US3827865A - Fibered metal powders - Google Patents
Fibered metal powders Download PDFInfo
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- US3827865A US3827865A US00059555A US5955570A US3827865A US 3827865 A US3827865 A US 3827865A US 00059555 A US00059555 A US 00059555A US 5955570 A US5955570 A US 5955570A US 3827865 A US3827865 A US 3827865A
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- 229910052751 metal Inorganic materials 0.000 title abstract description 48
- 239000002184 metal Substances 0.000 title abstract description 47
- 239000000843 powder Substances 0.000 title abstract description 30
- 239000000835 fiber Substances 0.000 abstract description 47
- 238000000034 method Methods 0.000 abstract description 11
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 17
- 239000002131 composite material Substances 0.000 description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 14
- 229910052802 copper Inorganic materials 0.000 description 14
- 239000010949 copper Substances 0.000 description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 13
- 229910052715 tantalum Inorganic materials 0.000 description 13
- 238000002386 leaching Methods 0.000 description 10
- 239000003990 capacitor Substances 0.000 description 8
- 239000011159 matrix material Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000009792 diffusion process Methods 0.000 description 7
- 230000008901 benefit Effects 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 238000005482 strain hardening Methods 0.000 description 4
- 239000002887 superconductor Substances 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- 229910052718 tin Inorganic materials 0.000 description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000007596 consolidation process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- IYRDVAUFQZOLSB-UHFFFAOYSA-N copper iron Chemical compound [Fe].[Cu] IYRDVAUFQZOLSB-UHFFFAOYSA-N 0.000 description 2
- CIYRLONPFMPRLH-UHFFFAOYSA-N copper tantalum Chemical class [Cu].[Ta] CIYRLONPFMPRLH-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 239000010955 niobium Substances 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000003870 refractory metal Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 229910000951 Aluminide Inorganic materials 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- CFJRGWXELQQLSA-UHFFFAOYSA-N azanylidyneniobium Chemical compound [Nb]#N CFJRGWXELQQLSA-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- KAYZQFIFFVGBSR-UHFFFAOYSA-N bis(lambda2-stannanylidene)niobium Chemical compound [Nb].[Sn].[Sn] KAYZQFIFFVGBSR-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- WUUZKBJEUBFVMV-UHFFFAOYSA-N copper molybdenum Chemical compound [Cu].[Mo] WUUZKBJEUBFVMV-UHFFFAOYSA-N 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- KJSMVPYGGLPWOE-UHFFFAOYSA-N niobium tin Chemical compound [Nb].[Sn] KJSMVPYGGLPWOE-UHFFFAOYSA-N 0.000 description 1
- 229910000657 niobium-tin Inorganic materials 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- -1 titanium hydride Chemical compound 0.000 description 1
- 229910000048 titanium hydride Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
- 229910000634 wood's metal Inorganic materials 0.000 description 1
Images
Classifications
-
- 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
- B22F3/002—Manufacture of articles essentially made from metallic fibres
-
- 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
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
- Y10T428/12153—Interconnected void structure [e.g., permeable, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
- Y10T428/1216—Continuous interengaged phases of plural metals, or oriented fiber containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12424—Mass of only fibers
Definitions
- FIBERED METAL POWDERS Original Filed Bax-ch 29, 1967 2 Sheets-Sheet 1 POWDERS OF FIRST METAL vAOuuM IMPREGNATE MOLTEN WITH SECOND METAL ECOND METAL I g'gfi; 'fgg'g ELONGATE TO ROO' A V I I ORAw TO C ROLL TO B wIRE SHEET II DIFFUSION D REACTION (2) USE As V LEACH OUT COMPOSITE SECOND METAL I I 1 USE As USE AS METAL FELT COMPOSITE RE IMPREGNATE E r V (b) SEPARATE DIFFUSION A FIBERS REACTION Aug. 6, 1 7Q w.
- the present invention relates to metal fibers or filaments useful for a variety of purposes including capacitors, filters, structural reinforcement.
- the fibers are particularly of the class of hard metals having high strength and high temperature use capability (having at least 50% room temperature strength at 500 C.) and extraordinarily small diameter as on the order of a micron or less, while having continuous length of several times diameter and as high as ten inches.
