Classifications

• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C1/00—Making non-ferrous alloys
  • C22C1/10—Alloys containing non-metals
  • C22C1/1084—Alloys containing non-metals by mechanical alloying (blending, milling)
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B22—CASTING; POWDER METALLURGY
  • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
  • B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
  • B22F1/05—Metallic powder characterised by the size or surface area of the particles
  • B22F1/054—Nanosized particles
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B22—CASTING; POWDER METALLURGY
  • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
  • B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
  • B22F1/07—Metallic powder characterised by particles having a nanoscale microstructure
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C1/00—Making non-ferrous alloys
  • C22C1/04—Making non-ferrous alloys by powder metallurgy
  • C22C1/0433—Nickel- or cobalt-based alloys
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C1/00—Making non-ferrous alloys
  • C22C1/10—Alloys containing non-metals
  • C22C1/1094—Alloys containing non-metals comprising an after-treatment
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C19/00—Alloys based on nickel or cobalt
  • C22C19/03—Alloys based on nickel or cobalt based on nickel
  • C22C19/05—Alloys based on nickel or cobalt based on nickel with chromium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C30/00—Alloys containing less than 50% by weight of each constituent
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C30/00—Alloys containing less than 50% by weight of each constituent
  • C22C30/02—Alloys containing less than 50% by weight of each constituent containing copper
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
  • C22C32/001—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
  • C22C32/0015—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents
  • C22C32/0026—Matrix based on Ni, Co, Cr or alloys thereof
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C33/00—Making ferrous alloys
  • C22C33/02—Making ferrous alloys by powder metallurgy
  • C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
  • C22C33/0278—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
  • C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
  • C22F1/10—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of nickel or cobalt or alloys based thereon
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B22—CASTING; POWDER METALLURGY
  • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
  • B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
  • B22F2998/10—Processes characterised by the sequence of their steps
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B22—CASTING; POWDER METALLURGY
  • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
  • B22F2999/00—Aspects linked to processes or compositions used in powder metallurgy
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
  • C22C32/001—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
  • C22C32/0015—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents

Definitions

• the invention relates to phase separating powders and methods of identifying them.
• Sintered nanocrystalline materials are often subjected to pressure or other postsintering processing techniques to achieve higher density materials.
• a method of designing a metal alloy powder having a miscibility gap at low temperature can include identifying a first metal element and a second metal to form a metal alloy, selecting a third metal having a miscibility gap with the metal alloy, and mechanically alloying the third metal and the metal alloy to form a metal alloy powder having a nanoscale grain size.
• the metal alloy powder can be engineered to have a phase separation temperature at which diffusion of the third metal occurs to phase separate as a nanoscale phase.
• the nanoscale phase can redissolve at a transition temperature higher than the phase separation temperature.
• the metal alloy can be a nano-phase separating powder.
• the first metal can include nickel.
• the second metal can include chromium, cobalt, vanadium, silver, molybdenum, tungsten, or iron.
• the third metal can include copper.
• the metal alloy powder can include manganese.
• the metal alloy powder can include vanadium.
• the metal alloy powder can include molybdenum.
• the metal alloy powder can include tungsten.
• the metal alloy powder can include silver.
• the metal alloy powder can include zirconium.
• the metal alloy powder can include iron.
• the metal alloy can include a ternary nano-phase separating powder.
• the metal alloy can include a quaternary nano-phase separating powder.
• the first metal can have a concentration of about 25 at% to about 95 at% of the alloy.
• the second metal can have a concentration of about 25 at% to about 95 at% of the alloy.
• the third metal can have a concentration of about 5 at% to about 50 at% of the alloy.
• the metal alloy powder can include an oxygen scavenging metal.
• a method of nano-phase separation sintering of a powder can include providing a fine grained powder including a first metal element and a second metal forming a metal alloy and a third metal having a miscibility gap with the metal alloy, and sintering the fine grained powder to form a sintered product.
• a metal alloy powder for sintering can include a mechanically alloyed powder including a first metal element and a second metal forming a metal alloy and a third metal having a miscibility gap with the metal alloy.
• the fine grained powder can be a mechanically alloyed powder.
• the sintered product achieves at least 80% density at low temperatures without the need for an applied pressure during the sintering.
• the sintered product achieves at least 90% density at low temperatures without the need for an applied pressure during the sintering.
• the mechanically alloyed powder is a nano-phase separating powder.
• the mechanically alloyed powder can include nickel, chromium, iron, copper, vanadium, molybdenum, tungsten, silver, zirconium, or combinations thereof.
