Self-healing environmental barrier coating

Abstract

An environmental barrier coating, comprising a substrate containing silicon; an environmental barrier layer applied to the substrate; the environmental barrier layer comprising an oxide matrix; an oxidant getter phase interspersed throughout the oxide matrix; and a self-healing phase interspersed throughout the oxide matrix.

Claims

1. An environmental barrier coating system, comprising: a substrate containing silicon; an environmental barrier layer applied to said substrate; said environmental barrier layer comprising an oxide matrix; an oxidant getter phase interspersed throughout said oxide matrix; and a self-healing phase interspersed throughout said oxide matrix; wherein said self-healing phase comprises a composition of CaO-AlO.sub.1.5-SiO.sub.2 in the ranges 1-25 mol % CaO, 1-25 mol % AlO.sub.1.5, 50-99 mol % SiO.sub.2.

2. The environmental barrier coating system of claim 1, wherein said substrate comprises a ceramic matrix composite material.

3. The environmental barrier coating system of claim 1, wherein said environmental barrier layer comprises a SiO.sub.2 rich phase.

4. The environmental barrier coating system of claim 1, wherein said self-healing phase comprises a glass phase.

5. The environmental barrier coating system of claim 1, wherein said oxidant getter phase comprises Si.sub.xO.sub.yC.sub.z where 0.5≤x <1; 0≤y <2; 0≤z <2.

6. The environmental barrier coating system of claim 1, wherein said self-healing phase comprises a material having properties of being in thermodynamic equilibrium with a SiO.sub.2 during operation at predetermined temperatures.

7. The environmental barrier coating system of claim 1, wherein said self-healing phase comprises a material having properties of flowing into cracks formed in said oxide matrix during operation at predetermined temperatures.

8. The environmental barrier coating system of claim 1, wherein said self-healing phase comprises a material having properties of flowing into cracks formed in said oxide matrix during operation at predetermined temperatures of from 1800 (982° C.) -3000 degrees Fahrenheit (1650° C.).

9. The environmental barrier coating system of claim 1, wherein said substrate comprises at least one of a turbine vane and a turbine blade.

10. The environmental barrier coating system of claim 1, further comprising: a protective layer applied on said environmental barrier layer.

11. An environmental barrier coating system, comprising: a substrate containing silicon; an environmental barrier layer applied to said substrate; said environmental barrier layer comprising an oxide matrix; an oxidant getter phase interspersed throughout said oxide matrix; and a self-healing phase interspersed throughout said oxide matrix; wherein said self-healing phase comprises a composition of alkaline earth-alumino silicates in which the total alkaline earth (AE) concentration is between 1-25% AE, 1-25mol % AlO.sub.1.5, and 50-99mol % SiO.sub.2.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

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

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

(3) FIGS. 3a-3c illustrate diagrams of an exemplary composition.

(4) FIGS. 4a-4c illustrate diagrams of an exemplary composition.

(5) FIGS. 5a-5c illustrate diagrams of an exemplary composition.

(6) FIG. 6 illustrates a diagram of an exemplary composition.

DETAILED DESCRIPTION

(7) 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 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 static and rotating components and portions of combustors, and the like.

(8) 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, and alloys of zirconium, hafnium, titanium, chromium, tungsten, boron, platinum, and tantalum.

(9) Referring also to FIG. 2, an environmental barrier layer 18 can be applied to the substrate 12 on a surface 20. A protective layer 22 can be applied on the environmental barrier layer 18. The protective layer 22 is configured to resist recession of the Si-containing volatile species when exposed to water vapor or steam. In an exemplary embodiment, the protective layer 22 can include binary or multicomponent oxides such as HfO.sub.2, ZrO.sub.2, or Gd.sub.2Hf.sub.2O.sub.7, Gd.sub.2Zr.sub.2O.sub.7, refractory metal oxides. In other exemplary embodiments, the protective layer 22 can include silicates with low(er) SiO.sub.2 activities. In another exemplary embodiment the protective layer 22 can include (rare earth) RE-monosilicates, disilicates and (alkaline earth) AE alumino silicates, silicates of Hafnium and zirconium.

(10) 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 SiO.sub.2 rich phase and a self-healing phase 28 that can include a glass phase.

(11) In an exemplary embodiment, the composition of the self-healing phase can include 15% CaO, 10% AlO.sub.1.5, 75% SiO.sub.2. The thermodynamically equilibrated phase constitution of this composition is shown in FIG. 3.

(12) Another exemplary embodiment is 10% CaO, 5% AlO.sub.1.5, 85% SiO.sub.2. The thermodynamically equilibrated phase constitution of this composition is shown in FIG. 4.

(13) In an exemplary embodiment, the composition of the oxide matrix 24 dictates the mole fraction of the glass and the SiO.sub.2. The self-healing phase 28 can include a material having properties that are in thermodynamic equilibrium with SiO.sub.2 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 SiO.sub.2 itself, as well as any representative glass/glass ceramics such as barium alumino silicate (BAS), barium-magnesium alumino silicate (BMAS), lithium alumino silicate (LAS), strontium alumino silicate (SAS). In another exemplary embodiment, the volume fraction and viscosity of the self-healing liquid phase is shown in FIGS. 3-6. FIGS. 3a-3c show the diagram for the composition of 15 CaO, 10 AlO.sub.1.5-75 SiO.sub.2. FIGS. 4a-4c show the diagram for the composition 10 CaO, 5 AlO.sub.1.5-85 SiO.sub.2. FIGS. 5a-5c shows the diagram for the composition 2 BaO, 3 MgO, 10 AlO.sub.1.5-85 SiO.sub.2. FIG. 6 shows the diagram for the composition 7 YO.sub.1.5, 13AlO.sub.1.5-80SiO.sub.2.

