GB2285632A - Thermal barrier coating system for superalloy components - Google Patents
Thermal barrier coating system for superalloy components Download PDFInfo
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- GB2285632A GB2285632A GB8520732A GB8520732A GB2285632A GB 2285632 A GB2285632 A GB 2285632A GB 8520732 A GB8520732 A GB 8520732A GB 8520732 A GB8520732 A GB 8520732A GB 2285632 A GB2285632 A GB 2285632A
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- coating
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- ceramic
- alumina
- aluminide
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- 229910000601 superalloy Inorganic materials 0.000 title claims abstract description 42
- 239000012720 thermal barrier coating Substances 0.000 title claims abstract description 41
- 238000000576 coating method Methods 0.000 claims abstract description 80
- 229910000951 Aluminide Inorganic materials 0.000 claims abstract description 72
- 239000011248 coating agent Substances 0.000 claims abstract description 71
- 238000009792 diffusion process Methods 0.000 claims abstract description 49
- 239000000919 ceramic Substances 0.000 claims abstract description 40
- 230000003647 oxidation Effects 0.000 claims abstract description 20
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 20
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 42
- 239000010410 layer Substances 0.000 claims description 41
- 238000005524 ceramic coating Methods 0.000 claims description 39
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 38
- 239000000758 substrate Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 30
- 230000001464 adherent effect Effects 0.000 claims description 12
- 229910052782 aluminium Inorganic materials 0.000 claims description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 12
- 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 10
- 241000588731 Hafnia Species 0.000 claims description 8
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 claims description 8
- 229910001233 yttria-stabilized zirconia Inorganic materials 0.000 claims description 8
- 238000010894 electron beam technology Methods 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052703 rhodium Inorganic materials 0.000 claims description 5
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 238000007740 vapor deposition Methods 0.000 claims description 4
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 4
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910052863 mullite Inorganic materials 0.000 claims description 3
- 150000004767 nitrides Chemical class 0.000 claims description 3
- 230000001681 protective effect Effects 0.000 claims description 3
- 239000002344 surface layer Substances 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 3
- 238000011065 in-situ storage Methods 0.000 claims 2
- 238000010952 in-situ formation Methods 0.000 claims 1
- 239000011247 coating layer Substances 0.000 abstract description 15
- 230000006872 improvement Effects 0.000 abstract description 3
- 230000008569 process Effects 0.000 description 16
- 230000004888 barrier function Effects 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052735 hafnium Inorganic materials 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 238000005240 physical vapour deposition Methods 0.000 description 4
- 229920006384 Airco Polymers 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000004901 spalling Methods 0.000 description 3
- 229910002076 stabilized zirconia Inorganic materials 0.000 description 3
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 238000005269 aluminizing Methods 0.000 description 2
- 238000010420 art technique Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910010293 ceramic material Inorganic materials 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000013077 target material Substances 0.000 description 2
- 238000005019 vapor deposition process Methods 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910002515 CoAl Inorganic materials 0.000 description 1
- 229910015372 FeAl Inorganic materials 0.000 description 1
- 229910000943 NiAl Inorganic materials 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910033181 TiB2 Inorganic materials 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910000907 nickel aluminide Inorganic materials 0.000 description 1
- WCSXVKQKODOOCM-UHFFFAOYSA-N nickel platinum Chemical compound [Ni][Pt][Ni] WCSXVKQKODOOCM-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005382 thermal cycling Methods 0.000 description 1
- -1 titanium diboride Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
- C23C14/5806—Thermal treatment
- C23C14/5813—Thermal treatment using lasers
-
- 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
- C23C10/60—After-treatment
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/08—Oxides
- C23C14/083—Oxides of refractory metals or yttrium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/58—After-treatment
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01D—NON-POSITIVE DISPLACEMENT MACHINES OR ENGINES, e.g. STEAM TURBINES
- F01D5/00—Blades; Blade-carrying members; Heating, heat-insulating, cooling or antivibration means on the blades or the members
- F01D5/12—Blades
- F01D5/28—Selecting particular materials; Particular measures relating thereto; Measures against erosion or corrosion
- F01D5/288—Protective coatings for blades
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T50/00—Aeronautics or air transport
- Y02T50/60—Efficient propulsion technologies, e.g. for aircraft
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Optics & Photonics (AREA)
- General Engineering & Computer Science (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
An improvement in a thermal barrier coating for superalloy turbine engine components subjected to high operating temperatures, such as turbine airfoils, e.g., vanes and blades, is disclosed which eliminates the expensive MCrAlY oxidation resistant bond coating underlayer for a columnar grained ceramic thermal barrier coating. In accordance with my present invention, a relatively low cost thermal barrier coating system for superalloy turbine components is provided which utilizes a diffusion aluminide coating layer as the oxidation resistant bonding surface for the columnar grained ceramic insulating coating.
