EP0924309A2 - Tantalum-containing nickel base superalloy - Google Patents

Tantalum-containing nickel base superalloy Download PDF

Info

Publication number
EP0924309A2
EP0924309A2 EP98309980A EP98309980A EP0924309A2 EP 0924309 A2 EP0924309 A2 EP 0924309A2 EP 98309980 A EP98309980 A EP 98309980A EP 98309980 A EP98309980 A EP 98309980A EP 0924309 A2 EP0924309 A2 EP 0924309A2
Authority
EP
European Patent Office
Prior art keywords
tantalum
nickel
alloys
base superalloy
essentially
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP98309980A
Other languages
German (de)
French (fr)
Other versions
EP0924309A3 (en
Inventor
Keh-Minn Chang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Publication of EP0924309A2 publication Critical patent/EP0924309A2/en
Publication of EP0924309A3 publication Critical patent/EP0924309A3/en
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/03Alloys based on nickel or cobalt based on nickel
    • C22C19/05Alloys based on nickel or cobalt based on nickel with chromium
    • C22C19/051Alloys based on nickel or cobalt based on nickel with chromium and Mo or W
    • C22C19/056Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 10% but less than 20%
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/0433Nickel- or cobalt-based alloys

Definitions

  • This invention is directed to nickel base superalloys and in particular to such alloys which contain tantalum and a ⁇ strengthening phase.
  • ⁇ strengthened nickel base superalloys are extensively employed in high performance environment articles.
  • the problems with such alloys relate to the high solvus temperature of the ⁇ phase. This temperature usually has a value very close to the incipient melting point of the alloy.
  • Direct hot isostatic pressing of superalloy powder has been used to produce large components in a near-net shape in order to reduce material use and machining waste.
  • current processing routes include blank die compaction followed by extrusion and Forging.
  • the most undesirable time-dependent crack growth behavior occurs when a hold-time is imposed at peak stress during the cycle, i.e., when the maximum tensile stress is held constant for a period of time.
  • a forged nickel-base superalloy article body having fatigue crack growth rates at elevated temperature essentially independent of frequency of cyclical stress applied thereto in which the alloy composition consists essentially of, in weight percent, about 14-22 cobalt 10-14 chromium 2-6 molybdenum 3-5 aluminum 3-5 titanium 0.5-6 tantalum 0-.6 zirconium 0.01-0.1 boron 0.03-0.1 carbon balance essentially nickel
  • this invention is directed to ⁇ ' strengthened nickel base superalloy compositions which can be forged and heat treated to exhibit essentially time independent fatigue crack resistance in combination with high tensile and rupture strength properties.
  • Articles can be manufactured from these alloys using conventional cast and wrought technology, but powder processing techniques are preferred.
  • the alloys of this invention consist essentially of nickel, chromium, cobalt, molybdenum, aluminum, titanium, zirconium, tantalum and boron.
  • the ⁇ ' precipitate phase is present in an amount ranging from about 40 to about 60 percent by volume. These alloys are free of the gamma double prime phase.
  • the forged alloy has a grain structure that is predominantly equiaxed with the grain size being about ASTM 5-8 and exhibits fatigue crack growth rates that are substantially independent of the frequency of fatigue stress intensity with or without intermittent periods during which maximum tensile stress is held. This fatigue cracking resistance is demonstrated at temperatures in excess of 1200°F.
  • compositional range, in weight percent, of the alloys included within the scope of this invention is set out in Table 1 below.
  • cobalt 14-22 chromium 10-14 molybdenum 2-6 aluminum 3-5 titanium 3-5 tantalum 0.5-6 zirconium 0-.6 boron 0.01-0.1 carbon 0.03-0.1 nickel balance
  • the alloy as embodied by the invention has an alloy composition consisting essentially of: 17.7-18.0 cobalt 11.8-12 chromium 3.9-4.0 molybdenum 3.9-4.0 aluminum 3.9-4.0 titanium 3.8-4.0 tantalum 0.17-0.3 zirconium about 0.03 carbon 0.01-0.04 boron balance essentially nickel.
  • the alloy compositions are selected so as developed from about 40 to about 60 volume percent of the ⁇ ' precipitate phase. This volume fraction of the ⁇ ' precipitate has been found to provide the required degree of forgeability in the ingot.
  • Standard superalloy melting procedures can be used to prepare the alloy in powder form.
  • Vacuum induction melting, vacuum arc remelting or electroslag refining or remelting can be used to prepare ingots of the alloy compositions which are converted to powder by conventional atomization techniques followed by compaction and formation of the near net shape article.
