JPH05315121A - Manufacture of ferrite - Google Patents

Manufacture of ferrite

Info

Publication number
JPH05315121A
JPH05315121A JP4114549A JP11454992A JPH05315121A JP H05315121 A JPH05315121 A JP H05315121A JP 4114549 A JP4114549 A JP 4114549A JP 11454992 A JP11454992 A JP 11454992A JP H05315121 A JPH05315121 A JP H05315121A
Authority
JP
Japan
Prior art keywords
ferrite
calcined
oxide
product
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.)
Granted
Application number
JP4114549A
Other languages
Japanese (ja)
Other versions
JP3239439B2 (en
Inventor
Koichi Watanabe
浩一 渡辺
Koji Yasumura
浩治 安村
Shigeru Yamanaka
繁 山中
Yoshio Onaka
良雄 尾中
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP11454992A priority Critical patent/JP3239439B2/en
Publication of JPH05315121A publication Critical patent/JPH05315121A/en
Application granted granted Critical
Publication of JP3239439B2 publication Critical patent/JP3239439B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To provide the manufacture of a ferrite, which can lessen the dispersion of sintering density in every lot of ferrites simply. CONSTITUTION:46-51mol% iron oxide (Fe2O3), 11-16mol% nickel oxide (NiO, etc.), 28-34mol% zinc oxide (ZnO, etc.), and 3-13mol% copper oxide (CuO, etc.) are combined and mixed. The mixed material is roughly halved into two groups, and the respective groups are calcined for two hours at temperatures of 1100+ or -50 deg.C and 850+ or -50 deg.C so as to manufacture a first calcined substance (1100+ or -50 deg.C) and a second calcined substance (850+ or -50 deg.C). These two calcined substances are mixed and baked by specified quantities. Hereby, even if the baking temperature is dispersed, specified cavity ratio can be gotten.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は筒型ロータリートランス
用コア等に用いられるフェライトの製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing ferrite used in a core for a cylindrical rotary transformer or the like.

【0002】[0002]

【従来の技術】ビデオテープレコーダ等のヘッドシリン
ダーに装着されるロータリートランス用コアは、平板型
と筒型の2種類がある。後者のロータリートランス用コ
アは焼結したフェライトコアをインナーコアとアウター
コアに切削して仕上げている。それらの寸法精度は、外
径,内径及び溝幅は±20μm以内の要求がなされてい
る。一方これら部材に用いられるフェライトは一般的に
酸化鉄,酸化ニッケル,酸化亜鉛に酸化銅を加え、混合
し、仮焼し、適当なバインダを加え、造粒したものを金
型を用いて、所定の形状にプレス成形した後、焼結する
ことによって製造されている。
2. Description of the Related Art There are two types of rotary transformer cores mounted on a head cylinder of a video tape recorder, such as a flat plate type and a cylindrical type. The latter rotary transformer core is made by cutting a sintered ferrite core into an inner core and an outer core. Regarding their dimensional accuracy, the outer diameter, inner diameter, and groove width are required to be within ± 20 μm. On the other hand, the ferrite used in these members is generally iron oxide, nickel oxide, zinc oxide with copper oxide added, mixed, calcined, added with an appropriate binder, and then granulated, using a metal mold It is manufactured by press-forming into the shape of and then sintering.

【0003】しかしながら上記のような寸法精度に加工
するフェライトは、その加工性及びその他の特性を考慮
しなければならない。フェライト内の焼結密度が99%
以上であればコア強度としては良好であるが、切削加工
を施す時には硬いために、切削砥石の送り速度を低速に
して、フェライトが割れないように注意しなければなら
ないので作業性が悪い。この作業性の向上のためにフェ
ライトの焼結密度を小さくすることが考えられる。
However, the workability and other characteristics of the ferrite processed to the above dimensional accuracy must be taken into consideration. Sintered density in ferrite is 99%
If it is above, the core strength is good, but since it is hard when cutting is performed, it is necessary to reduce the feed speed of the cutting grindstone and take care not to crack the ferrite, so workability is poor. It is conceivable to reduce the sintered density of ferrite in order to improve the workability.

【0004】[0004]

【発明が解決しようとする課題】しかしながら前記従来
の構成では、フェライトを所定の焼結密度に制御するに
は焼結温度を±2℃未満にしなければならなかったので
非常に製造が困難であった。従って焼結密度の同じもの
を作製しようとしてもロット毎に焼結密度のばらつきが
生じるという問題点があった。
However, in the above conventional structure, the sintering temperature must be kept below ± 2 ° C. in order to control the ferrite to a predetermined sintering density, so that it is very difficult to manufacture. It was Therefore, there is a problem that even if an attempt is made to produce the same sintered density, the sintered density varies from lot to lot.

