US2179810A - Finely divided magnetic substance - Google Patents

Finely divided magnetic substance Download PDF

Info

Publication number
US2179810A
US2179810A US158758A US15875837A US2179810A US 2179810 A US2179810 A US 2179810A US 158758 A US158758 A US 158758A US 15875837 A US15875837 A US 15875837A US 2179810 A US2179810 A US 2179810A
Authority
US
United States
Prior art keywords
magnetic
finely divided
iron
mixed crystals
magnetic substance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US158758A
Inventor
Brill Rudolf
Schoenemann Karl
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Application granted granted Critical
Publication of US2179810A publication Critical patent/US2179810A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets 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
    • H01F1/14Magnets 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
    • H01F1/20Magnets 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
    • H01F1/22Magnets 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
    • H01F1/24Magnets 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

Definitions

  • the present invention relates to the production of magnetic substances in finely divided form the particles of which are characterized by a very small and uniform grain size.
  • magnetic substances of the said kind may be obtained by preparing mixed crystals from oxides of magnetic metals and oxidic additional substances capable of forming mixed crystals with the said oxides, reducing the resulting mixed crystals and then mechanically comminuting the reduction product, as for example in an edge mill or ball mill.
  • mixed crystals are commonly meant solid solutions in which the crystal lattice of one component contains one or more other components of the solid solution.
  • An oxidic additional substances there are chosen such as are more diflicultly reducible than the employed oxides of magnetic metals.
  • the presence of the additional substances in the form of mixed crystal components has the result that the magnetic substances, when being formed by the reduction of the mixed crystals, are produced and remain in a very finely crystallized state, because any rigid adhering together of the single small crystals and their recrystallization are prevented by the intercalation of the foreign substance.
  • the mixed crystals it is preferable to start from a solution which contains a suitable compound both of the magnetic and the additional elements and to precipitate simultaneously the oxides of the magnetic metal and the oxidic additional substances.
  • the obtained mixture is preferably subjected to a strong heat treatment in order to render the mixed crystal formation as complete as possible.
  • a homogeneous mixed crystal is produced for example from the before-mentioned mixture NiO-FeO-CoO-MgO.
  • reduction which is preferably performed with hydrogen, a magnesium oxide containing nickel-iron-cobalt alloy is obtained.
  • Another method for the preparation of the mixed crystals consists in starting from the magnetic metals themselves and subjecting them after the addition of the foreign substances capable of forming mixed crystals, to an oxidizing fusion, the fused product then being reduced.
  • the above-mentioned aluminum oxide containing nickel-iron-cobalt alloy can be advantageously prepared.
  • an addition of from 2 or5 to per cent of foreign substances is suillciezf. Also greater amounts may be used, but the I afford no particular advantages.
  • the metallic mass obtained by the reduction and comminution consists, even when the reduction has been effected at temperatures exceeding the recrystallization temperature of the magnetic metal, of very small crystallites the size of which may be down to 10- centimeter or less. For example by pulverizing iron prepared in the said manner there may be obtained an iron powder the particle size of which is $4 millimeter or less.”
  • Magnetic substances prepared according to this invention are very suitable for the preparation of sound record carriers for electromagnetic sound recording and reproduction, for which purpose flnely divided magnetic metals are embedded in a non-magnetic supporting mass or are applied to the same. They are also suitable for other electromagnetic purposes, as for example for the preparation of mass cores for Pupin coils, induction coils and the like.
  • Example 1 From a solution containing 10 per cent of cobaltous chloride and 0.5 per cent of magnesium chloride, after the addition of a small amount of hydrazine, the hydroxides of cobalt and magnesium are precipitated by means of caustic soda solution. The precipitate is washed and dried and heated for, 2 hours at from 800 to 1000 C. and then cooled in an atmosphere of carbonv dioxide. The mixed crystals of cobalt oxide-and magnesium oxide thus formed are reduced at 400 C. with hydrogen. The reductionproduct is cooled in a stream of carbon dioxide to avoid spontaneous ignition and then ground for a long time in a ball mill. The particles 01' the cobalt-powder-containing magnesium oxide thus obtained have a size oi ,4 millimeter.
  • Example 2 40 kilograms of pig iron with an addition 01' 3 kilograms of lime are burnt in a stream of oxygen. After cooling, the'tused cake, consisting of mixed crystals of CaO.-Fez0s with F8304 in the spinel structure, is broken up into pieces of the size of nuts and reduced by means of hydrogen at a temperature of 600 C. An iron is thus obtained which contains CaO and a little unchanged CaOFezO; in fine, homogeneous distribution. The material is cooled in a, stream of nitrogen and comminuted to a fine powder, first in an edge mill and then in a ball mill.
  • Example 3 A mixture consisting of 94 per cent of iron powder, 2 per cent of aluminum powder and 4 per cent of calcium oxide is burnt in a stream of oxygen. After cooling, the fused cake, is broken up and reduced with hydrogen at 500 0. The
  • Example 4 A-solution 6:255 parts of potassium hydroxide; in 300i) parts of water'is'added to a solution of 145.4 parts of Ni (NO:)i.6Hand'404parts'of -Fe(NOa)a.9H:O in-1000 parts of .water; The mixture is boiled for 5 .minutes.
  • the precipitate thusproduced is washed with water and after drying heated for 4 hours at'750' C. 20 parts of parts of aluminum powder.
  • the process of producing magnetic substances in finely divided form which comprises simultaneously precipitating from a solution at least one hydroxide oi. a magnetic metal and smaller amounts of at least one additional hydroxide which when in oxidic state is capable of forming mixed crystals with the oxide oi the said magnetic metal, subjecting the precipitate to a heat treatment in order to produce the mixed crystals, reducing said oxide of a magnetic metal contained in the mixed crystals but not the additional oxidic substance and commlnuting the reduction product.
  • the process 01' producing magneticsubstances in finely divided form which comprises subjecting at least one magnetic metal together with smaller amounts oil at least one additional substance which, when in the oxidic 'form, is capable of forming mixed.- crystals with the oxide of the said metal, to an oxidizing fusion-subjecting the fusion product to such a reducing treatment as is sufiicient for: practically coinpletely reducing the oxide or the said magnetic metal contained in the fusion product, but insufiicient for reducing the oxidic iorm of the said additional substance, and ccmminuting the reduction product.

