CA1202768A - Method for forming braze-bonded abrasive turbine blade tip - Google Patents
Method for forming braze-bonded abrasive turbine blade tipInfo
- Publication number
- CA1202768A CA1202768A CA000413020A CA413020A CA1202768A CA 1202768 A CA1202768 A CA 1202768A CA 000413020 A CA000413020 A CA 000413020A CA 413020 A CA413020 A CA 413020A CA 1202768 A CA1202768 A CA 1202768A
- Authority
- CA
- Canada
- Prior art keywords
- braze
- grit
- superalloy
- substrate
- titanium
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- 229910000601 superalloy Inorganic materials 0.000 claims abstract description 49
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 27
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000010936 titanium Substances 0.000 claims abstract description 27
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 27
- 239000000843 powder Substances 0.000 claims abstract description 23
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 19
- 239000000956 alloy Substances 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 10
- 238000004026 adhesive bonding Methods 0.000 claims abstract description 5
- 238000000576 coating method Methods 0.000 claims description 45
- 239000011248 coating agent Substances 0.000 claims description 40
- 239000011159 matrix material Substances 0.000 claims description 16
- 239000004568 cement Substances 0.000 claims description 14
- 238000009736 wetting Methods 0.000 claims description 13
- 238000005219 brazing Methods 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 239000002002 slurry Substances 0.000 claims description 9
- -1 titanium hydride Chemical compound 0.000 claims description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052796 boron Inorganic materials 0.000 claims description 6
- 229910000048 titanium hydride Inorganic materials 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052735 hafnium Inorganic materials 0.000 claims description 4
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 4
- 239000007791 liquid phase Substances 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- 150000004678 hydrides Chemical class 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000012071 phase Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims 14
- 239000002904 solvent Substances 0.000 claims 5
- 239000011230 binding agent Substances 0.000 claims 4
- 229910052987 metal hydride Inorganic materials 0.000 claims 3
- 150000004681 metal hydrides Chemical class 0.000 claims 3
- 238000001704 evaporation Methods 0.000 claims 2
- 238000003892 spreading Methods 0.000 claims 2
- 238000005520 cutting process Methods 0.000 claims 1
- QSGNKXDSTRDWKA-UHFFFAOYSA-N zirconium dihydride Chemical compound [ZrH2] QSGNKXDSTRDWKA-UHFFFAOYSA-N 0.000 claims 1
- 229910000568 zirconium hydride Inorganic materials 0.000 claims 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 abstract description 2
- 239000007789 gas Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 238000007665 sagging Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000003522 acrylic cement Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- 239000004830 Super Glue Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000004901 spalling Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910003470 tongbaite Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/02—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
- B23K35/0222—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
- B23K35/0244—Powders, particles or spheres; Preforms made therefrom
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/32—Selection of soldering or welding materials proper with the principal constituent melting at more than 1550 degrees C
- B23K35/327—Selection of soldering or welding materials proper with the principal constituent melting at more than 1550 degrees C comprising refractory compounds, e.g. carbides
-
- 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
- C23C24/00—Coating starting from inorganic powder
- C23C24/08—Coating starting from inorganic powder by application of heat or pressure and heat
- C23C24/10—Coating starting from inorganic powder by application of heat or pressure and heat with intermediate formation of a liquid phase in the layer
- C23C24/103—Coating with metallic material, i.e. metals or metal alloys, optionally comprising hard particles, e.g. oxides, carbides or nitrides
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
METHOD FOR FORMING
BRAZE-BONDED ABRASIVE TURBINE BLADE TIP
Abstract of the Disclosure In a preferred embodiment, a turbine blade tip is coated with an abrasive for wear forming a seal track in a gas turbine engine by gluing a self-sustaining preform comprising abrasive alumina grit and nickel-base superalloy braze powder onto the tip and heating to braze the grit to the tip.
The preferred grit is titanium coated to strengthen bonding between the alumina and the braze alloy.
BRAZE-BONDED ABRASIVE TURBINE BLADE TIP
Abstract of the Disclosure In a preferred embodiment, a turbine blade tip is coated with an abrasive for wear forming a seal track in a gas turbine engine by gluing a self-sustaining preform comprising abrasive alumina grit and nickel-base superalloy braze powder onto the tip and heating to braze the grit to the tip.
The preferred grit is titanium coated to strengthen bonding between the alumina and the braze alloy.
Description
:l~Z~;~7~1~
METHOD FOR FORMING
BRAZE-BONDED ABRASIVE TURBINE BI~DE TIP
Background of the Invention This invention relates to an abrasive coating applied to a gas turbine blade tip for wear forming a seal track in a sta-tionary shroud. More particularly, this invention relates to a method for coating a turbine blade tip by brazing abrasive grit to the tip using a composite preform.