• sintering can include nano-phase separation sintering.
• the metal alloy powder can include: NiCu having 5 at% to 20 at% Cr; NiCu having 5 at% to 45 at% Fe; NiCu having 5 at% to 45 at% Co; NiFeCu having 5at% or 8at% Mn; NiCu having 5 at% to 15 at% V; or NiCu having 5at% to 45 at% Co.
• the mechanically powder is a quaternary nano-phase separating powder.
• the metal alloy powder can include NiCu having 5at% to 45 at% Co and up to 5at% Mn.
• a sintered product can include the powder described above.
• FIG. 1A is a schematic illustrating nano-phase separation sintering, including phase separation, neck formation, sintering and den si fi cation.
• FIG. IB depicts a phase diagram
• FIG. 1C is a schematic illustrating an example of the general process described herein.
• FIG. 2A depicts a Ni-Cu phase diagram.
• FIG. 2B is a graph illustrating a behavior of the system.
• FIG. 3 depicts a phase diagram
• FIG. 4A is a graph showing densification rate.
• FIG. 4B is a graph showing change in relative density.
• FIG. 5A depicts a Ni-Cr phase diagram.
• FIG. 5B depicts a Cu-Cr phase diagram.
• FIG. 6A depicts a Ni-Cu phase diagram at 5 at% Cr.
• FIG. 6B depicts a Ni-Cu phase diagram at 10 at% Cr.
• FIG. 6C depicts a Ni-Cu phase diagram at 15 at% Cr.
• FIG. 6D depicts a phase diagram of 60 at% Ni and 15% Cr.
• FIG. 6E is a table showing the compositions of stable phases at 550°C.
• FIG. 6F is a graph showing the temperature dependence of densification at 5°C/min to
• FIG. 7A depicts a Ni-Fe phase diagram.
• FIG. 7B depicts a Cu-Fe phase diagram.
• FIG. 8A depicts a Ni-Cu phase diagram at 5 at% Fe.
• FIG. 8B depicts a Ni-Cu phase diagram at 20 at% Fe.
• FIG. 8C depicts a Ni-Cu phase diagram at 42 at% Fe.
• FIG. 8D depicts a Ni-Cu phase diagram at 42at% Fe.
• FIG. 8E is a table showing the compositions of stable phases at 550°C.
• FIG. 8F is a graph showing the temperature dependence of densification at 5°C/min to
• FIG. 8G is a graph showing the change in relative density over time at 5°C/min heating.
• FIG. 8H is a graph showing the temperature dependence of densification at 10°C/min to 1000°C and 40°C/min cooling.
• FIG. 81 is a graph showing the change in relative density over time at 5°C/min heating to a final relative density of 0.5864%.
• FIG. 8J is a graph showing the temperature dependence of densification at 15°C/min to 1000°C and 40°C/min cooling.
• FIG. 8K is a graph showing the change in relative density over time at 15°C/min heating to a final relative density of 0.5477%.
• FIG. 8L is a graph showing the temperature dependence of densification at 20°C/min to 1000°C and 40°C/min cooling.
• FIG. 8M is a graph showing the change in relative density over time at 20°C/min heating to a final relative density of 0. 4276%.
• FIG. 8N is a graph showing the temperature dependence of densification at 5°C/min to 1100°C and 40°C/min cooling.
• FIG. 80 is a graph showing the change in relative density over temperature at 5°C/min heating.
• FIG. 8P is a graph showing the change in relative density over time at 5°C/min heating.
• FIG. 8Q is a graph showing the temperature dependence of densification at 10°C/min to 1100°C and 40°C/min cooling.
• FIG. 8R is a graph showing the change in relative density over temperature at 10°C/min heating.
• FIG. 8S is a graph showing the change in relative density over time at 15°C/min.
• FIG. 8T is a graph showing the temperature dependence of densification at 20°C/mino 1100°C and 40°C/min cooling.
• FIG. 8U is a graph showing the temperature dependence of densification at 20°C/mino 1100°C and 40°C/min cooling.
• FIG. 8V is a graph showing the change in relative density over time at 20°C/min.
• FIG. 9A depicts a Ni-Co phase diagram.
• FIG. 9B depicts a Cu-Co phase diagram.
• FIG. 10A depicts a Ni-Cu phase diagram at 5 at% Co.
• FIG. 10B depicts a Ni-Cu phase diagram at 20 at% Co.
• FIG. 10C depicts a Ni-Cu phase diagram at 44 at% Co.
• FIG. 11 A depicts a Ni-V phase diagram.
