JPH0779043B2 - Mn-Zn ferrite - Google Patents

Mn-Zn ferrite

Info

Publication number
JPH0779043B2
JPH0779043B2 JP4084563A JP8456392A JPH0779043B2 JP H0779043 B2 JPH0779043 B2 JP H0779043B2 JP 4084563 A JP4084563 A JP 4084563A JP 8456392 A JP8456392 A JP 8456392A JP H0779043 B2 JPH0779043 B2 JP H0779043B2
Authority
JP
Japan
Prior art keywords
khz
weight
magnetic permeability
ferrite
frequency
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
JP4084563A
Other languages
Japanese (ja)
Other versions
JPH0696933A (en
Inventor
豊 樋口
等 上田
勝之 城口
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.)
Hitachi Metals Ltd
Original Assignee
Hitachi 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 Hitachi Ferrite Ltd filed Critical Hitachi Ferrite Ltd
Publication of JPH0696933A publication Critical patent/JPH0696933A/en
Publication of JPH0779043B2 publication Critical patent/JPH0779043B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

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

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、高透磁率で低損失なM
n―Zn系フェライトを提供することを目的とする。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to M having high magnetic permeability and low loss.
It is an object to provide an n-Zn ferrite.

【0002】[0002]

【従来の技術】高透磁率を有するMn―Zn系フェライ
トは、Fe2O3、ZnO、MnOを主成分として構成
され、この主成分に対し、種々の添加物(Bi、Ca、
V)を加えた材料となっていた。
2. Description of the Related Art Mn--Zn type ferrite having a high magnetic permeability is mainly composed of Fe2O3, ZnO and MnO, and various additives (Bi, Ca,
It was a material to which V) was added.

【0003】このMn―Zn系フェライトは、トランス
やノイズフィルタ等の磁心として用いられ、高透磁率特
性を利用して部品の小型化が進められている。
This Mn--Zn type ferrite is used as a magnetic core of a transformer, a noise filter, etc., and miniaturization of parts is being promoted by utilizing its high magnetic permeability characteristics.

【0004】[0004]

【発明が解決しようとする課題】例えばノイズフィルタ
用の磁心として、高周波(〜500kHz)まで高い透
磁率を有する材料の要求が強まってきた。
For example, as a magnetic core for a noise filter, there has been an increasing demand for a material having a high magnetic permeability up to a high frequency (up to 500 kHz).

【0005】ところが、従来のMn―Zn系フェライト
の場合、透磁率の周波数特性が悪く、高周波になると透
磁率が低下し、高周波での損失が増大するといった問題
点があった。
However, in the case of the conventional Mn-Zn type ferrite, there is a problem that the frequency characteristic of magnetic permeability is poor, the magnetic permeability decreases at high frequencies, and the loss at high frequencies increases.

【0006】本発明は、上記の事を鑑みて、高周波で高
透磁率のMn―Zn系フェライトを得ることを目的とす
る。
In view of the above, the present invention has a high frequency and a high frequency.
The purpose is to obtain a Mn-Zn ferrite having magnetic permeability .

【0007】[0007]

【課題を解決するための手段】本発明は、Mn―Zn系
フェライトにおいて、副成分としてCaOを0.05〜
0.12重量%、Bi2O3を0.04重量%以下(但
し、0重量%を含まない)、SiO2を0.01〜0.
02重量%(但し、0.01重量%を含まない)含有し
ているMn―Zn系フェライトであり、高周波で高い初
透磁率を有するものである。
According to the present invention, CaO is added as an auxiliary component in an Mn--Zn system ferrite in an amount of 0.05 to 0.05.
0.12 wt%, Bi2O3 is 0.04 wt% or less (however, 0 wt% is not included), and SiO2 is 0.01 to 0.
It is a Mn-Zn-based ferrite containing 02% by weight (not including 0.01% by weight), and has a high initial magnetic permeability at high frequencies.

【0008】本発明において、副成分量を限定した理由
は、CaO、Bi2O3、SiO2が所定量より少ない
と損失が増大し、CaOが所定量より多いと透磁率が低
くなり、Bi2O3、SiO2が所定量より多いと異常
焼結が起こり、好ましくないからである。
In the present invention, the reason for limiting the amounts of subcomponents is that when CaO, Bi2O3, and SiO2 are less than a predetermined amount, the loss increases, and when CaO is more than a predetermined amount, the magnetic permeability decreases and Bi2O3 and SiO2 are present. This is because if the amount is larger than the fixed amount, abnormal sintering will occur, which is not preferable.