- the invention relates to such filaments as separate entities, in loose bundles (i.e. a metal felt) or as incorporated in reinforced matrices and to the process of making them.
- the present invention involves as a principal object the production of metal fibers of sub-micron size by a new process which is capable of being used with high temperature metals such as tantalum.
- FIG. 1 is a block diagram of the process of the invention.
- FIG. 2 is a copy of a photomicrograph of a composite according to the invention.
- FIG. 3 is a copy of a photomicrograph of a metal felt according to the invention.
- the fibers of the invention are made and used by the following process described with reference to FIG. 1 which is a block diagram of the process.
- the metal may be any of tantalum, niobium, molybdenum, tungsten, iron or stainless steels, titanium, nickel, aluminum, chromium, beryllium, magnesium oxide, titanium hydride and fabricable aluminides and silicides.
- the invention would also be of particular utility and distinctly advantageous benefit in fibering other hard metal elements, compounds or alloys which have softening temperatures in excess of about 1000 C.
- the starting powder size is variable depending upon subsequent processing and reactivity of the powders.
- the invention has been practiced successfully for instance with tantalum powders as large as minus mesh and as small as a few microns diameter.
- the powder is consolidated into a compact by pressing and sintering or sintering in a mold.
- a melt of a second metal is provided in vacuum or inert atmosphere and the powder compact of the first metal is impregnated by dipping in the melt.
- the compact is degassed and purified to enhance its wettability and ductility.
- the second metal may be any of aluminum, copper, nickel, Woods metal, tin, indium, mercury, or any other metal which meets the following criteria with respect to the first metal under the conditions of impregnation:
- the impregnated compact is then worked down to an elongated rod form or the like e.g. plate or cylinder (round or rectangular cross section) by swaging or forging. During this process the adjacent particles of hard metal in the compact begin to form long fibers within the matrix of the second metal.
- rod or cylinder or plate may be used or fabricated into a useful product in any of the following ways:
- a rod can be drawn for several passes before rolling.
- a wire or sheet can be heated for diffusion reaction.
- a re-impregnated article can be used as a composite, with or without a diffusion reaction, or releached.
- fibers of alloys or compounds can be formed even though such alloys are too brittle to be fibered directly.
- Another alternative in the scope of the invention is to form a loose fiber bundle or separate fiber ((a) or (b) above) and expose it to an oxidizing or nitriding atmosphere.
- fibers of aluminum oxide or aluminum nitride can be made for use in reinforced composite structures.
- fibers of tantalum or niobium nitride can be made for use as superconductors.
- the fiber diameters are so small as to favor the formation of the above compounds in single crystal form which is especially desirable.
- each fiber is derived from a single powder particle and its length is dependent on the degree of diameter reduction. For instance, an 8 micron diameter powder particle fibered to 0.1 microns diameter will have a length of about one inch, a 30 micron diameter particle fibered to 0.1 microns diameter will have a length of about seventy inches. Further cold working to finer fiber diameters would increase the length. In most applications of the invention, useful fibers will have a length of ten times the diameter of the fiber or longer (as high as 10 times for extreme cases).
- the felts of the invention are characterized by substantial cross-linking by metallurgical bonds between tangentially contacting fibers corresponding in part to the bonds between powders in the original powder compact skeleton and corresponding in part to new bonds formed during cold working the impregnated compact down to an elongated article, the new bonds being essentially an extension or stretching out of the old bonds.
- FIG. 2 shows longitudinal section photomicrograph of a composite in the form of a wire of .039 inch diameter at 133 times magnification.
- the composite has elongated reinforcing tantalum fibers in a matrix of copper.
- the starting material for the fibered metal was coarse melting grade powder minus 12 and plus 60 mesh pressed at 18,000 p.s.i. and sintered at 2300 C. for one hour to produce a compact of 61% density.
- FIG. 3 shows a longitudinal section photomicrograph of a tantalum metal felt, encapsulated in a molding resin for microscope examination, at 266 times magnification.
- the tantalum was made from nominal 8 micron diameter powders (minus mesh and plus 5 microns) which was consolidated to a compact of about 50% density and then impregnated with copper and then swaged to rod and rolled to sheet after which the copper was leached out in a nitric acid bath. Upon leaching the metal felt ballooned up to several times its original volume.