In a gas turbine engine~ gas flow between a tip of a rotating blade and a cooperating stationary shroud reduces efficiency and power. It is therefore desired to minimi~e clearance between the tip and the shroud to seal against gas flow. One method for accomplishing this is to employ an abrasive grit coating on one or more blade tips of a rotor to wear form a seal track in the shroud. The coatings comprise grit mechanically held, for example, in an electroplated metal matrix. A major problem with this method is that the grit tends to spall during turbine operations. Also, nickel-base superalloy is preferred for blade use but contains a plurality of minor constituents and is not suited for plating.
Thus, the coating and the blade are composed of different metals. Furthermore, a method is desired that is more suitable for mass production and provides more uniform thickness and grit dis-tribution.
Therefore, it is an object of this :invention to provide an improved method for coating a turbine blade with an abrasive for wear forming a seal track in a cooperating shroud within a gas turbine engine, which abrasive comprises refractory grit tightly bonded within a braze metal matrix to resist spalling.
More particularly, it is an object of this invention to provide a method for coating a superalloy turbine blade tip with abrasive grit braze bonded ~L2~
within a superalloy matrix haviny substantially the composition of the blad~ superalloy. The method not only tightly bonds the grit within the superalloy matrix, but also forms an integral braze bond between the coating superalloy and the blade superalloy. In one aspect of this invention, the grit is coated prior to brazing with a metallic braze-wetting agent, perferably titanium, that forms a strong metallurgical bond between the grit and the coating superalloy.
It is a further object of this invention to provide an impro~ed method for readily applying a spall-resistant, abrasive grit coating to a turbine blade tip, which method is adapted for commercial production. The method comprises brazing a grit-cont~;ning preform to the tip. The grit concentration and thickness is readily controlled in the preform to produce a uniform composition and thickness in the coating. An additional feature of this invention is that the pre~orm is readily sized and shaped to produce a coating having a desired pattern.
Summary of the Invention In a preferred embodiment, these and other objects are accomplished by forming a sheet comprising abrasive alumina grit and nickel-base superalloy braze powder and employing the preform sheet to braze the yrit to a tip surface of a nickel-base superalloy turbine blade. The alumina grit particles have a titanium coating that improves braze-wetting and substantially strengthens bonding between the alumina and braze alloy. Approximately equal volume portions of the grit and a nickel-base superalloy braze powder are slurried with a vaporizable liquid organic cement and spread into a uniform layer. After the cement sets, the layer forms a self-sustaining sheet that is suitably cut and glued onto a turbine blade tip.
The blade tip and attached preform are slowly heated to vaporize the cement and thereafter to melt the braze alloy, whereupon the melt forms a continuous phase surrounding the grit and wetting the blade tip.
Upon solidification, the grit is entrapped in a superalloy matrix that is integrally braze bonded to the blade tip, thereby forming a spall-resistant abrasive coating.
In a preferred coating of the invention, the metal matrix not only mechanically holds the grit, but it is also believed that the titanium on the grit interacts with the alumina and the braze superalloy to produce a strong metallurgical bond therebetween. The superalloy portion of the coating is integrally bonded to the superalloy of the blade and has substantially the same composition. The use of a braze-grit compo-site preform results in uniform grit distribution and thickness in the coating. In addition, the preform is readily shaped to produce a desired coating pattern.
Furthermore, the use of the preform and operations such as gluing and brazing are well suited for production.
Detailed Description of the Preferred Embodiment In accordance with this invention, an abrasive coating is applied to a gas turbine engine blade cast of a nickel~base superalloy. The preferred alloy consists of, by weight, 10 percent tungsten, 10 percent cobalt, 9 percent chromium, 5.5 percent aluminum, 1.5 percent tantalum, 1.5 percent titanium, 1.0 percent hafnium, 0.02 percent boron, 2.5 percent molybdenum, 0.15 percent carbon, 0.05 percenk zirconium and the balance nickel and is commercially available under the trade designation MAR M247* A preferred blade extends radially from a hub having a center * trademark 3 , 1q e~
t7~
axis about which it is adapted to rotate within a gas turbine engine~ The blade comprises a tip remote from the hub and havlng a substantially flat, axially parallel surface that is intended to lie proximate to a stationary shroud surface in the engine and to be coated with abrasive to wear form a seal track in the shroud. The coating is suitably applied to an individually cast blade tip prior to assembly in a hub. Alternately, the coating may be applied to one or more blade tips of an integrally cast rotor. ~n a surprising aspect of this invention, it has been found that coatings may be simultaneously brazed to blades diametrically arranged on a hub without sagging.
