Search Results (512)

Chromophore domains were proposed in a previous work as the mediators of self-healing of optical properties in dye-doped polymers. A statistical mechanical model based on domains matches all observed self-healing dynamics as a function of dye concentration, temperature and light intensity. This suggests that domains are responsible. However, there is no direct observation of domains, nor has their physical morphology been determined. This work reports the first observation of domains in a self-healing polymer using Resonant Soft X-ray Scattering (RSoXS), which gives a domain size in the range of 39.3 Å to 62.8 Å. This range includes the domain model’s prediction of an average domain size of roughly 30 molecules, which is about 56 Å, if the molecules form a loosely packed ball. X-ray scattering of samples of concentration spanning from neat polymer to the saturation limit of Disperse Orange 11 (DO11) dye in poly (methyl methacrylate) (PMMA) polymer shows domains in the expected size scales, with the mode of the effective scattering width varying little with concentration. However, for constant domain shape, the mode peak would decrease in q with increasing concentration, according to the domain model. This work suggests that the domain shape might change with concentration, which warrants further investigations of domain topology and geometry. The important evidence presented in this work is the direct experimental observation of domains, which is central to self-healing models. Full article

The development of materials for the remediation and monitoring of water environments remains a significant challenge in the field of environment and materials science. In this study, a nickel-based coordination polymer, [Ni(L)(H₂O)₃]_n·nH₂O (1), was synthesized employing 4,4′-(1H,1′H-[2,2′-biimidazole]-1,1′-diyl)dibenzoic acid (H₂L). Single-crystal X-ray diffraction analysis showed that L²⁻ ligands connect Ni²⁺ ions into 1D Z-shaped chains via two coordination modes. The chains are further assembled into a 3D supramolecular structure through hydrogen bonding interactions. The photocatalytic test showed that complex 1 could effectively degrade the organic dye methylene blue (MB). Under the conditions of catalyst dosage 5 mg, MB initial concentration 20 ppm and pH 7, the degradation efficiency reached 87.7% within 180 min. In addition, complex 1 can be used for the electrochemical detection of norfloxacin (NOR) by differential pulse voltammetry (DPV), exhibiting a linear response in the concentration range of 2–197 μM and the detection limit (LOD) of 1.74 μM. These results demonstrate that complex 1 has bifunctional properties of photocatalytic degradation of organic dyes and electrochemical sensing of antibiotic NOR, making it a promising candidate material for the synergistic treatment of complex pollutants. Full article

In the aspect of water purification, a photoactive hybrid material based on reduced graphite oxide (RGO) with covalently, coordinatively, and through van der Waals interactions bonded zirconium(IV) phthalocyanine (PcZr) is proposed. In the material, the phthalocyanine complex plays the role of photosensitizer, while RGO is considered a carrier, ensuring high surface area and supporting PcZr activation. The central metal atom of PcZr directly interacts with lateral active oxygen-containing surface groups of graphite oxide, mainly –OH and –COOH. Thus, the proposed method of synthesis under solvothermal conditions allowed obtaining a relatively high concentration of the dye (0.2 wt.%) in the system based on a partially reduced and exfoliated graphite oxide. Optical studies confirmed the presence of PcZr through absorption and luminescence spectra. Additionally, effective generation of reactive oxygen species was demonstrated by testing the transformation of a dye indicator (diphenylisobenzofuran). Photocatalytic activity of the system was confirmed by photooxidizing selected organic dyes (methylene blue, Rhodamine B, Brilliant Green, and Eriochrome Black T) in a water medium, tested in slightly acidic conditions under red light. The greatest overall decrease in absorption during the photodegradation test was observed for Brilliant Green, reaching 88% after 3 h of irradiation. Full article

Metal-organic frameworks (MOFs), a class of crystalline porous materials featuring a high specific surface area, tunable pore structures, and functional surfaces, exhibit remarkable potential in fluorescent sensing. This review systematically summarizes recent advances in the construction strategies, sensing mechanisms, and applications of MOF-based fluorescent sensors. It begins by highlighting the diverse degradation pathways that MOFs encounter in practical applications, including hydrolysis, acid/base attack, ligand displacement by coordinating anions, photodegradation, redox processes, and biofouling, followed by a detailed discussion of corresponding stabilization strategies. Subsequently, the review elaborates on the construction of sensors based on individual MOFs and their composites with metal nanomaterials, MOF-on-MOF heterostructures, covalent organic frameworks (COFs), quantum dots (QDs), and fluorescent dyes, emphasizing the synergistic effects of composite structures in enhancing sensor performance. Furthermore, key sensing mechanisms such as fluorescence quenching, fluorescence enhancement, Stokes shift, and multi-mechanism coupling are thoroughly examined, with examples provided of their application in detecting biological analytes, environmental pollutants, and food contaminants. Finally, future directions for MOF-based fluorescent sensors in food safety, environmental monitoring, and clinical diagnostics are outlined, pointing to the development of high-performance, low-cost MOFs; the integration of multi-technology platforms; and the construction of intelligent sensing systems as key to enabling their practical deployment and commercialization. Full article

