Search Results (854)

Background/Objectives: Magnetic nanoparticles, particularly iron oxide-based materials, such as magnetite (Fe₃O₄), have gained significant attention as contrast agents in medical imaging This study aimsto syntheze and characterize Fe₃O₄-based core–shell nanostructures, including Fe₃O₄@TiO₂ and Fe₃O₄@SiO₂, and to evaluate their potential as tunable contrast agents for diagnostic imaging. Methods: Fe₃O₄, Fe₃O₄@TiO₂, and Fe₃O₄@SiO₂ nanoparticles were synthesized via co-precipitation at varying temperatures from iron salt precursors. Fourier transform infrared spectroscopy (FTIR) was used to confirm the presence of Fe–O bonds, while X-ray diffraction (XRD) was employed to determine the crystalline phases and estimate average crystallite sizes. Morphological analysis and particle size distribution were assessed by scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX) and transmission electron microscopy (TEM). Magnetic properties were investigated using vibrating sample magnetometry (VSM). Results: FTIR spectra exhibited characteristic Fe–O vibrations at 543 cm⁻¹ and 555 cm⁻¹, indicating the formation of magnetite. XRD patterns confirmed a dominant cubic magnetite phase, with the presence of rutile TiO₂ and stishovite SiO₂ in the coated samples. The average crystallite sizes ranged from 24 to 95 nm. SEM and TEM analyses revealed particle sizes between 5 and 150 nm with well-defined core–shell morphologies. VSM measurements showed saturation magnetization (Ms) values ranging from 40 to 70 emu/g, depending on the synthesis temperature and shell composition. The highest Ms value was obtained for uncoated Fe₃O₄ synthesized at 94 °C. Conclusions: The synthesized Fe₃O₄-based core–shell nanomaterials exhibit desirable structural, morphological, and magnetic properties for use as contrast agents. Their tunable magnetic response and nanoscale dimensions make them promising candidates for advanced diagnostic imaging applications. Full article

High-titanium steel contains an elevated titanium content, which promotes the formation of abundant non-metallic inclusions in molten steel at high temperatures, including titanium oxides, sulfides, and nitrides. These inclusions adversely affect continuous casting operations and generate substantial internal/surface defects in cast slabs, ultimately compromising product performance and service reliability. Therefore, stringent control over the size, distribution, and population density of inclusions is imperative during the smelting of high-titanium steel to minimize their detrimental effects. In this paper, samples of high titanium steel (0.4% Ti, 0.004% N) casting billets were analyzed by industrial test sampling and full section comparative analysis of the samples at the center and quarter position. Using the Particle X inclusions, as well as automatic scanning and analyzing equipment, the number, size, location distribution, type and morphology of inclusions in different positions were systematically and comprehensively investigated. The results revealed that the primary inclusions in the steel consisted of TiN, TiS, TiC and their composite forms. TiN inclusions exhibited a size range of 1–5 µm on the slab surface, while larger particles of 2–10 μm were predominantly observed in the interior regions. Large-sized TiN inclusions (5–10 μm) are particularly detrimental, and this problematic type of inclusion predominantly concentrates in the interior regions of the steel slab. A gradual decrease in TiN inclusion number density was identified from the surface toward the core of the slab. Thermodynamic and kinetic calculations incorporating solute segregation effects demonstrated that TiN precipitates primarily in the liquid phase. The computational results showed excellent agreement with experimental data regarding the relationship between TiN size and solidification rate under different cooling conditions, confirming that increased cooling rates lead to reduced TiN particle sizes. Both enhanced cooling rates and reduced titanium content were found to effectively delay TiN precipitation, thereby suppressing the formation of large-sized TiN inclusions in high-titanium steels. Full article

In order to improve the hydrogen storage properties of Laves phase AB₂-type alloys, a series of Ti_1−xZr_xMn_1.0Cr_0.85Fe_0.1 (x = 0.1–0.5) alloys were prepared by arc melting. The effects of Zr content on microstructure and hydrogen storage properties was investigated in detail. Crystal structure characterizations confirmed that all the alloys exhibit a single-phase C14 Laves structure, and the lattice parameters increase with increasing Zr content. The hydrogen storage measurements of the alloys indicate that with increasing Zr content, the hydrogen storage capacity initially increases and then decreases. The hydrogen absorption and desorption measurements of the alloys were performed by a Sieverts-type apparatus. Pressure–composition–temperature (P-C-T) tests at various temperatures showed that all the alloys display sloped plateaus. Increasing Zr content results in a gradual decrease in hydrogen absorption and desorption plateau pressures. Moreover, these alloys exhibit varying degrees of hysteresis, which also becomes more pronounced with a rise in Zr content. In summary, the Ti_0.7Zr_0.3Mn_1.0Cr_0.85Fe_0.1 alloy demonstrates the best comprehensive hydrogen storage capacity. Further investigation on the cyclic performance of the Ti_0.7Zr_0.3Mn_1.0Cr_0.85Fe_0.1 alloy was conducted. It was found that the alloy particles undergo significant pulverization after hydrogenation cycles, but the alloy maintained good phase structure stability and hydrogen storage performance. Full article

