jointly act to enhance the overall performance of the catalyst. Finally, solutions to the deactivation problem of NC catalysts are proposed, and the future research directions are explored to meet the increasingly stringent environmental protection requirements and promote the development of related technologies. Full article

To promote sustainable wastewater treatment, this study developed an eco-friendly and low-cost ozone catalyst using natural zeolite for the advanced treatment of petrochemical wastewater. The Ca-Cu/zeolite catalyst (0.75 mol/kg Ca and 0.25 mol/kg Cu) demonstrated high efficiency in catalytic ozonation, achieving 55.52% TOC removal under optimized conditions (ozone dosage: 108.0 mg/(L·h), catalyst dosage: 406.0 g/L, reaction time: 90 min). Compared to ozonation alone, the catalyst enhanced oxidation rates by 10 times, promoting ozone decomposition into reactive oxygen species (e.g., OH and ¹O₂) while improving gas–liquid–solid mass transfer for efficient pollutant mineralization. Remarkably, the natural zeolite-based catalyst exhibited superior sustainability: compared to conventional alumina-based catalysts, its production cost (4000–4500 CNY/ton) is 44–53% lower, while its carbon footprint (533.7 kg CO₂/ton) is reduced by 45.4%. This work presents a sustainable, low-carbon, and economically viable catalytic ozonation solution, contributing to the development of green and cost-effective industrial wastewater treatment technologies. Full article

Biologically treated swine farm wastewater still contains high levels of refractory organics, humic substances and antibiotic residues, posing environmental risks and limiting opportunities for water reuse. Wastewater treatment by ozonation alone suffers from low mass transfer efficiency and selective oxidation. To overcome these limitations, a catalytic ozonation process (O₃/Fe²⁺/H₂O₂) was applied and optimized using Response Surface Methodology (RSM) based on single-factor experiments and Central Composite Design (CCD) for advanced swine farm wastewater treatment. The optimal conditions ([O₃] = 25.0 mg/L, [Fe²⁺] = 25.9 mg/L, [H₂O₂] = 41.1 mg/L) achieved a COD removal of 44.3%, which was 86.8% higher than that of ozonation alone, and increased TOC removal to 29.5%, indicating effective mineralization. Biodegradability (BOD₅/COD) of swine farm wastewater effluent increased from 0.01 to 0.34 after the catalytic ozonation treatment. Humic-like and fulvic-like substances were removed by 93.7% and 95.4%, respectively, and antibiotic degradation was significantly accelerated and enhanced. The synergistic process improved ozone utilization efficiency by 33.1% and removed 53.95% of total phosphorus through Fe³⁺-mediated coprecipitation. These findings demonstrate that with catalytic ozone decomposition and production of hydroxyl radicals, the O₃/Fe²⁺/H₂O₂ system effectively integrates enhanced ozone utilization efficiency, radical synergy, and simultaneous pollutant removal, providing a cost-effective and technically feasible strategy for advanced swine farm wastewater treatment and safe reuse. Full article

The development of efficient and sustainable advanced oxidation processes (AOPs) for organic pollutant removal is of great significance for water purification. In this study, a CoFeNi-layered double hydroxide (CoFeNi-LDH) catalyst was synthesized and applied for the simultaneous activation of peroxymonosulfate (PMS) and ozone to degrade rhodamine B (RhB) in aqueous solution. The CoFeNi-LDH/PMS/ozone system achieved a remarkable RhB removal efficiency of 95.2 ± 1.2% within 8 min under neutral pH conditions. Systematic parametric studies revealed that synergistic interactions among CoFeNi-LDH, PMS, and ozone contributed to the generation of reactive oxygen species (ROS), primarily sulfate radicals (SO₄^•−) and singlet oxygen (¹O₂), as confirmed by EPR and quenching experiments. Density functional theory (DFT) calculations demonstrated that ozone enhanced PMS adsorption and activation at CoFeNi catalytic sites. The catalyst exhibited robust magnetic recyclability and structural stability after repeated use. This work highlights a synergistic catalytic strategy for PMS/ozone activation, offering an effective and environmentally friendly platform for dye wastewater remediation. Full article

