Arc Melting Method Research Articles

Influence of atomic substitution on the structural stability and half-metallicity of Fe2-xCrxCoSi (x = 0 to 1) alloys

Bulk Fe2-xCrxCoSi (x = 0, 0.25, 0.5, 0.75, and 1) Heusler alloys have been prepared by arc melting method. Alloys with 0.0 ≤ x ≤ 0.75 show a highly ordered phase pure XA structure. However, 17 % of an impurity (A15 phase) was detected in the alloy with x = 1. The saturation magnetization (Ms) and Curie temperature (TC) decreased linearly with an increase in Cr content for alloys with x ≤ 0.75. Ms measured at 5 K followed the Slater–Pauling rule for half-metals. Ab initio calculations with the GGA + U approach revealed that spin polarization (P) increased with an increase in Cr and eventually reached 100 % for the alloys with x = 0.5. Though Fe-Co disorder affects P, it is still high (>98 %) for alloys with x ≥ 0.5. Despite the smaller bandgap (0.61 eV) of Fe1.5Cr0.5CoSi than FeCrCoSi (0.91 eV), it has higher Ms, elevated TC, and 100 % P. These factors, coupled with the challenges associated with obtaining phase pure FeCrCoSi alloy, make Fe1.5Cr0.5CoSi a preferred candidate for spintronic device applications.

Stacking ensemble learning assisted design of Al-Nb-Ti-V-Zr lightweight high-entropy alloys with high hardness

To improve the accuracy and efficiency of machine learning models in predicting and designing the mechanical properties and designing of lightweight high-entropy alloys, we have trained multi-classification machine learning models using stacking ensemble method. This ensembled model achieves high prediction accuracy of 0.9457 and good anti-overfitting performance. Two candidate high-entropy alloys with high hardness from the predicted results (Al0.38Ti0.36V0.05Zr0.16Nb0.05 and Al0.51Ti0.28V0.04Zr0.16Nb0.01) were selected to prepare bulk samples using arc melting method. The experimentally measured micro Vickers hardness of two samples were 723.7 HV and 691.0 HV respectively, and only slightly lower than the hardness values predicted by the model, with an error of less than 8 %. The phase structure of the samples, which is a mixture of HCP and FCC, also agrees well with the predicted results. This indicates that our machine learning approaches is highly effective in predicting the hardness of high-entropy alloys, with accuracy that has been experimentally verified, thereby significantly enhancing the efficiency of designing new lightweight high-hardness high-entropy alloys.

Advanced multi-component FeCoCuAlMo intermetallic electrocatalysts for efficient and sustainable hydrogen evolution in alkaline freshwater and seawater

Electrolyzing seawater to produce hydrogen is a promising sustainable energy production technology. The current non-precious metal-based hydrogen evolution reaction (HER) electrocatalysts demonstrate inadequate catalytic activity and poor stability in seawater electrolyte. Therefore, developing stable and efficient non-precious metal-based HER electrocatalysts is a major challenge for achieving sustainable green energy development. This work reports a multi-component intermetallic catalyst FeCoCuAlMo prepared by arc melting and chemical dealloying methods. The electrocatalytic hydrogen evolution performance of catalysts with varying atomic ratios (FeCoCu)20(Al70Mo30)80, (FeCoCu)30(Al70Mo30)70, (FeCoCu)40(Al70Mo30)60, and (FeCoCu)50(Al70Mo30)50 in alkaline seawater and alkaline electrolyte was studied. The findings indicate that these catalysts primarily consist of AlMo3 and (Cu0.35Fe0.35Co0.3)Al, among which the dealloyed (FeCoCu)30(Al70Mo30)70 exhibits excellent catalytic activity with overpotentials of 137.54 and 116.91 mV at a current density of 100 mA/cm2 in alkaline seawater and alkaline electrolyte, respectively, outperforming most catalysts. Additionally, it demonstrated long-term stability in alkaline seawater and alkaline electrolyte for 250 and 400 h without significant decay at overpotentials of 236 mV and 276 mV, respectively. This improved performance can be attributed to the unique structure of the multi-component intermetallic compound, which provides good thermodynamic stability and synergistic effects among its constituents, thereby enhancing HER performance. Within this multi-component intermetallic compound, AlMo3 particles serve as the primary conductive medium to accelerate electron transfer, while (Cu0.35Fe0.35Co0.3)Al serves as the main active site, resulting in a stable structure that provides the catalyst with high catalytic activity and good stability. Thus, the (FeCoCu)30(Al70Mo30)70 electrocatalyst is a promising candidate for seawater electrolysis aimed at hydrogen production.

