Search Results (205)

Advanced oxidation processes (AOPs) have been widely applied to treat textile wastewater, in which synthetic dyes are among the main pollutants. Some of these processes, such as the Fenton reaction, exhibit enhanced efficiency when coupled with radiation sources, particularly when combined with a compound parabolic concentrator (CPC). In this study, a UV-A photo-Fenton process assisted by CPC, constructed using reused fluorescent lamps as reaction tubes and operating with recirculation was applied to treat real textile wastewater. A preliminary factorial design was employed to optimize reagent concentrations, identifying optimal conditions of 2647.8 g·L⁻¹ of H₂O₂ and 15 mg·L⁻¹ of Fe²⁺. Overall, the use of the CPC led to an increase in photon availability, resulting in COD degradation efficiencies of 83%, corresponding to an ~19% relative increase in treatment efficiency, compared to the system without the CPC, as well as 79% removal efficiency for apparent color and 57% for turbidity. Results demonstrate that the CPC-assisted UV-A photo-Fenton process is an efficient and robust approach for treating real textile wastewater. Meanwhile, the reuse of fluorescent lamps represents a low-cost, environmentally sustainable alternative that contributes to waste valorization and process intensification. Full article

This study develops a visible-light-driven heterogeneous Fenton-like system for the efficient degradation and detoxification of the persistent fluoroquinolone antibiotic gatifloxacin (GAT) in water. Three Fe-based metal–organic frameworks (MIL-53(Fe), MIL-88A(Fe), and MIL-101(Fe)) were synthesized and systematically evaluated as catalysts in a visible-light/H₂O₂ process. The three MOFs were systematically characterized, and a comparative analysis was conducted to elucidate how their structural differences influence catalytic performance. Among three MOFs, MIL-88A(Fe) exhibited superior photocatalytic activity, stability, recyclability, and low energy consumption in the visible-light-driven photo-Fenton process, which was attributed to its favorable structural and photo-induced redox properties. Under the optimal conditions (pH 7.2, H₂O₂ dosage of 1.2 mL·L⁻¹, and catalyst loading of 0.1 g·L⁻¹), 95.6% of GAT was degraded within 90 min. Radical scavenging experiments demonstrated that hydroxyl radicals (•OH) dominated the oxidation process. Based on intermediate identification, plausible degradation pathways were proposed, accompanied by a pronounced reduction in the ecological risks of transformation products. Furthermore, toxicity assays revealed that both the antibacterial activity and acute toxicity of the treated solutions were significantly alleviated. Overall, the Light/MIL-88A(Fe)/H₂O₂ system offers an effective and sustainable strategy for the removal and detoxification of fluoroquinolone antibiotics from aquatic environments. Full article

Persistent organic pollutants, such as Rhodamine B (RhB), pose significant environmental and health risks, necessitating the development of advanced oxidation technologies for effective removal. While heterogeneous photo-Fenton catalysts are known for their high degradation efficiency, their practical application is often limited by complex synthesis processes, catalyst detachment, and difficult recovery. This study proposes an innovative laser-induced, one-step synthesis strategy to fabricate metal/carbon nanocomposite catalytic layers directly onto flexible carbon paper. The as-prepared composites exhibit strong interfacial interaction between metal nanoparticles and the carbon matrix, as indicated by XPS analysis, and demonstrate enhanced catalytic activity in the UV/H₂O₂ system. Notably, the integrated composites exhibit exceptional catalytic activity in the UV/H₂O₂ system, achieving complete degradation of a 20 mg/L RhB solution within just 1.5 h. The enhanced performance is attributed to the facilitated Fe³⁺/Fe²⁺ cycling and efficient generation of hydroxyl radicals (·OH), although the underlying charge separation mechanism requires further investigation with techniques such as photoluminescence spectroscopy and transient photocurrent measurements. This work not only demonstrates the high activity and stability of the photo-Fenton catalyst but also provides a green, rapid fabrication approach for the development of efficient and integrable catalytic devices for wastewater treatment. Full article

