EP1111091A1 - Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article - Google Patents
Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article Download PDFInfo
- Publication number
- EP1111091A1 EP1111091A1 EP00311496A EP00311496A EP1111091A1 EP 1111091 A1 EP1111091 A1 EP 1111091A1 EP 00311496 A EP00311496 A EP 00311496A EP 00311496 A EP00311496 A EP 00311496A EP 1111091 A1 EP1111091 A1 EP 1111091A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- coating
- substrate
- vapor deposition
- overlay
- transition metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 82
- 239000011248 coating agent Substances 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 41
- 229910000951 Aluminide Inorganic materials 0.000 title claims abstract description 25
- 239000000758 substrate Substances 0.000 claims abstract description 27
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000000919 ceramic Substances 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 238000005229 chemical vapour deposition Methods 0.000 claims abstract description 12
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 12
- 150000003624 transition metals Chemical class 0.000 claims abstract description 12
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000009713 electroplating Methods 0.000 claims abstract description 10
- 239000001301 oxygen Substances 0.000 claims abstract description 10
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 10
- 239000007921 spray Substances 0.000 claims abstract description 8
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 7
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 6
- 239000010703 silicon Substances 0.000 claims abstract description 6
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 6
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims abstract description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 24
- 229910052759 nickel Inorganic materials 0.000 claims description 12
- 230000003647 oxidation Effects 0.000 claims description 10
- 238000007254 oxidation reaction Methods 0.000 claims description 10
- 238000005260 corrosion Methods 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 claims description 9
- 239000010941 cobalt Substances 0.000 claims description 8
- 229910017052 cobalt Inorganic materials 0.000 claims description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 8
- 229910000601 superalloy Inorganic materials 0.000 claims description 8
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 6
- 238000005269 aluminizing Methods 0.000 claims description 6
- 238000005240 physical vapour deposition Methods 0.000 claims description 6
- 238000001912 gas jet deposition Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 238000005524 ceramic coating Methods 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 238000004544 sputter deposition Methods 0.000 claims description 3
- 229910002076 stabilized zirconia Inorganic materials 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- 239000010948 rhodium Substances 0.000 claims description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 claims description 2
- CMIHHWBVHJVIGI-UHFFFAOYSA-N gadolinium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[Gd+3].[Gd+3] CMIHHWBVHJVIGI-UHFFFAOYSA-N 0.000 claims 2
- 239000012720 thermal barrier coating Substances 0.000 abstract description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 5
- 230000004888 barrier function Effects 0.000 abstract description 4
- -1 platinum Chemical class 0.000 abstract description 3
- 239000007789 gas Substances 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 230000001464 adherent effect Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000012159 carrier gas Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 229910000510 noble metal Inorganic materials 0.000 description 3
- 229910001233 yttria-stabilized zirconia Inorganic materials 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000005328 electron beam physical vapour deposition 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
- 238000007750 plasma spraying Methods 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 229910001011 CMSX-4 Inorganic materials 0.000 description 1
- 229910017709 Ni Co Inorganic materials 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 102220106802 rs139353014 Human genes 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Images
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
- 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
- C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
- C23C28/34—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
- C23C28/345—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
- C23C28/3455—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer with a refractory ceramic layer, e.g. refractory metal oxide, ZrO2, rare earth oxides or a thermal barrier system comprising at least one refractory oxide layer
-
- 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
- C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
- C23C10/02—Pretreatment of the material to be coated
-
- 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
- C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
- C23C28/32—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
- C23C28/321—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer with at least one metal alloy layer
- C23C28/3215—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer with at least one metal alloy layer at least one MCrAlX layer
-
- 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
- C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
- C23C28/34—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
- C23C28/345—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
Definitions
- the present invention relates generally to oxidation and corrosion resistant coatings, and relates more particularly to aluminide coatings containing one or more active elements and improved oxidation and corrosion resistance.
- Overlay coatings are widely used in high temperature and/or corrosive environments, for example in gas turbine engines, as a stand alone coating, e.g., to provide high temperature corrosion and oxidation resistance to the underlying substrate, and also as an adherent bond coat for a subsequently-applied ceramic thermal barrier coatings.
- a typical overlay coating is an MCr, MCrAl or MCrAlY coating, such as a coating disclosed in commonly-owned U.S. Pat. No. 4,585,481 and Reissue No. 32,121, both to Gupta et al.
- the M is selected from the group including nickel, cobalt and iron or combinations of these elements.
- the Y typically indicates yttrium but may also include silicon and/or other active elements such as hafnium.
- Overlay coatings are generally, although not necessarily, applied by plasma spraying. See, e.g., U.S. Pat. Nos. 4,321,311 and 4,585,481 and Reissue No. 32,121. Application of overlay coatings by other applications, including but not limited to, electron-beam physical vapor deposition, chemical vapor deposition, cathodic arc and electroplating are also possible. While the bond coat thickness may vary depending upon the particular component and application, the illustrated bond coat typically has a thickness of less than about 5 mils, although thicker or thinner coatings are also used.
- Aluminide coatings are also used in high temperature and/or corrosive environments, for example in gas turbine engines, as a stand alone coating, e.g., to provide high temperature corrosion and oxidation resistance to the underlying substrate, and as an adherent bond coat for a subsequently-applied ceramic thermal barrier coating.
- Some aluminide coatings also include one or more noble metals, which enhance erosion and/or corrosion resistance. See, e.g., U.S. Pat. No. 5,856,027 to Murphy.
- Aluminide coatings, including those containing noble metal(s) are traditionally applied by a pack process or by chemical vapor deposition (CVD).
- the article to be coated is usually initially electroplated with a noble metal, and is then placed in a pack containing a source of aluminum, an activator, e.g., halide, and inert materials, e.g., alumina.
- the pack and article are then heated, forming vapors of the aluminum, which reacts with the nickel or cobalt in the article to form the aluminide.
- the coatings may be further heat treated to obtain desired coating properties.
- individual generators produce aluminum vapors, and the vapors are conveyed into a chamber to a heated article to be coated where the vapors condense and react with the nickel or cobalt in the article to form the aluminide.
