US3545944A - Composite metal article having an intermediate bonding layer of nickel aluminide - Google Patents
Composite metal article having an intermediate bonding layer of nickel aluminide Download PDFInfo
- Publication number
- US3545944A US3545944A US751629*A US3545944DA US3545944A US 3545944 A US3545944 A US 3545944A US 3545944D A US3545944D A US 3545944DA US 3545944 A US3545944 A US 3545944A
- Authority
- US
- United States
- Prior art keywords
- coating
- nickel
- abradable
- engine
- spraying
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/08—Metallic material containing only metal elements
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12458—All metal or with adjacent metals having composition, density, or hardness gradient
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12479—Porous [e.g., foamed, spongy, cracked, etc.]
Definitions
- This invention relates in general to the tip-sealing of rotating elements in gas turbine engines and more particularly to an improved abradable gas seal construction for such engines. It contemplates a process whereby a structurally reliable abradable coating is applied to engine stator assemblies by thermal spraying techniques.
- the efficiency of a gas turbine engine is dependent to some extent upon the control of gas leakage between stages in both the compressor and turbine sections of the engine.
- the engine is typically designed and manufactured to very precise dimensional tolerances, it is necessary to provide a sufiicient cold clearance between the tips of the rotating elements and the surrounding stator assembly to accommodate the differential thermal growth between the parts as the engine assumes is normal operating temperature.
- To this cold clearance must be added the usual manufacturing tolerances plus an additional safety factor to provide for limited engine operation at temperatures in excess of the design temperature.
- the requisite clearances thus provided are, however, generally not sufiicienitly close to permit the engine to operate at its maximum theoretical efficiency.
- an object of this invention to provide an abradable coating which is characterized by a high strength bond with the metal substrate and good structural integrity in the elevated temperature environment of a high performance jet engine. This objective is achieved by providing a coating in which the composition varies as a function of its depth.
- This technique contemplates varying the compositions of coating powders introduced to a spray gun as the coating is effected on the metal substrate, or varying the respective spray rates of a plurality of spray guns, to form an intermetall'ic at the substrate surface and an abradable composition at the outer surface of the coating, gradually phasing from one composition to another as the coating is produced.
- the abradable surface of the coating must be selected in accordance with the anticipated environment in which it is to be run.
- a suitable surface material must be readily penetrated by the rotating blade with a minimum of blade wear, and yet must Withstand, in jet engine applications, the erosive and corrosive effects of the hot engine gases.
- Abrasion of a material by a high speed rotating knifeedge occurs either as a result of the material being pushed aside or as a result of particles being broken away.
- Soft materials are abraded by the first method and friable materials by the second method. It should be noted, however, that friable materials generally have reduced strength properties and are therefore not suitable for abradable coatings unless supported by a matrix of stronger materials.
- the abradability of materials may be increased by decreasing the material density and increasing the porosity, although each of these factors reduces the strength of the coating and the resistance of the material to erosion. Further, the abradability may be increased by annealing.
- the hardness of nickel for example, is reduced from a Vickers hardness of over 200 to less than by annealing at 900 F.
- the abradability may be increased by introducing porosity into the coating, and this has been demonstrated to be the preferable method.
- the abradability index increases with the volume percent of pores, provided the pore size remains constant, but excessive porosity will reduce the mechanical and bond strengths below the desirable levels.
- Several methods have been utilized to introduce porosity to the material, one such method being the addition of a salt to the coating material as applied which may subsequently be leached from the formed coating.
- An alternate method of effecting porosity is to introduce a material into the coating as applied which may subsequently be removed by an oxidation process.
- a third method contemplates the addition of a constituent to the coating mixture, such as boron nitride, which will form a brittle compound at the interparticle boundaries.
- Flame spraying is a coating process in which powdered material is injected into a flame, melted, and subsequently carried in the molten state and deposited on a substrate by a gas jet.
- the flame is produced by the combustion of hydrogen or acetylene with oxygen or air.
- the carrier gas is usually air or one of the inert gases.
