METHOD FOR PRODUCING A MULTIFILAMENT NB3SN SUPERCONDUCTING WIRE
20170221608 · 2017-08-03
Inventors
- Michael Field (Hoboken, NJ, US)
- Hanping Miao (Edison, NJ, US)
- Carlos Sanabria (Tallahassee, FL, US)
- Jeffrey Parrell (Mountainside, NJ, US)
Cpc classification
Y02E40/60
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
C22C27/02
CHEMISTRY; METALLURGY
C22F1/18
CHEMISTRY; METALLURGY
B21C1/02
PERFORMING OPERATIONS; TRANSPORTING
International classification
C22F1/18
CHEMISTRY; METALLURGY
B21C1/02
PERFORMING OPERATIONS; TRANSPORTING
C22C27/02
CHEMISTRY; METALLURGY
Abstract
Methods for producing a multifilament Nb.sub.3Sn superconducting wire having a Jc value of at least 2000 A/mm.sup.2 at 4.2 K and 12 T by a) packing a plurality of Cu encased Nb rods within a first matrix which is surrounded by an intervening Nb diffusion barrier and a second matrix on the other side of the barrier remote from the rods thereby forming a packed subelement for the superconducting wire; b) providing a source of Sn within the subelement; c) assembling the metals within the subelement, the relative sizes and ratios of Nb, Cu and Sn being selected such that (i) the Nb fraction of the subelement cross section including and within the diffusion barrier is from 50 to 65% by area; (ii) the atomic ratio of the Nb to Sn including and within the diffusion barrier of the subelement is from 2.7 to 3.7; (iii) the ratio of the Sn to Cu within the diffusion barrier of the subelement is such that the Sn wt %/(Sn wt %+Cu wt %) is 45%-65%; (iv) the Cu to Nb local area ratio (LAR) of the Cu-encased Nb rods is from 0.10 to 0.30; (v) the Nb diffusion barrier being fully or partially converted to Nb.sub.3Sn by subsequent heat treatment; and (vi) the thickness of the Nb diffusion barrier is greater than the radius of the Nb portions of the Cu encased Nb rods; and d) assembling the subelements in a further matrix and reducing the assemblage to wire form such that (i) the multifilamentary Nb.sub.3Sn superconducting wire is formed of a plurality of the subelements, each having a Nb diffusion barrier to thereby form a wire having a distributed barrier design; (ii) the Nb portions of the copper encased Nb rods in the final wire are of diameter from 0.5 to 7 μm before reaction, and (iii) the Nb diffusion barrier that is fully or partially converted to Nb.sub.3Sn by heat treatment is from 0.8 to 11 μm thickness before reaction; and e) heat treating the final size wire from step d) to form the Nb.sub.3Sn superconducting phases, and multifilament Nb.sub.3Sn superconducting wires made thereby are described herein.
Claims
1. A method for producing a multifilament Nb.sub.3Sn superconducting wire comprising: a) packing a plurality of Cu encased Nb rods within a matrix which is surrounded by an intervening Nb diffusion barrier and a further matrix on the other side of the barrier remote from the rods, to thereby form a packed subelement for the superconducting wire; b) providing a source of Sn within the subelement; c) assembling the metals within the subelement the relative sizes and ratios of Nb, Cu and Sn being selected such that c1) the Nb fraction of the subelement including and within the diffusion barrier is 50-65% by area, c2) the atomic ratio of the Nb to Sn including and within the diffusion barrier of the subelement is between 2.7 and 3.7, c3) the ratio of the Sn to Cu within the diffusion barrier of the subelement is such that the Sn wt %/(Sn wt % +Cu wt %) is 45%-65%, c4) the Cu to Nb local area ratio of the Cu-encased Nb rods is 0.10-0.50, c5) the Nb diffusion barrier being fully or partially converted to Nb.sub.3Sn by heat treatment, and c6) the thickness of the Nb diffusion barrier is larger than the radius of the Nb portions of the Cu encased Nb rods; d) assembling the subelements in a further matrix and reducing the assemblage to wire form such that d1) the multifilamentary Nb.sub.3Sn superconducting wire is comprised of a plurality of the subelements each having a Nb diffusion barrier to thereby form a wire having a distributed barrier design, d2) the Nb portions of the copper encased Nb rods in the final wire are of diameter between 0.5-7 μm before reaction, and d3) the Nb diffusion barrier that is fully or partially converted to Nb3Sn by heat treatment is 0.8-11 μm thick before reaction; and e) heat treating the final size wire from step d) to form the Nb.sub.3Sn superconducting phase.
