WO2004056508A1 - Composition pulverulente faiblement ferromagnetique comprenant des particules isolees et un lubrifiant selectionne dans un groupe comprenant des organo-silanes, -titanates, -aluminates et zirconates et son procede de production - Google Patents

Composition pulverulente faiblement ferromagnetique comprenant des particules isolees et un lubrifiant selectionne dans un groupe comprenant des organo-silanes, -titanates, -aluminates et zirconates et son procede de production Download PDF

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Publication number
WO2004056508A1
WO2004056508A1 PCT/SE2003/002067 SE0302067W WO2004056508A1 WO 2004056508 A1 WO2004056508 A1 WO 2004056508A1 SE 0302067 W SE0302067 W SE 0302067W WO 2004056508 A1 WO2004056508 A1 WO 2004056508A1
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WIPO (PCT)
Prior art keywords
composition according
group
iron
powder
compound
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PCT/SE2003/002067
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English (en)
Inventor
Mikhail Kejzelman
Björn SKARMAN
Paul Skoglund
Ola Andersson
Per Knutsson
Hilmar Vidarsson
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Höganäs Ab
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Filing date
Publication date
Application filed by Höganäs Ab filed Critical Höganäs Ab
Priority to JP2004562232A priority Critical patent/JP4886987B2/ja
Priority to BR0317661-4A priority patent/BR0317661A/pt
Priority to AT03781264T priority patent/ATE473064T1/de
Priority to MXPA05006847A priority patent/MXPA05006847A/es
Priority to EP03781264A priority patent/EP1575726B1/fr
Priority to DE60333309T priority patent/DE60333309D1/de
Priority to AU2003288880A priority patent/AU2003288880B8/en
Priority to CA2505381A priority patent/CA2505381C/fr
Publication of WO2004056508A1 publication Critical patent/WO2004056508A1/fr

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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
    • H01F1/147Alloys characterised by their composition
    • H01F1/14708Fe-Ni based alloys
    • H01F1/14733Fe-Ni based alloys in the form of particles
    • H01F1/14741Fe-Ni based alloys in the form of particles pressed, sintered or bonded together
    • H01F1/1475Fe-Ni based alloys in the form of particles pressed, sintered or bonded together the particles being insulated
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • B22F1/105Metallic powder containing lubricating or binding agents; Metallic powder containing organic material containing inorganic lubricating or binding agents, e.g. metal salts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/16Metallic particles coated with a non-metal
    • 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
    • H01F1/26Magnets 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus 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
    • H01F41/02Apparatus 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
    • H01F41/0206Manufacturing of magnetic cores by mechanical means
    • H01F41/0246Manufacturing of magnetic circuits by moulding or by pressing powder

