JPH02257526A - Manufacture of oxide superconductor - Google Patents
Manufacture of oxide superconductorInfo
- Publication number
- JPH02257526A JPH02257526A JP1080049A JP8004989A JPH02257526A JP H02257526 A JPH02257526 A JP H02257526A JP 1080049 A JP1080049 A JP 1080049A JP 8004989 A JP8004989 A JP 8004989A JP H02257526 A JPH02257526 A JP H02257526A
- Authority
- JP
- Japan
- Prior art keywords
- oxide
- melting
- laser beam
- fiber
- oxide superconductor
- 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
Classifications
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E40/00—Technologies for an efficient electrical power generation, transmission or distribution
- Y02E40/60—Superconducting electric elements or equipment; Power systems integrating superconducting elements or equipment
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、酸化物超電導体の製造方法に係り、特に結晶
の配向性、すなわち超電導特性に優れた線状の酸化物超
電導体の製造方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for producing an oxide superconductor, and particularly a method for producing a linear oxide superconductor having excellent crystal orientation, that is, excellent superconducting properties. Regarding.
(従来の技術)
近年、酸化物超電導物質の開発が著しい速度で進められ
ており、La系、Y系、旧糸、Tl系等の超電導物質の
利用が有力視されている。(Prior Art) In recent years, the development of oxide superconducting materials has progressed at a remarkable speed, and the use of superconducting materials such as La-based, Y-based, old yarn, and Tl-based materials is considered to be promising.
しかしながら、これらの物質はその超電導特性に異方性
、すなわち結晶方位による特性の差が著しく、通常の合
成法によって得られた原料粉末を成型後焼結しただけで
はランダムな結晶方位のものしか得られないため、実用
的レベルに達する電気的、磁気的特性が得られないとい
う問題がある。However, these materials have anisotropy in their superconducting properties, that is, there are significant differences in properties depending on the crystal orientation, and simply molding and sintering the raw material powder obtained by normal synthesis methods only yields materials with random crystal orientation. Therefore, there is a problem in that electrical and magnetic properties that reach a practical level cannot be obtained.
上記の問題を解決する方法として、酸化物超電導物質を
溶融し、この融体を温度勾配を有する電気炉内で相対的
に移動させて結晶成長させることにより結晶の配向性を
高めることが試みられている。As a method to solve the above problem, an attempt has been made to increase crystal orientation by melting an oxide superconducting material and moving this melt relatively in an electric furnace with a temperature gradient to grow crystals. ing.
また、超電導体、たとえば線状の超電導体中にフローテ
ィングゾーンを形成して溶融、凝固させることにより結
晶の配向性を高めることも試みられている。Furthermore, attempts have been made to improve crystal orientation by forming a floating zone in a superconductor, such as a linear superconductor, and melting and solidifying the superconductor.
[発明が解決しようとする課題]
しかしながら、前者の溶融温度勾配結晶化法では温度勾
配の設定に限界があり、熱伝導により大きな勾配を炉内
に形成することが不可能なため、結晶配向の制御が困難
であるという難点を有する。[Problem to be solved by the invention] However, in the former melting temperature gradient crystallization method, there is a limit to the setting of the temperature gradient, and it is impossible to form a large gradient in the furnace by heat conduction, so it is difficult to change the crystal orientation. It has the disadvantage that it is difficult to control.
一方、後者のフローティングゾーンによる方法において
は、液相から安定に結晶化する相しか得られない上、そ
の成長速度は数印〜数11111/hrと極めて遅いと
いう難点を有する。特にこの方法においては、Y−Ba
−Cu−0系酸化物の場合、溶融→再結晶によって絶縁
物質であるY 2 BaCu0x相が生成され、超電導
物質であるYBa2 Cu30x相が生成されないとい
う致命的な欠点を有する。On the other hand, the latter method using a floating zone has the drawback that only a phase that stably crystallizes from the liquid phase can be obtained, and the growth rate thereof is extremely slow, ranging from several marks to several 11111/hr. In particular, in this method, Y-Ba
In the case of -Cu-0 based oxides, a fatal drawback is that the Y2BaCu0x phase, which is an insulating material, is produced by melting and recrystallization, but the YBa2 Cu30x phase, which is a superconducting material, is not produced.
本発明は上記の難点を解決するためになされたもので、
レーザビームを用いて結晶の配向性、すなわち超電導特
性に優れた線状の酸化物超電導体を製造する方法を提供
することをその目的とする。The present invention has been made to solve the above-mentioned difficulties.