Effect of Er2O3 and Y2O3 on microstructure and mechanical properties of Ti2AlNb alloy

Rare earth oxides can significantly refine the microstructure of the cast alloys and improve their mechanical properties. In this study, Er2O3 and Y2O3 particles were chosen to add into the Ti2AlNb-based alloy with vacuum non-consumable arc melting method. For the Er2O3 particles, it has obvious dissolution and re-precipitation characteristics during melting. While for the Y2O3 particles, they are more stable, and aggregated and grew up during melting. These two kinds of Er2O3 or Y2O3 both have obvious refinement effects on the B2 grains due to their heterogeneous nucleation. Specially, adding Er2O3 particles can promote the decomposition of the B2 and α2 phases and the increases of the O-phase content. But adding the Y2O3 particles can inhibits the B2 decomposition and just only promotes the α2 decomposition into the O-phase. Additionally, the TAC-Er2O3 ingot shows the worst mechanical properties at room-temperature due to its large size and grain boundary segregation of the Er2O3 reinforcements. Conversely, the TAC-Y2O3 alloy exhibits excellent strength and ductility whatever at room- and high- temperatures owing to its fine grain strengthening and effective strengthening of the second precipitated Y2O3 phases.

Tuning conduction properties and clarifying thermoelectric performance of P-type half-heusler alloys TiNi1−xCoxSn (0 ≤ x ≤ 0.15)

TiNiSn is an N-type thermoelectric material with a high-power factor composed of low toxicity and abundant elements. TiNiSn also shows P-type electrical conduction by hole doping. In this study, we tune the conduction properties of TiNi1−xCoxSn (0 ≤ x ≤ 0.15) with Co substitution at the Ni site. The samples were prepared by the arc melting method, and thermoelectric properties were investigated up to 800 K. The results of the Hall effect and the Seebeck coefficient measurements indicate that the majority of charge carriers changes from electrons to holes at x ≥ 0.03, suggesting that Co acts as an acceptor. We report for the first time that Ti0.994Ni1.00Co0.051Sn1.01 exhibits ZT = 0.12 at 675 K. This work reveals that Ti0.994Ni1.00Co0.051Sn1.01 could be a potential P-type thermoelectric material operating at high temperatures.

Microstructure evolution and mechanical properties of NiAlCrFeMo high entropy superalloy after different annealing treatment

A novel NiAlCrFeMo high entropy superalloy was prepared using the vacuum arc melting method, followed by annealing at 800 °C, 1000 °C, and 1200 °C for 10 h. The microstructural characteristics and mechanical properties of the alloy after annealing were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Vickers hardness testing, and high-temperature tensile testing. The results indicate that the as-cast alloy consists of dendritic γ+γ′ phases and interdendritic B2-type β phase, with hemispherical α-Cr phases present within the β phase. Compared to the as-cast status, the volume fraction of the β phase in the annealed state increased from 18.52 % to 26.13 %. Notably, at 800 °C/10h, acicular γp’ phases precipitated within the β phase. The alloy exhibited varying degrees of improvement in both strength and ductility after annealing. The specimen annealed at 800 °C/10h showed the highest strength (σYS = 181.06 MPa) and good ductility (εEI = 12.45 %), with strength increasing by approximately 13.10 % compared to the as-cast status. This improvement is attributed to the coarsening of the α-Cr phase, the transformation in γ′ morphology, and the precipitation of acicular γp’ phase. At 1200 °C/10h, all precipitates dissolved into the matrix, resulting in the lowest strength (σYS = 134.08 MPa) and the highest ductility (εEI = 15.54 %).

Microstructures and corrosion behaviors under sodium chloride aqueous conditions of Co-free non-equiatomic Al0.32CrFeTi0.73(Ni1.50-xMox) (x=0, 0.23) high entropy alloys

High entropy alloys (HEAs) were prepared using a vacuum arc melting method. The effect of Mo partially substituting Ni on the crystal structure and corrosion behaviors was studied. The results show that the HEAs exhibited a multiphase complex crystal structure which was composed of a BCC matrix and several intermetallic phases. The HEAs showed good corrosion resistance despite multiphase heterogeneity. But cyclic polarization showed that the HEAs were susceptible to pitting corrosion. Selective corrosion of Cr-depleted phases after polarization tests was attributed to the galvanic corrosion between Cr-depleted and Cr-rich phases. The spontaneous passive films on the HEAs surface were characterized by p-type semiconductor. Existence of Mo element of the HEAs accelerated passivation reaction kinetics, improved the stability of passive film, accordingly, acquired better general and pitting corrosion resistance.

