US3704508A - Process for compacting metallic powders - Google Patents
Process for compacting metallic powders Download PDFInfo
- Publication number
- US3704508A US3704508A US118562A US3704508DA US3704508A US 3704508 A US3704508 A US 3704508A US 118562 A US118562 A US 118562A US 3704508D A US3704508D A US 3704508DA US 3704508 A US3704508 A US 3704508A
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- US
- United States
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- container
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- mixture
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/0433—Nickel- or cobalt-based alloys
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/1208—Containers or coating used therefor
Definitions
- the present invention is concerned with a method of consolidating metallic powders such as nickel base alloy powders, for example, which dispense with the need for high pressure or the complicated and expensive apparatus employed commonly in high pressure metal compacting techniques. More specifically, the present invention is concerned with a method by which metallic powders are consolidated by heating the powder in the presence of an electron donor compound such as boric acid to a temperature just below the solidus point of the metallic powder.
- metal alloys that are reactive such as beryllium, and/or titanium, zirconium, etc.
- electron donor compounds have not been known in the prior art which are compatible with super-alloy materials such as nickel or chrome, or with beryllium and which might permit the manufacturing of a suitable alloy.
- the particle size of the super-alloy or exotic metals to be reconstituted be less than about one-half micron, it has been found that the present process is successful with particle sizes up to about 140 mesh (US. Standard Sieve).
- the blending of the fine metallic powder with the boric acid-methanol solution is carried out by adding about 0.0l5 0.1 weight percent boric acid based on the weight of the metallic powder in a solution which is, for example, about a 0.5-3 percent solution of boric acid in methanol.
- a solution which is, for example, about a 0.5-3 percent solution of boric acid in methanol.
- the powder can also be contained in a receptacle of the desired shape made of a metal foil such as aluminum.
- Articles produced by the process of the present invention can be of essentially any desired configuration including various fonns which could not be produced, or produced only with great difficulty and expense, by conventional powder metallurgy techniques. These articles which are produced according to the present invention have a theoretical density exceeding 99 percent, no interconnected porosity and exhibit grain growth and a total absence of powder particles.
- the consolidated articles produced by this invention can be subjected to a further additional "forging operation by heating the articles to an elevated temperature below the solidus point of the metal in a forging die and effecting up to as much as about a 20 percent reduction in volume.
- Typical of the alloys and super-alloys which can be prepared according to the present invention are those containing high percentages of a nickel, chromium, and cobalt with small or lesser amounts of zirconium, titanium, tungsten, and molybdenum, beryllium, and hafinum.
- the process of the present invention is applicable to all alloys heretofore known in the art as well as to some novel alloys not heretofore prepared successfully; or if prepared at all, only with great difficulty.
- EXAMPLE 1 A super-alloy powder consisting of 18 percent chromium, 18.5 percent cobalt, 4 percent molybdenum, 2.9 percent titanium, 2.9 percent aluminum, 0.05 percent zirconium, 0.006 percent boron and the balance nickel, was passed through a set of sieves so that the entire blend was -l40mesh (US. Standard), and this graded super-alloy powder was then placed into a vacuum retort and saturated with a solution of boric acid and methanol. The solution comprised of 200 cc. of methanol to 3 grams boric acid.
- the contents of the vacuum retort were then stirred in order to coat each individual particle with the electron donor boric acid solution.
- a rubber stopper was placed into the mouth of the retort and had a provision for a Centigrade thermometer.
- the retort was connected by the means of a rubber hose to a vacuum pump and evacuated to remove the condensible vapors generated by the solution. During the evacuation the temperature dropped to a l5 C.', as the degree of outgassing decreased, the contents in the retort reached room temperature.
- the vacuum retort, while still under vacuum, was then heated to 800 F. to remove entrapped gasses which were not removed during the initial evacuation.
- the powder was vibrated into a standard cylindrical boro silicate pyrex glass container.
