Search Results (583)

Green synthesis represents a sustainable, reliable, and eco-friendly approach for producing various materials and nanomaterials, including metal and metal oxide nanoparticles. This environmentally conscious method has garnered significant attention from materials scientists. In recent years, interest in plant-mediated nanoparticle synthesis has grown markedly, owing to advantages such as enhanced product stability, low synthesis costs, and the use of non-toxic, renewable resources. This review specifically focuses on the green synthesis of metal oxide nanoparticles using plant extracts, highlighting five key oxides: TiO₂, ZnO, WO₃, CuO, and Fe₂O₃, which are prepared through various plant-based methods. The release of toxic effluents like synthetic dyes into the environment poses serious threats to aquatic ecosystems and human health. Therefore, the application of biosynthesized nanoparticles in removing such pollutants from industrial wastewater is critically examined. This paper discusses the synthesis routes, characterization techniques, green synthesis methodologies, and evaluates the photocatalytic performance and dye degradation mechanisms of these plant-derived nanoparticles. Full article

Nanosized titanium dioxide is widely used by the industry, e.g., in pigments, suncreams, and food colors. Its environmental and biological effects have been investigated in the past; however, few studiesd have focused on its crystal structure-specific effects. In our experiments, the toxicity of two types of synthetic nanoparticles was examined on primary neural cultures with different cell compositions using MTT and LDH assays. Primary murine cell cultures containing only astroglia cells originated from two brain regions, as well as mixed neurons and glia cells or microglia cells exclusively, were treated with anatase (15.8 ± 1.7 nm average diameter) and rutile (46.7 ± 2.2 nm average length and 13.7 ± 0.7 nm average diameter) TiO₂ nanoparticles at varying concentrations for 24 or 48 h. Our results show that neither anatase nor rutile nanoparticles reduced viability in cell cultures containing a mixture of neurons and glial cells, independently of the applied concentration and treatment time. Rutile but not anatase form induced cell death in cortical astroglia cultures already at 24 h of treatment above 10 µg/mL, while hippocampus-derived glial cultures were much less sensitive to rutile. The rutile form also damaged microglia. These findings suggest that products containing rutile-form nano-titanium particles may pose a targeted risk to astroglia and microglial cells in the central nervous system. Full article

Dye-contaminated wastewater has become one of the most severe environmental challenges due to the non-biodegradability and toxicity of synthetic dyes. While photocatalytic degradation is considered a green and efficient technology for wastewater purification, conventional TiO₂ suffers from limited light utilization and rapid electron–hole recombination. In this exploration, Ag-TiO₂-RGO nanocomposites were successfully fabricated and systematically investigated by XRD, SEM, TEM, XPS, Raman, and PL spectroscopy. The incorporation of Ag nanoparticles and reduced graphene oxide (RGO) synergistically improved charge separation and transfer efficiency. Photocatalytic activity was evaluated using different dyes as pollutants under visible light irradiation. Among the samples, Ag-TiO₂-RGO-3% exhibited the highest RhB degradation efficiency of 99.5% within 75 min, with a rate constant (K) of 0.05420 min⁻¹, which was nearly three times higher than that of pure TiO₂. The photocatalyst also showed excellent reusability with only minor efficiency loss after five cycles, and its activity remained stable across a wide pH range. Radical trapping experiments revealed that •O₂⁻ served as the dominant reactive species, with additional contributions from •OH and photogenerated holes (h⁺). A possible photocatalytic mechanism was proposed, in which Ag nanoparticles and RGO effectively suppressed electron–hole recombination and accelerated the formation of reactive oxygen species for efficient dye mineralization. These findings demonstrate that Ag-TiO₂-RGO-3% is a promising photocatalyst with high activity, stability, and environmental adaptability for wastewater remediation. Full article