- the efficiency and quality of the coating processes depends on the flame temperature and heat production rate, the gas flow rates, the powder feed rate, and the distance between the substrate and the spray gun. Adjustment of the gas flow rates changes the combustion rate and the time that the powder particles remain in the combustion zone. Changing the substrate-to-gun distance changes the particle cooling time before impact and is probably the most important spraying parameter.
- Plasma spraying is similar to flame spraying except that the heat is derived from an electrical arc and no combustion products are produced. Considerably more energy is generated during plasma spraying than during flame spraying, however, and the temperature produced is 40,000 F. whereas the maximum temperature produced by flame spraying is about 3600 F. As a result, the coatings produced by the two processes have somewhat different properties. For example, salt added to metallic powders to produce porosity is vaporized during plasma spraying and consequently its usefulness as a porosity developer is lost.
- Flame spraying has been demonstrated to be somewhat more suitable than plasma spraying in the application of abradable coatings since less energy is added during the process, and the resulting coating is softer and less dense.
- the flame spraying process has been shown to be the most suitable method of applying abradable coatings, it has nevertheless been necessary to develop special spraying techniques and coating compositions before truly suitable coatings are obtained.
- Early experiments revealed that an adequate bond could not be formed between the abradable coatings, for example, porous nickel, and the metal substrate. Mechanical methods, such as knurling the substrate, have been attempted but were found to be impractical.
- the bond strength is weakened by thermal stresses which develop at the coating-substrate interface and, although the coefficients of thermal expansion may be similar, the stresses are developed during the formation of the bond while the coating material and the substrate are at different temperatures. Consequently, it was found necessary to interpose between the substrate and the abradable material an intermediate medium to improve the bonding to the substrate. It was further found necessary to effect a gradual phasing of one component into the other as a function of the coating thickness in order to eliminate shear planes therein which lead to laminar separation in the coating.
- nickel and chromium were selected as the most suitable abradable materials since they were known to have melting points in excess of 2000 F. and were further known to be compatible with the corrosive engine gases. Ceramics were not seriously considered since they are inherently brittle and not easily bonded to the non-rotating engine parts. Alloys are generally unsuitable because of their tendency to form low melting point eutectics or hard metallurgical phases which reduces the abradability. Mixtures of nickel and silver, however, have been determined to be suitable candidate materials since no alloy or solid solution is formed therebetween. The metals palladium, platinum, and rhodium are known to possess the requisite temperature and corrosion resistance characteristics but are not suitable for engine applications because of their cost.
- the intermediate medium selected to form the bridge between substrate and the abradable surface is nickel aluminide which will bond metallurgically to the substrate if properly applied.
- the nickel aluminide phase of the coating is formed on the substrate by means of a plasma spray utilizing nickel-coated aluminum powders, known commercially as METCO 404, as the feed material, the powder analyzing at approximately 80% nickel and aluminum. Since the nickel and aluminum mixture in this 4 form is both exothermic and synergistic, it will form a strong metallurgical bond with the metal substrate when applied from a plasma gun.
- This process is suitable for effecting a coating on a variety of metal substrates, the only requirement being the establishment of a metallurgical bond between the substrate and the intermediate medium.
- the nickel coated aluminum powders applied by plasma spray techniques are known to bond to nickel base alloys, steels, aluminum, titanium, tantalum and columbium.
- a porous nickel abradable surface has been applied to engine parts utilizing the above-mentioned technique by gradually phasing the coating from nickel aluminide to a nickel salt mixture and subsequently leaching out the salt after formation of the coating.
- the highest abradability was exhibited in tests on a coating with a porous surface containing 33% nickel but the excessive porosity resulted in a significant reduction in structural integrity.
- the optimum nickel concentration in the abradable surface has been established at between 50 and volume percent nickel.
- Nickel powder% by weight (68.6% by volume) Salt (sodium chloride)-10% by weight (31.4% by volume) Aluminum phosphate1 cc. per 8 grams salt The powders fed to the flame spraying apparatus were prepared in the indicated proportions and were thoroughly blended,
- the finer powders were shown to be more suitable for spraying. It is also advisable to abrade particles from a coating which are fine enough not to damage downstream engine parts. Accordingly, the powders utilized were in the range of 200-250 mesh.
