US20060016191A1 - Combined effusion and thick TBC cooling method - Google Patents
Combined effusion and thick TBC cooling method Download PDFInfo
- Publication number
- US20060016191A1 US20060016191A1 US10/897,788 US89778804A US2006016191A1 US 20060016191 A1 US20060016191 A1 US 20060016191A1 US 89778804 A US89778804 A US 89778804A US 2006016191 A1 US2006016191 A1 US 2006016191A1
- Authority
- US
- United States
- Prior art keywords
- stabilized
- yttria
- depositing
- tbc
- thermal barrier
- 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.)
- Abandoned
Links
- 238000001816 cooling Methods 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 claims abstract description 101
- 239000000758 substrate Substances 0.000 claims abstract description 59
- 238000005553 drilling Methods 0.000 claims abstract description 47
- 238000000151 deposition Methods 0.000 claims abstract description 36
- 230000011218 segmentation Effects 0.000 claims abstract description 27
- 239000012720 thermal barrier coating Substances 0.000 claims description 151
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 34
- 241000588731 Hafnia Species 0.000 claims description 29
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 claims description 29
- 238000000576 coating method Methods 0.000 claims description 27
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 claims description 27
- 239000011248 coating agent Substances 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 24
- 239000010987 cubic zirconia Substances 0.000 claims description 16
- 238000009527 percussion Methods 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 13
- 239000007921 spray Substances 0.000 claims description 10
- 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 9
- 238000003754 machining Methods 0.000 claims description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 6
- CMIHHWBVHJVIGI-UHFFFAOYSA-N gadolinium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[Gd+3].[Gd+3] CMIHHWBVHJVIGI-UHFFFAOYSA-N 0.000 claims description 6
- 238000010894 electron beam technology Methods 0.000 claims description 5
- 238000005240 physical vapour deposition Methods 0.000 claims description 5
- 230000000087 stabilizing effect Effects 0.000 claims description 5
- 238000011105 stabilization Methods 0.000 claims description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 3
- 241000968352 Scandia <hydrozoan> Species 0.000 claims description 3
- 239000000292 calcium oxide Substances 0.000 claims description 3
- 235000012255 calcium oxide Nutrition 0.000 claims description 3
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims description 3
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 3
- 239000000395 magnesium oxide Substances 0.000 claims description 3
- PLDDOISOJJCEMH-UHFFFAOYSA-N neodymium(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Nd+3].[Nd+3] PLDDOISOJJCEMH-UHFFFAOYSA-N 0.000 claims description 3
- HJGMWXTVGKLUAQ-UHFFFAOYSA-N oxygen(2-);scandium(3+) Chemical compound [O-2].[O-2].[O-2].[Sc+3].[Sc+3] HJGMWXTVGKLUAQ-UHFFFAOYSA-N 0.000 claims description 3
- FKTOIHSPIPYAPE-UHFFFAOYSA-N samarium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[Sm+3].[Sm+3] FKTOIHSPIPYAPE-UHFFFAOYSA-N 0.000 claims description 3
- -1 ytterbia Chemical compound 0.000 claims description 3
- 238000007750 plasma spraying Methods 0.000 claims 3
- 238000005336 cracking Methods 0.000 abstract description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 12
- 239000000919 ceramic Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 8
- 229910001233 yttria-stabilized zirconia Inorganic materials 0.000 description 8
- 229910000601 superalloy Inorganic materials 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000873 masking effect Effects 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000009760 electrical discharge machining Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000003628 erosive effect Effects 0.000 description 3
- 238000004901 spalling Methods 0.000 description 3
- 229910000951 Aluminide Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 229910052727 yttrium Inorganic materials 0.000 description 2
- 229910000943 NiAl Inorganic materials 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910002076 stabilized zirconia Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical group [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23R—GENERATING COMBUSTION PRODUCTS OF HIGH PRESSURE OR HIGH VELOCITY, e.g. GAS-TURBINE COMBUSTION CHAMBERS
- F23R3/00—Continuous combustion chambers using liquid or gaseous fuel
- F23R3/02—Continuous combustion chambers using liquid or gaseous fuel characterised by the air-flow or gas-flow configuration
- F23R3/04—Air inlet arrangements
- F23R3/06—Arrangement of apertures along the flame tube
-
- 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
-
- 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
-
- 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/18—After-treatment
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23M—CASINGS, LININGS, WALLS OR DOORS SPECIALLY ADAPTED FOR COMBUSTION CHAMBERS, e.g. FIREBRIDGES; DEVICES FOR DEFLECTING AIR, FLAMES OR COMBUSTION PRODUCTS IN COMBUSTION CHAMBERS; SAFETY ARRANGEMENTS SPECIALLY ADAPTED FOR COMBUSTION APPARATUS; DETAILS OF COMBUSTION CHAMBERS, NOT OTHERWISE PROVIDED FOR
- F23M5/00—Casings; Linings; Walls
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23M—CASINGS, LININGS, WALLS OR DOORS SPECIALLY ADAPTED FOR COMBUSTION CHAMBERS, e.g. FIREBRIDGES; DEVICES FOR DEFLECTING AIR, FLAMES OR COMBUSTION PRODUCTS IN COMBUSTION CHAMBERS; SAFETY ARRANGEMENTS SPECIALLY ADAPTED FOR COMBUSTION APPARATUS; DETAILS OF COMBUSTION CHAMBERS, NOT OTHERWISE PROVIDED FOR
- F23M2900/00—Special features of, or arrangements for combustion chambers
- F23M2900/05004—Special materials for walls or lining
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23R—GENERATING COMBUSTION PRODUCTS OF HIGH PRESSURE OR HIGH VELOCITY, e.g. GAS-TURBINE COMBUSTION CHAMBERS
- F23R2900/00—Special features of, or arrangements for continuous combustion chambers; Combustion processes therefor
- F23R2900/03041—Effusion cooled combustion chamber walls or domes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T50/00—Aeronautics or air transport
- Y02T50/60—Efficient propulsion technologies, e.g. for aircraft
Definitions
- the present invention generally relates to methods and apparatus for cooling components exposed to high temperatures, such as components of a gas turbine engine. More particularly, this invention relates to cooling methods and apparatus combining effusion cooling and thick thermal barrier coating (TBC).
- TBC thick thermal barrier coating
- Gas turbine engine components such as combustors, turbine blades, vanes, nozzles and shrouds, are exposed to temperatures that can reduce the operating life of the components. Effusion cooling and TBCs have been used extensively to improve component life.
- Effusion cooling comprises an array of effusion cooling holes through the component wall.
- a supply of cooling air is passed through the holes from the cooler surface of the component to the surface exposed to higher temperatures.
- the cooling air actively cools the component wall by convection taking place in the hole and film cooling after the cooling air is discharged.
- the cooling holes are typically formed by conventional drilling techniques such as electrical-discharge machining (EDM) and laser machining, or with complex casting techniques.
- a TBC can be applied on the surface of the component that is exposed to higher temperatures.
- TBCs comprise ceramic thermal protective coatings, such as yttria stabilized zirconia, and are applied to the surface of the component to insulate the component from a high temperature source, such as a hot combustion effluent.
- a high temperature source such as a hot combustion effluent.
- a masking material is positioned in the cooling holes prior to TBC application to prevent the TBC from entering the cooling holes.
- chipping and cracking often occurs along the edge due to the high cohesive strength of the TBCs in a direction horizontal to the plane of the substrate.
- the force needed to remove the masking material can cause a portion of the TBC to be pulled off the coated section of the substrate.
- the loss of a portion of coating material exposes the corresponding portion of the component to very high in-service temperatures.
- chipping and cracking along the edge can serve as crack propagation sites for further degradation throughout the coating.
- Another method comprises a water jet containing an abrasive media, such as particles with sharp corners and edges, for excess TBC removal.
- an abrasive media such as particles with sharp corners and edges
- the erosion and abrasion caused by the abrasive particles in the water jet at pressures adequate to remove the TBC deposit also damages the cooling hole. Additionally, for some applications, the abrasive media cannot be reused and must be disposed of, which increases production costs.
- Another water jet method uses a very high-pressure water jet. The TBC accumulated in a cooling hole is removed by projecting the jet toward the uncoated surface of the hole, with the component itself serving as a mask to prevent the jet from eroding the coating. Although this method may reduce coating erosion, further improvements are still needed.
- the method comprises laser drilling the effusion holes such that the diameter of the holes is larger on the side on which the TBC is to be deposited.
- a combustor was provided with effusion holes having 0.02′′ diameters on the “cold” side and 0.03′′ diameters on the “hot” side.
- a metallic bond coat was applied to a thickness of about 0.004-0.006′′.
- a TBC was deposited by plasma spray to a thickness of about 0.008-0.010′′.
- the TBC deposited in the cooling holes in this example did not reduce fluid flow through the holes, this method may not be suitable for some applications.
- a TBC coating of about 0.015′′ did reduce fluid flow through the passage. For thick TBCs, further improvements are still needed.
- cooling holes are often machined by EDM and laser drilling after deposition of the bond coat but prior to application of the TBC. After TBC application, a hole-cleaning step is necessary to remove the excess TBC.
