US3528861A - Method for coating the superalloys - Google Patents
Method for coating the superalloys Download PDFInfo
- Publication number
- US3528861A US3528861A US731649A US3528861DA US3528861A US 3528861 A US3528861 A US 3528861A US 731649 A US731649 A US 731649A US 3528861D A US3528861D A US 3528861DA US 3528861 A US3528861 A US 3528861A
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- Prior art keywords
- coating
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- superalloys
- cobalt
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- Expired - Lifetime
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- 238000000576 coating method Methods 0.000 title description 33
- 239000011248 coating agent Substances 0.000 title description 29
- 238000000034 method Methods 0.000 title description 14
- 229910000601 superalloy Inorganic materials 0.000 title description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 24
- 229910045601 alloy Inorganic materials 0.000 description 15
- 239000000956 alloy Substances 0.000 description 15
- 229910052742 iron Inorganic materials 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 239000011651 chromium Substances 0.000 description 11
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 10
- 229910052804 chromium Inorganic materials 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 229910052727 yttrium Inorganic materials 0.000 description 9
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229910052761 rare earth metal Inorganic materials 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 239000011324 bead Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 150000002910 rare earth metals Chemical class 0.000 description 4
- 238000005482 strain hardening Methods 0.000 description 4
- 239000010936 titanium Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 238000005422 blasting Methods 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000005480 shot peening Methods 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000684 Cobalt-chrome Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910018487 Ni—Cr Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910000946 Y alloy Inorganic materials 0.000 description 1
- WAIPAZQMEIHHTJ-UHFFFAOYSA-N [Cr].[Co] Chemical compound [Cr].[Co] WAIPAZQMEIHHTJ-UHFFFAOYSA-N 0.000 description 1
- 238000005270 abrasive blasting Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000011825 aerospace material Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- -1 at the composition Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000010952 cobalt-chrome Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000005486 sulfidation Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
- C23C14/5806—Thermal treatment
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/03—Alloys based on nickel or cobalt based on nickel
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/10—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of nickel or cobalt or alloys based thereon
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/14—Metallic material, boron or silicon
- C23C14/16—Metallic material, boron or silicon on metallic substrates or on substrates of boron or silicon
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
- C23C14/5886—Mechanical treatment
-
- 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
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F17/00—Multi-step processes for surface treatment of metallic material involving at least one process provided for in class C23 and at least one process covered by subclass C21D or C22F or class C25
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T50/00—Aeronautics or air transport
- Y02T50/60—Efficient propulsion technologies, e.g. for aircraft
Definitions
- the present invention relates to improved methods of processing various alloys, particularly the nickel-base and cobalt-base superalloys, to provide a corrosion resistant coating thereon of long term durability.
- a coating composition for the nickel-base and cobalt-base alloys which comprises iron, chromium, aluminum, and yttrium or a rare earth particularly at the composition, by weight, 20-50 percent chromium, 10-20 percent aluminum, 0.03-2 percent yttrium/rare earth, balance iron.
- the present invention is particularly effective in eliminating the deterimental intergranular precipitate which has been found to occur during the deposition cycle of the coating process.
- This invention describes an improved coating process for imparting long term corrosion resistance to various alloys, including the nickel-base and cobalt-base superalloys.
- a cold-working/heat-treatment sequence to minimize the size and effect of any undesirable intergranular precipitate which may be formed in the deposition process.
- coated articles are coldworked by shot peening, particularly glass bead blasting.
- articles formed from the nickel-base and cobalt-base alloys are: coated with a composition comprising iron, chromium, aluminum and yttrium or a rare earth; heat treated following coating; cold-worked; and heat treated to effect recrystallization.
- articles formed from the nickel-base and cobalt base superalloys are: coated in a vacuum chamber to a thickness of 0.003-0.005 inch with a composition comprising, by weight, 25-29 percent chromium, 12-14 percent aluminum, 0.6-0.9 percent yttrium, balance iron; following coating, the articles are heated to about 1900 F. for 4 hours in a non-oxidizing atmosphere, and cooled; the coated surfaces are dry glass bead peened; and, following peening the coated parts are held at about 1975 F. for 4 hours in a non-oxidizing atmosphere.