- the pyrex container was vibrated to such a point where there was approximately 64-68 percent tap density.
- the powder filled pyrex container was then connected to a vacuum pump and simultaneously evacuated and vibrated.
- the tubulated pyrex container which contained the powder, was placed on a ring stand and the tubulated end of the container connected to a vacuum pump. While under vacuum the entire pyrex container was heated to approximately 1100 F. to preclude further the possibility of entrapped gasses. While under vacuum the tubulated end of the powder filled pyrex container was then heated and sealed.
- the prepared pyrex container was next placed into a graphite crucible, and this assembly then placed into a standard air furnace for heat treatment. Heating was effected by heating from room temperature to 2280 F. as fast as the furnace would allow and held at that particular temperature for four to 6 hours.
- the heat treating cycle had been completed, the heat was turned off and the specimen allowed to cool to approximately 1200 F. at which time it was removed from the furnace and air cooled.
- the container reached a temperature of approximately 600 F., the pyrex glass spalled off to give a part which was approximately 99+ percent theoretical density and was a duplicate of the shape in which it was processed in.
- the powder preform was finally forged at 2100 F. and reduced approximately 20 percent at which time the forging preform had a density of 100 percent of theoretical.
- a process for consolidating particles of a metallic powder to form a unitary article therefrom comprising:
- said metallic powder comprises more than 50 percent of a metal selected from the group consisting of nickel, chromium and cobalt and less than 50 percent of a metal selected from the group consisting of zirconium, titanium, tungsten, molybdenum and mixtures thereof.
- a process as claimed in claim 1 wherein said step of heating to a temperaturebelow the solidus comprises heating the mixture to a temperature about l00-200 F. below the melting point of the metallic powder.
- Aprocess as claimed in claim 1 wherein said mixture is heated to drive off said condensible vapors and entrained gases at a temperature up to about 1 100 F.
- a process as claimed in claim 1 wherein said step of heating to drive ofi said condensible vapors and entrained gases is accomplished by heating said mixture in a first container at a temperature and for a time sufficient to drive off said condensible vapors and heating the resulting mixture in a second container at a temperature and for a time sufficient to drive off said entrained gases.
- a process as claimed in claim 12 including the step of vibrating said mixture prior to heating in said second container.
- said dilute solution includes about 0.015-0.l percent by weight of boric acid based on the weight of said metallic powder.
- a process as claimed in claim 21 wherein said forging comprises heating said article to a temperature below the solidus point of said powder and reducing the volume of said article up to about 20 percent.
- a procie ss as claimed in claim 23 including the further step of forging said unitary article by heating said article to a temperature below the solidus point of said powder and reducing the volume of said article up to about 20 percent.
- a process as claimed in claim 24 wherein said mixture is heated to drive 011' said condensible vapors and entrained gases at a temperature up to about 1 F. and said heating to a temperature below the solidus is continued for about 4 to 10 hours.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
Claims (26)
- 2. A process as claimed in claim 1 wherein said metallic powder is beryllium.
- 3. A process as claimed in claim 1 wherein said metallic powder comprises a mixture of more than one metal.
- 4. A process as claimed in claim 3 wherein said metallic powder comprises more than 50 percent of a metal selected from the group consisting of nickel, chromium and cobalt and less than 50 percent of a metal selected from the group consisting of zirconium, titanium, tungsten, molybdenum and mixtures thereof.
- 5. A process as claimed in claim 1 wherein said step of heating to a temperature below the solidus comprises heating the mixture to a temperature about 100*-200* F. below the melting point of the metallic powder.
- 6. A process as claimed in claim 1 wherein said step of heating to below the solidus is continued for about 4 to 10 hours.
- 7. A process as claimed in claim 1 wherein said metallic powder has a particle size of up to about 140 mesh.
- 8. A process as claimed in claim 7 wherein said metallic powder has a particle size less than about one-half micron.