The sustainable valorization of electrolytic manganese residue (EMR) and fly ash (FA) presents critical environmental challenges. This study systematically investigates the performance optimization of EMR-FA ceramic composites through the coordinated regulation of raw material ratios, sintering temperatures, and additive effects. While the composite with 85 g FA exhibits the highest mechanical strength, lowest porosity, and minimal water absorption, the formulation consisting of 45 wt% EMR, 40 wt% FA, and 15 wt% kaolin is identified as a balanced composition that achieves an effective compromise between mechanical performance and solid waste utilization efficiency. Sintering temperature studies revealed temperature-dependent property enhancement, with controlled sintering at 1150 °C preventing the over-firing phenomena observed at 1200 °C while promoting phase evolution. XRD-SEM analyses confirmed accelerated anorthite formation and the morphological transformations of FA spherical particles under thermal activation. Additive engineering demonstrated that 8 wt% CaO addition enhanced structural densification through hydrogrossular crystallization, whereas Na₂SiO₃ induced sodium-rich calcium silicate phases that suppressed anorthite development. Contrastingly, ZrO₂ facilitated zircon nucleation, while TiO₂ enabled progressive performance enhancement through amorphous phase modification. This work establishes fundamental phase–structure–property relationships and provides actionable engineering parameters for sustainable ceramic production from industrial solid wastes. Full article

The development of non-noble metal catalysts for gas-phase propylene epoxidation with H₂/O₂ remains challenging due to their inadequate activity and stability. Herein, we report a Cs⁺-modified Ni/TS-1 catalyst (9%Ni-Cs/TS-1), which exhibits unprecedented catalytic performance, giving a state-of-the-art PO formation rate of 382.9 g_PO·kg_cat⁻¹·h⁻¹ with 87.8% selectivity at 200 °C. The catalyst stability was sustainable for 150 h, far surpassing reported Ni-based catalysts. Ni/TS-1 exhibited low catalytic activity. However, the Cs modification significantly enhanced the performance of Ni/TS-1. Furthermore, the intrinsic reason for the enhanced performance was elucidated by multiple techniques such as XPS, N₂ physisorption, TEM, ²⁹Si NMR, NH₃-TPD-MS, UV–vis, and so on. The findings indicated that the incorporation of Cs⁺ markedly boosted the reduction of Ni, enhanced Ni⁰ formation, strengthened Ni-Ti interactions, reduced acid sites to inhibit PO isomerization, improved the dispersion of Ni nanoparticles, reduced particle size, and improved the hydrophobicity of Ni/TS-1 to facilitate propylene adsorption/PO desorption. The 9%Ni-Cs/TS-1 catalyst demonstrated exceptional performance characterized by a low cost, high activity, and long-term stability, offering a viable alternative to Au-based systems. Full article

The laser cladding (LC) of titanium matrix composite coatings (TMCCs) on titanium components not only effectively enhances the wear resistance, fatigue resistance, corrosion resistance, and biocompatibility of titanium and its alloys, but also circumvents the incompatibility and low bonding strength issues associated with other metallic composite coatings. While the incorporation of ceramic particles is a critical strategy for improving the coating performance, the limited interfacial bonding strength between ceramic particles and the matrix has historically constrained its advancement. To further elevate its performance and meet the demands of components operating in harsh environments, researchers worldwide have employed LC to synthesize in situ hard ceramic reinforcements such as TiC, TiB, TiN, and others within TMCCs on titanium substrates. This approach successfully addresses the aforementioned challenges, achieving coatings that combine a high interfacial bonding strength with superior mechanical properties. This paper provides a comprehensive review of the processing techniques, phase composition, microstructure, and mechanical properties of in situ-synthesized ceramic-reinforced TMCCs via LC on titanium components, with a focused summary of their strengthening mechanisms. Furthermore, it critically discusses the challenges and future prospects for advancing this technology. Full article