Paracetamol (PAR) was selected as an emerging micropollutant model to evaluate the effectiveness of the photo-Fenton process using natural Bandjéli ore (BO) as a heterogeneous source of iron. An aliquot of 1 mL of the activated product was introduced into 200 mL of an aqueous solution of paracetamol at a defined concentration. The tests were conducted in a double-jacketed glass photoreactor (0.2 L), continuously stirred and equipped with two UVA PL-L lamps (36 W, λ = 365 nm), with the temperature maintained at 20 °C and the pH around 2.4. The photo-Fenton process was applied with different initial paracetamol concentrations (10–50 mg/L), different ${\mathrm{H}}_2{\mathrm{O}}_2/\mathrm{P}\mathrm{A}\mathrm{R}$ initial molar ratios (10:1 and 5:1), and different ferric ion concentrations (2.84–4.73 mg/L). Under these conditions, complete disappearance of the parent compound (paracetamol) was achieved in less than 3 h for iron contents below 5 mg/L, in compliance with the discharge standards applicable in France and Togo. Inhibition tests with propan-2-ol highlighted the predominant role of hydroxyl radicals and the secondary involvement of superoxide radicals in the subsequent stages. Taken together, these results demonstrate that Bandjéli iron ore is an effective, sustainable, and economically advantageous alternative to commercial iron salts for implementing the photo-Fenton process in the decontamination of water polluted by organic micropollutants. Full article

Solar advanced oxidation processes (AOPs) utilising parabolic trough concentrators (PTCs) present a promising approach for the sustainable removal of recalcitrant contaminants from wastewater. This mini-review critically evaluates 25 peer-reviewed studies employing PTC-AOP systems for the degradation of chemical pollutants and microbial pathogens. Reported applications include photolysis, photo-Fenton and photocatalysis for the treatment of synthetic dyes, contaminants of emerging concern, industrial effluents, heavy metals and pathogenic microorganisms. A performance-oriented comparison based on normalised indicators is introduced. The time required for one order-of-magnitude reduction (corresponding to 90% removal; τ₉₀) reveals a significant mineralisation setback, where parent-compound degradation outpaces total organic carbon removal. The PTC concentration ratio and photon utilisation metrics highlight substantial variability in reactor design (geometry, materials, optical performance), which directly influences the treatment kinetics. Overall, PTC-AOP systems demonstrate strong potential as a polishing step within hybrid wastewater treatment. Future research should prioritise the standardisation of performance metrics, the catalyst design suited for high-photon and -temperature operation, and the integration into scalable and climate-resilient solar wastewater treatment. Full article

Constructed wetlands (CWs) are signified as green, self-sustaining systems for wastewater treatment. To date, their conventional designs struggle with slow kinetics and poor removal of refractory pollutants. This review redefines CWs as photo-reactive engineered systems, integrating near-neutral Fenton and photo-Fenton processes and in-situ oxidant generation to overcome diffusion limits, acid dosing, and sludge formation. By coupling catalytic fillers, solar utilization, and plant–microbe–radical (ROS) synergies, the approach enables intensified pollutant degradation while preserving the low-energy nature of CWs. Bibliometric trends indicate a sharp rise in studies linking CWs with advanced oxidation and renewable energy integration, confirming the emergence of a circular treatment paradigm. A decision framework is proposed that aligns material selection, reactor hydrodynamics, and solar light management with sustainability indicators such as energy efficiency, Fe-leach budget, and ROS-to-photon yield. This synthesis bridges environmental biotechnology with solar-driven catalysis, paving the way for next-generation eco-engineered wetlands capable of operating efficiently beyond the classical Fenton constraints. This work introduces the concept of “Constructed Wetlands Beyond the Fenton Limit”, where CWs are reimagined as photo-reactive circular systems that unify catalytic, biological, and solar processes under near-neutral conditions. It provides the first integrated decision matrix and performance metrics connecting catalyst design, ROS efficiency, and circular sustainability that offers a scalable blueprint for real-world hybrid wetland applications. Full article

