US2864734A - Magnetic flake core and method of - Google Patents
Magnetic flake core and method of Download PDFInfo
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- US2864734A US2864734A US2864734DA US2864734A US 2864734 A US2864734 A US 2864734A US 2864734D A US2864734D A US 2864734DA US 2864734 A US2864734 A US 2864734A
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- Prior art keywords
- flakes
- core
- cores
- magnetic
- alfenol
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 142
- 229910052742 iron Inorganic materials 0.000 claims description 68
- 229910045601 alloy Inorganic materials 0.000 claims description 60
- 239000000956 alloy Substances 0.000 claims description 60
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 54
- 229910052782 aluminium Inorganic materials 0.000 claims description 52
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 claims description 42
- 238000010438 heat treatment Methods 0.000 claims description 26
- 239000011162 core material Substances 0.000 description 152
- BLXVTZPGEOGTGG-UHFFFAOYSA-N 2-[2-(4-nonylphenoxy)ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCO)C=C1 BLXVTZPGEOGTGG-UHFFFAOYSA-N 0.000 description 50
- 229910001017 Alperm Inorganic materials 0.000 description 50
- 239000000843 powder Substances 0.000 description 34
- 230000035699 permeability Effects 0.000 description 32
- 238000004519 manufacturing process Methods 0.000 description 28
- 239000011248 coating agent Substances 0.000 description 22
- 238000000576 coating method Methods 0.000 description 22
- 239000002245 particle Substances 0.000 description 22
- 239000000463 material Substances 0.000 description 20
- 229910000889 permalloy Inorganic materials 0.000 description 20
- 238000005096 rolling process Methods 0.000 description 20
- 239000000696 magnetic material Substances 0.000 description 18
- 239000011230 binding agent Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- PNEYBMLMFCGWSK-UHFFFAOYSA-N al2o3 Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 229910052718 tin Inorganic materials 0.000 description 12
- ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 12
- 229910000831 Steel Inorganic materials 0.000 description 10
- 239000010959 steel Substances 0.000 description 10
- 230000004907 flux Effects 0.000 description 8
- 238000009413 insulation Methods 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 8
- 229910052725 zinc Inorganic materials 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000002349 favourable Effects 0.000 description 6
- 238000004804 winding Methods 0.000 description 6
- 229910001268 Ferrocerium Inorganic materials 0.000 description 4
- 229910001200 Ferrotitanium Inorganic materials 0.000 description 4
- GNTDGMZSJNCJKK-UHFFFAOYSA-N Vanadium(V) oxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 238000005056 compaction Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 4
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 239000011733 molybdenum Substances 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 230000001681 protective Effects 0.000 description 4
- 230000000171 quenching Effects 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- 229910000760 Hardened steel Inorganic materials 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N Sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 238000000498 ball milling Methods 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000003247 decreasing Effects 0.000 description 2
- 230000005347 demagnetization Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- -1 ferrous alloy Chemical class 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000004482 other powder Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000012256 powdered iron Substances 0.000 description 2
- 239000012254 powdered material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002035 prolonged Effects 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F41/00—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
- H01F41/02—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
- H01F41/0206—Manufacturing of magnetic cores by mechanical means
- H01F41/0246—Manufacturing of magnetic circuits by moulding or by pressing powder
-
- 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
- H01F1/12—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 soft-magnetic materials
- H01F1/14—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 soft-magnetic materials metals or alloys
- H01F1/20—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder
- H01F1/22—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together
- H01F1/24—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together the particles being insulated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/16—Metallic particles coated with a non-metal
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/04—Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
-
- 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
- H01F1/12—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 soft-magnetic materials
- H01F1/33—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 soft-magnetic materials mixtures of metallic and non-metallic particles; metallic particles having oxide skin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C2202/00—Physical properties
- C22C2202/02—Magnetic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S75/00—Specialized metallurgical processes, compositions for use therein, consolidated metal powder compositions, and loose metal particulate mixtures
- Y10S75/954—Producing flakes or crystals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
Definitions
- This invention relates to magnetic cores used with inductance coils, electronic filter networks, resonant circuits, transformers and the like.
- the invention relates to a new magnetic core material and to a method of producing said material and cores from said material.
- Prior art magnetic cores have usually been manufactured from Molybdenum-Permalloy either in the form of thin solid material rolled or stacked to produce the desired shape or from the powdered material compacted into the desired shape with an insulation binder.
- the Mo-Permallo-y cores made from the thin solid materials while giving a high value for permeability also give high power losses.
- the cores made from powdered Mo- Permalloy while giving low power losses also give a low permeability.
- the Mo-Permallo-y cores are prepared from a Permalloy containing about 2% molybdenum, 81% nickel and the remainder iron. The manufacture of these 2-81 Mo-Permalloy cores, therefore, results in the use for this purpose yearly of a considerable tonnage of s "ategically important, scarce and expensive nickel and molybdenum.
