Fiber-reinforced self-healing environmental barrier coating

Information

  • Patent Grant
  • 11668198
  • Patent Number
    11,668,198
  • Date Filed
    Friday, August 3, 2018
    6 years ago
  • Date Issued
    Tuesday, June 6, 2023
    a year ago
Abstract
An environmental barrier coating system for a turbine component, including an environmental barrier layer applied to a turbine component substrate containing silicon; the environmental barrier layer comprising an oxide matrix surrounding a fiber-reinforcement structure and a self-healing phase interspersed throughout the oxide matrix; wherein the fiber-reinforcement structure comprises at least one first fiber bundle oriented along a load bearing stress direction of said turbine component substrate; wherein the fiber-reinforcement structure comprises at least one second fiber bundle oriented orthogonal to the at least one first fiber bundle orientation; wherein the fiber-reinforcement structure comprises at least one third fiber woven between the at least one first fiber bundle and the at least one second fiber bundle.
Description
BACKGROUND

The disclosure relates to an article comprising a substrate containing silicon and an environmental barrier coating (EBC) which functions as a protective environmental barrier coating and inhibits the formation of gaseous species of Si, particularly Si(OH)x when the article is exposed to a high temperature, steam-laden environment.


Ceramic materials containing silicon and metal alloys containing silicon have been proposed for structures used in high temperature applications as, for example, gas turbine engines, heat exchangers, internal combustion engines, and the like. A particularly useful application for these materials is for service in gas turbine engines which operate at high temperatures in steam-laden environments. The ceramic materials that operate within the gas turbine are exposed to an environment in which jet fuel is combusted. As a result of the combustion, the temperature is high and steam (vapor phase water) and oxygen are present.


It has been found that these silicon containing substrates can recede and lose mass as a result of a formation of volatile Si species, particularly Si(OH)x and SiO when exposed to high temperature, steam laden environments. For example, silicon carbide when exposed to a lean fuel environment of approximately 1 ATM pressure of water vapor at 1200° C. will exhibit weight loss and recession at a rate of approximately 6 mils per 1000 hrs.


It is believed that the process involves oxidation of the silicon carbide to form silica on the surface of the silicon carbide followed by reaction of the silica with steam to form volatile species of silicon such as Si(OH)x. Naturally it would be highly desirable to provide an external barrier coating for silicon containing substrates which would inhibit the formation of volatile silicon species, Si(OH)x and SiO, and thereby reduce recession and mass loss.


SUMMARY

In accordance with the present disclosure, there is provided an environmental barrier coating, comprising an environmental barrier layer applied to a substrate containing silicon; the environmental barrier layer comprising an oxide matrix surrounding a fiber-reinforcement structure and a self-healing phase interspersed throughout the oxide matrix.


In another and alternative embodiment, the substrate comprises a ceramic matrix composite (CMC) material.


In another and alternative embodiment, the fiber-reinforcement structure comprises a continuous weave of fibers.


In another and alternative embodiment, the fiber-reinforcement structure comprises a SiC material composition.


In another and alternative embodiment, the fiber-reinforcement structure comprises at least one first fiber bundle oriented along a load bearing stress direction of the substrate.


In another and alternative embodiment, the substrate comprises a turbine blade, and the load bearing stress direction is oriented along a root to tip direction.


In another and alternative embodiment, the substrate comprises at least one of a turbine vane and a turbine blade, and the load bearing stress direction is oriented along the contour of a platform fillet.


In another and alternative embodiment, the fiber-reinforcement structure comprises at least one second fiber bundle oriented orthogonal to the first fiber bundle orientation.


In another and alternative embodiment, the fiber-reinforcement structure comprises at least one third fiber woven between the first fiber bundle and the second fiber bundle.


In another and alternative embodiment, the fiber-reinforcement structure comprises fibers that are oxygen getter loading materials.


In another and alternative embodiment, the fiber-reinforcement structure comprises fibers that are coated with an interface coating.


