US3649225A - Composite coating for the superalloys - Google Patents
Composite coating for the superalloys Download PDFInfo
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- US3649225A US3649225A US877321A US3649225DA US3649225A US 3649225 A US3649225 A US 3649225A US 877321 A US877321 A US 877321A US 3649225D A US3649225D A US 3649225DA US 3649225 A US3649225 A US 3649225A
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- 239000002131 composite material Substances 0.000 title claims abstract description 14
- 238000000576 coating method Methods 0.000 title abstract description 68
- 239000011248 coating agent Substances 0.000 title abstract description 51
- 229910000601 superalloy Inorganic materials 0.000 title abstract description 23
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 37
- 239000011651 chromium Substances 0.000 claims abstract description 37
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000000758 substrate Substances 0.000 claims abstract description 30
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 25
- 239000011229 interlayer Substances 0.000 claims abstract description 22
- 239000010410 layer Substances 0.000 claims abstract description 19
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 17
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims abstract description 17
- 230000003647 oxidation Effects 0.000 claims abstract description 16
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 16
- 239000010941 cobalt Substances 0.000 claims abstract description 9
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 22
- 239000000956 alloy Substances 0.000 claims description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 229910017052 cobalt Inorganic materials 0.000 claims description 6
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 12
- 229910000531 Co alloy Inorganic materials 0.000 abstract description 3
- 229910000640 Fe alloy Inorganic materials 0.000 abstract description 3
- 229910000990 Ni alloy Inorganic materials 0.000 abstract description 3
- 239000000470 constituent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 229910002543 FeCrAlY Inorganic materials 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 229910000951 Aluminide Inorganic materials 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000005254 chromizing Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000004901 spalling Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- 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
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- 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
- C23C14/5806—Thermal 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
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
- C23C28/02—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material
- C23C28/023—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material only coatings of metal elements only
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/938—Vapor deposition or gas diffusion
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12743—Next to refractory [Group IVB, VB, or VIB] metal-base component
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12778—Alternative base metals from diverse categories
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12806—Refractory [Group IVB, VB, or VIB] metal-base component
- Y10T428/12826—Group VIB metal-base component
- Y10T428/12847—Cr-base component
- Y10T428/12854—Next to Co-, Fe-, or Ni-base component
Definitions
- CoCrAlY coating comprising, by weight, 19-24 percent chromium, 13-17 percent aluminum, 0.6-0.9 percent yttrium, balance cobalt, hereinafter referred to as the CoCrAlY coating.
- a NiCrAlY coating comprising, by weight, 20-35 percent chromium, 15-20 percent aluminum, 0.050.3 percent yttrium, balance nickel is disclosed in application Ser. No. 734,740 filed June 5, 1968. All of the above coating alloys are resistant of oxidation, thermal spalling, and to interdifiusion with the substrate when compared to alternative coating schemes. However, it has been found that even with these advanced coatings there exists a measure of coating-substrate interdiffusion.
- a composite coating comprising a chromium or predominantly chromium interlayer at the superalloy surface to be protected and an outer layer of highoxidation resistance comprising an alloy of iron, cobalt or nickel containing selected amounts of chromium, aluminum and a rare earth element such as yttrium.
- the composite coating comprises an interlayer of chromium and an outer layer consisting essentially of, by weight, 25-29 percent chromium, 12-14 percent aluminum, 0.60.9 percent yttrium, balance iron.
- the composite coating comprises an interlayer of chromium and an outer layer consisting essentially of, by weight, 19-24 percent chromium, 13-17 percent aluminum, 0.60.9 percent yttrium, balance cobalt.
- component surface protection Prior to the generation of the FeCrAlY, CoCrAlY and NiCrAlY coating alloys, and as currently provided in production jet engines, component surface protection has nonnally been provided by exposing the substrate to aluminum or aluminum vapor at high temperature and promoting a reaction of the aluminum with one or more of the substrate constituents to form protective aluminides.
