JPS60137830A - Production of ferrite of mn-zn system - Google Patents

Production of ferrite of mn-zn system

Info

Publication number
JPS60137830A
JPS60137830A JP58247567A JP24756783A JPS60137830A JP S60137830 A JPS60137830 A JP S60137830A JP 58247567 A JP58247567 A JP 58247567A JP 24756783 A JP24756783 A JP 24756783A JP S60137830 A JPS60137830 A JP S60137830A
Authority
JP
Japan
Prior art keywords
ferrite
mno
production
loss
mol
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
Application number
JP58247567A
Other languages
Japanese (ja)
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 JP58247567A priority Critical patent/JPS60137830A/en
Publication of JPS60137830A publication Critical patent/JPS60137830A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compounds Of Iron (AREA)
  • Soft Magnetic Materials (AREA)

Abstract

PURPOSE:In production of ferrite of Mn-Zn system, to obtain ferrite having improved magnetic characteristics (especially magnetic loss characteristics), by using MnO.OH as a MnO source. CONSTITUTION:In production of ferrite of Mn-Zn system having a basic composition consisting of 50-70mol% Fe2O3, 10-40mol% MnO, and 5-30mol% ZnO, given amounts of Fe2O3, ZnO, and MnO.OH are blended with other components (CaO, SiO2, ZrO2, and CeO2), calcined, crushed, molded, calcined in a nitrogen gas atmosphere having a controlled oxygen concentration, to prepare ferrite of Mn-Zn system. The above-mentioned ferrite of Mn-Zn system has smaller loss than one using MnCO3 as a MnO source and improved magnetic characteristics.

Description

【発明の詳細な説明】 この発明は、すぐれた磁気特性、特に低磁気損失特性を
有するMn −Zη系フェライトを製造できる方法に係
り、lln −Zn系フェライトの製造方法にd3番ノ
る配合原料のr′1nOWAの改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a Mn-Zn ferrite having excellent magnetic properties, particularly low magnetic loss properties, and a method for producing an lln-Zn ferrite using a blended raw material number d3. This invention relates to the improvement of r'1nOWA.

Mn −7,n系フェライトは、通信機器、電子計算機
、V T R1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。
Mn-7,n-based ferrite is widely used in various consumer devices such as communication equipment, electronic computers, and VTR1 magnetic heads, and has been improved according to each application.

今日の機器の小型化並びに高性能化のため、まずまず、
磁気損失の少ない磁性材料がめられている。
Due to the miniaturization and high performance of today's equipment,
Magnetic materials with low magnetic loss are being used.

かかるI′In−ZTl系フェライトにおいて、磁気損
失の少ない材料を得る方法として、電気抵抗を大きくす
ることにより、磁気特性の向上を計ってきたが、磁気損
失の低減化については、未だ十分に満足できるものとは
言えない。
In this I'In-ZTl ferrite, attempts have been made to improve the magnetic properties by increasing the electrical resistance as a way to obtain a material with low magnetic loss, but the reduction in magnetic loss has not yet been fully satisfied. I can't say it's possible.

この発明は、上記のMn −Zn系フェライトの現状に
鑑み、ず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系フエライ1〜を目的としてい
る。
In view of the current state of Mn--Zn-based ferrites, the present invention aims at providing Mn--ZTI-based ferrites 1 to 1 that provide superior magnetic properties, and particularly have low magnetic loss properties.

この発明は、Mn −Znn系フシイ[〜の磁気損失の
低減化を計るために、配合原料である従来使用のl″I
n Co 3に代えてMn0・OH配合使用することを
特徴とする。
In order to reduce the magnetic loss of Mn-Znn-based adhesive [...], the present invention aims to reduce the magnetic loss of
It is characterized by using a mixture of Mn0 and OH in place of nCo3.

すなわち、この発明は、Fe2O350〜70モル%。That is, in this invention, Fe2O350 to 70 mol%.

l″InO1(1〜40モル%。l″InO1 (1-40 mol%.

ZnO3〜3〇七ル%、からなる基本組成を有するIn
n−ZTIフエライr〜の製造方法において、配合原料
のr′lnO源どしてr’:no・OHを使用すること
を特徴どJるMn −Zn系フェライトの製造方法であ
る。
In having a basic composition of 3 to 307% ZnO
In the method for producing n-ZTI ferrite, r':no.OH is used as the r'lnO source of the compounded raw material.

Mn −Zn系フェライトの基本組成を、Fe2O35
G・〜70モル%、Mn010〜40モル%、ZnO3
〜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 basic composition of Mn-Zn ferrite is Fe2O35
G・~70 mol%, Mn010~40 mol%, ZnO3
The reason for setting the content 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.

この発明において、対象とするMn −Zn系フェライ
トには上記の基本組成を有するものに、下記の種々の添
加物を含有させ、焼結温度を高くしても、異常組織が起
りにくく、すぐれた低磁気損失特性が得られる。
In this invention, the target Mn-Zn ferrite has the above-mentioned basic composition and contains the following various additives, and even if the sintering temperature is increased, abnormal structures are difficult to occur and it has excellent properties. Low magnetic loss characteristics can be obtained.

この発明によるjan −znフェライトは、上記の基
本組成に添加物として、 CaOO,005〜0.3wt%。
The JAN-ZN ferrite according to the present invention includes CaOO, 0.005 to 0.3 wt% as an additive to the above basic composition.

Nb2050.005〜0.’25wt%。Nb2050.005~0. '25wt%.

S、020,001〜2wt%。S, 020,001-2 wt%.

VO0,01〜2111t%。VO0.01~2111t%.

/V2O30,01〜2wt%。/V2O30.01~2wt%.

Coo O,01〜2wt%。Coo O, 01-2wt%.

CuO0001〜o、2wt%。CuO0001~o, 2wt%.

ZrO20,01〜0,2wt%。ZrO20.01-0.2 wt%.

5nO20,01〜1wt%。5nO20.01-1 wt%.

Coo20.01〜0.2wt%。Coo20.01-0.2wt%.

TLO20,01〜 1.0wt%。TLO20.01~1.0wt%.

BL203 0.01〜0,2wt%。BL203 0.01-0.2wt%.

Ta205 o、oos〜0,2wt%。Ta205 o,oos~0.2wt%.

MgQ 0.01〜1.0wt%。MgQ 0.01-1.0wt%.

の1種または2種以上を含有するものである。It contains one or more of the following.

以下に、実施例を示し、この発明の効果を明らかにする
Examples will be shown below to clarify the effects of this invention.

配合原料にFe2O3、ZTIO、MnO・OHを用い
て、Fe2O353モル%、 MnO31モル%、 Z
nO16モル%。
Using Fe2O3, ZTIO, and MnO・OH as blending raw materials, Fe2O353 mol%, MnO3 1 mol%, Z
nO 16 mol%.

なる基本組成となるように秤量し、ざらに、Cab。Weigh it so that it has a basic composition of

SLO,ZrO2,−02を、第1表に示ず如く添加し
、配合、混合したのち、900℃で仮焼成した。その後
ボールミルで粉砕し、外径36mmX内仔240un 
X高さemm寸法のリング状に成型し、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。得られた焼成品の磁気特性を測定し、その結
果を第1表に示す。
SLO, ZrO2, -02 were added as shown in Table 1, blended and mixed, and then calcined at 900°C. After that, it was ground in a ball mill to make an outer diameter of 36mm and an inner diameter of 240un.
It was molded into a ring shape with dimensions of x height em and fired at 1250°C for 3 hours in a nitrogen gas atmosphere with controlled oxygen concentration. The magnetic properties of the obtained fired product were measured and the results are shown in Table 1.

また、比較のため、tlno源として、従来のMll 
Co 3を使用した以外は上記の条件でリング状の焼成
体を製造し、同様に磁気特性を測定した。
For comparison, we also used conventional Mll as a tlno source.
A ring-shaped fired body was manufactured under the above conditions except that Co 3 was used, and its magnetic properties were similarly measured.

なお、第1表におけるコア損失は、上記リング状焼成品
を巻線し、100kH7の交流電流を流し、2000G
のときのコア損失を測定した。
In addition, the core loss in Table 1 is calculated by winding the above ring-shaped fired product and passing an alternating current of 100kHz to 2000G.
The core loss was measured when

第1表より明らかな如く、この発明の製造方法に係るM
n −Zn系フェライト・は、コア損失の低減、磁気特
性の改善が茗しいことが分る。
As is clear from Table 1, M according to the manufacturing method of the present invention
It can be seen that n-Zn-based ferrite is effective in reducing core loss and improving magnetic properties.

以下余白 第1表Below margin Table 1

Claims (1)

【特許請求の範囲】 1 F1120350〜70モル%、11no10〜4
0モル%。 Zn0 5〜30モル%、からなる基本組成を有するI
nn−Znnフシイ1への製造方法において、配合原料
の11nO源として肖0・OHを使用することを特徴と
する肯−Zn系フェライトの製造方法。
[Claims] 1 F1120350-70 mol%, 11no10-4
0 mol%. I having a basic composition consisting of 5 to 30 mol% of Zn0
A method for producing nn-Zn ferrite, characterized in that the method for producing nn-Zn ferrite 1 uses 0.OH as a source of 11nO in the compounded raw material.
JP58247567A 1983-12-24 1983-12-24 Production of ferrite of mn-zn system Pending JPS60137830A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58247567A JPS60137830A (en) 1983-12-24 1983-12-24 Production of ferrite of mn-zn system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58247567A JPS60137830A (en) 1983-12-24 1983-12-24 Production of ferrite of mn-zn system

Publications (1)

Publication Number Publication Date
JPS60137830A true JPS60137830A (en) 1985-07-22

Family

ID=17165411

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58247567A Pending JPS60137830A (en) 1983-12-24 1983-12-24 Production of ferrite of mn-zn system

Country Status (1)

Country Link
JP (1) JPS60137830A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01129403A (en) * 1987-11-16 1989-05-22 Sony Corp High-frequebnc high-permeability magnetic material
EP0551907A2 (en) * 1992-01-14 1993-07-21 Matsushita Electric Industrial Co., Ltd. An oxide magnetic material
US5846448A (en) * 1994-04-27 1998-12-08 Tdk Corporation Ferrite and ferrite core for power supply
EP1547988A1 (en) * 2002-09-26 2005-06-29 TDK Corporation Ferrite material

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS501398A (en) * 1973-05-10 1975-01-08

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS501398A (en) * 1973-05-10 1975-01-08

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01129403A (en) * 1987-11-16 1989-05-22 Sony Corp High-frequebnc high-permeability magnetic material
EP0551907A2 (en) * 1992-01-14 1993-07-21 Matsushita Electric Industrial Co., Ltd. An oxide magnetic material
EP0551907A3 (en) * 1992-01-14 1994-07-13 Matsushita Electric Ind Co Ltd An oxide magnetic material
US5518642A (en) * 1992-01-14 1996-05-21 Matsushita Electric Industrial Co., Ltd. Oxide magnetic material
EP0716053A2 (en) * 1992-01-14 1996-06-12 Matsushita Electric Industrial Co., Ltd. An oxide magnetic material
EP0716053A3 (en) * 1992-01-14 1996-07-03 Matsushita Electric Ind Co Ltd
US5846448A (en) * 1994-04-27 1998-12-08 Tdk Corporation Ferrite and ferrite core for power supply
EP1547988A1 (en) * 2002-09-26 2005-06-29 TDK Corporation Ferrite material
EP1547988A4 (en) * 2002-09-26 2007-12-05 Tdk Corp Ferrite material

Similar Documents

Publication Publication Date Title
KR0131840B1 (en) Magnetic oxidel of ni-cu-zn system
US20020008336A1 (en) Ferrite material, method of manufacturing the same and deflection yoke core made from the material
JPH0238537B2 (en)
KR100420897B1 (en) Process for preparation of oxide magnetic compact
JPH0430726B2 (en)
JPS60137830A (en) Production of ferrite of mn-zn system
JPH0521859B2 (en)
US3415751A (en) Manganese-zinc ferrites
JPS6111892B2 (en)
JPS60262404A (en) Manufacture of mn-zn ferrite
JPH01101610A (en) Chip inductor
JPH07142222A (en) Low-loss mn-zn soft ferrite
US5053156A (en) Process for producing ferrite powder for ferrite magnets
JPH09295862A (en) Low loss ferrite material and signal chip inductor using the same
JPS6253446B2 (en)
JPS60132302A (en) Oxide magnetic material
JP2802839B2 (en) Oxide soft magnetic material
JP2510788B2 (en) Low power loss oxide magnetic material
JPH02129063A (en) Oxide magnetic material
JP2939035B2 (en) Soft magnetic oxide substance
JPH0350124A (en) Magnetic core of mn-zn ferrite
KR100302071B1 (en) Method for preparing soft magnetic ferrite
JPH03212906A (en) Manufacture of high frequency low loss ferrite for power supply
JPS6314406A (en) Oxide magnetic material
JP3552794B2 (en) Method for producing low-loss oxide magnetic material