US2419847A - Powdered iron magnetic core - Google Patents
Powdered iron magnetic core Download PDFInfo
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- US2419847A US2419847A US538482A US53848244A US2419847A US 2419847 A US2419847 A US 2419847A US 538482 A US538482 A US 538482A US 53848244 A US53848244 A US 53848244A US 2419847 A US2419847 A US 2419847A
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- 239000012256 powdered iron Substances 0.000 title description 19
- 239000011162 core material Substances 0.000 description 43
- 239000002253 acid Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- -1 alcohol ester Chemical class 0.000 description 11
- 238000004804 winding Methods 0.000 description 11
- 239000004927 clay Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 7
- 238000005266 casting Methods 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 239000011810 insulating material Substances 0.000 description 4
- 239000004342 Benzoyl peroxide Substances 0.000 description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 239000004135 Bone phosphate Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- PVLVQTYSRICFCB-TYYBGVCCSA-N (e)-but-2-enedioic acid;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.OC(=O)\C=C\C(O)=O PVLVQTYSRICFCB-TYYBGVCCSA-N 0.000 description 1
- PVLVQTYSRICFCB-ODZAUARKSA-N (z)-but-2-enedioic acid;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.OC(=O)\C=C/C(O)=O PVLVQTYSRICFCB-ODZAUARKSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- VVYDVQWJZWRVPE-UHFFFAOYSA-L dimethyltin(2+);diiodide Chemical compound C[Sn](C)(I)I VVYDVQWJZWRVPE-UHFFFAOYSA-L 0.000 description 1
- DFQSWFGKYUFIFW-UHFFFAOYSA-N dipropyl 2-methylidenebutanedioate Chemical compound CCCOC(=O)CC(=C)C(=O)OCCC DFQSWFGKYUFIFW-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 1
- NZHHDFRSEQSGLN-ZRDIBKRKSA-N tris(prop-2-enyl) (e)-prop-1-ene-1,2,3-tricarboxylate Chemical compound C=CCOC(=O)C\C(C(=O)OCC=C)=C/C(=O)OCC=C NZHHDFRSEQSGLN-ZRDIBKRKSA-N 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Images
Classifications
-
- 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
- H01F1/26—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 by macromolecular organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/4902—Electromagnet, transformer or inductor
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/4902—Electromagnet, transformer or inductor
- Y10T29/49073—Electromagnet, transformer or inductor by assembling coil and core
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/4902—Electromagnet, transformer or inductor
- Y10T29/49075—Electromagnet, transformer or inductor including permanent magnet or core
- Y10T29/49076—From comminuted material
Definitions
- My invention relates to powdered iron bonded magnetic cores, and to an improved method of making such a core.
- Another object of my invention i-s to provide an improved method of forming a. powdered iron bonded core.
- FIG. 1 illustrates a mold apparatus in which my iniproved core is formed
- Fig. 2 illustrates a core produoed in the mold of Fig. 1
- Fig. 3 iilustrates a. modified mold construction for producing a mcdification of the core illus'- trated in Fig. 2
- Fig. 4 illustrates the core produced in the mold of Fig. 3.
- My improved core is formed by mixing powdered iron of suitable fineness with a suitable insulating material such as clay.
- a suitable insulating material such as clay.
- the clay is employed so as to prevent relative high eddy currents, but if the eddy currents are not material the clay or similar insulating material may be omitted.
- the mixture of powdered iron and clay is then mixed with any suitable heat hardenable substantiaily solventless liquid binding material such as esters of saturated monohydric alcohols and unsaturated monob'asic carboxylic acid.
- any suitable heat hardenable substantiaily solventless liquid binding material such as esters of saturated monohydric alcohols and unsaturated monob'asic carboxylic acid.
- Polymerizable comDOsitions comprising (1) a polymerizable polyhydrlc 'alcohol ester of an s oiaims. (ci. 175-121) alpha-unsaturated alpha, beta-polycarboxylic acid, e. g., diethylene glycol maleate, diethylene glycol fumarate, etc., and (2) a polymeriable monohydric alcohol ester oi' an alpha-unsaturated alpha,beta-polycarboxylic acid, e. g., diethyl fumarate, dipropyl itaconate, diallyl maleate, diallyl itaconate, etc.
