Auxiliary material for superconductive material

Superconductor technology: apparatus – material – process – High temperature devices – systems – apparatus – com- ponents,... – Superconducting wire – tape – cable – or fiber – per se

Reexamination Certificate

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C148S431000

Reexamination Certificate

active

06760606

ABSTRACT:

DESCRIPTION
1. Technical Field of the Invention
The present invention relates to an auxiliary material for use with a superconductive material to improve the mechanical deflection property of a tape-like or a wire-like superconductive material. In detail, this invention relates to a tape material or a pipe material containing Ag as a base material, particularly to a superconductor auxiliary material (i.e., an auxiliary material for use with a superconductive material) which, by virtue of its specific Ag alloy composition and upon being subjected to a specific oxidation treatment, can offer an excellent thermal stability, i.e., the auxiliary material will not be softened under a severe condition of a heat energy, thereby ensuring an excellent mechanical strength.
2. Background Art
As far as superconductive materials are concerned, in recent years, the public's concern has been shifted from metallic superconductive materials to oxide superconductive materials. This is because the oxide superconductive materials, by virtue of their height critical temperatures and their strong magnetic fields, have been found to have a broad use in various ways, with one example being that an oxide superconductive material can be used in a conductor such as a tape-like conductor and a wire-like conductor.
Here, since oxide conductive materials usually belong to ceramic category, they are often brittle. Accordingly, if an oxide superconductive material is to be put into practical use, it is required that a metal material be formed into a tape and used as an auxiliary material for the superconductive material, thereby forming a multi-layered composite structure. Alternatively, such a multi-layered composite structure may be filled into a pipe, so as to improve its mechanical deflection property.
However, an auxiliary material for use with a superconductive material is required not only to be able to strengthen the superconductive material, but also to have a flexibility which is regarded as an important aspect. Further, such an auxiliary material is not allowed to have a crack and a break. As a result, there have been appeared in the commercial market various auxiliary materials formed through different experiments for obtaining various desired properties.
On the other hand, for use as such auxiliary materials, there have been known many kinds of alloy materials each containing Ag as its main component. In this way, a reason as to why several sorts of alloy elements should be added in a superconductor auxiliary material can be explained as: it is because Ag fails to provide a sufficient thermal stability and a sufficient mechanical strength.
Several conventional superconductor auxiliary materials may be described as follows. At first, Japanese Patent Application Publication Laid-Open No. 6-283056 discloses that an Ag alloy serving as a metal base material contains at least one of Mg, Ni, Ti, Mn, Au and Cu, with Mg and Ni being 1 atom % or less, Ti and Mn being 0.5 atom % or less, Au being 30 atom % or less, Cu being 2 atom % or less.
In addition, Japanese Patent Application Publication Laid-Open No.8-241635 has disclosed that at least one of MgO and NiO contained in Ag alloy is converted to Mg and/or Ni, thereby indicating a material containing 0.01 to 0.5 mass % of at least one of Mg and Ni. This prior art teaches that a silver alloy after having been treated in a wire drawing treatment is oxidized in an atmospheric air at 800 to 900° C. for 5 to 50 hours, and the surface of the silver alloy has been oxidized only at a depth of 70 &mgr;m.
However, with regard to the above Prior art, it is difficult to ensure that the above described auxiliary materials for use with superconductive materials can exactly offer a sufficient mechanical strength, a sufficient flexibility and a sufficient softness, all of which are needed as an auxiliary material for use with a superconductive material. Namely, with regard to the above first prior art, when a superconductive material is caused to fill into a pipe material, crack will occur in a pipe during a wire drawing process, causing the pipe to be broken. On the other hand, with regard to the above second prior art, although there is not a problem in relation to a softness during processing, it is usually considered that a desired mechanical strength will become insufficient under a severe condition of a heat energy.
DISCLOSURE OF THE INVENTION
In view of the above, it is an object of the present invention to provide an improved alloy for use as a superconductor auxiliary material which has a sufficient mechanical strength, a sufficient flexibility and a sufficient softness.
The inventor of the present invention, after having carried out a great deal of research for the purpose of solving the above problems, has found that in order to improve the durability and the mechanical strength (to be resistant against a heat energy) of a superconductor auxiliary material, an effective method is to disperse oxides of Mg and Ni in a base material containing Ag as a main component, with the dispersion being effected by virtue of internal oxidation. The object of the present invention is to prevent the occurrence of a crack or damage even within an internal oxide, and such an object has been achieved by virtue of a specific composition and a specific internal oxidation method.
An invention according to claim
1
is a pipe-like or tape-like Ag alloy auxiliary material for use in a process for treating a superconductive material, characterized in that Ag is used as a base material, MgO alone or MgO and NiO formed by internal oxidation are dispersed in the Ag base material, wherein MgO is 0.03 to 3.3 wt % and a balance is Ag, or MgO is 0.01 to 1.7 wt %, NiO is 0.02 to 1.3 wt % and a balance is Ag.
In this way, the present invention is formed by dispersing MgO and NiO through an internal oxidation. This constitution is not at all disclosed in the above described prior art. That is, the above described first prior art is that whose oxidation is carried out in an atmospheric air which is different from that used in the present invention. Moreover, the first prior art does not inherently teach an oxide amount specified in the present invention. On the other hand, the above described second prior art is that which is capable of oxidizing the surface of Ag material at a depth of only 70 &mgr;m. The present invention is significantly different from this prior art in that the present invention employs an Ag alloy before combining a superconductive material with an auxiliary material, with Mg and Ni being internally oxidized under a specific condition, thereby forming an auxiliary material which failed to be obtained in the above Prior art.
Here, the alloy composition used in the present invention is such that when only MgO is dispersed in Ag material, the weight ratio of MgO is 0.03 to 3.3 wt %. On the other hand, when MgO and NiO are both dispersed, the weight ratios of MgO and NiO are respectively in a range of 0.01 to 1.7 wt % and a range of 0.02 to 1.3 wt %. The reason for these weight ratio ranges may be explained as follows. Namely, if MgO and NiO are respectively less than 0.01 wt % and less than 0.02 wt %, it will be difficult to improve the mechanical strength. On the other hand, if the weight ratios are respectively more than 1.7 wt % and more than 1.3 wt %, the material will have an undesirably high hardness, rendering it difficult to process the material.
Furthermore, a method according to the present invention for manufacturing the superconductor auxiliary material is characterized in that; after a base material consisting of either an Ag-Mg composition or an Ag—Mg—Ni composition has been dissolved and cast, the base material is rolled or subjected to a pipe drawing treatment, and in a process of being formed into a predetermined thickness and a predetermined length, the base material is subjected to an internal oxidation which is carried out at a temperature of 650 to 850° C. and continued for 20 to 80 hours in an oxygen atmosphere having a pressure of 3 to 10 atm, fol

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