JPS6177304A - Manufacture of mn-zn ferrite - Google Patents

Manufacture of mn-zn ferrite

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Publication number
JPS6177304A
JPS6177304A JP59199138A JP19913884A JPS6177304A JP S6177304 A JPS6177304 A JP S6177304A JP 59199138 A JP59199138 A JP 59199138A JP 19913884 A JP19913884 A JP 19913884A JP S6177304 A JPS6177304 A JP S6177304A
Authority
JP
Japan
Prior art keywords
cao
added
alkaline earth
silicate
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.)
Granted
Application number
JP59199138A
Other languages
Japanese (ja)
Other versions
JPH0436564B2 (en
Inventor
Yoshihiro Suenaga
末永 義弘
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.)
Proterial Ltd
Original Assignee
Sumitomo Special Metals Co Ltd
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 Sumitomo Special Metals Co Ltd filed Critical Sumitomo Special Metals Co Ltd
Priority to JP59199138A priority Critical patent/JPS6177304A/en
Publication of JPS6177304A publication Critical patent/JPS6177304A/en
Publication of JPH0436564B2 publication Critical patent/JPH0436564B2/ja
Granted legal-status Critical Current

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

Abstract

PURPOSE:To attain exellent magnetic characteristics without producing abnormal crystal formation, by adding CaO, and one kind of alkali metals, alkaline earth metals, and silicate of Zr or Al of predetermined amounts into principal composition consisting of Fe2O3, MnO, ZnO of predetermined proportions, and by fine- grinding, molding, and sintering them. CONSTITUTION:After CaO of 0.01-0.2wt% and one kind of alkali metal,s alkaline earth metals, and silicate of Zr or Al of 0.005-0.2wt% are added into calcined raw material of principal composition consisting of FeO3 of 50-70mol %, MnO of 10-40mol%, and ZnO of 5-30mol%, they are fine-ground, molded, and sintered. CaO is added for the purpose of providing low magnetic loss. Adding one kind of a alkali metals, alkaline earth metals, and silicate of Al or Zr can prevent large-size crystal formation which would be produced by being added in the form of SiO2, and can attain excellent magnetic characteristics.

Description

【発明の詳細な説明】 利用産業分野 この発明は、Mn −ZTI系フェライトの製造方法に
係り、高い焼結温度でも異常結晶組織を生成することな
く、すぐれた磁気特性、特に低磁気損失特性を有するh
−zη系フェライトの製造方法に関する。
[Detailed description of the invention] Industrial field of application The present invention relates to a method for manufacturing Mn-ZTI ferrite, which produces excellent magnetic properties, especially low magnetic loss properties, without producing abnormal crystal structures even at high sintering temperatures. have h
-Regarding a method for manufacturing zη-based ferrite.

背景技術 tln −Zn系フェライトは、通信機器、電子計算機
、VTR,磁気ヘッド等、各種民生用機器に多用され、
それぞれの用途に応じた改良が施されている。
BACKGROUND TECHNOLOGY tln-Zn ferrite is widely used in various consumer devices such as communication equipment, electronic computers, VTRs, and magnetic heads.
Improvements have been made to suit each application.

今日の機器の小型化並びに高性能化のため、ますます、
磁気損失の少ない磁性材料が求められている。
Due to the miniaturization and higher performance of today's equipment,
There is a need for magnetic materials with low magnetic loss.

かかるMn −ZTI系フェライトにおいて、残留損。In such Mn-ZTI ferrite, residual loss.