- other methods have included cooling hole formation after TBC deposition, these methods are unsuitable when a thick TBC is desired.
- Laser drilling is prone to spalling the brittle ceramic TBC by cracking the interface between the component substrate and the ceramic. The spalling off severely reduces the sealing effectiveness and the insulative characteristics of the ceramic coating, causing component failure and expensive repairs.
- EDM cannot be used to form cooling holes in a component having a TBC because the ceramic is electrically nonconducting.
- cooling hole formation after TBC application may avoid excess TBC deposits, the described methods are unsuitable for some applications, especially for applications requiring thick TBC.
- TBC comprises a thick TBC, for example a TBC having a thickness greater than about 0.02 inches. Further, methods are needed wherein cooling hole masking and/or cleaning processes are unnecessary.
- a method of cooling comprises the steps of providing a substrate; depositing a thermal barrier coating to a thickness of at least about 0.020 inches onto the substrate to produce a coated material; and forming an effusion array through the coated material.
- a method of cooling a combustor comprises the steps of applying a bond coat to the combustor; depositing a thermal barrier coating to a thickness greater than about 0.020 inch onto the bond coat such that a segmentation microcracked coating is produced; and machining at least one effusion hole through the segmentation microcracked coating and the combustor.
- a method of cooling a combustor comprises the steps of applying a bond coat to the combustor; depositing a thermal barrier coating onto the bond coat such that a segmentation microcracked coating having a thickness between about 0.020 and about 0.050 inches is produced, the thermal barrier coating comprising a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia; and laser drilling at least one effusion hole through the segmentation microcracked coating and the combustor.
- a method of forming an effusion hole comprises the steps of providing a substrate having a thermal barrier coating, the thermal barrier coating having a columnar crack structure and a thickness between about 0.020 and about 0.100 inches; and laser drilling at least one effusion hole through the substrate.
- a method of cooling a substrate comprises the steps of depositing a thermal barrier coating on the substrate to a thickness of at least about 0.02 inches such that a coated material having a columnar crack structure is produced; and drilling at least one effusion hole through the coated material.
- an apparatus for a gas turbine engine comprises a combustor having a segmentation microcracked thermal barrier coating and a plurality of effusion holes therethrough, the segmentation microcracked thermal barrier coating having a thickness between about 0.020 and about 0.100 inches.
- FIG. 1 is a flow chart of a method for combined effusion and thick TBC cooling according to an embodiment of the present invention
- FIG. 2 is a perspective view of a combustor according to one embodiment of the present invention.
- FIG. 3 is a close-up cross-sectional view of FIG. 2 ;
- FIG. 4 is a close-up view of FIG. 3 ;
- FIG. 5 is a cross-sectional view of a TBC coated substrate according to one embodiment of the present invention.
- FIG. 6 is a boxplot of TBC-bond coating interface crack length (inch) vs laser pulse power setting (Joules) according to one embodiment of the present invention
- FIG. 7 a is a cross-sectional view of an on-the-fly laser drilled TBC coated substrate according to one embodiment of the present invention.
- FIG. 7 b is a close-up cross-sectional view of FIG. 7 a;
- FIG. 8 is a boxplot of TBC-bond coating interface crack length vs laser defocus, which is the laser focus distance above the TBC surface, according to one embodiment of the present invention.
- FIG. 9 a is a cross-sectional view of stationary percussion laser drilled TBC coated substrate according to one embodiment of the present invention.
- FIG. 9 b is a close-up cross-sectional view of FIG. 9 a;
- FIG. 10 is a cross-sectional view of effusion holes drilled using a variety of pulses according to one embodiment of the present invention.
- FIG. 11 is a close-up cross-sectional view of the hole produced by a series of 20 laser pulses in FIG. 10 ;
- FIG. 12 is a close-up cross-sectional view of a hole drilled with 12 laser pulses using a 0.080′′ defocus, a pulse power of 12 joules, and a pulse duration of 0.5 microsecond, according to one embodiment of the present invention.
- the present invention generally provides combined effusion and thick TBC cooling methods and apparatus.
- the cooling methods and apparatus according to the present invention may find beneficial use in many industries including aerospace, automotive, and electricity generation.
- the present invention may be beneficial in applications including manufacturing and repair of aerospace and automotive components, such as turbine engines, combustors, nozzles, shrouds and vanes. This invention may be useful in any fluid cooled component application.
- the present invention provides a combined effusion and thick TBC cooling method and apparatus. Unlike the prior art, a thick TBC may be deposited prior to effusion hole formation, making a step of removing TBC deposit from the effusion holes unnecessary.
- cooling holes are machined by laser drilling after deposition of the bond coat but prior to application of the thick TBC because laser machining is prone to spalling the brittle ceramic TBC by cracking the interface between the component substrate and the ceramic.
- the present invention provides a method comprising laser drilling the cooling holes into the substrate after a thick TBC has been deposited.
- the TBC of the present invention may be deposited such that the TBC has a columnar crack structure comprising a plurality of segmentation microcracks. The segmentation microcracks may reduce cracking and chipping of the TBC during the laser drilling process.
- the method 20 may comprise a step 21 of providing a substrate, a step 22 of applying a bond coat, a step 23 of depositing a TBC to produce a TBC coated substrate, and a step 24 of laser drilling at least one effusion hole through the TBC coated substrate.
- the step 21 of providing a substrate 30 may comprise providing a combustor 40 , shown in FIG. 2 .
- a bond coat 31 may be applied to the combustor 40 , better seen in FIGS. 3-4 .
- a TBC 32 may be deposited onto the bond coat 31 and a plurality of effusion holes 34 may be laser drilled through the TBC coated substrate (coated material 35 ).
- the substrate 30 of step 21 may comprise any component exposed to high temperatures.
- Useful components may include gas turbine engine components, for example combustors, vanes and shrouds.
- the substrate 30 may comprise a metal or a metal alloy, such as nickel based and cobalt based superalloys.
- Useful nickel based and cobalt based superalloy substrates may comprise sheet metal, equiaxed, DS (directionally solidified) and SC (single crystal) investment castings as well as other forms of these superalloys, such as forgings, pressed superalloy powder components, machined components, and other forms.
- Useful nickel based superalloys may include HA230TM (available from Haynes International), Rene' alloy N5TM (available from General Electric), MarM247TM (available from Martin Marietta), PWA 1422TM (available from Pratt Whitney), PWA 1480TM (available from Pratt Whitney), PWA 1484TM (available from Pratt Whitney), Rene' 80TM (available from General Electric), Rene' 142TM (available from General Electric), SC 180TM (available from Honeywell) and others.
- Useful cobalt based superalloys may include HA188TM (available from Haynes International) and MarM509TM available from Martin Marietta and others.
- the bond coat 31 of step 22 may be applied to the surface of the substrate 30 to improve TBC adhesion.
- the bond coat 31 may grade the thermal expansion mismatch between the TBC 32 and the substrate 30 .
- the bond coat 31 may comprise an additional metallic layer.
- the bond coat 31 may include oxidation-resistant coatings such as MCrAlX (where M is iron, cobalt and/or nickel, and X is yttrium or another rare earth or reactive element such as hafnium, silicon, etc.), and diffusion coatings such as diffusion aluminides that contain aluminum intermetallics, for example NiAl and (Ni,Pt)Al.
- useful bond coats 31 may include NiCrAlY and NiCoCrAlY.
- the composition of a useful bond coat 31 may depend on factors including the composition of the substrate 30 .
- the thickness of a useful bond coat 31 may depend on factors including the composition of the bond coat 31 , the application and the composition of the substrate 30 .
- a bond coat 31 comprising NiCrAlY may be applied to a thickness between about 0.003 and about 0.008 inches on a substrate 30 comprising HA230TM (Haynes International) for a combustor application.
- the bond coat 31 may be applied by any known method, such as by plasma spray.
- a bond coat comprising MCrAlY may be deposited by air plasma spray (APS), inert gas shrouded plasma spray, low pressure (vacuum) plasma spray (LPPS), or high velocity oxyfuel (HVOF) techniques.
- the bond coating may also be applied to the substrate by the electron beam evaporation-physical vapor deposition (EB-PVD) process.
- the bond coat 31 may be positioned between the substrate 30 and a TBC 32 .
- the bond coating may be either an MCrAlY or an intermetallic coating, such as a Pt-aluminide. Bond coatings for EB-PVD TBCs are disclosed U.S. Pat. No. 4,321,311 and U.S. Pat. No. 5,514,482, which are incorporated herein by reference.
- the TBC 32 of step 23 may comprise a thermal-insulating ceramic material.
- the composition of a useful TBC 32 may comprise a stabilized zirconia, such as yttria-stabilized zirconia (YSZ).
- the TBC 32 may comprise one or more oxides.
- Useful oxides may include zirconia, hafnia, yttria, scandia, ytterbia, neodymia, samaria, gadolinia, magnesia, calcia, ceria, alumina, tantala and others.
- a useful TBC 32 may comprise zirconia stabilized with about 18% to about 22% by weight yttria.
- Another useful TBC 32 may comprise hafnia with about 18% to about 22% by weight yttria.
