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Showing papers on "Carbide published in 1972"


Journal ArticleDOI
TL;DR: In this paper, time-temperature-precipitation diagrams were determined between 400° and 900°C for up to 3000 hr as a function of carbon content, solution treatment temperature, and cold work.
Abstract: Although Type 316 austenitic stainless steel is widely used in steam generating plants and nuclear reactors the knowledge about aging reactions, nature of precipitates, and precipitation kinetics during high temperature exposure is limited. Time-temperature-precipitation (TTP) diagrams were determined between 400° and 900°C for up to 3000 hr as a function of carbon content, solution treatment temperature, and cold work. The nucleation and growth phenomena, morphology, and composition of the various carbide (M23C6, M6C) and intermetallic phases (σ, χ, η were determined. The complex sequence of phase instabilities can be explained on the basis of the carbon content, effect of molybdenum and chromium on the carbon solubility, thermodynamic stability of the phases, and the kinetics of the various precipitation reactions.

658 citations


Journal ArticleDOI
J. Gurland1
TL;DR: In this article, the initiation of fracture in the microstructure at room temperature was observed in tension, compression and torsion, and cracks formed in the carbide particles in a direction normal to the tensile strain imposed upon the particles by the deforming matrix.

280 citations


Journal ArticleDOI
TL;DR: A martensitic steel containing 1.13 wt. %C was tempered at 120°C for 1-100 days and the structure and morphology of precipitated carbide were studied by electron microscopy and selected area diffraction as discussed by the authors.

237 citations


Journal ArticleDOI
01 May 1972
TL;DR: In this article, it was shown that the Widmanstatten morphology of upper bainite is inessential to the classification of a eutectoid structure as bainitic ferrite with respect to carbon.
Abstract: The authors debate three topics central to the controversies which have enveloped the bainite reaction ever since it was first recognized as a distinctive mode of austenite decomposition. These include: “what is bainite?”, “the growth mechanism of the ferritic component of bainite”, and “the sources of bainitic carbide precipitation.” RFH concludes that bainite is the product of a shear transformation. Individual bainite plates are suggested to grow substantially more rapidly than volume diffusion-control allows, but a constraint such as the build-up of volume strain energy limits the extent of their growth. This mechanism of growth ensures extensive supersaturation of bainitic ferrite with respect to carbon. Whether or not carbides precipitate in association with bainite plates and whether the carbide is cementite ore, however, is a complex question in competitive reaction kinetics. New experimental evidence is presented to demonstrate thate carbide precipitated in lower bainite dissolves upon heating above the kinetic-B stemperature in an alloy steel containing 1.5 pct Si. This result is taken to support the existence of the metastable eutectoid reactionγ ⇌ α + e atca 350°C. HIA and KRK define bainite as the product of a nonlamellar eutectoid reaction. On this view, carbide precipitation thus plays an essential, rather than an ancillary role. Development of the Widmanstatten morphology by the ferritic component of bainite is shown to be inessential to the classification of a eutectoid structure as bainite. When this morphology is present, however, it is concluded to grow by the ledge mechanism, without the participation of shear, at rates of the order of or less than those allowed by volume diffusion-control. New experimental evidence is presented to show that the lengthening and thickening kinetics of individual plates within sheaves of upper bainite are consistent with this description. The results of a new calculation indicate that the initial carbon content of bainite plates lies between theα/α + Fe3C) and the extrapolatedα/(α+ γ) phase boundaries, in agreement with expectation from the ledge mechanism of growth.

236 citations


Journal ArticleDOI
TL;DR: Activated reactive evaporation as discussed by the authors is a new process developed for the high rate deposition of compounds, and it circumvents problems associated with direct evaporation of compounds. But it is not suitable for high rate compound synthesis, since the reaction has to be activated by ionization of the reacting species.
Abstract: Activated reactive evaporation is a new process developed for the high rate deposition of compounds. It circumvents problems associated with direct evaporation of compounds. Metal vapors from high rate evaporation sources are reacted with a gas in the vapor phase to form and deposit compounds. The vapor phase reaction has to be activated by ionization of the reacting species, i.e., metal vapor and gas in the reaction zone. The steps of compound synthesis and compound deposition are thus separated. Control of deposit stoichiometry, e.g., [C/M] ratio for TiC synthesis is readily achieved by controlling the relative amounts of reactants. Results on the synthesis of carbides, oxides, and nitrides are presented.

