Search Results (415)

Photocatalysis is considered to be a very promising method for the degradation of organic matter, because its process of degrading organic matter is safe. However, some problems such as weak absorption of visible light and electronic-hole recombination easily are obviously drawbacks. In this paper, three different morphologies of Bi₅O₇I (nanoball, nanosheet, and nanotube) were successfully prepared by solvothermal method, which was used for the degradation of Rhodamine B (RhB). Comparing the photocatalytic effect of three different morphologies and concluding that the optimal morphology was the Bi₅O₇I nanoball (97.8% RhB degradation within 100 min), which was analysed by the characterisation tests. Free radical trapping experiments were tested, which revealed that the main roles in the degradation process were singlet oxygen (¹O₂) and holes (h⁺). The degradation pathways of RhB were analyzed in detail. The photo/electrochemical parts of the three materials were analysed and explained the degradation mechanism of RhB degradation. This investigate provides a very valuable guide for the development of multiple morphologies of bismuth-based photocatalysts for removing organic dyes in aquatic environment. Full article

In this study, the BPTCD/g-C₃N₄ heterojunction photocatalyst was successfully prepared by the hydrothermal method. BPTCD (3,3′,4,4′-benzophenone tetracarboxylic dianhydride) is immobilised on the surface of g-C₃N₄ by non-covalent π-π stacking. The BPTCD/g-C₃N₄ heterojunction photocatalyst is an all-organic photocatalyst with significantly improved photocatalytic performance compared with g-C₃N₄. BPTCD/g-C₃N₄-60% was able to effectively degrade MO solution (10 mg/L) to 99.9% and 82.8% in 60 min under full spectrum and visible light. The TOC measurement results indicate that MO can ultimately be decomposed into H₂O and CO₂ through photocatalytic action. The photodegradation of methyl orange by BPTCD/g-C₃N₄ composite materials under sunlight is mainly attributed to the successful construction of the heterojunction structure and its excellent π-π stacking effect. Superoxide radicals (^•O₂⁻) were found to be the main active species, while ^•OH and h⁺ played a secondary role. The synthesised BPTCD/g-C₃N₄ also showed excellent stability in the activity of photodegradation of MO in wastewater, with the performance remaining above 90% after three cycles. The mechanism of the photocatalytic removal of MO dyes was also investigated by the trap agent experiments. Additionally, BPTCD/g-C₃N₄-60% demonstrated exceptional photodegradation performance in the degradation of methylene blue (MB). BPTCD/g-C₃N₄ heterojunctions have great potential to degrade organic pollutants in wastewater under solar irradiation conditions. Full article

Retinoids are used in cosmetics as anti-aging ingredients, along with other substances. However, due to limitations in use (such as photodegradation), it seems necessary to look for retinoid alternatives to be applied in cosmetic products. Bakuchiol, a natural alternative of retinoids, isolated from Psolarea corylifolia, is one such compound. It has great cosmetic potential and its mechanism of action is not yet fully explored. From the point of view of the bioactive compound, it is also essential to develop a method for rapid quality control of cosmetic preparations containing bakuchiol. The aim of this study was to apply and compare methods for the quantification of bakuchiol in cosmetic products using UV-Vis, ¹H qNMR, and HPLC. The results show the possibility of using the ¹H NMR method in the routine quality control of cosmetics with bakuchiol because of its comparable results with HPLC analysis and significantly shorter analysis time. Full article

