Special features of the α → γ transformation in powder carbon steels

The structural state of powder steels after sintering depends on the technological regimes of their production and can markedly affect the transformations in subsequent heat treatment. The effect of the technological regimes on the nature of the transformation is investigated.Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 3, pp. 14–16, March, 1996.     

Thermoelastic transformation in Cu - Al - Mn alloys

Heat treatment of Cu - 10%Al - Mn alloys with a low concentration of manganese can be accompanied by a transformation. The effect of manganese on the temperature range of this transformation and its kinetics is investigated.Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 8, pp. 5 – 6, August, 1996.     

Electrochemical Behavior of Nickel Hydride in Sodium Hydroxide Solutions

Electrochemical behavior of nickel hydride Ni₂H (-phase) is studied in 0.01–1 N NaOH by using common (VA) and cyclic (CVA) voltammetry, chronocoulometry, amperometry, and potentiometry. The limiting anodic and cathodic currents in VA and CVA curves are caused by the hydride decomposition via the following scheme Ni₂H -phase Ni + H_abs, where the intermediate -phase contains 0.003 at. % H, that is, one tenth that in the saturated -phase (0.03 at. %). At open circuit, the hydride maintains the equilibrium hydrogen potential. In the first 30 min, the hydrogen ionization from hydride is limited by solid-state diffusion and, later, the hydride decomposition. The anodic process involves ionization of sorbed hydrogen, while the cathodic process represents its electrochemical desorption: H₂O + H_ads + e H₂ + OH^–. The hysteresis observed in the cathodic CVA and open-circuit chronograms of the hydride potential in the beginning of anodic dissolution reflect the changes in the surface coverage of hydride with adsorbed hydrogen. The rate constant of hydride decomposition k, the rate Vitself, and the equilibrium constant K are as follows: k = k = 8 × 10^–5 s^–3, V = 3 × 10^–5 C/cm², and K = 10. The kinetic parameters of hydrogen electrochemical ionization from the hydride are b _a = 0.12 V and = 0.5.     

Developing Concepts of Chromium Functions in the Passivation and Pitting of Fe–Cr Alloys

The passivability and pitting resistance of Fe–(0–100)Cr alloys in deaerated acidic sulfate environments (at a concentration of sulfate ions of 0.1 to 1.0 mol/l and pH from 0.5 to 1.8) and neutral borate buffer solutions with a chloride concentration of 0.003 mol/l and pH 7.3 are studied with the use of steady-state and pulse electrochemical methods. Four critical alloy compositions corresponding to the sharp changes in the passivability, repassivability, and pitting resistance of the alloys are discussed: 6.5; 11; 17; and 27% Cr. Based on considering the alloys as purely mechanical mixtures with no sign of any order so that a chromium atom can occupy any lattice point with a probability proportional to the bulk chromium content, the following hypothesis is put forward. It is the crystallographic and electronic structure of Fe–Cr alloys that forms the main reason for the existence of the mentioned critical concentrations. Upon reaching certain critical compositions, chromium atoms either occupy positions in each coordination sphere (6.5% Cr), each elementary cell of an scc lattice (11% Cr), or each quasirhombohedral pore (17% Cr); or a superlattice compound appears (27% Cr).     

Interdiffusion Behavior of Ni–Cr–Al–Y Coatings Deposited by Arc-Ion Plating

Ni–Cr–Al–Y coatings were deposited on the Ni3Al–base superalloys IC-6 and K17 by arc-ion plating. The results indicated that a small amount of substrate atoms, such as Co, Ti, Mo, etc., existed in the Ni–Cr–Al–Y coatings near the substrates, probably due to sputter and antisputter. For the alloy K17, the impeding effect of Al was not obvious, because the temperatures of the substrate and the coating were high (420–480°C) during the deposition process and interdiffusion was accelerated. However, for alloy IC-6 which contains Al, as well as a high concentration of Mo, the diffusion of Cr was impeded. Vacuum heat treatment at 1050°C drastically increased diffusivities and the presence of Al and Mo was not enough to prevent some Cr diffusion. Thus, the coating became more uniform and close to the desired composition.     

