This disclosure relates to processes for manufacturing gamma TiAl alloys (hereinafter “γ-TiAl”) and, more particularly, to direct rolling of γ-TiAl alloys to form sheets.
Powder metallurgy and ingot metallurgy are two commonly used processes to produce γ-TiAl sheets as illustrated in the flowcharts of
For the powder metallurgy process shown in
For ingot metallurgy process shown in
Consequently, there exists a need for a process for forming sheets of γ-TiAl alloys.
In accordance with the present invention, a process for producing sheets of γ-TiAl is disclosed. This process broadly comprises forming a melt of a γ-TiAl alloy; casting the γ-TiAl alloy to form an as-cast γ-TiAl alloy; encapsulating the as-cast γ-TiAl alloy to form an as-cast γ-TiAl alloy preform; and rolling the as-cast γ-TiAl alloy preform to form a sheet comprising γ-TiAl.
In accordance with the present invention, an article made from a sheet produced in accordance with the process of the present invention is also disclosed.
In accordance with the present invention, a preform broadly comprising an as-cast γ-TiAl alloy material disposed in a canning material, wherein the as-cast γ-TiAl alloy material comprises a shape suitable for being rolled into a sheet, is also disclosed.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
a is a flowchart representing a powder metallurgy process of the prior art for fabricating γ-TiAl sheets;
b is a flowchart representing an ingot metallurgy process of the prior art for fabricating γ-TiAl sheets;
Like reference numbers and designations in the various drawings indicate like elements.
The process of the present invention produces articles comprising γ-TiAl by directly rolling encapsulated as-cast γ-TiAl alloy preforms into the articles. Unlike prior art processes for manufacturing γ-TiAl articles, an as-cast γ-TiAl alloy preform of the present invention does not undergo additional process steps such as atomizing, hot isostatically pressing, extruding or conditioning, prior to being encapsulated. Once the γ-TiAl alloy is cast as a preform, the as-cast γ-TiAl alloy preform is encapsulated and directly rolled to form articles comprising γ-TiAl.
For purposes of explanation, the following definitions are provided. “As-cast γ-TiAl alloy” means the γ-TiAl alloy cast material without having undergone any subsequent process steps such as, for example, atomizing, hot isostatically pressing, conditioning, extruding and the like. “As-cast γ-TiAl alloy preform” means the as-cast γ-TiAl alloy having a shape suitable for being rolled in a conventional rolling process and encapsulated with a canning material and, optionally, a thermal barrier material disposed therebetween. As used herein, the term “thermal barrier material” means a barrier material that acts as a thermal barrier and insulates the as-cast γ-TiAl alloy preform.
Referring now to
Various γ-TiAl alloys, for example, binary γ-TiAl and other γ-TiAl alloys, may be employed using the process of the present invention. Suitable γ-TiAl alloys contain Ti and Al and may also contain Cr, Nb, Ta, W, Mn, B, C and Si in amounts sufficient to impart characteristics to the γ-TiAl alloy sheets such as improved ductility, creep resistance, oxidation resistance, impact resistance and the like. The various γ-TiAl alloys may generally comprise the following materials in atomic weight percent:
Referring now to steps 2a and 2b of
Referring now to step 3 of
Referring now to a step 4 of
Experimental Section
Sample 1
A γ-TiAl ingot having the composition 54-Ti 46-Al (in at. %) was prepared by double melted VAR casting process, each ingot having a diameter of 180 mm and a length of 410 mm. The cast γ-TiAl ingot was cut into cast γ-TiAl plates of 7 in.×12 in.×½ in. using an electro-discharge machining process. Each cast γ-TiAl plate was polished with sand paper to remove the decast layer. Each cast γ-TiAl plate was encapsulated with a titanium thermal barrier. Each encapsulated cast γ-TiAl plate was preheated for one hour at 538° C. (1000° F.) and at a pressure of 1×10−5 torr. Each encapsulated cast γ-TiAl plate was hot rolled under a non-oxidizing atmosphere at a temperature of 1260° C. (2300° F.). Each encapsulated cast γ-TiAl plates were again preheated and hot rolled until achieving cast γ-TiAl sheets having a thickness of 100 mils. The encapsulation material was removed and the cast γ-TiAl sheets were ground to a thickness of 40 mils. The final cast γ-TiAl sheets size was 24 in.×12 in.×40 mils. The microphotograph of
Sample 2
