Search Results (2,754)

Water pollution caused by antibiotics is a growing problem. Therefore, photodegradation by efficient catalysts is an environmentally friendly technology that can effectively degrade organic pollutants in water. In this work, a method was innovatively used to prepare a ternary heterostructure of plasmon-enhanced Ag-CuO/TiO₂. The composite was synthesized through a facile stepwise strategy involving the formation of CuO nanorods, TiO₂ coating, and subsequent deposition of Ag nanoparticles on their surface using AgNO₃, enabling intimate interfacial contact among the different components. The prepared samples were characterized by XRD, HRTEM, XPS, and UV-Vis. The chemical composition of the composite Ag-CuO/TiO₂ showed a Cu/Ti atomic ratio of 2.58, as well as a Ag/Cu ratio of 0.91. The UV-Vis spectrum reveals the largest absorption peak at 550 nm for the composite Ag-CuO/TiO₂. The prepared Ag-CuO/TiO₂ composites were applied to the visible-light degradation of tetracycline hydrochloride, with the photocatalytic degradation rate reaching 80.7% under the optimal conditions within 60 min, which is significantly better than CuO and CuO/TiO₂ without silver nanoparticles. Capture experiments indicated that h⁺ are involved during the course of the photodegradation and that h⁺ are the main active substances. Furthermore, the proposed mechanism for the photodegradation of the Ag-CuO/TiO₂ composites is given. It has potential applications in the treatment of organic pollutants in water. Full article

With the growing severity of water pollution, conventional treatment technologies are increasingly unable to satisfy the demand for deep purification. Catalytic wastewater treatment has emerged as an effective strategy for degrading refractory pollutants because of its high efficiency, mild operating conditions, and environmentally friendly nature. This review systematically summarizes recent progress in catalytic materials for wastewater treatment, covering four major categories: metal-based materials, carbon-based materials, multicomponent composites, and photo/electrocatalytic systems. Particular attention is given to their design strategies, structural characteristics, and performance advantages. On this basis, the full mechanistic chain is discussed, from interfacial adsorption and activation to reactive-species generation, including both radical and non-radical pathways, intermediate transformation, and macroscopic reaction kinetics. The review also highlights representative applications in practical wastewater streams, including textile dyeing and pharmaceutical, chemical, landfill leachate, and municipal tailwater treatment, thereby demonstrating the engineering potential of catalytic technologies. At the same time, several critical challenges remain, including insufficient long-term material stability, incomplete mechanistic understanding in complex water matrices, limited adaptability to real wastewater, and the high cost of large-scale preparation. Future research should therefore focus on the development of highly stable, low-cost, and interference-resistant catalytic materials, deeper mechanistic elucidation through in situ characterization and theoretical calculations, stronger integration with membrane separation, biological treatment, photovoltaic or electrochemical processes, and the establishment of standardized evaluation protocols and life-cycle assessment frameworks. These efforts will accelerate the transition of catalytic wastewater treatment toward greener, smarter, and more practical engineering applications. Full article

