USRE32714E - Method of producing high performance permanent magnets - Google Patents
Method of producing high performance permanent magnets Download PDFInfo
- Publication number
- USRE32714E USRE32714E US06/854,125 US85412586A USRE32714E US RE32714 E USRE32714 E US RE32714E US 85412586 A US85412586 A US 85412586A US RE32714 E USRE32714 E US RE32714E
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- particles
- master alloy
- rare earth
- iaddend
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
- H01F1/047—Alloys characterised by their composition
- H01F1/053—Alloys characterised by their composition containing rare earth metals
- H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
- H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
- H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
- H01F1/0575—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together
- H01F1/0577—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together sintered
Definitions
- the present invention relates to permanent magnets and more particularly to a method of producing such magnets with high performance without the use of cobalt.
- Coercivity is the strength of an external field needed to demagnetize the permanent magnet and energy product is a composite of the strength of the magnet and its coercivity.
- magnets have been produced from the iron, boron and rare earth compound by conventional methods of producing magnets in which the ternary compound is melted and cast, the casting is crushed and milled to produce a powder of the desired small particle size, the particles of the powder are field oriented and compacted into the desired size and shape, the compacted powder is sintered at a temperature of at least 1000° C. for a sufficient time period--typically about one hour, and the sintered product is heat treated at about 630° C. for about one hour to enhance and in fact account for a large fraction of the magnetic characteristics of the product. While frequently producing acceptable magnets of the desired parameters, this method has numerous disadvantages and deficiencies.
- a more specific object of the present invention is to provide an inexpensive method of producing high performance permanent magnets using iron, boron and a rare earth which may be processed in air prior to sintering and which results in the production of a very low number of unacceptable magnets or rejects.
- the method of the present invention which includes the admixing of particles of a master alloy, consisting of Fe 2 B, with Fe powder and particles of a rare earth, such as neodymium or praseodymium.
- the admixture is then compacted into the desired size and shape and an intermetallic compound of the master alloy, Fe powder and rare earth is formed by sintering, under strictly controlled atmosphere, time and temperature which permits control of the particle size of the resultant magnet to provide a very small particle size and concomitant high magnetic parameters.
- the magnet formed by the sintering of the compacted admixture is heat treated to enhance the magnetic characteristics thereof.
- the method of the present invention includes the formation of particles of a master alloy which is stable and avoids the oxidation problems heretofore encountered in the production of sintered magnets using powders of the ternary compound itself.
- the master alloy we have chosen is Fe 2 B which is oxidation-resistant and can therefore be milled in air.
- the master alloy (Fe 2 B) powder is produced by melting of the master alloy and casting into ingots by conventional melting and casting techniques well-known to metallurgists.
- the cast ingots are then crushed by a jaw crusher to a particle size of about 1 mm and these particles are then milled by known milling techniques to a maximum particle size of 50 microns.
- the method of the present invention also uses elemental iron powder (Fe) which is commercially available and relatively inexpensive. Additionally, such iron powder is stable and may be stored and handled in air. Similarly, the rare earth is employed in elemental form as available powder or is freshly ground from ingots into particles large enough to preclude rapid oxidation in air.
- the particle size of the elemental rare earth used in the method of the present invention is not critical whereas in prior methods the particle size of the ternary compound is extremely critical.
- the rare earth may be any one of or a combination of the rare earths which react favorably with the iron and boron to produce a major phase of at least one intermetallic compound of the Fe-R-B type having a crystal structure of the substantially tetragonal system.
- Such rare earths include neodymium, praseodymium, gadolinium, samarium, cerium and possibly others.
- the master alloy powder is admixed with the Fe powder and rare earth particles (typically filings) to produce an admixture in which, for example, the iron (Fe) comprises about 75 to 82 atomic %, the boron comprises about 6 to 10 atomic % and the rare earth comprises about 12 to 16 atomic %.
- This admixture is then compacted into the desired size and shape under a pressure of about 50,000 to 100,000 psi.
