US3022163A - Ductile niobium base alloy - Google Patents
Ductile niobium base alloy Download PDFInfo
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- US3022163A US3022163A US814100A US81410059A US3022163A US 3022163 A US3022163 A US 3022163A US 814100 A US814100 A US 814100A US 81410059 A US81410059 A US 81410059A US 3022163 A US3022163 A US 3022163A
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- Prior art keywords
- alloy
- niobium
- zirconium
- base alloy
- titanium
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- 229910052758 niobium Inorganic materials 0.000 title claims description 23
- 239000010955 niobium Substances 0.000 title claims description 23
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 title claims description 23
- 229910045601 alloy Inorganic materials 0.000 title description 59
- 239000000956 alloy Substances 0.000 title description 59
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 16
- 239000010936 titanium Substances 0.000 claims description 15
- 229910052719 titanium Inorganic materials 0.000 claims description 15
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 12
- 229910052750 molybdenum Inorganic materials 0.000 claims description 12
- 239000011733 molybdenum Substances 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 19
- 230000003647 oxidation Effects 0.000 description 19
- 238000007254 oxidation reaction Methods 0.000 description 19
- 229910052726 zirconium Inorganic materials 0.000 description 19
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 13
- 229910052804 chromium Inorganic materials 0.000 description 13
- 239000011651 chromium Substances 0.000 description 13
- 239000007789 gas Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229910000753 refractory alloy Inorganic materials 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910001182 Mo alloy Inorganic materials 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- -1 nobium Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C27/00—Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
- C22C27/02—Alloys based on vanadium, niobium, or tantalum
Definitions
- This invention relates to a niobium base alloy having outstanding ductility, as well as excellent fabricab lity and high temperature oxidation resistance. It pertains particularly to a refractory metal alloy of this type which is designed for gas turbine engine components which reach temperatures up to 2000 F. under conditions where except onally high strength is not a primary requirement.
- the nickel base alloy and cobalt base alloy components commonly used today in gas turbine engines for aircraft normally have maximum service temperatures of approximately 1800 F. to 1900 F. This limitation necessarily restricts the performance and efiiciency of these engines.
- Refractory metals such as nobium, tungsten, molybdenum and chromium, have satisfactory high melting temperatures and sufiicient potential availability to warrant investigation for turbine engine applications.
- each of these metals exhibits poor ox dation resistance at temperatures of 2000 F. or above.
- Such metals are therefore unsatisfactory when exposed to extremely hot oxidizing gases, and prior attempts to correct this deficiency by adding small amounts of various alloying elements were generally unsuccessful. Some of the resultant alloys still did not possess'adequate oxidation resistance at the very high temperatures under consideration, while others were excess vely brittle.
- a principal object of the present invention is to provide a refractory alloy whi-h can be em ployed as a fabricated component of a turbine engine at temperatures up to 2000 F. because of its oxidation resistance at such temperatures and which possesses exceptional ductlity.
- Such an alloy also must have the necessary fabricability and a melting point of at least 3000 F.
- a refractory alloy comprising about to titanium, 9% to 11% molybdenum, 4% to 8% chromium, 1% to 5% zirconium and the balance (56% to 71%) substantially all niobium.
- Optimum results are obtainable when the alloy contains approximately 7% to 8% chromium and the zirconium content is maintained within the range of 3% to 5%.
- the molybdenum serves to materially increase the oxidation resistance of the niobium base alloy and also contributes to its hot strength.
- the molybdenum content is lower than about 9% or higher than approximately 11%, the oxidation resistance of the alloy is no ticeably reduced.
- Titanium further improves resistance to high temperature oxidation, although it is also necessary in order to ,provide the niobium base alloy with the desired amount of ductility. If the amount of titanium present is less than about 15%, the oxidation resistance of the alloy is inadequate. On the other hand, when more than 20% titanium is present the alloy becomes soft and weak.
- chromium contributes to the oxidation resistance of the n obium base alloy as well as increasing its hot strength.
- a chromium content of at least 4% is necessary for oxidation resistance, but if more than approximately 8% chromium is included, the microstructure of the alloy becomes unstable and the alloy is relatively brittle.
- the addition of about 7% to 8% chromium is desirable to achieve maximum oxidation resis'tance.
- the zirconium measurably increases the strength of the niobium base alloy, and at least 1% zirconium is necessary to maintain this property at an adequate level because of the high titanium content of the alloy. It is preerable to use 3% to 5% zirconium in order to meet strength requirements, particularly when the t'tanium content is near the upper end of the aforementioned range. If more than 5% zirconium is present, the niobium base alloy becomes susceptible to atmospheric contamination to an excessive extent. The alloy can tolerate this relatively high zirconium content because the substantial amount of titanium present raises the level at which atmospheric contamination would occur.