- U.S. Pat. No. Re 32,121 describes forming an MCrAIY (M including nickel, cobalt or a combination) bond coat by plasma spraying, with the MCrAIY composition including about 0.1 - 0.7 % silicon, and 0.1 - 2 % hafnium.
- U.S. Pat. No. 4,897,315 describes a plasma sprayed NiCoCrAIY overlay, which is then aluminized to form an aluminide coating on the substrate.
- U.S. Pat. No. 5,658,614 describes a platinum aluminide (without an MCrAIY) coating formed by electroplating the platinum onto the substrate, and then aluminizing by CVD.
- a method for improving the corrosion and oxidation resistance of a substrate.
- the method includes providing a superalloy substrate, and an overlay coating including at least one oxygen active element which is applied onto the substrate by an overlay step.
- Platinum or other Series VIII transition metal is applied onto the overlay coating, typically but not necessarily by electroplating.
- the overlay coating and metal is then aluminized, for example by chemical vapor deposition.
- a ceramic thermal barrier coating may also be applied.
- a coated article is also disclosed.
- a substrate having an aluminide coating in accordance with the present invention is illustrated by the reference numeral 10.
- the coating may serve as a stand alone coating, e.g., for high temperature oxidation resistance, or as an adherent bond coat for a subsequently-applied thermal barrier such as a layer of ceramic material, e.g., stabilized zirconia.
- a ceramic layer is applied over the aluminide to form a thermal barrier.
- the ceramic layer may be a stabilized zirconia, such as is disclosed in commonly owned U.S. Pat. 4,321,311 to Strangman or Ser. No. 09/164,700 to Maloney both of which are commonly owned with the present invention and are expressly incorporated by reference herein.
- a substrate 12 is typically composed of nickel, cobalt and /or iron base superalloy material.
- an overlay coating 14 such as an MCrAI type coating is first applied to the substrate, preferably by low pressure plasma spray and together with one or more oxygen active elements such as hafnium, yttrium and silicon or other oxygen active element.
- a metal for example a Series VIII transition metal such as platinum is then deposited, preferably by electroplating, and is aluminized to form an adherent alumina layer 16.
- the article may also be heat treated to provide the coating with desired properties, e.g., improved mechanical properties. As indicated in FIG.
- the present invention provides coatings having improved properties, e.g., corrosion and oxidation resistance and durability relative to prior coatings. While the invention illustrated below is used with a nickel base, cobalt base or iron base superalloy material, the invention is not limited to use with these materials.
- Typical compositions of such alloys are shown in Table 1.
- Exemplary U.S. Patents describing columnar and single crystal and directionally solidified alloys include 4,209,348; 4,643,782; 4,717,432; 4,719,080 and 5,068,084, each of which is expressly incorporated by reference herein.
- Cooling holes which may be positioned on one or more portions of a turbine blade, may be provided for flowing cooling air over the specific portions of the airfoil during operation, as is known generally in the art.
- Rene N4 and CMSX-2 are described in the prior art.
- the active element(s) is applied by a conventional overlay process, and may or may not contain other elements, e.g., as part of an MCr or MCrAI overlay coating.
- an overlay coating such as an MCrAI is applied to the substrate surface by a conventional overlay process, such as by low pressure plasma spray.
- Application of the overlay by other applications is also possible, including but not limited to, electron-beam physical vapor deposition, cathodic arc, electroplating, sputtering and physical vapor deposition.
- M indicates nickel, cobalt, iron and mixtures thereof.
- the bond coat preferably also includes at least one oxygen active element, e.g., yttrium, hafnium, silicon or others.
- the present invention preferably includes an overlay coating having a thickness of between about 1 - 5 mils (0.001 - 0.005 inches, (25.4-127 ⁇ m), although coatings of other thicknesses may also be used.
- An exemplary overlay coating (described further in an example below) which we have used successfully is a NiCoCrAl coating with added Y, Hf and/or Si.
- the coating is composed in weight percentage of about 5 - 40 Cr, 8 - 35 Al, up to 2 Y, 0.1 - 7 Si, 0.1 - 5.5 Hf, balance Ni and/or Co.
- One or more Series VIII transition metals are then deposited on the MCrAl coating.
- the final coating should contain in weight percent about 1- 30 of such metal, e.g., Pt, more preferably about 5 - 20 and as described below we have obtained good results with about 10 - 11 PT in the final coating.
- the metal(s) is deposited by electroplating, in a known manner, but those skilled in the art will recognize that the transition metal may be applied with the application of the overlay coating. Plating the metal to a thickness of about 0.05 - 0.15 mils (1.3-3.8 ⁇ m) should provide a final coating with the above-desired transition metal content.
- platinum While we prefer to use platinum in connection with the present invention, other metals may also be employed such as palladium, iridium, rhodium, ruthenium and osmium or combinations of these elements. Plating processes are known generally and are not described here in detail. Alternatively, the metal may be applied by jet vapor deposition (JVD), see e.g., U.S. Pat. 4,788,082 and other patents assigned to Jet Process Corporation, which are expressly incorporated herein by reference, by cathodic arc or by CVD.
- JVD jet vapor deposition
- a coating gas has a composition including some amount, in vol. % of a carrier gas, such as hydrogen, and an amount, in vol. %, of an aluminum containing gas.
- the coating gas may be formed by passing a carrier gas over a source of aluminum. The above process is adjusted as desired to provide a given quantity of aluminum on the part surface.
- the coating gas is then impinged upon the heated substrate, at a given delivery rate, with the substrate typically being heated to between about 1800 - 2200 F (982 - 1204°C) and preferably about 1950 - 2000F (1065 - 1093°C)
- the coated part is diffusion heat treated, although in some cases the diffusion heat treatment may not be necessary.
- the diffusion heat treatment preferably includes heating the component to a temperature, typically about 1975 F (1079°C) for a sufficient time, for example about 3 hours, followed by a precipitation heat treatment, for example at about 1600 °F (871°C) for about 16 hours.
- the temperatures and times may vary depending upon composition and desired properties with higher temperatures generally associated with shorter times.
- coatings in accordance with the present invention may be employed to provide stand alone coatings or bond coats for subsequently-applied ceramic thermal barrier coating.
- Typical ceramics are zirconia based, and may be partially or fully stabilized with additions of yttria or other appropriate stabilizer.