The object of the present invention is to provide a method for manufacturing a linear oxide superconductor with excellent crystal orientation, that is, excellent superconducting properties, using a laser beam.
[課題を解決するための手段]
上記目的を達成するために、本発明の酸化物超電導体の
製造方法は、酸化物超電導物質あるいは酸化物超電導物
質を構成する元素を含む原料物質を溶融し、これを紡糸
してファイバ状またはテープ状の線状体を形成する工程
と、前記線状体にレーザビームを照射し、この照射によ
り形成される溶融帯域を急速に移動させるようにしたも
のである。[Means for Solving the Problems] In order to achieve the above object, the method for producing an oxide superconductor of the present invention includes melting an oxide superconducting material or a raw material containing an element constituting the oxide superconducting material, The process involves spinning this to form a fiber- or tape-shaped linear body, irradiating the linear body with a laser beam, and rapidly moving the melted zone formed by this irradiation. .
本発明における酸化物超電導物質としては特に限定され
ず、たとえばLa−Ba−Cu−0系、La−8r−C
a−Cu−0系、Y−Ba−Cu−0系、B1−8r−
Ca−Cu−0系、Tl−Ba−Ca−Cu−0系等の
酸化物を挙げることができる。The oxide superconducting material in the present invention is not particularly limited, and includes, for example, La-Ba-Cu-0, La-8r-C
a-Cu-0 series, Y-Ba-Cu-0 series, B1-8r-
Examples include oxides such as Ca-Cu-0 type and Tl-Ba-Ca-Cu-0 type.
また、酸化物超電導物質を構成する元素を含む原料物質
としては、これ等の元素を含む酸化物、炭酸塩、硝酸塩
、金属石けん等が用いられ、−例を挙げればY−Ba−
Cu−0系の場合、Y2O5、BaC03、CuO’が
使用される。In addition, as the raw material containing the elements constituting the oxide superconducting material, oxides, carbonates, nitrates, metal soaps, etc. containing these elements are used; for example, Y-Ba-
In the case of Cu-0, Y2O5, BaC03, and CuO' are used.
本発明におけるレーザビームは、Ar、 YAG 。The laser beam in the present invention is Ar or YAG.
CO2等のCW(連続)レーザによって形成され、特に
線状体の軸方向に垂直な断面において対称的な温度分布
が形成されるように複数本照射し、がつビーム径が相互
に重なり合うように照射することが好ましい。このため
断面円形のファイバに対して同心円状の温度分布を形成
するように、等角度で多数本のレーザビームをファイバ
中心へ向がって照射することが行われる。レーザビーム
としては、たとえばビーム径20μ■φ程度のものを使
用して、50μ日程度の長さの溶融帯域を形成し、線状
体(あるいはビーム)を1−10cIII / see
程度の速度で移動させる。It is formed by a CW (continuous) laser such as CO2, and is irradiated with multiple lasers so that a symmetrical temperature distribution is formed especially in the cross section perpendicular to the axial direction of the linear body, so that the beam diameters overlap each other. Irradiation is preferred. For this reason, multiple laser beams are irradiated toward the fiber center at equal angles so as to form a concentric temperature distribution on the fiber having a circular cross section. For example, a laser beam with a beam diameter of about 20 μΦ is used to form a melting zone with a length of about 50 μ days, and the linear body (or beam) is heated at 1-10 cIII/see.
Move at a moderate speed.
[作用]
本発明においてioよ、融体から紡糸されるアモルファ
ス、単結晶等のファイバーがレーザビームにより非常に
狭い帯域で急速に溶融、凝固せしめられるため、非常に
大きな温度勾配を達成することができ、これにより非常
に高い配向性を有する結晶が得られ、超電導特性に優れ
た線状体を得ることができる。さらに長尺化も容易に達
成される。[Operation] In the present invention, since the amorphous, single crystal, etc. fiber spun from the melt is rapidly melted and solidified in a very narrow band by the laser beam, it is possible to achieve a very large temperature gradient. As a result, crystals with extremely high orientation can be obtained, and linear bodies with excellent superconducting properties can be obtained. Further, lengthening can be easily achieved.
