JP6536790B2 - Ferrite core, electronic component, and power supply device - Google Patents
Ferrite core, electronic component, and power supply device Download PDFInfo
- Publication number
- JP6536790B2 JP6536790B2 JP2015049587A JP2015049587A JP6536790B2 JP 6536790 B2 JP6536790 B2 JP 6536790B2 JP 2015049587 A JP2015049587 A JP 2015049587A JP 2015049587 A JP2015049587 A JP 2015049587A JP 6536790 B2 JP6536790 B2 JP 6536790B2
- Authority
- JP
- Japan
- Prior art keywords
- ppm
- ferrite core
- terms
- amount
- core
- 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.)
- Active
Links
- 229910000859 α-Fe Inorganic materials 0.000 title claims description 47
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 36
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 19
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 18
- 239000011787 zinc oxide Substances 0.000 claims description 18
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 13
- 229910006404 SnO 2 Inorganic materials 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 8
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical group [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 239000011162 core material Substances 0.000 description 67
- 239000000843 powder Substances 0.000 description 31
- 230000004907 flux Effects 0.000 description 22
- 230000000694 effects Effects 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 238000001354 calcination Methods 0.000 description 8
- 238000010304 firing Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 230000002159 abnormal effect Effects 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000008187 granular material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 229910052596 spinel Inorganic materials 0.000 description 3
- 239000011029 spinel Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910020599 Co 3 O 4 Inorganic materials 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000013016 damping Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910004140 HfO Inorganic materials 0.000 description 1
- 229910021380 Manganese Chloride Inorganic materials 0.000 description 1
- GLFNIEUTAYBVOC-UHFFFAOYSA-L Manganese chloride Chemical compound Cl[Mn]Cl GLFNIEUTAYBVOC-UHFFFAOYSA-L 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 235000002867 manganese chloride Nutrition 0.000 description 1
- 239000011565 manganese chloride Substances 0.000 description 1
- 229940099607 manganese chloride Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/34—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 non-metallic substances, e.g. ferrites
- H01F1/342—Oxides
- H01F1/344—Ferrites, e.g. having a cubic spinel structure (X2+O)(Y23+O3), e.g. magnetite Fe3O4
-
- 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
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02M—APPARATUS FOR CONVERSION BETWEEN AC AND AC, BETWEEN AC AND DC, OR BETWEEN DC AND DC, AND FOR USE WITH MAINS OR SIMILAR POWER SUPPLY SYSTEMS; CONVERSION OF DC OR AC INPUT POWER INTO SURGE OUTPUT POWER; CONTROL OR REGULATION THEREOF
- H02M3/00—Conversion of dc power input into dc power output
- H02M3/22—Conversion of dc power input into dc power output with intermediate conversion into ac
- H02M3/24—Conversion of dc power input into dc power output with intermediate conversion into ac by static converters
- H02M3/28—Conversion of dc power input into dc power output with intermediate conversion into ac by static converters using discharge tubes with control electrode or semiconductor devices with control electrode to produce the intermediate ac
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3284—Zinc oxides, zincates, cadmium oxides, cadmiates, mercury oxides, mercurates or oxide forming salts thereof
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
- Compounds Of Iron (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Dc-Dc Converters (AREA)
Description
本発明は、100℃近傍の飽和磁歪が低く、駆動時の音鳴きが抑制され、且つ、飽和磁束密度が高いフェライトコアに関するものである。 The present invention relates to a ferrite core having a low saturation magnetostriction near 100 ° C., suppressing noise during driving, and having a high saturation magnetic flux density.
電源用トランスなどの磁心材料として、フェライト焼結体が使用されている。コア(磁心)を形成するフェライト焼結体は、フェライトコアと呼ばれ、Mn及びZnを含有するMnZn系フェライトが広く使用されている。また、近年では電源の小型化に伴い高温で高い飽和磁束密度が求められている。 A ferrite sintered body is used as a core material for a power source transformer or the like. The ferrite sintered body which forms a core (magnetic core) is called a ferrite core, and MnZn ferrite containing Mn and Zn is widely used. Also, in recent years, high saturation magnetic flux density has been required at high temperature as the power supply is miniaturized.
たとえば特許文献1のフェライトではFe2O3:52〜56mol%、ZnO:6〜14mol%、NiO:4mol%以下、CoO:0.01〜0.6mol%、残部が実質的にMnOの組成となる基本成分に対して、外枠量でSiO2:0.0050〜0.0500wt%及びCaO:0.0200〜0.2000wt%を含有し、さらに、Ta2O5、ZrO2、Nb2O5、V2O5、K2O、TiO2、SnO2及びHfO2のうちから選ばれる少なくとも1種の添加成分を所定量含有し、かつ、高い飽和磁束密度を有することを特徴としている。 For example, in the ferrite of Patent Document 1, the composition of Fe 2 O 3 : 52 to 56 mol%, ZnO: 6 to 14 mol%, NiO: 4 mol% or less, CoO: 0.01 to 0.6 mol%, and the balance substantially MnO The outer frame amounts of SiO 2 : 0.0050 to 0.0050 wt% and CaO: 0.0200 to 0.2000 wt% with respect to the basic components to be contained, and further Ta 2 O 5 , ZrO 2 , Nb 2 O 5 , characterized in that it contains a predetermined amount of at least one additive component selected from V 2 O 5 , K 2 O, TiO 2 , SnO 2 and HfO 2 and has a high saturation magnetic flux density.
一方、電源の駆動時に発生する音鳴きについても重要であり、たとえば特許文献2では複数の脚部を持つコアの脚と脚の間に制振材を挟むことによって、トランス鳴きが低減または防止されるトランスを提供することを特徴としている。 On the other hand, it is also important for the noise generated at the time of driving the power source. For example, in Patent Document 2, the transformer noise is reduced or prevented by sandwiching the damping material between the legs of the core having a plurality of legs. It is characterized by providing a transformer.
音鳴きは磁歪振動することが原因であると一般的に知られている。特許文献2では音鳴きは低減しているものの、音鳴きの原因である磁歪を低減しているものではなく根本的な解決の方法とはいえない。また、制振材を用いることにより、製造時のコストや手間がかかってしまうという問題もある。 It is generally known that the noise is caused by magnetostrictive vibration. Although the noise reduction is reduced in Patent Document 2, it does not reduce the magnetostriction which is the cause of the noise, and it can not be said to be a fundamental solution method. In addition, there is also a problem that the use of the damping material increases the cost and labor at the time of manufacture.
