Patent Application
20160215631
This invention relates to articles comprising an environmental barrier coating (EBC), for example, high-temperature machine components. More particularly, this invention relates to coating systems and articles comprising the same for protecting machine components from exposure to high-temperature environments. This invention also relates to methods for making and protecting articles.
High-temperature materials, such as, for example, ceramics, alloys, and intermetallics, offer attractive properties for use in structures designed for service at high temperatures in such applications as gas turbine engines, heat exchangers, and internal combustion engines, for example. However, the environments characteristic of these applications often contain reactive species, such as water vapor, which at high temperatures may cause significant degradation of the material structure. For example, water vapor has been shown to cause significant surface recession and mass loss in silicon-bearing materials. The water vapor reacts with the structural material at high temperatures to form volatile silicon-containing species, often resulting in unacceptably high recession rates.
Environmental barrier coatings (EBC's) are applied to silicon-bearing materials and other material susceptible to attack by reactive species, such as high temperature water vapor. EBC's provide protection by prohibiting contact between the environment and the surface of the material. EBC's applied to silicon-bearing materials, for example, are designed to be relatively stable chemically in high-temperature, water vapor-containing environments. One exemplary conventional EBC system, as described in U.S. Pat. No. 6,410,148, comprises a silicon or silica bond layer applied to a silicon-bearing substrate; an intermediate layer comprising mullite or a mullite-alkaline earth aluminosilicate mixture deposited over the bond layer; and a top layer comprising an alkaline earth aluminosilicate deposited over the intermediate layer. In another example, U.S. Pat. No. 6,296,941, the top layer is a yttrium silicate layer rather than an alumino silicate. U.S. Pat. No. 6,299,988 and U.S. Publication No. 2011/0052925 also describe EBC's.
The above coating systems can provide suitable protection for articles in demanding environments, but opportunities for improvement in coating performance exist. Implementation of different materials in EBC's offers an opportunity for use in an expanded array of applications and environments, yet use of different materials can also result in new technical problems that can detrimentally impact the integrity of an EBC and/or the article comprising the EBC.
Therefore, there is a need for articles protected by improved coating systems that offer utility in expanded applications, without sacrificing the integrity of the EBC and/or the article. There is also a further need for methods to produce these articles economically and reproducibly.
In one aspect, the invention provides an article comprising a substrate, a substantially hermetic sealing layer disposed on the substrate, and a porous transition layer disposed on the substrate between the sealing layer and the substrate, wherein the article comprises one or more openings extending through the substrate to the porous transition layer.
In a second aspect, the invention provides a method for making an article. The method includes: disposing a bondcoat over a substrate, disposing a porous transition layer over the bondcoat, disposing a sealing layer over the porous transition layer, wherein the sealing layer comprises a rare earth silicate or an alkaline-earth aluminosilicate, and forming one or more openings, the openings extending through the substrate and bondcoat to the porous transition layer. In embodiments that do not include a bondcoat, the method does not comprise disposing a bondcoat over the substrate.
In some embodiments, the method further comprises: disposing an intermediate layer over the porous transition layer, the intermediate layer comprising a barrier material that is substantially inert with respect to silica; and optionally disposing a topcoat over the sealing layer.
These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings, wherein:
As used herein, the substantially hermetic sealing layer, which may be referred to herein as a “sealing layer,” refers to a layer/coating, or multiple layers/coatings, that can prevent gases in the environment from accessing the substrate from the coated side. The term “substantially hermetic” as used herein means that the coating has a gas permeability that is below about 2×10−14 cm2 (about 2×10−6 Darcy), the detection limit of commonly used measurement techniques. In some non-limiting embodiments, the sealing layer comprises material (“sealing material”) capable of forming a flowable phase, such as a liquid or a glassy phase, at or above a known temperature (“sealing temperature”) that is below a melting temperature of the bulk of the coating. This liquid or glassy phase has a viscosity at the sealing temperature suitable to allow the flowable phase to flow into and at least partially fill defects such as cracks and pores, thereby enhancing the ability of the coating to block the movement of detrimental species from the external environment into the substrate. Examples of non-limiting sealing layers that may be used in the present invention are described, for example, in U.S. Publication No. 2011/0052925.