In this study, we delve into the intricate microstructural features of Ti-6Al-4V alloy additively manufactured and heat-treated at 800 °C for 4 h. Our in-depth analysis will enable us to gain a better understanding of the β-Ti precipitation process, its dependence on temperature, and its ultimate effect on the overall mechanical properties. As well as α-Ti martensite grains and β-Ti particles interspersed in the α-Ti grain boundaries, there is a third microstructural feature, overlooked by many researchers. This feature is observed as nano-sized particles homogeneously embedded inside the α-Ti laths. Using high-resolution transmission electron microscopy, we reveal that these nano-sized features do not constitute a different phase. Instead, they define isolated regions of α-Ti in its relaxed form, surrounded by the heavily strained form of the α-Ti phase. This phenomenon is a result of the “incomplete” precipitation of the β-Ti phase following the heat treatment stage. The straining of the α-Ti phase appears as a shift in the equilibrium atomic position. Full article

This study investigates the industrial potential of red gypsum (RG), a major by-product of titanium dioxide (TiO₂) production, for the development of thermoplastic polypropylene (PP)-based composites via melt extrusion, targeting agricultural applications. Prior to compounding, RG was thermally treated at approximately 200 °C to remove residual moisture and chemically bound water, resulting in its anhydrous form (CaSO₄). PP/RG composites were then formulated with RG loadings up to 20 wt.%, employing stearic acid (SA) as a compatibilizer. The resulting materials were thoroughly characterized and successfully processed through industrial-scale injection molding up to 250 °C. Morphological and FTIR analyses confirmed the role of SA in enhancing both filler dispersion and interfacial adhesion between RG and the PP matrix. SEM images revealed finer and more uniformly distributed RG particles, resulting in a reduced loss of ductility and elongation at break typically associated with filler addition. Specifically, the Young’s Modulus increased from 1.62 GPa (neat PP) up to 3.21 GPa with 20 wt.% RG and 0.6 wt.% SA. The addition of 0.6 wt.% SA also helped limit the reduction in stress at break from 46.68 MPa (neat PP) to 34.05 MPa and similarly mitigated the decrease in Charpy impact energy, which declined slightly from 2.66 kJ/m² (neat PP) to 2.24 kJ/m² for composites containing 20 wt.% RG. Preliminary phytotoxicity was assessed using germination tests on Lepidium sativum L. seeds. Eluates from both untreated and SA-treated RG powders resulted in germination indices below 80%, indicating phytotoxicity likely due to high sulfate ion concentrations. In contrast, eluates from composite pellets exhibited germination indices equal to or exceeding 100%, demonstrating the absence of phytotoxic effects. These results highlight the suitability of the developed composites for applications in floriculture and horticulture. The optimized composite pellets were successfully processed via injection molding to manufacture plant pots, which exhibited a dark brown coloration, confirming the effective pigmenting function of RG. These results demonstrate the potential of red gypsum to serve both as a functional filler and pigment in PP composites, providing a sustainable alternative to iron oxide pigments and promoting the valorization of industrial waste through resource recovery. Full article

Membrane fouling poses a significant challenge in the widespread adoption and cost-effective operation of membrane technology. Among different strategies to mitigate fouling, dynamic membrane (DM) technology has emerged as a promising one for effective control and mitigation of membrane fouling. Silicon carbide (SiC) membranes have attracted considerable attention as membrane materials due to their remarkable advantages, yet membrane fouling is still inevitable in challenging separation tasks, such as oil-in-water (O/W) emulsion separation, and thus effective mitigation of membrane fouling is essential to maximize their economic viability. This study investigates the use of pre-deposited oxide DMs to mitigate the fouling of SiC membranes during the separation of O/W emulsions. Among five screened oxides (Fe₂O₃, SiO₂, TiO₂, ZrO₂, Al₂O₃), SiO₂ emerged as the most effective DM material due to its favorable combination of particle size, negative surface charge, hydrophilicity, and underwater oleophobicity, leading to minimized oil droplet adhesion via electrostatic repulsion to DM surfaces and enhanced antifouling performance. Parameter optimization in dead-end mode revealed a DM deposition amount of 300 g/m², a transmembrane pressure (TMP) of 0.25 bar, and a backwashing pressure of 2 bar as ideal conditions, achieving stable oil rejection (~93%) and high pure water flux recovery ratios (FRR, >90%). Cross-flow filtration outperformed dead-end mode, maintaining normalized permeate fluxes of ~0.4–0.5 (cf. ~0.2 in dead-end) and slower FRR decline, attributed to reduced concentration polarization and enhanced DM stability under tangential flow. Optimal cross-flow conditions included a DM preparation time of 20 min, a TMP of 0.25 bar, and a flow velocity of 0.34 m/s. The results establish SiO₂-based DMs as a cost-effective strategy to enhance SiC membrane longevity and efficiency in O/W emulsion separation. Full article

