Re-type oxide superconducting wire and process for producing the same
View Patent ↗A RE-type oxide superconducting wire having excellent angular dependence for magnetic field of Jc is obtained by finely dispersing magnetic flux pinning centers into a superconductor. A mixed solution which comprises a metal-organic complex solution including a metal element which composes a RE-type oxide superconductor whose Ba content is reduced and a metal-organic complex solution including at least one or more kinds of metals which are selected from Zr, Ce, Sn, or Ti which has a larger affinity for Ba is coated onto an intermediate layer of a composite substrate, and the assembly is then calcined to disperse artificially and finely oxide particles (magnetic flux pinning centers) including Zr. Thus, the angular dependence for magnetic field (Jc ,min /Jc ,max ) of Jc can be remarkably improved.
1. A RE-type oxide superconducting wire comprising a REBa y Cu 3 O z -type superconductor which is formed on an intermediate layer formed onto a substrate, wherein
said RE comprises an element selected from the group consisting of Y, Nd, Sm, Gd and Eu,
y is <2, and
oxide particles of 50 nm or less including Zr are dispersed as magnetic flux pinning centers in said superconductor.
2. A RE-type oxide superconducting wire comprising a REBa y Cu 3 O z -type superconductor which is formed on an intermediate layer formed onto a substrate, wherein
said RE has a composition of RE=A 1−x B x ,
wherein each of A and B is at least one element selected from the group consisting of Y, Nd, Sm, Gd and Eu,
y is <2, and
oxide particles of 50 nm or less including Zr are dispersed as magnetic flux pinning centers in said superconductor.
3. A RE-type oxide superconducting wire comprising a REBa y Cu 3 O z -type superconductor which is formed on an intermediate layer formed onto a substrate, wherein
said RE is Y 1−x Sm x ,
y is <2, and
oxide particles including Sm and oxide particles of 50 nm or less including Zr are dispersed as magnetic flux pinning centers into said superconductor.
4. The RE-type oxide superconducting wire according to claim 1 , wherein
1.3<y<1.8.
5. The RE-type oxide superconducting wire according to claim 1 , wherein
the oxide particles are 5-30 nm.
6. The RE-type oxide superconducting wire according to claim 3 , wherein
the oxide particles are 5-30 nm.
7. The RE-type oxide superconducting wire according to claim 1 , wherein
the amount of Zr is 0.5-10 mole % of the metal content.
8. The RE-type oxide superconducting wire according to claim 7 , wherein
the amount of Zr is 0.5-5 mole % of the metal content.
9. A process for producing a RE-type oxide comprising a step of forming a REBa y Cu 3 O z -type superconductor by a preliminary calcination heat-treatment after coating a raw material solution on an intermediate layer formed on a substrate, and subsequently heating to form a superconductor, wherein
the raw material solution is a mixed solution which comprises (1) a metal-organic complex solution including RE (wherein RE is a metal element selected from the group consisting of Y, Nd, Sm, Gd and Eu), Ba and Cu, and (2) a metal-organic complex solution including one or more metals selected from the group consisting of Zr, Ce, Sn and Ti
y is <2, and
oxide particles of 50 nm or less including Zr, Ce, Sn or Ti are dispersed as magnetic flux pinning centers in said superconductor.
10. A process for producing a RE-type oxide superconducting wire comprising a step of forming a REBa y Cu 3 O z -type superconductor by a preliminary calcination heat-treatment after coating a raw material solution on the intermediate layer formed on a substrate, and subsequently heating to form a superconductor, wherein
the raw material solution is a mixed solution which comprises (1) a metal-organic complex solution including RE (wherein RE is RE=A 1−x B x and A and B are elements selected from the group consisting of Y, Nd, Sm, Gd and Eu), Ba and Cu, and (2) a metal-organic complex solution including at least one metal selected from the group consisting of Zr, Ce, Sn and Ti,
y is <2, and
oxide particles of 50 nm or less including Zr, Ce, Sn or Ti are dispersed as magnetic flux pinning centers in said superconductor.
11. A process for producing a RE-type oxide superconducting wire comprising a step of forming a REBa y Cu 3 O z -type superconductor by a preliminary calcination heat-treatment after coating a raw material solution after coating a raw material solution on an intermediate layer formed on a substrate, and subsequently heating to form a superconductor, wherein
the raw material solution is a mixed solution which comprises (1) a metal-organic complex solution including RE (wherein RE is Y 1−x Sm x ), Ba and Cu, and (2) a metal-organic complex solution including at least one metal selected from the group consisting of Zr, Ce, Sn and Ti which has a larger affinity for Ba is used as said raw material solution,
y is <2, and
first oxide particles including Sm and second oxide particles of 50 nm or less including Zr, Ce, Sn or Ti are dispersed as magnetic flux pinning centers in said superconductor.
12. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
1.3<y<1.8.
13. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the magnetic flux pinning centers are the second oxide particles and wherein the second oxide particles include Zr and are 5-30 nm.
14. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the magnetic flux pinning centers are the first oxide particles including Sm and the second oxide particles including Zr of 5-30 nm.
15. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the amount of Zr is 0.5-10 mole % of the metal content.
16. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the amount of Zr is 0.5-5 mole % of the metal content.
17. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more RE compounds selected from trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
18. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the metal-organic complex solution including Ba comprises an organic solvent and a trifluoroacetate (TFA), salt of Ba.
19. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more Cu compounds selected from naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
20. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more Zr compounds of trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
21. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt, and neodecanoic acid salt of at least one metal selected from Ce, Sn and Ti.
22. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the preliminary calcination heat-treatment is at a temperature of 400-500 degrees C.
23. The process for producing the RE-type oxide superconducting wire according to claim 22 , wherein
the preliminary calcination heat-treatment is in an atmosphere of a water vapor partial pressure of 3-76 Torr and an oxygen partial pressure of 300-760 Torr.
24. The process for producing the RE-type oxide superconducting wire according to claim 11 , wherein
the heat treatment for formation of the superconductor is at a temperature of 700 to 800 degrees C.
25. The process for producing the RE-type oxide superconducting wire according to claim 24 , wherein
the heat treatment for formation of the superconductor is in an atmosphere of a water vapor partial pressure of 30-100 Torr and an oxygen partial pressure of 0.05-1 Torr.
26. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
1.3<y<1.8.
27. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the magnetic flux pinning centers are the second oxide particles and wherein the second oxide particles include Zr and are 5-30 nm.
28. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the amount of Zr is 0.5-10 mole % of the metal content.
29. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more RE compounds selected from trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
30. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the metal-organic complex solution including Ba comprises an organic solvent and a trifluoroacetate (TFA) salt of Ba.
31. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more Cu compounds selected from naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
32. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more Zr compounds of trifluoroacetate (TFA salt), naphthenate, octylic acid salt levulinic acid salt and neodecanoic acid salt.
33. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more of trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt of at least one metal selected from Ce, Sn or Ti.
34. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the preliminary calcination heat-treatment is at a temperature of 400-500 degrees C.
35. The process for producing the RE-type oxide superconducting wire according to claim 34 , wherein
the preliminary calcination heat-treatment is in an atmosphere of a water vapor partial pressure of 3-76 Torr and an oxygen partial pressure of 300-760 Torr.
36. The process for producing the RE-type oxide superconducting wire according to claim 9 , wherein
the heat treatment for formation of the superconductor is at a temperature of 700 to 800 degrees C.
37. The process for producing the RE-type oxide superconducting wire according to claim 36 , wherein
the heat treatment for formation of the superconductor is in an atmosphere of a water vapor partial pressure of 30-100 Torr and an oxygen partial pressure of 0.05-1 Torr.
38. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
1.3<y<1.8.
39. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the amount of Zr is 0.5-10 mole % of the metal content.
40. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more RE compounds selected from trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
41. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the metal-organic complex solution including Ba comprises an organic solvent and a trifluoroacetate (TFA) salt of Ba.
42. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the metal-organic complex solution (1) comprises an organic solvent and one or more Cu compounds selected from naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt.
43. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more Zr compounds of trifluoroacetate (TFA salt), naphthenate, octylic acid salt levulinic acid salt and neodecanoic acid salt.
44. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the metal-organic complex solution (2) comprises an organic solvent and one or more of trifluoroacetate (TFA salt), naphthenate, octylic acid salt, levulinic acid salt and neodecanoic acid salt of at least one metal selected from Ce, Sn or Ti.
45. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the preliminary calcination heat-treatment is at a temperature of 400-500 degrees C.
46. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the preliminary calcination heat-treatment is in an atmosphere of a water vapor partial pressure of 3-76 Torr and an oxygen partial pressure of 300-760 Torr.
47. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
the heat treatment for formation of the superconductor is at a temperature of 700 to 800 degrees C.
48. The process for producing the RE-type oxide superconducting wire according to claim 10 , wherein
1.3<y<1.8.