そこで本発明の目的は、従来技術が抱えている上述した課題を解決できるフェライトコアを提供することにある。特に100℃における磁歪を小さくすることで駆動時の音鳴きを抑え、且つ、高い飽和磁束密度を示すフェライトコアを提供することにある。 Therefore, an object of the present invention is to provide a ferrite core that can solve the above-described problems of the prior art. In particular, the object of the present invention is to provide a ferrite core exhibiting high saturation magnetic flux density by suppressing the generation of noise during driving by reducing the magnetostriction at 100 ° C.
かかる目的のもと、本発明者等はMnZn系フェライトに含まれる主成分として酸化鉄、酸化マンガン、酸化亜鉛、副成分として酸化ニッケル、酸化コバルトおよび酸化チタンの組成に着目してその特性について鋭意研究を行った。その結果、100℃において飽和磁歪が小さく、駆動時の音鳴きを抑え、かつ、高い飽和磁束密度を実現できることを見出し、本発明を完成させるに至った。 For this purpose, the present inventors focused on the composition of iron oxide, manganese oxide and zinc oxide as main components contained in MnZn ferrite and nickel oxide, cobalt oxide and titanium oxide as auxiliary components and are keenly aware of their characteristics. I did research. As a result, it has been found that saturation magnetostriction is small at 100 ° C., noise at the time of driving can be suppressed, and high saturation magnetic flux density can be realized, and the present invention has been completed.
すなわち、本発明に係るフェライトコアは、酸化鉄をFe2O3換算で51.5〜54.5mol%、酸化亜鉛をZnO換算で7.0〜11.5mol%、残部が酸化マンガンである主成分を含むMnZn系フェライトであって、この主成分に対して、NiをNiO換算で500〜10000ppmを含むこと、TiをTiO2換算で100〜6000ppmを含むこと、CoをCoO換算で500〜4000ppm含むことを特徴とするフェライトコアである。 That is, the ferrite core according to the present invention is mainly composed of 51.5 to 54.5 mol% of iron oxide in terms of Fe 2 O 3 , 7.0 to 11.5 mol% of zinc oxide in terms of ZnO, and the balance being manganese oxide. Mn-Zn-based ferrite containing a component, containing 500 to 10000 ppm of Ni in terms of NiO, 100 to 6000 ppm of Ti in terms of TiO 2 and 500 to 4000 ppm of Co based on CoO with respect to the main component It is a ferrite core characterized by including.
また本発明のフェライトコアにおいて、副成分として、主成分に対してSiをSiO2換算で50〜300ppm及びCaをCaCO3換算で200〜3000ppm含むことが好ましい。 Further, in the ferrite core of the present invention, it is preferable that 50 to 300 ppm of Si in terms of SiO 2 and 200 to 3000 ppm of Ca in terms of CaCO 3 be contained in the main component as minor components.
さらに本発明のフェライトコアにおいて、副成分として、主成分に対してNbをNb2O5換算で50〜750ppm、TaをTa2O5換算で50〜1500ppm、VをV2O5換算で50〜1000ppm、SnをSnO2換算で500〜8000ppmを1種または2種以上含むことが好ましい。 In addition the ferrite core of the present invention, as an accessory component, a Nb calculated as Nb 2 O 5 with respect to the main component 50~750Ppm, the Ta in Ta 2 O 5 in terms 50~1500Ppm, the V in terms of V 2 O 5 50 It is preferable to contain 1000 ppm, and one or two or more types of Sn in an amount of 500 to 8000 ppm in terms of SnO 2 .
100℃における飽和磁歪を低減することで駆動時の音鳴きを抑えることができ、且つ、高い飽和磁束密度を実現できる。 By reducing the saturation magnetostriction at 100 ° C., noise during driving can be suppressed, and a high saturation magnetic flux density can be realized.
はじめに、本発明における成分の限定理由を説明する。
本発明のフェライトコアは主成分としてのFe量をFe2O3換算で51.5〜54.5mol%とする。なお、以下では、Fe量をFe2O3換算で、との表記を単に、Fe2O3量等と表記する。Fe2O3量が51.5mol%未満だと、100℃における飽和磁歪は低減されるが飽和磁束密度が小さくなってしまう。一方、Fe2O3量が54.5mol%を超えると100℃における飽和磁歪が大きくなってしまう。したがって、本発明ではFe2O3量を51.5〜54.5mol%とする。好ましい量は51.5〜54mol%である。
First, the reasons for limitation of the components in the present invention will be described.
In the ferrite core of the present invention, the amount of Fe as the main component is 51.5 to 54.5 mol% in terms of Fe 2 O 3 . In the following, the expression of the amount of Fe in terms of Fe 2 O 3 is simply expressed as the amount of Fe 2 O 3 or the like. If the amount of Fe 2 O 3 is less than 51.5 mol%, the saturation magnetostriction at 100 ° C. is reduced but the saturation magnetic flux density is reduced. On the other hand, when the amount of Fe 2 O 3 exceeds 54.5 mol%, saturation magnetostriction at 100 ° C. becomes large. Therefore, in the present invention, the amount of Fe 2 O 3 is set to 51.5 to 54.5 mol%. The preferred amount is 51.5 to 54 mol%.
ZnO量も飽和磁束密度及び飽和磁歪に影響を与える。ZnO量が7.0mol%より少ないと飽和磁歪が大きくなってしまう。ZnOが11.5mol%を超えると100℃における飽和磁束密度が小さくなってしまう。したがって本発明ではZnO量を7.0〜11.5mol%とする。本発明のフェライトコアは主成分として、上記以外に不可避的不純物を除いて残部がMnOから構成される。 The amount of ZnO also affects the saturation magnetic flux density and saturation magnetostriction. When the amount of ZnO is less than 7.0 mol%, saturation magnetostriction becomes large. When ZnO exceeds 11.5 mol%, the saturation magnetic flux density at 100 ° C. becomes small. Therefore, in the present invention, the amount of ZnO is set to 7.0 to 11.5 mol%. The ferrite core of the present invention is mainly composed of MnO except the above-described unavoidable impurities.
次に本発明における副成分について説明する。
本発明のフェライトコアは、副成分として、Ni量をNiO換算で500〜10000ppmとする。NiOは磁歪を抑制するのに有効であり、その効果を得るために主成分に対して500ppm以上添加する。但し、添加量が多すぎると、飽和磁束密度が小さくなってしまう。したがって本発明ではNiO量を10000ppm以下とする。好ましい量は2000〜10000ppmである。
Next, the subcomponents in the present invention will be described.
