JPS59156920A - Magnetic oxide material - Google Patents

Magnetic oxide material

Info

Publication number
JPS59156920A
JPS59156920A JP58027367A JP2736783A JPS59156920A JP S59156920 A JPS59156920 A JP S59156920A JP 58027367 A JP58027367 A JP 58027367A JP 2736783 A JP2736783 A JP 2736783A JP S59156920 A JPS59156920 A JP S59156920A
Authority
JP
Japan
Prior art keywords
oxide
oxide material
magnetic oxide
magnetic
weight
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
JP58027367A
Other languages
Japanese (ja)
Other versions
JPS6256088B2 (en
Inventor
Masao Ishiwaki
石脇 将男
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
Nippon Ferrite 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 Nippon Ferrite Ltd filed Critical Nippon Ferrite Ltd
Priority to JP58027367A priority Critical patent/JPS59156920A/en
Publication of JPS59156920A publication Critical patent/JPS59156920A/en
Publication of JPS6256088B2 publication Critical patent/JPS6256088B2/ja
Granted legal-status Critical Current

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

Abstract

PURPOSE:To obtain a magnetic oxide material having high magnetic permeability, causing only a small loss, and suitable for use as the material of the iron core of a converter for communications equipment by blending ferric oxide, manganese oxide and zinc oxide as principal components with specified metallic oxides. CONSTITUTION:This magnetic oxide material is obtd. by blending 50-56mol% Fe2O3 (A), 22-39mol% MnO (B) and 8-25mol% ZnO (C) as principal components with 0.003-0.1wt% CaO (D) and 0.003-0.05wt% Bi2O3 (E) as secondary components.

Description

【発明の詳細な説明】 本発明は、通信機用の変成器磁心として使用するのに適
する高初透磁率と低損失特性を有する酸化物磁性材料に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oxide magnetic material having high initial permeability and low loss characteristics suitable for use as a transformer core for communication equipment.

近年、d子装置の小型化が進んでいるが、これに対して
電子装置に使用される電子部品についても小型化が要求
されている。この要求に従って本発明者は、高透磁率か
つ低損失インダクタンス素子′の開発に従事し、本発明
をするに至つた。
2. Description of the Related Art In recent years, miniaturization of d-sensor devices has progressed, and in response there has been a demand for miniaturization of electronic components used in electronic devices. In response to this demand, the present inventor engaged in the development of a high magnetic permeability and low loss inductance element, and came up with the present invention.

本発明は、上記の事よシ、高透磁率と低損失な特性を有
する酸化物磁性材料を提供するものである。
In addition to the above, the present invention provides an oxide magnetic material having high magnetic permeability and low loss characteristics.

即ち、酸化第二鉄(FeyOg )、酸化マンガン(M
nO)、酸化亜鉛(ZnO)を主成分とし、酸化力にシ
ラA (Cab) 0.003〜0.1重量%、酸化く
スマス(BizOi) 0.005〜0.05重量%お
よび酸化バナジウム(v20す0.003〜0.1重、
1%を複合添加することによって、高透磁率かつ低損失
な酸化物磁性材料を得るものである。
That is, ferric oxide (FeyOg), manganese oxide (M
The main component is zinc oxide (ZnO), and its oxidizing power includes 0.003 to 0.1% by weight of Cab, 0.005 to 0.05% by weight of BizOi, and vanadium oxide ( v20su 0.003~0.1 weight,
By adding 1% of the compound, an oxide magnetic material with high magnetic permeability and low loss can be obtained.

以下。図面によ)詳細に本発明を説明する。below. The invention will now be explained in detail (with reference to the drawings).