【0009】[0009]

【実施例】Fe2O3 53モル%、MnO 27モル
%、ZnO 20モル%を主成分とし、これにCaO、
Bi2O3、SiO2を表1に示す分量含有する原料を
作製し、これを850℃で2時間仮焼し、その後ボール
ミルで8時間粉砕し、リング状に圧縮成形し、1380
℃5時間酸素濃度5%で焼成した。また、実施例と同様
の試料作製工程において焼成条件(焼成温度、焼成雰囲
気)を変えて各試料を作製した。そのコアの100kH
zと500kHzの初透磁率μi、100kHzでのt
anδ/μi及び100kHzにおける初透磁率μiを
Aとし、500kHzにおける初透磁率μiをBとした
とき、(A−B)/Aで示される100kHzに対する
500kHzにおける初透磁率μiの変化率△μi/μ
iを表1に示す。この表1において、本発明の範囲内の
ものは実施例とし、範囲外のものは比較例としている。
Examples Fe2O3 53 mol%, MnO 27 mol%, ZnO 20 mol% were the main components, and CaO,
A raw material containing Bi2O3 and SiO2 in the amounts shown in Table 1 was prepared, calcined at 850 ° C. for 2 hours, crushed with a ball mill for 8 hours, and compression-molded into a ring shape.
Baking was carried out at 5 ° C. for 5 hours at an oxygen concentration of 5%. In addition, each sample was prepared by changing the baking conditions (baking temperature, baking atmosphere) in the same sample manufacturing process as in the example. 100kH of the core
z and initial permeability μi of 500 kHz, t at 100 kHz
anδ / μi and initial permeability μi at 100 kHz
A, and the initial permeability μi at 500 kHz was B.
At 100 kHz indicated by (A−B) / A
Change rate of initial permeability μi at 500 kHz Δμi / μ
i is shown in Table 1. In Table 1, those within the range of the present invention are examples, and those outside the range are comparative examples.

【0010】[0010]

【表1】 [Table 1]

【0011】また、実施例(試料No.8)と比較例
(試料No.10)の透磁率の周波数特性を図1に示
す。この図1及び表1に示されるとおり、本発明の実施
例は、高周波でも透磁率の高い材料であることがわか
る。これと同時に損失の小さい材料であることもわか
る。
Further, the frequency characteristics of magnetic permeability of the example (Sample No. 8) and the comparative example (Sample No. 10) are shown in FIG. As shown in FIG. 1 and Table 1, it is understood that the examples of the present invention are materials having high magnetic permeability even at high frequencies. At the same time, it can be seen that the material has low loss.

【0012】また、含有するCaO、Bi2O3、Si
O2は、CaOは0.05〜0.12重量%、Bi2O
3は0.04重量%以下(但し、0重量%を含まな
い)、SiO2を0.01〜0.02重量%(但し、
0.01重量%を含まない)の範囲内であれば、表1に
示した実施例とほぼ類似の特性が得られることがわかっ
た。
Further, CaO, Bi2O3 and Si contained
O2 is 0.05 to 0.12 wt% CaO, Bi2O
3 is 0.04% by weight or less (not including 0% by weight), and SiO2 is 0.01 to 0.02% by weight (however,
It was found that the characteristics similar to those of the examples shown in Table 1 can be obtained within the range of 0.01% by weight).

【0013】但し、焼成温度が1350〜1380℃の
範囲内であれば、そのときの酸素濃度は1%を超えるこ
とが必要である。酸素濃度が1%以下のときは、周波数
500kHzの初透磁率の低下や相対損失係数tanδ
/μiの増大を招く。
However, if the firing temperature is in the range of 1350 to 1380 ° C., the oxygen concentration at that time must exceed 1%. When the oxygen concentration is 1% or less, the initial magnetic permeability at a frequency of 500 kHz decreases and the relative loss coefficient tan δ.
/ Μi increases.

