US3084064A - Abradable metal coatings and process therefor - Google Patents
Abradable metal coatings and process therefor Download PDFInfo
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- US3084064A US3084064A US83192759A US3084064A US 3084064 A US3084064 A US 3084064A US 83192759 A US83192759 A US 83192759A US 3084064 A US3084064 A US 3084064A
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- abradable
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01D—NON-POSITIVE DISPLACEMENT MACHINES OR ENGINES, e.g. STEAM TURBINES
- F01D11/00—Preventing or minimising internal leakage of working-fluid, e.g. between stages
- F01D11/08—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator
- F01D11/12—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part
- F01D11/122—Preventing or minimising internal leakage of working-fluid, e.g. between stages for sealing space between rotor blade tips and stator using a rubstrip, e.g. erodible. deformable or resiliently-biased part with erodable or abradable material
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
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- 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
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- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S277/00—Seal for a joint or juncture
- Y10S277/935—Seal made of a particular material
- Y10S277/939—Containing metal
- Y10S277/94—Alloy
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Definitions
- This invention relates to a nongalling coating material and more specifically concerns an abradable metal coating and a process for producing same.
- Another object of the invention is to provide a coating that can flake off in relatively uniform particles when subjected to sufficiently high forces along its surface without galling or tearing.
- the present invention is a novel abradable metal coating that flakes off in powder form when subjected to stifliciently high forces along its surface. It not only imparts the desired abradable coating properties to a suitable base material, but possesses other beneficial properties such as oxidation resistance and suitable melting point.
- the novel coating of the invention comprises a maior component constituting the metal phase of the coating and consisting of one or more metals, and a minor component consisting of a high melting finelydivlded powder substantially uniformly distributed in the metal phase of the major component.
- the major component may be composed of one or more metals or alloys having desirable coating properties with respect to melting point, corrosion resistance, and oxidation resistance. For example, if a relatively low melting point abradable coating is desired, aluminum is preferred. For higher melting point coatings. metal such as nickel, stainless steel, Nichrome, Monel or other suitable alloys are preferred as the major component.
- the high melting dispersed powder examples include boron nitride, carbon, graphite, and magnesium oxide.
- the powder should be of a material which is not melted by the process used to apply the coating.
- the ratio of metal phase content to high melting point powder content of the coating product will depend upon the desired end use of the abradable coating.
- a metal phase having incorporated therein between approximately 2% and 20% by weight of finely divided high melting point powder is preferred, although higher and lower amounts of powder may be employed, depending upon the particular powder and base metal.
- a low percentage by weight of powder is dispersed in the metal phase of a relatively soft coating material, and higher weight percent powder contents are employed in coatings of relatively harder material.
- the higher melting additive content is about 2 to 5 weight percent.
- the additive content may be as much as 15 to 20%.
- An important feature of the invention involves the process of applying the abradable coating to the surface of a baseplate.
- an undercoat of metal is first applied to the baseplate.
- This metal undercoat preferably comprises one or more layers, each about 0.003-0005 inch thick. it is conveniently of the same metal as the metal phase of the final abradable coating, but it could be of any metal which is compatible with the adjacent metals in the baseplate and abradable coating.
- the baseplate is preferably heated to about 400600 F. in order to obtain the most satisfactory bond strength between coating and baseplate.
- the coating material can be applied by various processes employing a high temperature, high velocity means of application.
- Such methods are disclosed, for example, in US. Patents Nos. 2,714,563, 2,861,900 and 2,847,555 and US. applications, Serial No. 706,099, filed December 30, 1957, now abandoned, Serial No. 706,135, filed December 30, 1957, now abandoned, Serial No. 850,444, filed November 2, 1959, now US. Patent No. 3,016,447, and Serial No. 521,041, filed July 11, 1955, now Pat. No. 2,920,001.
- the preferred process of applying the novel coating comprises feeding the metal phase material in wire or rod form into the efiluent from a high temperature, high velocity burner in the manner described in copending application Serial No. 521,041.
- This eflluent traveling at velocities greater than 2000 ft./sec. melts the wire to form finely divided molten metal particles and then rapidly impinges them on the baseplate, or part being plated, with such force that a firm bond results.
- the high melting point dispersed material is simultaneously introduced, preferably in powder form, into the combustion chamber of the burner, is discharged into the burner effluent and mixes with the molten metal phase particles prior to impingement on the baseplate.
