US3649225A - Composite coating for the superalloys - Google Patents

Composite coating for the superalloys Download PDF

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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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chromium
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interlayer
aluminum
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Alfred E Simmons Jr
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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • C23C14/16Metallic material, boron or silicon on metallic substrates or on substrates of boron or silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5806Thermal treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5886Mechanical treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating 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
    • C23C28/02Coating 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
    • C23C28/023Coating 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
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/938Vapor deposition or gas diffusion
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12736Al-base component
    • Y10T428/12743Next to refractory [Group IVB, VB, or VIB] metal-base component
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12778Alternative base metals from diverse categories
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12806Refractory [Group IVB, VB, or VIB] metal-base component
    • Y10T428/12826Group VIB metal-base component
    • Y10T428/12847Cr-base component
    • Y10T428/12854Next 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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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)

  1. 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.
  2. 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.
  3. 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.
US877321A 1969-11-17 1969-11-17 Composite coating for the superalloys Expired - Lifetime US3649225A (en)

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US3755887A (en) * 1971-11-12 1973-09-04 Continental Can Co Method of making cobalt alloy steel composite article
US3849865A (en) * 1972-10-16 1974-11-26 Nasa Method of protecting the surface of a substrate
US3869779A (en) * 1972-10-16 1975-03-11 Nasa Duplex aluminized coatings
US3904382A (en) * 1974-06-17 1975-09-09 Gen Electric Corrosion-resistant coating for superalloys
US3918139A (en) * 1974-07-10 1975-11-11 United Technologies Corp MCrAlY type coating alloy
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US3957454A (en) * 1973-04-23 1976-05-18 General Electric Company Coated article
US4005989A (en) * 1976-01-13 1977-02-01 United Technologies Corporation Coated superalloy article
US4022587A (en) * 1974-04-24 1977-05-10 Cabot Corporation Protective nickel base alloy coatings
US4029477A (en) * 1975-10-29 1977-06-14 General Electric Company Coated Ni-Cr base dispersion-modified alloy article
US4080486A (en) * 1973-04-02 1978-03-21 General Electric Company Coating system for superalloys
US4109061A (en) * 1977-12-08 1978-08-22 United Technologies Corporation Method for altering the composition and structure of aluminum bearing overlay alloy coatings during deposition from metallic vapor
US4144380A (en) * 1976-06-03 1979-03-13 General Electric Company Claddings of high-temperature austenitic alloys for use in gas turbine buckets and vanes
US4148936A (en) * 1976-12-23 1979-04-10 General Electric Company Method for diffusion coating an Fe-Ni base alloy with chromium
FR2407272A1 (en) * 1977-10-31 1979-05-25 Howmet Turbine Components PROCESS FOR OBTAINING ARTICLES RESISTANT TO CORROSION AT HIGH TEMPERATURE
US4218007A (en) * 1979-02-22 1980-08-19 General Electric Company Method of diffusion bonding duplex sheet cladding to superalloy substrates
DE3229293A1 (en) * 1981-08-05 1983-03-24 United Technologies Corp., 06101 Hartford, Conn. COVERINGS FOR SUPER ALLOYS
EP0082660A1 (en) * 1981-12-18 1983-06-29 United Kingdom Atomic Energy Authority Apparatus for use in liquid alkali environment
US4743514A (en) * 1983-06-29 1988-05-10 Allied-Signal Inc. Oxidation resistant protective coating system for gas turbine components, and process for preparation of coated components
WO1989007159A1 (en) * 1988-02-05 1989-08-10 Siemens Aktiengesellschaft Metallic object, in particular gas turbine blade with protective coating
US4963440A (en) * 1987-07-09 1990-10-16 Kabushiki Kaisha Kobe Seiko Sho Al-Cr alloy vapor-deposited material
US5197852A (en) * 1990-05-31 1993-03-30 General Electric Company Nozzle band overhang cooling
US5384200A (en) * 1991-12-24 1995-01-24 Detroit Diesel Corporation Thermal barrier coating and method of depositing the same on combustion chamber component surfaces
US5500252A (en) * 1992-09-05 1996-03-19 Rolls-Royce Plc High temperature corrosion resistant composite coatings
US5499905A (en) * 1988-02-05 1996-03-19 Siemens Aktiengesellschaft Metallic component of a gas turbine installation having protective coatings
US5987882A (en) * 1996-04-19 1999-11-23 Engelhard Corporation System for reduction of harmful exhaust emissions from diesel engines
EP1033417A1 (en) * 1999-03-04 2000-09-06 Siemens Aktiengesellschaft Process and apparatus for coating a product, especially a high temperature gas turbine component
US6256984B1 (en) * 1996-04-19 2001-07-10 Engelhard Corporation System for reduction of harmful exhaust emissions from diesel engines
US6391479B1 (en) * 2000-12-21 2002-05-21 General Electric Company Coating interlayer for improved compatibility between HR-120 and aluminum-containing oxidation resistant metallic coatings
US6422008B2 (en) 1996-04-19 2002-07-23 Engelhard Corporation System for reduction of harmful exhaust emissions from diesel engines
US6655369B2 (en) 2001-08-01 2003-12-02 Diesel Engine Transformations Llc Catalytic combustion surfaces and method for creating catalytic combustion surfaces
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US20120321905A1 (en) * 2009-12-29 2012-12-20 Friedhelm Schmitz Nano and micro structured ceramic thermal barrier coating

