CN101168442A - High-performance MgB2 superconducting material and preparation method thereof - Google Patents
High-performance MgB2 superconducting material and preparation method thereof Download PDFInfo
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- CN101168442A CN101168442A CNA2007101223990A CN200710122399A CN101168442A CN 101168442 A CN101168442 A CN 101168442A CN A2007101223990 A CNA2007101223990 A CN A2007101223990A CN 200710122399 A CN200710122399 A CN 200710122399A CN 101168442 A CN101168442 A CN 101168442A
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- 239000000463 material Substances 0.000 title claims abstract description 33
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 229910020073 MgB2 Inorganic materials 0.000 title abstract description 8
- 239000000843 powder Substances 0.000 claims abstract description 73
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims abstract description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229910052786 argon Inorganic materials 0.000 claims abstract description 15
- 239000007789 gas Substances 0.000 claims abstract description 12
- 229910052742 iron Inorganic materials 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 8
- IYRDVAUFQZOLSB-UHFFFAOYSA-N copper iron Chemical compound [Fe].[Cu] IYRDVAUFQZOLSB-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000009413 insulation Methods 0.000 claims description 14
- 238000007789 sealing Methods 0.000 claims description 11
- 238000005096 rolling process Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 3
- 239000002131 composite material Substances 0.000 abstract description 3
- 238000005303 weighing Methods 0.000 description 12
- 238000012856 packing Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 230000002427 irreversible effect Effects 0.000 description 6
- 239000002887 superconductor Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000007792 addition Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000002019 doping agent Substances 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000005245 sintering Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 2
- 239000011858 nanopowder Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000013459 approach Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910021392 nanocarbon Inorganic materials 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
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- Superconductors And Manufacturing Methods Therefor (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The invention relates to an MgB2 superconductive material, which is characterized in being composed of Mg, B, C, and SiC. And a relative preparation is characterized in that according to mol ratio (0.8-0.975):(1.8-1.95):(0.010-0.15):(0.010-0.15) to prepare and mix Mg powder, B powder, C nanometer powder, and SiC nanometer powder uniformly to be filled into an iron tube or iron-copper composite tube to be sealed, rotationally forges, draws and rolls to obtain MgB2 superconductive material containing C and SiC nanometer powder, or tablets the raw powder mixed uniformly via a tablet press, to obtain MgB2 superconductive block containing C and SiC nanometer powder, arranges obtained band or block in a vacuum furnace, vacuums and fills argon gas, keeps temperature for 0.2-3h at 600-1200DEG C, and obtains MgB2 superconductive material containing C nanometer powder and SiC nanometer powder. The inventive MgB2 superconductive material has better performance under magnetic field, with better repeatability.
Description
Technical field
The present invention relates to a kind of high-performance MgB
2Superconducting material and preparation method thereof.
Background technology
MgB
2Have higher transition temperature, bigger coherence length, crystal boundary and do not have weak connection, characteristics such as simple in structure, with low cost.These advantages make MgB
2Become the strongest rival of material who is applied in the 20K-30K temperature range.Particularly in a low field, as at magnet for magnetic resonant imaging application facet, MgB
2Show great advantage, had data to show, MgB
2Practicability will bring billions of economic benefits, and owing to can under the refrigeration mechanism cool condition, work MgB
2Application will promote the popularization of magnetic resonance imager greatly, have crucial meaning for the raising of the vast rural people's medical level of China.
Yet the MgB of present preparation
2The critical current density of material is compared also lower with cryogenic superconductor with the A15 superconductor.Critical current density is the key characteristic that can a kind of superconducting material of decision large-scale application, film or block MgB
2Superconductor under null field, have higher critical current density (when 4.2K, J
c＞10
6A/cm
2When 20K, J
c＞5 * 10
5A/cm
2), but in certain magnetic field, MgB
2What critical current density was rapid along with the increase of magneticstrength reduces, and shows the irreversible field than enlightening, only is 4-5T as irreversible the value of pure MgB2 superconductor under 20K.In order to improve MgB
2Critical current density under certain magnetic field can adopt methods such as neutron (proton) bombardment, chemical corrosion, mechanical workout, doping, and since mix have easier fast, can carry out characteristics such as even modification, become present raising MgB
2The main method of material superconductivity.