Titanium and its alloys are widely used in biomedical implants due to their favorable mechanical properties and corrosion resistance; however, their natural surface lacks sufficient bioactivity and antibacterial performance. Micro-arc oxidation is a promising approach to producing bioactive coatings, and the incorporation of nanoparticles such as TiO₂ may further improve their functionality. This study aimed to determine the optimal TiO₂ nanoparticle concentration in the micro-arc oxidation electrolyte that ensures coating stability and biological safety. Calcium–phosphate coatings were fabricated on commercially pure titanium using micro-arc oxidation with two TiO₂ concentrations: 0.5 wt.% (MAO 1) and 1 wt.% (MAO 2). Surface morphology, porosity, and phase composition were analyzed by scanning electron microscopy, energy-dispersive spectroscopy, and X-ray diffraction. Corrosion resistance was evaluated via potentiodynamic polarization in NaCl and Ringer’s solutions, while biocompatibility was assessed in vitro using HOS human osteosarcoma cells and MTT assays. Increasing the TiO₂ content to 1% decreased coating porosity (13.7% vs. 26.3% for MAO 1), enhanced corrosion protection, and reduced the friction coefficient compared to bare titanium. However, MAO 2 exhibited high cytotoxicity (81% cell death) and partial structural degradation in the biological medium. MAO 1 maintained integrity and showed no toxic effects (3% cell death). These results suggest that 0.5% TiO₂ is the optimal concentration, providing a balance between corrosion resistance, mechanical stability, and biocompatibility, supporting the development of safer implant coatings. Full article

The increasing environmental presence of metal oxide nanoparticles (NMOPs) raises concerns regarding their influence on biological wastewater treatment. This study comparatively evaluates the structural and biological effects of zinc oxide (ZnO-NPs) and titanium dioxide (TiO₂-NPs) nanoparticles on activated sludge from a wastewater treatment plant. Experimental exposure covered nanoparticle concentrations of 0.05–0.3 g/L and contact times up to 180 min, with analysis of enzymatic activity (dehydrogenase activity, TTC-SA method), sludge settleability, and particle size distribution. Inhibition of microbial metabolic activity was observed in a clear dose- and time-dependent manner, with ZnO-NPs showing stronger toxicity than TiO₂-NPs. At the highest dose (0.3 g/L), enzymatic activity nearly disappeared after 90 min (0.04 µg TPF/mg MLSS). Both nanoparticles caused floc fragmentation, decreased sludge volume index (SVI), and increased the proportion of ultrafine particles (<0.3 µm). ZnO-NPs induced more severe destabilization, while TiO₂-NPs showed partial re-aggregation of suspended particles at higher concentrations. Additionally, particle size distribution in the supernatant was analyzed, revealing distinct aggregation and fragmentation patterns for ZnO- and TiO₂-NPs. These structural and functional alterations suggest potential risks for treatment efficiency, including reduced nutrient removal and impaired sludge settleability. The study provides a comparative contribution to understanding toxicity mechanisms of ZnO- and TiO₂-NPs and emphasizes the need to monitor NMOPs in wastewater and to develop mitigation strategies to ensure stable plant operation Full article

Emerging organic contaminants (EOCs), including polychlorinated bisphenyls (PCBs), pharmaceuticals, personal care products, pesticides, polycyclic aromatic hydrocarbons (PAH), and dyes, are among the most hazardous pollutants found in water bodies and sediments. These substances pose serious threats to the environment and human health due to their high toxicity, long-range mobility, and bioaccumulation potential. Although various methods for degradation of organic pollutants exist, photocatalysis using ultraviolet (UV) and visible light (VIS) has emerged as a promising approach. However, its practical applications remain limited due to challenges such as the use of powdered photocatalysts, which complicates their removal and recycling in industrial settings, and the restricted solar availability of UV light (~4% of the solar spectrum). This review investigates the effectiveness of hybrid electrospun conductive polymer nanofibers on metal oxide photocatalysts such as TiO₂ and ZnO (including doped and co-doped forms) and fabricated via mono- or coaxial electrospinning, in the degradation of EOCs in water under visible light. Furthermore, strategies to enhance the fabrication of these hybrid electrospun conductive nanofibers as visible-light-responsive photocatalysts, such as the inclusion of dopants and/or plasmonic materials, are discussed. Finally, the current challenges and future research directions related to electrospun nanofibers combined with photocatalysts for the degradation of EOCs in water treatment applications are outlined. Full article

