US3918998A - Method for producing superconducting wire and products of the same - Google Patents
Method for producing superconducting wire and products of the same Download PDFInfo
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- US3918998A US3918998A US342895A US34289573A US3918998A US 3918998 A US3918998 A US 3918998A US 342895 A US342895 A US 342895A US 34289573 A US34289573 A US 34289573A US 3918998 A US3918998 A US 3918998A
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 239000011159 matrix material Substances 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 46
- 239000002131 composite material Substances 0.000 claims abstract description 40
- 229910000906 Bronze Inorganic materials 0.000 claims abstract description 26
- 239000002887 superconductor Substances 0.000 claims abstract description 25
- 239000010974 bronze Substances 0.000 claims abstract description 24
- 238000009792 diffusion process Methods 0.000 claims abstract description 18
- 239000010955 niobium Substances 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 16
- 239000000463 material Substances 0.000 claims abstract description 14
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 13
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 11
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 10
- 239000002184 metal Substances 0.000 claims abstract description 10
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052718 tin Inorganic materials 0.000 claims abstract description 9
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 8
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 8
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims description 14
- 238000005275 alloying Methods 0.000 claims description 10
- 229910000765 intermetallic Inorganic materials 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims 2
- 229910000657 niobium-tin Inorganic materials 0.000 claims 1
- 229910000999 vanadium-gallium Inorganic materials 0.000 claims 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 abstract description 10
- 238000000137 annealing Methods 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- 239000010949 copper Substances 0.000 description 11
- 239000000314 lubricant Substances 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 239000012300 argon atmosphere Substances 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910002804 graphite Inorganic materials 0.000 description 5
- 239000010439 graphite Substances 0.000 description 5
- 238000005482 strain hardening Methods 0.000 description 5
- 238000005491 wire drawing Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910020012 Nb—Ti Inorganic materials 0.000 description 2
- 238000005253 cladding Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- -1 e.g. Inorganic materials 0.000 description 2
- 239000001307 helium Substances 0.000 description 2
- 229910052734 helium Inorganic materials 0.000 description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 2
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910001281 superconducting alloy Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002470 thermal conductor Substances 0.000 description 2
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- 229920006384 Airco Polymers 0.000 description 1
- LFVLUOAHQIVABZ-UHFFFAOYSA-N Iodofenphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(I)C=C1Cl LFVLUOAHQIVABZ-UHFFFAOYSA-N 0.000 description 1
- 229910020018 Nb Zr Inorganic materials 0.000 description 1
- 229910001275 Niobium-titanium Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010622 cold drawing Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- ZYTNDGXGVOZJBT-UHFFFAOYSA-N niobium Chemical compound [Nb].[Nb].[Nb] ZYTNDGXGVOZJBT-UHFFFAOYSA-N 0.000 description 1
- RJSRQTFBFAJJIL-UHFFFAOYSA-N niobium titanium Chemical compound [Ti].[Nb] RJSRQTFBFAJJIL-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
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- 238000012545 processing Methods 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N60/00—Superconducting devices
- H10N60/01—Manufacture or treatment
- H10N60/0184—Manufacture or treatment of devices comprising intermetallic compounds of type A-15, e.g. Nb3Sn
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S505/00—Superconductor technology: apparatus, material, process
- Y10S505/80—Material per se process of making same
- Y10S505/812—Stock
- Y10S505/814—Treated metal
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S505/00—Superconductor technology: apparatus, material, process
- Y10S505/80—Material per se process of making same
- Y10S505/815—Process of making per se
- Y10S505/822—Shaping
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S505/00—Superconductor technology: apparatus, material, process
- Y10S505/825—Apparatus per se, device per se, or process of making or operating same
- Y10S505/884—Conductor
- Y10S505/887—Conductor structure
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S505/00—Superconductor technology: apparatus, material, process
- Y10S505/825—Apparatus per se, device per se, or process of making or operating same
- Y10S505/917—Mechanically manufacturing superconductor
- Y10S505/918—Mechanically manufacturing superconductor with metallurgical heat treating
- Y10S505/919—Reactive formation of superconducting intermetallic compound
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49014—Superconductor
Definitions
- ABSTRACT A method for producing a composite superconducting wire including one or more strands of high-field Type 11 superconductor embedded in a conductive matrix of normal material and the product of the said method.
- a composite body is prepared which includes a matrix in which are embedded one or more rods of a metal which is capable of forming a high-field Type II superconductor upon high temperature extruded to an intermediate diameter. and then is hot drawn to a final diameter at temperatures exceeding about 100C. by multiple passes through drawing dies. the composite being reduced in crosssectional area approximately 15 to 2092 per draw. in a preferred mode of practicing the invention.
- the rods comprise vanadium or niobium. with the matrix being respeo tively gallium-bronze or tin-bronze. and the supercoir ductive strands being formed by high temperature diffusion of the gallium or tin into the rods subsequent to drawing.
- Composite superconducting wire characterized by multiple longitudinally extending strands of high-field superconducting alloy in a surrounding matrix of copper or similar good thermal conductor, has found increasing application for use in the coils of superconducting magnets capable of producing extremely high magnetic fields.
- Composite superconducting wire of the foregoing type is typically produced by initial preparation of a billet comprised of a copper extrusion can which contains a plurality of close-packed hexagonally-formed rod inserts.
- Each such rod insert may typically consist of a central round rod of a Type ll superconductor, such as a niobium-titanium alloy, surrounded by one or more concentric tubes of high purity OFHC copper, the unit being drawn to a cohesive hexagonal bar before insertion into the extrusion can.
- the can containing the packed rods is suitably sealed at its ends and thereupon subjected to extrusion or swaging and drawing opera tions, which gradually reduce the diameter of the billet 1 and of the contained inserts.
- the final very small diameter fine wire achieved by this technique contains the individual strands of the superconductor alloy in the surrounding copper matrix.
- the drawing operations cited are, for reasons to be set forth below, conducted at room temperature, and during the course of such mechanical working of the said billet, annealing may be required between draws, in order to remove the effects of cold work and maintain the required ductility for additional reduction in area.