So far, improve MgB by mixing
2The best dopant of material property effect is nanometer C (Ma Y W etc., the Significantly enhanced critical current densities in MgB that people such as Ma Yanwei finds
2Tapes made by ascaleable nanocarbon addition route, Applied Physics Letters, 88 (2006) 072502) and people such as the Dou Shixue nano SiC (Dou.S.X etc., the Enhancement of the critical current density and fluxpinning of MgB that attempt
2Superconductor by nanoparticle SiC doping, AppliedPhysics Letters, 81 (2002) 3419).A large amount of experimental results show that nanometer C and nano SiC doping can increase substantially MgB
2The upper critical field of bulk and irreversible field are introduced a large amount of effective pinning center simultaneously, thereby are made MgB
2The critical current density of material in magnetic field also is improved.After for example mixing through SiC, MgB
2The critical current density of band can reach 2.5 * 10
4A/cm
2[Matsumoto A etc., Effect of impurity additions on the microstructures andsuperconducting properties of in situ processed MgB
2Tapes, Supercond.Sci.Technol.17 (2004) S319-S323)], through MgB after the C doping
2The critical current density of band can reach 2.1 * 10
4A/cm
2[Ma Y W etc., Large irreversibility field in nanoscale C-doped MgB
2/ Fe tape conductors, Supercond.Sci.Technol.20 (2007) L5-L7)].
Summary of the invention
The objective of the invention is in order to overcome existing MgB
2Lower critical current density lower shortcoming in superconducting material magnetic field provides a kind of high-performance MgB that has
2Superconducting material and preparation method thereof.It is composite mixed that preparation method of the present invention adopts nanometer C and these two kinds the most effective dopants of SiC to carry out, and makes MgB
2Superconducting material obtains the raising effect of two kinds of dopants simultaneously, and then significantly improves MgB
2The critical current density of material.
MgB of the present invention
2The superconducting material component is Mg, B, C and SiC, and its constitutive molar ratio is: Mg: B: C: SiC=(0.8-0.975): (1.6-1.95): (0.010-0.15): (0.010-0.15).
Preparation method of the present invention is as follows:
The present invention adds nanometer C powder at raw material Mg powder in the B powder, nano SiC powder, material purity are commercially available chemical pure, and the mol ratio of its composition is: Mg: B: C: SiC=(0.8-0.975): (1.6-1.95): (0.010-0.15): (0.010-0.15).
With the Mg powder, the B powder, nanometer C powder, the nano SiC powder is according to mol ratio (0.8-0.975): (1.8-1.95): (0.010-0.15): (0.010-0.15) prepare and mix, pack in iron pipe or the iron copper multiple-unit tube sealing back with 10% deformation rate successively swage in order, drawing, rolling, obtain containing the MgB of C and SiC
2Superconducting line strips.Perhaps the raw material powder that mixes is carried out compressing tablet with tabletting machine, obtain containing the MgB of C and SiC
2Superconductive block.The wire strip or the bulk that obtain are placed in the vacuum oven, charge into argon gas after vacuumizing,, finally obtain containing the MgB of C and SiC 600 ℃-1200 ℃ insulations 0.5-3 hour
2Superconducting material.
In general, improve MgB
2The approach of material superconductivity has following two kinds, and a kind of is to improve MgB
2The upper critical field of material and irreversible field, another kind is to improve MgB
2The flux pinning ability of material.C and SiC are composite mixed for improving MgB
2Current capability under the wire strip High-Field has good effect, is that mainly it has following characteristics:
At first, C and SiC mix and have the effect of crystal grain thinning.The existence of a large amount of crystal boundaries has a very important role for the flux pinning ability that improves material in the crystal.The second phase impurity of introducing that mixes in addition also can play the effect that improves the flux pinning ability.
Secondly, lattice distortion that C and SiC doping can cause and C substitute B's, improve MgB
2The upper critical field of material and irreversible field.Simultaneously, experiment confirm has been arranged, C or SiC mix for improving MgB
2The compactness of material has remarkable effect.
The present invention adopts commercially available Mg powder, B powder, C nano powder, and the SiC nano powder adopts above-mentioned molar ratio, preparation technology and thermal treatment process can prepare the MgB that contains C and SiC that performances such as critical current density, irreversible field all are significantly improved
2Superconducting line strips.MgB with the inventive method preparation
2The critical current density of superconducting tape is 3.6 * 10
4A/cm
2(4.2K, 10T) about, and repeatability is fine, (4.2K, under the 10T condition, current density reaches 2.5 * 10 far above the best level of present World Report
4A/cm
2) [Matsumoto A etc., Effect of impurity additions on themicrostructures and superconducting properties of in situ-processed MgB
2Tapes, Superconductor Science and Technology, 17 (2004) S319], and the cost expense is far below people's such as Matsumoto A product.If the long wire strip of the MgB2 that this method is used to prepare will greatly promote MgB
2The industrialization process of material.