2. The method in accordance with claim 1 further comprising f) alloying the Nb or the Cu or the Sn with Ta or Ti or both after heat treatment to form (Nb,Ta).sub.3Sn, (Nb,Ti).sub.3Sn or (Nb,Ti,Ta).sub.3Sn.
3. The method in accordance with claim 2 where f) alloying the Nb or Cu or Sn with an element or compound for the purpose strengthening the composite.
4. The method in accordance with claim 1 wherein the Nb alloy fraction of the subelement is preferably 55%-60% by area.
5. The method in accordance with claim 1 wherein the Nb barrier fraction of the total Nb content of the subelement is between 20-50%, preferably 25-35% by area.
6. The method in accordance with claim 1 wherein the atomic ratio of the Nb alloy to Sn alloy in the subelement is between 3.1 and 3.6.
7. The method in accordance with claim 1 wherein the ratio of the copper to tin alloy in the subelement is such that the Sn wt %/(Sn wt % +Cu wt %) within the diffusion barrier is preferably 50-60%.
8. The method in accordance with claim 1 wherein the Cu to Nb local area ratio of the copper-encased Nb rods is preferably 0.15-0.45.
9. The method in accordance with claim 1 wherein the Nb portions of the copper encased Nb rods in the final wire are 1-5 μm before reaction.
10. The method in accordance with claim 1 wherein the Nb diffusion barrier that is fully or partially converted to Nb.sub.3Sn by heat treatment is 1.5-8 μm thick before reaction.
11. The method in accordance with claim 1 wherein the Sn is diffused into the Nb rods by a heat treatment process that minimizes dissolution of the Nb in the annulus region with pre-reaction stages at 180° C.-220° C. for 24-100 hours, followed by 340° -410° C. for 24-50 hours, followed by Nb.sub.3Sn formation stage at 625° C.-725° C. for 12-200 hours.
12. The method in accordance with claim 11, where a fourth stage is added to the heat treatment sequence prior to the Nb.sub.3Sn reaction stage, of 560°-580° C. for 24-200 hours.
13. The method in accordance with claim 1 wherein the Cu encased Nb rods are formed into hexagonal cross sectioned rods for use in packing the subelement.
14. The method in accordance with claim 1 wherein the matrix contains Cu.
15. The method in accordance with claim 1 wherein the matrix contains a low tin bronze.
16. The method in accordance with claim 15 wherein the matrix contains Cu 0.1-2.5 wt % Sn.
17. The method in accordance with claim 1 wherein at least 50% of the Nb portions of the copper encased Nb rods in the final wire have a diameter of less than about 2.5 μm.
18. The method in accordance with claim 1 wherein the Nb in Cu local area ratio (LAR) is adjusted or graded to provide a higher LAR in or near the center and a lower LAR near the periphery, near to or proximate to the barrier.
19. A multifilament Nb.sub.3Sn superconducting wire having a critical current density of at least 2,000 A/mm.sup.2 at temperature of 4.2 K and in a magnetic field of 12 T produced by the method of claim 1.