Description
Thermal Barrier Coating System for Superalloy Components AC An improvement in a thermal barrier coating for superalloy turbine engine components subjected to high operating temperatures, such as turbine airfoils, e.g., vanes and blades, is disclosed which eliminates the expensive MCrAlY oxidation resistant bond coating underlayer for a columnar grained ceramic thermal barrier coating. In accordance with my present invention, a relatively low cost thermal barrier coating system for superalloy turbine components is provided which utilizes a diffusion aluminide coating layer as the oxidation resistant bonding surface for the columnar grained ceramic insulating coating.
BACKGROUND OP THE INVENTION
Gas turbine engine fuel efficiency typically improves as turbine gas temperatures increase. Consequently, air-cooled superalloy airfoils have been developed to enhance engine performance. Purther improvements in turbine performance and component durability can be obtained by the use of protective thermal barrier coatings which insulate the component and inhibit oxidation and hot corrosion (accelerated oxidation by fuel and air Impurities such as sulfur and salt) of the superalloy.
A particular type of ceramic coating which is adherent to the metallic component but yet resistant to spalling during thermal cycling, is known as a columnar grained ceramic thermal barrier coating. The ceramic coating layer has a columnar grained microstructure and is bonded to the metal structure.
Porosity between the individual columns permits the columnar grained coating to expand and contract without developing stresses sufficient to induce spalling.
In accordance with present practice, the metallic article to be protected with the thermal barrier ceramic coating must first be coated with an adherent
MCrAlY (M = Ni, Co, Be) bond coating under layer which is compositionally tailored to grow an adherent, predominately aluminum oxide scale, which inhibits oxidation of the superalloy and provides a satisfactprvniirj face for the ceramic coating layer.
The cost of the MCrAlY underlayer, which is normally applied by vapor deposition or other conventional coating techniques, adds substantially to the total cost of the thermal barrier coating system.
DISCUSSION OF ThE PRIOR ART
My patents No. 4,321,311; 4,401,697 and 4,405,659 and those of Ulion and
Ruckle, 4,321,310 and 4,405,660 disclose a thermal barrier coating system for a superalloy, formed by first applying a 1 to 10 mil thick MCrAlY vapor deposition coating on the superalloy substrate followed by the formation of a thin, thermally grown aluminum oxide (alumina) layer to which the columnar grain ceramic thermal barrier coating, e8. zirconia stabilized with yttria oxide, is applied.
When using thermal barrier coatings of the type described in my patent
No. 4,321,311, it is common practice to also coat internal aircooling passages with a diffusion aluminide coating to inhibit oxidation at those locations.
During application of the aluminide coating to internal surfaces, external component surfaces will also be coated with a diffusion aluminide unless they are masked. Patent No. 4,005,989 teaches that an aluminide coating layer under an MCrAIY coating will increase coating durability. Consequently, my patent No. 4,321,311 also teaches that an MCrAlY coating over a diffusion aluminide coating will provide an acceptable surface for subsequent application of a columnar grained ceramic thermal barrier coating layer.
Reissue Patent No. 31,339 discloses the application of a MCrAlY bond coat to the superalloy substrate, by plasma spraying, followed by application of an aluminide coating on the MCrAlY bond coating, followed by hot isostatic pressure treatment of the assemblage.
None of the above references, however, suggest that a columnar grained ceramic thermal barrier coating will perform satisfactorily if applied directly to a diffusion aluminide coating formed on the superalloy substrate.
DISCLOSURE OP TBE MENTION In many instances, lower cost diffusion aluminide coatings are sufficient to provide required oxidation resistance to both internal and external surfaces of turbine airfoils. However, an insulative ceramic layer On the external airfoil surfaces will further improve component durability by reducing both metal temperatures and the magnitude of thermal strains in the metal. Alternatively, the benefit of a ceramic layer can be utilized to increase turbine performance by permitting cooling air requirements to be reduced or by allowing turbine inlet temperatures to be increased.
In my prior patent No. 4,321,311, I utilized an MOrAlY bond coating to both inhibit oxidation and provide a bonding surface for the ceramic layer. In most gas turbine applications, however, it is not necessary to use an expensive
MCrAlY coating to inhibit oxidation. It was subsequently discovered that for several superalloys it is not necessary to utilize an MCrAIY coating layer to develop an adherent alumina scale, which is necessary for ceramic layer adhesion.In several Instances, it was discovered that a lower cost diffusion aluminide coating could thermally grow an alumina scale with sufficient adhesion for e viable bonding surface. Consequently, the cost of a thermal barrier coating can be significanUy reduced in those instances where the diffusion aluminide coating provides an edequate bonding surface.
