JPH0437607A - Oxide superconducting material - Google Patents
Oxide superconducting materialInfo
- Publication number
- JPH0437607A JPH0437607A JP2143110A JP14311090A JPH0437607A JP H0437607 A JPH0437607 A JP H0437607A JP 2143110 A JP2143110 A JP 2143110A JP 14311090 A JP14311090 A JP 14311090A JP H0437607 A JPH0437607 A JP H0437607A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- oxygen
- superconducting material
- layers
- oxide superconducting
- 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
- Inorganic Compounds Of Heavy Metals (AREA)
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明(よ 高い超伝導転移温度を持つ酸化物超伝導材
料に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to oxide superconducting materials with higher superconducting transition temperatures.
従来の技術
超伝導材料は その超伝導転移温度以下で、l)電気抵
抗がゼロである、 2)完全反磁性であ衣3〉ジョセフ
ソン効果があゑ といった 他の材料にない特性を持っ
ており、電力輸送 発電風核融合プラズマ閉じ込へ 磁
気浮上列東 磁気シールドミ 高速コンピュータ等の幅
広い応用が期待されている。ところ力(従来の金属系超
伝導材料で(よ 超伝導転移温度は最も高いものでも2
3に程度であり、実使用時には高価な液体ヘリウムと犬
がかりな断熱装置を使って冷却しなければならず、工業
上大きな問題であっ旭 このだぬ より高温で超伝導体
となる材料の探索が行われてい九1986年i;
Bednorz (へ’ビノルッ) と Mulle
r (ミlラー)により約40にという高い超伝導転
移温度をもつ酸化物系超伝導材料(La+−zSrz
)2cuoうが見い出され それ以後 YBaa Cu
s Ox、B1−8r−Ca−Cu−Q。Conventional technology superconducting materials have properties that other materials do not have, such as 1) zero electrical resistance below their superconducting transition temperature, 2) complete diamagnetic property and 3) Josephson effect. It is expected to have a wide range of applications, including power transport, wind power generation, fusion plasma confinement, magnetic levitation arrays, magnetic shielding, and high-speed computers. However, the superconducting transition temperature of conventional metallic superconducting materials is 2.
In actual use, it must be cooled using expensive liquid helium and a complicated insulation device, which is a major industrial problem. was carried out in 1986;
Bednorz and Mulle
Oxide-based superconducting materials (La+-zSrz) with a high superconducting transition temperature of about 40
) 2 cuo was found and since then YBaa Cu
sOx, B1-8r-Ca-Cu-Q.
Tl−Ba−Ca−Cu−0なとてあいついでより高い
温度での超伝導転移が報告されている。現在、これらの
材料の製造法 物性、応用等に関して多くの研究がなさ
れていも
発明が解決しようとする課題
超伝導転移温度(以下、Toと称する)が高いはど、冷
却が容易となり、また同じ温度で使用した場合の臨界電
流密度や臨界磁場も大きくなる事が予想され 応用範囲
も広がるものと期待される力(上記従来の構成では高い
超伝導転移温度を持つ安定した超伝導材料か得られにく
いという課題を有してい九
本発明は 上記従来の課題を解決するもので、100に
以上のT・を有する新しい酸化物超伝導材この目的を達
成するために本発明の酸化物超伝導材料1tT1と酸素
からなる一原子層と、 B。Superconducting transitions at higher temperatures have been reported for Tl-Ba-Ca-Cu-0. Currently, much research has been conducted on the manufacturing methods, physical properties, applications, etc. of these materials, but the problem that the invention aims to solve is that the higher the superconducting transition temperature (hereinafter referred to as To), the easier cooling becomes, and the same It is expected that the critical current density and critical magnetic field will increase when used at high temperatures, and the range of applications is expected to expand. To achieve this object, the present invention solves the above-mentioned conventional problems and uses a new oxide superconducting material having a T of more than 100. a monoatomic layer consisting of 1tT1 and oxygen; B.
