The present disclosure relates to coating interfaces, and more particularly, but not exclusively, to coating interfaces on composite substrates.
Ceramic matrix composite (CMC) materials may be useful in a variety of contexts where mechanical and thermal properties are important. For example, components of high temperature mechanical systems, such as gas turbine engines, may be made from CMCs. CMCs may be resistant to high temperatures, but some CMCs may react with some elements and compounds present in the operating environment of high temperature mechanical systems, such as water vapor. These reactions may damage the CMC and reduce mechanical properties of the CMC, which may reduce the useful lifetime of the component. Thus, in some examples, a CMC component may be coated with various coatings, which may reduce exposure of the CMC component to elements and compounds present in the operating environment of high temperature mechanical systems.
In some examples, the disclosure describes techniques for improving the adhesion between a substrate and an applied coating layer by forming a plurality of microscopic grooves on the outer surface of the substrate where each respective groove includes an anchor tooth that curves outward from the outer surface of the substrate along an edge of the respective groove to at least partially enclose the groove. In some examples each respective anchor tooth may resemble an ocean wave pattern (e.g., a spilling wave or plunging wave) and may provide an interlocking pattern with the applied coating layer to at least partially mechanically adhere the coating layer to the substrate.
In some examples, the disclosure describes an article including a substrate including a ceramic or a ceramic matrix composite including silicon carbide, where the substrate defines an outer substrate surface and a plurality of grooves formed in the outer substrate surface, where each respective groove of the plurality of grooves exhibits an anchor tooth that spans an edge of the respective groove, and where the plurality of grooves define an average groove width less than about 20 micrometers. The article also includes a coating formed on the outer surface of the substrate, where the coating at least partially fills the plurality of grooves of the substrate.
In some examples, the disclosure describes a method for forming an article, the method includes forming a plurality of grooves on an outer substrate surface of a substrate, where the substrate includes a ceramic or a ceramic matrix composite comprising silicon carbide, where each respective groove of the plurality of grooves exhibits an anchor tooth that spans an edge of the respective groove, and where the plurality of grooves define an average groove width of less than about 20 micrometers.
The details of one or more examples are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.
In general, the disclosure describes techniques for forming a plurality of microscopic grooves on the outer surface of a substrate where each respective groove includes an anchor tooth that curves outward from the outer surface of the substrate along an edge of the groove to at least partially enclose the groove. In some examples the respective anchor teeth may resemble an ocean wave pattern (e.g., a spilling wave or plunging wave). The formed groove and anchor tooth structure may provide an interlocking pattern with the subsequent coating layer to at least partially mechanically adhere the subsequent coating layer to the CMC substrate.
In some examples, the plurality of grooves may be formed using laser ablation in which the respective anchor teeth are formed as a result of ablated substrate material solidifying along the edge of a respective groove. The laser ablation process may reduce the chance of the substrate cracking during processing (e.g., compared to using mechanical machining to form grooves in a surface of a CMC). Laser ablation may also result in a cleaner outer surface compared to other processing techniques (e.g., grit blasting), which may also improve the adhesion between the substrate and a subsequent coating layer. Additionally or alternatively, the laser ablation process may reduce the amount of heat applied to the outer surface of the substrate compared to mechanical machining of the surface, thereby reducing the likelihood of the underlying reinforcement material of the substrate becoming oxidized. For example, due to the microscopic size of the plurality of grooves (e.g., having a groove width of less than 20 micrometers), the amount of heat applied to the substrate during the ablation process is relatively low in comparison to alternative machining techniques (e.g., forming macroscopic topical features).
Article 10 may include any applicable structure that may benefit from the improved adhesion established by the groove and anchor tooth structure. In some examples, article 10 may be a component of a high temperature mechanical system. For example, article 10 may be a gas turbine engine component configured to operate in high temperature environments, e.g., operating at temperatures of 1900° to 2100° F. In some examples, article 10 may be a component of a gas turbine engine that is exposed to hot gases, including, for example, a seal segment, a blade track, an airfoil, a blade, a vane, a combustion chamber liner, or the like.