The increasing presence of synthetic dyes in aquatic environments presents a serious threat to ecosystems and human health. This study investigates the potential of natural biomaterials, specifically fish-derived components extracted from Cyprinus carpio (fish bladder and fish scales), for the simultaneous retention and degradation of a potentially toxic dye: Malachite Green (MG). The biomaterials were characterized using X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, thermogravimetric analysis (TGA), and high-performance liquid chromatography with mass spectrometry detection (HPLC-MS) for degradation monitoring. Batch adsorption experiments were conducted under varying biomaterial dosage, contact time and pH. Results demonstrated that all tested biomaterials exhibited significant adsorption capacities, with fish scales (FS) achieving a maximum removal efficiency of 91.2%, and fish bladder (FB) reaching 82% under optimal conditions. In catalytic ozonation tests, the fish scales impregnated with vanadium (FS-V) catalyst demonstrated significantly higher degradation efficiency, reaching 63.84% at an ozone flow rate of 0.5 g O₃·h⁻¹. The comparative analysis highlights the multifunctionality of these eco-friendly biomaterials, offering both pollutant capture and partial degradation. These findings suggest that low-cost, naturally derived biomaterials can serve as effective alternatives to synthetic adsorbents in water treatment applications, contributing to sustainable environmental remediation strategies. Full article

Dyes in wastewater are an environmental issue due to the persistent nature of these compounds. This comparative study examined the efficiency of ozonation and catalytic ozonation using Fe³⁺/O₃ for the degradation of two selected dyes, Methylene Blue (MB) and Methyl Orange (MO). For MB, ozonation alone achieved 65% degradation within the maximum reaction time of 15 min, whereas 100% degradation was obtained with the Fe³⁺/O₃ method in the same time. On the other hand, for MO, ozonation alone resulted in 85% degradation within 15 min, while the Fe³⁺/O₃ method achieved 100% degradation in 10 min. The effect of Fe³⁺ dose was also investigated, and 3 ppm was found to be the most efficient. The scavenger effect highlighted that ^•OH radicals were the dominant species for degradation. For MB, the highest degradation rate was observed at pH 9, which is attributed to catalyzed ozone decomposition, thereby enhancing the generation of ^•OH radicals to a higher concentration. For MO, the degradation rate was highest at pH 5. LC-MS analysis was performed to explore MB degradation products formed during Fe³⁺/O₃ treatment. Five main degradation products were observed, with the main pathway involving the generation of P1, P2, and P3. Based on the results, the Fe³⁺/O₃ method is considered efficient for wastewater treatment. This study highlights the Fe³⁺/O₃ method as a sustainable solution for the degradation of dyes from textile wastewater. Full article

The production of alumina produces red mud (RM), a highly alkaline solid waste. The majority of it is disposed of in landfills, which seriously pollutes the environment. It needs to be recycled and handled with care to protect the environment. RM is a promising raw material for wastewater and waste gas treatment owing to its high alkalinity and abundant metal compounds. It can efficiently remove diverse pollutants while facilitating large-scale utilization of RM resources. Reviews of the use of RM resources to create catalysts for environmental governance are, nevertheless, scarce. Therefore, this paper analyzes and summarizes the pertinent research on RM-based catalysts to remove pollutants from the environment based on journal literature related to RM resource utilization from 2015 to 2025. This study reviews the application of RM-based catalysts for degrading pollutants in wastewater and exhaust gases via advanced oxidation processes (AOPs)—including photocatalysis, Fenton-like catalysis, ozonation catalysis, and persulfate catalysis—as well as catalytic oxidation, chemical looping combustion (CLC), and selective catalytic reduction (SCR). The paper emphasizes the analysis of modification strategies and catalytic mechanisms of RM-based catalysts in environmental remediation and examines the environmental risks and corresponding mitigation measures related to their preparation from RM resources. Finally, it outlines that future research should prioritize green, low-energy modification processes; catalytic systems for the synergistic removal of multiple pollutants; and efficient, recyclable separation and recovery technologies. These directions aim to promote the sustainable application of RM in large-scale environmental remediation and to achieve the integrated advancement of resource utilization and ecological protection. Full article