- Useful TBCs 32 may also include stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia.
- Stabilizing oxides may comprise yttria, scandia, ytterbia, neodymia, samaria, gadolinia, magnesia, calcia, ceria, tantala, and other oxides to the compositional extent that they are soluble within the cubic or tetragonal phases of zirconia and hafnia.
- concentration of the stabilizing oxide or oxides can be between the minimum solubility limit for full-stabilization of the tetragonal phase and the maximum solubility limit for full-stabilization of the cubic phase.
- the composition of a useful TBC 32 may depend on factors including application.
- the conductivity of a TBC 32 comprising 20% yttria stabilized zirconia may be about 60% of the conductivity of a TBC comprising 7% yttria stabilized zirconia.
- Useful TBCs 32 may be deposited to a thickness between about 0.020 and about 0.100 inches.
- the TBC 32 may be deposited to a thickness between about 0.020 and about 0.050 inches.
- the TBC 32 may be deposited by plasma spray techniques such that the TBC 32 has a columnar crack structure.
- the TBCs 32 may be deposited by known methods. A useful method for depositing the TBC 32 is disclosed in U.S. Pat. No. 5,073,433, which is incorporated herein by reference.
- a TBC 32 deposited by the '433 method may provide a TBC 32 having a columnar crack structure.
- a columnar crack structure may comprise a TBC 32 having a plurality of segmentation microcracks 33 , as seen in FIG. 5 .
- a segmentation microcrack 33 as defined herein, is a crack in the coating if extended to contact the surface of the substrate will form an angle of from about 30° to about 0° with a line extended from a contact point normal to the surface of the substrate.
- a TBC having a columnar crack structure is a TBC having at least about 20 segmentation microcracks per linear inch measured in a line parallel to the surface of the substrate and in a plane perpendicular to the substrate.
- a useful method of depositing the TBC 32 may provide a TBC 32 having a plurality of homogeneously dispersed segmentation microcracks 33 (segmentation microcracked TBC).
- TBCs 32 having segmentation microcracks 33 may have a lower thermal conductivity than a dense ceramic of the same composition as a result of the presence of microstructural defects and pores at and between grain boundaries of the TBC microstructure. Any method of depositing the TBC 32 that provides a TBC 32 having a columnar crack structure may be useful with the present invention.
- EB-PVD is another known method (U.S. Pat. No. 4,321,311 and U.S. Pat. No. 5,514,482) to deposit TBCs 32 .
- the EB-PVD process results in a thermal barrier coating with a finely-segmented columnar-grain ‘ceramic rug’ microstructure, which provides compliance for accommodating laser drilling strains.
- the microstructure of a TBC deposited by EB-PVD may comprise columnar grains with intercolumnar gaps.
- the method 20 may comprise a step 24 of laser drilling at least one effusion hole 34 through the coated material 35 .
- the effusion holes 34 may be formed by known laser drilling methods.
- the step 24 may comprise stationary percussion laser drilling.
- the percussion method uses a series of laser energy pulses to drill the hole.
- the step 24 may comprise percussion on-the-fly laser drilling.
- a percussion on the fly method is particularly advantageous for economically drilling laser holes.
- the percussion on the fly method creates a line of percussion holes by rapidly moving the workpiece under the timed pulses of a laser. For example, when an annular combustion liner is rotated under a stationary laser's lens at a fixed speed, a line of 360 holes may be created by timing the laser pulses to occur after each degree of the liner's rotation.
- a useful method for forming the effusion holes 34 may comprise laser drilling through the TBC 32 coated substrate 30 (coated material 35 ) in a one step process.
- the '474 method is a two-step laser drilling process.
- the first step produces a counterbore to reduce the extent of the overhanging TBC 32 and the second step drills through the substrate 30 .
- the step 24 of laser drilling may provide a plurality of effusion holes 34 through the TBC 32 coated substrate 30 .
- the microstructure of the segmentation microcracked TBC 32 may reduce cracking and chipping of the TBC 32 during the step 24 of laser drilling. This may be because the strain-tolerant grain structure may be able to expand and contract without causing damaging stresses that lead to spallation.
- the useful number and orientation of the effusion holes 34 may vary with application.
- the effusion holes 34 may be configured such that an airflow passing through an array of effusion holes 34 distributes a cooling film over the component surface. Due to mechanical limitations, the effusion holes 34 typically are drilled at an angle ranging from about 15° to about 90° relative to the surface.
- Computational fluid dynamic (CFD) analysis may be useful in determining the desired effusion array configuration for a particular application.
- the diameter of a useful effusion hole 34 may be between about 0.010 and about 0.050 inches. For some applications, the diameter of a useful effusion hole 34 may be between about 0.015 and about 0.025 inches.
- a substrate comprising HA230TM (available from Haynes International) was formed into a 8′′ ⁇ 12′′ diameter cylinder.
- a bond coat comprising NiCrAlY, which had a nominal composition of 31 weight % Cr, 11 wt % Al, 0.5 wt % Y, and the balance Ni, was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches.
- a TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. (Indianapolis, Ind.) to a thickness of 0.040 plus or minus 0.003 inches.
- the coated cylinder was laser drilled using conventional percussion on-the-fly laser drilling techniques.
- the TBC crack length vs laser pulse power setting (Joules) is shown in FIG. 6 .
- the holes each had a nominal diameter of 0.020 inch.
- the laser defocus which is the distance of the lens focal point above the ceramic surface, was 0.08 inch.
- power setting 15.0 Joules resulted in TBC cracks ranging from about 0.00 to about 0.04 inch.
- FIGS. 7 a and 7 b show cross-sectional views of the percussion on-the-fly laser drilled TBC coated substrate (15 J, defocus 0.08′′).
- a TBC crack 36 interface crack
- a TBC interface crack 36 is a crack in a direction parallel to the plane of the substrate 30 .
- a substrate comprising HA230TM (available from Haynes International) was formed into a 8′′ ⁇ 12′′ diameter cylinder.
- a bond coat comprising NiCrAlY was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches.
- a TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. to a thickness of 0.040 plus or minus 0.003 inches.
- the coated cylinder was laser drilled using conventional stationary percussion laser drilling techniques.
- the TBC interface crack length vs laser defocus relationship is shown in FIG. 8 .
- Four holes were drilled for each laser defocus settings of 0.080, 0.125 and 0.250 inch.
- Three holes were drilled for the defocus setting of 0.500 inch.
- the holes each had a nominal diameter of 0.020 inch.
- laser defocus setting of 0.250 inch produced TBC interface cracks 36 ranging from about 0.005 to about 0.045 inches.
- FIGS. 9 a and 9 b show cross-sectional views of the stationary percussion drilled TBC coated substrate (9.4 J, 0.25 defocus).
- a TBC interface crack 36 less than about 0.03 inches in length can be seen.
- a substrate comprising HA230TM (available from Haynes International) was formed into a 8′′ ⁇ 12′′ diameter cylinder.
- a bond coat comprising NiCrAlY was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches.
- a TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. to a thickness of 0.040 plus or minus 0.003 inches.
- the coated strip was laser drilled using conventional stationary percussion laser drilling techniques. The holes were drilled at laser pulse process settings of 9.4 J, 0.5 microsecond, 0.25′′ defocus. A variety of pulses were used to drill four partial holes, shown in FIG. 10 .
- FIG. 11 shows a close-up cross-sectional view of an effusion hole drilled at 12 J, 0.5 ⁇ sec, 0.080′′ defocus, and 12 pulses. As can be seen, TBC crack formation was reduced.
- the present invention provides improved cooling methods and apparatus using effusion cooling and a thick TBC. Further, an improved method for providing an effusion hole array through a thick TBC coated substrate is provided.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- General Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Physics & Mathematics (AREA)
- Ceramic Engineering (AREA)
- Coating By Spraying Or Casting (AREA)
Abstract
A method for combined effusion and thick TBC cooling comprises a providing a substrate, depositing a thick TBC onto the substrate and laser drilling an array of effusion holes through the TBC coated substrate. The thick TBC has a columnar crack structure, which gives compliance and spall resistance. The microstructure of the segmentation microcracked TBC reduces cracking and chipping of the TBC during effusion hole laser drilling.
Description
- The invention was made with Government support under contract with the US Army (DAAE07-02-3-0002). The Government has certain rights in this invention.
- The present invention generally relates to methods and apparatus for cooling components exposed to high temperatures, such as components of a gas turbine engine. More particularly, this invention relates to cooling methods and apparatus combining effusion cooling and thick thermal barrier coating (TBC).
- Gas turbine engine components, such as combustors, turbine blades, vanes, nozzles and shrouds, are exposed to temperatures that can reduce the operating life of the components. Effusion cooling and TBCs have been used extensively to improve component life.
- Effusion cooling comprises an array of effusion cooling holes through the component wall. A supply of cooling air is passed through the holes from the cooler surface of the component to the surface exposed to higher temperatures. The cooling air actively cools the component wall by convection taking place in the hole and film cooling after the cooling air is discharged. The cooling holes are typically formed by conventional drilling techniques such as electrical-discharge machining (EDM) and laser machining, or with complex casting techniques.