Structure-Selective Dissolution of Al–Fe–Ni Bronze in Chloride Electrolyte

The selectivity of the anodic dissolution of the iron-rich phases of . 9-4-4-1 cast bronze in 0.5 N NaCl + 0.01 N HCl was studied. X-ray diffraction analysis revealed that the Fe₃Al and ₁-phases present at the surface of the initial bronze become predominantly etched during the early period of anodic dissolution at E = –0.12 V (NHE). According to electrochemical and analytical data, the above phases dissolve at this potential most rapidly. The x-ray diffraction data agree well with the results obtained by atomic absorption analysis of the solution.     

Mechanisms of the effect of vanadium,niobium, and titanium doping on the structure and properties of low-pearlite steels

Conclusions The favorable effect of doping with carbonitride-forming elements-vanadium, niobium, and titanium — on the structure and properties of low-pearlite steels subjected to controlled rolling is due to the change of the structural state of hot-deformed austenite, of the temperature range and nature of the -transformation, of the phase composition of the steel, and of the state of the -solid solution caused by the alloying with these elements.The ambiguous effect of doping with vanadium, niobium, and titanium on the strength and ductile properties of low-pearlite steel is due to the different degree of dispersion hardening, refinement of the ferrite grain, refinement of the solid solution, the ratio of the structural components, and the nature of the products of the -transformation.The newly devised economically alloyed low-pearlite steel 09G2FB for gas pipes with large diameter after controlled rolling with deformation at the concluding stage in the biphase +-region has a unique complex of mechanical properties satisfying the stringent requirements concening pipes intended for operation under conditions of the Far North.I. P. Bardin Central Scientific-Research Institute of Ferrous Metallurgy. Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 11, pp. 13–22, November, 1984.     

Isothermal formation of the ε-phase after phase hardening in ferromanganese alloys

Conclusions The investigations carried out show that isothermal formation of the -phase can be controlled not only by alloying, but also by means of repeated phase transitions. Reduction of the temperature at which the formation of the -phase commences intensifies the isothermal transformation near the martensite point and at room temperature. The latter is valid if the -transformation during continuous cooling begins not lower than the temperature at which the isothermal soaking is carried out, otherwise the intensity of the isothermal process decreases, and the lower the commencement of the -transformation with respect to the temperature isothermal line, the more the intensity drops. It was found that if the -phase forms at –60, –70°C, there is a complex dependence between the rate of the isothermal process and the temperature.It was demonstrated that when the -transformation temperature is fairly low, austenite can be supercooled by rapid cooling and the -phase may form during heating. Given the same supercooling rate, the transformation of austenite into -phase during heating is more complete when the heating rate is slow.It was noticed that if in continuous cooling the -phase forms at –60, –70°C, preliminary supercooling broadens the temperature range over which the isothermal -transformation is observed. The intensity of the process is influenced by the heating rate after supercooling.It was found that the maximum amount of -phase forming in the alloy G19 during continuous cooling after repeated phase transitions and subsequent isothermal soaking does not exceed 50–55%.It was discovered that isothermal soaking at room temperature in between repeated phase transitions intensifies the stabilization of the austenite.Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 4, pp. 2–8, April, 1965     

Recrystallization of maraging alloys

Conclusions In the maraging alloys investigated the transformation is not accompanied by refining of the original grains. The coarse-grained structure is eliminated by recrystallization of austenite at 900–1000°C, which occurs mainly by means of grain boundary migration.Physics of Metals Institute. Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 4, pp. 10–12, April, 1969.     

A Microstructural Study of Preferential Oxidation at the Grain Boundaries of Ni–Cr Alloys

The oxidation behavior of alloy grain boundaries in model Ni–Cr alloys was investigated. Two binary alloys with nominal wt.% compositions of Ni–10Cr and Ni–20Cr were used. Oxidation was performed in air for 50 hr at 1000°C. The grain boundaries intersecting the alloy surface in Ni–10Cr did not exhibit oxidation, whereas the alloy formed a thick (60 m) oxide layer which formed inwardly. The grain boundaries in this alloy showed a passivating influence at the adjacent regions and retarded oxide formation. An examination of the Ni–20Cr cross section revealed preferential oxidation to a depth of 65 m at the alloy grain boundaries intersecting its surface, while the oxide at the surface was a few micrometers thick. It is noted that the extent to which the grain-boundary oxidation differs from the alloy surface oxidation depends on the Cr content of the alloy. It is also considered that the grain-boundary oxidation behavior in different Ni–Cr alloys changes as a function of Cr content.     