This study aims to evaluate the potential of Lemna minor (common duckweed) for the removal of galaxolide (HHCB) from polluted water, a compound commonly used in consumer products such as perfumes and detergents. The focus was to identify the optimal conditions for removal, determine the removal efficiency, and elucidate the mechanisms involved. The experiment was conducted by cultivating Lemna minor using as a cultivation medium synthetic sewage and laboratory solutions (MilliQ water) containing galaxolide at two levels of concentration (1034 µg·L⁻¹ and 2326 µg·L⁻¹). The plants were exposed to light for 16 h a day and grown at pH 5. Removal efficiency was assessed through liquid chromatography (HPLC) with fluorescence detection (FLD). Kinetics of observed process was modelled using a pseudo-first-order equation. The study of the HHCB decay mechanism included determining the contributions to the final effect of the following processes occurring simultaneously: sorption on the plant surface, photodegradation, and uptake by Lemna. The removal efficiency (RE%) of galaxolide by Lemna minor was 99.7% when aqueous standard solution was used as the cultivation medium after 14 days, and between 97.8% and 98.6% in the case of wastewater samples. Sorption onto plants surface, photodegradation, and uptake by the plants were identified as the primary mechanisms for HHCB removal. Toxicity studies revealed that galaxolide exposure adversely affected Lemna minor growth, altering photosynthetic pigments (chlorophyll and carotenoid) levels. Full article

The use of semiconductors for photocatalytic degradation of organic pollutants has garnered considerable attention as a promising solution to environmental challenges. Compared to TiO₂, BiPO₄ exhibits superior photocatalytic activity. However, its large band gap restricts its light absorption to the UV region. One effective technique for extending BiPO₄’s absorption wavelength into the visible spectrum is the construction of the heterostructure. This study aimed to synthesize monodisperse BiPO₄ nanorods via a solvothermal approach and fabricate BiPO₄/g-C₃N₄ heterojunctions with varying loadings through in situ deposition. Tetracyclines were employed as the target pollutant to evaluate the photocatalytic performance and stability of the prepared materials. The results indicated that 5 wt% of composite exhibited better photocatalytic performance than single catalysts, which showed the highest photodegradation efficiency of approximately 98% for tetracyclines. The prepared bi-photocatalyst presented favorable stability under sunlight irradiation, the photocatalytic activity of which remained almost unchanged after four cycles. The enhanced photocatalytic activity was attributed to the synergistic effect. Additionally, the possible degradation mechanism was elucidated utilizing the semiconductor energy band theory. Overall, this work presents new perspectives on synthesizing innovative and efficient visible-light-driven photocatalysts. It also offers a mechanistic analysis approach by integrating theoretical calculations with experimental observations. Full article

Polyethersulfone (PES) membranes are essential in separation processes; however, their inherent hydrophobicity can limit their effectiveness in water-intensive applications. This study aims to enhance PES membranes by modifying them with a NiFe₂O₄–nanoclay composite nanoparticle to improve both their hydrophilicity and photocatalytic potential as a photocatalytic membrane. The nanoparticles were synthesized using the sol–gel auto-combustion method and incorporated into PES membranes through mixed-matrix embedding (1 wt% and 3 wt%) and surface coating. X-ray diffraction confirmed the cubic spinel structure of the composite nanoparticles, which followed the second order kinetic reaction during the photodegradation–adsorption of crystal violet. The mixed-matrix membranes displayed a remarkable 170% increase in water flux and a 25% improvement in mechanical strength, accompanied by a slight decrease in contact angle at 1 wt% of nanoparticle loading. In contrast, the surface-coated membranes demonstrated a significant reduction in contact angle to 18°, indicating a highly hydrophilic surface and increased roughness. All membranes achieved high dye removal rates of 98–99%, but only the coated membrane system exhibited approximately 50% photocatalytic degradation, following mixed kinetics. These results highlight the critical importance of surface modification in advancing PES membranes, as it significantly reduces fouling and enhances water–material interaction qualities essential for future filtration and photocatalytic applications. Exploring hybrid strategies that combine both embedding and coating approaches may yield even greater synergies in membrane functionality. Full article