Air-cooled turbine blades are typically aluminized on internal surfaces to inhibit oxidation. However, since the diffusion aluminizing process is multidirectional, it can provide an aluminide layer on the entire blade, in. both interior and exterior, and in many instances this diffusion aluminide coating provides adequate oxidation resistance. In accordance with my present invention, it has been found that the ceramic thermal barrier coating may be applied directly to the diffusion aluminide coating, thus eliminating the expensive MCrAlY coating layer. The ceramic thermal barrier coating, in contrast to the aluminide application process, is applied by a line-of-sight process which coats only the desired portion of the component, i.e. the exterior portion of the airfoil.
Although coatings of this invention have been thusfar developed for their thermal barrier benefits, other uses can also be anticipated. In particular, thin
ceramic coatings (eg. stabilized zirconia, zircon) applied on top of diffusion
aluminides have potential value in inhibiting hot corrosion attack of the
component by fuel and air impurities (eg., sulfur and salt). Subsequent
densification of the outer surface of the columnar ceramic layer (e.g. by laser
glazing) would increase the surface density and hardness and thus provide a
barrier to inhibit both hot corrosion and erosion from ingested sand or
combustor produced carbon particles.
BRIEF DESCRIPTION OF THE DRAWINGS
My invention will be described hereinafter with reference to the
accompanying drawings, wherein: Figure 1 is a cross sectional view of a magnified schematic drawing of the
coating of the invention;
Figure 2 is a photomicrograph of a superalloy substrate coated in
accordance with my invention; and Pigure 3 is a photograph showing turbine blades coated in accordance with
this invention.
DESCRIPTION OP TBE PREPERRED EMBODIMENT
My present invention involves a thermal barrier coated turbine component
which include two inter-related layers on the superalloy substrate. The base
metal or substrate of my present invention may be nickel, cobalt or iron base
high temperature alloys used for turbine airfoil applications, i.e. blades or
vanes. My present invention is particularly applicable to hafnium and/or
zirconium containing superalloys such as MAR-M247, IN-100 and MAR-M 509,
the compositions of which are shown in Table 1.
TABLE I
ALLOY Mo W Ta Al Ti Cr Co Hf V Zr C B Ni
Mar-M247 .65 10 3.3 5.5 1.05 8.4 10 1.4 - .055 .15 .15 bal.
IN-100 3.0 - - 5.5 4.7 9.5 15.0 1.0 .06 .17 .015 bal.
Mar-M509 - 7.0 3.5 - 0.25 23.4 Bal. - - .5 .6 - 10.0
Diffusion aluminide coatings have adequate oxide scale adhesion on hafnium and/or zirconium containing superalloys. Oxide scale adhesion may be promoted for coatings of my present invention on superalloys which do not contain hafnium, or a similar element, such as La, by the use of complex diffusion aluminides; i.e. aluminide coatings containing additions of elements which promote oxide scale adhesion, such as Pt, Rh, Si, and Hf.
The diffusion aluminide coating used in connection with my present invention can be applied by standard commercially available aluminide processes whereby aluminum is reacted at the substrate surface to form an aluminum intermetallic compound which provides a reservoir for the alumina scale oxidation resistant layer. Thus the aluminide coating is predominately composed of aluminum intermetallic [eg. NiAl, CoAl, FeAl and (Ni, Co, Fe)A1 phases] formed by reacting aluminum vapor species, aluminum rich alloy powder or surface layer with the substrate elements in the outer layer of the superalloy component. This layer is typically well bonded to the substrate.Aluminiding may be accomplished by one of several conventional prior art techniques, such as, the pack cementation process, spraying, chemical vapor deposition, electrophoresis, sputtering, and slurry sintering with an aluminum rich vapor and appropriate diffusion heat treatments. The aluminiding layer may be applied at a temperature from room temperature to 21000P depending upon the particular aluminiding process employed. The aluminiding layer for my present invention, should be applied to a thickness of about 1 to 5 mils.
Other beneficial elements can also be incorporated into diffusion aluminide coatings by a variety of processes. Beneficial elements include Pt,
Si, Hf and oxide particles, such as alumina, yttria, hafnia, for enhancement of alumia scale adhesion, Cr and Mn for hot corrosion resistance, Rh, Ta and Cb for diffusional stability and/or oxidation resistance and Ni, Co for increasing ductility or incipient melting limits. These elements can be added to the surface of the component prior to aluminizing by a wide range of processes including electroplating, pack cementation, chemical vapor deposition, powder metal layer deposition, thermal spray or physical vapor deposition processes.
Some methods of coating, such as slurry fusion, permit some or all of the benefical coating elements, including the aluminum, to be added concurrently.
Other processes, such-as chemical vapor aepab;lL1,, Smrr pedR cementation, can be modified to concurrently apply elements such as Si and Cr with the aluminum. In addition, it is obvious to those skilled in the art that diffusion aluminide coatings will contain all elements present within the surface layer of the substrate.
In the specific case of platinum modified diffusion aluminide coating layers, the coating phases adjacent to the alumina scale will be platinum aluminide and/or nickelplatinum aluminide phases (on a Niobase superalloy).