ヒステリシス損、渦電流損の少ない材料を得る方法とし
て、従来、アルカリ金属、アルカリ土類金属の酸化物あ
るいはAl2O3、ZrO2及びCaOを含有するMn
 −ZTI系フェライトが提案され、さらには、CaO
と5LO2の複合添加により、電気抵抗を大きくし、磁
気特性を向上させる手段がよく知られていた。しかし、
材料の密度を向上させるために、焼結温度を高くすると
、異常な焼結反応が起り、焼結組織が大きな結晶と小さ
な結晶との混在状態を呈し、磁気特性の劣化を招来しや
すい問題があった。
Conventionally, as a method for obtaining materials with low hysteresis loss and eddy current loss, oxides of alkali metals and alkaline earth metals or Mn containing Al2O3, ZrO2 and CaO have been used.
-ZTI-based ferrite has been proposed, and furthermore, CaO
A well-known method is to increase the electrical resistance and improve the magnetic properties by adding 5LO2 and 5LO2 in combination. but,
When the sintering temperature is raised to improve the density of the material, an abnormal sintering reaction occurs, resulting in a sintered structure that is a mixture of large and small crystals, which can easily lead to deterioration of magnetic properties. there were.

一般に、Mi  Zn系フェライトの製造において、基
本組成の原料に対して、添加物を仮焼前の粉砕時に、あ
るいは基本組成の仮焼原料の粉砕時に、単独酸化物の形
にて単体あるいは複合添加し、その後に成型、焼成ある
いはさらに、熱間静水圧プレス処理されていた。しかし
、従来製造方法においては、上記組成のフェライトの磁
気特性を向上させるには限度があり、今日切望されてい
る磁気特性、特にすぐれた低磁気損失特性を有する1−
7Tl系フエライトが19られなかった。
In general, in the production of MiZn-based ferrite, additives are added singly or in combination in the form of single oxides to the raw material of the basic composition during pulverization before calcination, or during the pulverization of the calcination raw material of the basic composition. After that, it was molded, fired, or further subjected to hot isostatic pressing. However, with conventional manufacturing methods, there is a limit to improving the magnetic properties of ferrite with the above composition, and 1-
7Tl-based ferrite was not detected.

発明の目的 この発明は、上述のMn −ZTI系フェライトの現状
に鑑み、高い焼結温度でも異常結晶組織を生成すること
なく、すぐれた磁気特性が得られ、特に低磁気損失特性
を有するMn −ZTI系フェライトを目的として、r
−Zn系フェライトの磁気特性を向」ニさせることがで
きる製造方法を目的としている。
Purpose of the Invention In view of the current state of the Mn-ZTI ferrite described above, the present invention has been made to develop a Mn-ZTI ferrite that can obtain excellent magnetic properties even at high sintering temperatures without forming an abnormal crystal structure, and has especially low magnetic loss properties. For the purpose of ZTI ferrite, r
The object of the present invention is to provide a manufacturing method that can improve the magnetic properties of Zn-based ferrite.

発明の構成と効果 この発明は、一般に実施されているMn −Zn系フェ
ライトの製造工程、すなわち、基本組成の原litに対
して、添加物を仮焼前の混合時に添加するか、あるいは
基本組成原料粉砕時に添加し、ついで成型、焼結あるい
は、さらに熱間静水圧プレス処理する工程について、特
に、添加物原料の配合処理について種々検討した結果、
CaOと、アルカリ金属、アルカリ土類金属あるいはZ
r、AIの珪酸塩の1種からなる添加物原料を、基本組
成の仮焼原料の粉砕時に配合添加し、これを微粉砕した
のち、成型、焼結あるいは、さらに、熱間静水圧プレス
処理することにより、従来の製造り法に比べて一段と磁
気特性が向上したMn−Zn系フェライトが得られるこ
とを知見したものである。
Structure and Effects of the Invention The present invention utilizes the commonly practiced manufacturing process of Mn-Zn ferrite, that is, adding additives to the original lit of the basic composition during mixing before calcination, or changing the basic composition. As a result of various studies on the process of adding raw materials during pulverization and then molding, sintering, or further hot isostatic pressing, in particular, the process of blending additive raw materials, we found that:
CaO and alkali metal, alkaline earth metal or Z
An additive raw material consisting of one type of silicate of AI is mixed and added during the pulverization of the calcined raw material of the basic composition, and after being finely pulverized, it is molded, sintered, or further subjected to hot isostatic pressing treatment. It has been discovered that by doing so, it is possible to obtain Mn--Zn-based ferrite with much improved magnetic properties compared to conventional manufacturing methods.