In some embodiments, a bondcoat 204 is disposed over substrate 202, between the sealing layer 210 and the substrate 202. Bondcoat 204 may be used, for example, to mitigate thermal stresses or to inhibit chemical reactions between, e.g., substrate 202 and sealing layer 210. In some embodiments, bondcoat 204 is a nonoxide layer that serves as an oxygen getter that inhibits and/or prevents oxidation of the substrate.
In some embodiments, such as, for example, where substrate 202 is a silicon-bearing material, the bondcoat 204 may comprise silicon. For example, bondcoat 204, in some embodiments, comprises elemental silicon or a silicide. In some embodiments, bondcoat 204 comprises silicon carbide and/or silicon nitride. In some embodiments, bond coat 204 comprises a carbide, nitride, and/or silicide.
In various applications, articles (e.g., articles comprising environmental barrier coatings (EBCs)) for substrates (e.g., silicon carbide-based ceramic matrix composites) employ silicon as the bondcoat (i.e., a silicon bond coat). However, this can limit the temperature application of, e.g., an EBC/CMC system to below the melting point of silicon. Accordingly, in some embodiments, the bondcoat comprises a material that is more refractory than silicon. Such embodiments offer utility in that they allow articles (e.g., turbines that use ceramic matrix composites (CMCs) on, e.g., hot-section parts), to benefit from a higher firing temperature.
Many potential options for a refractory bondcoat generate a gaseous reaction product upon oxidation. For example, carbides oxidize to release carbon monoxide or carbon dioxide, nitrides oxidize to release nitrogen gas, and some silicides oxidize to release metal oxides that may, in some cases, be in a gaseous state. These gaseous reaction products cause spallation in traditional EBC's because they include a hermetic layer and therefore do not permit permeation of these gaseous products. As a result, gas bubbles build up underneath the hermetic layer(s), which, overtime, lead to spallation of the EBC. Thus, while expanded, non-silicon bond coats offer advantages such as expanded temperature applications, they can also introduce new problems, such as potential article spallation due to gas bubbles caused by gaseous reactant products, thereby necessitating new EBC/CMC design.
The present invention addresses, inter alia, the problem of spallation due to bubbles caused by gaseous reactant products via the inclusion of porous transition layer 208, which is disposed on substrate 202 between the sealing layer 210 and the substrate 202, and by inclusion of one or more openings 212 extending through the substrate 202 to the porous transition layer 208. As shown in the embodiment depicted in
The porosity of porous transition layer 208 allows for redistribution of gaseous reaction product. The porous transition layer comprises an oxide or non-oxide ceramic or a combination thereof, which is thermally and chemically compatible with the substrate and the sealing layer. For example, in the case that the substrate is composed of silicon carbide based CMC, and the component within the sealing layer right next to the porous layer is composed of rare earth silicate, the porous layer in some embodiment can be a rare earth silicate. In another embodiment it can be silicon carbide. Persons having ordinary skill in the art will readily recognize that the desired porosity of the porous transition layer may change depending on the intended application of the inventive article, and the on the nature of the other materials used in the article (e.g., on the nature of the bond coat, where present). While the porous transition layer may have any porosity that effectuates the intended purpose of the layer, in some embodiments, the porous transition layer has a porosity of 10 to 90% (e.g., 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 90%), including any and all ranges and subranges therein (e.g., 15-85%, 12-75%, etc.), preferably 20˜50%. In some embodiments, the porous transition layer will have a specified, and optionally pre-determined average pore diameter, which again, may vary depending on application and nature of the inventive article. In some embodiments, the porous transition layer has an average pore diameter of 0.1 to 100 μm (e.g., 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 μm), including any and all ranges and subranges therein (e.g., 0.1 to 20 μm, 0.1 to 15 μm, etc.).
The chemical composition and physical features of the porous layer described as above are subject to change during the service of the article, and thereby may drift out of the ranges specified above. For example, sintering and coarsening may occur which lead to reduced porosity and increased pore diameter. In the case that silicon carbide is used to form the porous layer, oxidation will turn this layer into a silica based layer partially or entirely. The material that is used to make the porous layer can be applied in its pure form, or in mixture with a second phase or as an alloy with a minor dopant, to enhance the property of the layer according to specific application requirements.