- 2-81 Mo- Permalloy powder cores are sensitive to high humidity and require a protective coating to provide humidity stability. They also require the addition of a component to provide temperature stability.
- the 12-81 lvio- Permalloy powder cores also require heat treatment in a protective atmosphere. All of the above result in processing complications with attendant increases in costs and in safety hazards.
- an object of the present invention to provide a new and useful magnetic material for use in the manufacture of magnetic cores having high permeability and low power lossses.
- Another object is to provide a magnetic core material utilizing only non-strategic materials.
- a further object is to provide a magnetic core hav- Patented Dec. 16, 1958 ing high permeability and low power losses which contains only non-strategic materials.
- a still further object is to provide magnetic cores which are magnetically stable under varying environmental conditions.
- Another object is to provide a method of manufacturing a new magnetic core material which is simple and inexpensive.
- Still another object is to provide a method of manufacturing new and useful magnetic cores which method is simple, inexpensive and safe.
- powder of the extremely hard and brittle high aluminum content iron base alloys are converted to the flake form, subjected to heat treatment to provide an insulating coating on the particles, compacted to form a core of the desired configuration, and the core heat treated to obtain the desired magnetic properties.
- Alfenol type alloys i. e. iron base alloys having from 10 to 17 percent aluminum content
- iron base alloys having from 10 to 17 percent aluminum content
- Alfenol type alloys containing from 10 to 17 percent aluminum may be employed as desired.
- the chill cast ingots may be ground, however, by placing the ingot between two mild steel sheets and cold rolling them to lumps approximately /2 to 1 inch in size.
- the coarse powder may then be pulverized by prolonged ball milling in a steel mill using hardened steel balls.
- the particle size should be minus 30 plus 60 mesh although particles of any desired size may be used.
- the particles of Alfenol may be flaked by rolling the hot powder between the rolls of a six inch diameter standard Z-high laboratory rolling mill at a temperature below the melting point of the alloy.
- the powder is preheated preferably to a temperature between 400-500 C and vibrated into the rolls which have been preheate to approximately C., thereby resulting in a rolling operation carried out at about 200 C. which tempera- ,ture has been found to produce the best vresults.
- the flaked Alfenol particles are then sieved to obtain flakes of the preferred size minus 30 plus 60 mesh. If the flake thickness is too large they may be rerolled to obtain a high core permeability. It has been found that the best results were obtained on the Alfenol flakes when the ratio of average particle diameter to the average particle thickness is at least twenty to one.
- Alfenol flakes develop a self insulating coating of chiefly aluminum oxide when heated in air.
- the temperature and time requirement for developing this insulation depends on the alloy composition and the previous history of the flakes.
- the heat treatment is preferably carried out at a temperature between 400 C. to 900 C. for a period of from minutes to four hours in air atjatrnospberic pressure. The higher the temperature the less the tin e interval required.
- the heat treatment recommended for 16-Alfenol is one-half hour at 500 C. in air. 13.92 Alfenol requires three hours at 500 C. or one-half hour at 700 C. to establish the insulating oxide coating.
- the flakes may be cooled to room temperature to facilitate handling if desired but further processing may also be carried out on the hot particles if desired.
- insulating material may be added to the flaked Alfenol to further reduce the power losses with a consequent loss in permeability if it is so desired.
- Up to 3% by Weight of sodium silicate may be added for this purpose or sufficient hydrolyzed tetra-ethylsilicate inv ethyl alcohol suflicient to leave a coating of silicon dioxide of up to 3% by weight of the flakes may be used as. insulation.
- powdered tin, aluminum, zinc or lead may be added to the flaked Alfenol up to 3% by weight of the total mass.
- powdered tin, aluminum, zinc or lead may be added to the flaked Alfenol up to 3% by weight of the total mass.
- 1% by weight of atomized tin or aluminum powder it has been found preferable to add 1% by weight of atomized tin or aluminum powder and thoroughly blend the dry mixture before compacting.
- the larger mesh size flakes require a material with more bonding power and better insulating qualities.
- 1% by weight of vanadium pentoxide may be added to the flakes in a water slurry.
- the combination of flake and oxide is thoroughly mixed while wet and the water evaporated by heating the mixture. With this oxide binder a core made from minus 18 plus mesh flake possessed good strength after heat treatment. 7
- the flakes Before compacting it is necessary that the flakes be arranged in the die so that their shortest axis is perpendicular to the flux direction. This provides the most favorable magnetic path and the highest resistance to eddy currents. This may be accomplished by allowing the flakes to fall freely into a feed funnel that is revolving at a constant rate.