The diffusion aluminide coating in accordance with my present invention provides aluminum rich intermetallic phase(s) at the surface of the substrate which serve as an aluminum reservoir for subsequent alumina scale growth. An alumina scale or layer is utilized in my present invention between the diffusion aluminide coating and the ceramic layer to provide both oxidation resistance and a bonding surface for the ceramic layer. The alumina layer may be formed before the ceramic thermal barrier coating is applied or formed during application of the thermal barrier columnar grained coating. The alumina scale can also be grown subsequent to the application of the ceramic coating by heating the coated article in an oxygen containing atmosphere at a temperature consistent with the temperature capability of the superalloy, or by exposure to the turbine environment.The suSmicron thick alumina scale will thicken on the aluminide surface by heating the material to normal turbine exposure conditions. The thickness of the alumina scale is preferably suSmieron (up to about one micron).
The thermal barrier coating which is applied as the final coating layer in my present invention, is a columnar grained ceramic coating which is tightly bonded to the underlying alumina film on the aluminide coating, which is applied to the substrate. The columnar grains are oriented substantially perpendicular to the surface of the substrate with interstices between the individual columns extending from the surface of the thermal barrier coating down to or near (within a few microns) the alumina film on the aluminide coating. The columnar grained structure of this type of thermal barrier coating minimizes any stresses associated with the difference in the ocoefficients of thermal expansion between the substrate and the thermal barrier coating, which would otherwise cause a failure in a derse or continuous ceramic thermal barrier coating.When he the cledThte tae expands (or contracts) at a greater rate than the ceramic thermal barrier coating. Gaps between the ceramic columnar grains permit the grains to expand and contract without producing sufficient stress to induce spilling or cracking of the thermal barrier coating. This limits the stress at the interface between the substrate and the thermal barrier coating, thus preventing fractures in the ceramic coating.
The columnar grain thermal barrier coating used in my present invention may be any of the conventional ceramic compositions used for this purpose.
Currently the strain-tolerant zirconia coatings are believed to be particularly effective as thermal barrier coatings; however, my present invention is equally applicable to other ceramic thermal barrier coatings. A preferred ceramic coating is the yttria stabilized zirconia coating. These zirconia ceramic layers have a thermal conductivity that is about 1 and one-half orders of magnitude lower than that of the typical superalloy substrate such as MAR-M247. The zirconia may be stablized with CaO, MgO, Ce02 as well as Y203. Other ceramics which are believed to be useful as the columnar type coating materials within the scope of my present invention are alumina, ceria, hafnia (yttria-stabilized), mullite, zirconium silicate and certain borides and nitrides, e.g. titanium diboride, and silicon nitride.
The columnar ceramic material may have some degree of solid solubility with the alumina scale. Also the particular ceramic material selected for use as the columnar grain thermal barrier coating should be stable in the high temperature environment of a gas turbine.
The ceramic layer may be applied by a prior art technique which provides an open columnar microstructure, preferably the electron beam evaporationphysical vapor deposition process. The thickness of the ceramic layer may vary from 1 to 1000pm but is typically in the 50 to 300pm range for typical thermal barrier applications.
The electron beam evaporation-physical vapor deposition process for applying the thermal barrier coating is a modification of the standard high-rate vapor deposition process for metallic coatings. Power to evaporate the ceramic coating material is provided by a highenergy electron beam gun. The zirconia vapor produced by evaporation of the zirconia target material, condenses onto the turbine airfoil component to form the thermal barrier coating. Zirconia coating deposition rates are typically in the range of about 0.01 to 1.0 mils per minute. The parts to be coated are preheated in a load lock by either radiant or electron beam heat sources and/or heated in the coating chamber prior to exposure to the ceramic vapor.During coating, the component temperature is typically maintained in the 1500 to 21 000F range. Since zirconia becomes somewhat oxygen deficient due to partial dissociation during evaporation in a vacuum, oxygen is also bled into the yttria-stablized zirconia vapor cloud to minimize any deviation from stoichiometry during coating.
By my present invention the ceramic thermal barrier coating is applied directly to the diffusion aluminide metallic coating.
In accordance with my present invention, ceramic coatings on turbine airfoils accommodate large strains without developing stresses of a sufficient
magnitude to cause spalling. This strain tolerance is achieved by the above
mentioned microstructural discontinuities within the columnar grained ceramic
insulative layer, which permits the ceramic-layer strain to be accommodated
with minimal stress on the ceramic to metal interface region.
Figure 1 is a schematic cross-sectional line drawing showing a coating in
accordance with my present invention, wherein the aluminide coating 5 is
applied to the superalloy substrate 6 and an adherent alumina scale layer 7 is
formed on the aluminide coating 5. The columnar grain ceramic layer 8
overlays the alumina layer 7.