すなわち、この発明は、 Fe20350〜70モル%。That is, this invention: Fe20350-70 mol%.

Mn010〜40モル%。Mn010-40 mol%.

ZTIO5〜30モル%。ZTIO 5-30 mol%.

からなる基本組成に対し、 CaO0.01wt%〜0.2wt%と、アルカリ金属
、アルカリ土類金属 あるいは Zr、Hの珪酸塩の1種0.005wt%〜
0.2wt%を、 上記基本組成の仮焼原料に配合添加し、微粉砕したのち
成型、焼結することを特徴とする門nZηフエライ1〜
の製造方法である。
With respect to the basic composition consisting of: 0.01 wt% to 0.2 wt% of CaO and 0.005 wt% to one type of silicate of alkali metal, alkaline earth metal, or Zr, H
0.2wt% is blended and added to the calcined raw material having the above basic composition, which is pulverized, then molded and sintered.
This is a manufacturing method.

この発明において、すぐれた磁気特性の門n −Zn系
フェライトが得られる理由は、以下のとおりである。
The reason why an n-Zn ferrite with excellent magnetic properties can be obtained in this invention is as follows.

水系フェライトの透磁率を大きくし、保磁力を小さくし
、カリ磁気損失を小さくするため、添加物として、Ca
0.5LO2とアルカリ金属あるいはアルカリ土類金属
の酸化物、またはM2O3、ZrO2などを複合添加し
、焼結密度を上げるため、高温度で焼結するが、前記添
加物は、結晶粒界に遍在して、高い電気抵抗を有する層
が形成される。しかしながら、5LOpは一般に粗大結
晶組織を誘起し易、 く、高い電気抵抗層を澗滅するた
め、磁気損失を劣化させていたのである。そこで、この
5LO2を、添加物のアルカリ金属、アルカリ土類金属
あるいは7.r、AJの珪酸塩の形にて添加すると、高
温度の焼結においても、粗大結晶組織が生成され難くな
り、均一な結晶組織が得られ、すぐれた磁気特性が得ら
れるのである。
In order to increase the magnetic permeability, reduce the coercive force, and reduce the potash magnetic loss of water-based ferrite, Ca is added as an additive.
0.5LO2 and oxides of alkali metals or alkaline earth metals, or M2O3, ZrO2, etc. are added in combination and sintered at high temperatures to increase the sintered density. A layer with high electrical resistance is formed. However, 5LOp generally tends to induce a coarse crystal structure and destroys a high electrical resistance layer, resulting in a deterioration of magnetic loss. Therefore, this 5LO2 can be used as additives such as alkali metals, alkaline earth metals, or 7. When r, AJ is added in the form of a silicate, a coarse crystal structure is hardly generated even during high temperature sintering, a uniform crystal structure is obtained, and excellent magnetic properties are obtained.

この発明においてアルカリ金属の珪酸塩は、t11a2
Sし03、K2SLOaが好ましく、また、アルカリ土
類金属の珪酸塩としては、Ca si Oa、Mg5L
Os、Ba5jO3,5rSLOsが好ましい。
In this invention, the alkali metal silicate is t11a2
Ca si Oa, Mg5L are preferable, and as alkaline earth metal silicates, Ca si Oa, Mg5L are preferable.
Os, Ba5jO3,5rSLOs are preferred.

組成の限定理由 この発明による酸化物磁性材料において、基本組成並び
に添加物の組成を限定した理由を以下に説明する。
Reason for Limiting the Composition The reason for limiting the basic composition and the composition of additives in the oxide magnetic material according to the present invention will be explained below.

Mn −Zn系フェライトの基本組成を、Fe2035
o〜70モル%、 MnO10〜40モル%。
The basic composition of Mn-Zn ferrite is Fe2035
o to 70 mol%, MnO 10 to 40 mol%.