- the nickel powder was previously reduced in a hydrogen-rich atmosphere to control the oxygen content since powders with an oxygen content of 3 percent or more do not spray effectively.
- Aluminum phosphate was added to the mixture to bind the salt crystals to the metallic powder. Without the binder, the salt separates from the metallic powder in the vibrating hoppers used in conjunction with the spraying equipment.
- Nickel aluminide powder
- Colmonoy spray gun Oxygen-27 c.f.h.
- Inconel engine parts to be coated were grit blasted to roughen the surface. Silicon carbide #24 grit was used for this purpose.
- the surface to be coated was rotated at approximately 47 inches per minute at a distance of approximately four inches from the plasma gun and preheated to 200 F. using the plasma torch with the powder feed turned off.
- the nickel aluminide was applied to the rotating part to a thickness of .003.005 inch and, while the plasma gun application of nickel aluminide was continued, the nickel-salt mixture was simultaneously phased in as a separate stream from the flame gun, the nickel aluminide feed rate being gradually decreased while the nickel-salt feed rate was increased.
- the transition from nickel aluminide to nickelsalt was effected within .015.020 inch of the Inconel substrate.
- the nickel-salt application was then continued until the desired abradable surface thickness was attained. Although this is a function of the design requirements, the abradable surface was generally .025 inch thick after machining.
- the salt inclusions in the coating were then leached out with agitated water at 180 F.
- the salt removal is preferably undertaken before any machining of the coating has been performed since metal flow during machining tends to entrap salt particles.
- any necessary machining was performed followed by annealing at 1300" F. to eliminate the surface work hardening produced in the machining operation.
- a composite comprising a metallized aircraft engine component fabricated from a high temperature nickelbase alloy having an abradable surface coating thereon, the composite comprising a base formed of a nickelbase alloy, an intermediate bonding zone of nickel aluminide metallurgically bonded to said base, and an outer layer of porous nickel of 2050 volume percent porosity, said outer layer being bonded to the nickel aluminide intermetallic layer by a bond zone that increases in porous nickel as it recedes from the intermediate layer.
Description
United States Patent Int. Cl. B32b 15/00 US. Cl. 29-197 1 Claim ABSTRACT OF THE DISCLOSURE In a jet engine assembly, an abradable sealing surface between the tips of rotating elements and the surrounding assembly, featuring the use of a bonding medium and a porous nickel abradable coating wherein a graded sealing surface is achieved.
This is a division of the Emanuelson et a1. application, Ser. No. 43 8,734, filed Mar. 10, 1965.
This invention relates in general to the tip-sealing of rotating elements in gas turbine engines and more particularly to an improved abradable gas seal construction for such engines. It contemplates a process whereby a structurally reliable abradable coating is applied to engine stator assemblies by thermal spraying techniques.
The efficiency of a gas turbine engine is dependent to some extent upon the control of gas leakage between stages in both the compressor and turbine sections of the engine. Although the engine is typically designed and manufactured to very precise dimensional tolerances, it is necessary to provide a sufiicient cold clearance between the tips of the rotating elements and the surrounding stator assembly to accommodate the differential thermal growth between the parts as the engine assumes is normal operating temperature. To this cold clearance must be added the usual manufacturing tolerances plus an additional safety factor to provide for limited engine operation at temperatures in excess of the design temperature. The requisite clearances thus provided are, however, generally not sufiicienitly close to permit the engine to operate at its maximum theoretical efficiency.
In an effort to remedy this condition, it has been proposed to utilize an abradable surface on the assembly surrounding the rotating elements and to permit the knifeedge of the rotor system to penetrate into the coating as a result of thermal expansion, thereby permitting the rotor to seat itself against the stator assembly with what is essentially a zero clearance. The result is considerably better sealing and consequently better efliciency than that provided by conventional air seals. A typical abradable seal construction of this type is shown in the patent to Koehring 2,930,521.