Figure 2 is a photomicrograph of a zirconia insulative layer deposited on
superalloy substrate in accordance with my present invention. In this thermal
barrier coating system, a diffusion aluminide oxidation resistant layer 10 was
deposited directly on the Mar-M 247 superalloy substrate 12 and a yttria
stabilized zirconia thermal barrier coating 14 was applied to the substrate. As
may be seen from Figure 2, a thin alumina film 16 is formed between the
diffusion aluminide coating and the zirconia coating. The Hf content of the
superalloy substrate enhances the adhesion of the alumina layer formed on the
aluminide and to which the zirconia layer is adherred.
Figure 3 is a photograph of a turboprop engine turbine showing high
pressure turbine blades mounted in disc 20. Blades 22 and 24 shown as whitish,
have been coated in accordance with my present invention with yttria
stabilized zirconia. The blades are shown subsequent to 240 hours service in a
TPE 331-10 Turbo-orop Engine.
EXAMPLE 1
TPE 331-10 turboprop engine high pressure turbine blades of IN-100 alloy were coated with a diffusion alummide plus EOPVD yttria-stabilized zirconia system. The commercially available Chromalloy RT-21 pack cementation diffusion nickel aluminide coating was applied to a nominal thickness of 2 mils.
Pollowing application of the diffusion aluminide coating layer, the yttria (approximately 20%) stabilized zirconia coating layer was applied to the surface of the aluminide coated blades, by the commercial Airco Temescal EOPVD process. The thickness of the zirconia coating was also 2 mils. The ceramic coating was applied by evaporating a yttria-stabilized zirconia ingot with power provided by a high-energy electron beam gun focused magnetically onto the zirconia target, which was the vapor source. The cloud of zirconia vapor is produced by the evaporation of the zirconia target material and vapor from this cloud condensed onto the blades at a rate of about 0.2 mil/min. to form the ceramic coating layer. Substrate temperature during coating was about 1S000F.
The coated blades were then installed in the TPE 331-10 engine and successfully tested for 240 hours of engine operating time. Pigure 3 shows the blades after the test, confirming that the blades were in good condition after the 240 hour engine test.
EXAMPLE 2
A burner rig specimen of MAR-M247 was diffusion aluminide coated with the Chromalloy RT-21 pack cementation process to a nominal thickness of 2 mils and then a 5 mil thick Y203 stabilized zirconia coating applied by a commercial Airco Temescal EB-PVD process. A second burner rig specimen was diffusion aluminide coated with Chromalloy's RT 22 process which provides a Pt-modified aluminide coating, and the same columnar grained ceramic coating applied. The burner rig specimens were subjected to a test cycle comprising 4 minutes at 21000F followed by 2 minutes of forced air cooling.
The specimens withstood 400 cycles over a 40 hour period.
EXAMPLE 3
ATF3-6 turbofan engine high pressure turbine paired-vanes of the MAR-M 509 alloy were coated with a diffusion aluminide plus EB-PVD yttria-stabilized zirconia system in accordance with this invention. The commercially available chromalloy RT-l 9 pack cememtation diffusion cobalt aluminide coating was applied to a nominal thickness of 2 mils. Following application of the diffusion aluminide coating layer, the yttria-stabilized (approximately 20%) zirconia coating layer was applied to the surface of the aluminide coated vanes by a commercially available Airco Temescal ESPVD process. The nominal thickness of the zirconia coating was 3 to 8 mils.
These thermal barrier coated paired vanes were concurrently evaluated with paired vanes coated with only the diffusion aluminide for 217 hours in an
ATF 36 test engine. Post-test examination indicated that the durability of the thermal barrier coated vanes was increased relative to the vanes without the insulative zirconia coating layer.
While my present invention has been described herein with a certain degree of particularity In reference to certain specific coating and alloy compositions which were formulated and tested, it is to be understood that the scope of my invention is not limited thereto, but should be afforded the iull scope of the appended claims.
Claims (20)
1. A superalloy article having a ceramic thermal barrier coating, comprising:
(a) a superalloy substrate,
(b) an adherent diffusion aluminide bond coating applied to said
substrate and forming a reservoir of aluminum for the formation of
an alumina protective scale on said aluminide coated substrate, and
(c) a columnar grained ceramic coating bonded to said aluminide
alumina coating.
2. The article of Claim 1 wherein said diffusion aluminide coating is from 0.5 to 5 mils thick.
3. The article of Claim 1 wherein the ceramic coating is from 0.5 to 50 mils thick.
4. The article of Claim 1 wherein said diffusion aluminide coating is modified by at least one of the elements selected from the group consisting of
Pt, Rh, Si, Hf, Cr, Mn, Ta, and Cb.
5. The article of Claim 1 wherein said diffusion aluminide coating is modified by dispersed particles selected from the group consisting of alumina, yttria or hafnia.
6. The article of Claim 1 having an MCrAlY overlay coating applied to the superalloy substrate under the diffusion aluminide coating.
7. The article of Claim 1 wherein an adherent alumina layer is formed between said aluminide coating and said ceramic coating.
