JPH0710744B2 - Low loss oxide magnetic material - Google Patents

Low loss oxide magnetic material

Info

Publication number
JPH0710744B2
JPH0710744B2 JP63178718A JP17871888A JPH0710744B2 JP H0710744 B2 JPH0710744 B2 JP H0710744B2 JP 63178718 A JP63178718 A JP 63178718A JP 17871888 A JP17871888 A JP 17871888A JP H0710744 B2 JPH0710744 B2 JP H0710744B2
Authority
JP
Japan
Prior art keywords
ppm
magnetic material
oxide magnetic
loss
low loss
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.)
Expired - Lifetime
Application number
JP63178718A
Other languages
Japanese (ja)
Other versions
JPH0230660A (en
Inventor
彦宏 当金
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP63178718A priority Critical patent/JPH0710744B2/en
Priority to GB8915563A priority patent/GB2220935B/en
Priority to DE3922997A priority patent/DE3922997A1/en
Priority to KR1019890010092A priority patent/KR920001163B1/en
Priority to US07/381,302 priority patent/US4985167A/en
Publication of JPH0230660A publication Critical patent/JPH0230660A/en
Priority to GB9209763A priority patent/GB2253843B/en
Priority to GB9209762A priority patent/GB2253842B/en
Publication of JPH0710744B2 publication Critical patent/JPH0710744B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Magnetic Ceramics (AREA)
  • Soft Magnetic Materials (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、ディスプレイモニタ等の電源用磁心に用い
るのに適したMn-Zn系フェライトからなる低損失酸化物
磁性材料に関するものである。
Description: TECHNICAL FIELD The present invention relates to a low-loss oxide magnetic material made of Mn—Zn ferrite suitable for use in a magnetic core for a power supply such as a display monitor.

〔従来の技術〕[Conventional technology]

従来この種の電源用フェライトとしては、本出願人が特
公昭53-28634号で提案したMn-Zn系フェライトがある。
このMn-Zn系フェライトはCaO、SiO2、ClおよびSnF2を添
加して電力損失の低減を図ったものである。
Conventionally, as this kind of power supply ferrite, there is Mn-Zn type ferrite proposed by the applicant in Japanese Patent Publication No. 53-28634.
This Mn-Zn system ferrite has CaO, SiO 2 , Cl and SnF 2 added to reduce power loss.

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

ところで近年、ディスプレイモニタ等の高解像度化、民
生用カラーテレビの大画面化等の要求により、これらに
使用される電源は、動作周波数の高周波化ならびに高負
荷化が進展している。
By the way, in recent years, due to demands for higher resolution of display monitors and the like and larger screens of color televisions for consumer use, power supplies used for these have been increasing in operating frequency and load.

しかしながら、従来のMn-Zn系フェライトでは電力損失
が増大し、電源の温度上昇が著しく、信頼性の低下が大
きいという問題点があった。
However, the conventional Mn-Zn ferrite has a problem that power loss increases, the temperature of the power supply rises remarkably, and the reliability decreases greatly.

この発明は、上記問題点を解決するため、高周波、高負
荷においても電力損失を著しく改善した低損失Mn-Zn系
フェライトからなる低損失酸化物磁性材料を提供するこ
とを目的とするものである。
In order to solve the above problems, it is an object of the present invention to provide a low-loss oxide magnetic material composed of a low-loss Mn-Zn ferrite, which has significantly improved power loss even at high frequencies and high loads. .

〔課題を解決するための手段〕[Means for Solving the Problems]

この発明の低損失酸化物磁性体は、Fe2O352〜56モル
%、MnO 32〜42モル%およびZnO 5〜15モル%を主成分
とし、これにPを10〜70ppm、SiO2を100〜300ppm、CaO
を200〜2000ppm副成分として同時に含むことにより、上
記従来技術の問題点を解決したものである。
The low-loss oxide magnetic material of the present invention is mainly composed of Fe 2 O 3 52 to 56 mol%, MnO 32 to 42 mol% and ZnO 5 to 15 mol%, to which P is added at 10 to 70 ppm and SiO 2 is added. 100-300ppm, CaO
The above-mentioned problems of the prior art are solved by simultaneously containing 200 to 2000 ppm as a subcomponent.

〔作用〕[Action]

この発明の低損失酸化物磁性材料は、Mn-Zn系フェライ
トからなるもので、Fe2O3、MnOおよびZnOを主成分と
し、副成分としてPを10〜70ppm、SiO2を100〜300ppm、
CaOを200〜2000ppmの重量比でそれぞれ複合添加したも
のであり、各成分を酸化物の状態で配合し、または酸化
物となる塩の形で配合し、焼成して得られる。
The low-loss oxide magnetic material of the present invention is composed of Mn-Zn based ferrite and contains Fe 2 O 3 , MnO and ZnO as main components, P as an auxiliary component of 10 to 70 ppm, SiO 2 of 100 to 300 ppm,
CaO is a composite addition of CaO at a weight ratio of 200 to 2000 ppm, and is obtained by blending each component in the state of an oxide or in the form of a salt to be an oxide and firing.