Ca、 Cuおよび酸素からなるペロブスカイト型構造
を基本とする層とが交互に配列されている層状構造物に
おいて、BL Ca、 Cuおよび酸素の層中にC
uと酸素とから成る二次元平面が2枚存在する層と3枚
存在する他の層とがあり、これら両層がTlと酸素から
なる一原子層を介して交互に配列されている構成を有し
ている。In a layered structure in which layers based on a perovskite structure consisting of Ca, Cu, and oxygen are arranged alternately, BL contains C in the layers of Ca, Cu, and oxygen.
There is a layer in which there are two two-dimensional planes made of u and oxygen, and another layer in which there are three, and these two layers are arranged alternately through monoatomic layers made of Tl and oxygen. have.
作用
この構成により、120に以上の高いToを有する酸化
物超伝導材料が得られ九
実施例
以下本発明の一実施例について説明すも出発原料として
、純度99%以上のTl2O3、BaCO3、CaCO
3、CuO(7)粉末を用いん これらの粉末のう板B
aCO3とCuOを、Ba: Cu= 1: 1の比
率となるように秤量し 振動ミルにて直径2mmのZr
O2ボールを用し\ エタノールを分散媒として1時間
粉砕混合しf島 混合終了後、分散媒を含む全量を乾燥
機中で120℃で乾燥させ九 得られた粉末を900℃
で5時皿 空気中で仮焼した後、振動ミルにて前述と同
様の方法で30分間粉砕L120℃で乾燥させ1.
この仮焼粉末をX線回折により分析1.、 BaCu
O2か生成している事を確認し九次に同様の方法で、C
aCO3とCuOを秤量・混合し950℃の仮焼てCa
2CuO3の粉末を合成し九 このBaCu0a粉末と
Ca2Cub3粉末およびTl2O3、CuO粉末を所
定の比となるようにそれぞれ秤量しtも秤量粉末をらい
かい機により1時間粉砕混合し九 混合終了後、この粉
末の0.4g を15 mmx 5mmの金型中で70
0kg/cm2の圧力で一軸加圧成形しな これにより
得られた成形体をAu箔で包ムさらに石英チューブ中に
減圧状態で封じ込教 電気炉にて750〜950℃で1
〜128時間焼成し總 昇降温速度はいずれも300℃
/hとした超伝導の評価として、直流4端子法(測定電
流10 mA)により電気抵抗の温度変化を、5QUI
D (外部磁場100e)で磁化率をそれぞれ測定した
第1表に作製した試料の組成(Tl: Ba: Ca:
Cuのモル比)と焼成条件を示す。さらに 第2表に
X線回折で調べた試料中の超伝導相を示す。第2表中の
4桁の数字はそれぞれTl: Ba: Ca: Cuの
モル比を示している。゛またそれぞれを回折パターンの
低角側(3°≦2θ≦10°)に現われるピーク強度の
大きな順に並べ九 *印は17.6人の周期構造を示す
本発明の結晶相である。Effect: With this configuration, an oxide superconducting material having a high To of 120 or more can be obtained.9 Examples Hereinafter, an example of the present invention will be described.
3. Using CuO(7) powder These powder plates B
Weigh aCO3 and CuO so that the ratio of Ba: Cu = 1: 1, and use a vibration mill to make Zr with a diameter of 2 mm.
Using an O2 ball, pulverize and mix for 1 hour using ethanol as a dispersion medium. After mixing, dry the entire amount including the dispersion medium at 120°C in a dryer. 9. Heat the resulting powder at 900°C.
After calcining in the air, the powder was crushed in a vibrating mill for 30 minutes in the same manner as described above and dried at 120°C.1.
Analysis of this calcined powder by X-ray diffraction1. , BaCu
Confirm that O2 is being generated, and use the same method as the ninth
Weigh and mix aCO3 and CuO and calcinate at 950℃ to make Ca
Synthesize 2CuO3 powder.Weigh this BaCu0a powder, Ca2Cub3 powder, Tl2O3, and CuO powder so that they are in a predetermined ratio, and pulverize and mix the weighed powders for 1 hour using a sieve machine.9 After mixing, this powder 0.4g of 70g in a 15mm x 5mm mold
Uniaxial pressure molding was performed at a pressure of 0 kg/cm2.The resulting molded body was wrapped in Au foil and sealed in a quartz tube under reduced pressure.