- the billet is appropriately reduced, in a manner similar to that indicated for the Nb-Ti composite wire, and after the desired fine diameter composite wire is achieved, the resultant product is subjected to a prolonged heating schedule which serves to diffuse the gallium or tin into the central conductor to form the desired superconducting alloy thereat.
- the Lorentz force acting on a flux line is such that if such line is not pinned to the wire, it will start to move, generating localized heating which may initiate transition to the normal state.
- lattice imperfections introduced by plastic deformation, and inhomogeneities in alloy composition are capable of providing pinning sites that restrain movement of the flux lines.
- Cold-working techniques utilized in accordance with the foregoing processes serve to generate the desired lattice imperfections thereby providing pinning sites.
- the rods of the composite body are an alloy-type material, such as Nb-Zr or Nb-Ti, encased in a pure copper matrix
- the requirements for annealing are not too stringent.
- intermetallic compounds such as V Ga or Nb sn
- the Ga-bronze or Snbronze matrices present in the composites being drawn work-harden very rapidly. Therefore, the composite being worked will typically require intermediate an nealing after each two or three draws or every 40% reduction in cross-sectional area where cold-drawing is indeed utilized.
- the complex process of producing small diameter multifllament superconducting wire of which the annealing is but a part includes the steps of wire-drawing, placing the wire in an annealing furnace, annealing the wire in an inert atmosphere for a period of time, cooling the wire in a manner to prevent surface oxidation, stringing the annealed wire through a wire-drawing machine, drawing the wire, and then repeating the entire operation after the material has work hardened. Accordingly, it will be appreciated that the time required where annealing must be effected every two or three draws, together with the attendant expense, renders a process such as this completely economically prohibitive for practical production operations.
- a composite billet is initially formed, consisting of a conductive matrix of normal material in which are embedded one or more rods of a metal which is capable of forming a high-field Type II superconductor upon high temperature reac tion with a component of said matrix.
- the metallic rods are embedded in a matrix of copper, or other good thermal conductor such as silver or gold, containing in alloy the second element of the superconducting strands to be formed.
- the composite billet is extruded to an intermediate diameter, and thereafter drawn at temperatures over about lC and typically in the ap proximate range of l00 to 300C, to a final diameter, by reducing the cross-sectional area approximately -20% per draw.
- the upper temperature limit is controlled by the stability of the wire drawing lubricant and ultimately by oxidation of the surface of the wire.
- high temperature lubricants such as molybdenum disulfide or graphite, and an inert gas shield
- the high-field superconductors such as the in termetallic compounds V Ga and Nb Sn, are formed after drawing by high temperature reaction and diffusion.
- the drawing process may be effectively carried out without frequent intermediate annealing: in general such an anneal is required not more frequently than every 10 to 12 draws.
- a pro-annealed ll0-strand vanadium in Ga-bronze matrix wire (l4.85% Ga overall) can be hot-drawn from 57 to 13 mils at 218C with only one additional intermediate anneal.
- the resultant product is found to be essentially equivalent to wire formed from the same billet where such billet is cold-drawn.
- the initial stages of the method in accordance with the present invention may be substantially identical with methodology utilized in the prior art for preparation of composite superconducting wire.
- the primary requirement for the billet is that it include a conductive matrix of normal material which encases or surrounds longitudinally extending rods of a material which is capable of forming the desired high-field Type I] superconductor upon high temperature reaction with a component of the matrix.
- the billet can be assembled in any practical manner, which will yield the aforementioned construction.
- a body of the desired matrix alloy may be initially cast and longitudinal passages then formed therein by boring or drilling, with the rods thereupon being inserted within the passages to provide the desired billet construction.
- Bronze alloys constitute the matrix material employed in this preferred embodiment.
- a bronze matrix is defined as a copper based alloy containing the material which forms the desired high-field Type [I superconductor as the principal added element.
- a billet is initially prepared including a plurality of close-packed rods mounted within a bronze extrusion can, which billet is evacuated and sealed at both ends prior to extrusion and drawing.
- Methodology of this general type is disclosed at various places in the art, including, for example, in U.S. Pat. No. 3,618,205.
- the composite wire to be formed is of the preferred type, including multiple strands of a Type II high-field intermetallic compound superconductor in a bronze matrix
- hexagonally-shaped metallic rods are initially prepared including one element of the superconductor material to be formed.
- the rods in particular, comprise a central core of the metallic element contained within a surrounding tubular cladding of a bronze alloy, e.g., copper and the other element of the superconductor.
- the rods will consist of a core of vanadium surrounded by a tubular cladding of Ga bronze, i.e., copper containing about l570 gallium.
- Ga bronze i.e., copper containing about l570 gallium.
- a plurality of such rods are thus close-packed (the rods are initially worked to a hexagonal cross-section) within the surrounding extrusion can, so that the resulting billet consists in the aggregate of, for example, vanadium rod cores surrounded by a matrix of Ga bronze.
- the initial billet will essentially comprise longitudinally extending elements of niobium encased within a matrix of Sn-bronze.
- Billets of the type described above may be initially extruded at relatively elevated temperatures, e.g., on the order of 500C, and may then be cold-drawn at room temperature to an intermediate diameter, from which point hot-drawing to a final desired diameter is accomplished.
- relatively elevated temperatures e.g., on the order of 500C
- cold-drawn at room temperature to an intermediate diameter, from which point hot-drawing to a final desired diameter is accomplished.
- EXAMPLE I A 1.050 inch diameter extruded billet containing 1 l0 strands of vanadium in a gallium-bronze (about 15% Ga by weight) matrix was cold drawn to 0.205 inch diameter using a reduction in area of about 13-20% per draw. Work-hardening of the matrix required annealing in an argon atmosphere for one hour at 500C after every 2 or 3 draws.
- the 0.205 inch wire was then drawn down to 8 mils in accordance with the method of this invention by the following schedule:
- V Ga reaction zone area was derived from planimeter measurements made on photomicrographs of the center and the edge of a cross-section of this 8 mil diameter wire.