  • phase transition temperature of the alloy composition will depend upon obtaining accurate information on the phase transition temperature of the alloy composition.
  • Several different methods are available for determining the phase transition temperature of the superalloy. Differential thermal analysis is one such method.
  • a second method requires metallographic examination of the series of samples which are cold rolled to about 30% reduction and then heat treated at various temperatures around the expected phase transition temperature. Each of these methods is carried out on samples of the alloy.
  • the ⁇ ' precipitate solvus of an alloy composition of this invention is frequently in the range of from about 1050 to about 1175°C.
  • Figure 1a is a graphic representation of fatigue crack growth resistance for the alloys shown in Table 1 at 1200°F.
  • Figure 1b is a graphic representation of fatigue crack growth resistance for the same alloys obtained at 1400°F.
  • Figures 1a and 1b illustrate that the crack growth resistance advantage for the alloys in this invention over niobium containing alloys and other selected alloys. At 1200°F most alloys do not exhibit time dependent crack growth. However, at 1400°F many alloys exhibit faster crack growth with longer tensile hold times. The 1400°F crack growth rates for the alloys of this invention do not depend strongly on the hold time. Thus, the crack growth resistance of this class of alloys is superior to that of prior art alloys and other alloys with similar compositions containing niobium.
  • Ingots consisting essentially of the following composition were prepared by a vacuum induction melting and casting procedure: cobalt 14-22 chromium 10-14 molybdenum 2-6 aluminum 3-5 titanium 3-5 tantalum 0.5-6 zirconium 0-.6 boron 0.01-0.1 carbon 0.03-0.1 nickel balance
  • the alloy as embodied by the invention, has an alloy composition consisting essentially of: 17.7-18.0 cobalt 11.8-12 chromium 3.9-4.0 molybdenum 3.9-4.0 aluminum 3.9-4.0 titanium 3.8-4.0 tantalum 0.17-0.3 zirconium about 0.03 carbon 0.01-0.04 boron balance essentially nickel.
  • the alloy as embodied by the invention, has an alloy composition consisting essentially of: 17.5-18.5 cobalt 11.5-12.5 chromium 3.7-4.3 molybdenum 3.8-4.2 aluminum 3.8-4.2 titanium 3.7-4.3 tantalum 0.2-0.3 zirconium 0.01-0.04 carbon 0.01-0.04 boron balance essentially nickel.
  • a powder was prepared by melting ingots of the selected composition in an argon gas atmosphere and atomizing the liquid metal using argon gas for atomization. The powder was sieved to remove particles coarser than 150 mesh.
  • the -150 mesh powder was transferred to consolidation cans for initial densification using a closed die compaction procedure at a temperature of about 150°F below the ⁇ ' solvus. This was followed by extrusion using a 7:1 extrusion reduction ratio at a temperature approximately 100°F below the ⁇ ' solvus to produce a fully dense extrusion.
  • the extrusions were then solution treated or annealed at a temperature above the ⁇ ' solvus temperature in the range of about 2140°F to about 2160°F for about 1 hour.
  • This solvus solution treatment completely dissolves the ⁇ ' phase and forms a well annealed structure.
  • the solution treatment also recrystallizes and coarsens the fine grain billet structure and permits controlled reprecipitation of the ⁇ ' during subsequent heat treatment and processing.
  • the solution treated extrusions were then rapidly cooled for the solution treatment temperature using a controlled quench.
  • This quench is performed at a rate sufficient to develop a uniform distribution of ⁇ ' throughout the article.
  • a controlled fan helium quench having a cooling rate of about 250°F per minute was used.
  • the alloy was aged at a temperature of about 1500°F to 1550°F for about 4 hours.
  • a preferred temperature range for this aging treatment is about 1515°F to about 1535°F. Aging promotes uniform distribution of additional ⁇ ' and is particularly suited for an alloy designed for operating service at temperatures of about 1500 °F.
  • Solution treating can be carried out at any temperature above which the ⁇ ' phase dissolves in the gamma matrix and below the incipient melting temperature of the alloy.
  • the particular temperature at which ⁇ ' first begins to dissolve in the matrix is referred to as the ⁇ solvus temperature.
  • the temperature range between the ⁇ ' solvus temperature and the incipient melting temperature is generally referred to as the supersolvus temperature range. This temperature range will vary depending upon the composition of the superalloy.
  • the alloys of this invention were solution treated in the range of about 1175°C to 1200°C for about 1 hour. This solution treatment was followed by an aging treatment at a temperature of about 700°C to about 800°C for about 4-12 hours.