- the titanium in the alloy appears to oxidize and enter into solid solution w th niobium oxide to form a protective oxide layer which inhibits further oxide penetration of the alloy.
- a two-layer surface oxide is thus formed, the inner layer appearing to be the more beneficial in'restricting additional oxide penetration.
- var'ous other elements can be included in the niobium base a1- loy without detracting from its mechanical properties.
- aluminum slightly improves the oxidation resistance of the alloy without reducing its hot strength. If the aluminum content is raised above this level, however, it embrittles the alloy by promoting the formation of an unstable miscrostructure.
- a small quantity of carbon serves to somewhat increase the strength and hot workability of the niobium base alloy, particularly when the zirconium content is relatively high. Large amounts of zirconium have a tendency to promote subsurface contaimination of the alloy by absorbing oxygen in solid solution.
- carbon may advantageously be added to the alloy and apparently combines with the zirconium to form zrconium carbide, thereby inhibiting this contamination. If more than 2% carbon is added, on the other hand, the room temperature ductility of the alloy is reduced to an undesirable extent.
- zirconium content of the alloy When the zirconium content of the alloy is at a lower level, a small amount of boron, usually less than 0.01%, may be included in the alloy to further improve its hot workability to some degree. As indicated above, zircon um appears to absorb and/or react with oxygen at the alloy surface. Therefore, with the higher zirconium content alloy there is no need to add boron, which improves alloy ductility by apparently modifying grain boundary contaminants.
- niobium base alloy has been prepared by alloying high purity elemental raw materials in an inert atmosphere of argon plus helium. It was found that the constitutents of the alloy may be added either simultaneously or successively. Melting was accomplished with a nonconsumable tungsten electrode electric arc. After solidification of the alloy, it was crushed to fine particle size and re-melted in the above-described manner and cast in ingot form. This ingot was enclosed in a container formed of an alloy of molybdenum plus 0.5% titanium, heated to approximately 2700 F., and extruded.
- Sound extrusions may be obtained with the nobium base alloy of this invention by direct extrusion of the cast ingot, the extruded alloy having a fibrous appearing cold worked structure. Subsequent further working has been readily accomplished by both swaging and rolling. This highly ductile alloy therefore can easily be made into sheet material.
- Test bars were mach'ned from this extruded niobium base alloy bar stock and tested in an argon atmosphere at a temperature of 2000 F. under a load of 10,000 psi to evaluate the hot ductility of the alloy.
- a highly ductile, oxidation-resistant sheet metal article formed of an alloy comprising about 15% to 20% titanium, 9% to 11% molybdenum, 4% to 8% chromum, 1% to 5% zirconium and the balance substantially all niobium.
- molybdenum and 1% zirconium was reduced 80% in area and had a 125% elongation atlrupture.
- typical commercially available nickel base alloys used in sheet form for similar purposes, have materially 'lessstrength than the alloy of this invention.
- a commercial alloy consisting of 0.04% car bon, 0.5% manganese, 7% iron, 14.5% aluminum, 2.5% titanium,. 1% niobium plus tantalum I and the balance nickel, has a l0-hour stress-rupture life at l800 F. while under a load of only 4,000 p.s.i.
- The'new alloy thus'may be beneficially used for turbine engine components other than those which are subjected to extremely high stresses.
- niobium' base alloy of the present invention possesses a combine tion of good oxidation resistance at extreme temperatures chromiun, 0.7%'
- a sheet metal article characterized by outstanding ductility and oxidation resistance at elevated temperatures, said article being formed of analloy consisting essentially of about 15% to 20% titan'um,'9% to 11% molybdenum, 7% to 8% chromium, 3%'to.5% zirconium and the balance substantially all niobium.
- a gas turbine engine sheet metal component characterized by outstanding room and high temperature ductil ty and oxidation resistance upon exposure to oxidizing gases at a. temperature of 2000 F., said sheet metal being formed of'an alloy comprising about 56% to 71% niobium, 15% to 20% titanium, 9% to 11% molybdenum, 4% to 8% chromium and 1% to 5% zirconium.