- the V Ga reaction zone area was calculated as the difference be tween the total strand area and the unreacted strand area.
- the total V Ga reaction zone area is ascertained.
- In order to determine critical current density for a specific magnetic field level divide the critical current at that level by the total V Ga reaction zone area.
- Samples of this wire were annealed, mounted on graphite spools to be used for testing, and heated in vacuum for 120 hours at 600C in order to form the in termetallic compound V Ga on the periphery of each strand. After this high temperature reaction, testing at the boiling point of helium was conducted.
- a single strand niobium in 10% Sn, 90% copper, matrix billet was made by induction melting pure tin and OFHC copper in a graphite tube in an argon atmosphere, lowering a niobium rod into the center of the tube and cooling. After zone remelting the solidified bronze billet to eliminate bubbles and cavities, a billet 8.7 inches long and 0.558 inch diameter was obtained. The billet was homogenized at 500C for two hours in argon and water quenched. It was then hot-drawn at 100 to 110C from 0.558 inch to 0.140 inch diameter, with anneals (and quench) at 0.273 inch and 0.140 inch diameters.
- drawing temperatures exceed about 100C.
- drawing temperature being formed is V Ga
- a preferable operating range for drawing is from about 200 to 300C although higher temperatures may indeed be utilized.
- the composite product being formed is to be Nb Sn
- a drawing temperature of about "C was proven to be satisfactory.
- the wire Prior to drawing, the wire is typically preheated to a temperature close to that at which it will be drawn, This can be effected in any convenient manner, e.g., through use of inductive heating via an induction coil, by passage of the wire through a radiant tube, or so forth.
- a factor governing the upper temperature limit for this invention is the stability of the wire drawing lubricant employed during warm drawing.
- a low temperature lubricant such as one with a petroleum base
- these lubricants are stable up to about 300C. Therefore, for obvious safety reasons the hot drawing temperature should be maintained well below this temperature.
- high temperature lubricants such as graphite or molybdenum disulfide
- hot drawing temperatures up to approximately 600C can be practiced. Therefore, the se lection of a drawing lubricant is a controlling factor for determining the temperature at which hot drawing is conducted.
- a commercial fatty acid base wire drawing lubricant was modified by adding 5% M08 This modification permitted satisfactory hot drawing temperatures up to 350C. When hot drawing was conducted above this temperature, the wire surface oxidized and the lubricant appeared to decompose. It is quite probable that by increasing the amount of M05 a higher drawing temperature could be employed.
- pinning sites are formed as the result of lattice imperfections created by cold work. Since the niobium and vanadium rod inserts have substantially higher tensile strength levels than the matrix material, what might be considered hot working for the matrix is still cold working for the inserts. Therefore, pinning sites are still induced into the inserts. Once induced, these sites remain as lattice imperfections after subsequent processing, such as hot drawing and high temperature diffusion.
- a method for producing a composite superconducting wire including a high-field Type ll superconducting strand embedded in a conductive metallic ma trix of normal material comprising the steps of:
- assembling a composite body including a rod surrounded by said matrix, said rod comprising a metal which forms an intermetallic compound characterized as a high-field Type II superconductor upon high temperature diffusion reaction with an alloying element of said matrix;
- said rod comprises a metal selected from the group consisting of niobium and vanadium.
- rods comprise vanadium and wherein said matrix consists essentially of a bronze containing gallium as the principal alloying element.
- rods comprise niobium and wherein said matrix consists essentially of a bronze containing tin as the principal alloying element.
- thermoforming step is conducted at temperatures in the range of about C to about 600C and the range within which substantial diffusion takes place is at least about 600C.
- PRODUCTS should be -PRODUCT- 2.
- line 8 after "temperature” insert --reaction with a component of said matrix.
- the body is-- Signed and Scaled this thirtieth D f March 1976 [SEAL] Arrest.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
Abstract
A method for producing a composite superconducting wire including one or more strands of high-field Type II superconductor embedded in a conductive matrix of normal material and the product of the said method. A composite body is prepared which includes a matrix in which are embedded one or more rods of a metal which is capable of forming a high-field Type II superconductor upon high temperature reaction with a component of said matrix. The body is extruded to an intermediate diameter, and then is hot-drawn to a final diameter at temperatures exceeding about 100*C, by multiple passes through drawing dies, the composite being reduced in cross-sectional area approximately 15 to 20% per draw. In a preferred mode of practicing the invention, the rods comprise vanadium or niobium, with the matrix being respectively gallium-bronze or tin-bronze, and the superconductive strands being formed by high temperature diffusion of the gallium or tin into the rods subsequent to drawing.
Description
United States Patent [19;
Marancik et al.
[75] Inventors; William G. Marancik; Frederick T.
Ormand, both of Basking Ridge. NJ.
[73] Assignee: Airco, lnc., Montvale. NJ.
[22] Filed: Mar. 19. 1973 [211 Appl. No: 342.895
[52] U.S. Cl 148/115 R; 29/599; 148/127; 174/126 CP; 174/D1G. 6 [51] Int. Cl. ..C2ld 9/52; HOlv 11/14 [58] Field of Search. 29/199, 599; 148/127. 11.5 R; 174/126 CP, DIG. 6; 335/216 [56] References Cited UNITED STATES PATENTS 3.465.429 9/1969 Barber et a1. 39/599 3.625.662 12/1971 Roberts et a1. 174/D1G.f\ 3.728.165 4/1973 Howlett 29/599 X 3.731.374 5/1973 Sucnaga 29/599 1 Nov. 11, 1975 Primury E.\'uminerC. W. Lanham Assistant Eranu'nerD. C. Reile). lll
Attorney. Agent. or Firm-Larry R. Cassett'. Edmund W. Bopp; H. Hume Mathews [57] ABSTRACT A method for producing a composite superconducting wire including one or more strands of high-field Type 11 superconductor embedded in a conductive matrix of normal material and the product of the said method. A composite body is prepared which includes a matrix in which are embedded one or more rods of a metal which is capable of forming a high-field Type II superconductor upon high temperature extruded to an intermediate diameter. and then is hot drawn to a final diameter at temperatures exceeding about 100C. by multiple passes through drawing dies. the composite being reduced in crosssectional area approximately 15 to 2092 per draw. in a preferred mode of practicing the invention. the rods comprise vanadium or niobium. with the matrix being respeo tively gallium-bronze or tin-bronze. and the supercoir ductive strands being formed by high temperature diffusion of the gallium or tin into the rods subsequent to drawing.