ZnO5〜30モル%とした理由は、これ以外の組成で
は、透磁率が極めて小さくなり、また、保磁力も大きく
なりすぎて軟質磁性材料として実用的でないためである
The reason why the ZnO content is 5 to 30 mol % is that if the composition is other than this, the magnetic permeability will be extremely low and the coercive force will also be too large to be practical as a soft magnetic material.

CaOは、低磁気損失を得るために添加するが、0.0
1 wt%未満では電気抵抗が小さくなり、所要の磁気
特性が得られず、また、0,2wt%を越える添加では
、高密度化のため焼結温度を高くすると、異常組織が発
生しやすくなるため、0.01 wt%から0.2wt
%wt%とする。
CaO is added to obtain low magnetic loss, but 0.0
If it is less than 1 wt%, the electrical resistance becomes small and the required magnetic properties cannot be obtained, and if it is added more than 0.2 wt%, abnormal structures are likely to occur when the sintering temperature is increased to increase the density. Therefore, from 0.01 wt% to 0.2 wt
%wt%.

アルカリ金属、アルカリ土類金属またはM、Zrの珪酸
塩の1種を添加することは、この発明の特徴であり、5
id2の形で添加するために生成する粗大結晶組織が防
止され、すぐれた磁気特性が得られるため添加するが、
0.005wt%未満では上記効果が少なく、また、0
.2wt%を越えると、高密度化のために焼成温度を高
くした際に逆に粗大結晶組織を生成してしまうため、0
,005wt%〜0.2wt%の添加とする。
It is a feature of this invention that one of silicates of alkali metals, alkaline earth metals or M, Zr is added, and 5
It is added in the form of id2, which prevents the formation of a coarse crystal structure and provides excellent magnetic properties.
If it is less than 0.005wt%, the above effect will be small, and if it is less than 0.005wt%,
.. If it exceeds 2 wt%, a coarse crystal structure will be generated when the firing temperature is increased to increase the density.
,005wt% to 0.2wt%.

また、この発明における主原料、添加物には、焼成によ
り酸化物となる化合物を使用することができる。
Further, as the main raw materials and additives in this invention, compounds that become oxides upon firing can be used.

実施例 Fe2O353モル%、閂n031モル%、 ZnO1
6モル%。
Example Fe2O3 53 mol%, bar n0 31 mol%, ZnO1
6 mol%.

からなる基本組成の原料を配合、混合したのち、850
℃で仮焼成した。
After blending and mixing raw materials with a basic composition of 850
Temporary firing was performed at ℃.

上記の基本組成仮焼原料を、ボールミルで粉砕する際1
に、基本組成に対して、第1表に示す如く、CaOに、
Zr5LOt、/V 203 3SL 02、Na2S
iO3、K2Sε0.の複合添加、 また、第2表に示す如く、CaOに、Ca5LO2、M
g SL O3、Ba Si o8、Sr SL 02
の複合添加の形で、添加物原料を配合、混合粉砕した。
When pulverizing the above basic composition calcined raw material with a ball mill, 1
For the basic composition, as shown in Table 1, CaO,
Zr5LOt, /V 203 3SL 02, Na2S
iO3, K2Sε0. In addition, as shown in Table 2, to CaO, Ca5LO2, M
g SL O3, Ba Si o8, Sr SL 02
Additive raw materials were blended, mixed and ground in the form of a composite addition.

その後、外径36mmX内径24mmX高さ6mm寸法
のリング状に成型し、さらに、酸素濃度を制御した窒素
ガス雰囲気で、1250℃、3時間の条件で焼成した。
Thereafter, it was molded into a ring shape with dimensions of 36 mm outer diameter x 24 mm inner diameter x 6 mm height, and was further fired at 1250° C. for 3 hours in a nitrogen gas atmosphere with controlled oxygen concentration.

得られた焼成品の磁気特性を測定し、その結果を第1表
と第2表に示す。
The magnetic properties of the obtained fired product were measured and the results are shown in Tables 1 and 2.

