This invention relates generally to the field of materials technology, and more specifically to a wear alloy coating applied by a cold spray process.
It is well known to apply a wear alloy coating to a substrate material to improve its resistance to abrasion, galling, hammering, moisture erosion, solid particle erosion or other types of wear. “Hard facing” is defined in Materials Handbook, Ninth Edition, Volume 3, published by The American Society of Metals, on pages 563-567, as “the process of applying, by welding, plasma spraying or flame plating, a layer, edge or point of wear-resistant metal onto a metal part to increase its resistance to abrasion, erosion, galling, hammering or other form of wear.” Nonferrous alloys are also used for wear applications, both as wrought parts and as coatings, as discussed on pages 589-594 of the same Materials Handbook. The term “wear alloy” as used herein is meant to include both the hard facing materials discussed on pages 563-567 and the nonferrous alloys discussed on pages 589-594 of the Material Handbook.
Wear alloys are frequently used in applications where systematic lubrication against abrasion is not feasible or is inadequate to give a desired service life to a component. New parts may be provided with a wear alloy coating in selected areas and worn parts may be refaced multiple times before replacement of the entire part becomes necessary, thereby reducing the lifetime cost of the part.
Hard facing materials are classified in Materials Handbook into five major groups defined primarily according to total alloy content (elements other than iron). Generally, as the group number increases from Group 1 to Group 5, the alloy content, wear resistance and cost will all increase. Groups 1, 2 and 3 hard facing materials are ferrous materials generally contain a total alloy content of less than 50%. Group 4 materials contain from 50-100% alloy content, typically nickel-based and cobalt-based alloys with alloying elements of nickel, chrome, cobalt, boron and tungsten. Group 5 materials consist of hard granules of carbide distributed in a metal matrix. The carbide may be tungsten carbide, titanium carbide, chromium carbide or tantalum carbide. The metal matrix may be a ductile material such as iron, cobalt or nickel. Carbide based wear resistant materials are often used in applications of severe low stress abrasion where cutting edge retention is needed. Low stress wear resistance is an important component of a carbide material's performance. Some carbide systems, such as those with chromium carbide, also afford significant high temperature oxidation/corrosion resistance while retaining excellent wear resistance properties.
Nonferrous wear alloys may be wrought cobalt-base alloys (such as commercial brands sold under the names of Stellite 6B, Stellite 6K, Haynes 25 and Tribaloy T-400), beryllium-copper alloys (for example C17200) and certain aluminum bronzes (C60800, C61300 and C61400 soft ductile alloys and very hard proprietary die alloys).
Welding, brazing and flame spraying techniques have been used to apply wear alloy coatings. Brazed materials are limited in their potential uses by the melting temperature of the braze alloy. A welded or flame sprayed wear alloy coating may be subject to cracking upon its application due to the shrinkage cracking of these relatively brittle coating materials. Furthermore, the heat input during the application of a wear alloy coating may cause warping of a relatively thin substrate member such as a turbine blade. The heat input from the application of a wear alloy coating may melt or otherwise metallurgical degrade properties of an underlying single crystal or directionally stabilized substrate material or a proximate brazed joint.
Dilution is the interalloying of the wear alloy and the base metal, and it is usually expressed as the percentage of base metal in the deposited wear alloy. A dilution of 10% means that the deposit contains 10% base metal and 90% wear alloy. As dilution increases, the hardness, wear resistance and other desirable properties of the deposit are reduced. The amount of dilution may vary depending upon the deposition process being used and the thickness of the coating. One known technique used to control the amount of dilution it to deposit a buffer layer between the base metal and the wear alloy.
For applications requiring a thick layer of hard face coating material, several coating layers may be used. However, highly alloyed deposits are likely to spall if applied to a thickness of more than 6 mm (¼ inch) as a result of interfaces created within the coating by splat boundaries between sprayed layers or brittle phases between welded layers.
These and other advantages of the invention will be more apparent from the following description in view of the drawings that show:
U.S. Pat. No. 5,302,414 dated Apr. 12, 1994, incorporated by reference herein, describes a cold gas-dynamic spraying process for applying a coating, also referred to herein as a cold spray process. That patent describes a process and apparatus for accelerating solid particles having a size from about 1-50 microns to supersonic speeds in the range of 300-1,200 meters per second and directing the particles against a target surface. When the particles strike the target surface, the kinetic energy of the particles is transformed into plastic deformation of the particles, and a bond is formed between the particles and the target surface. This process forms a dense coating with little or no thermal effect on the underlying target surface.
