WO2013031243A1 - 磁性材料およびコイル部品 - Google Patents
磁性材料およびコイル部品 Download PDFInfo
- Publication number
- WO2013031243A1 WO2013031243A1 PCT/JP2012/050058 JP2012050058W WO2013031243A1 WO 2013031243 A1 WO2013031243 A1 WO 2013031243A1 JP 2012050058 W JP2012050058 W JP 2012050058W WO 2013031243 A1 WO2013031243 A1 WO 2013031243A1
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- Prior art keywords
- magnetic material
- metal particles
- particles
- oxide
- bonds
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Images
Classifications
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- 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
-
- 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
- H01F1/147—Alloys characterised by their composition
- H01F1/14766—Fe-Si based alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/33—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials mixtures of metallic and non-metallic particles; metallic particles having oxide skin
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F17/00—Fixed inductances of the signal type
- H01F17/0006—Printed inductances
- H01F17/0033—Printed inductances with the coil helically wound around a magnetic core
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F17/00—Fixed inductances of the signal type
- H01F17/04—Fixed inductances of the signal type with magnetic core
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F27/00—Details of transformers or inductances, in general
- H01F27/24—Magnetic cores
- H01F27/255—Magnetic cores made from particles
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F17/00—Fixed inductances of the signal type
- H01F17/04—Fixed inductances of the signal type with magnetic core
- H01F2017/048—Fixed inductances of the signal type with magnetic core with encapsulating core, e.g. made of resin and magnetic powder
Definitions
- the present invention relates to a magnetic material that can be used mainly as a core in a coil, an inductor, and the like, and a coil component using the magnetic material.
- a coil component such as an inductor, a choke coil, or a transformer has a magnetic material and a coil formed inside or on the surface of the magnetic material.
- Ferrite such as Ni—Cu—Zn ferrite is generally used as the material of the magnetic material.
- this type of coil component is required to have a large current (high rated current).
- a soft magnetic alloy such as an Fe—Cr—Si alloy or an Fe—Al—Si alloy from the conventional ferrite.
- the density is higher than ferrite.
- the volume resistivity of the material itself is much lower than conventional ferrite.
- Patent Document 1 discloses a composite magnetic material using particles made of an Fe—Al—Si alloy with an alumina coating formed around it.
- Patent Document 2 discloses a composite magnetic body that includes a metal magnetic powder and a thermosetting resin, and the metal magnetic powder is present at a predetermined filling rate.
- An object of the present invention is to provide a magnetic material that is formed of a soft magnetic alloy particle compact and can improve mechanical strength, and a coil component that uses the magnetic material.
- the magnetic material of the present invention comprises a particle compact formed by molding metal particles having an oxide film.
- the metal particles are made of a Fe-Si-M soft magnetic alloy (where M is a metal element that is more easily oxidized than iron).
- the metal particles in the particle molded body are bonded to each other by the bonding between the metal particles adjacent to each other and the oxide films of the respective metal particles.
- At least a part of the bonds between the oxide films is a bond made of a crystalline oxide, and preferably at least a part of the bond made of the crystalline oxide is continuously lattice-bonded.
- the bonds between the oxide films are generated by heat treatment.
- various coil components using the magnetic material as an element body are provided.
- a magnetic material having high strength can be obtained.
- the bonds include oxides that are continuously lattice-bonded, the strength can be further improved.
- FIG. 1A is a cross-sectional view schematically showing the fine structure of the magnetic material of the present invention.
- FIG. 1B is a partially enlarged view of FIG. It is a schematic cross section of the multilayer inductor as a coil component. It is a typical exploded view of a multilayer inductor. It is a powder X-ray-diffraction pattern of the particle compact obtained in the Example.
- the magnetic material is formed of a particle compact obtained by molding predetermined particles.
- the magnetic material is an article that plays the role of a magnetic path in a coil component such as a coil / inductor, and typically takes the form of a core or the like in the coil component.
- FIG. 1 is a sectional view schematically showing the fine structure of the magnetic material of the present invention.
- the particle compact 1 is microscopically grasped as an aggregate formed by combining a large number of metal particles 11 that were originally independent.
- the individual metal particles 11 are formed with an oxide film 12 over almost the entire periphery thereof, and the insulating properties of the particle molded body 1 are ensured by the oxide film 12.
- Adjacent metal particles 11 constitute a particle compact 1 having a certain shape mainly by bonding oxide films 12 around each metal particle 11 to each other. In part, metal portions of adjacent metal particles 11 may be bonded to each other.
- the particle molded body 1 is substantially free of a matrix made of an organic resin and a matrix made of a glass component.
- the oxide film 12 formed over almost the whole of the individual metal particles 11 may be formed at the stage of raw material particles before forming the particle molded body 1.
- an oxide film may be generated in the molding process using raw material particles that do not have an oxide film or have very few.
- the presence of the oxide film 12 can be recognized as a difference in contrast (brightness) in a photographed image of about 3000 times by a scanning electron microscope (SEM).
- SEM scanning electron microscope
- the bonds between the particles are mainly bonds 22 between the oxide films 12.
- the presence of the bonds 22 between the oxide films 12 can be clearly seen, for example, by visually confirming that the oxide films 12 of the adjacent metal particles 11 are in the same phase in an SEM observation image magnified about 3000 times. Judgment can be made.
- the presence of the bond 22 between the oxide coatings 12 improves the mechanical strength and insulation.
- At least some of the many bonds 22 present in the particle molded body 1 are made of a crystalline oxide.
- the presence of the crystalline oxide as well as the bonding 22 between the oxide films 12 becomes stronger, and as a result, the strength of the particle compact 1 can be improved. . *
- the bond 22 between the oxide coatings 12 is an oxide having crystallinity means that, for example, an X-ray diffraction pattern of the particle compact 1 is acquired and a diffraction peak of the corresponding crystalline oxide exists. It can be specified by confirming.
- the bonds 22 present in the particle compact 1 are made of a crystalline oxide that is continuously lattice-bonded.
- FIG. 1B the continuous lattice coupling in the coupling 22 is emphasized and depicted.
- Continuous lattice bonding means that when the oxide film 12 of each adjacent metal particle 11 forms the bond 22, the end of one metal particle 11 in the bond 22 extends to the end of the other metal particle 11. It means that there is a crystal lattice. In other words, when the oxide films 12 respectively covering the adjacent metal particles 11 form the bond 22, the two metal particles 11 are not integrated crystallographically only in the vicinity of the bond point but in a wider area.
- the oxide film 12 possessed by is integrated crystallographically to form a bond 22.
- the presence of continuous lattice bonding in this way can improve the strength of the particle compact 1 more effectively.
- the existence of the continuous lattice coupling is, for example, by visually recognizing a striped pattern integral with the coupling 22 in a bright field image of STEM (approximately 10,000 times) as schematically depicted in FIG. Can be confirmed. *
- the oxide coatings 12 of the adjacent metal particles 11 are bonded to each other over the entire particle molded body 1.
- Such a form is also one embodiment of the present invention.
- a bond (not shown) between the metal particles 11 may exist without passing through a bond between the oxide films 12.
- the adjacent metal particles 11 may partially have a form in which neither the oxide coatings 12 nor the metal particles 11 are bonded to each other and merely physically contacted or approached.
- a heat treatment is performed at a predetermined temperature, which will be described later, in an atmosphere in which oxygen is present (eg, in the air) when the particle molded body 1 is manufactured.
- the oxide film 12 is generated by the heat treatment, so that the oxide film 12 can easily form the bonds 22 having continuous lattice bonds.
- the metal portion at the stage of the raw material particles is oxidized by heat treatment to form the oxide film 12, whereby the bonds 22 having continuous lattice bonds can be easily formed. Become. *
- the bonds 22 between the oxide films 12 may exist in the particle molded body 1.
- the bonds 22 between the oxide films 12 described above for example, in an SEM observation image magnified about 3000 times, it is visually recognized that adjacent metal particles 11 have bonding points while maintaining the same phase. Thus, the presence of a metal bond can be clearly determined. The magnetic permeability can be further improved by the presence of the metal bond.
- particles having a small oxide film are used as the raw material particles, the temperature and the oxygen partial pressure are adjusted as described later in the heat treatment for manufacturing the particle compact 1, or the raw material particles Adjusting the molding density at the time of obtaining the particle compact 1 from the above.
- Each metal particle 11 is mainly composed of a specific soft magnetic alloy.
- the metal particles 11 are made of a Fe—Si—M soft magnetic alloy.
- M is a metal element that is easier to oxidize than iron, and typically includes chromium, aluminum, titanium, and the like, preferably chromium or aluminum.
- the metal particles are relatively soft, so that the molding density can be increased by deformation of the particles. Moreover, this can produce many bonds between oxide films.
- the Si content in the Fe—Si—M soft magnetic alloy is preferably 0.5 to 7.0 wt%, and more preferably 2.0 to 5.0 wt%.
- a high Si content is preferable in terms of high resistance and high magnetic permeability, and a low Si content is based on good moldability.
- the chromium content in the Fe—Si—M soft magnetic alloy is preferably 2.0 to 15 wt%, and more preferably 3.0 to 6.0 wt%.
- the presence of chromium reduces the magnetic properties before heat treatment, which is a physical property of raw material particles, but suppresses excessive oxidation during heat treatment. Therefore, when there is much Cr, the effect of increasing the magnetic permeability by heat treatment is increased, and the specific resistance after heat treatment is lowered. In consideration of these, the preferred range is proposed. *
- the content of aluminum in the Fe—Si—M soft magnetic alloy is preferably 2.0 to 15 wt%, and more preferably 3.0 to 6.0 wt%.
- the presence of aluminum is preferable in that it forms a passive state during heat treatment to suppress excessive oxidation and develop strength and insulation resistance.
- the amount of aluminum is small. The above preferable range is proposed in consideration of the above. Note that the preferable content of each metal component in the Fe—Si—M soft magnetic alloy is described assuming that the total amount of the alloy components is 100 wt%. In other words, the composition of the oxide film is excluded from the calculation of the preferable content.
- the remainder other than Si and metal M is preferably iron except for inevitable impurities.
- metals that may be contained other than Fe, Si, and M include manganese, cobalt, nickel, and copper.
- the chemical composition of the alloy constituting each metal particle 11 in the particle compact 1 is obtained, for example, by photographing a cross section of the particle compact 1 using a scanning electron microscope (SEM) and analyzing the composition by energy dispersive X-ray analysis ( EDS) can be calculated by the ZAF method.
- SEM scanning electron microscope
- EDS energy dispersive X-ray analysis
- the size of the individual raw material particles is substantially equal to the size of the metal particles constituting the particle compact 1 in the finally obtained magnetic material.
- d50 is preferably 2 to 30 ⁇ m, more preferably 2 to 20 ⁇ m, and further preferably 3 to 13 ⁇ m in consideration of the magnetic permeability and the intra-granular eddy current loss.
- the d50 of the raw material particles can be measured by a measuring device using laser diffraction / scattering. *
- the raw material particles are preferably particles produced by an atomizing method. As described above, in forming the bond 22 via the oxide film 12 in the particle molded body 1, it is preferable that the portion that was a metal in the raw material particle stage is oxidized by heat treatment. Therefore, an oxide film may be present on the raw material particles, but it is preferable that the raw material particles do not exist excessively. Examples of means for reducing the oxide film of the raw material particles include subjecting the raw material particles to a heat treatment in a reducing atmosphere and a chemical treatment such as removal of the surface oxide layer with an acid. *
- PF20-F manufactured by Epson Atmix Co., Ltd., SFR-FeSiAl manufactured by Nippon Atomizing Co., Ltd., etc. are commercially available. What has been used can also be used.
- the method for obtaining the molded body from the raw material particles there is no particular limitation on the method for obtaining the molded body from the raw material particles, and any known means in the production of the particle molded body can be appropriately adopted.
- a manufacturing method in the case where the coil component is a multilayer inductor will be exemplified.
- a coating machine such as a doctor blade or a die coater
- a magnetic paste (slurry) prepared in advance is applied to the surface of a base film made of a resin or the like. This is dried with a dryer such as a hot air dryer to obtain a green sheet.
- the magnetic paste includes metal particles 11, typically a polymer resin as a binder, and a solvent.
- the magnetic paste preferably contains a polymer resin as a binder.
- the type of the polymer resin is not particularly limited, and examples thereof include polyvinyl acetal resins such as polyvinyl butyral (PVB).
- the type of solvent for the magnetic paste is not particularly limited, and for example, glycol ethers such as butyl carbitol can be used.
- the blending ratio of soft magnetic alloy particles, polymer resin, solvent and the like in the magnetic paste can be adjusted as appropriate, and the viscosity of the magnetic paste can be set accordingly. *
- the green sheet may be rolled.
- a calendar roll, a roll press, etc. can be used for rolling. Rolling is performed, for example, at a load of 1800 kgf or more, preferably 2000 kgf or more, more preferably 2000 to 8000 kgf, for example, at 60 ° C. or more, preferably 60 to 90 ° C. *
- the green sheet is punched to form through holes (through holes) in a predetermined arrangement.
- the arrangement of the through holes is set so that when the sheets are laminated, a coil is formed by the through holes filled with the conductor and the conductor pattern.
- conventional techniques can be used as appropriate, and specific examples will be described in the following embodiments with reference to the drawings. *
- a conductor paste is preferably used for filling the through holes and for printing the conductor pattern.
- the conductive paste contains conductive particles, typically a polymer resin as a binder, and a solvent. *
- Silver particles or the like can be used as the conductor particles.
- d50 is preferably 1 to 10 ⁇ m on a volume basis.
- the d50 of the conductor particles is measured using a particle size / particle size distribution measuring apparatus (for example, Microtrack manufactured by Nikkiso Co., Ltd.) using a laser diffraction scattering method. *
- the conductive paste preferably contains a polymer resin as a binder.
- the type of the polymer resin is not particularly limited, and examples thereof include polyvinyl acetal resins such as polyvinyl butyral (PVB).
- the kind of the solvent of the conductor paste is not particularly limited, and for example, glycol ether such as butyl carbitol can be used.
- the blending ratio of the conductor particles, polymer resin, solvent, etc. in the conductor paste can be adjusted as appropriate, and the viscosity of the conductor paste can be set accordingly. *
- the conductor paste is printed on the surface of the green sheet and dried with a dryer such as a hot air dryer to form a conductor pattern corresponding to the coil. To do. During printing, a part of the conductor paste is also filled in the above-described through hole. As a result, the conductor paste filled in the through hole and the printed conductor pattern constitute the shape of the coil. *
- the green sheets after printing are stacked in a predetermined order using an adsorption conveyance machine and a press machine, and thermocompression bonded to produce a laminate. Subsequently, using a cutting machine such as a dicing machine or a laser processing machine, the laminated body is cut into a component body size to produce a pre-heat treatment chip.
- a cutting machine such as a dicing machine or a laser processing machine
- the chips before heat treatment are heat-treated in an oxidizing atmosphere such as air.
- This heat treatment usually includes a binder removal process and an oxide film formation process.
- the binder removal process is performed at a temperature at which the polymer resin used as the binder disappears, for example, at a temperature of about 300 ° C. for about 1 hour.
- Examples of the oxide film forming process include conditions of about 750 ° C. and about 2 hours.
- the fine gaps are usually filled with a mixture of a solvent and a binder. These disappear in the binder removal process, and after the binder removal process is completed, the fine gap changes to pores. Further, in the pre-heat-treatment chip, there are many fine gaps between the conductor particles. This fine gap is filled with a mixture of solvent and binder. These also disappear in the binder removal process.
- the alloy particles 11 are densely formed to form the particle compact 1.
- the oxide films 12 on the surfaces of the alloy particles 11 are bonded to each other by the bonds 22.
- at least some of the bonds 22 are made of crystalline oxide and are preferably continuously lattice-bonded.
- the conductor particles are sintered to form a coil. Thereby, a multilayer inductor is obtained.
- external terminals are formed after the heat treatment.
- a coating machine such as a dip coating machine or a roller coating machine
- a conductor paste prepared in advance is applied to both ends in the longitudinal direction of the component body, and this is applied to a temperature of about 600 ° C. using a heating device such as a firing furnace.
- the external terminals are formed by performing the baking process under the condition of about 1 hr.
- the conductor paste for the external terminals the above-described paste for printing a conductor pattern or a paste similar thereto can be used as appropriate.
- an organic resin As a binder, it is preferable to add an organic resin as a binder. It is preferable to use an organic resin made of an acrylic resin, a butyral resin, a vinyl resin, or the like having a thermal decomposition temperature of 500 ° C. or less because the binder hardly remains after heat treatment.
- a known lubricant may be added during molding. Examples of the lubricant include organic acid salts, and specific examples include zinc stearate and calcium stearate.
- the amount of the lubricant is preferably 0 to 1.5 parts by weight, more preferably 0.1 to 1.0 parts by weight with respect to 100 parts by weight of the raw material particles. A lubricant amount of zero means that no lubricant is used.
- a binder and / or lubricant is optionally added to the raw material particles and stirred, and then formed into a desired shape.
- a pressure of 5 to 10 t / cm 2 is applied. At this stage, there is a very high possibility that neither the bond 22 between the oxide films nor the metal bond is generated.
- the oxygen concentration during heating is preferably 1% or more, which facilitates the formation of both bonds 22 and metal bonds between oxide films.
- the oxygen concentration in the air (about 21%) can be given in consideration of the manufacturing cost.
- the heating temperature is preferably 600 ° C. or higher from the viewpoint of easily forming the oxide film 12 made of a crystalline oxide and easily forming the bonds 22 having continuous lattice bonds between the oxide films 12. From the viewpoint of increasing the magnetic permeability by moderately suppressing the presence of metal bonds, the temperature is preferably 900 ° C. or lower.
- the heating temperature is more preferably 700 to 800 ° C.
- the heating time is preferably 0.5 hours or longer from the viewpoint that the bonds 22 between the oxide films 12 can easily form continuous lattice bonds. From the viewpoint of facilitating the formation of metal bonds as well as the bonds 22 between the oxide films 12, the heating time is preferably 0.5 to 3 hours.
- the obtained particle molded body 1 may have voids 30 therein.
- a polymer resin (not shown) may be impregnated in at least a part of the voids 30 present inside the particle molded body 1.
- the pressure of the production system may be lowered by immersing the particle molded body 1 in a liquid material of the polymer resin such as a polymer resin in a liquid state or a solution of the polymer resin. Examples thereof include a method in which a liquid material of a polymer resin is applied to the particle molded body 1 and soaked into the voids 30 near the surface.
- the polymer resin include organic resins such as epoxy resins and fluororesins, and silicone resins without particular limitation. *
- the magnetic material which consists of the particle compact 1 obtained in this way can be used as a component of various electronic components.
- a coil component may be formed by using the magnetic material of the present invention as a core and winding an insulating coated conductor around it.
- various coil components can be obtained by using the magnetic material of the present invention as an element body and forming a coil inside or on the surface.
- the multilayer inductor described above is also an aspect of the coil component.
- the coil component may be of various mounting forms such as surface mounting type and through-hole mounting type, and means for obtaining the coil component from the magnetic material, including means for configuring the coil component of those mounting forms, Any known manufacturing technique in the field can be appropriately adopted.
- FIG. 2 is a schematic cross-sectional view of a multilayer inductor as a coil component.
- the coil component 40 includes a rectangular parallelepiped component main body 41 and a pair of external terminals 44 and 45 provided at both ends in the length direction of the component main body 41.
- the component main body 41 includes a magnetic material 1 composed of a rectangular parallelepiped shaped particle compact 1 and a spiral coil 43 covered with the magnetic material 1, and both ends of the coil 43 are opposed to two external terminals. 44, 45.
- FIG. 3 is a schematic exploded view of the multilayer inductor.
- the magnetic material 1 has a structure in which a total of 20 magnetic layers ML1 to ML6 are integrated, has a length of about 3.2 mm, a width of about 1.6 mm, and a height of about 0.8 mm. .
- Each of the magnetic layers ML1 to ML6 has a length of about 3.2 mm, a width of about 1.6 mm, and a thickness of about 40 ⁇ m.
- This magnetic material 1 is formed mainly of Fe—Cr—Si alloy particles which are soft magnetic alloy particles.
- the magnetic material 1 contains neither a glass component nor a resin cured product.
- the composition of the Fe—Cr—Si alloy particles is 92 wt% Fe, 4.5 wt% Cr, and 3.5 wt% Si.
- the d50 of the Fe—Cr—Si alloy particles is 10 ⁇ m, d10 is 3 ⁇ m, and d90 is 16 ⁇ m.
- d10, d50 and d90 are parameters expressing the volume-based particle size distribution. *
- the coil 43 has a structure in which a total of five coil segments CS1 to CS5 and a total of four relay segments IS1 to IS4 connecting the coil segments CS1 to CS5 are spirally integrated, and the number of turns Is about 3.5.
- the coil 43 is mainly obtained by heat-treating silver particles, and the volume-based d50 of the silver particles used as a raw material is 5 ⁇ m. *
- the four coil segments CS1 to CS4 have a U shape, and the one coil segment CS5 has a strip shape.
- Each coil segment CS1 to CS5 has a thickness of about 20 ⁇ m and a width of about 0.2 mm. It is.
- the uppermost coil segment CS1 has a continuous L-shaped lead portion LS1 used for connection to the external terminal 44, and the lowermost coil segment CS5 is used for connection to the external terminal 45.
- An L-shaped lead portion LS2 is continuously provided.
- Each of the relay segments IS1 to IS4 has a column shape penetrating the magnetic layers ML1 to ML4, and each has a diameter of about 15 ⁇ m. *
- Each external terminal 44 and 45 extends to each end face in the length direction of the component main body 41 and four side faces in the vicinity of the end face, and the thickness thereof is about 20 ⁇ m.
- One external terminal 44 is connected to the edge of the lead portion LS1 of the uppermost coil segment CS1
- the other external terminal 45 is connected to the edge of the lead portion LS2 of the lowermost coil segment CS5.
- the external terminals 44 and 45 were obtained mainly by heat-treating silver particles having a volume-based d50 of 5 ⁇ m. *
- a magnetic paste composed of 85 wt% of the Fe—Cr—Si alloy, 13 wt% of butyl carbitol (solvent), and 2 wt% of polyvinyl butyral (binder) was prepared. Using a doctor blade, this magnetic paste was applied to the surface of a plastic base film, and this was dried with a hot air dryer at about 80 ° C. for about 5 minutes. In this way, a green sheet was obtained on the base film. The base film and the green sheet were rolled with a calender roll at a load of about 70 ° C. and 2000 kgf. Thereafter, the green sheet was cut to obtain first to sixth sheets corresponding to the magnetic layers ML1 to ML6 (see FIG. 3) and having a size suitable for multi-cavity.
- the first sheet corresponding to the magnetic layer ML1 was punched to form through holes corresponding to the relay segment IS1 in a predetermined arrangement.
- through holes corresponding to the relay segments IS2 to IS4 were formed in a predetermined arrangement in the second to fourth sheets corresponding to the magnetic layers ML2 to ML4, respectively.
- a conductor paste consisting of 85 wt% of the Ag particles, 13 wt% of butyl carbitol (solvent), and 2 wt% of polyvinyl butyral (binder) is printed on the surface of the first sheet. Then, this was dried with a hot air dryer under conditions of about 80 ° C. and about 5 minutes, and a first printed layer corresponding to the coil segment CS1 was produced in a predetermined arrangement. Similarly, second to fifth printed layers corresponding to the coil segments CS2 to CS5 were formed in a predetermined arrangement on the surfaces of the second to fifth sheets. *
- the first to fourth sheets provided with the printing layer and the filling unit, the fifth sheet provided only with the printing layer, and the printing layer and the filling unit are provided using an adsorption conveyance machine and a press.
- This laminated body was cut into a component body size with a cutting machine to obtain a chip before heat treatment. *
- a conductive paste containing 85 wt% of the above silver particles, 13 wt% of butyl carbitol (solvent) and 2 wt% of polyvinyl butyral (binder) is applied to both ends in the length direction of the component body 41, Baking treatment was performed in a baking furnace under conditions of about 600 ° C. and about 1 hr. As a result, the solvent and the binder disappeared, the silver particles were sintered, the external terminals 44 and 45 were formed, and the coil component was obtained.
- FIG. 4 is an obtained powder X-ray diffraction pattern. Presence of respective peaks at 2 ⁇ of about 33 °, about 36 °, about 50 °, and about 55 ° due to the oxide was confirmed. Furthermore, the strength of the particle compact was measured. The strength measurement method and measurement results are as follows. With respect to the strength of the obtained multilayer inductor as a device, a three-point bending rupture stress was measured.
- a load W was measured when the measuring object was broken by applying a load in the height direction to the measuring object having a height dimension of h and a depth dimension of b.
- M is the distance between two fulcrums that support the measurement object on the opposite side of the surface to which the load is applied.
Abstract
Description
の組成は除外している。
41の長さ方向の両端部に設けられた1対の外部端子44、45とを有している。部品本体41は、直方体形状の粒子成形体1からなる磁性材料1と、磁性材料1によって覆われた螺旋状のコイル43とを有しており、コイル43の両端はそれぞれ対向する2つの外部端子44、45に接続している。
Claims (6)
- 酸化被膜を有する金属粒子が成形されてなる粒子成形体からなり、 前記金属粒子はFe-Si-M系軟磁性合金(但し、Mは鉄より酸化し易い金属元素である。)からなり、 前記粒子成形体中の前記金属粒子は、互いに隣接する金属粒子と、それぞれが有する酸化被膜どうしの結合によって結合されており、 前記酸化被膜どうしの結合の少なくとも一部は結晶性の酸化物からなる結合である、 磁性材料。
- 前記結晶性の酸化物からなる結合の少なくとも一部は連続的に格子結合している請求項1記載の磁性材料。
- 前記酸化被膜どうしの結合は熱処理によって生成されたものである請求項1又は2記載の磁性材料。
- 素体の内部あるいは表面にコイルを有するコイル部品であって、 前記素体として、 酸化被膜を有する金属粒子が成形されてなる粒子成形体からなり、 前記金属粒子はFe-Si-M系軟磁性合金(但し、Mは鉄より酸化し易い金属元素である。)からなり、 前記粒子成形体中の前記金属粒子は、互いに隣接する金属粒子と、それぞれが有する酸化被膜どうしの結合によって結合されており、 前記酸化被膜どうしの結合の少なくとも一部は結晶性の酸化物からなる結合である、磁性材料を用いたコイル部品。
- 前記結晶性の酸化物からなる結合の少なくとも一部は連続的に格子結合している請求項4記載のコイル部品。
- 前記酸化被膜どうしの結合は熱処理によって生成されたものである請求項4又は5記載のコイル部品。
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CN201280041704.2A CN103765529B (zh) | 2011-08-26 | 2012-01-05 | 磁性材料及线圈零件 |
US14/241,240 US11972885B2 (en) | 2011-08-26 | 2012-01-05 | Magnetic material and coil component |
KR1020147002025A KR101490772B1 (ko) | 2011-08-26 | 2012-01-05 | 자성 재료 및 코일 부품 |
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JP2011184223A JP5082002B1 (ja) | 2011-08-26 | 2011-08-26 | 磁性材料およびコイル部品 |
JP2011-184223 | 2011-08-26 |
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JP (1) | JP5082002B1 (ja) |
KR (1) | KR101490772B1 (ja) |
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US11972885B2 (en) | 2024-04-30 |
TW201310473A (zh) | 2013-03-01 |
KR20140038539A (ko) | 2014-03-28 |
CN103765529A (zh) | 2014-04-30 |
JP2013045985A (ja) | 2013-03-04 |
CN103765529B (zh) | 2016-09-14 |
JP5082002B1 (ja) | 2012-11-28 |
CN106158222B (zh) | 2021-06-22 |
US20140225703A1 (en) | 2014-08-14 |
CN106158222A (zh) | 2016-11-23 |
TWI501262B (zh) | 2015-09-21 |
KR101490772B1 (ko) | 2015-02-06 |
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