- the present invention was developed primarily to increase the oxidation, sulfidation, erosion and thermal shock resistance of gas turbine blades and vanes formed of the nickel-base and cobalt-base superalloys.
- the superalloys will be understood to be those strong, high temperature materials which find particular utility in the very demanding environments. Representative of these alloys are those identified in the industry as follows:
- Alloy Composition (percent by weight) IN 10 Cr, 15 Co, 4.5 Ti, 5.5 A1, 3 Mo, .17 C, .75 V, .075 Zr, .015 B, balance Ni MAR-M200 9 or, 10 Co, 2 Ti, 5 A1, 12.5 w, .15 C, 1 Nb, .05 Zr, .015 B, balance
- the characteristic of the typical superalloy is its basis as a nickel-chromium or cobalt-chromium solid solution with additions of aluminum, titanium and/or of refractory metals for strengthening, and carbon, boron and zironium to promote creep-rupture ductility.
- the effect of the detrimental precipitate is eliminated with a corresponding increase in useful coating life by compressively stressing the coating through cold-working and subsequently heat treating the coating to cause recrystallization.
- This treatment which is preferably performed utilizing shot peening or glass bead blasting, breaks up the precipitate into small particles which are more easily taken into solution by heat treatment and which are, in any event, more homogeneously distributed throughout the coating. Accordingly, exposure of the substrate to corrosive attack along the line of the intergranular precipitate is prevented.
- the surfaces to be coated are first thoroughly cleaned free of all dirt, grease and other objectionable foreign matter, then conditioned by abrasive blasting followed by power flushing with clean water.
- the coating is achieved by vapor deposition from a molten pool of the coating alloy in a vacuum chamber held at 10- Torr or better.
- the melt chemistry is preferably of the following composition:
- the parts are preheated in the vacuum chamber at 1750 F. for 5 minutes before deposition is commenced and maintained at temperature during coating. Deposition time varies somewhat but is controlled to obtain the preferred coating thickness for the exterior of blades and vanes of 0.003-0.005, excluding diffused zone. Subsequent cooling to below 1000 F. is accomplished in a non-oxidizing atmosphere at a rate equivalent to'air cooling. Following coating, the parts are heated to 1900 F. in vacuum; held at heat for 4 hours; and cooled in a non-oxidizing atmosphere at a rate equivalent to air coolmg.
- coated surfaces are then dry glass bead peened using 0.007-0.011 inch diameter beads with an intensity equivalent to N, the peening being conducted in accordance with the provisions of the Aerospace Materials Specifications AMS 2430B.
- the post-peening heat treatment involves heating to 1975 F. in dry argon, dry hydrogen or vacuum, holding at heat for 4 hours, and cooling at a rate equivalent to air cooling.
- Blades and vanes so processed exhibit a uniform coatin-g having a thickness, excluding diffused zone, of 0.003- 0.005 inch.
- the diffused zone for the nickel-base superalloys is 0.0010.002 inch and for the cobalt-base alloys 0.005-00015 inch.
- the method of imparting high temperature corrosion resistance to the nickel-base and cobalt-base alloys which comprises the steps of coating the alloys with a composition consisting essentially of, by weight, 2050 percent chromium, 10-20 percent aluminum, 0.03-2 percent selected from the group consisting of yttrium and the rare earth elements, balance iron;
- the coating consists essentially of, by weight, about 25-29 percent chromium, 12-14 percent aluminum, O.60.9 yttrium, balance iron, to a thickness of at least 0.003 inch.