Graphitic carbon nitride (g-C₃N₄) is emerging as one of the most promising non-metallic semiconductors for the degradation of pollutants in water by photocatalytic processes. Its exceptional reduction–oxidation (redox) potentials and adequate band gap of approximately 2.7 eV give it the ability to absorb in the visible light range. However, the characteristic sensitivity to light absorption is limited, leading to rapid recombination of electron–hole pairs. Therefore, different strategies have been explored to optimize this charge separation, among which the formation of heterostructures based on g-C₃N₄ is highlighted. This review addresses recent advances in photocatalysis mediated by g-C₃N₄ heterostructures, considering the synthesis methods enabling the optimization of the morphology and active interface of these materials. Next, the mechanisms of charge transfer are discussed in detail, with special emphasis on type II, type S, and type Z classifications and their influence on the efficiency of photodegradation. Subsequently, the progress in the application of these photocatalysts for the degradation of water pollutants, such as toxic organic dyes, pharmaceutical pollutants, pesticides, and per- and polyfluoroalkyl substances (PFAS), are analyzed, highlighting both experimental advances and remaining challenges. Finally, future perspectives oriented towards the optimization of heterostructures, the efficiency of synthesis methods, and the practical application of these in photocatalytic processes for environmental remediation. Full article

This article focuses on the possibility of using biodegradable polymer-composite materials in additive manufacturing via fused deposition modelling (FDM) 3D printing. The main objective was to experimentally verify the technical feasibility of the repeated use of recycled PLA and PLA composites containing 10% natural coffee-ground (CG) filler in a print–degradation–recycling–print cycle. Special attention was paid to simulated ultraviolet radiation as a degradation factor affecting the materials’ mechanical properties. Pure PLA and PLA_CG were compared at four levels of degradation time and after subsequent recycling. The results show that the inclusion of coffee-ground filler slightly reduces the initial strength but enhances the 3D-printed material’s resistance to UV degradation and thus extends its functional service life. Unlike pure PLA, which loses its processability after 12 weeks, PLA_CG retains structural integrity and mechanical functionality. The research confirms the potential of recycled PLA composites with natural fillers for sustainable manufacturing and supports their use within a circular economy framework. Full article

In this study, AgI/Ag₃PO₄/WO₃ ternary composite photocatalysts with dual Z-scheme heterojunction were fabricated via the in situ loading of Ag₃PO₄ onto WO₃ followed by anion exchange. Compared to single photocatalysts and binary composites, the AgI/Ag₃PO₄/WO₃ composites exhibited enhanced photocatalytic activity in the photodegradation of chlortetracycline hydrochloride (CTC) under visible-light irradiation. Notably, the AAW-40 photocatalyst, which contained an AgI/Ag₃PO₄ molar ratio of 40%, degraded 75.7% of the CTC within 75 min. Moreover, AAW-40 demonstrated an excellent performance in the cyclic degradation of CTC over four cyclic degradation experiments. The separation and transfer kinetics of the AgI/Ag₃PO₄/WO₃ composite were investigated with photoluminescence spectroscopy, time-resolved photoluminescence spectroscopy, and electrochemical measurements. The improved photocatalytic performance was primarily due to the creation of a silver-bridged dual Z-scheme heterojunction, which facilitated the efficient separation of photoinduced electron–hole pairs, retained the strong reducing capability of electrons in AgI, and ensured the strongly oxidizing nature of the photoexcited holes in WO₃. The dual Z-scheme charge-transfer mechanism was further validated using in situ X-ray photoelectron spectroscopy. This study provides a foundation for developing innovative dual Z-scheme photocatalytic systems aimed at the efficient degradation of antibiotics in wastewater. Full article