- Fibers obtained from rod or wire are found to be essentially circular in cross-section and fibers obtained from sheet are found to be rectangular in cross-section.
- the term diameter as used herein refers to diameter of a circle or width of a rectangle.
- EXAMPLE 1 A mold was filled with tantalum powder of about 8 micron nominal diameter (-100 mesh and plus 5 microns) and the powder was sintered in the mold at 1500 C. for 20 minutes to form a green compact. Then sintering was completed by removing the compact from the mold and heating at 2300 C. for one hour to complete consolidation of the powder. The density of the compact was 8.22 gms./cc. or 49.5% of theoretical density. The compact was vacuum impregnated with copper by dipping in a molten copper bath at 117 0 C. for 5 minutes under a vacuum of about l0 torr. The impregnated compact (.35 inches diameter by 4 inches long) was enclosed in an iron pipe and then swaged to .125 inches diameter.
- the jacket was removed and the rod was then further swaged to .080 inches diameter. After swaging, the rod was then leached in nitric acid to remove the copper. The leached compact left a bundle of interwoven tantalum fibers in the form of a felt.
- Thi metal felt was rinsed and removed from the leach bath.
- the felt was anodized and formed into a capacitor anode and tested for capacitor properties in a wet electrolyte.
- the formation voltage was 200 volts and the capacitance was 30.6 microfarads and on a specific weight basis 6120 microfarad-volts per gram.
- the felt had a dissipation factor of 32.19% making it an over-all operable capacitor anode.
- Tantalum felts were made as in Example 1 but with the difference that the compact was rolled to .010 inch thick sheet before leaching. The felt exhibited a vigorous swelling up with a volume increase and density decrease of 5-10 times during leaching and floated on the leaching bath. A capacitor formed from the felt at volts had 7965 microfarad-volts per gram specific capacitance.
- EXAMPLE 3 Felts were made as in Examples 1 and 2 with the difference that consolidation of the tantalum powder was accomplished by pressing at 18,000 p.s.i. and then sintering at 2250 C. for one hour and that some rods were drawn to wire. Densities of 60-80% of theoretical were obtained in the original compact. Upon leaching the final composite article of this type, the felt did not swell up. However, high values of capacitance were still obtained indicating substantial formation of new surface as in Examples 1 and 2 (surface enhancement of about 2.5 times).
- EXAMPLE 4 Several fibers from the felts of Examples 1 and 2 were encapsulated in epoxy resin and measured to yield an individual fiber diameter indication of .0002 cm. diameter. The Example 2 fibers were 5 to 10 times as long as the diameter of the fiber; the Example 1 fibers were continuous over much longer lengths.
- EXAMPLE 5 Several compacts made essentially as in Examples 1 and 2 were rolled or drawn to the final sizes indicated below for testing of their composite material properties. These tantalum reinforced copper composites were in the form of .020 inch diameter wire and as .010 inch thick sheet, both as worked and after being heated (350 C. for 1 hour to anneal the copper). The results for these specimens and for comparison, the properties of tantalum and copper, per se, are given in Table 1:
- EXAMPLE 6 A molybdenum-copper composite was made and tested in the same manner as the tantalum-copper composites of Example 5 and formed into .06 and .08 in. wire which displayed ultimate tensile strengths of 81,700 and 108,000 p.s.i., respectively.
- EXAMPLE 8 Iron powder of 270 mesh was mold sintered at 800 C. for 20 minutes and then finally sintered at 1150 C. for 1 hour to a density of 3.45 grams per cc. (45% theoretical) impregnated as above and worked to .025 inch wire and leached to form a fibrous bundle of iron fibers .0015 cm. diameter, quite continuous and having a surface layer of copper-iron alloy overlaid by residual copper but with a substantial core of pure iron in the fibers.
- the best mode of using the invention is believed to be selection of a tantalum-copper pair to produce a tantalum felt suitable for use as a capacitor anode.
- surface enhancement and work hardening it is a further useful advantage of the invention that it may be practiced if desired, with relatively coarse melting grade tantalum powder in the original compact rather than the conventional fine grain capacitor grade powder and the desired surface area increase can be obtained in the fiberpowder.