The ferrite core of the present invention has an amount of Ni of 500 to 10,000 ppm in terms of NiO as a minor component. NiO is effective for suppressing the magnetostriction, and in order to obtain the effect, it is added in an amount of 500 ppm or more based on the main component. However, if the addition amount is too large, the saturation magnetic flux density is reduced. Therefore, the amount of NiO is made 10000 ppm or less in the present invention. The preferred amount is 2000-10000 ppm.
本発明のフェライトコアは、副成分として、Ti量をTiO2換算で100〜6000ppmとする。TiO2は4価のTiイオンとしてスピネル格子中のFeと置換して磁歪を低減できる。その効果を得るためには主成分に対し100ppm以上添加する。但し、添加量が多すぎると、飽和磁束密度が小さくなる。したがって本発明ではTiO2量を6000ppm以下とする。好ましい量は1000〜3000ppmである。 The ferrite core of the present invention has a Ti content of 100 to 6000 ppm in terms of TiO 2 as an accessory component. TiO 2 can be substituted for Fe in the spinel lattice as tetravalent Ti ions to reduce magnetostriction. In order to obtain the effect, 100 ppm or more is added to the main component. However, when the addition amount is too large, the saturation magnetic flux density decreases. Therefore, in the present invention, the amount of TiO 2 is set to 6000 ppm or less. The preferred amount is 1000 to 3000 ppm.
本発明のフェライトコアは、副成分として、Co量をCoO換算で500〜4000ppmとする。CoOは磁歪を抑制するのに有効であり、その効果を得るために主成分に対して500ppm以上添加する。但し、その添加量が多すぎると、飽和磁束密度が小さくなってしまう。したがって本発明では、CoO量を4000ppm以下とする。好ましいCoO量は500〜3000ppmである。 The ferrite core of the present invention has a Co content of 500 to 4000 ppm in terms of CoO as an accessory component. CoO is effective in suppressing the magnetostriction, and in order to obtain the effect, it is added in an amount of 500 ppm or more to the main component. However, if the amount added is too large, the saturation magnetic flux density will be reduced. Therefore, in the present invention, the amount of CoO is set to 4000 ppm or less. The preferred amount of CoO is 500 to 3000 ppm.
また、Ni、Ti、Coは同時に添加することでその効果はさらに高まる。NiやCoはスピネル結晶中のBサイトに固溶することで磁歪抑制効果が得られる。しかし、これらを単体で添加すると、BサイトだけではなくAサイトにも固溶してしまい、添加量に対して十分な効果が得られない。しかし、Tiを同時に添加することでNiやCoがBサイトに固溶しやすくなり単体で添加するよりも大きい磁歪抑制効果を得ることができると考えられる。 Moreover, the effect is further enhanced by simultaneously adding Ni, Ti and Co. By dissolving Ni and Co in the B site in the spinel crystal, the magnetostriction suppressing effect can be obtained. However, when these are added alone, they are not only dissolved at the B site but also at the A site, and a sufficient effect can not be obtained with respect to the addition amount. However, by simultaneously adding Ti, it is considered that Ni and Co are easily dissolved in the B site, and it is possible to obtain a greater magnetostriction suppressing effect than adding it alone.
本発明のフェライトコアは、上述した組成を適宜選択することにより100℃における飽和磁束密度が380mT以上と高く、且つ、100℃における飽和磁歪を低減し駆動時の音鳴きを抑えることができる。 In the ferrite core of the present invention, the saturation magnetic flux density at 100 ° C. is as high as 380 mT or more, and the saturation magnetostriction at 100 ° C. can be reduced to suppress the noise at the time of driving.
本発明では次のように副成分を制限することでコア損失を抑えることができる。
本発明のフェライトコアは、副成分として、SiO2を50〜300ppm及びCaCO3を200〜3000ppmの範囲内で含むことができる。Si及びCaは、結晶粒界に偏析して高抵抗層を形成して低損失に寄与するとともに焼結助剤として焼結密度を向上する効果を有する。SiがSiO2換算で50ppm未満、あるいはCaがCaCO3換算で200ppm未満だと上記効果を十分に得ることができない。また、SiがSiO2換算で300ppm、あるいはCaがCaCO3換算で3000ppmを超えると、異常粒成長によるコア損失の劣化が大きくなる。SiO2は50〜150ppm及びCaCO3は500〜2000ppmとすることが好ましく、さらにSiO2は75〜125ppm及びCaCO3は800〜1600ppmとすることが好ましい。
In the present invention, core loss can be suppressed by limiting subcomponents as follows.
The ferrite core of the present invention can contain 50 to 300 ppm of SiO 2 and 200 to 3000 ppm of CaCO 3 as accessory components. Si and Ca are segregated at grain boundaries to form a high resistance layer to contribute to low loss and have the effect of improving the sintering density as a sintering aid. If Si is less than 50 ppm in terms of SiO 2 , or Ca is less than 200 ppm in terms of CaCO 3 , the above effects can not be sufficiently obtained. Further, when Si exceeds 300 ppm in terms of SiO 2 , or Ca exceeds 3000 ppm in terms of CaCO 3 , deterioration of core loss due to abnormal grain growth becomes large. It is preferable to set 50 to 150 ppm of SiO 2 and 500 to 2000 ppm of CaCO 3 , and more preferably, 75 to 125 ppm of SiO 2 and 800 to 1600 ppm of CaCO 3 .
本発明のフェライトコアは、副成分として、Nb2O5を50〜750ppm及びTa2O5を50〜1500ppmの範囲内で含むことができる。Nb及びTaは粒界抵抗を高める働きがある成分である。NbがNb2O5換算で50ppm未満、あるいはTaがTa2O5を換算で50ppm未満では改善効果がない。また、NbがNb2O5換算で750ppmを超え、あるいはTaがTa2O5換算で1500ppmを超えると異常粒成長によりコア損失が大きくなるため、Nb2O5を50〜750ppm及びTa2O5を50〜1500ppmの範囲に限定した。含有量が多くなると異常粒成長を起こすためNb2O5を100〜300ppm及びTa2O5を100〜600ppmの範囲で含有させるのが好ましい。 The ferrite core of the present invention can contain, as auxiliary components, 50 to 750 ppm of Nb 2 O 5 and 50 to 1500 ppm of Ta 2 O 5 . Nb and Ta are components having the function of increasing the grain boundary resistance. When Nb is less than 50 ppm in terms of Nb 2 O 5 , or Ta is less than 50 ppm in terms of Ta 2 O 5 , no improvement effect is obtained. In addition, if Nb exceeds 750 ppm in terms of Nb 2 O 5 or Ta exceeds 1500 ppm in terms of Ta 2 O 5 , core loss is increased due to abnormal grain growth, so 50 to 750 ppm of Nb 2 O 5 and Ta 2 O 5 5 was limited to the range of 50 to 1500 ppm. When the content is increased, it is preferable to contain 100 to 300 ppm of Nb 2 O 5 and 100 to 600 ppm of Ta 2 O 5 in order to cause abnormal grain growth.