Levofloxacin is an antibiotic classified as an emerging contaminant. Its presence in aquatic environments represents potential risks to ecosystems and human health, making its removal during wastewater treatment of relevant importance. Here, we present a comprehensive kinetic analysis of levofloxacin photodegradation under UVB solar irradiation, with emphasis on the influence of pH and dissolved oxygen, two conditions that can vary widely in wastewater and impact treatment efficiency. We also investigated the formation and role of reactive oxygen species in the degradation mechanism, as well as the cytotoxicity and antibacterial activity of photoproducts. Our findings reveal that the efficiency of levofloxacin photodegradation is highly dependent on environmental conditions; it requires neutral or slightly alkaline pH and a high concentration of dissolved oxygen, a situation not always observed in contaminated waters. Several reactive oxygen species are generated, with singlet oxygen being the most reactive with the antibiotic. We report for the first time the singlet oxygen quantum yield from levofloxacin. Bioassays demonstrated that photoproducts neither exhibit antibacterial activity nor induce significant cytotoxicity. Our study suggests that UVB treatment of contaminated effluent containing levofloxacin could be an effective and environmentally safe strategy for the antibiotic degradation under certain conditions of pH and dissolved oxygen. Full article

Durable polyamidoamine (PAA) coatings were covalently grafted onto cotton by applying a water-soluble, glycine-based PAA (M-GLY) through a radical polymerization mechanism. M-GLY oligomers of different chain lengths, terminated with bisacrylamide groups, were synthesized via polyaddition of N,N′-methylenebisacrylamide and glycine at molar ratios of 1:0.9, 1:0.85, and 1:0.8. Cotton strips were then impregnated with differently concentrated (10 and 20 wt.%) aqueous solutions of the M-GLY oligomers in the presence of potassium persulfate, which oxidized cellulose and generated radicals that initiated polymerization of the M-GLY terminals, thereby enabling covalent grafting onto cotton. This process yielded M-GLY-grafted cotton (COT-g-M-GLY) with 2–15% add-on levels. Scanning electron microscopy revealed uniform surface coverage and penetration of the coating into fiber interiors. Grafting did not alter cellulose crystallinity—65% vs. 64% for grafted and virgin cotton. However, thermogravimetric analysis showed that COT-g-M-GLY exhibited lower thermo-oxidative stability than M-GLY-adsorbed cotton (COT/M-GLY) at similar add-ons. Flame-retardancy tests indicated that COT-g-M-GLY reduced the burning rate (by 10% to 30%) but did not achieve self-extinguishing behavior, unlike COT/M-GLY. Despite this, COT-g-M-GLY provided good protection against UV-induced photodegradation. After accelerated UVA–UVB exposure, cotton samples with 10% M-GLY add-on showed a significantly reduced yellowing rate compared to untreated cotton, as confirmed by spectrophotometric analysis. Full article

ZnO/WO₃ coatings were synthesized by the plasma electrolytic oxidation of zinc in an alkaline phosphate electrolyte (supporting electrolyte, SE) with the addition of WO₃ particles or tungstosilicic acid (WSiA, H₄SiW₁₂O₄₀) at concentrations of up to 1.0 g/L. These coatings were intended for the decomposition of methyl orange (MO) through photocatalysis. The morphology, chemical composition, crystal structure and absorption properties of the coatings were investigated using scanning electron microscopy, energy dispersive X-ray spectroscopy, wavelength-dispersive X-ray spectroscopy, X-ray diffraction, photoelectron spectroscopy and diffuse reflectance spectroscopy. Under artificial sunlight, the PA of the coatings was investigated using MO decomposition. The photocatalytic activity (PA) of the ZnO/WO₃ coatings was higher than that of the ZnO obtained in SE. The decrease in the recombination rate of photo-generated electron/hole pairs due to the coupling of ZnO and WO₃ is related to the increased PA. The PA for ZnO and the most photocatalytically active ZnO/WO₃ was around 72% and 96%, respectively, after 8 h of irradiation. A mechanism for MO photo-degradation by the ZnO/WO₃ photocatalyst was also proposed. Full article

