Temperature Dependence of the γ/γ′ Interfacial Energy in Binary Ni–Al Alloys

Published data on the coarsening kinetics of γ′ (Ni₃Al) precipitates in binary Ni–Al alloys aged at 12 temperatures ranging from 773 K to 1073 K are analyzed to provide a comprehensive evaluation of the temperature dependence of the γ/γ′ interfacial free energy, σ. The data are analyzed using equations of the trans-interface-diffusion-controlled (TIDC) theory of coarsening, with temporal exponent n = 2.4. The results show that σ decreases with increasing temperature, T. A linear empirical equation is fitted to the data on σ vs T; it extrapolates to σ = 0 in the liquid region of the Ni–Al phase diagram, as it should do. A quantitative temperature-dependent transition radius, r_trans, is calculated; it depends on the product of the interface width and the ratio of the chemical diffusion coefficients in the γ phase and interface regions. Applying the TIDC coarsening equations to calculate σ is justified when the average radius, 〈r〉, satisfies the condition 〈r〉 < r_trans, which is valid for all the data used in the fit. The data on σ vs T are compared with theoretical predictions. The results are discussed in the context of previous work, as well as with values of σ obtained through analyses using the equations of traditional LSW coarsening kinetics, n = 3.

     

Temperature–Composition Dependence of Thermodynamic Mixing Functions of Co–Cr–Cu–Fe–Ni Melts

Powder Metallurgy and Metal Ceramics - In the framework of the CALPHAD method, a thermodynamic database was developed for calculating the thermodynamic properties of liquid alloys in the...     

Effect of Cr and Ni/Fe Ratio on the Microstructure and Mechanical Properties of γ′-Strengthened Ni–Fe-Based Alloys

Metallurgical and Materials Transactions A - To continue to meet the future materials’ requirements for advanced power generation systems, enhancing the mechanical properties and long-term...     

Influence of the Oxygen Induced Surface Segregation Process of Solutes on the Anti-corrosion Properties of the Fe–Cr and Fe–Cr–Si Alloys

Metallurgical and Materials Transactions A - The influence of the oxygen-induced surface segregation process of Cr and Si solutes on the anti-corrosion properties of Fe–Cr and...     

Effect of Microstructure,Strain Rate,and Elevated Temperature on the Compression Property of Fe–Co–Ni–Cr–Zr Alloy

Metallurgical and Materials Transactions A - Eutectic high-entropy alloys with FCC solid solution phase and hard Laves phase can be used as potential structural materials to meet the service...     

Sintering of Tungsten and Tungsten Heavy Alloys of W–Ni–Fe and W–Ni–Cu: A Review

Tungsten is a refractory metal possessing good mechanical properties of high strength, high yield point, and high resistance to creep. Therefore, tungsten and its alloys are used in many high temperature applications. Due to the high melting point, they are generally processed through powder metallurgy method. The powders are compacted using die pressing or isostatic pressing. The compacts are sintered in a sintering furnace to achieve high density, thereby, making the metal suitable for further processing. This article reviews the recent research findings of consolidating tungsten and its alloys (W–Ni–Fe and W–Ni–Cu), from preparation of powder alloys to sintering of the compact. The advances in sintering are based on the objective of achieving good densification of the metal at lower temperature and at faster rate. The use of microwave sintering and spark plasma sintering techniques resulted in significant reduction in sintering time and producing products of good mechanical properties.     

Centrifugal Metallothermic SHS of Cast Co–Cr–Fe–Ni–Mn–(Х) Alloys

Russian Journal of Non-Ferrous Metals - A relatively new approach to obtaining metal materials containing several principal elements in equiatomic concentrations which look promising for replacing...     

