JPH01257162A - Porcelain composition - Google Patents

Porcelain composition

Info

Publication number
JPH01257162A
JPH01257162A JP63085887A JP8588788A JPH01257162A JP H01257162 A JPH01257162 A JP H01257162A JP 63085887 A JP63085887 A JP 63085887A JP 8588788 A JP8588788 A JP 8588788A JP H01257162 A JPH01257162 A JP H01257162A
Authority
JP
Japan
Prior art keywords
temperature
oxide
resistivity
composition
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
Application number
JP63085887A
Other languages
Japanese (ja)
Inventor
Hiroshi Ouchi
宏 大内
Masahiro Ito
昌宏 伊藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP63085887A priority Critical patent/JPH01257162A/en
Publication of JPH01257162A publication Critical patent/JPH01257162A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E40/00Technologies for an efficient electrical power generation, transmission or distribution
    • Y02E40/60Superconducting electric elements or equipment; Power systems integrating superconducting elements or equipment

Landscapes

  • Superconductors And Manufacturing Methods Therefor (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は抵抗体磁器組成物、とくに酸化バリウム(Ba
O)と酸化ストロンチウム(SrO)と酸化ツリウム(
Ttn 203 )および酸化銅(CaO)の成分で構
成される抵抗体磁器組成物に関し、室温での抵抗率(ρ
3゜。)が小さいのみならず、室温からオンセット臨界
温度(TcO)までの抵抗率(ρCo)が小さく、さら
に液体窒素温度以下において抵抗率が零を示す超伝導体
磁器を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to resistor ceramic compositions, particularly barium oxide (Ba
O), strontium oxide (SrO), and thulium oxide (
Regarding the resistive ceramic composition composed of the components Ttn 203 ) and copper oxide (CaO), the resistivity at room temperature (ρ
3°. ), the resistivity (ρCo) from room temperature to the onset critical temperature (TcO) is small, and the resistivity is zero below the liquid nitrogen temperature.

従来の技術 近年、ベドノ’、 /V ツ(Bedno r z )
とミューラー(Muller)により、Ba−La−C
u−0系における高温超伝導体材料の可能性が1986
年のツァイトシュリフト フィア フィツク(Zeit
schriftfiir  Physik ) Ba4
巻 189頁に発表された。
Conventional technology In recent years, Bedno', /V tsu (Bednorz)
and Muller, Ba-La-C
The possibility of high-temperature superconductor materials in the u-0 system was discovered in 1986.
Zeitschrift Fear Fitzk (Zeit)
scriftfiir Physik) Ba4
Published in Volume 189.

この報告では材料の抵抗率(ρ)が急激に低下し始める
オンセット臨界温度(TcO)は絶対温度3O度付近で
あるが、抵抗率が零となるオフセット臨界温度(TC)
は絶対温度13度と低く、この材料では冷却剤に高価な
液体ヘリウムを必要とするため実用化に対する大きな障
害となっていた。また、本材料を室温からオンセット臨
界温度までの範囲で低抵抗の導伝性材料として使用する
ときは電力損失をできるだけ小さくするだめに材料の密
度が大きく抵抗率のより小さい材料が望ましい。
In this report, the onset critical temperature (TcO) at which the resistivity (ρ) of the material begins to rapidly decrease is around 30 degrees absolute, but the offset critical temperature (TC) at which the resistivity becomes zero
The absolute temperature of this material is as low as 13 degrees Celsius, and this material requires expensive liquid helium as a coolant, which has been a major obstacle to its practical application. Furthermore, when this material is used as a conductive material with low resistance in the range from room temperature to the onset critical temperature, it is desirable to use a material with high density and low resistivity in order to minimize power loss.

発明が解決しようとする課題 これらの課題を解決するために、材料の密度が大きくよ
シ高温のTcと室温からTcoまでの温度範囲でより小
さいρを持つ材料を開発することが要望されている。
Problems to be Solved by the Invention In order to solve these problems, it is desired to develop a material that has a high density, a high temperature Tc, and a smaller ρ in the temperature range from room temperature to Tco. .

本発明は上記の欠点を改善するためになされたものであ
り、焼結した材料の密度が大きく、室温からオンセント
臨界温度までの抵抗率が小さく、さらに安価な液体窒素
の温度で超伝導特性を示すTcの高い新規な磁器組成物
を提供するものである。
The present invention was made to improve the above-mentioned drawbacks, and the sintered material has a high density, a low resistivity from room temperature to the on-cent critical temperature, and superconducting properties at the temperature of inexpensive liquid nitrogen. The present invention provides a novel ceramic composition having a high Tc.

