Bulk oxide superconductor and method of production of bulk oxide superconductor

Abstract

The present invention has as its problem the provision of a bulk oxide superconductor which has a high workability and high critical current density characteristic regardless of the external conditions and solves the problem by limiting the amount of addition of Ag to 5 mass % or less, using the QMG method to produce a bulk superconductor and thereby obtain a single crystal-like bulk superconductor of a structure with parts where Ag particles are present and parts where Ag particles are not present made to adjoin each other.

Claims

1. A method of production of a bulk oxide superconductor comprising heating a precursor of a bulk oxide superconductor to form a semimolten state and bringing a seed crystal into contact with it to obtain a single crystal-like REBa.sub.2Cu.sub.3O.sub.7-x phase in which RE.sub.2BaCuO.sub.5 phases are finely dispersed, said method of production of the bulk oxide superconductor comprising adding Ag: 0.5 to 4.6 mass % to said precursor of a bulk oxide superconductor and heating it to become a semimolten state, then bringing a seed crystal into contact with said semimolten state precursor and gradually cooling to make said precursor solidify into a single crystal shape.

2. The method of production of the bulk oxide superconductor according to claim 1 further comprising working said bulk oxide superconductor into a bar shape so that parts where Ag is present sandwich a part where Ag is not present.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIGS. 1A and 1B are views showing an example of the appearance of a bulk oxide superconductor prepared from a seed crystal by a relatively small amount of addition of Ag and an example of the state of distribution of Ag particles at the cross-section. FIG. 1A is a conceptual view showing a bulk oxide superconductor grown from a seed crystal. FIG. 1B is a view showing the state of a cross-section at a broken line position of FIG. 1A.

(2) FIGS. 2A to 2C are views showing an example of the appearance of a bulk oxide superconductor prepared from a seed crystal by an amount of addition of Ag of over 5 mass % and an example of the state of distribution of Ag particles at the cross-section. FIG. 2A is a conceptual view showing a bulk oxide superconductor grown from a seed crystal. FIG. 2B is a view showing the state of a cross-section at a position of a broken line A of FIG. 2A. FIG. 2C is a view showing the state of a cross-section at a position of a broken line B of FIG. 2A.

(3) FIGS. 3A to 3C are conceptual views for explaining a bulk oxide superconductor prepared in Example 1 and a current lead element cut out in a bar shape. FIG. 3A is a view showing an example of a bulk oxide superconductor grown from a seed crystal (Ag: 3 mass % added. Diameter: about 37 mm). FIG. 3B is a view showing the state of a cross-section at positions of 5 mm and 10 mm from the top of FIG. 3A. FIG. 3C is a view showing a bar-shaped sample worked so that the two end parts become regions where Ag particles precipitate.

(4) FIGS. 4A to 4C are conceptual views for explaining a bulk oxide superconductor fabricated in Example 2 and a current lead element cut out in a bar shape. FIG. 4A is a view showing an example of a bulk oxide superconductor grown from a seed crystal (Ag: 4 mass % added. Diameter: about 45 mm). FIG. 4B is a view showing the state of a cross-section at positions of 5 mm and 10 mm from the top of FIG. 4A. FIG. 4C is a view showing a bar-shaped sample worked so that the two end parts become regions where Ag particles precipitate.

DESCRIPTION OF EMBODIMENTS

(5) The bulk oxide superconductor used in the present invention is preferably one having the structure of single crystal-like REBa.sub.2Cu.sub.3O.sub.7-x in which nonsuperconducting phases such as RE.sub.2BaCuO.sub.5 phases (211 phases) etc. are finely dispersed (so-called QMG material). Here, single crystal-like means not a perfect single crystal, but a state including defects not obstructing practical use such as small inclination grain boundaries. The RE at the REBa.sub.2Cu.sub.3O.sub.7-x phase (123 phase) and RE.sub.2BaCuO.sub.5 phases (211 phase) is a rare earth element selected from Y, La, Nd, Sm, Eu, Gd, Dy, Ho, Er, Tm, Yb, and Lu and combinations of the same. The 123 phase containing La, Nd, Sm, Eu, and Gd is outside the 1:2:3 stoichiochemical composition. Ba is partially substituted at the RE sites. Further, in the nonsuperconducting phases, that is, 211 phases, as well, it is known that La and Nd are somewhat different from Y, Sm, Eu, Gd, Dy, Ho, Er, Tm, Yb, and Lu, the ratio of metal elements becomes a non-stoichiochemical composition, and the crystal structure differs.