163 citations


Journal ArticleDOI
TL;DR: In this paper, the authors show that the carbide contiguity in a given alloy develops towards an equilibrium value, which is directly related to the dihedral angle between carbide grains and therefore to the relative values of the interfacial energy and the contiguous boundary energy.
Abstract: Measurements have been made of the contiguity, the dihedral angle, and the continuity of the carbide phase in alloys of a number of transition-metal carbides with cobalt, which were prepared by liquid-phase sintering. During sintering, the carbide contiguity in a given alloy develops towards an equilibrium value, which is directly related to the dihedral angle between carbide grains and therefore to the relative values of the interfacial energy and the contiguous boundary energy. A direct relationship between the contiguity and the angle of contact of the liquid on the carbide, however, does not exist. The contiguity at the start of sintering depends to some extent on the history of the specimen before liquid-phase sintering and in most cases is higher than the equilibrium value. Observations were made which indicate that the carbide grains in the majority of cemented carbides exist as a continuous skeleton. Arguments are presented to show that neither the presence of such a skeleton nor the prese...

138 citations


Journal ArticleDOI
TL;DR: In this paper, the activity of carbon in austenitic Fe-Mo-C, Fe-Cr-C and Fe-V-C alloys has been studied by equilibration with controlled CH4-H2 atmospheres at temperatures in the range 850° to 1200°C.
Abstract: The activity of carbon in austenitic Fe-Mo-C, Fe-Cr-C, and Fe-V-C alloys has been studied by equilibration with controlled CH4-H2 atmospheres at temperatures in the range 850° to 1200°C. The observations included a number of compositions in the two-phase fields, γ + carbide. Equations are given for the activity coefficient of carbon as a function of temperature and composition in the austenite field and from these the other thermodynamic properties of the solution may be computed as desired. The phase boundaries γ/γ + carbide were determined by breaks in the isoactivity lines. This was supplemented in the case of Fe-Mo-C alloys by metallographic linear analysis of equilibrated samples. The results confirm certain published phase diagrams and discredit others.

100 citations


Patent
09 Aug 1972
TL;DR: An ion plating method and product therefrom wherein ions of a metal are implanted into or/and plated onto a substrate to increase the hardness of the surface is described in this article.
Abstract: An ion plating method and product therefrom wherein ions of a metal are implanted into or/and plated onto a substrate to increase the hardness of the surface. After plating, the product can be reacted with carbon, boron, nitrogen or another metal, thereby forming the carbide, boride, nitride or metal compound of the plating metal coating. Hardening of the product by quenching follows which produces a cutting tool of superior qualities.

99 citations


Patent
T Kniff1
12 Sep 1972
TL;DR: In this paper, a massive hard carbide element is fitted to a steel holder which is reciprocated to drive the element against a formation to be broken, and a shrink fitted therein or brazed thereto.
Abstract: An impacting tool in which a massive hard carbide element is fitted to a steel holder which is reciprocated to drive the element against a formation to be broken. The massive carbide element can be press fitted in the steel holder or shrink fitted therein or brazed thereto and, furthermore, the carbide element can be fitted to a steel sleeve adapted for being secured to a steel holder as by threading or brazing.

