Search Results (608)

Microplastics are an increasing concern due to their widespread occurrence in aquatic environments worldwide. The lack of a harmonised protocol for their reliable quantification remains a major challenge in current scientific efforts. This study presents a comparative evaluation of three protocols for the detection and quantification of microplastics in aqueous samples. The protocols were assessed based on quantification efficiency, risk of particle degradation, staining performance, operational complexity, and cost per sample. Protocol A combined Rhodamine B and ethanol staining with NaCl-based density separation, demonstrating strong isolation performance while maintaining minimal chemical hazards and moderate cost (2.45€ per sample) that could be further reduced to 0.45€ per sample by substituting reagent-grade NaCl with table salt. Protocol B offered moderate isolation capacity and presented the highest risk of particle fragmentation, likely due to the use of acetone and high-temperature digestion. Protocol C, based on the combined use of Nile Red and ZnCl₂, also presented a risk of particle fragmentation, resulting in the highest MP count for small and hydrophobic particles. In addition, its high cost (15.23€ per sample) limits its suitability for routine application. Full article

Water pollution caused by increasing industrial and human activity remains a serious environmental challenge, especially due to the persistence of organic contaminants in aquatic systems. Photocatalysis offers a promising and eco-friendly solution, but in the case of bismuth oxide (Bi₂O₃) there is still a limited understanding of how structural and morphological features influence photocatalytic performance. In this work, a straightforward hydrothermal synthesis method followed by controlled calcination was developed to produce phase-pure α- and β-Bi₂O₃ with tunable morphologies. By varying the hydrothermal temperature and reaction time, distinct structures were successfully obtained, including flower-like, broccoli-like, and fused morphologies. XRD analyses showed that the final crystal phase depends solely on the calcination temperature, with β-Bi₂O₃ forming at 350 °C and α-Bi₂O₃ at 500 °C. SEM and BET analyses confirmed that morphology and surface area are strongly influenced by the hydrothermal conditions, with the flower-like β-Bi₂O₃ exhibiting the highest surface area. UV–Vis spectroscopy revealed that β-Bi₂O₃ also has a lower bandgap than its α counterpart, making it more responsive to visible light. Photocatalytic tests using Rhodamine B showed that the flower-like β-Bi₂O₃ achieved the highest degradation efficiency (81% in 4 h). Kinetic analysis followed pseudo-first-order behavior, and radical scavenging experiments identified hydroxyl radicals, superoxide radicals, and holes as key active species. The catalyst also demonstrated excellent stability and reusability. Additionally, Methyl Orange (MO), a more stable and persistent azo dye, was selected as a second model pollutant. The flower-like β-Bi₂O₃ catalyst achieved 73% degradation of MO at pH = 7 and complete removal under acidic conditions (pH = 2) in less than 3 h. These findings underscore the importance of both phase and morphology in designing high-performance Bi₂O₃ photocatalysts for environmental remediation. Full article

This work analyzes the performance of a photoreactor built with UV-LED technology. For this task, a UV-LED wavelength of 365 nm was used as an irradiation source, and it was electrically and spectrally characterized to ensure correct operation. To evaluate the functionality, the photoreactor was tested on the degradation of Rhodamine B (Rh B), a dye commonly used in the textile industry. The experiment was conducted under optimal conditions, using a concentration of 17 ppm of Rh B and 100 mg of zinc oxide (ZnO) as a photocatalyst in a glass reactor. The mixture was continuously stirred for 120 min, achieving 99.42% efficiency. The results showed that the UV-LED photoreactor performs well in activating ZnO for the removal of Rh B from the solution, highlighting its potential for treating textile industry wastewater. The use of LEDs offers advantages such as energy efficiency and lower environmental impact compared to traditional UV lamps. ZnO, known for its reactivity under UV light, acted as a stable photocatalyst, ensuring complete degradation of the dye without producing harmful by-products. This method provides an efficient approach to dye removal in wastewater treatment, promoting cleaner and more sustainable industrial practices. Full article