Design and characterization of novel Ti-8Mo-xFe-yCu alloys as implant materials: Evaluation of biocompatibility, mechanical properties, and antibacterial potential

Titanium and its alloys are highly desirable materials for biomedical metallic implants due to their superior specific strength, excellent corrosion resistance, and exceptional biocompatibility. Among these alloys, Ti6Al4V is widely used in practical biomedical applications because it offers an excellent combination of strength, fracture toughness, and corrosion resistance. However, recent research has revealed limitations in its biocompatibility attributed to the presence of toxic elements such as Al and V. In addition, it has been reported that Ti6Al4V is costly due to the addition of Vanadium and has the potential for post-implant inflammation. As a result, researchers have been investigating new biomedical beta-Ti alloys using biocompatible, affordable, and easily accessible beta-stabilizers like Mo, Fe, and Cu, to achieve similar performance as Ti6Al4V alloys. The present study aims to develop a novel biomedical alloy through the arc melting method, to obtain an implant material possessing low elastic moduli, biocompatibility, and antibacterial properties to mitigate the risk of post-implant inflammation. Microstructural analysis was conducted using microscopy and x-ray diffraction, while the mechanical properties were evaluated through micro vickers hardness testing machine and elastic moduli measurement utilizing the impulse excitation technique. Cytotoxicity assessment was performed using the (Cell Counting Kit-8) CCK-8 method, followed by an examination of the alloy's antibacterial properties using the point counting method. β-Ti single phase was obtained in this study with the addition of ≥1% Fe and ≥1% Cu. The Ti-8Mo-2Fe-2Cu alloy was found to have the lowest elastic moduli of 95 GPa. Electrochemical measurements show that the Ti-8Mo- xFe- yCu alloys have a lower corrosion current density of around 0.319–2.317 µA/cm2 compared to Ti6Al4V of 16.543 µA/cm2. The Ti-8Mo-1Fe-3Cu, Ti-8Mo-3Fe-1Cu, and Ti-8Mo-3Fe-3Cu alloys have comparable biocompatibility with Ti6Al4V with the viability of mesenchymal stem cells (MSCs) above 75% and have a positive antibacterial response. Ti-8Mo-3Fe-3Cu alloy demonstrates the most favorable blend of microstructure, mechanical attributes, corrosion resistance, cell viability, and antibacterial properties as an alternate biomaterial for implant applications.

Hysteresis gap-shrinking and structural effects of minor Al and Ti modifications on binary CuAl-based high-temperature shape memory alloys

Cu-based shape memory alloys (SMAs), except for exhibiting shape recovery, superelasticity, and high damping, are desirable because these smart materials have higher electrical and thermal conductivity and much lower prices than NiTi SMAs. However, they also have some downsides in mechanical strength and brittleness (mostly stemming from their coarse grain structure) and thermal instability. Therefore, adding some grain refining elements to these SMAs to improve their shape memory effect (SME), and thermal, structural, and mechanical properties is a widespread and simple way that significantly affects their martensitic phase transitions, structure, and mechanical properties. One of these grain-refining elements is titanium. Its thermal conductivity is lower than those of Cu and Al elements and has a low solubility in Cu-matrix. Besides the effects of small Al variations, the use of minor amounts of titanium in binary CuAl-base alloys can show impressive effects on all characteristics of these shape memory alloys, such as shape memory effect properties, martensitic transformation kinetics parameters, and microstructural features. In this research work, CuAlTi ternary high-temperature shape memory alloys (HTSMAs) with new compositions were produced by the arc melting method without a complicating use of Mn or Ni components in usual ternary CuAlMn and CuAlNi shape memory alloys. Thermal analyses of the prepared samples of the alloys were investigated by using differential scanning calorimetry (DSC) and differential thermal analysis (DTA) measurements. In contrast, x-ray diffraction (XRD) test results and optical micrographs were used for analyzing the structure of the alloy samples. The effect of different amounts of low soluble and grain refining Ti element on the binary CuAl alloy system was investigated.

Effect of Mo Content on the Structural, Mechanical, and Tribological Properties of New Zr-Nb-Mo Alloys Obtained by Combining Powder Metallurgy and Vacuum Arc Melting Methods.

