US3152891A - High strength niobium-base alloys - Google Patents

High strength niobium-base alloys Download PDF

Info

Publication number
US3152891A
US3152891A US7072A US707260A US3152891A US 3152891 A US3152891 A US 3152891A US 7072 A US7072 A US 7072A US 707260 A US707260 A US 707260A US 3152891 A US3152891 A US 3152891A
Authority
US
United States
Prior art keywords
niobium
alloys
molybdenum
vanadium
base alloys
Prior art date
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.)
Expired - Lifetime
Application number
US7072A
Inventor
Richard T Begley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CBS Corp
Original Assignee
Westinghouse Electric Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Westinghouse Electric Corp filed Critical Westinghouse Electric Corp
Priority to US7072A priority Critical patent/US3152891A/en
Priority to GB13153/62A priority patent/GB914862A/en
Priority to GB41748/60A priority patent/GB914861A/en
Application granted granted Critical
Publication of US3152891A publication Critical patent/US3152891A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/02Alloys based on vanadium, niobium, or tantalum

Definitions

  • molybdenum-base alloys are the only materials commercially available with strength properties comparable to the niobium-base alloys described in this application.
  • these molybdenum-base alloys have much poorer oxidation resistance than pure nobium, have approximately 25% higher density, and are quite difficult to fabricate.
  • the niobiumbase alloys offer much promise in this field of high temperature alloys. While pure niobium has a high melting point (2468 'C.), an intermediate density (8.56 gms./cc.), and a low ductile-brittle transition temperature, it does not possess entirely adequate high temperature properties.
  • niobium-base alloys having substantial ductility at room temperature, and high temperature strength, the alloys including predetermined amounts of at least one of the elements vanadium, molybdenum, zirconium, and hafnium.
  • a further object of this invention is to provide niobiumbase alloys having substantial ductility at room temperature and high temperature strength including, in predetermined amounts, the elements vanadium and molybdenum.
  • niobium one of the other elements of the group, and the balance being niobium.
  • the molybdenum present will not exceed 20% by Weight.
  • Highly useful binary, ternary, and quaternary niobium-base alloys may be prepared. In some cases, a part of the molybdenum in the ternary and higher component niobium-base alloys may be re placed by tungsten.
  • alloys of this invention comprise, by weight, from 0.5% to 20% Vanadium, from 0.5% to 20% molybdenum, from 0.1% to 5% zirconium, and the balance essentially niobium with small amounts of impurities.
  • alloys which has been found to be useful which comprises, by weight, from 4% to 6% vanadium from 4% to 6% molybdenum, from 0.75% to 1.25% zirconium, and the balance essentially niobium with small amounts of impurities.
  • An additional alloy of this invention comprises, by weight, from 0.5% to 20% vanadium, from 0.5% to 20% molybdenum, and the balance essentially nobium with small amounts of impurities.
  • useful alloys comprising from 4% to 6% vanadium, from 4% to 6% molybdenum, and the balance niobium.
  • Another ternary alloy of this invention comprises, by weight, from 3% to 15% molybdenum, from 3% to 15% hafnium, and the balance essentially niobium with small amounts of impurities.
  • a binary alloy of this invention comprises from 5% to 40% vanadium, and the balance essentially niobium with small amounts of impurities.
  • Another useful alloy of this invention comprises from 1% to 40% hafnium, and the balance essentially niobium.
  • the operating temperature range which is of particular interest for the above alloys is from 1800 F. to 2400 F.
  • the alloys of this invention were prepared employing essentially conventional non-consumable arc melting techniques. The melting was conducted under a protective atmosphere of argon. In the following Table I properties of several of the alloys, together with their nominal compositions, are set forth:
  • Table II PROPERTIES or PURE NIOBIUM The data presented in Tables I and II were obtained from fully recrystallized material, and all high temperature testing (except as noted) was performed in vacuum.
  • alloy A has over 4 times the strength of pure niobium at 2000 F. in addition to satisfactory ductility.
  • Alloy B which includes 1% zirconium, has even better high temperature strength.
  • the other alloys of Table I have at least twice the high temperature strength ofpure niobium.
  • vanadium is a most potent strengthener and also improves oxidation resistance.
  • Molybdenum is a strengthener though somewhat less eitective than vanadium, and it, too. improves oxidation resistance.
  • Zirconium and hafnium function primarily as strengtheners.
  • niobium employed in the alloys of this invention will contain the normal impurities carbon, oxygen, nitrogen, tantalum, silicon, iron, and titanium in a total amount of about 1% or less.
  • niobium-base alloys having an exceedingly useful combination of properties with substantial ductility at room temperature and very attractive high temperature strength properties.
  • a niobium-base alloy suitable for use at elevated temperatures consisting of, by weight, from 4% to 6% vanadium, from 4% to 6% molybdenum, from 0.75% to 1.25% zirconium, and the balance essentially niobium With small amounts of incidental impurities.
  • a high-strength alloy for use at elevated temperatures consisting of, by weight, from 0.5% to 20% vanadium, from 0.5% to 20% molybdenum, and the balance essentially niobium with small amounts of impurities.
  • a high-strength alloy for use at elevated tempera- 30 tures consisting of, by weight, from 4% to 6% vanadium,