- Polymerizable compositions comprising (1) a polymerizable 4polyhydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxylic acid and (2) a polymerlza'ole polyester obtained by esterifying an aromatic polycarboxylic acid or anhydride with. an unsaturated monohydric alcohol, e. g., diallyl phthalate.
- Polymerizable compositions comprising (1) a polymerizable polyhydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxylic acid and (2) and .an unsaturated monohydric alcohol triester of a tribasic acid, specically triallyl phosphate, trialiyl citrate, triailyl tricarballylate or triallyl aconitate. y
- a suitaloie moimt o eatalyst with the solventless bon' .terial is, about 3 per cent by Weight of total a ;cant of bonding material emplofeitl. ;any r' catalyst may be empioyed such e such as benzoyl peroxidc.
- Any lens of powdered iron insulation material soiyentless binder may be employed and I have found that a mixture including about 8 parts of ciay, 66 parts iron, and 26 parts binder produces a very desirable core.
- Fig. 1 I have illustrated somewhat diagrammatically a mold having similar portions i and ll which fit into a base 2, in' which mold 'the materials described above may be poured from a vessel
- the mixture is preheated before introducing into the mold to a temperature just below the polymerization temperature of the resin binder, and for the materials mentioned above the mixture is heated to about degrees C. for about 5 minutes while it is being agitated. The mixture is then poured into the mold to produce the core.
- the mold Sin order to pre'vent the mixture from chilling when it is poured into the mold, the mold is preheated to at least the temperature that the mixture has, such as around, to degrees by the use of heating coils H and 15. The mold is maintained at the temperature of about 100 degrees for a few minutes and then raised to above the polymerization temperature of the binder, such as being raised to about 130 degrees for a suitable time such as 1 hour. After the mold has cooled the two halves and li may be disassembled leaving 9, core
- the resulting core formed in the manner described above has better electrical characteristics than a similar core formed of powdered iron bonded together with chrome silicate.
- Tests of such cores were made by connecting the primary of a transformer having the powdered iron core in series with a capacitance to form a series resonant circuit and the highest voltage induced in the secondary winding of the transformer which also surrounded the core was measured.
- the transformer core having the powdered iron bonded together with chrome silicate was formed by mixing 300 mesh powdered iron with sufiicient chrome silicate, the core being hardened under heat and pressure.
- a transformer having such a core when tested in the resonant circuit described above had a maximum induced voltage in the secondary of about 10,000 volts, while a transformer having a core formed according to my invention with a similar amount of powdered iron had a maximum induced voltage in the secondary of about 18,000 volts. It will be appreciated that the difference in voltages is a. measure of the relative eflioiencies of the two types of cores, and my imprcved core was therefore considerably more .
- suitable slots may be placed in the outer surface of the core for the reception of a winding such as the low voltage primary winding turns.
- a winding such as the low voltage primary winding turns.
- the mold -sections 10 and ll have their inner surfaces suitably slotted so as to produce the winding slots in the outer surface of the core, as is illustrated in Fig. 2. If winding slots are desired in a powdered iron core formed according to past practice by the application of pressure,
- a winding if desired may be cast into the core formed according to my invention, and in Fig. 3 I have illustrated a mold having portions 18 and
- Fig. 4 illustrates a core 2
- a mechanically strong uncompressed magnetic core material comprising particles of powdered magnetic material bonded together by a polymerized alcohol ester of carbonlic acid.
- a hard mechanically strong pressure free low loss magnetic core casting comprising a mixture of powdered magnetic material and powdered insulating material bonded together by a polymerized polyhydrio alcohol ester of an alphaunsaturated alpha,beta-polycarboxylic acid and a catalyst.
- a hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts binder and 8 parts clay, said binder comprising, by weight, substantially 97 parts polymerized polyhydric alcohol ester of alphaunsaturated alpha,beta-polycarboxylic acid and 3 parts catalytic peroxide.