In another and alternative embodiment, the interface coating is selected from the group consisting of boron nitride, silicon carbide, an oxide and carbon.


In another and alternative embodiment, the matrix comprises a multi-phase mixture.


In another and alternative embodiment, the multi-phase mixture comprises SiO2.


In another and alternative embodiment, the self-healing phase comprises a glass phase.


In another and alternative embodiment, the self-healing phase comprises a material having properties of being in thermodynamic equilibrium with SiO2 during operation at predetermined temperatures.


In another and alternative embodiment, the self-healing phase comprises a material having properties of flowing into cracks formed in the matrix during operation at predetermined temperatures of between 1000° C. and 2000° C.


In another and alternative embodiment, the environmental barrier coating further comprises an oxygen getter phase interspersed throughout the matrix.


In another and alternative embodiment, the environmental barrier coating further comprises a protective layer applied on the environmental barrier coating.


The disclosure relates to a continuous fiber-reinforced, self-healing environmental barrier coating that prevents the ingress of oxygen and steam. The disclosed coating can increase durability with respect to conventional coatings. This coating consists of an oxide matrix and continuous fibers in a woven structure. The oxide matrix is a multi-phase mixture consisting of at least a SiO2 rich phase and a glass phase. In alternative embodiments, the oxide matrix can be a single phase material that may not include a self-healing functionality. The composition of the glass phase is chosen to be in thermodynamic equilibrium with SiO2 and to be sufficiently fluid at high temperatures to flow into cracks in the coating, which imparts ‘self-healing functionality.’ The fibers could be SiC, in some instances coated with an interface coating, such as boron nitride or silicon carbide, oxide (e.g. Nextel™ 720) or carbon.


Other details of the coating are set forth in the following detailed description and the accompanying drawings wherein like reference numerals depict like elements.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a cross section of an exemplary coating on a substrate containing silicon according to the disclosure.



FIG. 2 is a cross section of an exemplary coating on a substrate containing silicon according to the disclosure.



FIG. 3 is cross section of the exemplary coating on a substrate containing silicon according to the disclosure.





DETAILED DESCRIPTION

Referring now to FIG. 1, there is illustrated an environmental barrier coating 10 formed over a substrate 12 of an article 14, configured to inhibit the formation of gaseous species of silicon when the article 14 is exposed to a high temperature, steam-laden environment. The coating 10 can be designed for maximum protection between 1100° C. and 1700° C. The substrate 12 can be associated with articles 14 such as, at least one of a turbine vane and a turbine blade, and particularly a gas turbine engine component, such as components in the hot section of the gas turbine engine, including rotating components and portions of combustors, shrouds, and the like.


The substrate 12 of the article 14 can include portions that experience certain forces that result in a load bearing stress often oriented in a particular direction, i.e., a load bearing stress direction 16 of the substrate 12 of the article 14, illustrated as an arrow 16. It is contemplated that the load bearing stress direction 16 can be oriented in a variety of directions as well as multiple directions depending on the design of the substrate 12 and service of the article 14 in the gas turbine engine.


In an exemplary embodiment the load bearing stress direction 16 can be oriented from a root 18 of the article 14 to a tip 20 of the article 14, such as a blade root to a blade tip. In another exemplary embodiment, the load bearing stress direction 16 can be oriented along a contour of a fillet between a platform and an airfoil portion of the article 14, such as a blade/vane platform fillet 22. As illustrated in FIG. 3, the root to tip direction can be understood as orthogonal to the plane of the page shown in the bundle of fibers 38.