Abstract

A tantalum-containing nickel base superalloy strengthened by γ precipitates has greatly improved temperature capability, with a fatigue cracking resistance substantially independent of the fatigue frequency and waveform up to about 1500°F.

Description

  • This invention is directed to nickel base superalloys and in particular to such alloys which contain tantalum and a γ strengthening phase.
  • Despite fabrication problems, γ strengthened nickel base superalloys are extensively employed in high performance environment articles. In general, the problems with such alloys relate to the high solvus temperature of the γ phase. This temperature usually has a value very close to the incipient melting point of the alloy.
  • Direct hot isostatic pressing of superalloy powder has been used to produce large components in a near-net shape in order to reduce material use and machining waste. However, current processing routes include blank die compaction followed by extrusion and Forging.
  • Considerable effort has been expended in developing alloys and techniques for use in powder metallurgy and processing. Superalloy compositions providing improved resistance to fatigue crack growth at elevated temperatures are particularly useful in making shaped articles by various powder processes.
  • Crack propagation rate in high strength superalloy bodies depends on applied stress and crack length. These factors combine to provide a crack growth driving force referred to as stress intensity which is proportional to the applied stress multiplied by the square root of crack length (K= Yσ(a)1/2)).
  • The most undesirable time-dependent crack growth behavior occurs when a hold-time is imposed at peak stress during the cycle, i.e., when the maximum tensile stress is held constant for a period of time.
  • Various nickel base alloy compositions are representative of alloying situations in which many of the same elements are combined to achieve distinctly different functional relationships between the elements which provide the alloy system with different physical and mechanical characteristics. However, it is still not possible for workers in the art to predict with any degree of accuracy the physical and mechanical properties that will be displayed by certain concentrations of commonly known elements used in varying combinations to form such alloys even though such combinations may fall within broader more generalized teachings disclosed in the art. This inability to predict is particularly noticeable.
  • Certain objectives for forgeable nickel base superalloys are known. In the first place, it is important to minimize the time dependence of fatigue crack resistance and to secure values of strength at room and elevated temperature and creep properties that are reasonably comparable to those of known powder processed alloys. It is also important to reduce processing difficulties encountered in previous metal working procedures.
  • According to the invention, there is provided a forged nickel-base superalloy article body having fatigue crack growth rates at elevated temperature essentially independent of frequency of cyclical stress applied thereto in which the alloy composition consists essentially of, in weight percent, about
    14-22 cobalt
    10-14 chromium
    2-6 molybdenum
    3-5 aluminum
    3-5 titanium
    0.5-6 tantalum
    0-.6 zirconium
    0.01-0.1 boron
    0.03-0.1 carbon
    balance essentially nickel
  • Thus, this invention is directed to γ' strengthened nickel base superalloy compositions which can be forged and heat treated to exhibit essentially time independent fatigue crack resistance in combination with high tensile and rupture strength properties. Articles can be manufactured from these alloys using conventional cast and wrought technology, but powder processing techniques are preferred.
  • The alloys of this invention consist essentially of nickel, chromium, cobalt, molybdenum, aluminum, titanium, zirconium, tantalum and boron. The γ' precipitate phase is present in an amount ranging from about 40 to about 60 percent by volume. These alloys are free of the gamma double prime phase. The forged alloy has a grain structure that is predominantly equiaxed with the grain size being about ASTM 5-8 and exhibits fatigue crack growth rates that are substantially independent of the frequency of fatigue stress intensity with or without intermittent periods during which maximum tensile stress is held. This fatigue cracking resistance is demonstrated at temperatures in excess of 1200°F.
  • The compositional range, in weight percent, of the alloys included within the scope of this invention is set out in Table 1 below.
    cobalt 14-22
    chromium 10-14
    molybdenum 2-6
    aluminum 3-5
    titanium 3-5
    tantalum 0.5-6
    zirconium 0-.6
    boron 0.01-0.1
    carbon 0.03-0.1
    nickel balance
  • Further, the alloy as embodied by the invention, has an alloy composition consisting essentially of:
    17.7-18.0 cobalt
    11.8-12 chromium
    3.9-4.0 molybdenum
    3.9-4.0 aluminum
    3.9-4.0 titanium
    3.8-4.0 tantalum
    0.17-0.3 zirconium
    about 0.03 carbon
    0.01-0.04 boron
    balance essentially nickel.
  • The alloy compositions are selected so as developed from about 40 to about 60 volume percent of the γ' precipitate phase. This volume fraction of the γ' precipitate has been found to provide the required degree of forgeability in the ingot.
  • Standard superalloy melting procedures can be used to prepare the alloy in powder form.
  • Vacuum induction melting, vacuum arc remelting or electroslag refining or remelting can be used to prepare ingots of the alloy compositions which are converted to powder by conventional atomization techniques followed by compaction and formation of the near net shape article.