- a hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered. iron, 26 parts binder and 8 parts clay, said binder comprising, .by weight, substantially 9'7 parts polymerized polyhydrlc alcohol ester of an alphaunsaturated alpha,beta-polycarbowlic acid and a polymerizable monohydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxyllc acid and 3 parts benzoyl peroxide as a Catalyst.
- a hard mechanlcally strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts .binder and 8 parts clay, said binder comprising, by weight. substantially 97 parts polymerized polyhydric alcohol ester of an alphaunsaturated alpha,beta-polycarboiwlic acid and a polyester obtained by esterifying an aromatic polycarboxylic acid or anhydride with an unsaturated monohydric alcohol and 3 parts benzoyl peroxide as a Catalyst.
- a hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts binder and 8 parts clay, said binder comprising, ⁇ by weight, substantially 97 parts polymerized polyhydrio alcohol ester of an alphaunsaturated alpha,beta-polycarboxy1ic acid and an unsaturated monohydric alcohol triester of a tribasic acid and 3 parts benzoyl peroxide as a Catalyst.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Soft Magnetic Materials (AREA)
Description
w April 29, 1947' A. F. MITT'ERMAIER -2,419,847
POWERED IRON MAGNETIC CORE Filed June 2. 1944 Figi Patente Apr. 29, 1947 UNITE STATES PA FFMIE or to General Electric of New York Company, a corporation Application June 2, 1944, Serial No. 538,482
My invention relates to powdered iron bonded magnetic cores, and to an improved method of making such a core.
It has been customary to form electromagnetic cores particularly for high frequency application of powdered iron which is bonded together with suitable material,l such as a phenolic condensation product, varnishes, chrome silicate, and waxes. The iron particles have also been insulai'ed from each other -by mixing the powdered iron with an insulating material such as clay before the powder is bonded together with a bindcr. Cores which I formed according to past practice, however, by the use of high pressure had relatively high core losses and were not consistent in electrical characteristics.
It is therefore an object of my invention to provide an improved powdered iron bonded core.
Another object of my invention i-s to provide an improved method of forming a. powdered iron bonded core. i
Further objects and advantages of my Invention will 'become apparent from the following description referring to the accompanying drawing, and the features of novelty which characterize my invention will be pointed out with particularity in the ciaims annexed to and forming a part. of this specification.
In the -drawing, Fig. 1 illustrates a mold apparatus in which my iniproved core is formed; Fig. 2 illustrates a core produoed in the mold of Fig. 1; Fig. 3 iilustrates a. modified mold construction for producing a mcdification of the core illus'- trated in Fig. 2, and Fig. 4 illustrates the core produced in the mold of Fig. 3.
My improved core is formed by mixing powdered iron of suitable fineness with a suitable insulating material such as clay. The clay is employed so as to prevent relative high eddy currents, but if the eddy currents are not material the clay or similar insulating material may be omitted. The mixture of powdered iron and clay is then mixed with any suitable heat hardenable substantiaily solventless liquid binding material such as esters of saturated monohydric alcohols and unsaturated monob'asic carboxylic acid. Further examples of such materials are given in applications for Nordlander and Hargraves, S. N. 302,164, and Nordlander, S. N. 302,165 and S. N. 302,166. These further examples are listed below as follows:
Polymerizable comDOsitions comprising (1) a polymerizable polyhydrlc 'alcohol ester of an s oiaims. (ci. 175-121) alpha-unsaturated alpha, beta-polycarboxylic acid, e. g., diethylene glycol maleate, diethylene glycol fumarate, etc., and (2) a polymeriable monohydric alcohol ester oi' an alpha-unsaturated alpha,beta-polycarboxylic acid, e. g., diethyl fumarate, dipropyl itaconate, diallyl maleate, diallyl itaconate, etc.
Polymerizable compositions comprising (1) a polymerizable 4polyhydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxylic acid and (2) a polymerlza'ole polyester obtained by esterifying an aromatic polycarboxylic acid or anhydride with. an unsaturated monohydric alcohol, e. g., diallyl phthalate.
