The present invention is directed to a process of forming or refurbishing an aluminum diffusion coating. More particularly, the present invention is directed to a process for forming or refurbishing an aluminide coating by (1) selective removal of the diffusion coating and (2) minimizing the base metal removal.
Higher operating temperatures for gas turbines are continuously sought in order to increase their efficiency. However, as operating temperatures increase, the high temperature durability of the components of the turbine must correspondingly increase. Significant advances in high-temperature capabilities have been achieved through the formulation of nickel and cobalt-based superalloys, though without a protective coating components formed from superalloys typically cannot withstand long service exposures if located in certain sections of a gas turbine, such as the turbine or combustor. One such type of coating is referred to as an environmental coating, i.e., a coating that is resistant to oxidation and hot corrosion. Environmental coatings that have found wide use include diffusion aluminide coatings formed by diffusion processes, such as a pack cementation, vapor phase processes and slurry processes.
Though significant advances have been made with environmental coating materials and processes for forming such coatings, there is the inevitable requirement to repair these coatings under certain circumstances. For example, removal may be necessitated by erosion or thermal degradation of the diffusion coating, refurbishment of the component on which the coating is formed, or an in-process repair of the diffusion coating or a thermal barrier coating (if present) adhered to the component by the diffusion coating. Known repair processes completely remove the diffusion aluminide coating by treatment with an acidic solution capable of interacting with and removing both the additive and diffusion coatings.
Removal of the entire aluminide coating, which includes the diffusion zone, results in the removal of a portion of the substrate surface. For gas turbine engine blade and vane airfoils, removing the diffusion zone can cause alloy depletion of the substrate surface and, for air-cooled components, excessively thinned walls and drastically altered airflow characteristics to the extent that the component must be scrapped. Therefore, rejuvenation processes have been developed for situations in which a diffusion aluminide coating must be refurbished in its entirety, but removal of the coating is not desired or allowed because of the effect on component life. Known rejuvenation processes, as shown in
From the above, it can be appreciated that improved methods for refurbishing a diffusion aluminide coating are desired. A method that can refurbish a coated article by forming diffusion aluminide coatings on metallic substrates that does not suffer from one or more of the above drawbacks would be desirable in the art.
In one embodiment, a method for selective aluminide diffusion coating removal. The method includes diffusing aluminum into a substrate surface of a component to form a diffusion coating. The diffusion coating includes an aluminum-infused additive layer and an interdiffusion zone. The diffusion coating is solution heat treated at a temperature and for a time sufficient to dissolve at least a portion of the interdiffusion zone. Thereafter the aluminum-infused additive layer is selectively removed.
In another embodiment, a method for aluminide diffusion coating removal from a substrate of a gas turbine component. The method includes removing the component from a gas turbine after operation of the gas turbine. The component includes a diffusion coating having an aluminum-infused additive layer and an interdiffusion zone. The diffusion coating is solution heat treated at a temperature and for a time sufficient to dissolve at least a portion of the interdiffusion zone. Thereafter the aluminum-infused additive layer is selectively removed.
In another embodiment, an aluminide diffusion coated turbine component. The aluminide diffusion coated turbine component includes a substrate including a nickel-based or cobalt-based superalloy. The coated turbine component having an aluminide diffusion coating on a surface of the substrate. The aluminide diffusion coating has a dissolved interdiffusion zone. The dissolved interdiffusion zone is resistant to removal.
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 is a process for forming or refurbishing a diffusion aluminide coating with selective removal of the diffusion coating. Embodiments of the present disclosure, in comparison to similar concepts failing to include one or more of the features disclosed herein, minimize base materials loss and permit retention of wall thickness in components, permit easy processing with available methods, such as light grit blasting or short term acid dips, reduce the risk of chemical corrosive attacks to metallic substrates (e.g., intergranular attack (IGA) or pitting or alloy depletion), reduce the risk of component dimensional distortion, reduce scrap rate and facilitate subsequent processing, such as welding, brazing and re-coating repair.