A preferred abrasive grit consists of alumina A1203 particles sized to about 100 mesh~
The particles are coated with a metallic titanium film by vapor deposition. About 100 ~arts by weight alumina grit are blended with about 10 parts fine titanium hydride powder. The titanium hydride powder is sized to -325 mesh. The mixture is placed in a refractory alumina crucible and covered with a refractory perforated blanket suitable to contain the po~ders ~hile allowing gases to escape.
The covered crucible is then slowly heated in a ; vacuum furnace evacuated to a pressure less than about 5 x 10 torr. At about 400C, the titanium hydride decomposes to form hydrogen gas and metallic titanium. ~ slow heating rate is desired to allow the hydrogen to escape from the crucible without disrupting the powder. After the hydride is decomposed, the temperature is increased to about 1250C, whereat titanium vapor pressure increases and titanium is deposited onto nearby grit surfaces. The titanium film improves wetting of the surface by a nickel-base ,., -~ ~
~; ~
superalloy braze melt. It is also believed that the titanium interacts with the braze alloy and the alumina to form a strong metallurgical bondO
The tltanium-coated grit is then mixed with approximately an e~ual volume of finer braze alloy powder sized to -1~0 mesh. The preEerred braze alloy consists of, by weight, 10.8 percent tungsten, 10 percent chromium, 9.7 percent cobalt, 5.5 percent aluminum, 3.1 percent tantalum, 2.5 percent silicon, 1.6 percent titanium, 1.4 percent hafnium, 1.1 percent boron, 0.6 percent molybdenum, 0.17 percent carbon, 0.05 percent zirconium and the balance nickel. This alloy is essentially similar to MAR M247* but is modified to adapt the alloy for brazing, particularly by relatively high additions of silicon and boron that reduce the liquidus temperature and improve melt flow properties.
The mixture of grit and braze alloy powder is then formed into a self-sustaining sheet. The mixture is slurried with solvent-base vaporizable acrylic cement commercially available from Wall Colmonoy Corporation under the trade designation Nicrobraz~ The cement is of a type particularly formulated as a vehicle for bonding braze powder to metal surfaces in typical metal-metal brazing operations. A minimum volume of cement sufficient to form a pourable slurry is added to the powder.
The slurry is poured onto a sheet formed of a non-stick polytetrafluoroethylene material and covered with a similar sheet. The sandwich assembly is rolled -to spread the slurry into a layer having a uniform thickness of about 1.5 millimeters.
After rolling, the cover sheet is peeled away to expose the slurry layer to the air for drying. After the cement has sufficiently set so that the layer is * trademark 5 , f~s ~Z~Z71~13 self-sustaining, the botkom sheet is peeled away to further aid drying. Drying for about one hour at room temperature is generally adequate. The dried sheet is self-sustaining and sui~able for forming an abrasive coating. However, an acrylic lac~uer may be sprayed onto the sheet surfaces to prevent cracking and to stiffen the sheet for convenient handling.
The grit-braze sheet is cut using an abrasive silicon carbide wheel into a size and shape corresponding to a desired pattern of the abrasive coating on the blade tip. The preform is then glued onto the blade tip with a cyanoacrylate adhesive. Any overhang is trimmed by grinding. A
liquid stop-off alumina oxide slurry is painted onto the sides of the blade adjacent the tip to prevent brazing there.
Brazing is carried out in a vacuum furnace.
An individual blade is typically vertically oriented with the preform-bearing tip up. However, it has been found that brazing is also suitably carried out when a blade is oriented horizontally, without the preform falling off upon heating or the coating sagging, even though the tip surface is vertically oriented. Thus, two or more blades of an assembled or integrally cast rotor may be simultaneously coated by this invention.
The furnace is evacuated to less than 10 5 torr and initially slowly heated to vaporize the acrylic cement and cyanoacrylate glue. Thereafter, the temperature is raised to about 1230C and held for about 10 to 20 minutes to melt the braze alloy~
Upon melting, the braze alloy forms a liquid phase surrounding the alumina grit and wetting the blade tip. The melt wets and reacts with the titanium-coated '.,~
alumina particle surfaces in a manner that produces a strong bond upon cooling. Af-ter the braze powder has wet the grit surfaces and the blade tip, -the temperature is cooled to abou-t 1090C for five to ten minutes to set -the alloy to prevent sagging or flowing. Thereafter, the temperature is raised to about 1150C for 20 to 60 minutes. During this time, elements added to modify the superalloy for brazing, particularly boron and silicon, di~fuse into the blade and become substantially uniformly distributed in the coating and the cast blade near the tip.