The persistent release of synthetic dyes such as methylene blue (MB) into aquatic environments poses a significant ecological hazard due to their chemical stability and toxicity. In recent years, the application of engineered composite photocatalysts has emerged as a potent solution for efficient dye degradation under visible and UV light. This review comprehensively summarizes various advanced composites, including carbon-based, metal-doped, and heterojunction materials, tailored for MB degradation. Notably, composites such as TiO₂/C-550, WS₂/GO/Au, and MOF-derived α-Fe₂O₃/ZnO achieved near-complete degradation (>99%) within 30–150 min, while others, like ZnO/JSAC-COO⁻ and Ag/TiO₂/CNT, displayed enhanced charge separation and stability over five consecutive cycles. Band gap engineering (ranging from 1.7 eV to 3.2 eV) and reactive oxygen species (·OH, ·O₂⁻) generation were key to their photocatalytic performance. This review compares the structural attributes, synthetic strategies, and degradation kinetics across systems, highlighting the synergistic role of co-catalysts, surface area, and electron mobility. This work offers systematic insight into the state-of-the-art composite photocatalysts and provides a comparative framework to guide future material design for wastewater treatment applications. Full article

Triclosan (TCS), a persistent antimicrobial and endocrine-disrupting compound, is commonly found in surface and groundwater due to incomplete removal by conventional wastewater treatment. This study evaluated its fate in authentic rainwater runoff collected from a state road using rubber tiles made from recycled tires that were either uncoated (RRT) or coated with TiO₂ via the sol–gel method (SGT). Pollutants were analyzed by a high-resolution liquid chromatography–quadrupole time-of-flight mass spectrometry system (LC/MS QTOF) before and after treatment in a flat-plate cascade reactor under UV-A irradiation. After 120 min SGT achieved >50% TCS removal, while RRT achieved ~44%. Further analysis identified degradation products (chlorocatechole, quinone, and transient dioxin-like species). ECOSAR predictions indicated moderate to high toxicity for some degradation products, but their transient and low-abundance detection suggests that photocatalysis suppresses accumulation, ultimately yielding less harmful products such as benzoic acid. These findings highlight the dual role of TiO₂-coated rubber tiles: improving material durability while enabling photocatalytic degradation. Full article

The discharge of printing and dyeing wastewater has become a key concern in global water pollution control due to its high pollutant concentration, dark color, refractory biodegradability and toxic characteristics. Photoelectrocatalytic (PEC) technology has gained widespread attention as it can effectively treat refractory organic pollutants. In this study, titanium dioxide (TiO₂)–bismuth vanadate (BiVO₄) composite materials were synthesized through the sol–gel/solvothermal hybrid method, and layered heterojunction structures were fabricated via sol–gel precursor preparation followed by spin-coating deposition. The PEC degradation efficiency of rhodamine B (RhB) was systematically evaluated under varying operational conditions in the presence of TiO₂-BiVO₄. The four-layer BiVO₄/four-layer TiO₂ material showed the optimal catalytic activity among the tested structures, achieving an 80.3% removal of RhB under an applied bias of 4 V and illumination intensity of 14,000 lx. Through the equilibrium adjustment of the Fermi levels, the type Ⅱ heterostructure was formed. Moreover, superoxide radical (O₂⁻) was identified as the predominant reactive oxygen species driving the degradation mechanism. Mechanistic analysis revealed that RhB degradation was accomplished through deethylation, benzene ring cleavage, and subsequent ring-opening mineralization. This study prepared an efficient PEC material, which provides a theoretical basis for the PEC treatment of printing and dyeing wastewater. Full article