The applicants have found that a cold spray process may be used advantageously to apply and to control the material properties of a wear alloy coating. Furthermore, a cold spray process may be used to apply wear alloy materials in applications where traditional brazed or weld-applied coatings are not practical. A wear alloy coating may be applied to a component surface by a cold spray coating process to increase the surface resistance to wear, erosion, cavitation, and severe low stress abrasion while retaining cutting edge retention and good high temperature properties, high toughness, excellent corrosion and oxidation resistance, as well as excellent resistance to thermal shock and impact. Particles of the coating material are directed at a high speed against the surface to be coated. The particles deform upon impact with the surface, causing them to adhere to each other and to the target surface.
As illustrated in
A cold spraying process will produce a wear alloy material coating that approaches 100% density and includes no linear interfaces. As a result, there is a reduced chance of spalling when highly alloyed coatings such as Group 4 or Group 5 hard facing materials are applied by cold spraying to a depth exceeding ¼ inch than there would be when such coatings are applied by a prior art thermal technique. This makes it possible to produce a component 10 having a high alloy coating 14 with a depth exceeding 0.25 inch, such as 0.375 or 0.5 inch.
Because a cold spray process imparts only a small amount of heat to the underlying substrate material 12, it is possible to apply a wear alloy coating using a cold spray process in applications where it would not be possible using prior art thermal techniques. In one embodiment, a wear alloy coating material in particle form 16 is directed toward a target surface 18 of a substrate material 12 that is either a directionally solidified material or a single crystal metal material. The velocity of the particles is sufficiently high to cause the particles to deform and to adhere to the target surface 18 without recrystallization of the directionally solidified or single crystal metal substrate material 12. In another embodiment, the component 10 may have a brazed joint, and the particles are directed to a target surface 18 proximate the brazed joint at a velocity sufficiently high to cause the particles 16 to deform and to adhere mechanically to the target surface 18 without metallurgical degrading the properties of the brazed joint. Furthermore, no heat-treating of the component is required after the coating deposition, unlike prior art thermal processes.
In one embodiment, a mixture of particles 16 is prepared to include 75-96 wt. % carbide particles 26 and the remainder particles 22 of cobalt, iron, nickel and/or alloys thereof. The particles are manufactured by processes known in the art such as spray drying or melt spinning processes. The size range of the particles may be controlled to be within any desired size range, for example from 2 microns to 50 microns. Because carbides have a significantly higher hardness than the matrix material, the carbide particles 26 will experience a reduced amount of deformation compared to the matrix material particles 22 upon impact with the target surface 18. The carbide particles 26 will adhere to the target surface 18 as they embed themselves upon impact and as they are surrounded by the deforming matrix material particles 26. As a result, the size and quantity of the carbide particles 26 contained in a Group 5 hard face material coating 14 may be controlled more accurately by using a cold spray process than with prior art thermal techniques wherein the size of the carbide particles can vary significantly as a function of the rate of cooling/solidification of the material. A preferred size range and/or quantity of carbide particles may be predetermined for a particular application in order to optimize the performance of the coating under particular erosion wear or oxidation/corrosion conditions. When applied by a cold spray process, the average size of the carbide granules 22 distributed in a matrix 20 of metal such as nickel, cobalt or iron may be selectively less than or greater than the average size range that would be obtained by prior art casting techniques. Moreover, the size and distribution of carbide particles 22 may be made purposefully uniform (
Other combinations of particle types and sizes may be used to produce a wear alloy coating having particularly desired properties. Particles of a wear alloy material may be combined with particles of one or a plurality of other types of materials. In a further embodiment, particles 20 of a wear alloy material may be combined with particles 22 of a ceramic material to form a coating layer 14 having improved temperature capabilities resulting from the presence of the ceramic material. Alternatively, second material particles 22 may be a superalloy material such as nickel based superalloy IN738. A superalloy material may be used exclusively or in part as the matrix material.