Article 200 includes openings 212, which extend through the substrate 202 to the porous transition layer 208. The openings 212 serve as escape holes for gaseous species, which are first redistributed through porous transition layer 208. The openings 212 may be created in any desired or art/acceptable fashion. For example, in some embodiments, the openings 212 are created by drilling through the layer(s) preceding the porous transition layer 208 (e.g., drilling through substrate 202 and bond coat 204). In some embodiments, the openings 212 extend into the porous transition layer 208. The one or more openings 212 may have equivalent or differing diameters, and diameters may be selected depending on the nature and application of the article. In some embodiments, the one or more openings have an average diameter of 1 to 1000 μm (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 μm), including any and all ranges and subranges therein (e.g., 1-20 μm, 2 to 40 μm, etc.). While reference is made above to an average diameter, the cross section of the opening can be of any shape, including but not limited to circular, oval, square, rectangular, triangular, or any other regular or irregular geometry. The spacing between the openings can be periodical or random, and can range from 10 μm to 100 mm, depending on the application requirements. Longitudinally the openings can be straight or tortuous through the substrate and the coating layers.
Upon, for example, oxidation of the bond coat, gaseous product is conducted through the porous transition layer 208 to the openings 212, from which the gaseous product escapes.
In some embodiments, an intermediate layer (not shown) may be disposed between sealing layer 210 and bond coat 204 (e.g., between the sealing layer 210 and the porous transition layer 208, or between the porous transition layer 208 and the bondcoat 204). In some embodiments, the bond coat 204 comprises silicon or silicon oxide, and the intermediate layer comprises a barrier material that is substantially inert with respect to silicon oxide to promote chemical stability in the coating system. “Substantially inert” means that there is at most only incidental interaction (solubility or reactivity) between silica and the barrier material. Rare-earth disilicates, such as disilicates of yttrium, ytterbium, lutetium, scandium, and other rare-earth elements, are non-limiting examples of suitable barrier materials.
As shown in
The thickness of any of the various coating layers described above is generally chosen to provide adequate protection for a given service time while keeping thermal stresses to a sustainable level. Moreover, coating thickness may also be determined by the ability of a selected coating method to produce a continuous layer over the deposition area. Non-limiting examples of approximate thickness ranges for the various coatings include the following: for the sealing layer, from about 25 micrometers to about 1000 micrometers; for the porous transition layer, from about 25 micrometers to about 1000 micrometers; for the bondcoat, from about 25 micrometers to about 200 micrometers; for the intermediate layer, from about 50 micrometers to about 100 micrometers; for the topcoat layer, from about 50 micrometers to about 500 micrometers. For the dual-layer topcoat embodiment described above, the yttrium monosilcate outer layer can be from about 25 micrometers to about 50 micrometers in certain embodiments.
The coatings described above can be deposited using coating technology that may result in a substantial amount of cracking and internal open porosity. Plasma spray technology and slurry-based coating processes are examples of coating methods that generate coatings with such features. In such cases, the presence of the sealing layer serves to considerably enhance the hermeticity, and thus the efficacy of protection, of the coating. Moreover, in some embodiments the sealing layer may be effective in sealing cracks or other damage to the coating that may occur after processing, including for instance damage created during installation of components, or service of components.
In order to activate the optional self-sealing nature of the sealing layer, the sealing layer may be heated to the sealing temperature (described above) at which at least a portion of the sealing layer will flow; the flowable portion thus moves into cracks and pores and, upon solidification, seals off these defects that would otherwise serve as pathways for detrimental species, such as water vapor, from the environment to the substrate. Depending upon the nature of the coating, the economics of the processing, and other factors, the heating step may be performed immediately after depositing the sealing layer, after all coatings have been deposited but prior to putting the finished article into service, or even during service itself if the service temperature is allowed to be sufficiently high.