- For additional thermal and/or environmental resistance, a TBC can be applied on the surface of the component that is exposed to higher temperatures. TBCs comprise ceramic thermal protective coatings, such as yttria stabilized zirconia, and are applied to the surface of the component to insulate the component from a high temperature source, such as a hot combustion effluent. When TBC application occurs after cooling hole formation, a significant amount of TBC can be deposited in the cooling holes. The TBC deposits in the cooling holes can detrimentally affect the service life of the component because the TBC can alter the shape and reduce the size of the cooling holes. Methods for removing TBC from the cooling holes and/or reducing the amount of TBC deposited into the cooling holes have been described.
- In one method a masking material is positioned in the cooling holes prior to TBC application to prevent the TBC from entering the cooling holes. When the masking material is removed, chipping and cracking often occurs along the edge due to the high cohesive strength of the TBCs in a direction horizontal to the plane of the substrate. The force needed to remove the masking material can cause a portion of the TBC to be pulled off the coated section of the substrate. In the case of turbine engine components, the loss of a portion of coating material exposes the corresponding portion of the component to very high in-service temperatures. Additionally, chipping and cracking along the edge can serve as crack propagation sites for further degradation throughout the coating.
- Another method comprises a water jet containing an abrasive media, such as particles with sharp corners and edges, for excess TBC removal. The erosion and abrasion caused by the abrasive particles in the water jet at pressures adequate to remove the TBC deposit also damages the cooling hole. Additionally, for some applications, the abrasive media cannot be reused and must be disposed of, which increases production costs. Another water jet method uses a very high-pressure water jet. The TBC accumulated in a cooling hole is removed by projecting the jet toward the uncoated surface of the hole, with the component itself serving as a mask to prevent the jet from eroding the coating. Although this method may reduce coating erosion, further improvements are still needed.
- A method for reducing the TBC deposited in the cooling hole is disclosed in U.S. Pat. No. 6,620,457. In the described method, the TBC is applied in a direction such that the deposited TBC only partially blocks the holes. Unfortunately, following TBC deposition, this method also requires the holes to be cleaned by a water jet process.
- A method that requires neither a water jet nor a masking material has been described in U.S. Pat. No. 5,941,686. The method comprises laser drilling the effusion holes such that the diameter of the holes is larger on the side on which the TBC is to be deposited. In one example, a combustor was provided with effusion holes having 0.02″ diameters on the “cold” side and 0.03″ diameters on the “hot” side. A metallic bond coat was applied to a thickness of about 0.004-0.006″. A TBC was deposited by plasma spray to a thickness of about 0.008-0.010″. Although the TBC deposited in the cooling holes in this example did not reduce fluid flow through the holes, this method may not be suitable for some applications. Using the same relative sizes for the “cold” side of about 0.02″ and the “hot” side of about 0.03″, a TBC coating of about 0.015″ did reduce fluid flow through the passage. For thick TBCs, further improvements are still needed.
- Another cooling method combining effusion holes and TBC has been described in U.S. Pat. No. 6,573,474. In the disclosed method, the holes were drilled in a two-step process after the TBC was deposited. In the first step a counterbore was laser drilled to a depth that extended through the ceramic topcoat but not substantially into the workpiece. In the second step a smaller diameter hole was drilled through the workpiece. The two-step drilling process was found to reduce or avoid the formation of a recast bubble at the intersection of the TBC and substrate. In the disclosed example the TBC was deposited to a thickness between 0.009 and 0.014 inches, and the typical thickness for combustion liner TBC was described as between 0.003 and 0.010 inches. Unfortunately, thicker TBCs are desired for some applications.
- When depositing a sufficiently thick TBC to thermally insulate such hot section components as combustor liners, cooling holes are often machined by EDM and laser drilling after deposition of the bond coat but prior to application of the TBC. After TBC application, a hole-cleaning step is necessary to remove the excess TBC. Although other methods have included cooling hole formation after TBC deposition, these methods are unsuitable when a thick TBC is desired. Laser drilling is prone to spalling the brittle ceramic TBC by cracking the interface between the component substrate and the ceramic. The spalling off severely reduces the sealing effectiveness and the insulative characteristics of the ceramic coating, causing component failure and expensive repairs. EDM cannot be used to form cooling holes in a component having a TBC because the ceramic is electrically nonconducting. Although cooling hole formation after TBC application may avoid excess TBC deposits, the described methods are unsuitable for some applications, especially for applications requiring thick TBC.
- As can be seen, there is a need for improved combined effusion and TBC cooling methods and apparatus. Additionally, improved methods are needed wherein the TBC comprises a thick TBC, for example a TBC having a thickness greater than about 0.02 inches. Further, methods are needed wherein cooling hole masking and/or cleaning processes are unnecessary.
- In one aspect of the present invention, a method of cooling comprises the steps of providing a substrate; depositing a thermal barrier coating to a thickness of at least about 0.020 inches onto the substrate to produce a coated material; and forming an effusion array through the coated material.
- In another aspect of the present invention, a method of cooling a combustor comprises the steps of applying a bond coat to the combustor; depositing a thermal barrier coating to a thickness greater than about 0.020 inch onto the bond coat such that a segmentation microcracked coating is produced; and machining at least one effusion hole through the segmentation microcracked coating and the combustor.
- In yet another aspect of the present invention, a method of cooling a combustor comprises the steps of applying a bond coat to the combustor; depositing a thermal barrier coating onto the bond coat such that a segmentation microcracked coating having a thickness between about 0.020 and about 0.050 inches is produced, the thermal barrier coating comprising a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia; and laser drilling at least one effusion hole through the segmentation microcracked coating and the combustor.
- In still another aspect of the present invention, a method of forming an effusion hole comprises the steps of providing a substrate having a thermal barrier coating, the thermal barrier coating having a columnar crack structure and a thickness between about 0.020 and about 0.100 inches; and laser drilling at least one effusion hole through the substrate.
- In a further aspect of the present invention, a method of cooling a substrate comprises the steps of depositing a thermal barrier coating on the substrate to a thickness of at least about 0.02 inches such that a coated material having a columnar crack structure is produced; and drilling at least one effusion hole through the coated material.
- In still another aspect of the present invention, an apparatus for a gas turbine engine comprises a combustor having a segmentation microcracked thermal barrier coating and a plurality of effusion holes therethrough, the segmentation microcracked thermal barrier coating having a thickness between about 0.020 and about 0.100 inches.
- These and other features, aspects and advantages of the present invention will become better understood with reference to the following drawings, description and claims.
-
FIG. 1 is a flow chart of a method for combined effusion and thick TBC cooling according to an embodiment of the present invention; -
FIG. 2 is a perspective view of a combustor according to one embodiment of the present invention; -
FIG. 3 is a close-up cross-sectional view ofFIG. 2 ; -
FIG. 4 is a close-up view ofFIG. 3 ; -
FIG. 5 is a cross-sectional view of a TBC coated substrate according to one embodiment of the present invention; -
FIG. 6 is a boxplot of TBC-bond coating interface crack length (inch) vs laser pulse power setting (Joules) according to one embodiment of the present invention; -
FIG. 7 a is a cross-sectional view of an on-the-fly laser drilled TBC coated substrate according to one embodiment of the present invention; -
FIG. 7 b is a close-up cross-sectional view ofFIG. 7 a; -
FIG. 8 is a boxplot of TBC-bond coating interface crack length vs laser defocus, which is the laser focus distance above the TBC surface, according to one embodiment of the present invention; -
FIG. 9 a is a cross-sectional view of stationary percussion laser drilled TBC coated substrate according to one embodiment of the present invention; -
FIG. 9 b is a close-up cross-sectional view ofFIG. 9 a; -
FIG. 10 is a cross-sectional view of effusion holes drilled using a variety of pulses according to one embodiment of the present invention; -
FIG. 11 is a close-up cross-sectional view of the hole produced by a series of 20 laser pulses inFIG. 10 ; and -
FIG. 12 is a close-up cross-sectional view of a hole drilled with 12 laser pulses using a 0.080″ defocus, a pulse power of 12 joules, and a pulse duration of 0.5 microsecond, according to one embodiment of the present invention. - The following detailed description is of the best currently contemplated modes of carrying out the invention. The description is not to be taken in a limiting sense, but is made merely for the purpose of illustrating the general principles of the invention, since the scope of the invention is best defined by the appended claims.
- The present invention generally provides combined effusion and thick TBC cooling methods and apparatus. The cooling methods and apparatus according to the present invention may find beneficial use in many industries including aerospace, automotive, and electricity generation. The present invention may be beneficial in applications including manufacturing and repair of aerospace and automotive components, such as turbine engines, combustors, nozzles, shrouds and vanes. This invention may be useful in any fluid cooled component application.
- The present invention provides a combined effusion and thick TBC cooling method and apparatus. Unlike the prior art, a thick TBC may be deposited prior to effusion hole formation, making a step of removing TBC deposit from the effusion holes unnecessary. In prior art methods, cooling holes are machined by laser drilling after deposition of the bond coat but prior to application of the thick TBC because laser machining is prone to spalling the brittle ceramic TBC by cracking the interface between the component substrate and the ceramic. Unlike the prior art, the present invention provides a method comprising laser drilling the cooling holes into the substrate after a thick TBC has been deposited. The TBC of the present invention may be deposited such that the TBC has a columnar crack structure comprising a plurality of segmentation microcracks. The segmentation microcracks may reduce cracking and chipping of the TBC during the laser drilling process.
