Search Results (152)

The widely utilized TiO₂ nanoparticles (NPs) tend to accumulate in wastewater and affect microbial growth. This work investigated the impacts of prolonged TiO₂ NP addition to filamentous aerobic granular sludge (AGS) using two identical sequencing batch reactors (SBRs, R1 and R2). R1 (the control) had no TiO₂ NP addition. In this reactor, filamentous bacteria from large AGS grew rapidly and extended outward, the sludge volume index (SVI₃₀) quickly increased from 41.2 to 236.8 mL/g, mixed liquid suspended solids (MLSS) decreased from 4.72 to 0.9 g/L, and AGS disintegrated on day 40. Meanwhile, the removal rates of COD and NH₄⁺-N both exhibited significant declines. In contrast, 5–30 mg/L TiO₂ NPs was added to R2 from day 21 to 100, and the extended filamentous bacteria were effectively controlled on day 90 under a 30 mg/L NP dosage, leading to significant reductions in COD and NH₄⁺-N capabilities, particularly the latter. Therefore, NP addition was stopped on day 101, and AGS became dominant in R2, with an SVI₃₀ and MLSS of 48.5 mL/g and 5.67 g/L on day 130. COD and NH₄⁺-N capabilities both increased to 100%. Microbial analysis suggested that the dominant filamentous bacteria—Proteobacteria, Bacteroidetes, and Acidobacteria—were effectively controlled by adding 30 mg/L TiO₂ NPs. XRF analysis indicated that 11.7% TiO₂ NP accumulation made the filamentous bacteria a framework for AGS recovery and operation without NPs. Functional analysis revealed that TiO₂ NPs had stronger inhibitory effects on nitrogen metabolism compared to carbon metabolism, and both metabolic pathways recovered when NP addition was discontinued in a timely manner. These findings offer critical operational guidance for maintaining the stable performance of filamentous AGS systems treating TiO₂ NP wastewater in the future. Full article

The contamination of aquatic ecosystems by the micropollutants in wastewater discharges is currently a critical issue. Therefore, the development of novel treatment processes and materials is essential to ensure the availability of safe water. The present study aims to develop a photocatalytic material composed of silver nanoparticles (Ag-NPs)-doped TiO₂ supported on a Pyrex^® plate (TiO₂@Ag-NPs) exhibiting catalytic activity under visible irradiation (λ > 400 nm). The effects of Ag-NPs doping on the TiO₂ matrix, the resistance of the coating at the catalyst/substrate interface, and the photocatalytic degradation efficiency of the photocatalyst for a micropollutant (diuron) of the pesticide family were studied. The photocatalyst was characterised using X-ray diffraction, scanning electron microscopy, ultraviolet–visible spectrophotometry, and scratch tests. The solution concentrations were monitored using high-performance liquid chromatography and total organic carbon analyses. A 32% diuron removal was achieved using photocatalytic TiO₂@Ag-NPs under visible irradiation, whereas undoped TiO₂ showed no activity. Furthermore, the effects of the nanoparticle growth mode on the photocatalytic activity of TiO₂@Ag-NPs were explored. The presence of a TiO₂ sublayer ensured the adhesion of the coating and promoted the dispersion of nanoparticles within the matrix. It ensured chemical continuity (TiO₂@Ag-NPs/Pyrex^®), reduced the bandgap, and decreased electron–hole pair recombination. Full article