【0005】本発明は前記従来の問題点を解決するもの
で、簡単にフェライトのロット毎の焼結密度のばらつき
を小さくすることができるフェライトの製造方法を提供
することを目的としている。
The present invention solves the above-mentioned problems of the prior art, and an object of the present invention is to provide a method for producing ferrite which can easily reduce the variation in the sintered density of the ferrite from lot to lot.

【0006】[0006]

【課題を解決するための手段】この目的を達成するため
に、酸化鉄,酸化ニッケル,酸化亜鉛,酸化銅を含む原
料を1100±50℃で仮焼した第1の仮焼物と、その
原料を850±50℃で仮焼した第2の仮焼物を混合
し、焼結させた。
In order to achieve this object, a first calcined product obtained by calcining a raw material containing iron oxide, nickel oxide, zinc oxide, and copper oxide at 1100 ± 50 ° C. and its raw material are used. A second calcined product calcined at 850 ± 50 ° C. was mixed and sintered.

【0007】[0007]

【作用】この構成により、焼結温度で空孔率(焼結密
度)を制御するのではなく、仮焼物の混合によって制御
できる。
With this configuration, the porosity (sintering density) can be controlled by mixing the calcined product, not by controlling the sintering temperature.

【0008】[0008]

【実施例】以下本発明の一実施例におけるフェライトの
製造方法について説明する。
EXAMPLE A method for producing ferrite in one example of the present invention will be described below.

【0009】先ず酸化鉄(Fe23等)46〜51モル
%と、酸化ニッケル(NiO等)11〜16モル%、酸
化亜鉛(ZnO等)28〜34モル%、酸化銅(CuO
等)3〜12モル%とを配合し、混合する。本実施例で
は前記組成を組み合わせて100モル%としたが、この
組成以外に他の組成(不純物等)が多少含まれても効果
は変わらない。混合した原料を約半分ずつ2つのグルー
プに分け、それぞれのグループを1100±50℃と8
50±50℃の温度で2時間仮焼して第1の仮焼物(1
100±50℃)及び第2の仮焼物(850±50℃)
を作製した。
First, 46 to 51 mol% of iron oxide (Fe 2 O 3 etc.), 11 to 16 mol% of nickel oxide (NiO etc.), 28 to 34 mol% of zinc oxide (ZnO etc.) and copper oxide (CuO).
Etc.) 3 to 12 mol% and blended. In this embodiment, the above composition was combined to make 100 mol%, but the effect is not changed even if some other composition (impurities etc.) is contained in addition to this composition. Divide the mixed raw materials into two groups of about half each, and set each group at 1100 ± 50 ℃ and 8
The first calcinated product (1
100 ± 50 ° C) and second calcined product (850 ± 50 ° C)
Was produced.

【0010】以下前記2つの仮焼温度に設定した理由を
以下に述べる。1150℃以上で仮焼を20分以上行う
とZnOの昇華が起こるためか、本焼成時のZnの組成
ずれが−0.5〜−2.0モル%程度発生し、所定の組
成が得られないことと、仮焼後のペレットの硬度がビッ
カース硬度で700kg/mm 2以上になってしまうた
めに、粉砕時間が1100℃で仮焼したペレットに較べ
ミル粉砕(20μm以下)までに達するのに3倍以上時
間が掛かるために好ましくない。また仮焼温度が105
0℃以下の場合、ミル粉砕(20μm以下)を行い、本
焼成1120±15℃で焼結した時に、密度が98%以
上になってしまい空孔を残す目的を達成できなくなる。
The reasons for setting the above two calcination temperatures are as follows.
It will be described below. Calcination at 1150 ° C or higher for 20 minutes or longer
Or ZnO sublimation may occur, the composition of Zn at the time of main firing
Deviation occurs about -0.5 to -2.0 mol%, and
And the hardness of the pellet after calcination is
Curse hardness 700kg / mm 2It was over
In comparison with pellets that were calcinated at a crushing time of 1100 ° C
More than 3 times to reach mill grinding (20μm or less)
It is not preferable because it takes time. The calcination temperature is 105
If the temperature is 0 ° C or lower, perform milling (20 μm or less) and
When sintered at 1120 ± 15 ° C, the density is 98% or less.
It will be on the top and the purpose of leaving holes cannot be achieved.

【0011】また低温側の仮焼温度を850±50℃に
した理由は、仮焼温度が800℃未満であると仮焼後に
フェライトの結晶構造であるスピネル化が完全に進んで
いないことが確認された。従ってスピネル構造になって
いない仮焼物で成形を行うと本焼成時に20%を越える
収縮が発生し、クラックの発生率が大きくなるからであ
る。また900℃以上で仮焼すると、本焼成時の温度を
高くしなければならず、経済的でないとともに、炉の寿
命も短くなる。
The reason for setting the calcination temperature on the low temperature side to 850 ± 50 ° C. is that if the calcination temperature is less than 800 ° C., the spinelization, which is the crystal structure of ferrite, does not proceed completely after calcination. Was done. Therefore, when molding is performed using a calcined product that does not have a spinel structure, shrinkage of more than 20% occurs during main firing, and the crack generation rate increases. In addition, if calcination is performed at 900 ° C. or higher, the temperature during the main calcination must be increased, which is not economical and shortens the life of the furnace.

【0012】前記のように作製された第1及び第2の仮
焼物を以下の重量比で混合して5つのサンプルを作製し
た。
Five samples were prepared by mixing the first and second calcined products produced as described above in the following weight ratios.

【0013】 サンプルA 第1の仮焼物:第2の仮焼物=1:1 サンプルB 第1の仮焼物:第2の仮焼物=1:2 サンプルC 第1の仮焼物:第2の仮焼物=1:3 サンプルD 第1の仮焼物:第2の仮焼物=1:4 サンプルE 第1の仮焼物:第2の仮焼物=1:5 これらのサンプルをそれぞれボールミルで湿式粉砕を1
6時間施し、有機バインダ(ポリビニルアルコール等)
を加え、スプレードライヤー等の手法を用いて98%以
上乾燥し造粒させる。この時この乾燥物の粒径は80μ
m〜200μmである。そしてこの乾燥物を1120±
10℃で焼成を行った。この結果それぞれのサンプルに
おいて以下のような空孔率を有するフェライトを作製で
きた。
Sample A First Calcinated Product: Second Calcinated Product = 1: 1 Sample B First Calcinated Product: Second Calcinated Product = 1: 2 Sample C First Calcinated Product: Second Calcinated Product = 1: 3 Sample D 1st calcination product: 2nd calcination product = 1: 4 Sample E 1st calcination product: 2nd calcination product = 1: 5 These samples were wet-milled with a ball mill to 1
Apply for 6 hours, organic binder (polyvinyl alcohol, etc.)
Is added, and dried by a method such as a spray dryer to 98% or more to granulate. At this time, the particle size of this dried product is 80μ.
It is m-200 micrometers. And this dried product is 1120 ±
Firing was performed at 10 ° C. As a result, ferrite having the following porosity could be produced in each sample.

【0014】 サンプルA 空孔率 10〜13% サンプルB 空孔率 8〜12% サンプルC 空孔率 6〜 7% サンプルD 空孔率 4〜 5% サンプルE 空孔率 1〜 3% ここで注目すべき点は、焼成温度が±10℃ばらついて
も上記と同じような空孔率を得ることができる点であ
る。従来の製造方法であれば焼成温度を±2℃以内に制
御しなければ所定の空孔率を得ることができないが、本
実施例のような製造方法によれば焼成温度が多少ばらつ
いても所定の空孔率を得ることができる。また実験の結
果、焼成温度が±30℃のばらつきを有しても同様の空
孔率を得ることができる。
Sample A Porosity 10 to 13% Sample B Porosity 8 to 12% Sample C Porosity 6 to 7% Sample D Porosity 4 to 5% Sample E Porosity 1 to 3% where It should be noted that the same porosity as above can be obtained even if the firing temperature varies by ± 10 ° C. In the conventional manufacturing method, a predetermined porosity cannot be obtained unless the firing temperature is controlled within ± 2 ° C. However, according to the manufacturing method of this embodiment, even if the firing temperature varies to some extent, The porosity of can be obtained. Further, as a result of the experiment, the same porosity can be obtained even if the firing temperature has a variation of ± 30 ° C.

【0015】次に上記サンプルの諸特性を(表1)に示
す。
Next, various characteristics of the above sample are shown in (Table 1).

【0016】[0016]

【表1】 [Table 1]

【0017】この(表1)から分かるように本実施例の
フェライトの製造方法では、空孔率を簡単に制御するこ
とができ、しかもそれらの他の特性を劣化させることは
ない。
As can be seen from this (Table 1), in the ferrite manufacturing method of this embodiment, the porosity can be easily controlled and the other characteristics thereof are not deteriorated.

