US2565058A - Ceramic magnetic materials with high saturation-flux density - Google Patents

Ceramic magnetic materials with high saturation-flux density Download PDF

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Publication number
US2565058A
US2565058A US95581A US9558149A US2565058A US 2565058 A US2565058 A US 2565058A US 95581 A US95581 A US 95581A US 9558149 A US9558149 A US 9558149A US 2565058 A US2565058 A US 2565058A
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United States
Prior art keywords
flux density
zno
high saturation
mgo
saturation
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Expired - Lifetime
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US95581A
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English (en)
Inventor
Albers-Schoenberg Ernst
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Steatite Research Corp
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Steatite Research Corp
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Publication date
Application filed by Steatite Research Corp filed Critical Steatite Research Corp
Priority to US95581A priority Critical patent/US2565058A/en
Priority to GB11667/50A priority patent/GB668700A/en
Priority to DEST1079A priority patent/DE907995C/de
Priority to FR1018561D priority patent/FR1018561A/fr
Priority to CH288263D priority patent/CH288263A/de
Priority to NL78165D priority patent/NL78165C/xx
Application granted granted Critical
Publication of US2565058A publication Critical patent/US2565058A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/26Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
    • C04B35/2608Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead
    • C04B35/2625Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead containing magnesium

Definitions

  • This invention relates to a ferromagnetic ceramic material with a high saturation-flux density and method of making the same.
  • An object of this invention is to provide a method of making a ceramic magnetic material with a high saturation-flux density.
  • Another object of the invention is to provide a ceramic magnetic material with a high saturation-flux density.
  • Another object of the invention is to provide a ceramic magnetic material with a relatively high Curie point and a high saturation-flux density, and process of making the same.
  • Another object of the invention is to provide a ceramic magnetic material with a relatively low temperature coefficient, a relatively high Curie point and a high saturation-flux density and a process of making the same.
  • ferrite compounds have been developed and described in the technical literature, i. e., ferromagnetic oxides of the general formula MFe2O4, where M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • ferromagnetic oxides of the general formula MFe2O4 where M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • M represents a bivalent metal, as, for instance, manganese, copper or magnesium.
  • ferrite compounds which forms crystals of the same shape as the magnetite, F6304, has a different magnetic permeability, ohmic resistance, Curie point and magnetic losses.
  • these compounds or suitable mixtures of them cover a range ofin
  • a high initial permeability is desirable but according to the present invention it has been found that by sacrificing a certain amount of the high initial permeability property, other very valuable properties are obtained. It might be expected that higher Curie points could be obtained from compositions having a medium or low initial permeability but the particular composition employed in the present invention is very unusual in that it has a high saturation-flux density which exceeds that of the high permeability bodies.
  • the ferrite compounds of this invention have an initial permeability between 200 and 350, small magnetic losses over the frequency range of 60 cs. to about 10 mos, a Curie point of 250 C. or
  • a peculiarity of these materials is the fact that they show a high saturation flux-density of at least 3750 up to more than 000 exceeding the saturation fiux-density of the high permeability bodies.
  • the high saturation bodies are fired at fairlyhigh temperatures between Seger cones 7 and 10 and cooled in air, i. e. without applying a protective atmosphere.
  • the various components or compounds adapted to form the components of the final product during firing are combined in the proper proportions.
  • the manganese oxide component of the final product is preferably added in the form of manganese dioxide and when lithium oxide is employed as a component it is added in the form of the carbonate, etc. During firing these compounds are reduced to the required oxides.
  • the "mol ratio refers to the final product
  • the composition refers to the mix before firing.
  • the powders are preferably ground to a very fine particle size, for example, less than 0.010 m. m.
  • the final pulverized mixed powder is wet with an aqueous binder which may be just ordinary water or may contain emulsified waxes or other plasticizers or binding agents.
  • Enough of the aqueous binder is added to make the mix coherent when placed under pressure and the mix is thereafter molded.