- the molding pressure preferably from 80125 tons per sq. in., is applied at right angles to the plane of the flakes. Hardened three section dies are required to withstand the high pressures and for ease of ejection of the pressed core. 7
- the cores are heat treated to develop the best magnetic properties.
- the core is heated to a temperature between 400-800 C. and then cooled rapidly to disorder the magnetic material so as to improve the permeability.
- the core may be water quenched or cooled slowly.
- cores having vanadium pentoxide for a binder it is necessary to heat the cores to 675 C. to melt the oxide and then cool them to 575 C. before quenching.
- the basic magnetic properties of cores formed in accordance with the invention may be measured by means of a single layer winding upon a toroidal specimen of the material.
- the permeability and total losses can be determined from R. F. bridge measurements of the current, inductance and resistance of the toroidal winding.
- the permeability ,u of the core is:
- L is the inductance of the coil in henrys
- N is the number of turns in the test winding
- A is the cross section of the core in square centimeters
- Dm is the mean diameter of the toroid in centimeters.
- the flux density B (in gauss) in the core is given by:
- Alfenol flake toroidal cores were prepared in accordance with the invention and compared with 2-81 Mo- Permalloy and Alfenol powder cores.
- the cores were of a commercially standard size, viz., O. D. 1.060", I. D. 0.580 and about 0.25 thick.
- Table I lists the magnetic properties of typical Alfenol flake, Alfenol powder and 2-81 Mo-Permallo-y powder COIBS.
- the Alfenol flake cores are, therefore, a higher permeability than magnetic powder cores. They have lower losses than magnetic tape or laminated cores. Only non-critical and inexpensive components are needed in making the alloys. No addition agents are required indicates the to provide insulation. In addition the process of manufacture of the material and the cores from said material requires no protective atmosphere thus resulting in a manufacturing process which is sim le and less costly and hazardous than that required for the manufacture of comparative magnetic cores.
- the flake Alfenol cores are, therefore, high density, high permeability cores suitable as non-strategic alternates for Mo-Permalloy cores for low frequency applications.
- a magnetic material for use in the manufacture of magnetic cores and the like comprising flakes of a ferrous alloy containing frpm to 17 percent aluminum.
- balance being essentially iron.
- a magnetic core comprising flakes of an iron base alloy containing from 10 to 17 percent aluminum the balance being essentially iron and wherein the flakes are provided with an insulating coating of aluminum oxide.
- a magnetic core comprising compacted flakes of an iron base alloy containing from 10 to 17 percent aluminum the balance of the flakes being essentially iron, wherein the flakes are provided with an insulating coating of aluminum oxide and a binder selected from the group consisting of tin, lead, zinc and aluminum is disposed between the flakes.
- the method of preparing a magnetic material for use in the manufacture of magnetic cores and the like comprising forming flakes of an iron base alloy containing from 10 to 17 percent aluminum, a small amount of embrittling agent selected from the group consisting of ferrocerium and ferrotitanium, and the balance essentially iron, by rolling a powder of the alloy at about 200 C.
- the method of preparing a magnetic material for use in the manufacture of magnetic cores and the like comprising rolling a powder of an iron base alloy containing from 10 to 17 percent aluminum the balance being essentially iron at a temperature of about 200 C. to form flakes of said alloy and heating said flakes in air for a period of from minutes to four hours at a temperature between 400 to 900 C.
- the method of preparing a magnetic core comprising forming flakes by rolling at about 200 C. an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron, heat treating the flakes of the alloy at a temperature between 400 C. and 900 C. for a period of from 15 minutes to 4 hours to form an insulating coating of aluminum oxide on the flakes, adding up to 3% by weight of a metal binder selected from the group consisting of lead, zinc, tin, and aluminum, compacting the flakes into the desired core configuration, and heat treating the compacted flake core at a temperature from 400 C. to 800 C.
- the method of preparing a magnetic core comprising forming flakes of an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron by rolling a powder of said alloy at about 200 C., heat treating the flakes at a temperature from 400 C. to 900 C. for a period of from 15 minutes to 4 hours, mixing with the flakes a small amount of metal binder selected from the group consisting of tin, zinc, lead and aluminum, compacting said flakes into the desired core configuration, andheat treating the compacted flake core at a temperature from 400 C. to 800 C.
- the method of preparing a magnetic core comprising forming flakes of an iron base alloy containing 10 to 17 percent aluminum and the balance essentially iron by rolling a powder of said alloy at about 200 C., heating said flakes to a temperature between 400 to 900 C. for a period of from 15 minutes to 4 hours, compacting said flakes into the desired core configuration, and heat treating the compacted flake core at a temperature of from 400 C. to 800 C.