• FIG 1 IB depicts a Cu-V phase diagram.
• FIG. 12A depicts a Ni-Cu phase diagram at 6 at% V.
• FIG. 12B depicts a Ni-Cu phase diagram at 10 at% V.
• FIG. 12C depicts a Ni-Cu phase diagram at 13 at% V.
• FIG. 12D depicts a Ni-Cu phase diagram and 13 at% V. At 15 at% Cu.
• FIG. 12E is a table showing the stable phases at 1150°C.
• FIG. 12F is a graph showing the temperature dependence of the densification rate for 10 at 5°C/min to 1200°C and 40°C/min cooling.
• FIG. 12G is a graph showing the temperature dependences of the change in relative density.
• FIG. 13 is a chart showing the diffusion rates and temperature range for metals described herein.
• FIG. 14A depicts a phase diagram for Fe-Cu with 40 at% Ni from an Fe database.
• FIG. 14B depicts a phase diagram for Fe-Cu with 40 at% Ni from a Ni database.
• FIG. 14C depicts a phase diagram for Fe-Cu with 40 at% Ni from a Cu database.
• FIG. 14D depicts a phase diagram for Fe-Cu with 40 at% Ni from a high entropy alloy database.
• FIG. 15 depicts a Cr-Cu phase diagram at 60 at% Ni.
• FIG. 16 depicts a Co-Cu phase diagram at 40 at% Ni.
• FIG. 17 depicts a Cu-V phase diagram at 75 at% Ni.
• FIGS. 18A, 18B and 18C are graphs showing densification after pretreatment with hydrogen at different heating rates.
• FIG. 19 is a graph showing the impact on density of 5 at% and 8 at% Mn to a Ni-Fe- Cu composition.
• FIG. 20 is a graph showing the densification behavior of the addition of Mn in a 37.5 at% Ni - 37.5 at% Co - 20 at% Cu - 5 at% Mn composition heated to 1200°C.
• FIGS. 21, 22, 23 and 24 are micrographs of the composition of FIG. 20.
• FIGS. 25-28 are graphs showing the mechanical properties of the sintered products of 37.5 at% Ni 37.5 at% Fe 20 at% Cu 5 at% Mn.
• Ternary, and higher order, metal alloys are designed to serve as structural metals both in cryogenic and high temperature applications.
• the more specific properties of these alloys can include the capability to be rapidly sintered from powder and achieve full density at low temperatures without the need for an applied pressure during the sintering process, which enables the processability of these alloys in additive manufacturing operations in bulk form.
• design a Ni based alloy suitable for use in space applications can be primarily made up of Ni to replace Inconel/superalloys.
• the materials can lead to improved processing. For example, accelerated (low-temperature) sintering from powder can allow for 3D printing using bound metal deposition without sag of structure.
• the materials can also have improved mechanical properties. Nanocrystallinity can provide increased strength and lightweighting structure over Inconel. The materials show improved thermal stability and scalability of the sintered parts/components.
• Nanophase sintering demonstrates the need for the secondary phase to be transient. It can be important to avoid a contiguious secondary phase which can cause to a material to fail without harnessing the hard-won gains in Ni. Importantly, the Ni-Cu system thermodynamically it meets the criteria. However, kinetically diffusion is too slow in pure Ni-Cu allows in the two- phase region, which forms necks due to the low transus temperature.
• Rapid densification can be achieved through nano-phase separation and the design of ternary Ni systems, quaternary Ni systems, or higher order Ni systems.
• the Ni-Cu phase diagram exhibits a miscibility gap having a Ni- and a Cu-rich phase at low temperatures and a single phase at temperatures above 400 °C over the entire compositional range.
• the phase separating element is Cu to form interparticle necks between the powders.
• Cu is chosen, because it i) precipitates into a second phase at low temperatures, ii) has a relatively small activation energy for diffusion in Ni and a lower melting temperature, which makes it favorable to create new precipitates at the interparticle necks, and iii) promotes rapid diffusion of Ni into the interparticle necks after reaching the single solid-solution phase field. It thus satisfies all proposed thermodynamic criteria for nanophase separation.
• a third element can be chosen to elevate the transus temperature and to extend the two-phase field (miscibility gap) of the binary system Ni-Cu.
• Exemplary, calculated pseudo-binary phase diagrams for the systems containing various alloying amounts of Fe, Cr, Mn, V, W, Ag, Mo, or Co are described herein. Any of these ternary, or higher order, Ni phase diagrams can exhibit a two-phase field and a single-phase field at higher temperatures for a certain compositional range, like the binary Ni- Cu system. Any of these ternary or greater systems exhibits a transition from a dual to a single phase-field for a range of compositions that is taking place at a higher temperature than for any possible composition in the binary system Ni-Cu.