  • Any molding device such as a steel die or a ceramic extruding machine may be employed. After molding the articles are fired at Seger cones 7-10 and cooled. No special precautions are required during cooling.
  • Example 1 The mix is ballmilled and moistened and plasticized by an addition of 4% of a wax-water emulsion.
  • the wax-water emulsion contains 50% of wax.
  • the mix is then molded by pressing and fired at about Seger-cone 9. 1 After firing the molded article is cooled in air at room temperature.
  • the physical properties of this material are shown in the following table:
  • Example 3 A mix is made up of the following components: Mol ratio: .09 MgO:.4 MnO:.34 ZnO:.l7 NiO: about 1 F6203.
  • a ferromagnetic ceramic material consisting mainly of iron oxide compounds of the magnetitetype, suitable for the use at frequencies between 60 cs. and about 10 mos. composed of the bivalent metal oxides MgO MnO, ZnO and MO and F6203 in the mol ratio of .05-.15 MgO:.2-.4 MnO:.3-.4 ZnO:.l5-.4 Nioiabout 1.0 FezOs, the total mol ratio of said bivalent metal oxides to F6203 being approximately 1:1 said material having a Curie point of at least 250 C., an initial permeability between 200 and 350, a saturation-flux density of at least 3750 and a temperature coemcient of a of 25 to 35% (measured on a toroid) between room temperature and C.
  • a process of making a ferromagnetic ceramic material having small magnetic losses over a frequency range of 60 cycles to 10 megacycles and a high saturation-flux density comprising the steps of grinding and mixing together cornponents adapted to yield after firing the bivalent metal oxides MgO, MnO, ZnO and MO and F6203 in the mol ratio of .05-.15 NIgOLZ-fl MnO:.3-.4 ZnO:.15-.4 NiO:about 1.0 F8203, the total mol ratio of said bivalent metal oxides to F8203 being approximately 1:1 moistening the powdered mix with an aqueous binding composition, molding the resulting plastic mix to the desired shape, firing the molded article at Seger cones 7-10 to produce a ferromagnetic molded product having a Curie point of at least 250 (3., an initial perineability of 200-350, a saturation flux density of at least 3750 and a temperature coefficient of U. of 25-35% (measured on a toroid) between
  • a process of making a ferromagnetic ceramic material having small magnetic losses over a frequency range of 60 cycles to 10 megacycles and a high saturation-flux density comprising the steps of grinding and mixing the metallic oxides MgO, Win02, ZnO, 'rliO, and FezOa in the mol ratio of .O -.5 MgO:.2-.4 manganese oxide calculated as lvIn :.3-.4 ZnO:.15-.4 NiO:about 1.0 FezOa, the mol ratio of the iron to the total amount of the other said metals being approximately 2:1 moistening the powdered mix with water, molding the resulting plastic mix to the desired shape, firing the molded article Seger cones 7-10 and permitting it to cool in air to produce a ferromagnetic molded product having a Curie point of at least 250 (3., an initial permeability of #0 of 200-350, a saturation flux density of at least 3750 and a temperature coefficient of p. of 25-35%
  • a process of making a ferromagnetic ceramic material having small magnetic losses over a frequency range of 50 cycles to 10 megacycles and a high saturation-flux density comprising the steps of grinding and mixing the metallic oxides MgO, M1102, ZnO, Ni(), and FezOs, the mol ratio of the iron to the total amount of the other said metals being approximatel 2:1 nioistening the powdered mix with water, adding a wax as a plasticizer, molding the resultant plastic mix to the desired shape, firing the molded article at Seger cones 7-10 and permitting it to cool in air to produce a ferromagnetic molded product having a Curie point of at least 250 0., an initial permeability of t of 200-350, a saturation flux density of at least 3750 and a temperature coefficient of n of 25-35% (measured on a toroid) between room temperature and 125 C.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Soft Magnetic Materials (AREA)
  • Magnetic Ceramics (AREA)
US95581A 1949-05-26 1949-05-26 Ceramic magnetic materials with high saturation-flux density Expired - Lifetime US2565058A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US95581A US2565058A (en) 1949-05-26 1949-05-26 Ceramic magnetic materials with high saturation-flux density
GB11667/50A GB668700A (en) 1949-05-26 1950-05-10 Ceramic magnetic materials with high saturation flux density
DEST1079A DE907995C (de) 1949-05-26 1950-05-18 Ferromagnetisches, hauptsaechlich aus Eisenoxydverbindungen vom Magnetit-Typ bestehendes keramisches Material und seine Herstellung
FR1018561D FR1018561A (fr) 1949-05-26 1950-05-24 Matière céramique ferromagnétique
CH288263D CH288263A (de) 1949-05-26 1950-05-25 Keramischer, ferromagnetischer körper mit einer hohen Sättigungsinduktion und Verfahren zu dessen Herstellung.
NL78165D NL78165C (fr) 1949-05-26 1950-05-26

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US95581A US2565058A (en) 1949-05-26 1949-05-26 Ceramic magnetic materials with high saturation-flux density

Publications (1)

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US2565058A true US2565058A (en) 1951-08-21

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US95581A Expired - Lifetime US2565058A (en) 1949-05-26 1949-05-26 Ceramic magnetic materials with high saturation-flux density

Country Status (6)

Country Link
US (1) US2565058A (fr)
CH (1) CH288263A (fr)
DE (1) DE907995C (fr)
FR (1) FR1018561A (fr)
GB (1) GB668700A (fr)
NL (1) NL78165C (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2670331A (en) * 1951-09-28 1954-02-23 Steatite Res Corp Magnesium-zinc ceramic ferrite containing copper
US2773039A (en) * 1952-11-24 1956-12-04 Steatite Res Corp Magnetically strong ferromagnetic magnesium-zinc type of ferrite
DE1008181B (de) * 1952-02-15 1957-05-09 Steatite Res Corp Ferromagnetische Ferrite
US2830162A (en) * 1954-06-22 1958-04-08 Raytheon Mfg Co Heating method and apparatus
US2961407A (en) * 1954-06-30 1960-11-22 Gen Electric Mixed ferrite composition
US2981690A (en) * 1957-06-18 1961-04-25 Steatite Res Corp Ferrites with square hysteresis loops
US2981903A (en) * 1954-02-26 1961-04-25 Bell Telephone Labor Inc Gyromagnetic wave transmission devices
US3023165A (en) * 1956-08-17 1962-02-27 Bell Telephone Labor Inc Magnesium ferrite containing aluminum and method of making same
US3031407A (en) * 1959-03-24 1962-04-24 Ibm Method of producing ferrite bodies

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2382136A (en) * 1943-03-13 1945-08-14 Henry L Crowley & Company Inc Ceramic bodies and method of producing same
US2452531A (en) * 1943-05-31 1948-10-26 Hartford Nat Bank & Trust Co Process of manufacturing a magnetic material and magnetic core

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE227787C (fr) *
US2452529A (en) * 1941-10-24 1948-10-26 Hartford Nat Bank & Trust Co Magnet core
NL61937C (fr) * 1941-10-24 1948-11-15
CH239838A (de) * 1942-06-16 1945-11-15 Philips Nv Verfahren zur Herstellung magnetischer Kerne und nach diesem Verfahren hergestellter Kern.
CH265894A (de) * 1943-03-10 1949-12-31 Philips Nv Verfahren zur Herstellung eines ferromagnetischen Spulenmantels.
US2452530A (en) * 1943-05-15 1948-10-26 Hartford Nat Bank & Trust Co Magnetic core
CH260717A (de) * 1943-05-31 1949-03-31 Philips Nv Verfahren zur Herstellung eines magnetischen Kernes, und nach diesem Verfahren hergestellter magnetischer Kern.
AT164420B (de) * 1944-07-06 1949-11-10 Philips Nv Magnetischer Kern aus einem ferromagnetischen Ferrit

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2382136A (en) * 1943-03-13 1945-08-14 Henry L Crowley & Company Inc Ceramic bodies and method of producing same
US2452531A (en) * 1943-05-31 1948-10-26 Hartford Nat Bank & Trust Co Process of manufacturing a magnetic material and magnetic core

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2670331A (en) * 1951-09-28 1954-02-23 Steatite Res Corp Magnesium-zinc ceramic ferrite containing copper
DE1008181B (de) * 1952-02-15 1957-05-09 Steatite Res Corp Ferromagnetische Ferrite
US2773039A (en) * 1952-11-24 1956-12-04 Steatite Res Corp Magnetically strong ferromagnetic magnesium-zinc type of ferrite
US2981903A (en) * 1954-02-26 1961-04-25 Bell Telephone Labor Inc Gyromagnetic wave transmission devices
US2830162A (en) * 1954-06-22 1958-04-08 Raytheon Mfg Co Heating method and apparatus
US2961407A (en) * 1954-06-30 1960-11-22 Gen Electric Mixed ferrite composition
US3023165A (en) * 1956-08-17 1962-02-27 Bell Telephone Labor Inc Magnesium ferrite containing aluminum and method of making same
US2981690A (en) * 1957-06-18 1961-04-25 Steatite Res Corp Ferrites with square hysteresis loops
US3031407A (en) * 1959-03-24 1962-04-24 Ibm Method of producing ferrite bodies

Also Published As

Publication number Publication date
NL78165C (fr) 1955-06-15
DE907995C (de) 1954-04-01
CH288263A (de) 1953-01-15
FR1018561A (fr) 1953-01-09
GB668700A (en) 1952-03-19

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