20. A multifilament Nb.sub.3Sn superconducting wire having a critical current density of at least 3,000 A/mm.sup.2 at temperature of 4.2 K and in a magnetic field of 12 T produced by the method of claim 1.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0037] The methods described herein provide three particular advantages over the methods described in the prior art. First, the “Nb in Cu local area ratio (LAR)” may be adjusted or graded inside a billet to provide superior properties to the multifilament Nb.sub.3Sn superconducting wire. The “Nb in Cu local area ratio (LAR)” may not be a single, static value through the subelement. The LAR may be adjusted or graded within a billet to provide different effects in the final product. The LAR may be adjusted or graded to provide a higher LAR in or near the center and a lower LAR near the periphery, near to or proximate to the barrier. This may result in improving the current at small subelement dimensions. Varying the LAR in or near the center, closest to the copper annulus, may change the dynamics of subsequent bronze formation and the formation of the Nb—Cu—Sn ternary phase which acts as a regulatory membrane. Varying the LAR may also create circuitous routes for Sn diffusion through the subelement. This may result in delaying the reaction at smaller sizes and preserving the residual resistivity ratio (RRR) due to the minimum reaction times that are specified due to requirements to achieve coil heat treatment homogeneity.
[0038] Second, providing at least a certain percentage of Nb filaments having smaller dimensions, i.e. finer with more rows, may provide improved current in the resulting multifilament Nb.sub.3Sn superconducting wire. For instance, providing at least 25%, 33%, 50%, 67%, 75%, 80% or 90% or so of the Nb filaments having a diameter of less than about 1.0 μm or 1.5 μm or 2.0 μm or 2.5 μm or 3.0 μm or 4.0 μm or 5.0 μm may be particularly advantageous.
[0039] Third, while a copper containing matrix may be used in the methods described herein, the matrix may be a low tin bronze (Cu 0.1-2.5 wt % Sn, or Cu 0.2-1.5 wt % Sn or Cu 0.5-1.0 wt % Sn or Cu 0.7 wt % Sn). Such a matrix may provide superior dynamics of the reaction effectively speeding the reaction up among other beneficial effects.
Definitions
[0040] For purposes of the present specification, the following terms shall have the meanings set forth:
[0041] By “critical current density” is meant the maximum measured supercurrent divided by the overall wire diameter at a specified temperature and magnetic field. This is the key figure of merit for a superconductor.
[0042] By “non-copper critical current density” is meant the maximum measured supercurrent divided by the overall wire diameter at a specified temperature and magnetic field discounting the copper stabilizing region. As most Nb.sub.3Sn strands are integrated with a non-superconducting copper stabilizer region, this value removes for comparison the area fraction of copper stabilizer so that the properties of the superconducting package region can be compared between conductors of differing copper stabilizer fractions.
[0043] By “layer critical current density” is meant the maximum measured supercurrent divided by the overall wire diameter at a specified temperature and magnetic field discounting both the stabilizing copper on the outside of the diffusion barrier and the unreacted residual bronze phase (see, infra) and void space on the inside of the diffusion barrier. This value removes both the stabilizing copper on the outside of the diffusion barrier (see, infra) and the unreacted residual bronze phase (see, infra) and void space on the inside of the diffusion barrier. This leaves as the cross sectional area only the amount of Nb.sub.3Sn after reaction. If the quality of the Nb.sub.3Sn phase is poor, it will have a lower critical current density than the same amount of high quality Nb.sub.3Sn. The methods described herein produce high overall critical current density in part because the layer critical current density is higher than previously achieved in Nb.sub.3Sn wires.
[0044] By “subelement” is meant the elements that are grouped together to form the final restack. In a “distributed barrier” design, rods of copper-encased Nb and a tin source are assembled in a diffusion barrier of Nb before restacking in a copper tube. The elements that are grouped together to form the final restack are called subelements. It is the restack that is drawn to the final wire. The subelements are the key building blocks of the final wire. As ideally this outer Cu tube is inert during the reaction sequence, all the important activity (diffusion and reaction) occurs inside the subelement. Key features of the methods described herein are the metal area and size ratios within the subelement.
[0045] By “local area ratio” or LAR is meant the area or volume ratio of the Cu to Nb in the local region of the filament pack region of the subelement.
[0046] Internal tin wire requires Sn diffusion through Cu to react with the Nb. In doing so various bronze phases are formed, each having specific ratios of Sn and Cu. However Sn wt %/((Sn wt %+Cu wt %), refers to a value that would be the overall weight ratio of Sn to Sn+Cu within the diffusion barrier of the subelement, even if it does not represent a true bronze phase in existence. It is instead used to illustrate how much overall Sn is available to react with the Nb within the subelement.
