US3554817A - Cast nickel-columbium-aluminum alloy - Google Patents

Cast nickel-columbium-aluminum alloy Download PDF

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US3554817A
US3554817A US808956A US3554817DA US3554817A US 3554817 A US3554817 A US 3554817A US 808956 A US808956 A US 808956A US 3554817D A US3554817D A US 3554817DA US 3554817 A US3554817 A US 3554817A
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alloy
eutectic
percent
nickel
columbium
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Earl R Thompson
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Raytheon Technologies Corp
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United Aircraft Corp
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    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B21/00Unidirectional solidification of eutectic materials
    • C30B21/02Unidirectional solidification of eutectic materials by normal casting or gradient freezing

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  • the present invention relates in general to the nickelbase alloys and, more particularly, to a nickel-columbiumaluminum alloy at about the eutectic composition, as directionally solidied to provide a lamellar microstructure.
  • the present invention makes available the strongest nickel-base alloy known. It includes, as its essential component, the eutectic alloy existing between the intermetallic compounds Ni3A1 and Ni3Cb at about 33 Weight percent Ni2A1, as directionally solidified to provide a controlled lamellar microstructure.
  • FIG. 1 is a photomicrograph of a transverse section of a Ni3Al-Ni3Cb eutectic alloy unidirectionally solidified at a rate of 2.2 cm./hr.
  • FIG. 2 is a photomicrograph of the same alloy in longitudinal section, clearly revealing the pronounced anisotropy of the ingot as evidenced by the lamellar microstructure thereof.
  • FIG. 3 is a graph comparing the tensile strength of the Ni3Al-Ni3Cb alloy as directionally solidified with an advanced cast nickel-base superalloy.
  • FIG. 4 is a plot of the Larson-Miller parameter curves for rupture comparing the aligned NiSAl-NisCb eutectic with an advanced cast nickel-base superalloy.
  • a eutectic existing in the nickel-columbium-aluminum alloy system occurs at about the composition, by weight, 72.5 percent nickel, 23.1 percent columbium and 4.4 percent aluminum.
  • This alloy exhibits pseudo-binary belce havior between the Ni3Al and the Ni3Cb intermetallic compounds at about 33 weight percent Ni3A1 and, upon plane front solidiiication, produces a controlled lamellar microstructure containing about 44 volume percent of NiaCb within the Ni3A1 matrix.
  • the phase alignment is clearly evident from the photomicrographs of FIGS. 1 and 2.
  • nickel-base superalloys may be strengthened by precipitates of 'y', a phase based on the Ni3A intermetallic.
  • a precipitate is found in the typical nickel-base superalloy such as B-1900 which has a nominal composition, by weight, of 8 percent chromium, 10 percent cobalt, 1 percent titanium, 6 percent aluminum, 6 percent molybdenum, 0.11 percent carbon, 4.3 percent tantalum, 0.15 percent boron, 0.07 percent zirconium, balance essentially nickel.
  • the alloy of the present invention is hereinafter referred to as the eutectic alloy. It will be understood, however, that, particularly in connection with the mechanical property considerations, this term is utilized to refer to the Ni3Al-Ni3Cb eutectic alloy as unidirectionally solidified to yield an aligned, lamellar microstructure.
  • the eutectic temperature of the present alloy lies at about 2336 F., and the solid solubility of the NisCb phase within the 'y' phase extends to about 40 weight percent columbium, while the solubility of NiAl in the NiaCb phase is less than about 4 weight percent.
  • the eutectic exhibits coupled plane front growth when solidified unidirectionally at 2 cm./hr., growing with a lamellar morphology at a lamellar spacing of approximately 4 microns.
  • Tensile and creep-rupture specimens were ground from the unidirectionally solidified ingots such that the load would be applied parallel to the direction of growth.
  • the specimens typically were formed 'with gage sections having a diameter and length off 0.140 and 1.1 inch, respectively.
  • Tensile tests were performed with a Tinius-Olsen four screw machine. Creep rupture testing was carried out in air under constant load.
  • the longitudinal tensile properties of the eutectic alloy were measured as a function of temperature and the results are reported in Table I.
  • the tensile strength of the alloy is strain-rate dependent at 2000 F.
  • Time-temperature rupture data for the present alloy and the B-l900 alloy is presented in FIG. 4 as a Larson- Miller plot assuming a constant of for both alloys.
  • the superiority of the eutectic alloy to B-l900 is evident.
  • the directionally-solidied Ni3Al-Ni3Cb eutectic alloy exhibits rupture strengths in excess of those of any reported nickel-base alloy.
  • the room temperature elastic modulus and 0.2 percent offset compressive yield strength have been established at 34X l0G p.s.i. and 200,000 p.s.i., respectively. Failure in compression occurs at a strain of approximately 10 percent and a stress of 340,000 p.s.i., both ductile flow and interfacial cleavage occurring in the process.
  • the lamellar morphology of the alloy is thermally stable at least to temperatures as high as 2200o F. Specimens which were heat treated for up to 200 hours at 2200 F. showed no measurable coarsening of the lamellae.
  • alloys which deviate from the true eutectic compositions may nevertheless be capable of solidilication to produce the desired lamellar microstructure.
  • unidirectional solidiication of eutectics has shown that such alloy frequently comprise a eutectic portion and a proeutectic portion, Le., a portion which does not undergo a eutectic reaction.
  • the resulting castings of such alloys often comprise a lamellar microstructure, as described herein, having distributed therein relatively large proeutectic crystals throughout the lamellar microstructure in either random or uniform distribution.
  • deviations from or additions to the basic eutectic composition may be made as long as they do not interfere with the basic coupled plane front growth mechanism by which the lamellar microstructure is formed. Such deviations may be advisable in certain applications to impart or improve a specific property of the basic alloy. Even in such cases, however, the strength advantages to be achieved from a major portion comprising the Ni3Al-Ni3Cb eutectic will be desirable.
  • a cast Ni base alloy containing Al and Cb contains a multiphase lamellar microstructure, a first phase consisting essentially of the Ni3Al intermetallic compound, a second phase consisting essentially of the NiaCb intermetallic compound, the first and second phases consisting of lamellae arranged in alternation in the cast article and in substantial alignment over a major portion of the length thereof.
  • a cast gas turbine engine blade or vane which comprises an alloy consisting essentially of about 33 weight percent NiaAl, balance Ni3Cb unidirectionally solidified parallel to the tensile axis of the blade or vane to produce a lamellar microstructure wherein the NiaAl and NiaCb components comprises respective lamellar phases which are arranged in alternation in the microstructure.
  • the alloy is solidified in a direction substantially parallel to the designed tensile axis of the component.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Turbine Rotor Nozzle Sealing (AREA)
  • Manufacture Of Alloys Or Alloy Compounds (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

