Search Results (316)

Ti-bearing blast furnace slag (TBS), a byproduct of vanadium–titanium magnetite smelting, serves as an important secondary resource for titanium recovery. However, the complex mineralogical composition and finely dispersed nature of titanium in TBS present significant challenges for efficient extraction. This review systematically examines four major titanium extraction routes: hydrometallurgical leaching, pyrometallurgical smelting, molten salt electrolysis, and selective precipitation, focusing on their limitations and recent improvements. For instance, conventional acid leaching suffers from acid mist release, a colloidal formation that hinders titanium recovery, and waste acid pollution. The adoption of concentrated sulfuric acid roasting activation effectively suppresses acid mist emission and prevents colloidal generation. Pyrometallurgical approaches are hampered by high energy consumption and substantial carbon emissions, which can be alleviated through the use of gaseous reductants to enhance reaction efficiency and reduce environmental impact. Molten electrolysis faces issues such as polarization and undesirable dendritic deposition; these are mitigated by employing liquid metal cathodes integrated with vacuum distillation to achieve high-purity titanium products. Selective precipitation struggles with strict crystallization conditions and low separation efficiency, though advanced techniques like supergravity separation show improved extraction performance. We propose an integrated technical strategy termed “Online conditioning driven by waste heat-mineral phase reconstruction-directional crystallization-optimized liberation.” This approach utilizes the inherent waste heat of slag combined with electromagnetic stirring to enhance homogeneity and promote efficient titanium recovery, offering a sustainable and scalable solution for industrial TBS treatment. Full article

Ti150 has potential applications in aeroengine components. However, the lack of research on its flame resistance, combustion behavior, and mechanisms makes it difficult to assess the risk of “titanium fire” and leaves fire protection design without theoretical support. This study aimed to determine the combustion resistance of Ti150 and elucidate its combustion behavior and mechanisms to address these issues. Through comparative Promoted Ignition-Combustion (PIC) tests between Ti150 and TC11 alloys, microstructural characterization, and thermodynamic/kinetic analyses, the following conclusions were drawn. Ti150 alloy exhibited a higher critical oxygen pressure and a higher ignition temperature but a significantly faster burning velocity, compared with TC11 alloy. The relationship between pressure and ignition temperature was in good agreement with the modified Frank-Kamenetskii ignition model. The ignition activation energy of Ti150 alloy was determined to be 118.41 kJ/mol, which was approximately 21% higher than that of TC11 alloy (97.72 kJ/mol). Moreover, post-combustion microstructural observations of Ti150 alloy revealed a higher oxygen content in the melting zone and an enrichment of Zr at the solid–liquid interface, both of which contribute to the higher burning velocity of Ti150 alloy compared with TC11 alloy. Full article

Titanium–manganese alloys have emerged as a promising option of β-phase titanium alloys, which have recently gained popularity thanks to their exceptional cold strength, deformability, and high specific strength. In this study, the vacuum arc melting process was used to obtain a Ti3Mn alloy, and its behavior in three physiological conditions was analyzed: at room temperature, simulated fever conditions (at 40 °C), and simulated severe infection conditions (pH = 1.2). Optical and scanning electron microscopy were employed to study the effect of Mn addition on the Ti-base alloy microstructure. It was observed the formation of fine precipitates of Mn2Ti, localized at the grain boundaries, allow for the increase in microhardness and blocked their growth. The beta phase of titanium was obtained as fine lamellae with a low level of porosity. The microhardness values were higher than those reported for cp-Ti. The electrochemical tests have shown a high resistance to corrosion in the three analyzed conditions. On the sample’s surface, there is a passive bilayer film, composed of a porous one being in contact with the physiological liquid and a compact one in contact with the bulk alloy. The results obtained suggest that Ti3Mn alloy can be a promising low-cost biomaterial for biomedical applications. Full article

The determination of uncertainty in porosity analysis based on X-ray computed tomography (XCT) images is currently the focus of research. This study aims to contribute to that by investigating the variation in porosity analysis resulting only from the segmentation and data analysis and by focusing on metal parts produced by different additive manufacturing processes, partially fabricated with intended porosity. Samples manufactured from aluminum, titanium alloy and nickel-chromium-based feedstock by liquid metal jetting (LMJ), laser-based powder bed fusion (PBF-LB) and directed energy deposition (DED) were scanned by XCT. The reconstructed volumes were distributed to four operators with different experience levels using Avizo, Dragonfly, Image J/Fiji, IPSDK Explorer, and VG Studio Max for porosity analysis. It was found that for all parts, the majority of operators chose a global manual threshold for image segmentation. Depending on the characteristics of the pores in the investigated samples, relative standard uncertainties up to 12% and 38% were observed for the LMJ and PBF-LB parts. For the part produced by DED, which showed the lowest overall porosity, relative standard uncertainties between 70% and 89% were observed for different image qualities; all were affected by the presence of artefacts investigated on purpose. Full article