97 citations


Journal ArticleDOI
TL;DR: In this paper, the hardness of the cubic transition-metal carbides was examined as a function of the Knoop indenter orientation on the (001) surfaces of the carbides titanium, vanadium, zirconium, and niobium.
Abstract: Hardness has been examined as a function of indenter orientation on the (001) surfaces of the cubic transition-metal carbides titanium carbide, vanadium carbide, zirconium carbide and niobium carbide. To emphasize the observed anisotropy a Knoop indenter was used. Experiments have been performed in the temperature range -196 to 610$^{\circ}$C. The anisotropy curves obtained at each temperature have been analysed in terms of operative slip systems. Three different temperature regimes for the anistropy have been identified. These correspond to the {110} $\langle 1\overline{1}0\rangle $ slip systems for the low-temperature regime, the {111} $\langle 1\overline{1}0\rangle $ slip system for the high-temperature regime and a combination of these two systems for the intermediate-temperature regime. To explain this change in slip system it is proposed that an important temperature dependent change in bonding occurs. A qualitative model is suggested for this change in which an increased density of high mobility electrons increasingly screens the directional covalent bonds as the temperature is raised.

89 citations


Journal ArticleDOI
R.C. Henderson1, Rohe F. Helm1
TL;DR: In this article, a SiH 4 pyrolysis at moderate temperatures (823 −983 °C) and low pressure (0.15 −0.02 torr) was used to demonstrate that the absence of detectable impurities was the necessary surface condition to obtain such material.

Patent
R Newman1, K Cross1, J Cavanagh1
17 Jan 1972
TL;DR: In this article, a plasma-sprayed coating for increasing the vibration damping capacity of metal alloys is presented. But the coating consists of a outermost layer portion formed of an oxide ceramic or refractory carbide and an intermediate portion formed by a mixture of one of the above alloys and the material forming the outermost layers.
Abstract: Nickel, cobalt, aluminum, iron-nickel, molybdenum, and titanium alloy articles are provided with a plasma sprayed coating for increasing the vibration damping capacity thereof. The coating consists of a outermost layer portion formed of an oxide ceramic or refractory carbide and an intermediate portion formed of a mixture of one of the above alloys and the material forming the outermost layer. In the preferred embodiment, the intermediate portion consists of two or more discrete layers, with the layers having decreasing alloy content and increasing oxide ceramic content toward the outermost layer portion.

Journal ArticleDOI
TL;DR: In this paper, the microstructural changes that occur during the liquid-phase sintering of VC-Co alloys were studied and it was found that considerable growth of the carbide grains takes place and that this growth can be described by the equation:
Abstract: A study was made of the microstructural changes that occur during the liquid-phase sintering of VC-Co alloys. It was found that considerable growth of the carbide grains takes place and that this growth can be described by the equation: $$\bar d^3 - \bar d_o^3 = Kt$$

Journal ArticleDOI
TL;DR: In this paper, the surface of monocrystalline silicon was chemically converted with hydrocarbon to polycrystalline β-silicon carbide, and the growth mechanism was investigated by means of 14C tracer method.
Abstract: The surface of monocrystalline silicon was chemically converted with hydrocarbon to polycrystalline β‐silicon carbide, and the growth mechanism was investigated by means of 14C tracer method. It is shown that the growth of the silicon carbide layer is due to diffusion of silicon through the SiC layer so that the Si–SiC conversion is taking place at the surface of the sample. Dependence of layer thickness on carbidizing time and on hydrocarbon concentration in the carrier gas hydrogen was measured.

Journal ArticleDOI
TL;DR: In this article, the Mossbauer effect was used to investigate the cementite state in cold-worked steel, and an intensive dissociation of cementite was found at plastic deformation of the steel with the structure of plate perlite.
Abstract: The Mossbauer effect was used to investigate the cementite state in cold-worked steel. An intensive dissociation of cementite is found at plastic deformation of the steel with the structure of plate perlite. For deformation of 93% this dissociation amounts to 50%. The effect of dissociation was not observed in the steel with granular perlite. The fact that cementite dissociates at deformation may be explained by the increase of bond energy between C atoms and dislocations as compared to that for carbon in the cementite lattice. Alloying with the elements which decrease the bond of dislocations and substitutional impurities has the result that the cementite becomes much more stable at deformation. This is shown on the example of steel containing cobalt. The latter fact influences strongly the mechanical properties of a cold worked steel. [Russian text ignored].