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Powder Metallurgy (AREA)
  • Turbine Rotor Nozzle Sealing (AREA)

Description

United States Patent 3,152,891 HIGH STRENGTH NIOBIUM-BASE ALLOYS Richard T. Begley, Verona, Pa., assignor to Westinghouse Electric Corporation, East Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Filed Feb. 8, 1960, Ser. No. 7,072 4 Claims. (Cl. 75-174) This invention is directed to high strength niobiumbase alloys particularly intended for service at elevated temperatures.
The trend toward high operating temperatures in jet engines, missiles, gas turbines, and other heat engines has accelerated interest in the development of high temperature structural materials. At present, the primary obstacle to improved performance in many power generation and propulsion systems is the unavailability of materials with suflicient high temperature strength. There is also a continuing need for high temperature alloys for the construction of chemical reactors, oil refining equipment and the like. Much effort has been expended in this field to obtain a material having a combination of high temperature strength and corrosion resistance, and adequate ductility at room temperatures so that they'are reasonably workable and usable at room temperature.
At the present time, molybdenum-base alloys are the only materials commercially available with strength properties comparable to the niobium-base alloys described in this application. However, these molybdenum-base alloys have much poorer oxidation resistance than pure nobium, have approximately 25% higher density, and are quite difficult to fabricate.
In accordance with the present invention the niobiumbase alloys offer much promise in this field of high temperature alloys. While pure niobium has a high melting point (2468 'C.), an intermediate density (8.56 gms./cc.), and a low ductile-brittle transition temperature, it does not possess entirely adequate high temperature properties.
It is, accordingly, an object of this invention to provide niobium-base alloys having substantial ductility at room temperature, and high temperature strength, the alloys including predetermined amounts of at least one of the elements vanadium, molybdenum, zirconium, and hafnium.
It is another object of this invention to provide niobium-base alloys having substantial ductility at room temperature and high temperature strength in which predetermined amounts of the elements vanadium and molybdenum are present, and also incorporating zirconium in predetermined amounts.
A further object of this invention is to provide niobiumbase alloys having substantial ductility at room temperature and high temperature strength including, in predetermined amounts, the elements vanadium and molybdenum.
It is also an object of this invention to provide alloys having good ductility at room temperature and high elevated temperature strength including in predetermined amounts, the elements niobium and hafnium.
Other objects of this invention will, in part, be. obvious and will, in part, appear hereinafter.
one of the other elements of the group, and the balance being niobium. The molybdenum present will not exceed 20% by Weight. Highly useful binary, ternary, and quaternary niobium-base alloys may be prepared. In some cases, a part of the molybdenum in the ternary and higher component niobium-base alloys may be re placed by tungsten.
Certain of the alloys of this invention comprise, by weight, from 0.5% to 20% Vanadium, from 0.5% to 20% molybdenum, from 0.1% to 5% zirconium, and the balance essentially niobium with small amounts of impurities. Within this broad range, there is a range of alloys which has been found to be useful which comprises, by weight, from 4% to 6% vanadium from 4% to 6% molybdenum, from 0.75% to 1.25% zirconium, and the balance essentially niobium with small amounts of impurities.
An additional alloy of this invention comprises, by weight, from 0.5% to 20% vanadium, from 0.5% to 20% molybdenum, and the balance essentially nobium with small amounts of impurities. Within this broad range there is a range of useful alloys comprising from 4% to 6% vanadium, from 4% to 6% molybdenum, and the balance niobium.