(6) The above-mentioned substitution by the Ba element tends to cause the critical temperature to decline. Further, in an environment with a smaller oxygen partial pressure, substitution by the Ba element tends to be suppressed.

(7) The 123 phase is formed by a peritectic reaction between the 211 phases and a liquid phase comprised of a composite oxide of Ba and Cu, that is, the reaction of
211 phases+liquid phase (composite oxide of Ba and Cu).fwdarw.123 phase
Further, due to this peritectic reaction, the temperature Tf at which the 123 phase is formed (Tf: 123 phase formation temperature) is substantially related to the ion radius of the RE element and becomes lower along with the reduction in the ion radius. Further, the Tf tends to fall along with a low oxygen atmosphere and addition of Ag.

(8) A material comprised of a single crystal-like 123 phase in which 211 phases are finely dispersed can be formed since when the 123 phase is grown by crystal growth, the unreacted 211 grains are left in the 123 phase. That is, a QMG material can be formed by a reaction shown by:
211 phases+liquid phase (composite oxide of Ba and Cu).fwdarw.123 phase+211 phases
The fine dispersion of the 211 phases in the QMG material is extremely important from the viewpoint of improvement of the critical current density (Jc). By adding a fine amount of at least one of Pt, Rh, or Ce, particle growth of the 211 phases in the semimolten state (state comprised of 211 phases and liquid phase) is suppressed and as a result the 211 phases in the material are refined to about 1 m. The amount of addition, from the viewpoint of the amount at which the effect of refining appears and the material costs, is preferably Pt: 0.2 to 2.0 mass %, Rh: 0.01 to 0.5 mass %, and Ce: 0.5 to 2.0 mass %. The added Pt, Rh, and Ce partially form solid solutions in the 123 phase. Further, the elements which cannot form solid solutions form composite oxides with Ba and Cu and are scattered in the QMG material.

(9) Further, a bulk oxide superconductor forming a magnet has to have a high critical current density even in a magnetic field. To satisfy this condition, a single crystal-like 123 phase not containing large inclination grain boundaries forming weak bonds in a superconductive manner is necessary. Further, to obtain a high Jc characteristic, pinning centers for stopping the action of the magnetic flux become necessary. What function as the pinning centers are the finely dispersed 211 phases. These are preferably dispersed in large numbers in finer form. As stated above, Pt, Rh, and Ce act to promote the refining of the 211 phases. Further, as pinning sites, the possibility of BaCeO.sub.3, BaSiO.sub.3, BaGeO.sub.3, BaSnO.sub.3, etc. is known. Further, the 211 phases and other nonsuperconducting phases finely disperse in the easily cleavable 123 phase and thereby mechanically strengthen the superconductor and have important actions in the bulk material.

(10) The ratio or the 211 phases in the 123 phase is preferably 5 to 35 vol % from the viewpoint of the Jc characteristic and mechanical strength. Further, a QMG material generally contains 50 to 500 m or so voids in 5 to 20 vol %. Furthermore, when adding Ag, depending on the amount of addition, the case is included of 1 to 500 m or so Ag or Ag compounds in over 0 vol % to 25 vol %.

(11) Further, the oxygen loss (x) of the material after crystal growth shows the temperature change of the semiconductor resistance at about 0.5. Depending on the RE, by annealing at 350 C. to 600 C. at 100 hours or so in an oxygen atmosphere, oxygen is taken into the material, the oxygen loss (x) becomes 0.2 or less, and a good superconducting characteristic is exhibited.

(12) Effect of Addition of Ag

(13) Next, the effect of addition of Ag in the QMG material will be explained. In general, it is important to efficiently and inexpensively produce a good quality superconducting bulk material suitable for the conditions of use. It is possible to say that causing fine dispersion of expensive Ag only at required parts is an economically advantageous technique.

(14) However, to make Ag segregate at specific locations of an Ag bulk oxide superconductor, advanced crystal growth technology keeping down the amount of addition of Ag and anticipating changes in crystal growth temperature is also necessary. It is believed there has not been such a technical idea in the past. Further, when applied to a current lead element or other current carrying device, it is necessary to coat the electrode parts of the current carrying device with Ag to lower the contact resistance, so it is desirable to make Ag particles disperse in the material. However, on the other hand, it is necessary to suppress the entry of heat between electrodes of a current carrying device, so it is necessary to eliminate Ag particles with a large heat conductivity.

