Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing MgB2 superconducting material

A technology of superconducting materials and organic acids, which is applied in the field of preparation of MgB2 superconducting materials, can solve the problems of increased preparation cost, easy to be peeled off, and increased specific surface area, so as to enhance electron scattering intensity, overcome oxidation and even spontaneous combustion, and improve Effect of Flux Pinning Force

Inactive Publication Date: 2010-06-23
INST OF ELECTRICAL ENG CHINESE ACAD OF SCI
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, it is worth noting that the particle size of magnesium powder can be reduced to submicron level after high-energy ball milling. During the ball milling process, the oxide layer on the surface is easily peeled off, resulting in a sharp increase in specific surface area and a sharp increase in activity. Once in contact with oxygen or water vapor in the air, it is easy to oxidize or even spontaneously ignite; at the same time, fine boron powder is also very easy to absorb oxygen and be oxidized, which will undoubtedly seriously affect the performance of superconducting materials, and also bring new problems to the preparation process. considerable risk
In order to prevent the oxidation of magnesium powder after ball milling, some research groups are preparing MgB 2 When superconducting materials, the original powder is always kept under the protection of argon atmosphere ([W.Haessler et al, Superconducting MgB2 Tapes Prepared Using Mechanically Alloyed Nanocrystalline PrecursorPowder, Trans.Appl.Supercond.17(2007)2919]), but this obviously increases The complexity and difficulty of the actual operation lead to a sharp increase in the preparation cost, and at the same time, due to the limited argon protection space, the preparation efficiency of superconducting materials is low
In addition, some research groups use organic solvents such as acetone or ethanol to carry out wet ball milling on the original powder to prevent oxidation, but acetone or ethanol is extremely volatile, and once volatilized, the original powder will be completely exposed to the air again, so there is no Very effective in preventing oxidation

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing MgB2 superconducting material
  • Method for preparing MgB2 superconducting material

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0012] (1) Weigh Mg powder and B powder according to molar ratio Mg: B=1: 2, Mg powder purity is 95%, 70 microns, and B powder purity is 90%, 1-2 microns, weighs simultaneously the quality is Mg powder Dissolve benzoic acid with a total mass of 5% of B powder in 5 mL of ethanol, mix the benzoic acid ethanol solution with Mg powder and B powder, and ball mill for 1 hour; then heat-preserve and dry at 80°C for 1 hour in a vacuum drying oven;

[0013] (2) Tablet the gained powder to obtain MgB 2 superconducting bulk;

[0014] (3) Put the obtained block in a vacuum furnace, under vacuum, heat treatment temperature is 650 ℃, keep warm for 0.5 hours, and finally obtain MgB 2 superconducting material.

example 2

[0016] Weigh the Mg powder and the B powder according to the molar ratio Mg: B=1: 2, the Mg powder purity is 99.99%, 0.5 micron, the B powder purity is 99.9999%, 1-2 micron, and the weighing quality is the Mg powder and the B powder The 30% magnesium stearate of total mass is dissolved in 50mL acetone, after the magnesium stearate acetone solution is mixed with Mg powder and B powder, ball milling 10 hours, then in a vacuum oven at 50 ℃ of temperature insulation drying 5 hours; put the obtained powder into the iron-copper composite tube, and after sealing, carry out swaging and drawing successively with a deformation rate of 5%, to obtain MgB 2 Superconducting wire; place the obtained wire in a vacuum furnace, under the protection of argon, heat treatment at a temperature of 950°C, and keep it warm for 2 hours to finally obtain MgB 2 superconducting material.

example 3

[0018] Weigh Mg powder and B powder according to the molar ratio Mg: B=1: 2, Mg powder purity is 99.8%, 44 microns, B powder purity is 92%, 1-2 microns, and weighing quality is Mg powder and B powder simultaneously 5% of the total mass of stearic acid was dissolved in 10mL of acetone, the stearic acid acetone solution was mixed with Mg powder and B powder, ball milled for 2 hours, and then dried in a vacuum oven at a temperature of 70°C for 2 hours; Put the obtained powder into a pure iron pipe, and after sealing, carry out swaging, drawing and rolling with a deformation rate of 5% in sequence to obtain MgB 2 Superconducting tape; put the obtained tape in a vacuum furnace, under the protection of argon, heat treatment temperature is 950 ℃, keep it warm for 1 hour, and finally get MgB 2 superconducting material. The critical current density of the obtained strip was 4.02×10 3 A / cm 2 (4.2K, 10T).

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a process for preparing MgB2 superconductive material, wherein according to mol ratio Mg:B=1:2, the invention weights Mg powder and B powder, and weights organic acid or organic acid salt at 5-30% weight of total Mg powder and B powder, to be dissolved in 5-50mL acetone or alcohol, mixes the solution with Mg powder and B powder, to be ball milled for 1-10h, to be dried ina vacuum drying box, tablets the powder, to obtain MgB2 superconductive block, or fills the powder into metal tube or metal composite tube, to be sealed and rotationally forged, drawn or rolled with 5% deformation ratio, to obtain MgB2 superconductive band, arranges the superconductive block or band into a vacuum furnace, under vacuum to argon gas protection and thermal treatment temperature as 650-950DEG C, to keep temperature for 0.5-2h, to obtain MgB2 superconductive material. The inventive MgB2 superconductive material can effectively overcome the oxidation and self-combustion problems ofhigh-energy ball milled refined magnesium powder, and the invention adds doping material to significantly improve the superconductivity of the MgB2 superconductive material.

Description

technical field [0001] The present invention relates to a kind of MgB 2 Methods for the preparation of superconducting materials. Background technique [0002] Since the discovery of a new type of superconductor magnesium diboride (MgB) with a superconducting transition temperature as high as 39K in 2001, 2 ) Since then, scientists from various countries have conducted a large number of in-depth studies. At present, in the preparation of high-performance MgB 2 Among the wire and strip methods, the in-situ (in-situ) powder tube (Powder-In-Tube) technology is the most convenient and practical one, but its critical current density (Jc) is still low. Studies have shown that the particle size of the original powder has an effect on the MgB 2 The critical current density of superconducting materials plays an important role. The sample prepared by the Japanese research group using submicron or nanoscale magnesium powder can reach a higher critical current density ([Yamada H.Hi...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): H01L39/12C01B35/04
Inventor 王栋樑马衍伟高召顺张现平禹争光王雷王军红
Owner INST OF ELECTRICAL ENG CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products