- the high velocity burner efiluent and molten metal particles could be directed through a gaseous suspension of high melting point powder particles prior to impingement on the baseplate.
- Still another method involves incorporating the powder into the metal wire prior to introduction into the coating apparatus.
- a spot test used to determine degree of abradability is to take a blunt tool and scratch the surface of the coating. Powdery material consisting of small flakes will be removed from an abradable coating while the surface of a non-abradable coating will simply be scratched with no metal removal or will gall and tear.
- EXAMPLE I Aluminum-Boron Nitride Abradabie Coating
- the plating apparatus comprised a throat combustion burner having an unconstricted combustion chamber /4- in. ID. and 4-in. long.
- Acetylene at 160 c.f.h. and oxygen at 230 c.f.h. were fed to the burner, combusted and discharged as a high temperature effluent having velocity greater than 2000 ft./sec.
- Aluminum wire having -in. dia. was fed at 13.5 grams/min. into the efiluent from the burner where it melted and formed finely-divided metal particles which were in turn impinged on a baseplate.
- This baseplate consisted of a steel ring 4-in. dia. and %-in.
- the boron nitride flow is reduced to less than 1.0 gram/ min. while maintaining the other coating conditions constant, the resulting coating loses its abradability. If the boron nitride flow is increased above 4.0 grarns/min., the resulting coating is too weak and unreliable.
- EXAMPLE II Aluminum-Graphite Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of aluminum 0003-0005 in. thick was applied to a heated baseplate. The abradable coating was applied using feed rates of 13.5 grams/ min. for the in. diameter aluminum wire and 17 grams/min. for graphite powder. The resulting 0.070-in. thick coating was easily abraded.
- Example III Nickel-Chromium-Boron Nitride Abradable Coating
- An undercoat of nickel 0.0030.00-5 in. thick was applied to the heated baseplate followed by a second coat of Nichrome V Ni20% Cr) of same thickness.
- the final abradable coating was applied using feed rates of 25 grams/min. for the 0.063-in. dia. Nichrome V wire and 6.0 grams/ min. for the boron nitride powder.
- the resulting 0.060- in. thick coating had desirable abradable characteristics up to about 1400" F.
- EXAMPLE IV Nic'ke[Chromium-Graphite Abradable Coating
- An undercoat of nickel 0003-0005 in. thick was applied to a heated baseplate.
- the abradable coating was applied using feed rates of 25 grams/min. for the 0.063-in. dia. Nichrome V wire and 14.0 grams/min. for the graphite powder.
- the resulting 0.050-1'n. thick coating was easily abraded.
- Example V Nickel-Chromiron-Magnesium Oxide Abradable Coating
- An undercoat of nickel 0.0030.005-in. thick was applied to a heated baseplate followed by the abradable coating. Feed rates of 25 grams/min. for the .063-in. dia. Nichrome V wire and 10.0 grams/min. for the magnesium oxide powder were employed. The resulting .O30-in. thick coating had desirable abradable characteristics.
- EXAM PLE VI N ickel-C opper-I ron-G rap] ite A bradable C ating
- An undercoat of nickel 0.0030.005 in. thick was first applied to a heated baseplate.
- the abradable coating was applied using feed rates of 27 grams/min. for the .063-in. dia. Monel metal (60% nickel-33% copper-6.5% iron) wire and 8.0 grams/min. for the graphite powder. This .030-in. thick final coating was easily abraded.
- Example I Nickel-Carbon Abradable Coating
- An undercoat of nickel 0.003-0.005-in. thick was first applied to a heated baseplate.
- An abradable coating was then applied to the undercoat by feeding 0.063-in. dia. nickel wire at 17 grams/min. into the high velocity burner efiiuent and passing the molten metal particles through a gaseous suspension of carbon particles prior to impinging on the baseplate.
- An article comprising a structure having thereon a coating which produces a powder-like scraping when scratched with suflicient force along its surface consisting essentially of metallically bonded metal particles defining a fused metal phase having substantially uniformly incorporated therein in a non-fused relationship, particles of a high melting powder in minor amounts between 2 and by weight, there being lesser amounts of high melting powder in said metal phase when said metal phase consists of relatively low melting metal than when said metal phase consists of relatively high melting metal.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of aluminum and said high melting point powder consisting of boron nitride.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of aluminum and said high melting point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of boron nitride.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of iron, chromium and nickel and said high melting point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel, copper and iron and said high meling point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel, chromium and aluminum and said high melting point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of nickel and said high melting point powder consisting of graphite.