- 9. A process as claimed in claim 1 wherein said mixture is heated to drive off said condensible vapors and entrained gases at a temperature up to about 1100* F.
- 10. A process as claimed in claim 1 wherein said container is a borosilicate glass container.
- 11. A process as claimed in claim 1 wherein said container has the shape of the desired unitary article.
- 12. A process as claimed in claim 1 wherein said step of heating to drive off said condensible vapors and entrained gases is accomplished by heating said mixture in a first container at a temperature and for a time sufficient to drive off said condensible vapors and heating the resulting mixture in a second container at a temperature and for a time sufficient to drive off said entrained gases.
- 13. A process as claimed in claim 12 wherein said mixture is heated in said first container at a temperature up to about 800* F. and in said second container at a temperature up to about 1100* F.
- 14. A process as claimed in claim 12 wherein said second container is a borosilicate glass container.
- 15. A process as claimed in claim 12 wherein said second container has the shape of the desired unitary article.
- 16. A process as claimed in claim 12 including the step of vibrating said mixture prior to heating in said second container.
- 17. A process as claimed in claim 16 wherein said container is vibrated to a tap density of about 65-68 percent.
- 18. A process as claimed in claim 1 wherein said container is sealed prior to heating to a temperature below the solidus.
- 19. A process as Claimed in claim 1 wherein said dilute solution includes about 0.015-0.1 percent by weight of boric acid based on the weight of said metallic powder.
- 20. A process as claimed in claim 19 wherein said dilute solution comprises about 0.5-3 percent by weight of boric acid in methanol.
- 21. A process as claimed in claim 1 including the further step of forging said unitary article after removal thereof from said container.
- 22. A process as claimed in claim 21 wherein said forging comprises heating said article to a temperature below the solidus point of said powder and reducing the volume of said article up to about 20 percent.
- 23. A process as claimed in claim 1 wherein said metallic powder has a particle size of up to about 140 mesh, and said dilute solution includes about 0.015-1 percent by weight of boric acid based on the weight of said metallic powder.
- 24. A process as claimed in claim 23 including the further step of forging said unitary article by heating said article to a temperature below the solidus point of said powder and reducing the volume of said article up to about 20 percent.
- 25. A process as claimed in claim 24 wherein said mixture is heated to drive off said condensible vapors and entrained gases at a temperature up to about 1100* F. and said heating to a temperature below the solidus is continued for about 4 to 10 hours.
- 26. A process as claimed in claim 25 wherein said dilute solution comprises about 0.5-3 percent by weight of boric acid in methanol and said container is a borosilicate container.
- 27. A product made by the process of claim 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11856271A | 1971-02-24 | 1971-02-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3704508A true US3704508A (en) | 1972-12-05 |
Family
ID=22379377
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US118562A Expired - Lifetime US3704508A (en) | 1971-02-24 | 1971-02-24 | Process for compacting metallic powders |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3704508A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4227927A (en) * | 1978-04-05 | 1980-10-14 | Cyclops Corporation, Universal-Cyclops Specialty Steel Division | Powder metallurgy |
| US4407775A (en) * | 1981-04-27 | 1983-10-04 | The United States Of America As Represented By The Secretary Of The Interior | Pressureless consolidation of metallic powders |
| US4693863A (en) * | 1986-04-09 | 1987-09-15 | Carpenter Technology Corporation | Process and apparatus to simultaneously consolidate and reduce metal powders |