Description

Patented Nov. 14, 1939 'FINELY DIVIDED MAGNETIC SUBSTANCE Rudolf Brill and Karl Schoenemann, Heidelberg, Germany, amignorl. to I. G. Farbenindustrie Aktiengeaellachaft, on the Main,
Germany No Drawing. Application August 12 1937, Se-
Germany Septem rial No. 158,758. In 1935 4 Clalml. (CI. 75-55) The present invention relates to the production of magnetic substances in finely divided form the particles of which are characterized by a very small and uniform grain size.
We have found that magnetic substances of the said kind may be obtained by preparing mixed crystals from oxides of magnetic metals and oxidic additional substances capable of forming mixed crystals with the said oxides, reducing the resulting mixed crystals and then mechanically comminuting the reduction product, as for example in an edge mill or ball mill. By the term mixed crystals are commonly meant solid solutions in which the crystal lattice of one component contains one or more other components of the solid solution. An oxidic additional substances there are chosen such as are more diflicultly reducible than the employed oxides of magnetic metals. The oxides of the alkaline earth metals, including magnesium, or of aluminum or titanium, have proved especially suitable.
The presence of the additional substances in the form of mixed crystal components has the result that the magnetic substances, when being formed by the reduction of the mixed crystals, are produced and remain in a very finely crystallized state, because any rigid adhering together of the single small crystals and their recrystallization are prevented by the intercalation of the foreign substance.
According to our invention it is possible to produce for example finely divided powder of iron, nickel or the like and also powders of magnetic alloys, for example nickel-iron or nickeliron-cobalt, when employing mixtures of oxides of several magnetic metals. Such a mixture is NiO-FeO-CoO and a suitable oxidic additional substance to form mixed crystals together with the mixture is in this case MgO. As another suitable mixture which also yields a magnetic nickel-iron-cobalt alloy may be mentioned NiO.FB203F304CO304 and as additional substance A1203.
For the preparation of the mixed crystals it is preferable to start from a solution which contains a suitable compound both of the magnetic and the additional elements and to precipitate simultaneously the oxides of the magnetic metal and the oxidic additional substances. The obtained mixture is preferably subjected to a strong heat treatment in order to render the mixed crystal formation as complete as possible. In this manner a homogeneous mixed crystal is produced for example from the before-mentioned mixture NiO-FeO-CoO-MgO. By the following reduction which is preferably performed with hydrogen, a magnesium oxide containing nickel-iron-cobalt alloy is obtained.
Another method for the preparation of the mixed crystals consists in starting from the magnetic metals themselves and subjecting them after the addition of the foreign substances capable of forming mixed crystals, to an oxidizing fusion, the fused product then being reduced. By this method the above-mentioned aluminum oxide containing nickel-iron-cobalt alloy can be advantageously prepared. In most cases an addition of from 2 or5 to per cent of foreign substances is suillciezf. Also greater amounts may be used, but the I afford no particular advantages.
The metallic mass obtained by the reduction and comminution consists, even when the reduction has been effected at temperatures exceeding the recrystallization temperature of the magnetic metal, of very small crystallites the size of which may be down to 10- centimeter or less. For example by pulverizing iron prepared in the said manner there may be obtained an iron powder the particle size of which is $4 millimeter or less." 1
Magnetic substances prepared according to this invention are very suitable for the preparation of sound record carriers for electromagnetic sound recording and reproduction, for which purpose flnely divided magnetic metals are embedded in a non-magnetic supporting mass or are applied to the same. They are also suitable for other electromagnetic purposes, as for example for the preparation of mass cores for Pupin coils, induction coils and the like.
The following examples will further illustrate how the said invention may be carried out in practice, but the invention is not restricted to these examples.
Example 1 From a solution containing 10 per cent of cobaltous chloride and 0.5 per cent of magnesium chloride, after the addition of a small amount of hydrazine, the hydroxides of cobalt and magnesium are precipitated by means of caustic soda solution. The precipitate is washed and dried and heated for, 2 hours at from 800 to 1000 C. and then cooled in an atmosphere of carbonv dioxide. The mixed crystals of cobalt oxide-and magnesium oxide thus formed are reduced at 400 C. with hydrogen. The reductionproduct is cooled in a stream of carbon dioxide to avoid spontaneous ignition and then ground for a long time in a ball mill. The particles 01' the cobalt-powder-containing magnesium oxide thus obtained have a size oi ,4 millimeter.
Example 2 40 kilograms of pig iron with an addition 01' 3 kilograms of lime are burnt in a stream of oxygen. After cooling, the'tused cake, consisting of mixed crystals of CaO.-Fez0s with F8304 in the spinel structure, is broken up into pieces of the size of nuts and reduced by means of hydrogen at a temperature of 600 C. An iron is thus obtained which contains CaO and a little unchanged CaOFezO; in fine, homogeneous distribution. The material is cooled in a, stream of nitrogen and comminuted to a fine powder, first in an edge mill and then in a ball mill.
Example 3 A mixture consisting of 94 per cent of iron powder, 2 per cent of aluminum powder and 4 per cent of calcium oxide is burnt in a stream of oxygen. After cooling, the fused cake, is broken up and reduced with hydrogen at 500 0. The
reduction product is cooled in a stream of hydrogen, then for a short time treated with a stream. of carbon dioxideand finallycomminuted to 9. ill... powder as describedin Example 2. V
Example 4 A-solution 6:255 parts of potassium hydroxide; in 300i) parts of water'is'added to a solution of 145.4 parts of Ni (NO:)i.6Hand'404parts'of -Fe(NOa)a.9H:O in-1000 parts of .water; The mixture is boiled for 5 .minutes.
The precipitate thusproduced is washed with water and after drying heated for 4 hours at'750' C. 20 parts of parts of aluminum powder.
the obtained product whichvconsists of NiQFezOa, are mixed with parts of iron powder and 2 v The mixture is burnt in a stream of oxygen. The fused cake is then treated as described in Example 3. Thus an iron-nickel alloy with a nickel content of 5 per cent is obtained in the form ofa very finely divided powder."
1. The process of producing magnetic subreduced state.
2. The process of producing magnetic substances in finely divided form which comprises simultaneously precipitating from a solution at least one hydroxide oi. a magnetic metal and smaller amounts of at least one additional hydroxide which when in oxidic state is capable of forming mixed crystals with the oxide oi the said magnetic metal, subjecting the precipitate to a heat treatment in order to produce the mixed crystals, reducing said oxide of a magnetic metal contained in the mixed crystals but not the additional oxidic substance and commlnuting the reduction product.
3. The process 01' producing magneticsubstances in finely divided form which comprises subjecting at least one magnetic metal together with smaller amounts oil at least one additional substance which, when in the oxidic 'form, is capable of forming mixed.- crystals with the oxide of the said metal, to an oxidizing fusion-subjecting the fusion product to such a reducing treatment as is sufiicient for: practically coinpletely reducing the oxide or the said magnetic metal contained in the fusion product, but insufiicient for reducing the oxidic iorm of the said additional substance, and ccmminuting the reduction product. v
4. As a new article of manufacture magnetic substances especially suitable. tor; the manufacture of sound record cairierainqfinely divided form which have been prepared in accordance with'the process defined in claim 1.
' RUDQLF BRHL. 1
KARL SCHOENEMANN.
US158758A 1935-09-18 1937-08-12 Finely divided magnetic substance Expired - Lifetime US2179810A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2179810X 1935-09-18

Publications (1)

Publication Number Publication Date
US2179810A true US2179810A (en) 1939-11-14

Family

ID=7988821

Family Applications (1)

Application Number Title Priority Date Filing Date
US158758A Expired - Lifetime US2179810A (en) 1935-09-18 1937-08-12 Finely divided magnetic substance

Country Status (1)

Country Link
US (1) US2179810A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2497268A (en) * 1944-07-26 1950-02-14 Electro Chimie Metal Permanent magnets and method for the obtention of the same
US2531445A (en) * 1945-11-23 1950-11-28 Int Standard Electric Corp Manufacture of magnetic bodies from compressed powdered materials
US2575099A (en) * 1950-02-18 1951-11-13 Henry L Crowley & Company Inc Magnetic compositions
US2762700A (en) * 1949-08-23 1956-09-11 Richard J Brooks Production of ferrous chloride and metallic iron powder
US2783207A (en) * 1952-05-22 1957-02-26 Electro Chimie Metal Preparation of powders suitable for the manufacture of permanent magnets
US2873512A (en) * 1955-10-13 1959-02-17 Sprague Electric Co Ferro magnetic core materials and methods of producing same
US2970112A (en) * 1955-05-03 1961-01-31 Lignes Telegraphiques And Tele Ferromagnetic materials with rectangular hysteresis cycle and method for their manufacture
US2982731A (en) * 1957-06-13 1961-05-02 Sylvania Electric Prod Modified nickel ferrite

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2497268A (en) * 1944-07-26 1950-02-14 Electro Chimie Metal Permanent magnets and method for the obtention of the same
US2531445A (en) * 1945-11-23 1950-11-28 Int Standard Electric Corp Manufacture of magnetic bodies from compressed powdered materials
US2762700A (en) * 1949-08-23 1956-09-11 Richard J Brooks Production of ferrous chloride and metallic iron powder
US2575099A (en) * 1950-02-18 1951-11-13 Henry L Crowley & Company Inc Magnetic compositions
US2783207A (en) * 1952-05-22 1957-02-26 Electro Chimie Metal Preparation of powders suitable for the manufacture of permanent magnets
US2970112A (en) * 1955-05-03 1961-01-31 Lignes Telegraphiques And Tele Ferromagnetic materials with rectangular hysteresis cycle and method for their manufacture
US2873512A (en) * 1955-10-13 1959-02-17 Sprague Electric Co Ferro magnetic core materials and methods of producing same
US2982731A (en) * 1957-06-13 1961-05-02 Sylvania Electric Prod Modified nickel ferrite

Similar Documents

Publication Publication Date Title
US2736708A (en) Magnetic compositions
US2179810A (en) Finely divided magnetic substance
US2651105A (en) Manufacture of permanent magnets
JPS6036081B2 (en) Permanent magnets and their manufacturing method
US2463413A (en) Manufacture of permanent oxide magnets
US2734034A (en) Magnetic compositions
US2783207A (en) Preparation of powders suitable for the manufacture of permanent magnets
US1669648A (en) Magnetic material
US2445648A (en) Method of producing powdered metal
US2689168A (en) Production of gamma ferric oxide
US1878589A (en) Manufacture of nickel iron alloys
US5925166A (en) Process for obtaining iron or iron-based powders by organic liquid phase precipitation
JPH05271852A (en) Production of rare earth magnet alloy
US3306742A (en) Method of making a magnetic sheet
JPS5841727A (en) Manufacture of fine ferrite powder
US4865660A (en) Rare-earth element/cobalt type magnet powder for resin magnets
US2660522A (en) Method for the manufacture of permanent magnets
US2557059A (en) Method of concentrating the iron content of iron ores
US1739052A (en) Production of finely-divided metallic materials
JPS60114503A (en) Manufacture of processed product of mother alloy powder
JPH10261514A (en) Magnetic material
JP3796680B2 (en) Electromagnetic wave absorbing material
US2261425A (en) Method of making paramagnetic materials
US1747854A (en) Magnetic structure
JPS6131601B2 (en)