Patent
22 Feb 1972
TL;DR: In this article, a hard facing wear pad usable by brazing to a digger tooth or the like is provided, which is from 70 to 85 percent by volume particles of cemented metal carbide in a metal matrix having a melting point not substantially higher than the melting point of the metal cementing the carbide.
Abstract: A hard facing wear pad usable, for example, by brazing to a digger tooth or the like is provided in practice of this invention. The wear pad is from 70 to 85 percent by volume particles of cemented metal carbide in a metal matrix having a melting point not substantially higher than the melting point of the metal cementing the carbide. The cemented carbide particles are in the size range of from about 6 to 30 U.S. Sieve, and the thickness of the pad is within limits determined by the cemented carbide particle size.

Patent
03 Nov 1972
TL;DR: In this article, a sintered hard metal body (e.g., a cutting insert) is provided as to wear resistance by depositing thereon an intermediate thin coating of a metallic carbide or metallic nitride free from binder metal.
Abstract: A sintered hard metal body (e.g., a cutting insert) is provided as to wear resistance by depositing thereon an intermediate thin coating of a metallic carbide or metallic nitride free from binder metal and applying over this intermediate coating a thin ceramic coating free from binder metal.

Journal ArticleDOI
TL;DR: The fracture surface energies of polycrystalline silicon carbides were measured at room temperature using the double-cantilever-beam, notched-beam and work-of-fracture methods as discussed by the authors.
Abstract: The fracture surface energies of 5 polycrystalline silicon carbides were measured at room temperature using the double-cantilever-beam, notched-beam, and work-of-fracture methods. All methods yielded comparable fracture surface energies,

Journal ArticleDOI
TL;DR: In this paper, it was shown that refractory metals Nb, Ta, Mo, and W dissolve C, N, and O by forming interstitial solid solutions and the concentration of these components can be increased or decreased by annealing treatments, depending on the partial pressure of gases such as N2, O2, H2O, CH4, or CO and on the temperature of the specimen.
Abstract: The refractory metals Nb, Ta, Mo, and W dissolve C, N, and O by forming interstitial solid solutions The concentration of these components can be increased or decreased by annealing treatments, depending on the partial pressure of gases such as N2, O2, H2O, CH4, or CO and on the temperature of the specimen New results in binary and ternary systems combined with those obtained in the last few years now provide most of the data needed for the thermochemical analysis of the solid solution phases and for the establishment of p-T-c phase diagrams The mechanisms of the gas-metal reactions and the general feature of the constitution diagrams are similar for all refractory metals However, marked differences exist between group Va metals niobium and tantalum and group VIa metals molybdenum and tungsten in the absolute values and temperature dependence of the equilibrium pressure of gaseous species and therefore also in the amount of gas absorbed The data now available for the estimation of the final content of interstitials in solid solution after annealing treatments are compiled and discussed

Patent
15 Sep 1972
TL;DR: Hard, dense composite ceramic bodies of titanium diboride, boron carbide, silicon carbide and silicon, having a wide variety of utilities, are produced by forming a mixture of the three materials into a desired shape to obtain a coherent green body which is siliconized by heating it in contact with silicon to a temperature above the melting point of silicon as mentioned in this paper.
Abstract: Hard, dense composite ceramic bodies of titanium diboride, boron carbide, silicon carbide and silicon, having a wide variety of utilities, are produced by forming a mixture of titanium diboride, boron carbide and a temporary binder into a desired shape to obtain a coherent green body which is siliconized by heating it in contact with silicon to a temperature above the melting point of silicon, whereupon the molten silicon infiltrates the body and reacts with some of the boron carbide therein to produce silicon carbide in situ.