【0014】また、焼成温度が1250〜1350℃の
範囲内であれば、そのときの酸素濃度は1%以下であ
る。酸素濃度が1%を超えると、初透磁率の低下を招
く。尚、含有する副成分のうち、CaOが0.05〜
0.08重量%の範囲で周波数100kHzに対する5
00kHzにおけるμiの変化率△μi/μiは10%
以下となり、特に高周波まで高い透磁率を得ることがで
きる。このときの焼成条件は、焼成温度1250〜13
50℃、酸素濃度1%以下である。
If the firing temperature is in the range of 1250 to 1350 ° C., the oxygen concentration at that time is 1% or less. When the oxygen concentration exceeds 1%, the initial magnetic permeability is lowered. Incidentally, CaO is 0.05 to
5 for frequency 100 kHz in the range of 0.08% by weight
Change rate of μi at 00kHz Δμi / μi is 10%
Below, it is possible to obtain a high magnetic permeability, especially up to a high frequency. The firing conditions at this time are firing temperatures of 1250 to 13
It is 50 ° C. and the oxygen concentration is 1% or less.

【0015】[0015]

【発明の効果】本発明によれば、高周波(500kH
z)まで高い透磁率を有し、しかも100kHzと50
0kHzでの透磁率の変化が小さいMn―Zn系フェラ
イトを得ることができる。
According to the present invention, a high frequency (500 kHz)
z) has a high magnetic permeability, and at 100 kHz and 50
It is possible to obtain a Mn—Zn-based ferrite with a small change in magnetic permeability at 0 kHz .

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

【図1】本発明に係る実施例と比較例との透磁率の周波
数特性である。
FIG. 1 is a frequency characteristic of magnetic permeability of an example according to the present invention and a comparative example.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭62−278162(JP,A) 特開 昭59−156920(JP,A) 特開 昭61−42105(JP,A) 特開 平6−140230(JP,A) 特開 平5−330906(JP,A) 特公 昭51−49019(JP,B2) 特公 昭53−18718(JP,B1) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) Reference JP-A-62-278162 (JP, A) JP-A-59-156920 (JP, A) JP-A-61-42105 (JP, A) JP-A-6- 140230 (JP, A) JP-A-5-330906 (JP, A) JP 51-49019 (JP, B2) JP 53-18718 (JP, B1)

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 Mn―Zn系フェライトにおいて、副成
分としてCaOを0.05〜0.12重量%、Bi23
を0.04重量%以下(但し、0重量%を含まない)、
SiO2を0.01〜0.02重量%(但し、0.01
重量%を含まない)含有し、初透磁率μiが周波数10
0kHzにおいて5000以上、500kHzにおいて
4000以上であることを特徴とするMn―Zn系フェ
ライト。
1. A Mn—Zn-based ferrite containing 0.05 to 0.12% by weight of CaO as a secondary component and Bi 2 O 3
0.04% by weight or less (excluding 0% by weight),
SiO 2 0.01 to 0.02% by weight (however, 0.01
Content is not included) and the initial permeability μi is 10
A Mn-Zn-based ferrite characterized by having a frequency of 5000 or more at 0 kHz and a frequency of 4000 or more at 500 kHz.
【請求項2】 Mn―Zn系フェライトにおいて、副成
分としてCaOが0.05〜0.08重量%、Bi 2 3
を0.04重量%以下(但し、0重量%を含まない)、
SiO 2 を0.01〜0.02重量%(但し、0.01
重量%を含まない)含有し、初透磁率μiが周波数10
0kHz及び500kHzにおいて5000以上、周波
数100kHzにおける初透磁率μiに対する周波数5
00kHzにおける初透磁率μiの変化率が10%以下
であることを特徴とするMn―Zn系フェライト。
2. A by-product of Mn--Zn ferrite
CaO is 0.05 to 0.08% by weight, Bi 2 O 3
0.04% by weight or less (excluding 0% by weight),
SiO 2 0.01 to 0.02% by weight (however, 0.01
Content is not included) and the initial permeability μi is 10
5000 or more at 0 kHz and 500 kHz, frequency
Frequency 5 for initial permeability μi at several 100 kHz
Change rate of initial permeability μi at 00 kHz is 10% or less
Mn-Zn ferrite, characterized in that it.
JP4084563A 1991-03-07 1992-03-05 Mn-Zn ferrite Expired - Lifetime JPH0779043B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP3-69238 1991-03-07
JP3069238A JPH05330906A (en) 1991-03-07 1991-03-07 Mn-zn-based ferrite