この発明の低損失酸化物磁性材料は電力損失を著しく低
減でき、130kHz程度の周波数領域でも充分な低損失特性
を実現可能である。また変成器の磁心に使用した場合、
稼動時に発熱が伴うが、この発明の低損失フェライトは
60℃ないし100℃程度の温度範囲で電力損失が最も低く
なるよう設定が可能である。このため実働時の電力損失
を少なくすることができる。
The low-loss oxide magnetic material of the present invention can remarkably reduce the power loss, and can realize a sufficiently low-loss characteristic even in the frequency region of about 130 kHz. When used as a transformer core,
Although it generates heat during operation, the low-loss ferrite of the present invention
The power loss can be set to be lowest in the temperature range of 60 ℃ to 100 ℃. Therefore, power loss during actual operation can be reduced.

〔発明の実施例〕Example of Invention

以下、この発明の実施例について説明する。 Examples of the present invention will be described below.

Fe2O353.5モル%、MnO38.5モル%およびZnO8.0モル%を
主成分とする原料を仮焼した後、微粉砕して得たフェラ
イト粉末に副成分としてH3PO479ppm(Pとして30pp
m)、SiO2を200ppm、CaCO3を1640ppm(CaOとして1000pp
m)の割合で添加混合の上、結合剤としてポリビニール
アルコール溶液を加え造粒後、外径60mm、内径40mm、高
さ10mmのリング状試料に成形圧1ton/cm2で成形した。た
だし、これらの添加物は予め原料に含まれているものを
分析し、添加量が全体として上記値となるように調整し
た。この試料を酸素濃度を制御したN2雰囲気中で1350
℃、2時間本焼成を行った。
Fe 2 O 3 53.5 mol%, MnO 38.5 mol% and ZnO 8.0 mol% were calcined and then finely pulverized to obtain a ferrite powder, and H 3 PO 4 79 ppm (P As 30pp
m), SiO 2 200ppm, CaCO 3 1640ppm (CaO 1000pp
m) was added and mixed, a polyvinyl alcohol solution was added as a binder, and the mixture was granulated and molded into a ring-shaped sample having an outer diameter of 60 mm, an inner diameter of 40 mm and a height of 10 mm at a molding pressure of 1 ton / cm 2 . However, as for these additives, those contained in the raw material were analyzed in advance, and the addition amounts were adjusted so as to be the above values as a whole. This sample was subjected to 1350 in an N 2 atmosphere with controlled oxygen concentration.
Main firing was performed at 2 ° C. for 2 hours.

この試料を周波数25kHz、磁束密度2000Gauss、100℃の
測定条件において電力損失を測定した結果、60mW/cm3
あった。この時の波形は正弦波である。また、10kHz、1
0T、10mAにおける初透磁率μiを測定した結果1883であ
った。
The power loss of this sample was measured at a frequency of 25 kHz, a magnetic flux density of 2000 Gauss and a temperature of 100 ° C., and the result was 60 mW / cm 3 . The waveform at this time is a sine wave. Also, 10kHz, 1
As a result of measuring the initial magnetic permeability μi at 0 T and 10 mA, it was 1883.

さらに主成分を同一とし、また試料作成の方法も同一手
順とし、副成分を変化させ、電力損失、μiを測定した
結果を表1に示す。
Further, Table 1 shows the results of measuring the power loss and μi with the same main component and the same sample preparation method with different subcomponents.

この表1中の電力損失およびμiの測定条件は実施例1
と同様である。
The conditions for measuring the power loss and μi in Table 1 are as in Example 1.
Is the same as.

以上の結果から、P、SiO2およびCaOを複合添加するこ
とにより、電力損失が大幅に改善され、低損失酸化物磁
性材料が得られることが明らかである。
From the above results, it is apparent that the combined addition of P, SiO 2 and CaO significantly improves the power loss and obtains a low loss oxide magnetic material.

ただし副成分のPが10ppmよりも少ない場合、結晶粒径
が小さく、また70ppmより多い場合は大きくなるため、
電力損失が共に大きくなり、不適当である。
However, if P as an accessory component is less than 10 ppm, the crystal grain size will be small, and if it is more than 70 ppm, it will be large.
It is inappropriate because the power loss increases together.

副成分のSiO2は100ppmより少ない場合も、300ppmより多
い場合も共に電気抵抗は減少し、電力損失が増大するた
め不適当である。CaOは2000ppmより多いと結晶粒径は小
さくなるが、ヒステリシスロスが増大するため電力損失
は大きくなる。CaOが200ppmより少なくなると結晶粒界
層が薄くなり、エディカレントロスが増大するため不適
当である。また本発明における上記副成分は本焼成前に
おいて含まれていれば、その添加はどの工程にて行って
も差し支えない。
When the content of SiO 2 as a sub-component is less than 100 ppm or more than 300 ppm, the electrical resistance decreases and the power loss increases, which is unsuitable. When CaO is more than 2000 ppm, the crystal grain size becomes small, but the hysteresis loss increases and the power loss increases. When CaO is less than 200 ppm, the grain boundary layer becomes thin and eddy current loss increases, which is not suitable. Further, if the above-mentioned subcomponents in the present invention are contained before the main calcination, the addition may be carried out in any step.