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

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

A strong interaction between Bi³⁺ and ZnO was used to successfully sensitize ZnO nanorods with quantum dots (QDs) of Bi₂O₃ through three different strategies. Although the Bi₂O₃ QDs had similar particle size distributions, their photocatalytic performance varied significantly, prompting the investigation of factors beyond particle size. The study revealed that the photochemical method selectively deposited Bi₂O₃ QDs onto electron-rich ZnO sites, providing a favorable pathway for efficient electron–hole separation and transfer. Consequently, abundant h⁺ and ·OH radicals were generated, which effectively degraded Rhodamine B (RhB). As demonstrated in the RhB degradation experiments, the Bi₂O₃/ZnO nanorod catalyst achieved an 89.3% degradation rate within 120 min, significantly outperforming catalysts with other morphologies. The photoluminescence (PL) and time-resolved photoluminescence (TRPL) results indicated that the Bi₂O₃/ZnO heterostructure constructed an effective interface to facilitate the spatial separation of photogenerated charge carriers, which effectively prolonged their lifetime. The electron paramagnetic resonance (EPR) results confirmed that the ·OH radicals played a key role in the degradation process. Full article

This study investigated the enhancement of Cu₂MnSnS₄ (CMTS) thin films’ photocatalytic properties through potassium (K) doping for rhodamine B degradation under visible light. K-doped CMTS films synthesized using spray pyrolysis technology achieved a 98% degradation efficiency within 120 min. The physical property improvements were quantitatively validated through X-ray diffraction (XRD) analysis, which confirmed enhanced crystallinity. Scanning electron microscopy (SEM) revealed significant modifications in surface morphology as a function of potassium content, highlighting its influence on film growth dynamics. Optical characterization demonstrated a pronounced reduction in transmittance, approaching negligible values at 7.5% potassium doping, and a narrowed optical band gap of 1.41 eV, suggesting superior light absorption capabilities. Photocatalytic performance was significantly enhanced, achieving a Rhodamine B degradation efficiency of up to 98% at 7.5% doping. These enhancements collectively improved the material’s light-harvesting capabilities and charge separation efficiency, positioning K-doped CMTS as a highly effective photocatalyst compared to other ternary and quaternary materials. Full article

A simple method for synthesizing novel Pd-In₂O₃/BiVO₄ composites by using a hydrothermal technique is proposed. The synthesized samples showed a monoclinic phase and featured homogeneously dispersed Pd and BiVO₄ dopants on In₂O₃, as confirmed by XRD, SEM, and XPS analyses. The Pd-In₂O₃/BiVO₄ composite exhibited notable improvements, such as broadened visible-light absorption (up to 596.1 nm) and a narrowed band gap (2.08 eV vs. 2.82 eV for pure In₂O₃), a more compact and integrated morphology observed by SEM, which are expected to promote improved light harvesting and facilitate charge separation during photocatalysis. Under visible-light irradiation, the optimized 1 wt% Pd-In₂O₃/BiVO₄ achieved 99% degradation of Rhodamine B (10 mg/L) within 40 min, while pure In₂O₃ showed less than 10% removal after 60 min—highlighting the strong synergistic effect of dual doping. Additionally, the composite demonstrated excellent stability and reusability over multiple cycles. A plausible photocatalytic mechanism for this process is proposed, providing insights into the design of efficient photocatalysts for wastewater treatment. Full article

Spherical Cu₂O nanoparticles were obtained by reducing copper acetate in N,N-dimethylformamide (DMF) system using glucose as the reducing agent and polyvinylpyrrolidone (PVP) as the surfactant, with which spherical PdCu nanocatalysts were thus synthesized by disproportionation. The catalyst was used for the activation of peroxymonosulfate (PMS) and showed an excellent degradation effect on rhodamine B and methylene blue-contained printing and dyeing wastewater with good stability. Additionally, the surface morphology analysis of the catalyst was carried out by SEM and TEM. The structure was characterized by XRD and FT-IR. The valence state and composition of the catalyst were characterized by XPS. The catalytic performance of the prepared catalysts was investigated with methylene blue and rhodamine B used as target pollutants. The results showed that the catalytic reduction efficiency of PdCu nanocatalyst for the two pollutants could reach 99% at 20 °C, when catalyst concentration was 60 mg/L and PMS concentration was 1.0 g/L and 0.6 g/L, respectively. The degradation efficiency of the catalyst was significantly reduced when Cl⁻, ${\mathrm{H}\mathrm{C}\mathrm{O}}_3^{-}$ and HA were present in the water. The degradation efficiency was above 90% when the pH was in the range of 5–11. The excellent performance of the PdCu/PMS system in the treatment of RhB-contained wastewater was further confirmed by taking into account of the data of free radical quenching experiment and the results of electron paramagnetic resonance (EPR) experiment. After three cycles, the removal rate of MB and RhB could still be maintained at more than 90%, which proved its excellent recyclability due to its remarkable stability and efficiency. Full article