- Exemplary ceramic coatings composed of yttria stabilized zirconia (YSZ) are described, for example, in commonly-owned U.S. Pat. Nos. 4,321,311, 5,262,245.
- the ceramic may be applied by EB-PVD, by plasma spray or by another suitable method.
- Samples were prepared using superalloy substrates in accordance with preferred embodiments and some were also coated with a standard, zirconia based columnar ceramic thermal barrier coating.
- the overlay coating as described above was applied by low pressure plasma spray, and then plated with platinum in a known manner.
- the samples were aluminized using a coating gas included about 80 vol. % of a carrier gas, such as hydrogen, and about 20 vol. %, of an aluminum containing gas, in this case AlCl 3 .
- the coating gas was formed by passing HCI over a source of aluminum at about 600 C.
- the coating gas was impinged upon the heated substrate, at a delivery rate of about 224 standard cubic feet per minute, with the substrate heated to a nominal temperature of between about 1950-2000 F (1065-1093°C).
- Some of the samples were then coated with a ceramic thermal barrier coating composed of yttria stabilized zirconia, as taught for example in the above referenced '311 patent to Strangman, while other samples were tested
- Coated articles in accordance with the present invention have been tested in a burner rig apparatus. Testing indicated that the present invention coatings, which tests included samples having a subsequently applied thermal insulating layer, are about 2 - 3 times more durable than current TBC's. The inventive coated articles were also tested as stand alone coatings, e.g., no overlying ceramic layer, and also demonstrate improved protection and durability.
- the samples were tested in high temperature burner rigs.
- the test cycles comprised 117 minute exposure at 2150 degree F (1176°C) followed by 3 minute air cooling per cycle together with standard platinum aluminides.
- the samples prepared in accordance with the present method exhibited improved lives over the samples including the standard aluminides by a factor of about 2.5.
- composition of the final coating in accordance with the most preferred embodiments is, in weight percent, between about 1-30 Pt, 2-4.5 Si, 13-14 A1, 1-5.5 Hf, remainder Ni, Co, and Cr, and more preferably 10 - 11 Pt, 2.6 - 4.2 Si, 13.4 - 13.6 Al, 3.9 - 5.3 Hf, remainder Ni, Co, and Cr.
- Other compositional ranges should also provide for significantly improved lives over known aluminide coatings (with or without a thermal barrier coating).
- the present invention provides significant advantages over prior processes.
- the improved process enables the production of active element containing aluminide coatings having significantly more consistent compositions, and thus significantly more consistent properties and improved durability.
- the quality of the resulting coatings are thus similarly improved.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Coating By Spraying Or Casting (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
- Electroplating Methods And Accessories (AREA)
Abstract
Description
- The present invention relates generally to oxidation and corrosion resistant coatings, and relates more particularly to aluminide coatings containing one or more active elements and improved oxidation and corrosion resistance.
- Overlay coatings are widely used in high temperature and/or corrosive environments, for example in gas turbine engines, as a stand alone coating, e.g., to provide high temperature corrosion and oxidation resistance to the underlying substrate, and also as an adherent bond coat for a subsequently-applied ceramic thermal barrier coatings. A typical overlay coating is an MCr, MCrAl or MCrAlY coating, such as a coating disclosed in commonly-owned U.S. Pat. No. 4,585,481 and Reissue No. 32,121, both to Gupta et al. The M is selected from the group including nickel, cobalt and iron or combinations of these elements. The Y typically indicates yttrium but may also include silicon and/or other active elements such as hafnium. Overlay coatings are generally, although not necessarily, applied by plasma spraying. See, e.g., U.S. Pat. Nos. 4,321,311 and 4,585,481 and Reissue No. 32,121. Application of overlay coatings by other applications, including but not limited to, electron-beam physical vapor deposition, chemical vapor deposition, cathodic arc and electroplating are also possible. While the bond coat thickness may vary depending upon the particular component and application, the illustrated bond coat typically has a thickness of less than about 5 mils, although thicker or thinner coatings are also used.
- Aluminide coatings are also used in high temperature and/or corrosive environments, for example in gas turbine engines, as a stand alone coating, e.g., to provide high temperature corrosion and oxidation resistance to the underlying substrate, and as an adherent bond coat for a subsequently-applied ceramic thermal barrier coating. Some aluminide coatings also include one or more noble metals, which enhance erosion and/or corrosion resistance. See, e.g., U.S. Pat. No. 5,856,027 to Murphy. Aluminide coatings, including those containing noble metal(s), are traditionally applied by a pack process or by chemical vapor deposition (CVD). In a typical "in pack" process, the article to be coated is usually initially electroplated with a noble metal, and is then placed in a pack containing a source of aluminum, an activator, e.g., halide, and inert materials, e.g., alumina. The pack and article are then heated, forming vapors of the aluminum, which reacts with the nickel or cobalt in the article to form the aluminide. The coatings may be further heat treated to obtain desired coating properties. In a typical CVD process, individual generators produce aluminum vapors, and the vapors are conveyed into a chamber to a heated article to be coated where the vapors condense and react with the nickel or cobalt in the article to form the aluminide.
- It is generally accepted that it is difficult to produce active element containing aluminides of consistent quality. It is also generally accepted that it is at least as difficult to consistently produce aluminide coatings containing more than one active element.
- Numerous patents describe various overlay and aluminide coating compositions and processes. Exemplary patents are identified below.
- U.S. Pat. No. Re 32,121 describes forming an MCrAIY (M including nickel, cobalt or a combination) bond coat by plasma spraying, with the MCrAIY composition including about 0.1 - 0.7 % silicon, and 0.1 - 2 % hafnium.
- U.S. Pat. No. 4,897,315 describes a plasma sprayed NiCoCrAIY overlay, which is then aluminized to form an aluminide coating on the substrate.
- U.S. Pat. No. 5,658,614 describes a platinum aluminide (without an MCrAIY) coating formed by electroplating the platinum onto the substrate, and then aluminizing by CVD.
- It is a general object of the present invention to provide a coating having improved properties.
- It is another object to provide an aluminide coating, and a process for applying an aluminide, having improved durability.
- It is still another object to provide a repeatable process for forming active element(s) containing aluminide coatings that produces high quality coatings more consistently.
- According to one aspect of the invention, a method is disclosed for improving the corrosion and oxidation resistance of a substrate. The method includes providing a superalloy substrate, and an overlay coating including at least one oxygen active element which is applied onto the substrate by an overlay step. Platinum or other Series VIII transition metal is applied onto the overlay coating, typically but not necessarily by electroplating. The overlay coating and metal is then aluminized, for example by chemical vapor deposition. A ceramic thermal barrier coating may also be applied. A coated article is also disclosed.
- Certain preferred embodiments of the present invention will now be described by way of example only and with reference to the accompanying drawings, in which:
- FIG. 1 is a photomicrograph of a coating of a preferred embodiment, including a ceramic coating.
- FIG. 2 is a flow diagram illustrating a preferred process for fabricating the coating of the present invention.
-
- Turning now to FIG. 1, a substrate having an aluminide coating in accordance with the present invention is illustrated by the reference numeral 10. The coating may serve as a stand alone coating, e.g., for high temperature oxidation resistance, or as an adherent bond coat for a subsequently-applied thermal barrier such as a layer of ceramic material, e.g., stabilized zirconia. In the embodiment illustrated in FIG. 1, a ceramic layer is applied over the aluminide to form a thermal barrier. The ceramic layer may be a stabilized zirconia, such as is disclosed in commonly owned U.S. Pat. 4,321,311 to Strangman or Ser. No. 09/164,700 to Maloney both of which are commonly owned with the present invention and are expressly incorporated by reference herein.
- A substrate 12 is typically composed of nickel, cobalt and /or iron base superalloy material. As described further below with reference to FIG. 2, an overlay coating 14 such as an MCrAI type coating is first applied to the substrate, preferably by low pressure plasma spray and together with one or more oxygen active elements such as hafnium, yttrium and silicon or other oxygen active element. A metal, for example a Series VIII transition metal such as platinum is then deposited, preferably by electroplating, and is aluminized to form an adherent alumina layer 16. The article may also be heat treated to provide the coating with desired properties, e.g., improved mechanical properties. As indicated in FIG. 3, the present invention provides coatings having improved properties, e.g., corrosion and oxidation resistance and durability relative to prior coatings. While the invention illustrated below is used with a nickel base, cobalt base or iron base superalloy material, the invention is not limited to use with these materials.
- Typical compositions of such alloys are shown in Table 1. Exemplary U.S. Patents describing columnar and single crystal and directionally solidified alloys include 4,209,348; 4,643,782; 4,717,432; 4,719,080 and 5,068,084, each of which is expressly incorporated by reference herein. Cooling holes, which may be positioned on one or more portions of a turbine blade, may be provided for flowing cooling air over the specific portions of the airfoil during operation, as is known generally in the art.
COMPOSITION OF COLUMNAR AND SINGLE CRYSTAL ALLOYS Alloy Type Ni Co Cr Al Mo Ta W Re Hf Ti Nb PWA 1422 DS Bal. 10 9 5 - - 12 - 1.6 2 1 DS R80H DS Bal. 9.5 14 3 4 - 4 - 0.75 4.8 - CM247LC DS Bal. 9.2 8.1 5.6 0.5 3.2 9.5 - 1.4 0.7 - PWA 1480 SC Bal. 5 10 5 - 12 4 - - 1.5 - PWA 1484 SC Bal. 10 5 5.65 1.9 8.7 5.9 3 0.1 - - Rene' N5 SC Bal. 7.5 7 6.2 1.5 6.5 5 3 0.15 - - CMSX-4 SC Bal. 9 6.5 5.6 0.6 6.5 6 3 0.1 1 - - Other alloys include, for example, Rene N4 and CMSX-2, which are described in the prior art.
- Generally, the active element(s) is applied by a conventional overlay process, and may or may not contain other elements, e.g., as part of an MCr or MCrAI overlay coating. In accordance with the present invention, an overlay coating such as an MCrAI is applied to the substrate surface by a conventional overlay process, such as by low pressure plasma spray. Application of the overlay by other applications is also possible, including but not limited to, electron-beam physical vapor deposition, cathodic arc, electroplating, sputtering and physical vapor deposition. As is known, M indicates nickel, cobalt, iron and mixtures thereof. The bond coat preferably also includes at least one oxygen active element, e.g., yttrium, hafnium, silicon or others. As applied, the present invention preferably includes an overlay coating having a thickness of between about 1 - 5 mils (0.001 - 0.005 inches, (25.4-127 µm), although coatings of other thicknesses may also be used.
- An exemplary overlay coating (described further in an example below) which we have used successfully is a NiCoCrAl coating with added Y, Hf and/or Si. In broad terms, the coating is composed in weight percentage of about 5 - 40 Cr, 8 - 35 Al, up to 2 Y, 0.1 - 7 Si, 0.1 - 5.5 Hf, balance Ni and/or Co.
- One or more Series VIII transition metals are then deposited on the MCrAl coating. We believe that the final coating should contain in weight percent about 1- 30 of such metal, e.g., Pt, more preferably about 5 - 20 and as described below we have obtained good results with about 10 - 11 PT in the final coating. Preferably the metal(s) is deposited by electroplating, in a known manner, but those skilled in the art will recognize that the transition metal may be applied with the application of the overlay coating. Plating the metal to a thickness of about 0.05 - 0.15 mils (1.3-3.8 µm) should provide a final coating with the above-desired transition metal content. While we prefer to use platinum in connection with the present invention, other metals may also be employed such as palladium, iridium, rhodium, ruthenium and osmium or combinations of these elements. Plating processes are known generally and are not described here in detail. Alternatively, the metal may be applied by jet vapor deposition (JVD), see e.g., U.S. Pat. 4,788,082 and other patents assigned to Jet Process Corporation, which are expressly incorporated herein by reference, by cathodic arc or by CVD.
- Aluminum is then applied to the part. While we prefer to use chemical vapor deposition to aluminize the part, jet vapor deposition, physical vapor deposition or other suitable deposition may also be employed. While CVD aluminizing processes are known generally and are not described here in detail, a coating gas has a composition including some amount, in vol. % of a carrier gas, such as hydrogen, and an amount, in vol. %, of an aluminum containing gas. The coating gas may be formed by passing a carrier gas over a source of aluminum. The above process is adjusted as desired to provide a given quantity of aluminum on the part surface. The coating gas is then impinged upon the heated substrate, at a given delivery rate, with the substrate typically being heated to between about 1800 - 2200 F (982 - 1204°C) and preferably about 1950 - 2000F (1065 - 1093°C)
- After aluminizing, the coated part is diffusion heat treated, although in some cases the diffusion heat treatment may not be necessary. Using the above example, the diffusion heat treatment preferably includes heating the component to a temperature, typically about 1975 F (1079°C) for a sufficient time, for example about 3 hours, followed by a precipitation heat treatment, for example at about 1600 °F (871°C) for about 16 hours. The temperatures and times may vary depending upon composition and desired properties with higher temperatures generally associated with shorter times. A resulting coating is illustrated in FIG. 1, which includes a subsequently applied, columnar grain, ceramic thermal barrier layer.
- As noted above, coatings in accordance with the present invention may be employed to provide stand alone coatings or bond coats for subsequently-applied ceramic thermal barrier coating. Typical ceramics are zirconia based, and may be partially or fully stabilized with additions of yttria or other appropriate stabilizer. Exemplary ceramic coatings composed of yttria stabilized zirconia (YSZ) are described, for example, in commonly-owned U.S. Pat. Nos. 4,321,311, 5,262,245. The ceramic may be applied by EB-PVD, by plasma spray or by another suitable method.
- Samples were prepared using superalloy substrates in accordance with preferred embodiments and some were also coated with a standard, zirconia based columnar ceramic thermal barrier coating. The overlay coating as described above was applied by low pressure plasma spray, and then plated with platinum in a known manner. The samples were aluminized using a coating gas included about 80 vol. % of a carrier gas, such as hydrogen, and about 20 vol. %, of an aluminum containing gas, in this case AlCl3. The coating gas was formed by passing HCI over a source of aluminum at about 600 C. The coating gas was impinged upon the heated substrate, at a delivery rate of about 224 standard cubic feet per minute, with the substrate heated to a nominal temperature of between about 1950-2000 F (1065-1093°C). Some of the samples were then coated with a ceramic thermal barrier coating composed of yttria stabilized zirconia, as taught for example in the above referenced '311 patent to Strangman, while other samples were tested without such a ceramic coating.
- Coated articles in accordance with the present invention have been tested in a burner rig apparatus. Testing indicated that the present invention coatings, which tests included samples having a subsequently applied thermal insulating layer, are about 2 - 3 times more durable than current TBC's. The inventive coated articles were also tested as stand alone coatings, e.g., no overlying ceramic layer, and also demonstrate improved protection and durability.
- The samples were tested in high temperature burner rigs. The test cycles comprised 117 minute exposure at 2150 degree F (1176°C) followed by 3 minute air cooling per cycle together with standard platinum aluminides. The samples prepared in accordance with the present method exhibited improved lives over the samples including the standard aluminides by a factor of about 2.5.
- As a result of the testing, we believe that the composition of the final coating in accordance with the most preferred embodiments is, in weight percent, between about 1-30 Pt, 2-4.5 Si, 13-14 A1, 1-5.5 Hf, remainder Ni, Co, and Cr, and more preferably 10 - 11 Pt, 2.6 - 4.2 Si, 13.4 - 13.6 Al, 3.9 - 5.3 Hf, remainder Ni, Co, and Cr. Other compositional ranges should also provide for significantly improved lives over known aluminide coatings (with or without a thermal barrier coating).
- The present invention provides significant advantages over prior processes. The improved process enables the production of active element containing aluminide coatings having significantly more consistent compositions, and thus significantly more consistent properties and improved durability. The quality of the resulting coatings are thus similarly improved.
- While the present invention has been described above in some detail, numerous variations and substitutions may be made without departing from the scope of the invention as defined by the following claims. Accordingly, it is to be understood that the invention has been described by way of illustration and not by limitation.
Claims (18)
- A method of improving the corrosion and oxidation resistance of a substrate, comprising the steps of:providing a superalloy substrate;applying an MCrAl overlay coating including at least one oxygen active element onto the substrate by an overlay step;applying a Series VIII transition metal onto the overlay coating; andaluminizing the overlay coating and metal.
- A method of improving the oxidation resistance of a substrate, comprising the steps of:providing a substrate composed of nickel base and/or cobalt base superalloy material;applying an overlay coating including at least one oxygen active element onto the substrate by low pressure plasma spray;applying a Series VIII transition metal onto the substrate by electroplating; andaluminizing the bond coat, at least one oxygen active element and the metal by chemical vapor deposition to form an aluminide on the substrate.
- The method of claim 2, wherein the overlay coating is also composed of yttrium, hafnium and/or silicon.
- The method of claim 1 or 3, wherein the overlay coating has a nominal composition in weight percent of about 5 - 40 Cr, 8 - 35 Al, up to 2 Y, 0.1 - 7 Si, 0.1-5.5 Hf, balance Ni and/or Co.
- The method of any preceding claim, wherein the step of applying the overlay coating with the at least one oxygen active element is by a process selected from the group consisting of air plasma spray, low pressure plasma spray, sputtering, cathodic arc, electroplating, and physical vapor deposition.
- The method of any preceding claim, wherein the step of applying the transition metal is performed using a process selected from the group consisting of electroplating, jet vapor deposition, physical vapor deposition, sputtering and cathodic arc.
- The method of any preceding claim, wherein the step of aluminizing is performed by a process selected from the group consisting of chemical vapor deposition, jet vapor deposition, and physical vapor deposition.
- The method of any preceding claim, wherein the Series VIII transition metal is selected from the group consisting of platinum, palladium, iridium, rhodium, ruthenium and osmium.
- The method of claim 8, wherein the metal is platinum.
- The method of any preceding claim, further comprising the step of heat treating the article.
- The method of any preceding claim, further comprising the step of depositing a thermally insulating ceramic on the aluminide.
- The method of claim 11, wherein the ceramic coating is composed of a stabilized zirconia.
- The method of claim 12, wherein the zirconia is stabilized by yttria or by gadolinia.
- The method of any preceding claim, wherein the resulting coating has a nominal composition in weight percent of about 5 - 40 Cr, 8 - 35 Al, 5 - 20 Series VIII transition metal, up to 2 Y, 0.1 - 7 Si, 0.1 - 5.5 Hf, balance Ni and/or Co.
- The method of claim 14, wherein the coating has a nominal composition of about 9 - 12 Pt, 13 - 14 Al, 3.95.5 Hf, 2.5 - 4.5 Si, balance Ni, Co and Cr.
- A superalloy article having a coating with improved oxidation and corrosion resistance and durability, made in accordance with the method of any preceding claim.
- A superalloy article having a coating comprising a nominal composition in weight percent of 5 - 40 Cr, 8-35 Al, 5 - 20 Series VIII transition metal, up to 2 Y, 0.1 - 7 Si, 0.1 - 5.5 Hf, balance Ni and/or Co.
- An article as claimed in claim 17, wherein the coating has a nominal composition of 9 - 12 Pt, 13 - 14 Al, 3.9 - 5.5 Hf, 2.5 - 4.5 Si, balance Ni, Co and Cr.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17282499P | 1999-12-21 | 1999-12-21 | |
US172824P | 1999-12-21 | ||
US09/735,223 US20020132132A1 (en) | 2000-12-12 | 2000-12-12 | Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1111091A1 true EP1111091A1 (en) | 2001-06-27 |
EP1111091B1 EP1111091B1 (en) | 2010-06-23 |
Family
ID=26868500
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00311496A Expired - Lifetime EP1111091B1 (en) | 1999-12-21 | 2000-12-20 | Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1111091B1 (en) |
JP (1) | JP2002115081A (en) |
DE (1) | DE60044574D1 (en) |
SG (1) | SG98436A1 (en) |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1347079A2 (en) * | 2002-03-18 | 2003-09-24 | General Electric Company | Article for high temperature service and method for manufacture |
WO2003057944A3 (en) * | 2002-01-10 | 2004-07-15 | Alstom Technology Ltd | Mcraly bond coating and method of depositing said mcraly bond coating |
EP1491659A1 (en) * | 2003-06-26 | 2004-12-29 | ALSTOM Technology Ltd | A method of depositing a coating system |
EP1507019A1 (en) * | 2003-08-11 | 2005-02-16 | General Electric Aviation Service Operation (PTE) Ltd. | Upgrading aluminide coating on used turbine engine component |
WO2006026456A1 (en) * | 2004-08-26 | 2006-03-09 | Honeywell International Inc. | Chromium and active elements modified platinum aluminide coatings |
WO2006071507A1 (en) * | 2004-12-29 | 2006-07-06 | Honeywell International Inc. | Low cost inovative diffused mcraly coatings |
EP1795623A1 (en) * | 2005-11-14 | 2007-06-13 | Sulzer Metco AG | Coating process of an article with modified platinum aluminide and component |
EP1953252A1 (en) * | 2007-01-09 | 2008-08-06 | General Electric Company | Alloy compositions of the MCrAlY type and articles comprising the same |
DE102009010026A1 (en) * | 2009-02-21 | 2010-08-26 | Mtu Aero Engines Gmbh | Component, useful for flow machine, comprises a metal alloy comprising base material, where the component is coated with portion of adhesive layer comprising nickel-chromium-aluminum-yttrium alloy and a surface layer comprising zirconia |
US7846243B2 (en) | 2007-01-09 | 2010-12-07 | General Electric Company | Metal alloy compositions and articles comprising the same |
US7875370B2 (en) | 2006-08-18 | 2011-01-25 | United Technologies Corporation | Thermal barrier coating with a plasma spray top layer |
US7931759B2 (en) | 2007-01-09 | 2011-04-26 | General Electric Company | Metal alloy compositions and articles comprising the same |
EP2022869A3 (en) * | 2007-08-02 | 2011-07-06 | United Technologies Corporation | Method for forming active-element aluminide diffusion coatings |
US8123967B2 (en) | 2005-08-01 | 2012-02-28 | Vapor Technologies Inc. | Method of producing an article having patterned decorative coating |
CN101307442B (en) * | 2002-06-27 | 2012-04-11 | 通用电气公司 | Method for making high-temperature articles |
US8334056B2 (en) | 2003-05-16 | 2012-12-18 | Iowa State University Research Foundation, Inc. | High-temperature coatings with Pt metal modified γ-Ni + γ′-Ni3Al alloy compositions |
WO2013071086A1 (en) * | 2011-11-09 | 2013-05-16 | General Electric Company | Alloys for bond coatings and articles incorporating the same |
US8821654B2 (en) | 2008-07-15 | 2014-09-02 | Iowa State University Research Foundation, Inc. | Pt metal modified γ-Ni+γ′-Ni3Al alloy compositions for high temperature degradation resistant structural alloys |
CN109989058A (en) * | 2013-11-13 | 2019-07-09 | 应用材料公司 | High purity metal top coating for semiconductor processing components |
CN114672859A (en) * | 2022-03-11 | 2022-06-28 | 沈阳梅特科航空科技有限公司 | Platinum modified aluminide coating capable of being used as thermal barrier coating bonding layer and preparation process thereof |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1428982B1 (en) * | 2002-12-06 | 2009-02-04 | ALSTOM Technology Ltd | A method of depositing a local MCrAIY-coating |
US7927722B2 (en) * | 2004-07-30 | 2011-04-19 | United Technologies Corporation | Dispersion strengthened rare earth stabilized zirconia |
JP5857794B2 (en) * | 2012-02-27 | 2016-02-10 | 株式会社Ihi | Metal material with diffusion layer and method for producing the same |
TWI574840B (en) * | 2014-09-12 | 2017-03-21 | 香港浸會大學 | Sapphire thin film coated flexible substrate |
CN112458351B (en) * | 2020-10-22 | 2021-10-15 | 中国人民解放军陆军装甲兵学院 | High compressive strength nickel-cobalt-based high temperature alloy |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3692554A (en) * | 1969-12-05 | 1972-09-19 | Deutsche Edelstahlwerke Ag | Production of protective layers on cobalt-based alloys |
US3979273A (en) * | 1975-05-27 | 1976-09-07 | United Technologies Corporation | Method of forming aluminide coatings on nickel-, cobalt-, and iron-base alloys |
USRE32121E (en) | 1981-08-05 | 1986-04-22 | United Technologies Corporation | Overlay coatings for superalloys |
US4788082A (en) | 1984-02-13 | 1988-11-29 | Schmitt Jerome J | Method and apparatus for the deposition of solid films of a material from a jet stream entraining the gaseous phase of said material |
US4897315A (en) | 1985-10-15 | 1990-01-30 | United Technologies Corporation | Yttrium enriched aluminide coating for superalloys |
EP0386386A1 (en) * | 1989-03-06 | 1990-09-12 | United Technologies Corporation | Process for producing Yttrium enriched aluminide coated superalloys |
US4962005A (en) * | 1988-10-26 | 1990-10-09 | Office National D'etudes Et De Recherches Aerospatiales | Method of protecting the surfaces of metal parts against corrosion at high temperature, and a part treated by the method |
EP0587341A1 (en) * | 1992-09-05 | 1994-03-16 | ROLLS-ROYCE plc | High temperature corrosion resistant composite coatings |
US5427866A (en) * | 1994-03-28 | 1995-06-27 | General Electric Company | Platinum, rhodium, or palladium protective coatings in thermal barrier coating systems |
US5658614A (en) | 1994-10-28 | 1997-08-19 | Howmet Research Corporation | Platinum aluminide CVD coating method |
EP0845547A1 (en) * | 1996-11-30 | 1998-06-03 | ROLLS-ROYCE plc | A thermal barrier coating for a superalloy article and a method of application thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6129991A (en) * | 1994-10-28 | 2000-10-10 | Howmet Research Corporation | Aluminide/MCrAlY coating system for superalloys |
US5716720A (en) * | 1995-03-21 | 1998-02-10 | Howmet Corporation | Thermal barrier coating system with intermediate phase bondcoat |
-
2000
- 2000-12-19 SG SG200007530A patent/SG98436A1/en unknown
- 2000-12-20 DE DE60044574T patent/DE60044574D1/en not_active Expired - Lifetime
- 2000-12-20 EP EP00311496A patent/EP1111091B1/en not_active Expired - Lifetime
- 2000-12-21 JP JP2000388097A patent/JP2002115081A/en active Pending
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3692554A (en) * | 1969-12-05 | 1972-09-19 | Deutsche Edelstahlwerke Ag | Production of protective layers on cobalt-based alloys |
US3979273A (en) * | 1975-05-27 | 1976-09-07 | United Technologies Corporation | Method of forming aluminide coatings on nickel-, cobalt-, and iron-base alloys |
USRE32121E (en) | 1981-08-05 | 1986-04-22 | United Technologies Corporation | Overlay coatings for superalloys |
US4788082A (en) | 1984-02-13 | 1988-11-29 | Schmitt Jerome J | Method and apparatus for the deposition of solid films of a material from a jet stream entraining the gaseous phase of said material |
US4897315A (en) | 1985-10-15 | 1990-01-30 | United Technologies Corporation | Yttrium enriched aluminide coating for superalloys |
US4962005A (en) * | 1988-10-26 | 1990-10-09 | Office National D'etudes Et De Recherches Aerospatiales | Method of protecting the surfaces of metal parts against corrosion at high temperature, and a part treated by the method |
EP0386386A1 (en) * | 1989-03-06 | 1990-09-12 | United Technologies Corporation | Process for producing Yttrium enriched aluminide coated superalloys |
EP0587341A1 (en) * | 1992-09-05 | 1994-03-16 | ROLLS-ROYCE plc | High temperature corrosion resistant composite coatings |
US5427866A (en) * | 1994-03-28 | 1995-06-27 | General Electric Company | Platinum, rhodium, or palladium protective coatings in thermal barrier coating systems |
US5658614A (en) | 1994-10-28 | 1997-08-19 | Howmet Research Corporation | Platinum aluminide CVD coating method |
EP0845547A1 (en) * | 1996-11-30 | 1998-06-03 | ROLLS-ROYCE plc | A thermal barrier coating for a superalloy article and a method of application thereof |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003057944A3 (en) * | 2002-01-10 | 2004-07-15 | Alstom Technology Ltd | Mcraly bond coating and method of depositing said mcraly bond coating |
US7264887B2 (en) | 2002-01-10 | 2007-09-04 | Alstom Technology Ltd. | MCrAlY bond coating and method of depositing said MCrAlY bond coating |
EP1347079A3 (en) * | 2002-03-18 | 2004-03-31 | General Electric Company | Article for high temperature service and method for manufacture |
EP1347079A2 (en) * | 2002-03-18 | 2003-09-24 | General Electric Company | Article for high temperature service and method for manufacture |
CN101307442B (en) * | 2002-06-27 | 2012-04-11 | 通用电气公司 | Method for making high-temperature articles |
US8334056B2 (en) | 2003-05-16 | 2012-12-18 | Iowa State University Research Foundation, Inc. | High-temperature coatings with Pt metal modified γ-Ni + γ′-Ni3Al alloy compositions |
EP1491659A1 (en) * | 2003-06-26 | 2004-12-29 | ALSTOM Technology Ltd | A method of depositing a coating system |
EP1507019A1 (en) * | 2003-08-11 | 2005-02-16 | General Electric Aviation Service Operation (PTE) Ltd. | Upgrading aluminide coating on used turbine engine component |
WO2006026456A1 (en) * | 2004-08-26 | 2006-03-09 | Honeywell International Inc. | Chromium and active elements modified platinum aluminide coatings |
US7229701B2 (en) | 2004-08-26 | 2007-06-12 | Honeywell International, Inc. | Chromium and active elements modified platinum aluminide coatings |
WO2006071507A1 (en) * | 2004-12-29 | 2006-07-06 | Honeywell International Inc. | Low cost inovative diffused mcraly coatings |
US8123967B2 (en) | 2005-08-01 | 2012-02-28 | Vapor Technologies Inc. | Method of producing an article having patterned decorative coating |
EP1795623A1 (en) * | 2005-11-14 | 2007-06-13 | Sulzer Metco AG | Coating process of an article with modified platinum aluminide and component |
US7875370B2 (en) | 2006-08-18 | 2011-01-25 | United Technologies Corporation | Thermal barrier coating with a plasma spray top layer |
CN101220435B (en) * | 2007-01-09 | 2012-11-28 | 通用电气公司 | Metal alloy compositions and articles comprising the same |
US7931759B2 (en) | 2007-01-09 | 2011-04-26 | General Electric Company | Metal alloy compositions and articles comprising the same |
US7846243B2 (en) | 2007-01-09 | 2010-12-07 | General Electric Company | Metal alloy compositions and articles comprising the same |
US7727318B2 (en) | 2007-01-09 | 2010-06-01 | General Electric Company | Metal alloy compositions and articles comprising the same |