In this study, silver nanoparticles (Ag NPs) were synthesized on the surface of rutile-phase titanium dioxide (R-TiO₂) using a plasma-assisted technique. Comprehensive analyses were conducted to investigate the structural, morphological, optical, and electrical properties of the synthesized nanocomposites. Transmission electron microscopy (TEM) images revealed the uniform decoration of Ag NPs (average size: 29.8 nm) on the R-TiO₂ surface. X-ray diffraction (XRD) confirmed the polycrystalline nature of the samples, with decreased diffraction peak intensity indicating reduced crystallinity due to Ag decoration. The Williamson–Hall analysis showed increased crystallite size and reduced tensile strain, suggesting grain growth and stress relief. Raman spectroscopy revealed quenching and broadening of R-TiO₂ vibrational modes, likely due to increased oxygen vacancies. X-ray photoelectron spectroscopy (XPS) confirmed successful plasma-assisted deposition and the coexistence of Ag⁰ and Ag⁺ states, enhancing surface reactivity. UV-Vis spectroscopy demonstrated enhanced light absorption across the spectral range, attributed to localized surface plasmon resonance (LSPR), and a reduced optical bandgap. Dielectric properties, including dielectric constants, loss factor, and AC conductivity, were evaluated across frequencies (4–8 MHz) and temperatures (20–240 °C). The AC conductivity results indicated correlated barrier hopping (CBH) and overlapping large polaron tunneling (OLPT) as the primary conduction mechanisms. Composition-dependent dielectric behavior was interpreted through the Coulomb blockade effect. These findings suggest the potential of plasma assisted Ag NP-decorated R-TiO₂ nanostructures for photocatalysis, sensor and specific electro electrochemical systems applications. Full article

Solar-driven catalytic oxidation processes for the removal of toxic gaseous pollutants have attracted considerable scientific attention, and there is a strong desire to improve the mass transfer, photogenerated charge separation, and O₂ activation by regulating the structure of the photocatalyst. Initially, functionalized graphene–TiO₂ mesoporous hollow nanofibers have been controllably fabricated by a coaxial electrospinning technique, in which functionalized graphene is controllably prepared through a sequential diazonium functionalization and silane modification and ensures its uniform distribution among TiO₂ nanoparticles (NPs). Subsequently, the ultrafine Ag NPs are primarily anchored onto the surface of graphene by an in situ frozen photodeposition strategy, producing Ag/functionalized graphene–TiO₂ mesoporous hollow nanofibers (Ag/SiG-TO MPHNFs). The optimal Ag/SiG-TO MPHNFs exhibit 3.9-fold and 4.6-fold enhancements in CO photooxidation compared with TO MPHNFs and P25 TiO₂, respectively. The enhanced photoactivity can be attributed to three factors: the creation of the mesoporous hollow structure accelerates mass transfer, the incorporation of graphene facilitates the transfer of photogenerated electrons from TiO₂ to graphene, and the anchoring of Ag NPs improves O₂ activation. Full article

Piezo-photocatalysis is a promising solution to address both water pollution and the energy crisis. However, the recombination of electron–hole pairs often leads to poor performance, rendering current piezoelectric photocatalysts unsuitable for industrial water treatment. To overcome this issue, oxygen vacancies (V) and Ag nanoparticles (NPs) are introduced into Bi₄Ti₃O₁₂ (BTO) nanosheets, forming Schottky junctions (BTO-V/Ag). These 2D/3D structures offer more exposed active sites, shorter carrier separation distances, and improved piezo-photocatalytic performance. Additionally, the photothermal effect of Ag NPs supplies additional energy to counteract adsorption changes caused by active species, promoting the generation of more active species. The rate constant of the optimized BTO-V/Ag-2 in the piezo-photocatalytic degradation of nizatidine (NZTD) was 4.62 × 10⁻² min⁻¹ (with a removal rate of 98.34%), which was 4.32 times that of the initial BTO. Moreover, the composite catalyst also showed good temperature and pH response. This study offers new insights into the regulatory mechanisms of piezo-photocatalysis at the Schottky junction. Full article