- An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of magnesium oxide.
- a coated body comprising a base member and a metallic coating having good antigalling properties, bonded thereto, said coating consisting of a fused metal phase consisting of interbonded particles of a fused metal having incorporated therein dispersed non-fused refractory particles in quantities of from 2 to 20% by weight, said coating being abradable upon the application of a firm force across the surface thereof.
- a method of producing an abradable metal coating coating on a base material comprising applying to said base material an undercoating of a metal bondably compatible with the coating desired, impinging a high velocity high temperature stream of molten metal phase coating material against said undercoating to form a firm bond therewith, and simultaneously introducing about 2 to 20% by weight of a high melting point powder into said stream of metal phase coating material prior to impingement on the undercoat.
- a method of producing an abradable metal coating on a base material comprising: forming a high velocity stream consisting of molten particles of a metal to be deposited, impinging said stream against the surface of the base material to be coated, forming a second high velocity stream consisting of molten particles of said metal and unmelted particles of a high melting point powder, impinging said stream at high velocity against the base material to fuse the molten metal particles into a metallically bonded mass having interspersed therethrough in an amount between 2 and 20 percent by weight and in non-fused relationship, said particles of high melting point powder, and maintaining said base material and coating at a temperature between 400 F. and 600 F. during said coating method.
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Description
United tates 3,084,064 ABRADABLE METAL COATENGS AND PROtZESS THEREFOR Lewis M. Cowden, Indianapolis, and Joseph R. Clark,
Brownsburg, Ind, assignors to Union Carbide Corporation, a corporation of New York No Drawing. Filed Aug. 6, 1959, Ser. No. 831,927 13 Claims. (Ci. ill-71) This invention relates to a nongalling coating material and more specifically concerns an abradable metal coating and a process for producing same.
Designers of turbines, for example, are confronted by the formidable problem of reducing the clearance space between the turbine blade and the turbine housing. This represents a substantial physical barrier to increasing the turbine speed. If the clearance is reduced, the amount of gas that escapes, which represents available energy that has not been fully utilized, becomes less, leading to an increase in efliciency.
In view of the growing number of turbines for jet engines, the emphasis on closer tolerances is increasing. The development of new materials that can be applied as coatings to housings and that are adapted to closely conform to the path of the blade tip with a minimum of clearance will enable engineers to wring greater speeds from smaller turbines.
We have attempted to minimize the clearance between the blade and the housing of a turbine by coating the inside diameter of the housing with various coating materials of sufiicient thickness to establish contact with the blade, and then allowing the blade to rotate and cut a path through the coating. Up to now, this procedure has been unsatisfactory due to galling and tearing of the coating under the forces generated by the rotating blades.
It is, therefore, an important object of the present invention to provide a novel coating material capable of being applied as a coating to a suitable base material and adapted to suitably abrade when subjected to sutficiently high forces along its surfaces.
Another object of the invention is to provide a coating that can flake off in relatively uniform particles when subjected to sufficiently high forces along its surface without galling or tearing.
Other objects, features and advantages of the present invention will be apparent from the following detailed description of a preferred embodiment thereof.
The present invention is a novel abradable metal coating that flakes off in powder form when subjected to stifliciently high forces along its surface. It not only imparts the desired abradable coating properties to a suitable base material, but possesses other beneficial properties such as oxidation resistance and suitable melting point.
The novel coating of the invention comprises a maior component constituting the metal phase of the coating and consisting of one or more metals, and a minor component consisting of a high melting finelydivlded powder substantially uniformly distributed in the metal phase of the major component.
The major component may be composed of one or more metals or alloys having desirable coating properties with respect to melting point, corrosion resistance, and oxidation resistance. For example, if a relatively low melting point abradable coating is desired, aluminum is preferred. For higher melting point coatings. metal such as nickel, stainless steel, Nichrome, Monel or other suitable alloys are preferred as the major component.
Among the materials that have been found to be eminently suitable as the high melting dispersed powder are boron nitride, carbon, graphite, and magnesium oxide. Preferably, the powder should be of a material which is not melted by the process used to apply the coating.