- the green compacts composed of the compacted admixture of the master alloy powder, the Fe powder and the filings of the rare earth are then sintered in a vacuum of 10 -4 Torr or an argon atmosphere at a temperature within the range of about 700° C. to about 1000° C. for a time period within the approximate range of a fraction of an hour to 36 hours. Sintering at this temperature and time causes the compacted powders and particles to react to form a magnetic material which includes a major phase of at least one intermetallic compound of the Fe-R-B type having a crystal structure of the tetragonal system.
- Our experiments using neodymium as the rare earth component have shown that one such intermetallic compound formed is Fe 14 Nd 2 B. Additionally, we have discovered that sintering temperature and time within these ranges permit the particle size of the Fe 14 Nd 2 B crystallites to be controlled to produce the small particle size necessary to achieve high coercivity.
- the magnetic material produced by the sintering of the green compacts has substantial magnetic properties without subsequent heat treatment or annealing.
- heat treatment or annealing at a temperature of about 550° C. to about 650° C. for a sufficient time, such as about a fraction of 1 hour to about 2 hours will enhance these magnetic properties and produce a permanent magnet with high coercivity.
- Magnetic material has been produced by admixing sufficient amounts of master alloy particles, Fe powder and Neodymium particles to provide a composition (in atomic %) of 77 Fe, 15 Nd, 8B, compacting this admixture under a pressure of 100,000 psi without the use of a binder or die lubricant, and sintering in a vacuum of 10 -4 Torr for 4 hours at 800° C.
- the magnetic material was magnetized in a maximum field of 12 kOe and had H ci of 6 kOe. This material was then annealed for 1 hour at 600° C. and then had a H ci of 7.5 kOe.
- Magnetic material has also been produced by the above procedure except compaction was under pressure of 50,000 psi, sintering was conducted in a vacuum of 10 -4 Torr for 24 hours at 700° C. and annealing was performed for 2 hours at 600° C.
- This magnetic material had a coercivity (H ci ) .[.or.]. .Iadd.of .Iaddend.7 kOe.
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- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
Abstract
A method of producing .Iadd.permanent magnet material for .Iaddend.high performance permanent magnets is disclosed in which particles of a master alloy consisting of Fe2 B having a maximum particle size of 50 microns is admixed with Fe powder and particles of a rare earth capable of combining with Fe and B to form a tetragonal compound of Fe14 R2 B type. The admixture is compacted and a magnetic material is formed of the master alloy, Fe powder and .[.rate.]. .Iadd.rare .Iaddend.earth particles which includes a major phase of at least one intermetallic compound of the Fe-R-B type having a crystal structure of the substantially tetragonal system and while the particle size of the crystal structure is controlled by sintering the compacted admixture at a temperature of about 700° C. to 1000° C. for from a fraction of an hour to 36 hours. The magnetic material is then annealed at a temperature of about 550° C. to 650° C. for a fraction of an hour to 2 hours.
Description
The present invention relates to permanent magnets and more particularly to a method of producing such magnets with high performance without the use of cobalt.
There are a number of parameters that measure the performance of permanent magnets. The most important of these parameters are coercivity and energy product. Coercivity is the strength of an external field needed to demagnetize the permanent magnet and energy product is a composite of the strength of the magnet and its coercivity.
Until recently, permanent magnets formed of combinations of samarium and cobalt provided the highest parameters of coercivity and energy product. However, cobalt is a strategic material and the main source of cobalt in the United States is southern Africa, particularly Zaire, and political considerations frequently affect the availability and price of cobalt. Additionally, samarium--cobalt magnets are very expensive and their high price has limited their use for many applications.
Because of the foregoing there has been a search for an effective alternative to samarium--cobalt magnets which would provide high coercivity and energy product without the disadvantages of the samarium--cobalt magnets. Recently, such an effective substitute was proposed and this substitute utilizes a ternary compound of iron, boron and a light rare earth, such as neodymium.
Heretofore, magnets have been produced from the iron, boron and rare earth compound by conventional methods of producing magnets in which the ternary compound is melted and cast, the casting is crushed and milled to produce a powder of the desired small particle size, the particles of the powder are field oriented and compacted into the desired size and shape, the compacted powder is sintered at a temperature of at least 1000° C. for a sufficient time period--typically about one hour, and the sintered product is heat treated at about 630° C. for about one hour to enhance and in fact account for a large fraction of the magnetic characteristics of the product. While frequently producing acceptable magnets of the desired parameters, this method has numerous disadvantages and deficiencies.