Polymerizable compositions comprising (1) a polymerizable polyhydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxylic acid and (2) and .an unsaturated monohydric alcohol triester of a tribasic acid, specically triallyl phosphate, trialiyl citrate, triailyl tricarballylate or triallyl aconitate. y
In order to prodiice a. core which will not ice ruhbery, ii have found it is desirable to use a suitaloie moimt o eatalyst with the solventless bon' .terial, is, about 3 per cent by Weight of total a ;cant of bonding material emplofeitl. ;any r' catalyst may be empioyed such e such as benzoyl peroxidc. Any lens of powdered iron insulation material soiyentless binder may be employed and I have found that a mixture including about 8 parts of ciay, 66 parts iron, and 26 parts binder produces a very desirable core.
In Fig. 1 I have illustrated somewhat diagrammatically a mold having similar portions i and ll which fit into a base 2, in' which mold 'the materials described above may be poured from a vessel |3 to produce a core. In order to insure that the mixture will fill all parts of the mold, the mixture is preheated before introducing into the mold to a temperature just below the polymerization temperature of the resin binder, and for the materials mentioned above the mixture is heated to about degrees C. for about 5 minutes while it is being agitated. The mixture is then poured into the mold to produce the core. Sin order to pre'vent the mixture from chilling when it is poured into the mold, the mold is preheated to at least the temperature that the mixture has, such as around, to degrees by the use of heating coils H and 15. The mold is maintained at the temperature of about 100 degrees for a few minutes and then raised to above the polymerization temperature of the binder, such as being raised to about 130 degrees for a suitable time such as 1 hour. After the mold has cooled the two halves and li may be disassembled leaving 9, core |6 as is illustrated in Fig. 2.
I have found that the resulting core formed in the manner described above has better electrical characteristics than a similar core formed of powdered iron bonded together with chrome silicate. Tests of such cores were made by connecting the primary of a transformer having the powdered iron core in series with a capacitance to form a series resonant circuit and the highest voltage induced in the secondary winding of the transformer which also surrounded the core was measured. The transformer core having the powdered iron bonded together with chrome silicate was formed by mixing 300 mesh powdered iron with sufiicient chrome silicate, the core being hardened under heat and pressure. A transformer having such a core when tested in the resonant circuit described above had a maximum induced voltage in the secondary of about 10,000 volts, while a transformer having a core formed according to my invention with a similar amount of powdered iron had a maximum induced voltage in the secondary of about 18,000 volts. It will be appreciated that the difference in voltages is a. measure of the relative eflioiencies of the two types of cores, and my imprcved core was therefore considerably more eficient.
Not only will my improved core have efflcient electrical characteristics, but by casting the ingredients in the manner described above, suitable slots il may be placed in the outer surface of the core for the reception of a winding such as the low voltage primary winding turns. It will be seen that the mold -sections 10 and ll have their inner surfaces suitably slotted so as to produce the winding slots in the outer surface of the core, as is illustrated in Fig. 2. If winding slots are desired in a powdered iron core formed according to past practice by the application of pressure,
not only is a much more electrically ineflicient core produced but the core will be formed first with a cylindrical surface, after which the core is machined to produce the Slots, and unless the powdered iron is bonded very solidly together the ridges 'between the slots may crumble.
A winding if desired may be cast into the core formed according to my invention, and in Fig. 3 I have illustrated a mold having portions 18 and |9 filled with a mixture of iron, clay and solventless binder, as is described above. 'I'he mixture is, of course, heated and before it hardens a winding 20 is inserted so as to be cast into the core. Insteacl of introducing the winding 20 into a heated mixture in the mold, the winding may be previously inserted in the mold and then the mixture poured in and then polymerized around the winding. Fig. 4 illustrates a core 2| forzned with the winding 20 cast therein.
Although I have shown and described particular embodiments of my invention, I do not desire to be limited to the particular embodiments described, and I intend in the appended claims to cover all modifications which do not depart from the spirit and scope of my invention.
What 1 claim as new and desire to secure by Letters Patent of the United States is;
1. A mechanically strong uncompressed magnetic core material comprising particles of powdered magnetic material bonded together by a polymerized alcohol ester of carbonlic acid.