" atent O 3,084,064 Patented Apr. 2, 1963 ice The ratio of metal phase content to high melting point powder content of the coating product will depend upon the desired end use of the abradable coating. A metal phase having incorporated therein between approximately 2% and 20% by weight of finely divided high melting point powder is preferred, although higher and lower amounts of powder may be employed, depending upon the particular powder and base metal. Generally, a low percentage by weight of powder is dispersed in the metal phase of a relatively soft coating material, and higher weight percent powder contents are employed in coatings of relatively harder material. For example, when a relatively soft coating material such as aluminum is used, the higher melting additive content is about 2 to 5 weight percent. On the other hand, if a coating of Nichrome is desired, the additive content may be as much as 15 to 20%.
An important feature of the invention involves the process of applying the abradable coating to the surface of a baseplate. In order to obtain good bond strength between the abradable coating and the baseplate, an undercoat of metal is first applied to the baseplate. This metal undercoat preferably comprises one or more layers, each about 0.003-0005 inch thick. it is conveniently of the same metal as the metal phase of the final abradable coating, but it could be of any metal which is compatible with the adjacent metals in the baseplate and abradable coating. During the entire coating operation of applying both the undercoat and final abradable layer the baseplate is preferably heated to about 400600 F. in order to obtain the most satisfactory bond strength between coating and baseplate.
The coating material can be applied by various processes employing a high temperature, high velocity means of application. Such methods are disclosed, for example, in US. Patents Nos. 2,714,563, 2,861,900 and 2,847,555 and US. applications, Serial No. 706,099, filed December 30, 1957, now abandoned, Serial No. 706,135, filed December 30, 1957, now abandoned, Serial No. 850,444, filed November 2, 1959, now US. Patent No. 3,016,447, and Serial No. 521,041, filed July 11, 1955, now Pat. No. 2,920,001.
The preferred process of applying the novel coating comprises feeding the metal phase material in wire or rod form into the efiluent from a high temperature, high velocity burner in the manner described in copending application Serial No. 521,041. This eflluent traveling at velocities greater than 2000 ft./sec. melts the wire to form finely divided molten metal particles and then rapidly impinges them on the baseplate, or part being plated, with such force that a firm bond results. The high melting point dispersed material is simultaneously introduced, preferably in powder form, into the combustion chamber of the burner, is discharged into the burner effluent and mixes with the molten metal phase particles prior to impingement on the baseplate. As an alternative, the high velocity burner efiluent and molten metal particles could be directed through a gaseous suspension of high melting point powder particles prior to impingement on the baseplate. Still another method involves incorporating the powder into the metal wire prior to introduction into the coating apparatus.
While we do not wish to be limited by the following theory, it is believed that the abradable characteristics of our novel coating are caused by the dispersed material preventing the formation of a solid, dense, strongly cohesive metal phase. For this reason, it is desired that the dispersed material not be molten during formation of the coating. Otherwise, a fused or inter-metallic bond between the metal phase and the dispersed material could be strengthened and form a coating which would gall or tear instead of uniformly flaking. Under our preferred coating conditions, some of the high melting point material applied to the coating area may not be deposited since it may not be molten.
A spot test used to determine degree of abradability is to take a blunt tool and scratch the surface of the coating. Powdery material consisting of small flakes will be removed from an abradable coating while the surface of a non-abradable coating will simply be scratched with no metal removal or will gall and tear.
In order to indicate still more fully the nature of the present invention, the following examples of typical procedures are set forth, it being understood that these examples are presented as illustrative only and that they are not intended to limit the scope of the invention.
EXAMPLE I Aluminum-Boron Nitride Abradabie Coating The plating apparatus comprised a throat combustion burner having an unconstricted combustion chamber /4- in. ID. and 4-in. long. Acetylene at 160 c.f.h. and oxygen at 230 c.f.h. were fed to the burner, combusted and discharged as a high temperature effluent having velocity greater than 2000 ft./sec. Aluminum wire having -in. dia. was fed at 13.5 grams/min. into the efiluent from the burner where it melted and formed finely-divided metal particles which were in turn impinged on a baseplate. This baseplate consisted of a steel ring 4-in. dia. and %-in. wide which was heated to 400-600 F. This coating operation was continued until a layer of aluminum 0003-0005 in. thick was deposited on the inner surface of the ring. The aluminum wire feed was then continued and finely-divided boron nitride powder at 2 grams/min. was introduced by means of a 40 c.f.h. nitrogen carrier gas stream into the combustion burner throat. The resulting mixture of aluminum and boron nitride particles were then impinged on the aluminum undercoat to form a coating about 0.080 in. thick. This outer coating was analyzed to contain 97 weight percent aluminum. The coated ring was mounted in a lathe and rotated at 800 rpm. while a blunt-edged tool was forced onto the coated surface. The coating abraded satisfactorily and formed small particles which readily flaked off. A similar coating was successfully applied to the compressor housing of a jet engine.