12 Claims. N0 Drawings METHOD FOR PRODUCING SUPERCONDUCTING WIRE AND PRODUCT OF THE SAME BACKGROUND OF THE INVENTION This invention relates generally to the field of superconductivity, and more specifically relates to the method for manufacture of composite superconducting wire and the resulting product.
Composite superconducting wire characterized by multiple longitudinally extending strands of high-field superconducting alloy in a surrounding matrix of copper or similar good thermal conductor, has found increasing application for use in the coils of superconducting magnets capable of producing extremely high magnetic fields.
Composite superconducting wire of the foregoing type is typically produced by initial preparation ofa billet comprised of a copper extrusion can which contains a plurality of close-packed hexagonally-formed rod inserts. Each such rod insert may typically consist of a central round rod ofa Type ll superconductor, such as a niobium-titanium alloy, surrounded by one or more concentric tubes of high purity OFHC copper, the unit being drawn to a cohesive hexagonal bar before insertion into the extrusion can. The can containing the packed rods is suitably sealed at its ends and thereupon subjected to extrusion or swaging and drawing opera tions, which gradually reduce the diameter of the billet 1 and of the contained inserts. The final very small diameter fine wire achieved by this technique contains the individual strands of the superconductor alloy in the surrounding copper matrix. The drawing operations cited are, for reasons to be set forth below, conducted at room temperature, and during the course of such mechanical working of the said billet, annealing may be required between draws, in order to remove the effects of cold work and maintain the required ductility for additional reduction in area.
In the case of several of the more significant highfield Type ll conductors, the procedure outlined above may not be readily employed. in particular, intermetallic compounds such as V Ga and Nb Sn, which are among the presently recognized more useful Type II superconductors, are so brittle in nature, that the drawing processes are ineffective in working them. Indeed, taking recognition of this problem, it has been proposed to prepare composite superconducting wire based upon such high-field intermetallic Type ll superconductors, by preparing a billet structure similar to that described above, but utilizing as the rod inserts a central core of vanadium or niobium surrounded by a matrix of Gabronze or of Sn-bronze. Pursuant to this approach the billet is appropriately reduced, in a manner similar to that indicated for the Nb-Ti composite wire, and after the desired fine diameter composite wire is achieved, the resultant product is subjected to a prolonged heating schedule which serves to diffuse the gallium or tin into the central conductor to form the desired superconducting alloy thereat.
Pursuant to the foregoing procedures, it will be appreciated that sound reasons are present for supposing that the drawing operations shall usually be conducted at room temperature. In particular, it is known that in the case of a Type II superconductor, the strength of the attainable magnetic field when such wire is used in an electro-magnet is limited, because the superconducting state of the winding is impaired at a critical current by its own magnetic field. The transition of the coil to the normal state, furthermore, occurs at much smaller critical current than that corresponding to the upper critical field. Such result obtains because of interaction of the flux lines created in the wire by the magnetic field, and the current by which the coil is operated. In particular, the Lorentz force acting on a flux line is such that if such line is not pinned to the wire, it will start to move, generating localized heating which may initiate transition to the normal state. Aside from the use in composite wires ofa highly conductive matrix of normal material to minimize such localized heating, it is known that lattice imperfections introduced by plastic deformation, and inhomogeneities in alloy composition, are capable of providing pinning sites that restrain movement of the flux lines. Cold-working techniques utilized in accordance with the foregoing processes serve to generate the desired lattice imperfections thereby providing pinning sites.
In the case where the rods of the composite body are an alloy-type material, such as Nb-Zr or Nb-Ti, encased in a pure copper matrix, the requirements for annealing are not too stringent. Where, however, it is desired to obtain intermetallic compounds such as V Ga or Nb sn, much more difficult problems occur. In particular, it unfortunately is true that the Ga-bronze or Snbronze matrices present in the composites being drawn, work-harden very rapidly. Therefore, the composite being worked will typically require intermediate an nealing after each two or three draws or every 40% reduction in cross-sectional area where cold-drawing is indeed utilized. This requirement for frequent annealing" must furthermore be viewed in the context of the overall operation being conducted, if its full detrimental impact is to be appreciated. Indeed the complex process of producing small diameter multifllament superconducting wire of which the annealing is but a part, includes the steps of wire-drawing, placing the wire in an annealing furnace, annealing the wire in an inert atmosphere for a period of time, cooling the wire in a manner to prevent surface oxidation, stringing the annealed wire through a wire-drawing machine, drawing the wire, and then repeating the entire operation after the material has work hardened. Accordingly, it will be appreciated that the time required where annealing must be effected every two or three draws, together with the attendant expense, renders a process such as this completely economically prohibitive for practical production operations.
In accordance with the foregoing, it may be regarded as an object of the present invention, to provide a method for manufacture of composite superconducting wire based upon high-field Type II superconductors resulting in a superior product, whereby the time required for reducing a composite billet to a desired cross-section is vastly reduced, with commensurate saving in attendant expense.
It is a further object of the present invention, to provide a method for drawing a composite billet including rods of metal to be formed into high-field Type II superconducting strands, whereby work-hardening of the matrix containing the element to be alloyed with the rod is minimized during drawing of the composite material, and wherein the formation of adequate pinning sites in the ultimate superconductor product remains unimpaired.