- a sheet metal component for a gas turbine engine characterized by excellent ductility and oxidation resistance upon exposure to oxidizing gases at a temperature of 2000 F., said component being formed of an alloy consist'ng essentially of about 15 to 20% titanium, 9%
- the alloy has a melting point materially in excess of 3000. F., the desired minimum temperature hereinbefore mentioned.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Turbine Rotor Nozzle Sealing (AREA)
Description
United States Patent 3,022,163 DUCTILE NIOBIUM BASE ALLOY Neil M. Lottridge, Jr., Warren, and Douglas G. McCullough, Rochester, Mich, assignors to General Motors Corporation, Detroit, Mich., a corporation of Delaware No Drawing. Filed May 18, 1959, Ser. No. 814,100 Claims. (Cl. 75-174) This invention relates to a niobium base alloy having outstanding ductility, as well as excellent fabricab lity and high temperature oxidation resistance. It pertains particularly to a refractory metal alloy of this type which is designed for gas turbine engine components which reach temperatures up to 2000 F. under conditions where except onally high strength is not a primary requirement.
The nickel base alloy and cobalt base alloy components commonly used today in gas turbine engines for aircraft normally have maximum service temperatures of approximately 1800 F. to 1900 F. This limitation necessarily restricts the performance and efiiciency of these engines. Refractory metals, such as nobium, tungsten, molybdenum and chromium, have satisfactory high melting temperatures and sufiicient potential availability to warrant investigation for turbine engine applications. However, each of these metals exhibits poor ox dation resistance at temperatures of 2000 F. or above. Such metals are therefore unsatisfactory when exposed to extremely hot oxidizing gases, and prior attempts to correct this deficiency by adding small amounts of various alloying elements were generally unsuccessful. Some of the resultant alloys still did not possess'adequate oxidation resistance at the very high temperatures under consideration, while others were excess vely brittle.
Consequently, a principal object of the present invention is to provide a refractory alloy whi-h can be em ployed as a fabricated component of a turbine engine at temperatures up to 2000 F. because of its oxidation resistance at such temperatures and which possesses exceptional ductlity. Such an alloy also must have the necessary fabricability and a melting point of at least 3000 F.
These and other objects are attained in accordance with this invention with a refractory alloy comprising about to titanium, 9% to 11% molybdenum, 4% to 8% chromium, 1% to 5% zirconium and the balance (56% to 71%) substantially all niobium. Optimum results are obtainable when the alloy contains approximately 7% to 8% chromium and the zirconium content is maintained within the range of 3% to 5%.
The molybdenum serves to materially increase the oxidation resistance of the niobium base alloy and also contributes to its hot strength. When the molybdenum content is lower than about 9% or higher than approximately 11%, the oxidation resistance of the alloy is no ticeably reduced.
Titanium further improves resistance to high temperature oxidation, although it is also necessary in order to ,provide the niobium base alloy with the desired amount of ductility. If the amount of titanium present is less than about 15%, the oxidation resistance of the alloy is inadequate. On the other hand, when more than 20% titanium is present the alloy becomes soft and weak.
Likewise, chromium contributes to the oxidation resistance of the n obium base alloy as well as increasing its hot strength. A chromium content of at least 4% is necessary for oxidation resistance, but if more than approximately 8% chromium is included, the microstructure of the alloy becomes unstable and the alloy is relatively brittle. The addition of about 7% to 8% chromium is desirable to achieve maximum oxidation resis'tance.
The zirconium measurably increases the strength of the niobium base alloy, and at least 1% zirconium is necessary to maintain this property at an adequate level because of the high titanium content of the alloy. It is preerable to use 3% to 5% zirconium in order to meet strength requirements, particularly when the t'tanium content is near the upper end of the aforementioned range. If more than 5% zirconium is present, the niobium base alloy becomes susceptible to atmospheric contamination to an excessive extent. The alloy can tolerate this relatively high zirconium content because the substantial amount of titanium present raises the level at which atmospheric contamination would occur. The titanium in the alloy appears to oxidize and enter into solid solution w th niobium oxide to form a protective oxide layer which inhibits further oxide penetration of the alloy. A two-layer surface oxide is thus formed, the inner layer appearing to be the more beneficial in'restricting additional oxide penetration.
Small amounts of var'ous other elements, usually less than 2% or 3%, can be included in the niobium base a1- loy without detracting from its mechanical properties. For example, up to 2% or 3% aluminum slightly improves the oxidation resistance of the alloy without reducing its hot strength. If the aluminum content is raised above this level, however, it embrittles the alloy by promoting the formation of an unstable miscrostructure. A small quantity of carbon serves to somewhat increase the strength and hot workability of the niobium base alloy, particularly when the zirconium content is relatively high. Large amounts of zirconium have a tendency to promote subsurface contaimination of the alloy by absorbing oxygen in solid solution. Under these circumstances, carbon may advantageously be added to the alloy and apparently combines with the zirconium to form zrconium carbide, thereby inhibiting this contamination. If more than 2% carbon is added, on the other hand, the room temperature ductility of the alloy is reduced to an undesirable extent.