Considering the high demand for innovative solutions in medicine, a major increase in interest in biomaterials research has been noticed, with the most significant advancements in metals and their alloys. Titanium-based alloys are one of the most recognised in the scientific community but do not represent the only way to achieve optimal results. Zirconium alloys for medical applications are a novelty with significant research potential based on their outstanding properties, which may be of value for medicine. The aim of the present study was to obtain new biomedical Zr-Nb-Mo alloys with varying ratios of their respective elements-Zr and Mo-using combined powder metallurgy (PM) and arc melting (VAM) methods. The obtained samples underwent microstructure analysis using an optical microscope (OM) and a scanning electron microscope (SEM). The study of element distribution was conducted with energy dispersive spectroscopy (EDS), whereas the phase composition was determined using X-ray diffraction (XRD). Mechanical properties were examined with a Micro Combi Tester MCT3, whereas tribological properties were assessed with a TRN Tribometer, and Ringer's solution was used as a lubricant. Additionally, the wear tracks of the studied samples were observed using the SEM. The research results indicated that increased Mo content conduced to microstructure refinement and homogeneity. Furthermore, the higher content of this element contributed to the growth of the HVIT, HIT, and EIT parameters, together with the improvement in the tribological performance of the alloys. XRD analysis revealed that the obtained samples were multiphase, and raising the Mo addition promoted the formation of new phases, including a ternary phase-Zr0.9Nb0.66Mo1.44 (Fd3¯m). The chemical composition study showed uneven distribution of niobium and areas of uneven mutual distribution of zirconium and molybdenum.

Investigation of bio-corrosion behavior, structural and thermal properties of Ni20Ti50Sn30 high-temperature shape memory alloy

In this study, Ni20Ti50Sn30 (atomic %) sample was prepared using the arc melting method. Some thermodynamic parameters (phase transformation temperatures, PTT; enthalpy, ΔH; and phase transformation hysteresis, H) obtained from the phase transformations of the alloy were determined using differential scanning calorimetry (DSC). The sample exhibited high-temperature shape memory alloy (HTSMA) properties. X-ray (XRD) analysis was performed to determine the crystal structure properties at the alloy. The presence of B2, B19′, Ti2Ni, β-Ti, Ni3Sn4, TiNiSn and Ti3Sn phases was identified through X-ray analysis of the alloy. Scanning electron microscopy (SEM) was used to examine the pre- and post-corrosion surface morphologies of the sample, with EDX analysis being performed to reveal chemical structure determinations (matrix phases, precipitates and weathering zones). The presence of dendritic arms was observed, while martensite plates were absent in all SEM images. Particularly in the SEM image taken after corrosion, it was noted that the TiO2 layer placed on the surface of the matrix rich in Ti elements altered the surface morphology of the alloy. The presence of Ti and O elements in the post-corrosion EDX analysis confirmed the existence of this layer. Biocompatibility studies of the alloy were conducted using potentiodynamic corrosion tests and electrochemical impedance spectroscopy (EIS) methods. It was determined that the NiTiSn sample was in the excellent stability class according to corrosion standards.

Magnetic properties and magnetocaloric effect in the multiple rare-earth-containing MRE2Cu2In compounds

In this study, two Mo2FeB2-type multiple rare-earth-containing MRE2Cu2In (MRE = Dy1/3Ho1/3Er1/3 and Ho1/3Er1/3Tm1/3; space group P4/mbm, No. 127) compounds are prepared via arc-melting method and systematically determined regarding their structural and magnetic properties, magnetic phase transition (MPT), and magnetocaloric (MC) performances. They undergo typical second-order MPT at low temperatures. The MC effect and MC performances of the present MRE2Cu2In compounds at low temperatures are assessed using magnetic entropy changes, refrigerant capacity, and temperature-averaged entropy changes. The values of these parameters are comparable to most updated candidate materials for low-temperature magnetic cooling, making the present MRE2Cu2In compounds considerable for practical applications.

New lightweight and super-hard refractory high-entropy alloys developed by a high-throughput method

Lightweight refractory high-entropy alloy (LRHEA) is one of potential structural materials in aerospace industry for its excellent high-temperature comprehensive properties and low density. In this work, a new high-throughput method to develop LRHEAs was proposed. The equimolar HfNbTaTiZr alloy was immersed with melting pure aluminum for a given time, and a thick layer with composition gradient was obtained. Further characterizations of the layer result in relations between composition and nanohardness or Young's modulus, which facilitate the selection of the optimal composition with desired properties. Finally, three LRHEAs were designed and casted into bulk samples with arc-melting method. The alloys show superhigh Vickers hardness of 8.29–9.56 GPa and low densities of 6.27–7.08 g/cm3, showing great potentials in applications as wear-resistant materials. The high-throughput method developed here may also accelerate the development of new LRHEAs.