- a further useful aspect of the invention is the above described feature of swelling When the original compact is made in low density (4060% theoretical) and/or when a high degree of working is put into the composite. The swelling of the metal felt, when utilized makes it easier to refill the felt with an anodizing medium and electrolyte.
- niobium-tin pair could be utilized to obtain interconnected niobium fibers in a tin matrix with a better degree of interconnection between fibers than is obtainable in the process of the above described Speidel patent. Then .the composite could be heated for diffusion reaction to form a niobium stannide superconductor subsequent to which residual tin would be leached out and replaced with copper by re-impregnation to provide a higher conductivity matrix for electrical stability of the superconductor.
- a high degree of control of the final product is obtainable. For instance, use of coarse melt grade powders or low density consolidation of the original compact (40- 60%) tend to limit the number of cross-link bonds formed between fibers thereby enhancing the swelling up of fibers upon leaching the matrix metal and enhancing the ease of separation of fibers.
- the felt having enhanced internal surface area compared to the original porous compact.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Powder Metallurgy (AREA)
Abstract
HARD METAL POWDER COMPACTS ARE SINTERED AND IMPREGNATED WITH A SOFTER METAL. THE COMPACTS ARE REDUCED TO ROD, WIRE OF SHEET. IN THE PROCESS FINE FIBERS OF THE HARD METAL POWDER ARE FORMED.
Description
8- 1974 R. W. DOUGLASS ,8*?,65
FIBERED METAL POWDERS Original Filed Bax-ch 29, 1967 2 Sheets-Sheet 1 POWDERS OF FIRST METAL vAOuuM IMPREGNATE MOLTEN WITH SECOND METAL ECOND METAL I g'gfi; 'fgg'g ELONGATE TO ROO' A V I I ORAw TO C ROLL TO B wIRE SHEET II DIFFUSION D REACTION (2) USE As V LEACH OUT COMPOSITE SECOND METAL I I 1 USE As USE AS METAL FELT COMPOSITE RE IMPREGNATE E r V (b) SEPARATE DIFFUSION A FIBERS REACTION Aug. 6, 1 7Q w. DOUGLASS FIBERED METAL POWDERS Original Filed Each 29, 1967 2 Sheets-Sheet a I NVENTOR WARD W 0045 atent Patented Aug. 6, 1974 1m. (:1. 1122f 3/26 U.S. c1. 29-192 1 Clalm ABSTRACT OF THE DISCLOSURE Hard metal powder compacts are sintered and impregnated with a softer metal. The compacts are reduced to rod, wire or sheet. In the process fine fibers of the hard metal powder are formed.
This application is a division of my earlier application, Ser. No. 807,129, filed Mar. 13, 1969, now abandoned, which was in turn a continuation of my application Ser. No. 626,773, filed Mar. 29, 1967, now abandoned. Other related copending applications are Ser. No. 74,962, filed Sept. 24, 1970, now US. Pat. 3,729,794, Ser. No. 869,404, filed Mar. 13, 1969, now US. Pat. 3,681,063, as a division of 626,773, Ser. No. 839,024, filed July 3, 1969, now abandoned, as a division and continuation-in-part of Ser. No. 626,773 and 807,129 and 869,404, now US. Pat. 3,681,063, and Ser. No. 196,812, filed Nov. 8, 1971, now US. Pat. 3,742,369, as a division of said Ser. No. 839,024, now abandoned, Ser. No. 199,065, filed Nov. 15, 1971 as a continuation of Ser. No. 839,024, now US. Pat. 3,740,- 834, also is a related copending application.
The present invention relates to metal fibers or filaments useful for a variety of purposes including capacitors, filters, structural reinforcement. The fibers are particularly of the class of hard metals having high strength and high temperature use capability (having at least 50% room temperature strength at 500 C.) and extraordinarily small diameter as on the order of a micron or less, while having continuous length of several times diameter and as high as ten inches.
The invention relates to such filaments as separate entities, in loose bundles (i.e. a metal felt) or as incorporated in reinforced matrices and to the process of making them.