THE PSEUDO-BINARY EUTECTIC ALLOY OCCURING BETWEEN THE INTERMETALLIC COMPOUND NI3AL AND NI3CB IS UNIDIRECTIONALLY SOLIDIFIED INTO A CASTING CHARACTERIZED BY AN ALIGNED, LAMELLAR MICROSTRUCTURE.

Description

$1.151?,'1971 E. R. THOMPSON l 3,554,817
v CSII :NICKELCOLUMBIUM-ALUMINUM ALLOY y Filed nai-cen 2o. 1969 '2 sheets-sheet 1 Maf/avra@ Jan. 12, 1971 E. R. THOMPSON CAST NICKEL-COLUMBIUMALUMINUM ALLOY 2 Sheets-Sheet 2 Filed Mal-n zo, 1969 United States Patent O 3,554,817 CAST NICKEL-COLUMBIUM-ALUMINUM ALLOY Earl R. Thompson, Glastonbury, Conn., assignor to United Aircraft Corporation, East Hartford, Conn., a corporation of Delaware Filed Mar. 20, 1969, Ser. No. 808,956 Int. Cl. B22d 21/00; (122e 15/00 U.S. Cl. 148--32 8 Claims ABSTRACT OF THE DISCLOSURE The pseudo-binary eutectic alloy occurring between the intermetallic compounds NigAl and NiaCb is unidirectionally solidified into a casting characterized by an aligned, lamellar microstructure.
BACKGROUND OF THE INVENTION The present invention relates in general to the nickelbase alloys and, more particularly, to a nickel-columbiumaluminum alloy at about the eutectic composition, as directionally solidied to provide a lamellar microstructure.
The demands of todays technology require a continuous search for new alloys adapted to high temperature structural applications. One of the areas to which considerable research and development activity has been furnished is that of the fibrous composite materials. Strengthening of metal matrices has been accomplished utilizing a variety of reinforcing materials, including vapor grown oxide, carbide and nitride whiskers, carbon and refractory metal wires.
It is known that many of the eutectic-type alloys respond to plane front solidification to produce phasealigned microstructures, as described in the patent to Kraft 3,124,452 which shares a common assignee with the present invention. In some cases, casting of the eutectic alloys as described by Kraft has produced in situ strengthening of a metal matrix by a stiffer, less ductile phase and has avoided many of the difiiculties normally encountered in the fabrication and use of composite materials produced by other methods.
SUMMARY OF THE INVENTION The present invention makes available the strongest nickel-base alloy known. It includes, as its essential component, the eutectic alloy existing between the intermetallic compounds Ni3A1 and Ni3Cb at about 33 Weight percent Ni2A1, as directionally solidified to provide a controlled lamellar microstructure.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a photomicrograph of a transverse section of a Ni3Al-Ni3Cb eutectic alloy unidirectionally solidified at a rate of 2.2 cm./hr.
FIG. 2 is a photomicrograph of the same alloy in longitudinal section, clearly revealing the pronounced anisotropy of the ingot as evidenced by the lamellar microstructure thereof.
FIG. 3 is a graph comparing the tensile strength of the Ni3Al-Ni3Cb alloy as directionally solidified with an advanced cast nickel-base superalloy.
FIG. 4 is a plot of the Larson-Miller parameter curves for rupture comparing the aligned NiSAl-NisCb eutectic with an advanced cast nickel-base superalloy.
DESCRIPTION OF THE PREFERRED IEMBODIMENTS A eutectic existing in the nickel-columbium-aluminum alloy system occurs at about the composition, by weight, 72.5 percent nickel, 23.1 percent columbium and 4.4 percent aluminum. This alloy exhibits pseudo-binary belce havior between the Ni3Al and the Ni3Cb intermetallic compounds at about 33 weight percent Ni3A1 and, upon plane front solidiiication, produces a controlled lamellar microstructure containing about 44 volume percent of NiaCb within the Ni3A1 matrix. The phase alignment is clearly evident from the photomicrographs of FIGS. 1 and 2.
It is Well recognized in the high temperature alloy development field that nickel-base superalloys may be strengthened by precipitates of 'y', a phase based on the Ni3A intermetallic. Such a precipitate is found in the typical nickel-base superalloy such as B-1900 which has a nominal composition, by weight, of 8 percent chromium, 10 percent cobalt, 1 percent titanium, 6 percent aluminum, 6 percent molybdenum, 0.11 percent carbon, 4.3 percent tantalum, 0.15 percent boron, 0.07 percent zirconium, balance essentially nickel.