Photochemical degradation is a major removal pathway for pharmaceutical pollutants in water, and dissolved organic matter (DOM) in water is an important factor affecting this process. This study investigates the differential effects of seasonally-varied dissolved organic matter (DOM) from Songhua River and Liao River on the photodegradation of pharmaceutical pollutants, using levofloxacin (LFX), sulfamethoxazole (SMZ), and ibuprofen (IBP) as target compounds. The results demonstrated that summer and autumn DOM inhibited the photodegradation of LFX and SMZ through light screening and dynamic quenching effects, with inhibition rates of 35.1% and 55.5%, respectively, whereas winter DOM enhanced degradation through photo-oxidation mechanisms. DOM from Songhua River and Liao River significantly promoted the photodegradation of IBP. Quenching experiments showed differences in the contributions of photochemically reactive intermediates (PPRIs) to the photodegradation of different target pollutants, with hydroxyl radicals (•OH) dominating LFX photodegradation (48.79% contribution), excited triplet states of DOM (³DOM*) dominating SMZ photodegradation (85.20% contribution), and singlet oxygen (¹O₂) dominating IBP photodegradation (79.89% contribution). The photodegradation pathways were elucidated by measuring the photodegradation by-products of the target pollutants: LFX mainly underwent piperazine ring cleavage and oxidative decarboxylation, SMZ underwent isoxazole ring opening and deamination during photodegradation, and IBP underwent photodecarboxylation and oxidation reactions. Under the influence of the DOM from the Songhua River and Liao River, the generation of multiple photodegradation by-products led to an increasing trend in the acute toxicity of target pollutants to luminescent bacteria. This investigation elucidates the dual regulatory mechanisms of natural aquatic DOM on both photo-induced degradation pathways and toxicity evolution dynamics of pharmaceutical contaminants, which is of great significance for understanding the photochemical transformation behavior and risk assessment of pharmaceutical pollutants in aquatic environments. Full article

TiO₂ mesoporous supports were obtained by the sol–gel method from different precursors (titaniumethoxide, isopropoxide, or butoxide) in the presence of nonionic, cationic, and anionic surfactants. Among these samples, those obtained from Ti isopropoxide, Brij58 w/o activated carbon (AC), were selected as supports. Photocatalysts were obtained by modifying these supports with Ag, Fe, and AgFe (each metal around 1% mass). The characterization results showed a stronger influence of titania precursors, surfactants, and AC on the texture and an insignificant effect on the crystalline structure and morphology of the obtained materials. X-ray photoelectron spectroscopy revealed the effects of AC and Fe on the Ag⁰ concentration and of Ag on Fe-reduced species. Based on this information, the results obtained by H₂-TPR, UV–Vis, Raman, and photoluminescence spectroscopy were explained. The performance of the photocatalysts was evaluated in the degradation of Congo Red (CR) and Crystal Violet (CV) dyes under UV and visible light. The Ag-TiO₂ sample exhibited the best activity in degrading CR at acidic pH and in degrading CV under basic conditions. In visible light, we observed the significant effects of the surface plasmon resonance, AC, Ag, and Fe on the activity in CR photodegradation. The proposed kinetics and mechanisms complete the study of the reactions. Full article

Water pollution by persistent organic and inorganic contaminants constitutes a significant problem for ecosystems and public health. Organic substances such as dyes, pharmaceutical residues, pesticides, and phenolic compounds are increasingly detected in water due to industrial and agricultural activities. Alongside these, toxic heavy metals contribute to the complexity of water treatment challenges. Conventional remediation methods often fall short due to high operational costs or limited efficiency. In this context, photocatalysis has emerged as a promising approach for pollutant degradation in water under light irradiation. In this sense, covalent organic frameworks (COFs), a class of porous, crystalline materials formed by the covalent linkage of organic units, offer great advantages as photocatalysts. Their tunable electronic properties, structural diversity, and high stability under aqueous conditions make them ideal for visible light-driven processes. This review explores the structural features that govern the photocatalytic activity of COFs, including conjugation, bandgap modulation, and donor–acceptor structures. Mechanistic insights into photocatalytic degradation are also discussed. Finally, examples of pre-designed COFs are presented with their application in the photodegradation of water pollutants, and their main reactive oxygen species (ROS) involved in the photodegradation mechanism. Overall, this review aims to provide a foundation for the rational design of COFs in advanced water treatment technologies. Full article