A three-year (January 2020–December 2022) daily dataset of 16 polycyclic aromatic hydrocarbons (PAHs) collected in parallel with PM_2.5 and a suite of meteorological variables at a coastal Mediterranean urban site in southern Italy (Pomigliano d’Arco, Campania) is presented and analysed. Raw PAH time series were decomposed into a long-term trend component (LT), a seasonal component (ST), and a residual component (RT) using an iterative missing-value-robust Kolmogorov–Zurbenko (KZ) moving-average filter. Spearman rank correlations between PAH concentrations and four meteorological predictors (mean temperature, relative humidity, mean wind speed, and maximum wind speed) were computed for each congener. Diagnostic molecular ratios—Fla/(Fla + Pyr), BaP/BghiP, Indeno[1,2,3-cd]pyrene/(IcdP + BghiP), and BaA/(BaA + Chr)—were evaluated seasonally and interpreted jointly with an information-theoretic Bayesian mixture modelling procedure (SNOB/MML) and with the documented susceptibility of some PAH ratios, especially BaP-containing ratios, to atmospheric ageing, phase repartitioning and summer photodegradation. Total PAH concentrations (sum of 16 congeners) ranged from <1 ng m⁻³ in summer to 46 ng m⁻³ during winter high-pollution episodes, with BaP peaking at ≈6.7 ng m⁻³. Because BaP was measured in the PM_2.5 fraction, comparisons with the EU annual target value of 1 ng m⁻³ established for PM₁₀-bound BaP are treated as indicative context only, not as formal compliance statements. Pronounced seasonal variability was driven primarily by residential heating emissions, and the incremental lifetime cancer risk (ILCR) for inhalation exposure reached $1.03\times {10}^{-4}$ (95% CI: $0.88$–$1.20\times {10}^{-4}$) during the heating season under a continuous outdoor-exposure worst-case scenario. The absolute ILCR magnitude is conditional on the selected TEF scheme and on the adopted BaP unit-risk coefficient; under an additional indoor-dominated scenario (16 h day⁻¹, infiltration factor 0.6), the corresponding risk remained above the conventional ${10}^{-6}$ benchmark. An anomalous near-background PAH signal during spring 2020 is attributed to the COVID-19 national lockdown, which reduced total PAH concentrations by approximately 85% relative to the seasonal component predicted by the iterative moving-average filter for the same calendar window. Source apportionment via diagnostic ratios identifies residential/biomass combustion as the dominant cold-season source and vehicular emissions as the prevailing warm-season source. These results provide a novel characterisation of PAH pollution dynamics in the undersampled southern Mediterranean and provide evidence to support targeted abatement policies. Full article

In this research work, Ag-doped and undoped TiO₂ nanocomposites were prepared through a sol–gel method, using diethanolamine as a solvent. From the evolution of various characterized techniques (XRD, FT-IR, SEM and TGA analysis), it was found that Ag-TiO₂ nanocomposites have a mixture of rutile and anatase phases of titania. The catalytic performance of the Ag-TiO₂ nanocomposites was evaluated for Eriochrome Black T (EBT) photodegradation. To determine the photocatalytic efficiency of the nanocomposites, different factors including pH (2–12), catalytic dose (2–12 mg), reaction time (0–180 min) and concentration (2–10 mg/L) were investigated. The calcined Ag-TiO₂ showed high degradation (94%) for EBT at a low pH for 0.01 g of catalyst using 10 mg/L of dye solution. The kinetic study revealed that the photocatalytic degradation process obeys pseudo second-order kinetics. To investigate antibacterial effects, different bacteria such as Enterococcous, Staph Avrius, serritia and Escherichia E. coli were utilized. A total of 200 mg of calcined Ag-TiO₂ nanocomposite showed optimum activities against bacterial strains. Full article

Surface-enhanced Raman scattering (SERS) offers exceptional sensitivity for trace contaminant detection; conventional noble-metal substrates suffer from high cost, signal irreproducibility, and poor chemical stability. While semiconductor alternatives are promising, their performance is fundamentally limited by sluggish interfacial charge-transfer kinetics under static band alignment. To overcome these limitations, we introduced a new strategy centred on a high carrier generation rate (HCGR). By integrating TiOPc, a material that exhibits strong Ti–O bond polarisation and a high HCGR, with atomically thin MoS₂, we constructed a hybrid platform that drives efficient charge transfer via HCGR-enabled kinetic pumping, surpassing traditional thermodynamic band engineering. This HCGR-driven efficient CT mechanism primarily amplifies SERS through enhanced chemical mechanisms (CM) with minor electromagnetic contributions, achieving an enhancement factor (EF) of 10⁷. The platform can detect methylene blue (MB) and rhodamine 6G (R6G) at concentrations as low as 10⁻¹⁴ M and 10⁻¹³ M, respectively, demonstrating excellent repeatability (RSD = 7.2%) and stability over 60 days. Additionally, efficient CT accelerated MB photodegradation under UV light, achieving complete decomposition within 80 min. The practical applicability of the platform is evidenced by detecting Hg²⁺ (LOD: 10⁻¹¹ M) and malachite green in tap/lake water (LODs: 10⁻¹² M/10⁻¹⁰ M). This work establishes HCGR-driven efficient CT as the next generation of semiconductor SERS platforms. It provides a scalable route toward low-cost, reusable sensors for real-time, in situ monitoring of industrial effluents and the dynamic pollutant degradation of pollutants in environmental monitoring. Full article