When the zirconium content of the alloy is at a lower level, a small amount of boron, usually less than 0.01%, may be included in the alloy to further improve its hot workability to some degree. As indicated above, zircon um appears to absorb and/or react with oxygen at the alloy surface. Therefore, with the higher zirconium content alloy there is no need to add boron, which improves alloy ductility by apparently modifying grain boundary contaminants.
The above-described niobium base alloy has been prepared by alloying high purity elemental raw materials in an inert atmosphere of argon plus helium. It was found that the constitutents of the alloy may be added either simultaneously or successively. Melting was accomplished with a nonconsumable tungsten electrode electric arc. After solidification of the alloy, it was crushed to fine particle size and re-melted in the above-described manner and cast in ingot form. This ingot was enclosed in a container formed of an alloy of molybdenum plus 0.5% titanium, heated to approximately 2700 F., and extruded. Sound extrusions may be obtained with the nobium base alloy of this invention by direct extrusion of the cast ingot, the extruded alloy having a fibrous appearing cold worked structure. Subsequent further working has been readily accomplished by both swaging and rolling. This highly ductile alloy therefore can easily be made into sheet material.
Test bars were mach'ned from this extruded niobium base alloy bar stock and tested in an argon atmosphere at a temperature of 2000 F. under a load of 10,000 psi to evaluate the hot ductility of the alloy. The elongation chromium, l%'
. 4 scope of the invention is not to be limited thereby except as defined bythe following claims.
For example, a test bar of an alloy We claim:
1. A highly ductile, oxidation-resistant sheet metal article formed of an alloy comprising about 15% to 20% titanium, 9% to 11% molybdenum, 4% to 8% chromum, 1% to 5% zirconium and the balance substantially all niobium.
molybdenum and 1% zirconium was reduced 80% in area and had a 125% elongation atlrupture.
This alloy demonstrated a life of 16.1 hours to rupture under these 7 test conditions. We have also evaluated these alloys from the standpoint of oxidation resistance. For example, an alloy composed of about 60.5% niobium, titanium, 7.5 chromium, 10% molybdenum, 5% zirconium, 1% aluminum and 1% carbon had a total surface metalloss of less than 5 mils in thickness after 100 hours cyclic exposure in air at a temperature of 2000 F. The other alloys previously mentioned exh bited similar oxidation resistance. When subjectedto the foregoing stress-rupture test, a test-bar of the alloy containing 60.5% niobium'had a life of 13.7 hours with 68.7% elongation at rupture and a reduction in area of 54.4%
'In comparison, typical commercially available nickel base alloys, used in sheet form for similar purposes, have materially 'lessstrength than the alloy of this invention. For example, a commercial alloy consisting of 0.04% car bon, 0.5% manganese, 7% iron, 14.5% aluminum, 2.5% titanium,. 1% niobium plus tantalum I and the balance nickel, has a l0-hour stress-rupture life at l800 F. while under a load of only 4,000 p.s.i. Hence the strength of our alloy compares favorably with the strength of sheet materials heretofore employed in high temperature applications. The'new alloy thus'may be beneficially used for turbine engine components other than those which are subjected to extremely high stresses.
'The aforementioned data also show that the niobium' base alloy of the present invention possesses a combine tion of good oxidation resistance at extreme temperatures chromiun, 0.7%'
2. A sheet metal article characterized by outstanding ductility and oxidation resistance at elevated temperatures, said article being formed of analloy consisting essentially of about 15% to 20% titan'um,'9% to 11% molybdenum, 7% to 8% chromium, 3%'to.5% zirconium and the balance substantially all niobium.
3. A gas turbine engine sheet metal component characterized by outstanding room and high temperature ductil ty and oxidation resistance upon exposure to oxidizing gases at a. temperature of 2000 F., said sheet metal being formed of'an alloy comprising about 56% to 71% niobium, 15% to 20% titanium, 9% to 11% molybdenum, 4% to 8% chromium and 1% to 5% zirconium.
4. A sheet metal component for a gas turbine engine characterized by excellent ductility and oxidation resistance upon exposure to oxidizing gases at a temperature of 2000 F., said component being formed of an alloy consist'ng essentially of about 15 to 20% titanium, 9%
to 11% molybdenum, 4% to 8% chromium, 3% to 5% zirconium and the balance substantially all niobium.