The substrate 12 can be constructed from materials containing silicon and can be a ceramic matrix composite material, a silicon ceramic substrate or a silicon containing metal alloy. In an exemplary embodiment, the substrate 12 can be silicon containing ceramic material such as, for example, silicon carbide, silicon nitride, silicon oxy-nitride and silicon aluminum oxy-nitride. In accordance with a particular embodiment, the silicon containing ceramic substrate comprises a silicon containing matrix with reinforcing materials 24 such as fibers, particles and the like and, more particularly, a silicon based matrix which is fiber-reinforced. Particularly suitable ceramic substrates are a silicon carbide coated silicon carbide fiber-reinforced silicon carbide particle and silicon matrix, a carbon fiber-reinforced silicon carbide matrix and a silicon carbide fiber-reinforced silicon nitride matrix. Particularly useful silicon-metal alloys for use as substrates for the article 14 can include molybdenum-silicon alloys, niobium-silicon alloys, iron-silicon alloys, and aluminum-silicon alloys.


Referring also to FIG. 2 and FIG. 3, an environmental barrier layer 26 can be applied to the substrate 12. A protective layer 28 can be applied on the environmental barrier layer 26. The protective layer 28 is configured to resist vaporization when exposed to steam. In an exemplary embodiment, the protective layer can be a rare earth disilicate, such as Y2Si2O7, Yb2Si2O7; a rare earth monosilicate, such as Y2SiO5, Yb2SiO5, HfSiO4, ZrSiO4, HfO2, BSAS (BaxSr1-xAl2Si2O8 where x may be 0.25).


The environmental barrier layer 26 can include an oxide matrix 30 surrounding a fiber-reinforcement structure 32 and a self-healing phase 34 interspersed throughout the oxide matrix 30. In an alternative embodiment, the oxide matrix 30 can be a single phase without self-healing phase present. In another embodiment, the oxide matrix 30 can include a multi-phase mixture, such as SiO2 rich phase. The self-healing phase 34 can include a glass phase. The self-healing phase 34 can include a material having properties that are in thermodynamic equilibrium with SiO2 during operation at predetermined temperatures. The self-healing phase 34 comprises a material having properties of flowing into cracks 48 formed in the matrix 30 during operation at those predetermined temperatures. The self-healing phase 34 can be sufficiently fluid at high temperatures to flow into cracks 48 in the coating 10, which imparts a self-healing functionality. Between 1000° C. and 2000° C. these materials can exist as mixtures of solid and liquid phases. The temperature at which liquid formation occurs can be controlled by the chemical composition. In an exemplary embodiment, liquid formation initiates between 1150° C. and 1500° C., with the volume fraction of liquid increasing with temperature. The viscosity of the liquid phase can vary from 0.1 to 100,000 Pa*s with the exemplary viscosity varying between 10-10,000 Pa*s. An example of the self-healing phase 34 can include a mixture of BaMg2Al6Si9O30 and SiO2. Another example can include the mixture of CaAl2Si2O8, CaSiO3 and SiO2. Another example includes the mixture of Y2Si2O7, Al2O3 and SiO2. Alternatively, the materials listed above could be premixed and processed to form a glass. The initial composition of the glass could be: 2% BaO, 3% MgO, 10% AlO1.5, 85% SiO2, or 8% CaO, 17% AlO1.5 75% SiO2, or 10% YO1.5, 10 AlO1.5, 80% SiO2.


An oxygen getter phase 36 can also be interspersed throughout the oxide matrix 30. The oxygen getter phase 36 can comprise an oxy-carbide material. In an exemplary embodiment, the oxy-carbide material can include a glass that contains oxygen and carbon and silicon dioxide as well as particles of amorphous carbon and silicon carbide.


The fiber-reinforcement structure 32 can include a continuous weave of fibers. In an exemplary embodiment, the fiber-reinforcement structure 32 comprises a SiC material composition. The fiber-reinforcement structure 32 can include at least one first fiber bundle 38 oriented along the load bearing stress direction 16 of the substrate 12. In an exemplary embodiment, the first fiber bundle 38 can be oriented from blade root 18 to blade tip 20 and aligned along the root to tip direction, so as to provide structural support along the same orientation as the load bearing stress direction 16. In another exemplary embodiment, the first fiber bundle 38 can be oriented along the load bearing stress direction 16 oriented along the contour of the blade/vane platform fillet 22.