Electrocatalytic urea synthesis offers great potential for sustainable strategies through CO₂ and NO₃⁻ reduction reactions. However, the development of high-performance catalysts is often hampered by the complexity of synthetic methodologies and the unresolved nature of C-N coupling pathways. In this study, we present a copper–indium co-doped titanium dioxide (CuIn-TiO₂) catalyst that exhibits remarkable efficacy in enhancing the synergistic reduction of CO₂ and NO₃⁻ to produce urea. The bimetallic CuIn site functions as the primary active site for the C-N coupling reaction, achieving a urea yield rate of 411.8 μg h⁻¹ mg_cat⁻¹ with a Faradaic efficiency of 6.7% at −0.8 V versus reversible hydrogen electrode (vs. RHE). A body of experimental and theoretical research has demonstrated that the nanoscale particles enhance the density of active sites and improve the feasibility of reactions on the surface of TiO₂. The co-doping of Cu and In has been shown to significantly enhance electronic conductivity, increase the adsorption affinity for *CO₂ and *NO₃⁻, and promote the C-N coupling process. The CuIn-TiO₂ catalyst has been demonstrated to effectively promote the reduction of NO₃⁻ and CO₂, as well as accelerate the C-N coupling reaction. This effect is a result of a synergistic interaction among the catalyst’s components. Full article

Aluminum, boron, and titanium microalloyed into high-strength low-alloy boron steel exhibit a complex interplay, competing for nitrogen, with titanium demonstrating the highest affinity, followed by boron and aluminum. This competition affects the formation and distribution of nitrides, impacting the microstructure and mechanical properties of the steel. Titanium protects boron from forming BN and facilitates the nucleation of acicular ferrite, enhancing toughness. The segregation of boron to grain boundaries, rather than its precipitation as boron nitride, promotes the formation of martensite and thus the through-hardenability. Aluminum nitride is critical in controlling grain size through a pronounced pinning effect. In this study, we employ energy- and wavelength-dispersive X-ray spectroscopy and computer-aided particle analysis to analyze the phase content of 12 high-purity vacuum induction-melted samples. The primary objective of this study is to correctly describe the microstructural evolution in the Fe-Al-B-Ti-C-N system using the Calphad approach, with special emphasis on correctly predicting the dissolution temperatures of nitrides. A multicomponent database is constructed through the incorporation of available binary and ternary descriptions, employing the Calphad approach. The experimental findings regarding the solvus temperature of the involved nitrides are employed to validate the accuracy of the thermodynamic database. The findings offer a comprehensive understanding of the relative phase stabilities and the associated interplay among the involved elements Al, B, and Ti in the Fe-rich corner of the system. The type and size distribution of the stable nitrides in microalloyed steel have been demonstrated to exert a substantial influence on the properties of the material, thereby rendering accurate predictions of phase stabilities of considerable relevance. Full article

Current research on the synthesis of isonicotinic acid (INA) has focused on the development of catalysts by mixing transition metal oxides such as vanadium, titanium and zirconium in the desired molar ratio. These materials have good catalytic activity (CA) but have drawbacks, including low resistance to deactivation and limited ability to control reaction selectivity. In the present study, two- and three-component catalysts containing vanadium were successfully synthesized and their compositions and properties were studied. The experimental results showed that the efficiency of V-Ti-Mn-O catalyst was superior to V-Ti-O. Selectivity analysis showed that V-Ti-Mn-O was the most efficient catalyst, reaching a maximum value of 67.17% at 320 °C. Scanning electron microscope (SEM), Raman spectroscopy and X-ray diffraction (XRD) were used to characterize the catalysts. The corresponding experimental results showed that the superior performance of the V-Ti-Mn-O catalyst was attributed to both the smaller size of the catalyst particles and their more uniform distribution. In the oxidation of 4-methylpyridine (4-MP), the V-Ti-O catalyst showed lower CA and stability compared to the V-Ti-Mn-O catalyst, which can be attributed to its limited CA and potential deactivation at higher temperatures, probably due to excessive oxidation. Full article