Another ternary alloy of this invention comprises, by weight, from 3% to 15% molybdenum, from 3% to 15% hafnium, and the balance essentially niobium with small amounts of impurities.
A binary alloy of this invention comprises from 5% to 40% vanadium, and the balance essentially niobium with small amounts of impurities.
Another useful alloy of this invention comprises from 1% to 40% hafnium, and the balance essentially niobium.
The operating temperature range which is of particular interest for the above alloys is from 1800 F. to 2400 F.
The alloys of this invention were prepared employing essentially conventional non-consumable arc melting techniques. The melting was conducted under a protective atmosphere of argon. In the following Table I properties of several of the alloys, together with their nominal compositions, are set forth:
TABLE I PROPERTIES or Nb-BASE ALLOYS Indicates analysis.
While all of the alloys listed in the above table have relatively good high temperature strength, particularly striking is the important improvement in this property displayed by the zirconium-containing Alloy B, which 7 also retains substantial ductility.
To further indicate the improvement over pure niobium realized in the alloys of this invention, certain properties of pure niobium are presented in Table II for purposes of comparison.
Table II PROPERTIES or PURE NIOBIUM The data presented in Tables I and II were obtained from fully recrystallized material, and all high temperature testing (except as noted) was performed in vacuum.
As can be seen from Tables I and II, the alloy A has over 4 times the strength of pure niobium at 2000 F. in addition to satisfactory ductility. Alloy B, which includes 1% zirconium, has even better high temperature strength. The other alloys of Table I have at least twice the high temperature strength ofpure niobium.
In the alloys of this invention vanadium is a most potent strengthener and also improves oxidation resistance. Molybdenum is a strengthener though somewhat less eitective than vanadium, and it, too. improves oxidation resistance. Zirconium and hafnium function primarily as strengtheners.
The oxidation resistance of Alloy A was determined and compared with oxixdation data obtained under the same test condition as on pure niobium. These data are set forth in Table III below:
Table III OXIDATION DATA Composition (Wt. percent) Temp. Time Wt. gain F.) (hrs) mgJcm.
Nb 2,000 2 75.9 Nb5Y5Mo- 2,000 2 23.2
prepared by standard arcmelting techniques, and electron beam melting, and ingots of the alloys may be hot worked by conventional methods such as forging, extrusion, rolling, and swaging. 5 tective atmosphere, such as the indicated argon, or
In melting, an inert provacuum, should be employed. The niobium employed in the alloys of this invention will contain the normal impurities carbon, oxygen, nitrogen, tantalum, silicon, iron, and titanium in a total amount of about 1% or less.
Thus, there have been disclosed niobium-base alloys having an exceedingly useful combination of properties with substantial ductility at room temperature and very attractive high temperature strength properties.
It will be understood by those skilled in the art that although the present invention has been described in connection with preferred alloys, modifications and variations may be employed without departing from the underlying spirit and scope of the invention.
I claim as my invention:
1. A niobium-base alloy suitable for use at elevated temperatures consisting of, by weight, from 4% to 6% vanadium, from 4% to 6% molybdenum, from 0.75% to 1.25% zirconium, and the balance essentially niobium With small amounts of incidental impurities.
2. A high-strength alloy for use at elevated temperatures consisting of, by weight, from 0.5% to 20% vanadium, from 0.5% to 20% molybdenum, and the balance essentially niobium with small amounts of impurities.
3. A high-strength alloy for use at elevated tempera- 30 tures consisting of, by weight, from 4% to 6% vanadium,
purities.
References Cited in the file of this patent UNITED STATES PATENTS Bomberger Jan. 14, 1958 Hix Feb. 4, 1958 Wainer Apr. 21, 1959 FOREIGN PATENTS France Apr. 6, 1959 OTHER REFERENCES Miller: Tantalum and Niobium, Academic Press Inc, New York, March, 1952.
Gonser and Sherwood: Technology of Columbium, John Wiley and Sons, Inc., New York, 1958, pages 87-97.