As shown in
In one embodiment, the component including the aluminum-infused additive layer 107 is subjected to conditions, such as turbine operation, that result in diffusion of aluminum into the substrate surface 103. The component including the diffusion coating 105, as shown in
After the component is provided having the diffusion coating 105, the component is subjected to a solution heat treatment (step 303). Solution heat treatment includes a heat treatment at a temperature and for a time sufficient to dissolve at least a portion of the interdiffusion zone 109 into the substrate 101 to form a dissolved interdiffusion zone 201. Suitable temperatures for the solution heat treatment include, but are not limited to, 2000° F. to 2300° F. or 2100° F. to 2250° F. or 2100° F. to 2200° F. Suitable times for the solution heat treatment include, but are not limited to, 1 to 4 hours, 2 to 4 hours or 2 to 3 hours. In one embodiment, the solution heat treatment includes heating at a temperature about 2100° F. for a time of about 2 hours. In another embodiment, the solution heat treatment includes heating at a temperature about 2200° F. for a time of about 2.5 hours. The specific temperature and times for the solution heat treatment vary depending on the material of the substrate 101 and the material of the aluminide diffusion coating 105. The dissolution mechanism may include, but is not limited to, incipient melting of the interdiffusion zone 109 into the substrate 101.
After dissolution of at least a portion of the interdiffusion zone 109, the additive layer is selectively removed (step 305). As used herein, the term “selective removal” of the aluminide coating refers to the removal of at least a portion of the aluminum-infused additive layer 107, while removing only a very small portion or none of dissolved interdiffusion zone 201. Suitable methods for selective removal of the additive layer include, but are not limited to, grit blasting, water jet abrasive stripping, laser ablation and acid dipping. Suitable processes for grit blasting include light grit blasting using, for example, 220# grit at 40-60 PSI. Suitable methods for selective removal also include acid dips in acids, such as, HCl, a mixture of HCl and H3PO4, HCl and H2SO4, and HNO3 and H3PO4. Other removal techniques includes additive coating removal (ACR) methods, as recited in U.S. Pat. No. 6,758,914, which is hereby incorporated by reference in its entirety. In one embodiment, the selective removal includes an acid dipping for short periods of time, for example, a single cycle in an acid solution of 20-40 weight percent nitric acid solution to permit the acid to react with the aluminum-infused additive layer 107. Selective removal of at least a portion of the additive layer includes a reduction in the thickness of the component of less than 0.3 mils, less than 0.2 mils or less than 0.1 mils, as measured from the position of the substrate surface 103 prior to diffusing the aluminum.
Subsequent to the selective removal, the process may further include deposition of an aluminide bond coat or aluminide diffusion coating, such as an aluminum-infused additive layer. In one embodiment, the deposition is provided prior to returning the component to service. The deposition may include the same aluminum-infused additive layer present on the component having the diffusion coating. Alternatively, the deposition may include a material different than the aluminum-infused additive layer originally formed on the component. The deposition process may include any known process for providing aluminide diffusion coatings.
While the invention has been described with reference to one or more embodiments, 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. In addition, all numerical values identified in the detailed description shall be interpreted as though the precise and approximate values are both expressly identified.
Filing Document | Filing Date | Country | Kind |
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PCT/CN2014/087417 | 9/25/2014 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2016/045043 | 3/31/2016 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
5222282 | Sukonnik et al. | Jun 1993 | A |
5366765 | Milaniak | Nov 1994 | A |
5667663 | Rickerby et al. | Sep 1997 | A |
6036995 | Kircher et al. | Mar 2000 | A |
6174448 | Das et al. | Jan 2001 | B1 |
6334907 | Das | Jan 2002 | B1 |
6482469 | Spitsberg et al. | Nov 2002 | B1 |
6719853 | Buergel et al. | Apr 2004 | B2 |
7093335 | Conner et al. | Aug 2006 | B2 |
8021491 | Kool et al. | Sep 2011 | B2 |
8252376 | Buergel et al. | Aug 2012 | B2 |
8383214 | Schaepkens et al. | Feb 2013 | B2 |
8449262 | Strangman | May 2013 | B2 |
8475598 | Cetel et al. | Jul 2013 | B2 |
20100062180 | Tuppen et al. | Mar 2010 | A1 |
Number | Date | Country |
---|---|---|
101613819 | Dec 2009 | CN |
103382544 | Nov 2013 | CN |
0 713 957 | May 1996 | EP |
0 814 179 | Dec 1997 | EP |
2 401 115 | Nov 2004 | GB |
Entry |
---|
International Search Report and Written Opinion issued in connection with corresponding PCT Application No. PCT/CN2014/087417 dated Jun. 17, 2015. |
Extended European Search Report and Opinion issued in connection with corresponding EP Application No. 14902582.7 dated Apr. 25, 2018. |
Number | Date | Country | |
---|---|---|---|
20170081977 A1 | Mar 2017 | US |