8. The article of Claim 1 wherein said ceramic coating is yttriastabilized zirconia.
9. The article of Claim 1 wherein said ceramic coating is zirconia stabilized with at least one oxide selected from the group consisting of CaO,
MgO, and CeO2.
10. The article of Claim 1 wherein said ceramic coating is selected from the group consisting of alumina, ceria, yttria stebilized hafnia, zirconium silicate or mullite.
11. The article of Claim 1 wherein said ceramic coating is selected from the group consisting of borides and nitrides.
12. The article of Claim 1 wherein up to 0.1 mil of the ceramic adjacent to the alumina scale has a denser microstructure, which may vary from equiaxed grains to columnar grains with the balance of the ceramic coating having a fully columnar grained microstructure.
13. The article of Claim 1 wherein the exterior of the ceramic coating is densified by glazing.
14. The method for producing a superalloy article having an adherent ceramic thermal barrier coating thereon, comprising the steps:
(a) providing a superalloy substrate with a clean surface;
(b) applying a diffusion aluminide layer to the clean superalloy
substrate surface, and
(c) applying a columnar grained ceramic coating to the diffusion
aluminide layer on said superalloy substrate.
15. The method of Claim 14 including the step of forming an adherent alumina layer on said diffusion aluminide coating.
16. The method of Claim 15 wherein said alumina layer is formed on said aluminide coating by heat treating the ceramic coated article in an oxygen containing atmosphere at a temperature of between 1600 and 21000F.
17. The method of Claim 14 including the step of modifying the substrate surface by applying a material selected from the group consisting of
h
Pt, R@, Si, Hf, Cr, Ta, Cb, alumina, yttria, hafnia, or a MCrAIY surface layer, prior to aluminiding.
18. The method of Claim 14 including the step of densifying the exterior of the ceramic coating by electron beam glazing.
19. The method of Claim 14 including the step of densifying the exterior of the ceramic coating by laser glazing.
20. A method for producing a superalloy article substantially as hereinbefore described with references to the Examples.
20. The method of Claim 14 wherein said columnar grained ceramic coating is applied by vapor deposition.
Amendments to the claims have been filed as follows 1. A superalloy article having a ceramic thermal barrier coating on at least a portion of its surface, comprising:
(a) a superalloy substrate,
(b) an adherent diffusion aluminide coating applied to said portion of the substrate and adapted to be a reservoir of aluminum for the subsequent in situ formation by oxidation of an alumina protective scale on said aluminide coated substate; and
(c) a columnar grained ceramic coating bonded directly to said aluminide coating or said subsequently formed alumina scale and adapted to allow in situ oxidation of said aluminide to alumina.
2. An article according to claim 1, wherein the diffusion aluminide coating is from 0.5 to 5 mils thick.
3. An article according to claim 1 or 2, wherein the ceramic coating is from 0.5 to 50 mils thick.
4. An article according to any one of the preceding claims, wherein the diffusion aluminide coating is modified by at least one of the elements selected from the group consisting of Pt, Rh, Si, Hf, Cr, Mn, Ta, and Cb.
5. An article according to any one of the preceding claims, wherein the diffusion aluminide coating is modified by dispersed particles selected from the group consisting of alumina, yttria or hafnia.
6. An article according to any one of the preceding claims, wherein the ceramic coating is yttria-stabilized zirconia.
7. An article according to any one of claims 1 to 5, wherein the ceramic coating is zirconia stabilized with at least one oxide selected from the group consisting of CaO,
MgO, and CeO2.
8. An article according to any one of claims 1 to 5, wherein the ceramic coating is selected from the group consisting of alumina, cera, yttria-stabilized hafnia, zirconium silicate or mullite.
9. An article according to any one of claims 1 to 5, wherein the ceramic coating is selected from the group consisting of borides and nitrides.
10. An article according to any one of the preceding claims, wherein up to 0.1 mil of the ceramic adjacent to the alumina scale has a denser microstructure, which may vary from equiaxed grains to columnar grains with the balance of the ceramic coating having a fully columnar grained microstructure.
11. An article according to any one of the preceding claims, wherein the exterior of the ceramic coating is densified by glazing.
12. A method for producing a superalloy article having an adherent ceramic thermal barrier coating thereon, comprising the steps of:
(a) providing a superalloy substrate with a clean surface;
(b) applying a diffusion aluminide layer to at least a portion of the clean superalloy substrate surface, and
(c) applying a columnar grained ceramic coating directly to the diffusion aluminide layer on said superalloy substrate.
13. A method according to claim 12, including the further step of forming, in situ, an adherent alumina layer on the diffusion aluminide coating by oxidation thereof.
14. A method according to claim 13, wherein the alumina layer is formed on the aluminide coating by heat treating the ceramic coated article in an oxygen containing atmosphere at a temperature of between 1600 and 2100-F.
