|Publication number||US3434811 A|
|Publication date||Mar 25, 1969|
|Filing date||Feb 26, 1965|
|Priority date||Feb 26, 1965|
|Publication number||US 3434811 A, US 3434811A, US-A-3434811, US3434811 A, US3434811A|
|Original Assignee||Gen Electric|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (6), Classifications (10)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 3,434,811 TUNGSTEN-HAFNIUM-OXYGEN ALLOYS Stephen Foldes, Cleveland, Ohio, assignor to General Electric Company, a corporation of New York No Drawing. Filed Feb. 26, 1965, Ser. No. 435,725 Int. Cl. B22f 3/10; C22c 27/00 US. Cl. 29-1825 5 Claims ABSTRACT OF THE DISCLOSURE The present invention relates generally to tungsten-base alloys useful in high temperature applications, and more specifically relates to such alloys containing both hafnium and oxygen in material amounts.
Previously known alloys of tungsten containing hafnium generally also include carbon in combination with the hafnium constituent. All alloys are subject to limitations on their utility due to their mechanical and metallurgical characteristics. In particular, the utilities of known tungsten-hafnium-carbon alloys have limits de pending upon the fabricability of the metal, especially in the alloys containing larger amounts of hafnium and carbon, and also depending on such other factors as stability of hafnium carbides in the tungsten matrix. Each of these factors can be affected strongly by the contained amounts and proportions of alloying additives including and in addition to hafnium and carbon.
Although in certain cases one alloy system cannot be categorically stated to be superior to another, it often can be determined that certain properties of one type of alloy are significantly more useful in certain applications than are related properties of another type of alloy. Thus, it is desirable to provide different types of alloy systems that may be found to be superior in certain applications to known alloy systems.
Accordingly, it is an object of the present invention to provide tungsten-base alloys containing dispersoids, which alloys are different from and in some aspects superior to many known tungsten-base alloys in certain characteristics.
It is further the object of the invention to provide such alloys that are superior to many known tungsten-base alloys in workability and fabricability.
Still another object of the invention is to provide such alloys which are superior to many known tungsten-base alloys in applications at elevated temperatures.
Briefly stated, the present invention in one form provides tungsten-hafnium-oxygen alloys having desirable characteristics different from, and in some cases superior to presently known alloys. Alloys of the invention contain, by weight, about: 1-7% hafnium, 0.030.l2% oxygen, not more than of metal selected from the group consisting of columbium, molybdenum, tantalum, rhenium and mixtures thereof, not more than 2% of metal selected from the group consisting of zirconium, titanium and vanadium and mixtures thereof, and not more than 0.25% boron, the balance essentially all tungsten. Preferably, the oxygen content of the alloys of the invention is 0.06-0.09%. The elements specified in amount not more than certain percentages are entirely optional, and the term not more than is meant to include an amount of zero. Specifically preferred alloys of the invenice tion include the preferred range of oxygen content along with hafnium in amounts of about 1%, 2.9 or 3%, and 6.6 or 7%. Percentages herein are given by weight except where specified otherwise.
By the use of large amounts of oxygen which, even in smallest amounts, was considered by the prior art to be deleterious and to render alloys unusable, the alloys of the present invention are provided with strengths and stabilities that are quite useful and in some cases superior to those previously generally known in tungsten-base alloys. While previously known alloys were considered to require that oxygen contents be no more than 50 or even 35 parts per million by weight (p.p.m.), I have foun that the alloys of the invention beneficially contain oxygen within the limits of 300-1200 p.p.m., and preferably 600900 p.p.m. oxygen.
Alloys of the invention have been prepared by mixing together freshly reduced tungsten metal powders and hafnium hydride powders according to predetermined nominal compositions, pressing them into compacts and sintering in vacuum. An analysis of the starting materials is presented in Table I below with the quantities given in p.p.m. except where expressed otherwise.
TABLE I.ANALYTIOAL DATA AND PARTICLE SIZE OF STARTING MATERIAL In addition to the impurities noted in the table, the tungsten contained less than 10 ppm. of other impurities. These materials were premixed in a twin shell blender, and then thoroughly blended for about four hours in a tungsten rod mill. Compacts were then made by hydrostatic pressing in a rubber sleeve at a pressure of about 35,000 p.s.i.
Following a vacuum pre-sintering treatment at 1050 C. for two hours, the ingots were finally sintered at 2800 C. for two hours in a dynamic vacuum of less than 10- torr. Above the dissociation temperature of hafnium hydride of about 600 C., the small amounts of tungsten oxide on the surface of the tungsten metal powder continued to evaporate and react with the nascent hafnium surfaces, thus resulting in a significant pickup of oxygen by hafnium during sintering. Since material quantities of carbon were not present in the compacts, the oxygen became usefully associated with the hafnium rather than being volatilized out of the compact. The hafnium oxide dispersoid particles thus formed perform a useful function in greatly strengthening the alloys while also allowing them to be worked at elevated temperatures. Subsequent to the sintering operation, the alloys were analyzed, and the results of these tests are presented in Table II below. The values are in p.p.-m. except for hafnium which is expressed in percentages.
TABLE IL-ALLOY COMPOSITIONS AND ANALYSES Analysis O N H The sintered ingots were from 92-95% of theoretical density. They were machined to cylinders one inch in diameter by 2.5 inches long with a 45 chamfered nose. The cylinders were extruded at a 10:1 ratio to 0.350 inch diameter rods in a high energy rate extrusion apparatus. Hardness and grain size measurements were taken on the as-extruded alloys and are presented in Table III below. VPH stands for Vickers pyramid hardness.