- the method of preparing a magnetic core comprising compacting flakes of an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron and provided with a dense insulating coating of aluminum oxide into the desired core configuration, heating said compacted flake core to a temperature between 400 to 800 C. and rapidly cooling said core.
- the method of preparing a magnetic core cornprising forming flakes of an iron base alloy containing approximately 16 percent aluminum and the balance essentially iron, by rolling a powder of said alloy at about 200 C., heating said flakes to approximately 500 C. for one-half hour, compacting said flakes into the desired core configuration, heating said compacted flake core to approximately 625 C. and water quenching said core.
Description
MAGNETIC FLAKE CORE AND METHOD OF PREPARATION Edmond Adams and Albert M. Syeles, Silver Spring, and William M. Hubbard, Hyattsville, Md., assignors to the United States of America as represented by the Secretary of the Navy No Drawing. Application May 20, 1957 Serial No. 660,431
15 Claims. (Cl. 148-104) (Granted under Title 35, U. 5. Code (1952), see. 266) The invention described herein may be manufactured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties thereon or therefor.
This invention relates to magnetic cores used with inductance coils, electronic filter networks, resonant circuits, transformers and the like.
More specifically the invention relates to a new magnetic core material and to a method of producing said material and cores from said material.
Prior art magnetic cores have usually been manufactured from Molybdenum-Permalloy either in the form of thin solid material rolled or stacked to produce the desired shape or from the powdered material compacted into the desired shape with an insulation binder. The Mo-Permallo-y cores made from the thin solid materials while giving a high value for permeability also give high power losses. The cores made from powdered Mo- Permalloy while giving low power losses also give a low permeability. in addition the Mo-Permallo-y cores are prepared from a Permalloy containing about 2% molybdenum, 81% nickel and the remainder iron. The manufacture of these 2-81 Mo-Permalloy cores, therefore, results in the use for this purpose yearly of a considerable tonnage of s "ategically important, scarce and expensive nickel and molybdenum.
in addition to the above disadvantages, 2-81 Mo- Permalloy powder cores are sensitive to high humidity and require a protective coating to provide humidity stability. They also require the addition of a component to provide temperature stability. The 12-81 lvio- Permalloy powder cores also require heat treatment in a protective atmosphere. All of the above result in processing complications with attendant increases in costs and in safety hazards.
Attempts to find a suitable alternate or substitute for the 2-81 Mo-Permalloy cores have been heretofore unsuccessful. The general requirements for a powdered core are quite severe and diflicult to meet all respects. The core permeability should be reasonably high and stable with respect to changes in frequency, induced flux density, temperature, humidity, time and accidental direct current overloads. Total core losses (eddy current, hysteresis and residual) should be as low as possible. Besides these electrical requirements, the core must be sufficiently strong to withstand handling and shock in manufacture and use. In addition, the core manufacturing process must be economical i. e. the material must be fairly easy to grind, insulate, compact and heat treat.
It is, therefore, an object of the present invention to provide a new and useful magnetic material for use in the manufacture of magnetic cores having high permeability and low power lossses.
Another object is to provide a magnetic core material utilizing only non-strategic materials.
,A further object is to provide a magnetic core hav- Patented Dec. 16, 1958 ing high permeability and low power losses which contains only non-strategic materials.
A still further object is to provide magnetic cores which are magnetically stable under varying environmental conditions.
Another object is to provide a method of manufacturing a new magnetic core material which is simple and inexpensive.
Still another object is to provide a method of manufacturing new and useful magnetic cores which method is simple, inexpensive and safe.
Other objects and the attendant advantages of the invention will become apparent to those skilled in the art as the invention is disclosed in the following detailed description.
The above mentioned objects are achieved in accordance with the invention by the production of magnetic core by the compaction of flakes of finely divided high aluminum content iron base alloys.
It has been known for some time that when iron particles are converted into the form of flakes, i. e. shaped particles whose length and width are greater than their thickness, and the flaked iron particles layered uniformly in a die cavity so that they can be compressed while taining a high inter-laminary resistance than the permeability of'the powdered iron core could be improved and the eddy current losses lowered. The permeability is believed to be improved by the more favorable penetration of the flux at various levels of the applied field. The eddy current losses are believed to be lowered by the presence of a greater number of air gaps perpendicular to the plane of the pressed flake laminates. Because of their high electrical losses, however, flake iron cores have not proved satisfactory for most purposes when compared with other powder cores. Other iron base alloys such as Alfenol having good magnetic properties were considered impossible to roll because of their inherent qualities of hardness, brittleness and lack of ductility.
In accordance with the present invention, powder of the extremely hard and brittle high aluminum content iron base alloys are converted to the flake form, subjected to heat treatment to provide an insulating coating on the particles, compacted to form a core of the desired configuration, and the core heat treated to obtain the desired magnetic properties.