If the boron nitride flow is reduced to less than 1.0 gram/ min. while maintaining the other coating conditions constant, the resulting coating loses its abradability. If the boron nitride flow is increased above 4.0 grarns/min., the resulting coating is too weak and unreliable.
EXAMPLE II Aluminum-Graphite Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of aluminum 0003-0005 in. thick was applied to a heated baseplate. The abradable coating was applied using feed rates of 13.5 grams/ min. for the in. diameter aluminum wire and 17 grams/min. for graphite powder. The resulting 0.070-in. thick coating was easily abraded.
The above described aluminum-boron nitride and aluminum-graphite coatings are satisfactory for use at relatively low temperatures.
The following examples describe formation of abradable coatings which retain their useful properties at tem peratures as high as 1400 F. These coatings find utility in the turbine sections of commercial jet engines which operate at higher temperatures than the compressor section.
EXAMPLE III Nickel-Chromium-Boron Nitride Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0.0030.00-5 in. thick was applied to the heated baseplate followed by a second coat of Nichrome V Ni20% Cr) of same thickness. The final abradable coating was applied using feed rates of 25 grams/min. for the 0.063-in. dia. Nichrome V wire and 6.0 grams/ min. for the boron nitride powder. The resulting 0.060- in. thick coating had desirable abradable characteristics up to about 1400" F.
EXAMPLE IV Nic'ke[Chromium-Graphite Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0003-0005 in. thick was applied to a heated baseplate. The abradable coating was applied using feed rates of 25 grams/min. for the 0.063-in. dia. Nichrome V wire and 14.0 grams/min. for the graphite powder. The resulting 0.050-1'n. thick coating was easily abraded.
EXAMPLE V Nickel-Chromiron-Magnesium Oxide Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0.0030.005-in. thick was applied to a heated baseplate followed by the abradable coating. Feed rates of 25 grams/min. for the .063-in. dia. Nichrome V wire and 10.0 grams/min. for the magnesium oxide powder were employed. The resulting .O30-in. thick coating had desirable abradable characteristics.
EXAM PLE VI N ickel-C opper-I ron-G rap]: ite A bradable C ating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0.0030.005 in. thick was first applied to a heated baseplate. The abradable coating was applied using feed rates of 27 grams/min. for the .063-in. dia. Monel metal (60% nickel-33% copper-6.5% iron) wire and 8.0 grams/min. for the graphite powder. This .030-in. thick final coating was easily abraded.
EXAMPLE VII Nickel-Chromium-Aluminum-Graphite Coating EXAMPLE VIII Iron-Chromium-Nickel-Graphite Abradabie Cvating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0.003-0.005 in. thick was first applied to a heated baseplate. The final coating was applied using feed rates of 24 grams/min. of .063-in. dia. Type 302 Stainless Steel (iron-carbon alloy containing 17-19% Cr and 8.10% Ni) wire and 12 gram/min. graphite powder. The resulting 0.020-in. thick coating was easily abraded.
EXAMPLE IX Nickel-Carbon Abradable Coating The same apparatus and burner operating conditions were used as described in Example I. An undercoat of nickel 0.003-0.005-in. thick was first applied to a heated baseplate. An abradable coating was then applied to the undercoat by feeding 0.063-in. dia. nickel wire at 17 grams/min. into the high velocity burner efiiuent and passing the molten metal particles through a gaseous suspension of carbon particles prior to impinging on the baseplate.
It will be understood that modifications and variations may be efiected without departing from the spirit and scope of the invention.
What is claimed is:
1. An article comprising a structure having thereon a coating which produces a powder-like scraping when scratched with suflicient force along its surface consisting essentially of metallically bonded metal particles defining a fused metal phase having substantially uniformly incorporated therein in a non-fused relationship, particles of a high melting powder in minor amounts between 2 and by weight, there being lesser amounts of high melting powder in said metal phase when said metal phase consists of relatively low melting metal than when said metal phase consists of relatively high melting metal.
2. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of aluminum and said high melting point powder consisting of boron nitride.
3. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of aluminum and said high melting point powder consisting of graphite.
4. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of boron nitride.
5. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of graphite.
6. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of iron, chromium and nickel and said high melting point powder consisting of graphite.
7. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel, copper and iron and said high meling point powder consisting of graphite.
8. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel, chromium and aluminum and said high melting point powder consisting of graphite.
9. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of nickel and said high melting point powder consisting of graphite.
10. An article comprising a structure having thereon a coating according to claim 1, said metal phase consisting of an alloy of nickel and chromium and said high melting point powder consisting of magnesium oxide.
11. A coated body comprising a base member and a metallic coating having good antigalling properties, bonded thereto, said coating consisting of a fused metal phase consisting of interbonded particles of a fused metal having incorporated therein dispersed non-fused refractory particles in quantities of from 2 to 20% by weight, said coating being abradable upon the application of a firm force across the surface thereof.
12. A method of producing an abradable metal coating coating on a base material comprising applying to said base material an undercoating of a metal bondably compatible with the coating desired, impinging a high velocity high temperature stream of molten metal phase coating material against said undercoating to form a firm bond therewith, and simultaneously introducing about 2 to 20% by weight of a high melting point powder into said stream of metal phase coating material prior to impingement on the undercoat.
13. A method of producing an abradable metal coating on a base material comprising: forming a high velocity stream consisting of molten particles of a metal to be deposited, impinging said stream against the surface of the base material to be coated, forming a second high velocity stream consisting of molten particles of said metal and unmelted particles of a high melting point powder, impinging said stream at high velocity against the base material to fuse the molten metal particles into a metallically bonded mass having interspersed therethrough in an amount between 2 and 20 percent by weight and in non-fused relationship, said particles of high melting point powder, and maintaining said base material and coating at a temperature between 400 F. and 600 F. during said coating method.
References Cited in the file of this patent UNITED STATES PATENTS 2,178,529 Calkins et al. Oct. 31, 1939 2,261,228 Cockrum Nov. 4, 1941 2,694,647 Cole Nov. 16, 1954 2,714,563 Poorman et al Aug. 2, 1955 2,775,531 Montgomery et al. Dec. 25, 1956 2,861,900 Smith et al Nov. 25, 1958 2,903,375 Peras Sept. 8, 1959 2,964,420 Poor-man et a1. Dec. 13, 1960 3,016,311 Stackhouse Jan. 9, 1962
Claims (1)
12. A METHOD OF PRODUCING AN ABRADABLE METAL COATING COATING ON A BASE MATERIAL COMPRISING APPLYING TO SAID BASE MATERIAL AN UNDERCOATING OF A METAL BONDABLY COMPATIBLE WITH THE COATING DESIRED, IMPINGING A HIGH VELOCITY HIGH TEMPERATURE STREAM OF MOLTEN METAL PHASE COATING MATERIAL AGAINST SAID UNDERCOATING TO FORM A FIRM BOND THEREWITH, AND SIMULTANEOUSLY INTRODUCING ABOUT 2 TO 20% BY WEIGHT OF A HIGH MELTING POINT POWDER INTO SAID STREAM OF METAL PHASE COATING MATERIAL PRIOR TO IMPINGEMENT ON THE UNDERCOAT.
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Cited By (24)
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US3413136A (en) * | 1965-03-10 | 1968-11-26 | United Aircraft Corp | Abradable coating |
DE2031616A1 (en) * | 1969-07-01 | 1971-01-21 | Metco Ine Westbury (Long Island) NY (VStA) | Flame spray powder |
US4072797A (en) * | 1974-08-28 | 1978-02-07 | Laboratoire Suisse De Recherches Horlogeres | Diffusion barrier and separation substance for metal parts adjoining each other in an oxygen free atmosphere |
FR2388776A1 (en) * | 1977-04-26 | 1978-11-24 | Sherritt Gordon Mines Ltd | MIXED POWDER WITH METAL COATING AND PROCESS OF PREPARATION |
US4268564A (en) * | 1977-12-22 | 1981-05-19 | Allied Chemical Corporation | Strips of metallic glasses containing embedded particulate matter |
FR2507729A1 (en) * | 1981-06-12 | 1982-12-17 | Snecma | JOINT THAT CAN BE USED BY ABRASION AND METHOD OF MAKING SAME |