Embodiment
Example 1
Preparation (MgB
2)
0.92C
0.04SiC
0.04Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.92: 1.84: 0.04: 0.04 accurate weighing also mixes, the diameter of packing into be in 8 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 900 ℃ of insulations 1 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.The critical current density of the band that makes is 3.6 * 10
4A/cm
2(4.2K, 10T).
Example 2
Preparation (MgB
2)
0.975C
0.015SiC
0.013Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.975: 1.95: 0.015: 0.013 accurate weighing also mixes, the diameter of packing into be in 8 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 800 ℃ of insulations 1 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.The critical current density of the band that makes is 8.4 * 10
3A/cm
2(4.2K, 14T).
Example 3
Preparation (MgB
2)
0.8C
0.1SiC
0.1Superconducting wire.With the Mg powder, the B powder, nanometer C powder, nano SiC powder were according to mol ratio 0.8: 1.6: 0.1: 0.1 accurate weighing also mixes, the diameter of packing into be in 20 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, obtain diameter and be 1.0 millimeters wire rod.With wire rod 700 ℃ of insulations 0.5 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting wire.
Example 4
Preparation (MgB
2)
0.95C
0.015SiC
0.035Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder is according to mol ratio accurate weighing in 0.95: 1.9: 0.01 5: 0.035 and mix, the diameter of packing into be in 16 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 700 ℃ of insulations 0.5 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.
Example 5
Preparation (MgB
2)
0.95C
0.025SiC
0.025Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.95: 1.9: 0.025: 0.025 accurate weighing also mixes, the external diameter of packing into be in 12 millimeters the iron copper multiple-unit tube sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 650 ℃ of insulations 1 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.
Example 6
Preparation (MgB
2)
0.8C
0.085SiC
0.115Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.8: 1.6: 0.085: 0.115 accurate weighing also mixes, the diameter of packing into be in 8 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 600 ℃ of insulations 1.5 hours in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.
Example 7
Preparation (MgB
2)
0.8C
0.115SiC
0.085Superconducting wire.With the Mg powder, the B powder, nanometer C powder, nano SiC powder were according to mol ratio 0.8: 1.6: 0.115: 0.085 accurate weighing also mixes, the external diameter of packing into be in 8 millimeters the iron copper multiple-unit tube sealing back with 10% deformation rate swage in order, drawing, obtain diameter and be 1.0 millimeters wire rod.With band 650 ℃ of insulations 1 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting wire.
Example 8
Preparation (MgB
2)
0.975C
0.02SiC
0.005Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.975: 1.95: 0.02: 0.005 accurate weighing also mixes, the diameter of packing into be in 8 millimeters the iron pipe sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 700 ℃ of insulations 0.5 hour in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.
Example 9
Preparation (MgB
2)
0.975C
0.015SiC
0.01Superconducting tape.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.975: 1.95: 0.015: 0.01 accurate weighing also mixes, the external diameter of packing into be in 18 millimeters the iron copper multiple-unit tube sealing back with 10% deformation rate swage in order, drawing, rolling, obtain wide 3.7 millimeters, thick 0.5 millimeter band.With band 600 ℃ of insulations 1.5 hours in the argon gas vacuum oven of atmosphere that flows, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconducting tape.
Example 10
Preparation (MgB
2)
0.95C
0.025SiC
0.015Superconductive block.With the Mg powder, the B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.95: 1.9: 0.025: 0.015 accurate weighing also mixes, carry out in the normal pressure argon atmospher, carrying out sintering behind the compressing tablet with tabletting machine, 800 ℃ of insulations 2 hours, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconductive block.
Example 11
Preparation (MgB
2)
0.8C
0.15SiC
0.05Superconductive block.With the Mg powder, B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.8: 1.6: 0.15: 0.05 accurate weighing also mixes, and carries out carrying out sintering behind the compressing tablet in the normal pressure argon atmospher with tabletting machine, 600 ℃ of insulations 1.5 hours, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconductive block.
Example 12
Preparation (MgB
2)
0.9C
0.015SiC
0.085Superconductive block.With the Mg powder, B powder, nanometer C powder, the nano SiC powder was according to mol ratio 0.9: 1.8: 0.015: 0.085 accurate weighing also mixes, and carries out carrying out sintering behind the compressing tablet in the normal pressure argon atmospher with tabletting machine, 900 ℃ of insulations 3 hours, in vacuum oven, be cooled to room temperature then, obtain containing the MgB of C and SiC
2Superconductive block.
This technology is used in the explanation of above example can the good wire strip of processability, is MgB
2The superconducting material practical application provides material foundation.