This study optimized a homogeneous photo-Fenton process for the simultaneous degradation of the emerging pesticides atrazine and methomyl in water using Response Surface Methodology (RSM). A synthetic agricultural effluent containing 2.0 mg L⁻¹ of each pesticide (COD = 103.2 mg O₂ L⁻¹; TOC = 26.1 mg C L⁻¹; BOD₅ = 45.8 mg O₂ L⁻¹) was treated in a recirculating UV–H₂O₂/Fe²⁺ reactor. A 2³ factorial design with replication and five central points identified the H₂O₂/Fe²⁺ ratio and irradiation time as the main factors controlling mineralization, achieving up to 88.9% COD removal in the best screening run. Steepest-ascent experiments were then performed to approach the region of maximum response, followed by a rotatable Central Composite Design (20 runs). The resulting quadratic model explained 98.14% of the COD variance (R² = 0.9814; adjusted R² = 0.9646; predicted R² = 0.8591; CV = 0.2736%) and predicted a maximum COD removal of 94.5% at a volumetric flow rate of 0.466 L min⁻¹, a Fenton ratio of 12.713 mg mg⁻¹, and a treatment time of 71.0 min. Experimental validation under these optimized conditions yielded highly reproducible removals of 94.2 ± 0.04% COD and 81% TOC, confirming the predictive capability of the RSM model and demonstrating a high degree of organic mineralization. The response surfaces revealed that increasing the Fenton ratio enhances oxidation up to an optimum, beyond which hydroxyl-radical self-scavenging slightly decreases efficiency. Overall, the integration of multivariable experimental design and RSM provided a robust framework to maximize photo-Fenton performance with moderate reagent consumption and operating time, consolidating this process as a viable alternative for the mitigation of pesticide-laden agricultural wastewaters. Full article

Photo-Fenton advanced oxidation processes are promising and sustainable approaches for water treatment, particularly under visible-light irradiation. In this study, Cu-Fe bimetallic catalysts supported on silica and γ-alumina were developed for visible-light-driven photo-Fenton reactions, with emphasis on the influence of metal ratios and support-metal interactions on charge–carrier dynamics and hydroxyl radical formation. Comprehensive characterization (XRD, TEM, UV-Vis DRS, PL, TCSPC, and EPR) revealed stronger metal–support interactions and higher metal dispersion on γ-alumina, while silica-supported catalysts showed CuO aggregation at higher Cu loadings. Catalytic performance was evaluated using coumarin oxidation as both a model reaction and a quantitative probe for ^•OH radical generation. Alumina-supported catalysts exhibited superior activity, and ^•OH production increased with increasing Cu content on both supports. Importantly, iron was found to play a dual role: low Fe loading enhances photo-Fenton activity, whereas higher Fe content promotes charge–carrier recombination, leading to reduced activity under visible-light irradiation. These results highlight how the interplay between Fe/Cu ratio and support material governs charge dynamics and provides clear guidelines for the rational design of efficient heterogeneous photo-Fenton catalysts. Full article

The photo-Fenton process has been widely studied for the treatment of organic pollutants and disinfection in a wide range of scenarios. Nevertheless, its efficiency decreased when applied to complex matrices, as in the case of most advanced oxidation processes. Despite the interferences caused by different anions, the photo-Fenton is able to obtain good degradation values for pollutants and microorganisms, especially in combination with other methods; however, it depends on the matrix to be treated. Due to the lack of studies and reviews in this field, this paper reviewed the outcome of the inorganic ions present on highly saline water matrices (more than 1 g L⁻¹ of chlorides, fluorides, bromides, sulphates, carbonates or bicarbonates, borates, phosphates and nitrates/nitrites) on the Fenton-based processes, focusing on their outcome on iron speciation and their scavenger effect. Also, the most relevant works so far for the abatement of microcontaminants and disinfection by this process on highly saline matrices have been revised. Special emphasis is on the efficiency of the process, considering the relevant industries referred to. Full article