(15) The inventors studied in detail the amount of addition of Ag, the heat treatment conditions, and the crystal growth process and investigated in depth and elucidated the segregation behavior of Ag in a material to thereby reach the present invention. When the amount of addition of Ag in the 123 phase and 211 phases, mixed powder of Ag or Ag.sub.2O powder, or precursor of the shaped article, that is, bulk oxide superconductor, is less than 5 mass %, Ag dissolves in the liquid phase when heated to a semimolten state. Further, they discovered that if bringing a seed crystal into contact with this liquid phase to cause crystal growth, Ag particles will not segregate near the seed crystal. Furthermore, along with crystal growth, the concentration of Ag in the liquid phase rises. For example, in the case of a Gd-based material, the inventors discovered that if the concentration of Ag in the liquid phase exceeds about 5 mass %, Ag particles will precipitate.

(16) In the semimolten state before crystal growth [211 phases+liquid phase (composite oxide of Ba and Cu)], Ag dissolves in the liquid phase to a certain extent. For example, when mixing a Gd-based 123 phase powder and a Gd-based 211 powder in a 3:1 ratio and heating them to a semimolten state, the amount of Ag dissolving in the liquid phase component is about 5 mass % of the mixed powder. This amount changes depending on the amount and composition of the liquid phase in the semimolten state. The greater the liquid phase component, the greater the amount of Ag dissolved. Further, there is also somewhat of a dependency on the crystal growth temperature. The higher the crystal growth temperature, the greater the amount of Ag dissolved tends to become.

(17) Therefore, for example, in the case of the above Gd-based material with an amount of addition of Ag of 3 mass %, since the amount of addition of Ag is less than 5 mass %, the added Ag completely dissolves in the liquid phase. Next, when bringing a seed crystal into contact with this from this state to cause crystal growth, at the initial stage of crystal growth, as explained below, crystal growth (peritectic reaction) proceeds in the state with no Ag particles contained.
211 phase+liquid phase (composite oxide of Ba and Cu).fwdarw.123 phase

(18) At this time, almost no Ag forms a solid solution in the crystal phase, so the concentration of Ag in the liquid phase increases along with the crystal growth. If crystal growth proceeds and the concentration of Ag in the precursor exceeds about 5 mass %, 1 to 10 m or so fine Ag particles precipitate from the liquid phase and are taken into the crystal phase. At this time, a structure is obtained in which 1 to 10 m or so fine Ag particles are dispersed in a volume ratio of several percent. Due to the above, the upper limit of the concentration of Ag in the precursor (amount of addition) is made 5 mass %. To secure many parts where Ag particles are not present, it is better to lower the Ag concentration, but if doing so, the workability is sacrificed. Therefore, the lower limit of the Ag concentration is made 0.1 mass %. To secure such an effect, the upper limit is preferably made 4.8 mass %, more preferably made 4.6 mass %. Similarly, the lower limit is preferably made 0.5 mass %, more preferably is made 1 mass %.

(19) Due to the above process, it is possible to obtain a structure where parts where Ag particles are present and parts where Ag particles are not present adjoin each other. Furthermore, viewed three-dimensionally, it is possible to obtain a structure in which parts where Ag particles are present surround parts where Ag particles are not present. Note that, here, the dispersion means the state where the precipitated Ag particles are present at certain extents of intervals from each other without aggregating.

(20) For example, when placing a single seed crystal 2 on the surface of the center part of a single bulk material (precursor) 1 and growing a crystal such as shown in FIG. 1A, at the initial stage of crystal growth, that is, at the bulk, the center part of the surface does not contain Ag particles, but a material is obtained where the peripheral parts contain 1 to 10 m or so fine Ag particles. Further, the crystal growth proceeds along with rectangular facets, so due to such a series of processes of crystal growth, regions containing fine Ag particles 4 are formed around the rectangular regions not containing Ag particles 3 shown in FIG. 1B.

(21) The particle size of Ag particles is a relatively fine 1 to 3 m or so near the boundaries between the regions containing Ag particles and regions not containing Ag particles, but the particle size of the Ag particles tends to become larger the further from the boundaries. This is because in the region far from the boundaries, the saturated state of the Ag at the liquid phase is held for a long period of time and as a result nuclei for precipitation of Ag particles easily form and Ag particles grow starting from these nuclei, so the particle size becomes larger. In the regions far from the comparative boundaries, many Ag particles of a particle size of 10 m or so are seen. Due to such a phenomenon, a situation arises where 1 to 10 m or so Ag particles surround regions not containing Ag particles.

(22) The starting temperature of the crystal growth of a bulk oxide superconductor containing Ag changes by the amount of addition of Ag. For example, in the case of a Gd-based material, in the air atmosphere, the crystal growth temperature falls along with the amount of addition, e.g., when the amount of addition of Ag is 0 mass %, it is about 1040 C., when 1 mass %, it is about 1034 C., and when 2 mass %, it is about 1025 C. Further, the drop in crystal growth temperature tends to become saturated from an amount of addition of Ag near 7 mass %, e.g., when 5 mass %, it is about 1010 C., when 7 mass %, it is about 1004 C., and when 10 mass %, it is about 1004 C.

(23) The crystal growth of the 123 phase is crystal growth while maintaining relatively stable facets when the difference of the starting temperature of this crystal growth and the actual growth temperature, that is, the supercooling degree, is 10 C. or less, so a good quality bulk oxide superconductor is obtained. Therefore, for example, for a material to which Ag: 2 mass % is added, if growing the crystal to the shaped article as a whole, if making the furnace temperature at the initial stage of crystal growth a condition several percent lower than 1025 C., the Ag is concentrated at the surrounding parts of the bulk material. Further, to obtain a structure in which Ag particles are dispersed, gradually cooling down to at least several degrees centigrade lower than 1010 C. is necessary. It is necessary to produce a bulk oxide superconductor while maintaining a good crystallinity while lowering the crystal temperature in accordance with the concentration of Ag due to crystal growth. A material in a condition where the starting temperature of crystal growth does not change along with crystal growth, for example, a material to which Ag: 10 mass % is added, differs in heat treatment (method of production) on this point.

(24) On the other hand, for example, in the case of a Gd-based material with an amount of addition of Ag of 5 mass % to less than 10 mass %, part of the added Ag dissolves in the liquid phase, but part is trapped as liquid Ag particles in the shaped article in the semimolten state. The size of the Ag particles at this time is determined by the size of the Ag particles added to the mixed powder of the 123 powder and the 211 phase powder, the size of the Ag.sub.2O powder, or the size of the secondary particles formed by aggregation of these particles. With normal sieving etc., most particles become 30 to 300 m or so.

(25) If crystal growth starts by such a composition, at the crystal growth ends, the Ag which dissolved in the liquid phase is absorbed at the relatively large 30 to 300 m or so Ag particles of the liquid. For this reason, 1 to 10 m or so fine Ag particles become hard to precipitate. Almost all is taken into the crystal phase as large 30 to 300 m or so Ag particles. As a result, a bulk oxide superconductor in which 30 to 300 m or so Ag particles are dispersed is obtained.

(26) Further, for example, if the above Gd-based material with an amount of addition of Ag of 5 mass %, the added Ag substantially completely dissolves in the liquid phase. Next, when growing a crystal from a seed crystal by such a composition, if holding the rectangular facets, 1 to 10 m or so fine Ag particles are precipitated at the regions grown in the [100], [010], [001] directions at the facet surface and the rectangular region of the center part.

(27) In this regard, at the parts of the corners of the crystal phases, that is, the nearby regions grown in the [110], [101], [111] directions (width 0.2 to 1.0 mm), regions in which 1 to 10 m or so fine Ag particles are not contained are formed. For example, as shown in FIG. 2A, when using a seed crystal 2 for crystal growth, a structure such as shown in FIGS. 2B and 2C having regions 4 containing fine Ag particles and straight line regions 5 not containing Ag particles is formed. In the straight line regions 5 not containing Ag particles, it appears that either the Ag precipitated along with the crystal growth again dissolves into the liquid phase or the precipitated liquid Ag particles are pushed by the facets of the corner parts.

(28) The crystal phase is black in color, while the Ag particles have a metallic luster, so by roughly polishing the sample surface by abrasive paper etc., it is possible to visually discriminate between regions containing Ag particles and regions not containing them. In relatively small-sized bulk oxide superconductors as well, it is possible to discern any respective 100 mm.sup.3 or so regions as well.