- A method of the present invention is shown in
FIG. 1 . Themethod 20 may comprise astep 21 of providing a substrate, astep 22 of applying a bond coat, astep 23 of depositing a TBC to produce a TBC coated substrate, and astep 24 of laser drilling at least one effusion hole through the TBC coated substrate. In one embodiment of the present invention, thestep 21 of providing asubstrate 30 may comprise providing acombustor 40, shown inFIG. 2 . Abond coat 31 may be applied to thecombustor 40, better seen inFIGS. 3-4 . ATBC 32 may be deposited onto thebond coat 31 and a plurality of effusion holes 34 may be laser drilled through the TBC coated substrate (coated material 35). - The
substrate 30 ofstep 21, as shown inFIG. 5 , may comprise any component exposed to high temperatures. Useful components may include gas turbine engine components, for example combustors, vanes and shrouds. Thesubstrate 30 may comprise a metal or a metal alloy, such as nickel based and cobalt based superalloys. Useful nickel based and cobalt based superalloy substrates may comprise sheet metal, equiaxed, DS (directionally solidified) and SC (single crystal) investment castings as well as other forms of these superalloys, such as forgings, pressed superalloy powder components, machined components, and other forms. Useful nickel based superalloys may include HA230™ (available from Haynes International), Rene' alloy N5™ (available from General Electric), MarM247™ (available from Martin Marietta), PWA 1422™ (available from Pratt Whitney), PWA 1480™ (available from Pratt Whitney), PWA 1484™ (available from Pratt Whitney), Rene' 80™ (available from General Electric), Rene' 142™ (available from General Electric), SC 180™ (available from Honeywell) and others. Useful cobalt based superalloys may include HA188™ (available from Haynes International) and MarM509™ available from Martin Marietta and others. - The
bond coat 31 ofstep 22 may be applied to the surface of thesubstrate 30 to improve TBC adhesion. Thebond coat 31 may grade the thermal expansion mismatch between theTBC 32 and thesubstrate 30. Thebond coat 31 may comprise an additional metallic layer. Thebond coat 31 may include oxidation-resistant coatings such as MCrAlX (where M is iron, cobalt and/or nickel, and X is yttrium or another rare earth or reactive element such as hafnium, silicon, etc.), and diffusion coatings such as diffusion aluminides that contain aluminum intermetallics, for example NiAl and (Ni,Pt)Al. For nickel-based superalloy substratesuseful bond coats 31 may include NiCrAlY and NiCoCrAlY. The composition of auseful bond coat 31 may depend on factors including the composition of thesubstrate 30. The thickness of auseful bond coat 31 may depend on factors including the composition of thebond coat 31, the application and the composition of thesubstrate 30. For example, abond coat 31 comprising NiCrAlY may be applied to a thickness between about 0.003 and about 0.008 inches on asubstrate 30 comprising HA230™ (Haynes International) for a combustor application. Thebond coat 31 may be applied by any known method, such as by plasma spray. For example, a bond coat comprising MCrAlY may be deposited by air plasma spray (APS), inert gas shrouded plasma spray, low pressure (vacuum) plasma spray (LPPS), or high velocity oxyfuel (HVOF) techniques. The bond coating may also be applied to the substrate by the electron beam evaporation-physical vapor deposition (EB-PVD) process. Thebond coat 31 may be positioned between thesubstrate 30 and aTBC 32. - If the TBC is applied by the electron beam evaporation-physical vapor deposition process, the bond coating may be either an MCrAlY or an intermetallic coating, such as a Pt-aluminide. Bond coatings for EB-PVD TBCs are disclosed U.S. Pat. No. 4,321,311 and U.S. Pat. No. 5,514,482, which are incorporated herein by reference.
- The
TBC 32 ofstep 23 may comprise a thermal-insulating ceramic material. The composition of auseful TBC 32 may comprise a stabilized zirconia, such as yttria-stabilized zirconia (YSZ). TheTBC 32 may comprise one or more oxides. Useful oxides may include zirconia, hafnia, yttria, scandia, ytterbia, neodymia, samaria, gadolinia, magnesia, calcia, ceria, alumina, tantala and others. Auseful TBC 32 may comprise zirconia stabilized with about 18% to about 22% by weight yttria. Anotheruseful TBC 32 may comprise hafnia with about 18% to about 22% by weight yttria.Useful TBCs 32 may also include stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia. Stabilizing oxides may comprise yttria, scandia, ytterbia, neodymia, samaria, gadolinia, magnesia, calcia, ceria, tantala, and other oxides to the compositional extent that they are soluble within the cubic or tetragonal phases of zirconia and hafnia. The concentration of the stabilizing oxide or oxides can be between the minimum solubility limit for full-stabilization of the tetragonal phase and the maximum solubility limit for full-stabilization of the cubic phase. - The composition of a
useful TBC 32 may depend on factors including application. For example, the conductivity of aTBC 32 comprising 20% yttria stabilized zirconia may be about 60% of the conductivity of a TBC comprising 7% yttria stabilized zirconia.Useful TBCs 32 may be deposited to a thickness between about 0.020 and about 0.100 inches. For some applications, theTBC 32 may be deposited to a thickness between about 0.020 and about 0.050 inches. TheTBC 32 may be deposited by plasma spray techniques such that theTBC 32 has a columnar crack structure. - The TBCs 32 may be deposited by known methods. A useful method for depositing the
TBC 32 is disclosed in U.S. Pat. No. 5,073,433, which is incorporated herein by reference. ATBC 32 deposited by the '433 method may provide aTBC 32 having a columnar crack structure. A columnar crack structure may comprise aTBC 32 having a plurality ofsegmentation microcracks 33, as seen inFIG. 5 . Asegmentation microcrack 33, as defined herein, is a crack in the coating if extended to contact the surface of the substrate will form an angle of from about 30° to about 0° with a line extended from a contact point normal to the surface of the substrate. As defined herein, a TBC having a columnar crack structure (or segmented columnar structure) is a TBC having at least about 20 segmentation microcracks per linear inch measured in a line parallel to the surface of the substrate and in a plane perpendicular to the substrate. A useful method of depositing theTBC 32 may provide aTBC 32 having a plurality of homogeneously dispersed segmentation microcracks 33 (segmentation microcracked TBC).TBCs 32 havingsegmentation microcracks 33 may have a lower thermal conductivity than a dense ceramic of the same composition as a result of the presence of microstructural defects and pores at and between grain boundaries of the TBC microstructure. Any method of depositing theTBC 32 that provides aTBC 32 having a columnar crack structure may be useful with the present invention. - EB-PVD is another known method (U.S. Pat. No. 4,321,311 and U.S. Pat. No. 5,514,482) to
deposit TBCs 32. The EB-PVD process results in a thermal barrier coating with a finely-segmented columnar-grain ‘ceramic rug’ microstructure, which provides compliance for accommodating laser drilling strains. The microstructure of a TBC deposited by EB-PVD may comprise columnar grains with intercolumnar gaps. - The
method 20 may comprise astep 24 of laser drilling at least oneeffusion hole 34 through thecoated material 35. The effusion holes 34 may be formed by known laser drilling methods. Thestep 24 may comprise stationary percussion laser drilling. The percussion method uses a series of laser energy pulses to drill the hole. Thestep 24 may comprise percussion on-the-fly laser drilling. A percussion on the fly method is particularly advantageous for economically drilling laser holes. The percussion on the fly method creates a line of percussion holes by rapidly moving the workpiece under the timed pulses of a laser. For example, when an annular combustion liner is rotated under a stationary laser's lens at a fixed speed, a line of 360 holes may be created by timing the laser pulses to occur after each degree of the liner's rotation. A useful method for forming the effusion holes 34 may comprise laser drilling through theTBC 32 coated substrate 30 (coated material 35) in a one step process. - Another useful drilling method is described in U.S. Pat. No. 6,573,474, which is incorporated herein by reference. The '474 method is a two-step laser drilling process. The first step produces a counterbore to reduce the extent of the overhanging
TBC 32 and the second step drills through thesubstrate 30. Thestep 24 of laser drilling may provide a plurality of effusion holes 34 through theTBC 32coated substrate 30. The microstructure of thesegmentation microcracked TBC 32 may reduce cracking and chipping of theTBC 32 during thestep 24 of laser drilling. This may be because the strain-tolerant grain structure may be able to expand and contract without causing damaging stresses that lead to spallation. - The useful number and orientation of the effusion holes 34 may vary with application. The effusion holes 34 may be configured such that an airflow passing through an array of effusion holes 34 distributes a cooling film over the component surface. Due to mechanical limitations, the effusion holes 34 typically are drilled at an angle ranging from about 15° to about 90° relative to the surface. Computational fluid dynamic (CFD) analysis may be useful in determining the desired effusion array configuration for a particular application. The diameter of a
useful effusion hole 34 may be between about 0.010 and about 0.050 inches. For some applications, the diameter of auseful effusion hole 34 may be between about 0.015 and about 0.025 inches. - A substrate comprising HA230™ (available from Haynes International) was formed into a 8″×12″ diameter cylinder. A bond coat comprising NiCrAlY, which had a nominal composition of 31 weight % Cr, 11 wt % Al, 0.5 wt % Y, and the balance Ni, was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches. A TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. (Indianapolis, Ind.) to a thickness of 0.040 plus or minus 0.003 inches. The coated cylinder was laser drilled using conventional percussion on-the-fly laser drilling techniques. The TBC crack length vs laser pulse power setting (Joules) is shown in