本発明のフェライトコアは、副成分として、V2O5を50〜1000ppmの範囲内で含むことができる。Vは粒界抵抗を高める働きがある成分である。VがV2O5を換算で50ppm未満では改善効果がない。また、VがV2O5換算で1000ppmを超えると異常粒成長によりコア損失が大きくなるため、V2O5を50〜1000ppmの範囲に限定した。含有量が多くなると異常粒成長を起こすためV2O5を100〜500ppmの範囲で含有させるのが好ましい。 The ferrite core of the present invention can contain V 2 O 5 in the range of 50 to 1000 ppm as an accessory component. V is a component having a function to increase intergranular resistance. When V is less than 50 ppm in terms of V 2 O 5 , there is no improvement effect. Also, V is because the core loss increases due to abnormal grain growth exceeds 1000ppm in terms of V 2 O 5, with limited V 2 O 5 in the range of 50 to 1000 ppm. It is preferable to contain V 2 O 5 in a range of 100 to 500 ppm because abnormal grain growth occurs when the content is increased.
本発明のフェライトコアは、副成分として、SnO2を500〜8000ppm含むことができる。SnO2は、一部粒界に存在し焼結後の冷却過程で粒界再酸化を助長して損失を低下させる成分である。SnO2は4価のイオンとしてスピネル格子の原子とも置換してボトム温度を低下させる働きもある。しかしながら、添加量が多すぎると異常粒成長を引き起こして損失が高くなるため、SnO2は500〜8000ppm、の範囲で含有させる。好ましくは、SnO2を1000〜3000ppmの範囲で含有させる。なお、これらの成分は必ずしも酸化物の形で添加する必要はなく、たとえば、炭酸塩の形で混合してもかまわない。 The ferrite core of the present invention can contain 500 to 8000 ppm of SnO 2 as an accessory component. SnO 2 is a component that is partially present in grain boundaries and promotes grain boundary re-oxidation in the cooling process after sintering to reduce loss. SnO 2 also acts as a tetravalent ion to replace atoms of the spinel lattice to lower the bottom temperature. However, if the addition amount is too large, abnormal grain growth is caused to increase loss, so SnO 2 is contained in the range of 500 to 8000 ppm. Preferably, SnO 2 is contained in the range of 1000 to 3000 ppm. These components do not necessarily have to be added in the form of oxides, and may be mixed, for example, in the form of carbonates.
本発明のフェライトコアは、上述した組成を適宜選択することにより100℃における損失を抑えることができる。 The ferrite core of the present invention can suppress the loss at 100 ° C. by appropriately selecting the above-mentioned composition.
次に、本発明によるフェライトコアにとって好適な製造方法を説明する。
主成分の原料としては、酸化物又は加熱により酸化物となる化合物の粉末を用いる。具体的には、Fe2O3粉末、Mn3O4粉末及びZnO粉末等を用いることができる。各原料粉末の平均粒径は0.1〜3μmの範囲で適宜選択すればよい。主成分の原料粉末を湿式混合した後、仮焼きを行う。仮焼きの温度は800〜1100℃の範囲内での所定温度とすればよい。仮焼きの安定時間は0.5〜5時間の範囲で適宜選択すればよい。仮焼き後、仮焼き材を例えば、平均粒径0.5〜3μm程度まで粉砕する。なお、本発明では、上述の主成分の原料に限らず、2種以上の金属を含む複合酸化物の粉末を主成分の原料としてもよい。例えば、塩化鉄、塩化マンガンを含有する水溶液を酸化培焼することによりFe、Mnを含む複合酸化物の粉末が得られる。この粉末とZnO粉末を混合して主成分原料としてもよい。このような場合には、仮焼きは不要である。
Next, a manufacturing method suitable for the ferrite core according to the present invention will be described.
As a raw material of the main component, a powder of an oxide or a compound which becomes an oxide upon heating is used. Specifically, Fe 2 O 3 powder, Mn 3 O 4 powder, ZnO powder or the like can be used. The average particle diameter of each raw material powder may be appropriately selected in the range of 0.1 to 3 μm. After wet mixing of the raw material powder of the main component, calcination is performed. The temperature of the pre-baking may be a predetermined temperature within the range of 800 to 1100 ° C. The stabilization time of calcination may be appropriately selected in the range of 0.5 to 5 hours. After calcination, the calcined material is crushed, for example, to an average particle diameter of about 0.5 to 3 μm. In the present invention, not only the raw material of the above-described main component, but also a powder of a composite oxide containing two or more metals may be used as the raw material of the main component. For example, oxidation and calcination of an aqueous solution containing iron chloride and manganese chloride gives a powder of a composite oxide containing Fe and Mn. The powder and the ZnO powder may be mixed to form the main component material. In such a case, preliminary baking is unnecessary.
仮焼き後に副成分を添加する。仮焼き後の添加には、仮焼き材に副成分の原料を添加して上記粉砕を行ってもよいし、仮焼き材の粉砕後に副成分の原料を添加、混合することができる。ただし、NiO、TiO2、CoOについては、主成分の原料とともに仮焼きに供することもできる。
副成分の原料として、酸化物又は加熱により酸化物となる化合物の粉末を用いることもできる。具体的には、NiO粉末、Co3O4粉末、TiO2粉末、SiO2粉末、CaCO3粉末、Nb2O5粉末、Ta2O5粉末、SnO2粉末等を用いることができる。
The auxiliary components are added after calcination. For the addition after the calcination, the raw material of the auxiliary component may be added to the calcined material and the above-mentioned pulverization may be performed, or the raw material of the auxiliary component can be added and mixed after the calcination of the calcined material. However, NiO, TiO 2 and CoO can also be subjected to calcination together with the main component material.
An oxide or a powder of a compound that becomes an oxide upon heating can also be used as a raw material of the accessory component. Specifically, NiO powder, Co 3 O 4 powder, TiO 2 powder, SiO 2 powder, CaCO 3 powder, Nb 2 O 5 powder, Ta 2 O 5 powder, SnO 2 powder or the like can be used.
