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, aqueous (water and/or steam) 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 particular useful application for these materials is for use in gas turbine engines which operate at high temperatures in aqueous environments.
It has been found that these silicon containing structures can recess and lose mass as a result of formation of volatile silicon species, particularly Si(OH)x and SiO when exposed to high temperature, aqueous environments.
It is believed that the process involves oxidation of the silicon-containing structure to form silica on the surface followed by reaction of the silica with steam to form volatile species of silicon such as Si(OH)x. It would be highly desirable to provide an external harrier 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.
In accordance with the present disclosure, there is provided a process of coating a substrate containing silicon with an environmental barrier coating, comprising altering a surface of the substrate; and applying an environmental barrier layer to the surface of the substrate.
In another and alternative embodiment, the substrate comprises a ceramic matrix composite material.
In another and alternative embodiment, the altering step comprises at least one of a chemical process and a physical process.
In another and alternative embodiment, the surface is exposed to at least one of an intense ultraviolet light, a plasma, a laser, ion beam, and electron beam.
In another and alternative embodiment, the altering step comprises at least one of altering a chemical structure of the surface and altering a chemical function of the surface.
In another and alternative embodiment, the surface has organic contaminants, and wherein the altering step removes the organic contaminants.
In another and alternative embodiment, the substrate comprises at least one of a turbine vane and a turbine blade.
In another and alternative embodiment, the process further comprises applying a protective layer on the environmental barrier layer.
In another and alternative embodiment, the altering step comprises modifying textures of the surface through at least one of a chemical exposure, a physical addition of material, a physical removal of material; wherein the texture modification results in a surface topology.
In another and alternative embodiment, the surface topology can be created by at least one of embedding particles into the surface, directional deposition and mechanical removal of surface material.
In another and alternative embodiment, the mechanical removal comprises at least one of creating divots in the surface, creating lines in the surface.
In another and alternative embodiment, the divots and the lines can be arranged in at least one of patterns and randomly arranged.
In another and alternative embodiment, the process further comprises creating the surface topology by mechanical removal of material by at least one of a particle ablation, a laser ablation and chemical etching.
In another and alternative embodiment, the process further comprises utilizing a contact mask for isolating a predetermined area for adhesion of the environmental barrier coating.
In another and alternative embodiment, the process further comprises utilizing a contact mask for isolating a predetermined area for promoting chemical vapor infiltration growth during coating.
In another and alternative embodiment, the surface topology comprises characteristics that enhance bonding.
In another and alternative embodiment, the characteristics that enhance bonding are selected from the group consisting of a chemical uniformity, OH or Cr—Si group activity and a surface tortuosity, roughness and angularity.
In another and alternative embodiment, the surface tortuosity comprises at least one of a roughness and angularity.
In another and alternative embodiment, the surface topology is one of pre-determined in particular patterns, or randomly arranged.
In another and alternative embodiment, the environmental barrier layer comprises an oxidant getter phase, the oxidant getter phase is selected from the group consisting of silicon oxycarbide and elemental silicon.
In another and alternative embodiment, the environmental barrier layer comprises at least one of (rare earth) RE-monosilicates, disilicates and (alkaline earth) AE alumino silicates, silicates of Hafnium and zirconium, and oxides of Hafnium or zirconium.
In another and alternative embodiment, the environmental barrier layer comprises an oxide matrix and an oxidant getter phase interspersed throughout the oxide matrix, the oxide matrix contains a self-healing phase that contains at least one of doped silicates, compatible metals/metal alloys, non-oxide glasses, silica, and glass/glass ceramics comprising BAS, BMAS, LAS, SAS.
Other details of the coating are set forth in the following detailed description and the accompanying drawings wherein like reference numerals depict like elements.