For the sake of brevity, the alloy of the present invention is hereinafter referred to as the eutectic alloy. It will be understood, however, that, particularly in connection with the mechanical property considerations, this term is utilized to refer to the Ni3Al-Ni3Cb eutectic alloy as unidirectionally solidified to yield an aligned, lamellar microstructure.
The eutectic temperature of the present alloy lies at about 2336 F., and the solid solubility of the NisCb phase within the 'y' phase extends to about 40 weight percent columbium, while the solubility of NiAl in the NiaCb phase is less than about 4 weight percent. The eutectic exhibits coupled plane front growth when solidified unidirectionally at 2 cm./hr., growing with a lamellar morphology at a lamellar spacing of approximately 4 microns. Numerous off-eutectic castings were made to demonstrate that a lamellar morphology could be attained, as suggested by Kraft, supra, and an examination of these off-eutectic specimens showed that the nucleating phase for the eutectic is the Ni3Cb phase and that dendrites of the y phase are haloed by the NiaCb phase from which the eutectic grains grow.
Master melts of eutectic compositions were made in alumina crucibles and chill cast in copper molds. The resulting ingots were unidirectionally solidified vertically within a resistively heated graphite tube furnace under a dynamic argon atmosphere. The molten eutectic alloy was contained in a 1A inch diameter 99.7 percent recrystallized alumina, cylindrical Crucible held in graphite sleeve which separated the Crucible bottom from a water cooled brass plug by one inch of graphite. Crucible lowering rates of about 2 cm./hr. and liquid superheats of about 300 C. were generally employed, with a resultant thermal gradient in the liquid of approximately 70 C./ cm.
Tensile and creep-rupture specimens were ground from the unidirectionally solidified ingots such that the load would be applied parallel to the direction of growth. The specimens typically were formed 'with gage sections having a diameter and length off 0.140 and 1.1 inch, respectively. Tensile tests were performed with a Tinius-Olsen four screw machine. Creep rupture testing was carried out in air under constant load.
The longitudinal tensile properties of the eutectic alloy were measured as a function of temperature and the results are reported in Table I. The tensile strength of the alloy is strain-rate dependent at 2000 F.
TABLE 1I Final elongation, percent,
Time to rupture, lrr.
Time t Stress, p.s.i. 1%, hr.
Temp., F.
Time-temperature rupture data for the present alloy and the B-l900 alloy is presented in FIG. 4 as a Larson- Miller plot assuming a constant of for both alloys. The superiority of the eutectic alloy to B-l900 is evident. Moreover, the directionally-solidied Ni3Al-Ni3Cb eutectic alloy exhibits rupture strengths in excess of those of any reported nickel-base alloy.
The room temperature elastic modulus and 0.2 percent offset compressive yield strength have been established at 34X l0G p.s.i. and 200,000 p.s.i., respectively. Failure in compression occurs at a strain of approximately 10 percent and a stress of 340,000 p.s.i., both ductile flow and interfacial cleavage occurring in the process.
The lamellar morphology of the alloy is thermally stable at least to temperatures as high as 2200o F. Specimens which were heat treated for up to 200 hours at 2200 F. showed no measurable coarsening of the lamellae.
In assessing the strength characteristics of the NaaAl- NiaCb eutectic alloy, it will be remembered that the testing was performed in air. In extended testing at high temperatures in air an oxide scale was produced which at times was significant in terms of the loss in specimen cross-section, amounting to approximately ten percent for 500 hours at 2000 F. Accordingly, the superiority in strength of this alloy, while far surpassing that of the advanced nickel-base superalloys in air, nevertheless was diminished for comparative purposes by the effects of the oxidation. AOf course, it is normal to provide surface protection to the vast majority of the nickel-base superalloys in dynamic oxidizing environments at high temperature.
Those alloys which deviate from the true eutectic compositions may nevertheless be capable of solidilication to produce the desired lamellar microstructure. Experience with the unidirectional solidiication of eutectics has shown that such alloy frequently comprise a eutectic portion and a proeutectic portion, Le., a portion which does not undergo a eutectic reaction. The resulting castings of such alloys often comprise a lamellar microstructure, as described herein, having distributed therein relatively large proeutectic crystals throughout the lamellar microstructure in either random or uniform distribution.
In general, deviations from or additions to the basic eutectic composition may be made as long as they do not interfere with the basic coupled plane front growth mechanism by which the lamellar microstructure is formed. Such deviations may be advisable in certain applications to impart or improve a specific property of the basic alloy. Even in such cases, however, the strength advantages to be achieved from a major portion comprising the Ni3Al-Ni3Cb eutectic will be desirable.
While the invention has been described in detail with relation to specific preferred embodiments and examples, in its broader aspects it is not limited thereto, for obvious modifications will occur to those skilled in the art.
What is claimed is:
1. A cast Ni base alloy containing Al and Cb contains a multiphase lamellar microstructure, a first phase consisting essentially of the Ni3Al intermetallic compound, a second phase consisting essentially of the NiaCb intermetallic compound, the first and second phases consisting of lamellae arranged in alternation in the cast article and in substantial alignment over a major portion of the length thereof.
2. A metallic article according to claim 1 wherein the lamellae are arranged in substantial alignment with each other and with the major tensile strength axis of the article.
3. A cast Ni base alloy containing Al and Cb characterized by an aligned lamellar microstructure over the major portion of the length thereof formed from an alloy which consists essentially of the pseudo-binary eutectic between the Ni3Al and NiaCb intermetallic compounds.
4. A metallic article according to claim 3 wherein the alloy consists essentially of about 33 weight percent Ni3Al, balance Ni3Cb.
5. A cast gas turbine engine blade or vane which comprises an alloy consisting essentially of about 33 weight percent NiaAl, balance Ni3Cb unidirectionally solidified parallel to the tensile axis of the blade or vane to produce a lamellar microstructure wherein the NiaAl and NiaCb components comprises respective lamellar phases which are arranged in alternation in the microstructure.
6. The method of forming gas turbine engine components which comprises:
melting an alloy which consists essentially of about 72 percent nickel, 23 percent columbium and 4 percent aluminum; and
unidirectionally solidifying the alloy utilizing a solidification rate about 2 cm./hr. to produce a lamellar microstructure.
7. The method according to claim 6 wherein:
the alloy is solidified in a direction substantially parallel to the designed tensile axis of the component.
8. The metthod according to claim 6 wherein:
about 300 C. superheat is provided in the alloy in the solidication process.
References Cited UNITED STATES PATENTS 3,124,452 3/1964 Kraft 75-135 3,434,827 3/1969 Lemkey 75-135X 3,434,892 3/1969 Heimke 14S-31.57
CHARLES N. LOVELL, Primary Examiner U.S. Cl. X.R.
75-l35, 175.5; 148-3; l64--l22
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3767479A (en) * 1972-02-14 1973-10-23 Gen Electric Multicomponent eutectics for high temperature applications
US3793008A (en) * 1972-03-01 1974-02-19 Gen Electric Monocarbide fiber-reinforced iron-base superalloy composite eutectic castings and method
US3793010A (en) * 1972-01-27 1974-02-19 United Aircraft Corp Directionally solidified eutectic type alloys with aligned delta phase
US4288259A (en) * 1978-12-04 1981-09-08 United Technologies Corporation Tantalum modified gamma prime-alpha eutectic alloy
US4543235A (en) * 1982-09-22 1985-09-24 United Technologies Corporation Eutectic superalloy compositions and articles
US4859416A (en) * 1986-03-17 1989-08-22 Stuart Adelman Superalloy compositions and articles
US20090136381A1 (en) * 2007-11-23 2009-05-28 Rolls-Royce Plc Ternary nickel eutectic alloy
US11525172B1 (en) 2021-12-01 2022-12-13 L.E. Jones Company Nickel-niobium intermetallic alloy useful for valve seat inserts

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0546150U (en) * 1991-11-12 1993-06-18 東京コスモス電機株式会社 Portable wireless phone

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3793010A (en) * 1972-01-27 1974-02-19 United Aircraft Corp Directionally solidified eutectic type alloys with aligned delta phase
US3767479A (en) * 1972-02-14 1973-10-23 Gen Electric Multicomponent eutectics for high temperature applications
US3793008A (en) * 1972-03-01 1974-02-19 Gen Electric Monocarbide fiber-reinforced iron-base superalloy composite eutectic castings and method
US4288259A (en) * 1978-12-04 1981-09-08 United Technologies Corporation Tantalum modified gamma prime-alpha eutectic alloy
US4543235A (en) * 1982-09-22 1985-09-24 United Technologies Corporation Eutectic superalloy compositions and articles
US4859416A (en) * 1986-03-17 1989-08-22 Stuart Adelman Superalloy compositions and articles
US20090136381A1 (en) * 2007-11-23 2009-05-28 Rolls-Royce Plc Ternary nickel eutectic alloy
US8858874B2 (en) 2007-11-23 2014-10-14 Rolls-Royce Plc Ternary nickel eutectic alloy
US11525172B1 (en) 2021-12-01 2022-12-13 L.E. Jones Company Nickel-niobium intermetallic alloy useful for valve seat inserts

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GB1271181A (en) 1972-04-19
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SE354876B (en) 1973-03-26
DE2013074A1 (en) 1970-10-08
DE2013074B2 (en) 1972-08-31

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