[0047] The “Nb in Cu local area ratio (LAR)” may not be a single, static value through the subelement. The LAR may be adjusted or graded within a billet to provide different effects in the final product. The LAR may be adjusted or graded to provide a higher LAR in or near the center and a lower LAR near the periphery, near to or proximate to the barrier. This may result in improving the current at small subelement dimensions. Varying the LAR in or near the center may change the dynamics of bronze formation and the formation of the ternary phase which acts as a regulatory membrane. Varying the LAR may also create circuitous routes for Sn diffusion through the subelement. This may result in delaying the reaction at smaller sizes and preserving the residual resistivity ratio (RRR).
[0048]
[0049] By “atomic Nb: Sn” is meant the atomic ratio of Nb to Sn. Ideally this is 3:1 to form stoichiometric Nb.sub.3Sn. If extra unreacted Nb barrier is to be left over after the heat treatment sequence, this value must be greater than 3:1. A layer of unreacted Nb barrier is often desired to prevent Sn from diffusing into the matrix Cu outside of the diffusion barrier, and lowering the wire residual resistivity ratio (RRR) and stability. If this value is much greater than 3:1, then there is much more Nb in the subelement than is needed to form Nb.sub.3Sn, and although the RRR will be high, there is wasted space within the subelement, lowering the non-Cu critical current density.
[0050] In the methods described herein, the selection of Nb.sub.3Sn wire design parameters incorporates an understanding of the factors that result in high J.sub.c. The design combines high Nb and Sn fractions, necessary to achieve a high Nb.sub.3Sn fraction in the final wire, with a small Cu fraction, but one still suitable to meet the nine objectives listed below. This caveat means that the Cu must have the proper distribution and/or alloying elements that result in a thorough conversion of the Nb to a high quality Nb.sub.3Sn microstructure.
[0051] For purposes of the methods described herein, the important materials details of the wire design that influence the J.sub.c include the following: [0052] 1. The Nb area fraction including and within the Nb diffusion barrier of the subelement; [0053] 2. The Nb to Sn atomic ratio including and within the Nb diffusion barrier of the subelement; [0054] 3. The area ratio of Sn to Cu within the “non-Cu fraction” Sn wt %/(Sn wt %+Cu wt %) within the Nb barrier envelope of the subelement; [0055] 4. The area ratio of Cu and Nb in the filament package (Local Area Ratio); [0056] 5. A distributed barrier (infra) approach, as opposed to a single diffusion barrier approach; [0057] 6. The Nb diffusion barrier that can be reacted to form Nb.sub.3Sn; [0058] 7. The ratio of Nb diffusion barrier thickness to filament diameter, and thus the Nb distribution (fractions) between filaments and outer diffusion barrier; [0059] 8. Nb filament and Nb barrier ring absolute size in final wire; and [0060] 9. Minimizing the dissolution of Nb filament in a Sn rich environment and excessive Nb.sub.3Sn grain growth during heat treatment while fully converting the filaments to Nb.sub.3Sn.
[0061] Regarding the Nb area fraction including and within the Nb diffusion barrier of the subelement, the Nb area fraction must be maximized in the non-copper region in the subelement (i.e. inside and including the Nb diffusion barrier), but it is limited by the amounts of Cu and Sn simultaneously required in the non-copper region. The Nb fraction comes from the diffusion barrier and the enclosed Nb filament pack region. The individual Nb filaments are created by combining Nb with some form of Cu cladding. Often this is by extrusion of a Nb ingot in a Cu jacket which is reduced and formed to hexagonal cross section by wire drawing for ease of fabrication. However, it can be formed by wrapping Cu foil on round rods and assembling a pack of round monofilaments. The details of the assembly are not critical. However, it is critical that the area fraction of Nb including and within the diffusion barrier is from 50-65% of the area specified.