- the oxidation protection is effected, not by a coatingsubstrate reaction, but rather by the coating alloy per se.
- the coating alloy of itself is oxidation-resistant and relatively immune to thermal spalling and no intermediate coatings are required in terms of the basic function which the coating is to provide, nor in fact is any interdiffusion of substrate or intermediate layer constituents into the coating desired.
- an interlayer of chromium is provided to specifically reduce the outer coating-substrate interdifiusion and by so doing to improve the durability of the coating as demonstrated by an increased operating lifetime for a component so coated.
- the durability of the FeCrAlY-type coatings have been found to be limited not by deficiencies in the oxidationerosion resistance of the coatings per se, but rather is a function of the extent of aluminum depletion in the coating resultant from the coating-substrate interdifi'usion, particularly at temperatures in excess of about 2,000 F.
- chromium interlayer may be produced by any of the available methods for generating such coatings or surface layers including electroplating, electroplating plus diffusion heat treatment, pack cementation, plasma spray, slurry spray, or any other technique providing a predominantly chromium layer at or on the substrate surface. It is relatively immaterial how the interlayer formed subject, however, to the requirement that the process be one yielding an interlayer composed primarily of chromium.
- the FeCrAlY-type outer coatings are typically applied utilizing vacuum vapor deposition methods and apparatus. As explained, the efficacy of these coatings is dependent upon the correct coating alloy composition being deposited on the surface to be protected. These coatings are characterized by high-melting points as alloyed and by diverse melting points insofar as the elemental constituents are concerned. Care must taken in the coating formation process to provide all of the desired coating alloy species in the correct proportions in the coating as applied. Satisfactory results have been attained by vapor deposition in a vacuum utilizing an electron beam heat source, as suggested in the U.S. Pat. No. to Steigerwald 2,746,420.
- EXAMPLE Various nickel-base and cobalt-base superalloy parts to be coated were embedded in a pack of blended powders composed of, by weight, 84.5 percent alumina, 15 percent chromium, and 0.5 percent ammonium chloride. After purging with argon, the pack was sealed and the parts were chromized at 2,l F. for 4 hours. In general, surface buildups of 0002-0005 in. resulted from pack chromizing under these conditions.
- parts were mounted in the vacuum chamber of electron beam melting apparatus, preheated, and coated by vapor deposition from a molten pool of coating material in a vacuum of Torr or better to typical outer coating thicknesses of 0001-0005 in.
- the coated cobalt-base substrates were heat treated at 1,900 F. for about an hour in vacuum with a cool in a nonoxidizing atmosphere at a rate equivalent to air cool.
- the nickel-base superalloy substrates after coating, and the cobalt-base superalloy substrates after coating and heat treatment, as coated, were dry glass bead peened at N for about 2 minutes in accordance with AMS 2,430. Subsequent to peening the coated parts were heated to 1,975 F. in dry argon or hydrogen, or vacuum; held at heat for 4 hours; and cooled at a rate equivalent to air coolmg.
- CoCrAlY coating in the composite coating consisted of:
- a composite article resistant to oxidation at high temperature comprising:
- a substrate selected from the group consisting of the hightemperature nickel-base and cobalt-base alloys having strengths suitable for structural applications in a gas turbine engine environment,
- an interlayer adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
- the chromium content is 1 5-30 weight percent
- the aluminum content is l0-20 weight percent
- the rare earth element is yttrium
- the yttrium content is at least 0.1 weight percent.
- a coated gas turbine engine component comprising:
- a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys,
- an interlayer adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
- the outer layer consisting essentially of, by weight, 25-29 percent chromium, 10-14 percent aluminum, 0.4-0.9 percent yttrium, balance substantially iron.
