The present invention is directed to a process for forming a diffusion coating on a substrate. More particularly, the present invention is directed to a process for forming a diffusion coating on a substrate utilizing a covering composition to enclose a slurry against the substrate during formation of the diffusion coating.
Gas turbines include components, such as buckets (blades), nozzles (vanes), combustors, shrouds, and other hot gas path components which are coated to protect the components from the extreme temperatures, chemical environments and physical conditions found within the gas turbines. Certain coating systems, such as diffusion coatings, may be formed by applying a layer of coating precursor material to the area of a substrate to be coated, and subjecting the coating precursor material and the substrate to conditions suitable for forming the coating system.
The formation of coating systems may be incomplete or inefficient, however, due the interaction of the coating precursor material with the external environment in addition or in lieu of the interaction of the coating precursor material with the desired substrate. In one example, formation of a diffusion coating may be inhibited or incomplete due to the release of coating-forming gas or vapor from the coating precursor material to the exterior environment without the gas or vapor contacting the substrate surface to be coated. Further, such incomplete or inhibited coating may be exacerbated when the surface to be coated includes narrow channels, cracks in the substrate surface, or other reduced-access areas.
In an exemplary embodiment, a process for forming a diffusion coating on a substrate includes preparing a slurry including a donor metal powder, an activator powder, and a binder, and applying the slurry to the substrate. The slurry is dried on the substrate, forming a slurry layer on the substrate. A covering composition is applied over the slurry layer, and the covering composition is dried, forming at least one covering layer enclosing the slurry layer against the substrate. The slurry layer and the at least one covering layer are heated to form the diffusion coating on the substrate, the diffusion coating including an additive layer and an interdiffusion zone disposed between the substrate and the additive layer.
Other features and advantages of the present invention will be apparent from the following more detailed description of the preferred embodiment, taken in conjunction with the accompanying drawings, which illustrate, by way of example, the principles of the invention.
Wherever possible, the same reference numbers will be used throughout the drawings to represent the same parts.
Provided are processes for forming diffusion coatings on substrates. Embodiments of the present disclosure, in comparison to processes not utilizing one or more features disclosed herein, decrease costs, increase process efficiency, increase operating lifetime, increase coating uniformity, increase crack coating penetration, add diffusion coating around cracks to prevent crack propagation, ensure a uniform coating, or a combination thereof.
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In one embodiment, the at least one covering layer 400 partially covers the slurry layer 200. In another embodiment, the at least one covering layer 400 fully covers the slurry layer 200. In yet another embodiment, the at least one covering layer 400 and the substrate 100 enclose the slurry layer 200. In a further embodiment, the at least one covering layer 400 and the substrate 100 hermetically enclose the slurry layer 200.
Applying the at least one covering layer 400 over the slurry layer 200 may increase the uniformity of the diffusion coating 500 relative to a comparable process lacking the at least one covering layer 400. In one embodiment, the diffusion coating 500 has heightened uniformity. As used herein, “heightened uniformity” indicates that the diffusion coating 500 covers the substrate 100 without break throughout the area which was covered by the at least one covering layer 400, and the thickness of the diffusion coating 500 (including both the additive layer 502 and the interdiffusion zone 504) does not vary across the diffusion coating 500 by more than about 50% of the greatest thickness of the diffusion coating 500. In another embodiment, the diffusion coating 500 is substantially uniform. As used herein, “substantially uniform” indicates that the diffusion coating 500 covers the substrate 100 without break throughout the area which was covered by the at least one covering layer 400, and the thickness of the diffusion coating 500 (including both the additive layer 502 and the interdiffusion zone 504) does not vary across the diffusion coating 500 by more than about 25% of the greatest thickness of the diffusion coating 500. In yet another embodiment, the diffusion coating 500 is essentially uniform. As used herein, “essentially uniform” indicates that the diffusion coating 500 covers the substrate 100 without break throughout the area which was covered by the at least one covering layer 400, and the thickness of the diffusion coating 500 (including both the additive layer 502 and the interdiffusion zone 504) does not vary across the diffusion coating 500 by more than about 10% of the greatest thickness of the diffusion coating 500. In another embodiment, the diffusion coating 500 is uniform. As used herein, “uniform” indicates that the diffusion coating 500 covers the substrate 100 without break throughout the area which was covered by the at least one covering layer 400, and the thickness of the diffusion coating 500 (including both the additive layer 502 and the interdiffusion zone 504) does not vary across the diffusion coating 500 by more than about 5% of the greatest thickness of the diffusion coating 500.