[0062] Regarding the Nb to Sn atomic ratio including and within the Nb diffusion barrier of the subelement, an ideal Nb to Sn atomic ratio within the subelement should be close to the atomic ratio of Nb.sub.3Sn, 3:1. However, practical considerations impact this ratio, as full conversion to Nb.sub.3Sn would, because of naturally occurring variations of thickness of the barrier tube, result in tin diffusion to the stabilization matrix. This leakage in turn lowers RRR and stability of the wire, making it difficult to achieve the theoretical critical current without quenching the sample. Therefore, in practice this minimum ratio is about 3.3:1, but less than about 3.7:1 to minimize the underutilized wire cross-section consisting of unreacted Nb. A value of below 3:1 does not prevent J.sub.c of at least 2000 A/mm.sup.2 (4.2 K, 12 T) if other key parameters are in place, but it does greatly decrease RRR and make it an impractical conductor. The understanding and control of this parameter are important to the methods described herein.
[0063] Regarding the area ratio of Sn to Cu within the “non-Cu fraction” Sn wt %/(Sn wt %+Cu wt %) within the Nb barrier envelope of the subelement, the Sn wt %/(Sn wt %+Cu wt %) within the diffusion barrier is a critical parameter. Values are needed above about 45%, and up to about 65%, but preferably from 50%-60% in order for the Sn to react quickly with the Nb alloy to form a very high quality Nb.sub.3Sn phase. Regarding the non-copper J.sub.c, the effect of the Sn wt %/(Sn wt %+Cu wt %) within the diffusion barrier in the internal tin wire is illustrated in
[0064] Regarding the area ratio of Cu and Nb in the filament package (Local Area Ratio), the local area ratio (LAR) must be small, preferably in the range of from 0.10 to 0.30. Minimizing LAR is critical to enhancing item 1, the amount of Nb that can be located in the subelement. However, LAR must be greater than zero as Cu is needed to act as a diffusion network for tin. The lack of a copper diffusion network in “tube process” internal tin is why that process failed to deliver high J.sub.c despite high Sn wt %/(Sn wt %+Cu wt %) within the diffusion barrier.
[0065] Regarding a distributed barrier approach, as opposed to a single diffusion barrier approach, a distributed barrier of Nb is used. The term “distributed barrier” refers to a strand design where each subelement has its own diffusion barrier, as opposed to a diffusion barrier around the entire collection of subelements as seen in many internal tin wires such as the internal tin designs proposed for the ITER fusion tokamak project. One prior art internal tin wire made in commercial quantities by the distributed barrier method, the “Modified Jelly Roll,” is described by U.S. Pat. Nos. 4,262,412 and 4,414,428, the disclosures of which are herein incorporated by reference. The distributed barrier approach allows for lower Cu fractions within the subelement. This feature enhances the Sn wt %/(Sn wt %+Cu wt %) within the diffusion barrier because in the single barrier approach, due to practical handling concerns, a significant amount of copper must be left on the outside of a subelement before it can be restacked in a barrier. This in turn dilutes the Sn wt %/(Sn wt %+Cu wt %). In the methods described herein, the distributed barrier also provides for a continuous web of high conductivity copper between all of the subelements, enhancing electrical stability. The single barrier construction is electrically meta-stable or unstable with respect to current carrying capacity, especially at higher J.sub.c levels. An illustration of a distributed barrier wire is shown in
[0066] Regarding a Nb diffusion barrier that can be reacted to form Nb.sub.3Sn, a reactable Nb ring is used as the diffusion barrier. This feature is key to maximizing the Nb content in the non-copper portion of the wire. Many internal tin wire designs feature an inert Ta diffusion barrier, but this uses valuable space in the subelement cross-section. Using Nb, this space may be converted to a useful superconductor. However, the Nb must be thick enough so that not all of it reacts, thus preventing tin from diffusing into the copper stabilizer matrix. Achieving this proper balance is one of the benefits of the methods described herein.