To improve the combustion performance of boron powder, a method was developed for synthesizing boron–magnesium–titanium (B-Mg-Ti) ternary composite powders with controlled metal content. Boron–magnesium (B-Mg) base materials were first prepared via electrical explosion, followed by the incorporation of titanium powder at varying mass fractions (1 wt.%, 3 wt.%, 5 wt.%, and 7 wt.%) through mechanical ball milling. Field emission scanning electron microscopy (FE-SEM) revealed that the addition of titanium promoted a more uniform dispersion of magnesium within the boron agglomerates. Moreover, nanoscale titanium particles were observed to be embedded on the particle surfaces, confirming successful microscale composite formation. Particle size distribution was measured using a Malvern 3000 laser particle size analyzer, and results showed that the particle size of the ternary composites decreased gradually with increasing titanium content. Specific surface area was determined via the Brunauer–Emmett–Teller (BET) method, with all samples exhibiting values greater than 15 m²/g, indicating good surface reactivity. Furthermore, the rheological behavior of the B-Mg-Ti composite powders, when combined with terminal hydroxyl polybutadiene (HTPB)—a typical binder in solid propellants—was evaluated. Viscosity measurements were conducted using a rotational rheometer at constant temperatures of 20 °C and 70 °C. The results demonstrated a marked decrease in viscosity with increasing titanium content, suggesting that titanium incorporation enhances the flowability of the composite powders. This study systematically evaluated the influence of titanium content on the structural and physicochemical properties of B-Mg-Ti composite powders, thereby providing a valuable experimental foundation for the optimized design of boron-based combustion systems and the enhancement of their processing and application performance. Full article

This study investigates the microstructure and mechanical properties of Inconel 718, a nickel-based alloy, reinforced with ceramic phases via additive manufacturing. Two reinforcement strategies were explored: in situ formation of ceramic phases through titanium powder addition, and direct incorporation of Cr₂O₃ and TiO₂ ceramic particles. Both approaches significantly modified the alloy’s microstructure and elemental distribution. The in situ formation method produced leaf-like Ti-rich precipitates (up to 70.13 wt%), while direct ceramic addition suppressed the preferred orientation of the Laves phase and promoted the formation of NbC precipitates. Microhardness increased by 19.4% with titanium addition, compared to a modest 1.3% improvement with direct ceramic addition. Tensile testing revealed that titanium powder enhanced ultimate tensile strength but reduced elongation, whereas direct ceramic addition led to decreases in both strength and ductility. Wear resistance evaluation showed that direct ceramic addition yielded superior performance, evidenced by the lowest friction coefficient (0.514) and smallest wear volume (16,290,782 μm³). These findings demonstrate the effectiveness of ceramic reinforcement strategies in optimizing the mechanical and tribological behavior of additively manufactured Inconel 718, and offer valuable guidance for the development of wear-resistant components such as those used in hydraulic support systems. Full article

Photodegradation is a sustainable green technology that has been studied worldwide, especially for wastewater treatment. The calcination temperature has an important impact on the physicochemical properties of the prepared photocatalysts. In this study, a ternary photocatalyst of Cu₂O/WO₃/TiO₂ (CWT) was successfully synthesized using an ultrasonic-assisted hydrothermal technique, and the calcination temperature was varied from 500 to 800 °C. The characterization outcomes proved that the anatase phase titanium dioxide (TiO₂) in the CWT composite transformed to rutile phase TiO₂ when the calcination temperature reached 700 °C and 800 °C. The surface area of the CWT composite decreased from 35.77 to 8.09 m².g⁻¹ and the particle size of the CWT composite increased from 39.11 to 180.25 nm with an increasing calcination temperature from 500 to 800 °C. Photoelectrochemical (PEC) studies showed the charge-transfer resistance of 208.10 Ω, electron lifetime of 32.48 ms, current density of 1.40 mA.cm⁻², transient photovoltage of 0.53 V, and p-n heterojunction properties for CWT-500. Reactive Black 5 (RB5) was used as the model pollutant to examine the photodegradation performance. The photodegradation rate of CWT-500 was the highest (0.70 × 10⁻² min⁻¹) due to its large surface area, effective separation of photoexcited electron-hole pairs, and low photoexcited charge carrier recombination rate. Full article