Related Child Applications (2)

Application Number Title Priority Date Filing Date
JP6331624A Division JP2731357B2 (en) 1994-12-08 1994-12-08 Method for producing Mn-Zn ferrite
JP6331625A Division JP2731358B2 (en) 1994-12-08 1994-12-08 Method for producing Mn-Zn ferrite

Publications (2)

Publication Number Publication Date
JPH0696933A JPH0696933A (en) 1994-04-08
JPH0779043B2 true JPH0779043B2 (en) 1995-08-23

Family

ID=13396974

Family Applications (2)

Application Number Title Priority Date Filing Date
JP3069238A Pending JPH05330906A (en) 1991-03-07 1991-03-07 Mn-zn-based ferrite
JP4084563A Expired - Lifetime JPH0779043B2 (en) 1991-03-07 1992-03-05 Mn-Zn ferrite

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP3069238A Pending JPH05330906A (en) 1991-03-07 1991-03-07 Mn-zn-based ferrite

Country Status (1)

Country Link
JP (2) JPH05330906A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05330906A (en) * 1991-03-07 1993-12-14 Hitachi Ferrite Ltd Mn-zn-based ferrite

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5149019A (en) * 1974-10-25 1976-04-27 Victor Company Of Japan Bideoteepurekoodano batsuteryoryokeihosochi
JPS5318718A (en) * 1976-08-02 1978-02-21 Toshin Chemical Co Preparation of sodium salt of cephalothin
JPS59156920A (en) * 1983-02-21 1984-09-06 Nippon Ferrite Ltd Magnetic oxide material
JPS6142105A (en) * 1984-08-02 1986-02-28 Tdk Corp Manganese-zinc system ferrite material and magnetic core for high frequency power supply transformer
JPS62278162A (en) * 1986-05-23 1987-12-03 株式会社トーキン Oxide ferrite composition and manufacture
JPH05330906A (en) * 1991-03-07 1993-12-14 Hitachi Ferrite Ltd Mn-zn-based ferrite
JPH06140230A (en) * 1991-05-16 1994-05-20 Tokin Corp Manufacture of low-loss oxide magnetic material

Also Published As

Publication number Publication date
JPH0696933A (en) 1994-04-08
JPH05330906A (en) 1993-12-14

Similar Documents

Publication Publication Date Title
KR100389821B1 (en) MnZn ferrite production process, MnZn ferrite, and ferrite core for power supplies
JPH09306716A (en) Sintered ferrite material and manufacture thereof
JP2002134312A (en) Magnetic material and coil part using the same
JPH081844B2 (en) High frequency low loss ferrite for power supply
JP3635410B2 (en) Method for producing manganese-zinc based ferrite
JPH0779043B2 (en) Mn-Zn ferrite
JP2731358B2 (en) Method for producing Mn-Zn ferrite
JP2731357B2 (en) Method for producing Mn-Zn ferrite
JP3042627B2 (en) Low loss ferrite
JPH0433755B2 (en)
JP2556917B2 (en) Manufacturing method of high frequency and low loss ferrite for power supply
JP2802839B2 (en) Oxide soft magnetic material
JP2907253B2 (en) High permeability Mn-Zn ferrite
JP2726388B2 (en) High magnetic permeability high saturation magnetic flux density Ni-based ferrite core and method of manufacturing the same
JP3454472B2 (en) Manganese-zinc ferrite and method for producing the same
JP2000299217A (en) High permeability oxide magnetic material
WO2023182133A1 (en) MnZn-BASED FERRITE
JP2627676B2 (en) Manufacturing method of oxide magnetic material
JP3044666B2 (en) Low loss ferrite for power supply
JP2001348226A (en) Magnetic ferrite material
JP2963067B2 (en) Low loss ferrite
JPH0555463B2 (en)
JP2000091114A (en) High permeability oxide magnetic material
JPH11228217A (en) Mn-zn ferrite
JP3128656B2 (en) Method for producing magnetic oxide

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080823

Year of fee payment: 13

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090823

Year of fee payment: 14

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090823

Year of fee payment: 14

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100823

Year of fee payment: 15

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100823

Year of fee payment: 15

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110823

Year of fee payment: 16

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110823

Year of fee payment: 16

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120823

Year of fee payment: 17

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120823

Year of fee payment: 17