BACKGROUND Metal felts and fine metal wires or fibers or filaments used in such felts are known in the art as indicated in Pats. 2,903,787 and 3,178,280. These felts are made from standard cold reduced metal wires which are limited to minimum diameters on the order of .001.010 inches or less by the inherent vulnerabilitites of standard wire drawing processes or from shavings from metal blocks which are characterized by many surface defects. Much finer wires can be made by extrusion as indicated in Pat. 3,199,- 331 to Allen. But production by this process is substantially limited as a practical matter to low melting metals and alloys (e.g. tin). Other prior art of interest is Buehler, US. Pat. 3,124,455 and the Speidel, Levy and Wulfi' work cited below.
The present invention involves as a principal object the production of metal fibers of sub-micron size by a new process which is capable of being used with high temperature metals such as tantalum.
It is a further object of the invention to provide an economical method of making metal fibers on the order of 10 microns or less, and preferably sub-micron, in diameter with a single series of processing steps; i.e. free of the expensive supplementary or recycling processing involved, for instance, in Speidel, US. Pat. 3,256,118, Levy, US. Pat. 3,029,496 and Wulff, January 1966 Journal of Applied Physics, p. 5.
It is a further object of the invention to provide work hardened fibers by a production process free of the need for intermediate anneals as required in the above patents of Allen and Levy, and for use in composites providing a high degree of work hardening in final product form, with or without a final low anneal for stress relief of the matrix only.
Other objects, features and advantages of the present invention will in part be obvious and will in part appear hereinafter.
DESCRIPTION The invention is now described with respect to typical specific embodiments thereof and with reference to the accompanying drawings wherein:
FIG. 1 is a block diagram of the process of the invention.
FIG. 2 is a copy of a photomicrograph of a composite according to the invention.
FIG. 3 is a copy of a photomicrograph of a metal felt according to the invention.
The fibers of the invention are made and used by the following process described with reference to FIG. 1 which is a block diagram of the process. First, powders of the metal to be fibered are obtained. The metal may be any of tantalum, niobium, molybdenum, tungsten, iron or stainless steels, titanium, nickel, aluminum, chromium, beryllium, magnesium oxide, titanium hydride and fabricable aluminides and silicides. The invention would also be of particular utility and distinctly advantageous benefit in fibering other hard metal elements, compounds or alloys which have softening temperatures in excess of about 1000 C. The starting powder size is variable depending upon subsequent processing and reactivity of the powders. The invention has been practiced successfully for instance with tantalum powders as large as minus mesh and as small as a few microns diameter. The powder is consolidated into a compact by pressing and sintering or sintering in a mold. Then a melt of a second metal is provided in vacuum or inert atmosphere and the powder compact of the first metal is impregnated by dipping in the melt. During both the sintering and impregnating steps the compact is degassed and purified to enhance its wettability and ductility.
The second metal may be any of aluminum, copper, nickel, Woods metal, tin, indium, mercury, or any other metal which meets the following criteria with respect to the first metal under the conditions of impregnation:
(1) readily wet the skeleton structure of the sintered compact of the first metal; (2) not alloy extensively with the first metal;
(3) have similar hardness and fabrication characteristics to the extent necessary for co-working;
(4) be easily removable from the compact by chemical or thermal means.
The impregnated compact is then worked down to an elongated rod form or the like e.g. plate or cylinder (round or rectangular cross section) by swaging or forging. During this process the adjacent particles of hard metal in the compact begin to form long fibers within the matrix of the second metal.
At this point, the rod or cylinder or plate may be used or fabricated into a useful product in any of the following ways:
A(1)-Removing the matrix metal and (a) using directly as a filter or with further fabrication as a capacitor (b) separating out individual fibers (c) re-impregnating the fibered article A-(2)--Using the rod directly as a composite structural element B-Rolling the rod to sheet prior to 1) or (2) above CDrawing the rod to wire prior to (1) or (2) above DHeating the rod for diffusion reaction between the hard metal fibers and the matrix metal prior to (l) or (2) above.