Ammonia is one of the common inorganic pollutants in surface waters. It can come from a wide range of sources through the discharge of wastewater (industry, agriculture, and municipal waters). Catalytic ozonation reaction can efficiently remove ammonia nitrogen without introducing other pollutants and improve the nitrogen selectivity of reaction products by controlling the reaction conditions. Catalysts based on silver nanoparticles (Ag NPs) have shown excellent O₃ decomposition performance; therefore, they are promising catalysts for catalytic ammonia ozonation due to their high reactivity, stability, and selectivity to N₂. In this study, we synthesized well-defined silver nanoparticles (Ag NPs) using a modified alkaline polyol method and then dispersed them on solid oxide supports (Fe₃O₄, TiO₂, and WO₃). Before being deposited on the oxide support, the silver nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV-VIS spectroscopy. The obtained catalysts, Ag_Fe₃O₄, Ag_TiO₂, and Ag_WO₃ were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), BET surface area analysis, UV-VIS spectroscopy, temperature-programmed reduction (H₂-TPR), and temperature-programmed desorption (TPD) of CO₂ and NH₃. It has been demonstrated that the nature of the support significantly influences the physicochemical properties of the catalysts, as well as their catalytic performance in ammonia ozonation reaction. Full article

In recent years, nanomaterials have gained special attention for removing contaminants from wastewater. Nanoparticles (NPs), such as carbon-based materials and metal oxides, exhibit exceptional adsorption capacity and antimicrobial properties for wastewater treatment. Their unique properties, including reactivity, high surface area, and tunable surface functionalities, make them highly effective adsorbents. They can remove contaminants such as organics, inorganics, pharmaceuticals, medicine, and dyes by adsorption mechanisms. In this review, the effectiveness of different types of carbon-based NPs, including carbon nanotubes (CNTs), graphene-based nanoparticles (GNPs), carbon quantum dots (CQDs), carbon nanofibers (CNFs), and carbon nanospheres (CNSs), and metal oxides, including copper oxide (CuO), zinc oxide (ZnO), iron oxide (Fe₂O₃), titanium oxide (TiO₂), and silver oxide (Ag₂O), in the removal of different contaminants from wastewater has been comprehensively evaluated. In addition, their synthesis methods, such as physical, chemical, and biological, have been described. Based on the findings, CNPs can remove 75 to 90% of pollutants within two hours, while MONPs can remove 60% to 99% of dye in 150 min, except iron oxide NPs. For future studies, the integration of NPs into existing treatment systems and the development of novel nanomaterials are recommended. Hence, the potential of NPs is promising, but challenges related to their environmental impact and their toxicity must be considered. Full article

Bacterial infections are a common cause of clinical complications associated with the use of orthodontic microimplants. Biofilm formation on their surfaces and subsequent infection of peri-implant tissues can result in either exfoliation or surgical removal of these medical devices. In order to improve the properties of microimplants, hybrid coatings enriched with silver nanoparticles, calcium, and phosphorus were investigated. The present study aimed to assess the microstructure of commercially available microimplants composed of a medical TiAlV (Ti6Al4V) alloy covered with organic–inorganic layers obtained by the sol–gel method using the dip-coating technique. The microstructures and elemental surface compositions of the sterile, etched, and layer-modified microimplants were characterized by scanning electron microscopy with X-ray energy-dispersive spectroscopy (SEM-EDS). Elements such as silver (Ag), calcium (Ca), phosphorus (P), silicon (Si), oxygen (O), and carbon (C) were detected on the microimplant’s surface layer. The SEM observations revealed that control microimplants (unetched) had smooth surfaces with only manufacturing-related embossing, while etching in hydrofluoric acid increased the surface roughness and introduced fluoride onto the microimplants. Layers with only silver nanoparticles reduced the roughness of the implant surface, and no extrusion was observed, while increased roughness and emerging porosity were observed when the layers were enriched with calcium and phosphorus. The highest roughness was observed in the microimplants etched with AgNPs and CaP, while the AgNPs-only layer showed a reduction in the roughness average parameter due to lower porosity. Enhancing the effectiveness of microimplants can be achieved by applying selective surface treatments to different parts. By keeping the outer tissue contact area smooth while making the bone contact area rough to promote stronger integration with bone tissue, the overall performance of the implants can be significantly improved. Full article