Alfenol type alloys, i. e. iron base alloys having from 10 to 17 percent aluminum content, may be prepared by melting electrolytic iron under a vacuum of about 250 microns and subsequently adding ferroaluminum alloy or aluminum to the molten iron. Small amounts of ferrocerium or ferrotitanium may be added to the melt to embrittle the Alfenol for easier grinding. Alfenol type alloys containing from 10 to 17 percent aluminum may be employed as desired.
High aluminum content Alfenol slabs without embrittling agents are extremely difficult to grind. The chill cast ingots may be ground, however, by placing the ingot between two mild steel sheets and cold rolling them to lumps approximately /2 to 1 inch in size. The coarse powder may then be pulverized by prolonged ball milling in a steel mill using hardened steel balls. Preferably the particle size should be minus 30 plus 60 mesh although particles of any desired size may be used.
The particles of Alfenol may be flaked by rolling the hot powder between the rolls of a six inch diameter standard Z-high laboratory rolling mill at a temperature below the melting point of the alloy. The powder is preheated preferably to a temperature between 400-500 C and vibrated into the rolls which have been preheate to approximately C., thereby resulting in a rolling operation carried out at about 200 C. which tempera- ,ture has been found to produce the best vresults.
The flaked Alfenol particles are then sieved to obtain flakes of the preferred size minus 30 plus 60 mesh. If the flake thickness is too large they may be rerolled to obtain a high core permeability. It has been found that the best results were obtained on the Alfenol flakes when the ratio of average particle diameter to the average particle thickness is at least twenty to one.
Because of the high aluminum content Alfenol flakes develop a self insulating coating of chiefly aluminum oxide when heated in air. The temperature and time requirement for developing this insulation depends on the alloy composition and the previous history of the flakes. The heat treatment is preferably carried out at a temperature between 400 C. to 900 C. for a period of from minutes to four hours in air atjatrnospberic pressure. The higher the temperature the less the tin e interval required. The heat treatment recommended for 16-Alfenol is one-half hour at 500 C. in air. 13.92 Alfenol requires three hours at 500 C. or one-half hour at 700 C. to establish the insulating oxide coating. At the end of the heat cycle the flakes may be cooled to room temperature to facilitate handling if desired but further processing may also be carried out on the hot particles if desired.
At this point insulating material may be added to the flaked Alfenol to further reduce the power losses with a consequent loss in permeability if it is so desired. Up to 3% by Weight of sodium silicate may be added for this purpose or sufficient hydrolyzed tetra-ethylsilicate inv ethyl alcohol suflicient to leave a coating of silicon dioxide of up to 3% by weight of the flakes may be used as. insulation.
in order to increase the density of the compact and thereby to increase the permeability thereof, and to act as a binder, powdered tin, aluminum, zinc or lead may be added to the flaked Alfenol up to 3% by weight of the total mass. For the smaller mesh size flakes it has been found preferable to add 1% by weight of atomized tin or aluminum powder and thoroughly blend the dry mixture before compacting. The larger mesh size flakes require a material with more bonding power and better insulating qualities. For this purpose 1% by weight of vanadium pentoxide may be added to the flakes in a water slurry. The combination of flake and oxide is thoroughly mixed while wet and the water evaporated by heating the mixture. With this oxide binder a core made from minus 18 plus mesh flake possessed good strength after heat treatment. 7
Before compacting it is necessary that the flakes be arranged in the die so that their shortest axis is perpendicular to the flux direction. This provides the most favorable magnetic path and the highest resistance to eddy currents. This may be accomplished by allowing the flakes to fall freely into a feed funnel that is revolving at a constant rate.
The molding pressure, preferably from 80125 tons per sq. in., is applied at right angles to the plane of the flakes. Hardened three section dies are required to withstand the high pressures and for ease of ejection of the pressed core. 7
After compaction the cores are heat treated to develop the best magnetic properties. The core is heated to a temperature between 400-800 C. and then cooled rapidly to disorder the magnetic material so as to improve the permeability. v
For le -Alfenol the best heat treatment has been found to be /2 hour at 625 C. followed by a water quench. For 13.92-A1feno1 the most favorable was found to be a Water quench from 575 C. The method of cooling depends on the composition of the alloys and the properties desired in the core. Where the aluminum content is over 12 percent the core should be Water quenched.
For aluminum contents less than 12% the core may be water quenched or cooled slowly. In the case of cores having vanadium pentoxide for a binder it is necessary to heat the cores to 675 C. to melt the oxide and then cool them to 575 C. before quenching.