Journal ArticleDOI
TL;DR: In this article, the scattering of collimated beams of helium, deuterium, neon, and argon is reported from two tungsten carbide surfaces which form on the (110) face of Tungsten and some comments on the sort of periodic potential which is likely to give rise to diffractive scattering of atoms are given.
Abstract: The scattering of collimated beams of helium, deuterium, neon, and argon are reported from two tungsten carbide surfaces which form on the (110) face of tungsten. On a (3× 5) surface both helium and deuterium give sharp, well‐defined diffraction peaks corresponding to the (2, 0), (1, 0), (0, 0), (1, 0), (2, 0) directions along the 5 spacing. No diffraction is observed on the (1× 1) carbide surface or the clean metal surface which is also (1× 1). Fractions scattered in the specular ray, (0, 0), as high as 55% have been observed from the carbide surfaces. The scattering of neon is in the inelastic regime and argon is trapping dominated. Analysis of the scattering in combination with the LEED suggests a dense carbide, perhaps WC, with a Debye temperature of 1200°K or higher. This diffractive scattering is the first reported on a surface other than alkali halides and some comments on the sort of periodic potential which is likely to give rise to diffractive scattering of atoms are given.

Journal ArticleDOI
01 Aug 1972
TL;DR: In this paper, the origin of extra spots in electron diffraction patterns taken from retained austenite and martensite in Fe-7 pct Al-2 pct C has been investigated.
Abstract: The origin of “extra” spots in electron diffraction patterns taken from retained austenite and martensite in Fe-7 pct Al-2 pct C has been investigated. The present interpretation differs from that of previous investigators. It is concluded that a high density of fine carbide precipitates 50A in diameter is responsible for the extra reflections. The precipitates have the perovskite structure and grow epitaxially in the austenite during quenching. When martensite forms at a lower temperature, the precipitates are transformedin situ.


Patent
16 Jun 1972
TL;DR: In this article, a process and apparatus for the production of carbide films at high rates by physical vapor deposition is described, where the metal is evaporated in a vacuum chamber by an electron beam, the hydrocarbon gas is introduced into the chamber, and the metal vapor atoms and gas atoms are activated by electrons deflected from the electron beam to the reaction zone by a low voltage electrode at the react zone.
Abstract: Process and apparatus for the production of carbide films at high rates by physical vapor deposition. The metal is evaporated in a vacuum chamber by an electron beam, the hydrocarbon gas is introduced into the chamber, and the metal vapor atoms and gas atoms are activated by electrons deflected from the electron beam to the reaction zone by a low voltage electrode at the reaction zone. The reaction takes place primarily in the vapor phase in the reaction zone, rather than on the substrate. A high reaction efficiency is obtained with the activated atoms and a deposition rate in the range of 1 to 12 micrometers per minute and higher is achieved.

Patent
R Sara1
10 Jul 1972
TL;DR: In this article, the composites are characterized by improved thermal cycling characteristics and are produced by coating a plurality of carbon fibers first with a thin, continuous layer of nickel, and then with a second thin continuous overcoating of a metal capable of diffusing through the nickel coating and reacting with carbon to form a metal carbide; and then hot pressing the dual-coated fibers for a time and at a temperature and pressure sufficient to bond them together and diffuse at least a portion of the carbide-forming metal surface layer through the Nickel undercoating and effect reaction between said
Abstract: Composite articles having a nickel base metal matrix reinforced with a plurality of high strength, high modulus carbon fibers having a thin, intermediate layer of a metal carbide disposed upon at least a portion of the fiber surfaces. Such composites are characterized by improved thermal cycling characteristics and are produced by coating a plurality of carbon fibers first with a thin, continuous layer of nickel, and then with a second thin, continuous overcoating of a metal capable of diffusing through the nickel coating and reacting with carbon to form a metal carbide; and then hot pressing the dual-coated fibers for a time and at a temperature and pressure sufficient to bond them together and diffuse at least a portion of the carbide-forming metal surface layer through the nickel undercoating and effect reaction between said carbide-forming metal and said carbon fibers to produce a metal carbide coating on at least a portion of the surface of the fibers.