Referring now to
The substrate 12 can be constructed from materials containing silicon and can be a ceramic matrix composite material, a monolithic ceramic, a silicon-based or silicon-containing 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, alkaline earth or rare earth silicate glasses or glass ceramics and combinations thereof. Examples can include barium strontium alumino silicate, strontium alumino silicate, lithium alumino silicate, aluminosilicate, mullite, yttrium silicate, ytterbium silicate, and the like. In accordance with a particular embodiment, the silicon-containing ceramic substrate comprises a silicon-containing matrix with reinforcing materials 16 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 fiber-reinforced silicon carbide 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, zirconium, hafnium, titanium, chromium, tungsten, boron, platinum, tantalum, Ti—Si alloys and Mo—Si, Nb—Si and Fe—Si alloys.
Referring also to
The environmental barrier layer 18 can include an oxide matrix 24 and an oxidant getter phase 26 interspersed throughout the oxide matrix 24. The oxide matrix 24 can include a multi-phase mixture, such as SiO2 rich phase and a self-healing phase 28 that can include a glass phase.
In an exemplary embodiment, the composition of the oxide matrix 24 dictates the mole fraction of the glass and the SiO2. The self-healing phase 28 can include a material having properties that are in thermodynamic equilibrium with SiO2 during operation at predetermined temperatures. The self-healing phase 28 comprises a material having properties of flowing into cracks 30 formed in the matrix 24 during operation at those predetermined temperatures. The self-healing phase 28 can be sufficiently fluid at high temperatures to flow into the cracks 30 in the coating 10, which imparts a self-healing functionality. In an exemplary embodiment, the self-healing phase 28 can include doped silicates, compatible metals/metal alloys, non-oxide glasses, the SiO2 itself, as well as any representative glass/glass ceramics such as BAS, BMAS, LAS, SAS.
The environmental barrier layer 18 can be present on the substrate 12 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 5 mils.
In an exemplary embodiment the oxidant getter phase 26 can comprise, silicon oxycarbide, SixOyCz where 0.5≤x<1; 0≤y<2; 0≤z<2. In another exemplary embodiment, the oxidant getter phase comprises elemental silicon. The composition can include up to 100% silicon. The elemental silicon can improve coating adhesion.
It is advantageous to apply the environmental barrier layer 18 to the surface 20 of the substrate 14 after the surface 20 has been treated and prepared. The surface can have organic contaminants. The organic contaminants can be removed from the surface 20 via techniques, such as, plasma treatment. In order to obtain good adhesion of the environmental barrier layer 18 to the surface 20 it can be advantageous to enhance the properties of the surface 20.
Referring also to
In an exemplary embodiment, the surface 20 can be exposed to an intense ultraviolet light, a plasma, a laser, ion beam, or electron beam. The exposure can alter the surface 20 by at least one of chemical structure or chemical function. It is also contemplated that the surface 20 can be etched to modify the properties of the surface 20.
In addition to the chemo-alteration of the surface 20, the surface 20 can have a texture modified through at least one of a chemical exposure, physical addition of material, physical removal of material resulting in a surface topology 32 that can enhance or enable adhesion of the environmental barrier layer 18.
In an exemplary embodiment, the surface topology 32 can be created by embedding particles 34, by directional deposition 36, with/without a mask 38, and mechanical removal of surface material. The mechanical removal 40 can include the creation of divots 42 or lines 44 in patterns or randomly arranged.
In another exemplary embodiment, the surface topology 32 can be created by mechanical removal 40 of material by particle ablation, laser ablation, chemical etching, and the like.
The contact mask 38, can be utilized for isolating a predetermined area for adhesion 46 and/or for promoting chemical vapor infiltration growth during coating.
The surface topology 32 can include characteristics that enhance bonding, such as chemical uniformity, OH or Cr—Si group activity, surface tortuosity, such as, roughness and angularity. The surface topology 32 can be pre-determined in particular patterns, such as a herring bone, or other pattern, or randomly arranged as shown in
In an exemplary embodiment, the surface 20 of the composite to be coated is made via a CVI process, mechanically roughening the surface prior to a final CVI treatment that creates enhanced roughness resulting in significantly better adherence of the environmental barrier layer 18.