Several permutations of the foregoing can be made. For instance a rod can be drawn for several passes before rolling. A wire or sheet can be heated for diffusion reaction. Similarly a re-impregnated article can be used as a composite, with or without a diffusion reaction, or releached. With diffusion reactions, fibers of alloys or compounds can be formed even though such alloys are too brittle to be fibered directly. Another alternative in the scope of the invention is to form a loose fiber bundle or separate fiber ((a) or (b) above) and expose it to an oxidizing or nitriding atmosphere. In this way fibers of aluminum oxide or aluminum nitride can be made for use in reinforced composite structures. Also fibers of tantalum or niobium nitride can be made for use as superconductors. In these applications it is of special interest that the fiber diameters are so small as to favor the formation of the above compounds in single crystal form which is especially desirable.
The fibers of the invention are characterized in that each fiber is derived from a single powder particle and its length is dependent on the degree of diameter reduction. For instance, an 8 micron diameter powder particle fibered to 0.1 microns diameter will have a length of about one inch, a 30 micron diameter particle fibered to 0.1 microns diameter will have a length of about seventy inches. Further cold working to finer fiber diameters would increase the length. In most applications of the invention, useful fibers will have a length of ten times the diameter of the fiber or longer (as high as 10 times for extreme cases).
The felts of the invention are characterized by substantial cross-linking by metallurgical bonds between tangentially contacting fibers corresponding in part to the bonds between powders in the original powder compact skeleton and corresponding in part to new bonds formed during cold working the impregnated compact down to an elongated article, the new bonds being essentially an extension or stretching out of the old bonds.
FIG. 2 shows longitudinal section photomicrograph of a composite in the form of a wire of .039 inch diameter at 133 times magnification. The composite has elongated reinforcing tantalum fibers in a matrix of copper. The starting material for the fibered metal was coarse melting grade powder minus 12 and plus 60 mesh pressed at 18,000 p.s.i. and sintered at 2300 C. for one hour to produce a compact of 61% density.
FIG. 3 shows a longitudinal section photomicrograph of a tantalum metal felt, encapsulated in a molding resin for microscope examination, at 266 times magnification. The tantalum was made from nominal 8 micron diameter powders (minus mesh and plus 5 microns) which was consolidated to a compact of about 50% density and then impregnated with copper and then swaged to rod and rolled to sheet after which the copper was leached out in a nitric acid bath. Upon leaching the metal felt ballooned up to several times its original volume.
Fibers obtained from rod or wire are found to be essentially circular in cross-section and fibers obtained from sheet are found to be rectangular in cross-section. The term diameter as used herein refers to diameter of a circle or width of a rectangle.
The practice of the invention is further illustrated by the following non-limiting Examples.
EXAMPLE 1 A mold was filled with tantalum powder of about 8 micron nominal diameter (-100 mesh and plus 5 microns) and the powder was sintered in the mold at 1500 C. for 20 minutes to form a green compact. Then sintering was completed by removing the compact from the mold and heating at 2300 C. for one hour to complete consolidation of the powder. The density of the compact was 8.22 gms./cc. or 49.5% of theoretical density. The compact was vacuum impregnated with copper by dipping in a molten copper bath at 117 0 C. for 5 minutes under a vacuum of about l0 torr. The impregnated compact (.35 inches diameter by 4 inches long) was enclosed in an iron pipe and then swaged to .125 inches diameter. The jacket was removed and the rod was then further swaged to .080 inches diameter. After swaging, the rod was then leached in nitric acid to remove the copper. The leached compact left a bundle of interwoven tantalum fibers in the form of a felt.
Thi metal felt was rinsed and removed from the leach bath. The felt was anodized and formed into a capacitor anode and tested for capacitor properties in a wet electrolyte. The formation voltage was 200 volts and the capacitance was 30.6 microfarads and on a specific weight basis 6120 microfarad-volts per gram. The felt had a dissipation factor of 32.19% making it an over-all operable capacitor anode.
EXAMPLE 2 Tantalum felts were made as in Example 1 but with the difference that the compact was rolled to .010 inch thick sheet before leaching. The felt exhibited a vigorous swelling up with a volume increase and density decrease of 5-10 times during leaching and floated on the leaching bath. A capacitor formed from the felt at volts had 7965 microfarad-volts per gram specific capacitance.