Foremost among these disadvantages and deficiencies is the necessity that many of the steps of this method be carried out in an inert gas atmosphere, such as argon, because powders of the ternary compound are highly oxidative and cannot be processed in air. Additional disadvantages are non-reproducibility of the product, the complexity of the method, and powder handling problems caused by oxidation. Due to these many disadvantages and deficiencies, the prior method is expensive and results in a relatively high number of unacceptable magnets or rejects being produced.
With the foregoing in mind, it is an object of the present invention to provide a method of producing high performance permanent magnets from iron, boron and a rare earth which obviates the disadvantages and deficiencies of prior methods.
A more specific object of the present invention is to provide an inexpensive method of producing high performance permanent magnets using iron, boron and a rare earth which may be processed in air prior to sintering and which results in the production of a very low number of unacceptable magnets or rejects.
The foregoing objects are accomplished by the method of the present invention which includes the admixing of particles of a master alloy, consisting of Fe2 B, with Fe powder and particles of a rare earth, such as neodymium or praseodymium. The admixture is then compacted into the desired size and shape and an intermetallic compound of the master alloy, Fe powder and rare earth is formed by sintering, under strictly controlled atmosphere, time and temperature which permits control of the particle size of the resultant magnet to provide a very small particle size and concomitant high magnetic parameters. Finally, the magnet formed by the sintering of the compacted admixture is heat treated to enhance the magnetic characteristics thereof.
The method of the present invention includes the formation of particles of a master alloy which is stable and avoids the oxidation problems heretofore encountered in the production of sintered magnets using powders of the ternary compound itself. The master alloy we have chosen is Fe2 B which is oxidation-resistant and can therefore be milled in air.
The master alloy (Fe2 B) powder is produced by melting of the master alloy and casting into ingots by conventional melting and casting techniques well-known to metallurgists. The cast ingots are then crushed by a jaw crusher to a particle size of about 1 mm and these particles are then milled by known milling techniques to a maximum particle size of 50 microns.
The method of the present invention also uses elemental iron powder (Fe) which is commercially available and relatively inexpensive. Additionally, such iron powder is stable and may be stored and handled in air. Similarly, the rare earth is employed in elemental form as available powder or is freshly ground from ingots into particles large enough to preclude rapid oxidation in air. The particle size of the elemental rare earth used in the method of the present invention is not critical whereas in prior methods the particle size of the ternary compound is extremely critical.
The rare earth may be any one of or a combination of the rare earths which react favorably with the iron and boron to produce a major phase of at least one intermetallic compound of the Fe-R-B type having a crystal structure of the substantially tetragonal system. Such rare earths include neodymium, praseodymium, gadolinium, samarium, cerium and possibly others.
The master alloy powder is admixed with the Fe powder and rare earth particles (typically filings) to produce an admixture in which, for example, the iron (Fe) comprises about 75 to 82 atomic %, the boron comprises about 6 to 10 atomic % and the rare earth comprises about 12 to 16 atomic %. This admixture is then compacted into the desired size and shape under a pressure of about 50,000 to 100,000 psi.
The green compacts composed of the compacted admixture of the master alloy powder, the Fe powder and the filings of the rare earth are then sintered in a vacuum of 10-4 Torr or an argon atmosphere at a temperature within the range of about 700° C. to about 1000° C. for a time period within the approximate range of a fraction of an hour to 36 hours. Sintering at this temperature and time causes the compacted powders and particles to react to form a magnetic material which includes a major phase of at least one intermetallic compound of the Fe-R-B type having a crystal structure of the tetragonal system. Our experiments using neodymium as the rare earth component have shown that one such intermetallic compound formed is Fe14 Nd2 B. Additionally, we have discovered that sintering temperature and time within these ranges permit the particle size of the Fe14 Nd2 B crystallites to be controlled to produce the small particle size necessary to achieve high coercivity.