- a coated gas turbine engine component comprising:
- a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys,
- an interlayer adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
- the outer layer consisting essentially of, by weight, 21-25 percent chromium, 10-1 5 percent aluminum, 0.4-0.9 percent yttrium, balance substantially cobalt.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Improved operating lifetimes are provided for the superalloys through use of a composite coating comprising a chromium or chromium-rich interlayer adjacent the superalloy substrate surface and an oxidation-resistant outer layer comprising an alloy of iron, cobalt and/or nickel alloyed with selected amounts of chromium, aluminum and yttrium.
Description
United States Patent Simmons, Jr.
[45] Mar. 14, 1972 [54] COMPOSITE COATING FOR THE 3,041,040 6/1962 Levinstein ....29/ 198 SUPERALLOYS 2,861,327 11/1958 Bechtold ....29/19s 3,552,953 l/197l Lemkey... ....75/l7l [721 lnvemorl Alfred slmmons, East Hartford 3,215,512 11/1965 Coad ..29/191 Conn.
[73] Assignee: United Aircraft Corporation, East Hart- Primary Emfniner flyland Bizot ford, Conn. Attorney-Richard N. James [22] Filed: NOV. 17, 196 [57] ABSTRACT [21] Appl. No.: 877,321
Improved operating lifetimes are provided for the superalloys [52] U.S. Cl. ..29/194, 29/1966, 29/198 hr gh use of a omp ite coa ing comprising a chromium or [51] Int. Cl ..B32b 15/00 chromium-rich interlayer adjacent the superalloy substrate [58] Field of Search ..29/ 198, 194, 196.6; 75/171 surface and an oxidation-resistant outer layer comprising an alloy of iron, cobalt and/or nickel alloyed with selected [56] References Cited amounts of chromium, aluminum and yttrium.
UNlTED STATES PATENTS 4 Claims, 1 Drawing Figure 2,993,264 7/1961 Grenoble ..29/198 KVPPf/l/T f/V/Nf fifQV/Pf/Wf/VZJ l \1 Q 1% Q \s COMPOSITE COATING FOR THE SUPERALLOYS BACKGROUND OF THE INVENTION The present invention relates in general to high-temperature, oxidation-resistant coatings for the superalloys, particularly as applied to gas turbine engine components.
A limiting factor in the application of many of the superalloys to demanding environments such as those encountered by jet engine hardware is their susceptibility to high-temperature oxidation and corrosion. For this reason these alloys are generally provided with suitable surface coatings for increased oxidation resistance. For current operating conditions the most widely used coatings have been provided by reacting aluminum with the alloy to form surface aluminides which preferentially oxidize to form surface oxides through which the transport rates of the oxidizing species are low. Typical of processes of this type is that described in the US. Pat. No. to Joseph 3,102,044.
Both turbine blade and vane life in existing engines, and the extent of power increases requiring higher engine operating temperatures, are largely limited by the durability of the coatings. In the past, the inadequacy of current coatings to give long term protection against corrosion at very high temperatures has prevented use of some of the stronger nickelbase alloys, such as B-l900, in applications where their properties otherwise indicate the desirability of their use.
At high temperatures in the dynamic oxidizing environment of a gas turbine engine, temperature fluctuations caused by the mixing of hot combustion gases with cooler secondary air, or those associated with variations in engine power levels, give rise to thermally induced strains in the coatings at the metaloxide interface which are sufficiently large to spall the protective oxide layer. Furthermore, at a temperature of about 2,000 F nickel and the nickel-base superalloys begin to exhibit a great alloying affinity for the usual coating constituents, and particularly for aluminum, as recognized in the US. Pat. No. to Maxwell 3,450,212. Thus, a loss of coating protection in a dynamic oxidizing environment at very high temperature, involves both an inward and an outward loss of one or more of the protective species.