問題点を解決するだめの手段 W化バ!Jt ム(Bad)と酸化ストロンチウム(S
rO)と酸化ツリウム(Tm2O3)と酸化銅(CuO
)で構成される組成において、その組成式をTm(Ba
1−.5rx)2Cu3O7と表わしたとき、その成分
組成をモル分率で。くx≦0.75の範囲とする。
The only way to solve the problem is to make it double! Jt (Bad) and strontium oxide (S)
rO), thulium oxide (Tm2O3), and copper oxide (CuO
), the compositional formula is Tm(Ba
1-. 5rx) When expressed as 2Cu3O7, its component composition is expressed in mole fraction. x≦0.75.

作  用 」1記の組成物は室温からオンセット臨界温度まですぐ
れた抵抗体磁器であり、また液体窒素中で超伝導体磁器
になる。
The composition described in item 1 of "Operation" is a resistive porcelain with excellent resistance from room temperature to the onset critical temperature, and also becomes a superconducting porcelain in liquid nitrogen.

実施例 出発原料には化学的に高純度のB a COs (99
−5%以上) +  S r C0−5(99%以上)
、Tm203(99,9%)およびCu0(99,5%
以上)を所定の組成になるように秤量し、めのうボール
を備えたポリエチレン製のボールミルで水トドもに17
時時間式混合した。この混合物をボールミルとり出して
乾燥したのち粉末をアルミナ質るつぼに入れ空気中にお
いて900℃の温度で5時間仮焼した。得られた仮焼物
はめのう乳鉢とめのう乳棒を備えだ捕潰機により粉砕し
た。粉砕の終った粉末に対してバインダーとしてプロピ
ルアルコールを5重量%添加して均質としたのち32メ
ソシユのふるいを通して整粒.しだ。整粒粉体は金型と
油圧プレスを用いて成形圧力s o o ky/cdで
矩形棒さや鉢の中に入れたのち、酸素中において900
〜11oo′Cの範囲内の温度で6時間保持して焼成し
、表に示す配合組成の抵抗体磁器を得た。円板試料から
重量と寸法を測定し密度を算出した。
The starting materials for the examples include chemically highly purified B a COs (99
-5% or more) + S r C0-5 (99% or more)
, Tm203 (99,9%) and Cu0 (99,5%
(above) was weighed out to the specified composition, and then milled in a polyethylene ball mill equipped with an agate ball.
Mixed time-wise. This mixture was taken out of a ball mill and dried, and then the powder was placed in an alumina crucible and calcined in air at a temperature of 900° C. for 5 hours. The obtained calcined product was crushed using a crusher equipped with an agate mortar and an agate pestle. After grinding, 5% by weight of propyl alcohol was added as a binder to the powder to make it homogeneous, and the powder was then passed through a 32 sieve sieve for granulation. Shida. The sized powder was put into a rectangular rod or pot using a mold and a hydraulic press at a molding pressure of 900 ky/cd, and then heated in oxygen at 900 °C.
It was held and fired at a temperature within the range of ~11oo'C for 6 hours to obtain a resistor ceramic having the composition shown in the table. The weight and dimensions of the disk samples were measured and the density was calculated.

矩形棒の試料には直径Oi2flの絶縁被覆銅線を60
回巻き、LCRメータを用いて周波数10 kHzでイ
ンダクタンスの温度変化(gi体窒素温度から室温まで
)による変化を測定した。これらの試料の室温における
インダクタンスの値は4〜6μHであった。液体窒素温
度近傍でインダクタンスが急激に減少する(3イル%)
試料については矩形棒の長辺に垂直な両端面と長辺部に
1On+の幅をあけて4端子状の電極を金蒸着又は焼付
銀の方法で取付け、一定電流(10mA)の下での抵抗
の温度変化(液体窒素温度から室温まで)を測定した。
For the rectangular bar sample, 60 insulated copper wires with a diameter of Oi2fl were used.
The change in inductance due to temperature change (from gi body nitrogen temperature to room temperature) was measured at a frequency of 10 kHz using an LCR meter. The inductance values of these samples at room temperature were 4 to 6 μH. Inductance decreases rapidly near liquid nitrogen temperature (3%)
For the sample, 4-terminal electrodes were attached with a width of 1 On+ on both end faces perpendicular to the long side of the rectangular rod and on the long side using gold evaporation or baked silver, and the resistance under a constant current (10 mA) was measured. The temperature change (from liquid nitrogen temperature to room temperature) was measured.