The increasing use of recycled polypropylene (rPP) in technical and outdoor applications requires strategies to limit photo-oxidative degradation while maintaining adequate performance after reprocessing. In this work, the photo-oxidative stability of rPP films was investigated under accelerated weathering conditions, focusing on the effect of a commercially available additive, Nexamite^® R201 (NEX), previously shown to partially restore PP molecular weight after reprocessing. Films of rPP and rPP containing 5 wt.% NEX were produced by cast extrusion and exposed to cyclic UVA irradiation and water condensation in a QUV chamber, and the evolution of the functional and structural degradation of the materials was monitored as a function of aging time. Spectroscopical analyses showed progressive oxidation in both systems, with carbonyl growth starting after an induction period of about 200 h. A faster increase in the carbonyl index was observed for rPP containing NEX, indicating that the additive does not improve chemical oxidative resistance under the adopted conditions. However, NEX significantly enhanced the retention of mechanical properties during aging, with higher elongation and stress at break compared with unmodified rPP, thus delaying embrittlement. Overall, the results show that the investigated additive effectively mitigates the loss of mechanical integrity during photo-aging, likely as a consequence of the macromolecular restructuring induced during reprocessing. Full article

Three types of graphene–single crystal titanium dioxide composite (GR–TiO₂SCs) were prepared using the hydrothermal method, employing TiF₄ and graphite as raw materials with hydrofluoric acid serving as the morphology-directing agent. The phase composition and morphological features of the resultant composites were systematically characterized by X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy and X-ray diffraction. These complementary characterization results clearly demonstrate that graphene and TiO₂ single crystals have been successfully hybridized to form a well-defined heterostructure, rather than a simple physical mixture. Photocatalytic performances were evaluated by monitoring the photodegradation behaviors of methylene blue, rhodamine B, and methyl orange solutions under simulated light irradiation, with real-time concentration variations recorded by UV–visible absorption spectroscopy. The composite sample in which TiO₂SCs were in situ grown and uniformly anchored onto graphene oxide substrates effectively suppressed the self-stacking and agglomeration of individual crystallites, thus delivering the best photocatalytic response. Increased exposure of the active catalytic interfaces of TiO₂SCs was found to play a key role in elevating the overall photocatalytic activity. The hierarchical assembly protocol developed in this work provides a feasible pathway for the rational design of functional composites with controllable microstructures and tailored properties, which can be further extended to the development of advanced sensing materials. Full article

Currently, the search continues for solutions for the treatment of water contaminated by toxic compounds such as chlorophenols that are used in the manufacture of pesticides, insecticides, and the paper industry, among others, and that are considered persistent in the environment, in addition to being extremely toxic, especially 2,4,6-trichlorophenol, which is potentially carcinogenic. In this work, the use of thermally activated Co/Fe hydrotalcites as photocatalysts is presented. The catalysts were characterized by differential thermal and thermogravimetric analysis, X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, N₂ physisorption, diffuse reflectance spectroscopy and photoluminescence. The catalysts were tested in the photo-assisted degradation of 80 mg/L of 2,4,6-trichlorophenol. The catalytic structures present are Co/Fe simple and mixed oxides. The results of the photocatalytic activity show that the materials have good photocatalytic activity with a degradation efficiency of 2,4,6-trichlorophenol, reaching a maximum capacity of 65% for oxides derived from hydrotalcites with a Co/Fe ratio of 2 and calcined at 500 °C, exceeding the activity shown by the reference catalyst, high-performance commercial titanium dioxide. The photocatalytic activity studied for the catalyst with the highest percentage of degradation is attributed to the presence of holes, as well as to the formation of oxidizing species such as superoxide and hydroxyl radicals that are determinants in the degradation mechanism. Full article