Isothermal Oxidation of α2-Ti3Al

The isothermal oxidation behavior of binary Ti–25 at.% Al was studiedat 1073, 1173, and 1273 K in air and oxygen with emphasis on themicrostructure of the subsurface zone underneath the external oxidescale. Thermogravimetric analysis, acoustic-emission (AE) analysis, lightmicroscopy, scanning electron microscopy (SEM), atomic force microscopy(AFM), and cross-sectional transmission electron microscopy (TEM) werecarried out. Three layers could be identified in the subsurface regionconsisting of an internal oxidation zone of -Al₂O₃,and -Ti, a ternary phase with the empirical formulaTi–21Al–15O (at.%), and an oxygen penetration zone consisting of₂-Ti₃Al(O).     

On the oxidation ofα-Fe andε-Fe2 N1−z II. Residual strains and blisters in the oxide layer

The development of residual strains in the iron-oxide layers growing on -Fe and -Fe₂N_1–z at 673 K in O₂ at 1 atm was investigated by X-ray diffraction at room temperature. After correction for thermal-strain development due to cooling after oxidation, it was found that tensile growth strains occur in magnetite and compressive growth strains occur in hematite. The growth strains in the oxides on -Fe are (in absolute sense) 2–3 times as large as those in the oxides on -Fe₂N_1–z. Buckling of the oxide layer occurs in the case of an -Fe substrate, which is attributed mainly to relaxation of the growth strains in magnetite and hematite. Thermal-strain development during cooling enhances the tendency for buckling. Buckling is not observed for oxide layers on -Fe₂N_1–z, which could be due to the smaller values of absolute strain in the oxide layer on -nitride. The absolute values of the growth strains in the oxide layer on -nitride being smaller is attributed to microstructural changes in the nitride layer during oxidation.     

Protection of Sintered Steels against Corrosion in Neutral Media with an N-M-1 Inhibitor

The effect of an N-M-1 inhibitor (a salt of cyclohexylamine and C₁₀ to C₁₆ aliphatic acids) on the corrosion of sintered powder steels 13 and 141 (with the 14 to 17% porosity) in distilled or tap water at 20 to 80°C, as well as in 0.05 M Na₂SO₄ solution, is studied by gravimetric and electrochemical methods. The protective concentration of the inhibitor is lower in distilled, than in tap water or sodium sulfate solution. The protective action decreased with an increase in temperature. In tap water or sodium sulfate solution, the corrosion-inhibiting effect is weaker for 13 than for 141.     

The Influence of Ozone on the Electrochemical and Corrosion Behavior of Metals in Acid Media

The corrosion–electrochemical behavior of 092, 0817, 1017132 steels, 0628 alloy, and such metals as aluminum, chromium, and nickel are investigated in ozonized acid media. The effect of ozone on the corrosion–electrochemical properties of these metals are shown to be ambiguous.     

Improving the quality of forged propellers of alloy D1

Conclusion The working life and operational reliability of airplane propellers made of alloy D1 can be improved by manufacturing them from degassed aluminum with 0.3% Fe and 0.2% Si.Translated from Metallovedenie i termicheskaya Obrabotka Metallov, No. 5, pp. 8–9, May, 1974.     

Effects of the composition and low-temperature thermomechanical treatment on the mechanical properties of structural steels

Conclusions The investigation of the effect of thermomechanical treatment on the mechanical properties of steels with different compositions makes it possible to put in evidence the effect of alloyed elements. The addition of up to 1.2–1.5% Si (particularly with vanadium) makes it possible to increase the tempering temperature to 350°C without significantly decreasing the strengthening effect of low-temperature thermomechanical treatment. An increase of the concentration of chromium from 1.5 to 3–5% also increases the resistance of the steel. In steel containing 3–5% Cr and also molybdenum, vanadium, and tungsten, the effect of low-temperature thermomechanical treatment is retained after tempering at temperatures up to 500°C, the plasticity remaining rather high. Low-temperature thermomechnical treatment of batches 8 and 10 followed by tempering at 500°C resulted in the following mechanical characteristics: _b=240–255 kg/mm² when =10–13% and =30–35%; after tempering at 350°C _b=255–265 kg/mm², ₅=8–12%, and =28–36%.Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 4, pp. 36–40, April, 1963     

Thermal Resistance of Low-Alloyed Chromium Alloys

The oxidation kinetics of low-alloyed -2 and 1-17 chromium alloys is investigated at a temperature from 1273 to 1673 K for 1000 h. It is shown that even at a temperature from 1473 to 1673 K the heat resistance of these alloys is higher than that of the 648 nickel-containing alloy at a temperature from 1273 to 1373 K. This allows to recommend the alloys as heat-resistant materials operating at a temperature up to 1573 K.     

Influence of the Anion Nature and the Metal-to-Additive Ratio on the Effectiveness of ε-Caprolactam during Cadmium Electrodeposition

The rate and mechanism of cadmium(II) electroreduction from electrolytes containing -caprolactam were found to significantly depend on the metal-to-additive ratio. Whatever the anion nature, the process sharply accelerates in the presence of an excess of cadmium cations, which form activated surface complexes with adsorbed -caprolactam molecules as bridging ligands. With an excess of the additive, metal depolarization due to the "-effect still persists in perchlorate media; in iodide solutions, -caprolactam inhibits this process. The formation of a dense adsorbed film composed of -caprolactam molecules and I^– anions at the electrode ensures a high throwing power of the electrolyte and makes it possible to obtain uniform elastic organocadmium plating.     

Control of the phase composition and nitrogen content in the nitride layer in the nitriding of the steel 38Kh2MYuA

It is known that in order to obtain a high-hardness, wear- and corrosion-resistant article a nitrided layer of nitride (+)-phases should be formed on its surface. However, in some cases, for example, in nitriding high-speed die steels and steel 38Kh2MYuA, the formation of brittle nitride surface layers should be eliminated and only a zone of internal nitriding (a+ + MN) should be formed in order to provide the requisite hardness and wear resistance. The article concerns preparation of nitrided layers with different compositions on the widely used 38Kh2MYuA nitralloy.     

Two-phase ferritic-martensitic steels

Conclusions The results of laboratory and production experiments showed that the main condition for providing the necessary combination of properties of two-phase ferritic-martensitic steels (high tensile strength, low yield strength, high plasticity and work hardenability) is obtaining the specified quantity of the hardening phase (martensite) in the structure (20–28% M to obtain _t 550 MPa or 10–18% M for _t 450 MPa). The specified ratio of the structural constituents under conditions of mass production of two-phase ferritic-martensitic steels may be guaranteed only with the use of steels containing carbon and alloy elements within the necessary limits and also with strict observance of the heat-treatment cycle. Without the use of metallographic measurements as the criteria for obtaining the optimum structural condition in addition to the required values of strength and plasticity it is necessary to use the _0.2/_t ratio, which must not be greater than 0.5–0.6 with the absence of yield points on the tensile curve (without special temper rolling).As the result of the combination of work done in the Central Scientific-Research Institute of Ferrous Metallurgy together with plants of the Ministries of Ferrous Metallurgy and of the Automobile Industry at present the production is being introduced and experimental production lots of heat-treated two-phase steels of the following types with guaranteed mechanical properties are being supplied:At the Novolipetsk Metallurgical Combine cold-rolled 0.7–2.0-mm sheet of 06KhG(S)Yu and 06G2SYu steels with _0.2 = 260–320 MPa, _t 550 MPa, ₄ 30%, and _0.2/_t 0.5–0.6.At the Cherepovets Metallurgical Combine hot-rolled 2–6-mm sheet of 09G2(S) steel with _0.2 = 260–320 MPa, _t 550 MPa, ₄ 25%, and _0.2/_t 0.5–0.6.At the Beloretsk Metallurgical Combine (billets melted and rolled at the Cherepovets Metallurgical Combine) heat-treated cold-drawn wire up to 10.5 mm in diameter of 06KhGR steel with _0.2 250 MPa, _t 530 MPa, and ₁₀ 30%.For successful development of the production and use of two-phase ferritic-martensitic steels the combined work of the designers of machine building plants on determination of the most effective types of parts, of engineers on correction of the method taking into consideration the specifics of the properties of two-phase ferritic-martensitic steels, and of users on determining the service properties of parts of these steels is necessary. The fulfillment of such a combination of work will make possible th timely formulation of the further work of the metallurgical industry and determination of the required volume and product range of rolled products of two-phase ferritic-martensitic steels.I. P. Bardin Central Scientific-Research Institute of Ferrous Metallurgy. Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 11, pp. 25–29, November, 1984.