Ti Content Research Articles

Study on the Corrosion Resistance of Electrodeposited NiW/TiO2 Composite Coating and Its Application in Methylene Blue Degradation in Simulated Wastewater

NiW/TiO2 composite coatings were electrodeposited on the surface of Q235B steel to investigate the effect of different TiO2 particle concentrations on the deposition rate, thickness, chemical composition, and surface morphology of the composite coatings. The corrosion resistance of the NiW/TiO2 composite coatings and their photocatalytic degradation of methylene blue in simulated wastewater were examined and verified. The NiW/TiO2 composite coating electrodeposited from a plating solution with 15g/L TiO2 particle exhibited the fastest deposition rate (402mg/h) and the largest thickness (23.92 μm). All electrodeposited NiW/TiO2 composite coatings comprised C, Ti, Ni and W, with granular surface morphology. Increasing the TiO2 particle concentration in the plating solution enhanced the mass transfer rate of Ni ions, thereby increasing the Ni and Ti contents in the composite coating. However, at an excessive TiO2 particle concentration of 20g/L, the viscosity increased and the transfer rate of particles and nickel ions decreased, resulting in a decrease in the Ni and Ti contents in the composite coating. Among all NiW/TiO2 composite coatings, the NiW/TiO2 composite coating electrodeposited from a plating bath containing 15g/L TiO2 particle demonstrated optimal corrosion resistance with the most positive corrosion potential (-0.533V) and the lowest corrosion current density (8.6×10-6 A/cm2). The electrodeposited NiW/TiO2 composite coatings effectively degraded the methylene blue in the simulated wastewater, achieving an optimal degradation efficiency of 60.7%.

Lattice energy transfer from homo-crystalline substitution for enhanced piezo-photocatalytic CO2 conversion

The rapid recombination of carriers and large activation energy of CO2 compromise the efficiency of CO2 photoreduction. Herein, SrTiO3 (STO) with different molar ratios of La3+ and Al3+ double-site homo-crystalline substitution is prepared by a ball-milling molten salt method. The concentration of Ti3+ and excess oxygen vacancies decrease to improve the catalytic activity. Meanwhile, the double sites act as electron transfer platforms for easy electron transfer from the bulk phase to the surface to foster CO2 photoreduction. Not only that, the energy transfer due to doping-induced lattice distortion can potentially enhance the photocatalytic activity. A piezoelectrically polarized electric field is introduced to further expedite charge transport. As a result, the activity of La, Al-STO piezo-photocatalytic CO2 reduction is improved to 39.17 µmol g-1h−1, which is more than seven times better than that of the pure STO. Furthermore, CO2 adsorbs spontaneously on the catalysts because the thermodynamic energy barrier decreases due to the piezoelectric force, which is verified by density-functional theory calculation. This study reveals the great potential of double-site homo-crystalline substitution of STO pertaining to the charge transport kinetics and thermodynamics of the catalytic reaction in the piezo-photocatalytic CO2 process.

Effect of Ti addition on the microstructure and corrosion behavior of laser cladding AlCoCrFeNi high-entropy alloy coatings

AlCoCrFeNi high-entropy alloys (HEAs) has higher strength and wear resistance but poorer corrosion resistance. In the present investigation, the AlCoCrFeNi HEAs containing titanium(Ti) were fabricated via laser cladding to enhance the corrosion resistance properties of the coating and the influence of the Ti content on the microstructure of the coatings was investigated. The results show that the microstructure of the coating changed from a single BCC phase to a BCC+B2 phase with the addition of Ti. The Laves phases appeared within the coating when the Ti content was beyond 0.5 mol ratio. As an excellent corrosion-resistant element, Ti promoted the formation of a passive film and enhanced the corrosion resistance of the HEAs coating. The corrosion resistance of the coating first increased and then decreased with the addition of Ti, and the AlCoCrFeNiTi0.5 coating exhibited optimal corrosion resistance.

Metal concentration in bottom sediments for a tropical river, geological or anthropogenic source?

