This invention relates to fabrication of turbine engine components by forming a metal skin over a core structure with a mechanically interlocking skin/core interface. It particularly relates to fabrication of turbine blades and vanes with subsurface cooling channels.
Components in the hot gas path of gas turbines, such as rotating blades and stationary vanes, have been produced by metal casting. Cooling passages can be formed in the component by placing pre-formed inserts in the mold. Such inserts are typically made from oxide ceramics. A high-temperature material such as ceramic is required to withstand the molten metal temperatures during pouring. After solidification of the casting the inserts are removed. This can be done for example by dissolving them with a caustic solution. However, ceramics are brittle. If an insert is too thin it can break during pouring or solidification of the metal, resulting in a defective component. This is especially true of directionally solidified (DS) and single crystal (SX) cast components, in which the mold is withdrawn slowly from the furnace during solidification, which increases the amount of tine that the insert is exposed to the molten metal.
Pre-formed ceramic inserts are expensive, and are limited as to the size and complexity of cooling passages that can be produced. Small passages or tortuous circuits would require inserts that are thin, and therefore delicate. In some turbine airfoils and other components it is desirable to provide numerous small cooling channels just below the component surface. One approach is first to cast an airfoil core structure of a superalloy. Grooves are then formed in the outer surface of the core, either during casting or by machining. A superalloy skin is formed separately and bonded to the core, covering the grooves to form sub-surface cooling passages. Transient liquid phase (TLP) bonding has been used for this, in which a foil, powder, or tape, made of a low melting point variant of the airfoil core material is placed between the skin and the core. Upon heating, the TLP partially melts, fusing the skin to the core. This process can use a smaller gap and a higher temperature than soldering or brazing. The TLP material contains melting point depressants such as silicon and/or boron. However, the size of skin that can be accurately formed and bonded has been a limitation of this process.
The assignee of the present invention has invented a process for forming the skin in place on the metallic core, as described in U.S. Pat. No. 5,875,549. Grooves may be formed in the surface of the core. A fugitive filler material such as a ceramic paste is placed in the grooves. The fugitive material is smoothed flush with the core surface, and then a skin of metal is deposited on the surface of the core and the fugitive material. The skin bonds to the core surface between the grooves. The fugitive material is removed, leaving subsurface cooling channels.
However, even with a diffusion bonding heat treatment, the bond interface between the skin and core is weaker than the material of the skin or the core because no grain growth occurs across the bond line. A stronger bond interface is desired.
The invention is explained in the following description in view of the drawings that show:
The inventors have devised a method and mechanism for forming a metal skin in place on a cast metal core structure using mechanical interlocks in the skin/core interface that simulate and approximate an interlocking internal grain structure across the bond line.
The scale of the pits is significant, because thermally deposited coatings tend to follow the features of the underlying substrate. Larger pits would produce a dimpled outer skin surface, which would be disadvantageous for airfoil applications. Alternately, grooves could be used instead of pits. However, grooves form continuous lines of discontinuity that can seed a crack in the substrate, whereas pits do not form such lines. Also grooves do not block bond shear in the direction of the grooves, whereas pits have 360-degree walls, so they block bond shear in all directions.
The skin may be applied to the core by known coating deposition techniques, such as plasma spraying, low-pressure plasma spraying, high velocity oxy-fuel (HVOF) spraying, or cold spraying. Mar M002, CM247, and Haynes 230 powders are commercially available from suppliers of thermal spray powders. Spray parameters similar to those known for bond coats may be used.
For example, a 25 micron thick layer of TLP (using Amdry 775 powder) may be sprayed via HVOF onto the CM247 core. The core is then HVOF-sprayed with a 1 mm thick skin of Haynes 230 (using Ni-517-5 powder). The component may then be maintained at 1080 to 1150 degrees Centigrade for 1-4 hours, resulting in metallic diffusion bonding and migration of the melting-point depressants away from the bond interface, leaving a continuous, heat tolerant interface.
Different processes may be used for the TLP layer and the skin. For example, a thin film deposition process may be used for the TLP, while a thermal spray process may be used for the skin. Herein “thin film deposition process” means a process that deposits one or more layers, with each layer being less than 10 microns thick. This includes processes known as atomic layer deposition, chemical vapor deposition, pulsed laser deposition, plating, cathodic arc deposition, molecular beam epitaxy, and other known deposition processes. By using a thin film deposition process for the TLP layer 40, the pits 24 may be filled without blocking the pit opening with spray particles. But using a thermal spray process for the skin provides layering thick enough to smooth over the relatively small pits to form an aerodynamically smooth outermost surface.
After the skin 42 is formed on the core/filler surfaces, the filler 36 is removed from the grooves, for example by exposure to a caustic solution. Methods of removing the filler material using a caustic solution are known in the investment casting art. These methods include a low or high temperature salt bath of potassium hydroxide or through the use of an autoclave. When the filler is removed from the grooves, the skin and substrate of the core structure 30 remain. This forms subsurface cooling channels 35 just below and adjacent to the skin 42 as later shown.
61—Cast a component core structure;
62—Form grooves in an outer surface of the core structure;
63—Fill the grooves with a sacrificial filler material;
64—Form pits in the outer surface of the core structure;
65—Deposit a transient liquid phase material on the surface of the core structure;
66—Deposit a skin on the surface of the core structure, over the TLP material;
67—Heat the assembly to form a diffusion bond between the skin and the core structure, and to diffuse melting-point depressants of the TLP material away from the bond interface;
68—Remove the sacrificial filler to leave subsurface channels under and adjacent to the skin.
In some embodiments of the invention, the grooves/channels may be omitted and/or a TLP layer may be omitted.
While various embodiments of the present invention have been shown and described herein, it will be obvious that such embodiments are provided by way of example only. Numerous variations, changes and substitutions may be made without departing from the invention herein. Accordingly, it is intended that the invention be limited only by the spirit and scope of the appended claims.
Development for this invention was supported in part by Contract No. DE-FC26-05NT42644, awarded by the United States Department of Energy. Accordingly, the United States Government may have certain rights in this invention.
Number | Name | Date | Kind |
---|---|---|---|
3806276 | Aspinwall | Apr 1974 | A |
5328331 | Bunker et al. | Jul 1994 | A |
5419971 | Skelly et al. | May 1995 | A |
5484258 | Isburgh et al. | Jan 1996 | A |
5640767 | Jackson et al. | Jun 1997 | A |
5875549 | McKinley | Mar 1999 | A |
6060174 | Sabol et al. | May 2000 | A |
6074706 | Beverley et al. | Jun 2000 | A |
6508000 | Burke et al. | Jan 2003 | B2 |
6514046 | Morrison et al. | Feb 2003 | B1 |
6709230 | Morrison et al. | Mar 2004 | B2 |
6805535 | Tiemann | Oct 2004 | B2 |
7182580 | Bostanjoglo et al. | Feb 2007 | B2 |
7182581 | Bostanjoglo et al. | Feb 2007 | B2 |
7247002 | Albrecht et al. | Jul 2007 | B2 |
20080160269 | Stamm | Jul 2008 | A1 |
20080298975 | James et al. | Dec 2008 | A1 |
Number | Date | Country | |
---|---|---|---|
20110192024 A1 | Aug 2011 | US |