  • Subsequent mechanical and thermal manufacturing processing will depend upon obtaining accurate information on the phase transition temperature of the alloy composition. Several different methods are available for determining the phase transition temperature of the superalloy. Differential thermal analysis is one such method. A second method requires metallographic examination of the series of samples which are cold rolled to about 30% reduction and then heat treated at various temperatures around the expected phase transition temperature. Each of these methods is carried out on samples of the alloy. The γ' precipitate solvus of an alloy composition of this invention is frequently in the range of from about 1050 to about 1175°C.
  • The invention will now be described in greater detail, by way of example, with reference to the drawings in which:-
  • Figure 1a is a graphic representation of fatigue crack growth resistance for the alloys shown in Table 1 at 1200°F.
  • Figure 1b is a graphic representation of fatigue crack growth resistance for the same alloys obtained at 1400°F.
  • Figures 1a and 1b illustrate that the crack growth resistance advantage for the alloys in this invention over niobium containing alloys and other selected alloys. At 1200°F most alloys do not exhibit time dependent crack growth. However, at 1400°F many alloys exhibit faster crack growth with longer tensile hold times. The 1400°F crack growth rates for the alloys of this invention do not depend strongly on the hold time. Thus, the crack growth resistance of this class of alloys is superior to that of prior art alloys and other alloys with similar compositions containing niobium.
  • Ingots consisting essentially of the following composition were prepared by a vacuum induction melting and casting procedure:
    cobalt 14-22
    chromium 10-14
    molybdenum 2-6
    aluminum 3-5
    titanium 3-5
    tantalum 0.5-6
    zirconium 0-.6
    boron 0.01-0.1
    carbon 0.03-0.1
    nickel balance
  • Further, the alloy, as embodied by the invention, has an alloy composition consisting essentially of:
    17.7-18.0 cobalt
    11.8-12 chromium
    3.9-4.0 molybdenum
    3.9-4.0 aluminum
    3.9-4.0 titanium
    3.8-4.0 tantalum
    0.17-0.3 zirconium
    about 0.03 carbon
    0.01-0.04 boron
    balance essentially nickel.
  • Also, the alloy, as embodied by the invention, has an alloy composition consisting essentially of:
    17.5-18.5 cobalt
    11.5-12.5 chromium
    3.7-4.3 molybdenum
    3.8-4.2 aluminum
    3.8-4.2 titanium
    3.7-4.3 tantalum
    0.2-0.3 zirconium
    0.01-0.04 carbon
    0.01-0.04 boron
    balance essentially nickel.
  • A powder was prepared by melting ingots of the selected composition in an argon gas atmosphere and atomizing the liquid metal using argon gas for atomization. The powder was sieved to remove particles coarser than 150 mesh.
  • The -150 mesh powder was transferred to consolidation cans for initial densification using a closed die compaction procedure at a temperature of about 150°F below the γ' solvus. This was followed by extrusion using a 7:1 extrusion reduction ratio at a temperature approximately 100°F below the γ' solvus to produce a fully dense extrusion.
  • The extrusions were then solution treated or annealed at a temperature above the γ' solvus temperature in the range of about 2140°F to about 2160°F for about 1 hour. This solvus solution treatment completely dissolves the γ' phase and forms a well annealed structure. The solution treatment also recrystallizes and coarsens the fine grain billet structure and permits controlled reprecipitation of the γ' during subsequent heat treatment and processing.
  • The solution treated extrusions were then rapidly cooled for the solution treatment temperature using a controlled quench. This quench is performed at a rate sufficient to develop a uniform distribution of γ' throughout the article. A controlled fan helium quench having a cooling rate of about 250°F per minute was used. Following quenching, the alloy was aged at a temperature of about 1500°F to 1550°F for about 4 hours. A preferred temperature range for this aging treatment is about 1515°F to about 1535°F. Aging promotes uniform distribution of additional γ' and is particularly suited for an alloy designed for operating service at temperatures of about 1500 °F.
  • In order to achieve properties and microstructures which are necessary for the alloys of the present invention, the processing of the superalloy is important. Although a metal powder was produced which was subsequently processed using compaction and extrusion methods followed by a heat treatment it should be understood by those skilled in the art that other methods and associated heat treatments which produce the specific composition, grain size, and microstructure can be used to provide the benefits of this invention.
  • Solution treating can be carried out at any temperature above which the γ' phase dissolves in the gamma matrix and below the incipient melting temperature of the alloy. The particular temperature at which γ' first begins to dissolve in the matrix is referred to as the γ solvus temperature. The temperature range between the γ' solvus temperature and the incipient melting temperature is generally referred to as the supersolvus temperature range. This temperature range will vary depending upon the composition of the superalloy. The alloys of this invention were solution treated in the range of about 1175°C to 1200°C for about 1 hour. This solution treatment was followed by an aging treatment at a temperature of about 700°C to about 800°C for about 4-12 hours.
  • While the embodiments described herein are preferred, it will be appreciated from the specification that various combinations of elements, variations or improvements therein may be made by those skilled in the art are within the scope of the appended claims.