• Thermo-Calc Software can be used to assess the equilibrium bulk phase diagrams of the ternary, or higher order, nano-phase separating Ni alloys with all of the following described characteristics and properties, such as volume fraction and chemical composition of the involved phases. Calculations, for example, Thermo-Calc, can be used as design tool to identify and predict potential alloy candidates for nano-phase separating ternary, or higher order, Ni systems.
• Criteria to identify alloying elements for the design of ternary, or higher order, nanophase separating Ni alloys can include one or more of the following features.
• the third alloying element should extend the thermodynamic stability of the low-temperature miscibility gap phase field of the binary system Ni-Cu, while maintaining a single phase solid-solution at high homologous temperatures of the alloy. Another factor to consider is a low-temperature miscibility gap is comprised of a Ni and a Cu-rich containing phase.
• a ternary, or higher order, alloying element can be chosen to elevate the transition temperature from a dual to single phase to such a degree that the thermodynamic equilibrium is reached. For example, phase decomposition into a dual-phase structure can kinetically take place.
• a heating cycle to the desired temperature can include initial (phase separation) and secondary (interdiffusion, redissolution) densification take place at 500-700 °C and above 850 °C, respectively, reaching full density at a temperature of 1100 °C. Temperature and heating rate details can vary, as discussed herein and as understood in practice.
• the methods and materials described herein can be useful in commercial applications.
• the ternary, or higher order, nano-phase separating Ni alloys can be designed to facilitate rapid consolidation of powder in bulk form without application of pressure during sintering, which are suitable characteristics for the application in additive manufacturing processes.
• the sintered ternary, or higher order, Ni alloys can be used as structural alloys in many applications that require high thermal, mechanical and corrosive stability, such as for components of turbines, engines and nuclear reactors.
• the simplified processibility of the ternary, or higher order, Ni alloys can reduce the complexity of 3d printing typically associated with Ni-base superalloys, which can require an additional isothermal precipitation treatment to adjust appropriate phase fraction of a dual-phase structure.
• the technology is of special interest for high technology and space applications, because they plan on incorporating components printed from powders of these ternary or greater Ni alloys.
• a favored printing technique will be bound metal deposition, which can enable large scale production of components with relative complex geometries and shapes.
• a method of designing a metal alloy powder having a miscibility gap at low temperature can include identifying a first metal element and a second metal to form a metal alloy, selecting a third metal having a miscibility gap with the metal alloy, and mechanically alloying the third metal and the metal alloy to form a metal alloy powder having a nanoscale grain size.
• a Ni-Cu alloy can include one or more of a third metal, which can be chromium, cobalt, vanadium, silver, molybdenum, tungsten, or iron.
• the third metal is selected based on the ternary phase diagram properties that will allow nano-phase separation to occur, as described herein.
• iron can be a preferred metal in the alloy.
• chromium can be a preferred metal in the alloy.
• cobalt can be a preferred metal in the alloy.
• vanadium can be a preferred metal in the alloy.
• silver can be a preferred metal in the alloy.
• molybdenum can be a preferred metal in the alloy.
• tungsten can be a preferred metal in the alloy.
• the composition of the metal alloy can be selected to be a nano-phase separating powder, such as a ternary nano-phase separating powder or a quaternary nano-phase separating powder.
• the alloy can include an oxygen scavenging metal.
• the oxygen scavenging metal can be at a low concentration of the alloy, for example, 5 at%, 4 at%, 3 at%, 2 at%, 1 at%, or lower.
• the oxygen scavenging metal can be manganese or zirconium.
• the oxygen scavenging metal can be added to a ternary alloy to for a quaternary alloy.
• the metal alloy powder can be engineered to have a phase separation temperature at which diffusion of the third metal occurs to phase separate as a nanoscale phase. Moreover, it can be preferred that the nanoscale phase can redissolve at a transition temperature higher than the phase separation temperature.
• the mechanical alloying is performed at a relatively low temperature.
• the mechanical alloying e.g., ball milling
• the mechanical alloying is performed while the particles are at a temperature of less than or equal to 150° C, less than or equal to 100° C, less than or equal to 75° C, less than or equal to 50° C, less than or equal to 40° C, less than or equal to 35° C, less than or equal to 30° C, less than or equal to 25° C, or less than or equal to 20° C.