Revealing the Role of Cerium on Precipitation Behavior of In Situ TiC Particles and Wear Resistance of High-Titanium Wear-Resistant Steels

Compared to conventional martensitic wear-resistant steels of the same hardness, high-titanium wear-resistant steels with in situ TiC particles can significantly improve wear resistance. However, micron-sized TiC particles will decrease the toughness of high-titanium wear-resistant steels. Here, in order to improve wear resistance without reducing impact toughness, we incorporate 0.0025% cerium elements into high-titanium wear-resistant steels. Compared with no cerium steel, the steel containing cerium is demonstrating comparable mechanical properties, with the yield strength of 1283 MPa and impact toughness of 35.6 J, and the wear performance of the steel containing cerium is 1.78 times that of the steel with no cerium. The results show that with the addition of cerium the effective grain size of the steel decreases, and yield strength and toughness increase. The addition of cerium can form intermetallic compounds of Ce₂O₂S, which are used as heterogeneous nuclear particles in TiC to form rare earth composite particles calculated by the 2D mismatch theoretical model of Bramfitt. As the average spacing of the reinforcing phase particles in the steel decreases, the effective grain size of the steel decreases, and the number of reinforcing phase particles increases, the wear resistance of the steel with the addition of cerium is optimized.     

Effect of Vacuum Hot Pressing Temperature on the Mechanical and Tribological Properties of the Fe–Cu–Ni–Sn–VN Composites

Powder Metallurgy and Metal Ceramics - The mechanical (hardness and elastic modulus) and tribological (friction force and wear rate) properties of the Fe–Cu–Ni–Sn–VN...     

Research on Nitrogen Solubility of Fe–Cr–Mn–V–N System Alloys in Liquid and Solid Phases

In this paper, the thermodynamic model of nitrogen solubility in vanadium nitrogen microalloyed high strength weathering steels of Fe–Cr–Mn–V–N system, according to Hillert’s model for Gibbs energy of its various phases, was established and validated. In the model, the effect of the nitrogen partial pressure on the activity coefficient and the lattice structure characteristics of the vanadium nitrogen precipitated phase were considered. It would be of guiding significance for the design and smelting of Fe–Cr–Mn–V–N system alloys. Based on the established model, the nitrogen contents in \(\delta\), \(\gamma\), \(\alpha\) phase and liquid were calculated as a function of the temperature for Fe–Cr–Mn–V–N system alloys. The results show that: first, the maximum solubility of nitrogen in the solidification process is obviously affected by the phase transition when there is a sudden change in the solubility of nitrogen at the phase transition point. The maximum nitrogen solubility of the molten steel in the delta phase region determines whether nitrogen bubbles are formed during the solidification process. The nitrogen solubility is lowest in the solid–liquid region (about 1673 K). Secondly, the increase of Cr and Mn content is beneficial to improve nitrogen solubility in liquid and solid phases. However, the increase of V content mainly affects the nitrogen solubility in the solid phase because the nitrogen in this temperature range is precipitated in the form of vanadium nitride, as the second phase plays a role in strengthening. In addition, the alloying element Mn has a significant effect on nitrogen solubility since the Mn element is the promoting element of austenitic formation. During the solidification process, the delta ferrite region gradually reduces and may disappear with increasing Mn content. Therefore, increasing the Mn content of the alloy system in the design of alloy composition, can reduce the precipitation trend of the nitrogen during the solidification process, which can effectively avoid bubble formation in high nitrogen weathering steels. Lastly, with the increase in the nitrogen partial pressure, the solubility of nitrogen increases during the liquid and solid phases.     

The Structure and Phase Composition Acquired by Fe–Ti–Ni–C Alloys in Thermal Synthesis

Powder Metallurgy and Metal Ceramics - The structure and phase composition of Fe–Ti–Ni–C alloys produced in situ by thermal synthesis at 1200°C using TiH2, Fe, graphite, and...     

In Situ Observation of the Lengthening Rate of Bainite Sheaves During Continuous Cooling Process in a Fe–C–Mn–Si Superbainitic Steel

The evolution of lengthening rate of bainite sheaves during continuous cooling process in a Fe–C–Mn–Si superbainitic steel was investigated by in situ observation on high-temperature laser scanning confocal microscope. The lengthening rates of bainite sheaves in three temperature ranges were calculated. The results indicate that the lengthening rate of bainite sheaves continuously decreases with the decrease of temperature during continuous cooling process. The lengthening rate of bainite sheaf depends on undercooling, transformation temperature, the diffusion of carbon atoms and the carbon content in parent austenite etc. The lengthening rate at high temperature is large due to the favorable carbon diffusion, smaller carbon content and less plastic deformation in untransformed austenite. Additionally, the microstructures after different isothermal holding temperatures were analyzed, indicating that the larger lengthening rate of bainite sheaves due to the high isothermal transformation temperature does not mean more amount of bainite transformation. Lower bainitic transformation temperature results in more and finer bainite plates.     

Grain coarsening in FeNiCr alloys and the influence of second phase particles

The effects of second phase particles, e.g. M₂₃C₆, MC and M(C, N) carbides on the grain growth phenomenon of FeNiCr alloys have been determined. Various theoretical models on grain coarsening have been compared. The grain size at all stages of grain coarsening was dependent on the undissolved carbide particle size (r), the volume fraction (f), and the nature of the carbides. The nature of M₂₃C₆ carbides varied, since Fe, Ni and Mo entered the M₂₃C₆ unit cell; and complex carbides such as (Cr₁₅Fe₄Ni₂Mo₂)C₆ were formed. Gladman's equation was verified for predicting the observed grain size values to a significant degree, and other models were less successful.     

Comparison of the Effect of Ni,Mn, Fe,and Si Additives on the Microstructure and Phase Composition of Hypereutectic Aluminum–Calcium Alloys

Russian Journal of Non-Ferrous Metals - A comparative analysis of the phase composition and morphology of primary crystals in hypereutectic alloys of the Al–Ca–Ni–X system (where...     

Effects of Nickel on the Oxide/Metal Interface Morphology and Oxidation Rate During High-Temperature Oxidation of Fe–Cu–Ni Alloys

Steel produced in an electric arc furnace (EAF) contains a high amount of Cu that causes a surface-cracking phenomenon called surface hot shortness. Ni reduces the risk for surface hot shortness, and this work focuses on investigating the following two phenomena caused by Ni during oxidation at 1150 °C for Fe–Cu–Ni alloys: (1) the decrease in oxidation rate and (2) the formation of a wavy liquid-Cu/oxide and of liquid-Cu/γ-iron (γFe) interfaces, which promote Cu occlusion into the scale. Thermogravimetry, scanning electron microscopy, and transmission electron microscopy-energy dispersive spectroscopy techniques were applied. A numerical model also was developed to explain the experimental results. High Ni contents cause higher liquid-Cu/γFe interface nickel concentrations and more potential for an interface breakdown. The decrease in oxidation rate by adding nickel can be explained qualitatively by the decrease in Fe cation transport through the wüstite layer.     

Effect of zirconium on the oxygen solubility in liquid nickel and Ni–Fe melts

The oxygen solubility in liquid nickel containing zirconium is studied experimentally for the first time at 1873 K. The equilibrium constants of the reaction of interaction between zirconium and oxygen dissolved in liquid nickel, the interaction parameters characterizing these solutions, and the zirconium activity coefficient in nickel at infinite dilution are found. The equilibrium constants of the reaction of interaction between zirconium and oxygen dissolved in the melt, the Gibbs energy of the reaction of interaction between zirconium and oxygen, and the interaction parameters characterizing these solutions are calculated at 1873 K for a wide composition range of Ni–Fe alloys. The oxygen solubility in various Ni–Fe melts containing zirconium is found at 1873 K. The deoxidizing capacity of zirconium increases as the iron content increases to 30% and decreases at higher iron content in the melt. This can be explained by the fact that an increase in the iron content lead to, on the one hand, a strengthening of the bonding forces of oxygen atoms in a melt and, on the other hand, to a significant weakening of the bonding forces of zirconium atoms with the base metal.