EXAMPLE 3 Felts were made as in Examples 1 and 2 with the difference that consolidation of the tantalum powder was accomplished by pressing at 18,000 p.s.i. and then sintering at 2250 C. for one hour and that some rods were drawn to wire. Densities of 60-80% of theoretical were obtained in the original compact. Upon leaching the final composite article of this type, the felt did not swell up. However, high values of capacitance were still obtained indicating substantial formation of new surface as in Examples 1 and 2 (surface enhancement of about 2.5 times).
EXAMPLE 4 Several fibers from the felts of Examples 1 and 2 were encapsulated in epoxy resin and measured to yield an individual fiber diameter indication of .0002 cm. diameter. The Example 2 fibers were 5 to 10 times as long as the diameter of the fiber; the Example 1 fibers were continuous over much longer lengths.
EXAMPLE 5 Several compacts made essentially as in Examples 1 and 2 were rolled or drawn to the final sizes indicated below for testing of their composite material properties. These tantalum reinforced copper composites were in the form of .020 inch diameter wire and as .010 inch thick sheet, both as worked and after being heated (350 C. for 1 hour to anneal the copper). The results for these specimens and for comparison, the properties of tantalum and copper, per se, are given in Table 1:
TABLE 1 Example 5 Ultimate tensile sample: strength, p.s.i.
(a) .01.020 inch diameter wire as worked 160,000195,000 (b) Wire with stress relief 150,000-172,000
(c) Sheet, as worked 99,000-127,000
(d) Sheet, stress relieved 93,000 (e) Pure tantalum, as worked (.005 and .015 inch thick sheet) 104,000-116,000 (f) Pure copper, as worked (.005 and .015 inch thick sheet) 59,000-60,500
EXAMPLE 6 A molybdenum-copper composite was made and tested in the same manner as the tantalum-copper composites of Example 5 and formed into .06 and .08 in. wire which displayed ultimate tensile strengths of 81,700 and 108,000 p.s.i., respectively.
EXAMPLE 7 Tantalum felts made as in Examples 4 and 2 were tested for tensile strength after leaching out the copper. The results are in Table 2.
TABLE 2 Ultimate tensile Example sample: strength, p.s.i. (a) .01 in. sheet 114,700 (b) .04 in. wire 90,000
EXAMPLE 8 Iron powder of 270 mesh was mold sintered at 800 C. for 20 minutes and then finally sintered at 1150 C. for 1 hour to a density of 3.45 grams per cc. (45% theoretical) impregnated as above and worked to .025 inch wire and leached to form a fibrous bundle of iron fibers .0015 cm. diameter, quite continuous and having a surface layer of copper-iron alloy overlaid by residual copper but with a substantial core of pure iron in the fibers.
' EXAMPLE 9 Before leaching, the iron-copper composite Wire of Example 8 was tested for tensile strength and this was found to be 160,000 p.s.i.
EXAMPLE 10 Leaching experiments were conducted and a solution of five parts ammonium hydroxide in one part hydrogen peroxide was found to be superior to nitric acid for selectively leaching copper from the iron to free the iron fibers from the composites.
The best mode of using the invention is believed to be selection of a tantalum-copper pair to produce a tantalum felt suitable for use as a capacitor anode. In addition to the above indicated advantages of ease of processing, surface enhancement and work hardening it is a further useful advantage of the invention that it may be practiced if desired, with relatively coarse melting grade tantalum powder in the original compact rather than the conventional fine grain capacitor grade powder and the desired surface area increase can be obtained in the fiberpowder. A further useful aspect of the invention is the above described feature of swelling When the original compact is made in low density (4060% theoretical) and/or when a high degree of working is put into the composite. The swelling of the metal felt, when utilized makes it easier to refill the felt with an anodizing medium and electrolyte.
The extension to other species of the above advantages and variations in processing and still other advantages and variations will be obvious to those skilled in the art from the description herein. For instance, a niobium-tin pair could be utilized to obtain interconnected niobium fibers in a tin matrix with a better degree of interconnection between fibers than is obtainable in the process of the above described Speidel patent. Then .the composite could be heated for diffusion reaction to form a niobium stannide superconductor subsequent to which residual tin would be leached out and replaced with copper by re-impregnation to provide a higher conductivity matrix for electrical stability of the superconductor.