FR2545537A1 (en) * | 1983-05-06 | 1984-11-09 | Mtu Muenchen Gmbh | TURBOCHARGER COMPRISING A RUNNING TRIM |
DE3447470A1 (en) * | 1983-12-27 | 1985-07-04 | United Technologies Corp., Hartford, Conn. | MATERIAL FOR A GRINDABLE SEAL, ITS USE IN TURBINES AND METHOD FOR THE PRODUCTION THEREOF |
US4546047A (en) * | 1981-01-14 | 1985-10-08 | United Technologies Corporation | Composite tape preform for abradable seals |
WO1988003854A1 (en) * | 1986-11-26 | 1988-06-02 | Sundstrand Corporation | Composite, method of forming a composite, and article of manufacture |
US4813965A (en) * | 1988-02-29 | 1989-03-21 | Nuclear Metals, Inc. | Brazed porous coating and improved method of joining metal with silver material |
EP0416954A1 (en) * | 1989-09-08 | 1991-03-13 | Toyota Jidosha Kabushiki Kaisha | Abradable material for a turbo machine |
US5024884A (en) * | 1984-12-24 | 1991-06-18 | United Technologies Corporation | Abradable seal having particulate erosion resistance |
EP0459114A1 (en) * | 1990-05-10 | 1991-12-04 | The Perkin-Elmer Corporation | Aluminium and boron nitride thermal spray powder |
US5153021A (en) * | 1990-03-23 | 1992-10-06 | Rolls-Royce Plc | Abradable seal coating and method of making the same |
US5196471A (en) * | 1990-11-19 | 1993-03-23 | Sulzer Plasma Technik, Inc. | Thermal spray powders for abradable coatings, abradable coatings containing solid lubricants and methods of fabricating abradable coatings |
US5536022A (en) * | 1990-08-24 | 1996-07-16 | United Technologies Corporation | Plasma sprayed abradable seals for gas turbine engines |
US5976695A (en) * | 1996-10-02 | 1999-11-02 | Westaim Technologies, Inc. | Thermally sprayable powder materials having an alloyed metal phase and a solid lubricant ceramic phase and abradable seal assemblies manufactured therefrom |
US6410159B1 (en) | 1999-10-29 | 2002-06-25 | Praxair S. T. Technology, Inc. | Self-bonding MCrAly powder |
US20040023056A1 (en) * | 2002-06-14 | 2004-02-05 | Snecma Moteurs | Metallic material that can be worn away by abrasion; parts, casings, and a process for producing said material |
US20090136740A1 (en) * | 2007-11-28 | 2009-05-28 | Reynolds George H | Article having composite layer |
WO2014095887A1 (en) | 2012-12-18 | 2014-06-26 | Commissariat à l'énergie atomique et aux énergies alternatives | Process for coating a substrate with an abradable ceramic material, and coating thus obtained |
US20160186595A1 (en) * | 2014-12-29 | 2016-06-30 | United Technologies Corporation | Compressor abradable material seal with tailored wear ratio and desirable erosion resistance |
US11156358B2 (en) * | 2018-11-20 | 2021-10-26 | Serendipity Technologies Llc | Furnace apparatus |
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Cited By (35)
Publication number | Priority date | Publication date | Assignee | Title |
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US3413136A (en) * | 1965-03-10 | 1968-11-26 | United Aircraft Corp | Abradable coating |
DE2031616A1 (en) * | 1969-07-01 | 1971-01-21 | Metco Ine Westbury (Long Island) NY (VStA) | Flame spray powder |
FR2048433A5 (en) * | 1969-07-01 | 1971-03-19 | Metco Inc | |
US4072797A (en) * | 1974-08-28 | 1978-02-07 | Laboratoire Suisse De Recherches Horlogeres | Diffusion barrier and separation substance for metal parts adjoining each other in an oxygen free atmosphere |
FR2388776A1 (en) * | 1977-04-26 | 1978-11-24 | Sherritt Gordon Mines Ltd | MIXED POWDER WITH METAL COATING AND PROCESS OF PREPARATION |
US4268564A (en) * | 1977-12-22 | 1981-05-19 | Allied Chemical Corporation | Strips of metallic glasses containing embedded particulate matter |
US4546047A (en) * | 1981-01-14 | 1985-10-08 | United Technologies Corporation | Composite tape preform for abradable seals |
FR2507729A1 (en) * | 1981-06-12 | 1982-12-17 | Snecma | JOINT THAT CAN BE USED BY ABRASION AND METHOD OF MAKING SAME |
EP0067746A1 (en) * | 1981-06-12 | 1982-12-22 | Societe Nationale D'etude Et De Construction De Moteurs D'aviation, "S.N.E.C.M.A." | Abradable rub strip and method of making the same |