SUMMARY or INVENTION Now, in accordance with the present invention, the foregoing objects. and others as will become apparent in the course of the ensuing specification, are achieved in a method according to which a composite billet is initially formed, consisting of a conductive matrix of normal material in which are embedded one or more rods of a metal which is capable of forming a high-field Type II superconductor upon high temperature reac tion with a component of said matrix. The metallic rods are embedded in a matrix of copper, or other good thermal conductor such as silver or gold, containing in alloy the second element of the superconducting strands to be formed. The composite billet is extruded to an intermediate diameter, and thereafter drawn at temperatures over about lC and typically in the ap proximate range of l00 to 300C, to a final diameter, by reducing the cross-sectional area approximately -20% per draw. The upper temperature limit is controlled by the stability of the wire drawing lubricant and ultimately by oxidation of the surface of the wire. By the utilization of high temperature lubricants such as molybdenum disulfide or graphite, and an inert gas shield, the composite can be drawn at approximately 600C. The high-field superconductors, such as the in termetallic compounds V Ga and Nb Sn, are formed after drawing by high temperature reaction and diffusion. By utilizing the relatively hot drawing temperatures indicated, the drawing process may be effectively carried out without frequent intermediate annealing: in general such an anneal is required not more frequently than every 10 to 12 draws. Typically, for example, a pro-annealed ll0-strand vanadium in Ga-bronze matrix wire (l4.85% Ga overall) can be hot-drawn from 57 to 13 mils at 218C with only one additional intermediate anneal. The resultant product is found to be essentially equivalent to wire formed from the same billet where such billet is cold-drawn.
DESCRIPTION OF PREFERRED EMBODIMENT The initial stages of the method in accordance with the present invention may be substantially identical with methodology utilized in the prior art for preparation of composite superconducting wire. The primary requirement for the billet is that it include a conductive matrix of normal material which encases or surrounds longitudinally extending rods of a material which is capable of forming the desired high-field Type I] superconductor upon high temperature reaction with a component of the matrix. The billet can be assembled in any practical manner, which will yield the aforementioned construction. For example, a body of the desired matrix alloy may be initially cast and longitudinal passages then formed therein by boring or drilling, with the rods thereupon being inserted within the passages to provide the desired billet construction.
Bronze alloys constitute the matrix material employed in this preferred embodiment. As used herein, a bronze matrix is defined as a copper based alloy containing the material which forms the desired high-field Type [I superconductor as the principal added element.
in a typical procedure, a billet is initially prepared including a plurality of close-packed rods mounted within a bronze extrusion can, which billet is evacuated and sealed at both ends prior to extrusion and drawing. Methodology of this general type is disclosed at various places in the art, including, for example, in U.S. Pat. No. 3,618,205. Where the composite wire to be formed is of the preferred type, including multiple strands of a Type II high-field intermetallic compound superconductor in a bronze matrix, hexagonally-shaped metallic rods are initially prepared including one element of the superconductor material to be formed. The rods, in particular, comprise a central core of the metallic element contained within a surrounding tubular cladding of a bronze alloy, e.g., copper and the other element of the superconductor.
Assuming the superconductor strands to be formed are, for example, V Ga, the rods will consist of a core of vanadium surrounded by a tubular cladding of Ga bronze, i.e., copper containing about l570 gallium. A plurality of such rods are thus close-packed (the rods are initially worked to a hexagonal cross-section) within the surrounding extrusion can, so that the resulting billet consists in the aggregate of, for example, vanadium rod cores surrounded by a matrix of Ga bronze. Similarly where, for example, Nb Sn is to be formed, the initial billet will essentially comprise longitudinally extending elements of niobium encased within a matrix of Sn-bronze.
Billets of the type described above may be initially extruded at relatively elevated temperatures, e.g., on the order of 500C, and may then be cold-drawn at room temperature to an intermediate diameter, from which point hot-drawing to a final desired diameter is accomplished. The conditions of drawing and the methodolity utilized is set forth in the following Examples:
EXAMPLE I A 1.050 inch diameter extruded billet containing 1 l0 strands of vanadium in a gallium-bronze (about 15% Ga by weight) matrix was cold drawn to 0.205 inch diameter using a reduction in area of about 13-20% per draw. Work-hardening of the matrix required annealing in an argon atmosphere for one hour at 500C after every 2 or 3 draws.
The 0.205 inch wire was then drawn down to 8 mils in accordance with the method of this invention by the following schedule:
a. Hot-draw to 72 mils, drawing temperature 20022 1C, annealed in an argon atmosphere for one hour at 500C;
b. Hot-draw to 25 mils, same drawing temperature and annealing cycle as in (a);
c. Hot-draw to 10 mils, same drawing temperature and annealing cycle as in (a);
d. Hot-draw to 8 mils 200-221C.
Samples of this 8 mil V and Ga-bronze matrix wire were reacted at 600C for 3, 4, 5, 6, 7 and ll days in an argon atmosphere in order to form the desired intermetallic compound V Ga on the periphery of each strand. The 5 day reaction time gave the best performance, viz. a critical current of l l. 17 amps at 79 kilo Gauss.
To determine critical current density required an ac curate measurement of the V Ga reaction zone area. This area was derived from planimeter measurements made on photomicrographs of the center and the edge of a cross-section of this 8 mil diameter wire. The V Ga reaction zone area was calculated as the difference be tween the total strand area and the unreacted strand area. By multiplying the reaction zone area by the numdrawing temperature ber of strands in the wire, the total V Ga reaction zone area is ascertained. In order to determine critical current density for a specific magnetic field level, divide the critical current at that level by the total V Ga reaction zone area.
By utilizing this procedure, the superconducting properties of this wire measured at the boiling point of He are at 79 K Gauss, critical current (lc) 11.17 amps and critical current density (.lc) 4.31 X amp/cm? EXAMPLE II A 0.205 inch diameter wire as produced in Example I above (that is cold-drawn from a 1.050 inch extruded billet) was drawn down to 13 mils in accordance with the method of this invention by the following schedule:
a. Hot-draw to 57 mils, drawing temperature 200-2l8C, annealed in an argon atmosphere for one hour at 500C.
b. Hot-draw to 19.5 mils, same drawing temperature and annealing cycle as in (a);
c. Hot-draw to 200-2l8C.