While in theory such an abradable surface may be seen to have great potential in improving engine performance, current techniques and abradable seal structures have not been entirely satisfactory in their practical application to high performance jet engines. In general, the problems that have arisen in the use of abradable coatings are attributable to the lack of structural strength in the coating itself and in its poor adherence to the metal substrate to which it is applied.
It is, therefore, an object of this invention to provide an abradable coating which is characterized by a high strength bond with the metal substrate and good structural integrity in the elevated temperature environment of a high performance jet engine. This objective is achieved by providing a coating in which the composition varies as a function of its depth.
It is a further object of this invention to provide a procedure for effecting such a coating utilizing thermal spraying techniques.
It is a still further object to provide a technique for varying the characteristics of the coating as a function of its depth .without introducing shear planes therein. This technique contemplates varying the compositions of coating powders introduced to a spray gun as the coating is effected on the metal substrate, or varying the respective spray rates of a plurality of spray guns, to form an intermetall'ic at the substrate surface and an abradable composition at the outer surface of the coating, gradually phasing from one composition to another as the coating is produced.
These and other objects and advantages of the present invention will be evident or will be discussed in connection the following description.
It is axiomatic that the abradable surface of the coating must be selected in accordance with the anticipated environment in which it is to be run. A suitable surface material must be readily penetrated by the rotating blade with a minimum of blade wear, and yet must Withstand, in jet engine applications, the erosive and corrosive effects of the hot engine gases.
Abrasion of a material by a high speed rotating knifeedge occurs either as a result of the material being pushed aside or as a result of particles being broken away. Soft materials are abraded by the first method and friable materials by the second method. It should be noted, however, that friable materials generally have reduced strength properties and are therefore not suitable for abradable coatings unless supported by a matrix of stronger materials.
The abradability of materials may be increased by decreasing the material density and increasing the porosity, although each of these factors reduces the strength of the coating and the resistance of the material to erosion. Further, the abradability may be increased by annealing. The hardness of nickel, for example, is reduced from a Vickers hardness of over 200 to less than by annealing at 900 F.
As has been indicated, the abradability may be increased by introducing porosity into the coating, and this has been demonstrated to be the preferable method. The abradability index increases with the volume percent of pores, provided the pore size remains constant, but excessive porosity will reduce the mechanical and bond strengths below the desirable levels. Several methods have been utilized to introduce porosity to the material, one such method being the addition of a salt to the coating material as applied which may subsequently be leached from the formed coating. An alternate method of effecting porosity is to introduce a material into the coating as applied which may subsequently be removed by an oxidation process. A third method contemplates the addition of a constituent to the coating mixture, such as boron nitride, which will form a brittle compound at the interparticle boundaries.
Although several methods of applying the coatings are available, the most satisfactory results have been obtained by means of thermal spraying. This process is inherently flexible since it permits the coating material to be selected and premixed in powder form before spraying, and because close control can be exercised over, the spraying process.
Flame spraying is a coating process in which powdered material is injected into a flame, melted, and subsequently carried in the molten state and deposited on a substrate by a gas jet. The flame is produced by the combustion of hydrogen or acetylene with oxygen or air. The carrier gas is usually air or one of the inert gases. The efficiency and quality of the coating processes depends on the flame temperature and heat production rate, the gas flow rates, the powder feed rate, and the distance between the substrate and the spray gun. Adjustment of the gas flow rates changes the combustion rate and the time that the powder particles remain in the combustion zone. Changing the substrate-to-gun distance changes the particle cooling time before impact and is probably the most important spraying parameter.
Plasma spraying is similar to flame spraying except that the heat is derived from an electrical arc and no combustion products are produced. Considerably more energy is generated during plasma spraying than during flame spraying, however, and the temperature produced is 40,000 F. whereas the maximum temperature produced by flame spraying is about 3600 F. As a result, the coatings produced by the two processes have somewhat different properties. For example, salt added to metallic powders to produce porosity is vaporized during plasma spraying and consequently its usefulness as a porosity developer is lost.