Claims (3)

  1. A forged nickel-base superalloy article body having fatigue crack growth rates at elevated temperature essentially independent of frequency of cyclical stress applied thereto in which the alloy composition consists essentially of, in weight percent, about 14-22 cobalt 10-14 chromium 2-6 molybdenum 3-5 aluminum 3-5 titanium 0.5-6 tantalum 0-.6 zirconium 0.01-0.1 boron 0.03-0.1 carbon balance essentially nickel
  2. The forged nickel-base superalloy body of claim 1 wherein the alloy composition consists essentially of: 17.7-18.0 cobalt 11.8-12 chromium 3.9-4.0 molybdenum 3.9-4.0 aluminum 3.9-4.0 titanium 3.8-4.0 tantalum 0.17-0.3 zirconium about 0.03 carbon 0.01-0.06 boron balance essentially nickel.
  3. The forged nickel-base superalloy body of claim 1 wherein the alloy composition consists essentially of: 17.5-18.5 cobalt 11.5-12.5 chromium 3.7-4.3 molybdenum 3.8-4.2 aluminum 3.8-4.2 titanium 3.7-4.3 tantalum 0.2-0.3 zirconium 0.01-0.04 carbon 0.01-0.04 boron balance essentially nickel.
EP98309980A 1997-12-17 1998-12-04 Tantalum-containing nickel base superalloy Withdrawn EP0924309A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99190097A 1997-12-17 1997-12-17
US991900 1997-12-17

Publications (2)

Publication Number Publication Date
EP0924309A2 true EP0924309A2 (en) 1999-06-23
EP0924309A3 EP0924309A3 (en) 1999-09-08

Family

ID=25537700

Family Applications (1)

Application Number Title Priority Date Filing Date
EP98309980A Withdrawn EP0924309A3 (en) 1997-12-17 1998-12-04 Tantalum-containing nickel base superalloy

Country Status (1)

Country Link
EP (1) EP0924309A3 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009112380A1 (en) * 2008-03-14 2009-09-17 Siemens Aktiengesellschaft Nickel base alloy and use of it, turbine blade or vane and gas turbine
CN101899595A (en) * 2009-05-29 2010-12-01 通用电气公司 Nickel based super alloy reaches by its member of making
EP2256222A1 (en) * 2009-05-29 2010-12-01 General Electric Company Nickel-base superalloys and components formed thereof
CN115821117A (en) * 2022-11-29 2023-03-21 江西宝顺昌特种合金制造有限公司 GH4141 high-temperature alloy and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5662749A (en) * 1995-06-07 1997-09-02 General Electric Company Supersolvus processing for tantalum-containing nickel base superalloys

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5662749A (en) * 1995-06-07 1997-09-02 General Electric Company Supersolvus processing for tantalum-containing nickel base superalloys