Conjugated microporous polymers (CMP) are advanced photocatalytic systems for degrading organic dyes. However, their potential and efficiency are often limited by rapid electron–hole pair (e⁻/h⁺) recombination. To overcome this limitation, this study proposes a strategy that involves designing a Mott–Schottky heterojunction and integrating graphene sheets with a near-zero bandgap into the CMP-1 framework, resulting in a non-covalent graphene/CMP (GCMP) heterojunction composite. GCMP serves two main functions: physical adsorption and photocatalytic absorption that uses visible light energy to trigger and degrade the organic dye. GCMP effectively degraded four dyes with both anionic and cationic properties (Rhodamine B; Nile Blue; Congo Red; and Orange II), demonstrating stable recyclability without losing its effectiveness. When exposed to visible light, GCMP generates reactive oxygen species (ROS), primarily singlet oxygen (¹O₂), and superoxide radicals (^•O₂), degrading the dye molecules. These findings highlight GCMP’s potential for real-world applications, offering a metal-free, cost-effective, and environmentally friendly solution for wastewater treatment. Full article

Nowadays, there is an urgent need for efficient photocatalysts and adsorbents for environmentally relevant applications. This study investigates the effect of polyaniline (PANI) on the structure and performance of carbonized nanocomposites composed of PANI and TiO₂ nanotubes (NTs), focusing on their photocatalytic degradation efficiency and dye adsorption capacity. The hypothesis was that PANI forms conductive carbon domains and stabilizes the anatase phase during thermal treatment, enhancing the performance of TiO₂-NTs as photocatalysts. Nanocomposites based on PANI and TiO₂-NTs (TTP) were synthesized through chemical oxidative polymerization of aniline (ANI) in the presence of TiO₂-NTs using two TiO₂/ANI molar ratios of 50 and 150 and subsequently carbonized at 650 °C, yielding CTTP-50 and CTTP-150. The novel CTTP composites and carbonized pristine TiO₂-NTs (CTNT) were characterized by various techniques, including TEM, UV-Vis diffuse reflectance, Raman spectroscopy, XRD, and TGA. Their performance regarding dye adsorption and photocatalytic degradation under visible light was evaluated with Acid Orange 7, Methylene Blue, and Rhodamine B. CTTP-150 exhibited the highest adsorption capacity and photodegradation rate, attributed to the synergistic effect of PANI, which stabilizes the TiO₂ phase and enhances visible-light absorption and adsorption. Full article

A cellulose-based material with high adsorption capacity and surface area was developed by selecting appropriate copolymer monomers for structural design. This material was used for selective dye adsorption in wastewater treatment. The copolymer was characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and Fourier-transform infrared spectroscopy (FTIR) to investigate its microstructure, structure, thermal stability, and thermal decomposition. We explored the factors affecting dye adsorption, including dye type, adsorption reaction time, initial dye concentration, copolymer dosage, temperature, and the acidity or alkalinity of the reaction environment. The results showed that as the adsorption reaction time increased, the amount of adsorbed Rhodamine B dye gradually increased, and the initial stage (0–20 min) increased rapidly. When the initial dye concentration was 15 mg/L, the adsorption capacity (q_e) was at its maximum (3.67 mg/g). In addition, when the amount of copolymer used was 5 mg/10 mL, the adsorption capacity (q_e) was the highest (12.37 mg/g). High-temperature conditions were favorable for adsorption, with the maximum adsorption capacity (q_e) at 35 °C (13.48 mg/g). The prepared copolymer exhibited significant adsorption performance in acidic environments (pH = 3). The polymer adsorbed with dye was degraded by UV irradiation, avoiding secondary pollution caused by recycling. Full article

