JP2008169072A - Mn-Zn FERRITE - Google Patents
Mn-Zn FERRITE Download PDFInfo
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- JP2008169072A JP2008169072A JP2007003480A JP2007003480A JP2008169072A JP 2008169072 A JP2008169072 A JP 2008169072A JP 2007003480 A JP2007003480 A JP 2007003480A JP 2007003480 A JP2007003480 A JP 2007003480A JP 2008169072 A JP2008169072 A JP 2008169072A
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- 229910000859 α-Fe Inorganic materials 0.000 title claims abstract description 15
- 230000004907 flux Effects 0.000 claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 5
- 229910052742 iron Inorganic materials 0.000 claims abstract description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 18
- 239000000463 material Substances 0.000 description 10
- 239000011787 zinc oxide Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 239000011701 zinc Substances 0.000 description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- VASIZKWUTCETSD-UHFFFAOYSA-N manganese(II) oxide Inorganic materials [Mn]=O VASIZKWUTCETSD-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000011802 pulverized particle Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
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Abstract
Description
本発明は、電源用トランス等の磁心に用いられる、100kHz〜1MHzの広い周波数帯域で損失が少なく、且つ高飽和磁束密度を有するフェライト材料に関するものである。 The present invention relates to a ferrite material that is used for a magnetic core of a power transformer or the like and has a low loss and a high saturation magnetic flux density in a wide frequency band of 100 kHz to 1 MHz.
従来のMn−Znフェライトは、例えば100kHz程度の周波数において高透磁率で且つ低損失な材料という様に、使用する駆動周波数を限定する材料が多い。またトランスの小型化に対しては高磁束密度であることが肝心である。近年、電源用トランスの小型化、駆動周波数の高周波数化が進み、高飽和磁束密度と共に、高調波による損失等の理由から、より広い周波数帯域における損失の低減が求められている。しかし、先だって例に挙げた様な従来の材料では高周波帯域で損失が高くなり、逆に高周波帯域で低損失な材料となれば飽和磁束密度が低くなる欠点があった。 Many conventional Mn—Zn ferrites limit the driving frequency to be used, for example, a material having high permeability and low loss at a frequency of about 100 kHz. In addition, high magnetic flux density is important for transformer miniaturization. In recent years, power transformers have been downsized and driving frequency has been increased, and reduction of loss in a wider frequency band has been demanded for reasons such as loss due to harmonics as well as high saturation magnetic flux density. However, the conventional materials as previously mentioned have the disadvantage that the loss becomes high in the high frequency band, and conversely the saturation magnetic flux density becomes low if the material is low loss in the high frequency band.
高周波帯域のフェライト材料として、例えば300kHz〜数MHzの周波数でMn−Zn系フェライトに様々な添加物を含有させて低損失を示す材料が特開平6−310320公報などで開示されている。これらのような高周波帯域用材料は、主に低損失化を意図しており、同様に重要であるトランスの小型化に係わる飽和磁束密度への配慮が十分ではなく、逆に特開2003-128458公報で開示されている様な高飽和磁束密度材料は、高周波帯域の損失への配慮が十分ではなかった。
100kHz〜1MHzの広い周波数帯域で低損失且つ高飽和磁束密度を両立する材料は、一般的に難しい。高周波帯域で低損失にするには焼成温度を下げ、結晶成長を抑制する方法があるが飽和磁束密度を低下させる問題がある。また、飽和磁束密度を充分得るためには基本組成であるFe2O3含有量を多くすることが知られているが、この場合電力損失の最小値(Pcv min)が低温側に移動し、損失が増大するなど実用的でなかった。
It is generally difficult to make a material that achieves both low loss and high saturation magnetic flux density in a wide frequency band of 100 kHz to 1 MHz. To reduce the loss in the high frequency band, there is a method of lowering the firing temperature and suppressing crystal growth, but there is a problem of lowering the saturation magnetic flux density. Further, in order to obtain a sufficient saturation magnetic flux density, it is known to increase the content of Fe 2 O 3 which is a basic composition. In this case, the minimum value of power loss (Pcv min) moves to the low temperature side, Loss increased and was not practical.
本発明は上記問題点を解決し、広い周波数帯域で低損失及び高飽和磁束密度を有するMn−Znフェライトを提供しようとするものである。 The present invention is intended to solve the above problems and to provide a Mn—Zn ferrite having a low loss and a high saturation magnetic flux density in a wide frequency band.