(29) The Ag particles dispersed in the material act to suppress the progression of cracks in the crystal phase, so by adding Ag into a superconductor, it is considered that there is a tendency for the mechanical strength to increase. Further, there is the effect of suppressing the progression of cracks in the crystal phase, so at the time or grinding and cutting, the workability of the material increases and the resistance to chipping and other defects increases. For this reason, when applied to a bulk magnet, when precisely working the outer circumferential part of the bulk oxide superconductor by a 0.1 mm or so precision for reinforcement, by the outer ring, it is extremely desirable to have a structure in which Ag is dispersed.

(30) Further, by working this bulk oxide superconductor into a bar shape, it is possible to prepare an oxide superconductor current lead element where the center part does not contain Ag particles, but the peripheral parts contain 1 to 10 m or so fine Ag particles. At this time, the two end parts where the Ag coating is provided have Ag particles finely dispersed, while the center part does not contain Ag particles. In this way, it is possible to apply an Ag coating at the electrode parts of a current carrying device at the two end parts to efficiently lower the contact resistance and sufficiently suppress entry of heat between electrodes.

EXAMPLES

Example 1

(31) Purity 99.9% reagents Gd.sub.2O.sub.3, BaO.sub.2, and CuO were mixed to give a molar ratio of Gd:Ba:Cu metal elements of 10:14:20 (that is, molar ratio of 123 phase:211 phases of final structure of 3:1). Furthermore, a mixed powder to which CeO.sub.2: 1.0 mass % and Ag.sub.2O: 3 mass % (converted to Ag of about 2.8 mass %) were added was prepared. The mixed powders were calcined once at 900 C. for 8 hours. The calcined powders were filled in inside diameter 50 mm cylindrical molds and formed into thickness about 30 mm disk shapes to prepare Gd-based shaped articles. Further, Sm.sub.2O.sub.3 and Yb.sub.2O.sub.3 were used by the same method as the above shaped articles to prepare thickness 4 mm Sm-based and Yb-based disk shape shaped articles. Further, the shaped articles were compressed by an isostatic hydraulic press by about 100 MPa.

(32) Further, in the preparation of comparative materials of Sm-based, Yb-based, Gd-based shapes (precursors), shaped articles of precursors not containing Ag (Sm-based, Yb-based, Gd-based) prepared by not adding Ag.sub.2O were prepared.

(33) Next, the precursors of the invention example were stacked on an alumina support in the order of the Sm-based, Yb-based, and Gd-based shaped articles (precursors) from the bottom and were placed in a furnace. These precursors were raised in temperature in the air up to 700 C. over 15 hours, up to 1040 C. over 160 hours, and further up to 1120 C. over 1 hour, held there for 30 minutes, then lowered in temperature down to 1030 C. over 1 hour and held there for 1 hour. During that time, a Sm-based seed crystal prepared in advance was used and the seed crystal placed on the semimolten state precursors. Regarding the orientation of the seed crystal, the cleaved surface was placed on the precursors so that the c-axis became the normal line of the disk shaped precursor. After this, the assembly was cooled in the air down to 1025 to 1000 C. over 120 hours to grow the crystal. Further, the assembly was cooled down to room temperature over about 35 hours to obtain an outside diameter about 37 mm, thickness about 22 mm Gd-based single crystal-like bulk oxide superconductor.

(34) Further, a comparative example of precursors not containing Ag were also similarly placed in a furnace. After heat treatment up to similar seeding, they were cooled down to 1045 to 1025 C. over 120 hours to grow a crystal and thereby similarly obtain a comparative material of a Gd-based single crystal-like bulk oxide superconductor.

(35) Next, the obtained sample of the invention example, as shown in FIG. 3A, was cut at positions of 5 mm, 10 mm, and 15 mm from the top surface carrying the seed crystal 31, annealed by oxygen annealing (held in an oxygen stream at 400 C. for 80 hours), then polished on the surfaces and observed in structure. As a result, the pieces respectively had structures of single crystal-like GdBa.sub.2Cu.sub.3O.sub.y-x phases in which Gd.sub.2BaCuO.sub.5 phases (211 phases) were finely dispersed. At the positions of 5 mm and 10 mm from the top surfaces, as shown in FIG. 3B, regions 32 not containing Ag particles could be observed in the approximately 26 mm square regions at the center parts of the samples while regions 33 in which fine Ag particles are contained could be observed at the peripheries. That is, in about 3400 mm.sup.3 regions, almost no precipitation of Ag particles was seen while in the surrounding about 2000 mm.sup.3 regions, the dispersion of Ag was seen. The particle size of most of the Ag particles was 1 to 10 m, while the area ratio of the Ag particles was about 5%. Further, the closer to the peripheral parts, the larger the particle size tended to become. However, at the 15 mm position, the facets became disturbed and recessed facets were formed in the crystal growth direction, so it was confirmed that Ag particles precipitated at the center parts together with the peripheral parts.

(36) Next, a sample cut out from a position 5 to 10 mm from the top surface was worked to an outside diameter 36.0+0.0 to 0.1 mm and thickness 4.50.1 mm precision. The outer circumferential part contained Ag particles, so the sample could be worked without chipping. Further, to this sample, an inside diameter 36.0+0.1 to 0.0 mm, outside diameter 40.00.1 mm, height 4.50.1 mm SUS ring was fit and fastened by a resin. Next, this was cooled in a 2.0 T magnetic field in liquid nitrogen (77K). The outside magnetic field was removed, then the trapped magnetic flux distribution was measured whereupon a concentric magnetic flux density distribution and 1.2 T magnetic flux density were confirmed at the sample surface. Due to this, it could be confirmed that crystals of the superconducting phase (123 phase) were connected to the sample as a whole and the c-axes were aligned.

(37) Further, a comparative example of the Gd-based sample not containing Ag was similarly cut out from a position of 5 to 10 mm from the top surface to obtain a sample which was similarly worked to an outside diameter of 36.0+0.0 to 0.1 mm and thickness 4.50.1 mm precision, but chipping was confirmed in three locations. Further, this sample was similarly measured for trapped magnetic flux distribution, whereupon the 0.95 T maximum magnetic flux density was confirmed. Due to this comparative experiment, it could be confirmed that the material of the invention example is better than the comparative material.

(38) Next, a sample of the invention example cut out from a position 0 to 5 mm from the top surface, as shown in FIG. 3C, was shaved in thickness from about 5 mm to 2.0 mm, then a width 8 mm, length about 34 mm bar-shaped sample was cut out so that the two end parts became regions where Ag particles precipitated. Further, at the regions where Ag particles precipitated at the two end parts of this bar-shaped sample, thickness 2 m Ag films were formed by sputtering. These were heat treated to make the Ag films closely contact the bar-shaped sample, then copper electrodes were soldered to these parts. The bar-shaped sample as a whole was sandwiched between glass fiber-reinforced plastic and screwed with them, then solidified by a resin to prepare a current lead. This current lead can carry 1500 A at 77K. It could be confirmed to sufficiently function as a current lead.

Example 2

(39) Purity 99.9% reagents Y.sub.2O.sub.3, BaO.sub.2, and CuO were mixed to give a molar ratio of Gd:Ba:Cu metal elements of 13:17:24 (that is, molar ratio of 123 phase:211 phase of final structure of 7:3). Furthermore, a mixed powder to which CeBaO.sub.3: 1.5 mass % and Ag.sub.2O: 4 mass % (converted to Ag about 3.7 mass %) were added was prepared. The mixed powders were calcined once at 900 C. for 8 hours. The calcined powders were filled into inside diameter 60 mm cylindrical molds and formed into thickness about 35 mm disk shapes to prepare Y-based shaped articles. Further, Sm.sub.2O.sub.3 and Yb.sub.2O.sub.3 were used by the same method as the above shaped articles to prepare thickness 4 mm Sm-based and Yb-based disk shape shaped articles. Furthermore, the shaped articles were compressed by an isostatic hydraulic press by about 100 MPa.

(40) Further, in the preparation of comparative materials of Sm-based, Yb-based, Y-based shapes (precursors), shaped articles of precursors not containing Ag (Sm-based, Yb-based, Gd-based) prepared by not adding Ag.sub.2O were prepared.

(41) Next, the precursors of the invention example were stacked on an alumina-based support in the order of Sm-based, Yb-based, and Y-based shapes (precursors) from the bottom and were placed inside a furnace. These precursors were raised in temperature in the atmosphere up to 700 C. over 15 hours, up to 1040 C. over 160 hours, and up to 1100 C. over 1 hour and held there for 30 minutes, then were lowered in temperature down to 1020 C. over 1 hour and held there for 1 hour. During that time, Sm-based seed crystal prepared in advance was used and the seed crystal placed on the semimolten state precursors. Regarding the orientation of the seed crystal, the cleaved surface was placed on the precursors so that the c-axis became the normal line of the disk shaped precursor. After this, the assembly was cooled in the air down to 990 to 970 C. over 140 hours to grow the crystal. Further, the assembly was cooled down to room temperature over about 35 hours to obtain an outside diameter about 45 mm, thickness about 26 mm Y-based single crystal-like bulk oxide superconductor.

(42) Further, a comparative example of precursors not containing Ag were similarly arranged in a furnace, were heated treated until similar seeding, then were cooled down to 1005 to 990 C. over 140 hours to grow a crystal and similarly obtain a comparative example of a Y-based single crystal-like oxide superconducting material.

(43) Next, the obtained sample of the invention example, as shown in FIG. 4A, was cut at positions of 5 mm, 10 mm, and 15 mm from the top surface carrying the seed crystal 41, annealed by oxygen annealing (held in oxygen stream at 400 C. for 80 hours), then polished on the surfaces and observed in structure. As a result, the pieces respectively had structures of single crystal-like YBa.sub.2Cu.sub.3O.sub.7-x phases in which Y.sub.2BaCuO.sub.5 phases (211 phases) were finely dispersed. At the positions of 5 mm and 10 mm from the top surfaces, as shown in FIG. 4B, regions 42 not containing Ag particles could be observed in the approximately 23 mm square regions at the center parts of the samples while regions 43 in which fine Ag particles are contained could be observed at the peripheries. That is, in about 2600 mm.sup.3 regions, almost no precipitation of Ag particles was seen while in the surrounding about 7600 mm.sup.3 regions, the dispersion of Ag was seen. The particle size of most of the Ag particles was 1 to 10 m, while the area ratio of the Ag particles was about 5%. Further, the closer to the peripheral parts, the larger the particle size tends to become. Near the sample surface, 20 m or so particles could also be seen. However, at the 15 mm position, the facets became disturbed and recessed facets are formed in the crystal growth direction, so it was confirmed that Ag particles precipitated at the center parts together with the peripheral parts.

(44) Next, a sample cut out from a position 5 to 10 mm from the top surface was worked to an outside diameter 44.0+0.0 to 0.1 mm and thickness 4.50.1 mm precision. The outer circumference part contained Ag particles, so the sample could be worked without chipping. Further, to this sample, an inside diameter 44.0+0.1 to 0.0 mm, outside diameter 45.00.1 mm, height 4.50.1 mm SUS ring was fit and fastened by a resin. Next, this was cooled in a 3.0 T magnetic field in liquid nitrogen (77K). The outside magnetic field was removed, then the trapped magnetic flux distribution was measured whereupon a concentric magnetic flux density distribution and 1.25 T magnetic flux density were confirmed at the sample surface. Due to this, it could be confirmed that crystals of the superconducting phase (123 phase) were connected to the sample as a whole and the c-axes were aligned.

(45) Further, a comparative example of the Y-based sample not containing Ag was similarly cut out from a position of 5 to 10 mm from the top surface to obtain a sample which was then similarly worked to an outside diameter 44.0+0.0 to 0.1 mm and thickness 4.50.1 mm precision, but chipping was confirmed at five locations. Further, this sample was similarly measured for trapped magnetic flux distribution, whereupon the 1.10 T maximum magnetic flux density was confirmed. Due to this comparative experiment, it could be confirmed that material of the invention example is better than the comparative material.

(46) Next, a sample of the invention example cut out from a position 0 to 5 mm from the top surface, as shown in FIG. 4C, was shaved in thickness from about 5 mm to 2.0 mm, then a width 8 mm, length about 42 mm bar-shaped sample was cut out so that the two end parts become regions in which Ag particles precipitated. Further, at the regions where Ag particles precipitated at the two end parts of this bar-shaped sample, thickness 2 m Ag films were formed by sputtering. These were heat treated to make the Ag films closely contact the bar-shaped sample, then copper electrodes were soldered to these parts. The bar-shaped sample as a whole was sandwiched between glass fiber-reinforced plastic and screwed with them, then solidified by a resin to prepare a current lead. This current lead can carry 1500 A at 77K. It could be confirmed to sufficiently function as a current lead.

INDUSTRIAL APPLICABILITY

(47) The bulk oxide superconductor according to the present invention can be utilized for a superconducting magnet. Further, a superconducting magnet can be applied to a linear motor or can be utilized as an alternative to current permanent magnets.

REFERENCE SIGNS LIST

(48) 2. seed crystal 3. rectangular region not containing Ag particles 4. region containing fine Ag particles 5. straight line region not containing Ag particles