This work optimizes the energetic performance of 2,4,6-trinitrotoluene (TNT) abatement in water using a sono-photo-Fenton-like (SPF) process coupled with nano zero-valent iron (nZVI). A response–surface methodology (RSM) with a five-level central composite design (CCD) was applied to concurrently minimize specific energy consumption (SEC) from ultrasound (US) and UV irradiation while maximizing TNT removal. The optimal conditions were US power 80 W for 2 min and UV power 10 W for 6 min, yielding 73.95% TNT removal with SEC = 101.19 kWh kg⁻¹ TNT removed. The analysis of variance (ANOVA) test revealed that US power had the greatest effect on removal efficiency, whereas UV and US exposure times predominantly influenced SEC. Relative to the other Fenton-like configurations examined, the optimized SPF achieved superior removal at lower SEC and enabled enhanced iron recovery compared with photo-Fenton process using Fe²⁺. When applied to actual “yellow” wastewater, the optimized SPF again outperformed the photo-Fenton process using Fe²⁺, reducing SEC from 380.77 to 252.60 kWh kg⁻¹ and increasing treatment efficiency. The high-power/short-duration US paired with a low-power/short-duration UV regime provides a favorable efficacy–energy trade-off and supports pilot-scale deployment. Full article

Hydrogen peroxide (H₂O₂) is a key oxidant for green chemical processes, yet its catalytic utilization and activation efficiency remain limited by material instability and uncontrolled radical release. Here, we report a dual-functional, hollow conductive polymer nanostructure that enables selective modulation of H₂O₂ reactivity through interfacial physicochemical design. Hollow polypyrrole nanospheres functionalized with carboxyl groups (PPy@PyCOOH) were synthesized via a one-step Fe²⁺/H₂O₂ oxidative copolymerization route, in which H₂O₂ simultaneously served as oxidant, template, and reactant. The resulting structure exhibits enhanced hydrophilicity, rapid redox degradability (>80% optical loss in 60 min (82.5 ± 4.1%, 95% CI: 82.5 ± 10.2%), 10 mM H₂O₂, pH 6.5), and strong electronic coupling to reactive oxygen intermediates. Subsequent tannic acid–copper (TA–Cu) coordination produced a conformal metal–polyphenol network that introduces a controllable Fenton-like catalytic interface, achieving a 50% increase in ROS yield (1.52 ± 0.08-fold vs. control, 95% CI: 1.52 ± 0.20-fold) while maintaining stable photothermal conversion under repeated NIR cycles. Mechanistic analysis reveals that interfacial TA–Cu complexes regulate charge delocalization and proton–electron transfer at the polymer–solution boundary, balancing redox catalysis with energy dissipation. This work establishes a sustainable platform for H₂O₂-driven redox and photo-thermal coupling, integrating conductive polymer chemistry with eco-friendly catalytic pathways. Full article

The photo-Fenton process is an advanced oxidation method widely employed in environmental remediation. Herein, we developed a novel metal–organic framework@hydrogen-bonded organic framework (MOF/HOF) composite with excellent photo-Fenton-like activity for the efficient degradation of organic dye methylene blue (MB). Cu-based MOF (CuBTC) was firstly prepared via the solvothermal method, then melamine (MA) and trimesic acid (TMA)-based HOF (MA-TMA) was grown in situ on CuBTC with hydrogen bonding interactions to produce the MOF/HOF composite CuBTC-MA. The CuBTC-MA composite could catalyze H₂O₂ to produce active substances for efficient MB degradation. The degradation rate constant of the CuBTC-MA composite was 4.4 times and 16.7 times higher than that of CuBTC and MA-TMA. The remarkably enhanced performance was attributed to the synergistic effect between the efficient separation of electron–holes supported by the type-II heterojunction structure of the CuBTC-MA composite and the Cu(I)/Cu(II) inter-conversion. The CuBTC-MA composite demonstrated exceptional repeatability and maintained a stable performance across a broad pH range. This study provided a novel paradigm for engineering heterogeneous MOF/HOF heterostructures, demonstrating significant potential in advancing photo-Fenton-like catalytic systems for the efficient environmental remediation of organic pollutants through synergistic charge separation and radical generation mechanisms. Full article