Claims (2)

1. A NIOBIUIM-BASE ALLOY SUITABLE FOR USE AT ELEVATED TEMPERATURES CONSISTING OF , BY WEIGHT, FROM 4% TO 6% VANADIUM, FROM 4% TO 6% MOLYBDENUM, FROM 0.75% TO 1.25% ZIRCONIUM, AND THE BALANCE ESSENTIALLY NIOBIUM WITH SMALL AMOUNTS OF INCIDENTAL IMPURITIES.
4. A HIGH-STRENGTH ALLOY FOR USE AT ELEVATED TEMPERATURES CONSISTING OF, BY WEIGHT, FROM 3% TO 15% MOLYBDENUM, FROM 3% TO 15% HAFNIUM, AND THE BALANCE ESSENTIALLY NIOBIUM WITH SMALL AMOUNTS OF INCIDENTAL IMPURITIES.
US7072A 1960-02-08 1960-02-08 High strength niobium-base alloys Expired - Lifetime US3152891A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US7072A US3152891A (en) 1960-02-08 1960-02-08 High strength niobium-base alloys
GB13153/62A GB914862A (en) 1960-02-08 1960-12-05 High strength niobium-base alloys
GB41748/60A GB914861A (en) 1960-02-08 1960-12-05 High strength niobium-base alloys

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7072A US3152891A (en) 1960-02-08 1960-02-08 High strength niobium-base alloys

Publications (1)

Publication Number Publication Date
US3152891A true US3152891A (en) 1964-10-13

Family

ID=21724065

Family Applications (1)

Application Number Title Priority Date Filing Date
US7072A Expired - Lifetime US3152891A (en) 1960-02-08 1960-02-08 High strength niobium-base alloys

Country Status (2)

Country Link
US (1) US3152891A (en)
GB (2) GB914862A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4836849A (en) * 1987-04-30 1989-06-06 Westinghouse Electric Corp. Oxidation resistant niobium alloy
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 (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2819960A (en) * 1956-11-15 1958-01-14 Rem Cru Titanium Inc Formable acid resistant titanium alloys
US2822268A (en) * 1956-08-01 1958-02-04 Du Pont Compositions of matter
US2883282A (en) * 1957-05-21 1959-04-21 Horizons Inc Protection of niobium from oxidation
FR1190580A (en) * 1956-11-14 1959-10-14 Du Pont Niobium-molybdenum alloys

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2822268A (en) * 1956-08-01 1958-02-04 Du Pont Compositions of matter
FR1190580A (en) * 1956-11-14 1959-10-14 Du Pont Niobium-molybdenum alloys
US2819960A (en) * 1956-11-15 1958-01-14 Rem Cru Titanium Inc Formable acid resistant titanium alloys
US2883282A (en) * 1957-05-21 1959-04-21 Horizons Inc Protection of niobium from oxidation

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4836849A (en) * 1987-04-30 1989-06-06 Westinghouse Electric Corp. Oxidation resistant niobium alloy
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

Also Published As

Publication number Publication date
GB914862A (en) 1963-01-09
GB914861A (en) 1963-01-09

Similar Documents

Publication Publication Date Title
US3164465A (en) Nickel-base alloys
US3366478A (en) Cobalt-base sheet alloy
US3030206A (en) High temperature chromiummolybdenum alloy
US3753699A (en) Refractory metal alloys for use in oxidation environments
US3293030A (en) Nickel-base alloys
US2850385A (en) Molybdenum-base alloy
US3027255A (en) High strength niobium base alloys
US2996379A (en) Cobalt-base alloy
US3152891A (en) High strength niobium-base alloys
US2868640A (en) Titanium alloys
US2798806A (en) Titanium alloy
JPS6057498B2 (en) molybdenum alloy
US3918965A (en) Iridium-hafnium alloy
US3346379A (en) Niobium base alloy
US3177076A (en) Forgeable high temperature cast alloys
US3183085A (en) Tantalum base alloys
US3166414A (en) Tantalum base alloys
JPS6137347B2 (en)
US2622023A (en) Titanium-base alloys
US3022163A (en) Ductile niobium base alloy
US3140943A (en) Tantalum base alloys
US2162596A (en) Furnace heating element
US2575915A (en) Nickel base high-temperature alloy
US3249429A (en) Tantalum brazing alloy
US3046109A (en) High temperature niobium base alloy