主成分及び副成分からなる混合粉末は、後の成型工程を円滑に実行するために顆粒に造粒される。造粒は例えばスプレードライヤを用いて行うことができる。混合粉末に適当な結合材、例えばポリビニルアルコール(PVA)を少量添加し、これをスプレードライヤで噴霧、乾燥する。得られる顆粒の粒径は80〜300μm程度とすることが好ましい。 The mixed powder consisting of the main component and the accessory components is granulated into granules in order to smoothly carry out the subsequent molding process. Granulation can be performed using, for example, a spray dryer. A small amount of a suitable binder such as polyvinyl alcohol (PVA) is added to the mixed powder, which is sprayed with a spray dryer and dried. The particle size of the obtained granules is preferably about 80 to 300 μm.
得られた顆粒は、例えば所定形状の金型を有するプレスを用いて所望の形状に成型され、この成型体は焼成工程に供される。
焼成工程においては、焼成温度と焼成雰囲気を制御する必要がある。焼成温度は1250〜1500℃の範囲から適宜選択することができるが、本発明のフェライトコアの効果を十分引き出すには、1300〜1400℃の範囲で焼成することが好ましい。焼成雰囲気は、窒素と酸素の混合雰囲気において、酸素分圧を適宜調整すればよい。
The obtained granules are formed into a desired shape using, for example, a press having a mold having a predetermined shape, and the formed body is subjected to a firing step.
In the firing step, it is necessary to control the firing temperature and the firing atmosphere. The firing temperature can be appropriately selected from the range of 1250 to 1500 ° C., but in order to sufficiently bring out the effect of the ferrite core of the present invention, the firing is preferably performed in the range of 1300 to 1400 ° C. As the firing atmosphere, the partial pressure of oxygen may be appropriately adjusted in a mixed atmosphere of nitrogen and oxygen.
焼成された本発明によるフェライトコアは、93%以上、さらに好ましくは95%以上の相対密度を得ることができる。
本発明により得られたフェライトコアはトランスに用いることが可能であり、本発明により得られたトランスは、スイッチング電源装置に用いることが可能である。
The fired ferrite core according to the present invention can obtain a relative density of 93% or more, more preferably 95% or more.
The ferrite core obtained by the present invention can be used in a transformer, and the transformer obtained by the present invention can be used in a switching power supply device.
図1(a)は、本実施形態に係るE字型フェライトコア(磁心)を示す斜視図である。図1(a)に示すように、E字型のフェライトコア10は、E型コアなどと呼ばれ、トランスなどに使用される。フェライトコア10のようなE型コアが採用されたトランスとしては、図1(b)に示すような、内部に2つのE型コアが対向配置されたものが知られている。
FIG. 1A is a perspective view showing an E-shaped ferrite core (magnetic core) according to the present embodiment. As shown in FIG. 1A, the
図2は、スイッチング電源装置の構成を示すブロック図である。 FIG. 2 is a block diagram showing the configuration of the switching power supply device.
図2に示すスイッチング電源装置200は、直流入力電圧Vinを直流出力電圧Voutに変換するための装置(DC/DCコンバーター)であり、直流出力電圧Vinに含まれるノイズ成分を除去する入力フィルタ201と、入力フィルタ201の出力を交流に変換するスイッチング回路202と、スイッチング回路202の出力を変圧するトランス203と、トランス203の出力を直流に変換する整流回路204と、整流回路の出力を平滑化する平滑回路205とを備えている。このような構成を有するスイッチング電源装置200において、トランス203のコアとして本発明によるコアを用いれば、トランス203にて発生する音鳴きを抑制できることから、スイッチング電源装置200の騒音問題を解決することができる。
Switching
図2に示したスイッチング電源装置200は、特に自動車用のスイッチング電源装置として利用することが好適である。
The switching
図3は、スイッチング電源装置200を備えた自動車の主要部分を概略的に示すブロック図である。
FIG. 3 is a block diagram schematically showing a main part of a vehicle provided with switching
図3に示すように、スイッチング電源装置200を自動車用に用いた場合、スイッチング電源装置200は、高圧バッテリー210と電気機器220及び低圧バッテリー230との間に設けられ、高圧バッテリー210より供給される約144Vや約288Vの高電圧を約14Vに降圧してこれを電気機器220に供給するとともに、低圧バッテリー230を充電する役割を果たす。電気機器220としては、自動車に備えられるエアコンやオーディオ等が挙げられる。
As shown in FIG. 3, when the switching
高圧バッテリー210への充電は、発電装置240より供給される電力によって行われる。また、高圧バッテリー210の出力はモータ250にも供給され、モータ250は、高圧バッテリー210より供給される高電圧(約144Vや約288V)に基づいて駆動系260を駆動する。尚、燃料電池車においては燃料電池本体が発電装置240となり、ハイブリッド車においてはモータ250が発電装置240を兼ねることになる。
The
以上、本発明の好ましい実施形態について説明したが、本発明は、上記の実施形態に限定されることなく、本発明の主旨を逸脱しない範囲で種々の変更が可能であり、それらも本発明の範囲内に包含されるものであることはいうまでもない。 Although the preferred embodiments of the present invention have been described above, the present invention is not limited to the above-described embodiments, and various modifications can be made without departing from the spirit of the present invention. It is needless to say that they are included in the scope.
以下、本発明を具体的な実施例に基づいて説明する。
主成分の原料としてFe2O3粉末、Mn3O4粉末及びZnO粉末、副成分の原料としてNiO粉末、TiO2粉末、Co3O4粉末、SiO2粉末、CaCO3粉末、Nb2O5粉末、V2O5粉末、Ta2O5粉末及びSnO2粉末を用いた。主成分の組成、副成分の組成を表1〜3に示す。また、表1、2は表に示した材料の他にSiO2を100ppm、CaCO3を1000ppm、Nb2O5を200ppmを添加した。これらの粉末を湿式混合した後、大気中、900℃で3時間仮焼きした。
得られた混合物にバインダを加え、顆粒化した後、成型してトロイダル形状の成型体、I型形状の成型体、及び、E型形状の成型体を得た。得られた成型体を酸素分圧制御下において、温度1300℃(安定部5時間、安定部酸素分圧2%)で焼成することにより、トロイダル形状のフェライトコア(外径20mm、内径10mm、厚さ5mm)、I字型形状のフェライトコア(長さ70mm、幅8mm、厚さ8mm)及びE字型形状のフェライトコア(長さ40mm、高さ15mm、幅5mm)を得た。
Hereinafter, the present invention will be described based on specific examples.