Samples of this wire were annealed, mounted on graphite spools to be used for testing, and heated in vacuum for 120 hours at 600C in order to form the in termetallic compound V Ga on the periphery of each strand. After this high temperature reaction, testing at the boiling point of helium was conducted.
Critical current density was again ascertained from planimeter measurements as hereinbefore described in Example I.
The superconducting properties of this wire measured at the boiling point of helium are:
a. At 79 K Gauss, critical current (1c) 23 amps. and critical current density (Jc) 4.9 X l0 amp/cm;
b. At 40 K Gauss, critical current (1c) 41 amps. and critical current density (Jc) 8.7 X l0 amp/cm EXAMPLE [1] Although for most practical application, multiple strand composite superconductive wire is preferred, the methodology of the invention is not limited to its use with multiple strand constructions.
For purposes of the present Example, a single strand niobium in 10% Sn, 90% copper, matrix billet was made by induction melting pure tin and OFHC copper in a graphite tube in an argon atmosphere, lowering a niobium rod into the center of the tube and cooling. After zone remelting the solidified bronze billet to eliminate bubbles and cavities, a billet 8.7 inches long and 0.558 inch diameter was obtained. The billet was homogenized at 500C for two hours in argon and water quenched. It was then hot-drawn at 100 to 110C from 0.558 inch to 0.140 inch diameter, with anneals (and quench) at 0.273 inch and 0.140 inch diameters. Resultant samples were then hot-drawn at 200C from 0.140 inch to 0.010 inch diameter, with anneals at mils, and mounted on graphite spools for high temperature reaction treatments. Various samples were then held at 900C for 6.5, 8 and 10. hours in an argon atmosphere in order to form the desired intermetallic compound Nb Sn on the periphery of each strand. These samples had critical currents of 1.36, 2.07 and 3.51 amps at 79 kilo Gauss.
Good results in accordance with the invention are obtained when the drawing temperatures exceed about 100C. Where the multi-strand composite product 13 mils, drawing temperature being formed is V Ga, a preferable operating range for drawing is from about 200 to 300C although higher temperatures may indeed be utilized. When the composite product being formed is to be Nb Sn, a drawing temperature of about "C was proven to be satisfactory. Prior to drawing, the wire is typically preheated to a temperature close to that at which it will be drawn, This can be effected in any convenient manner, e.g., through use of inductive heating via an induction coil, by passage of the wire through a radiant tube, or so forth. A factor governing the upper temperature limit for this invention is the stability of the wire drawing lubricant employed during warm drawing. For example, if a low temperature lubricant is used, such as one with a petroleum base, these lubricants are stable up to about 300C. Therefore, for obvious safety reasons the hot drawing temperature should be maintained well below this temperature. However, by the utilization of high temperature lubricants such as graphite or molybdenum disulfide, hot drawing temperatures up to approximately 600C can be practiced. Therefore, the se lection ofa drawing lubricant is a controlling factor for determining the temperature at which hot drawing is conducted.
A commercial fatty acid base wire drawing lubricant was modified by adding 5% M08 This modification permitted satisfactory hot drawing temperatures up to 350C. When hot drawing was conducted above this temperature, the wire surface oxidized and the lubricant appeared to decompose. It is quite probable that by increasing the amount of M05 a higher drawing temperature could be employed.
With respect to the formation of pinning sites, it is believed that hot drawing does not adversely affect the formation of such sites. it is well known that pinning sites are formed as the result of lattice imperfections created by cold work. Since the niobium and vanadium rod inserts have substantially higher tensile strength levels than the matrix material, what might be considered hot working for the matrix is still cold working for the inserts. Therefore, pinning sites are still induced into the inserts. Once induced, these sites remain as lattice imperfections after subsequent processing, such as hot drawing and high temperature diffusion.
The precise metallurgical theory that will explain the success of this invention is not known. However, the restoration of ductility by hot drawing with the concommittant reduced effect of work hardening can best be explained as a form of recovery. Recovery is defined on page 10 of the A.S.M. Metals Handbook, 1948 Edi tion, as the removal of residual stresses by localized plastic flow as the result of low-temperature annealing operations; performed on cold worked metals without altering the grain structure or strength properties substantially. The effect of recovery is that residual stresses imparted by cold work are greatly reduced, thereby permitting additional mechanical work without elaborate annealing procedures.
While the present invention has not particularly set forth in terms of specific embodiments thereof, it will be understood in view of the present disclosure, that numerous variations upon the invention are now enabled to those skilled in the art, which variations yet reside within the scope of the present teaching. Accordingly, the invention is to be broadly construed and limited only by the scope and spirit of the claims now appended hereto.
We claim:
I. A method for producing a composite superconducting wire including a high-field Type ll superconducting strand embedded in a conductive metallic ma trix of normal material, comprising the steps of:
assembling a composite body including a rod surrounded by said matrix, said rod comprising a metal which forms an intermetallic compound characterized as a high-field Type II superconductor upon high temperature diffusion reaction with an alloying element of said matrix;
extruding said composite to an intermediate diameter; hot drawing said intermediate diameter composite to a final diameter by multiple passes through drawing dies at temperatures above about lC but below the diffusion temperature range within which sub stantial diffusion occurs between the alloying element of said matrix and the material of said rod. said composite being reduced in cross-sectional area appproximately to per draw; and
subjecting said composite at said final diameter to reaction at a high temperature within said diffusion temperature range for an extended period required for substantial diffusion of said matrix alloying element into said rod and the formation ofa superconducting layer adjacent the interface between said matrix and said rod.
2. A method according to claim I, wherein said rod comprises a metal selected from the group consisting of niobium and vanadium.
3. A method in accordance with claim 2, wherein said rods are multiple in number, whereby multi-strand superconducting wire is formed.
4. A method in accordance with claim 3, wherein said rods comprise vanadium and wherein said matrix consists essentially of a bronze containing gallium as the principal alloying element.