Ageing radically alters the physicochemical properties of microplastics, significantly increasing their affinity for environmental pollutants. However, the slow nature of natural degradation necessitates the development of efficient laboratory protocols. This study establishes an accelerated ageing methodology that reflects natural dynamics by comparing Polyethene terephthalate microplastics (PET MPs) exposed to sunlight (3 months) with those exposed to laboratory UV-C radiation (varying lamp numbers and 24–336 h). scanning electron microscopy (SEM) imaging confirmed progressive surface degradation, including increased roughness, micro-cavities, and erosion. Photo-oxidation was evidenced by an increase in the carbonyl index (CI) from 7.43 ± 0.30 to 8.97 ± 0.35 (UV-aged) and 11.45 ± 0.45 (sun-aged). Furthermore, crystallinity significantly decreased from 59.5% to 54.4% and 16.6%, respectively, while the point of zero charge (pH_PZC) shifted from near neutral (6.5–7.0) to below 2.0. Notably, high-intensity, short-term UV-C exposure accelerated surface functionalization, enhancing cadmium adsorption capacity (q_e = 1.9 mg/g). The laboratory protocol provides rapid reactivation on the surface, serving as a proxy for prolonged sunlight exposure. Consequently, these findings offer a framework for assessing heavy metal uptake and the broader environmental implications of microplastics in aquatic environments. This understanding supports pollutant evaluation and sustainable water management for aquatic ecosystem protection. Full article

The pharmaceutical industry is a major source of pollution in wastewater effluents, characterized by chemical residues that are complex and difficult to degrade. Naproxen, a commonly detected drug in sewage effluents, exceeds safe concentrations for aquifers and is highly persistent, posing significant risks to aquatic life and ecosystems. This drug is known to cause long-term side effects in humans, such as gastrointestinal ulcers and nephrosis, associated with frequent and prolonged use. Additionally, the recent pandemic has led to a marked increase in drug consumption over a short period, exacerbating environmental contamination. Titanium dioxide has been extensively used as a photocatalyst in recent decades, proving effective in reducing these emerging pollutants. In this study, TiO₂ doped with cerium was synthesized using the sol–gel method, with cerium concentrations varied at 1, 3, 5, and 10% by weight. The resulting nanocatalysts were characterized through nitrogen physisorption, scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV-Vis diffuse reflectance spectroscopy. Photocatalytic activity was assessed using a UV-Vis spectrophotometer to monitor the degradation of the drugs. XRD analysis confirmed the crystallinity and anatase phase of TiO₂. UV-Vis diffuse reflectance spectra indicated a decrease in bandgap energy of up to 3.00 eV compared to pure TiO₂. The materials demonstrated significant degradation of naproxen (NPX) and acetaminophen (ACTP), both prepared at 30 ppm, over a 6 h reaction period. Full article

