[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US3166833A - Production of heavy metal objects by powder metallurgy - Google Patents

Production of heavy metal objects by powder metallurgy Download PDF

Info

Publication number
US3166833A
US3166833A US191746A US19174662A US3166833A US 3166833 A US3166833 A US 3166833A US 191746 A US191746 A US 191746A US 19174662 A US19174662 A US 19174662A US 3166833 A US3166833 A US 3166833A
Authority
US
United States
Prior art keywords
powder
metal
powder metallurgy
borohydride
production
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
US191746A
Inventor
Alfred R Globus
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.)
Consolidated Astronautics Inc
Original Assignee
Consolidated Astronautics Inc
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 Consolidated Astronautics Inc filed Critical Consolidated Astronautics Inc
Priority to US191746A priority Critical patent/US3166833A/en
Application granted granted Critical
Publication of US3166833A publication Critical patent/US3166833A/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
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/045Alloys based on refractory metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0047Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
    • C22C32/0073Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only borides

Definitions

  • the invention more particularly relates to improvements in the process of forming metal objects from titanium, zirconium, tantalum, tungsten, molybdenum and chromium powders, to a novel powder composition used in such process, and to the object's formed by the process.
  • a powder of a metal of the aforementioned group is first compacted into the desired shape of the object to be formed, as for example by pressing in a die at pressures between 10 and 50 tons per square inch.
  • the compacting solidifies the powder into what is referred to as a green briquette, which has sufficient structural strength to withstand the further treatment. After the compacting the green briquette may be trimmed or cut, as necessary, or otherwise finished. It is then sintered into the final object, preferably in a vacuum furnace.
  • One object of this invention is to improve the mechanical properties, as Well as the chemical and wearresistant characteristics of objects produced by the aforementioned process.
  • an alkali metal borohydride is admixed with the metal powder in an amount of about 1-5%, and preferably 1-3%, by weight, calculated as boron, prior to the compacting of the powder into the green briquette.
  • alkali metal borohydrides may be used, including sodium, potassium, lithium, cesium, and rubidium borohydrides, but sodium, potassium or lithium borohydrides are preferred due to their greater availability and lesser cost.
  • the starting metal powder used in the process is the conventional powder used for the production of titanium, zirconium, tantalum, timgsten, molybdenum, or chromium objects by powder metallurgy.
  • the powder should have a mesh size of above 325 mesh, U.S. standard screen size, and should preferably have a mesh size between -100 and +200 mesh, though still coarser powder may be used.
  • the Starting metal powder should preferably have an oxygen content of 0.5% or less.
  • the alkali metal borohydride is thoroughly incorporated and mixed with this powder, as for example by milling.
  • the powder is then compacted into the form of a green briquette in the conventional manner, preferably using pressures to produce a density of about 60-80% of the theoretical, as for example pressures between 10 and tons per square inch.
  • the green briquettes are then trimmed or cut, as necessary, in the conventional manner and sintered in a high vacuum furnace at a temperature 3,166,833 Patented Jan. 26, 1965 of at least 1600 F.
  • temperatures of between 1800 and 2000 F. are preferably used
  • temperatures between about 2000 and 2500 F. are preferably used.
  • the vacuum in the furnace is preferably maintained at 1 to 2 microns Hg.
  • the preferable sintering time is about 4 hours, but as high as 24 hours or longer may be employed.
  • the heating time in hours may be calculated by multiplying the percentage of boron, added as borohydride, by 1 /2 to 2.
  • the alkali metal borohydride decomposes and reacts during the sintering,'liberating the alkali metal, which combines with the oxygen, carrying the same off and thus acting as a deoxidizing agent while the boron combines with the metal to form a stable boride.
  • the hydrogen is apparently liberated, and furthermore the overall hydrogen content of the metal is reduced because of the heating in a high vacuum.
  • the objects formed in accordance with the invention have improved mechanical properties, as well as chemical and wear-resistant characteristics.
  • Example 1 A quantity of sodium borohydride, sufficient to add about 2% by weight of boron, was mixed with zirconium metal powder having an oxygen content of 0.3%, and a mesh size between and +200 mesh. The powder was compacted in a die, at a pressure of about 20 tons per square inch, into the form of a small crucible having a density of about 70% of the theoretical. The crucible was trimmed to remove any jagged edges remaining after the compacting, and the green briquette was sintered in a vacuum furnace for about 4 hours at a temperature of about 2100 F. The crucible formed showed improved tensile strength and chemical resistance, as well as increased wear-resistance because of an increase in hardness. The metal of the crucible showed a reduced oxygen content of 0.07%
  • Example 2 Titanium metal powder of a mesh size between -200 and +200 mesh, and with an oxygen content of 0.25%, and a hydrogen content of 0.018% was milled With po tassium borohydride in an amount supplying about 3% boron, based on the titanium. The powder was then compacted by pressing in a die with punches into the form of a rocket nozzle. The pressure was sufficient to produce a density of about 70% of the theoretical. The green briquette was then trimmed to remove rough edges and imperfections, and was sintered in a vacuum furnace at a temperature of about 2200 F. for about 4 hours. The finished product showed an oxygen content of 0.05% and a hydrogen content of 0.009%. As compared with an identical object produced without the potassium boro hydride, it showed marked improvement (22%) in tensile strength.
  • Example 3 The above examples are repeated using, in turn, chromium, molybdenum, tantalum and tungsten powder, and lithium, cesium and rubidium borohydride, with the sintering being effected at a temperature between about 2000 and 2200 F. Improved products are obtained in each case as compared with the product produced in the identical manner but without the alkali metal borohydride.
  • the invention is particularly applicable for producing, for example, gears, bearings, cams, pump parts, turbine blades, valve parts, hydraulic equipment, jet engine parts, etc.
  • a powder material for powder metallurgy comprising a powder of a metal selected from the group consisting of titanium, zirconium, tantalum, tungsten, molybdenum and chromium, having a particle size above about 325 mesh and containing an alkali metal borohydride intimately admixed therewith in an amount of about 1-5% by weight boron.
  • a powderaccording to claim 8 having a mesh size between about and 200 mesh.
  • said powder containing an alkali'metal borohydride in an amount of about 15 by weight boron.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Powder Metallurgy (AREA)