Sol-gel spin coating method was employed for depositing TiO₂ and Ag-doped TiO₂ films. The effects of Ag doping and the annealing temperatures (300–600 °C) were studied with respect to their structural, morphological, vibrational, and optical properties. Field Emission Scanning Electron microscopy (FESEM) investigation exhibited the grained, compact structures of TiO₂-based films. Ag incorporation resulted in a rougher film surface. X-ray diffraction (XRD) results confirmed the formation of Ag nanoparticles and AgO phase, along with anatase and rutile TiO₂, strongly depending on Ag concentration and technological conditions. AgO fraction diminished after high temperature annealing above 500 °C. The vibrational properties were characterized by Fourier Transform Infrared (FTIR) spectroscopy. It was found that silver presence induced changes in IR bands of TiO₂ films. UV–VIS spectroscopy revealed that the embedment of Ag NPs in titania matrix resulted in higher absorbance across the visible spectral range due to local surface plasmon resonance (LSPR). Ag doping reduced the optical band gap of sol-gel TiO₂ films. The optical and plasmonic modifications of TiO₂:Ag thin films by the number of layers and different technological conditions (thermal and UV treatment) are discussed. Full article

The applications of nanotechnology in the field of water treatment are rapidly expanding and have harvested significant attention from researchers, governments, and industries across the globe. This great interest stems from the numerous benefits, properties, and capabilities that nanotechnology offers in addressing the ever-growing challenges related to water quality, availability, and sustainability. This review paper extensively studies the applications of several nanomaterials including: graphene and its derivative-based adsorbents, CNTs, TiO₂ NPs, ZnO NPs, Ag NPs, Fe NPs, and membrane-based nanomaterials in the purification of drinking water. This, it is hoped, will provide the water treatment sector with efficient materials that can be applied successfully in the water purification process to help in addressing the worldwide water scarcity issue. Full article

As an important trace molecular detection technique, surface-enhanced Raman scattering (SERS) has been extensively investigated, while the realization of simple, low-cost, and controllable fabrication of wafer-scale, flexible SERS-active substrates remains challenging. Here, we report a facile, low-cost strategy for fabricating wafer-scale SERS substrates based on Ag-TiO₂ nanoparticle–film hybrids by combining dip-coating and UV light array photo-deposition. The results show that a centimeter-scale Ag nanoparticle (AgNP) film (~20 cm × 20 cm) could be uniformly photo-deposited on both non-flexible and flexible TiO₂ substrates, with a relative standard deviation in particle size of only 5.63%. The large-scale AgNP/TiO₂ hybrids working as SERS substrates show high sensitivity and good uniformity at both the micron and wafer levels, as evidenced by scanning electron microscopy and Raman measurements. In situ bending and tensile experiments demonstrate that the as-prepared flexible AgNP/TiO₂ SERS substrate is mechanically robust, exhibiting stable SERS activity even in a large bending state as well as after more than 200 tensile cycles. Moreover, the flexible AgNP/TiO₂ SERS substrates show excellent performance in detecting sub-micrometer-sized plastics (≤1 μm) and low-concentration organic pollutants on complex surfaces. Overall, this study provides a simple path toward wafer-scale, flexible SERS substrate fabrication, which is a big step for practical applications of the SERS technique. Full article

Titanium dioxide (TiO₂) is a prevalent food additive, yet comprehensive data on particle size and dietary exposure are lacking in China. Transmission electron microscopy results revealed that the quantitative proportion of nanoparticles (NPs) in food-additive TiO₂ was 37.7%, with a mass fraction of 9.89%. Laboratory test results showed that among the domestic products surveyed, candies excluding gum-based candies contained the highest content of TiO₂. Using consumption data from the China Health and Nutrition Survey in 2018, the average dietary exposure for TiO₂ and TiO₂ NPs in the Chinese population were calculated at 34.84 and 3.44 μg/kg bw/day, respectively. The primary dietary sources were puffed food and powdered drinks. Exposure varied significantly across age and region, with children and Inner Mongolia residents having the highest intake. TiO₂ NP exposure showed a negative correlation with age. Despite this, the dietary exposure risk of TiO₂ NPs for the Chinese population remains deemed acceptable. Full article