- composition consisting essentially of, by weight, 20-50 percent chromium, 10- 20 percent aluminum, 0.03-2 percent selected from the group consisting of yttrium and the rare earth elements, balance iron;
- the coat ing consists essentially of, by weight, about 2529 percent chromium, 12-l4 percent aluminum, 0.6-0.9 percent yttrium, balance iron to a thickness of 0.0030.005 inch.
- coating is accomplished by vapor deposition from a molten pool of the coating composition in a vacuum chamber.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Physical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
Description
United States Patent 01 fee US. Cl. 148-115 7 Claims ABSTRACT OF THE DISCLOSURE A method of coating the superalloys, particularly with an iron/chromium/aluminum/yttrium alloy, including cold-Working and subsequent heat treatment of the coating to minimize the size of the intergranular precipitate and thereby prolong the useful life of the superalloy.
CROSS-REFERENCE TO RELATED APPLICATION This applicttion is related to and shares a common assignee with a copending application entitled Iron Base Coating for the Superalloys, Ser. No. 731,650, by F. P. Talboom, Jr. and J. Grafwallner.
BACKGROUND OF THE INVENTION The present invention relates to improved methods of processing various alloys, particularly the nickel-base and cobalt-base superalloys, to provide a corrosion resistant coating thereon of long term durability.
In the copending application entitled Iron Base Coating for the Superalloys, Ser. No. 731,650, mentioned previously, there is described a coating composition for the nickel-base and cobalt-base alloys which comprises iron, chromium, aluminum, and yttrium or a rare earth particularly at the composition, by weight, 20-50 percent chromium, 10-20 percent aluminum, 0.03-2 percent yttrium/rare earth, balance iron. The present invention is particularly effective in eliminating the deterimental intergranular precipitate which has been found to occur during the deposition cycle of the coating process.
SUMMARY OF THE INVENTION This invention describes an improved coating process for imparting long term corrosion resistance to various alloys, including the nickel-base and cobalt-base superalloys. In particular it contemplates, as part of a coating process, a cold-working/heat-treatment sequence, to minimize the size and effect of any undesirable intergranular precipitate which may be formed in the deposition process.
In the preferred process the coated articles are coldworked by shot peening, particularly glass bead blasting.
In the more preferred process, articles formed from the nickel-base and cobalt-base alloys are: coated with a composition comprising iron, chromium, aluminum and yttrium or a rare earth; heat treated following coating; cold-worked; and heat treated to effect recrystallization.
In the most preferred process, articles formed from the nickel-base and cobalt base superalloys are: coated in a vacuum chamber to a thickness of 0.003-0.005 inch with a composition comprising, by weight, 25-29 percent chromium, 12-14 percent aluminum, 0.6-0.9 percent yttrium, balance iron; following coating, the articles are heated to about 1900 F. for 4 hours in a non-oxidizing atmosphere, and cooled; the coated surfaces are dry glass bead peened; and, following peening the coated parts are held at about 1975 F. for 4 hours in a non-oxidizing atmosphere.
3,528,861 Patented Sept. 15 1970 DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention was developed primarily to increase the oxidation, sulfidation, erosion and thermal shock resistance of gas turbine blades and vanes formed of the nickel-base and cobalt-base superalloys. The superalloys will be understood to be those strong, high temperature materials which find particular utility in the very demanding environments. Representative of these alloys are those identified in the industry as follows:
Alloy: Composition (percent by weight) IN 10 Cr, 15 Co, 4.5 Ti, 5.5 A1, 3 Mo, .17 C, .75 V, .075 Zr, .015 B, balance Ni MAR-M200 9 or, 10 Co, 2 Ti, 5 A1, 12.5 w, .15 C, 1 Nb, .05 Zr, .015 B, balance The characteristic of the typical superalloy is its basis as a nickel-chromium or cobalt-chromium solid solution with additions of aluminum, titanium and/or of refractory metals for strengthening, and carbon, boron and zironium to promote creep-rupture ductility.