Substrate 12 of article 10 may be formed from various materials including, for example, a superalloy, a fiber reinforced composite, a ceramic matrix composite (CMC), a metal matrix composite, a hybrid material, combinations thereof, or the like. In some examples, substrate 12 may be a CMC substrate. In other examples, substrate 12 may include high temperature alloys based on Ni, Co, Fe, or the like.
In some examples, substrate 12 may include a ceramic or CMC material. In such examples, the ceramic or CMC material may include, for example, a silicon-containing ceramic, such as silica (SiO2), silicon carbide (SiC), silicon nitride (Si3N4), alumina (Al2O3), aluminosilicate, or the like. In some examples, the ceramic may be substantially homogeneous and may include substantially a single phase of material. In other examples, substrate 12 may include a matrix material and reinforcement material. Suitable matrix materials may include, for example, carbon, silicon carbide (SiC), silicon carbide aluminum boron silicide, silicon nitride (Si3N4), alumina (Al2O3), aluminosilicate, silica (SiO2), or the like. In some examples, the matrix material of the CMC substrate may include carbon, boron carbide, boron nitride, or resin (epoxy/polyimide). The matrix material may be combined with any suitable reinforcement materials including, for example, discontinuous whiskers, platelets, or particulates composed of SiC, Si3N4, Al2O3, aluminosilicate, SiO2, or the like. In some examples the reinforcement material may include continuous monofilament or multifilament fibers that include fibers of SiC. The reinforcement fibers may be woven or non-woven. In other examples, substrate 12 may include a metal alloy that includes silicon, such as a molybdenum-silicon alloy (e.g., MoSi2) or a niobium-silicon alloy (e.g., NbSi2).
Substrate 12 may be produced using any suitable means. For example, substrate 12 may be produced from a porous preform including reinforcement fibers. The porous preformed may be impregnated with a matrix material using e.g., resin transfer molding (RTM), chemical vapor infiltration (CVI), chemical vapor deposition (CVD), slurry infiltration, melt infiltration, or the like and/or heat treated to produce substrate 12.
Substrate 12 includes a plurality of grooves 18 formed on substrate surface 22. For example,
With the formation of each respective groove, e.g., groove 18a, two respective castoffs (e.g. 16a and 28a) are formed, one on each side of the newly formed groove 18a. In some examples, by placing adjacent grooves 18 sufficiently close together (e.g., in a rastering pattern), a castoff of a previously formed groove (e.g. castoff 28a of groove 18a) can be redefined to create an anchor tooth 16 for a respective groove of grooves 18. For example, as shown in
FIG. 2D shows a conceptual cross-sectional view of substrate 12 illustrating various parameters that may be used to characterize plurality of grooves 18 including, for example, a groove depth (D), a groove width (W), and a period between adjacent grooves (P). In some examples, plurality of grooves 18 may be configured to define a groove depth (D) of about 10 micrometers to about 30 micrometers (e.g., as measured perpendicularly from a lowest point of a groove to a highest point of a peak). In some examples, plurality of grooves 18 may be configured to define a groove width (W) of about 10 micrometers to about 20 micrometers, which, in some examples, may be defined by the width of the beam of ablation laser 26.
In some examples, plurality of grooves 18 may be configured to define a groove period (P) between adjacent grooves 18 of about 25 to about 100 micrometers (e.g., a groove period (P) of about 60 micrometers). In some examples, the selection of the groove period (P) may depend on the groove width (W). For example, narrow grooves (e.g., grooves 18 that define a groove width (W) of about 10 micrometers) may define a shorter groove period (P) to allow for the proper formation of the anchor tooth 16 for each respective groove of grooves 18. Additionally or alternatively, grooves 18 that are characterized by a larger groove width (W) (e.g., about 20 micrometers), may define a longer groove period (P) and still allow for the proper formation of each respective anchor tooth 16. In some examples, the groove depth (D), the groove width (W), and the groove period (P) may be defined as a result of the process parameters used to form plurality of grooves 18. In some examples, the groove depth (D), the groove width (W), and the groove period (P) may be non-uniform or varying in size. In other examples, plurality of grooves 18 may define a substantially uniform and repeating pattern. For example, forming grooves 18 via a laser ablation technique may allow for a high degree of control over the sizing and positioning of plurality of grooves 18, thereby establishing a substantially uniform and repeating pattern.