| EP0260812A3 (en) * | 1986-09-15 | 1988-11-17 | Inco Alloys International, Inc. | Production of water atomized powder metallurgy products |
| US4808225A (en) * | 1988-01-21 | 1989-02-28 | Special Metals Corporation | Method for producing an alloy product of improved ductility from metal powder |
| US4818482A (en) * | 1987-07-09 | 1989-04-04 | Inco Alloys International, Inc. | Method for surface activation of water atomized powders |
| US5009704A (en) * | 1989-06-28 | 1991-04-23 | Allied-Signal Inc. | Processing nickel-base superalloy powders for improved thermomechanical working |
| AU655951B2 (en) * | 1990-11-29 | 1995-01-19 | Corning Incorporated | Sintered metal bodies and manufacturing method therefor |
| EP0676483A1 (en) * | 1994-04-06 | 1995-10-11 | Special Metals Corporation | High strain rate deformation of nickel-base superalloy compact |
| US6042781A (en) * | 1991-12-04 | 2000-03-28 | Materials Innovation, Inc. | Ambient temperature method for increasing the green strength of parts |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA553284A (en) * | 1958-02-18 | Haller John | Process of making powdered metal articles without briquetting |
-
1971
- 1971-02-24 US US118562A patent/US3704508A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA553284A (en) * | 1958-02-18 | Haller John | Process of making powdered metal articles without briquetting |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4227927A (en) * | 1978-04-05 | 1980-10-14 | Cyclops Corporation, Universal-Cyclops Specialty Steel Division | Powder metallurgy |
| US4407775A (en) * | 1981-04-27 | 1983-10-04 | The United States Of America As Represented By The Secretary Of The Interior | Pressureless consolidation of metallic powders |
| US4693863A (en) * | 1986-04-09 | 1987-09-15 | Carpenter Technology Corporation | Process and apparatus to simultaneously consolidate and reduce metal powders |
| EP0260812A3 (en) * | 1986-09-15 | 1988-11-17 | Inco Alloys International, Inc. | Production of water atomized powder metallurgy products |
| US4818482A (en) * | 1987-07-09 | 1989-04-04 | Inco Alloys International, Inc. | Method for surface activation of water atomized powders |
| US4808225A (en) * | 1988-01-21 | 1989-02-28 | Special Metals Corporation | Method for producing an alloy product of improved ductility from metal powder |
| US5009704A (en) * | 1989-06-28 | 1991-04-23 | Allied-Signal Inc. | Processing nickel-base superalloy powders for improved thermomechanical working |
| AU655951B2 (en) * | 1990-11-29 | 1995-01-19 | Corning Incorporated | Sintered metal bodies and manufacturing method therefor |
| US5427601A (en) * | 1990-11-29 | 1995-06-27 | Ngk Insulators, Ltd. | Sintered metal bodies and manufacturing method therefor |
| US6042781A (en) * | 1991-12-04 | 2000-03-28 | Materials Innovation, Inc. | Ambient temperature method for increasing the green strength of parts |
| EP0676483A1 (en) * | 1994-04-06 | 1995-10-11 | Special Metals Corporation | High strain rate deformation of nickel-base superalloy compact |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: MSL ACQUISTION CORPORATION, A DE CORP.,STATELESS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CYCLOPS CORPORATION;REEL/FRAME:004807/0983 Effective date: 19870626 Owner name: MSL ACQUISTION CORPORATION, A DE CORP. Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:CYCLOPS CORPORATION;REEL/FRAME:004807/0983 Effective date: 19870626 |
|
| AS | Assignment |
Owner name: MELON BANK, N.A., ONE MELLON BANK CENTER, PITTSBUR Free format text: SECURITY INTEREST;ASSIGNOR:CYCLOPS CORPORATION;REEL/FRAME:004809/0868 Effective date: 19870930 |
|
| AS | Assignment |
Owner name: CYCLOPS CORPORATION Free format text: CHANGE OF NAME;ASSIGNOR:MSL ACQUISITION CORPORATION;REEL/FRAME:004832/0543 Effective date: 19880212 |
|
| AS | Assignment |
Owner name: PITTSBURGH NATIONAL BANK, FIFTH AVENUE AND WOOD ST Free format text: SECURITY INTEREST;ASSIGNOR:CYCLOPS CORPORATION;REEL/FRAME:004994/0581 Effective date: 19880727 |