[実施例]
図は本発明の方法に用いられる装置の一実施例を示す概
略図である。図において1は溶融ルツボ、2は溶融酸化
物、3は冷却器、4はファイバ、5はレーザビームを示
す。上記の溶融ルツボ1内にY−Ba−Cu−0系酸化
物(Y:Ba:Cu −1:2:3 )を収容し、ヒー
タ6によりルツボ内を、1200℃以上に加熱して酸化
物2を溶融させた。この融体の液面2′をガス7により
加圧しルツボ下部のダイス8より融体を約10CII/
seeで噴出させ、直ちに冷却器3内でガス冷却を施し
た後、レーザビーム5を外周より照射した。レーザビー
ムは出力5ooII1w、ビーム径20μ謹φの30本
を用い、外径100μmφのファイバ5の外周より等角
度で照射した。[Example] The figure is a schematic diagram showing an example of an apparatus used in the method of the present invention. In the figure, 1 is a melting crucible, 2 is a molten oxide, 3 is a cooler, 4 is a fiber, and 5 is a laser beam. A Y-Ba-Cu-0 based oxide (Y:Ba:Cu -1:2:3) is placed in the melting crucible 1, and the inside of the crucible is heated to 1200°C or higher using a heater 6 to form an oxide. 2 was melted. The liquid surface 2' of this melt is pressurized by gas 7, and the melt is pumped through the die 8 at the bottom of the crucible by about 10 CII/
See was ejected, and immediately after gas cooling was performed in the cooler 3, the laser beam 5 was irradiated from the outer periphery. Thirty laser beams were used, each having an output of 5ooII1w and a beam diameter of 20μmφ, and were irradiated at equal angles from the outer periphery of the fiber 5 having an outer diameter of 100μmφ.
このようにして得られた超電導線の軸方向の結晶の配向
性および臨界電流密度等を下表に示した。The axial crystal orientation, critical current density, etc. of the superconducting wire thus obtained are shown in the table below.
なお比較例として赤外線を用いたフローティングゾーン
法(単楕円赤外線加熱、1 、5 K%/)および電気
炉を用い゛た溶融温度勾配結晶化法30″C/cmの結
果を同表中に示した。As comparative examples, the results of the floating zone method using infrared rays (single elliptical infrared heating, 1,5 K%/cm) and the melting temperature gradient crystallization method using an electric furnace at 30"C/cm are shown in the same table. Ta.
(以下余白)
[発明の効果]
以上述べたように、本発明の酸化物超電導体の製造方法
によれば、高い結晶の配向性を有し、これにより臨界電
流密度の高い線状体が容品に得られる上、その制御も容
易であり、かつ製造速度も大きいため、実用的な方法と
してその価値は極めて大である。(The following is a blank space) [Effects of the Invention] As described above, according to the method for producing an oxide superconductor of the present invention, a linear body having a high crystal orientation and a high critical current density can be produced. It is extremely valuable as a practical method because it is easy to control, and the manufacturing speed is high.
図は本発明の方法に用いられる装置の一実施例を示す概
略図である。
1・・・・・・・・・溶融ルツボ
2・・・・・・・・・溶融酸化物
3・・・・・・・・・冷却器
4・・・・・・・・・ファイバ
5・・・・・・・・・レーザビーム
6・・・・・・・・・ヒータThe figure is a schematic diagram showing an embodiment of the apparatus used in the method of the present invention. 1... Melting crucible 2... Melting oxide 3... Cooler 4... Fiber 5. ......Laser beam 6...Heater
Claims (2)
成する元素を含む原料物質を溶融し、これを紡糸してフ
ァイバ状またはテープ状の線状体を形成する工程と、前
記線状体にレーザビームを照射し、この照射により形成
される溶融帯域を急速に移動させることを特徴とする酸
化物超電導体の製造方法。(1) A step of melting an oxide superconducting material or a raw material containing an element constituting the oxide superconducting material, and spinning this to form a fiber- or tape-like linear body, and applying a laser beam to the linear body. A method for producing an oxide superconductor, comprising irradiating a beam and rapidly moving a molten zone formed by the irradiation.
の酸化物超電導体の製造方法。(2) The method for manufacturing an oxide superconductor according to claim 1, wherein a plurality of laser beams are irradiated.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1080049A JPH02257526A (en) | 1989-03-30 | 1989-03-30 | Manufacture of oxide superconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1080049A JPH02257526A (en) | 1989-03-30 | 1989-03-30 | Manufacture of oxide superconductor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02257526A true JPH02257526A (en) | 1990-10-18 |
Family
ID=13707387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1080049A Pending JPH02257526A (en) | 1989-03-30 | 1989-03-30 | Manufacture of oxide superconductor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02257526A (en) |
-
1989
- 1989-03-30 JP JP1080049A patent/JPH02257526A/en active Pending
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