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JP2008169072A - Mn-Zn FERRITE - Google Patents

Mn-Zn FERRITE Download PDF

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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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loss
flux density
ferrite
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Takashi Nishikawa
崇 西川
Kazuyuki Yoneda
和之 米田
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Nippon Ceramic Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an Mn-Zn ferrite which is low loss and high saturation flux density in a wide frequency band of 100 kHz to 1 MHz. <P>SOLUTION: The main component composition of the Mn-Zn ferrite contains 53.0-58.0 mol% Fe<SB>2</SB>O<SB>3</SB>, 5.0-9.0 mol% ZnO and the balance MnO. The Mn-Zn ferrite simultaneously contains, as sub-components, 0.002-0.02 wt.% SiO<SB>2</SB>, 0.01-0.2 wt.% CaO, 0.01-0.1 wt.% V<SB>2</SB>O<SB>5</SB>, 0.01-0.1 wt.% Nb<SB>2</SB>O<SB>5</SB>, 0.3-1.5 wt.% MgO, and 0.1-0.5 wt.% CoO. <P>COPYRIGHT: (C)2008,JPO&INPIT

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。

特開平6−310320公報 特開2003−128458公報
As a ferrite material in a high frequency band, for example, Japanese Unexamined Patent Publication No. 6-310320 discloses a material exhibiting low loss by adding various additives to a Mn—Zn ferrite at a frequency of 300 kHz to several MHz. These materials for high-frequency bands are mainly intended for low loss, and similarly, the saturation magnetic flux density related to the miniaturization of the transformer, which is equally important, is not sufficient, and conversely, JP 2003-128458 A The high saturation magnetic flux density material as disclosed in the publication is not sufficient in consideration of the loss in the high frequency band.

JP-A-6-310320 JP 2003-128458 A


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Fe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%Fe、5.0〜9.0mol%ZnO、残部MnOからなり、副成分としてSiO 0.002〜0.02重量%、CaO 0.01〜0.2重量%、V 0.01〜0.1重量%、Nb 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/m以下、1MHz−50mTで500kW/m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SiO 0.007重量%、CaO 0.06重量%、V 0.04重量%、Nb 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/m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 , MgO 0. The mixture was added to 7 wt% and CoO 0.3 wt%, and pulverized with an attritor until the pulverized particle size became 1.7 μm. Polyvinyl alcohol was added to the pulverized powder and granulated, and the resulting granulated granules were formed into a toroidal shape having an outer diameter of 24 mm, an inner diameter of 19 mm, and a height of 10 mm. Thereafter, while maintaining the oxygen partial pressure at the peak temperature in the main firing, the temperature was maintained at 1350 ° C. for 4 hours, and then the temperature was lowered to obtain a sintered sample. Thus, the loss (100kHz-200mT, 1MHz-50mT, measurement temperature 23-120 degreeC) was measured for the obtained sample with the BH / Z analyzer (E5060A by HP company). Further, the saturation magnetic flux density at the maximum magnetic field of 1194 A / m was measured. Table 1 shows the Pcv min value of each composition and its temperature, and the saturation magnetic flux density 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, within the main component composition range of the present invention, Pcv min is in the range of 40 to 100 ° C., and at 100 kHz-200 mT and 1 MHz-50 mT, respectively, at 500 kW / m 3 or less. is there. Further, a saturation magnetic flux density of 530 mT or more at 23 ° C. and 430 mT or more at 100 ° C. is obtained.

Figure 2008169072
Figure 2008169072

(実施例2)Fe: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SiO 0.007重量%、CaO 0.06重量%、V 0.04重量%、Nb 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/m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.

Figure 2008169072
Figure 2008169072

主成分組成はFe、MnO、ZnOからなるMn−Znフェライトであり、53.0〜58.0mol%Fe、5.0〜9.0mol%ZnO、残部MnOの範囲に限定した。その理由は、Fe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SiO、CaO、V、Nb、MgO、CoOを同時に添加している。SiO、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、NbはSiO、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。VはNbが共存する場合、Nb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Fe、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.


実施例1における主成分組成の違いによるPcv温度特性(1MHz−50mT)を示す図である。It is a figure which shows the Pcv temperature characteristic (1MHz-50mT) by the difference in a main component composition in Example 1. FIG. 実施例2におけるMgO、CoO含有量の違いによるPcv温度特性(1MHz−50mT)を示す図である。It is a figure which shows the Pcv temperature characteristic (1MHz-50mT) by the difference in MgO in Example 2, and CoO content.

Claims (2)

主成分組成が53.0〜58.0mol%Fe、5.0〜9.0mol%ZnO、残部MnOからなり、副成分としてSiO 0.002〜0.02重量%、CaO 0.01〜0.2重量%、V 0.01〜0.1重量%、Nb 0.01〜0.1重量%、MgO 0.3〜1.5重量%、CoO 0.1〜0.5重量%を同時に含有することを特徴とするMn−Znフェライト。
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.
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/m以下、1MHz−50mTで500kW/m以下で、且つ飽和磁束密度が23℃で530mT以上、100℃で430mT以上であることを特徴とする請求項1に記載のMn−Znフェライト。 The minimum value of the loss in the 100kHz-200 mT and 1MHz-50mT (Pcv min) is in the 40 to 100 ° C., its value is in the 100kHz-200mT 500kW / m 3 or less, at 1MHz-50mT 500kW / m 3 or less, and saturation 2. The Mn—Zn ferrite according to claim 1, wherein the magnetic flux density is 530 mT or more at 23 ° C. and 430 mT or more at 100 ° C. 3.
JP2007003480A 2007-01-11 2007-01-11 Mn-Zn FERRITE Pending JP2008169072A (en)

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Cited By (5)

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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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JP2005236069A (en) * 2004-02-20 2005-09-02 Nippon Ceramic Co Ltd Mn-Zn FERRITE

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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)

* Cited by examiner, † Cited by third party
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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