Search Results (863)

This study investigates the significant impact of metal–support interactions on catalytic reaction mechanisms at the interface of oxide-supported metal nanoparticles. The distinct and contrasting effects of SiO₂ and TiO₂ supports on reaction dynamics using NaBD₄ were studied and focused on the relative yields of [HD]/[H₂] and [D₂]/[H₂]. The findings show a consistent increase in HD yields with rising [BD₄⁻] concentrations. Notably, the sequence of HD yield enhancement follows the order of TiO₂-Au⁰-NPs < Au⁰-NPs < SiO₂-Au⁰-NPs. Conversely, the rate of H₂ evolution during BH₄^- hydrolysis exhibits an inverse trend, with TiO₂-Au⁰-NPs outperforming the others, followed by Au⁰-NPs and SiO₂-Au⁰-NPs, demonstrating the opposing effects exerted by the TiO₂ and SiO₂ supports on the catalytic processes. Further, the catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) confirms the catalytic mechanism, with TiO₂-Au⁰-NPs demonstrating superior activity. The catalytic activity observed aligns with the order of TiO₂-Au⁰-NPs > Au⁰-NPs > SiO₂-Au⁰-NPs, suggesting that SiO₂ donates electrons to Au⁰-NPs, while TiO₂ withdraws them. It is of interest to note that two very different processes, that clearly proceed via different mechanisms, are affected similarly by the supports. This study reveals that the choice of support material influences catalytic activity, impacting overall yield and efficiency. These findings underscore the importance of selecting appropriate support materials for tailored catalytic outcomes. Full article

This research aims to evaluate the efficacy of Mouromtseff’s numbers in assessing the thermal transfer performance of titanium oxide (TiO₂) nanosized dispersions in convective heat transfer through a pipe. New experimental coefficients of convective heat transfer, thermophysical and rheological characterisation are carried out for TiO₂-based nanodispersions in an aqueous propylene glycol 30 vol% mixture at various nanoadditive mass loadings (from 0.25 to 2.0 wt%). Different Mouromtseff’s number formulations, including the Dittus–Boelter and Simons expressions, were obtained from experimental data of thermophysical properties, enabling concise analyses on the prospective improvement of heat transfer in cooling and heating systems. The morphology, particle size, and crystallinity of the anatase TiO₂ nanopowder were confirmed, and the stability of the nanofluids with various surfactants was evaluated, with PSS at a 1:4 mass ratio being optimal. Slight increments in thermal conductivity (up to 1.5%) and density (up to 1.3%) with nanoparticle loading were observed, while isobaric heat capacity presents a decreasing trend (less than 13%). Dynamic viscosity increases with higher nanoadditive concentrations, 8.8% for the 2.0 wt% A-TiO₂/PG:W 30:70 + PSS 1:4 nanofluid. The employed Dittus–Boelter and Simons expressions correctly predict a worsening of the convective heat transfer, but the percentages diverge slightly from experimental data. Full article

Recently, Pd catalysts supported on magnetic nanoparticles (MNPs) have attracted a great attention due to their ability of easy separation with an external magnet. Modification of MNPs is successfully used to obtain Pd magnetic catalysts with enhanced catalytic activity. In this work, we discussed the effect of titania content in TiO₂/MNPs support materials on catalytic properties of Pd@TiO₂/MNPs catalysts in phenylacetylene hydrogenation. TiO₂/MNPs composites were prepared by simple ultrasound-assisted mixing of TiO₂ and MNPs, synthesized by co-precipitation method. This was followed by deposition of palladium ions on the mixed metal oxides using NaOH as precipitant. The supports and catalysts were characterized using XRD, BET, STEM, EDX, XPS, and a SQUID magnetometer. Pd nanoparticles (5–6 nm) formed were found to be homogeneously distributed on support materials representing the well-mixed metal oxides with TiO₂ content of 10, 30, 50, or 70%wt. Testing of the catalysts in phenylacetylene hydrogenation showed that their activity increased with increasing TiO₂ content, and the process was faster in alkali medium (pH = 10). The hydrogenation rates of triple and double C–C bonds on Pd@70TiO₂/MNPs achieved 9.3 × 10⁻⁶ mol/s and 23.1 × 10⁻⁶ mol/s, respectively, and selectivity to styrene was 96%. The catalyst can be easily recovered with an external magnet and reused for 12 runs without significant degradation in the catalytic activity. The improved catalytic properties of Pd@70TiO₂/MNPs can be explained by the fact that the surface of the support is mainly composed of TiO₂ particles, affecting the state and size of Pd species. Full article