Wood coatings play a critical role in protecting wood substrates from environmental degradation, particularly ultraviolet (UV)-induced photodegradation. This review comprehensively examines the mechanisms of wood coating photodegradation, the factors influencing their durability, and current anti-aging strategies. Photodegradation arises from polymer chain scission, chemical structure reorganization, and photo-oxidation of lignin and cellulose, leading to coating chalking, cracking, gloss loss, and color changes, ultimately compromising wood mechanical properties and service life. Key anti-aging strategies include UV absorbers, which convert harmful UV radiation into heat; hindered amine light stabilizers (HALSs) that capture free radicals and quench excited-state molecules; barrier and shielding materials that form dense physical or nanostructured networks to block UV penetration and enhance mechanical and water resistance; and antioxidants that neutralize free radicals or decompose peroxides at the molecular level. Each approach can be employed individually or synergistically to enhance coating durability. Challenges remain in achieving long-term outdoor stability, balancing transparency and UV shielding, optimizing nanoparticle dispersion, and maintaining the activity of natural antioxidants. Future research should focus on multifunctional composite coatings integrating bio-based materials and nanotechnology, smart responsive systems, adaptive protection mechanisms, and standardized long-term evaluation protocols. These advancements will facilitate the development of high-performance, sustainable wood coatings and promote the value-added utilization of wood resources. Full article

UVA exposure elicits immediate and persistent pigment darkening of the skin, which is thought to result from the oxidation and polymerization of existing melanin and/or precursors. Melanocytes produce eumelanin and pheomelanin. Eumelanin consists of 5,6-dihydroxyindole (DHI) and 5,6-dihydroxyindole-2-carboxylic acid (DHICA), while pheomelanin consists of benzothiazine and benzothiazole units. Melanins can be analyzed by quantifying specific degradation products using HPLC. Specifically, eumelanin can be analyzed as pyrrole-2,3,5-tricarboxylic acid (PTCA) and pyrrole-2,3-dicarboxylic acid (PDCA), specific degradation products of DHICA and DHI, respectively. Benzothiazole pheomelanin can be analyzed as thiazole-2,4,5-tricarboxylic acid (TTCA), whereas benzothiazine pheomelanin is analyzed as 4-amino-3-hydroxyphenylalanine (4-AHP) and 3-amino-4-hydroxyphenylalanine (3-AHP). Upon UVA exposure, melanins undergo structural modifications. Eumelanin undergoes oxidative cleavage to free pyrrole-2,3,5-tricarboxylic acid (Free PTCA) and undergoes cross-linking to form pyrrole-2,3,4,5-tetracarboxylic acid (PTeCA). UVA exposure of pheomelanin induces oxidative conversion from the benzothiazine to the benzothiazole. Nevertheless, these structural modifications have never been previously characterized in human skin. In this study, we exposed ex vivo skin to increasing UVA1 doses (60, 90 and 120 J/cm²; n = 6 in triplicate) and characterized the induced pigment darkening before, immediately, and 2 h after exposure through colorimetry, HPLC and spectrophotometry. The results showed changes in the CIELAB colorimetric parameters, namely a decrease in Luminance L*, the yellow-blue component b* and the Individual Typology Angle (ITA) in UVA1-exposed samples, indicative of skin darkening. In parallel, UVA1 exposure induced significant modifications of the levels of absorbance at 500 nm (A500) and melanin markers PTCA, PTeCA, PDCA, TTCA, and 4-AHP, as well as in the ratios of various markers, such as PTeCA/PTCA, Free/Total PTCA, and TTCA/4-AHP, indicative of photooxidation/degradation of melanins. Our study provides the first evidence of UVA1-induced modifications of melanins associated with pigment darkening occurring in human skin. Full article