第1図および第2図は酸化第二鉄(p6x、Og、)5
2モルチ、酸化マンガン(rvinO)26モル係、酸
化亜鉛(Zn0) 22モル係から成る基本組成に、酸
化力に’/ +) A (Cab) 0.005−0.
1 重量価、酸化ビスマス(BizOi)0.005−
0.05 、in1%、dllll化ハクフA (Vz
Os) 0.Oo3〜0.os ffljt%を単独又
は複合添加し、混合、仮焼後1300°0で焼成した場
合の初透磁率μiacの特性曲線であシ、第1図はCa
Oを0,01Wt % トし、曲#1〜曲11+115
はそれぞれV t Osを0. 0.005、(1,0
50、IWt多添加したものであ)、第2図はVxOs
を0.01wt%とじ、曲線6〜曲線10はそれぞれC
aOを0.0,005.0,01.0,05.0,1w
t%添加したものでらる。又、第3図は第1図の、場合
の損失係数のグラフでhb、曲線11〜曲#!15ハソ
レソhV*osを0.0.005.0.01、o、as
O,1wt%添加したものであ)、第4図は第2図の場
合の損失係数のグラフであシ、曲1〜16〜曲線20は
、それぞれCaOを0.0.003、o、oi、0.0
5.0.1wt%添加したものである。図面より、酸化
カルシウム、酸化バナジウム単独の添加ではaiacの
向上が見られないが、酸化ビスマスとの複合添加によ、
90,005〜0,03wt%の範囲でaiacが著し
く向上することが判かる。
Figures 1 and 2 show ferric oxide (p6x, Og,)5
The basic composition consists of 2 mol. of manganese oxide (rvinO), 26 mol.
1 Weight value, bismuth oxide (BizOi) 0.005-
0.05, in1%, dlllllized Hakufu A (Vz
Os) 0. Oo3~0. Figure 1 shows the characteristic curve of the initial magnetic permeability μiac when os ffljt% is added singly or in combination, mixed, calcined and then fired at 1300°0.
O to 0.01Wt%, songs #1 to songs 11+115
are respectively V t Os 0. 0.005, (1,0
Figure 2 shows VxOs.
0.01wt%, curves 6 to 10 are C
aO 0.0,005.0,01.0,05.0,1w
t% added. Also, Fig. 3 is a graph of the loss coefficient in the case of Fig. 1, hb, curve 11 to song #! 15 hV*os 0.0.005.0.01, o, as
4 is a graph of the loss coefficient in the case of FIG. , 0.0
5.0.1 wt% was added. From the drawing, it can be seen that the addition of calcium oxide and vanadium oxide alone does not improve AIAC, but when combined with bismuth oxide,
It can be seen that the aiac is significantly improved in the range of 90,005 to 0.03 wt%.

また、Cab、 Bi zOi傾合添合添加シ、Ca0
0、C11−C,03wt%Bi2’s 0.005〜
0.05wt%の範囲でAiacをらまシ低丁させるこ
となく、損失が著しく小さくなる。又、v206、Bi
zOi腹。
In addition, Cab, BizOi gradient addition, Ca0
0, C11-C, 03wt% Bi2's 0.005~
In the range of 0.05 wt%, the loss is significantly reduced without causing Aiac to decrease. Also, v206, Bi
zOi belly.

合添加K x 9 VxOs o、 oos 〜0.0
5 wt% 、BixusO,005−0,05wt%
の範囲でaiacの低下をあまシ低下させることなく、
損失が小さくなる。
Combined addition K x 9 VxOs o, oos ~0.0
5 wt%, BixusO,005-0,05 wt%
without reducing the AIAC in the range of
Loss becomes smaller.

CaO1di20s 、 V2(J6複合添加によシ、
Ca00.01〜0.03wt%、Bit’s 0.0
05〜0.05wt俤、VxOs O,005〜0.0
5wt%の範囲でaiacをあまシ低下させることなく
、用失を著しく小さくすることができる。
CaO1di20s, V2 (by J6 composite addition,
Ca00.01-0.03wt%, Bit's 0.0
05~0.05wt, VxOs O,005~0.0
Within the range of 5 wt%, the loss of use can be significantly reduced without significantly lowering the aiac.

実施例 Fezes s2 モル%、MnO26モA/ %、Z
n022モルチから成る基本組成にCaOを0.01又
は0.0°2重−7%、Bit’sをo、oi m4%
、v2Qsを0.01又は0.02重遺饅複合添加し、
ボールミルで20時間混会し、800’Oで2時間仮焼
した後外径30ダ内径180、高さ°10nのリング状
試料に成形し、1300°0で4時間1.0%の酸素を
含む窒素雰囲気中で焼成したフェライトの1(lKHz
での透磁率(aiac)、磁気損失係数(tanδ/μ
1ac)を第1表に示す。
Example Fezes s2 mol%, MnO26mol A/%, Z
Basic composition consisting of n022 molti with CaO 0.01 or 0.0°2 weight-7%, Bit's o, oi m4%
, adding 0.01 or 0.02 of v2Qs,
After mixing in a ball mill for 20 hours and calcining at 800°C for 2 hours, it was molded into a ring-shaped sample with an outer diameter of 30°, an inner diameter of 180mm, and a height of 10nm. 1 (lKHz) of ferrite fired in a nitrogen atmosphere containing
magnetic permeability (aiac), magnetic loss coefficient (tanδ/μ
1ac) are shown in Table 1.

第1表 以上、詳記した如く、本発明によれば、高透磁率でsb
低損失である酸化物磁性材料を得ることができるもので
あシ、工業的に非常に有意義なものである。
As detailed in Table 1 and above, according to the present invention, sb with high magnetic permeability
Since it is possible to obtain an oxide magnetic material with low loss, it is of great industrial significance.

【図面の簡単な説明】[Brief explanation of drawings]

第1図〜第4図はPet’s 52モ#%、Mn026
モルチ、Zn022モルチを主成分とし、’CaO1B
i2’s 、VzOsを単独又は複合添加した場合のグ
ラフでsb、第1図はCaOを0.01wt%一定とし
た初透磁率のグラフであ’p 、dX 2図はVzOs
を0.01 wt%一定とした初透磁率のグラフであシ
、第3図は第1図の場合の損失係数のグラフでらシ、第
4図は第2図の場合の損失係・数のグラフである。 代理人 梶 原 弘1 二θ 第1図 θ     0.(N     O,03θ、058/
2θ3 (w−1%ン 第3図 Bix03(wt % ) 第2 目 第4 図 B; 203(Wl: % )
Figures 1 to 4 are Pet's 52Mo#%, Mn026
Molch, Zn022 morch as the main component, 'CaO1B
i2's is a graph when VzOs is added alone or in combination, sb, Figure 1 is a graph of initial magnetic permeability with CaO constant at 0.01 wt%'p, dX Figure 2 is a graph for VzOs
Figure 3 is a graph of the initial permeability with constant 0.01 wt%, Figure 3 is a graph of the loss coefficient in the case of Figure 1, and Figure 4 is the loss coefficient/number in the case of Figure 2. This is a graph of Agent Hiroshi Kajihara1 2θ Figure 1θ 0. (NO, 03θ, 058/
2θ3 (w-1% Fig. 3 Bix03 (wt %) 2nd Fig. 4 B; 203 (Wl: %)

Claims (1)

【特許請求の範囲】[Claims] 酸化第二鉄(Fears ) 5O−sH1酸化マンガ
ン(MnO) 22−39 %ル%、酸化亜鉛(ZnO
:’8〜25モルチを主成分とし、酸化カルシウム(C
ab) 0.003〜0.1重、t%、酸化ビスマス(
Bi20g ) 0.003〜0.05重量%、酸化バ
ナジ9 A (VzOII) 0.003〜0.1 J
it% ヲ副成分トして同時に含むことを特徴とする酸
化物磁性材料。
Ferric oxide (Fears) 5O-sH1 Manganese oxide (MnO) 22-39%, Zinc oxide (ZnO
:'8~25 molti as the main component, calcium oxide (C
ab) 0.003 to 0.1 weight, t%, bismuth oxide (
Bi20g) 0.003-0.05% by weight, vanadium oxide 9A (VzOII) 0.003-0.1J
An oxide magnetic material characterized in that it simultaneously contains two subcomponents.
JP58027367A 1983-02-21 1983-02-21 Magnetic oxide material Granted JPS59156920A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58027367A JPS59156920A (en) 1983-02-21 1983-02-21 Magnetic oxide material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58027367A JPS59156920A (en) 1983-02-21 1983-02-21 Magnetic oxide material

Publications (2)

Publication Number Publication Date
JPS59156920A true JPS59156920A (en) 1984-09-06
JPS6256088B2 JPS6256088B2 (en) 1987-11-24

Family

ID=12219072

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58027367A Granted JPS59156920A (en) 1983-02-21 1983-02-21 Magnetic oxide material

Country Status (1)

Country Link
JP (1) JPS59156920A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0696933A (en) * 1991-03-07 1994-04-08 Hitachi Ferrite Ltd Mn-zn ferrite
JPH06263447A (en) * 1993-03-05 1994-09-20 Hitachi Ferrite Ltd High permeability mn-zn ferrite

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5149079A (en) * 1974-10-25 1976-04-27 Nippon Mining Co ZAIRYOSHIKENSOCHI
JPS56160330A (en) * 1980-05-13 1981-12-10 Tohoku Metal Ind Ltd Magnetic oxide material
JPS6253446A (en) * 1985-08-30 1987-03-09 日産テクシス株式会社 Apparatus for driving weft yarn engaging body of weft yarn storage apparatus

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5149079A (en) * 1974-10-25 1976-04-27 Nippon Mining Co ZAIRYOSHIKENSOCHI
JPS56160330A (en) * 1980-05-13 1981-12-10 Tohoku Metal Ind Ltd Magnetic oxide material
JPS6253446A (en) * 1985-08-30 1987-03-09 日産テクシス株式会社 Apparatus for driving weft yarn engaging body of weft yarn storage apparatus

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0696933A (en) * 1991-03-07 1994-04-08 Hitachi Ferrite Ltd Mn-zn ferrite
JPH06263447A (en) * 1993-03-05 1994-09-20 Hitachi Ferrite Ltd High permeability mn-zn ferrite

Also Published As

Publication number Publication date
JPS6256088B2 (en) 1987-11-24

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