This work examined the influence of UV-A light modulation on the photocatalytic process coadjuvated with H₂O₂ to mineralize phenol in an aqueous solution. A fixed-bed batch photocatalytic reactor with a flat-plate geometry, irradiated by UV-A LEDs, was employed. The successful deposition of commercial TiO₂ PC105 on a steel plate (SP) was achieved, and the structured photocatalyst was characterized using Raman spectroscopy, specific surface area (SSA) measurements, and UV–vis DRS analysis. These analyses confirmed the formation of a titania coating in the anatase phase with a bandgap energy of 3.25 eV. Various LED-dimming techniques, with both fixed and variable duty cycle values, were tested to evaluate the stability of the photocatalyst’s activity and the influence of operating parameters during the mineralization of 450 mL of a phenol solution. The optimal operating parameters were identified as an initial phenol concentration of 10 ppm, a hydrogen peroxide dosage of 0.208 g L⁻¹, and triangular variable duty cycle light modulation. Under these conditions, the highest apparent phenol degradation kinetic constant (0.39 min⁻¹) and the total mineralization were achieved. Finally, the energy consumption for mineralizing 90% phenol in one cubic meter of treated water was determined, showing the greatest energy savings with triangular light modulation. Full article

TiO₂ nanoparticles (NPs) doped with W (W:TiO₂), double-doped with W and V (W&V:TiO₂), and loaded with noble metals (W:TiO₂ @Pt/Pd/Ag and W&V:TiO₂@Pt/Pd/Ag) were synthesized by laser pyrolysis followed by chemical impregnation and reduction. Due to its exceptional properties, TiO₂ is considered a key material being used in a wide range of applications. To improve its detection activity, the increase in the specific surface of the material, and the presence of defects in its structure play a decisive role. Doped and double-doped TiO₂ nanoparticles with dimensions in the range of 25–30 nm presented a mixture of phases corresponding to titania, with the anatase phase accounting for the majority (95%). By loading these nanoparticles with small particles of noble metals, a significant increase in the specific surface area by three or even five times the original values was achieved. Sensitive thin films for surface acoustic wave (SAW) sensors were made with the NPs, embedded in polyethyleneimine (PEI) polymer and deposited by spin-coating. Each sensor was tested at CH₄ concentrations between 0.4 and 2%, at room temperature, and the best results were obtained by the sensor with NPs doped with V and decorated with Pd, with a limit of detection (LOD) of 17 ppm, due to the strong catalytic effect of Pd. Full article

Titanium dioxide was synthesized via hydrolysis of titanium (IV) isopropoxide using a sol–gel method, under neutral or basic conditions, and heated in the microwave-assisted solvothermal reactor and/or high-temperature furnace. The phase composition of the prepared samples was determined using the X-ray diffraction method. The specific surface area and pore volumes were determined through low-temperature nitrogen adsorption/desorption studies. The photoactivity of the samples was tested through photocatalytic reduction of carbon dioxide. The composition of the gas phase was analyzed using gas chromatography, and hydrogen, carbon oxide, and methane were identified. The influence of pH and heat treatment on the physicochemical properties of titania-based materials during photoreduction of carbon dioxide have been studied. It was found that the photocatalysts prepared in neutral environment were shown to result in a higher content of hydrogen, carbon monoxide, and methane in the gas phase compared to photocatalysts obtained under basic conditions. The highest amounts of hydrogen were detected in the processes using photocatalysts heated in the microwave reactor, and double-heated photocatalysts. Full article

Hollow mesoporous hydroxyapatite (HM-HAP) composites coated with titania are prepared to increase the stability and catalytic performance of titania for azo dyes present in the wastewater system. In this work, HM-HAP particles were first synthesized by a hydrothermal method utilizing the CaCO₃ core as a template and then coated with titania to form TiO₂/HM-HAP composites. Utilizing SEM, XRD, XPS, BET, FTIR, EDS, UV–vis DRS spectroscopy, and point of zero charge (PZC) analysis, the coating morphological and physicochemical parameters of the produced samples were analyzed. The photocatalytic efficiency of the synthesized coated composites was assessed by the degradation of methyl red (MR) dye in water. The results indicated that TiO₂/HM-HAP particles could efficiently photodegrade MR dye in water under UV irradiation. The 20% TiO₂/HM-HAP coating exhibited high catalytic performance, and the degradation process was followed by the pseudo-first-order (PFO) kinetic model with a rate constant of 0.033. The effect of pH on the degradation process was also evaluated, and the maximum degradation was observed at pH 6. The analysis of degraded MR dye products was investigated using LC-MS and FTIR analysis. Finally, a good support material, HM-HAP for TiO₂ coatings, which provides a large number of active adsorption sites and has catalytic degradation performance for MR dye, was revealed. Full article