Fe 2 O 3 powder, Mn 3 O 4 powder and ZnO powder as raw materials for main component, NiO powder, TiO 2 powder, Co 3 O 4 powder, SiO 2 powder, CaCO 3 powder, Nb 2 O 5 as raw materials for auxiliary components Powder, V 2 O 5 powder, Ta 2 O 5 powder and SnO 2 powder were used. The composition of the main component and the composition of the subcomponents are shown in Tables 1 to 3. Further, Tables 1 and 2 and the SiO 2 was added 100 ppm, the CaCO 3 1000 ppm, the 200ppm the Nb 2 O 5 in addition to the materials shown in Table. After wet-mixing these powders, they were calcined at 900 ° C. for 3 hours in the atmosphere.
The obtained mixture was added with a binder, granulated, and then molded to obtain a toroidal-shaped molded body, an I-shaped molded body, and an E-shaped molded body. The resulting molded body is sintered at a temperature of 1300 ° C. (5 hours for stable part, 2% for oxygen partial pressure for stable part) under oxygen partial pressure control to obtain a toroidal shaped ferrite core (outer diameter 20 mm,
次に本発明の測定方法について説明する。
100℃における磁歪の測定は共和電業製の歪ゲージ(KFG:汎用箔ひずみゲージ)を用いて行った。I型のフェライトコアの中心部側面に歪ゲージを貼り付けた。Iコアを励磁して歪量が変化しなくなった時点における歪量の変化率の絶対値を飽和磁歪λsとした。なお、以下ではIコアを励磁して歪量が変化しなくなった時点における歪量の変化率の絶対値を飽和磁歪λs、との表記を単に飽和磁歪またはλsと表記する。
Next, the measuring method of the present invention will be described.
The measurement of magnetostriction at 100 ° C. was performed using a strain gauge (KFG: general-purpose foil strain gauge) manufactured by Kyowa Denki. A strain gauge was attached to the side of the center of the I-type ferrite core. The absolute value of the rate of change of strain amount when the I core was excited and the strain amount did not change was taken as the saturation magnetostriction λs. In the following description, the absolute value of the rate of change in strain amount when the I core is excited and the strain amount does not change is simply expressed as saturation magnetostriction λs as saturation magnetostriction or λs.
100℃における音鳴きはE型コア各組成を簡易無響箱内に設置して行った。測定はコアと騒音計のマイク先端部を30mm離れた位置に設置して行った。音圧レベルは小野測器製の騒音計(LA−5570)を用いて測定した。データはA特性変換後のオーバーオール値(OA値)を示す。A特性は、人間の聴感に基づいた音圧レベルを表す量として周波数の重みをつけた値である。OA値は、周波数分析された各音圧レベルの合計である。 The sounding at 100 ° C. was performed by setting each composition of E-shaped core in a simple anechoic box. The measurement was performed with the core and the tip of the microphone of the sound level meter placed 30 mm apart. The sound pressure level was measured using an Ono Sokki noise meter (LA-5570). The data indicates the overall value (OA value) after the A characteristic conversion. The A characteristic is a value obtained by weighting the frequency as an amount representing a sound pressure level based on human hearing. The OA value is the sum of each sound pressure level analyzed.
100℃における飽和磁束密度Bsはトロイダル形状のコアを、メトロン技研製直流磁化特性試験装置(SK−110)により、励磁磁界1194A/mの条件下で測定した。 The saturation magnetic flux density Bs at 100 ° C. was measured under a condition of an excitation magnetic field of 1194 A / m by using a toroidal-shaped core with a direct current magnetization characteristic test device (SK-110) manufactured by Metron Giken.
100℃におけるコア損失Pcvはトロイダル形状のフェライトコアを用いて、1次側5巻、2次側5巻の巻線を施し、100kHzの周波数で最大磁束密度200mTの条件下でIWATSU製BHアナライザー(SY−8217)により測定した。
以上の測定結果より、以下のことが判る。
表中の「−」はその材料を添加していないことを示している。
From the above measurement results, the following can be understood.
"-" In the table indicates that the material is not added.
(表1)
Fe2O3量が51.5mol%未満(比較例1、2参照)だと100℃における飽和磁束密度Bs(以下、100℃における、は省略)が380mTより小さくなってしまう。また、Fe2O3量が54.5mol%を超える(比較例7、8参照)と飽和磁歪が1.5×10−6より大きくなりOA値が45dBより大きくなってしまう。
また、ZnO量が7.0mol%未満(比較例3、5参照)では飽和磁歪が1.5×10−6より大きくなってしまいOA値が45dBより大きくなってしまう。また、ZnO量が11.5mol%を超える(比較例4、6参照)と飽和磁歪は小さくなるが飽和磁束密度Bsが380mTより小さくなってしまう。
(Table 1)
If the Fe 2 O 3 content is less than 51.5 mol% (see Comparative Examples 1 and 2), the saturation magnetic flux density Bs at 100 ° C. (hereinafter, omitted at 100 ° C.) becomes smaller than 380 mT. In addition, when the Fe 2 O 3 content exceeds 54.5 mol% (see Comparative Examples 7 and 8), the saturation magnetostriction becomes larger than 1.5 × 10 −6 and the OA value becomes larger than 45 dB.
In addition, when the amount of ZnO is less than 7.0 mol% (see Comparative Examples 3 and 5), the saturation magnetostriction becomes larger than 1.5 × 10 −6 and the OA value becomes larger than 45 dB. Further, when the amount of ZnO exceeds 11.5 mol% (see Comparative Examples 4 and 6), the saturation magnetostriction decreases but the saturation magnetic flux density Bs becomes smaller than 380 mT.