It has been discovered, as described in the copending application, that an alloy of the composition, by weight, 20-50 percent chromium, 10-20 percent aluminum, 0.03- 2 percent yttrium/rare earth, balance iron will provide long term corrosion protection to the superalloys when applied as a coating. However, the coating effectiveness has been found to be limited by the formation of an intergranular precipitate during the coating deposition cycle.
In accordance with the present invention the effect of the detrimental precipitate is eliminated with a corresponding increase in useful coating life by compressively stressing the coating through cold-working and subsequently heat treating the coating to cause recrystallization. This treatment, which is preferably performed utilizing shot peening or glass bead blasting, breaks up the precipitate into small particles which are more easily taken into solution by heat treatment and which are, in any event, more homogeneously distributed throughout the coating. Accordingly, exposure of the substrate to corrosive attack along the line of the intergranular precipitate is prevented.
In the preferred method of coating the nickel-base and cobalt-base turbine blades and vanes, the surfaces to be coated are first thoroughly cleaned free of all dirt, grease and other objectionable foreign matter, then conditioned by abrasive blasting followed by power flushing with clean water.
The coating is achieved by vapor deposition from a molten pool of the coating alloy in a vacuum chamber held at 10- Torr or better. The melt chemistry is preferably of the following composition:
The parts are preheated in the vacuum chamber at 1750 F. for 5 minutes before deposition is commenced and maintained at temperature during coating. Deposition time varies somewhat but is controlled to obtain the preferred coating thickness for the exterior of blades and vanes of 0.003-0.005, excluding diffused zone. Subsequent cooling to below 1000 F. is accomplished in a non-oxidizing atmosphere at a rate equivalent to'air cooling. Following coating, the parts are heated to 1900 F. in vacuum; held at heat for 4 hours; and cooled in a non-oxidizing atmosphere at a rate equivalent to air coolmg.
The coated surfaces are then dry glass bead peened using 0.007-0.011 inch diameter beads with an intensity equivalent to N, the peening being conducted in accordance with the provisions of the Aerospace Materials Specifications AMS 2430B.
The post-peening heat treatment involves heating to 1975 F. in dry argon, dry hydrogen or vacuum, holding at heat for 4 hours, and cooling at a rate equivalent to air cooling.
Blades and vanes so processed exhibit a uniform coatin-g having a thickness, excluding diffused zone, of 0.003- 0.005 inch. The diffused zone for the nickel-base superalloys is 0.0010.002 inch and for the cobalt-base alloys 0.005-00015 inch.
While the present invention has been described in connection with certain preferred embodiments, these will be understood to be illustrative only. Those modifications to the invention evident to those skilled in the art from the teachings herein will, in the true spirit of the invention, be embraced within the scope of the appended claims.
What is claimed is:
1. The method of imparting high temperature corrosion resistance to the nickel-base and cobalt-base alloys which comprises the steps of coating the alloys with a composition consisting essentially of, by weight, 2050 percent chromium, 10-20 percent aluminum, 0.03-2 percent selected from the group consisting of yttrium and the rare earth elements, balance iron;
cold-working the coated surfaces to fracture any intergranular precipitates formed in the coating process; and
heat treating the cold-worked alloys to effect recrystallization of the coating.
2. The method according to claim 1 wherein the coating consists essentially of, by weight, about 25-29 percent chromium, 12-14 percent aluminum, O.60.9 yttrium, balance iron, to a thickness of at least 0.003 inch.
3. The method of imparting corrosion resistance to articles formed from the nickel-base and cobalt-base super-alloys which comprises the steps of:
coating the articles with a composition consisting essentially of, by weight, 20-50 percent chromium, 10- 20 percent aluminum, 0.03-2 percent selected from the group consisting of yttrium and the rare earth elements, balance iron;
heat treating the coated articles at about 1900 F.;
peening the coated surfaces; and
heat treating the peened articles to effect recrystallization of the coating.
4. The method according to claim 3 wherein the recrystallization heat treatment is conducted at a temperature of about 1975 F.