Definitions

  • the present invention relates to new metal powder compositions. More specifically, the invention concerns a new iron-based powder which is useful for the preparation of soft magnetic materials having improved properties when used both at high and low frequencies . The invention also concerns a method for the manufacturing of soft magnetic composite materials prepared therefrom.
  • Soft magnetic materials are used for applications, such as core materials in inductors, stators and rotors for electrical machines, actuators, sensors and transformer cores.
  • soft magnetic cores such as rotors and stators in electric machines, are made of stacked steel laminates.
  • Soft Magnetic Composite, SMC materials are based on soft magnetic particles, usually iron- based, with an electrically insulating coating on each particle. By compacting the insulated particles optionally together with lubricants and/or binders using the traditionally powder metallurgy process, the SMC parts are obtained.
  • the SMC material can carry a three dimensional magnetic flux and as three dimensional shapes can be obtained by the compaction process.
  • Two key characteristics of an iron core component are its magnetic permeability and core loss characteristics.
  • the magnetic permeability of a material is an indication of its ability to become magnetised or its ability to carry a magnetic flux. Permeability is defined as the ratio of the induced magnetic flux to the magnetising force or field intensity.
  • the hysteresis loss is brought about by the necessary expenditure of energy to overcome the retained magnetic forces within the iron core component.
  • the eddy current loss is brought about by the production of electric currents in the iron core component due to the changing flux caused by alternating current (AC) conditions.
  • a high electrical resistivity of the component is desirable in order to minimise the eddy currents .
  • Desired component properties include e.g. a high permeability through an extended frequency range, low core losses, high saturation induction, and high strength. Normally an increased density of the component enhances all of these properties provided that a sufficient electrical resistivity can be maintained.
  • the desired powder properties include suitability for compression moulding techniques, which i.e. means that the powder can be easily moulded to a high density component, which can be easily ejected from the moulding equipment without damages on the component surface.
  • the present invention concerns a new ferromagnetic powder composition, which is suitable of compaction to high density composite components. More specifically the present invention concerns a powder composition comprising soft magnetic iron or iron-based core particles, the surface of which are surrounded by an electrically insulating in- organic coating and which composition also includes a lubricating amount of silanes, titanates, aluminates, or zirconates .
  • the present invention also includes a method of preparing high-density green, and optionally heat-treated, compacts from these compositions.
  • This method comprises the steps of providing the composition, optionally mixing said composition with additives, such as conventional lubricants (i.e. particular lubricants) and binders as well as flow- enhancing agents; uniaxially compacting in a die at high pressure and ejecting the green body, which may subsequently be heat-treated.
  • additives such as conventional lubricants (i.e. particular lubricants) and binders as well as flow- enhancing agents
  • the ferromagnetic powders used herein are made up of iron or an alloy containing iron optionally in combination with up to 20 % by weight of one or more of element selected from the group consisting of aluminium, silicon, chromium, niobium, molybdenum, nickel and cobalt.
  • the new powder is based on a base powder that consists of essentially pure iron.
  • This powder could be e.g. commercially available water-atomised or gas- atomised iron powders or reduced iron powders, such as sponge iron powders.
  • the powder particle shape could be round, irregular or flat.
  • Preferred electrically insulating coatings which may be used according to the invention, are thin phosphorous containing coatings of the type described in the US patent 6348265 which is hereby incorporated by reference. Also other, preferably inorganic coatings may be used, for example coatings based on Cr, Mg, Mo, Zn, Ni, or Co.
  • the lubricating agent used according to the invention is a type of organo-silanes, organo-titanates, organo- aluminates or organo-zirconates .
  • This class of substances is often referred to as surface modifying agents, coupling agents, or cross-linking agents depending on the chemical functionality of their linked groups.
  • the specific type of organo-silanes, organo- titanates, or ' gano-aluminates or organo-zirconates which are used according to the present invention and which may be referred to as organo-metallic compounds are distinguished by the presence of at least one hydrolysable group and at least one lubricating organic moiety. This type of compounds can be defined by the following general formula:
  • M is a central atom selected from Si, Ti, Al, and Zr; Ri is a hydrolysable group; R 2 is a group consisting of a lubricating organic moiety; wherein the sum of m+n must equal the coordination number of the central atom and where n is an integer >1 and m is an integer >1.
  • Ri is an alkoxy group having less than 12 C atoms. Preferred are those alkoxy groups, which have less than 6, and most preferred are alkoxy groups having 1-3 C atoms.
  • R may also be a chelate group, such as a residue of hydroxyacetic acid (-0C (0) ) -CH 2 0-) or a residue of ethylene glycol (-OCH 2 CH 2 0-) .
  • R 2 is an organic group including between 6-30, preferably 10-24 carbon atoms optionally including one or more hetero atoms selected from the group consisting of N, 0, S and P.
  • R 2 is a group consisting of an organic moiety, which is not easily hydrolysed and often lipophilic and can be a chain of an alkyl, ether, ester, phospho-alkyl, phospho-alkyl, phospho-lipid, or phospho-amine .
  • the phosphorous may be present as phosphato, pyrophosphato, or phosphito groups.
  • R 2 may be linear, branched, cyclic, or aromatic.
  • a preferred group of lubricating silanes according to the present invention are alkyl-alkoxy silanes and polyether- alkoxy silanes. Furthermore, promising results have been obtained with hexadecyl-trimethoxy silane, isopropyl- triisostearyl titanate, isopropyl-tri (dioctyl) phosphato titanate, neopentyl (diallyl) oxy-tri (dioctyl) hosphato zirconate, neopentyl (diallyl) oxy-trineodecanoyl zirconate, and diisobutyl-acetoacetyl aluminate .