The covering composition 300 may include any suitable additives, including, but not limited to, polymer adhesives, ceramic powders, viscosity thinning agents, or a combination thereof. In one embodiment, the covering composition 300 includes at least one polymer adhesive and at least one ceramic powder. Suitable viscosity thinning agents include, but are not limited to, NH4Cl, NH4F, NH4Br, and combinations thereof.
Applying the slurry 102 may include any suitable technique, including, but not limited to, spraying, dipping, painting, brushing, and combinations thereof. Applying the covering composition 300 may include any suitable technique, including, but not limited to spraying, painting, brushing, dipping, and combinations thereof.
The substrate 100 may include any suitable material composition, including, but not limited to, an iron-based superalloy, a nickel-based superalloy, a cobalt-based superalloy, or a combination thereof. The slurry 102 may be applied directly to the substrate 100. In another embodiment, the substrate 100 includes a bond coat. The slurry 102 may be applied directly to the bond coat. The bond coat may be any suitable material, including, but not limited to a MCrAlY, an aluminide diffusion coating, a chromide diffusion coating, or a combination thereof.
In one embodiment, heating the slurry layer 200 and the at least one covering layer 400 to form the diffusion coating 500 includes heating the slurry layer 200 and the at least one covering layer 400 to a temperature within a range of about 550° C. to about 1250° C., alternatively within a range of about 750° C. to about 1200° C., alternatively within a range of about 815° C. to about 1150° C. Heating the slurry layer 200 and the at least one covering layer 400 to form the diffusion coating 500 may include any heating duration, including, but not limited to, a duration of from about 0.5 hours to about 12 hours, alternatively about 2 hours to about 8 hours, alternatively about 4 hours to about 6 hours, alternatively less than about 8 hours, alternatively less than about 6 hours.
Forming the diffusion coating 500 having the additive layer 502 and the interdiffusion zone 504 may include forming the diffusion coating 500 as an additive coating which adds a metal onto the substrate 100, the added metal forming the additive layer 502 as well as interdiffusing with the substrate 100 to form the interdiffusion zone 504 between the substrate 100 and the additive layer 502.
In one embodiment, the process for forming the diffusion coating 500 on the substrate 100 further includes a pre-coating cleaning prior to applying the slurry 102. In another embodiment, the process for forming the diffusion coating 500 includes a post-coating cleaning while removing the at least one covering layer 400 from the diffusion coating 500 or after removing the at least one covering layer 400 from the diffusion coating 500. The post-coating cleaning may include any suitable technique, and may remove the at least one covering layer 400, residues of the at least one covering layer 400 remaining following the heating of the at least one covering layer 400 and the slurry layer 200, the covering composition 300, the slurry layer 200, the slurry 102, impurities, or a combination thereof. The suitable technique for cleaning may include, but is not limited to, ultrasonic cleaning in a solvent bath (e.g., water and a suitable reagent), water flushing, grit blasting, or a combination thereof.
The substrate may be any suitable substrate, including, but not limited to turbine components. Suitable turbine components include, but are not limited to buckets (blades), nozzles (vanes), shrouds, diaphragms, combustors, hot gas path components, or combinations thereof.
In one embodiment, the slurry 102 is an aluminizing slurry, and the donor metal powder includes a metallic aluminum alloy having a melting temperature higher than aluminum (melting point of about 660° C.), the binder includes at least one organic polymer gel, and the diffusion coating 500 formed is an aluminide diffusion coating including an aluminide additive layer as the additive layer 502 and an aluminide interdiffusion zone as the interdiffusion zone 504. The aluminizing slurry may include any suitable composition, including, but not limited to, a composition having, by weight, about 35% to about 65% of the donor metal powder, about 1% to about 50% of the activator powder, and about 25% to about 60% of the binder.