In a series of copending applications of the present assig'nee, there are described a number of coating compositions for the superalloys which have doubled the endurance of the coated components at high temperature and have in addition permitted engine performance increases associated with the higher temperatures of current interest. In application Ser. No. 731,650, filed May 23, 1968 for an Iron Base Coating for the Superalloys, now US, Pat. No. 3,542,530 there is described a preferred coating alloy comprising, by weight, 25-29 percent chromium, 12-14 percent aluminum, 0.6-0.9 percent yttrium, balance iron, hereinafter referred to as the FeCrAlY coating. In application Ser. No. 795,616 filed Jan. 31, 1969 for a Cobalt Base Coating for the Superalloys, there is described a preferred coating composition comprising, by weight, 19-24 percent chromium, 13-17 percent aluminum, 0.6-0.9 percent yttrium, balance cobalt, hereinafter referred to as the CoCrAlY coating. A NiCrAlY coating comprising, by weight, 20-35 percent chromium, 15-20 percent aluminum, 0.050.3 percent yttrium, balance nickel is disclosed in application Ser. No. 734,740 filed June 5, 1968. All of the above coating alloys are resistant of oxidation, thermal spalling, and to interdifiusion with the substrate when compared to alternative coating schemes. However, it has been found that even with these advanced coatings there exists a measure of coating-substrate interdiffusion.
It is known that, in some instances, improved coating performance may be obtained through coating processes involving multiple surface treatments. In the U.S. Pat. No. to Gibson 2,809,127, the surface of an alloy is first chromized and then aluminized to increase the oxidation resistance at high temperature. As in the case of Joseph, supra, the basic oxidation protection in Gibson is dependent upon the reaction of aluminum with the constituents of the substrate at the surface to be protected.
SUMMARY OF THE INVENTION It is the object of the present invention to provide an improved coating for the superalloys characterized by long term durability in dynamic oxidizing environments at very high temperatures. There is provided a composite coating comprising a chromium or predominantly chromium interlayer at the superalloy surface to be protected and an outer layer of highoxidation resistance comprising an alloy of iron, cobalt or nickel containing selected amounts of chromium, aluminum and a rare earth element such as yttrium.
In a preferred embodiment of the invention, the composite coating comprises an interlayer of chromium and an outer layer consisting essentially of, by weight, 25-29 percent chromium, 12-14 percent aluminum, 0.60.9 percent yttrium, balance iron.
In another preferred embodiment, the composite coating comprises an interlayer of chromium and an outer layer consisting essentially of, by weight, 19-24 percent chromium, 13-17 percent aluminum, 0.60.9 percent yttrium, balance cobalt.
BRIEF DESCRIPTION OF THE DRAWING The drawing is a chart comparing the various coatings for the nickel-base superalloys in terms of durability.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Prior to the generation of the FeCrAlY, CoCrAlY and NiCrAlY coating alloys, and as currently provided in production jet engines, component surface protection has nonnally been provided by exposing the substrate to aluminum or aluminum vapor at high temperature and promoting a reaction of the aluminum with one or more of the substrate constituents to form protective aluminides. In the FeCrAlY-type coating system, the oxidation protection is effected, not by a coatingsubstrate reaction, but rather by the coating alloy per se. The coating alloy of itself is oxidation-resistant and relatively immune to thermal spalling and no intermediate coatings are required in terms of the basic function which the coating is to provide, nor in fact is any interdiffusion of substrate or intermediate layer constituents into the coating desired. In the present composite coating, an interlayer of chromium is provided to specifically reduce the outer coating-substrate interdifiusion and by so doing to improve the durability of the coating as demonstrated by an increased operating lifetime for a component so coated.
Thus, the durability of the FeCrAlY-type coatings have been found to be limited not by deficiencies in the oxidationerosion resistance of the coatings per se, but rather is a function of the extent of aluminum depletion in the coating resultant from the coating-substrate interdifi'usion, particularly at temperatures in excess of about 2,000 F.