This work shows a sustainable methodology for the synthesis of biogenic materials designed for the removal and photodegradation of rhodamine B (RhB), a highly dangerous environmental pollutant that induces reproductive toxicity. The classical synthesis of MCM-41-ordered mesoporous materials was modified using biocompatible rice husk as the silica template. Iron was incorporated and the so-prepared biogenic photocatalysts were characterized by X-ray diffraction, N₂ adsorption–desorption isotherms, transmission electron microscopy, diffuse reflectance UV-Vis, surface pH, cyclic voltammetry, and Fourier transform infrared spectral analysis of pyridine adsorption. The photocatalytic performance of the materials was evaluated following the removal by adsorption and the photon-driven degradation of RhB. The adsorption capacity and photocatalytic activity of the biogenic materials were correlated with their properties, including iron content, texture, surface content, and electrochemical properties. The best biogenic material boosted the degradation rates of RhB under UV irradiation up to 4.7 and 2.2 times greater than the direct photolysis and the benchmark semiconductor TiO₂-P25. It can be concluded that the use of rice husks for the synthesis of biogenic Fe-modified mesoporous materials is a promising strategy for wastewater treatment applications, particularly in the removal of highly toxic organic dyes. Full article

Niobium oxides are promising materials for catalytic applications due to their unique structural versatility and surface chemistry. Nb₂O₅ nanomaterials were synthesized via a solvothermal method at 150 °C using niobium oxalate as a precursor. A comprehensive characterization of the material was performed using electron microscopy, X-ray diffraction, and Raman spectroscopy. The as-prepared nanoparticles primarily crystallized in a mixture of the TT-Nb₂O₅ phase (TT from the German Tief-Tief, meaning “low-low”) and niobic acid, while subsequent thermal treatment at 900 and 1100 °C induced a phase transformation to T-Nb₂O₅ and H-Nb₂O₅, respectively (T from the German Tief, meaning “low”, and H from Hoch, meaning “high”). The as-prepared samples consist of micro-coils composed of interconnected nanometer-scale fibers, whereas the morphology changes into rods when they are treated at 1100 °C. The photocatalytic performance of the nanoparticles was evaluated by comparing the as-prepared and thermally treated samples. The as-prepared nanoparticles exhibited the highest photocatalytic activity under visible illumination, achieving 100% degradation after 180 min. More interestingly, the treatment of the as-prepared material with H₂O₂ modified the surface species formed on the Nb₂O₅, altering the photocatalytic behavior under various illumination conditions. This sample showed the highest photocatalytic activity under UV illumination, reaching 100% degradation after 75 min. On the other hand, the calcined samples are practically inactive, attributed to the loss of active catalytic sites during thermal treatment and phase transformation. Full article

In this study, Bi₂MoO₆ nanoflowers with different molybdenum sources were in situ grown on the surface of g-C₃N₄ nanosheets (OCN) by a simple one-step solvothermal method. The effects of doping and different molybdenum sources on the photocatalytic degradation and bactericidal activity of Bi₂MoO₆/OCN were discussed. Among them, the solvothermal preparation of P-Bi₂MoO₆/OCN using phosphomolybdic acid as molybdenum source can make up for the shortcomings caused by the destruction of OCN structure by generating more lattice defects to promote charge separation and constructing Lewis acid/base sites to effectively improve the photocatalytic performance. In addition, by adding phosphoric acid to increase the P-doped content, more exposed alkaline active sites are induced on the surface of P-Bi₂MoO₆/OCN, as well as larger specific surface area and charge transfer efficiency, which further improve the photocatalytic performance. Finally, the optimized 16P-Bi₂MoO₆/OCN showed a degradation rate of 99.7% for 20 mg/L rhodamine B (RhB) within 80 min under visible light, and the antibacterial rates against E. coli, S. aureus and P. aeruginosa within 300 min were 99.58%, 98.20% and 97.48%, respectively. This study provides a reference for optimizing the synthesis of environmentally friendly, solar-responsive, photocatalytic sterilization materials from the perspective of preparation, raw materials and structure. Full article