(表2)
副成分であるNiOの量が500ppmより少ない(比較例9参照)と飽和磁歪が大きくなってしまいOA値が45dBより大きくなってしまう。また、NiO量が10000ppmを超える(比較例10参照)と飽和磁歪は小さくなるが飽和磁束密度Bsが380mTより小さくなってしまう。
副成分であるTiO2の量が100ppmより少ない(比較例11参照)と飽和磁歪が1.5×10−6より大きくなってしまい、OA値も45dBより大きくなってしまう。また、TiO2量が6000ppmを超える(比較例12参照)と磁歪は小さくなるが飽和磁束密度Bsが380mTより小さくなってしまう。
副成分であるCoOの量が500ppmより少ない(比較例13参照)と飽和磁歪が1.5×10−6より大きくなってしまいOA値が45dBより大きくなってしまう。また、CoO量が4000ppmを超える(比較例14参照)と飽和磁束密度Bsが380mTより小さくなってしまう。
(Table 2)
When the amount of NiO as the accessory component is less than 500 ppm (see Comparative Example 9), the saturation magnetostriction becomes large and the OA value becomes larger than 45 dB. When the amount of NiO exceeds 10000 ppm (see Comparative Example 10), the saturation magnetostriction decreases but the saturation magnetic flux density Bs becomes smaller than 380 mT.
When the amount of TiO 2 as the accessory component is less than 100 ppm (see Comparative Example 11), the saturation magnetostriction becomes larger than 1.5 × 10 −6 and the OA value becomes larger than 45 dB. When the amount of TiO 2 exceeds 6000 ppm (see Comparative Example 12), the magnetostriction decreases but the saturation magnetic flux density Bs becomes smaller than 380 mT.
When the amount of CoO which is an accessory component is less than 500 ppm (see Comparative Example 13), the saturation magnetostriction becomes larger than 1.5 × 10 −6 and the OA value becomes larger than 45 dB. In addition, when the amount of CoO exceeds 4000 ppm (see Comparative Example 14), the saturation magnetic flux density Bs becomes smaller than 380 mT.
以上に対して、Fe2O3量が51.5〜54.5mol%、ZnO量が7.0〜11.5mol%、残部MnOの主成分に対して、副成分としてNiO量を500〜10000ppm、TiO2量を100〜6000ppm及びCoOを500〜4000ppmを含む場合に、100℃における飽和磁歪が1.5×10−6以下、OA値が45dB以下、飽和磁束密度Bsが380mT以上という特性を得ることができる。 With respect to the above, the amount of Fe 2 O 3 is 51.5 to 54.5 mol%, the amount of ZnO is 7.0 to 11.5 mol%, and the balance of the main component of MnO is 500 to 10000 ppm of NiO as an accessory component. When the content of TiO 2 is 100 to 6000 ppm and CoO is 500 to 4000 ppm, the saturation magnetostriction at 100 ° C. is 1.5 × 10 −6 or less, the OA value is 45 dB or less, and the saturation magnetic flux density Bs is 380 mT or more. You can get it.
(表3)
他の副成分については以下の通りである。
SiO2及びCaCO3は、前述の通り、結晶粒界に偏析して高抵抗層を形成して低損失に寄与するとともに焼結助剤として焼結密度を向上する効果を有するが、表3に示すように、コア損失Pcvに影響を及ぼす。つまり、SiO2及びCaCO3を添加することにより、コア損失Pcvを低減することができるが、表3に示すように、添加しすぎるとコア損失が悪くなる(実施例20〜27参照)。そこで、SiO2及びCaCO3を添加する場合には、SiO2を50〜300ppm、CaCO3を200〜3000ppmとする。
また、Nb2O5及びTa2O5を添加することにより、コア損失Pcvを低減することができる(実施例28〜34参照)。しかし、SiO2及びCaCO3の場合と同様に添加しすぎるとコア損失が悪くなるので、最適な添加量の範囲はNb2O5を50〜750ppm以下、Ta2O5を50〜1500ppm以下とする。
また、V2O5を添加することにより、コア損失Pcvを低減することができる(実施例35〜37参照)。しかし、SiO2及びCaCO3の場合と同様に添加しすぎるとコア損失が悪くなるので、最適な添加量の範囲はV2O5を50〜1000ppm以下とする。
また、SnO2を添加することにより、コア損失Pcvを低減することができる(実施例38〜40参照)。しかし、SiO2をCaCO3の場合と同様に添加しすぎるとコア損失が悪くなるので、最適な添加量の範囲はSnO2を500〜8000ppm以下とする。
(Table 3)
The other subcomponents are as follows.
As described above, SiO 2 and CaCO 3 segregate at grain boundaries to form a high resistance layer to contribute to low loss and have the effect of improving the sintering density as a sintering aid, as shown in Table 3. As shown, it affects the core loss Pcv. That is, by adding SiO 2 and CaCO 3 , core loss Pcv can be reduced, but as shown in Table 3, core loss becomes worse if it is added too much (see Examples 20 to 27). Therefore, when SiO 2 and CaCO 3 are added, 50 to 300 ppm of SiO 2 and 200 to 3000 ppm of CaCO 3 are added.
Moreover, the core loss Pcv can be reduced by adding Nb 2 O 5 and Ta 2 O 5 (see Examples 28 to 34). However, similar to the case of SiO 2 and CaCO 3 , too much addition leads to poor core loss, so the range of optimum addition amount is 50 to 750 ppm or less for Nb 2 O 5 and 50 to 1500 ppm or less for Ta 2 O 5 Do.
Moreover, the core loss Pcv can be reduced by adding V 2 O 5 (see Examples 35 to 37). However, if it is added too much in the same manner as in the case of SiO 2 and CaCO 3, the core loss becomes worse, so the optimum addition amount range is 50 to 1000 ppm or less of V 2 O 5 .
Moreover, the core loss Pcv can be reduced by adding SnO 2 (see Examples 38 to 40). However, if SiO 2 is added too much as in the case of CaCO 3, the core loss becomes worse, so the optimum addition amount range is 500 to 8000 ppm or less of SnO 2 .
以上のように、本発明に係るフェライトコアは100℃近傍における飽和磁歪を低減することで駆動時のコアの音鳴きを十分に抑制でき、且つ、飽和磁束密度を高くすることができる。 As described above, the ferrite core according to the present invention can sufficiently suppress the ringing of the core during driving by reducing the saturation magnetostriction at around 100 ° C., and can increase the saturation magnetic flux density.
10フェライトコア(磁心)
11(中脚部)
12(コイル)
200スイッチング電源
10 Ferrite core (magnetic core)
11 (middle leg)
12 (coil)
200 switching power supply
Claims (5)
100℃における飽和磁歪λsが1.5×10 −6 以下であり、100℃におけるA特性変換後のオーバーオール値が45dB以下であることを特徴とするフェライトコア。 MnZn ferrite containing a main component in which iron oxide is 51.5 to 54.5 mol% in terms of Fe 2 O 3 , zinc oxide is 7.0 to 11.5 mol% in terms of ZnO, and the balance is manganese oxide, In this main component, Ni is contained 500 to 10000 ppm in NiO conversion, Ti is contained 100 to 6000 ppm in TiO 2 conversion, Co is contained 500 to 4000 ppm in CoO conversion, and V is converted to V 2 O 5 in 50~1000ppm seen including,
1. A ferrite core having a saturated magnetostriction λs at 100 ° C. of 1.5 × 10 −6 or less and an overall value after A characteristic conversion at 100 ° C. of 45 dB or less .