The increasing discharge of organic pollutants such as dyes and antibiotics poses severe threats to aquatic ecosystems and human health. Conventional wastewater treatment methods are often limited by high energy consumption, secondary pollution, or low efficiency under visible light. It is crucial to design novel photocatalysts that can simultaneously utilize visible photons and enable swift transport of photoinduced charge carriers to drive contaminant decomposition. Herein, novel BiOCl/MIL-121 composites were synthesized via a straightforward hydrothermal route. A suite of complementary microscopic and spectroscopic analyses, including SEM, TEM, XRD and XPS, were employed to elucidate the material’s composition. Furthermore, collective evidence from spectroscopic and electrochemical analyses confirms markedly improved light absorption and charge separation efficiency within the BiOCl/MIL-121 photocatalyst. The 5% BiOCl/MIL-121 composite achieved 93.7% removal of Rhodamine B in 60 min, exhibiting a high photocatalytic degradation rate. Similarly, 5% BiOCl/MIL-121 photodegraded 80.4% of tetracyclin, which was much better than that of BiOCl. A plausible interfacial charge-transfer mechanism was deduced from the band structure of the 5% BiOCl/MIL-121 composite and experimental evidence from radical scavenger studies. This study provides an effective strategy for constructing a composite photocatalyst and offers a green way for the efficient degradation of organic pollutants. Full article

In this study, nanostructured ferberites (FeWO₄) were synthesized via hydrothermal routes in an acidic medium. It was then investigated as an efficient photocatalyst for degrading organic dye molecules, with methylene blue (MB) as a model pollutant. The formation mechanism of ferberite revealed that the physical form of the precursor, FeSO₄·7H₂O, acts as a decisive factor in morphological evolution. Depending on whether it is in a solid or dilute solution form, two distinct nanostructures are produced: nanoplatelets and self-organized microspheres. Both structures are composed of stoichiometric FeWO₄ (Fe: 49%, W: 51%) in a single monoclinic phase (space group P2/c:1) with high purity and crystallinity. The p-type semiconductor behavior was confirmed using Mott–Schottky model and the optical analysis, resulting in small band gap energies (≈1.7 eV) favoring visible absorption light. Photocatalytic tests under simulated solar irradiation revealed rapid and efficient degradation in less than 10 min under near-industrial conditions (pH 5). This was achieved using only a ferberite catalyst and a low concentration of H₂O₂ (4 mM) without additives, dopants, or artificial light sources. Advanced studies based on photocurrent measurements, trapping and stability tests were carried out to identify the main reactive species involved in the photocatalytic process and better understanding of photodegradation mechanisms. These results demonstrate the potential of nanostructured FeWO₄ as a sustainable and effective photocatalyst for water purification applications. Full article

This work aims to apply polymeric PBAT/PLA fibers electrospun with TiO₂ in the photodegradation of the dye Red BF-4B in an aqueous solution and the dye’s subsequent reuse. Initially, the influence of the solution pH was evaluated, and the results showed more significant dye degradation at pH values below the pHpcz (7.42). Kinetic studies show that at 15 mg·L⁻¹, the highest percentage of degradation occurs at 600 min of reaction time; however, degradation equal to (or greater than) 65% was observed at all evaluated concentrations, with the kinetic data being well fitted by the pseudo-first-order model. Additional studies demonstrated the reuse of polymeric films for dye removal, with removal efficiencies ranging from 86.60% to 93.07% over six consecutive reuse cycles. Each cycle consisted of a 600 min removal process, simulating repeated practical applications. After the photocatalytic process, the polymeric fibers remained cylindrical, with several fractures. Diameter decreases of 31.61% and 7.95% were observed after the first and sixth cycles, respectively, with possible exposure of TiO₂. The vibrational spectra indicate changes in the bands at 1755 and 1714 cm⁻¹, attributed to C=O (PLA) and C-O (PBAT) stretches, respectively, suggesting a possible conformational change in the polymers. The thermal profiles showed only slight changes after the cycles. X-ray diffractograms indicate that degradation of the polymeric matrix leads to greater exposure of the embedded TiO₂ particles. The combined results from different characterization techniques provide evidence of the degradation of the polymeric material. Full article