The magnetic material produced by the sintering of the green compacts has substantial magnetic properties without subsequent heat treatment or annealing. However, such heat treatment or annealing at a temperature of about 550° C. to about 650° C. for a sufficient time, such as about a fraction of 1 hour to about 2 hours will enhance these magnetic properties and produce a permanent magnet with high coercivity.
Magnetic material has been produced by admixing sufficient amounts of master alloy particles, Fe powder and Neodymium particles to provide a composition (in atomic %) of 77 Fe, 15 Nd, 8B, compacting this admixture under a pressure of 100,000 psi without the use of a binder or die lubricant, and sintering in a vacuum of 10-4 Torr for 4 hours at 800° C. The magnetic material was magnetized in a maximum field of 12 kOe and had Hci of 6 kOe. This material was then annealed for 1 hour at 600° C. and then had a Hci of 7.5 kOe.
Magnetic material has also been produced by the above procedure except compaction was under pressure of 50,000 psi, sintering was conducted in a vacuum of 10-4 Torr for 24 hours at 700° C. and annealing was performed for 2 hours at 600° C. This magnetic material had a coercivity (Hci) .[.or.]. .Iadd.of .Iaddend.7 kOe.
In the specification, there has been set forth a preferred embodiment of the invention, and although specific terms are employed, they are used in a generic and descriptive sense and not for purposes of limitation.
Claims (10)
1. A method of producing .Iadd.permanent magnet material for .Iaddend.high performance permanent magnets characterized by an absence of cobalt, said method comprising the steps of
(a) admixing particles of a master alloy consisting of Fe2 B with Fe powder and particles of a rare earth capable of combining with Fe and B to form a .[.tetraganol.]. .Iadd.tetragonal .Iaddend.compound of Fe14 R2 B,
(b) compacting the admixture into a predetermined size and shape, and
(c) forming a magnetic material of the Fe2 B, Fe powder and rare earth which includes a major phase of at least one intermetallic compound consisting of Fe-R-B and having a .[.tetragoval.]. .Iadd.tetragonal .Iaddend.crystal structure while controlling the particle size of the crystal structure and imparting magnetic characteristics thereto by sintering the compacted admixture at a temperature within the range of about 700° C. to about 1000° C. for a time period within the range of about a fraction of 1 hour to 36 hours .[.to produce a permanent magnet with high coercivity.]. .Iadd.to produce magnetic material with high coercivity.Iaddend..
2. A method according to claim 1 wherein the particles of master alloy are formed by melting and casting the master alloy, and crushing and milling the casting.
3. A method according to claim 1 including heat treating the magnetic material at a temperature of about 550° C. to 650° C. for a time sufficient to enhance the magnetic characteristics thereof.
4. A method according to claim 1 wherein the particles of the master alloy are of a size no larger than about 50 microns.
5. A method of producing .Iadd.permanent magnet material for .Iaddend.high performance permanent magnets characterized by an absence of cobalt, said method comprising the steps of
(a) forming milled particles of a master alloy consisting of Fe2 B by melting and casting the master alloy and crushing and milling the cast master alloy to a particle size no larger than about 50 microns,
(b) admixing the master alloy particles with Fe powder and particles of a rare earth capable of combining with the Fe and B to form a tetragonal compound of Fe14 R2 B,
(c) compacting the admixture into a predetermined size and shape,
(d) forming a magnetic material of the Fe2 B, Fe powder and rare earth which includes a major phase of at least one intermetallic compound consisting of Fe-R-B and having a .[.tetrogonal.]. .Iadd.tetragonal .Iaddend.crystal structure while controlling the particle size of the crystal structure and imparting magnetic characteristics thereto by sintering the compacted admixture at a temperature within the range of about 700° C. to about 1000° C. for a time period within the range of about a fraction of 1 hour to 36 hours .[.to produce a permanent magnet with high coercivity.]. .Iadd.to produce magnetic material with high coercivity.Iaddend., and
(e) heat treating the magnetic material at a temperature of about 550° to 650° C. for about a fraction of an hour to two hours to enhance the magnetic characteristics thereof.