Baked for ~128 hours. Temperature increase/decrease rate was 300℃.
/h to evaluate the superconductivity, the temperature change in electrical resistance was measured using the DC 4-terminal method (measurement current 10 mA) at 5QUI.
Compositions of the prepared samples (Tl: Ba: Ca:
The molar ratio of Cu) and firing conditions are shown below. Furthermore, Table 2 shows the superconducting phases in the samples investigated by X-ray diffraction. The four-digit numbers in Table 2 each indicate the molar ratio of Tl:Ba:Ca:Cu. In addition, they are arranged in descending order of peak intensity appearing on the low-angle side (3°≦2θ≦10°) of the diffraction pattern.The * mark is the crystal phase of the present invention showing a periodic structure of 17.6 people.
(以下余白)
第1表
試料 組成
番号 Tl: Ba: Ca: Cu焼成
温度 時間
20゜
2、O:
2叶
20:
20:
:4.4
−4.4
:44
:4.4
・ 44
900℃
900℃
900℃
900℃
900℃
840℃
(ルj1余白)
第2表
試料番号
超伝導相
No、1 2223. 22122
2223、 1223
4 1223、 本1 2 2.5 3
.5. 12345 本1 2 2.5 3
.5. 1234. 12236 本1
2 2.5 3.5No、 6の試料は17.6人の周
期構造を示す結晶相のほぼ単相であった(ピーク強度は
小さいがCuOおよびCap CLIOJ も確S忍さ
れた )。 透過型電子顕微鏡(TEM)で観察したと
ころ 19.2人と16.0人間隔の層が交互に配列し
ている部分(少なくとも20対が一視野中に61t K
Mできる。)が観察され九
このようにして得られた本発明の一実施例における酸化
物超伝導材料のq No、6の試料の電気抵抗および
磁化率の温度特性を第1図に示す。 抵抗値の減少が1
26Kから始まり、122にでゼロとなっ九 また磁化
率についても 123に以下で大きな反磁化を示しな
Tl−Ba−Ca−Cu−0系において120に以上で
超伝導転移を起こす材料として(よ T12 Ba2C
a2Cu30x とTI+ Ba2CaaCuzOxか
知られている。 本発明の材料はT1+Ba2Ca2.
5Cu3.sOx と表記でき、 Tl−Ba−Ca−
Cu−0から成る120に以上で超伝導転移を起こす材
料として(友 人体に有害なT1の含有量か最も少な(
X。(Leaving space below) Table 1 Sample Composition number Tl: Ba: Ca: Cu Firing temperature Time 20°2, O: 2 leaves 20: 20: :4.4 -4.4 :44 :4.4 ・44 900℃ 900℃ 900℃ 900℃ 900℃ 840℃ (le j1 margin) Table 2 Sample number Superconducting phase No. 1 2223. 22122
2223, 1223 4 1223, Book 1 2 2.5 3
.. 5. 12345 books 1 2 2.5 3
.. 5. 1234. 12236 book 1
The samples No. 2, 2.5, 3.5 and No. 6 were almost single-phase crystals showing a periodic structure of 17.6 people (CuO and Cap CLIOJ were also clearly observed, although the peak intensity was small). When observed with a transmission electron microscope (TEM), the area where layers of 19.2 and 16.0 layers are arranged alternately (at least 20 pairs in one field of view are 61tK)
I can do M. ) was observed. Figure 1 shows the temperature characteristics of the electrical resistance and magnetic susceptibility of the thus obtained sample of the oxide superconducting material with q No. 6 in one embodiment of the present invention. The decrease in resistance value is 1
The magnetic susceptibility starts at 26K and becomes zero at 122K. Also, regarding the magnetic susceptibility, it is considered that the Tl-Ba-Ca-Cu-0 system exhibits a large demagnetization below 123K, and as a material that causes a superconducting transition above 120K. T12 Ba2C
a2Cu30x and TI+ Ba2CaaCuzOx are known. The material of the present invention is T1+Ba2Ca2.