This diffusion raises the liquidus tempexature of the coating to a level suitable for turbine engine operations.
The product coated tip compxises alumina grit tightly held within a nickel-base superalloy matrix, which matrix is tightly brazed to the cast superalloy of the blade. Superalloy in the coating and in -the blade has substantially the same composi-tion, particularly after diffusion during brazing.
Within the coating, the proportion of grit to alloy is essentially the same as formulated in the preform.
Also, uniform coating thickness is obtained, particu-larly for coatings on different bladesof a rotor.
If necessary, the coating may be ground to true up the blade dimensions or provide a desired contour.
In addition, the surface of the coating may be chemically ox electrochemically etched to better expose the grit to improve initial abrasiveness.
In the preferred embodiment, titanium is coated onto the grit to produce a strong metallurgical bond between the alumina and the braze alloy. It is believed that titanium deposited in immediate contact with the alumina surface bonds to oxygen in the alumina, essentially becoming part of the oxide 7~;~
stxucture. Titanium that is deposited further away remains substantially metallic. secause of its metallic nature, the titanium coming in contact with the braze melt improves wetting and itself alloys with the nickel-base superalloy. Thus, both the alumina titanium interface and the titanium-superalloy interface are strengthened by chemical bonding so that the overall grit-superalloy bond is stronger than mere mechanical joining. While titanium is preferably deposited onto the grit prior to mixing with the braze powder, improved bonding may also be obtained by includlng titanium hydride powder with uncoated grit and braze powder in a preform sheet, although titanium deposition is less efficient. Other metals, such as hafnium and zirconium, are also suitable for forming hydride-derived coatings that produce similar alumina-superalloy metallurgical bonds.
Other known abrasive oxides, carbides or nitrides may be substituted for the preferred alumina grit, including, for example, titania, zirconia or chromium carbide~ The coating preferably comprlses about equal portions of alumina grit and superalloy. At least about 30 percent by volume superalloy is believ~d necessary to adequately bond the grit particles into a cohesive coating. Coatings having greater than about 70 percent by volume alloy do not have adequate abrasive properties.
Although this invention has heen described in terms of certain emboaiments thereof, i-t is not in-tended to be limited to the above description, but rather only to the extent set forth in the claims that follow.
METHOD FOR FORMING
BRAZE-BONDED ABRASIVE TURBINE BI~DE TIP
Background of the Invention This invention relates to an abrasive coating applied to a gas turbine blade tip for wear forming a seal track in a sta-tionary shroud. More particularly, this invention relates to a method for coating a turbine blade tip by brazing abrasive grit to the tip using a composite preform.
In a gas turbine engine~ gas flow between a tip of a rotating blade and a cooperating stationary shroud reduces efficiency and power. It is therefore desired to minimi~e clearance between the tip and the shroud to seal against gas flow. One method for accomplishing this is to employ an abrasive grit coating on one or more blade tips of a rotor to wear form a seal track in the shroud. The coatings comprise grit mechanically held, for example, in an electroplated metal matrix. A major problem with this method is that the grit tends to spall during turbine operations. Also, nickel-base superalloy is preferred for blade use but contains a plurality of minor constituents and is not suited for plating.
Thus, the coating and the blade are composed of different metals. Furthermore, a method is desired that is more suitable for mass production and provides more uniform thickness and grit dis-tribution.
Therefore, it is an object of this :invention to provide an improved method for coating a turbine blade with an abrasive for wear forming a seal track in a cooperating shroud within a gas turbine engine, which abrasive comprises refractory grit tightly bonded within a braze metal matrix to resist spalling.
More particularly, it is an object of this invention to provide a method for coating a superalloy turbine blade tip with abrasive grit braze bonded ~L2~
within a superalloy matrix haviny substantially the composition of the blad~ superalloy. The method not only tightly bonds the grit within the superalloy matrix, but also forms an integral braze bond between the coating superalloy and the blade superalloy. In one aspect of this invention, the grit is coated prior to brazing with a metallic braze-wetting agent, perferably titanium, that forms a strong metallurgical bond between the grit and the coating superalloy.
It is a further object of this invention to provide an impro~ed method for readily applying a spall-resistant, abrasive grit coating to a turbine blade tip, which method is adapted for commercial production. The method comprises brazing a grit-cont~;ning preform to the tip. The grit concentration and thickness is readily controlled in the preform to produce a uniform composition and thickness in the coating. An additional feature of this invention is that the pre~orm is readily sized and shaped to produce a coating having a desired pattern.
Summary of the Invention In a preferred embodiment, these and other objects are accomplished by forming a sheet comprising abrasive alumina grit and nickel-base superalloy braze powder and employing the preform sheet to braze the yrit to a tip surface of a nickel-base superalloy turbine blade. The alumina grit particles have a titanium coating that improves braze-wetting and substantially strengthens bonding between the alumina and braze alloy. Approximately equal volume portions of the grit and a nickel-base superalloy braze powder are slurried with a vaporizable liquid organic cement and spread into a uniform layer. After the cement sets, the layer forms a self-sustaining sheet that is suitably cut and glued onto a turbine blade tip.
The blade tip and attached preform are slowly heated to vaporize the cement and thereafter to melt the braze alloy, whereupon the melt forms a continuous phase surrounding the grit and wetting the blade tip.
Upon solidification, the grit is entrapped in a superalloy matrix that is integrally braze bonded to the blade tip, thereby forming a spall-resistant abrasive coating.
In a preferred coating of the invention, the metal matrix not only mechanically holds the grit, but it is also believed that the titanium on the grit interacts with the alumina and the braze superalloy to produce a strong metallurgical bond therebetween. The superalloy portion of the coating is integrally bonded to the superalloy of the blade and has substantially the same composition. The use of a braze-grit compo-site preform results in uniform grit distribution and thickness in the coating. In addition, the preform is readily shaped to produce a desired coating pattern.
Furthermore, the use of the preform and operations such as gluing and brazing are well suited for production.
Detailed Description of the Preferred Embodiment In accordance with this invention, an abrasive coating is applied to a gas turbine engine blade cast of a nickel~base superalloy. The preferred alloy consists of, by weight, 10 percent tungsten, 10 percent cobalt, 9 percent chromium, 5.5 percent aluminum, 1.5 percent tantalum, 1.5 percent titanium, 1.0 percent hafnium, 0.02 percent boron, 2.5 percent molybdenum, 0.15 percent carbon, 0.05 percenk zirconium and the balance nickel and is commercially available under the trade designation MAR M247* A preferred blade extends radially from a hub having a center * trademark 3 , 1q e~
t7~
axis about which it is adapted to rotate within a gas turbine engine~ The blade comprises a tip remote from the hub and havlng a substantially flat, axially parallel surface that is intended to lie proximate to a stationary shroud surface in the engine and to be coated with abrasive to wear form a seal track in the shroud. The coating is suitably applied to an individually cast blade tip prior to assembly in a hub. Alternately, the coating may be applied to one or more blade tips of an integrally cast rotor. ~n a surprising aspect of this invention, it has been found that coatings may be simultaneously brazed to blades diametrically arranged on a hub without sagging.
A preferred abrasive grit consists of alumina A1203 particles sized to about 100 mesh~
The particles are coated with a metallic titanium film by vapor deposition. About 100 ~arts by weight alumina grit are blended with about 10 parts fine titanium hydride powder. The titanium hydride powder is sized to -325 mesh. The mixture is placed in a refractory alumina crucible and covered with a refractory perforated blanket suitable to contain the po~ders ~hile allowing gases to escape.
The covered crucible is then slowly heated in a ; vacuum furnace evacuated to a pressure less than about 5 x 10 torr. At about 400C, the titanium hydride decomposes to form hydrogen gas and metallic titanium. ~ slow heating rate is desired to allow the hydrogen to escape from the crucible without disrupting the powder. After the hydride is decomposed, the temperature is increased to about 1250C, whereat titanium vapor pressure increases and titanium is deposited onto nearby grit surfaces. The titanium film improves wetting of the surface by a nickel-base ,., -~ ~
~; ~
superalloy braze melt. It is also believed that the titanium interacts with the braze alloy and the alumina to form a strong metallurgical bondO
The tltanium-coated grit is then mixed with approximately an e~ual volume of finer braze alloy powder sized to -1~0 mesh. The preEerred braze alloy consists of, by weight, 10.8 percent tungsten, 10 percent chromium, 9.7 percent cobalt, 5.5 percent aluminum, 3.1 percent tantalum, 2.5 percent silicon, 1.6 percent titanium, 1.4 percent hafnium, 1.1 percent boron, 0.6 percent molybdenum, 0.17 percent carbon, 0.05 percent zirconium and the balance nickel. This alloy is essentially similar to MAR M247* but is modified to adapt the alloy for brazing, particularly by relatively high additions of silicon and boron that reduce the liquidus temperature and improve melt flow properties.
The mixture of grit and braze alloy powder is then formed into a self-sustaining sheet. The mixture is slurried with solvent-base vaporizable acrylic cement commercially available from Wall Colmonoy Corporation under the trade designation Nicrobraz~ The cement is of a type particularly formulated as a vehicle for bonding braze powder to metal surfaces in typical metal-metal brazing operations. A minimum volume of cement sufficient to form a pourable slurry is added to the powder.
The slurry is poured onto a sheet formed of a non-stick polytetrafluoroethylene material and covered with a similar sheet. The sandwich assembly is rolled -to spread the slurry into a layer having a uniform thickness of about 1.5 millimeters.
After rolling, the cover sheet is peeled away to expose the slurry layer to the air for drying. After the cement has sufficiently set so that the layer is * trademark 5 , f~s ~Z~Z71~13 self-sustaining, the botkom sheet is peeled away to further aid drying. Drying for about one hour at room temperature is generally adequate. The dried sheet is self-sustaining and sui~able for forming an abrasive coating. However, an acrylic lac~uer may be sprayed onto the sheet surfaces to prevent cracking and to stiffen the sheet for convenient handling.
The grit-braze sheet is cut using an abrasive silicon carbide wheel into a size and shape corresponding to a desired pattern of the abrasive coating on the blade tip. The preform is then glued onto the blade tip with a cyanoacrylate adhesive. Any overhang is trimmed by grinding. A
liquid stop-off alumina oxide slurry is painted onto the sides of the blade adjacent the tip to prevent brazing there.
Brazing is carried out in a vacuum furnace.
An individual blade is typically vertically oriented with the preform-bearing tip up. However, it has been found that brazing is also suitably carried out when a blade is oriented horizontally, without the preform falling off upon heating or the coating sagging, even though the tip surface is vertically oriented. Thus, two or more blades of an assembled or integrally cast rotor may be simultaneously coated by this invention.
The furnace is evacuated to less than 10 5 torr and initially slowly heated to vaporize the acrylic cement and cyanoacrylate glue. Thereafter, the temperature is raised to about 1230C and held for about 10 to 20 minutes to melt the braze alloy~
Upon melting, the braze alloy forms a liquid phase surrounding the alumina grit and wetting the blade tip. The melt wets and reacts with the titanium-coated '.,~
alumina particle surfaces in a manner that produces a strong bond upon cooling. Af-ter the braze powder has wet the grit surfaces and the blade tip, -the temperature is cooled to abou-t 1090C for five to ten minutes to set -the alloy to prevent sagging or flowing. Thereafter, the temperature is raised to about 1150C for 20 to 60 minutes. During this time, elements added to modify the superalloy for brazing, particularly boron and silicon, di~fuse into the blade and become substantially uniformly distributed in the coating and the cast blade near the tip.
This diffusion raises the liquidus tempexature of the coating to a level suitable for turbine engine operations.
The product coated tip compxises alumina grit tightly held within a nickel-base superalloy matrix, which matrix is tightly brazed to the cast superalloy of the blade. Superalloy in the coating and in -the blade has substantially the same composi-tion, particularly after diffusion during brazing.
Within the coating, the proportion of grit to alloy is essentially the same as formulated in the preform.
Also, uniform coating thickness is obtained, particu-larly for coatings on different bladesof a rotor.
If necessary, the coating may be ground to true up the blade dimensions or provide a desired contour.
In addition, the surface of the coating may be chemically ox electrochemically etched to better expose the grit to improve initial abrasiveness.
In the preferred embodiment, titanium is coated onto the grit to produce a strong metallurgical bond between the alumina and the braze alloy. It is believed that titanium deposited in immediate contact with the alumina surface bonds to oxygen in the alumina, essentially becoming part of the oxide 7~;~
stxucture. Titanium that is deposited further away remains substantially metallic. secause of its metallic nature, the titanium coming in contact with the braze melt improves wetting and itself alloys with the nickel-base superalloy. Thus, both the alumina titanium interface and the titanium-superalloy interface are strengthened by chemical bonding so that the overall grit-superalloy bond is stronger than mere mechanical joining. While titanium is preferably deposited onto the grit prior to mixing with the braze powder, improved bonding may also be obtained by includlng titanium hydride powder with uncoated grit and braze powder in a preform sheet, although titanium deposition is less efficient. Other metals, such as hafnium and zirconium, are also suitable for forming hydride-derived coatings that produce similar alumina-superalloy metallurgical bonds.
Other known abrasive oxides, carbides or nitrides may be substituted for the preferred alumina grit, including, for example, titania, zirconia or chromium carbide~ The coating preferably comprlses about equal portions of alumina grit and superalloy. At least about 30 percent by volume superalloy is believ~d necessary to adequately bond the grit particles into a cohesive coating. Coatings having greater than about 70 percent by volume alloy do not have adequate abrasive properties.
Although this invention has heen described in terms of certain emboaiments thereof, i-t is not in-tended to be limited to the above description, but rather only to the extent set forth in the claims that follow.
Claims (4)
1. A method for coating a superalloy substrate with an abrasive comprising attaching to the substrate a self-sustaining preform comprising metal-coated abrasive refractory grit and superalloy-base braze powder, said grit comprising refractory particles coated by a metal selected from the group consisting of titanium, hafnium and zirconium and effective to enhance wetting by a braze liquid, said preform further comprising a vaporizable organic binder bonding the grit and the braze powder, heating the preform to vaporize the organic binder and to melt the superalloy braze to form a continuous superalloy liquid phase surrounding and wetting the grit particles and wetting the substrate, and cooling the braze phase to entrap the grit in a superalloy matrix and to braze-bond the matrix to the substrate.
2. A method for applying an abrasive coating to a nickel-base superalloy substrate comprising gluing to the substrate a self-sustaining preform comprising titanium-coated abrasive alumina grit and superalloy-base braze powder, said grit comprising alumina particles having a braze-wettable titanium coating suitable for metallurgically bonding alumina to a superalloy, said preform further comprising a vaporizable organic binder bonding the grit and the braze powder together, slowly heating the preform to vaporize the organic binder and thereafter to melt the braze superalloy to form a continuous superalloy liquid phase wetting the substrate and surrounding the grit particles and wetting titanium-coated surfaces thereof, and cooling to solidify the superalloy braze phase to form an abrasive coating comprising alumina grit enclosed within and metallurgically bonded to a superalloy matrix and to braze-bond the matrix to the substrate.
3. A method for applying an abrasive coating to a nickel-base superalloy substrate comprising heating a mixture comprising abrasive alumina grit and a metal hydride in a vacuum to decompose the metal hydride and to deposit nascent metal onto the grit, the metal hydride being selected from the group consisting of titanium hydride, hafnium hydride and zirconium hydride, mixing the metal-coated grit and a nickel-base superalloy braze powder with a liquid comprising a relatively high temperature vaporizable organic cement dissolved in a relatively low temperature vaporizable solvent, said liquid being in an amount sufficient to form a spreadable slurry and containing sufficient cement to cohesively bond the grit and the braze powder together, spreading the braze-grit slurry to a desired thickness, evaporating the solvent from the slurry to bond the grit and the braze powder into a self-sustaining sheet, gluing the sheet to the substrate, heating the sheet and substrate to vaporize the cement and to melt the braze alloy to form a braze liquid phase that wets the substrate and surrounds the grit, wetting metal coated surfaces thereof, and cooling the substrate and braze liquid overlayer to solidify the braze liquid to form an abrasive coating comprising grit within a nickel-base superalloy matrix tightly bonded to the substrate.
4. A method for applying to a nickel-base superalloy gas turbine blade tip an abrasive coating of the type employed for wear-forming a seal track within a gas turbine engine, said method comprising heating a mixture comprising abrasive alumina grit and titanium hydride in a vacuum for a time and at a temperature sufficient to decompose the hydride and to deposit nascent titanium onto the grit surfaces to form a braze-wettable film adapted for metallurgi-cally bonding alumina and nickel-base superalloy, mixing the titanium-coated grit with approximately an equal volume portion of a braze powder consisting essentially of a nickel-base superalloy similar to the blade tip but containing boron and silicon in sufficient amounts to reduce the liquidus temperature for brazing, slurrying the grit-braze mixture in a liquid comprising an organic cement dissolved in a solvent, said solvent being vaporizable at ordinary temperatures to set the cement, said cement being vaporizable at elevated temperatures and being present in an amount sufficient to cohesively bond the grit-braze mixture together, spreading the slurry to a desired thickness, evaporating the solvent therefrom to set the cement to form a self-sustaining sheet composed of the grit and the braze powder, cutting the sheet to form a preform having a desired size and shape conforming to the blade tip, gluing the preform to the blade tip, heating the glued preform and blade tip to vaporize the cement and thereafter to melt the braze alloy to form a braze liquid wetting the blade tip and surrounding the grit, wetting the titanium-coated surfaces, cooling the blade tip and braze liquid to solidify the braze superalloy to metallurgically bond the grit within a nickel-base superalloy matrix and to braze-bond the superalloy matrix to the turbine blade tip, thereby forming an abrasive coating on the blade tip, and heating the coated blade at a temperature and for a time sufficient to diffuse boron and silicon from the superalloy matrix into the blade so as to produce a substantially uniform superalloy composition.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31848981A | 1981-11-05 | 1981-11-05 | |
US318,489 | 1981-11-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1202768A true CA1202768A (en) | 1986-04-08 |
Family
ID=23238391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000413020A Expired CA1202768A (en) | 1981-11-05 | 1982-10-07 | Method for forming braze-bonded abrasive turbine blade tip |
Country Status (2)
Country | Link |
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CA (1) | CA1202768A (en) |
GB (1) | GB2108534B (en) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4726101A (en) * | 1986-09-25 | 1988-02-23 | United Technologies Corporation | Turbine vane nozzle reclassification |
US4854196A (en) * | 1988-05-25 | 1989-08-08 | General Electric Company | Method of forming turbine blades with abradable tips |
US5359770A (en) * | 1992-09-08 | 1994-11-01 | General Motors Corporation | Method for bonding abrasive blade tips to the tip of a gas turbine blade |
US5264011A (en) * | 1992-09-08 | 1993-11-23 | General Motors Corporation | Abrasive blade tips for cast single crystal gas turbine blades |
JP3315919B2 (en) | 1998-02-18 | 2002-08-19 | 日本碍子株式会社 | Method for manufacturing a composite member composed of two or more different types of members |
WO1999055470A1 (en) * | 1998-04-25 | 1999-11-04 | Penn State Research Foundation | Method of applying hard-facing material to a substrate |
DE10000988A1 (en) * | 1999-02-17 | 2001-07-19 | Euromat Gmbh | Method for producing a protective layer on the surface of a component or the like workpiece, solder material for this and their use |
US20040124231A1 (en) * | 1999-06-29 | 2004-07-01 | Hasz Wayne Charles | Method for coating a substrate |
JP4367675B2 (en) | 1999-10-21 | 2009-11-18 | 日本碍子株式会社 | Adhesive composition for joining ceramic member and metal member, manufacturing method of composite member using the same composition, and composite member obtained by the manufacturing method |
DE10000989A1 (en) * | 2000-01-13 | 2001-07-19 | Euromat Gmbh | A method for producing a protective layer on the surface of a component o. The like. Workpiece, solder material therefor and their use |
US7331755B2 (en) * | 2004-05-25 | 2008-02-19 | General Electric Company | Method for coating gas turbine engine components |
DE102005030848A1 (en) * | 2005-07-01 | 2007-01-11 | Mtu Aero Engines Gmbh | Method for producing a blade tip armor |
US7653994B2 (en) * | 2006-03-22 | 2010-02-02 | General Electric Company | Repair of HPT shrouds with sintered preforms |
US20070295785A1 (en) * | 2006-05-31 | 2007-12-27 | General Electric Company | Microwave brazing using mim preforms |
EP2171124B1 (en) * | 2007-05-04 | 2011-09-14 | MTU Aero Engines AG | Method for manufacturing an abrasive coating on a gas turbine component |
US20100288977A1 (en) * | 2009-05-15 | 2010-11-18 | Metso Minerals, Inc. | Corrosion protection under influence of corrosive species |
US20150118060A1 (en) * | 2013-10-25 | 2015-04-30 | General Electric Company | Turbine engine blades, related articles, and methods |
DE102013223585A1 (en) * | 2013-11-19 | 2015-06-03 | MTU Aero Engines AG | Inlet lining based on metal fibers |
US10018056B2 (en) * | 2014-07-02 | 2018-07-10 | United Technologies Corporation | Abrasive coating and manufacture and use methods |
US10786875B2 (en) | 2014-07-02 | 2020-09-29 | Raytheon Technologies Corporation | Abrasive preforms and manufacture and use methods |
US10030527B2 (en) | 2014-07-02 | 2018-07-24 | United Technologies Corporation | Abrasive preforms and manufacture and use methods |
US10012095B2 (en) * | 2014-07-02 | 2018-07-03 | United Technologies Corporation | Abrasive coating and manufacture and use methods |
-
1982
- 1982-10-07 CA CA000413020A patent/CA1202768A/en not_active Expired
- 1982-10-27 GB GB08230705A patent/GB2108534B/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB2108534A (en) | 1983-05-18 |
GB2108534B (en) | 1985-07-24 |
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