The laser ablation process may be performed using any suitable ablation laser 26. In some examples, ablation laser 26 may include a plurality or operating parameters including a beam frequency, a beam power, a defocus value, and a travel speed. The operating parameters of ablation laser 26 may be configured to form plurality of grooves 18 that define the selected groove depth (D), groove width (W), and groove period (P). In some examples, the operating parameters of ablation laser 26 may be configured to have a beam frequency of less than about 200 Hz, a beam power of about 15 W to about 25 W, a defocus value of about −60 to about 50, and a cutting speed (e.g., the speed in which ablation laser 26 moves across in the x-y plane of substrate surface 22) of about 10 mm/s to about 200 mm/s.
In some examples, compared to mechanical machining, the laser ablation process may significantly reduce the chance of substrate 12 becoming cracked during the formation of plurality of grooves 18 by reducing the mechanical force applied to substrate surface 22 during processing. Additionally or alternatively, in some examples, due to the relatively small amount of material removed by ablation laser 26, the amount of heat applied and/or generated on substrate surface 22 may remain relatively low during the formation of plurality of grooves 18 compared to other machining techniques. By reducing the heat applied and/or generated on substrate 12 during the laser ablation process, the chance of the material of substrate 12 (e.g. fibers) becoming oxidized prior to the application of coating 14 may be significantly reduced compared to other processing techniques.
In some examples, ablation laser 26 may be configured to form plurality of grooves 18 on substrate surface 22 even when substrate surface 22 is non-planar. For example, in some examples the underlying structure of substrate 12 (e.g., the reinforcement fibers) may cause substrate surface 22 to be uneven or non-planar (e.g., mimicking the pattern of the reinforcement fibers). In such examples, ablation laser 26 may be configured to adjust the incident angle between the ablation beam and substrate surface 22 to produce plurality of grooves 18.
In some examples, a respective anchor tooth 16 on a respective groove 18 may be discontinuous (e.g., anchor tooth 16c may not traverse the entire length of groove 18b). For example, when each groove of plurality of grooves 18 is formed, the anchor tooth produced (e.g., anchor tooth 16c) for a respective groove (e.g., groove 18b) may exhibit a non-uniform and/or a discontinuous pattern along the edge of the respective groove 18b such that the anchor tooth 16c forms a plurality of anchor teeth along the respective groove 18b instead of a single continuous anchor tooth.
In some examples, each respective anchor tooth of anchor teeth 16 may be formed from molten substrate material that is displaced during the formation of grooves 18 and solidifies along the edge of the respective groove of grooves 18. In some examples, each respective anchor tooth of anchor teeth 16 may exhibit a spilling or a plunging wave-like pattern such that each respective anchor tooth of anchor teeth 16 curves outward from substrate surface 22 (e.g., anchor teeth 16c extends out in the z-axis/normal direction and curves in the negative x-axis direction of
Each groove of the plurality of grooves 18 may be formed on substrate surface 22 such that the grooves 18 progress across the substrate surface (e.g., progress in the x-y plane of
Returning to
In some examples, coating 14 may include a bond coat that includes any useful material to improve adhesion between substrate 12 and subsequent layers applied to the bond coat. For example, the bond coat may be formulated to exhibit desired chemical or physical attraction between substrate 12 and any subsequent coating applied to the bond coat. In some examples, the bond coat may include silicon metal, alone, or mixed with at least one other constituent including, for example, at least one of a transition metal carbide, a transition metal boride, or a transition metal nitride. Representative transition metals include, for example, Cr, Mo, Nb, W, Ti, Ta, Hf, or Zr. In some examples, the bond coat may additionally or alternatively include mullite (aluminum silicate, Al6Si2O13), silica, a silicide, or the like, alone, or in any combination (including in combination with one or more of silicon metal, a transition metal carbide, a transition metal boride, or a transition metal nitride).