FIG. 6 . For each power J setting, four holes were drilled. The holes each had a nominal diameter of 0.020 inch. The laser defocus, which is the distance of the lens focal point above the ceramic surface, was 0.08 inch. As can be seen, power setting 15.0 Joules resulted in TBC cracks ranging from about 0.00 to about 0.04 inch. -
FIGS. 7 a and 7 b show cross-sectional views of the percussion on-the-fly laser drilled TBC coated substrate (15 J, defocus 0.08″). A TBC crack 36 (interface crack) about 0.03 inches in length can be seen. ATBC interface crack 36 is a crack in a direction parallel to the plane of thesubstrate 30. - A substrate comprising HA230™ (available from Haynes International) was formed into a 8″×12″ diameter cylinder. A bond coat comprising NiCrAlY was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches. A TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. to a thickness of 0.040 plus or minus 0.003 inches. The coated cylinder was laser drilled using conventional stationary percussion laser drilling techniques. The TBC interface crack length vs laser defocus relationship is shown in
FIG. 8 . Four holes were drilled for each laser defocus settings of 0.080, 0.125 and 0.250 inch. Three holes were drilled for the defocus setting of 0.500 inch. The holes each had a nominal diameter of 0.020 inch. As can be seen, laser defocus setting of 0.250 inch produced TBC interface cracks 36 ranging from about 0.005 to about 0.045 inches. -
FIGS. 9 a and 9 b show cross-sectional views of the stationary percussion drilled TBC coated substrate (9.4 J, 0.25 defocus). ATBC interface crack 36 less than about 0.03 inches in length can be seen. - A substrate comprising HA230™ (available from Haynes International) was formed into a 8″×12″ diameter cylinder. A bond coat comprising NiCrAlY was applied by plasma spray to a thickness of 0.0055 plus or minus 0.0025 inches. A TBC comprising 20 weight % yttria stabilized zirconia was deposited by Praxair Surface Technology, Inc. to a thickness of 0.040 plus or minus 0.003 inches. The coated strip was laser drilled using conventional stationary percussion laser drilling techniques. The holes were drilled at laser pulse process settings of 9.4 J, 0.5 microsecond, 0.25″ defocus. A variety of pulses were used to drill four partial holes, shown in
FIG. 10 . These holes illustrate the propagation of percussion holes through the coating and initial penetration into the substrate. (These holes were not intended to penetrate the full thickness of the specimen.) Thefirst hole 51 was formed using a series of 20 pulses, thesecond hole 52 was formed using 25 pulses, thethird hole 53 was formed using 35 pulses, and theforth hole 54 was formed using 45 pulses. A close-up view of theforth hole 54 is shown inFIG. 11 .FIG. 12 shows a close-up cross-sectional view of an effusion hole drilled at 12 J, 0.5 μsec, 0.080″ defocus, and 12 pulses. As can be seen, TBC crack formation was reduced. - As can be appreciated by those skilled in the art, the present invention provides improved cooling methods and apparatus using effusion cooling and a thick TBC. Further, an improved method for providing an effusion hole array through a thick TBC coated substrate is provided.
- It should be understood, of course, that the foregoing relates to exemplary embodiments of the invention and that modifications may be made without departing from the spirit and scope of the invention as set forth in the following claims.
Claims (39)
1. A method of cooling comprising the steps of:
providing a substrate;
depositing a thermal barrier coating to a thickness of at least about 0.020 inches onto said substrate to produce a coated material; and
forming an array of effusion cooling holes through said coated material.
2. The method of claim 1 , wherein said step of depositing comprises plasma spraying such that said thermal barrier coating has a columnar crack microstructure comprising a plurality of segmentation microcracks.
3. The method of claim 1 , wherein said step of depositing comprises electron beam evaporation-physical vapor deposition such that said thermal barrier coating has a microstructure comprising a columnar grain structure with intercolumnar gaps.
4. The method of claim 1 , further comprising a step of applying a bond coat, such that said bond coat is between said substrate and said thermal barrier coating.
5. The method of claim 1 , wherein said step of depositing comprises depositing to a thickness between about 0.020 and about 0.100 inches.
6. The method of claim 1 , wherein said step of depositing comprises depositing to a thickness between about 0.020 and about 0.050 inches.
7. The method of claim 1 , wherein said step of forming comprises laser drilling through said coated material.
8. The method of claim 7 , wherein said laser drilling comprises a two-step laser drilling process and wherein a first step produces a counterbore.
9. The method of claim 1 , wherein said substrate comprises a combustor.
10. The method of claim 1 , wherein said step of depositing comprises depositing cubic zirconia stabilized with about 18% to about 22% by weight yttria.
11. The method of claim 1 , wherein said thermal barrier coating comprises a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia.
12. A method of cooling a combustor comprising the steps of:
applying a bond coat to said combustor;
depositing a thermal barrier coating to a thickness greater than about 0.020 inch onto said bond coat such that a segmentation microcracked coating is produced; and
machining at least one effusion hole through said segmentation microcracked coating and said combustor.
13. The method of claim 12 , wherein said step of machining comprises a first step of laser drilling a counterbore into said segmentation microcracked coating and a second step of laser drilling through said combustor.
14. The method of claim 12 , wherein said step of machining comprises stationary percussion laser drilling at an angle ranging from 15° to 90° relative to a surface of said combustor.
15. The method of claim 12 , wherein said step of machining comprises laser drilling at least one effusion hole having a diameter between about 0.01 and about 0.03 inches.
16. The method of claim 12 , wherein said step of applying comprises plasma spraying a material selected from the group consisting of NiCrAlY and NiCoCrAlY.
17. The method of claim 12 , wherein said step of depositing comprises depositing to a thickness between about 0.020 and about 0.100 inch.
18. The method of claim 12 , wherein said step of depositing comprises depositing a stabilized cubic zirconia.
19. The method of claim 18 , wherein said stabilized cubic zirconia has at least about 18% by weight yttria.
20. The method of claim 12 , wherein said thermal barrier coating comprises at least one stabilizing oxide and a material selected from the group consisting of zirconia and hafnia.
21. The method of claim 20 , wherein said at least one stabilizing oxide is selected from the group consisting of zirconia, hafnia, yttria, scandia, ytterbia, neodymia, samaria, gadolinia, magnesia, calcia, ceria, and tantala.
22. The method of claim 21 , wherein the concentration of said at least one stabilizing oxide is between the minimum solubility limit for full-stabilization of the tetragonal phase and the maximum solubility limit for full-stabilization of the cubic phase.
23. The method of claim 12 , wherein said step of depositing comprises a process selected from the group consisting of plasma spray, high velocity oxyfuel, and electron beam evaporation-physical vapor deposition.
24. A method of cooling a combustor comprising the steps of:
applying a bond coat to said combustor;
depositing a thermal barrier coating onto said bond coat such that a segmentation microcracked coating having a thickness between about 0.020 and about 0.050 inches is produced, said thermal barrier coating comprising a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia; and
laser drilling at least one effusion hole through said segmentation microcracked coating and said combustor.
25. The method of claim 24 , wherein said thermal barrier coating comprises cubic zirconia stabilized with about 18% and about 22% by weight Yttria.
26. A method of cooling a combustor comprising the steps of:
applying a bond coat to said combustor;
depositing a thermal barrier coating onto said bond coat such that a columnar grained coating having intercolumnar gaps is produced, said columnar grained coating having a thickness between about 0.020 and about 0.050 inches, said thermal barrier coating comprising a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia; and
laser drilling at least one effusion hole through said columnar grained coating and said combustor.
27. A method of forming an effusion hole comprising the steps of:
providing a substrate having a thermal barrier coating, said thermal barrier coating having a segmented columnar structure and a thickness between about 0.020 and about 0.100 inches; and
laser drilling at least one effusion hole through said substrate.
28. The method of claim 27 , wherein said step of laser drilling comprises stationary percussion laser drilling at an angle between about 15° and about 45° relative to a surface of said substrate.
29. The method of claim 27 , wherein said step of laser drilling comprises percussion on-the-fly laser drilling at an angle between about 15° and about 45° relative to a surface of said substrate.
30. The method of claim 27 , wherein said step of laser drilling comprises laser drilling a counterbore.
31. A method of cooling a substrate comprising the steps of:
depositing a thermal barrier coating on said substrate to a thickness of at least about 0.02 inches such that a coated material is produced; and
drilling at least one effusion hole through said coated material.