Description

United States Patent O "we 3,166,833 PRODUCTION OF HEAVY METAL OBJECTS BY POWDER METALLURGY Alfred R. Globus, New York, N.Y., assignor to Consolidated Astronautics Inc, Long Island City, N.Y., a corporation of Delaware No Drawing. Filed May 2, 1962, Ser. No. 191,746 Claims. (Cl. 29-1825) This invention relates to improvements for the production of heavy metal objects by powder metallurgy. The invention more particularly relates to improvements in the process of forming metal objects from titanium, zirconium, tantalum, tungsten, molybdenum and chromium powders, to a novel powder composition used in such process, and to the object's formed by the process.
It is known to produce metal objects of titanium, zirconium, tantalum, tungsten, molybdenum and chromium by the powder metallurgy process. In accordance with this process, a powder of a metal of the aforementioned group is first compacted into the desired shape of the object to be formed, as for example by pressing in a die at pressures between 10 and 50 tons per square inch. The compacting solidifies the powder into what is referred to as a green briquette, which has sufficient structural strength to withstand the further treatment. After the compacting the green briquette may be trimmed or cut, as necessary, or otherwise finished. It is then sintered into the final object, preferably in a vacuum furnace.
One object of this invention is to improve the mechanical properties, as Well as the chemical and wearresistant characteristics of objects produced by the aforementioned process.
These and still further objects will become apparent from the following description:
In accordance with the invention I have discovered that the properties, such as the mechanical, chemical, and wear-resistant characteristics of the articles produced by the above mentioned process, may be improved if an alkali metal borohydride is admixed with the metal powder in an amount of about 1-5%, and preferably 1-3%, by weight, calculated as boron, prior to the compacting of the powder into the green briquette.
Any of the known alkali metal borohydrides may be used, including sodium, potassium, lithium, cesium, and rubidium borohydrides, but sodium, potassium or lithium borohydrides are preferred due to their greater availability and lesser cost.
The starting metal powder used in the process is the conventional powder used for the production of titanium, zirconium, tantalum, timgsten, molybdenum, or chromium objects by powder metallurgy. The powder, however, should have a mesh size of above 325 mesh, U.S. standard screen size, and should preferably have a mesh size between -100 and +200 mesh, though still coarser powder may be used. The use of the relatively coarser powder, as indicated above, assures the escape of the gas evolved from the alkali borohydride during the sintering, and thus prevents an eruption or even explosion of the piece, which could occur if the same were compacted with too high a density to allow such gas to escape.
The Starting metal powder should preferably have an oxygen content of 0.5% or less. The alkali metal borohydride is thoroughly incorporated and mixed with this powder, as for example by milling.
The powder is then compacted into the form of a green briquette in the conventional manner, preferably using pressures to produce a density of about 60-80% of the theoretical, as for example pressures between 10 and tons per square inch. The green briquettes are then trimmed or cut, as necessary, in the conventional manner and sintered in a high vacuum furnace at a temperature 3,166,833 Patented Jan. 26, 1965 of at least 1600 F. In connection with chromium, molybdenum, tantalum and tungsten, temperatures of between 1800 and 2000 F. are preferably used, and in connection with titanium and zirconium, temperatures between about 2000 and 2500 F. are preferably used. The vacuum in the furnace is preferably maintained at 1 to 2 microns Hg. The preferable sintering time is about 4 hours, but as high as 24 hours or longer may be employed. Generally, as a rule of thumb, the heating time in hours may be calculated by multiplying the percentage of boron, added as borohydride, by 1 /2 to 2.
Apparently the alkali metal borohydride decomposes and reacts during the sintering,'liberating the alkali metal, which combines with the oxygen, carrying the same off and thus acting as a deoxidizing agent while the boron combines with the metal to form a stable boride. The hydrogen is apparently liberated, and furthermore the overall hydrogen content of the metal is reduced because of the heating in a high vacuum. The objects formed in accordance with the invention have improved mechanical properties, as well as chemical and wear-resistant characteristics.