本発明は、主成分組成が53.0〜58.0mol%Fe2O3、5.0〜9.0mol%ZnO、残部MnOからなり、副成分としてSiO2 0.002〜0.02重量%、CaO 0.01〜0.2重量%、V2O5 0.01〜0.1重量%、Nb2O5 0.01〜0.1重量%、MgO 0.3〜1.5重量%、CoO 0.1〜0.5重量%を同時に含有し、100kHz−200mT及び1MHz−50mTにおける損失の最小値(Pcv min)が40〜100℃にあり、その値が100kHz−200mTで500kW/m3以下、1MHz−50mTで500kW/m3以下で、飽和磁束密度が23℃で530mT以上、100℃で430mT以上であることを特徴とするMn−Znフェライト。
The present invention is mainly composed composition 53.0~58.0mol% Fe 2 O 3, 5.0~9.0mol % ZnO, the balance being MnO, SiO 2 0.002 to 0.02 wt% as an auxiliary component , CaO 0.01 to 0.2 wt%, V 2 O 5 0.01~0.1 wt%, Nb 2 O 5 0.01~0.1 wt%, MgO 0.3 to 1.5 wt% , CoO 0.1 to 0.5% by weight at the same time, the minimum loss (Pcv min) at 100 kHz-200 mT and 1 MHz-50 mT is 40-100 ° C., and the value is 500 kW / m at 100 kHz-200 mT. 3 or less, 1 MHz-50 mT, 500 kW / m 3 or less, a saturation magnetic flux density of 530 mT or more at 23 ° C., and 430 mT or more at 100 ° C.
本発明が提供するMn−Znフェライトは、スイッチング電源トランス等の磁心に適した、100kHz〜1MHz の広い周波数帯域において低損失かつ飽和磁束密度の高いMn−Znフェライト材料を提供することができる。 The Mn—Zn ferrite provided by the present invention can provide a Mn—Zn ferrite material having a low loss and a high saturation magnetic flux density in a wide frequency band of 100 kHz to 1 MHz suitable for a magnetic core such as a switching power supply transformer.
(実施例1)表1に示した組成となるように高純度の酸化鉄、酸化マンガン、酸化亜鉛を計量・混合し、大気中で950℃×2時間仮焼を行った。この仮焼原料に本発明請求項範囲内でSiO2 0.007重量%、CaO 0.06重量%、V2O5 0.04重量%、Nb2O5 0.04重量%、MgO 0.7重量%、CoO 0.3重量%となるように加え、アトライターで粉砕粒径が1.7μmとなるまで粉砕した。この粉砕粉にポリビニルアルコールを加え造粒し、得られた造粒顆粒を外径24mm、内径19mm、高さ10mmのトロイダル状に成形した。その後、本焼成においてピーク温度の酸素分圧をコントロールしながら、1350℃×4時間保持した後、降温することにより焼結サンプルを得た。このようにして得られた試料を、B−H/Zアナライザー(HP社製E5060A)にて、損失(100kHz−200mT、1MHz−50mT、測定温度23〜120℃)を測定した。また、最大磁界1194A/mにおける飽和磁束密度を測定した。表1に各組成のPcv min値とその温度、23℃及び100℃における飽和磁束密度を示す。また、1MHz−50mTの損失の温度特性を図1に示す。この表、図に示す結果から明らかなように、本発明の主成分組成範囲内ではPcv minが40〜100℃の範囲にあり、かつ100kHz−200mT、1MHz−50mTでそれぞれ500kW/m3以下である。更に飽和磁束密度が23℃で530mT以上、100℃で430mT以上が得られている。
Example 1 High-purity iron oxide, manganese oxide, and zinc oxide were weighed and mixed so as to have the composition shown in Table 1, and calcined at 950 ° C. for 2 hours in the atmosphere. Within the scope of the present invention, this calcined raw material is within a range of 0.002 wt% SiO 2 , 0.06 wt% CaO, 0.04 wt% V 2 O 5, 0.04 wt% Nb 2 O 5 ,
(実施例2)Fe2O3:55.5mol%、ZnO:7.0mol%残部MnOとなるように高純度の酸化鉄、酸化亜鉛、酸化マンガンを計量・混合し、大気中950℃×2時間仮焼を行った。この仮焼原料に本発明の請求項範囲内でSiO2 0.007重量%、CaO 0.06重量%、V2O5 0.04重量%、Nb2O5 0.04重量%となるように添加し、表2に示す分量を含有するようにMgO、CoOを添加した。その後、実施例1と同様にサンプルの作製、評価を行った。これらのPcv min温度とその値、23℃、100℃における飽和磁束密度を表2に示す。また、1MHz−50mTの損失の温度特性を図2に示す。この表、図に示す結果から明らかなように、本発明の副成分であるMgO、CoO添加範囲ではPcv minが40℃〜100℃の範囲にあり、かつ100kHz−200mT、1MHz−50mTでそれぞれ500kW/m3以下である。 (Example 2) Fe 2 O 3: 55.5mol %, ZnO: 7.0mol% pure iron oxide as the balance becomes MnO, zinc oxide, manganese oxide were weighed and mixed, atmospheric 950 ° C. × 2 Temporary calcining was performed. Within the scope of the present invention, the calcined raw material is 0.007 wt% SiO 2 , 0.06 wt% CaO, 0.04 wt% V 2 O 5, 0.04 wt% Nb 2 O 5. MgO and CoO were added so as to contain the amounts shown in Table 2. Thereafter, samples were prepared and evaluated in the same manner as in Example 1. Table 2 shows these Pcv min temperatures and their values, and saturation magnetic flux densities at 23 ° C. and 100 ° C. Moreover, the temperature characteristic of the loss of 1 MHz-50mT is shown in FIG. As is apparent from the results shown in this table and figure, in the MgO and CoO addition ranges of the present invention, Pcv min is in the range of 40 ° C. to 100 ° C., and 500 kW at 100 kHz-200 mT and 1 MHz-50 mT, respectively. / M 3 or less.