6. A method according to claim 5 wherein the rare earth comprises neodynium.
7. A method according to claim 6 wherein the compacted admixture is sintered at a temperature within the range of about 800° C. to about 900° C. for a time period within the range of about 0.25 hours to 10/hours.
8. A method according to claim 5 wherein the admixture is compacted under a pressure of about 75,000 psi.
9. A method according to claim 5 wherein the rare earth comprises praseodymium.
10. A method according to claim 5 wherein the rare earth comprises a mixture of neodymium and praseodymium.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/854,125 USRE32714E (en) | 1984-09-25 | 1986-04-21 | Method of producing high performance permanent magnets |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/654,655 US4541877A (en) | 1984-09-25 | 1984-09-25 | Method of producing high performance permanent magnets |
| US06/854,125 USRE32714E (en) | 1984-09-25 | 1986-04-21 | Method of producing high performance permanent magnets |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/654,655 Reissue US4541877A (en) | 1984-09-25 | 1984-09-25 | Method of producing high performance permanent magnets |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE32714E true USRE32714E (en) | 1988-07-19 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/854,125 Expired - Fee Related USRE32714E (en) | 1984-09-25 | 1986-04-21 | Method of producing high performance permanent magnets |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE32714E (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115010479A (en) * | 2022-06-23 | 2022-09-06 | 横店集团东磁股份有限公司 | Non-shrinkage nickel-copper-zinc ferrite material and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3821035A (en) * | 1972-05-01 | 1974-06-28 | Gen Electric | Sintered cobalt-neodymium-samarium intermetallic product and permanent magnets produced therefrom |
| US4152178A (en) * | 1978-01-24 | 1979-05-01 | The United States Of America As Represented By The United States Department Of Energy | Sintered rare earth-iron Laves phase magnetostrictive alloy product and preparation thereof |
| JPS54136520A (en) * | 1978-04-17 | 1979-10-23 | Seiko Instr & Electronics Ltd | Permanent magnet |
| US4211585A (en) * | 1976-03-10 | 1980-07-08 | Tokyo Shibaura Electric Co., Ltd. | Samarium-cobalt-copper-iron-titanium permanent magnets |
| EP0101552B1 (en) * | 1982-08-21 | 1989-08-09 | Sumitomo Special Metals Co., Ltd. | Magnetic materials, permanent magnets and methods of making those |
-
1986
- 1986-04-21 US US06/854,125 patent/USRE32714E/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3821035A (en) * | 1972-05-01 | 1974-06-28 | Gen Electric | Sintered cobalt-neodymium-samarium intermetallic product and permanent magnets produced therefrom |
| US4211585A (en) * | 1976-03-10 | 1980-07-08 | Tokyo Shibaura Electric Co., Ltd. | Samarium-cobalt-copper-iron-titanium permanent magnets |
| US4152178A (en) * | 1978-01-24 | 1979-05-01 | The United States Of America As Represented By The United States Department Of Energy | Sintered rare earth-iron Laves phase magnetostrictive alloy product and preparation thereof |
| JPS54136520A (en) * | 1978-04-17 | 1979-10-23 | Seiko Instr & Electronics Ltd | Permanent magnet |
| EP0101552B1 (en) * | 1982-08-21 | 1989-08-09 | Sumitomo Special Metals Co., Ltd. | Magnetic materials, permanent magnets and methods of making those |
Non-Patent Citations (2)
| Title |
|---|
| Chabin et al., (Nd, Sm, Gd) Fe B Ternary Systems, Dopov. Akad. Nauk, URSR, Ser. A:Fiz Mat. Tekh. Nauki, 1979(10), pp. 873 876. * |
| Chabin et al., (Nd, Sm, Gd)-Fe-B Ternary Systems, Dopov. Akad. Nauk, URSR, Ser. A:Fiz-Mat. Tekh. Nauki, 1979(10), pp. 873-876. |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115010479A (en) * | 2022-06-23 | 2022-09-06 | 横店集团东磁股份有限公司 | Non-shrinkage nickel-copper-zinc ferrite material and preparation method thereof |
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