The following examples are given by way of illustration and not limitation:
Example 1 A quantity of sodium borohydride, sufficient to add about 2% by weight of boron, was mixed with zirconium metal powder having an oxygen content of 0.3%, and a mesh size between and +200 mesh. The powder was compacted in a die, at a pressure of about 20 tons per square inch, into the form of a small crucible having a density of about 70% of the theoretical. The crucible was trimmed to remove any jagged edges remaining after the compacting, and the green briquette was sintered in a vacuum furnace for about 4 hours at a temperature of about 2100 F. The crucible formed showed improved tensile strength and chemical resistance, as well as increased wear-resistance because of an increase in hardness. The metal of the crucible showed a reduced oxygen content of 0.07%
Example 2 Titanium metal powder of a mesh size between -200 and +200 mesh, and with an oxygen content of 0.25%, and a hydrogen content of 0.018% was milled With po tassium borohydride in an amount supplying about 3% boron, based on the titanium. The powder was then compacted by pressing in a die with punches into the form of a rocket nozzle. The pressure was sufficient to produce a density of about 70% of the theoretical. The green briquette was then trimmed to remove rough edges and imperfections, and was sintered in a vacuum furnace at a temperature of about 2200 F. for about 4 hours. The finished product showed an oxygen content of 0.05% and a hydrogen content of 0.009%. As compared with an identical object produced without the potassium boro hydride, it showed marked improvement (22%) in tensile strength.
Example 3 The above examples are repeated using, in turn, chromium, molybdenum, tantalum and tungsten powder, and lithium, cesium and rubidium borohydride, with the sintering being effected at a temperature between about 2000 and 2200 F. Improved products are obtained in each case as compared with the product produced in the identical manner but without the alkali metal borohydride.
The invention is particularly applicable for producing, for example, gears, bearings, cams, pump parts, turbine blades, valve parts, hydraulic equipment, jet engine parts, etc.
While the invention has been described in detail with reference to certain specific embodiments, various changes and modifications which fall within the spirit of the invention and scope of the appended claims will become apparent to the skilled artisan. The invention is therefore only intended to 'be limited by the appended claims or their equivalents, wherein I have endeavored to claim all inherent novelty.
I claim: a a
1 In the process for producing metal objects by powder metallurgy, in which a powder of a metal selected from the group consisting of titanium, zirconium, tantalum, tungsten, molybdenum and chromium, is compacted into shape and thereafter sintered, the improvement which comprises admixing an alkali metal borohydride with the powder in an amount of about 15% by weight boron prior to said compacting.
2. Improvement according to claim 1 in which said alkali metal borohydride is admixed in an amount of about 13% by weight boron.
3. Improvement according to claim 1 in which said powder has a mesh size above about 325 mesh.
4. Improvement according to claim 3 in which said powder has a mesh size between about 100 and 200 mesh.
5. Improvement according to claim 1 in which said compacting is effected to about 60-80% of the theoretical density.
6. Improvement according to claim 1 in which said sintering is eifected at a temperature between about 1800 and 2200 F. in a vacuum furnace.
7. A powder material for powder metallurgy comprising a powder of a metal selected from the group consisting of titanium, zirconium, tantalum, tungsten, molybdenum and chromium, having a particle size above about 325 mesh and containing an alkali metal borohydride intimately admixed therewith in an amount of about 1-5% by weight boron.
8. A powder according to claim 7'in which said alkali metal borohydride is present in an amount of about 1'3% boron.
9. A powderaccording to claim 8 having a mesh size between about and 200 mesh.
10. An article sintered from a compacted metal powder selected from the group consisting of titanium, zirconium, tantalum, tungsten, molybdenum and chromium,
said powder containing an alkali'metal borohydride in an amount of about 15 by weight boron.
References Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