Additionally or alternatively, coating 14 may include an EBC, which may provide environmental protection, thermal protection, and/or CMAS-resistance to substrate 12. An EBC may include materials that are resistant to oxidation or water vapor attack, and/or provide at least one of water vapor stability, chemical stability and environmental durability to substrate 12. In some examples, the EBC may be used to protect substrate 12 against oxidation and/or corrosive attacks at high operating temperatures. For example, EBCs may be applied to protect the ceramic composites such as SiC based CMCs. An EBC coating may include at least one of a rare earth oxide, a rare earth silicate, an aluminosilicate, or an alkaline earth aluminosilicate. For example, an EBC coating may include mullite, barium strontium aluminosilicate (BSAS), barium aluminosilicate (BAS), strontium aluminosilicate (SAS), at least one rare earth oxide, at least one rare earth monosilicate (RE2SiO5, where RE is a rare earth element), at least one rare earth disilicate (RE2Si2O7, where RE is a rare earth element), or combinations thereof. The rare earth element in the at least one rare earth oxide, the at least one rare earth monosilicate, or the at least one rare earth disilicate may include at least one of Lu (lutetium), Yb (ytterbium), Tm (thulium), Er (erbium), Ho (holmium), Dy (dysprosium), Tb (terbium), Gd (gadolinium), Eu (europium), Sm (samarium), Pm (promethium), Nd (neodymium), Pr (praseodymium), Ce (cerium), La (lanthanum), Y (yttrium), or Sc (scandium). In some examples, the at least one rare earth oxide includes an oxide of at least one of Yb, Y, Gd, or Er.
In some examples, an EBC coating may include at least one rare earth oxide and alumina, at least one rare earth oxide and silica, or at least one rare earth oxide, silica, and alumina. In some examples, an EBC coating may include an additive in addition to the primary constituents of the EBC coating. For example, an EBC coating may include at least one of TiO2, Ta2O5, HfSiO4, an alkali metal oxide, or an alkali earth metal oxide. The additive may be added to the EBC coating to modify one or more desired properties of the EBC coating. For example, the additive components may increase or decrease the reaction rate of the EBC coating with CMAS, may modify the viscosity of the reaction product from the reaction of CMAS and the EBC coating, may increase adhesion of the EBC coating to substrate 12, may increase or decrease the chemical stability of the EBC coating, or the like.
In some examples, the EBC coating may be substantially free (e.g., free or nearly free) of hafnia and/or zirconia. Zirconia and hafnia may be susceptible to chemical attack by CMAS, so an EBC coating substantially free of hafnia and/or zirconia may be more resistant to CMAS attack than an EBC coating that includes zirconia and/or hafnia.
In some examples, the EBC coating may have a dense microstructure, a columnar microstructure, or a combination of dense and columnar microstructures. A dense microstructure may be more effective in preventing the infiltration of CMAS and other environmental contaminants, while a columnar microstructure may be more strain tolerant during thermal cycling. A combination of dense and columnar microstructures may be more effective in preventing the infiltration of CMAS or other environmental contaminants than a fully columnar microstructure while being more strain tolerant during thermal cycling than a fully dense microstructure. In some examples, an EBC coating with a dense microstructure may have a porosity of less than about 20 vol. %, such as less than about 15 vol. %, less than 10 vol. %, or less than about 5 vol. %, where porosity is measured as a percentage of pore volume divided by total volume of the EBC coating.
In some examples, the EBC may act as a thermal barrier coating (TBC). The TBC may include at least one of a variety of materials having a relatively low thermal conductivity, and may be formed as a porous or a columnar structure in order to further reduce thermal conductivity of the TBC and provide thermal insulation to substrate 12. In some examples, the TBC may include materials such as ceramic, metal, glass, pre-ceramic polymer, or the like. In some examples, the TBC may include silicon carbide, silicon nitride, boron carbide, aluminum oxide, cordierite, molybdenum disilicide, titanium carbide, stabilized zirconia, stabilized hafnia, or the like.