[0067] Regarding the ratio of Nb diffusion barrier thickness to filament diameter, and thus the Nb distribution (fractions) between filaments and outer diffusion barrier, the thickness of the Nb diffusion barrier must be sufficient to ensure that at some stage during the heat treatment the filaments are fully reacted yet the barrier is only partially reacted. Thus, additional time in the heat treatment is used to controllably react the fraction of barrier desired. However it should not be too thick. Otherwise, the non-copper region will have too large a fraction of unreacted Nb, reducing the non-copper J.sub.c. Preferably the barrier thickness to filament radius is between 1:1 to 6:1. The relationship between the thickness of the barrier and the filaments also dictates the barrier fraction of the non-copper portion of the subelement.
[0068] Regarding the Nb filament and Nb barrier ring absolute size in the final wire, the absolute size of the filaments and barrier is critical in determining if the Nb reacts completely within a practical heat treatment time. Typically for internal tin heat treatments, longer and/or higher temperature heat treatments results in larger Nb.sub.3Sn grain sizes and reduced layer critical current density at moderate magnetic fields, i.e. 12-16 Tesla. Therefore smaller Nb filaments allow a heat treatment to be chosen to minimize grain size throughout a fully reacted filament, yet react the barrier not fully but instead about 50-90%. Typically this Nb filament diameter must be at least 0.5 μm but no more than 7 μm in the finished wire condition, preferably from 1 μm to 5 μm.
[0069] In general, providing at least a certain percentage of Nb filaments having smaller dimensions, i.e. finer with more rows, may provide improved current in the resulting multifilament Nb.sub.3Sn superconducting wire. For instance, providing at least 25%, 33%, 50%, 67%, 75%, 80% or 90% or so of the Nb filaments having a diameter of less than about 1.0 μm or 1.5 μm or 2.0 μm or 2.5 μm or 3.0 μm or 4.0 μm or 5.0 μm may be particularly advantageous.
[0070] Regarding minimizing the dissolution of Nb filament in a Sn rich environment and excessive Nb.sub.3Sn grain growth during heat treatment while fully converting the filaments to Nb.sub.3Sn, the selection of a proper heat treatment is the final step needed to produce a high J.sub.c conductor. It is possible to choose all the proper design parameters but over or under react the wire by heat treatment so as to achieve less than optimum J.sub.c values. The heat treatment must be chosen so as to react all of the filaments and most, but not all of the diffusion barrier. This must be determined empirically as the optimal heat treatment for a fixed wire design varies by subelement size and thus wire diameter. Essentially independent of wire diameter, the first two sequences are typically 210° C. for about48 hours and 400° C. for about 48 hours. These two steps are needed to form the bronze phases and start the tin diffusion through the copper matrix. If these steps are omitted, the wire is subject to tin bursting, and if they are too lengthy, the tin rich bronze phases can dissolve Nb in the inner filament ring, reducing the Nb available for reaction. For subelements larger than about100 μm in finished wire, a 570° C. sequence for about48 hours is helpful to aid in tin diffusion. The Nb.sub.3Sn formation step is optimal between 625° C. and 725° C., with the length on the order of 10 to greater than 200 hours, depending on subelement size. A heat treatment study is needed to establish the optimal heat treatment per wire design.
[0071] It is well known in the literature that alloys of Nb (e.g. Nb—Ta, Nb—Ti, Nb—Ta—Ti) and/or alloys of Sn (e.g. Sn—Ti, Sn—Cu) are normally required to produce the highest J.sub.c strand. Nb and Sn alloy selection is also an important design parameter and some doping with e.g. Ta and/or Ti is useful to achieve the best properties. In addition, the fact that Ta doped Nb.sub.3Sn reacts more slowly than Ti doped Nb.sub.3Sn at the final heat treatment plateau if that plateau is around 630° C., can be used to create a more effective diffusion barrier by making the subelement diffusion barrier of Nb7.5 wt % Ta alloy and doping the filaments with Nb47 wt %Ti rods. Thus, when for subelements in the 20-70 micron range a relatively long heat treatment at approximately 630° C. results in a conductor having maximum J.sub.c and RRR.