A γ-TiAl ingot having the composition 48.5-Ti 46.5-Al 4-(Cr, Nb, Ta, B) (in at. %) was prepared by an induction skull melting casting process, each ingot having a diameter of 180 mm and a length of 410 mm. The cast γ-TiAl ingot was cut into cast γ-TiAl plates of 7 in.×12 in.×½ in. using an electro-discharge machining process. Each cast γ-TiAl plate was polished with sand paper to remove the decast layer. Each cast γ-TiAl plate was encapsulated with a titanium thermal barrier. Each encapsulated cast γ-TiAl plate was preheated for one hour at 538° C. (1000° F.) and at a pressure of 1×10−5 torr. Each encapsulated cast γ-TiAl plate was hot rolled under a non-oxidizing atmosphere at a temperature of 1260° C. (2300° F.). Each encapsulated cast γ-TiAl plates were again preheated and hot rolled until achieving cast γ-TiAl sheets having a thickness of 100 mils. The encapsulation material was removed and the cast γ-TiAl sheets were ground to a thickness of 40 mils. The final cast γ-TiAl sheet size was 24 in.×12 in.×40 mils. The microphotograph of
Sample 3
A commercially available 47 XD γ-TiAl cast plate having the composition 49-Ti 47-Al 2-Nb 2-Mn (in at. %) and 0.08% by volume of TiB2, and dimensions 4.8 in.×3.4 in.×0.6 in. Each cast γ-TiAl plate was encapsulated with a titanium thermal barrier. Each encapsulated cast γ-TiAl plate was preheated for one hour at 538° C. (1000° F.) and at a pressure of 1×10−5 torr. Each encapsulated cast γ-TiAl plate was hot rolled in a non-oxidizing atmosphere at a temperature of 1260° C. (2300° F.). Each encapsulated cast γ-TiAl plate was heated and hot rolled until achieving cast γ-TiAl sheets having a thickness of 100 mils. The encapsulation material was removed and the cast γ-TiAl sheets were ground to a thickness of 27 mils. The final cast γ-TiAl sheet size was 27 in.×6.3 in.×27 mils. The microphotograph of
As may be seen in the microstructures of Samples 1-3 in the microphotographs of
γ-TiAl alloys have high ductility at temperatures above the ductile-to-brittle temperature of 1300° F. (704° C.)-1400° F. (760° C.). γ-TiAl alloys also exhibit low strength at elevated temperatures and readily recrystallize under such conditions. Given these inherent characteristics of γ-TiAl alloys, as-cast γ-TiAl alloys preforms can be successfully rolled directly into thin sheets once encapsulated under isothermal temperature conditions. Encapsulating as-cast γ-TiAl alloy preforms without first subjecting the as-cast γ-TiAl alloy to additional process steps such as atomizing, hot isostatically pressing, extruding or conditioning eliminates costly and wasteful intermediate steps employed in prior art processes. It is estimated that the process of the present invention can effectively reduce process costs by upwards of 35% over the conventional powder metallurgy and ingot metallurgy processes.
γ-TiAl articles made by the direct rolling process of the present invention also exhibit enhanced physical properties over γ-TiAl articles made by the prior art processes. Conventional powder metallurgy processes include steps performed under atmospheres such as argon. It is recognized that atmospheric particles, for example, argon gas, become trapped within the γ-TiAl alloy. Once the argon particles diffuse, the resultant γ-TiAl alloy articles exhibit thermally induced porosity and poor ductility, lower temperature resistance and reduced impact resistance. The direct rolling process of the present invention avoids this danger by eliminating the additional process steps that lead to thermally induced porosity.
It is to be understood that the invention is not limited to the illustrations described and shown herein, which are deemed to be merely illustrative of the best modes of carrying out the invention, and which are susceptible to modification of form, size, arrangement of parts, and details of operation. The invention rather is intended to encompass all such modifications, which are within its spirit and scope as defined by the claims.
The Government of the United States of America may have rights in the present invention pursuant to Contract No. NAS326385 awarded by the National Aeronautics and Space Administration.
Number | Name | Date | Kind |
---|---|---|---|
5028491 | Huang et al. | Jul 1991 | A |
5284620 | Larsen, Jr. | Feb 1994 | A |
5411700 | Martin | May 1995 | A |
5424027 | Eylon | Jun 1995 | A |
6161285 | Eberhardt et al. | Dec 2000 | A |
6420051 | Appel et al. | Jul 2002 | B1 |
6669791 | Tetsui et al. | Dec 2003 | B2 |
Number | Date | Country |
---|---|---|
1072652 | Mar 1989 | JP |
2224803 | Sep 1990 | JP |
3-104833 | May 1991 | JP |
03 115549 | May 1991 | JP |
5186842 | Jul 1993 | JP |
5209243 | Aug 1993 | JP |
7251202 | Oct 1995 | JP |
8-225906 | Mar 1996 | JP |
08 225906 | Sep 1996 | JP |
8238503 | Sep 1996 | JP |
2001316743 | Nov 2001 | JP |
Number | Date | Country | |
---|---|---|---|
20070107202 A1 | May 2007 | US |