Industrial activities generate enormous quantities of polluted effluents, necessitating advanced methods of wastewater treatment to prevent potential environmental threats. Thus, the design of a novel photocatalytic reactor for industrial water decontamination, purification, and reuse is proposed as an efficient advanced oxidation technology. In this work, the development of the active reactor components is described, utilizing a two-step sol–gel technique to prepare a silica-titania trilayer coating on 3D-printed polymeric filters. The initial dip-coated SiO₂ insulator further protects and enhances the stability of the polymer matrix, and the subsequent TiO₂ layers endow the composite architecture with photocatalytic functionality. The structural and morphological characteristics of the modified photocatalytic filters are extensively investigated, and their performance is assessed by studying the photocatalytic degradation of the Triton X-100, a common and standard chemical surfactant, presented in the contaminated wastewater of the steel metal industry. The promising outcomes of the innovative versatile reactor pave the way for developing scalable, cost-effective reactors for efficient water treatment technologies. Full article

Black titania, a conductive ceramic material class, has garnered significant interest due to its unique optical and electrochemical properties. However, synthesising and properly characterising these structures pose a considerable challenge. This diverse material family comprises various titanium oxide phases, many of them non-stoichiometric. The term “black TiO₂” was first introduced in 2011 by Xiaobo Chen, but Arne Magneli’s groundbreaking discovery and in-depth investigation of black titania in 1957 laid the foundation for our understanding of this material. The non-stoichiometric black titanium oxides were then called the Magneli phases. Since then, the science of black titania has advanced, leading to numerous applications in photocatalysis, electrocatalysis, supercapacitor electrodes, batteries, gas sensors, fuel cells, and microwave absorption. Yet, the literature is rife with conflicting reports, primarily due to the inadequate analysis of black titania materials. This review aims to provide an overview of black titania nanostructures synthesis and the proper characterisation of the most common and applicable black titania phases. Full article

Steel structures located in subtropical marine climates face harsh conditions such as strong sunlight and heavy rain, and they are extremely corroded. In this study, a waterborne coating with excellent corrosion resistance, hydrophobic ability, high-temperature resistance and high density was successfully prepared by using modified nanoscale titania powders and grafted polymers. The effects of three modifiers on titania nanoparticles and waterborne coatings’ properties were studied independently. The experimental results showed that the activation index of the modification employing methacryloxy silane reached 97.5%, which achieved the best modification effect at 64.4 °C for 43.3 min. The waterborne coating with nanoscale titania modified by methacryloxy silane exhibited the best hydrophobic effect, with a drop contact angle of 115.4° and excellent heat resistance of up to 317.2 °C. The application of the waterborne modified coating in steel structures under subtropical maritime climates showed that the waterborne titania coatings demonstrated excellent resistance to corrosion, high temperatures and harsh sunlight, with a maximum service life of up to five years. Economic analysis indicated that, considering a conservative three-year effective lifespan, this coating could save more than 50% in cost compared with conventional industrial coatings. Finally, the strengthening mechanism of the polymer coatings with modified nanoscale titania was analyzed. Full article

Titania nanoparticles (NPs) find wide application in photocatalysis, photovoltaics, gas sensing, lithium batteries, etc. One of the most important synthetic challenges is maintaining control over the polymorph composition of the prepared nanomaterial. In the present work, TiO₂ NPs corresponding to anatase, rutile, or an anatase/rutile/brookite mixture were obtained at 80 °C by an inverse microemulsion method in a ternary system of water/cetyltrimethylammonium bromide/1-hexanol in a weight ratio of 17:28:55. The only synthesis variables were the preparation of the aqueous component and the nature of the Ti precursor (Ti(IV) ethoxide, isopropoxide, butoxide, or chloride). The materials were characterized with X-ray diffraction, scanning/transmission electron microscopy, N₂ adsorption–desorption isotherms, FTIR and Raman vibrational spectroscopies, and diffuse reflectance spectroscopy. The synthesis products differed significantly not only in phase composition, but also in crystallinity, textural properties, and adsorption properties towards water. All TiO₂ NPs were active in the photocatalytic decomposition of rhodamine B, a model dye pollutant of wastewater streams. The mixed-phase anatase/rutile/brookite nanopowders obtained from alkoxy precursors showed the best photocatalytic performance, comparable to or better than the P25 reference. The exceptionally high photoactivity was attributed to the advantageous electronic effects known to accompany multiphase titania composition, namely high specific surface area and strong surface hydration. Among the single-phase materials, anatase samples showed better photoactivity than rutile ones, and this effect was associated, primarily, with the much higher specific surface area of anatase photocatalysts. Full article