32. The method of claim 31 , wherein said step of depositing comprises forming a microstructure having a plurality of segmentation microcracks.
33. The method of claim 31 , wherein said step of depositing comprises forming a microstructure having a plurality of columnar grains with intercolumnar gaps.
34. The method of claim 31 , wherein said step of drilling comprises laser drilling.
35. The method of claim 31 , wherein said step of depositing comprises plasma spraying.
36. The method of claim 31 , wherein said step of depositing comprises electron beam evaporation-physical vapor deposition.
37. An apparatus for a gas turbine engine comprising:
a combustor having a segmentation microcracked thermal barrier coating and a plurality of effusion holes therethrough, said segmentation microcracked thermal barrier coating having a thickness between about 0.020 and about 0.100 inches.
38. The apparatus of claim 37 , wherein said segmentation microcracked thermal barrier coating comprises a material selected from the group consisting of stabilized cubic zirconia, stabilized cubic hafnia, stabilized tetragonal zirconia, stabilized tetragonal hafnia, yttria-stabilized cubic zirconia, yttria-stabilized cubic hafnia, yttria-stabilized tetragonal zirconia, and yttria-stabilized tetragonal hafnia.
39. The apparatus of claim 37 , wherein said segmentation microcracked thermal barrier coating comprises about 18% to about 22% by weight yttria.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/897,788 US20060016191A1 (en) | 2004-07-23 | 2004-07-23 | Combined effusion and thick TBC cooling method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/897,788 US20060016191A1 (en) | 2004-07-23 | 2004-07-23 | Combined effusion and thick TBC cooling method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20060016191A1 true US20060016191A1 (en) | 2006-01-26 |
Family
ID=35655676
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/897,788 Abandoned US20060016191A1 (en) | 2004-07-23 | 2004-07-23 | Combined effusion and thick TBC cooling method |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US20060016191A1 (en) |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050126001A1 (en) * | 2003-12-15 | 2005-06-16 | Hanley Gary L. | Process for removing thermal barrier coatings |
| US20070271925A1 (en) * | 2006-05-26 | 2007-11-29 | Pratt & Whitney Canada Corp. | Combustor with improved swirl |
| US20090199563A1 (en) * | 2008-02-07 | 2009-08-13 | Hamilton Sundstrand Corporation | Scalable pyrospin combustor |
| US20090226626A1 (en) * | 2006-07-28 | 2009-09-10 | General Electric Company | Method for concurrent thermal spray and cooling hole cleaning |
| US20100050650A1 (en) * | 2008-08-29 | 2010-03-04 | Patel Bhawan B | Gas turbine engine reverse-flow combustor |
| US20100272953A1 (en) * | 2009-04-28 | 2010-10-28 | Honeywell International Inc. | Cooled hybrid structure for gas turbine engine and method for the fabrication thereof |
| US20110287191A1 (en) * | 2010-05-18 | 2011-11-24 | C.R.M.A. | Production method of multilayer pieces comprising inclined holes and resistant to high thermal stresses, and use of the method for repairing pieces |
| WO2011144860A1 (en) * | 2010-05-18 | 2011-11-24 | C.R.M.A. | Method for manufacturing and/or repairing multi-layer parts which comprise angled holes and need to be able to withstand high thermal stress |
| US20120167573A1 (en) * | 2010-12-30 | 2012-07-05 | United Technologies Corporation | Thermal Barrier Coatings and Methods of Application |
| US20140120308A1 (en) * | 2012-10-30 | 2014-05-01 | General Electric Company | Reinforced articles and methods of making the same |
| CN104164643A (en) * | 2014-08-18 | 2014-11-26 | 南京理工大学 | Thermal barrier coating with bonding layer in net structure and preparation method of thermal barrier |
| US20150275682A1 (en) * | 2014-04-01 | 2015-10-01 | Siemens Energy, Inc. | Sprayed haynes 230 layer to increase spallation life of thermal barrier coating on a gas turbine engine component |
| US20160069569A1 (en) * | 2014-09-09 | 2016-03-10 | United Technologies Corporation | Film cooling circuit for a combustor liner |
| US20160069567A1 (en) * | 2014-09-09 | 2016-03-10 | United Technologies Corporation | Single-walled combustor for a gas turbine engine and method of manufacture |
| US20160209033A1 (en) * | 2015-01-20 | 2016-07-21 | United Technologies Corporation | Combustor dilution hole passive heat transfer control |
| WO2019006067A1 (en) * | 2017-06-29 | 2019-01-03 | Siemens Aktiengesellschaft | Method for constructing impingement/effusion cooling features in a component of a combustion turbine engine |
| US10386067B2 (en) * | 2016-09-15 | 2019-08-20 | United Technologies Corporation | Wall panel assembly for a gas turbine engine |
| US10934853B2 (en) | 2014-07-03 | 2021-03-02 | Rolls-Royce Corporation | Damage tolerant cooling of high temperature mechanical system component including a coating |
| US10995624B2 (en) * | 2016-08-01 | 2021-05-04 | General Electric Company | Article for high temperature service |
Citations (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4321310A (en) * | 1980-01-07 | 1982-03-23 | United Technologies Corporation | 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 |
| US5073433A (en) * | 1989-10-20 | 1991-12-17 | Technology Corporation | Thermal barrier coating for substrates and process for producing it |
| US5123248A (en) * | 1990-03-28 | 1992-06-23 | General Electric Company | Low emissions combustor |
| US5239823A (en) * | 1991-02-26 | 1993-08-31 | United Technologies Corporation | Multiple layer cooled nozzle liner |
| US5261223A (en) * | 1992-10-07 | 1993-11-16 | General Electric Company | Multi-hole film cooled combustor liner with rectangular film restarting holes |
| US5276963A (en) * | 1992-02-21 | 1994-01-11 | Coors Electronic Package Company | Process for obtaining side metallization and articles produced thereby |
| US5514482A (en) * | 1984-04-25 | 1996-05-07 | Alliedsignal Inc. | Thermal barrier coating system for superalloy components |
| US5674585A (en) * | 1995-11-15 | 1997-10-07 | United Technologies Corporation | Composite thermal insulation structure |
| US5771577A (en) * | 1996-05-17 | 1998-06-30 | General Electric Company | Method for making a fluid cooled article with protective coating |
| US6383602B1 (en) * | 1996-12-23 | 2002-05-07 | General Electric Company | Method for improving the cooling effectiveness of a gaseous coolant stream which flows through a substrate, and related articles of manufacture |
| US6408610B1 (en) * | 2000-07-18 | 2002-06-25 | General Electric Company | Method of adjusting gas turbine component cooling air flow |
| US6471881B1 (en) * | 1999-11-23 | 2002-10-29 | United Technologies Corporation | Thermal barrier coating having improved durability and method of providing the coating |
| US6573474B1 (en) * | 2000-10-18 | 2003-06-03 | Chromalloy Gas Turbine Corporation | Process for drilling holes through a thermal barrier coating |
| US6620457B2 (en) * | 2001-07-13 | 2003-09-16 | General Electric Company | Method for thermal barrier coating and a liner made using said method |
| US6655146B2 (en) * | 2001-07-31 | 2003-12-02 | General Electric Company | Hybrid film cooled combustor liner |
| US6663919B2 (en) * | 2002-03-01 | 2003-12-16 | General Electric Company | Process of removing a coating deposit from a through-hole in a component and component processed thereby |
| US6718774B2 (en) * | 2001-09-29 | 2004-04-13 | Rolls-Royce Plc | Fastener |
| US20040134897A1 (en) * | 2003-01-10 | 2004-07-15 | General Electric Company | Process of removing a ceramic coating deposit in a surface hole of a component |
| US20050013994A1 (en) * | 2003-07-16 | 2005-01-20 | Honeywell International Inc. | Thermal barrier coating with stabilized compliant microstructure |
-
2004
- 2004-07-23 US US10/897,788 patent/US20060016191A1/en not_active Abandoned
Patent Citations (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4321310A (en) * | 1980-01-07 | 1982-03-23 | United Technologies Corporation | 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 |
| US5514482A (en) * | 1984-04-25 | 1996-05-07 | Alliedsignal Inc. | Thermal barrier coating system for superalloy components |
| US5073433A (en) * | 1989-10-20 | 1991-12-17 | Technology Corporation | Thermal barrier coating for substrates and process for producing it |
| US5073433B1 (en) * | 1989-10-20 | 1995-10-31 | Praxair Technology Inc | Thermal barrier coating for substrates and process for producing it |
| US5123248A (en) * | 1990-03-28 | 1992-06-23 | General Electric Company | Low emissions combustor |
| US5239823A (en) * | 1991-02-26 | 1993-08-31 | United Technologies Corporation | Multiple layer cooled nozzle liner |
| US5276963A (en) * | 1992-02-21 | 1994-01-11 | Coors Electronic Package Company | Process for obtaining side metallization and articles produced thereby |