主成分組成はFe2O3、MnO、ZnOからなるMn−Znフェライトであり、53.0〜58.0mol%Fe2O3、5.0〜9.0mol%ZnO、残部MnOの範囲に限定した。その理由は、Fe2O3が53.0mol%以下になると飽和磁束密度の低下を招き、58.0mol%以上になると高周波帯域の損失が増大する。同様にZnOが5.0mol%以下になると飽和磁束密度の低下を招き、9.0mol%以上になると高周波帯域の損失が増大することから上記主成分組成に決定した。 The main component composition is Mn—Zn ferrite composed of Fe 2 O 3 , MnO and ZnO, and is limited to the range of 53.0 to 58.0 mol% Fe 2 O 3 , 5.0 to 9.0 mol% ZnO and the balance MnO. did. The reason is that when Fe 2 O 3 is 53.0 mol% or less, the saturation magnetic flux density is lowered, and when it is 58.0 mol% or more, the loss in the high frequency band is increased. Similarly, when the ZnO content is 5.0 mol% or less, the saturation magnetic flux density is lowered. When the ZnO content is 9.0 mol% or more, the loss in the high frequency band increases.
上記主成分組成に加え、副成分としてSiO2、CaO、V2O5、Nb2O5、MgO、CoOを同時に添加している。SiO2、CaOは互いに共存することによって粒界の比抵抗を高め、渦電流損失の低減に寄与しており、Nb2O5はSiO2、CaOと共に粒界に析出し、高抵抗相を形成し損失を低減させる。V2O5はNb2O5が共存する場合、Nb2O5によって誘起される粒内気孔や異常粒成長の発生を抑制し、結晶組成を粒径が微細で均一な組成となるように安定化して損失の悪化を抑える効果がある。そして、目標の飽和磁束密度を維持するFe2O3、MnO、ZnOの主組成にするとPcv minが40℃以下になるため、MgOを添加することによりPcv minを実用上有効な40〜100℃の範囲に収める。MgOはPcv minを高温に移動させる効果があると同時に、高周波帯域の損失を低減させる。CoOはMn−ZnフェライトにCo2+として固溶する事により、Co2+による正の磁気異方性とFe2+による負の磁気異方性が相殺しあい、結果的に絶対値および温度変化の小さい磁気異方性が発生し、低温から高温まで広い温度範囲にわたって温度特性の変動を減少させる効果があると共に、常温の飽和磁束密度を向上させる働きを持つ。これらの副成分は、焼成後酸化物となり得るものであれば、添加時の構造は問わない。また、その添加は本焼成前において含有されていればどの工程で行っても差し支えない。 In addition to the main component composition, SiO 2 , CaO, V 2 O 5 , Nb 2 O 5 , MgO, and CoO are added simultaneously as subcomponents. SiO 2 and CaO coexist with each other to increase the specific resistance of the grain boundary and contribute to the reduction of eddy current loss. Nb 2 O 5 precipitates at the grain boundary together with SiO 2 and CaO to form a high resistance phase. To reduce loss. When Nb 2 O 5 coexists, V 2 O 5 suppresses the occurrence of intragranular pores and abnormal grain growth induced by Nb 2 O 5 , so that the crystal composition has a fine and uniform grain size. It has the effect of stabilizing and suppressing the deterioration of loss. When the main composition of Fe 2 O 3 , MnO, and ZnO that maintains the target saturation magnetic flux density is used, Pcv min is 40 ° C. or lower. Therefore, by adding MgO, Pcv min is practically effective from 40 to 100 ° C. Within the range of MgO has the effect of moving Pcv min to a high temperature and at the same time reduces the loss in the high frequency band. When CoO is dissolved in Mn—Zn ferrite as Co 2+ , the positive magnetic anisotropy due to Co 2+ and the negative magnetic anisotropy due to Fe 2+ cancel each other, and as a result, the magnetism has a small absolute value and temperature change. Anisotropy occurs, and has the effect of reducing fluctuations in temperature characteristics over a wide temperature range from low temperature to high temperature, and has the function of improving the saturation magnetic flux density at room temperature. As long as these subcomponents can become oxides after firing, the structure at the time of addition is not limited. Moreover, the addition may be performed in any process as long as it is contained before the main firing.