TABLE III.HARDNESS AND GRAIN SIZE Extrusion Grain Size, VPH, Temp., 0. microns kgt/mmfi Nominal Composition:
W-lHi 2, 050 27 378 W3Ht 2, 100 7 477 W-7Ht 2, 310 9 517 TABLE IV.HIGH TEMPERATURE TENSILE DATA Temper- UTS, 0.2% YS, Elongation, ague, K s.i. K s.i. percent Nominal Composition:
1, 649 15. 4 8. 3 65. 1 W 1, 927 8. 9 4. 9 36. 8 2, 206 6. 3. 4 32. 4 1, 649 48. 2 30. 4 38. 2 W-lHf 1, 927 26. 9 18. 1 38. 6 2, 206 12. 6 11. 1 12.7 1, 649 63. 7 47. 20. 5 W-3Hf 1, 927 41. 4 36. 1 19. 9 2, 206 21. 0 18. 5 13. 8 1, 649 W-7Hf 1, 927 49. 1 30. 1 19. 5
It can be seen from the table that these alloys are significantly stronger than unalloyed tungsten at elevated temperatures. In addition, the alloy containing 7% hafnium is considerably stronger than most previously known tungsten-base alloys.
It is contemplated by the appended claims to cover any such modifications as fall within the true spirit of the scope of this invention.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. A sintered tungsten-base alloy consisting essentially of about, by weight: 17% hafnium, 0.03-0.12% oxygen, not more than 10% of metal selected from the group consisting of columbium, molybdenum, tantalum, rhenium and mixtures thereof, not more than 2% of metal selected from the group consisting of zirconium, titanium and vanadium and mixtures thereof, and not more than 0.25% of boron, the balance essentially all tungsten, said alloy containing hafnium oxide dispersoid particles there- 2. A sintered tungsten-base alloy consisting essentially of about, by weight: 17% hafnium, 0.06-0.09% oxygen, not more than 10% of metal selected from the group consisting of columbium, molybdenum, tantalum, rhenium and mixtures thereof, not more than 2% of metal selected from the group consisting of zirconium, titanium, and vanadium and mixtures thereof, and not more than 0.25% of boron, the balance essentially all tungsten, said alloy containing hafnium oxide dispersoid particles there- 3. A sintered tungsten-base alloy consisting essentially of about, by weight: 1% hafnium, 0.06-0.09% oxygen, the balance essentially all tungsten, said alloy containing hafnium oxide dispersoid particles therein.
4. A sintered tungsten-base alloy consisting essentially of about, by weight: 2.9% hafnium and 0.060.09% oxygen, the balance essentially all tungsten, said alloy containing hafnium oxide dispersoid particles therein.
5. A sintered tungsten-base alloy consisting essentially of about, by weight: 6.6% hafnium and 0.060.09% oxygen, the balance essentially all tungsten, said alloy containing hafnium oxide dispersoid particles therein.
References Cited UNITED STATES PATENTS 3,116,145 12/1963 Semchyshen -176 3,150,971 9/1964 Weisert et al. 75176 3,177,076 4/1965 Timmons et al. 75176 3,181,946 5/1965 McAndreW et al. 75174 3,243,291 3/1966 Dickinson 75-176 OTHER REFERENCES Nb, Ta, Mo and W Quarrell, Elsevier Publishing Company, N.Y., 1961, relied on pages 321 and 332.
Tungsten Alloys of High Melting Point, Kieffer et al., Journal of the Less Common Metals, vol. 1, 1959, relied on pages 19-33.
CHARLES N. LOVELL, Primary Examiner.
U.S. Cl. X.R. 75176
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3116145 *||Apr 30, 1962||Dec 31, 1963||American Metal Climax Inc||Tungsten-hafnium alloy casting|
|US3150971 *||Feb 25, 1959||Sep 29, 1964||Union Carbide Corp||High-temperature tungsten base alloys|
|US3177076 *||Jun 12, 1961||Apr 6, 1965||American Metal Climax Inc||Forgeable high temperature cast alloys|
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|US3243291 *||Oct 29, 1963||Mar 29, 1966||Gen Telephone & Elect||High-temperature alloy|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3637422 *||Jan 3, 1968||Jan 25, 1972||Atomic Energy Commission||Dispersion-hardened tungsten alloy|
|US4314007 *||Aug 6, 1979||Feb 2, 1982||Bbc Brown, Boveri & Company Limited||Composite shaped articles|
|US5049355 *||Apr 13, 1989||Sep 17, 1991||Schwarzkopf Development Corporation||Process for producing an ODS sintered alloy|
|US5604321 *||Jul 26, 1995||Feb 18, 1997||Osram Sylvania Inc.||Tungsten-lanthana alloy wire for a vibration resistant lamp filament|
|US5742891 *||Apr 4, 1996||Apr 21, 1998||Osram Sylvania Inc.||Tungsten-lanthana alloy wire for a vibration resistant lamp filament|
|WO1989009840A1 *||Apr 13, 1989||Oct 19, 1989||Metallwerk Plansee Gesellschaft M.B.H.||Process for producing an ods sintered alloy|
|U.S. Classification||75/233, 148/423, 75/235|
|International Classification||C22C32/00, C22C27/04, C22C27/00|
|Cooperative Classification||C22C32/0031, C22C27/04|
|European Classification||C22C27/04, C22C32/00C6|