The accumulation of aquatic organisms on submerged surfaces causes major economic and environmental impacts in marine ecosystems. Conventional antifouling biocides pose risks due to toxicity to non-target species and bioaccumulation. Nature-inspired compounds such as flavonoids have emerged as more sustainable alternatives. Aiming to assess the environmental impact of new antifouling flavonoids and to evaluate the toxicity of their transformation products, this study investigates the degradation of three promising antifouling flavonoids (chalcone CC345G and dihydrochalcones DH345 and DH345P) in aqueous matrices. Comprehensive abiotic and biotic degradation assays (hydrolysis, photodegradation, and biodegradation) were conducted. Appropriate liquid chromatography with UV detection methods were developed and validated to monitor the studies. The glycosylated chalcones bearing a triazole moiety CC345G revealed no detectable degradation under any of the experimental conditions. In contrast, both dihydrochalcones underwent significant abiotic degradation; DH345 was more susceptible to hydrolysis at pH 7.10 (17.41% degradation), while DH345P was more prone to photolysis in sterilized natural seawater at pH 8.82 (45.82–54.52% degradation), also showing substantial degradation in hydrolysis (24.34–42.41%) and biodegradation (33.43–41.07%). Overall, the prenylated dihydrochalcone DH345P exhibited the highest degradation rate among the tested compounds. Analysis with high-resolution mass spectrometry disclosed several transformation products in degradation assays, and one chemical structure was proposed. Preliminary ecotoxicity assessment performed on the degradation products using Artemia salina indicated low toxicity, suggesting minimal environmental impact. Full article

Piezo-enhanced photocatalysis is progressively considered an eco-friendly technology for contaminant removal, harvesting not only solar energy but also mechanical vibrations found in nature. Multiferroic materials present a coupled effect of various properties and can potentially increase the applicability of this process. In this study, Cr- doped bismuth ferrite thin film was deposited on SrTiO₃ substrate by HiPIMS, and its photo-, piezo-, and piezo-photocatalytic efficiencies in Rhodamine B (RhB) degradation were analyzed. The highest removal percentage was found under the simultaneous exposure of visible light and mechanical vibrations, reaching 86.2% after 180 min. The calculated efficiencies for photo- and piezocatalysis were 12.2% and 83.7%, respectively. The rate constant (k) for piezo-photocatalysis was 16.1 times higher than that found during photocatalytic experiments. To assess the contribution of each reactive species to the decomposition process, different reagents were added to the Rhodamine B contaminated solution. The results revealed that when p-benzoquinone was used, the degradation efficiency declined significantly from 86.2% to 37.6%, suggesting that superoxide radicals (O₂^•−) play a key role in decomposing RhB molecules. The structural, chemical, optical, and ferroelectric changes caused by the catalytic processes were analyzed and linked to the proposed degradation mechanisms. The poor photocatalytic efficiency was linked to an improper band structure and an improper polarization orientation of the ferroelectric domains in the as-deposited film. The degradation mechanisms in piezo-photocatalysis were driven partly by the band bending caused by mechanical vibrations and partly by the reorientation of the induced polarization of the domains in the unstrained film. Full article

Over the past 20 years, the iron-activated persulfate systems have been widely used for removing pharmaceuticals and personal care products (PPCPs) from water. However, slow Fe(III)/Fe(II) redox cycling and precipitation of iron, unless in very acidic conditions, were the main limitations. Thus, two ligand-assisted Fe(III)/persulfate systems, Fe(III)-acetohydroxamic acid (AHA)/peroxydisulfate (PDS) and Fe(III)-nitrilotriacetic acid (NTA)/peroxymonosulfate (PMS), were comparatively investigated for the degradation of atenolol (ATL) in this study. The experimental results showed that the Fe(III)-NTA/PMS system worked much better than the AHA system. However, the cost of PMS is higher than that of PDS, which should be considered. The primary advantage of the NTA system was its ability to overcome the pH limitations. It worked well over a wide pH range (3.0–10.0), whereas the AHA system could only be used in a narrower pH window (pH 2.4 to 6.5). The investigation of radicals that contributed to ATL degradation revealed that sulfate radicals (SO₄^•−) were dominant in the NTA system, while hydroxyl radicals (^•OH) and SO₄^•− were the primary and secondary radicals in the AHA system. These results provided useful insight into the comparative behavior of two ligand-assisted Fe(III)/persulfate systems for ATL degradation, with the Fe(III)-NTA/PMS system showing clear potential under neutral or near-neutral conditions, while Fe(III)-AHA/PDS may still represent a lower-cost option under acidic conditions. Full article