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009112380A1 (en) * 2008-03-14 2009-09-17 Siemens Aktiengesellschaft Nickel base alloy and use of it, turbine blade or vane and gas turbine
EP2103700A1 (en) * 2008-03-14 2009-09-23 Siemens Aktiengesellschaft Nickel base alloy and use of it, turbine blade or vane and gas turbine
CN101970702B (en) * 2008-03-14 2012-11-28 西门子公司 Nickel base alloy and use of it, turbine blade or vane and gas turbine
US7993101B2 (en) 2008-03-14 2011-08-09 Siemens Aktiengesellschaft Nickel base alloy and use of it, turbine blade or vane and gas turbine
EP2256222A1 (en) * 2009-05-29 2010-12-01 General Electric Company Nickel-base superalloys and components formed thereof
US8992700B2 (en) 2009-05-29 2015-03-31 General Electric Company Nickel-base superalloys and components formed thereof
JP2010275636A (en) * 2009-05-29 2010-12-09 General Electric Co <Ge> Nickel-base super alloy and component thereof
JP2010280986A (en) * 2009-05-29 2010-12-16 General Electric Co <Ge> Nickel-base superalloy and component formed thereof
EP2256223A1 (en) * 2009-05-29 2010-12-01 General Electric Company Nickel-base superalloys and components formed thereof
CN101899595A (en) * 2009-05-29 2010-12-01 通用电气公司 Nickel based super alloy reaches by its member of making
US8992699B2 (en) 2009-05-29 2015-03-31 General Electric Company Nickel-base superalloys and components formed thereof
CN101899594A (en) * 2009-05-29 2010-12-01 通用电气公司 Nickel based super alloy reaches by its member of making
CN101899594B (en) * 2009-05-29 2015-06-24 通用电气公司 Nickel-base superalloys and components formed thereof
CN101899595B (en) * 2009-05-29 2015-08-05 通用电气公司 Nickel based super alloy and the component be made up of it
CN104946933A (en) * 2009-05-29 2015-09-30 通用电气公司 Nickel-base superalloys and components formed thereof
US9518310B2 (en) 2009-05-29 2016-12-13 General Electric Company Superalloys and components formed thereof
CN115821117A (en) * 2022-11-29 2023-03-21 江西宝顺昌特种合金制造有限公司 GH4141 high-temperature alloy and preparation method thereof
CN115821117B (en) * 2022-11-29 2023-09-29 江西宝顺昌特种合金制造有限公司 GH4141 high-temperature alloy and preparation method thereof

Also Published As

Publication number Publication date
EP0924309A3 (en) 1999-09-08

Similar Documents

Publication Publication Date Title
EP0184136B1 (en) Fatigue-resistant nickel-base superalloys
JP3944271B2 (en) Grain size control in nickel-base superalloys.
US4957567A (en) Fatigue crack growth resistant nickel-base article and alloy and method for making
EP0292320B1 (en) Nickel base superalloy
US5558729A (en) Method to produce gamma titanium aluminide articles having improved properties
US11718897B2 (en) Precipitation hardenable cobalt-nickel base superalloy and article made therefrom
US5653828A (en) Method to procuce fine-grained lamellar microstructures in gamma titanium aluminides
US5584947A (en) Method for forming a nickel-base superalloy having improved resistance to abnormal grain growth
CN114921684B (en) High strength titanium alloy
US3767385A (en) Cobalt-base alloys
US5662749A (en) Supersolvus processing for tantalum-containing nickel base superalloys
US5393483A (en) High-temperature fatigue-resistant nickel based superalloy and thermomechanical process
JPS6339651B2 (en)
JP3145091B2 (en) Fatigue crack resistant nickel-base superalloy
US4386976A (en) Dispersion-strengthened nickel-base alloy
US5417781A (en) Method to produce gamma titanium aluminide articles having improved properties
AU2022224763B2 (en) Creep resistant titanium alloys
EP3572541B1 (en) Nickel-base superalloy
US20230151459A1 (en) Nickel-based alloy embodiments and method of making and using the same
EP0260512B1 (en) Method of forming fatigue crack resistant nickel base superalloys and products formed
US5584948A (en) Method for reducing thermally induced porosity in a polycrystalline nickel-base superalloy article
Sczerzenie et al. DEVELOPMENT OF LJDIMET 720 FOR HIGH STRENGTH DISK APPLICATIONS
US5556484A (en) Method for reducing abnormal grain growth in Ni-base superalloys
US5415712A (en) Method of forging in 706 components
EP0924309A2 (en) Tantalum-containing nickel base superalloy

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB IT

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

RIC1 Information provided on ipc code assigned before grant

Free format text: 6C 22C 19/05 A, 6C 22F 1/10 B, 6C 22C 1/04 B

17P Request for examination filed

Effective date: 20000308

AKX Designation fees paid

Free format text: DE FR GB IT

17Q First examination report despatched

Effective date: 20000522

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20001202