5. A method in accordance with claim 4, wherein said bronze contains about l5 weight percent gallium.
6. A method in accordance with claim 3, wherein said rods comprise niobium and wherein said matrix consists essentially of a bronze containing tin as the principal alloying element.
7. A method in accordance with claim 6, wherein said bronze contains about [0 weight percent tin.
8. A method in accordance with claim 1, wherein said high-field Type II superconductor consists essentially of V Ga.
9. A method in accordance with claim I, wherein said high-field Type ll superconductor consists essentially of Nb Sn.
10. A method in accordance with claim I, wherein said hot drawing step is conducted at temperatures in the range of about C to about 600C and the range within which substantial diffusion takes place is at least about 600C.
11. A method in accordance with claim 10, wherein said hot drawing step is conducted at temperatures in the range of about 100C to about 300C, and said diffusion step is carried out in a substantially inert environment.
12. A product by the process of claim 1.
UNITED STATES PA'ITQNT OFFICE CERTIFICATE OF CORRECTION PATENT NO, 3,918,998 DATED November 11, 1975 INVENTORtS) William G. Marancik &; Frederick T. Ormand It rs tertrfied that error appears m the above-identified patent and that said Letters Patent are hereby corrected as shown below:
1. In the Title, "PRODUCTS" should be -PRODUCT- 2. In the Abstract, line 8, after "temperature" insert --reaction with a component of said matrix.
The body is-- Signed and Scaled this thirtieth D f March 1976 [SEAL] Arrest.
RUTH C. MASON C. MARSHALL DANN Alftsring Ujfire Commissioner nj'larvnrs and Trademarks
Claims (12)
1. A METHOD FOR PRODUCING A COMPOSITE SUPERCONDUCTING WIRE INCLUDING A HIGH-FIELD TYPE II SUPERCONDUCTING STRAND EMBEDDED IN A CONDUCTIVE METALLIC MATRIX OF NORMAL MATERIAL, COMPRISING THE STEPS OF: ASSEMBLING A COMPOSITE BODY INCLUDING A ROD SURROUNDED BY SAID MATRIX, SAID ROD COMPRISING A METAL WHICH FORMS AN INTERMETALLIC COMPOUND CHARACTERIZED AS A HIGH-FIELD TYPE II SUPERCONDUCTOR UPON HIGH TEMPERATURE DIFFUSION REACTION WITH AN ALLOYING ELEMENT OF SAID MATRIX, EXTRUDING SAIC COMPOSITE TO AN INTERMEDIATE DIAMETER, HOT DRAWING SAID INTERMEDIATE DIAMETER COMPOSITE TO A FINAL DIAMETER BY MULTIPLE PASSES THROUGH DRAWING DIES AT TEMPERATURES ABOVE ABOUT 100*C BUT BELOW THE DIFFUSION TEMPERATURE RANGE WITHIN WHICH SUBSTANTIAL DIFFUSION OCCURS BETWEEN THE ALLOYING ELEMENT OF SAID MATRIX AND THE MATERIAL OF SAID ROD, SAID COMPOSITE BEING REDUCED IN CROSS-SECTIONAL AREA APPROXIMATELY 15 TO 20% PER DRAW, AND SUBJECTING SAID COMPOSITE AT SAID FINAL DIAMETER TO REACTION AT A HIGH TEMPERATURE WITHIN SAID DIFFUSION TEMPERATURE RANGE FOR AN EXTENDED PERIOD REQUIRED FOR SUBSTANTIAL DIFFUSION OF SAID MATRIX ALLOYING ELEMENT INTO SAID ROD AND THE FORMATION OF A SUPERCONDUCTING LAYER ADJACENT THE INTERFACE BETWEEN SAID MATRIX AND SAID ROD.
2. A method according to claim 1, wherein said rod comprises a metal selected from the group consisting of niobium and vanadium.
3. A method in accordance with claim 2, wherein said rods are multiple in number, whereby multi-strand superconducting wire is formed.
4. A method in accordance with claim 3, wherein said rods comprise vanadium and wherein said matrix consists essentially of a bronze containing gallium as the principal alloying element.
5. A method in accordance with claim 4, wherein said bronze contains about 15 weight percent gallium.
6. A method in accordance with claim 3, wherein said rods comprise niobium and wherein said matrix consists essentially of a bronze containing tin as the principal alloying element.
7. A method in accordance with claim 6, wherein said bronze contains about 10 weight percent tin.
8. A method in accordance with claim 1, wherein said high-field Type II superconductor consists essentially of V3Ga.
9. A method in accordance with claim 1, wherein said high-field Type II superconductor consists essentially of Nb3Sn.
10. A method in accordance with claim 1, wherein said hot drawing step is conducted at temperatures in the range of about 100*C to about 600*C and the range within which substantial diffusion takes place is at least about 600*C.
11. A method in accordance with claim 10, wherein said hot drawing step is conducted at temperatures in the range of about 100*C to about 300*C, and said diffusion step is carried out in a substantially inert environment.