15. A method according to any one of claims 12 to 14, including the step of modifying the substrate surface by applying a material selected from the group consisting of
Pt, Rh, Si, Hf, Cr, Ta, Cb, alumina, yttria and hafnia prior to aluminiding.
16. A method according to any one of claims 12 to 15, including the step of densifying the exterior of the ceramic coating by electron beam glazing.
17. A method according to any one of claims 12 to 15, including the step of densifying the exterior of the ceramic coating by laser glazing.
18. A method according to any one of claims 12 to 17, wherein the columnar grained ceramic coating is applied by vapor deposition.
19. A superalloy article as hereinbefore described with references to the Examples.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8520732A GB2285632B (en) | 1985-08-19 | 1985-08-19 | Thermal barrier coating system for superalloy components |
| FR8512633A FR2718464A1 (en) | 1985-08-19 | 1985-08-22 | Superalloy article and method of mfr. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8520732A GB2285632B (en) | 1985-08-19 | 1985-08-19 | Thermal barrier coating system for superalloy components |
| FR8512633A FR2718464A1 (en) | 1985-08-19 | 1985-08-22 | Superalloy article and method of mfr. |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8520732D0 GB8520732D0 (en) | 1995-03-15 |
| GB2285632A true GB2285632A (en) | 1995-07-19 |
| GB2285632B GB2285632B (en) | 1996-02-14 |
Family
ID=26224688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8520732A Expired - Lifetime GB2285632B (en) | 1985-08-19 | 1985-08-19 | Thermal barrier coating system for superalloy components |
Country Status (2)
| Country | Link |
|---|---|
| FR (1) | FR2718464A1 (en) |
| GB (1) | GB2285632B (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0792948A1 (en) * | 1996-02-29 | 1997-09-03 | Societe Nationale D'etude Et De Construction De Moteurs D'aviation "Snecma" | Thermal barrier coating with improved underlayer and articles having this thermal barrier coating |
| EP0814178A1 (en) * | 1996-06-19 | 1997-12-29 | ROLLS-ROYCE plc | A thermal barrier coating for a superalloy article and a method of application thereof |
| 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 |
| GB2322869A (en) * | 1997-03-04 | 1998-09-09 | Rolls Royce Plc | A coated superalloy article |
| US5824423A (en) * | 1996-02-07 | 1998-10-20 | N.V. Interturbine | Thermal barrier coating system and methods |
| US5981091A (en) * | 1994-12-24 | 1999-11-09 | Rolls-Royce Plc | Article including thermal barrier coated superalloy substrate |
| WO2001061067A1 (en) * | 2000-02-17 | 2001-08-23 | Anatoly Nikolaevich Paderov | Combined protective coating of parts made of heat resisting alloys |
| EP1184479A1 (en) * | 2000-08-28 | 2002-03-06 | Snecma Moteurs | Method of forming a reactive-element containing aluminide on a metallic substrate |
| WO2006036171A1 (en) * | 2004-09-16 | 2006-04-06 | Aeromet Technologies, Inc. | Superalloy jet engine components with protective coatings and method of forming such protective coatings on superalloy jet engine components |
| WO2006052277A3 (en) * | 2004-09-16 | 2007-02-15 | Aeromet Technologies Inc | Gas turbine engine components with aluminide coatings and method of forming such aluminide coatings on gas turbine engine components |
| US9133718B2 (en) | 2004-12-13 | 2015-09-15 | Mt Coatings, Llc | Turbine engine components with non-aluminide silicon-containing and chromium-containing protective coatings and methods of forming such non-aluminide protective coatings |
| WO2020172016A1 (en) * | 2019-02-20 | 2020-08-27 | General Electric Company | Dense abradable coating with brittle and abradable components |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9800511D0 (en) * | 1998-01-13 | 1998-03-11 | Rolls Royce Plc | A metallic article having a thermal barrier coating and a method of application thereof |
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| WO1981001983A1 (en) * | 1980-01-07 | 1981-07-23 | United Technologies Corp | Columnar grain ceramic thermal barrier coatings on polished substrates |
| US4321311A (en) * | 1980-01-07 | 1982-03-23 | United Technologies Corporation | Columnar grain ceramic thermal barrier coatings |
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| FR1351302A (en) * | 1962-03-23 | 1964-01-31 | Bbc Brown Boveri & Cie | Process for obtaining a base coat preparatory to the application of a ceramic coating on metal parts |
| GB1077735A (en) * | 1964-08-14 | 1967-08-02 | Power Jets Res & Dev Ltd | Coatings for metallic materials |
| CH1466870A4 (en) * | 1970-10-02 | 1977-08-15 | ||
| US3811959A (en) * | 1971-05-17 | 1974-05-21 | Chromalloy American Corp | Corrosion resistant coating system |