The environmental barrier layer 18 can be applied to the substrate 12 by use of suspension plasma spray, electron-beam physical vapor deposition, or an air plasma spray, as well as, slurry based method including dipping, painting and spraying.
The disclosed method can create a surface 20 that promotes strong adhesion that enables the capability of the environmental barrier coating system to endure higher thermal gradients, retain larger coating thickness design space, longer coating life, and higher resistance to spallation.
There has been provided a method of preparing a surface for an environmental barrier 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.
Number | Name | Date | Kind |
---|---|---|---|
5113582 | Monson | May 1992 | A |
5580837 | Dodds et al. | Dec 1996 | A |
5858181 | Jindal et al. | Jan 1999 | A |
6117560 | Maloney | Sep 2000 | A |
6210812 | Hasz | 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 | Mar 2009 | B2 |
7513955 | Kruger | Apr 2009 | B2 |
7622195 | Schlichting et al. | Nov 2009 | B2 |
7862901 | Darolia et al. | Jan 2011 | B2 |
7951459 | Tang | 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 | 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 |
20060115659 | Hazel et al. | Jun 2006 | A1 |
20080113218 | Schlichting et al. | May 2008 | A1 |
20090155554 | Gentleman et al. | Jun 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 |
20130122259 | Lee | May 2013 | A1 |
20130260130 | Taxacher et al. | Oct 2013 | A1 |
20140065408 | Strock et al. | Mar 2014 | A1 |
20140272310 | Lazur et al. | Sep 2014 | A1 |
20150118444 | Lipkin et al. | Apr 2015 | A1 |
20150167141 | Rozenweig et al. | Jun 2015 | A1 |
20150308276 | Kleinow | Oct 2015 | A1 |
20160160664 | Luthra 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 | May 2017 | A1 |
20170335118 | Tang et al. | Nov 2017 | A1 |
20180347049 | Oboodi et al. | Dec 2018 | A1 |
20180370862 | Kirby et al. | Dec 2018 | A1 |
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 |
3409653 | Dec 2015 | EP |
3130577 | Feb 2017 | EP |
3162783 | May 2017 | EP |
2013103425 | Jul 2013 | WO |
2014204480 | Dec 2014 | WO |
2017031163 | Feb 2017 | WO |
20190269023 | Apr 2019 | WO |
Entry |
---|
J. Kolitsch, H.J. Seifert, and F. Aldinger, “Phase Relationships in the Systems RE2O3—Al2O3—SiO2 (RE = Rare Earth Element , Y, and Sc)” Journal of Phase Equilibria, vol. 19, No. 5, 1998. |
European Search Report dated Jan. 3, 2020 issued for corresponding European Patent Application No. 19192124.6. |
European Search Report dated Dec. 6, 2019 issued for corresponding European Patent Application No. 19189903.8. |
European Search Report dated Jan. 7, 2020 issued for corresponding European Patent Application No. 19192131.1. |
European Search Report dated Jan. 13, 2020 issued for corresponding European Patent Application No. 19192162.6. |
Poerschke, D.L., et al., “Interaction of yttrium disilicate environmental barrier coatings with calcium-magnesium-iron alumino-sllicate melts”, Acta Materialia, vol. 145, Dec. 19, 2017 pp. 451-461. |
Ahlborg, N.L., et al., “Calcium-magnesium aluminosilicate (CMAS) reactions and degradation mechanisms of advanced environmental barrier coatings”, Surface & Coatings Technology, vol. 237, (2013) pp. 79-87. |
Zhao, H., et al., “Molten silicate reactions with plasma sprayed ytterbium silicate coatings”, Surface & Coatings Technology, vol. 288, Jan. 14, 2016, pp. 151-162. |
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 Sep. 10, 2020 issued for corresponding U.S. Appl. No. 14/711,902. |
Number | Date | Country | |
---|---|---|---|
20200055788 A1 | Feb 2020 | US |