The ever-increasing expansion of chemical industries produces a variety of common pollutants, including colors, which become a global and environmental problem. Using a nanocatalyst is one of the effective ways to reduce these organic contaminants. With this in mind, a straightforward and effective method for the production of a novel nanocatalyst based on lignin-derived carbon, titanium dioxide nanoparticles, and Ag particles (TiO₂/C/Ag) is described. The preparation of carbon and Ag particles (in sub-micro and nano size) was carried out by laser ablation in air. The nanocomposite was synthesized using a facile magnetic stirrer of TiO₂, C, and Ag. According to characterization methods, a carbon nanostructure was successfully synthesized through the laser irradiation of lignin. According to scanning electron microscope images, spherical Ag particles were agglomerated over the nanocomposite. The catalytic activities of the TiO₂/C/Ag nanocomposite were tested for the decolorization of methylene blue (MB) and Congo red (CR), employing NaBH₄ in a water-based solution at 25 °C. After adding fresh NaBH₄ to the mixture of nanocomposite and dyes, both UV absorption peaks of MB and CR completely disappeared after 10 s and 4 min, respectively. The catalytic activity of the TiO₂/C/Ag nanocomposite was also examined for the reduction of 4-nitrophenol (4-NP) using a NaBH₄ reducing agent, suggesting the complete reduction of 4-NP to 4-aminophenol (4-AP) after 2.30 min. This shows excellent catalytic behavior of the prepared nanocomposite in the reduction of organic pollutants. Full article

This study aims to improve the photocatalytic properties of titanium dioxide nanorods (TNRs) and other related nanostructures (dense nanorods, needle-like nanorods, nanoballs, and nanoflowers) by modifying them with silver nanoparticles (AgNPs). This preparation is carried out using a two-step method: sol–gel dip-coating deposition combined with hydrothermal crystal growth. Further modification with AgNPs was achieved through the photoreduction of Ag⁺ ions under UV illumination. The investigation explores the impact of different growth factors on the morphological development of TiO₂ nanostructures by modulating (i) the chemical composition, the water:acid ratio, (ii) the precursor concentration involved in the hydrothermal process, and (iii) the duration of the hydrothermal reaction. Morphological characteristics, including the length, diameter, and nanorod density of the nanostructures, were analyzed using scanning electron microscope (SEM). The chemical states were determined through use of the X-ray photoelectron spectroscopy (XPS) technique, while phase composition and crystalline structure analysis was performed using the Grazing Incidence X-ray Diffraction (GIXRD) method. The results indicate that various nanostructures (dense nanorods, needle-like nanorods, nanoballs, and nanoflowers) can be obtained by modifying these parameters. The photocatalytic efficiency of these nanostructures and Ag-coated nanostructures was assessed by measuring the degradation of the organic dye rhodamine B (RhB) under both ultraviolet (UV) irradiation and visible light. The results clearly show that UV light causes the RhB solution to lose its color, whereas under visible light RhB changes into rhodamine 110, indicating a successful photocatalytic transformation. The nanoball-like structures’ modification with the active metal silver (TNRs 4 Ag) exhibited high photocatalytic efficiency under both ultraviolet (UV) and visible light for different chemical composition parameters. The nanorod structure (TNRs 2 Ag) is more efficient under UV, but under visible-light photocatalyst, the TNRs 6 Ag (dense nanorods) sample is more effective. Full article

Volatile organic compounds (VOCs) are representative indoor air pollutants that negatively affect the human body owing to their toxicity. One of the most promising methods for VOC removal is photocatalytic degradation using TiO₂. In this study, the addition of carbon black (CB) and heavy metal nanoparticles (NPs) was investigated to improve the efficiency of a TiO₂-based photocatalytic VOC decomposition system combined with ultrasonic atomization and ultraviolet irradiation, as described previously. The addition of CB and Ag NPs significantly improved the degradation efficiency. A comparison with other heavy metal nanoparticles and their respective roles are discussed. Full article