Additionally or alternatively, the coating 14 may include an abradable layer. The abradable layer may include at least one of a rare earth oxide, a rare earth silicate, an aluminosilicate, or an alkaline earth aluminosilicate. For example, an EBC coating may include mullite, barium strontium aluminosilicate (BSAS), barium aluminosilicate (BAS), strontium aluminosilicate (SAS), at least one rare earth oxide, at least one rare earth monosilicate (RE2SiO5, where RE is a rare earth element), at least one rare earth disilicate (RE2Si2O7, where RE is a rare earth element), or combinations thereof. The rare earth element in the at least one rare earth oxide, the at least one rare earth monosilicate, or the at least one rare earth disilicate may include at least one of Lu (lutetium), Yb (ytterbium), Tm (thulium), Er (erbium), Ho (holmium), Dy (dysprosium), Tb (terbium), Gd (gadolinium), Eu (europium), Sm (samarium), Pm (promethium), Nd (neodymium), Pr (praseodymium), Ce (cerium), La (lanthanum), Y (yttrium), or Sc (scandium). In some examples, the at least one rare earth oxide includes an oxide of at least one of Yb, Y, Gd, or Er.
The abradable layer may be porous. Porosity of the abradable layer may reduce a thermal conductivity of the abradable layer and/or may affect the abradability of the abradable layer. In some examples, the abradable layer includes porosity between about 10 vol. % and about 50 vol. %. In other examples, the abradable layer includes porosity between about 15 vol. % and about 35 vol. %, or about 20 vol. %. Porosity of the abradable layer is defined herein as a volume of pores or cracks in the abradable layer divided by a total volume of the abradable layer (including both the volume of material in the abradable layer and the volume of pores/cracks in the abradable layer).
The abradable layer may be formed using, for example, a thermal spraying technique, such as, for example, plasma spraying. Porosity of the abradable layer may be controlled by the use of coating material additives and/or processing techniques to create the desired porosity. In some examples, substantially closed pores may be desired.
For example, a coating material additive that melts or burns at the use temperatures of the component (e.g., a blade track) may be incorporated into the coating material that forms the abradable layer. The coating material additive may include, for example, graphite, hexagonal boron nitride, or a polymer such as a polyester, and may be incorporated into the coating material prior to deposition of the coating material over outer surface layer 17 to form the abradable layer. The coating material additive then may be melted or burned off in a subsequent heat treatment, or during operation of the gas turbine engine, to form pores in the abradable layer. The post-deposition heat-treatment may be performed at up to about 1500° C.
The porosity of the abradable layer can also be created and/or controlled by plasma spraying the coating material using a co-spray process technique in which the coating material and coating material additive are fed into the plasma stream with two radial powder feed injection ports. The feed pressures and flow rates of the coating material and coating material additive may be adjusted to inject the material on the outer edge of the plasma plume using direct 90 degree angle injection. This may permit the coating material particles to soften but not completely melt and the coating material additive to not burn off but rather soften sufficiently for adherence in the abradable layer.
The groove and anchor tooth structure of substrate 12 may be formed using any suitable technique. For example,
The technique of
The technique of
The technique of
Substrate 70 was subsequently coated with a two layer system of silicon and ytterbium disilicate. Substrate 70 demonstrated improved adhesion at the substrate/coating interface evidenced by coating splat formations being tightly bonded to the substrate anchor tooth pattern with no sign of coating separation.
Substrate 90 was subsequently coated with a two layer system of silicon and ytterbium disilicate. Substrate 90 demonstrated improved adhesion at full coating thickness with no separation. The normal residual coating stress was negated by the surface topography which allows mechanical cementation of the coating particles.
Various examples have been described. These and other examples are within the scope of the following claims.
This application claims the benefit of U.S. Provisional Application No. 62/248,635 filed Oct. 30, 2015, which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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62248635 | Oct 2015 | US |