[0072] According to the methods described herein, the following parameters are instrumental in producing the desired properties in the subelements that are then incorporated into the composite wire structures: Sn wt %/(Sn wt %+Cu wt %) within the diffusion barrier is at least 45%, preferably 50-55%; and atomic Nb: Sn is equal to or greater than 2.7 but not more than 3.7, preferably about 3.45; the LAR is from 0.5 to 0.1; a distributed barrier design is used; a barrier that is reactable to Nb.sub.3Sn (i.e., Nb) is provided; a barrier that is thicker than the Nb filament 11 radius from
[0073]
[0074] Individual subelements 22 are best seen in the enlarged cross-sectional in
[0075] During the initial 210° C. stage of the heat treatment of wire 20, the Sn diffuses into the copper matrix, e.g., starting at 35, forming high Sn % bronze phases. During the 400° C. heat treatment stage, Sn further diffuses from 35 to the intervening copper 12. If the wire is heated directly to the Nb.sub.3Sn reaction stage without these pre-reaction sequences, the rapid conversion of tin from solid to liquid can lead to rapid differential expansion and the tin bursting through the subelement. One of the benefits of the methods described herein is that subelements of high Nb and Sn wt %/(Sn wt %+Cu wt %) can be successfully converted by heat treatment to form a large volume fraction of high quality Nb.sub.3Sn. Allocation of some Nb in both the reactable diffusion barrier and within a copper web containing Nb filaments is of prime importance to achieve a wire capable of high J.sub.c without the wire experiencing Sn bursting out of the subelement during heat treatment. The methods described herein thus eliminate a defect of the “tube process” whereby high Sn wt %/(Sn wt %+Cu wt %) wires experienced tin bursting.
[0076] For subelements larger than 100 μm, a 570° C. sequence for about 48 hours can be added to aid in tin diffusion to the filaments furthest from the tin source. During the 625° C. to 725° C. heat treatment stage, Cu—Sn phases react rapidly with the Nb filaments 11. The Nb barrier 31 also reacts during the 625° C. to 725° C. stage to contribute to the non-copper critical current density. The degree of barrier reaction is controlled by the temperature and length of the final heat treatment stage. It is up to the end user to trade off between critical current density and RRR, as increased reaction time eventually leads to decreased RRR. The Nb filaments 11 and barrier 31 constitute about 55% to 60% of the subelement area.
[0077] Table 1 summarizes the key parameters necessary to create the wire of this invention.
TABLE-US-00001 TABLE 1 Parameter Range Preferred Range Total Nb content 50-65% of Non-Cu 55-60% of Non-Cu Sn wt %/((Sn wt % + Cu wt %) 45-65% 50-60% within the diffusion barrier Local Area Ratio 0.10-0.50 0.15-0.45 Nb to Sn atomic ratio 2.7-3.7 3.1-3.6 Nb filament diameter 0.5-7 microns 1-5 microns Nb diff. barrier thickness 0.8-11 microns 1.5-8 microns Nb barrier fraction of Nb 20-50% 25-35%
[0078] The invention is further illustrated by the following Example, which, however, is to be deemed illustrative and not limiting the invention:
EXAMPLE 1
[0079] In the course of developing and refining the methods described herein, several different wires were prepared which illustrate the principles described above. The Nb alloy used for the filaments and the diffusion barriers was Nb7.5 wt % Ta, and the Sn alloy used was Sn0.7 wt % Cu. The bulk of the wire was fabricated to 0.7 mm or 0.8 mm diameter, although shorter lengths were made from 0.4 mm to 1.6 mm diameter, corresponding to a subelement size range of 35 μm-195 μm and a filament size range of 0.9 μm-5 μm. Final piece lengths were as good as or better than internal tin wire made by the Modified Jelly Roll process, with >1 km piece lengths routinely achievable in 0.7 mm and 0.8 mm diameter wire, demonstrating that the improved properties of the wires do not come at the expense of manufacturability. All the wires conformed to the preferred parameters listed in Table 1. The plot in
[0080] While the present invention has been described 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 teachings. Accordingly, the invention is to be broadly construed, and limited only by the scope and spirit of the claims now appended hereto.