5. The method according to claim 3 wherein the coat ing consists essentially of, by weight, about 2529 percent chromium, 12-l4 percent aluminum, 0.6-0.9 percent yttrium, balance iron to a thickness of 0.0030.005 inch.
6. The method according to claim 5 wherein coating is accomplished by vapor deposition from a molten pool of the coating composition in a vacuum chamber.
7. In the processes wherein the high temperature alloys are coated with composition providing long term corrosion resistance thereto, the improvement which comprises:
peening the surface of the coated alloy; and
subsequently heat treating the alloy to effect recrystallization of the coating.
References Cited UNITED STATES PATENTS 2,683,305 7/1954 Goetzel 29--527.2 2,871,150 l/1959 Fraser et al 148-l1.5 3,034,934 5/1962 Redden l4811.5
L. DEWAYNE RUTLEDGE, Primary Examiner W. W. STALLARD, Assistant Examiner US. Cl. X.R. 7247; 148l2
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73164968A | 1968-05-23 | 1968-05-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3528861A true US3528861A (en) | 1970-09-15 |
Family
ID=24940407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US731649A Expired - Lifetime US3528861A (en) | 1968-05-23 | 1968-05-23 | Method for coating the superalloys |
Country Status (7)
Country | Link |
---|---|
US (1) | US3528861A (en) |
BE (1) | BE732801A (en) |
CH (1) | CH540994A (en) |
DE (1) | DE1924092C2 (en) |
FR (1) | FR2010478B1 (en) |
GB (1) | GB1261261A (en) |
SE (1) | SE345145B (en) |
Cited By (40)
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US3951642A (en) * | 1974-11-07 | 1976-04-20 | General Electric Company | Metallic coating powder containing Al and Hf |
US3976436A (en) * | 1975-02-13 | 1976-08-24 | General Electric Company | Metal of improved environmental resistance |
US4071638A (en) * | 1974-11-07 | 1978-01-31 | General Electric Company | Method of applying a metallic coating with improved resistance to high temperature to environmental conditions |
US4086391A (en) * | 1975-06-23 | 1978-04-25 | United Technologies Corporation | Alumina forming coatings containing hafnium for high temperature applications |
US4151017A (en) * | 1976-05-07 | 1979-04-24 | Maschinenfabric Augsburg-Nurnberg Aktiengesellschaft | Method of producing heat-resistant parts |
US4168183A (en) * | 1978-06-23 | 1979-09-18 | University Of Delaware | Process for improving the fatigue properties of structures or objects |
FR2430461A1 (en) * | 1978-07-04 | 1980-02-01 | Bulten Kanthal Ab | ALLOY LAYER OBTAINED BY HOT SPRAYING AND METHOD FOR OBTAINING SAME |
DE3229293A1 (en) * | 1981-08-05 | 1983-03-24 | United Technologies Corp., 06101 Hartford, Conn. | COVERINGS FOR SUPER ALLOYS |
US4401697A (en) * | 1980-01-07 | 1983-08-30 | United Technologies Corporation | Method for producing columnar grain ceramic thermal barrier coatings |
US4405659A (en) * | 1980-01-07 | 1983-09-20 | United Technologies Corporation | Method for producing columnar grain ceramic thermal barrier coatings |
US4405660A (en) * | 1980-01-07 | 1983-09-20 | United Technologies Corporation | Method for producing metallic articles having durable ceramic thermal barrier coatings |
US4414249A (en) * | 1980-01-07 | 1983-11-08 | United Technologies Corporation | Method for producing metallic articles having durable ceramic thermal barrier coatings |
WO1994001244A1 (en) * | 1992-07-10 | 1994-01-20 | Sandvik Ab | Method of blasting cutting tool inserts and the resulting inserts |