In another exemplary embodiment, the fiber-reinforcement structure 32 comprises at least one second fiber bundle 40 oriented orthogonal to the first fiber bundle 38 orientation. In another exemplary embodiment, the fiber-reinforcement structure 32 comprises at least one third fiber 42 woven between the first fiber bundle 38 and the second fiber bundle 40. In an exemplary embodiment, the fiber-reinforcement structure 32 comprises fibers that comprise oxygen getter materials 44. In another exemplary embodiment, the fiber-reinforcement structure 32 comprises fibers that are coated with an interface coating 46. The interface coating 46 can include materials selected from the group consisting of boron nitride, silicon carbide, an oxide and carbon.


The environmental barrier layer 26 can be present on the article at a thickness of greater than or equal to about 0.5 mils (0.0005 inch), preferably between about 3 to about 30 mils and ideally between about 3 to about 8 mils.


The environmental barrier layer 26 can be applied by preparing the substrate 12 surface.


There are several methods that could be used to introduce a glass-ceramic into the fiber reinforcement structure 32 being provided for the environmental barrier coating 10. In one approach, a fiber preform can be infiltrated using a glass particulate suspension, which would be added to the fiber preform layer by soaking, spraying or other means, at ambient temperature. The infiltrated fabric or preform is placed adjacent to the silicon containing CMC substrate 12, and the assembly is heated. Pressure can be applied using graphite dies, powdered media such as carbon or boron nitride, and the like, in order to de-gas the environmental barrier layer 26 at temperatures suitable for melting the glass. The subsequent assembly can undergo annealing to obtain a desired microstructure.


In another exemplary embodiment, an alternate technique of assembly would be to place a fiber preform in contact with the silicon containing CMC substrate 12. The fiber perform can then be rigidized using a variety of techniques, including but not limited to adding a ceramic sol and freezing the substrate followed by freeze drying. The assembly is then placed into a graphite die which comprises an outer profile of the EBC coated article 14. Molten glass is then injected into the die and flows into and among the fibers of the preform. The assembly can then be cooled and (re)heated to a temperature suitable to promote the formation of the desired microstructure.


Alternative approaches to introducing oxide or silicate phases into a relatively thin fiber preform, can include but are not limited to spraying the preform with a suspension, followed by heating the surface via flame or plasma spraying molten oxide and/or silicate materials onto the preform, and the like. Generally, sharp temperature gradients between the substrate and the created layer should be avoided to enhance adherence.


A self-healing, fiber-reinforced oxidant barrier offers a robust mechanism for protecting load bearing materials in the hot-section of gas turbine engines. This disclosure describes the use of fiber reinforcements in the environmental barrier coating to increase durability. Additionally, the self-healing, multi-phase matrix that surrounds the fibers inhibits the permeability of oxidants through the coating. The fibers will also increase the creep resistance of the coating, enhancing durability on rotating components.


An environmental barrier coating prevents CMC recession caused by Si(OH)x formation. Interaction of the environmental barrier coating with the steam laden combustion environment results in the formation of Si(OH)x, but the rate of formation is much less than that of an uncoated SiC CMC.


There has been provided a coating. While the coating has been described in the context of specific embodiments thereof, other unforeseen alternatives, modifications, and variations may become apparent to those skilled in the art having read the foregoing description. Accordingly, it is intended to embrace those alternatives, modifications, and variations which fall within the broad scope of the appended claims.