The basic magnetic properties of cores formed in accordance with the invention may be measured by means of a single layer winding upon a toroidal specimen of the material. The permeability and total losses (eddy current, hysteresis and residual) can be determined from R. F. bridge measurements of the current, inductance and resistance of the toroidal winding. The permeability ,u of the core is:
where L is the inductance of the coil in henrys, N is the number of turns in the test winding, A is the cross section of the core in square centimeters and Dm is the mean diameter of the toroid in centimeters. The flux density B (in gauss) in the core is given by:
LI(1. .114 10 NA where I is the bridge current in ampere R. M. S. The
remainder or residual loss. Since rea H f Q the value of should be very low for a good core material.
Alfenol flake toroidal cores were prepared in accordance with the invention and compared with 2-81 Mo- Permalloy and Alfenol powder cores. The cores were of a commercially standard size, viz., O. D. 1.060", I. D. 0.580 and about 0.25 thick.
Table I lists the magnetic properties of typical Alfenol flake, Alfenol powder and 2-81 Mo-Permallo-y powder COIBS.
Table I Material Binder RI/J1 a 10 e 10 0x10 16 Alfenol Powder None 107 1, 162 16 14 37 7 120 +200 mesh. 16 Alfenol Flake 1% A1. 169 1, 598
-30+60 mesh. 13.92 Alfenol Powder None. 1, G37 1 -+200 mesh. 13.92 Alfenol Flake 1% Sun... 240 958 13 It 460 30+60 mesh. 13.92 Alfenol Flake 1% Sn 343 2,103 30 -18 1-30 mesh. 13.92 Alfenol Flake 1% 17205.. 308 1, 577 11 1 1 S56 18 +30 mesh. Mo-Permalloy -120 Ceramic" 537 1. 6 19 30 mesh.
From the foregoing it may be seen that because of the decreased number of air gaps and the improved demagnetization factor the permeability of the Alfenol cores is greatly increased by flaking.
The Alfenol flake cores, ma ufactured in accordance with the process of this invention have, therefore, a higher permeability than magnetic powder cores. They have lower losses than magnetic tape or laminated cores. Only non-critical and inexpensive components are needed in making the alloys. No addition agents are required indicates the to provide insulation. In addition the process of manufacture of the material and the cores from said material requires no protective atmosphere thus resulting in a manufacturing process which is sim le and less costly and hazardous than that required for the manufacture of comparative magnetic cores. The flake Alfenol cores are, therefore, high density, high permeability cores suitable as non-strategic alternates for Mo-Permalloy cores for low frequency applications.
It is to be understood that the invention may be prac ticed otherwise than as specifically described within the scope of the following claims.
We claim:
1. A magnetic material for use in the manufacture of magnetic cores and the like comprising flakes of a ferrous alloy containing frpm to 17 percent aluminum. the
balance being essentially iron.
2. The magnetic material of claim 1 in which the flakes are provided with an insulating coating.
3. The magnetic material of claim 2 in which the insulating coating is metallic oxide.
4. The magnetic material of claim 3 in which the metallic oxide coating is substantially aluminum oxide.
5. A magnetic core comprising flakes of an iron base alloy containing from 10 to 17 percent aluminum the balance being essentially iron and wherein the flakes are provided with an insulating coating of aluminum oxide.
6. A magnetic core comprising compacted flakes of an iron base alloy containing from 10 to 17 percent aluminum the balance of the flakes being essentially iron, wherein the flakes are provided with an insulating coating of aluminum oxide and a binder selected from the group consisting of tin, lead, zinc and aluminum is disposed between the flakes.
7. The method of preparing a magnetic material for use in the manufacture of magnetic cores and the like comprising forming flakes of an iron base alloy containing from 10 to 17 percent aluminum, a small amount of embrittling agent selected from the group consisting of ferrocerium and ferrotitanium, and the balance essentially iron, by rolling a powder of the alloy at about 200 C.
8. The method of preparing a magnetic material for use in the manufacture of magnetic cores and the like comprising rolling a powder of an iron base alloy containing from 10 to 17 percent aluminum the balance being essentially iron at a temperature of about 200 C. to form flakes of said alloy.
9. The method of preparing a magnetic material for use in the manufacture of magnetic cores and the like comprising rolling a powder of an iron base alloy containing from 10 to 17 percent aluminum the balance being essentially iron at a temperature of about 200 C. to form flakes of said alloy and heating said flakes in air for a period of from minutes to four hours at a temperature between 400 to 900 C.
10. The method of preparing a magnetic core comprising forming flakes by rolling at about 200 C. an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron, heat treating the flakes of the alloy at a temperature between 400 C. and 900 C. for a period of from 15 minutes to 4 hours to form an insulating coating of aluminum oxide on the flakes, adding up to 3% by weight of a metal binder selected from the group consisting of lead, zinc, tin, and aluminum, compacting the flakes into the desired core configuration, and heat treating the compacted flake core at a temperature from 400 C. to 800 C.