EP1953252A1 (en) * | 2007-01-09 | 2008-08-06 | General Electric Company | Alloy compositions of the MCrAlY type and articles comprising the same |
EP2022869A3 (en) * | 2007-08-02 | 2011-07-06 | United Technologies Corporation | Method for forming active-element aluminide diffusion coatings |
US8821654B2 (en) | 2008-07-15 | 2014-09-02 | Iowa State University Research Foundation, Inc. | Pt metal modified γ-Ni+γ′-Ni3Al alloy compositions for high temperature degradation resistant structural alloys |
DE102009010026A1 (en) * | 2009-02-21 | 2010-08-26 | Mtu Aero Engines Gmbh | Component, useful for flow machine, comprises a metal alloy comprising base material, where the component is coated with portion of adhesive layer comprising nickel-chromium-aluminum-yttrium alloy and a surface layer comprising zirconia |
WO2013071086A1 (en) * | 2011-11-09 | 2013-05-16 | General Electric Company | Alloys for bond coatings and articles incorporating the same |
CN109989058A (en) * | 2013-11-13 | 2019-07-09 | 应用材料公司 | High purity metal top coating for semiconductor processing components |
CN114672859A (en) * | 2022-03-11 | 2022-06-28 | 沈阳梅特科航空科技有限公司 | Platinum modified aluminide coating capable of being used as thermal barrier coating bonding layer and preparation process thereof |
CN114672859B (en) * | 2022-03-11 | 2024-05-17 | 沈阳梅特科航空科技有限公司 | Platinum modified aluminide coating capable of being used as thermal barrier coating bonding layer and preparation process thereof |
Also Published As
Publication number | Publication date |
---|---|
DE60044574D1 (en) | 2010-08-05 |
EP1111091B1 (en) | 2010-06-23 |
JP2002115081A (en) | 2002-04-19 |
SG98436A1 (en) | 2003-09-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20020132132A1 (en) | Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article | |
EP1111091B1 (en) | Method of forming an active-element containing aluminide as stand alone coating and as bond coat and coated article | |
US6933052B2 (en) | Diffusion barrier and protective coating for turbine engine component and method for forming | |
US6168874B1 (en) | Diffusion aluminide bond coat for a thermal barrier coating system and method therefor | |
US6344282B1 (en) | Graded reactive element containing aluminide coatings for improved high temperature performance and method for producing | |
EP0979881B1 (en) | Thermal barrier and overlay coating systems comprising composite metal/metal oxide bond coating layers | |
US6720038B2 (en) | Method of forming a coating resistant to deposits and coating formed thereby | |
US5624721A (en) | Method of producing a superalloy article | |
US6607611B1 (en) | Post-deposition oxidation of a nickel-base superalloy protected by a thermal barrier coating | |
US6974636B2 (en) | Protective coating for turbine engine component | |
US20100068556A1 (en) | Diffusion barrier layer and methods of forming | |
EP1254967A1 (en) | Improved plasma sprayed thermal bond coat system | |
US20070281103A1 (en) | MCrAIY BOND COATING AND METHOD OF DEPOSITING SAID MCrAIY BOND COATING | |
JP4855610B2 (en) | Oxidation resistant coating, related articles and methods | |
WO2006071507A1 (en) | Low cost inovative diffused mcraly coatings | |
JP5264156B2 (en) | Coating system including rhodium aluminide layer | |
JP2011512454A (en) | Superalloy article with coating | |
CA2292370C (en) | Improved coating and method for minimizing consumption of base material during high temperature service | |
EP1627937A2 (en) | Protected article having a layered protective structure overlying a substrate | |
JP2011510167A (en) | Thermal barrier coating system | |
US20020031683A1 (en) | Vapor phase co-deposition coating for superalloy applications | |
EP1123987A1 (en) | Repairable diffusion aluminide coatings | |
US6558813B2 (en) | Article having a protective coating and an iridium-containing oxygen barrier layer | |
JP2011509346A (en) | Thermal barrier coating construction method | |
EP1491659B1 (en) | A method of depositing a coating system |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): CH DE FR GB LI NL |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
17P | Request for examination filed |
Effective date: 20011205 |
|
AKX | Designation fees paid |
Free format text: CH DE FR GB LI NL |
|
17Q | First examination report despatched |
Effective date: 20061024 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): CH DE FR GB LI NL |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REF | Corresponds to: |
Ref document number: 60044574 Country of ref document: DE Date of ref document: 20100805 Kind code of ref document: P |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: VDEP Effective date: 20100623 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20100623 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20110324 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 60044574 Country of ref document: DE Effective date: 20110323 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20110831 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101231 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101231 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110103 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 60044574 Country of ref document: DE Representative=s name: SCHMITT-NILSON SCHRAUD WAIBEL WOHLFROM PATENTA, DE |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 60044574 Country of ref document: DE Representative=s name: SCHMITT-NILSON SCHRAUD WAIBEL WOHLFROM PATENTA, DE Ref country code: DE Ref legal event code: R081 Ref document number: 60044574 Country of ref document: DE Owner name: UNITED TECHNOLOGIES CORP. (N.D.GES.D. STAATES , US Free format text: FORMER OWNER: UNITED TECHNOLOGIES CORP., HARTFORD, CONN., US |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20191119 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20191122 Year of fee payment: 20 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R071 Ref document number: 60044574 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 Expiry date: 20201219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20201219 |