Since methanol has a significant health hazard due to its inherent toxicity, it is urgent to develop a method capable of rapid, sensitive, and continuous monitoring of methanol. The present study successfully synthesized a NiCo₂O₄/MIL-Ti₁₂₅ composite material and conducted a comprehensive analysis of its effectiveness for the detection of methanol employing cataluminescence (CTL) technology. The findings demonstrated that the composite material displays marked CTL in response to methanol, showcasing notable sensitivity, selectivity, and stability. The composite’s heterogeneous structure significantly improves the adsorption and reaction efficiency of methanol and further reduces the sensor’s working temperature. Under the optimal conditions of 215 °C and a flow rate of 300 mL/min, the CTL signal intensity is governed by the equation Y = 10.388X − 4.473 (R² = 0.982), with a detection limit as low as 0.431 ppm. The NiCo₂O₄/MIL-Ti₁₂₅ sensor exhibits high selectivity towards methanol. In addition, a relative standard deviation (RSD) of 4.95% demonstrates its excellent stability. Utilizing X-ray photoelectron spectroscopy (XPS), the study investigated the impact of elemental valence changes on the CTL process. We believe that the NiCo₂O₄/MIL-Ti₁₂₅ composite material, as a high-performance low-temperature CTL methanol sensor, is promising for applications. Full article

Endocytic uptake and lysosomal localization are suggested to be the key mechanisms underlying the toxicity of metal oxide nanoparticles (MONPs), with dissolution in the acidic milieu driving the response. In this study, we aimed to investigate if MONPs of varying solubility are similarly sequestered intracellularly, including in lysosomes and the role of the acidic lysosomal milieu on toxicity induced by copper oxide (CuO) nanoparticles (NPs), nickel oxide (NiO) NPs, aluminum oxide (Al₂O₃) NPs, and titanium dioxide (TiO₂) NPs of varying solubility in FE1 lung epithelial cells. Mitsui-7 multi-walled carbon nanotubes (MWCNTs) served as contrasts against particles. Enhanced darkfield hyperspectral imaging (EDF-HSI) with fluorescence microscopy was used to determine their potential association with lysosomes. The v-ATPase inhibitor Bafilomycin A1 (BaFA1) was used to assess the role of lysosomal acidification on toxicity. The results showed co-localization of all MONPs with lysosomes, with insoluble TiO₂ NPs showing the greatest co-localization. However, only acute toxicity induced by soluble CuO NPs was affected by the presence of BaFA1, showing a 14% improvement in relative survival. In addition, all MONPs were found to be associated with large actin aggregates; however, treatment with insoluble TiO₂ NPs, but not soluble CuO NPs, impaired the organization of F-actin and α-tubulin. These results indicate that MONPs are sequestered similarly intracellularly; however, the nature or magnitude of their toxicity is not similarly impacted by it. Future studies involving a broader variety of NPs are needed to fully understand the role of differential sequestration of NPs on cellular toxicity. Full article

Despite aggressive current therapies against glioblastoma (GB), residual tumor cells may remain at the edge of the surgical cavity after resection. These cells can rapidly proliferate, giving rise to tumor recurrence in more aggressive and drug-resistant forms. As photodynamic therapy (PDT) has advanced, it has emerged as an option to treat this brain tumor. The oncological basis of PDT involves the selective accumulation of a photosensitizer (PS) in the tumor, followed by its activation with electromagnetic radiation to generate reactive oxygen species (ROS), which induce tumor cell death. Given that first- and second-generation PSs present significant limitations, including poor tumor selectivity, suboptimal biodistribution, limited absorption within the therapeutic window, and slow systemic clearance, research has progressed toward the development of third-generation PSs based on nanotechnology to optimize their therapeutic properties. This review addresses the types of tumor cell death induced by PDT, as well as the advancements of PS design, focusing on titanium dioxide (TiO₂) and zinc oxide (ZnO) nanoparticles. These nanomaterials can be designed as carriers, encapsulating or conjugating conventional PSs, or act as PSs themselves, due to their favorable biocompatibility and intrinsic photoreactivity. Additionally, they can be functionalized with targeting ligands to achieve tumor-specific delivery, enhancing therapeutic selectivity while minimizing toxicity to healthy tissue. Overall, these nanotechnology-based PSs represent a versatile and promising therapeutic paradigm that warrants further investigation through basic research, supporting the development and potential clinical translation of a more precise and effective PDT-based intervention for glioblastoma, initially aimed at eliminating intra-surgical post-resection residual tumor cells. Full article