Flame spraying has been demonstrated to be somewhat more suitable than plasma spraying in the application of abradable coatings since less energy is added during the process, and the resulting coating is softer and less dense. Although the flame spraying process has been shown to be the most suitable method of applying abradable coatings, it has nevertheless been necessary to develop special spraying techniques and coating compositions before truly suitable coatings are obtained. Early experiments revealed that an adequate bond could not be formed between the abradable coatings, for example, porous nickel, and the metal substrate. Mechanical methods, such as knurling the substrate, have been attempted but were found to be impractical. In flame spraying the bond strength is weakened by thermal stresses which develop at the coating-substrate interface and, although the coefficients of thermal expansion may be similar, the stresses are developed during the formation of the bond while the coating material and the substrate are at different temperatures. Consequently, it was found necessary to interpose between the substrate and the abradable material an intermediate medium to improve the bonding to the substrate. It was further found necessary to effect a gradual phasing of one component into the other as a function of the coating thickness in order to eliminate shear planes therein which lead to laminar separation in the coating.
For turbine applications, nickel and chromium were selected as the most suitable abradable materials since they were known to have melting points in excess of 2000 F. and were further known to be compatible with the corrosive engine gases. Ceramics were not seriously considered since they are inherently brittle and not easily bonded to the non-rotating engine parts. Alloys are generally unsuitable because of their tendency to form low melting point eutectics or hard metallurgical phases which reduces the abradability. Mixtures of nickel and silver, however, have been determined to be suitable candidate materials since no alloy or solid solution is formed therebetween. The metals palladium, platinum, and rhodium are known to possess the requisite temperature and corrosion resistance characteristics but are not suitable for engine applications because of their cost.
The intermediate medium selected to form the bridge between substrate and the abradable surface is nickel aluminide which will bond metallurgically to the substrate if properly applied. The nickel aluminide phase of the coating is formed on the substrate by means of a plasma spray utilizing nickel-coated aluminum powders, known commercially as METCO 404, as the feed material, the powder analyzing at approximately 80% nickel and aluminum. Since the nickel and aluminum mixture in this 4 form is both exothermic and synergistic, it will form a strong metallurgical bond with the metal substrate when applied from a plasma gun.
While the deposited nickel aluminide forms an excellent base for a subsequent topcoat, it was found that laminar separation could occur at the nickel aluminideporous nickel interface during engine operation. Consequently a technique was developed whereby the coating was graded gradually from pure nickel aluminide at the substrate surface to pure nickel at the outer surface of the coating. This technique involves spraying each constituent separately, the nickel coated aluminum powder from a plasma gun and the nickel from a flame gun, but sequentially to produce the desired material gradient in the coating. Attempts to apply a graded coating with a single gun by changing the characteristics of the powders in the charge was unsatisfactory because the constituents required different spraying parameters. With different materials, however, particularly those having similar characteristics, there is no reason why a single gun could not be used for this purpose.
This process is suitable for effecting a coating on a variety of metal substrates, the only requirement being the establishment of a metallurgical bond between the substrate and the intermediate medium. For example, the nickel coated aluminum powders applied by plasma spray techniques are known to bond to nickel base alloys, steels, aluminum, titanium, tantalum and columbium.
A porous nickel abradable surface has been applied to engine parts utilizing the above-mentioned technique by gradually phasing the coating from nickel aluminide to a nickel salt mixture and subsequently leaching out the salt after formation of the coating.
The highest abradability was exhibited in tests on a coating with a porous surface containing 33% nickel but the excessive porosity resulted in a significant reduction in structural integrity. The optimum nickel concentration in the abradable surface has been established at between 50 and volume percent nickel.