(14) In an exemplary embodiment the oxidant getter phase can comprise, silicon oxycarbide, Si.sub.xO.sub.yC.sub.z where 0.5≤x<1; 0≤y<2; 0≤z<2.

(15) FIGS. 3a-3c and 4a-4c show thermodynamic calculations describing the CaO—AlO.sub.1.5—SiO.sub.2 (CAS) system. Two preferred embodiments of the self-healing matrix are considered in detail, 15 CaO, 10 AlO.sub.1.5-75 SiO.sub.2 and 10 CaO, 5 AlO.sub.1.5-85 SiO.sub.2. In an exemplary temperature range these compositions are 30-80% liquid phase. These calculations demonstrate that the volume fraction of liquid can be varied through changes of composition in the CaO—AlO.sub.1.5—SiO.sub.2 in the range 1-25% CaO, 1-25% AlO.sub.1.5, 50-99% SiO.sub.2. The viscosity of the liquid phase is generally greater than 100 Pa*s.

(16) With reference to chemical databases such as ‘Phase diagram for Ceramists’ Levin, E. M., C. R. Robbins, and H. F. McMurdie. “Phase Diagrams for Ceramists (The American Ceramic Society, Columbus, 1964). or through the use of the software FactSage™ it is understood that other alkaline earth-alumina silica systems, such as MgO—AlO.sub.1.5—SiO.sub.2, BaO—AlO.sub.1.5—SiO.sub.2, SrO—AlO.sub.1.5—SiO.sub.2 have a eutectic composition in SiO.sub.2 rich portion of the phase diagram and compositional ranges in which liquid+SiO.sub.2 are the equilibrium phases. The SiO.sub.2-liquid equilibria results in the formation of a liquid with viscosity greater than 100 Pa*s which simultaneously enables self-healing of cracks 30 without compromising mechanical integrity of the environmental barrier layer 18.

(17) Within the above specified composition range, in exemplary cases greater than 2 phases will be in thermodynamic equilibrium. For example, in the CAS system the composition 10 CaO, 10 AlO.sub.1.5-80 SiO.sub.2, liquid —SiO.sub.2 and CaAl.sub.2Si.sub.2O.sub.8 (anorthite) will be in equilibrium at temperatures greater than 1185° C. The presence of anorthite does not interfere with the effect that the SiO.sub.2-liquid equilibrium has on maintaining the viscosity of the liquid at the desired level of greater than 100 Pa*s.

(18) FIGS. 5a-5c show thermodynamic calculations in the BaO—MgO—AlO.sub.1.5—SiO.sub.2 system. A preferred embodiment of this system is 2 BaO, 3 MgO, 10 AlO.sub.1.5-85 SiO.sub.2 and is described in detail in FIGS. 5a-5c. Similar to the CAS system a liquid+SiO.sub.2 phase field exists, in this case BaAl.sub.2Si.sub.2O.sub.8 and Mg.sub.2Al.sub.4Si.sub.5O.sub.18 and possibly BaMg.sub.2Al.sub.6Si.sub.9O.sub.30 are in equilibrium. The key feature is a liquid phase that is equilibrated with SiO.sub.2 that has a viscosity of greater than 100 Pa*s.

(19) It can also be understood that other combinations of alkaline earth-alumina silicates in which the total alkaline earth (AE) concentration is between 1-25% AE, the 1-25 AlO.sub.1.5, and 50-99% SiO.sub.2 will form a similar distribution of phases.

(20) FIG. 6 shows thermodynamic calculations in the YO.sub.1.5—AlO.sub.1.5—SiO.sub.2 (YAS) system. An exemplary embodiment of this system is 7 YO.sub.1.5, 13 AlO.sub.1.5-80 SiO.sub.2 and is described in detail in FIG. 6. In the desired temperature range a Y—Al—Si—O liquid is in equilibrium with SiO.sub.2.

(21) The work of U. Kolitsch, H. J. Seifert, and F. Aldinger 1998 can be referenced for one to see that other rare earth, AlO.sub.1.5—SiO.sub.2 systems have silica rich eutectics that are in equilibrium with SiO.sub.2. For ra viscosity greater than 100 Pa*s re earths such as La, Gd, Nd, Sm, and the like.

(22) 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.

(23) The environmental barrier layer 18 can be applied by preparing a surface 20 of the substrate 14. The environmental barrier layer 18 can be applied to the substrate 12 by use of thermal spray methods, including air plasma spray, suspension plasma spray, low pressure or vacuum plasma spray, high velocity oxygen or air fuel spraying, and flame spraying, or, vapor deposition, including, atomic layer deposition, chemical vapor deposition, or electron-beam physical vapor deposition. In alternative embodiments, the environmental barrier layer 18 can be applied by slurry based methods including dip or spray coating, painting, electrophoretic deposition and the like.

(24) An advantage of utilizing the disclosed environmental barrier coating 10 is that the coating composition offers a robust composition for protecting components in the hot-section of gas turbine engines. The disclosed compositions form a multiphase matrix that consists of a liquid phase and silica at elevated temperatures. The compositions can be varied to create coatings with different properties for a desired application.

(25) There has been provided a protective 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.