Rehabilitation of fully or partially edentulous patients with dental implants represents one of the most frequently used surgical procedures. The work of Branemark, who observed that a piece of titanium embedded in rabbit bone became firmly attached and difficult to remove, introduced the concept of osseointegration and revolutionized modern dentistry. Since then, an ever-growing need for improved implant materials towards enhanced material–tissue integration has emerged. There is a strong belief that nanoscale materials will produce a superior generation of implants with high efficiency, low cost, and high volume. The aim of this review is to explore the contribution of nanomaterials in implantology. A variety of nanomaterials have been proposed as potential candidates for implant surface customization. They can have inherent antibacterial properties, provide enhanced conditions for osseointegration, or act as reservoirs for biomolecules and drugs. Titania nanotubes alone or in combination with biological agents or drugs are used for enhanced tissue integration in dental implants. Regarding immunomodulation and in order to avoid implant rejection, titania nanotubes, graphene, and biopolymers have successfully been utilized, sometimes loaded with anti-inflammatory agents and extracellular vesicles. Peri-implantitis prevention can be achieved through the inherent antibacterial properties of metal nanoparticles and chitosan or hybrid coatings bearing antibiotic substances. For improved corrosion resistance various materials have been explored. However, even though these modifications have shown promising results, future research is necessary to assess their clinical behavior in humans and proceed to widespread commercialization. Full article

This work demonstrates a completely wet-chemical procedure for the fabrication of a functional impedimetric humidity-sensing device on a titania (TiO₂) surface. Optically transparent anatase TiO₂ thin films were deposited on a glass substrate via dip-coating from a titanium tetraisopropoxide (TTIP)–acetylacetonate (AA)-based sol and surface-functionalized with a nickel oxide (NiO_x) layer by ultraviolet (UV) photodeposition. Photodeposition was employed to form the interdigitated electrode pattern on the TiO₂ surface as well through activation with a silver catalyst to promote electroless copper deposition. The relative humidity (RH) response of the pristine TiO₂- and NiO_x/TiO₂-functionalized sensors was studied by impedance (Z) measurements in the 15%–90% RH range. It was found that while NiO_x functionalization significantly dampens the RH–Z functional dependence, it improves its overall linearity and may successfully be employed for the purposeful design of titania-based sensing devices. Full article

Rolling is one of the most important processes in the metallurgical industry due to its versatility. Despite its inherent advantages, design and manufacturing by rolling still rely on trial-and-error-based optimizations, which reduces its efficiency. To minimize the cost and time spent on the development of new rolling schedules, various analytical and numerical methods have been used in recent years. Among other alternatives, simulations based on the finite element method (FEM) are the most widely used. This allows for the analysis of the feasibility of new rolling schedules considering metal alloys with different characteristics, process conditions, or the creation of new operations, as well as the optimization of existing ones. This paper presents a literature review including the latest developments in the field of numerical simulation of rolling processes, which have been classified according to the type of rolling into the following categories: flat rolling, shape rolling, ring rolling, cross-wedge rolling, skew rolling, and tube piercing. Full article

The behavior of technical nanoparticles at high temperatures was measured systematically to detect morphology changes under conditions relevant to the thermal treatment of end-of-life products containing engineered nanomaterials. The focus of this paper is on laboratory experiments, where we used a Bunsen-type burner to add titania and ceria particles to a laminar premixed flame. To evaluate the influence of temperature on particle size distributions, we used SMPS, ELPI and TEM analyses. To measure the temperature profile of the flame, we used coherent anti-Stokes Raman spectroscopy (CARS). The comprehensible data records show high temperatures by measurement and equilibrium calculation for different stoichiometries and argon admixtures. With this, we show that all technical metal oxide nanoparticle agglomerates investigated reform in flames at high temperatures. The originally large agglomerates of titania and ceria build very small nanoparticles (<10 nm/“peak 2”) at starting temperatures of <2200 K and <1475 K, respectively (ceria: T_melt = 2773 K, T_boil = 3873 K/titania: T_melt = 2116 K, T_boil = 3245 K). Since the maximum flame temperatures are below the evaporation temperature of titania and ceria, enhanced vaporization of titania and ceria in the chemically reacting flame is assumed. Full article