WO2005104144A1 - 臨界電流特性に優れたMgB2超電導線材の製造方法 - Google Patents
臨界電流特性に優れたMgB2超電導線材の製造方法 Download PDFInfo
- Publication number
- WO2005104144A1 WO2005104144A1 PCT/JP2005/007714 JP2005007714W WO2005104144A1 WO 2005104144 A1 WO2005104144 A1 WO 2005104144A1 JP 2005007714 W JP2005007714 W JP 2005007714W WO 2005104144 A1 WO2005104144 A1 WO 2005104144A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- wire
- mgb
- producing
- metal tube
- carbon
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 38
- 239000002184 metal Substances 0.000 claims abstract description 75
- 229910052751 metal Inorganic materials 0.000 claims abstract description 75
- 239000002994 raw material Substances 0.000 claims abstract description 41
- 239000008188 pellet Substances 0.000 claims abstract description 35
- 239000011248 coating agent Substances 0.000 claims abstract description 30
- 238000000576 coating method Methods 0.000 claims abstract description 30
- 239000000843 powder Substances 0.000 claims abstract description 29
- 238000010438 heat treatment Methods 0.000 claims abstract description 26
- 239000003575 carbonaceous material Substances 0.000 claims abstract description 22
- 239000011261 inert gas Substances 0.000 claims abstract description 9
- 239000011812 mixed powder Substances 0.000 claims abstract description 7
- 238000000748 compression moulding Methods 0.000 claims abstract description 6
- 239000010949 copper Substances 0.000 claims description 57
- 229910052802 copper Inorganic materials 0.000 claims description 55
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 54
- 238000004519 manufacturing process Methods 0.000 claims description 49
- 239000000463 material Substances 0.000 claims description 46
- 238000005491 wire drawing Methods 0.000 claims description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 36
- 229910002804 graphite Inorganic materials 0.000 claims description 22
- 239000010439 graphite Substances 0.000 claims description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 229910000975 Carbon steel Inorganic materials 0.000 claims description 7
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 7
- 229910000640 Fe alloy Inorganic materials 0.000 claims description 7
- 229910000990 Ni alloy Inorganic materials 0.000 claims description 7
- 239000010962 carbon steel Substances 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 239000010935 stainless steel Substances 0.000 claims description 7
- 229910001220 stainless steel Inorganic materials 0.000 claims description 7
- 239000007769 metal material Substances 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 238000011049 filling Methods 0.000 claims description 4
- 239000007770 graphite material Substances 0.000 claims description 2
- 230000001747 exhibiting effect Effects 0.000 abstract description 3
- 229910020073 MgB2 Inorganic materials 0.000 abstract 2
- 239000002245 particle Substances 0.000 description 21
- 229910052799 carbon Inorganic materials 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 229910003460 diamond Inorganic materials 0.000 description 8
- 239000010432 diamond Substances 0.000 description 8
- 230000004907 flux Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002887 superconductor Substances 0.000 description 5
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 238000011065 in-situ storage Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 238000011066 ex-situ storage Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000003507 refrigerant Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004453 electron probe microanalysis Methods 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- ALKZAGKDWUSJED-UHFFFAOYSA-N dinuclear copper ion Chemical compound [Cu].[Cu] ALKZAGKDWUSJED-UHFFFAOYSA-N 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B35/00—Boron; Compounds thereof
- C01B35/02—Boron; Borides
- C01B35/04—Metal borides
-
- 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
- H10N60/0856—Manufacture or treatment of devices comprising metal borides, e.g. MgB2
Definitions
- the present invention relates to a method for manufacturing a MgB superconducting wire, and relates to a power cable, a magnet, and a motor.
- the present invention relates to a manufacturing method capable of stably supplying superconducting wires applicable to power sources, generators, and the like at low cost.
- Patent document 1 Japanese Patent Application Laid-Open No. 2002-21916
- An object of the present invention is to develop a technology for converting MgB exhibiting such excellent characteristics into a wire.
- the powder sealing method is roughly classified into two types.
- such a metal tube filled with powder or pellets is also referred to as a sheath tube, and the material is also referred to as a sheath material.
- a superconducting breakdown phenomenon (called a superconducting entanglement) due to a flux jump, which is a phenomenon in which magnetic flux rapidly enters, occurs immediately after, as a sheath tube or a superconducting tangent.
- the present invention will be described by taking as an example a copper tube which has a high thermal conductivity and is effective in countermeasures against heat generation as a stabilizing material against the phenomenon.
- the present inventors have studied the superconducting material MgB by using a force Mg
- the reaction can be prevented by providing an intermediate layer of carbon, and carbon is contained in MgB.
- the wire rod (metal body) obtained by performing the wire drawing is further covered with another metal pipe and subjected to wire drawing.
- the metal pipe coated on the inside with a carbon-based material and the another metal pipe are the same or different types, and are made of copper, copper alloy, iron, iron alloy, carbon steel, stainless steel, And the nickel alloy force.
- the metal tube enclosing the pellet and the another metal tube are the same or different types, and copper, copper alloy, iron, iron alloy, carbon steel, stainless steel, nickel and nickel alloy are also selected.
- the wire obtained by the present invention had a critical current of 419 A and a critical current density of 460 kA / cm 2 in a self-magnetic field of 4.2 K in a short-length material.
- FIG. 1 A short sheet obtained by coating graphite powder inside the copper tube according to Example 1, filling the mixture with force, drawing, and then heat-treating at 600 ° C. for 2 hours.
- Single-core MgB wire rod
- Figure 3 shows a single-core MgB wire rod coated with graphite powder and a coating.
- the figure shows the result of elemental mapping of the cross section of a single-core MgB wire using EPMA.
- FIG. 4 A short single-core MgB wire rod prepared by coating graphite inside the copper tube according to Example 2 and then heat-treated at 500 to 800 ° C. for 2 hours each.
- FIG. 5 is an IV curve of a short single-core MgB wire rod prepared by coating a graphite paste on the inside of a copper tube according to Example 3 and then heat-treated at 600 ° C. for 2 hours. .
- FIG.6 A short single-core MgB / Cu wire (diameter 1.0mm) which was prepared by coating 5 to 15mol% of graphite paste inside the copper tube according to Example 5 and then heat-treated at 600 ° C for 2 hours. )
- FIG. 7 A short single-core MgB / Cu wire rod (diameter 0.8 mm) which was prepared by coating 0-15 mol% of graphite paste inside the copper tube according to Example 5 and then heat-treated at 600 ° C for 2 hours )
- the above-mentioned coating is an important step in the present invention in that the intended critical current characteristics are obtained.
- a carbon-based material is applied to the inside of a metal tube as a base material or to pellets obtained by compression molding.
- a carbon-based material in order to effectively suppress the reaction between the metal tube and Mg, particularly when the metal tube is a copper tube, and to reduce the reaction product that inhibits the critical current characteristics, the graphite material is used. It is preferable to select the material described above.
- a powdery or paste-like material is used as the raw material of the carbon-based material.
- coating is performed by dissolving it in an organic solvent. After coating, heat-treat and dry in an inert atmosphere.
- the thickness after drying is not particularly limited, but is preferably uniform if it is uniform, and 10 to 100 / ⁇ is sufficient for suppressing the reaction.
- the paste-like raw material may be used after being dissolved in an organic solvent, or may be directly applied to the inside of a metal tube or the surface of a pellet.
- the coating thickness is preferably 10 to 100 / ⁇ .
- the operation of applying the carbon-based material itself may be performed by an ordinary method.
- a mixture of powdered Mg and ⁇ powder materials or a mixture of powdered Mg and B powder materials with MgB is obtained.
- the mixed powder thus prepared is appropriately placed in a mold and compression-molded to form a pellet.
- the pellets are used for ease of handling and to ensure a constant raw material density over the entire length of the metal tube.
- Encapsulation of pellet in sheath tube The obtained pellet is sealed in a metal tube as a sheath tube. Specifically, in an inert atmosphere, the pellet is inserted into the metal tube sealed at one end from the other end, and the metal tube is sealed.
- the material of the tubular body is not particularly limited as long as it can secure a sufficient strength, but is usually iron, iron alloy, carbon steel, stainless steel, copper, copper alloy, or the like. -It is preferable to select one of nickel and nickel alloy.
- the sheath material for the stabilization copper and copper alloy may be mentioned as a substance which has a high thermal conductivity, a low electric resistivity, has excellent ductility, and is easily available. But MgB
- Cu and Mg may react during heat treatment to form compounds, but if it is desired to avoid the formation of compounds, stainless steel, nickel, nickel alloys, iron, iron alloys, carbon steel, etc. May be used.
- the metal tube into which the pellet has been inserted, prepared as described above, is subjected to wire drawing by swaging, roller dies, or the like.
- the wire drawing is not particularly limited even in the present invention, which is satisfactory according to a known method.
- the wire drawing may be performed in a plurality of times.
- the obtained wire may be further covered with another metal tube and further subjected to wire drawing.
- wires obtained by wire drawing It may be covered with another metal tube together with the metal material to be filled, and further subjected to wire drawing.
- the other metal tube described above may be copper, copper alloy, nickel, nickel alloy, iron, iron alloy, stainless steel, or the like. Steel or carbon steel power You can use some metal tubing that you chose.
- the wire (metal body) obtained by wire drawing is finished to a predetermined size, and optionally further wound in a coil shape, for example, in an inert atmosphere such as an Ar atmosphere, for example, Under a pressurized atmosphere of 2 atm or more, a heat treatment of heating for 1 to 2 hours at a temperature of 550 to 800 ° C, preferably 550 to 750 ° C, more preferably 580 to 680 ° C, Change Mg and B to MgB.
- the pressurized atmosphere is used to prevent the generation of voids, etc.
- the carbon film inside the metal tube serves as a protective layer for preventing the reaction between the metal tube and the raw material, thereby preventing generation of impurities.
- a copper tube having a thickness of 2.8 mm, a diameter of 12 mm, and a total length of 200 mm was plugged at one end with a graphite powder (purity of 99%, particle size of 44 m or less) on the inner wall thereof.
- a graphite powder purity of 99%, particle size of 44 m or less
- heat treatment was performed at 300 ° C for 1 hour in a heat treatment furnace in an Ar atmosphere to coat dalaphite on the inside of the copper tube. If heat treatment is performed in the atmosphere, the carbon constituting graphite may become CO and diffuse, so heat treatment in an inert atmosphere is required.
- powdered Mg having a particle size of 44 ⁇ m or less and powdered amorphous ⁇ having a particle size of 1 ⁇ m or less were blended at an element ratio of 1: 2 to obtain a first powder raw material.
- the mixed raw material thus obtained was formed into a pellet-shaped compression-molded product having a size of 6 x 10 mm in diameter using a dedicated mold.
- the green density was 1.6 g / cm 2 .
- pellet-shaped compression molded bodies that is, pellets, were sealed in the above-mentioned copper tube coated with graphite and having a thickness of 2.8 mm and a diameter of 12 mm.
- the pellet-enclosed copper tube thus obtained is then subjected to wire drawing.
- the wire drawing was performed using a conventional swaging machine.
- the copper tube was heated at 600 ° C for 2 hours under an atmosphere of Ar gas at 3 atm to carry out the reaction of Mg + 2B ⁇ MgB. I let you.
- Figure 1 shows the I-V characteristics of a short sample with a length of 30 mm measured by the four-terminal method, and the critical current was measured.
- the temperature 4.2K of the self-magnetic field shows the critical current value of more than 400A, the critical current density at this time reached 460kA / cm 2.
- the cross section of the wire is shown.
- the black area in the center is the superconducting material, and the white area surrounding it is copper sheath material.
- powdered Mg having a particle diameter of 44 ⁇ m or less and amorphous amorphous powder having a particle diameter of 1 ⁇ m or less were blended at an element ratio of 1: 2 to obtain a first powder raw material.
- the mixed raw material was prepared by adding diamond particles having a particle diameter of 0.1 ⁇ m or less to the mixed raw materials at a ratio of 0%, 3%, 6%, and 10%, respectively.
- the mixed raw material thus obtained was formed into a pellet-shaped compression molded body having a size of 6 ⁇ 10 mm in diameter using a dedicated mold.
- the green density was 1.6 g / cm 2 on average.
- pellet-shaped compression molded bodies are coated with graphite and then enclosed in a copper tube. Then, a total of four wire rod base materials (pellet-enclosed copper pipes) were prepared by adding 0%, 3%, 6%, and 10% of diamond particles.
- the copper tube was heated at 600 ° C for 2 hours under an atmosphere of Ar gas at 3 atm to carry out the reaction of Mg + 2B ⁇ MgB. I let you.
- Figure 2 shows the IV characteristics of the short sample with a length of 30 mm measured by the 4-terminal method in a 4.2 K self-magnetic field.
- the I-V curve obtained in Example 1 is additionally shown for comparison.
- the one having 6% diamond particles exhibited the best critical current characteristic.
- FIG. 3 also shows the results.
- the left side shows the case without coating
- the right side shows the case with coating.
- the area glowing white indicates the presence of the copper element.
- the coated sample has little penetration of copper element. This suggests that the graphite coating has the effect of reducing the reaction between elemental copper and Mg.
- a copper tube having a wall thickness of 2.8mm, a diameter of 12mm, and a total length of 200mm was plugged on one end with a graphite powder (purity of 99%, particle size of 44 ⁇ m or less) on its inner wall at a weight ratio of 1: 3. Then, the copper tube was horizontally rotated slowly with the other end lightly plugged, and the rotation was continued until acetone was evaporated and graphite was adhered to the inside of the tube.
- the mixed raw material thus obtained was formed into a pellet-shaped compression molded body having a size of 6 ⁇ 10 mm in diameter by using a dedicated mold.
- the green density was 1.6 g / cm 2 .
- pelletized compacts were coated with graphite and had a thickness of 2.8 mm and a diameter of 2.8 mm.
- the copper tube is heated at 500 ° C, 550 ° C, 650 ° C, 700 ° C, and 750 ° C in an atmosphere of Ar gas at 3 atm. , And heated at 800 ° C for 2 hours, Mg + 2B ⁇
- Figure 4 shows I-V curves of I_V characteristics measured by the four-terminal method for a short sample of 30 mm in length subjected to heat treatment at each temperature.
- the curve at 650 ° C almost coincides with the characteristic at 600 ° C shown in the examples.
- Example 3 [0059]
- a commercially available graphite paste (quick drying, for SEM, for XMA, solvent: n-butyl acetate) was directly applied to a coating material of a metal tube as a copper tube obtained by repeating Example 1. Coated on the surface.
- coating on the inside of the metal tube may cause uneven coating, and immediately after drying, the substance adhering to the inside of the metal tube may peel off and fall off.
- the graphite paste since the solvent has the effect of the adhesive, the effect of easily coating the metal pipe uniformly was obtained.
- Figure 5 shows the results of evaluating the IV characteristics of the obtained sample.
- a carbon molding was performed using a carbon vapor deposition apparatus on a compression-molded body, that is, a pellet obtained by compacting a mixed powder that was used to apply a coating material to a copper pipe by repeating the procedure of Example 1.
- a carbon vapor deposition apparatus on a compression-molded body, that is, a pellet obtained by compacting a mixed powder that was used to apply a coating material to a copper pipe by repeating the procedure of Example 1.
- the critical current exceeded 200 A, which was higher than the value without carbon deposition.
- the effect was smaller than when applied in a sheath tube. Further improvements are expected due to improved coating conditions.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006512603A JPWO2005104144A1 (ja) | 2004-04-22 | 2005-04-22 | 臨界電流特性に優れたMgB2超電導線材の製造方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004127309 | 2004-04-22 | ||
JP2004-127309 | 2004-04-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005104144A1 true WO2005104144A1 (ja) | 2005-11-03 |
Family
ID=35197244
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/007714 WO2005104144A1 (ja) | 2004-04-22 | 2005-04-22 | 臨界電流特性に優れたMgB2超電導線材の製造方法 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPWO2005104144A1 (ja) |
WO (1) | WO2005104144A1 (ja) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007157590A (ja) * | 2005-12-07 | 2007-06-21 | Hitachi Ltd | 高性能MgB2超電導線及び製造方法 |
JP2007172865A (ja) * | 2005-12-19 | 2007-07-05 | Showa Denko Kk | 超伝導体、超伝導線材、その製造方法及び用途 |
JP2008140556A (ja) * | 2006-11-30 | 2008-06-19 | Hitachi Ltd | MgB2超電導線材の製造方法 |
JP2011014304A (ja) * | 2009-06-30 | 2011-01-20 | Hitachi Ltd | 超電導線材 |
US20150111755A1 (en) * | 2012-04-26 | 2015-04-23 | The University Of Tokyo | Superconducting wire, superconducting wire precursor body and fabrication method thereof, and superconducting multi-core conductor precursor body |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003217370A (ja) * | 2002-01-23 | 2003-07-31 | Hitachi Cable Ltd | 二ホウ化マグネシウム超電導線材 |
JP2003331670A (ja) * | 2002-05-16 | 2003-11-21 | National Institute For Materials Science | MgB2超伝導線材の作製方法 |
JP2004047441A (ja) * | 2002-05-10 | 2004-02-12 | Edison Spa | MgB2製の中空フィラメントを基材とする超伝導線材の製法 |
JP2004111203A (ja) * | 2002-09-18 | 2004-04-08 | Internatl Superconductivity Technology Center | MgB2系超電導線材の作製方法 |
JP2005063768A (ja) * | 2003-08-08 | 2005-03-10 | Hitachi Cable Ltd | 金属シース超電導線材 |
JP2005063769A (ja) * | 2003-08-08 | 2005-03-10 | Hitachi Cable Ltd | 金属シース超電導線材及びその製造方法 |
-
2005
- 2005-04-22 WO PCT/JP2005/007714 patent/WO2005104144A1/ja active Application Filing
- 2005-04-22 JP JP2006512603A patent/JPWO2005104144A1/ja not_active Withdrawn
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003217370A (ja) * | 2002-01-23 | 2003-07-31 | Hitachi Cable Ltd | 二ホウ化マグネシウム超電導線材 |
JP2004047441A (ja) * | 2002-05-10 | 2004-02-12 | Edison Spa | MgB2製の中空フィラメントを基材とする超伝導線材の製法 |
JP2003331670A (ja) * | 2002-05-16 | 2003-11-21 | National Institute For Materials Science | MgB2超伝導線材の作製方法 |
JP2004111203A (ja) * | 2002-09-18 | 2004-04-08 | Internatl Superconductivity Technology Center | MgB2系超電導線材の作製方法 |
JP2005063768A (ja) * | 2003-08-08 | 2005-03-10 | Hitachi Cable Ltd | 金属シース超電導線材 |
JP2005063769A (ja) * | 2003-08-08 | 2005-03-10 | Hitachi Cable Ltd | 金属シース超電導線材及びその製造方法 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007157590A (ja) * | 2005-12-07 | 2007-06-21 | Hitachi Ltd | 高性能MgB2超電導線及び製造方法 |
JP4602237B2 (ja) * | 2005-12-07 | 2010-12-22 | 株式会社日立製作所 | 高性能MgB2超電導線及び製造方法 |
JP2007172865A (ja) * | 2005-12-19 | 2007-07-05 | Showa Denko Kk | 超伝導体、超伝導線材、その製造方法及び用途 |
JP2008140556A (ja) * | 2006-11-30 | 2008-06-19 | Hitachi Ltd | MgB2超電導線材の製造方法 |
JP2011014304A (ja) * | 2009-06-30 | 2011-01-20 | Hitachi Ltd | 超電導線材 |
US20150111755A1 (en) * | 2012-04-26 | 2015-04-23 | The University Of Tokyo | Superconducting wire, superconducting wire precursor body and fabrication method thereof, and superconducting multi-core conductor precursor body |
Also Published As
Publication number | Publication date |
---|---|
JPWO2005104144A1 (ja) | 2008-03-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7018954B2 (en) | Processing of magnesium-boride superconductors | |
EP1526586B1 (en) | Manufacturing method for superconducting wire | |
US20030036482A1 (en) | Processing of magnesium-boride superconductors | |
US20090197771A1 (en) | Method of manufacturing oxide superconducting wire, method of modifying oxide superconducting wire and oxide superconducting wire | |
Kumakura et al. | Superconducting Properties of Diffusion-Processed Multifilamentary ${\rm MgB} _ {2} $ Wires | |
JP5401487B2 (ja) | MgB2超電導線材 | |
JP2002373534A (ja) | 超電導線材とその作製方法及びそれを用いた超電導マグネット | |
Miao et al. | Studies of precursor composition effect on Jc in Bi‐2212/Ag wires and tapes | |
TW200834609A (en) | Production method of Bi-2223-based superconducting wire | |
WO2005104144A1 (ja) | 臨界電流特性に優れたMgB2超電導線材の製造方法 | |
WO2002069353A1 (en) | Superconducting borides and wires made thereof | |
JP2005310600A (ja) | MgB2線材の製造方法 | |
JP2008066168A (ja) | MgB2超伝導線材及びその製造法 | |
JP2003331660A (ja) | 金属シース超伝導体線材及び超電導コイル並びにその製造方法 | |
JP2007095367A (ja) | 二硼化マグネシウム超伝導体線材の作製方法 | |
JP5356132B2 (ja) | 超電導線材 | |
Atamert et al. | Novel superconducting MgB 2 wires made by continuous process | |
JP2004269268A (ja) | MgB2超伝導体の製造方法 | |
JP3945600B2 (ja) | Nb 3 Sn超伝導線材の製造方法 | |
JP4602237B2 (ja) | 高性能MgB2超電導線及び製造方法 | |
EP3503230A1 (en) | Magnesium diboride superconducting wire with magnesium coated iron sheath and method of obtaining | |
JP4925639B2 (ja) | Re123系酸化物超電導体とその製造方法 | |
Glowacki et al. | Comparative study of the continuous and batch thermal processing of MgB 2 wires | |
Yamamoto et al. | Processing of Low T c Conductors: The Compound MgB2 | |
JP4507899B2 (ja) | ビスマス系酸化物超電導線材およびその製造方法、該ビスマス系酸化物超電導線材を用いた超電導機器 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2006512603 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: DE |
|
122 | Ep: pct application non-entry in european phase |