12. A product by the process of claim 1.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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US342895A US3918998A (en) | 1973-03-19 | 1973-03-19 | Method for producing superconducting wire and products of the same |
DE19742412573 DE2412573B2 (en) | 1973-03-19 | 1974-03-15 | METHOD OF MANUFACTURING A DIVIDED SUPRALCONDUCTIVE WIRE |
FR7409137A FR2222776B1 (en) | 1973-03-19 | 1974-03-18 | |
JP49031391A JPS5026076A (en) | 1973-03-19 | 1974-03-19 | |
GB1209574A GB1451168A (en) | 1973-03-19 | 1974-03-19 | Method for producing superconducting wire |
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US342895A US3918998A (en) | 1973-03-19 | 1973-03-19 | Method for producing superconducting wire and products of the same |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2557840A1 (en) * | 1975-12-22 | 1977-06-30 | Battelle Institut E V | Superconductive multifilamentary composite - contg. superconductive alloyed vanadium or niobium wires in copper matrix |
US4101731A (en) * | 1976-08-20 | 1978-07-18 | Airco, Inc. | Composite multifilament superconductors |
US4177087A (en) * | 1976-03-23 | 1979-12-04 | United Kingdom Atomic Energy Authority | Manufacture of superconducting members |
US4224087A (en) * | 1978-09-14 | 1980-09-23 | National Research Institute For Metals | Method for producing Nb3 Sn superconductor |
US4224735A (en) * | 1979-03-23 | 1980-09-30 | Airco, Inc. | Method of production multifilamentary intermetallic superconductors |
US4324842A (en) * | 1978-12-05 | 1982-04-13 | The United States Of America As Represented By The United States Department Of Energy | Superconducting wire with improved strain characteristics |
US4343867A (en) * | 1979-12-19 | 1982-08-10 | The United States Of America As Represented By The United States Department Of Energy | Superconducting wire with improved strain characteristics |
US4414428A (en) * | 1979-05-29 | 1983-11-08 | Teledyne Industries, Inc. | Expanded metal containing wires and filaments |
US4501062A (en) * | 1982-02-27 | 1985-02-26 | Vacuumschmelze Gmbh | Stabilized super-conductor having a diffusion-inhibiting layer therein and method of producing same |
US4646428A (en) * | 1985-11-21 | 1987-03-03 | Oxford Superconducting Technology | Method of fabricating multifilament intermetallic superconductor |
US4687883A (en) * | 1985-09-06 | 1987-08-18 | Kernforschungszentrum Karlsruhe Gmbh | Method for producing superconductive wires |
US4860431A (en) * | 1988-02-17 | 1989-08-29 | Oxford Superconducting Technology | Fabrication of multifilament intermetallic superconductor using strengthened tin |
US5030614A (en) * | 1987-05-15 | 1991-07-09 | Omega Engineering, Inc. | Superconductor sensors |
US5228928A (en) * | 1991-02-07 | 1993-07-20 | The Furukawa Electric Co., Ltd. | Method of manufacturing Nb3 Sn superconducting wire |
US6534718B1 (en) * | 2001-01-30 | 2003-03-18 | Shahin Pourrahimi | Reinforcement of superconducting coils by high-strength materials |
US20040065468A1 (en) * | 1998-09-16 | 2004-04-08 | Seuntjens Jeffrey Michael | Composite noble metal wire |
EP1638151A1 (en) * | 2004-09-16 | 2006-03-22 | Bruker BioSpin AG | Method for producing a superconductive element |
Families Citing this family (2)
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DE2711496C3 (en) | 1977-03-16 | 1982-01-21 | Siemens AG, 1000 Berlin und 8000 München | Process for the manufacture of a superconductor |
DE2759640C2 (en) * | 1977-03-16 | 1983-02-24 | Siemens AG, 1000 Berlin und 8000 München | Process for the manufacture of a superconductor |
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Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
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DE2557840A1 (en) * | 1975-12-22 | 1977-06-30 | Battelle Institut E V | Superconductive multifilamentary composite - contg. superconductive alloyed vanadium or niobium wires in copper matrix |
US4177087A (en) * | 1976-03-23 | 1979-12-04 | United Kingdom Atomic Energy Authority | Manufacture of superconducting members |
US4101731A (en) * | 1976-08-20 | 1978-07-18 | Airco, Inc. | Composite multifilament superconductors |
US4224087A (en) * | 1978-09-14 | 1980-09-23 | National Research Institute For Metals | Method for producing Nb3 Sn superconductor |
US4324842A (en) * | 1978-12-05 | 1982-04-13 | The United States Of America As Represented By The United States Department Of Energy | Superconducting wire with improved strain characteristics |
US4224735A (en) * | 1979-03-23 | 1980-09-30 | Airco, Inc. | Method of production multifilamentary intermetallic superconductors |
US4414428A (en) * | 1979-05-29 | 1983-11-08 | Teledyne Industries, Inc. | Expanded metal containing wires and filaments |
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US4501062A (en) * | 1982-02-27 | 1985-02-26 | Vacuumschmelze Gmbh | Stabilized super-conductor having a diffusion-inhibiting layer therein and method of producing same |
US4687883A (en) * | 1985-09-06 | 1987-08-18 | Kernforschungszentrum Karlsruhe Gmbh | Method for producing superconductive wires |
US4646428A (en) * | 1985-11-21 | 1987-03-03 | Oxford Superconducting Technology | Method of fabricating multifilament intermetallic superconductor |
US5030614A (en) * | 1987-05-15 | 1991-07-09 | Omega Engineering, Inc. | Superconductor sensors |
US4860431A (en) * | 1988-02-17 | 1989-08-29 | Oxford Superconducting Technology | Fabrication of multifilament intermetallic superconductor using strengthened tin |
US5228928A (en) * | 1991-02-07 | 1993-07-20 | The Furukawa Electric Co., Ltd. | Method of manufacturing Nb3 Sn superconducting wire |
US20040065468A1 (en) * | 1998-09-16 | 2004-04-08 | Seuntjens Jeffrey Michael | Composite noble metal wire |
US6534718B1 (en) * | 2001-01-30 | 2003-03-18 | Shahin Pourrahimi | Reinforcement of superconducting coils by high-strength materials |
EP1638151A1 (en) * | 2004-09-16 | 2006-03-22 | Bruker BioSpin AG | Method for producing a superconductive element |
US20070227622A1 (en) * | 2004-09-16 | 2007-10-04 | Bruker Biospin Ag | Method for producing a superconductive element |
US7476281B2 (en) | 2004-09-16 | 2009-01-13 | Bruker Biospin Ag | Method for producing a superconductive element |
Also Published As
Publication number | Publication date |
---|---|
FR2222776B1 (en) | 1978-10-27 |
FR2222776A1 (en) | 1974-10-18 |
DE2412573B2 (en) | 1977-01-13 |
DE2412573A1 (en) | 1974-10-03 |
JPS5026076A (en) | 1975-03-18 |
GB1451168A (en) | 1976-09-29 |
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