Claims
  • 1. An environmental barrier coating system for a turbine component, comprising: an environmental barrier layer applied to a turbine component substrate containing silicon; said environmental barrier layer comprising an oxide matrix surrounding a fiber-reinforcement structure and a self-healing phase interspersed throughout said oxide matrix; wherein said fiber-reinforcement structure comprises at least one first fiber bundle oriented along a load bearing stress direction of said turbine component substrate; wherein said fiber-reinforcement structure comprises at least one second fiber bundle oriented orthogonal to said at least one first fiber bundle orientation; wherein said fiber-reinforcement structure comprises at least one third fiber woven between said at least one first fiber bundle and said at least one second fiber bundle.
  • 2. The environmental barrier coating of claim 1, wherein said turbine component substrate comprises a ceramic matrix composite material.
  • 3. The environmental barrier coating of claim 1, wherein said fiber-reinforcement structure comprises a continuous weave of fibers.
  • 4. The environmental barrier coating of claim 1, wherein said fiber-reinforcement structure comprises a SiC material composition.
  • 5. The environmental barrier coating of claim 1, wherein said turbine component substrate comprises a turbine blade, and said load bearing stress direction is oriented along a root to tip direction.
  • 6. The environmental barrier coating of claim 1, wherein said turbine component substrate comprises at least one of a turbine vane and a turbine blade, and said load bearing stress direction is oriented along a contour of a platform fillet.
  • 7. The environmental barrier coating of claim 1, wherein said fiber-reinforcement structure comprises fibers that are oxygen getter materials.
  • 8. The environmental barrier coating of claim 1, wherein said fiber-reinforcement structure comprises fibers that are coated with an interface coating.
  • 9. The environmental barrier coating of claim 8, wherein said interface coating is selected from the group consisting of boron nitride, silicon carbide, an oxide, and carbon.
  • 10. The environmental barrier coating of claim 1, wherein said matrix comprises a multi-phase mixture.
  • 11. The environmental barrier coating of claim 10, wherein said multi-phase mixture comprises SiO2.
  • 12. The environmental barrier coating of claim 1, wherein said self-healing phase comprises a glass phase.
  • 13. The environmental barrier coating of claim 1, wherein said self-healing phase comprises a material having properties of being in thermodynamic equilibrium with SiO2 during operation at predetermined temperatures.
  • 14. The environmental barrier coating of claim 1, wherein said self-healing phase comprises a material having properties of flowing into cracks formed in said matrix during operation at predetermined temperatures.
  • 15. The environmental barrier coating of claim 1, further comprising an oxygen getter phase interspersed throughout said matrix.
  • 16. The environmental barrier coating of claim 1, further comprising: a protective layer applied on said environmental barrier coating.
US Referenced Citations (99)
Number Name Date Kind
3532438 Palfreyman Oct 1970 A
5113582 Monson et al. May 1992 A
5580837 Dodds et al. Dec 1996 A
5858181 Jindal et al. Jan 1999 A
6117560 Maloney Sep 2000 A
6210182 Hasz et al. Apr 2001 B1
6228453 Fareed et al. May 2001 B1
6270852 Ulion et al. Aug 2001 B1
6284323 Maloney Sep 2001 B1
6296941 Eaton, Jr. et al. Oct 2001 B1
6579636 Oguri et al. Jun 2003 B2
6730422 Litton et al. May 2004 B2
6924040 Maloney Aug 2005 B2
7063894 Sun et al. Jun 2006 B2
7226672 Litton et al. Jun 2007 B2
7509735 Philip et al. Mar 2009 B2
7513955 Kruger et al. Apr 2009 B2
7622195 Schlichting et al. Nov 2009 B2
7862901 Darolia et al. Jan 2011 B2
7951459 Tang et al. May 2011 B2
7972657 Schlichting et al. Jul 2011 B2
8039113 Kirby et al. Oct 2011 B2
8062759 Fu et al. Nov 2011 B2
8084086 Hass et al. Dec 2011 B2
8111078 Yang et al. Feb 2012 B1
8119247 Kirby et al. Feb 2012 B2
8216689 Witz et al. Jul 2012 B2
8217087 Keller et al. Jul 2012 B1
8257559 Floyd et al. Sep 2012 B2
8273470 Kirby et al. Sep 2012 B2
8287635 Luccarelli et al. Oct 2012 B2
8343589 Kirby et al. Jan 2013 B2
8357454 Kulkarni et al. Jan 2013 B2
8470460 Lee Jun 2013 B2
8512874 Darolia et al. Aug 2013 B2
8529999 Maloney et al. Sep 2013 B2
8574721 Gero et al. Nov 2013 B2
8658255 Kirby et al. Feb 2014 B2
8658291 Kirby et al. Feb 2014 B2
8663378 Luccarelli et al. Mar 2014 B2
8673400 Kirby et al. Mar 2014 B2
8940417 Courcot et al. Jan 2015 B2
9034479 Nagaraj et al. May 2015 B2
9126873 Diss et al. Sep 2015 B2
9387512 Lee et al. Jul 2016 B2
9428650 Meschter et al. Aug 2016 B2
9611181 Tang et al. Apr 2017 B2
9713912 Lee Jul 2017 B2
9771811 Zhang et al. Sep 2017 B2
9926238 Louchet et al. Mar 2018 B2
9938839 Rosenzweig et al. Apr 2018 B2
9951630 Hass Apr 2018 B2
20060099358 Raybould et al. May 2006 A1
20060110609 Eaton et al. May 2006 A1
20060115659 Hazel et al. Jun 2006 A1
20070292616 Hazel Dec 2007 A1
20080113218 Schlichting et al. May 2008 A1
20090155554 Gentleman et al. Jun 2009 A1
20090186237 Lee Jul 2009 A1
20100129636 Cybulsky et al. May 2010 A1
20100129673 Lee May 2010 A1
20100154422 Kirby et al. Jun 2010 A1
20110014060 Bolcavage et al. Jan 2011 A1
20110217560 Ridgeway Sep 2011 A1
20110281107 Gero et al. Nov 2011 A1
20120244383 Meschter et al. Sep 2012 A1
20130122259 Lee May 2013 A1
20130210299 Zhang Aug 2013 A1
20130260130 Taxacher et al. Oct 2013 A1
20140065408 Strock et al. Mar 2014 A1
20140271208 Garcia-Crespo Sep 2014 A1
20140272310 Lazur et al. Sep 2014 A1
20150111063 Khan et al. Apr 2015 A1
20150118444 Lipkin et al. Apr 2015 A1
20150167141 Rozenweig et al. Jun 2015 A1
20150308276 Kleinow et al. Oct 2015 A1
20160130188 Louchet May 2016 A1
20160160664 Luthra et al. Jun 2016 A1
20160186580 Zaleski et al. Jun 2016 A1
20160214907 Shim et al. Jul 2016 A1
20160332922 Tang et al. Nov 2016 A1
20170022113 Opila Jan 2017 A1
20170073278 Landwehr et al. Mar 2017 A1
20170121232 Nelson et al. May 2017 A1
20170145560 Weaver et al. May 2017 A1
20170217842 Sato Aug 2017 A1
20170335118 Tang et al. Nov 2017 A1
20170342539 Sato et al. Nov 2017 A1
20180170811 Osada et al. Jun 2018 A1
20180305821 Wan et al. Oct 2018 A1
20180347049 Oboodi et al. Dec 2018 A1
20180370862 Kirby et al. Dec 2018 A1
20190084890 Weaver Mar 2019 A1
20200040746 Jackson et al. Feb 2020 A1
20200055788 Mikalsen et al. Feb 2020 A1
20200080430 Schmidt et al. Mar 2020 A1
20200123071 Ndamka et al. Apr 2020 A1
20200331817 Bianchi Oct 2020 A1
20220048828 Liu et al. Feb 2022 A1
Foreign Referenced Citations (17)
Number Date Country
102015205807 Oct 2016 DE
1044944 Oct 2000 EP
1806431 Jul 2007 EP
1900848 Mar 2008 EP
2189504 May 2010 EP
2192098 Jun 2010 EP
2388354 Nov 2011 EP
2615250 Jul 2013 EP
2644747 Oct 2013 EP
3130577 Feb 2017 EP
3162783 May 2017 EP
3409653 Dec 2018 EP
3954806 Feb 2022 EP
2013103425 Jul 2013 WO
2014204480 Dec 2014 WO
2017031163 Feb 2017 WO
2019069023 Apr 2019 WO
Non-Patent Literature Citations (25)
Entry
European Search Report dated Dec. 6, 2019 issued for corresponding European Patent Application No. 19189903.8.
European Search Report dated Jan. 13, 2020 issued for corresponding European Patent Application No. 19192162.6.
European Search Report dated Jan. 7, 2020 issued for corresponding European Patent Application No. 19192131.1.
European Search Report dated Jan. 3, 2020 issued for corresponding European Patent Application No. 19192124.6.
Poerschke, David L. et al: “Interaction of yttrium disilicate environment barrier coatings with calcium-magnesium-iron alumino-silicate melts”, Acta Materalia., vol. 145, Dec. 19, 2017, pp. 451-461.
Ahlborg, Nadia L., et al.: “Calcium-magnesium aluminosilicate (CMAS) reactions and degradation mechanisms of advanced environmental barrier coatings”, Surface and Coatings Technology, vol. 237, 2013, pp. 79-87.
Zhao, Hengbei et al: “Molten silicate reactions with plasma sprayed ytterbium silicate coatings”, Surace and Coatings Technology, vol. 288, Jan. 14, 2016, pp. 151-162.
Nikas, V. et al..(2015) Strong visible light emission from silicon-oxycarbide nanowire arrays prepared by electron beam lithography and reactive ion etching. Journal of Materials Research. 30. 1-8. (Year 2015).
U.S. Office Action dated Mar. 14, 2022 issued for corresponding U.S. Appl. No. 15/998,730.
U.S. Office Action dated Mar. 16, 2022 issued for corresponding U.S. Appl. No. 15/998,731.
U.S. Non-Final Office Action dated Mar. 11, 2020 for corresponding U.S. Appl. No. 15/998,736.
U.S. Non-final Office action dated Sep. 10, 2020 issued for corresponding U.S. Appl. No. 14/711,902.
U.S. Notice of Allowance dated Nov. 2, 2010 issued for corresponding U.S. Appl. No. 15/998,736.
U. Kolitsch, H.J. Seifert, and F. Aldinger, “Phase Relationships in the Systems RE2O3-AI2O3-SiO2 (RE = Rare Earth Element , Y, and Sc)” Journal of Phase Equilibria, vol. 19, No. 5, 1998.
European Office action dated Mar. 7, 2018 issued for corresponding EP Patent Application No. 15168227.5.
Latka, et al. “Thermal diffusivity and conductivity of yttria stabilized zirconia coatings obtained by suspension plasma spraying”, Surface & Coatings Technology 208 (2012), pp. 87-91, (Year 2012).
Fauchals, et al. “Understanding of Suspension DC Plasma Spraying of Finely Structured Coatings for SOFC”, IEEE Transactions on Plasma Science, vol. 33, No. 2, Apr. 2005, pp. 920-930. (Year: 2005).
Qu, et al., “Thermal Conductivity of the gadolinium calcium silicate apatites: Effect of Different Point Defect Types”, Acta Materialia vol. 59, (2011), pp. 3841-3850.
U.S. Non-final Office action dated Apr. 13, 2017 issued for corresponding U.S. Appl. No. 14/711,902.
U.S. Non-final Office action dated Aug. 1, 2019 issued for corresponding U.S. Appl. No. 14/711,902.
U.S. Final Office action dated Aug. 23, 2017 issued for corresponding U.S. Appl. No. 14/711,902.
U.S. Final Office action dated Dec. 11, 2019 issued for corresponding U.S. Appl. No. 14/711,902.
EP Search Report dated Sep. 28, 2015 issued for European Patent Application No. 15168227.5.
U.S. Non-Final Office Action dated Jul. 17, 2019 issued in U.S. Appl. No. 15/998,736.
U.S. Final Office Action dated Oct. 31, 2019 issued in U.S. Appl. No. 15/998,736.
Related Publications (1)
Number Date Country
20200040746 A1 Feb 2020 US