Claims (3)
1. high-performance MgB
2Superconducting material is characterized in that its component is Mg, B, C and SiC, and its constitutive molar ratio is: Mg: B: C: SiC=(0.8-0.975): (1.6-1.95): (0.010-0.15): (0.010-0.15).
2. one kind prepares the described MgB of claim 1
2The method of superconducting material, it is characterized in that, with the Mg powder, the B powder, nanometer C powder, nano SiC powder are according to mol ratio (0.8-0.975): (1.8-1.95): (0.010-0.15): (0.010-0.15) prepare and mix, in pack into iron pipe or the iron copper multiple-unit tube after the sealing, deformation rate with 10% is successively swaged in order, drawing, rolling, obtains containing the MgB of C and SiC
2Superconducting wire or band; Perhaps the raw material powder that mixes is carried out compressing tablet with tabletting machine, obtain containing the MgB of C and SiC
2Superconductive block.
3. according to the described MgB of claim 2
2The preparation method of superconducting material in the wire strip or bulk placement vacuum oven that it is characterized in that obtaining, charges into argon gas after vacuumizing, and 600 ℃-1200 ℃ insulations 0.2-3 hour, finally obtains containing the MgB of C and SiC
2Superconducting material.
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|---|---|---|---|
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|---|---|---|---|
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| Publication Number | Publication Date |
|---|---|
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| CN101168442B CN101168442B (en) | 2010-08-11 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102074309A (en) * | 2010-11-28 | 2011-05-25 | 上海大学 | Method for preparing magnesium diboride composite superconducting material |
| CN102190311A (en) * | 2010-03-12 | 2011-09-21 | 北京大学 | Method for preparing MgB2 superconducting material on basis of Mg(BH4)2 precursor |
| CN101591172B (en) * | 2009-06-26 | 2012-04-18 | 天津大学 | Metal Sn doped MgB2 superconductor and high-temperature rapid preparation method thereof |
| CN102543304A (en) * | 2011-12-20 | 2012-07-04 | 东南大学 | Method for preparing MgB2 superconducting wire |
| CN102718230A (en) * | 2012-05-17 | 2012-10-10 | 天津大学 | Layered MgB2 crystal structure and synthetic method thereof |
| CN106205861A (en) * | 2016-06-29 | 2016-12-07 | 西北有色金属研究院 | A kind of preparation method of graphene-supported multi-element doping magnesium diboride superconductive bulk |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060093861A1 (en) * | 2004-10-29 | 2006-05-04 | The Penn State Research Foundation | Method for producing doped, alloyed, and mixed-phase magnesium boride films |
| CN1933036A (en) * | 2005-09-13 | 2007-03-21 | 中国科学院电工研究所 | MgBz superconducting material and producing method thereof |
| CN1986407A (en) * | 2005-12-23 | 2007-06-27 | 中国科学院电工研究所 | Corbon-containing superconductive MgB2 material and its preparing process |
| CN1929044B (en) * | 2006-08-07 | 2010-09-22 | 中国科学院电工研究所 | MgB2 superconductive material containing Si element and C element and its preparing method |
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2007
- 2007-09-25 CN CN2007101223990A patent/CN101168442B/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101591172B (en) * | 2009-06-26 | 2012-04-18 | 天津大学 | Metal Sn doped MgB2 superconductor and high-temperature rapid preparation method thereof |
| CN102190311A (en) * | 2010-03-12 | 2011-09-21 | 北京大学 | Method for preparing MgB2 superconducting material on basis of Mg(BH4)2 precursor |
| CN102190311B (en) * | 2010-03-12 | 2013-03-06 | 北京大学 | Method for preparing MgB2 superconducting material on basis of Mg(BH4)2 precursor |
| CN102074309A (en) * | 2010-11-28 | 2011-05-25 | 上海大学 | Method for preparing magnesium diboride composite superconducting material |
| CN102543304A (en) * | 2011-12-20 | 2012-07-04 | 东南大学 | Method for preparing MgB2 superconducting wire |
| CN102543304B (en) * | 2011-12-20 | 2013-07-31 | 东南大学 | Method for preparing MgB2 superconducting wire |
| CN102718230A (en) * | 2012-05-17 | 2012-10-10 | 天津大学 | Layered MgB2 crystal structure and synthetic method thereof |
| CN106205861A (en) * | 2016-06-29 | 2016-12-07 | 西北有色金属研究院 | A kind of preparation method of graphene-supported multi-element doping magnesium diboride superconductive bulk |
| CN106205861B (en) * | 2016-06-29 | 2017-05-10 | 西北有色金属研究院 | Preparation method for graphene-loaded multielement-doped magnesium diboride superconducting bulk material |
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