• the mechanical working e.g., ball milling
• the mechanical alloying e.g., ball milling
• the mechanical alloying (e.g., ball milling) may be conducted for a time of greater than or equal to 6 hours (e.g., greater than or equal to 8 hours, greater than or equal to 10 hours, greater than or equal to 12 hours, or greater than or equal to 15 hours). In certain embodiments, the mechanical alloying (e.g., ball milling) may be conducted for a time of less than or equal to 18 hours. In some embodiments, the mechanical alloying (e g., ball milling) may be conducted for a time of 6 hour to 18 hours.
• the mechanical alloying e.g., ball milling
• an inert atmosphere for example, an argon atmosphere.
• the nanoscale feature or nanophase can be 100 nm, 90 nm, 80 nm, 70 nm, 60 nm, 50 nm, 40 nm, 30 nm, 20 nm, 10 nm, 5 nm or smaller.
• the nanophase, nanoscale feature, or nanocrystal can refer to the size of a crystal (or a “grain”) being less than or equal to about 1000 nm — e.g., 500 nm, 200 nm, 100 nm, 50 nm, 20 nm, 10 nm, 5 nm, 2 nm, etc.
• the grain size may be between 1000 nm and about 2 nm — e.g., about 500 nm and about 2 nm, about 200 nm and about 2 nm, about 100 nm and about 2 nm, about 50 nm and about 2 nm, about 30 nm and about 2 nm, about 20 and about 2 nm, about 10 nm and about 2 nm.
• the size may refer to the largest dimension of the grain.
• the size of the grains referred herein may be determined as an “average” and may be measured by any suitable techniques.
• the dimensions may refer the diameter, length, width, height, depending on the geometry of the grain.
• a stable nanocrystalline material may also refer to a material comprising an amorphous phase.
• the alloy can be composed of three, four or more metals. Each metal can have a concentration of about 25 at% (atomic percent) to about 95 at% of the alloy. When two metal components of a ternary alloy each has a concentration of about 25 at% to about 95 at% of the alloy, the third metal component can have a concentration of about 5 at% to about 50 at% of the alloy.
• each metal concentration can be at least 5 at%, at least 10 at%, at least 15 at%, at least 20 at%, at least 25 at%, at least 30 at%, at least 35 at%, at least 40 at%, at least 45 at%, at least 50 at%, at least 55 at%, at least 60 at%, at least 65 at%, at least 70 at%, at least 75 at%, at least 80 at%, at least 85 at%, at least 90 at%, or at least 95 at%.
• a method of nano-phase separation sintering of a powder can include providing a fine grained powder including a first metal element and a second metal forming a metal alloy and a third metal having a miscibility gap with the metal alloy, and sintering the fine grained powder to form a sintered product.
• a metal alloy powder for sintering can include a mechanically alloyed powder including a first metal element and a second metal forming a metal alloy and a third metal having a miscibility gap with the metal alloy.
• the sintered product achieves at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, or at least 98% density. These densities can be achieved at low temperatures without the need for an applied pressure during the sintering.
• sintering can include nano-phase separation sintering.
• sintering the plurality of particles involves heating the particles to a sintering temperature of less than or equal to 2200° C., less than or equal to 2000° C., less than or equal to 1900° C., less than or equal to 1800° C., less than or equal to 1700° C., less than or equal to 1600° C , less than or equal to 1500° C , less than or equal to 1400° C , less than or equal to 1300° C., less than or equal to 1200° C., less than or equal to 1100° C., less than or equal to 1000° C., less than or equal to 900° C., less than or equal to 850° C., less than or equal to 800° C., or less than or equal to 750° C.
• sintering the plurality of particles involves heating the particles to a sintering temperature of greater than or equal to 750° C., greater than or equal to 850° C., greater than or equal to 1000° C., greater than or equal to 1200° C., greater than or equal to 1450° C., or greater than or equal to 1600° C. Combinations of these ranges are also possible.
• sintering the plurality of particles involves heating the particles to a sintering temperature that is greater than or equal to 750° C. and less than or equal to 2200° C.
• the temperature of the sintered material is within these ranges for at least 10%, at least 25%, at least 50%, at least 75%, at least 90%, or at least 99% of the sintering time.
• sintering the plurality of particles involves maintaining the particles within the range of sintering temperatures for less than 72 hours, less than 48 hours, less than or equal to 24 hours, less than or equal to 12 hours, less than or equal to 6 hours, less than or equal to 4 hours, less than or equal to 3 hours, less than or equal to 2 hours, or less than or equal to 1 hour (and/or, in some embodiments, for at least 10 minutes, at least 20 minutes, at least 30 minutes, at least 50 minutes, at least 3 hours, or at least 6 hours). Combinations of these ranges are also possible.