Cutting CO₂ emissions is crucial to face of climate change, and one of the most tried and true means of post-combustion CO₂ capture is by way of chemical absorption. In this work, the effect of titanium dioxide (TiO₂) nanoparticles in a 25 wt% potassium carbonate (K₂CO₃) solution on solvent regeneration is investigated. This research follows the previous work in which the effect of nanofluids was evaluated on CO₂ absorption. Desorption was studied at three different temperatures (343.15, 348.15 and 353.15 K), using the absorbent fluid with and without 0.06 wt% TiO₂ nanoparticles. The results indicate that the nanofluid enhanced the CO₂ release rates, also reducing energy consumption. The mass transfer was intensified by the presence of nanoparticles, which in turn increased CO₂ diffusivity and influenced the liquid boundary layer, resulting in an enhanced desorption rate, because of the higher diffusivity. These enhancements were achieved with negligible modifications to the fluid properties, i.e., viscosity. In summary, application of TiO₂-enhanced K₂CO₃ solutions is a practical approach to enhance CO₂ removal performance and reduce operating costs such that CO₂ capture is beginning to be environmentally and economically more competitive for the existing system retrofit. Full article

Ultrahigh-temperature ceramic composites based on hafnium diboride have a wide range of applications, including as components for high-speed aircraft and energy generation and storage devices. Consequently, developing methodologies for their fabrication and studying their properties are of paramount importance, in particular in using them as an electrode material for energy storage devices with increased oxidation resistance. This study investigates the behavior of ceramic composites based on the HfB₂-HfO₂-SiC system, obtained using 15 vol% Ti₂AlC MAX-phase as a sintering component, under the influence of subsonic flow of dissociated air. It was determined that incorporating the modifying component (Ti₂AlC) altered the composition of the silicate melt formed on the surface during ceramic oxidation. This modification led to the observation of a protective antioxidant function. Consequently, liquation was observed in the silicate melt layer, resulting in the formation of spherical phase inhomogeneities in its volume with increased content of titanium, aluminum, and hafnium. It is hypothesized that the increase in the high-temperature viscosity of this melt prevents it from being carried away in the form of drops, even at a surface temperature of ~1900–2000 °C. Despite the established temperature, there is no sharp increase in its values above 2400–2500 °C. This is due to the evaporation of silicate melt from the surface. In addition, the electrochemical behavior of the obtained material in a liquid electrolyte medium (KOH, 3 mol/L) was examined, and it was shown that according to the value of electrical conductivity and specific capacitance, it is a promising electrode material for supercapacitors. Full article

The motivation for increasing the efficiency of renewable energy sources is the basic problem of ongoing research. Currently, intensive research is underway in technology based on the use of dye-sensitized solar cells (DSSCs). The aim of this work is to investigate the effect of modifying the iodide electrolyte with liquid crystals (LCs) known for the self-organization of molecules into specific mesophases. The current–voltage (I-V) and power–voltage (P-V) characteristics were determined for the ruthenium-based dyes N3, Z907, and N719 to investigate the influence of their structure and concentration on the efficiency of DSSCs. The addition of a nematic LC of 4-n-pentyl-4-cyanobiphenyl (5CB) to the iodide electrolyte influences the I-V and P-V characteristics. A modification of the I-V characteristics was found, especially a change in the values of short circuit current (I_SC) and open circuit voltage (V_OC). The conversion efficiency for cells with modified electrolyte shows a complex dependence that first increases and then decreases with increasing LC concentration. It may be caused by the orientational interaction of LC molecules with the titanium dioxide (TiO₂) layer on the photoanode. A too high concentration of LC may lead to a reduction in total ionic conductivity due to the insulating effect of the elongated polar molecules. 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