In this study, an analysis was carried out of the combustion of pellets made from chamomile and English ryegrass biomass, including those with the addition of kaolin and urea, in terms of their physical and chemical properties. During combustion tests with synchronized timing, the concentrations of CO₂, CO, NO, and SO₂ in the flue gases were measured, along with the temperatures of the supplied air and the flue gases. The addition of kaolin improved combustion parameters, reduced CO emissions, and stabilized the combustion process, despite the deterioration of the mechanical durability of the pellets. Combustion in the drop-in burner (type B tests) showed higher energy efficiency (CEI) and lower flue gas toxicity (TI) than in the grate system (type A tests). The SiO₂ content in the chamomile ash explained its higher resistance to slagging, confirmed by characteristic ash temperatures. Comparison with other biofuels (straw, hay, sawdust) showed similarities or advantages in terms of reducing CO, NO, and SO₂ emissions. NO emissions were lower for pellets with urea and kaolin added, although in the case of biomass with high nitrogen content these relationships require further improvement. The research results indicate the potential of herbaceous biomass as a fuel in local heating systems. However, modification of such fuels is also associated with the need for further research on reducing emissions during unstabilized combustion phases, with particular emphasis on the ignition phase. Full article

Nanofertilizers (NFs) and engineered nanoparticles (NPs) are increasingly used in agriculture, yet their environmental safety remains poorly understood. This study evaluated the comparative phytotoxicity of zinc oxide (ZnO), titanium dioxide (TiO₂), and clinoptilolite nanoparticles, three commercial nanofertilizers, and potassium dichromate (K₂Cr₂O₇) using Lactuca sativa seeds under adapted OECD-208 protocol conditions. Seeds were exposed to varying concentrations of each xenobiotic material (0.5–3% for NFs; 10–50% for NPs), with systematic assessment of seedling survival, root and hypocotyl length, dry biomass, germination index (GI), and median effective concentration (EC₅₀) values. Nanofertilizers demonstrated significantly greater phytotoxicity than engineered nanoparticles despite lower application concentrations. The toxicity ranking was established as NF1 > NF3 > NF2 > NM2 > NM1 > NM3, with NF1 being most toxic (EC₅₀ = 1.2%). Nanofertilizers caused 45–78% reductions in root length and 30–65% decreases in dry biomass compared with controls. GI values dropped to ≤70% in NF1 and NF3 treatments, indicating concentration-dependent growth inhibition. While nanofertilizers offer agricultural benefits, their elevated phytotoxicity compared with conventional nanoparticles necessitates rigorous pre-application safety assessment. These findings emphasize the critical need for standardized evaluation protocols incorporating both physiological and ecotoxicological endpoints to ensure safe xenobiotic nanomaterial deployment in agricultural systems. Full article

Platinum has emerged as an optimal catalyst for the selective hydrogenation of nitroarenes owing to its high hydrogenation activity, selectivity, and stability. In this study, we report the fabrication of platinum nanoparticles stabilized on a composite support consisting of gum acacia polymer (GAP) and TiO₂. It was engineered for the targeted reduction of nitroarenes to arylamines via selective hydrogenation in methanol at ambient temperature. The non-toxic and biocompatible properties of GAP enable it to act as a reducing and stabilizing agent during synthesis. The synthesized nanocatalyst was characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Morphological and structural analyses revealed that the fabricated catalyst consisted of minuscule Pt nanoparticles integrated within the GAP framework, accompanied by the corresponding TiO₂ nanoparticles. Inductively coupled plasma optical emission spectrometry (ICP-OES) was employed to ascertain the Pt content. The mild reaction conditions, decent yields, trouble-free workup, and facile separation of the catalyst make this method a clean and practical alternative to nitroreduction. Selective hydrogenation yielded an average arylamine production of 97.6% over five consecutive cycles, demonstrating the stability of the nanocatalyst without detectable leaching. Full article