• sintering the plurality of particles involves heating the particles to a first sintering temperature that is greater than or equal to 600° C. and less than or equal to 1100° C. for a sintering duration greater than or equal to 6 hours and less than or equal to 24 hours.
• the rate of heating can be 2° C/min, 3° C/min, 4° C/min, 5° C/min, 10° C/min, 15° C/min, or 20° C/min.
• grain size of the metal alloy powder and grain size of the sintered powder can be substantially the same.
• the grain size can be a nano-scale grain size.
• the powder can be a fine grained powder.
• the alloys described herein can be the alloys may be at least one of Ni — Cu — Fe, Ni — Cu— Co, Ni— Cu— Cr, Ni— Cu— V, Ni— Cu— Ag, Ni— Cu— Mo, Ni— Cu— W, Ni— Cu— Mn, Ni— Cu— Zr, Ni— Cu— Fe— Mn, Ni— Cu— Co— Mn, Ni— Cu— Cr— Mn, Ni— Cu— V— Mn, Ni — Cu — Ag — Mn, Ni — Cu — Mo — Mn, or Ni — Cu — W — Mn.
• the Ni content can be 1 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the Cu content can be 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the Fe content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the Co content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the Cr content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the V content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the Mo content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• the W content can be 1 at%, 2 at%, 3 at%, 4 at%, 5 at%, 6 at%, 7 at%, 8 at%, 9 at%, 10 at%, 11 at%, 13 at%, 14 at%, 15 at%, 20 at%, 30 at%, 35 at%, 40 at%, 45 at%, 50 at%, 55 at%, 60 at%, 65 at%, 70 at%, 75at%, 80 at%, 85 at%, 90 at%, or 95 at% of the composition.
• NiCu can have 5 at% to 20 at% Cr; NiCu can have 5 at% to 45 at% Fe; NiCu can have 5 at% to 45 at% Co; NiFeCu can have 5at% or 8at% Mn; NiCu can have 5 at% to 15 at% V; or NiCu can have 5at% to 45 at% Co.
• the metal alloy powder can include: NiCu having 5at%, 10at% 1 lat%, 12at%, 13at%, 14at%, 15at%, 16at%, 17at%, 18at%, or 19at% Cr; NiCu having 5 at%, 10at% 12at%, 14at%, 16at%, 18at%, 20at%, 22at%, 24at%, 26at%, 28at%, 30at%, 32at%, 34at%, 36at%, 38at%, 40at%, or 42at% Fe; NiCu having 5at%, 10at% 12at%, 14at%, 16at%, 18at%, 20at%, 22at%, 24at%, 26at%, 28at%, 30at%, 32at%, 34at%, 36at%, 38at%, 40at%, 42at%, or 44at% Co; NiFeCu having 5at% or 8at% Mn; NiCu having 6at%, 7at%, 8at%, 9at%, 10at%, 1 lat%
• the mechanically powder is a quaternary nano-phase separating powder.
• the metal alloy powder can include NiCu having 5at%, 10at% 12at%, 14at%, 16at%, 18at%, 20at%, 22at%, 24at%, 26at%, 28at%, 30at%, 32at%, 34at%, 36at%, 38at%, 40at%, 42at%, or 44at% Co and up to 5at% Mn.
• FIG. 1 A generalized requirements for nano-phase separation sintering are illustrated, including phase separation, neck formation, sintering and densification.
• the characteristics of the alloy are important to perform these steps. For example, nanocrystallinity can ensure rapid diffusion to the particle surface. Moreover, supersaturation can allow a desired second phase to form at necks. Mechanical alloying can facilitate both of these important factors.
• phase diagram suggests the interplay between concentration, tempature, phase separation, reduced surface energy and high solubility that least to the phase seperation enhanced sintering described herein.
• FIG. 1C illustrates an example of the general process example with Fe.
• Ternary and higher order Ni-Cu alloy systems are of particular interest. Requirements for the selection of the ternary element include the following.
• the ternary element should possess a high positive heat of mixing with Cu. This can increase the transition temperature from miscibility gap to the solid solution phase field.
• the ternary element should also ideally form a solid solution with Ni. This property can favor an interdiffusion as required for nano-phase separation sintering.
• FIG. 2A shows a Ni-Cu phase diagram.