The surface roughness of coating layer 14 may be affected by controlling the cold spray process parameters used to apply the coating 14. In some applications it may be desired to impart a predetermined degree of roughness to the surface of a component 10 in order to promote turbulent air flow over the surface, such as to promote mixing and heat transfer across the surface. Generally a higher impact velocity of the particles 16 will result in a smoother coating surface. In one application the component 10 is a part of a gas turbine engine exposed to hot combustion gases, and the surface roughness of coating 14 impacts the heat transfer between the hot gases and the coating 14 and underlying substrate material 12.
The process and coating described herein may be used in any application, and is especially useful for valves, steam turbine blades and vanes, combustion turbine z-notch shrouds, erosion shields and combustor basket spring clips. This process may further be used for mining applications, piston rings, cams, bushings, valves, thrust washers, cutting tool applications and other manufacturing applications for severe abrasion and wear conditions. For space applications, a thin coating of moly-disulfide material may be applied by cold spray to prevent localized cold welding under the low temperature, high local stress conditions of a spacecraft application. The coatings described herein may be applied in a factory or a field environment.
While the preferred 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 will occur to those of skill in the art 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.
This application is a divisional of U.S. application Ser. No. 10/210,719, filed Aug. 1, 2002 now U.S. Pat. No. 6,780,458. This application also claims benefit of the Aug. 1, 2001, filing date of U.S. provisional patent application No. 60/309,451; and further the Dec. 5, 2001, filing date of U.S. provisional patent application 60/336,825; and further the Jan. 30, 2001, filing date of U.S. patent application Ser. No. 09/774,550; and further the Dec. 5, 2000, filing date of U.S. patent application Ser. No. 09/729,844.
Number | Name | Date | Kind |
---|---|---|---|
3754976 | Babecki | Aug 1973 | A |
4340698 | De Jongh et al. | Jul 1982 | A |
4372404 | Drake | Feb 1983 | A |
4382811 | Lüscher | May 1983 | A |
4416421 | Browning | Nov 1983 | A |
4430360 | Bill | Feb 1984 | A |
4552784 | Chu | Nov 1985 | A |
4576874 | Spengler | Mar 1986 | A |
4610698 | Eaton | Sep 1986 | A |
4639399 | Aprigliano | Jan 1987 | A |
4714622 | Omori et al. | Dec 1987 | A |
4753094 | Spears | Jun 1988 | A |
4854196 | Mehan | Aug 1989 | A |
4880614 | Strangman | Nov 1989 | A |
5024884 | Otfinoski | Jun 1991 | A |
5059095 | Kushner | Oct 1991 | A |
5076897 | Wride et al. | Dec 1991 | A |
5180285 | Lau | Jan 1993 | A |
5210944 | Monson | May 1993 | A |
5302414 | Alkhimov | Apr 1994 | A |
5495979 | Sastri et al. | Mar 1996 | A |
5607561 | Gruver et al. | Mar 1997 | A |
5660320 | Hoffmuller et al. | Aug 1997 | A |
5665217 | Gruver et al. | Sep 1997 | A |
5702574 | Foster | Dec 1997 | A |
5704759 | Draskovich | Jan 1998 | A |
5763106 | Blanchard et al. | Jun 1998 | A |
5912087 | Jackson | Jun 1999 | A |
5928977 | Magnin et al. | Jul 1999 | A |
5932356 | Sileo et al. | Aug 1999 | A |
5952110 | Schell | Sep 1999 | A |
5997248 | Ghasripoor | Dec 1999 | A |
6015586 | Omori | Jan 2000 | A |
6060174 | Sabol | May 2000 | A |
6102656 | Nissley | Aug 2000 | A |
6106959 | Vance | Aug 2000 | A |
6194086 | Nenov | Feb 2001 | B1 |
6251494 | Schreiber | Jun 2001 | B1 |
6365222 | Wagner | Apr 2002 | B1 |
6469278 | Boyce | Oct 2002 | B1 |
6528123 | Cadden et al. | Mar 2003 | B1 |
Number | Date | Country |
---|---|---|
0 718 420 | Dec 1995 | EP |
8-333671 | Dec 1996 | JP |
2038411 | Jun 1995 | RU |
Number | Date | Country | |
---|---|---|---|
20040202885 A1 | Oct 2004 | US |
Number | Date | Country | |
---|---|---|---|
60309451 | Aug 2001 | US | |
60336825 | Dec 2001 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10210719 | Aug 2002 | US |
Child | 10836560 | US |