Sulfanilic acid (SA) is a representative sulfonated aromatic amine commonly found in industrial effluents, posing significant risks to both human health and the ecosystem. Efficient and cost-effective treatment of SA-containing wastewater is crucial for sustainable environmental management. This study investigates the performance of the photo-Fenton process in degrading SA-containing wastewater. Three process variables are selected to study their effects on percent total organic carbon (%TOC) removal and final pH (pH_Final): initial total organic carbon concentration (TOC₀) (150–250 mg/L), Fe²⁺ concentration (15–85 mg/L), and H₂O₂ concentration (1000–1500 mg/L). A combination of response surface methodology (RSM) and Box-Behnken design (BBD) is applied to examine both the individual and interactive effects of these variables. A total of 15 experimental trials are conducted, with the center point repeated three times. The results indicate significant interaction effects between Fe²⁺ and H₂O₂ concentrations on %TOC removal, while the interaction between TOC₀ and H₂O₂ concentration notably influences pH_Final. The optimal operating parameters to maximize %TOC removal within 45 min of operation are determined as a TOC₀ of 54.2 mg/L, an Fe²⁺ catalyst concentration of 33.7 mg/L, and an H₂O₂ concentration of 1403 mg/L. Under these conditions, the predicted %TOC removal and pH_Final were 89.2% and 2.93, respectively, which confirmed through validation experiments. Additionally, a correlation between pH_Final, TOC₀, and final TOC concentration (TOC_Final) is observed, leading to the development of a linear model capable of predicting TOC_Final based on TOC₀ and ${\mathrm{p}\mathrm{H}}_{\mathrm{F}\mathrm{i}\mathrm{n}\mathrm{a}\mathrm{l}}$ within the experimental space. The latter finding facilitates online monitoring of the process progress. Full article

The textile industry releases effluents containing toxic contaminants such as azo dyes, which severely affect water quality and aquatic ecosystems. This study optimized the Fe⁰/H₂O₂/UV photo-Fenton process through Response Surface Methodology (RSM) using a Box–Behnken design applied to real textile wastewater. The process relies on in situ hydroxyl radicals (•OH) generation, which degrades refractory organic compounds. Under optimal conditions (pH 3.5, 0.5 g Fe⁰, and 0.55 mL H₂O₂), the system achieved complete color removal, 91% aromatic structures degradation, and an 80% COD reduction within 3 h. Statistical validation indicated an excellent model fit (R² = 1.0; Q² = 1.0), with strong correlation between experimental and predicted results. Spectroscopic analyses (UV–Vis and FTIR) further confirmed the cleavage of chromophoric and aromatic structures, indicating efficient pollutant degradation. Overall, the findings indicate that the Fe⁰/H₂O₂/UV system is an effective and sustainable technology for treating textile wastewater, offering strong potential for industrial-scale application. Full article

Water pollution caused by synthetic dyes is a major environmental concern due to their stability, toxicity, and resistance to conventional wastewater treatments. This study presents a sustainable approach for synthesizing zinc oxide (ZnO) nanoparticles using artichoke biomass (waste) as a green precursor and enhancing their visible light photocatalytic activity through phosphorus doping. ZnO nanoparticles were successfully synthesized via a simple green route and doped with 3–6% phosphorus using NH₄H₂PO₄. The structural, morphological, and optical properties of the resulting P-ZnO were characterized by XRD, SEM/EDX, TEM, FTIR, and UV-Vis spectroscopy. (6 wt%) Phosphorus doping effectively reduced the band gap from 3.06 eV to 2.95 eV, extended light absorption into the visible range, and improved electron–hole separation, resulting in enhanced photocatalytic performance. The P-ZnO nanoparticles were evaluated for methylene blue (MB) degradation under visible light in a photo-Fenton-like process, with H₂O₂ as an oxidant. The degradation efficiency reached 87.05% with 6% P-ZnO and further increased to 92.35% upon addition of H₂O₂. Durability and reusability tests demonstrated that the 6% P-ZnO catalyst maintained its activity and structural integrity over four consecutive cycles, indicating negligible loss of efficiency and excellent resistance to surface poisoning. The photocatalytic activity was strongly impacted by the quantity of catalyst, solution pH, and initial dye levels, with optimal performance at 0.3 g/L catalyst loading, pH 3, and lower MB concentrations. Full article