• FIG. 2B illustrates a behavior of the system. For example, increased mobility leads to decreased undercooling and increased undercooling leads to decreased mobility.
• FIG. 3 shows the phase diagram for the system.
• the alloy was heated at different rates (5, 10, 15°C/min) up to 1000°C then cooled 40°C/min.
• FIG. 4A shows the densification rate at lOK/min to 1000°C, then 40K/min cooling.
• FIG. 4B shows the change in relative density.
• FIG. 5A is a Ni-Cr phase diagram.
• FIG. 5B is a Cu-Cr phase diagram.
• Other phase diagrams at other Cr concentrations can be found at FIGS. 6A-6C.
• FIG. 6A is a Ni-Cu phase diagram at 5 at% Cr.
• FIG. 6B is a Ni-Cu phase diagram at 10 at% Cr.
• FIG. 6C is a Ni-Cu phase diagram at 15 at% Cr.
• FIG. 6D An alloy of 60 at% Ni, 25 at% Cu and 15 at% Cr was studied.
• a phase diagram of 60 at% Ni and 15% Cr is shown in FIG. 6D.
• FIG. 6E is a table showing the compositions of stable phases at 550°C.
• FIG. 6F shows the temperature dependence of densification at 5°C/min to 1200°C and 40°C/min cooling.
• FIG. 7A is a Ni-Fe phase diagram.
• FIG. 7B is a Cu-Fe phase diagram.
• Other phase diagrams at other Fe concentrations can be found at FIGS. 8A-8C.
• FIG. 8A is a Ni-Cu phase diagram at 5 at% Fe.
• FIG. 8B is a Ni-Cu phase diagram at 20 at% Fe.
• FIG. 8C is a Ni-Cu phase diagram at 42 at% Fe.
• FIG. 8D is a Ni-Cu phase diagram at 42at% Fe.
• FIG. 8E is a table showing the compositions of stable phases at 550°C. One set of experiments were conducted at 15 at% Cu.
• FIG. 8F shows the temperature dependence of densification at 5°C/min to 945°C and 40°C/min cooling.
• FIG. 8G shows the change in relative density over time at 5°C/min heating.
• FIG. 8H shows the temperature dependence of densification at 10°C/min to 1000°C and 40°C/min cooling.
• FIG. 81 shows the change in relative density over time at 5°C/min heating to a final relative density of 0.5864%.
• FIG. 8J shows the temperature dependence of densification at 15°C/min to 1000°C and 40°C/min cooling.
• FIG. 8K shows the change in relative density over time at 15°C/min heating to a final relative density of 0.5477%.
• FIG. 8L shows the temperature dependence of densification at 20°C/min to 1000°C and 40°C/min cooling.
• FIG. 8M shows the change in relative density over time at 20°C/min heating to a final relative density of 0. 4276%.
• FIG. 8N shows the temperature dependence of densification at 5°C/min to 1100°C and 40°C/min cooling.
• FIG. 80 shows the change in relative density over temperature at 5°C/min heating.
• FIG. 8P shows the change in relative density over time at 5°C/min heating.
• FIG. 8Q shows the temperature dependence of densification at 10°C/min to 1100°C and 40°C/min cooling.
• FIG. 8R shows the change in relative density over temperature at 10°C/min heating.
• FIG. 8S shows the change in relative density overtime at 15°C/min.
• FIG. 8T shows the temperature dependence of densification at 20°C/min to 1100°C and 40°C/min cooling.
• FIG. 8U shows the temperature dependence of densification at 20°C/min to 1100°C and 40°C/min cooling.
• FIG. 8V shows the change in relative density over time at 20°C/min.
• FIG. 9A is a Ni-Co phase diagram.
• FIG. 9B is a Cu-Co phase diagram.
• Other phase diagrams at other Co concentrations can be found at FIGS. 10A-10C.
• FIG. 10A is a Ni-Cu phase diagram at 5 at% Co.
• FIG. 10B is a Ni-Cu phase diagram at 20 at% Co.
• FIG. 10C is a Ni-Cu phase diagram at 44 at% Co.
• a V alloy was studied.
• FIG. 11 A is a Ni-V phase diagram.
• FIG. 1 IB is a Cu-V phase diagram.
• Other phase diagrams at other V concentrations can be found at FIGS. 12A-12C.
• FIG. 12A is a Ni-Cu phase diagram at 6 at% V.
• FIG. 12A is a Ni-Cu phase diagram at 6 at% V.
• FIG. 12B is a Ni-Cu phase diagram at 10 at% V.
• FIG. 12C is a Ni-Cu phase diagram at 13 at% V.