EP0676481A2 (en) * | 1994-03-25 | 1995-10-11 | Ngk Insulators, Ltd. | Alloy for high resistivity heater |
EP1160352A1 (en) * | 2000-05-31 | 2001-12-05 | ALSTOM Power N.V. | Method of adjusting the size of cooling holes of a gas turbine component |
EP1251191A1 (en) | 2001-04-21 | 2002-10-23 | ALSTOM (Switzerland) Ltd | A method of repairing a ceramic coating |
US6569492B2 (en) | 2000-06-05 | 2003-05-27 | Alstom Ltd | Process for repairing a coated component |
WO2003057944A2 (en) | 2002-01-10 | 2003-07-17 | Alstom Technology Ltd. | Mcraly bond coating and method of depositing said mcraly bond coating |
US20040079648A1 (en) * | 2002-10-15 | 2004-04-29 | Alstom (Switzerland) Ltd. | Method of depositing an oxidation and fatigue resistant MCrAIY-coating |
US20040108019A1 (en) * | 2002-12-06 | 2004-06-10 | Alstom Technology Ltd. | Non-destructive testing method of determining the depletion of a coating |
US6773753B2 (en) | 2001-08-14 | 2004-08-10 | Alstom Technology Ltd | Process for treating a coated gas turbine part, and coated gas turbine part |
US20040159552A1 (en) * | 2002-12-06 | 2004-08-19 | Alstom Technology Ltd. | Method of depositing a local MCrAIY-coating |
US20040159376A1 (en) * | 2002-12-06 | 2004-08-19 | Alstom Technology Ltd | Non-destructive testing method of determining the service metal temperature of a component |
US20040163583A1 (en) * | 2002-12-06 | 2004-08-26 | Alstom Technology Ltd. | Method of depositing a local MCrAIY-coating |
US20040234808A1 (en) * | 2001-09-22 | 2004-11-25 | Alexander Schnell | Mcraly-coating |
US20040244676A1 (en) * | 2001-09-22 | 2004-12-09 | Alexander Schnell | Method of growing a mcraly-coating and an article coated with the mcraly-coating |
DE10337019A1 (en) * | 2003-08-12 | 2005-03-10 | Alstom Technology Ltd Baden | Blade of gas turbine, comprising ceramic protection coating with partially polished areas for reduced heat generation |
US6924045B2 (en) | 2001-05-25 | 2005-08-02 | Alstom Technology Ltd | Bond or overlay MCrAIY-coating |
EP1752553A2 (en) | 2005-08-04 | 2007-02-14 | United Technologies Corporation | Method for microstructure control of ceramic thermal spray coating |
US20070160873A1 (en) * | 2006-01-10 | 2007-07-12 | United Technologies Corporation | Thermal barrier coating compositions, processes for applying same and articles coated with same |
EP1829984A1 (en) | 2006-03-01 | 2007-09-05 | United Technologies Corporation | High Density Thermal Barrier Coating |
US20070231589A1 (en) * | 2006-04-04 | 2007-10-04 | United Technologies Corporation | Thermal barrier coatings and processes for applying same |
US20080113218A1 (en) * | 2006-01-10 | 2008-05-15 | United Technologies Corporation | Thermal barrier coating compositions, processes for applying same and articles coated with same |
US20080113217A1 (en) * | 2006-01-10 | 2008-05-15 | United Technologies Corporation | Thermal barrier coating compositions, processes for applying same and articles coated with same |
EP1939326A2 (en) | 2006-12-22 | 2008-07-02 | United Technologies Corporation | Process for preventing the formation of secondary reaction zone in susceptible articles, and articles manufactured using same |
EP2014786A1 (en) | 2007-07-11 | 2009-01-14 | United Technologies Corporation | Process for controlling fatigue debit of a coated article |
US20100098923A1 (en) * | 2006-10-05 | 2010-04-22 | United Technologies Corporation | Segmented abradable coatings and process (ES) for applying the same |
US20100159149A1 (en) * | 2008-12-24 | 2010-06-24 | United Technologies Corporation | Apparatus for reducing stress when applying coatings, processes for applying the same and their coated articles |
US20120222961A1 (en) * | 2010-12-30 | 2012-09-06 | Michel Shawn Smallwood | System, method, and apparatus for leaching cast components |
CN111041436A (en) * | 2019-11-15 | 2020-04-21 | 中国科学院宁波材料技术与工程研究所 | Fe-Cr-Al-Y protective coating for zirconium alloy protection and preparation method and application thereof |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1397066A (en) * | 1971-06-19 | 1975-06-11 | Rolls Royce | High temperature corrosion resistant alloys |
GB1521293A (en) * | 1975-03-06 | 1978-08-16 | Secr Defence | Production of alloys |
US4253884A (en) * | 1979-08-29 | 1981-03-03 | Special Metals Corporation | Treating nickel base alloys |
US4253885A (en) * | 1979-08-29 | 1981-03-03 | Special Metals Corporation | Treating nickel base alloys |
DE4226272C1 (en) * | 1992-08-08 | 1994-02-10 | Mtu Muenchen Gmbh | Process for treating MCrAlZ layers and components produced using the process |
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- 1969-05-09 GB GB23700/69A patent/GB1261261A/en not_active Expired
- 1969-05-12 DE DE19691924092 patent/DE1924092C2/en not_active Expired
- 1969-05-21 FR FR696916816A patent/FR2010478B1/fr not_active Expired
- 1969-05-21 SE SE7215/69A patent/SE345145B/xx unknown
- 1969-05-23 CH CH788869A patent/CH540994A/en not_active IP Right Cessation
Patent Citations (3)
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US2683305A (en) * | 1949-07-15 | 1954-07-13 | Sintercast Corp | Molybdenum coated article and method of making |
US2871150A (en) * | 1955-09-19 | 1959-01-27 | Westinghouse Electric Corp | Method of cladding molybdenum |
US3034934A (en) * | 1960-03-31 | 1962-05-15 | Gen Electric | Method for processing of refractory metals |
Cited By (69)
Publication number | Priority date | Publication date | Assignee | Title |
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US3951642A (en) * | 1974-11-07 | 1976-04-20 | General Electric Company | Metallic coating powder containing Al and Hf |
US4071638A (en) * | 1974-11-07 | 1978-01-31 | General Electric Company | Method of applying a metallic coating with improved resistance to high temperature to environmental conditions |
US3976436A (en) * | 1975-02-13 | 1976-08-24 | General Electric Company | Metal of improved environmental resistance |
US4086391A (en) * | 1975-06-23 | 1978-04-25 | United Technologies Corporation | Alumina forming coatings containing hafnium for high temperature applications |
US4151017A (en) * | 1976-05-07 | 1979-04-24 | Maschinenfabric Augsburg-Nurnberg Aktiengesellschaft | Method of producing heat-resistant parts |
US4168183A (en) * | 1978-06-23 | 1979-09-18 | University Of Delaware | Process for improving the fatigue properties of structures or objects |
FR2430461A1 (en) * | 1978-07-04 | 1980-02-01 | Bulten Kanthal Ab | ALLOY LAYER OBTAINED BY HOT SPRAYING AND METHOD FOR OBTAINING SAME |
US4405660A (en) * | 1980-01-07 | 1983-09-20 | United Technologies Corporation | Method for producing metallic articles having durable ceramic thermal barrier coatings |
US4401697A (en) * | 1980-01-07 | 1983-08-30 | United Technologies Corporation | Method for producing columnar grain ceramic thermal barrier coatings |
US4405659A (en) * | 1980-01-07 | 1983-09-20 | United Technologies Corporation | Method for producing columnar grain ceramic thermal barrier coatings |
US4414249A (en) * | 1980-01-07 | 1983-11-08 | United Technologies Corporation | Method for producing metallic articles having durable ceramic thermal barrier coatings |
DE3229293A1 (en) * | 1981-08-05 | 1983-03-24 | United Technologies Corp., 06101 Hartford, Conn. | COVERINGS FOR SUPER ALLOYS |
WO1994001244A1 (en) * | 1992-07-10 | 1994-01-20 | Sandvik Ab | Method of blasting cutting tool inserts and the resulting inserts |
US6132293A (en) * | 1992-07-10 | 2000-10-17 | Sandvik Ab | Method of blasting cutting tool inserts |
EP0676481A3 (en) * | 1994-03-25 | 1995-11-15 | Ngk Insulators Ltd | |
EP0676481A2 (en) * | 1994-03-25 | 1995-10-11 | Ngk Insulators, Ltd. | Alloy for high resistivity heater |
EP1160352A1 (en) * | 2000-05-31 | 2001-12-05 | ALSTOM Power N.V. | Method of adjusting the size of cooling holes of a gas turbine component |
US6623790B2 (en) * | 2000-05-31 | 2003-09-23 | Alstom (Switzerland) Ltd | Method of adjusting the size of cooling holes of a gas turbine component |
US6569492B2 (en) | 2000-06-05 | 2003-05-27 | Alstom Ltd | Process for repairing a coated component |
EP1251191A1 (en) | 2001-04-21 | 2002-10-23 | ALSTOM (Switzerland) Ltd | A method of repairing a ceramic coating |
US6890587B2 (en) | 2001-04-21 | 2005-05-10 | Alstom Technology Ltd | Method of repairing a ceramic coating |
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US6773753B2 (en) | 2001-08-14 | 2004-08-10 | Alstom Technology Ltd | Process for treating a coated gas turbine part, and coated gas turbine part |
US7094475B2 (en) | 2001-09-22 | 2006-08-22 | Alstom Technology Ltd | MCrAlY-coating |
US20040234808A1 (en) * | 2001-09-22 | 2004-11-25 | Alexander Schnell | Mcraly-coating |
US20040244676A1 (en) * | 2001-09-22 | 2004-12-09 | Alexander Schnell | Method of growing a mcraly-coating and an article coated with the mcraly-coating |
US7014923B2 (en) | 2001-09-22 | 2006-03-21 | Alstom Technology Ltd | Method of growing a MCrAlY-coating and an article coated with the MCrAlY-coating |
US20070281103A1 (en) * | 2002-01-10 | 2007-12-06 | Alstom Technology Ltd | MCrAIY BOND COATING AND METHOD OF DEPOSITING SAID MCrAIY BOND COATING |
US7264887B2 (en) | 2002-01-10 | 2007-09-04 | Alstom Technology Ltd. | MCrAlY bond coating and method of depositing said MCrAlY bond coating |
WO2003057944A2 (en) | 2002-01-10 | 2003-07-17 | Alstom Technology Ltd. | Mcraly bond coating and method of depositing said mcraly bond coating |
US20050003227A1 (en) * | 2002-01-10 | 2005-01-06 | Alstom Technology Ltd | MCrAIY bond coating and method of depositing said MCrAIY bond coating |
US20040079648A1 (en) * | 2002-10-15 | 2004-04-29 | Alstom (Switzerland) Ltd. | Method of depositing an oxidation and fatigue resistant MCrAIY-coating |
US20040108019A1 (en) * | 2002-12-06 | 2004-06-10 | Alstom Technology Ltd. | Non-destructive testing method of determining the depletion of a coating |
US20040163583A1 (en) * | 2002-12-06 | 2004-08-26 | Alstom Technology Ltd. | Method of depositing a local MCrAIY-coating |
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Also Published As
Publication number | Publication date |
---|---|
DE1924092C2 (en) | 1971-03-04 |
SE345145B (en) | 1972-05-15 |
FR2010478B1 (en) | 1974-06-14 |
FR2010478A1 (en) | 1970-02-20 |
BE732801A (en) | 1969-10-16 |
GB1261261A (en) | 1972-01-26 |
CH540994A (en) | 1973-08-31 |
DE1924092B1 (en) | 1970-07-30 |
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