11. The method of preparing a magnetic core comprising forming flakes of an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron by rolling a powder of said alloy at about 200 C., heat treating the flakes at a temperature from 400 C. to 900 C. for a period of from 15 minutes to 4 hours, mixing with the flakes a small amount of metal binder selected from the group consisting of tin, zinc, lead and aluminum, compacting said flakes into the desired core configuration, andheat treating the compacted flake core at a temperature from 400 C. to 800 C.
12. The method of preparing a magnetic core comprising forming flakes of an iron base alloy containing 10 to 17 percent aluminum and the balance essentially iron by rolling a powder of said alloy at about 200 C., heating said flakes to a temperature between 400 to 900 C. for a period of from 15 minutes to 4 hours, compacting said flakes into the desired core configuration, and heat treating the compacted flake core at a temperature of from 400 C. to 800 C.
13. The method of claim 12 wherein the compacted flake core is cooled rapidly after heat treating.
14. The method of preparing a magnetic core comprising compacting flakes of an iron base alloy containing 10 to 17 percent aluminum the balance essentially iron and provided with a dense insulating coating of aluminum oxide into the desired core configuration, heating said compacted flake core to a temperature between 400 to 800 C. and rapidly cooling said core.
15. The method of preparing a magnetic core cornprising forming flakes of an iron base alloy containing approximately 16 percent aluminum and the balance essentially iron, by rolling a powder of said alloy at about 200 C., heating said flakes to approximately 500 C. for one-half hour, compacting said flakes into the desired core configuration, heating said compacted flake core to approximately 625 C. and water quenching said core.
References Cited in the file of this patent UNITED STATES PATENTS 1,381,460 Harris June 14, 1921 2,300,336 Bozorth Oct. 27, 1942 FOREIGN PATENTS 625,627 Great Britain June 30, 1949 OTHER REFERENCES Sykes et al.: Journal of the Iron and Steel Institute, 1935, No. 1, pages 225-247. Published by the Iron and Steel Institute, London, England.
The Making, Shaping and Treating of Steel, 6th ed., 1951, pages 580-588 and 654. Published by the U. S. Steel Co., Pittsburgh, Pa.
Case et al.: Aluminum in Iron and Steel, 1953, pages 297-300. Published by John Wiley & Sons, Inc., New York, N. Y. l
Claims (1)
12. THE METHOD OF PREPARING A MAGNETIC CORE COMPRISING FORMING FLAKES OF AN IRON BASE ALLOY CONTAINING 10 TO 17 PERCENT ALUMINUM AND THE BALANCE ESSENTIALLY IRON BY ROLLING A POWDER OF SAID ALLOY AT ABOUT 200*C., HEATING SAID FLAKES TO A TEMPERATURE BETWEEN 400* TOO 900*C. FOR A PERIOD OF FROM 15 MINUTES TO 4 HOURS, COMPACTING SAID FLAKES INTO THE DESIRED CORE CONFIGURATION, AND HEAT TREATING THE COMPACTED FLAKE CORE AT A TEMPERATURE OF FROM 400*C. TO 800*C.
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Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
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US2992474A (en) * | 1958-11-17 | 1961-07-18 | Adams Edmond | Magnetic tape recorder heads |
US3099080A (en) * | 1957-07-01 | 1963-07-30 | Int Nickel Co | Method of converting metal powder into flake |
US3163527A (en) * | 1960-10-04 | 1964-12-29 | Alloys Res & Mfg Corp | Coating metal articles by powdered metals |
US3255052A (en) * | 1963-12-09 | 1966-06-07 | Magnetics Inc | Flake magnetic core and method of making same |
US3293007A (en) * | 1965-11-29 | 1966-12-20 | Carl S Wukusick | Steam corrosion-resistant iron-chromium-aluminum-yttrium alloys and process for making same |
US3661570A (en) * | 1970-04-03 | 1972-05-09 | Rca Corp | Magnetic head material method |
US3948690A (en) * | 1973-09-11 | 1976-04-06 | Westinghouse Electric Corporation | Molded magnetic cores utilizing cut steel particles |
US3998669A (en) * | 1974-09-20 | 1976-12-21 | Th. Goldschmidt Ag | Permanent magnet on the basis of cobalt-rare earth alloys and method for its production |
US4029501A (en) * | 1976-01-26 | 1977-06-14 | Rca Corporation | Method of preparing improved magnetic head material |
US4177089A (en) * | 1976-04-27 | 1979-12-04 | The Arnold Engineering Company | Magnetic particles and compacts thereof |
US4919734A (en) * | 1984-09-29 | 1990-04-24 | Kabushiki Kaisha Toshiba | Compressed magnetic powder core |
US5534361A (en) * | 1993-07-01 | 1996-07-09 | Dowa Mining Co., Ltd. | Ferromagnetic metal powder |
US5591535A (en) * | 1993-07-01 | 1997-01-07 | Dowa Mining Co., Ltd. | Ferromagnetic metal powder |
US20040042922A1 (en) * | 2002-09-04 | 2004-03-04 | Firooz Rasouli | Methods for modifying oxygen content of atomized intermetallic aluminide powders and for forming articles from the modified powders |
US20080096009A1 (en) * | 2004-06-24 | 2008-04-24 | University Of Delaware | High Frequency Soft Magnetic Materials With Laminated Submicron Magnetic Layers And The Methods To Make Them |
US20080100154A1 (en) * | 2006-10-27 | 2008-05-01 | Takao Imagawa | Compacted magnetic core with high resistance, manufacturing method thereof, and motor for electric car |
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US1381460A (en) * | 1919-12-31 | 1921-06-14 | Western Electric Co | Magnet-core |
US2300336A (en) * | 1940-08-07 | 1942-10-27 | Bell Telephone Labor Inc | Magnetic alloy of iron and aluminum |
GB625627A (en) * | 1947-08-06 | 1949-06-30 | Geoffrey Charles Gaut | Improvements in or relating to magnetisable divided bodies or compacts |
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Patent Citations (3)
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US1381460A (en) * | 1919-12-31 | 1921-06-14 | Western Electric Co | Magnet-core |
US2300336A (en) * | 1940-08-07 | 1942-10-27 | Bell Telephone Labor Inc | Magnetic alloy of iron and aluminum |
GB625627A (en) * | 1947-08-06 | 1949-06-30 | Geoffrey Charles Gaut | Improvements in or relating to magnetisable divided bodies or compacts |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
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US3099080A (en) * | 1957-07-01 | 1963-07-30 | Int Nickel Co | Method of converting metal powder into flake |
US2992474A (en) * | 1958-11-17 | 1961-07-18 | Adams Edmond | Magnetic tape recorder heads |
US3163527A (en) * | 1960-10-04 | 1964-12-29 | Alloys Res & Mfg Corp | Coating metal articles by powdered metals |
US3255052A (en) * | 1963-12-09 | 1966-06-07 | Magnetics Inc | Flake magnetic core and method of making same |
US3293007A (en) * | 1965-11-29 | 1966-12-20 | Carl S Wukusick | Steam corrosion-resistant iron-chromium-aluminum-yttrium alloys and process for making same |
US3661570A (en) * | 1970-04-03 | 1972-05-09 | Rca Corp | Magnetic head material method |
US3948690A (en) * | 1973-09-11 | 1976-04-06 | Westinghouse Electric Corporation | Molded magnetic cores utilizing cut steel particles |
US3998669A (en) * | 1974-09-20 | 1976-12-21 | Th. Goldschmidt Ag | Permanent magnet on the basis of cobalt-rare earth alloys and method for its production |
US4029501A (en) * | 1976-01-26 | 1977-06-14 | Rca Corporation | Method of preparing improved magnetic head material |
US4177089A (en) * | 1976-04-27 | 1979-12-04 | The Arnold Engineering Company | Magnetic particles and compacts thereof |
US4919734A (en) * | 1984-09-29 | 1990-04-24 | Kabushiki Kaisha Toshiba | Compressed magnetic powder core |
US5534361A (en) * | 1993-07-01 | 1996-07-09 | Dowa Mining Co., Ltd. | Ferromagnetic metal powder |
US5591535A (en) * | 1993-07-01 | 1997-01-07 | Dowa Mining Co., Ltd. | Ferromagnetic metal powder |
US20040042922A1 (en) * | 2002-09-04 | 2004-03-04 | Firooz Rasouli | Methods for modifying oxygen content of atomized intermetallic aluminide powders and for forming articles from the modified powders |
US6863862B2 (en) | 2002-09-04 | 2005-03-08 | Philip Morris Usa Inc. | Methods for modifying oxygen content of atomized intermetallic aluminide powders and for forming articles from the modified powders |
US20080096009A1 (en) * | 2004-06-24 | 2008-04-24 | University Of Delaware | High Frequency Soft Magnetic Materials With Laminated Submicron Magnetic Layers And The Methods To Make Them |
US20080100154A1 (en) * | 2006-10-27 | 2008-05-01 | Takao Imagawa | Compacted magnetic core with high resistance, manufacturing method thereof, and motor for electric car |
US7816820B2 (en) * | 2006-10-27 | 2010-10-19 | Hitachi, Ltd. | Compacted magnetic core with high resistance, manufacturing method thereof, and motor for electric car |
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