It was found that a substantial improvement in the endurance of the FeCrAlY-type coatings can be provided by interposing an interlayer of chromium or a predominantly chromium alloy between the outer coating and the substrate to act as a diffusion barrier therebetween, minimizing the depletion of aluminum in the outer coating by this mechanism. This chromium interlayer may be produced by any of the available methods for generating such coatings or surface layers including electroplating, electroplating plus diffusion heat treatment, pack cementation, plasma spray, slurry spray, or any other technique providing a predominantly chromium layer at or on the substrate surface. It is relatively immaterial how the interlayer formed subject, however, to the requirement that the process be one yielding an interlayer composed primarily of chromium.
The FeCrAlY-type outer coatings are typically applied utilizing vacuum vapor deposition methods and apparatus. As explained, the efficacy of these coatings is dependent upon the correct coating alloy composition being deposited on the surface to be protected. These coatings are characterized by high-melting points as alloyed and by diverse melting points insofar as the elemental constituents are concerned. Care must taken in the coating formation process to provide all of the desired coating alloy species in the correct proportions in the coating as applied. Satisfactory results have been attained by vapor deposition in a vacuum utilizing an electron beam heat source, as suggested in the U.S. Pat. No. to Steigerwald 2,746,420.
It should be noted that it is the unique combination comprising the composite coating that provides the coating endurance improvements established by test. One of the incidents of the undesirable coating-substrate interdiffusion, in addition to aluminum depletion in the coating, is contamination of the substrate by the coating constituents. The use of the chromium interlayer has been found not only to prevent such detrimental contamination by the coating elements but also to provide none of itself. In addition, the chromium interlayer adjacent the FeCrAlY coating has appeared to provide no observable detrimental effect on the coating alloy itself nor on its adherence to the substrate.
Tests conducted on several nickel-base superalloy substrates, including such superalloys as B4900, MAR M200, and NX 188, and on the cobalt-base superalloys such as MAR M302, have indicated that coating life improvements on the order of 50 percent are achieved, as graphically illustrated in the drawing.
EXAMPLE Various nickel-base and cobalt-base superalloy parts to be coated were embedded in a pack of blended powders composed of, by weight, 84.5 percent alumina, 15 percent chromium, and 0.5 percent ammonium chloride. After purging with argon, the pack was sealed and the parts were chromized at 2,l F. for 4 hours. In general, surface buildups of 0002-0005 in. resulted from pack chromizing under these conditions.
Subsequent to the chromizing operation, parts were mounted in the vacuum chamber of electron beam melting apparatus, preheated, and coated by vapor deposition from a molten pool of coating material in a vacuum of Torr or better to typical outer coating thicknesses of 0001-0005 in.
Following deposition of the outer coating, the coated cobalt-base substrates were heat treated at 1,900 F. for about an hour in vacuum with a cool in a nonoxidizing atmosphere at a rate equivalent to air cool. The nickel-base superalloy substrates after coating, and the cobalt-base superalloy substrates after coating and heat treatment, as coated, were dry glass bead peened at N for about 2 minutes in accordance with AMS 2,430. Subsequent to peening the coated parts were heated to 1,975 F. in dry argon or hydrogen, or vacuum; held at heat for 4 hours; and cooled at a rate equivalent to air coolmg.
A variety of superalloy substrates were provided with several composite coating combinations, particularly with respect to the outer coating composition. After extensive testing, it was determined that the preferred FeCrAlY outer coating chemistry conformed to the following:
Component percent by weight chromium 25-29 aluminum 10.5-12.5 yttrium 0.4-0.9
oxygen 0.03 max. nitrogen 0.01 max. hydrogen 0.01 max.
0.5 max.
remainder other elements, total iron The most preferred CoCrAlY coating in the composite coating consisted of:
broader aspects it is not limited to the exact details described, for obvious modifications will occur to those skilled in the art.
What is claimed is:
l. A composite article resistant to oxidation at high temperature comprising:
a substrate selected from the group consisting of the hightemperature nickel-base and cobalt-base alloys having strengths suitable for structural applications in a gas turbine engine environment,
an interlayer, adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
and an oxidation resistant outer layer thereover, bonded to the interlayer, which consists essentially of chromium, aluminum, at least one rare earth element, and at least one element selected from the group consisting of iron, cobalt, and nickel.
2. A composite article according to claim 1 wherein: in the outer layer,
the chromium content is 1 5-30 weight percent,
the aluminum content is l0-20 weight percent,
the rare earth element is yttrium,
and the yttrium content is at least 0.1 weight percent.
3. A coated gas turbine engine component comprising:
a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys,
an interlayer, adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
and an oxidation resistant outer layer superimposed on and bonded to the interlayer, the outer layer consisting essentially of, by weight, 25-29 percent chromium, 10-14 percent aluminum, 0.4-0.9 percent yttrium, balance substantially iron.
4. A coated gas turbine engine component comprising:
a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys,
an interlayer, adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys,
and an oxidation resistant outer layer superimposed on and bonded to the interlayer, the outer layer consisting essentially of, by weight, 21-25 percent chromium, 10-1 5 percent aluminum, 0.4-0.9 percent yttrium, balance substantially cobalt.
Claims (3)
- 2. A composite article according to claim 1 wherein: in the outer layer, the chromium content is 15-30 weight percent, the aluminum content is 10-20 weight percent, the rare earth element is yttrium, and the yttrium content is at least 0.1 weight percent.
- 3. A coated gas turbine engine component comprising: a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys, an interlayer, adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys, and an oxidation resistant outer layer superimposed on and bonded to the interlayer, the outer layer consisting essentially of, by weight, 25-29 percent chromium, 10-14 percent aluminum, 0.4-0.9 percent yttrium, balance substantially iron.
- 4. A coated gas turbine engine component comprising: a substrate selected from the group consisting of the high temperature, high-strength nickel-base and cobalt-base alloys, an interlayer, adjacent the substrate surface and bonded thereto, selected from the group consisting of chromium and its alloys, and an oxidation resistant outer layer superimposed on and bonded to the interlayer, the outer layer consisting essentially of, by weight, 21-25 percent chromium, 10-15 percent aluminum, 0.4-0.9 percent yttrium, balance substantially cobalt.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US87732169A | 1969-11-17 | 1969-11-17 |
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US3649225A true US3649225A (en) | 1972-03-14 |
Family
ID=25369728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US877321A Expired - Lifetime US3649225A (en) | 1969-11-17 | 1969-11-17 | Composite coating for the superalloys |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2861327A (en) * | 1956-09-12 | 1958-11-25 | Westinghouse Electric Corp | Applying protective metal coatings on molybdenum |
US2993264A (en) * | 1955-12-23 | 1961-07-25 | Gen Electric | Protective coating for molybdenum |
US3041040A (en) * | 1955-12-23 | 1962-06-26 | Gen Electric | Metal clad blade |
US3215512A (en) * | 1961-06-09 | 1965-11-02 | Texas Instruments Inc | Composite refractory articles |
US3552953A (en) * | 1969-01-10 | 1971-01-05 | United Aircraft Corp | Cobalt-chromium base alloy and articles produced therefrom |
-
1969
- 1969-11-17 US US877321A patent/US3649225A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2993264A (en) * | 1955-12-23 | 1961-07-25 | Gen Electric | Protective coating for molybdenum |
US3041040A (en) * | 1955-12-23 | 1962-06-26 | Gen Electric | Metal clad blade |
US2861327A (en) * | 1956-09-12 | 1958-11-25 | Westinghouse Electric Corp | Applying protective metal coatings on molybdenum |
US3215512A (en) * | 1961-06-09 | 1965-11-02 | Texas Instruments Inc | Composite refractory articles |
US3552953A (en) * | 1969-01-10 | 1971-01-05 | United Aircraft Corp | Cobalt-chromium base alloy and articles produced therefrom |
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