  • the amount of the compound is preferably present in amounts above 0.05%, such as in amounts of 0.05-0.5%, preferably 0.07-0.45%, and most preferably 0.08-0.4% by weight of the composition.
  • a too low amount of lubricating agent gives high density but results in poor ejection behaviour and may thus result in poor surface condition of the tool and/or SMC parts.
  • a too high amount may give excellent ejection behaviour but could render in low component densities.
  • the compound is present as a lubricating layer on the insulated particles . It should, however, be noted that the geometry of the component as well as the material and quality of the tool, have great impact on the surface condition of the SMC parts after ejection.
  • organo-silanes organo-titanates, or organo-aluminates
  • US patents 4820338 and 6537389 silanes, titanates or aluminates are used in order to accelerate a coupling between the magnetic powder particles and an electrically insulating organic binder polymer.
  • the powder particles do not have an inorganic coating.
  • the US patent 6537389 discloses a wide range of silicon-, aluminium-, or boron-containing compounds as molecular precursors for producing electrically insulating ceramics on soft magnetic powders.
  • the precursor compounds are converted by thermal treatments into ceramic, metallic or intermetallic end products to enhance temperature and solvent resistance.
  • the US patent 6537389 distinguishes from the present invention i.a. in that the organo- metallic compounds are used as precursors for producing chemically and thermally resistant coatings, and not as the key component that facilitates production of high density parts.
  • the precursor compounds described in the examples of US patent 6537389 do not include a lubricating moiety.
  • the lubricating compound (s) used according to the present invention can be used in such a way that it is dissolved or dispersed in a suitable solvent, e.g. an organic sol- vent, such as acetone or ethanol .
  • a suitable solvent e.g. an organic sol- vent, such as acetone or ethanol .
  • the obtained solution or dispersion is subsequently added to the iron based powder during mixing and optionally heating.
  • the solvent is finally evaporated optionally in vacuum.
  • the powder used has coarse particles i.e. the powder is essentially without fine particles.
  • the term "essentially without fine particles" is intended to mean that less than about 5 % of the iron or iron-based powder particles have size below 45 ⁇ m as measured by the method described in SS-EN
  • the term "essentially consisting” is intended to mean that at least 40 %, preferably at least 60 % of the particles have a particle size above 106 and 212 ⁇ m, respectively. So far the best results have been obtained with powders having an average particle size about 250 ⁇ m and only less than 3 % below 106 ⁇ m. The maximum particle size may be about 5 mm.
  • the particle size distribution for iron-based powders used at PM manufacturing is normally distributed with a Gaussian distribution with an average particle diameter in the region of 30 to 100 ⁇ m and about 10-30% less than 45 ⁇ m. Iron based powders essentially free from fine particles may be obtained by removing the finer fractions of the powder or by manufacturing a powder having the desired particle size distribution .
  • the iron or iron-based powder must not be mixed with a separate (particular) lubricant before it is transferred to the die.
  • external lubrication die wall lubrication
  • the invention does not exclude the possibility of, when it is of interest, to utilise conventional internal lubrication (in an amount up to 0.5% by weight), external lubrication or a combination of both.
  • the powder to be compacted may also include additives selected from the group consisting of binders, lubricants, and flow- enhancing agents.
  • additives selected from the group consisting of binders, lubricants, and flow- enhancing agents.
  • inorganic lubricants which may be used in addition to organic PM lubricants, are hexagonal boron nitride, and MoS 2 .
  • soft magnetic composite materials having a density of at least 7.45 g/cm 3 can be prepared by uniaxially compacting the new powder cor ⁇ - positions in a die at high compaction pressures and without die wall lubrication.
  • the green body When the green body has been ejected from the compaction tool it can be heat treated up to temperatures of about 700°C.
  • At high compaction pressure is intended to mean at pressures of about at least 800 MPa. More interesting results are obtained with higher pressures such as pressures above 900, more preferably above 1000, and most preferably above 1100 MPa.
  • Conventional compaction at high pressures, i.e. pressures above about 800 MPa, with conventionally used powders including finer particles are generally considered unsuitable due to the high forces required in order to eject the compacts from the die, the accompanying high wear of the die, and the fact that the surfaces of the components tend to be less shiny or dete- riorated. High electrical resistance can be obtained even though high compaction pressures are used to achieve the high density.
  • the ejection force is reduced at high pressures of about 1000 MPa, and that components having acceptable or even perfect surfaces may be obtained.
  • the compaction may be performed with standard equipment, which means that the new method may be performed without expensive investments.
  • the compaction is performed uni- axially and preferably in a single step at ambient or elevated temperature.
  • the compaction may be performed with the aid of a percussion machine (Model HYP 35-4 from Hydropulsor) as described in patent publication WO 02/38315.
  • the heat treatment may be performed at the temperatures normally used, e.g. up to temperatures of about 700°C in different types of atmospheres or at reduced pressure and optionally in the presence of steam. Prior to the heat treatment the pressed components may optionally be green machined and/or cleaned.
  • a main object of the present invention is to achieve high density products and to this end it is preferred to use coarse powders as described above. It has, however, also been found that these lubricating effects can also be obtained in combination with powders including higher amounts of fine particles i.e. the type of powders which are conventionally used in the PM industry today.
  • Example 3 and 5 below illustrates the lubricating effect of the organo-metallic compounds according to the present invention on both conventional powders and coarse powders . As can be observed high densities are obtained also with a conventional powder including higher amounts of fine particles.
  • Compositions including iron or iron- based powders with the particle size distributions which are normally used today and the lubricating agents according to the present invention may be of special interest for certain applications and are therefore also within the scope of the invention.
  • high density is intended to mean compacts having a density of about at least 7.45 g/cm 3 .
  • “High density” is not an absolute value.
  • a typical achievable density according to the state of the art for single heat-treated, single pressed components is about 7.2 g/cm 3 .
  • warm compaction an increase of about 0.2 g/cm 3 may be reached.
  • high density is intended to mean compacts having a density of about 7.45-7.65 g/cm 3 and above, depending on type and amount of additives used, and type of iron-based powder used. Components having lower densities can of course also be produced but are believed to be of less interest.
  • the advantage obtained by using the powder and method according to the present invention is that high- density SMC parts can be cost-efficiently produced. SMC parts with remarkably high magnetic induction levels together with low core losses can be obtained.
  • Other advantages are that the mechanical strength after heat treatment is increased and that, in spite of very high densities, compacted parts with high electrical resistance can be successfully ejected from the dies without negatively influence the finish of the die walls and/or on the surfaces of the compacted SMC parts. It is thus possible to obtain parts having excellent surface finish. These results can be obtained with a single compaction step. Examples of products of special interest for the new powder compacts are inductors, stators and rotors for electrical machines, actuators, sensors and transformer cores.
  • An iron-based water atomised powder (Somaloy 550TM, available from Hoganas AB, Sweden) was used as starting material. This powder has an average particle size between 212 and 425 ⁇ m and less than 5% of the particles have a particle size below 45 ⁇ m.
  • This powder which is a pure iron powder, the particles of which are electrically insulated by a thin phosphorus containing barrier, was treated with 0.2% by weight of a hexadecyl-trimethoxy silane as a lubricating agent.
  • the addition of the lubricating agent was performed as follows : hexadecyl- trimethoxy silane was diluted in ethanol to a 20% solution by weight and the solution was stirred during 60 minutes.
  • Rings with an inner diameter of 47 mm and an outer diameter of 55 mm and a height of 4 mm were uniaxially compacted in a single step at different compaction pressures 800, 1000 and 1200 MPa, respectively.
  • compaction pressures 800, 1000 and 1200 MPa respectively.
  • the green density is significantly higher for the powder according to the invention and magnetic properties are, hence, improved compared with the materials used in the comparative examples.
  • the comparative example also demonstrates that no or only minor improvements of the magnetic properties can be obtained by increasing the compaction pressure to 1000 MPa and 1200 MPa.
  • a very high purity water atomised iron-based powder the particles of which were provided with a thin insulating coating and which had a mean particle size above 212 ⁇ m was treated with 0.1% and 0.2% of hexadecyl- trimethoxysilane, respectively, according to the procedure in Example 1.
  • the same iron-based powder without any lubricating agent was used as a reference.
  • Cylindrical samples with a diameter of 25 mm and a height of 4 mm were compacted in an uniaxially press movement at a compaction pressure of 1000 MPa.
  • Table 2 shows the ejection energy needed for ejecting the components and the green density obtained.
  • the ejection energy is expressed as percentage of the ejection energy for the sample without lubricating agent.
  • the S-powder has about 14 % of the particles less than 45 ⁇ m and a weight average particle size of about 100 ⁇ m.
  • the C-powder has a significantly coarser particle size distribution with a weight average size of about 250 ⁇ m and less than 3% below 106 ⁇ m.
  • A-E Five different kinds of organo-silanes were used (A-E) : A Methyl-trimethoxy silane B Propyl-trimethoxy silane C Octyl-trimethoxy silane D Hexadecyl-trimethoxy silane E Polyethyleneether-trimethoxy silane with 10 ethylene ether groups
  • lubricant agent optionally mixed with conventionally used i.e. particular lubricants, can be of interest for some applications .
  • This example demonstrates the lubrication effect of organo-metallic compounds with different central atoms.
  • the lubrication effect of four different agents have been examined i.e. silane, titanate, zirconate and aluminate, having Si, Ti, Zr and Al as the central atom, respectively.
  • the various central atoms have different coordination numbers and chemical properties.
  • the chemical structure of the organo-metallic compound was selected so that the chain length of the lubricating group or groups (R 2 ) would 'show comparable properties which can be compared with those obtained with hexadecyl-trimethoxy silane (D) .
  • a high purity water atomised iron-based powder with a thin insulating coating were treated with 0.2% by weight of each organo-metallic compound as lubricating agent.
  • the obtained mixtures were compacted at 1100 MPa in a uniaxial press movement into slugs with a diameter of 25 mm and a height of 12 mm.
  • the dynamic ejection force per unit sliding area was measured and after ejection green surface finish was evaluated and density was measured as is shown below in table 4.
  • A-D organo-metallic agents
  • Cylindrical samples with a diameter of 25 mm and a weight of 50 grams were compacted in an uniaxially press move- ment at a compaction pressure of 1000 MPa and green densities above 7.6 g/cm 3 for all the samples were obtained.
  • This example illustrates the importance of the inorganic insulation.
  • a high purity iron powder the particles of which are electrically insulated by a thin phosphorus-containing barrier was compared with an identical powder without the phosphorous-based inorganic insulation. Both types of powders were subsequently treated with 0.2% by weight of hexadecyl-trimethoxy silane as a lubricating agent according to the invention.
  • Rings with an inner diameter of 45 mm and an outer diameter of 55 mm and a height of 5 mm were uniaxially compacted in a single step at compaction pressure 1100 MPa. After compaction the parts were heat treated at 500°C for 30 minutes in air. The electrical resistivity was measured by the four-point method.
  • the following table 6 shows electrical resistivity and density of composite components prepared of powders with and without insulated particles.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Electromagnetism (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Soft Magnetic Materials (AREA)
  • Powder Metallurgy (AREA)
  • Lubricants (AREA)
  • Silicon Polymers (AREA)

Abstract

La présente invention concerne une nouvelle composition pulvérulente ferromagnétique comprenant des particules possédant un noyau à base de fer faiblement ferromagnétique dont la surface est recouverte d'un enrobage non organique isolant, et un composé lubrifiant sélectionné dans le groupe comprenant des silanes, des titanates, des aluminates, des zirconates, ou des mélanges de ces derniers. L'invention concerne également un procédé destiné à la préparation de substances composites faiblement ferromagnétiques, utilisant cette nouvelle composition pulvérulente.
PCT/SE2003/002067 2002-12-23 2003-12-22 Composition pulverulente faiblement ferromagnetique comprenant des particules isolees et un lubrifiant selectionne dans un groupe comprenant des organo-silanes, -titanates, -aluminates et zirconates et son procede de production WO2004056508A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP2004562232A JP4886987B2 (ja) 2002-12-23 2003-12-22 絶縁粒子と、有機シラン、有機チタネート、有機アルミネート、及び有機ジルコネートから選択された潤滑剤とを含む軟磁性粉末組成物、並びにその調製方法
BR0317661-4A BR0317661A (pt) 2002-12-23 2003-12-22 Composição magnética macia em pó compreendendo partìculas isoladas e um lubrificante selecionado de organo-silanos, organo-titanatos, organo-aluminatos e organo-zirconatos e processo para preparação da mesma
AT03781264T ATE473064T1 (de) 2002-12-23 2003-12-22 Weichmagnetische pulverzusammensetzung mit isolierten teilchen und schmiermittel, ausgewählt aus organosilanen, -titanaten, -aluminaten und zirkonaten und verfahren für ihre herstellung
MXPA05006847A MXPA05006847A (es) 2002-12-23 2003-12-22 Composicion en polvo magnetica suave que comprende particulas aisladas y un lubricante seleccionado de organosilanos, titanatos, aluminatos y zirconatos y un procedimiento para su preparacion.
EP03781264A EP1575726B1 (fr) 2002-12-23 2003-12-22 Composition pulverulente faiblement ferromagnetique comprenant des particules isolees et un lubrifiant selectionne dans un groupe comprenant des organo-silanes, -titanates, -aluminates et zirconates et son procede de production
DE60333309T DE60333309D1 (de) 2002-12-23 2003-12-22 Weichmagnetische pulverzusammensetzung mit isolierten teilchen und schmiermittel, ausgewählt aus organosilanen, -titanaten, -aluminaten und zirkonaten und verfahren für ihre herstellung
AU2003288880A AU2003288880B8 (en) 2002-12-23 2003-12-22 Soft magnetic powder composition comprising insulated particles and a lubricant selected from organo-silanes, -titanates, -aluminates and zirconates and a process for their preparation
CA2505381A CA2505381C (fr) 2002-12-23 2003-12-22 Composition pulverulente faiblement ferromagnetique comprenant des particules isolees et un lubrifiant selectionne dans un groupe comprenant des organo-silanes, -titanates, -aluminates et zirconates et son procede de production

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0203851-1 2002-12-23
SE0203851A SE0203851D0 (sv) 2002-12-23 2002-12-23 Iron-Based Powder

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WO2004056508A1 true WO2004056508A1 (fr) 2004-07-08

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EP (1) EP1575726B1 (fr)
JP (2) JP4886987B2 (fr)
KR (1) KR101035757B1 (fr)
CN (1) CN100548541C (fr)
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009116938A1 (fr) * 2008-03-20 2009-09-24 Höganäs Ab (Publ) Composition de poudre ferromagnétique, et procédé de production correspondant
WO2011101276A1 (fr) * 2010-02-18 2011-08-25 Höganäs Ab Composition de poudre ferromagnétique et procédé de production associé
EP2966654A4 (fr) * 2013-03-08 2016-12-14 Ntn Toyo Bearing Co Ltd Poudre pour noyau magnétique ainsi que noyau en poudre, et procédés de fabrication de ceux-ci
CN113066630A (zh) * 2019-12-12 2021-07-02 株式会社村田制作所 软磁性材料和压粉成型体
US11948714B2 (en) 2019-12-12 2024-04-02 Murata Manufacturing Co., Ltd. Soft magnetic material and green compact

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0203851D0 (sv) * 2002-12-23 2002-12-23 Hoeganaes Ab Iron-Based Powder
EP2139630B1 (fr) * 2007-03-21 2013-05-15 Höganäs Ab (publ) Composites de polymères et de métal en poudre
JP5482097B2 (ja) * 2009-10-26 2014-04-23 Tdk株式会社 軟磁性材料、並びに、圧粉磁芯及びその製造方法
AT12021U1 (de) * 2010-04-14 2011-09-15 Plansee Se Beschichtungsquelle und verfahren zu deren herstellung
CN101982856B (zh) * 2010-09-21 2012-02-15 李延军 笔杆式汽车点火线圈内用软磁铁芯及其制作方法
CN102136330A (zh) * 2011-04-01 2011-07-27 钢铁研究总院 一种复合软磁材料及其制备方法
EP2509081A1 (fr) * 2011-04-07 2012-10-10 Höganäs AB Nouvelle composition et procédé
CN102909373A (zh) * 2012-09-15 2013-02-06 安徽省怀远县尚冠模具科技有限公司 一种模具冲压顶杆的制备方法
CN102896315B (zh) * 2012-09-15 2015-04-01 安徽省怀远县尚冠模具科技有限公司 一种模具上压板的制备方法
CN104217834B (zh) * 2013-06-03 2018-01-23 株式会社田村制作所 软磁性粉末组合物、芯、电抗器
CN105149601A (zh) * 2015-09-29 2015-12-16 四川有色金源粉冶材料有限公司 一种高比重合金喂料的制备方法
CN105108166B (zh) * 2015-09-29 2017-06-06 四川有色金源粉冶材料有限公司 一种注射成型用铁基合金粉末的制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4475946A (en) * 1982-09-08 1984-10-09 Fuji Photo Film Co., Ltd. Ferromagnetic metal particles of iron alloyed with Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Si, P, Mo, Sn, Sb and Ag coated with mono- or dialkoxysilanes
EP0205786A1 (fr) * 1985-06-26 1986-12-30 Kabushiki Kaisha Toshiba Noyau magnétique et procédé de fabrication
US4820338A (en) * 1983-11-16 1989-04-11 Kabushiki Kaisha Toshiba Magnetic powder composition
US5277980A (en) * 1988-06-07 1994-01-11 Matsushita Electric Industrial Co., Ltd. Mass of fine particles of inorganic material and a film of the fine inorganic particles
WO2001024205A1 (fr) * 1999-09-28 2001-04-05 Tokin Corporation Feuille magnetique composite et procede de fabrication correspondant

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002015912A (ja) * 2000-06-30 2002-01-18 Tdk Corp 圧粉磁芯用粉末及び圧粉磁芯
SE0203851D0 (sv) * 2002-12-23 2002-12-23 Hoeganaes Ab Iron-Based Powder
US20060096406A1 (en) * 2004-11-08 2006-05-11 Yao-Huang Liu Gear lever having a light emitting effect

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4475946A (en) * 1982-09-08 1984-10-09 Fuji Photo Film Co., Ltd. Ferromagnetic metal particles of iron alloyed with Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Si, P, Mo, Sn, Sb and Ag coated with mono- or dialkoxysilanes
US4820338A (en) * 1983-11-16 1989-04-11 Kabushiki Kaisha Toshiba Magnetic powder composition
EP0205786A1 (fr) * 1985-06-26 1986-12-30 Kabushiki Kaisha Toshiba Noyau magnétique et procédé de fabrication
US5277980A (en) * 1988-06-07 1994-01-11 Matsushita Electric Industrial Co., Ltd. Mass of fine particles of inorganic material and a film of the fine inorganic particles
WO2001024205A1 (fr) * 1999-09-28 2001-04-05 Tokin Corporation Feuille magnetique composite et procede de fabrication correspondant

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009116938A1 (fr) * 2008-03-20 2009-09-24 Höganäs Ab (Publ) Composition de poudre ferromagnétique, et procédé de production correspondant
US20110006246A1 (en) * 2008-03-20 2011-01-13 Hoganas Ab (Publ) Ferromagnetic powder composition and method for its production
CN101977712A (zh) * 2008-03-20 2011-02-16 霍加纳斯股份有限公司 铁磁粉末组合物及其制造方法
US8236420B2 (en) 2008-03-20 2012-08-07 Höganäs Ab (Publ) Ferromagnetic powder composition and method for its production
US20120292555A1 (en) * 2008-03-20 2012-11-22 Hoganas Ab (Publ) Ferromagnetic powder composition and method for its production
US8647743B2 (en) 2008-03-20 2014-02-11 Hoganas Ab (Publ) Ferromagnetic powder composition and method for its production
RU2510993C2 (ru) * 2008-03-20 2014-04-10 Хеганес Аб (Пабл) Порошковая ферромагнитная композиция и способ ее получения
WO2011101276A1 (fr) * 2010-02-18 2011-08-25 Höganäs Ab Composition de poudre ferromagnétique et procédé de production associé
US10741316B2 (en) 2010-02-18 2020-08-11 Höganäs Ab (Publ) Ferromagnetic powder composition and method for its production
EP2966654A4 (fr) * 2013-03-08 2016-12-14 Ntn Toyo Bearing Co Ltd Poudre pour noyau magnétique ainsi que noyau en poudre, et procédés de fabrication de ceux-ci
CN113066630A (zh) * 2019-12-12 2021-07-02 株式会社村田制作所 软磁性材料和压粉成型体
US11948714B2 (en) 2019-12-12 2024-04-02 Murata Manufacturing Co., Ltd. Soft magnetic material and green compact

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AU2003288880A1 (en) 2004-07-14
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PL376102A1 (en) 2005-12-12
KR101035757B1 (ko) 2011-05-20
CA2505381A1 (fr) 2004-07-08
CN1732059A (zh) 2006-02-08
CN100548541C (zh) 2009-10-14
CA2505381C (fr) 2011-12-13
EP1575726B1 (fr) 2010-07-07
ATE473064T1 (de) 2010-07-15
TW200422122A (en) 2004-11-01
JP4886987B2 (ja) 2012-02-29

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