1. IN THE PROCESS FOR PRODUCING METAL OBJECTS BY POWDER METALLURGY, IN WHICH A POWDER OF A METAL SELECTED FROM THE GROUP CONSISTING OF TITANIUM, ZIRCONIUM, TANTALUM, TUNGSTEN, MOLYBDENUM AND CHROMIUM, IS COMPACTED INTO SHAPE AND THEREAFTER SINTERED, THE IMPROVEMENT WHICH COMPRISES ADMIXING AN ALKALI METAL BOROHYDRIDE WITH THE POWDER IN AN AMOUNT OF ABOUT 1-5% BY WEIGHT BORON PRIOR TO SAID COMPACTING.
US191746A 1962-05-02 1962-05-02 Production of heavy metal objects by powder metallurgy Expired - Lifetime US3166833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US191746A US3166833A (en) 1962-05-02 1962-05-02 Production of heavy metal objects by powder metallurgy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US191746A US3166833A (en) 1962-05-02 1962-05-02 Production of heavy metal objects by powder metallurgy

Publications (1)

Publication Number Publication Date
US3166833A true US3166833A (en) 1965-01-26

Family

ID=22706782

Family Applications (1)

Application Number Title Priority Date Filing Date
US191746A Expired - Lifetime US3166833A (en) 1962-05-02 1962-05-02 Production of heavy metal objects by powder metallurgy

Country Status (1)

Country Link
US (1) US3166833A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3437526A (en) * 1962-08-27 1969-04-08 Asea Ab Sintered nickel boride electrode and fuel cell therewith
US3470030A (en) * 1965-06-21 1969-09-30 Asea Ab Method of manufacturing a porous electrode containing a boron compound
US3526485A (en) * 1968-03-23 1970-09-01 Feldmuehle Ag Metal filled bodies of sintered refractory oxides
US3947269A (en) * 1970-01-07 1976-03-30 Trw Inc. Boron-hardened tungsten facing alloy
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

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2735155A (en) * 1956-02-21 With an excess of boron
US2910357A (en) * 1956-02-09 1959-10-27 Nat Distillers Chem Corp Method of reducing metal halides
US2920360A (en) * 1956-10-03 1960-01-12 Westcott & Thomson Inc Apparatus for backing up a shell
US2936250A (en) * 1953-06-22 1960-05-10 Borolite Corp Cemented zirconium boride material having a protective chromium containing coating
US3052538A (en) * 1960-04-21 1962-09-04 Robert W Jech Titanium base alloys

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2735155A (en) * 1956-02-21 With an excess of boron
US2936250A (en) * 1953-06-22 1960-05-10 Borolite Corp Cemented zirconium boride material having a protective chromium containing coating
US2910357A (en) * 1956-02-09 1959-10-27 Nat Distillers Chem Corp Method of reducing metal halides
US2920360A (en) * 1956-10-03 1960-01-12 Westcott & Thomson Inc Apparatus for backing up a shell
US3052538A (en) * 1960-04-21 1962-09-04 Robert W Jech Titanium base alloys

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3437526A (en) * 1962-08-27 1969-04-08 Asea Ab Sintered nickel boride electrode and fuel cell therewith
US3470030A (en) * 1965-06-21 1969-09-30 Asea Ab Method of manufacturing a porous electrode containing a boron compound
US3526485A (en) * 1968-03-23 1970-09-01 Feldmuehle Ag Metal filled bodies of sintered refractory oxides
US3947269A (en) * 1970-01-07 1976-03-30 Trw Inc. Boron-hardened tungsten facing alloy
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

Similar Documents

Publication Publication Date Title
US3836355A (en) Steel powder containing phosphorus
US3749571A (en) Cold-pressed compositions
US2894838A (en) Method of introducing hard phases into metallic matrices
US3166833A (en) Production of heavy metal objects by powder metallurgy
US3120436A (en) Powdered metal article and method of making
US2526805A (en) Method of forming uranium carbon alloys
US3161949A (en) Refractory metal base alloys and method of making same
US3249410A (en) Process of making metal bonded diamond abrasive articles
US3278280A (en) Workable ruthenium alloy and process for producing the same
US2671953A (en) Metal body of high porosity
US2840891A (en) High temperature structural material and method of producing same
US2776468A (en) Ternary metal boride compositions
US3737290A (en) Sintered titanium alloy
US3357826A (en) Powder metallurgical production of chromium-containing alloys
US3196007A (en) Beryllium copper composition and method of producing green compacts and sintered articles therefrom
US3275564A (en) Process of fabrication of sintered compounds based on uranium and plutonium
US4407775A (en) Pressureless consolidation of metallic powders
US2902363A (en) Method of treating powdered metal
US3510276A (en) Sintered titanium carbide bodies
US2998641A (en) Titanium carbide-silver compositions
US2490570A (en) Pyrophoric alloys of lead and zirconium and sparking devices containing the same
US2909808A (en) Process of producing powdered or granular metallic material
US3167428A (en) Titanium powder metallurgy
US3497347A (en) Phosphorus containing iron powder
US2986807A (en) Metal bonded refractory