JPH04328806A - Manufacture of manganese-zinc ferrite - Google Patents
Manufacture of manganese-zinc ferriteInfo
- Publication number
- JPH04328806A JPH04328806A JP3124831A JP12483191A JPH04328806A JP H04328806 A JPH04328806 A JP H04328806A JP 3124831 A JP3124831 A JP 3124831A JP 12483191 A JP12483191 A JP 12483191A JP H04328806 A JPH04328806 A JP H04328806A
- Authority
- JP
- Japan
- Prior art keywords
- firing
- manganese
- ferrite
- magnetic permeability
- zinc ferrite
- 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.)
- Pending
Links
Landscapes
- Soft Magnetic Materials (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、マンガン−亜鉛系フェ
ライトの製造方法に関し、更に詳しく述べると、少量の
In2 O3 を添加し焼成することにより、短時間焼
成で高透磁率特性を呈する酸化物磁性材料の製造方法に
関するものである。[Industrial Application Field] The present invention relates to a method for manufacturing manganese-zinc ferrite, and more specifically, by adding a small amount of In2O3 and firing, the present invention produces an oxide that exhibits high magnetic permeability characteristics in a short firing time. The present invention relates to a method of manufacturing a magnetic material.
【0002】0002
【従来の技術】フェライトの透磁率を高くするためには
結晶の粒径を大きくすれば良いとされているが、そのた
めには高温長時間の焼成が必要となる。しかしマンガン
−亜鉛系フェライトのように亜鉛を含む場合には、あま
り長時間高温状態においておくと、その表面から酸化亜
鉛が蒸発するため逆に透磁率が低下する。そこで従来技
術によれば、焼成時にフェライト材料に同種のフェライ
ト粉体を被せるなど何らかのシールを施し、亜鉛が蒸発
しないように工夫した状態で焼成していた。BACKGROUND OF THE INVENTION It is believed that increasing the magnetic permeability of ferrite can be achieved by increasing the grain size of the crystals, but this requires firing at high temperatures and for long periods of time. However, if the material contains zinc, such as manganese-zinc ferrite, if it is left in a high temperature state for too long, the zinc oxide will evaporate from the surface, resulting in a decrease in magnetic permeability. Therefore, according to the prior art, during firing, the ferrite material is covered with the same type of ferrite powder or some other kind of sealing, and the ferrite material is fired in a devised state to prevent the zinc from evaporating.
【0003】しかし、この方法では数十時間といった長
時間焼成を行うため焼成コストが増大し、また焼成後に
シールを除去する作業が必要なため生産コストが高くな
り、全体として量産化には不向きである。[0003] However, this method requires firing for a long period of time, such as several tens of hours, which increases the firing cost, and the process of removing the seal after firing increases the production cost, making it unsuitable for mass production as a whole. be.
【0004】そこで、これらの欠点を解消できるものと
して、少量のMoO3 を添加するとともに、低酸素濃
度(0.01〜5%)で急速昇温(1100℃以上での
昇温速度が200〜600℃/時)を行い焼結させるマ
ンガン−亜鉛系フェライトの製造方法が開発された(特
開昭61−91908号公報参照)。[0004] Therefore, as a solution to these drawbacks, a small amount of MoO3 is added, and a low oxygen concentration (0.01 to 5%) is used to rapidly raise the temperature (the heating rate is 200 to 600 degrees Celsius at 1100°C or higher). A method for producing manganese-zinc ferrite has been developed in which the ferrite is sintered by sintering (1988-91908).
【0005】[0005]
【発明が解決しようとする課題】上記の急速昇温による
方法は高透磁率化及び高密度化の点で極めて有効である
が、低酸素濃度雰囲気中で焼成することから、使用でき
る焼成炉に制約があり、また焼成コストもかかる等の欠
点がある。[Problems to be Solved by the Invention] The method using rapid temperature rise described above is extremely effective in increasing magnetic permeability and density, but since firing is performed in an atmosphere with a low oxygen concentration, it is difficult to use a firing furnace that can be used. There are limitations and drawbacks such as high firing costs.
【0006】本発明の目的は、上記のような従来技術の
欠点を解消し、連続炉を用いた比較的短時間の焼成サイ
クルで、低コストで量産しうる高透磁率特性を呈するマ
ンガン−亜鉛系フェライトの製造方法を提供することで
ある。The object of the present invention is to solve the above-mentioned drawbacks of the prior art, and to create a manganese-zinc material that exhibits high magnetic permeability and can be mass-produced at low cost using a relatively short firing cycle using a continuous furnace. An object of the present invention is to provide a method for producing a ferrite-based ferrite.