EXAMPLE Nickel salt mixture:
Nickel powder% by weight (68.6% by volume) Salt (sodium chloride)-10% by weight (31.4% by volume) Aluminum phosphate1 cc. per 8 grams salt The powders fed to the flame spraying apparatus were prepared in the indicated proportions and were thoroughly blended,
Although abradability testing of coatings indicated that large grain sizes produced the more abradable coatings, the finer powders were shown to be more suitable for spraying. It is also advisable to abrade particles from a coating which are fine enough not to damage downstream engine parts. Accordingly, the powders utilized were in the range of 200-250 mesh.
The nickel powder was previously reduced in a hydrogen-rich atmosphere to control the oxygen content since powders with an oxygen content of 3 percent or more do not spray effectively.
Aluminum phosphate was added to the mixture to bind the salt crystals to the metallic powder. Without the binder, the salt separates from the metallic powder in the vibrating hoppers used in conjunction with the spraying equipment.
Nickel aluminide powder:
METCO 404 Spray equipment Giannini plasma spray gun SG1:
Current-550 amperes Arc gas flow (argon)SS c.f.h. Powder gas (argon)27 c.f.h.
Colmonoy spray gun: Oxygen-27 c.f.h.
Hydrogen58 c.f.h. Powder gas (nitrogen)-45 c.f.h.
Coating process After degreasing, Inconel engine parts to be coated were grit blasted to roughen the surface. Silicon carbide #24 grit was used for this purpose. The surface to be coated was rotated at approximately 47 inches per minute at a distance of approximately four inches from the plasma gun and preheated to 200 F. using the plasma torch with the powder feed turned off. The nickel aluminide was applied to the rotating part to a thickness of .003.005 inch and, while the plasma gun application of nickel aluminide was continued, the nickel-salt mixture was simultaneously phased in as a separate stream from the flame gun, the nickel aluminide feed rate being gradually decreased while the nickel-salt feed rate was increased. The transition from nickel aluminide to nickelsalt was effected within .015.020 inch of the Inconel substrate. The nickel-salt application was then continued until the desired abradable surface thickness was attained. Although this is a function of the design requirements, the abradable surface was generally .025 inch thick after machining.
The salt inclusions in the coating were then leached out with agitated water at 180 F. For engine applications it is essential that all of the exposed salt is removed from the finished coating since residual chlorine catalyzes a sulfidation reaction to which high temperature, high nickel content aircraft alloys are particularly vulnerable. For this reason, the salt removal is preferably undertaken before any machining of the coating has been performed since metal flow during machining tends to entrap salt particles.
After the salt has been removed, any necessary machining was performed followed by annealing at 1300" F. to eliminate the surface work hardening produced in the machining operation.
Over 150 engine parts were coated with abradable 6 materials and tested in experimental engines. An abradable porous nickel coating of 30 volume percent porosity bonded with nickel aluminide by the foregoing method was tested in the turbine section of an experimental engine and demonstrated a capability of over 200 hours of engine service. Analysis indicates that an improvement in turbine efliciency of at least 1 /2 percent is realized.
While a preferred process and abradable seal composition has been described, the present invention in its broader aspects is not limited thereto but departures may be made from such details within the scope of the accompanying claim.
We claim:
1. A composite comprising a metallized aircraft engine component fabricated from a high temperature nickelbase alloy having an abradable surface coating thereon, the composite comprising a base formed of a nickelbase alloy, an intermediate bonding zone of nickel aluminide metallurgically bonded to said base, and an outer layer of porous nickel of 2050 volume percent porosity, said outer layer being bonded to the nickel aluminide intermetallic layer by a bond zone that increases in porous nickel as it recedes from the intermediate layer.
References Cited UNITED STATES PATENTS 2,763,920 9/1956 Turner 29-198 3,041,040 6/1962 Levinstein 29--l98 3,129,069 4/1964 Hanink 29----l94 3,141,744 7/1964 Couch 29--197 3,337,427 8/1967 Whitfield 29--198 2,996,795 8/1961 Stout 29--191.2 3,322,515 5/1967 Dittrich 29-192 HYLAND BIZOT, Primary Examiner US. Cl. X.R. 29194
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US438734A US3413136A (en) | 1965-03-10 | 1965-03-10 | Abradable coating |
US75162968A | 1968-05-10 | 1968-05-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3545944A true US3545944A (en) | 1970-12-08 |
Family
ID=27031775
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US751629*A Expired - Lifetime US3545944A (en) | 1965-03-10 | 1968-05-10 | Composite metal article having an intermediate bonding layer of nickel aluminide |
Country Status (1)
Country | Link |
---|---|
US (1) | US3545944A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3879831A (en) * | 1971-11-15 | 1975-04-29 | United Aircraft Corp | Nickle base high temperature abradable material |
US4207024A (en) * | 1977-05-27 | 1980-06-10 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Composite seal for turbomachinery |
US4377371A (en) * | 1981-03-11 | 1983-03-22 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Laser surface fusion of plasma sprayed ceramic turbine seals |
US4405284A (en) * | 1980-05-16 | 1983-09-20 | Mtu Motoren-Und-Turbinen-Union Munchen Gmbh | Casing for a thermal turbomachine having a heat-insulating liner |
EP0170763A1 (en) * | 1984-06-09 | 1986-02-12 | Goetze Ag | Wear-resistant coating |
US4669955A (en) * | 1980-08-08 | 1987-06-02 | Rolls-Royce Plc | Axial flow turbines |
US5326647A (en) * | 1991-09-18 | 1994-07-05 | Mtu Motoren- Und Turbinen-Union | Abradable layer for a turbo-engine and a manufacturing process |
US5975845A (en) * | 1995-10-07 | 1999-11-02 | Holset Engineering Company, Ltd. | Turbomachinery abradable seal |
EP1420144A3 (en) * | 2002-11-15 | 2009-02-18 | Rolls-Royce Plc | Method of protecting a vibration damping coating from foreign object damage |
EP2711441A1 (en) * | 2012-09-21 | 2014-03-26 | Reinhausen Plasma GmbH | Device and method for creating a coating system |
US8876470B2 (en) | 2011-06-29 | 2014-11-04 | United Technologies Corporation | Spall resistant abradable turbine air seal |
FR3097562A1 (en) * | 2019-06-21 | 2020-12-25 | Safran Aircraft Engines | Method of manufacturing an abradable part of a turbomachine and an abradable part |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763920A (en) * | 1951-03-06 | 1956-09-25 | Thompson Prod Inc | Corrosion and impact-resistant article |
US2996795A (en) * | 1955-06-28 | 1961-08-22 | Gen Electric | Thermionic cathodes and methods of making |
US3041040A (en) * | 1955-12-23 | 1962-06-26 | Gen Electric | Metal clad blade |
US3129069A (en) * | 1956-10-11 | 1964-04-14 | Gen Motors Corp | Oxidation-resistant turbine blades |
US3141744A (en) * | 1961-06-19 | 1964-07-21 | Dwight E Couch | Wear-resistant nickel-aluminum coatings |
US3322515A (en) * | 1965-03-25 | 1967-05-30 | Metco Inc | Flame spraying exothermically reacting intermetallic compound forming composites |
US3337427A (en) * | 1966-06-27 | 1967-08-22 | Whitfield Lab Inc | Heat and chemical resistant metal alloy parts |
-
1968
- 1968-05-10 US US751629*A patent/US3545944A/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763920A (en) * | 1951-03-06 | 1956-09-25 | Thompson Prod Inc | Corrosion and impact-resistant article |
US2996795A (en) * | 1955-06-28 | 1961-08-22 | Gen Electric | Thermionic cathodes and methods of making |
US3041040A (en) * | 1955-12-23 | 1962-06-26 | Gen Electric | Metal clad blade |
US3129069A (en) * | 1956-10-11 | 1964-04-14 | Gen Motors Corp | Oxidation-resistant turbine blades |
US3141744A (en) * | 1961-06-19 | 1964-07-21 | Dwight E Couch | Wear-resistant nickel-aluminum coatings |