それらの実験結果を表に示す。なお、表において*を付
した試料は本発明の範囲外の比較例であり、これ以外の
試料が本発明の範囲内の実施例である。
The experimental results are shown in the table. In addition, the samples marked with * in the table are comparative examples outside the scope of the present invention, and the other samples are examples within the scope of the present invention.

表から明らかなように、本発明の範囲内のSrにより置
換した磁器組成物は焼結密度が犬きく、室温からオンセ
ット臨界温度までの範囲で抵抗率を小さくすることがで
きるとともに、液体窒素温度以下でオフセット臨界温度
Tcの高い材料が得られる。従って、本発明の磁器組成
物を用いることにより冷却剤として安価で豊富に利用で
きる液体窒素を用いて電気抵抗が零を示す超伝導特性を
容易に得ることができる。
As is clear from the table, the porcelain composition substituted with Sr within the scope of the present invention has a high sintering density, can reduce the resistivity in the range from room temperature to the onset critical temperature, and A material with a high offset critical temperature Tc can be obtained below this temperature. Therefore, by using the ceramic composition of the present invention, superconducting properties exhibiting zero electrical resistance can be easily obtained using liquid nitrogen, which is inexpensive and abundantly available, as a coolant.

本発明の組成範囲を限定した理由を説明すると、Sr○
の置換最xが0.75以上になると焼結密度が低下する
とともに室温およびオンセント臨界温度までの抵抗率が
犬きくなり面体窒素温度で超伝導特性も得られなくなる
。また、x=Oでは焼結密度が低くまだ室1偏の抵抗率
が大きいために本発明の範囲から除かれる。
To explain the reason why the composition range of the present invention is limited, Sr○
When the maximum substitution value x becomes 0.75 or more, the sintered density decreases and the resistivity at room temperature and up to the on-cent critical temperature becomes too high, making it impossible to obtain superconducting properties at the surface nitrogen temperature. Further, when x=O, the sintered density is low and the resistivity of the chamber is still large, so it is excluded from the scope of the present invention.

発明の効果 本発明の磁器組成物は高価な液体ヘリウムや水素を使用
することなく資源的に豊富で価格的に廉価な液体窒素を
冷却剤に使用することにより、液体窒素の温度で超伝導
特性が得られる。従って、本発明の磁器組成物は液体窒
素で冷却することにより核隔合炉やリニヤモーターカー
用の強力な磁場が作り出せる超伝導磁石や、ジョセフソ
ン素子などの超高速コンピュータ用素子や、大電力送電
線や超伝導印刷回路など幅広い分野での応用に適し、安
価で高性能の電子機器や回路部品を作ることができ工業
的に利用価値の著しく大きいものである。
Effects of the Invention The porcelain composition of the present invention has superconducting properties at the temperature of liquid nitrogen by using resource-rich and inexpensive liquid nitrogen as a coolant without using expensive liquid helium or hydrogen. is obtained. Therefore, the porcelain composition of the present invention can be used in superconducting magnets that can produce strong magnetic fields for nuclear isolation reactors and linear motor trains when cooled with liquid nitrogen, ultra-high-speed computer elements such as Josephson elements, and high-power It is suitable for application in a wide range of fields such as power transmission lines and superconducting printed circuits, and can be used to make inexpensive, high-performance electronic devices and circuit parts, making it extremely valuable industrially.

Claims (1)

【特許請求の範囲】 酸化バリウム(BaO)と酸化ストロンチウム(SrO
)と酸化ツリウム(Tm_2O_3)と酸化銅(CuO
)からなり、その組成式をTm(Ba_1_−_xSr
_x)_2Cu_3O_7と表わしたとき、その成分組
成がモル分率で 0<x≦0.75の範囲にあることを特徴とする磁器組
成物。
[Claims] Barium oxide (BaO) and strontium oxide (SrO
), thulium oxide (Tm_2O_3) and copper oxide (CuO
), whose compositional formula is Tm(Ba_1_−_xSr
_x) A porcelain composition characterized in that, when expressed as _2Cu_3O_7, its component composition is in the range of 0<x≦0.75 in terms of molar fraction.
JP63085887A 1988-04-07 1988-04-07 Porcelain composition Pending JPH01257162A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63085887A JPH01257162A (en) 1988-04-07 1988-04-07 Porcelain composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63085887A JPH01257162A (en) 1988-04-07 1988-04-07 Porcelain composition

Publications (1)

Publication Number Publication Date
JPH01257162A true JPH01257162A (en) 1989-10-13

Family

ID=13871415

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63085887A Pending JPH01257162A (en) 1988-04-07 1988-04-07 Porcelain composition

Country Status (1)

Country Link
JP (1) JPH01257162A (en)

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