In one embodiment, the donor metal powder of the aluminizing slurry form of the slurry 102 includes metallic aluminum alloyed with chromium, iron, another aluminum alloying agent, or a combination thereof, provided that the alloying agent does not deposit during the diffusion aluminizing process, but instead serves as an inert carrier for the aluminum of the donor material. In a further embodiment, the donor metal powder includes a chromium-aluminum alloy such as, but not limited to, by weight, about 10% to about 60% aluminum, balance chromium and incidental impurities. In another embodiment, the donor metal powder has a particle size of up to 100 mesh (149 μm), alternatively up to −200 mesh (74 μm). Without being bound by theory, it is believed that the donor metal powder being a fine powder reduces the likelihood that the donor metal powder will be lodged or entrapped within the substrate 100.
The activator powder of the aluminizing slurry form of the slurry 102 may include any suitable material, including, but not limited to, ammonium chloride, ammonium fluoride, ammonium bromide, another halide activator or combinations thereof. Suitable materials for the activator powder react with aluminum in the donor metal powder to form a volatile aluminum halide, such as, but not limited to, AlCl3 or AlF3, which reacts at the substrate 100 to deposit aluminum, which diffuses into the substrate 100.
The at least one organic polymer gel of the binder of the aluminizing slurry form of the slurry 102 may include, but is not limited to, a polymeric gel available under the name Vitta Braz-Binder Gel from the Vitta Corporation, and low molecular weight polyols such as polyvinyl alcohol. In one embodiment, the binder further includes a cure catalyst, an accelerant, or both, such as, but not limited to, sodium hypophosphite.
In one embodiment, the aluminizing slurry 102 form of the slurry 102 is free of inert fillers and inorganic binders. The absence of inert fillers and inorganic binders prevents such materials from sintering and becoming entrapped in the substrate 100.
The aluminizing slurry form of the slurry 102 may further include, by weight, about 1% to about 30% ceramic powder, about 1% to about 10% oxide removal agent, or a combination thereof. The ceramic powder may include any suitable material, including, but not limited to, aluminum oxide, chromium oxide, yttrium oxide, zirconium oxide, or a combination thereof. The oxide removal agent may include any suitable material, including, but not limited to, an acid such as acetic acid, hydrochloric acid, acids having acidities between acetic acid and hydrochloric acid, inclusive, or a combination thereof.
In one embodiment, the slurry 102 is a chromizing slurry, and the donor metal powder includes chromium. The chromizing slurry form of the slurry 102 further includes an inorganic salt having a melting point that is less than or equal to about 800° C., and the diffusion coating 500 formed is a chromide diffusion coating including a chromide additive layer as the additive layer 502 and a chromide interdiffusion zone as the interdiffusion zone 504. The chromizing slurry may include any suitable composition, including, but not limited to, a composition having, by weight, about 1% to about 60% of the donor metal powder, about 1% to about 70% of the inorganic salt, about 1% to about 30% of the activator powder, and at least about 1% of the binder.
In one embodiment, the chromizing slurry form of the slurry 102 includes a donor metal powder, an inorganic salt having a melting point that is less than or equal to about 800° C., an activator, and a binder, wherein the donor metal powder includes chromium. The donor metal powder may include chromium in the form for chromium powder, and may further include an aluminum powder. In one embodiment, the chromium powder includes an additive such as aluminum, cobalt, nickel, silicon, or mixtures thereof. The chromizing slurry form of the slurry 102 includes donor metal powder particles having any suitable size, including, but not limited to, particles having a mean diameter of about 1 to about 10 microns (i.e., micrometers (μm)) as measured using a conventional particle size analyzer.
The activator of the chromizing slurry form of the slurry 102 may be any suitable activator, including, but not limited to, ammonium halides, chromium halides, aluminum halides, and mixtures thereof. In one embodiment, the activator is NH4Cl, NH4F, NH4Br, CrCl2, CrCl3, AlCl3, or a combination thereof.
The binder of the chromizing slurry form of the slurry 102 may be any suitable binder which promotes cohesiveness of the chromizing slurry form of the slurry 102 and which decomposes when exposed to a predetermined temperature.
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While the invention has been described with reference to a preferred embodiment, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the appended claims.