• FIG. 12D is a Ni-Cu phase diagram and 13 at% V.
• FIG. 12E shows the stable phases at 1150°C.
• FIG. 12F shows the temperature dependence of the densifi cation rate for 10 at 5°C/min to 1200°C and 40°C/min cooling.
• FIG. 12G shows the temperature dependences of the change in relative density.
• FIG. 13 is a chart showing the diffusion rates and temperature range for metals described herein.
• FIG. 14A is a phase diagram for Fe-Cu with 40 at% Ni from an Fe database.
• FIG. 14B is a phase diagram for Fe-Cu with 40 at% Ni from a Ni database.
• FIG. 14C is a phase diagram for Fe-Cu with 40 at% Ni from a Cu database.
• FIG. 14D is a phase diagram for Fe-Cu with 40 at% Ni from a high entropy alloy database.
• FIG. 15 is a Cr-Cu phase diagram at 60 at% Ni.
• FIG. 16 is a Co-Cu phase diagram at 40 at% Ni.
• FIG. 17 is a Cu-V phase diagram at 75 at% Ni.
• Pretreatment of an alloy in a reducing atmosphere can improve the sintering performance of the alloy.
• pretreatment with hydrogen gas at 300°C for 24 hours can reduce swelling.
• FIGS. 18A, 18B and 18C show densification after pretreatment with hydrogen at different heating rates.
• oxygen scavenger can be included in an alloy.
• FIG. 19 shows the impact on density of 5 at% and 8 at% Mn to a Ni-Fe-Cu composition.
• FIG. 20 shows the densification behavior of the addition of Mn in a 37.5 at% Ni - 37.5 at% Co - 20 at% Cu - 5 at% Mn composition heated to 1200°C. Microstructures are shown in the images of FIGS. 21, 22, 23 and 24.
• Ni is selected as the base metal for its technological relevance, and because it occupies a unique position: for microcrystalline materials debinding easily precedes sintering, but for nanocrystalline materials the onset of sintering is at the low end of the debinding range, so that the conflation of organic burnout and sintering is expected to be nearly unavoidable.
• Nanocrystalline Ni-Fe alloy powders were produced through high-energy ball milling.
• Nickel powder Alfa Aesar, 99.9% purity, 3-7 pm particle size
• SPEX 8000D Mixer/Mill and with a ball-to-powder ratio of 10: 1 (5 g powder batch) with hardened steel vials and media.
• High-energy ball-milling was conducted in a glovebox maintained under an ultra-high purity Ar atmosphere to limit atmospheric oxygen contamination.
• approximately 5 weight percent (wt%) ethanol (C2H6O) was added as a process control agent (PC A). Note that this is the only organic species used in the present work, and is therefore the primary source of carbon in the system.
• the powder was milled for 20 h and then imaged using a Merlin Zeiss high-resolution scanning electron microscope (HR-SEM) in secondary electron (SE) mode to estimate the as- milled powder size of 51 (+ 23) pm.
• the average grain size was determined from the peak broadening corrected by the lattice strain using a classical Williamson-Hall analysis and instrumental contributions using a NIST LaB6 as reference.
• Ni-Fe solid solution alloy powders Although pure Ni is the input to this process, the wear of the steel media/vials for these milling conditions leads to the production of Ni-Fe solid solution alloy powders.
• the final composition of powders was determined using an energy-dispersive x-ray (EDX) spectrometry detector in the SEM, under the same conditions as described before. The accumulation of Fe contamination as function of ball-milling time. All of the powders reported in this paper were produced under the same 20 h milling conditions and have an iron content of 9.75 atomic percent (at%) ( ⁇ 0.41), which was generally confirmed by wavelength dispersive spectroscopy measurements. Wavelength dispersive spectroscopy (WDS) analysis was based on four separate measurements, which were all comparable.
• WDS Wavelength dispersive spectroscopy
• the ball-milled powders were pressed into cylindrical specimens with dimensions of approximately 6 and 1.5 mm for diameter and height, respectively, to an initial relative density in the range of - 55.8-58.9% using a uniaxial hydraulic press (model YLJ-15 L from MTI Corporation) with a pressure of - 400-450 MPa acting on the pellets, and no additional added binder phases.
• the initial relative densities of the pressed specimens were determined from the ratio of initial and theoretical density (8.80 g/cm 3 , accounting for the Fe content) based on mass and dimension measurements.
• TMA data are presented by converting a raw change in length into a relative density assuming an isotropic shape change, which was generally confirmed after each experiment with caliper measurements.

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