Cost-effective procedures usually cannot achieve complete removal of priority contaminants present in water at very low concentrations (as pesticides or pharmaceuticals). Advanced oxidation processes (AOPs) represent promising technologies for removing priority contaminants from water at trace concentrations, yet practical implementation remains limited due to technical and economic constraints. This study presents an innovative flow-through photodegradation device designed to overcome current limitations while achieving efficient contaminant removal at industrial scale. The device integrates a UVC 254 nm lamp-equipped flow chamber with automated dosing pumps for hydrogen peroxide and/or solid catalyst suspensions, coupled with a 30 nm porous membrane filtration system for catalyst recirculation. This configuration optimizes light–catalyst–pollutant contact while enabling combined catalytic processes. Performance evaluation using acesulfame (ACE) and iohexol (IHX) as model contaminants demonstrated rapid and effective removal. IHX degradation with UVC and 75 μM H₂O₂ achieved complete removal with t₉₅% = 7.23 ± 1.21 min (pseudo-order 0.25, t₁/₂ = 3.27 ± 0.39 min), while ACE photolysis (with UVC only) required t₉₅% = 14.88 ± 2.02 min (pseudo-order 1.27, t₁/₂ = 2.35 ± 0.84 min). The introduction of t₉₅% as a performance metric provides practical insights for near-complete contaminant removal requirements. Real-world efficacy was confirmed using tertiary wastewater treatment plant effluents containing 14 μg/L IHX, achieving complete removal within 8 min. However, carbamazepine degradation proved slower (t₉₅% > 74 h), highlighting the need for combined catalytic approaches for recalcitrant compounds. Spiking experiments (1000 μg/L) revealed concentration-dependent kinetics and synergistic effects between co-present contaminants. Analysis identified degradation byproducts consistent with previous studies, including tri-deiodinated iohexol (474.17 Da) intermediates. This scalable system, constructed from commercially available components, demonstrates potential for cost-effective industrial implementation. The modular design allows adaptation to various contaminants through adjustable AOP combinations (UV/H₂O₂, photocatalysts, ozone), representing a practical advancement toward addressing the gap between laboratory-scale photocatalytic research and full-scale water treatment applications. Full article

This study explores the adsorption and catalytic degradation of 2,4,6-trinitrotoluene (TNT) from aqueous solutions, using montmorillonite-based catalysts. Commercially, montmorillonite K10 was modified through aluminum pillaring (K10-Al-PILC), followed by vanadium intercalation (K10-Al-PILC-V) and ozone activation. A novel aspect of this work is the use of naturally contaminated water as the TNT source. The selected sample, collected from the Plaiul Arșiței–Cireșu–Leșunț region (Oituz, Bacau, Romania), originated from an area historically exposed to explosive residues, where TNT traces were previously identified. The adsorption performance of the materials was evaluated by varying adsorbent dosage, contact time, and solution pH. Catalytic ozonation experiments were conducted under different catalyst masses, ozone concentrations, and reaction times to assess degradation efficiency. The results demonstrated that aluminum pillaring significantly enhanced the adsorption capacity of the clay, while vanadium incorporation further improved both adsorption and catalytic activity. The vanadium-modified material exhibited superior performance in TNT removal, both through adsorption and oxidative degradation. Additionally, the catalytic ozonation process led to the formation of degradation products with reduced toxicity, confirming the potential of these materials for environmental remediation of nitroaromatic pollutants in real water systems. Full article