【0018】[0018]

【発明の効果】本発明は、酸化鉄,酸化ニッケル,酸化
亜鉛,酸化銅を含む原料を1100±50℃で仮焼した
第1の仮焼物と、その原料を850±50℃で仮焼した
第2の仮焼物を混合し、焼結させたことにより、焼結温
度で空孔率(焼結密度)を制御するのではなく、仮焼物
の混合によって制御できるので、簡単にフェライトのロ
ット毎の焼結密度のばらつきを小さくすることができ
る。
According to the present invention, a first calcined product obtained by calcining a raw material containing iron oxide, nickel oxide, zinc oxide and copper oxide at 1100 ± 50 ° C. and the raw material is calcined at 850 ± 50 ° C. By mixing and sintering the second calcined product, the porosity (sintering density) can be controlled not by the sintering temperature but by the mixing of the calcined product. It is possible to reduce the variation in the sintering density of.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 H01F 41/02 D 8019−5E (72)発明者 尾中 良雄 大阪府門真市大字門真1006番地 松下電器 産業株式会社内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Internal reference number FI Technical indication location H01F 41/02 D 8019-5E (72) Inventor Yoshio Onaka 1006 Kadoma, Kadoma, Osaka Prefecture Matsushita Denki Sangyo Co., Ltd.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】酸化鉄,酸化ニッケル,酸化亜鉛,酸化銅
を含む原料を1100±50℃で仮焼した第1の仮焼物
と、前記原料を850±50℃で仮焼した第2の仮焼物
を混合し、焼結させたことを特徴とするフェライトの製
造方法。
1. A first calcined product obtained by calcining a raw material containing iron oxide, nickel oxide, zinc oxide, and copper oxide at 1100 ± 50 ° C., and a second calcined substance obtained by calcining the raw material at 850 ± 50 ° C. A method for producing a ferrite, characterized in that the fired product is mixed and sintered.
【請求項2】酸化鉄を46〜51モル%、酸化ニッケル
を11〜16モル%、酸化亜鉛を28〜34モル%、酸
化銅を3〜12モル%で合わせて100モル%としたこ
とを特徴とする請求項1記載のフェライトの製造方法。
2. Iron oxide of 46 to 51 mol%, nickel oxide of 11 to 16 mol%, zinc oxide of 28 to 34 mol%, and copper oxide of 3 to 12 mol%, which are 100 mol% in total. The method for producing a ferrite according to claim 1, which is characterized in that.
【請求項3】第1の仮焼物と第2の仮焼物の割合を1:
1〜5としたことを特徴とする請求項2記載のフェライ
トの製造方法。
3. The ratio of the first calcined product to the second calcined product is 1:
The method for producing a ferrite according to claim 2, wherein the ferrite is 1 to 5.
【請求項4】焼結密度を90%〜99%にしたことを特
徴とする請求項3記載のフェライトの製造方法。
4. The method for producing a ferrite according to claim 3, wherein the sintered density is 90% to 99%.
JP11454992A 1992-05-07 1992-05-07 Ferrite manufacturing method Expired - Fee Related JP3239439B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11454992A JP3239439B2 (en) 1992-05-07 1992-05-07 Ferrite manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11454992A JP3239439B2 (en) 1992-05-07 1992-05-07 Ferrite manufacturing method

Publications (2)

Publication Number Publication Date
JPH05315121A true JPH05315121A (en) 1993-11-26
JP3239439B2 JP3239439B2 (en) 2001-12-17

Family

ID=14640574

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11454992A Expired - Fee Related JP3239439B2 (en) 1992-05-07 1992-05-07 Ferrite manufacturing method

Country Status (1)

Country Link
JP (1) JP3239439B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11243024A (en) * 1998-02-25 1999-09-07 Kyocera Corp Electrical equipment applicable to non-contact charger
JP2014189485A (en) * 2013-03-28 2014-10-06 Murata Mfg Co Ltd Ferrite calcinated powder, laminate type coil part, method of producing ferrite calcinated powder and method of producing laminate type coil part

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11243024A (en) * 1998-02-25 1999-09-07 Kyocera Corp Electrical equipment applicable to non-contact charger
JP2014189485A (en) * 2013-03-28 2014-10-06 Murata Mfg Co Ltd Ferrite calcinated powder, laminate type coil part, method of producing ferrite calcinated powder and method of producing laminate type coil part

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Publication number Publication date
JP3239439B2 (en) 2001-12-17

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