Claims (2)
The main component composition is 53.0 to 58.0 mol% Fe 2 O 3 , 5.0 to 9.0 mol% ZnO, and the balance MnO, with SiO 2 0.002 to 0.02 wt% and CaO 0. 01 to 0.2 wt%, V 2 O 5 0.01~0.1 wt%, Nb 2 O 5 0.01~0.1 wt%, MgO 0.3 to 1.5 wt%, CoO 0. An Mn-Zn ferrite containing 1 to 0.5% by weight at the same time.
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| JP2007003480A JP2008169072A (en) | 2007-01-11 | 2007-01-11 | Mn-Zn FERRITE |
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| JP2007003480A JP2008169072A (en) | 2007-01-11 | 2007-01-11 | Mn-Zn FERRITE |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016032001A1 (en) * | 2014-08-29 | 2016-03-03 | 日立金属株式会社 | MnZn FERRITE AND METHOD FOR PRODUCING SAME |
| WO2017164350A1 (en) * | 2016-03-25 | 2017-09-28 | 日立金属株式会社 | METHOD FOR PRODUCING MnZn-BASED FERRITE, AND MnZn-BASED FERRITE |
| CN112079562A (en) * | 2020-10-19 | 2020-12-15 | 江苏亨通光导新材料有限公司 | Sintering protection device for OVD (over-voltage-reduction) method deposition loose body |
| JP7406022B1 (en) | 2022-07-26 | 2023-12-26 | Jfeケミカル株式会社 | MnZnCo ferrite |
| WO2024262587A1 (en) * | 2023-06-21 | 2024-12-26 | 株式会社プロテリアル | MnZn-BASED SOFT FERRITE AND METHOD FOR PRODUCING SAME |
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| JPH05226137A (en) * | 1992-02-18 | 1993-09-03 | Matsushita Electric Ind Co Ltd | Oxide magnetic body material and its manufacture |
| JP2004196658A (en) * | 2004-02-16 | 2004-07-15 | Minebea Co Ltd | Manganese-zinc ferrite and method of manufacturing the same |
| JP2005236069A (en) * | 2004-02-20 | 2005-09-02 | Nippon Ceramic Co Ltd | Mn-Zn FERRITE |
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2007
- 2007-01-11 JP JP2007003480A patent/JP2008169072A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH05226137A (en) * | 1992-02-18 | 1993-09-03 | Matsushita Electric Ind Co Ltd | Oxide magnetic body material and its manufacture |
| JP2004196658A (en) * | 2004-02-16 | 2004-07-15 | Minebea Co Ltd | Manganese-zinc ferrite and method of manufacturing the same |
| JP2005236069A (en) * | 2004-02-20 | 2005-09-02 | Nippon Ceramic Co Ltd | Mn-Zn FERRITE |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016032001A1 (en) * | 2014-08-29 | 2016-03-03 | 日立金属株式会社 | MnZn FERRITE AND METHOD FOR PRODUCING SAME |
| US10304602B2 (en) | 2014-08-29 | 2019-05-28 | Hitachi Metals, Ltd. | MnZn-based ferrite and method for manufacturing the same |
| WO2017164350A1 (en) * | 2016-03-25 | 2017-09-28 | 日立金属株式会社 | METHOD FOR PRODUCING MnZn-BASED FERRITE, AND MnZn-BASED FERRITE |
| US10919809B2 (en) | 2016-03-25 | 2021-02-16 | Hitachi Metals, Ltd. | MnZn ferrite and its production method |
| CN112079562A (en) * | 2020-10-19 | 2020-12-15 | 江苏亨通光导新材料有限公司 | Sintering protection device for OVD (over-voltage-reduction) method deposition loose body |
| JP7406022B1 (en) | 2022-07-26 | 2023-12-26 | Jfeケミカル株式会社 | MnZnCo ferrite |
| WO2024024303A1 (en) * | 2022-07-26 | 2024-02-01 | Jfeケミカル株式会社 | Mnznco-based ferrite |
| JP2024016788A (en) * | 2022-07-26 | 2024-02-07 | Jfeケミカル株式会社 | MnZnCo ferrite |
| CN117769531A (en) * | 2022-07-26 | 2024-03-26 | 杰富意化学株式会社 | MnZnCo ferrite |
| WO2024262587A1 (en) * | 2023-06-21 | 2024-12-26 | 株式会社プロテリアル | MnZn-BASED SOFT FERRITE AND METHOD FOR PRODUCING SAME |
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