5Cu3. It can be written as sOx, Tl-Ba-Ca-
As a material that causes a superconducting transition in 120 or more consisting of Cu-0 (the content of T1, which is harmful to the friend body, is the lowest (
X.
発明の効果
以上のように本発明Lt、、 Tlまたは酸素からな
る一原子層と、Ba、 Ca、 Cuおよび酸素からな
るペロブスカイト型構造を基本とする層とが交互に配列
されている層状構造物において、BL CL Cu
および酸素の層中にCuと酸素とから成る二次元平面が
2枚存在する層と3枚存在する他の層とがあり、これら
両層がT1と酸素からなる一原子層を介して交互に配列
されており、120に以上の高いToを有し ま?、Z
、 Tl−Ba−Ca−Cu−0から成る120に以
上で超伝導転移を起こす材料の中で人体に有害なTlの
含有量が最も少ない優れた酸化物超伝導材料を実現でき
るものである。Effects of the Invention As described above, the present invention provides a layered structure in which monoatomic layers consisting of Lt, Tl or oxygen and layers based on a perovskite structure consisting of Ba, Ca, Cu and oxygen are arranged alternately. In, BL CL Cu
In the oxygen layer, there is a layer in which two two-dimensional planes made of Cu and oxygen exist, and another layer in which three two-dimensional planes exist, and these two layers are alternately interposed through a monoatomic layer made of T1 and oxygen. Is it arranged and has a high To of 120 or more? ,Z
, Tl-Ba-Ca-Cu-0, which is an excellent oxide superconducting material that has the lowest content of Tl, which is harmful to the human body, among the materials that undergo a superconducting transition at a temperature of 120 or more.
第1図は本発明の一実施例における酸化物超伝導材料の
電気抵抗および磁化率の温度特性図であ代理人の氏名
弁理士 粟野重孝 ほか]名第 1 図
温 度 CK)Figure 1 is a temperature characteristic diagram of electrical resistance and magnetic susceptibility of an oxide superconducting material in one embodiment of the present invention.
Patent attorney Shigetaka Awano et al.] Figure 1 Temperature CK)
Claims (1)
ム(Ba)、カルシウム(Ca)、銅(Cu)および酸
素からなるペロブスカイト型構造を基本とする層とが交
互に配列されている層状構造物において、Ba、Ca、
Cuおよび酸素の層中にCuと酸素とから成る二次元平
面が2枚存在する層と3枚存在する他の層とがあり、こ
れら両層がTlと酸素からなる一原子層を介して交互に
配列されている酸化物超伝導材料。A layered structure in which monoatomic layers consisting of thallium (Tl) and oxygen and layers based on a perovskite structure consisting of barium (Ba), calcium (Ca), copper (Cu) and oxygen are arranged alternately. In, Ba, Ca,
In the Cu and oxygen layer, there is a layer in which two two-dimensional planes made of Cu and oxygen exist, and another layer in which three two-dimensional planes exist, and these two layers alternate with one atomic layer made of Tl and oxygen interposed in between. An oxide superconducting material arranged in
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2143110A JPH0437607A (en) | 1990-05-31 | 1990-05-31 | Oxide superconducting material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2143110A JPH0437607A (en) | 1990-05-31 | 1990-05-31 | Oxide superconducting material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0437607A true JPH0437607A (en) | 1992-02-07 |
Family
ID=15331142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2143110A Pending JPH0437607A (en) | 1990-05-31 | 1990-05-31 | Oxide superconducting material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0437607A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5385882A (en) * | 1991-04-12 | 1995-01-31 | Alfred Univeristy | Process for preparing a thallium-containing superconductor |
| CN118894719A (en) * | 2024-07-05 | 2024-11-05 | 中国科学院物理研究所 | A single-phase Cu1234 superconductor and its preparation method |
-
1990
- 1990-05-31 JP JP2143110A patent/JPH0437607A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5385882A (en) * | 1991-04-12 | 1995-01-31 | Alfred Univeristy | Process for preparing a thallium-containing superconductor |
| CN118894719A (en) * | 2024-07-05 | 2024-11-05 | 中国科学院物理研究所 | A single-phase Cu1234 superconductor and its preparation method |
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