〔発明の効果〕〔The invention's effect〕

以上のように、この発明によれば、Fe2O3、MnOおよびZn
Oを主成分とし、副成分としてPを10〜70ppm、SiO2を10
0〜300ppmおよびCaOを200〜2000ppm複合添加した組成と
することにより、電力損失を著しく低減でき、このため
高周波ディスプレイモニタ、大画面カラーテレビ等の電
源の効率化、小形化に寄与でき、産業上極めて有益であ
る。
As described above, according to the present invention, Fe 2 O 3 , MnO and Zn
O is the main component, P is 10 to 70 ppm and SiO 2 is 10 as secondary components.
By adding 0 to 300 ppm and CaO to 200 to 2000 ppm in combination, power loss can be significantly reduced, which can contribute to higher efficiency and miniaturization of power supplies for high frequency display monitors, large screen color TVs, etc. It is extremely beneficial.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】Fe2O3 52〜56モル%、MnO 32〜42モル%お
よびZnO 5〜15モル%を主成分とし、これにPを10〜70p
pm、SiO2を100〜300ppmおよびCaOを200〜2000ppm副成分
として同時に含むことを特徴とする低損失酸化物磁性材
料。
1. Fe 2 O 3 52 to 56 mol%, MnO 32 to 42 mol% and ZnO 5 to 15 mol% as main components, and P to 10 to 70 p.
A low loss oxide magnetic material characterized by containing pm, SiO 2 of 100 to 300 ppm and CaO of 200 to 2000 ppm as auxiliary components at the same time.
JP63178718A 1988-07-18 1988-07-18 Low loss oxide magnetic material Expired - Lifetime JPH0710744B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP63178718A JPH0710744B2 (en) 1988-07-18 1988-07-18 Low loss oxide magnetic material
GB8915563A GB2220935B (en) 1988-07-18 1989-07-07 Magnetic oxide material
DE3922997A DE3922997A1 (en) 1988-07-18 1989-07-12 LOW LOSS OXIDE MAGNETIC MATERIAL
KR1019890010092A KR920001163B1 (en) 1988-07-18 1989-07-15 Low loss ferrite mage-netic materials
US07/381,302 US4985167A (en) 1988-07-18 1989-07-18 Low-loss oxide magnetic material
GB9209763A GB2253843B (en) 1988-07-18 1992-05-06 Magnetic oxide material
GB9209762A GB2253842B (en) 1988-07-18 1992-05-06 Magnetic oxide material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63178718A JPH0710744B2 (en) 1988-07-18 1988-07-18 Low loss oxide magnetic material

Publications (2)

Publication Number Publication Date
JPH0230660A JPH0230660A (en) 1990-02-01
JPH0710744B2 true JPH0710744B2 (en) 1995-02-08

Family

ID=16053350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63178718A Expired - Lifetime JPH0710744B2 (en) 1988-07-18 1988-07-18 Low loss oxide magnetic material

Country Status (1)

Country Link
JP (1) JPH0710744B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3389170B2 (en) * 1999-10-12 2003-03-24 ティーディーケイ株式会社 NiMnZn ferrite

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5229439A (en) * 1975-09-01 1977-03-05 Mitsubishi Heavy Ind Ltd Method of removing heterogeneous layer generated in heat resisting steel
JPS5328634A (en) * 1976-08-27 1978-03-17 Hitachi Cable Ltd Bonding of filmy materials
JPS58114401A (en) * 1981-12-28 1983-07-07 Tdk Corp Superlow loss ferrite for power source
JPS62219903A (en) * 1986-03-20 1987-09-28 Tohoku Metal Ind Ltd Manufacture of low loss oxide magnetic material
JPS62235221A (en) * 1986-04-02 1987-10-15 Japan Metals & Chem Co Ltd Production of high-purity iron oxide
JPS63116406A (en) * 1986-11-05 1988-05-20 Tdk Corp Ferrite core
JPH01294538A (en) * 1988-05-23 1989-11-28 Kemiraito Kogyo Kk Oxide iron for ferrite

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5229439A (en) * 1975-09-01 1977-03-05 Mitsubishi Heavy Ind Ltd Method of removing heterogeneous layer generated in heat resisting steel
JPS5328634A (en) * 1976-08-27 1978-03-17 Hitachi Cable Ltd Bonding of filmy materials
JPS58114401A (en) * 1981-12-28 1983-07-07 Tdk Corp Superlow loss ferrite for power source
JPS62219903A (en) * 1986-03-20 1987-09-28 Tohoku Metal Ind Ltd Manufacture of low loss oxide magnetic material
JPS62235221A (en) * 1986-04-02 1987-10-15 Japan Metals & Chem Co Ltd Production of high-purity iron oxide
JPS63116406A (en) * 1986-11-05 1988-05-20 Tdk Corp Ferrite core
JPH01294538A (en) * 1988-05-23 1989-11-28 Kemiraito Kogyo Kk Oxide iron for ferrite

Also Published As

Publication number Publication date
JPH0230660A (en) 1990-02-01

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