A high degree of control of the final product is obtainable. For instance, use of coarse melt grade powders or low density consolidation of the original compact (40- 60%) tend to limit the number of cross-link bonds formed between fibers thereby enhancing the swelling up of fibers upon leaching the matrix metal and enhancing the ease of separation of fibers.
For superconductor applications it is particularly desirable to use a fine grain powder and form the original compact to a higher density for forming maximum crosslinks between fibers.
Still other applications within the scope of the present invention will be apparent to those skilled in the art when aided by the foregoing description. The description is therefore intended to be read as illustrative and not in a limiting sense.
What is claimed is:
1. A felt of refractory metal fibers which are interconnected to each other by spaced metallurgical bond crosslinks,
as produced by impregnating a sintered refractory metal powder porous compact having powder-to-powder metallurgical bond cross-links between powder particles with a second metal in fluid form solidifying the second metal working the impregnated compact down to an elongated article to elongate the metal powders to fibers and to elongate the bonds and then removing the second metal,
to thereby produce an elongated felt product having a characteristic direction of elongation with interconnected fibers being therein which are similarly elongated with each fiber being derived from a single powder particle and the cross-links being derived in part from original powder cross-links,
the felt having enhanced internal surface area compared to the original porous compact.
References Cited UNITED STATES PATENTS 2,627,531 2/1953 Vogt 136-20 2,972,554 2/1961 Muskat et al. 11776 3,029,496 4/1962 Levi 29419 X 3,127,668 4/1964 Troy 29182 3,254,189 5/1966 Evaniscko, et al. 200166 C 3,310,387 3/1967 Sump et al 29-182 X 3,087,233 4/1963 Turnbull 29182 3,337,337 8/1967 Weeton et al 204 ALLEN B. CURTIS, Primary Examiner O. F. CRUTCHFIELD, Assistant Examiner
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US00059555A US3827865A (en) | 1969-03-13 | 1970-07-30 | Fibered metal powders |
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US80712969A | 1969-03-13 | 1969-03-13 | |
US00059555A US3827865A (en) | 1969-03-13 | 1970-07-30 | Fibered metal powders |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4502884A (en) * | 1983-10-27 | 1985-03-05 | Cabot Corporation | Method for producing fiber-shaped tantalum powder and the powder produced thereby |
US5217526A (en) * | 1991-05-31 | 1993-06-08 | Cabot Corporation | Fibrous tantalum and capacitors made therefrom |
US5245514A (en) * | 1992-05-27 | 1993-09-14 | Cabot Corporation | Extruded capacitor electrode and method of making the same |
US5264293A (en) * | 1992-01-02 | 1993-11-23 | General Electric Company | Composite structure with NbTiHf alloy matrix and niobium base metal |
US5277990A (en) * | 1992-01-02 | 1994-01-11 | General Electric Company | Composite structure with NbTiAl and high Hf alloy matrix and niobium base metal reinforcement |
US5304427A (en) * | 1992-07-02 | 1994-04-19 | General Electric Company | Composite structure with NBTIA1CRHF alloy matrix and niobium base metal reinforcement |
-
1970
- 1970-07-30 US US00059555A patent/US3827865A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4502884A (en) * | 1983-10-27 | 1985-03-05 | Cabot Corporation | Method for producing fiber-shaped tantalum powder and the powder produced thereby |
US5217526A (en) * | 1991-05-31 | 1993-06-08 | Cabot Corporation | Fibrous tantalum and capacitors made therefrom |
US5306462A (en) * | 1991-05-31 | 1994-04-26 | Cabot Corporation | Fibrous tantalum and capacitors made therefrom |
US5264293A (en) * | 1992-01-02 | 1993-11-23 | General Electric Company | Composite structure with NbTiHf alloy matrix and niobium base metal |
US5277990A (en) * | 1992-01-02 | 1994-01-11 | General Electric Company | Composite structure with NbTiAl and high Hf alloy matrix and niobium base metal reinforcement |
US5245514A (en) * | 1992-05-27 | 1993-09-14 | Cabot Corporation | Extruded capacitor electrode and method of making the same |
US5304427A (en) * | 1992-07-02 | 1994-04-19 | General Electric Company | Composite structure with NBTIA1CRHF alloy matrix and niobium base metal reinforcement |
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