5. A sheet metal article formedtrom a niobium base alloy having an outstanding combination of high temperature ductility, fabricablity and oxidation resistance at a temperature of 2000 F., said alloy consisting essentially of about 1 5% to 20% titanium, 9% to 11% molybdenum, 7% to 8% chromium, 1% to 5% zirconium, aluminum not-in excess of approximately 3%,
a carbon not in excess of approximately 2%, boron not in and outstanding ductility. The alloy has a melting point materially in excess of 3000. F., the desired minimum temperature hereinbefore mentioned.
While our invention has been described by means of certain specific examples, it is to be understood that the excess of approximately 0.01% and the balance substan tially all niobium. .1
References Cited in the file of this patent UNITED STATES PATENTS
Claims (1)
1. A HIGHLY DUCTILE, OXIDATION-RESISTANT SHEET METAL ARTICLE FORMED OF AN ALLOY COMPRISING ABOUT 15% TO 20% TITANIUM, 9% TO 11% MOLYBDENUM, 4% TO 8% CHROMUM. 1% TO 5% ZIRCOMIUM AND THE BALANCE SUBSTANTIALLY ALL NIOBIUM.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US814100A US3022163A (en) | 1959-05-18 | 1959-05-18 | Ductile niobium base alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US814100A US3022163A (en) | 1959-05-18 | 1959-05-18 | Ductile niobium base alloy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3022163A true US3022163A (en) | 1962-02-20 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US814100A Expired - Lifetime US3022163A (en) | 1959-05-18 | 1959-05-18 | Ductile niobium base alloy |
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| US (1) | US3022163A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3183085A (en) * | 1961-09-15 | 1965-05-11 | Westinghouse Electric Corp | Tantalum base alloys |
| US3830670A (en) * | 1970-12-18 | 1974-08-20 | Surface Technology Corp | Graded multiphase carburized materials |
| FR2669644A1 (en) * | 1990-11-26 | 1992-05-29 | Onera (Off Nat Aerospatiale) | INTERMETALLIC ALLOYS AND COMPOUNDS BASED ON NIOBIUM OR TANTALIUM WITH HIGH SPECIFIC RESISTANCE. |
| US5486242A (en) * | 1990-11-26 | 1996-01-23 | Office National D'etudes Et De Recherches Aerospatiales | Niobium or tantalum based high specific strength inter metallic compounds and alloys |
| US11198927B1 (en) * | 2019-09-26 | 2021-12-14 | United States Of America As Represented By The Secretary Of The Air Force | Niobium alloys for high temperature, structural applications |
| US11846008B1 (en) | 2019-09-26 | 2023-12-19 | United States Of America As Represented By Secretary Of The Air Force | Niobium alloys for high temperature, structural applications |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2882146A (en) * | 1957-09-27 | 1959-04-14 | Du Pont | High temperature niobium base alloy |
| US2883282A (en) * | 1957-05-21 | 1959-04-21 | Horizons Inc | Protection of niobium from oxidation |
-
1959
- 1959-05-18 US US814100A patent/US3022163A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2883282A (en) * | 1957-05-21 | 1959-04-21 | Horizons Inc | Protection of niobium from oxidation |
| US2882146A (en) * | 1957-09-27 | 1959-04-14 | Du Pont | High temperature niobium base alloy |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3183085A (en) * | 1961-09-15 | 1965-05-11 | Westinghouse Electric Corp | Tantalum base alloys |
| US3830670A (en) * | 1970-12-18 | 1974-08-20 | Surface Technology Corp | Graded multiphase carburized materials |
| FR2669644A1 (en) * | 1990-11-26 | 1992-05-29 | Onera (Off Nat Aerospatiale) | INTERMETALLIC ALLOYS AND COMPOUNDS BASED ON NIOBIUM OR TANTALIUM WITH HIGH SPECIFIC RESISTANCE. |
| WO1992009713A1 (en) * | 1990-11-26 | 1992-06-11 | Office National D'etudes Et De Recherches Aerospatiales | Niobium or tantalum based high specific strength inter metallic compounds and alloys |
| US5486242A (en) * | 1990-11-26 | 1996-01-23 | Office National D'etudes Et De Recherches Aerospatiales | Niobium or tantalum based high specific strength inter metallic compounds and alloys |
| US11198927B1 (en) * | 2019-09-26 | 2021-12-14 | United States Of America As Represented By The Secretary Of The Air Force | Niobium alloys for high temperature, structural applications |
| US11846008B1 (en) | 2019-09-26 | 2023-12-19 | United States Of America As Represented By Secretary Of The Air Force | Niobium alloys for high temperature, structural applications |
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