2. A hard mechanically strong pressure free low loss magnetic core casting comprising a mixture of powdered magnetic material and powdered insulating material bonded together by a polymerized polyhydrio alcohol ester of an alphaunsaturated alpha,beta-polycarboxylic acid and a catalyst.
3. A hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts binder and 8 parts clay, said binder comprising, by weight, substantially 97 parts polymerized polyhydric alcohol ester of alphaunsaturated alpha,beta-polycarboxylic acid and 3 parts catalytic peroxide.
4. A hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered. iron, 26 parts binder and 8 parts clay, said binder comprising, .by weight, substantially 9'7 parts polymerized polyhydrlc alcohol ester of an alphaunsaturated alpha,beta-polycarbowlic acid and a polymerizable monohydric alcohol ester of an alpha-unsaturated alpha,beta-polycarboxyllc acid and 3 parts benzoyl peroxide as a Catalyst.
5. A hard mechanlcally strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts .binder and 8 parts clay, said binder comprising, by weight. substantially 97 parts polymerized polyhydric alcohol ester of an alphaunsaturated alpha,beta-polycarboiwlic acid and a polyester obtained by esterifying an aromatic polycarboxylic acid or anhydride with an unsaturated monohydric alcohol and 3 parts benzoyl peroxide as a Catalyst.
6. A hard mechanically strong gravity compacted low loss magnetic core casting comprising, by weight, substantially 66 parts powdered iron, 26 parts binder and 8 parts clay, said binder comprising,` by weight, substantially 97 parts polymerized polyhydrio alcohol ester of an alphaunsaturated alpha,beta-polycarboxy1ic acid and an unsaturated monohydric alcohol triester of a tribasic acid and 3 parts benzoyl peroxide as a Catalyst.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PA'I'ENTS Number Name Date 2,230,228 Bandur Feb. 4, 1941 1,982,689 Polydorofi Dec. 4, 1934 2,273,891 Pollack et al. Feb. 24, 1942 2,195,362 Ellis Mar. 26, 1940 1,867,362 Lathrop July 12, 1932 1,881,711 Iratljirop Oct. 11, 1932 2,043,3i6`''I 'Buckley June 9, 1936 2,330,590 Kaschke Sept. 28, 1943 1,948,308 Neighbors Feb. 20, 1934 1,994,534 Robinson Mar. 19, 1935 FOREIGN PA'I'EN'IfS Number Country Date 647,072 French July 24, 1928
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US538482A US2419847A (en) | 1944-06-02 | 1944-06-02 | Powdered iron magnetic core |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US538482A US2419847A (en) | 1944-06-02 | 1944-06-02 | Powdered iron magnetic core |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2419847A true US2419847A (en) | 1947-04-29 |
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ID=24147103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US538482A Expired - Lifetime US2419847A (en) | 1944-06-02 | 1944-06-02 | Powdered iron magnetic core |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2419847A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2561495A (en) * | 1947-08-26 | 1951-07-24 | Rca Corp | High-loss magnetic core for high-frequency coils |
| US2568310A (en) * | 1948-03-30 | 1951-09-18 | Bendix Aviat Corp | Inductance coil structure |
| US2761939A (en) * | 1948-11-30 | 1956-09-04 | Metallurg Tech Et Commerciale | Apparatus for welding by means of electromagnetic induction heating |
| US2808630A (en) * | 1954-04-29 | 1957-10-08 | Westinghouse Electric Corp | Matchplate for the production of shell molds and process of making the same |
| US2901455A (en) * | 1954-08-09 | 1959-08-25 | Union Carbide Corp | Molding composition comprising synthetic resin and metallic filaments, articles molded therefrom and method of making same |
| US3659336A (en) * | 1970-01-30 | 1972-05-02 | Electronic Diversified Inc | Method of manufacturing an inductive device |
| US3813770A (en) * | 1973-04-19 | 1974-06-04 | Jetro Matic Ind Corp | Method of encapsulating coils |
| US3848331A (en) * | 1973-09-11 | 1974-11-19 | Westinghouse Electric Corp | Method of producing molded stators from steel particles |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR647072A (en) * | 1927-12-08 | 1928-11-20 | Magnet coil | |
| US1867362A (en) * | 1930-11-21 | 1932-07-12 | Bell Telephone Labor Inc | Insulation of metal bodies |
| US1881711A (en) * | 1931-08-14 | 1932-10-11 | Bell Telephone Labor Inc | Magnetic structure |
| US1948308A (en) * | 1931-12-11 | 1934-02-20 | Western Electric Co | Method of making magnetic bodies |
| US1982689A (en) * | 1931-03-16 | 1934-12-04 | Johnson Lab Inc | Magnetic core material |
| US1994534A (en) * | 1932-04-23 | 1935-03-19 | Rca Corp | Inductance coil and method of manufacture thereof |
| US2043346A (en) * | 1930-07-25 | 1936-06-09 | Bell Telephone Labor Inc | Submarine cable loading coil |
| US2195362A (en) * | 1936-05-21 | 1940-03-26 | Ellis Foster Co | Glycol-maleic acid resin and process of making same |
| US2230228A (en) * | 1940-01-06 | 1941-02-04 | Western Electric Co | Manufacture of magnetic cores |
| US2273891A (en) * | 1939-02-18 | 1942-02-24 | Pittsburgh Plate Glass Co | Method of polymerizing polymerizable materials containing more than one polymerizable grouping |
| US2330590A (en) * | 1939-05-19 | 1943-09-28 | Kaschke Kurt | Dust iron core |
-
1944
- 1944-06-02 US US538482A patent/US2419847A/en not_active Expired - Lifetime
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR647072A (en) * | 1927-12-08 | 1928-11-20 | Magnet coil | |
| US2043346A (en) * | 1930-07-25 | 1936-06-09 | Bell Telephone Labor Inc | Submarine cable loading coil |
| US1867362A (en) * | 1930-11-21 | 1932-07-12 | Bell Telephone Labor Inc | Insulation of metal bodies |
| US1982689A (en) * | 1931-03-16 | 1934-12-04 | Johnson Lab Inc | Magnetic core material |
| US1881711A (en) * | 1931-08-14 | 1932-10-11 | Bell Telephone Labor Inc | Magnetic structure |
| US1948308A (en) * | 1931-12-11 | 1934-02-20 | Western Electric Co | Method of making magnetic bodies |
| US1994534A (en) * | 1932-04-23 | 1935-03-19 | Rca Corp | Inductance coil and method of manufacture thereof |
| US2195362A (en) * | 1936-05-21 | 1940-03-26 | Ellis Foster Co | Glycol-maleic acid resin and process of making same |
| US2273891A (en) * | 1939-02-18 | 1942-02-24 | Pittsburgh Plate Glass Co | Method of polymerizing polymerizable materials containing more than one polymerizable grouping |
| US2330590A (en) * | 1939-05-19 | 1943-09-28 | Kaschke Kurt | Dust iron core |
| US2230228A (en) * | 1940-01-06 | 1941-02-04 | Western Electric Co | Manufacture of magnetic cores |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2561495A (en) * | 1947-08-26 | 1951-07-24 | Rca Corp | High-loss magnetic core for high-frequency coils |
| US2568310A (en) * | 1948-03-30 | 1951-09-18 | Bendix Aviat Corp | Inductance coil structure |
| US2761939A (en) * | 1948-11-30 | 1956-09-04 | Metallurg Tech Et Commerciale | Apparatus for welding by means of electromagnetic induction heating |
| US2808630A (en) * | 1954-04-29 | 1957-10-08 | Westinghouse Electric Corp | Matchplate for the production of shell molds and process of making the same |
| US2901455A (en) * | 1954-08-09 | 1959-08-25 | Union Carbide Corp | Molding composition comprising synthetic resin and metallic filaments, articles molded therefrom and method of making same |
| US3659336A (en) * | 1970-01-30 | 1972-05-02 | Electronic Diversified Inc | Method of manufacturing an inductive device |
| US3813770A (en) * | 1973-04-19 | 1974-06-04 | Jetro Matic Ind Corp | Method of encapsulating coils |
| US3848331A (en) * | 1973-09-11 | 1974-11-19 | Westinghouse Electric Corp | Method of producing molded stators from steel particles |
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