Hydrogen isotope effect on thermodynamic and kinetic properties of Pd based ternary alloys: Pd–Ag-M (M = Au, Zr)

Owing to the importance of hydrogen and its isotopes in energy sector, the present study investigates thermodynamic and kinetic hydrogen isotope effects on desorption reaction of newly synthesized Pd-based ternary alloy-hydrides/deuterides viz., Pd0.89Ag0.05M0.06 (M = Au, Zr)–H/D. Alloys were prepared by arc melting method followed by characterization using PXRD, SEM, TXRF and EDX techniques. The effect of hydrogen isotopes on thermodynamics of H2/D2 desorption reaction was investigated by generating pressure-temperature isotherms (PCIs) at various temperatures using a Sieverts' type volumetric apparatus. The PCT diagram of alloys depicts a single plateau which confirms desorption to be a one-step process. Both alloy systems display a normal isotope effect as indicated by higher plateau pressure for deuterides as compared to hydrides. The enthalpy and entropy changes for the desorption reactions were calculated using Van't Hoff equation. The separation factor derived from PCT data indicates that Pd0.89Ag0.05Au0.06 alloy has a significantly high separation factor as compared to other Pd based alloys reported in the literature. To get more insight into this behavior, non-isothermal kinetic analysis of H2/D2 desorption based on Differential Scanning Calorimeter (DSC) data acquired at four different heating rates was conducted and activation energies of desorption were calculated by invoking Kissinger's equation. The activation energies of alloys were found to be lower than that of palladium which explains the high separation factor of alloys as compared to Pd. The desired combination of higher separation factor and lower activation energy makes Pd0.89Ag0.05Au0.06 alloy a promising material for practical application in the separation of hydrogen isotopes via self-displacement gas chromatography (SDGC).

Effect of rare earth element Y content on microstructure, magnetic properties, and electrochemical properties of the as-annealed FeCoNiAl0.2Yx high-entropy alloys

FeCoNi high-entropy alloy (HEA) is widely used in the aerospace and chemical industry. However, the strength and corrosion resistance of the alloy still need to be improved. In this paper, FeCoNiAl0.2Yx (x = 0, 0.05, 0.1, 0.2, and 0.3 in mole ratio) high entropy alloys with different contents of rare earth (RE) element yttrium (Y) were prepared by the vacuum arc melting method, and then the alloys were subjected to annealing treatment at 800 °C/2h. The microstructure, hardness, magnetism, and corrosion performance of FeCoNiAl0.2Yx HEAs in the annealed state with different contents of element Y were analyzed. The results show that the annealed FeCoNiAl0.2Yx HEAs without the addition of element Y and after the addition of element Y both were composed of a face-centered cubic phase. The alloy showed a dendritic structure inside. The element Y was solidly dissolved in the alloys to refine the microstructure of the alloys, and the dendrites were gradually refined with the addition of Y. The Y element caused the phenomenon of lattice distortion inside the alloys, which led to the increase in the alloys’ hardness. The alloy with x = 0.2 showed the greatest exchange of magnetic atoms and the alloy with x = 0.05 showed the lowest coercivity. The alloy with x = 0.1 showed the lowest self-corrosion current density, the broadest passivation zone, the densest dendrites, the smallest grain spacing, and the weakest tendency for intergranular corrosion. The present study shows that the introduction of element Y improves the microstructural morphology, hardness, magnetism, and corrosion properties of FeCoNiAl0.2Yx HEAs in the annealed state.

Dually functional NiSi intermetallic compounds for the efficient hydrogenation and oxidation of cinnamaldehyde

Intermetallic compounds (IMCs) are promising catalysts for upgrading biomass-derived platform chemicals. Herein, bifunctional NiSi IMCs catalysts were developed for the hydrogenation and oxidation of cinnamaldehyde (CAL). A solvent-free arc-melting method was employed for the synthesis of NiSi IMCs within 5 min. The NiSi IMCs catalysts afforded 99 % conversion of CAL and presented ∼ 71 % yield of 2-phenyl propanol and ∼ 34 % yield of benzaldehyde for the hydrogenation and base-free oxidation of CAL, respectively. Moreover, NiSi IMCs could be used for five runs without deactivation. Characterizations and theoretical calculation results indicated the formation of intermetallic structure and the existence of Si vacancy sites, which could not only facilitate the efficient hydrogenation of CAL but also expose NiOx species as catalytic centers for the oxidation of CAL, leading to the high performance and stability in both hydrogenation and oxidation process.