This study centers on the adsorption–flotation coupling extraction of rubidium (Rb⁺) and cesium (Cs⁺) within a titanium silicate (CTS)–cetyltrimethylammonium bromide (CTAB) system, systematically investigating the impacts of pH, aeration rate, CTAB concentration, and flotation time on the extraction efficiency of these elements. Single-factor experiments revealed that the optimal flotation efficiency was achieved when the pH ranged from 6 to 10, the aeration rate was set at 1000 r/min, the CTAB concentration was 0.2 mmol/L, and the flotation duration was 18 min. Under these conditions, the adsorption capacities for Rb⁺ and Cs⁺ were recorded as 128.32 mg/g and 185.47 mg/g, respectively. Employing the response surface optimization method to analyze the interactive effects of these four factors, we found that their order of significance was as follows: pH > aeration rate > CTAB concentration > flotation time. The optimized parameters were determined as pH 8.64, bubble formation rate 1121 r/min, CTAB concentration 0.26 mmol/L, and flotation time 18.47 min. Under these refined conditions, the flotation efficiency for both CTS–Rb and CTS–Cs surpassed any single-factor experiment scenario, with the flotation efficiencies for Rb⁺ and Cs⁺ reaching 95.05% and 94.82%, respectively. This methodology effectively extracts Rb⁺ and Cs⁺ from low-concentration liquid systems, while addressing the challenges of solid–liquid separation for powdered adsorption materials. It holds significant theoretical and practical reference value for enhancing the separation processes of low-grade valuable components and boosting overall separation performance. Full article

Objectives: This study aimed to evaluate the effects of different titanium (Ti) anodized surfaces on soft tissue healing around dental implant abutments. Methods: Discs of machined (MC), pink anodized (PA) and yellow anodized (YA) surfaces were morphologically characterized and evaluated in vitro. Cell adhesion and collagen synthesis by human gingival fibroblasts (hGFs) were assessed to evaluate the regenerative potential of the surfaces under study. Their inflammatory potential was evaluated in THP-1 cell cultures by measuring cytokine secretion, and their proteomic adsorption patterns were characterized using nano-liquid chromatography mass spectrometry (nLC-MS/MS). Statistical significance was considered at 5%. In relation to proteomics, statistical differences were evaluated using the Student t-test with the Perseus application. Results: The anodization process resulted in a reduction in the surface roughness parameter (Ra) relative to the machined titanium (p < 0.05). No differences in hGF adhesion were found between the surfaces after one day. PA induced increased hGF collagen synthesis after 7 days (p < 0.05). The secretion of TNF-α was lower for anodized surfaces than for MC, and its concentration was lower for PA than for YA (p < 0.05). In turn, TGF-β was higher for PA and YA versus MC after one and three days of culture. A total of 176 distinct proteins were identified and 26 showed differences in adhesion between the anodized surfaces and MC. These differential proteins were related to coagulation, lipid metabolism, transport activity, plasminogen activation and a reduction in the immune response. Conclusions: Anodized Ti surfaces showed promising anti-inflammatory and regenerative potential for use in dental implant abutments. Anodization reduced surface roughness, increased collagen synthesis and lowered TNF-α secretion while increasing TGF-β levels compared to machined surfaces. Identified proteins related to coagulation and lipid metabolism supported these findings. Clinical relevance: Anodized surfaces could offer improved short-term peri-implant soft tissue healing over machined surfaces. The analysis of abutment surface, instead of implant surface, is a new approach that can provide valuable information. Full article

Low-surface-energy and wettability-based antifouling coatings have garnered increasing attention in marine applications owing to their environmentally friendly characteristics. However, their limited functionality often results in suboptimal long-term antifouling performance, particularly under dynamic marine conditions. To address these limitations, a polydimethylsiloxane (PDMS)-based slippery (PSL) coating was fabricated on TC4 titanium alloy by integrating surface silanization via (3-Aminopropyl)triethoxysilane (APTES), antimicrobial Ag-TiO₂ nanoparticles, laser-induced hierarchical microtextures, and silicone oil infusion. The resulting PSL coating exhibited excellent oil retention and stable interfacial slipperiness even after thermal aging. Compared with bare TC4, low-surface-energy Ag-containing coatings, Ag-containing superhydrophobic coatings, and conventional slippery liquid-infused porous surfaces (SLIPS), the PSL coating demonstrated markedly superior resistance to protein adsorption, bacterial attachment, and diatom settlement, indicating an enhanced synergistic antifouling effect. Furthermore, it significantly reduced the diatom concentration in the surrounding medium without complete eradication, underscoring its eco-friendly and non-disruptive antifouling mechanism. This study offers a scalable, durable, and environmentally benign antifouling strategy for marine surface protection. Full article

Catalytic methane decomposition offers an attractive and sustainable pathway for producing CO_x-free hydrogen and valuable carbon nanotubes. This work investigates the innovative use of liquid metals, particularly gallium and indium, as promoters for iron catalysts based on a titanium dioxide and alumina composite to improve this process even more. In a fixed-bed reactor operating at 800 °C and atmospheric pressure, all catalyst activities for methane decomposition were thoroughly assessed while keeping the gas hourly space velocity at 6 L/g h. Surface area and porosity, H₂-temperature programmed reduction/oxidation, X-ray diffraction, Raman spectroscopy, scanning transmission electron microscopy, and thermogravimetry analysis were utilized to investigate the physicochemical properties of the catalyst. The result showed that iron supported on a titanium-alumina catalyst exhibited higher activity, stability, and reproducibility with a methane conversion of 90% and hydrogen production of 81% after three cycles, with 240 min for each cycle and stability for 480 min. In contrast, the liquid metal-promoted catalysts improved the metal-support interaction and textural properties, such as surface area, pore volume, and particle dispersion of the catalysts. Still, the catalytic efficiency significantly improved. However, the gallium-promoted catalyst displayed excellent reusability. The characterization of the spent catalyst proved that both the iron supported on a titanium-alumina and its gallium-promoted derivative produced graphitic carbon; on the contrary, the indium-promoted catalyst produced amorphous carbon. These results demonstrate how liquid metal promoters can be used to adjust the characteristics of catalysts, providing opportunities for improved reusability and regulated production of carbon byproducts during methane decomposition. Full article

Niobium, with its unique properties, plays a key role in high-tech industries, but its recovery from secondary sources remains poorly studied. The kinetics of niobium leaching from niobium-containing middlings obtained via the water treatment of dust chamber sublimations of titanium chlorinators is considered in this study. The leaching process was conducted using a fluoride–sulphuric acid solution. The experiments were performed at 25–90 °C in agitation mode. Kinetic data were analysed using compression-core and mixed-control models, which made it possible to establish the limiting stages of the process. A mixed mechanism, including a chemical reaction on the surface and diffusion through a layer of products with an activation energy of 30.05 kJ/mol, was established. The niobium recovery degree increased from 35.25 to 93.5% as the temperature increased, highlighting its effect on the process. The insoluble residue, rich in titanium, and the liquid phase with niobium and zirconium have the potential for further processing. The results provide the basis to optimise technologies intended to recover niobium from man-made raw materials, contributing to an increase in resource efficiency. Full article

This paper presents the results of a study of the catalytic hydrogenation of phenanthrene using catalysts based on chrysotile modified with nickel and titanium (chrysotile/NiTi), as well as coal shale. Complex characterization of catalysts in terms of acid, texture and morphological properties was carried out. Pre-reduction in the catalysts has been found to increase the yield of partially and fully hydrogenated products, including tetrahydronaphthalene, trans-decalin and dihydrophenanthrene. Particular attention is paid to the role of coal shale as a donor source of hydrogen in thermolysis conditions. The results of hydrogenation revealed complex mechanisms of phenanthrene transformations, including partial saturation of aromatic rings, desulfurization and the formation of alkyl-substituted compounds. The obtained data emphasize the prospects of using the studied catalysts in the processes of processing heavy and solid hydrocarbon raw materials, which opens up opportunities for creating new technologies for the production of liquid fuel. Full article

Industrial growth led to the expansion of existing environmental problems, where different kinds of pollutants can enter the environment by many known routes, particularly through wastewater. Among other contaminants, pharmaceuticals, such as diazepam, once released, pose a significant challenge related to their removal from complex environmental matrices due to their persistence and potential toxicity. For this reason, it is a great challenge to find suitable methods for the treatment of wastewater. The aim of this paper was to investigate the stability of diazepam, subjecting it to various degradation processes (hydrolysis and photolysis), focusing on photocatalysis, an advanced oxidation process commonly used for the purification of industrial wastewater. The photocatalytic system consisted of UV-A and simulated solar irradiation with titanium dioxide (TiO₂) immobilized on a glass mesh as a photocatalyst, with an additional reaction performed in the presence of an oxidizing agent, i.e., hydrogen peroxide, to improve diazepam removal from water matrices. The kinetic rate of diazepam degradation was monitored with a high-performance liquid chromatograph coupled with a photodiode array detector (HPLC-PDA). The target compound was characterized as a hydrolytically and photolytically stable compound with t_1/2 = 25 h. The presence of an immobilized TiO₂ catalyst contributed significantly to the degradation of diazepam under the influence of UV-A and simulated solar radiation, with t_1/2 in the range of 1.61–2.56 h. Five degradation products of diazepam were identified at the laboratory scale by MS analysis (m/z = 267, m/z = 273, m/z = 301, m/z = 271, and m/z = 303), while the toxicity assessment revealed that diazepam exhibited developmental toxicity and a low bioaccumulation factor. The pilot-scale process resulted in significant improvements in diazepam degradation with the fastest degradation kinetics (0.6888 h⁻¹). These results obtained at the pilot scale highlight the potential for industrial-scale implementation, offering a promising and innovative solution for pharmaceutical removal from wastewater. Full article