US3322515A (en) * | 1965-03-25 | 1967-05-30 | Metco Inc | Flame spraying exothermically reacting intermetallic compound forming composites |
US3337427A (en) * | 1966-06-27 | 1967-08-22 | Whitfield Lab Inc | Heat and chemical resistant metal alloy parts |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3879831A (en) * | 1971-11-15 | 1975-04-29 | United Aircraft Corp | Nickle base high temperature abradable material |
US4207024A (en) * | 1977-05-27 | 1980-06-10 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Composite seal for turbomachinery |
US4405284A (en) * | 1980-05-16 | 1983-09-20 | Mtu Motoren-Und-Turbinen-Union Munchen Gmbh | Casing for a thermal turbomachine having a heat-insulating liner |
US4669955A (en) * | 1980-08-08 | 1987-06-02 | Rolls-Royce Plc | Axial flow turbines |
US4377371A (en) * | 1981-03-11 | 1983-03-22 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Laser surface fusion of plasma sprayed ceramic turbine seals |
EP0170763A1 (en) * | 1984-06-09 | 1986-02-12 | Goetze Ag | Wear-resistant coating |
US5326647A (en) * | 1991-09-18 | 1994-07-05 | Mtu Motoren- Und Turbinen-Union | Abradable layer for a turbo-engine and a manufacturing process |
US5975845A (en) * | 1995-10-07 | 1999-11-02 | Holset Engineering Company, Ltd. | Turbomachinery abradable seal |
EP1420144A3 (en) * | 2002-11-15 | 2009-02-18 | Rolls-Royce Plc | Method of protecting a vibration damping coating from foreign object damage |
US8876470B2 (en) | 2011-06-29 | 2014-11-04 | United Technologies Corporation | Spall resistant abradable turbine air seal |
EP2711441A1 (en) * | 2012-09-21 | 2014-03-26 | Reinhausen Plasma GmbH | Device and method for creating a coating system |
FR3097562A1 (en) * | 2019-06-21 | 2020-12-25 | Safran Aircraft Engines | Method of manufacturing an abradable part of a turbomachine and an abradable part |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5976695A (en) | Thermally sprayable powder materials having an alloyed metal phase and a solid lubricant ceramic phase and abradable seal assemblies manufactured therefrom | |
EP0725842B1 (en) | Plasma sprayed abradable seals for gas turbine engines | |
US4145481A (en) | Process for producing elevated temperature corrosion resistant metal articles | |
US3961098A (en) | Coated article and method and material of coating | |
US4198442A (en) | Method for producing elevated temperature corrosion resistant articles | |
US8266801B2 (en) | Method for producing abrasive tips for gas turbine blades | |
US7179507B2 (en) | Thermal spray compositions for abradable seals | |
USRE31339E (en) | Process for producing elevated temperature corrosion resistant metal articles | |
EP1583850B1 (en) | Thermal spray composition and method of deposition for abradable seals | |
CA1044643A (en) | Ductile corrosion resistant coating on a superalloy substrate | |
US3846159A (en) | Eutectic alloy coating | |
JPS6136061B2 (en) | ||
US3545944A (en) | Composite metal article having an intermediate bonding layer of nickel aluminide | |
US3896244A (en) | Method of producing plasma sprayed titanium carbide tool steel coatings | |
JP2001192862A (en) | A coating system for providing environmental protection to a metal substrate and its related method | |
US3957454A (en) | Coated article | |
JP2001152310A (en) | Method of improving oxidation resistance of metallic base material coated with thermal barrier coating | |
US7198858B2 (en) | Method of vibration damping in metallic articles | |
JP2001020052A (en) | Transition metal boride coating | |
US3779720A (en) | Plasma sprayed titanium carbide tool steel coating | |
US3413136A (en) | Abradable coating | |
US3143383A (en) | Means for preventing fretting erosion | |
JPH06212455A (en) | High loading coating structural member consisting of titanium-aluminide inter- metallic phase | |
JPS601396B2 (en) | Sealing member for gap control | |
US3573963A (en) | Method of coating nickel base alloys with a mixture of tungsten and aluminum powders |