100℃における飽和磁歪λsが1.5×10 −6 以下であり、100℃におけるA特性変換後のオーバーオール値が45dB以下であることを特徴とするフェライトコア。 MnZn ferrite containing a main component in which iron oxide is 51.5 to 54.5 mol% in terms of Fe 2 O 3 , zinc oxide is 7.0 to 11.5 mol% in terms of ZnO, and the balance is manganese oxide, In this main component, Ni is contained 500 to 10000 ppm in NiO conversion, Ti is contained 100 to 6000 ppm in TiO 2 conversion, Co is contained 500 to 4000 ppm in CoO conversion, and Sn is 500 for SnO 2 conversion. ~8000ppm seen including,
1. A ferrite core having a saturated magnetostriction λs at 100 ° C. of 1.5 × 10 −6 or less and an overall value after A characteristic conversion at 100 ° C. of 45 dB or less .
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2015049587A JP6536790B2 (en) | 2014-05-15 | 2015-03-12 | Ferrite core, electronic component, and power supply device |
KR1020150065372A KR20150131981A (en) | 2014-05-15 | 2015-05-11 | Ferrite core, electronic component, and power supply device |
CN201510250244.XA CN105097169B (en) | 2014-05-15 | 2015-05-15 | FERRITE CORE, electronic unit and supply unit |
KR1020170027805A KR20170029462A (en) | 2014-05-15 | 2017-03-03 | Ferrite core, electronic component, and power supply device |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014101497 | 2014-05-15 | ||
JP2014101497 | 2014-05-15 | ||
JP2015049587A JP6536790B2 (en) | 2014-05-15 | 2015-03-12 | Ferrite core, electronic component, and power supply device |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2015231938A JP2015231938A (en) | 2015-12-24 |
JP6536790B2 true JP6536790B2 (en) | 2019-07-03 |
Family
ID=54933684
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015049587A Active JP6536790B2 (en) | 2014-05-15 | 2015-03-12 | Ferrite core, electronic component, and power supply device |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP6536790B2 (en) |
KR (2) | KR20150131981A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7278787B2 (en) * | 2019-01-28 | 2023-05-22 | Njコンポーネント株式会社 | magnetic material |
KR102261729B1 (en) | 2019-07-19 | 2021-06-08 | 엘지이노텍 주식회사 | Magnetic core |
EP3767648B1 (en) * | 2019-07-19 | 2023-12-13 | LG Innotek Co., Ltd. | Magnetic core |
JP2022067365A (en) * | 2020-10-20 | 2022-05-06 | 株式会社トーキン | MnZn-based ferrite |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3917216B2 (en) * | 1996-08-14 | 2007-05-23 | Jfeケミカル株式会社 | Low loss ferrite core material |
JP3597673B2 (en) * | 1997-06-12 | 2004-12-08 | Jfeケミカル株式会社 | Ferrite material |
JP3968188B2 (en) * | 1999-03-30 | 2007-08-29 | Jfeケミカル株式会社 | Ferrite |
JP2004161500A (en) * | 2002-11-08 | 2004-06-10 | Jfe Chemical Corp | Manganese-zinc-nickel-based ferrite |
JP4244193B2 (en) * | 2004-01-30 | 2009-03-25 | Tdk株式会社 | Method for producing MnZn ferrite and MnZn ferrite |
JP5089963B2 (en) * | 2006-11-17 | 2012-12-05 | Jfeフェライト株式会社 | Method for producing MnZnNi ferrite |
JP2013118308A (en) | 2011-12-05 | 2013-06-13 | Sony Corp | Transformer and switching power supply device |
-
2015
- 2015-03-12 JP JP2015049587A patent/JP6536790B2/en active Active
- 2015-05-11 KR KR1020150065372A patent/KR20150131981A/en active Application Filing
-
2017
- 2017-03-03 KR KR1020170027805A patent/KR20170029462A/en active Search and Examination
Also Published As
Publication number | Publication date |
---|---|
JP2015231938A (en) | 2015-12-24 |
KR20150131981A (en) | 2015-11-25 |
KR20170029462A (en) | 2017-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6551057B2 (en) | Ferrite core, electronic component, and power supply device | |
JP6451742B2 (en) | MnZn-based ferrite and method for producing the same | |
JP6536790B2 (en) | Ferrite core, electronic component, and power supply device | |
JP6409553B2 (en) | Ferrite core, electronic component, and power supply device | |
JP2007112695A (en) | METHOD FOR PRODUCING Mn FERRITE | |
CN105097169B (en) | FERRITE CORE, electronic unit and supply unit | |
JP2016056044A (en) | Ferrite core, electronic component and electric power supply | |
JP2016141602A (en) | NiMnZn-BASED FERRITE | |
JP6330645B2 (en) | Ferrite core, electronic component, and power supply | |
JP6365288B2 (en) | Ferrite core, electronic component, and power supply device | |
JP5716381B2 (en) | Ferrite material | |
JP4799808B2 (en) | Ferrite composition, magnetic core and electronic component | |
JP2006298728A (en) | Mn-Zn-BASED FERRITE MATERIAL | |
JP2017145152A (en) | MnZnCo-BASED FERRITE | |
JP2012111675A (en) | Ferrite composition and electronic component | |
JP5810629B2 (en) | Ferrite composition and electronic component | |
JP5817118B2 (en) | Ferrite composition and electronic component | |
JP6311298B2 (en) | Ferrite composition, ferrite core and electronic component | |
JP5834408B2 (en) | Ferrite composition and electronic component | |
JP2015151299A (en) | Ferrite composition, ferrite core and electronic component | |
JP2013116833A (en) | Ferrite composition, ferrite core and electronic part | |
JP2012250858A (en) | Ferrite composition, and electronic component | |
JP2013014442A (en) | Ferrite composition and electronic component | |
JP2015174782A (en) | Ferrite composition, ferrite core, and electronic component | |
JP2015174781A (en) | Ferrite composition, ferrite core, and electronic component |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20171019 |
|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20180323 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180427 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180516 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20181204 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20190130 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20190508 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20190521 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6536790 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |