JPH01111702A - Production of room temperature superconductor from composite oxide utilizing irradiation - Google Patents
Production of room temperature superconductor from composite oxide utilizing irradiationInfo
- Publication number
- JPH01111702A JPH01111702A JP62269000A JP26900087A JPH01111702A JP H01111702 A JPH01111702 A JP H01111702A JP 62269000 A JP62269000 A JP 62269000A JP 26900087 A JP26900087 A JP 26900087A JP H01111702 A JPH01111702 A JP H01111702A
- Authority
- JP
- Japan
- Prior art keywords
- amt
- beams
- contg
- compound oxide
- room temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002887 superconductor Substances 0.000 title claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000002131 composite material Substances 0.000 title claims description 3
- 239000002245 particle Substances 0.000 claims abstract description 11
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 7
- 229910052706 scandium Inorganic materials 0.000 claims abstract description 6
- 238000006073 displacement reaction Methods 0.000 claims abstract 2
- 238000010894 electron beam technology Methods 0.000 claims abstract 2
- 238000010884 ion-beam technique Methods 0.000 claims abstract 2
- 230000005855 radiation Effects 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 8
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 3
- 150000002602 lanthanoids Chemical class 0.000 claims description 3
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims description 3
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 3
- 239000000843 powder Substances 0.000 abstract description 8
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 abstract description 4
- 239000007788 liquid Substances 0.000 abstract description 3
- 238000003825 pressing Methods 0.000 abstract description 2
- 238000010298 pulverizing process Methods 0.000 abstract description 2
- 239000007787 solid Substances 0.000 abstract description 2
- 239000010409 thin film Substances 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 230000001678 irradiating effect Effects 0.000 abstract 1
- HYXGAEYDKFCVMU-UHFFFAOYSA-N scandium(III) oxide Inorganic materials O=[Sc]O[Sc]=O HYXGAEYDKFCVMU-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 description 9
- 239000002243 precursor Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000010304 firing Methods 0.000 description 3
- 241000968352 Scandia <hydrozoan> Species 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- HJGMWXTVGKLUAQ-UHFFFAOYSA-N oxygen(2-);scandium(3+) Chemical compound [O-2].[O-2].[O-2].[Sc+3].[Sc+3] HJGMWXTVGKLUAQ-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- CNEWPRQQHICZBP-UHFFFAOYSA-N [O].[Cu].[Ba].[La] Chemical compound [O].[Cu].[Ba].[La] CNEWPRQQHICZBP-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 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
- 229910000311 lanthanide oxide Inorganic materials 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000001308 synthesis method 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
- H10N60/0884—Treatment of superconductor layers by irradiation, e.g. ion-beam, electron-beam, laser beam or X-rays
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Oxygen, Ozone, And Oxides In General (AREA)
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
- Manufacturing Of Electric Cables (AREA)
Abstract
Description
【発明の詳細な説明】
(イ〕 産業上の利用分野
この発明は次のように広い分野への応用ができる。(1
) 宇宙や地下空間での電力貯蔵のための超伝導体へ
の利用、■ 電気エネルギーの損失が少ない発電、送電
又は配電のための超伝導体への利用、(3基板上の常伝
導体薄膜へ放射線を照射して、超伝導回路及びジョセフ
ソン接合素子形成への利用、(4) その他超伝導を
応用する機器への利用。[Detailed description of the invention] (a) Industrial application field This invention can be applied to a wide range of fields as follows. (1)
) Use in superconductors for power storage in space or underground space; ■ Use in superconductors for power generation, transmission, or distribution with little electrical energy loss; irradiation with radiation to form superconducting circuits and Josephson junction elements; (4) use in other devices that apply superconductivity;
(ロフ 従来の技術
従来の電気設備や電子装置では、電気エネルギーの発熱
による多大な損失と発熱によるllI害が常に付きまと
い、このI+Tl!flを克服することは非常に困難で
あった。酸化物を焼結するだけの従来の超伝導体の製造
方法では、最近開発された酸化物高温超伝導体でさえ、
その臨界温度が絶対温度で約90°に以下であるため超
伝導体の実用化にはなお問題があった。(Roff) Conventional technology In conventional electrical equipment and electronic devices, there is always a huge loss due to heat generation of electrical energy and llI harm due to heat generation, and it is extremely difficult to overcome this I+Tl!fl. The traditional method of manufacturing superconductors, which involves simply sintering, is difficult to manufacture, even for recently developed oxide high-temperature superconductors.
Since its critical temperature is below about 90° in absolute terms, there are still problems in putting superconductors into practical use.
(ハ)発明が解決しようとする問題点
この発明は放射線照射を利用して液体窒素温度から室温
までの温度範囲で、超伝導現象が安定に発現する超伝導
体を製造することを目的とする。(c) Problems to be solved by the invention The purpose of this invention is to use radiation irradiation to produce a superconductor that stably exhibits superconductivity in a temperature range from liquid nitrogen temperature to room temperature. .
(ニ)問題を解決するための手段
従来の材料と技術では絶対温度が約100°に以上で安
定に超伝導環1を起こしうる焼結法による材料のwJ造
が不可能であった。以下にこの発明による高温で安定な
超伝導体を!+2造する方法を述べる。(d) Means for Solving the Problem With conventional materials and techniques, it has been impossible to produce a wJ using a sintering method that can stably form the superconducting ring 1 at an absolute temperature of about 100° or more. Below is a superconductor that is stable at high temperatures according to this invention! I will explain how to create +2.
1)先駆物質の合成法
■ イ ッ ト リ ウ ム 系 (Y−
Ba−Cu−0系)、スカンジウム系(Sc−Ba−C
u−0系)及びランタニド系(Ln−Ba−Cu−0系
)の複合酸化物が、焼成後ペロブスカイト構造を構成す
るようにするには、イツトリア(Y to s) 、ス
カンジア(SC201)、又はランタニドオキサイド(
L n 20 i>をそれぞれ炭酸バリウム(BaCO
,)及び酸化第2tjA(CuO)の粉末と調合するの
が基本である。そのためには、イオン半径や化学的性質
が近似のイツトリウム、スカンジウム又はランタニドの
元素量を1とすると、元素量比でバリウム2. WA3
の割合で混合し、次に述べるように焼成する。1) Synthesis method of precursor ■ Yttrium-based (Y-
Ba-Cu-0 system), scandium system (Sc-Ba-C
In order for the composite oxides of u-0 series) and lanthanide series (Ln-Ba-Cu-0 series) to constitute a perovskite structure after firing, ittria (Y to s), scandia (SC201), or Lanthanide oxide (
L n 20 i> respectively, barium carbonate (BaCO
, ) and oxidized secondary tjA (CuO) powder. To this end, if the elemental amount of yttrium, scandium, or lanthanide, which has similar ionic radius and chemical properties, is 1, then the elemental amount ratio of barium is 2. WA3
and baked as described below.
■ 調合済みの粉末は通常の混合粉砕機で混合及び粉砕
を行い、粒子径が約1ミクロン以下の均質な混合粉末と
する。この混合粉末を約1100〜1200’にの大気
中で約10h仮焼する。この仮焼粉末を再び粒子径約1
ミクロン以下に粉砕して仮焼済み粉末とする0次に高温
超伝導体を形成する手段は、超伝導体の形態にもよるが
、(1) 粉末、■ プレスによる固形体、(3)
基板上の薄膜、(4) 中空管への充てんなどの状
態で本焼成する。この焼成条件は超伝導体の形状、寸法
にもよるが、たとえば1200〜1400”Kの空気中
で約25hである。■ The blended powder is mixed and pulverized using an ordinary mixer and pulverizer to form a homogeneous mixed powder with a particle size of approximately 1 micron or less. This mixed powder is calcined in the atmosphere at about 1100-1200' for about 10 hours. This calcined powder is reused with a particle size of approximately 1
The means for forming a zero-order high temperature superconductor by pulverizing it to micron size or less to make a calcined powder depends on the form of the superconductor, but it depends on the form of the superconductor: (1) powder, ■ solid body by pressing, (3)
The thin film on the substrate, (4) is filled into a hollow tube, etc., and then subjected to main firing. The firing conditions depend on the shape and dimensions of the superconductor, but are, for example, about 25 hours in air at 1200-1400''K.
2)放射線による処理法
上記の焼成体に超伝導特性を発揮するのに必要な構造す
なわち超伝導相を生じさせるために、焼成体を、室温か
ら約600°にの温度範囲でヘリウムガス雰囲気中に保
持し、焼成体に対し放射線を照射する。適正な放射線の
照射量は、荷電粒子線で10′6〜10”個/ c m
”、又非荷電粒子線で1019〜l Q IS個/
c m ”の範囲に入る。照射量がこれらの上限を超え
ると超伝導相が破壊される。2) Radiation treatment method In order to generate the structure necessary for the above-mentioned fired body to exhibit superconducting properties, that is, a superconducting phase, the fired body is treated in a helium gas atmosphere at a temperature range from room temperature to approximately 600°. and irradiate the fired body with radiation. The appropriate radiation dose is 10'6 to 10'' particles/cm of charged particle beam.
”, and with uncharged particle beam 1019~l Q IS pieces/
cm'' range. If the irradiation dose exceeds these upper limits, the superconducting phase will be destroyed.
(ホ〕 作用
先駆物質に電気抵抗測定リード線を付け、放射線照射装
置内で、照射面と照射後の電気抵抗値を室温から20°
Kまでの冷却過程で長時間連続的に測定してそれぞれの
過程で電気抵抗の温度依存性を調べることにより第1図
と第2図を得た。第1図と第2図は、いずれも横軸に絶
対温度を、縦軸に電気抵抗¥1(Ω)をとったもので、
この発明の例として、ランタン−バリウム−銅−酸素系
へロブスカイト構造の複合酸化物に原子炉の放射線(中
性子線など)を照射する前と照射したt&の材料の電気
抵抗の温度変化を示したものである。第1図は比較的低
量の放射線照射の結果であり、第2図は第1図より高い
放射線照射の結果である。(e) Attach an electrical resistance measurement lead to the action precursor, and measure the electrical resistance value of the irradiated surface and after irradiation by 20° from room temperature in the radiation irradiation equipment.
Figures 1 and 2 were obtained by making continuous measurements over a long period of time during the cooling process to K and examining the temperature dependence of the electrical resistance during each process. In both Figures 1 and 2, the horizontal axis represents absolute temperature, and the vertical axis represents electrical resistance ¥1 (Ω).
As an example of this invention, temperature changes in the electrical resistance of the material before and after irradiation of a lanthanum-barium-copper-oxygen complex oxide with a helobskite structure with nuclear reactor radiation (neutron beam, etc.) are shown. It is something. FIG. 1 is the result of a relatively low dose of radiation, and FIG. 2 is the result of a higher dose of radiation than FIG.
両図において、材料の電気抵抗値は冷却過程で矢印のよ
うに変化していて、放射線照射により材料の超伝導性が
液体窒素温度から室温までの温度範囲で明らかに安定に
発現しているのがわかる。な明細書の浄書1
お第1表と第2表はそれぞれ第1図と第2図での先駆物
質に対する放射線照射の条件を示したものである。In both figures, the electrical resistance value of the material changes as shown by the arrow during the cooling process, and the superconductivity of the material clearly appears stably in the temperature range from liquid nitrogen temperature to room temperature due to radiation irradiation. I understand. Table 1 and Table 2 show the conditions for irradiation of the precursor materials in FIGS. 1 and 2, respectively.
第1図は放射照射量が比較的低い場合の、放射線照射前
の先駆物質の電気抵抗と温度の関係 (a)及び放射線
照射後の同物質の電気抵抗と温度の関係(bとC)を示
し、第2図は放射線照射量が比較的高い場合の、放射線
照射前の先駆物質の電気抵抗と温度の間係(a’)及び
放射線照射後の同物質の電気抵抗と温度の間係(b’と
c′)を示す。
手続補正歯(方式)
昭和63年2月12日Figure 1 shows the relationship between the electrical resistance and temperature of the precursor material before irradiation (a) and the relationship between the electrical resistance and temperature of the same material after irradiation (b and C) when the radiation dose is relatively low. Figure 2 shows the relationship between the electrical resistance and temperature of the precursor material before irradiation (a') and the relation between the electrical resistance and temperature of the precursor material after irradiation (a') when the radiation dose is relatively high. b' and c') are shown. Procedural correction tooth (method) February 12, 1988
Claims (1)
ウム系及びランタニド系複合酸化物に放射線すなわち原
子変位を起こしうる電子線、陽子線、重イオン線の荷電
粒子又は中性子線などの非荷電粒子を照射して、液体窒
素温度から室温までの温度範囲で安定に超伝導現象を発
現する超伝導体を製造する方法。1 Yttrium-based scandium-based and lanthanide-based composite oxides with a perovskite structure are irradiated with radiation, that is, charged particles such as electron beams, proton beams, and heavy ion beams that can cause atomic displacement, or uncharged particles such as neutron beams. A method for manufacturing superconductors that stably exhibit superconductivity in the temperature range from temperature to room temperature.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62269000A JPH01111702A (en) | 1987-10-24 | 1987-10-24 | Production of room temperature superconductor from composite oxide utilizing irradiation |
| IT67931/88A IT1224497B (en) | 1987-10-24 | 1988-10-18 | METHOD FOR THE PRODUCTION OF AN AMBIENT TEMPERATURE SUPERCONDUCTOR FROM A COMPOSITE OXIDE USING RADIATION IRRADIATION |
| GB8824505A GB2211497A (en) | 1987-10-24 | 1988-10-19 | Method of producing room-temperature superconductor |
| FR8813854A FR2622357A1 (en) | 1987-10-24 | 1988-10-21 | PROCESS FOR PRODUCING AMBIENT TEMPERATURE SUPERCONDUCTOR FROM COMPOUND OXIDE USING IRRADIATION BY RADIATION |
| DE3835989A DE3835989A1 (en) | 1987-10-24 | 1988-10-21 | METHOD FOR PRODUCING A ROOM TEMPERATURE SUPRALINE FROM AN OXIDE COMPOUND USING RADIATION WITH A PARTICULAR RADIATION |
| CN88107397.0A CN1033122A (en) | 1987-10-24 | 1988-10-22 | Using irradiation with radiation is prepared the method for normal temperature superconductor by composite oxides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62269000A JPH01111702A (en) | 1987-10-24 | 1987-10-24 | Production of room temperature superconductor from composite oxide utilizing irradiation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01111702A true JPH01111702A (en) | 1989-04-28 |
Family
ID=17466278
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62269000A Pending JPH01111702A (en) | 1987-10-24 | 1987-10-24 | Production of room temperature superconductor from composite oxide utilizing irradiation |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPH01111702A (en) |
| CN (1) | CN1033122A (en) |
| DE (1) | DE3835989A1 (en) |
| FR (1) | FR2622357A1 (en) |
| GB (1) | GB2211497A (en) |
| IT (1) | IT1224497B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04265221A (en) * | 1991-01-30 | 1992-09-21 | Gec Marconi Electron Syst Corp | Method for enhancing upper critical magnetic field of high temperature superconducting ceramic copper oxide perovskite |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4119707A1 (en) * | 1991-06-14 | 1992-12-17 | Siemens Ag | METHOD FOR PRODUCING A HIGH-TEMPERATURE SUPRAL-CONDUCTING COMPONENT AND HIGH-TEMPERATURE SUPRAL-CONDUCTING COMPONENT |
| US6465739B1 (en) | 1993-12-21 | 2002-10-15 | Finch International Limited | Very high temperature and atmospheric pressure superconducting compositions and methods of making and using same |
| JPH0891837A (en) * | 1994-09-16 | 1996-04-09 | Kokusai Chodendo Sangyo Gijutsu Kenkyu Center | Oxide superconductor and method for manufacturing the same |
| DE10007915A1 (en) * | 2000-02-21 | 2001-09-13 | Alcatel High Temperature Super | Material used, e.g., in the production of a sputtering target and as a superconductor contains lead, carbon and oxygen |
| US6799462B1 (en) | 2003-06-05 | 2004-10-05 | International Business Machines Corporation | Gravimetric measurement method and system |
| US6898970B2 (en) | 2003-06-05 | 2005-05-31 | International Business Machines Corporation | Inertial navigation device for ion propulsion driven spacecraft |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6433006A (en) * | 1987-04-08 | 1989-02-02 | Hitachi Ltd | Production of superconducting oxide and superconducting device |
| JPS6461373A (en) * | 1987-08-28 | 1989-03-08 | Matsushita Electric Industrial Co Ltd | Production of superconductor |
| JPS6487516A (en) * | 1987-09-29 | 1989-03-31 | Matsushita Electric Industrial Co Ltd | Production of thin film superconductor |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3346425A (en) * | 1964-04-01 | 1967-10-10 | Gen Electric | Superconductors |
| CA1328242C (en) * | 1987-05-18 | 1994-04-05 | Nobuhiko Fujita | Process for manufacturing a superconductor and a method for producing a superconducting circuit |
-
1987
- 1987-10-24 JP JP62269000A patent/JPH01111702A/en active Pending
-
1988
- 1988-10-18 IT IT67931/88A patent/IT1224497B/en active
- 1988-10-19 GB GB8824505A patent/GB2211497A/en not_active Withdrawn
- 1988-10-21 DE DE3835989A patent/DE3835989A1/en not_active Withdrawn
- 1988-10-21 FR FR8813854A patent/FR2622357A1/en active Pending
- 1988-10-22 CN CN88107397.0A patent/CN1033122A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6433006A (en) * | 1987-04-08 | 1989-02-02 | Hitachi Ltd | Production of superconducting oxide and superconducting device |
| JPS6461373A (en) * | 1987-08-28 | 1989-03-08 | Matsushita Electric Industrial Co Ltd | Production of superconductor |
| JPS6487516A (en) * | 1987-09-29 | 1989-03-31 | Matsushita Electric Industrial Co Ltd | Production of thin film superconductor |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04265221A (en) * | 1991-01-30 | 1992-09-21 | Gec Marconi Electron Syst Corp | Method for enhancing upper critical magnetic field of high temperature superconducting ceramic copper oxide perovskite |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1224497B (en) | 1990-10-04 |
| IT8867931A0 (en) | 1988-10-18 |
| CN1033122A (en) | 1989-05-24 |
| GB8824505D0 (en) | 1988-11-23 |
| GB2211497A (en) | 1989-07-05 |
| FR2622357A1 (en) | 1989-04-28 |
| DE3835989A1 (en) | 1989-05-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Zhang et al. | Synthesis of Bi2Sr2CaCu2Ox superconductors via direct oxidation of metallic precursors | |
| JPH01242418A (en) | High temperature superconductor and its manufacturing method | |
| Horita et al. | Cation diffusion in (La, Ca) CrO3 perovskite by SIMS | |
| JPH01111702A (en) | Production of room temperature superconductor from composite oxide utilizing irradiation | |
| JPS63222068A (en) | Device and system based on novel superconductive material | |
| JPH07302936A (en) | Method of increase of electric current transportation capacitance of high-temperature superconducting body | |
| JPH0259465A (en) | Manufacturing method of oxide high temperature superconductor | |
| Kovatcheva et al. | An X-ray and neutron diffraction study of cation substituted TlSr2CuO5 | |
| JPH06511551A (en) | Method for manufacturing a molded body of high temperature superconductor with high critical current | |
| CN105845269A (en) | High temperature superconducting material and method for preparing high temperature superconducting material | |
| JP2609460B2 (en) | Method for manufacturing molded body of ceramic oxide superconducting material | |
| Sergeev et al. | High-Temperature Superconducting Materials Based on Bismuth with a Low Critical Current | |
| JP2603688B2 (en) | Superconducting material reforming method | |
| Brown et al. | Photoemission spectroscopy of YBa2Cu3O6+ x | |
| JPH02279517A (en) | Superconductor | |
| JPH01164780A (en) | Method for modifying oxide superconductor | |
| JP2730043B2 (en) | Superconductor | |
| JP2716698B2 (en) | Method for producing superconducting oxide | |
| JPH02255526A (en) | Superconductor | |
| JPH02124715A (en) | Production of thallium base oxide superconductor | |
| JPH01257107A (en) | Production of superconducting material | |
| JPH03109213A (en) | Superconductor | |
| JPH04114915A (en) | Superconductor | |
| JPH02116619A (en) | Superconducting material | |
| Al-Shafei | High temperature ceramic superconductors: oxalate co-precipitation procedure for synthesis and influence of compositional variations |