Effects of composition complexity of single-phase concentrated solid solution alloys on He bubbles behavior

Three types of single-phase concentrated solid solution alloys (SP-CSAs) with compositions of NiCoFe, NiCoFeCr and NiCoFeCrMn were prepared using the vacuum arc melting method. The bulk samples were implanted by 100 keV helium ions to a fluence of 5 × 1016 ions/cm2 at 673 K. The transmission electron microscopy (TEM) is employed to systematically characterize helium bubbles along the depth of implantation. The observation results revealed that the He bubble density followed the sequence NiCoFeCr > NiCoFeCrMn > NiCoFe, and the bubble sizes exhibited the trend NiCoFe > NiCoFeCrMn > NiCoFeCr. For NiCoFe and NiCoFeCr, the higher the number complexity of components, the higher the density and the smaller the size of He bubbles. However, the introduction of Mn as a larger-sized atom appeared to increase the vacancy diffusivity and lower the melting temperature, consequently promoting helium bubble growth.

Effect of double substitution on hydrogen absorption-desorption properties of Ti2CrV alloy

Doubly substituted Ti2CrV alloy with composition Ti1.5Sc0.3CrVNi0.2 was prepared by arc melting method followed by annealing. The annealed alloy exists in body centred cubic (BCC) structure and shows fast kinetics for hydrogen absorption and desorption at room temperature. BCC phase of the alloy undergoes phase transformation to face centred cubic (FCC) hydride phase with H atoms occupying tetrahedral sites in the lattice, reaching an overall H/M ratio >2.2 (storage capacity ∼ 4 wt%). Storage capacity decreases by 40% in the 2nd cycle and then stabilizes at a value of ∼2.5 wt% for the subsequent 10 cycles. A drastic reduction in hydride desorption temperature upon double substitution (Sc and Ni substitution in Ti2CrV alloy) has been confirmed by DSC studies. Furthermore, the change in isotope effect in doubly substituted Ti2CrV alloy is discussed in light of thermal stabilities of the hydrides and deuterides.

Effect of Mo content on microstructure and mechanical properties of CoCrFeNi Series high-entropy alloys

In this paper, the microstructure and mechanical properties of CoCrFeNiMox (x = 0, 0.1, 0.3, 0.5, 0.7, and 1.0) high-entropy alloys (HEAs) prepared with high-vacuum arc melting method were studied in detail. After Mo-doping, the strengthening mechanism of HEAs mainly included the component segregation strengthening and the second phase strengthening. Cr and Mo elements were enriched at the grain boundary of HEAs, which leaded to the formation of σ phase and strengthens the alloys. The microhardness and strength increased with Mo contents, while the elongation decreased gradually. Among which, the higher microhardness, yield strength, and ultimate tensile strength of CoCrFeNiMo0.3 alloy reach 205.96 HV, 292.22 MPa, and 593.25 MPa, respectively, in compared with other alloys. More importantly, the percentage elongation of which remains 37.36%, and the microhardness distribution was uniform with an average value of 7.4 GPa and an elastic modulus of 263.6 GPa. The research findings presented in this paper could serve as a valuable theoretical basis and practical foundations for the strengthening efforts of face centered cubic (FCC) HEAs.

Hydrogen generation by hydrolysis of Sc–Sn alloy over a wide temperature range as low as 0 °C

A series of Sc–Sn alloys are prepared by the arc-melting method and their hydrogen generation performance of hydrolysis in pure water is investigated. It was found that only Sc element reacts with water in Sc–Sn alloy, while Sn element is retained as an elemental metal. The reaction temperature of Sc with water can be reduced below 0 °C after Sc and Sn are alloyed. The Sc3Sn2 alloy has the best hydrogen generation performance. Its hydrogen conversion rate is up to 90% at 0 °C for 100 min as well as when the water temperature dropped from 60 °C to 0 °C, the average conversion rate in the first 30 min only dropped from 19.95 mL/min∙g to 14.31 mL/min∙g. The hydrogen generation performance of Sc–Sn alloys depends on the reaction activity after Sc and Sn alloying, the effect of micro galvanic cells and the solidification microstructure in the alloy ingot.