【0007】[0007]
【課題を解決するための手段】上記の目的を達成できる
本発明は、従来一般に用いられている組成のマンガン−
亜鉛系フェライト材料に対して極く少量のIn2 O3
を添加し焼成する方法である。In2 O3 の添加
量は、主成分となるマンガン−亜鉛系フェライト材料に
対して0.02〜0.3重量%の範囲とする。ここで用
いるマンガン−亜鉛系フェライト材料は、通常、高透磁
率酸化物磁性材料として用いられているこの種の材料の
組成範囲とほぼ同様であり、Fe2 O3 50〜58
モル%、ZnO 3〜30モル%、残部がMnOであ
るような組成範囲から選ぶ。[Means for Solving the Problems] The present invention, which can achieve the above-mentioned objects, has a composition of manganese which has been generally used in the past.
Very small amount of In2 O3 in zinc-based ferrite material
This method involves adding and firing. The amount of In2O3 added is in the range of 0.02 to 0.3% by weight based on the manganese-zinc ferrite material which is the main component. The manganese-zinc ferrite material used here has a composition range that is almost the same as that of this type of material that is normally used as a high permeability oxide magnetic material, and has a composition range of 50 to 58 Fe2O3.
The composition is selected from a composition range in which ZnO is 3 to 30 mol% and the balance is MnO.
【0008】フェライトの焼成は、連続炉による24時
間以下の焼成サイクルで行うことができ、その際、特に
シール等を施す必要はない。また昇温速度や昇温・焼結
雰囲気に特に注意を払う必要はない。[0008] The firing of ferrite can be carried out in a continuous furnace in a firing cycle of 24 hours or less, and there is no need for special sealing or the like. Further, there is no need to pay particular attention to the temperature increase rate, temperature increase, and sintering atmosphere.
【0009】[0009]
【作用】上記の製造方法によって得られるマンガン−亜
鉛系フェライトの透磁率は従来品のそれよりも遙に向上
する。それは以下の理由による。In2 O3 は80
0℃以上で分解し、In2 Oが昇華する。昇華したイ
ンジウムの高原子価イオンが粒界近傍に存在することに
より、粒界近傍の金属イオンの空格子量が増加して粒界
の移動度が高まり、粒成長が促進させる。本発明で用い
るIn2 O3 は、同様の効果を示すPbO,Bi2
O3 ,MoO3 などに比べて昇華速度が小さいた
め、昇温速度や昇温雰囲気に注意を払う必要はなく、1
300℃以上の粒成長過程までInO2 の昇華量が抑
えられ、InO2 による粒成長促進効果が持続するこ
とになる。そして最終的には添加したインジウムの殆ど
は昇華してしまい粒界近傍に残らないため、粒界応力な
どによる透磁率の低下も見られず、透磁率が10,00
0程度もしくはそれ以上の高透磁率特性が発現する。[Function] The magnetic permeability of the manganese-zinc ferrite obtained by the above manufacturing method is much higher than that of conventional products. This is due to the following reasons. In2 O3 is 80
It decomposes at temperatures above 0°C and In2O sublimates. The presence of high-valent ions of sublimated indium near the grain boundaries increases the amount of vacancies of metal ions near the grain boundaries, increases the mobility of the grain boundaries, and promotes grain growth. In2O3 used in the present invention is similar to PbO, Bi2, which has similar effects.
Since the sublimation rate is lower than that of O3, MoO3, etc., there is no need to pay attention to the heating rate or heating atmosphere.
The amount of sublimation of InO2 is suppressed until the grain growth process reaches 300° C. or higher, and the grain growth promoting effect of InO2 is maintained. Finally, most of the added indium sublimes and does not remain near the grain boundaries, so there is no decrease in magnetic permeability due to grain boundary stress, and the magnetic permeability is 10,000.
A high magnetic permeability characteristic of about 0 or more is exhibited.
【0010】0010
【実施例】図1はマンガン−亜鉛系フェライト(Fe2
O3 53モル%,ZnO 20モル%,MnO
27モル%)にIn2 O3 を0〜0.4重量%添
加し、3種の条件で焼成を行ったときの透磁率を示して
いる。焼成条件を表1に示す。[Example] Figure 1 shows manganese-zinc ferrite (Fe2
O3 53 mol%, ZnO 20 mol%, MnO
The graph shows the magnetic permeability when 0 to 0.4% by weight of In2O3 was added to 27% by mole) and firing was performed under three conditions. Table 1 shows the firing conditions.
【0011】[0011]
【表1】[Table 1]
【0012】僅かなIn2 O3 の添加で透磁率は急
激に上昇する。焼成条件が変わっても、In2 O3
の添加量に対する透磁率の特性曲線は基本的には変化し
ない。しかし大気中で焼成を行う方(例A)が全体とし
て特性は向上する。In2 O3 の添加量が増大しす
ぎても透磁率は低下するから、より好ましくは0.03
〜0.2重量%程度とすることである。[0012] Addition of a small amount of In2O3 causes a rapid increase in magnetic permeability. Even if the firing conditions change, In2 O3
The characteristic curve of magnetic permeability with respect to the amount of addition does not basically change. However, the properties are improved overall when firing is performed in the atmosphere (Example A). If the amount of In2O3 added is too large, the magnetic permeability decreases, so it is more preferably 0.03.