また、比較のため、添加物原料を単独酸化物の形にて、
基本組成の仮焼原料の粉砕時に、添加粉砕する以外は、
基本組成、添加物配合量及び成型。
For comparison, we also used additive raw materials in the form of single oxides.
When pulverizing the calcined raw material of the basic composition, other than addition pulverization,
Basic composition, amount of additives, and molding.

焼成条件を本発明例(陽1〜12.25〜36)と同一
条件として、焼成した比較焼成品の磁気特性を測定し、
第1表と第2表に示ず。
The magnetic properties of the comparative fired products were measured under the same firing conditions as the inventive examples (positive 1 to 12.25 to 36),
Not shown in Tables 1 and 2.

なお、第1表と第2表におけるコア損失は、上記リング
状焼成品を巻線し、100k)−1zの交流電流を流し
、2000Gのときのコア損失を測定した。
The core loss in Tables 1 and 2 was determined by winding the ring-shaped fired product, passing an alternating current of 100k)-1z, and measuring the core loss at 2000G.

第1表と第2表より明らかな如く、この発明の特徴であ
る添加物原料をCaOと珪酸塩の形にて、基本組成粉砕
時に添加配合することにより、Mn −Zn系フェライ
トは、コア損失の低減、磁気特性の改善に著しい効果が
あることが分る。
As is clear from Tables 1 and 2, by adding and blending the additive raw materials in the form of CaO and silicate, which are the characteristics of this invention, at the time of pulverization of the basic composition, Mn-Zn-based ferrite can be made with low core loss. It can be seen that there is a remarkable effect on reducing the magnetic properties and improving the magnetic properties.

以下余白Margin below

Claims (1)

【特許請求の範囲】 Fe_2O_3 50モル%〜70モル%、MnO 1
0〜40モル%、 ZnO 5〜30モル%、 からなる基本組成に対し、 CaO 0.01wt%〜0.2wt%と、アルカリ金
属、アルカリ土類金属 あるいはZr、Alの珪酸塩の1種0.005wt%〜
0.2wt%を、 上記基本組成の仮焼原料に配合添加し、 微粉砕したのち成型、焼結することを特徴とするMn−
Zn系フェライトの製造方法。
[Claims] Fe_2O_3 50 mol% to 70 mol%, MnO 1
0 to 40 mol%, ZnO 5 to 30 mol%, CaO 0.01 wt% to 0.2 wt%, and one type of silicate of alkali metal, alkaline earth metal, or Zr, Al. .005wt%~
A Mn-
A method for manufacturing Zn-based ferrite.
JP59199138A 1984-09-21 1984-09-21 Manufacture of mn-zn ferrite Granted JPS6177304A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59199138A JPS6177304A (en) 1984-09-21 1984-09-21 Manufacture of mn-zn ferrite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59199138A JPS6177304A (en) 1984-09-21 1984-09-21 Manufacture of mn-zn ferrite

Publications (2)

Publication Number Publication Date
JPS6177304A true JPS6177304A (en) 1986-04-19
JPH0436564B2 JPH0436564B2 (en) 1992-06-16

Family

ID=16402771

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59199138A Granted JPS6177304A (en) 1984-09-21 1984-09-21 Manufacture of mn-zn ferrite

Country Status (1)

Country Link
JP (1) JPS6177304A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0254901A (en) * 1988-08-19 1990-02-23 Mitsubishi Electric Corp Low-loss oxide magnetic material
CN103172358A (en) * 2013-03-21 2013-06-26 电子科技大学 High-Bs and high-Tc MnZn ferrite material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0254901A (en) * 1988-08-19 1990-02-23 Mitsubishi Electric Corp Low-loss oxide magnetic material
CN103172358A (en) * 2013-03-21 2013-06-26 电子科技大学 High-Bs and high-Tc MnZn ferrite material and preparation method thereof

Also Published As

Publication number Publication date
JPH0436564B2 (en) 1992-06-16

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