Patent
25 Sep 1972
TL;DR: In this paper, a method of treating a nickel base alloy so as to produce an alloy having a structure characterized by dispersed discrete fine spherical carbides was proposed, and the method comprises the steps of casting an ingot of nickel base Alloy, homogenizing the ingot at a temperature of from 2,200* to 2,400* F, cooling the alloy at a rate which substantially precludes the precipitation of coarse and film-like carbides at temperatures above 1,900* F and at a second rate in which dispersed fine spheres precipitate at temperatures below 1,
Abstract: A method of treating a nickel base alloy so as to produce an alloy having a structure characterized by dispersed discrete fine spherical carbides. The method comprises the steps of casting an ingot of nickel base alloy, homogenizing the ingot at a temperature of from 2,200* to 2,400* F so as to dissolve primary carbides present in the alloy and increase the chemical homogeneity thereof, cooling the alloy at a rate which substantially precludes the precipitation of coarse and film-like carbides at temperatures above 1,900* F and at a second rate in which dispersed fine spherical carbides precipitate at temperatures below 1,900* F; and hot working the alloy at a temperature lower than that at which the primary carbides dissolve.

Patent
Erwin Rudy1
08 Sep 1972
TL;DR: In this paper, refractory metal-bonded carbide alloys for use as cutting tools and in other applications where high hardness and abrasion resistance are required.
Abstract: This invention relates to refractory metal bonded carbide alloys for use as cutting tools and in other applications where high hardness and abrasion resistance are required. The desired finegrain, lamellar microstructure is obtained preferably by casting eutectic, or near-eutectic composition alloys of a Group IVa metal (titanium, zirconium, hafnium), tungsten and carbon which may contain certain alloying and inert materials. For selected applications, the composites may be fabricated by powdermetallurgical techniques.

Patent
14 Feb 1972
TL;DR: In this article, a composition of material comprising a titanium molybdenum carbide and an iron group metal binder is described, which is particularly useful as a metal cutting tool.
Abstract: A composition of material comprising a titanium molybdenum carbide and an iron group metal binder is disclosed which is particularly useful as a metal cutting tool. The carbide phase of the composition is substantially richer in carbon than the prior art. For any given metal exchange ration, the carbide phase contains more carbon than the composition line TiC-Mo2C for the same ratio. Also, the carbide phase can contain higher amounts of molybdenum than was used in the prior art.

Journal ArticleDOI
TL;DR: The performance of TRISO-coated carbide fissile particles, of the type to be used in the large HTGR, correlates well with statistically based calculations of stresses in the SiC coating as discussed by the authors.
Abstract: The performance of TRISO-coated carbide fissile particles, of the type to be used in the large HTGR, correlates well with statistically based calculations of stresses in the SiC coating. Three coat...

Journal ArticleDOI
TL;DR: The binder phase of WC-Co cemented carbide is a Co-rich alloy in which tungsten and carbon are in solid solution as mentioned in this paper, and it is supersaturated with respect to Tungsten even after slow cooling from the sintering temperature.
Abstract: The binder phase of WC-Co cemented carbide is a Co-rich alloy in which tungsten and carbon are in solid solution. The binder phase is supersaturated with respect to tungsten even after slow cooling from the sintering temperature. In this study the binder phase contained 6% W in solid solution before heat-treatment at 650°C (923 K). Transmission electron microscopy on thin foils of binder phase showed that a finely dispersed. phase, α′, precipitated in the cubic binder phase. After long ageing times Co3W could be identified by X-ray diffraction methods. As no discontinuous , ‘cells’ of Co3W and ∊-Co could be observed, the following reaction is suggested.α-Co(W, C)→α-Co+α′→α-Co (C)+Co3W (needles)The precipitation of α′ was accompanied by an increase in hardness and a decrease in transverse rupture strength. The effects observed are consistent with those found during annealing of Co-rich cobalt-tungsten-carbon alloys (> 85% Co).