The content should be approximately 0.2% by weight.
【0013】[0013]
【発明の効果】本発明は上記のように、マンガン−亜鉛
系フェライトにIn2 O3 を少量添加し焼成する方
法であるから、InO2 の昇華が少ないため1300
℃以上での連続粒成長が促進され、しかも最終的にはI
nO2 の殆どは昇華してしまい粒界近傍に残らない。
このため、粒界応力などによる透磁率の低下も見られず
、10,000程度もしくはそれ以上の高透磁率が発現
する。そして、本発明方法では24時間以下の焼成サイ
クルで、しかも大気中昇温でも高透磁率磁性材料の量産
が可能であるため、焼成コストを大幅に下げることがで
きる。また本発明方法では上記のように、粒成長が促進
され、添加物も粒界に残らないから、フライバックトラ
ンス用コアのような高密度酸化物磁性も高性能化できる
。Effects of the Invention As described above, the present invention is a method in which a small amount of In2O3 is added to manganese-zinc ferrite and then fired.
Continuous grain growth is promoted above ℃, and finally I
Most of the nO2 sublimes and does not remain near the grain boundaries. Therefore, no decrease in magnetic permeability due to grain boundary stress is observed, and a high magnetic permeability of about 10,000 or more is exhibited. Furthermore, in the method of the present invention, high permeability magnetic materials can be mass-produced with a firing cycle of 24 hours or less and even at elevated temperature in the atmosphere, so the firing cost can be significantly reduced. Furthermore, as described above, in the method of the present invention, grain growth is promoted and additives do not remain at grain boundaries, so high-density oxide magnets such as cores for flyback transformers can also have high performance.
【図1】焼成条件をパラメータとしたIn2 O3 添
加量−透磁率特性線図。FIG. 1 is an In2O3 addition amount-magnetic permeability characteristic diagram with firing conditions as parameters.
Claims (1)
nO 3〜30モル%、残部がMnOである組成のマ
ンガン−亜鉛系フェライト材料に対して、In2 O3
を0.02〜0.3重量%添加し焼成することを特徴
とするたマンガン−亜鉛系フェライトの製造方法。[Claim 1] Fe2O3 50-58 mol%, Z
In2O3
A method for producing manganese-zinc ferrite, which comprises adding 0.02 to 0.3% by weight of manganese-zinc ferrite and firing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3124831A JPH04328806A (en) | 1991-04-27 | 1991-04-27 | Manufacture of manganese-zinc ferrite |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3124831A JPH04328806A (en) | 1991-04-27 | 1991-04-27 | Manufacture of manganese-zinc ferrite |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04328806A true JPH04328806A (en) | 1992-11-17 |
Family
ID=14895179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3124831A Pending JPH04328806A (en) | 1991-04-27 | 1991-04-27 | Manufacture of manganese-zinc ferrite |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04328806A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014123708A (en) * | 2012-11-20 | 2014-07-03 | Jfe Chemical Corp | MnZn FERRITE AND PROCESS OF MANUFACTURING THE SAME |
| JP2014123709A (en) * | 2012-11-20 | 2014-07-03 | Jfe Chemical Corp | MnZn FERRITE CORE AND PROCESS OF MANUFACTURING THE SAME |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4897093A (en) * | 1972-03-18 | 1973-12-11 | ||
| JPS5678429A (en) * | 1979-11-26 | 1981-06-27 | Hitachi Metals Ltd | Magnetic oxide material |
| JPS6191908A (en) * | 1984-10-12 | 1986-05-10 | Fuji Elelctrochem Co Ltd | Manufacture of high permeability oxide magnetic material |
-
1991
- 1991-04-27 JP JP3124831A patent/JPH04328806A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4897093A (en) * | 1972-03-18 | 1973-12-11 | ||
| JPS5678429A (en) * | 1979-11-26 | 1981-06-27 | Hitachi Metals Ltd | Magnetic oxide material |
| JPS6191908A (en) * | 1984-10-12 | 1986-05-10 | Fuji Elelctrochem Co Ltd | Manufacture of high permeability oxide magnetic material |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014123708A (en) * | 2012-11-20 | 2014-07-03 | Jfe Chemical Corp | MnZn FERRITE AND PROCESS OF MANUFACTURING THE SAME |
| JP2014123709A (en) * | 2012-11-20 | 2014-07-03 | Jfe Chemical Corp | MnZn FERRITE CORE AND PROCESS OF MANUFACTURING THE SAME |
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