The study analyzes data from a survey of metal concentrations in bottom sediments from both margins (left and right) of the lower main channel of the Orinoco River. This study aims to analyze metal concentrations in the bottom sediments of the lower Orinoco River with different geological settings and anthropological sources. El Almacen (ALM), Las Galderas (G), Los Castillos de Guayana (C), Ciudad Bolivar (CB), and Ciudad Guayana (CG) were the sampling sites. Freshwater physicochemical parameters pH, conductivity, and DO were measured in situ at each sample site. Twenty-four bottom sediment samples were collected with an Eckman grab, dried, and sieved. Trace elements Pb, Cr, Cu, Cd, Ti, and Co were measured in sediments with grain sizes <63μm. Bottom sediment analysis followed EPA method 3050B (digestion with HNO3 + HCl + H2O2). Statistical analyses included the Shapiro-Wilk test, Spearman correlation, Kruskal-Wallis test, and principal component analysis (PCA). Physicochemical parameters highlighted the marked difference between the left and the right river margins, reflecting the cross-channel heterogeneity due to the dissimilar geology and low horizontal mixing. Metal concentrations were generally low, with higher variations associated with urban and industrial sources. Pb, Cr, Cu, Cd, Ba, Ti, and Co concentrations did not generally indicate significant pollution, but potential contamination from sewage and industrial effluents was noted. The differences between the two river margins were common in all the sampling sites, reflecting the sources of water biochemistry related to geochemical origins in the Andes and the Guiana Shield, respectively. The study emphasizes the importance of sampling location within the river channel.

Medium-entropy Zr–Nb–Ti alloys with low magnetic susceptibility, high yield strength, and low elastic modulus through spinodal decomposition for bone-implant applications

Medium-entropy Zr–Nb–Ti (ZNT) alloys are being extensively investigated as load-bearing implant materials because of their exceptional biocompatibility and corrosion resistance, and low magnetic susceptibility. Nevertheless, enhancing their yield strength while simultaneously decreasing their elastic modulus presents a formidable obstacle, significantly constraining their broader utilization as metallic biomaterials. In this study, three medium-entropy ZNT alloys, i.e., Zr45Nb45Ti10, Zr42.5Nb42.5Ti15, and Zr40Nb40Ti20 (denoted ZNT10, ZNT15, and ZNT20, respectively), were designed based on the miscibility gap in the ZNT phase diagram and prepared by annealing of cold-rolled ingots. Their microstructures, mechanical properties, wear resistance, corrosion resistance, magnetic susceptibility, and biocompatibility were systematically studied. Spinodal decomposition occurred in the cold-rolled ZNT10 and ZNTi15 after annealing at 650°C for 2 h and resulted in nanoscale Zr-rich β1 and (Nb, Ti)-rich β2 phases, which significantly improved their yield strength and reduced their elastic modulus. The wear resistance of the alloys decreased with an increase in Ti content. Dense ZrO2, Nb2O5, and TiO2 oxide layers were formed during the polarization process in Hanks’ solution, which enhanced the corrosion resistance of the alloys. These ZNT alloys exhibited significantly lower magnetic susceptibility than medical Ti alloys. The ZNT alloys showed a cell viability of more than 94 % toward MG-63 cells after culturing for 3 d. Overall, the spinodal ZNT15 showed the best combination of mechanical properties, wear resistance, corrosion resistance, low magnetic susceptibility, and sufficient biocompatibility among the three alloys. Statement of SignificanceThis work reports on medium-entropy Zr–Nb–Ti (ZNT) alloys with heterostructure. Spinodal decomposition significantly improved their mechanical strength and reduced the elastic modulus of the alloys. The wear resistance of the ZNT alloys decreased with an increase in Ti content. Dense ZrO2, Nb2O5, and TiO2 oxide layers were formed during the polarization process in Hanks’ solution, which enhanced the corrosion resistance of the alloys. The ZNT alloys exhibited significantly lower magnetic susceptibility than medical Ti alloys. The ZNT alloys showed a cell viability of more than 94% toward MG-63 cells after culturing for 3 d. The results demonstrate that spinodal ZNT alloys have enormous potential as bone-implant materials due to their outstanding overall mechanical properties, high corrosion resistance, wear resistance, low magnetic susceptibility, and sufficient biocompatibility.

Tunable TiO2‐Heterophase Junctions for Studying and Enhancing Photocatalytic H2 Production Under Visible Light

AbstractPhotocatalytic performance of titanium dioxide under visible light was optimized by preparing heterophase compounds (containing two or more phases) by hydrolysis method using TiCl4 as a precursor with different concentrations (0.5, 0.7, 1, and 2) to adjust condensation modes of Ti4+. The structural and textural properties of the synthesized TiO2 multiphase were fully characterized by XRD, Raman scattering, FTIR, BET, MEB‐EDX, XPS, diffuse UV–vis, and EIS spectroscopy. The increase of TiCl4 amount precursor has a significant effect on the heterophase junctions of TiO2 structure and more especially on textural and structural properties. The best specific surface area (131 m2/g) is observed for the sample at high Ti‐content (2 in Ti4+). The anatase phase (79%) is detected only for 0.5 in Ti4+ sample. However, both rutile (R) and brookite (B) phases are present in 0.7, 1, and 2 Ti‐contents. On the one hand, the band gap of 2.9 eV allows titanium dioxide to be active under visible light. In addition, the presence of rutile/brookite heterophase junction contributes significantly to the improvement of active sites for photocatalytic reaction. The separation efficiency of photogenerated electrons and holes contributes to photocatalytic evolution performance under visible light for hydrogen production. The optimal sample (0.7 content in Ti+4 species) which presents in its structure 52% of rutile and 46% of brookite phases presented the highest photocatalytic activity with a 230 µmol/h of hydrogen generation, attributed to the heterophase junctions R52/B46, highly pore size 20.60 nm, and relatively small bandgap energy 2.974 eV. This work opens new horizons on the creation and study of a multiphase TiO2 that works under visible light in the fields of renewable energies and various other fields.

Geochronological and geochemical constraints on the multistage magmatic processes of the Lianhuashan batholith, South China: Implications for the petrogenesis and polymetallic mineralization

The Lianhuashan batholith, which is a composite pluton located in the middle part of a world-class giant tungsten (W) polymetallic belt of South China, hosts a huge reserve of more than 50000 t of W. Despite this great economic significance, the petrogenesis of each phases of the Lianhuashan batholith, as well as its temporal and genetic relationships to the W polymetallic mineralization, is still unclear. To address these questions, we conducted a comprehensive study for the Lianhuashan batholith, including LA-ICP-MS zircon U-Pb dating, whole-rock geochemical and in-situ mineral trace element analyses. Different from previous studies, four main granitic phases (G1 to G4) were identified. The biotite granite (G1) formed from 168.6 to 165.3 Ma, has the lowest Si content and high Al and Fe contents, and is significantly depleted in Ba, Sr, Ti, P, and Nb whereas enriched in U, Hf, Zr, and Y contents. In contrast, the two-mica granite (G2) and fine-grained muscovite granite (G3), formed from 162.8 to 160.5 Ma, exhibit similar characteristics including enrichment in La, Y, Hf, Th, U, and depletion in Ba, Sr, and P. The porphyritic granite (G4) is the latest magmatic phase and formed at 158.3 Ma. It is characterized by high K, Si, Th, U, Zr, Hf contents but low Al, Fe, Sr, P, and Ti contents. These features support that four main phases of the Lianhuashan batholith belong to S-type granites that experienced significant fractional crystallization, and display reduced and low temperature features. Combined with previously published studies, we suggest that the Lianhuashan batholith formed in an intraplate extensional setting triggered by the high-angle rollback subduction of the paleo-Pacific plate. The three early phases (i.e., G1–G3) are in turn more oxidized and are responsible for the transition from Sn- to W-dominated mineralization. In contrast, the G4 granite, characterized by lower oxygen fugacity, is resposible for Pb-Zn-Ag-U polymetallic mineralization.

Measurements of F1‐ Region Ionosphere State Variables at Arecibo Through Quasi Height‐Independent Exhaustive Fittings of the Incoherent Scatter Ion‐Line Spectra

AbstractWe discuss an exhaustive search approach to fit the incoherent scatter spectrum (ISS) in the F1‐region for molecular ion fraction (fm), ion temperature (Ti), and electron temperature (Te). The commonly used “full profile” approach for F1‐region measurements parameterizes the molecular ion fraction as a function of altitude and fits all the related heights for the state variables. In our approach, we fit the ISS at each height for fm, Ti, Te, and ion velocity (Vi) independently. Our exhaustive search method finds all the major local minima at each altitude. Although a parameterized function is used to guide the algorithm in finding the best solution, the fitting parameters retain their local characteristics. Despite that fitting fm, Ti, and Te without constraints requires Doppler shift to be accurately determined and the ISS signal‐to‐noise ratio higher than the full‐profile method, simulations show that Ti, Te, and fm can be recovered within a few percent accuracy with a moderate signal‐to‐noise ratio. We apply the exhaustive search approach to the Arecibo high‐resolution incoherent scatter radar data taken on 13 September 2014. The derived ion and electron temperatures are sensitive enough to reveal thermosphere gravity waves commonly seen in the electron density previously. Our method is more robust than previous height‐independent fitting methods. Comparison with another Arecibo program indicates our results are likely more accurate. Simultaneous high‐resolution measurements of Ti, Te, fm, Vi, and electron concentration (Ne) in our approach open new opportunities for synergistic studies of the F1‐region dynamics and chemistry.

Tracking hydrothermal particles from the ridge axis to the sediment column along the Endeavour segment of the Juan de Fuca Ridge

Elemental fluxes associated with mid-ocean ridge hydrothermal systems are thought to be important in the ocean budgets of many elements but quantitative models of these fluxes, and how they vary in space and time due to different boundary conditions, are in their infancy. This is especially true for non-conservative elements that can be involved in multiple processes transforming them between the dissolved and particulate phases both in the water column and after sedimentation. To help develop a more robust database for parameterizing the processes operating, we undertook a coupled sediment trap and sediment core study of hydrothermal sediments on the west flank of the Endeavour segment of the Juan de Fuca Ridge. Sediment traps deployed in the Main Endeavour Field (MEF) and 3 and 9 km southwest of this field, along the mean flow direction of the hydrothermal plume, show that the rate of change of the concentration of sulfide-associated elements (Cu, Zn, Cd, Pb, Ag, As, Mo) in sediment settling from the plume differs between elements. We interpret this as indicating both different dissolution rates of phases containing these elements and different rates of scavenging of these elements from seawater. Scavenging is most readily tracked using elements for which the scavenged fraction is large relative to the hydrothermally derived fraction. For such elements, the relative efficiency of scavenging from seawater (REE > Cr > Ni > V > P > U) matches that previously reported from the TAG system on the Mid-Atlantic ridge despite different vent fluid and seawater chemistries that are expected to lead to both differing roles of Fe-sulfide and Fe-oxyhydroxides and different Fe oxidation rates. In the sediment trap samples collected 9 km off-axis, but not in those collected 3 km off-axis, the Mn and Ti concentrations correlate strongly despite these samples having much higher Mn concentrations than background sediment. Since Ti is sourced almost entirely from background terrigenous material such a correlation was not expected. The most reasonable explanation for this is that aggregation of hydrothermally derived particles with terrigenous material settling through the water column controls removal of hydrothermally derived particles from the water column. Changes in sediment composition with depth in the off-axis sediment core, along with differences between the composition of material from the sediment core and the off-axis sediment traps, are interpreted as indicating large post-deposition changes in sediment composition. For example, much or all of the Mn, P, As and Mo carried to the sediments with hydrothermally derived particles is released back into the water column during diagenesis. In contrast, V and REE concentrations in the sediment core are higher than those in the off-axis sediment trap samples, which may be due to continued scavenging in a benthic boundary layer post-deposition. Overall these data are interpreted as indicating that the net loss of many elements from the non-buoyant plume may not be a proxy for loss from the ocean, and a better understanding of post-depositional processes in hydrothermal settings may be important in understanding cycling of the aforementioned elements, and likely others, in seawater.

Improving flexural performance of repaired C/C composites through Ti addition: Mechanism analysis

Ti-doped Ni-based solder was used as the repair agent to recover the flexural performance of the damaged carbon/carbon (C/C) composites. The effects of the contents of Ti on the microstructure, chemical compositions, and flexural strength were investigated. The thermal stress distribution and repair mechanism was studied by finite element analysis methods. The addition of an appropriate amount of Ti enhanced the wetting performance of the repair agent on the surface of C/C composites. Besides, the TiC hard particles formed at the interface provided strengthen effect, and form a gradient structure of coefficient of thermal expansion (CTE), thereby enhancing the interface bonding ability and improving the flexural performance of the repaired C/C composites. The flexural strength was the highest with a recovery rate of 92.6 % when the content of Ti was 5 wt%. This work provides a strategy for the engineering application and improving the damage repair of C/C composites.

MoS2/Ti Co-deposited Coatings and Their Fretting Wear Properties at Elevated Temperatures

Abstract Fretting wear refers to the damage phenomenon experienced by the mechanical components undergoing micro-amplitude relative slip at their contact region due to vibration. Titanium alloys find their extensive application in aerospace industry components such as splines and dovetail joints, where they experience fretting wear phenomenon. This research work investigates the effect of MoS2/Ti co-deposition coatings with varying Ti content, deposited on TC4 titanium alloy substrate using magnetron sputtering. Fretting wear tests were conducted at room temperature, 100 °C, and 200 °C, using a specially designed fretting test fixture with a ball-on-flat contact configuration, mounted on a servo-hydraulic fatigue testing machine. The results indicated that the coating becomes denser with an increase in the Ti content. The coating exhibited the highest hardness and better anti-fretting wear performance at room temperature. However, the effect of Ti content on the fretting wear behaviors changed at elevated temperatures. At the highest Ti content coating, excessive oxide particles were found at the worn surface at elevated temperatures, inducing an abrasive effect and localized cracks. However, coatings with moderate Ti content (9.62 at. %) effectively protected the substrate from significant wear at room temperature and maintained a low coefficient of friction at high temperatures without failure.

Modelling of blast furnace ironmaking process based on digital twin

AbstractThe blast furnace ironmaking process is a crucial step in the steel industry. Effectively modelling the blast furnaces is significant in ensuring smooth operation and accelerating the digitalisation transformation of blast furnaces. The authors focus on the mechanism modelling of the blast furnace operation process, using a digital twin model development platform to simulate the main reaction processes inside the blast furnaces. Under on‐site production conditions, Si, Mn and Ti contents of molten iron and the corresponding indicators for model accuracy are calculated. For Si, Mn, and Ti content, the Root Mean Square Error values are 0.0678, 0.0108 and 0.0093 for dataset 1, while 0.0933, 0.0120 and 0.0111 for dataset 2, respectively, indicating that the model has a small simulation error and high accuracy. By comparing the simulation results with accurate laboratory results, the model is validated to have satisfactory simulation reliability and compensates for the existing shortcomings in the blast furnace mechanism modelling field.

Influence of Al and Ti Alloying and Annealing on the Microstructure and Compressive Properties of Cr-Fe-Ni Multi-Principal Element Alloy

This study meticulously examines the influence of aluminum (Al) and titanium (Ti) on the genesis of self-generated ordered phases in high-entropy alloys (HEAs), a class of materials that has garnered considerable attention due to their exceptional multifunctionality and versatile compositional palette. By meticulously tuning the concentrations of Al and Ti, this research delves into the modulation of the in situ self-generated ordered phases’ quantity and distribution within the alloy matrix. The annealing heat treatment outcomes revealed that the strategic incorporation of Al and Ti elements facilitates a phase transformation in the Cr-Fe-Ni medium-entropy alloy, transitioning from a BCC (body-centered cubic) phase to a BCC + FCC (face-centered cubic) phase. Concurrently, this manipulation precipitates the emergence of novel phases, including B2, L21, and σ. This orchestrated phase evolution enacts a synergistic enhancement in mechanical properties through second-phase strengthening and solid solution strengthening, culminating in a marked improvement in the compressive properties of the HEA.

Genesis of high-grade lode gold shoot dominated by ore fluid overprinting during a ductile-brittle shear event

Lode gold deposits hosted by ductile-brittle shear zones account for more than one-third of the world’s gold production. High-grade ore shoots from this type of deposit are the most critical exploration targets. The ore shoots can form through the post-depositional deformation of auriferous sulfides or overprinting of ore fluids accompanied by coupled dissolution-reprecipitation (CDR) reactions. However, the mechanism that dominates ore shoot genesis remains unknown, primarily due to the controversial single progressive or polyphase nature of ore-bearing shear zones. Here, we report on geological and geochemical analyses we conducted at the large Hetai goldfield, South China, to construct an accurate gold upgrading model for the formation of ore shoots. Stages 1−3 of mineralization at Hetai show features typical of ductile shearing, while Stage 4 is characterized by quartz-sulfide veinlets in brittle fractures. 40Ar/39Ar ages of ca. 184 Ma and 157 Ma for the mineralization of stages 1 and 4 overlap with the regionally dextral ductile-brittle shear that occurred during ca. 210−162 Ma. Thus, the gold event at Hetai should have been controlled by a single progressive ductile-brittle shear episode, rather than polyphase structural events. The auriferous fluids at Hetai precipitated minor invisible gold in pyrites (mean 0.173 ppm) produced during stages 1−4 through fluid-rock interaction. The systematic increase of elements Au, As, Sb, Bi, Ag, and Cu and δ34S values in ductile-deformed pyrites from stages 1−3 indicate that early invisible gold upgrading should be the result of the post-depositional remobilization of auriferous sulfides during the long-lived ductile-brittle transition. Cataclastic pyrites hosting invisible gold from Stage 4 have zoned and porous mantles with elevated invisible gold (mean 0.503 ppm) and Sb, Bi, Pb, Co, Ni, and Ti contents. These pyrites are further replaced by chalcopyrite and pyrrhotite with increasing invisible gold, Co, and Ni contents. In addition, numerous visible native gold grains in Stage 4 are included in sulfides formed by replacement and develop along the microfractures and grain boundaries of these sulfides. We suggest the late invisible and visible gold upgrading events in Stage 4 can be attributed to the auriferous fluid superposition and subsequent replacement of pyrite via CDR reactions in a brittle regime. Therefore, the gold upgrading process at Hetai is jointly caused by the early remobilization induced by ductile-brittle deformation and the late ore fluid superposition with accompanying CDR reactions within a brittle domain. As the ore fluid superposition and CDR reactions in Stage 4 produce a significant amount of visible gold, they exert a first-order control on the genesis of ore shoots at Hetai. The refined model may be widely applicable to lode gold deposits elsewhere and can be used to identify regions with promising exploration targets.

Microstructure and properties behavior of in situ synthesized with high content (Ti, W) C reinforced In625 by two step-laser direct energy deposition

The formation of sensitive interface cracks and the difficulty in processing high-concentration Ni-based ceramic coatings via direct energy deposition (LDED) present major engineering challenges. To address these, high-quality In625/ceramic coatings with various mass contents of Ti, nickel-coated graphite (Ni3C), and WC were fabricated on QT250 using two-step laser directed energy deposition (TsLDED). The influence of the Ti/C: WC molar mass ratio on the bonding interface, microstructure, phase composition, and mechanical properties of the coatings was analyzed. The results indicated that grains at the In625/ceramic coating interface formed epitaxial growth, ensuring a robust bond. In situ synthesis of (Ti, W) C, WCx (WC and W2C), M23C6, and other precipitated phases were uniformly distributed, enhancing nucleation, refining microstructure, and improving mechanical properties. The addition of Ti facilitated the transformation of WCx to (Ti, W) C. High Ti and C concentrations promoted eutectic structure formation in the matrix phase, enhancing performance. The In625 + 56 % Ti – 14 % Ni3C – 30 % WC composite coating exhibited the highest microhardness and the lowest friction coefficient, with microhardness 5.61 and 3.6 times that of QT250 and In625 coatings, respectively, and a friction coefficient 0.3 times that of In625. Variations in the Ti/C: WC molar mass ratio directly affected the content, proportion, and type of (Ti, W) C, WCx, γ-Ni, and eutectic structures comprising M23C6, NiTix, Ni2W4C, Cr2Ti, and γ-Ni, influencing microstructure evolution and mechanical properties. The TsLDED process thus enables the preparation of In625/ceramic reinforced coatings with improved mechanical properties.

Theoretical Insights into Off-Stoichiometric Zr(x)Ti(1-x)IrSb Half-Heusler Alloys: A First Principle Calculations.

This study presents a theoretical investigation into the phase stability, electronic, and optical properties of off-stoichiometric Zr_{x}Ti_{1-x}IrSb (x = 0, 0.0625, 0.1875, 0.25, 0.50, 0.75, 1) compounds. Using first-principles calculations, we explore how varying Zr and Ti concentrations can tune the electronic and optical properties of these half-Heusler alloys. The Structural, optical, and electronic properties were meticulously analyzed with both the GGA-PBE and Meta-GGA-SCAN approximations, as implemented in the Vienna Ab initio Simulation Package (VASP). The dynamical stability of these compounds was assessed using the Phonopy package. Our findings reveal that these alloys exhibit semiconductor behavior with tunable band gaps, and their optical properties show significant variation across different compositions, particularly in the visible light range. The compounds also demonstrate robust dynamical stability, indicating their potential for practical applications in electronic and optoelectronic devices. These results underscore the versatility of Zr_{x}Ti_{1-x}IrSb alloys and highlight their promise for next-generation technology.

Effect of Nb and Ti additions on microstructure, hardness and wear properties of AlCoCrFeNi high-entropy alloy

The use of Nb and Ti in the development of high-performance alloys is strategically important for technological advancement. The effect of Nb and Ti additions on the microstructure, hardness and tribological properties of the High Entropy Alloy (HEA) AlCoCrFeNi was evaluated. The addition of 0.6 mol of Nb led to the formation of Laves phase, resulting in a B2/Laves type hypoeutectic microstructure. Conversely, increasing Ti concentration led to the formation of a dendritic microstructure, with interdendritic region composed of Cr-rich BCC-A2 and Fe-Ti rich Laves phase. The average hardness values obtained were 790 HV, 597 HV and 731 HV for AlCoCrFeNiNb0.6, AlCoCrFeNiTi0.5 and AlCoCrFeNiTi1.2 HEAs, respectively. The high hardness was attributed to the formation of the Laves phase and Cr-rich phases, in addition to solid solution hardening, as confirmed by the increase in the lattice parameter calculated by Rietveld refinement method for both B2 and BCC-A2 phases. While the three compositions exhibited comparable friction coefficient, the alloy containing Nb showed superior wear behavior. This was evidenced by the lower volume of material loss and the lower wear rate, which can be attributed to the fine and homogeneous hypoeutectic microstructure observed in the ingot’s cross section. The wear mechanisms were studied, characteristics features of abrasion and adhesion wear were observed.

Preparation and oxidative desulfurization performances of modified SBA-15 supported polyacid metal oxolates

In this study, eight composite catalysts were prepared by loading (CTAB)3H3[PW9V3O40] (active components) onto amino-functionalized mesoporous titanium silicate Ti-SBA-15(supports). In order to study the effects of different Ti contents and different active components on the catalytic performances of the catalysts, 30 %(CTAB)3H3[PW9V3O40]/NH2–Ti-SBA-X (X = 0, 25, 50, 75, 100) and X%(CTAB)3H3[PW9V3O40]/NH2–Ti-SBA-50 (X = 20, 40, 50) were obtained and characterized. The oxidative desulfurization performances of the composite catalysts were explored. It was found that catalyst 40 %(CTAB)3H3[PW9V3O40]/NH2–Ti-SBA-50 exhibits the optimal oxidative desulfurization performance. This is because the incorporation of SBA-15 with an appropriate amount of Ti (n(Si)/n(Ti) = 50) can improve the acidity and stability of mesoporous silica. The successful substitution of CTAB (n(CTAB)/n(H6PW9V3O40) = 3) in the active component can reduce the mass transfer resistance and speed up the reaction rate. 3-Aminopropyltriethyl silane (APTES) acts as a silane coupling agent to graft amino groups onto mesoporous molecular sieve SBA-15, which can enhance the interaction between heteropolyacids and carriers. Under the synergistic effect of the active component and the support, the total removal rate of the optimal catalyst with a total concentration of 1000 ppm sulfur compounds in the simulated fuel was 94.44 %. After four cycles, the total desulfurization rate of the catalyst can reach 91.28 %.

Effect of mechanical vibration on microstructure and performance of Fe-based composite coatings fabricated by underwater laser deposition technology

To solve the problem of the uneven composition and poor performance caused by water environment during the underwater laser deposition process, the mechanical vibration assisted underwater laser deposition technology was innovatively proposed, and Fe-based composite layer was successfully prepared. The microstructure, grain type and properties of Fe-based composite layer with and without mechanical vibration were studied and compared. The results showed that the mechanical vibration broke the grain and promoted the formation of more nuclei, which reduced the average grain size by 13.48 %. The solute located in the grain gap was transferred to the liquid molten pool by mechanical vibration, which reduced the Ti content in the intergranular precipitated phase Fe2Ti and made the Fe2Ti from coarse continuous distribution to fine discontinuous distribution. Additionally, the mechanisms of mechanical vibration promoting the performance of the composite were analyzed comprehensively. Compared with the composite without mechanical vibration, the composite with mechanical vibration had good corrosion resistance after 30 days of immersion, and the tribo-corrosion resistance was also improved. With the aid of mechanical vibration, the ultimate tensile strength and elongation of the composite were increased by 11.30 % and 22.08 %, respectively, due to the formation of recrystallized grains, high density high-angle grain boundaries, and fine intergranular precipitate. This study was expected to provide a new way to regulate the microstructure and properties of the underwater laser deposition layer, and promote the application of underwater laser deposition technology in marine engineering equipment.

Analyzing the Influence of Titanium Content in 5087 Aluminum Filler Wires on Metal Inert Gas Welding Joints of AA5083 Alloy

As the demand for lightweight structures in the transportation industry continues to rise, AA5083 aluminum alloy has become increasingly prominent due to its superior corrosion resistance and weldability. To facilitate the production of high-quality, intricate AA5083 components, 5087 aluminum filler wire is commonly utilized in metal inert gas (MIG) welding processes for industrial applications. The optimization of filler wire composition is critical to enhancing the mechanical properties of AA5083 MIG-welded joints. This study investigates the effects of modifying 5087 aluminum filler wires with different titanium (Ti) contents on the microstructure and weldability of AA5083 alloy plates using MIG welding. The influence of Ti contents was systematically analyzed through comprehensive characterization techniques. The findings reveal that the constitutional supercooling induced by the Ti element and the formation of Al3Ti facilitate the heterogeneous nucleation of α(Al), thereby promoting grain refinement. When the Ti content of 5087 filler wire is 0.1 wt.%, the grain size of the weld center was 78.48 μm. This microstructural enhancement results in the improved ductility of the AA5083 MIG-welded joints, with a maximum elongation of 16.64% achieved at 0.1 wt.% Ti addition. The hardness of the joints was the lowest in the weld center zone. This study provides critical insights into the role of Ti content in MIG welding and contributes to the advancement of high-performance filler wire formulations.