The sealing temperature is maintained for an effective time to allow time for the flowable material to reach and at least partially fill or otherwise seal off the defects. The length of time needed to achieve this is generally selected based on the number and nature of the defects to be sealed and the quantity of flowable material available in the sealing layer. In one embodiment, the sealing layer is heated to a sealing temperature in a range from about 950 degrees Celsius to about 1350 degrees Celsius for a time in the range from about 30 minutes to about 10 hours; in particular embodiments the time is in the range from about 30 minutes to about 4 hours. In some embodiments, the temperature is in the range from about 950 degrees Celsius to about 1050 degrees Celsius for a time in the range from about 30 minutes to about 4 hours, while in other embodiments the temperature is from about 1250 degrees Celsius to about 1350 degrees Celsius for a time in the range from about 30 minutes to about 4 hours. The heating step to seal the coating may be performed in air, vacuum, an inert atmosphere, or other environment, depending at least in part on the requirements of the materials being heated (i.e., the substrate and other coating layers, if present).
The method that is applied to deposit the porous layer is selected to fulfill the geometric requirements as described above. In some embodiments, the layer is applied by thermal spray with parameters selected to target a specific porosity, such as controlling the spray gun energy, standoff distance, and particle size of the powder feed. In other embodiments, a sacrificial phase is added to the powder feed to enhance the porosity. For example, organic particles such as but not limited to polystyrene particles, are added to the powder feed during the coating process, which can be burned off during subsequent steps and leave behind pores in the coating. In another example, a dissolvable salt is added and subsequently dissolved away to generate the pores. In yet another example, glass particles are added to the powder feed, after applying the layer, the glass phase is leached away by soaking the part in a hydrofluoric acid solution to leave behind a porous structure. In yet another example, a glass layer is deposited and then a subsequent heat-treatments is applied to lead to partial crystallization or phase separation of the glass, subsequently the coating is soaked in an acid solution to leach out one phase and leave behind a porous structure.
Similar technology can be applied in slurry coating, wherein either controlling parameters to facilitate partial sintering, or otherwise employment of a sacrificial phase can be used to achieve a structure that contain appropriate porosity. Partial sintering can be realized by solid phase or liquid sintering of coarse particle compact at lower temperatures, or use a bonding agent to facilitate necking with minimal volume shrinkage, or sintering of a multimodal powder mixture. Sacrificial phases, as stated above, can be an organic or carbonaceous phase, or a dissolvable salt or a glass phase that can be etched away. In general, any technologies known by those skilled in the art of making porous ceramics can be applied in this invention.
All publications and patent references cited in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fully set forth.
Subject matter incorporated by reference is not considered to be an alternative to any claim limitations, unless otherwise explicitly indicated.
Where one or more ranges are referred to throughout this specification, each range is intended to be a shorthand format for presenting information, where the range is understood to encompass each discrete point within the range as if the same were fully set forth herein.
It is to be understood that the above description is intended to be illustrative, and not restrictive. For example, the above-described embodiments (and/or aspects thereof) may be used in combination with each other. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the various embodiments without departing from their scope. While the dimensions and types of materials described herein are intended to define the parameters of the various embodiments, they are by no means limiting and are merely exemplary. Many other embodiments will be apparent to those of skill in the art upon reviewing the above description. The scope of the various embodiments should, therefore, be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled. In the appended claims, the terms “including” and “in which” are used as the plain-English equivalents of the respective terms “comprising” and “wherein.” Moreover, in the following claims, the terms “first,” “second,” and “third,” etc. are used merely as labels, and are not intended to impose numerical requirements on their objects. Further, the limitations of the following claims are not written in means-plus-function format and are not intended to be interpreted based on 35 U.S.C. §112, sixth paragraph, unless and until such claim limitations expressly use the phrase “means for” followed by a statement of function void of further structure. It is to be understood that not necessarily all such objects or advantages described above may be achieved in accordance with any particular embodiment. Thus, for example, those skilled in the art will recognize that the systems and techniques described herein may be embodied or carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other objects or advantages as may be taught or suggested herein.
While the invention has been described in detail in connection with only a limited number of embodiments, it should be readily understood that the invention is not limited to such disclosed embodiments. Rather, the invention can be modified to incorporate any number of variations, alterations, substitutions or equivalent arrangements not heretofore described, but which are commensurate with the spirit and scope of the invention. Additionally, while various embodiments of the invention have been described, it is to be understood that aspects of the disclosure may include only some of the described embodiments. Accordingly, the invention is not to be seen as limited by the foregoing description, but is only limited by the scope of the appended claims.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal language of the claims.