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US3755887A (en) * 1971-11-12 1973-09-04 Continental Can Co Method of making cobalt alloy steel composite article
US3849865A (en) * 1972-10-16 1974-11-26 Nasa Method of protecting the surface of a substrate
US3869779A (en) * 1972-10-16 1975-03-11 Nasa Duplex aluminized coatings
US4080486A (en) * 1973-04-02 1978-03-21 General Electric Company Coating system for superalloys
US3957454A (en) * 1973-04-23 1976-05-18 General Electric Company Coated article
US4022587A (en) * 1974-04-24 1977-05-10 Cabot Corporation Protective nickel base alloy coatings
DE2520192A1 (en) * 1974-05-13 1975-11-27 United Technologies Corp HEAT-RESISTANT NICOCRALY COATINGS
US3928026A (en) * 1974-05-13 1975-12-23 United Technologies Corp High temperature nicocraly coatings
US3904382A (en) * 1974-06-17 1975-09-09 Gen Electric Corrosion-resistant coating for superalloys
US3918139A (en) * 1974-07-10 1975-11-11 United Technologies Corp MCrAlY type coating alloy
US4029477A (en) * 1975-10-29 1977-06-14 General Electric Company Coated Ni-Cr base dispersion-modified alloy article
US4005989A (en) * 1976-01-13 1977-02-01 United Technologies Corporation Coated superalloy article
US4144380A (en) * 1976-06-03 1979-03-13 General Electric Company Claddings of high-temperature austenitic alloys for use in gas turbine buckets and vanes
US4148936A (en) * 1976-12-23 1979-04-10 General Electric Company Method for diffusion coating an Fe-Ni base alloy with chromium
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US4109061A (en) * 1977-12-08 1978-08-22 United Technologies Corporation Method for altering the composition and structure of aluminum bearing overlay alloy coatings during deposition from metallic vapor
US4218007A (en) * 1979-02-22 1980-08-19 General Electric Company Method of diffusion bonding duplex sheet cladding to superalloy substrates
DE3006103A1 (en) * 1979-02-22 1980-09-04 Gen Electric METHOD FOR DIFFUSION CONNECTING A DOUBLE SHEET COVER TO A SUPER ALLOY SUBSTRATE
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EP0082660A1 (en) * 1981-12-18 1983-06-29 United Kingdom Atomic Energy Authority Apparatus for use in liquid alkali environment
US4743514A (en) * 1983-06-29 1988-05-10 Allied-Signal Inc. Oxidation resistant protective coating system for gas turbine components, and process for preparation of coated components
US4963440A (en) * 1987-07-09 1990-10-16 Kabushiki Kaisha Kobe Seiko Sho Al-Cr alloy vapor-deposited material
GB2214934B (en) * 1987-10-09 1992-10-07 Kobe Steel Ltd Al-cr alloy vapor-deposited material
US5499905A (en) * 1988-02-05 1996-03-19 Siemens Aktiengesellschaft Metallic component of a gas turbine installation having protective coatings
WO1989007159A1 (en) * 1988-02-05 1989-08-10 Siemens Aktiengesellschaft Metallic object, in particular gas turbine blade with protective coating
US5197852A (en) * 1990-05-31 1993-03-30 General Electric Company Nozzle band overhang cooling
US5384200A (en) * 1991-12-24 1995-01-24 Detroit Diesel Corporation Thermal barrier coating and method of depositing the same on combustion chamber component surfaces
US5500252A (en) * 1992-09-05 1996-03-19 Rolls-Royce Plc High temperature corrosion resistant composite coatings
US5987882A (en) * 1996-04-19 1999-11-23 Engelhard Corporation System for reduction of harmful exhaust emissions from diesel engines
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US6793968B1 (en) 1999-03-04 2004-09-21 Siemens Aktiengesellschaft Method and device for coating a product
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