US4423097A (en) * | 1981-06-12 | 1983-12-27 | Societe Nationale D'etude Et De Construction De Moteurs D'aviation "S.N.E.C.M.A." | Abradable seal and its method of production |
FR2545537A1 (en) * | 1983-05-06 | 1984-11-09 | Mtu Muenchen Gmbh | TURBOCHARGER COMPRISING A RUNNING TRIM |
DE3447470A1 (en) * | 1983-12-27 | 1985-07-04 | United Technologies Corp., Hartford, Conn. | MATERIAL FOR A GRINDABLE SEAL, ITS USE IN TURBINES AND METHOD FOR THE PRODUCTION THEREOF |
US5024884A (en) * | 1984-12-24 | 1991-06-18 | United Technologies Corporation | Abradable seal having particulate erosion resistance |
US4817853A (en) * | 1986-11-26 | 1989-04-04 | Sundstrand Corporation | Composite, method of forming a composite, and article of manufacture |
WO1988003854A1 (en) * | 1986-11-26 | 1988-06-02 | Sundstrand Corporation | Composite, method of forming a composite, and article of manufacture |
US4813965A (en) * | 1988-02-29 | 1989-03-21 | Nuclear Metals, Inc. | Brazed porous coating and improved method of joining metal with silver material |
EP0416954A1 (en) * | 1989-09-08 | 1991-03-13 | Toyota Jidosha Kabushiki Kaisha | Abradable material for a turbo machine |
US5185217A (en) * | 1989-09-08 | 1993-02-09 | Toyota Jidosha Kabushiki Kaisha | Relatively displacing apparatus |
US5153021A (en) * | 1990-03-23 | 1992-10-06 | Rolls-Royce Plc | Abradable seal coating and method of making the same |
EP0459114A1 (en) * | 1990-05-10 | 1991-12-04 | The Perkin-Elmer Corporation | Aluminium and boron nitride thermal spray powder |
US5780116A (en) * | 1990-08-24 | 1998-07-14 | United Technologies Corporation | Method for producing an abradable seal |
US5536022A (en) * | 1990-08-24 | 1996-07-16 | United Technologies Corporation | Plasma sprayed abradable seals for gas turbine engines |
US5434210A (en) * | 1990-11-19 | 1995-07-18 | Sulzer Plasma Technik, Inc. | Thermal spray powders for abradable coatings, abradable coatings containing solid lubricants and methods of fabricating abradable coatings |
US5196471A (en) * | 1990-11-19 | 1993-03-23 | Sulzer Plasma Technik, Inc. | Thermal spray powders for abradable coatings, abradable coatings containing solid lubricants and methods of fabricating abradable coatings |
US5976695A (en) * | 1996-10-02 | 1999-11-02 | Westaim Technologies, Inc. | Thermally sprayable powder materials having an alloyed metal phase and a solid lubricant ceramic phase and abradable seal assemblies manufactured therefrom |
US6410159B1 (en) | 1999-10-29 | 2002-06-25 | Praxair S. T. Technology, Inc. | Self-bonding MCrAly powder |
US7128962B2 (en) * | 2002-06-14 | 2006-10-31 | Snecma Services | Metallic material that can be worn away by abrasion; parts, casings, and a process for producing said material |
US20040023056A1 (en) * | 2002-06-14 | 2004-02-05 | Snecma Moteurs | Metallic material that can be worn away by abrasion; parts, casings, and a process for producing said material |
US20090136740A1 (en) * | 2007-11-28 | 2009-05-28 | Reynolds George H | Article having composite layer |
US7998604B2 (en) | 2007-11-28 | 2011-08-16 | United Technologies Corporation | Article having composite layer |
WO2014095887A1 (en) | 2012-12-18 | 2014-06-26 | Commissariat à l'énergie atomique et aux énergies alternatives | Process for coating a substrate with an abradable ceramic material, and coating thus obtained |
US20160186595A1 (en) * | 2014-12-29 | 2016-06-30 | United Technologies Corporation | Compressor abradable material seal with tailored wear ratio and desirable erosion resistance |
US10060281B2 (en) * | 2014-12-29 | 2018-08-28 | United Technologies Corporation | Compressor abradable material seal with tailored wear ratio and desirable erosion resistance |
US11156358B2 (en) * | 2018-11-20 | 2021-10-26 | Serendipity Technologies Llc | Furnace apparatus |
US20220003409A1 (en) * | 2018-11-20 | 2022-01-06 | Serendipity Technologies Llc | Furnace apparatus |
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