This study details the sustainable synthesis and characterization of electrospun zinc oxide nanofibers, uniquely derived from industrial waste streams. Our approach leverages diverse industrial byproducts—specifically sal ammoniac skimming from hot-dip galvanizing, electric arc furnace dust, and galvanization flue dust—as sustainable raw materials. Following hydrometallurgical treatment with various leaching agents (HCl, (NH₄)₂CO₃, or H₂SO₄) to obtain zinc-rich leachates, electrospinning solutions were formulated. The resulting fibers were subsequently calcined, yielding three distinct ZnO-based materials. Comprehensive characterization by XRD, SEM-EDX, and TEM revealed that the choice of leaching strategy significantly influenced the resultant fibers’ morphology and chemical composition. To demonstrate the potential applicability of these waste-derived materials, their photocatalytic activity was assessed through the degradation of methylene blue dye under UVA irradiation. ZnO fibers derived from HCl leaching exhibited remarkable photodegradation capabilities, achieving nearly complete dye removal within 690 min at optimal catalyst-to-dye ratios. Conversely, the H₂SO₄-prepared sample displayed impaired efficiency, primarily due to the formation of an undesirable Al₂ZnO₄ phase stemming from high aluminum content in the input waste, a critical consideration for waste-to-product strategies. The results showed that the cost-effective ZnO fibers obtained by electrospinning from industrial waste products have potential for applications in photocatalytic water treatment. Full article

Natural dyes and pigments are gaining importance as a sustainable alternative to synthetic dyes. Sourced from renewable materials, they are known for their biodegradable and non-toxic properties, offering a diverse range of color profiles and applications across industries such as textiles, cosmetics, food, and pharmaceuticals. This manuscript discusses various aspects of natural dyes and pigments (derived from plants and microbes), including anthocyanins, flavonoids, carotenoids, lactones, and chlorophyll. Furthermore, it highlights the polyphenolic nature of these compounds, which is responsible for their antioxidant activity and contributes to their anticancer, antibacterial, antifungal, antiprotozoal, and immunomodulatory effects. However, natural dyes are often categorized as pigments rather than dyes due to their limited solubility, a consequence of their molecular characteristics. Consequently, this manuscript provides a detailed discussion of key structural challenges associated with natural dyes and pigments, including thermal decomposition, photodegradation, photoisomerization, cross-reactivity, and pH sensitivity. Due to these limitations, natural dyes are currently used in relatively limited applications, primarily in the food industry, and, to lesser extent, in textiles and coatings. Nevertheless, with ongoing research and technological innovations, natural dyes present a viable alternative to synthetic dyes, promoting a more sustainable and environmentally conscious future. Full article

The natural sunlight driven photocatalytic degradation of organic pollutants is a sustainable solution for water purification. The use of heterojunction nanocomposites in this process shows promise for improved photodegradation efficiency. In this work, nanocrystalline Zn₂SnO₄/SnO₂ obtained by the solid-state synthesis method was tested as a heterojunction photocatalyst material for the degradation of methylene blue (MB) and Rhodamine B (RhB) dyes as single and multicomponent systems in natural sunlight. Characterization of the structure and morphology of the synthesized nanocomposite using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDS), and photoluminescence (PL) spectroscopy confirmed the formation of Zn₂SnO₄/SnO₂ and heterojunctions between Zn₂SnO₄ and the SnO₂ nanoparticles. A photodegradation efficiency of 99.1% was achieved in 120 min with 50 mg of the photocatalyst for the degradation of MB and 70.6% for the degradation of RhB under the same conditions. In the multicomponent system, the degradation efficiency of 97.9% for MB and 53.2% for RhB was obtained with only 15 mg of the photocatalyst. The degradation of MB occurred through N-demethylation and the formation of azure intermediates and degradation of RhB occurred through sequential deethylation and fragmentation of the xanthene ring, both in single and multicomponent systems. 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

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

In the present study, a photodegradation technique was employed for the removal of methylene blue dye from aqueous solution using a tungsten oxide-based photocatalyst. The photocatalyst was synthesized via a green synthesis route utilizing a plant extract (PE) under acidic conditions. The synthesized photocatalyst was characterized by various spectroscopic and microscopic techniques that confirmed the presence of various functional groups on the catalyst surface and revealed a narrow bandgap of ~3.0 eV. The synthesized particles exhibited a nanoscale dimension ranging from 10 to 15 nm. The photocatalytic activity of the material was evaluated under ultraviolet light, visible light, and sunlight irradiation, demonstrating the efficient degradation of methylene blue under all light sources. Furthermore, catalysis reusability studies indicated excellent stability, with consistent photocatalytic performance observed after five successive cycles. Full article