| GB1384883A (en) * | 1972-01-11 | 1975-02-26 | Inst Metallurg Im Aa Baikova A | Method for applying nonmetallic coatings |
| US3837894A (en) * | 1972-05-22 | 1974-09-24 | Union Carbide Corp | Process for producing a corrosion resistant duplex coating |
| SE8000480L (en) * | 1979-02-01 | 1980-08-02 | Johnson Matthey Co Ltd | ARTICLE SUITABLE FOR USE AT HIGH TEMPERATURES |
| JPS5947382A (en) * | 1982-09-09 | 1984-03-17 | Usui Internatl Ind Co Ltd | Heat and corrosion resistant coated steel material |
| US5238752A (en) * | 1990-05-07 | 1993-08-24 | General Electric Company | Thermal barrier coating system with intermetallic overlay bond coat |
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- 1985-08-22 FR FR8512633A patent/FR2718464A1/en active Granted
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1981001983A1 (en) * | 1980-01-07 | 1981-07-23 | United Technologies Corp | Columnar grain ceramic thermal barrier coatings on polished substrates |
| US4321311A (en) * | 1980-01-07 | 1982-03-23 | United Technologies Corporation | Columnar grain ceramic thermal barrier coatings |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5981091A (en) * | 1994-12-24 | 1999-11-09 | Rolls-Royce Plc | Article including thermal barrier coated superalloy substrate |
| US5824423A (en) * | 1996-02-07 | 1998-10-20 | N.V. Interturbine | Thermal barrier coating system and methods |
| EP0792948A1 (en) * | 1996-02-29 | 1997-09-03 | Societe Nationale D'etude Et De Construction De Moteurs D'aviation "Snecma" | Thermal barrier coating with improved underlayer and articles having this thermal barrier coating |
| FR2745590A1 (en) * | 1996-02-29 | 1997-09-05 | Snecma | THERMAL BARRIER COATING WITH IMPROVED UNDERLAYER AND PARTS COATED BY SUCH A THERMAL BARRIER |
| US5843585A (en) * | 1996-02-29 | 1998-12-01 | Societe Nationale D'etude Et De Construction De Moteurs D'aviation "Snecma" | Thermal barrier coating with improved sub-layer and parts coated with said thermal barrier |
| EP0814178A1 (en) * | 1996-06-19 | 1997-12-29 | ROLLS-ROYCE plc | A thermal barrier coating for a superalloy article and a method of application thereof |
| RU2127772C1 (en) * | 1996-06-19 | 1999-03-20 | Роллс-Ройс плс | Multilayer heat barrier coating of base from superstrength alloy and method of its application |
| US5942337A (en) * | 1996-06-19 | 1999-08-24 | Rolls-Royce, Plc | Thermal barrier coating for a superalloy article and a method of application thereof |
| 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 |
| GB2322869A (en) * | 1997-03-04 | 1998-09-09 | Rolls Royce Plc | A coated superalloy article |
| WO2001061067A1 (en) * | 2000-02-17 | 2001-08-23 | Anatoly Nikolaevich Paderov | Combined protective coating of parts made of heat resisting alloys |
| EP1184479A1 (en) * | 2000-08-28 | 2002-03-06 | Snecma Moteurs | Method of forming a reactive-element containing aluminide on a metallic substrate |
| US6673709B2 (en) | 2000-08-28 | 2004-01-06 | Snecma Moteurs | Formation of an aluminide coating, incorporating a reactive element, on a metal substrate |
| WO2006036171A1 (en) * | 2004-09-16 | 2006-04-06 | Aeromet Technologies, Inc. | Superalloy jet engine components with protective coatings and method of forming such protective coatings on superalloy jet engine components |
| WO2006052277A3 (en) * | 2004-09-16 | 2007-02-15 | Aeromet Technologies Inc | Gas turbine engine components with aluminide coatings and method of forming such aluminide coatings on gas turbine engine components |
| US7901739B2 (en) | 2004-09-16 | 2011-03-08 | Mt Coatings, Llc | Gas turbine engine components with aluminide coatings and method of forming such aluminide coatings on gas turbine engine components |
| US8623461B2 (en) | 2004-09-16 | 2014-01-07 | Mt Coatings Llc | Metal components with silicon-containing protective coatings substantially free of chromium and methods of forming such protective coatings |
| US9133718B2 (en) | 2004-12-13 | 2015-09-15 | Mt Coatings, Llc | Turbine engine components with non-aluminide silicon-containing and chromium-containing protective coatings and methods of forming such non-aluminide protective coatings |
| WO2020172016A1 (en) * | 2019-02-20 | 2020-08-27 | General Electric Company | Dense abradable coating with brittle and abradable components |
| US11149354B2 (en) | 2019-02-20 | 2021-10-19 | General Electric Company | Dense abradable coating with brittle and abradable components |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2285632B (en) | 1996-02-14 |
| FR2718464B1 (en) | 1997-02-28 |
| GB8520732D0 (en) | 1995-03-15 |
| FR2718464A1 (en) | 1995-10-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 20050818 |