| US5261223A (en) * | 1992-10-07 | 1993-11-16 | General Electric Company | Multi-hole film cooled combustor liner with rectangular film restarting holes |
| US5674585A (en) * | 1995-11-15 | 1997-10-07 | United Technologies Corporation | Composite thermal insulation structure |
| US5771577A (en) * | 1996-05-17 | 1998-06-30 | General Electric Company | Method for making a fluid cooled article with protective coating |
| US5941686A (en) * | 1996-05-17 | 1999-08-24 | General Electric Company | Fluid cooled article with protective coating |
| US6383602B1 (en) * | 1996-12-23 | 2002-05-07 | General Electric Company | Method for improving the cooling effectiveness of a gaseous coolant stream which flows through a substrate, and related articles of manufacture |
| US6471881B1 (en) * | 1999-11-23 | 2002-10-29 | United Technologies Corporation | Thermal barrier coating having improved durability and method of providing the coating |
| US6408610B1 (en) * | 2000-07-18 | 2002-06-25 | General Electric Company | Method of adjusting gas turbine component cooling air flow |
| US6573474B1 (en) * | 2000-10-18 | 2003-06-03 | Chromalloy Gas Turbine Corporation | Process for drilling holes through a thermal barrier coating |
| US6620457B2 (en) * | 2001-07-13 | 2003-09-16 | General Electric Company | Method for thermal barrier coating and a liner made using said method |
| US6655146B2 (en) * | 2001-07-31 | 2003-12-02 | General Electric Company | Hybrid film cooled combustor liner |
| US6718774B2 (en) * | 2001-09-29 | 2004-04-13 | Rolls-Royce Plc | Fastener |
| US6663919B2 (en) * | 2002-03-01 | 2003-12-16 | General Electric Company | Process of removing a coating deposit from a through-hole in a component and component processed thereby |
| US20040134897A1 (en) * | 2003-01-10 | 2004-07-15 | General Electric Company | Process of removing a ceramic coating deposit in a surface hole of a component |
| US20050013994A1 (en) * | 2003-07-16 | 2005-01-20 | Honeywell International Inc. | Thermal barrier coating with stabilized compliant microstructure |
Cited By (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7805822B2 (en) * | 2003-12-15 | 2010-10-05 | Turbocombustor Technology, Inc. | Process for removing thermal barrier coatings |
| US20050126001A1 (en) * | 2003-12-15 | 2005-06-16 | Hanley Gary L. | Process for removing thermal barrier coatings |
| US20070271925A1 (en) * | 2006-05-26 | 2007-11-29 | Pratt & Whitney Canada Corp. | Combustor with improved swirl |
| US7628020B2 (en) * | 2006-05-26 | 2009-12-08 | Pratt & Whitney Canada Cororation | Combustor with improved swirl |
| US20090226626A1 (en) * | 2006-07-28 | 2009-09-10 | General Electric Company | Method for concurrent thermal spray and cooling hole cleaning |
| US7622160B2 (en) | 2006-07-28 | 2009-11-24 | General Electric Company | Method for concurrent thermal spray and cooling hole cleaning |
| US20090199563A1 (en) * | 2008-02-07 | 2009-08-13 | Hamilton Sundstrand Corporation | Scalable pyrospin combustor |
| US8407893B2 (en) | 2008-08-29 | 2013-04-02 | Pratt & Whitney Canada Corp. | Method of repairing a gas turbine engine combustor |
| US8001793B2 (en) | 2008-08-29 | 2011-08-23 | Pratt & Whitney Canada Corp. | Gas turbine engine reverse-flow combustor |
| US20100050650A1 (en) * | 2008-08-29 | 2010-03-04 | Patel Bhawan B | Gas turbine engine reverse-flow combustor |
| US20100272953A1 (en) * | 2009-04-28 | 2010-10-28 | Honeywell International Inc. | Cooled hybrid structure for gas turbine engine and method for the fabrication thereof |
| US20110287191A1 (en) * | 2010-05-18 | 2011-11-24 | C.R.M.A. | Production method of multilayer pieces comprising inclined holes and resistant to high thermal stresses, and use of the method for repairing pieces |
| WO2011144860A1 (en) * | 2010-05-18 | 2011-11-24 | C.R.M.A. | Method for manufacturing and/or repairing multi-layer parts which comprise angled holes and need to be able to withstand high thermal stress |
| FR2960242A1 (en) * | 2010-05-18 | 2011-11-25 | C R M A | PROCESS FOR MANUFACTURING MULTI-LAYER COMPONENTS HAVING INCLINED HOLES AND RESISTANT TO HIGH THERMAL CONSTRAINTS AND USE OF THE PROCESS FOR REPAIRING WORKPIECES |
| US20120167573A1 (en) * | 2010-12-30 | 2012-07-05 | United Technologies Corporation | Thermal Barrier Coatings and Methods of Application |
| US9139897B2 (en) * | 2010-12-30 | 2015-09-22 | United Technologies Corporation | Thermal barrier coatings and methods of application |
| US20140120308A1 (en) * | 2012-10-30 | 2014-05-01 | General Electric Company | Reinforced articles and methods of making the same |
| US9260788B2 (en) * | 2012-10-30 | 2016-02-16 | General Electric Company | Reinforced articles and methods of making the same |
| US20150275682A1 (en) * | 2014-04-01 | 2015-10-01 | Siemens Energy, Inc. | Sprayed haynes 230 layer to increase spallation life of thermal barrier coating on a gas turbine engine component |
| US10934853B2 (en) | 2014-07-03 | 2021-03-02 | Rolls-Royce Corporation | Damage tolerant cooling of high temperature mechanical system component including a coating |
| CN104164643A (en) * | 2014-08-18 | 2014-11-26 | 南京理工大学 | Thermal barrier coating with bonding layer in net structure and preparation method of thermal barrier |
| US20160069569A1 (en) * | 2014-09-09 | 2016-03-10 | United Technologies Corporation | Film cooling circuit for a combustor liner |
| US20160069567A1 (en) * | 2014-09-09 | 2016-03-10 | United Technologies Corporation | Single-walled combustor for a gas turbine engine and method of manufacture |
| US10731857B2 (en) * | 2014-09-09 | 2020-08-04 | Raytheon Technologies Corporation | Film cooling circuit for a combustor liner |
| US10788210B2 (en) * | 2014-09-09 | 2020-09-29 | Raytheon Technologies Corporation | Single-walled combustor for a gas turbine engine and method of manufacture |
| US20160209033A1 (en) * | 2015-01-20 | 2016-07-21 | United Technologies Corporation | Combustor dilution hole passive heat transfer control |
| US10132498B2 (en) * | 2015-01-20 | 2018-11-20 | United Technologies Corporation | Thermal barrier coating of a combustor dilution hole |
| US10995624B2 (en) * | 2016-08-01 | 2021-05-04 | General Electric Company | Article for high temperature service |
| US10386067B2 (en) * | 2016-09-15 | 2019-08-20 | United Technologies Corporation | Wall panel assembly for a gas turbine engine |
| WO2019006067A1 (en) * | 2017-06-29 | 2019-01-03 | Siemens Aktiengesellschaft | Method for constructing impingement/effusion cooling features in a component of a combustion turbine engine |
| US11092338B2 (en) | 2017-06-29 | 2021-08-17 | Siemens Energy Global GmbH & Co. KG | Method for constructing impingement/effusion cooling features in a component of a combustion turbine engine |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20060016191A1 (en) | Combined effusion and thick TBC cooling method | |
| CA2711175C (en) | Substrate features for mitigating stress | |
| US7078073B2 (en) | Method for repairing coated components | |
| US5723078A (en) | Method for repairing a thermal barrier coating | |
| US7371426B2 (en) | Method for repairing components using environmental bond coatings and resultant repaired components | |
| CA2464375C (en) | Method for applying or repairing thermal barrier coatings | |
| EP1685923B1 (en) | Repair and reclassification of superalloy components | |
| US7094444B2 (en) | Method for repairing coated components using NiAl bond coats | |
| US20030101587A1 (en) | Method for replacing a damaged TBC ceramic layer | |
| US20110048017A1 (en) | Method of depositing protective coatings on turbine combustion components | |
| US20160281204A1 (en) | Thermal barrier coating repair | |
| US20230228199A1 (en) | Slotted ceramic coating with a reactive phase coating disposed thereon for improved cmas resistance and methods of forming the same | |
| JP2006104577A (en) | Segmented gadolinia zirconia coating film, method for forming the same, segmented ceramic coating system and coated film component | |
| EP2519659A1 (en) | Nano and micro structured ceramic thermal barrier coating | |
| EP2431495A1 (en) | A method for forming thermal barrier coating and device with the thermal barrier coating | |
| JP2004190140A (en) | Method of depositing a local MCrAlY coating | |
| EP2423347A1 (en) | Method for forming a thermal barrier coating and a turbine component with the thermal barrier coating | |
| US8123464B2 (en) | Coating optimization process using a coupon and component comprising a coupon | |
| US20140255652A1 (en) | Surface having specially formed recesses and component |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: HONEYWELL INTERNATIONAL INC., NEW JERSEY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WOODCOCK, GREGORY O.;SILCOX, CHARLES P.;STRANGMAN, THOMAS E.;AND OTHERS;REEL/FRAME:015616/0599 Effective date: 20040721 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |