EP2971240B1 - Revêtement de barrière thermique hybride et son procédé de fabrication - Google Patents

Revêtement de barrière thermique hybride et son procédé de fabrication Download PDF

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Publication number
EP2971240B1
EP2971240B1 EP13878078.8A EP13878078A EP2971240B1 EP 2971240 B1 EP2971240 B1 EP 2971240B1 EP 13878078 A EP13878078 A EP 13878078A EP 2971240 B1 EP2971240 B1 EP 2971240B1
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EP
European Patent Office
Prior art keywords
layer
barrier coating
thermal barrier
forming
porosity
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EP13878078.8A
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German (de)
English (en)
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EP2971240A4 (fr
EP2971240A1 (fr
Inventor
Brian T HAZEL
David A. Litton
Michael J. Maloney
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RTX Corp
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United Technologies Corp
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • C23C4/134Plasma spraying
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/042Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material including a refractory ceramic layer, e.g. refractory metal oxides, ZrO2, rare earth oxides
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/10Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
    • C23C4/11Oxides

Definitions

  • the present disclosure relates to a thermal barrier coating for use on a turbine engine component and to a process of making the thermal barrier coating.
  • a thermal barrier coating (TBC) is created to meet one or more performance requirements including, but not liited to, spallation life, calcia-magnesia-alumina-silicate (CMAS) resistance, foreign object damage (FOD) resistance, erosion, and low conductivity.
  • CMAS calcia-magnesia-alumina-silicate
  • FOD foreign object damage
  • a turbine barrier coating is applied to a turbine engine component, such as a turbine blade/vane, to help the component withstand the relatively high temperatures of its operational environment.
  • TBCs are often formed using a singular coating process such as an electron beam physical vapor deposition (EB-PVD) process.
  • EB-PVD electron beam physical vapor deposition
  • a TBC may be formed from two separate EB-PVD layers formed from two different materials, such as 7 wt% yttria stabilized zirconia and gadolinia stabilized zirconia in order to improve the thermal conductivity properties of the coating.
  • the strain-tolerant columnar structure of an EB-PVD coating helps to increase the TBC spallation life.
  • a more porous TBC however may minimize the TBC thermal conductivity and possibly the thermal radiation through the coating.
  • TBC there is a porous outer layer over a more dense inner layer made by an EB-PVD process.
  • the two layers have different porosity levels.
  • Such a structure can be formed by changing the coating temperature. More power equals more density but also more temperature. It is also known to form a dense vertically cracked microstructure for the TBC where the deposition is conducted at a two inch stand-off for the dense layer and a six inch stand-off for the porous layer.
  • EP 2 341 166 discloses a TBC on a substrate, the TBC comprising a bond coat, a ceramic coating, and a ceramic layer.
  • US 2011/244216 A1 discloses a combination of SPS and APS methods for deposition of multilayer thermal barrier coatings on turbine components.
  • the applied materials comprise partially or fully YSZ as well as pyrochlores.
  • EP 2 336 381 A1 discloses a thermal barrier coating deposited by APS, consisting of a first 7YSZ layer and a second gadolinia stabilized zirconia layer with a porosity of 5-20 vol.%.
  • EP 2 450 465 A1 discloses a multilayer ceramic TBC deposited by APS, comprising an inner YSZ layer of low porosity, an intermediate YSZ layer with higher porosity than the inner layer and an outer porous layer of gadolinium zirconate.
  • the second layer has a porosity in the range of from 10 to 40%.
  • the first layer forming step comprises suspending a powder feedstock in a liquid suspension and injecting the powder feedstock and the suspension into a plasma jet under conditions where the first layer is formed with the strain-tolerant columnar microstructure.
  • the second layer forming step comprises changing spray parameters so as to form the porous and radiation thermally resistant second layer.
  • the second layer forming step comprises forming the second layer so as to have a porosity of from 10 to 40%.
  • the first and second layer forming steps comprise using a powdered feedstock having a particle size in the range of from 10nm to 10 micrometers
  • the first and second layer forming steps comprises using a powdered feedstock having a particle size in the range of from 10nm to 2.0 micrometers.
  • the turbine engine component may be any component which requires a thermal barrier coating such as a blade/vane.
  • the turbine engine component 10 may have a substrate 12 formed from any suitable material known in the art including, but not limited to, a nickel based alloy, a cobalt based alloy, a titanium based alloy, a ceramic material, and an organo-matrix composite material.
  • a thermal barrier coating 14 is deposited on the substrate 12.
  • the thermal barrier coating 14 has a first layer 16 which interfaces with the surface 18 of the substrate 12 and an outer second layer 20.
  • the first layer 16 is formed so as to have a strain-tolerant columnar microstructure at the interface with the surface 18 of the substrate.
  • the second layer 20 is formed to have a porous thermal conduction and radiant heat transfer resistant microstructure at an outer surface 22 of the thermal barrier coating.
  • the first layer 16 and the second layer 20 is formed from a material having the same composition.
  • Each of the layers 16 and 20 is formed from a 7 wt% yttria stabilized zirconia (7YSZ).
  • each of the layers 16 and 20 is formed using suspension plasma spray (SPS) technique such as that shown in FIG. 2 .
  • SPS suspension plasma spray
  • a powdered feedstock is suspended in a liquid suspension 30.
  • the powdered feedstock may be 7YSZ which may be suspended in ethanol, water, or other alcohols such as methanol.
  • the powdered feedstock may have a particle size in the range of from 10 nm to 10 micrometers mean size diameter. In another non-limiting embodiment, the particles size may be in the range of from 10 nm to 2.0 micrometers.
  • the powdered feedstock in the suspension is injected into a plasma jet 32 created by a plasma torch 34 and thus deposited onto the substrate 12.
  • the spray conditions are such that the first layer 16 is formed to have the desired strain tolerant columnar microstructure.
  • the deposition technique may have a short stand off (similar to that used in dense vertically cracked coatings) and high power/enthalpy plasma conditions.
  • the spray conditions may be changed so as to form the second layer 20 with the porous thermal conduction and radiant heat transfer resistant microstructure.
  • porosity (1) the angle of the spray nozzle could be changed from normal relative to the surface on which the layer 20 is being deposited; (2) the stand off may be increased; and/or (3) the plasma power/enthalpy may be reduced. More porosity in the second layer 20 than in the first layer 16 creates a reduction in thermal conductivity.
  • the second layer 20 may have a reduction of at least 10% in thermal conductivity. This may come purely from a porosity increase or a change in the structure from columnar to more splat like. An increase in porosity increases the erosion rate. A useful limit may be 10 to 40% porosity in the second layer 20.
  • the columnar structure SPS gives a thermal cyclic spallation resistance similar to EB-PVD (much higher than APS and higher than dense vertically cracked). Erosion is a function of porosity content and can be greater or less than EB-PVD (generally higher than APS and more like dense vertically cracked). Thermal conductivity, as discussed above, follows the porosity content.
  • the spray conditions are discreetly or incrementally changed throughout the spray run.
  • the spray conditions are changed so that a continuously graded microstructure is formed where there is the strain-tolerant columnar microstructure at the interface with the substrate 12 for thermal barrier coating spallation resistance and a porous thermal conduction and radiation thermally resistant layer at the outer surface 22.
  • thermal barrier coating can be formed using a single piece of equipment and in a single coating.
  • Another advantage is that one can easily change the composition of the second layer 20 so that it is different than the composition of the first layer 16. This can easily be done by changing the composition of the feedstock being injected into the plasma jet.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Coating By Spraying Or Casting (AREA)

Claims (8)

  1. Revêtement de barrière thermique (14) appliqué à un composant de moteur à turbine (10) ayant un substrat (2), ledit revêtement comprenant :
    une première couche (16) qui a une microstructure en colonne tolérante à la contrainte au niveau d'une interface avec le substrat pour résistance à la spallation ; et
    une seconde couche (20) qui est poreuse, thermiquement résistante au rayonnement et à la conduction au niveau d'une surface extérieure du revêtement de barrière thermique ;
    dans lequel il y a une microstructure échelonnée en continu de l'interface vers la surface extérieure ;
    dans lequel lesdites première et seconde couches sont formées à partir du même matériau ;
    dans lequel chacune desdites première et seconde couches est formée à partir de 7 % en poids de zircone stabilisée par de l'oxyde d'yttrium ; et
    dans lequel ladite première couche a une première conductibilité thermique et ladite seconde couche a une seconde conductibilité thermique qui est au moins 10 % inférieure à la première conductibilité thermique.
  2. Revêtement de barrière thermique selon la revendication 1, dans lequel ladite seconde couche présente une porosité dans la plage de 10 à 40 %.
  3. Procédé pour appliquer un revêtement de barrière thermique (14) à un composant de moteur à turbine (10) comprenant :
    la formation d'une première couche (16) qui a une microstructure en colonne tolérante à la contrainte au niveau d'une interface de la première couche et d'un substrat en utilisation une technique de pulvérisation de plasma en suspension ;
    la formation d'une seconde couche (20) qui est poreuse et thermiquement résistante au rayonnement au niveau d'une surface extérieure du revêtement de barrière thermique en utilisant ladite technique de pulvérisation de plasma en suspension ;
    la formation d'une microstructure échelonnée en continu de ladite interface vers ladite surface extérieure ;
    dans lequel lesdites étapes de formation de première et seconde couches comprennent la formation desdites couches à partir du même matériau ;
    dans lequel chacune desdites première et seconde couches est formée à partir de 7 % en poids de zircone stabilisée par de l'oxyde d'yttrium ; et
    dans lequel ladite étape de formation de seconde couche comprend la formation de ladite seconde couche avec plus de porosité que la première couche de manière à ce qu'elle ait une conductibilité thermique qui est au moins 10 % inférieure à une conductibilité thermique de ladite première couche.
  4. Procédé selon la revendication 3, dans lequel ladite étape de formation de première couche comprend la suspension d'une charge de poudre dans une suspension liquide et l'injection de ladite charge de poudre et de ladite suspension dans un jet de plasma dans des conditions où ladite première couche est formée avec ladite microstructure en colonne tolérante à la contrainte.
  5. Procédé selon la revendication 4, dans lequel ladite étape de formation de seconde couche comprend le changement de paramètres de pulvérisation de manière à former ladite seconde couche poreuse et thermiquement résistante au rayonnement.
  6. Procédé selon la revendication 3, dans lequel ladite étape de formation de seconde couche comprend la formation de ladite seconde couche de manière à avoir une porosité de 10 à 40 %.
  7. Procédé selon la revendication 3, dans lequel lesdites étapes de formation de première et seconde couches comprennent l'utilisation d'une charge de poudre ayant une taille de particule dans la plage de 10 nm à 10 micromètres.
  8. Procédé selon la revendication 7, dans lequel lesdites étapes de formation de première et seconde couches comprennent l'utilisation d'une charge de poudre ayant une taille de particule dans la plage de 10 nm à 2 micromètres.
EP13878078.8A 2013-03-14 2013-12-30 Revêtement de barrière thermique hybride et son procédé de fabrication Active EP2971240B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361781656P 2013-03-14 2013-03-14
PCT/US2013/078186 WO2014143363A1 (fr) 2013-03-14 2013-12-30 Revêtement de barrière thermique hybride et son procédé de fabrication

Publications (3)

Publication Number Publication Date
EP2971240A1 EP2971240A1 (fr) 2016-01-20
EP2971240A4 EP2971240A4 (fr) 2016-12-21
EP2971240B1 true EP2971240B1 (fr) 2018-11-21

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US (2) US20160017475A1 (fr)
EP (1) EP2971240B1 (fr)
WO (1) WO2014143363A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4534512A1 (fr) * 2023-10-06 2025-04-09 RTX Corporation Système de revêtement de barrière thermique et radiatif multiphase

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Publication number Priority date Publication date Assignee Title
FR3043411B1 (fr) * 2015-11-09 2017-12-22 Commissariat Energie Atomique Revetement ceramique multicouche de protection thermique a haute temperature, notamment pour application aeronautique, et son procede de fabrication
US10436042B2 (en) 2015-12-01 2019-10-08 United Technologies Corporation Thermal barrier coatings and methods
JP6908973B2 (ja) * 2016-06-08 2021-07-28 三菱重工業株式会社 遮熱コーティング、タービン部材、ガスタービン、ならびに遮熱コーティングの製造方法

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JP3872632B2 (ja) * 2000-06-09 2007-01-24 三菱重工業株式会社 遮熱コーティング材、それを適用したガスタービン部材およびガスタービン
US20090110953A1 (en) * 2007-10-29 2009-04-30 General Electric Company Method of treating a thermal barrier coating and related articles
DE102008007870A1 (de) * 2008-02-06 2009-08-13 Forschungszentrum Jülich GmbH Wärmedämmschichtsystem sowie Verfahren zu seiner Herstellung
US20110143043A1 (en) * 2009-12-15 2011-06-16 United Technologies Corporation Plasma application of thermal barrier coatings with reduced thermal conductivity on combustor hardware
US20110151219A1 (en) * 2009-12-21 2011-06-23 Bangalore Nagaraj Coating Systems for Protection of Substrates Exposed to Hot and Harsh Environments and Coated Articles
EP2341166A1 (fr) 2009-12-29 2011-07-06 Siemens Aktiengesellschaft Barrière thermique ceramique nano- et microstructurée
JP2010255121A (ja) * 2010-07-20 2010-11-11 Mitsubishi Heavy Ind Ltd 皮膜材料
EP2450465A1 (fr) * 2010-11-09 2012-05-09 Siemens Aktiengesellschaft Système de couche poreux doté d'une couche intérieure poreuse
US9017792B2 (en) * 2011-04-30 2015-04-28 Chromalloy Gas Turbine Llc Tri-barrier ceramic coating
US20130260132A1 (en) * 2012-04-02 2013-10-03 United Technologies Corporation Hybrid thermal barrier coating

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4534512A1 (fr) * 2023-10-06 2025-04-09 RTX Corporation Système de revêtement de barrière thermique et radiatif multiphase

Also Published As

Publication number Publication date
WO2014143363A1 (fr) 2014-09-18
US20180282853A1 (en) 2018-10-04
US20160017475A1 (en) 2016-01-21
EP2971240A4 (fr) 2016-12-21
EP2971240A1 (fr) 2016-01-20

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