JPH02102506A - Manufacture of magnetic material for permanent magnet - Google Patents

Manufacture of magnetic material for permanent magnet

Info

Publication number
JPH02102506A
JPH02102506A JP63254944A JP25494488A JPH02102506A JP H02102506 A JPH02102506 A JP H02102506A JP 63254944 A JP63254944 A JP 63254944A JP 25494488 A JP25494488 A JP 25494488A JP H02102506 A JPH02102506 A JP H02102506A
Authority
JP
Japan
Prior art keywords
mixed
permanent magnet
magnetic material
hours
powder
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
JP63254944A
Other languages
Japanese (ja)
Inventor
Kazuhiko Fujiwara
一彦 藤原
Giichi Kawashima
川島 義一
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP63254944A priority Critical patent/JPH02102506A/en
Publication of JPH02102506A publication Critical patent/JPH02102506A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To manufacture the magnetic material for a permanent magnet having high magnetic force by a method wherein raw material powder is mixed so as to obtain Sr[Zn(LiFe)0.5]Fe16O27, the mixed powder is calcined, finely ground, a wet pulverizing work is conducted by adding a fluoride, thermoplastic resin is added to the W-type ferrite, which is retreated in the atmospheric air, and they are kneaded. CONSTITUTION:Each powder of SrCo3, ZnO, Li2CO3 and Fe2O3 is used as raw materials, the materials are mixed so as to obtain the sample composition of Sr[Zn(LiFe)0.5]Fe16O27. The mixture is calcined in the atmospheric air at 1100 to 1600 deg.C for 5 to 9 hours, then it is pulverized to the grain diameter of 1mm or less, a wet grinding work is conducted by adding a fluoride of 1 to 3wt.%, and a heat treatment is conducted again in the atmospheric air at the temperature of 600 to 1400 deg.C for 1 to 6 hours. Thermoplastic resin of 5 to 50-wt.% is mixed to and kneaded with the obtained W-type ferrite. As a result, a magnetic material for permanent magnet having high magnetic force can be manufactured.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、W型フェライトに熱可塑性樹脂5〜50重量
%を混合混練することで、高磁力を有する永久磁石用磁
性材料の製造方法に関するものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for producing a magnetic material for permanent magnets having high magnetic force by mixing and kneading 5 to 50% by weight of a thermoplastic resin with W-type ferrite. It is something.

(従来の技術) 特開昭57−18303号公報に記載のごとくW型フェ
ライトとは基本的には下記式に示される化学量論的組成
を有するフェライト相を意味する。
(Prior Art) As described in JP-A-57-18303, W-type ferrite basically means a ferrite phase having a stoichiometric composition represented by the following formula.

MAi”F e ”O,。MAi”F e”O,.

(式中M=Ba1SrまたはPb A”=Fe、Zn、Cu1N i、Mn5Mgまたはこ
れらの混合物) W型7エライトの内 A ”= F e ”であるW型
フェライトについては飽和磁化の値が通常のM型フェラ
イト(MO・n F e 20 s  式中:M−Ba
(In the formula, M = Ba1Sr or Pb A" = Fe, Zn, Cu1N i, Mn5Mg or a mixture thereof) Of the W-type 7 ferrites, the W-type ferrite with A " = Fe " has a saturation magnetization value that is normal. M-type ferrite (MO・n Fe 20 s where: M-Ba
.

Sr又はPb、n−5〜6なる化学量論的組成を有する
もの)より大きいことは知られている。
Sr or Pb, which has a stoichiometric composition of n-5 to 6), is known to be larger.

しかしながらW型7エライトは2価の金属イオンを含む
ため焼成時MFeW相が不安定となり、そのため酸素分
圧を厳しく制御して焼成及び焼鈍を行う必要があり、ま
た保持力がM型フェライトに比べて大巾に低下すること
から未だ実用化には至っておらず、従って上述したW型
フェライトを磁性粉とし、これに熱可塑性樹脂を混合混
練したプラスチック磁性材料は工業的に使用できるよう
には至っていない。
However, since W-type 7 ferrite contains divalent metal ions, the MFeW phase becomes unstable during firing. Therefore, it is necessary to strictly control the oxygen partial pressure during firing and annealing, and the holding power is lower than that of M-type ferrite. However, it has not yet been put into practical use due to the large drop in magnetic flux, and therefore, plastic magnetic materials made by mixing and kneading the above-mentioned W-type ferrite with magnetic powder and thermoplastic resin have not yet been able to be used industrially. not present.

(発明が解決しようとする課題) 本発明は、上記のごと〈従来からある欠点を解消して、
飽和磁化σ、が大きく且つ保持力IHcも大きいW型フ
ェライトを磁性粉とし、これに熱可塑性樹脂を5〜50
重量%重量%線することで高磁力を有する永久磁石とな
る磁性材料の製造方法を提供するものである。
(Problems to be Solved by the Invention) The present invention solves the conventional drawbacks as described above,
A W-type ferrite with a large saturation magnetization σ and a large coercive force IHc is used as magnetic powder, and a thermoplastic resin is added to it to
The present invention provides a method for manufacturing a magnetic material that becomes a permanent magnet having high magnetic force by weight% weight%.

(課題を解決するための手段) 本発明は、S rcOs 、Zn0SL 12cOx、
FezO,の各粉末を原料とし、試料組成S r  [
Z n(L i F e)+ i]F e tasty
  となるように混合して、大気中で1100〜160
0℃、5〜9時間仮焼し、その後粒径1mm以下に粉砕
し、弗化物を1〜3重量%添加し湿式粉砕し、再び大気
中で600〜1400℃の温度で1〜6時間熱処理した
W型フェライトに熱可塑性樹脂を5〜50重量%添加し
混練することを特徴とする永久磁石用磁性材料の製造方
法である。
(Means for solving the problems) The present invention provides S rcOs , Zn0SL 12cOx,
Using each powder of FezO, as a raw material, the sample composition S r [
Z n (L i Fe) + i] Fe delicious
Mix it so that it becomes 1100-160 in the air.
Calcined at 0℃ for 5 to 9 hours, then crushed to a particle size of 1 mm or less, added 1 to 3% by weight of fluoride, wet crushed, and heat treated again in the air at a temperature of 600 to 1400℃ for 1 to 6 hours. This method of manufacturing a magnetic material for a permanent magnet is characterized in that 5 to 50% by weight of a thermoplastic resin is added to the W-type ferrite and kneaded.

本発明において用いられる弗化物とはCaF2.5rF
1及びBaF、の1種又は2種以上の組み合わせである
The fluoride used in the present invention is CaF2.5rF
1 and BaF, or a combination of two or more thereof.

又熱可塑性樹脂としてはナイロン6、ナイロン12或い
はこれらのコポリマーなどのポリアミド樹脂、ポリエチ
レン、ポリプロピレンなどのポリオレフィン樹脂、ポリ
塩化ビニル樹脂、エチレン酢酸ビニル共重合体樹脂、エ
チレンエチルアクリレート樹脂、ポリフェニレンサルフ
ァイド樹脂などをいう。
Examples of thermoplastic resins include polyamide resins such as nylon 6, nylon 12, or copolymers thereof, polyolefin resins such as polyethylene and polypropylene, polyvinyl chloride resins, ethylene vinyl acetate copolymer resins, ethylene ethyl acrylate resins, polyphenylene sulfide resins, etc. means.

またW型フェライトを樹脂との相溶性を上げるためシラ
ン系或いはチタネート系の表面処理剤でフェライトを前
処理しても何ら差し支えのあるものではない。
Furthermore, there is no problem in pre-treating the ferrite with a silane-based or titanate-based surface treatment agent in order to improve the compatibility of the W-type ferrite with the resin.

また熱可塑性樹脂を混合していることにより、押出成形
、射出成形が可能となり、従来よりある焼結磁石より軽
量で複雑な形状を有する永久磁石を製造することができ
る。
Further, by mixing a thermoplastic resin, extrusion molding and injection molding are possible, and it is possible to manufacture a permanent magnet that is lighter than conventional sintered magnets and has a complicated shape.

(実施例) S r [Z n(L i F e)o、i]F e 
tasty  の組成を有するようにSrCO3、Zn
○、Li1CO,、Fe、O,の各粉末を混合し、大気
中で1330℃、7時間仮焼する。これをボールミル中
でエタノールの存在下に粒径1+am以下に粉砕した。
(Example) S r [Z n (L i Fe) o, i] Fe
SrCO3, Zn so as to have a composition of delicious
○, Li1CO,, Fe, and O powders were mixed and calcined in the atmosphere at 1330°C for 7 hours. This was ground in a ball mill in the presence of ethanol to a particle size of 1+am or less.

この粉砕生成物にSrF、を2重量%(実施例1)[比
較例1は無添加]添加して20時時間式粉砕後、大気中
で900°0.2時間熱処理した。得られI;磁性粉に
ナイロン12を12重量%混合し、2軸押比機で混練し
ペレット状にした。その後射出成形機で磁場成形を行い
、直流型磁束計で磁気特性を測定した。
To this pulverized product, 2% by weight of SrF (Example 1) [no additive was added in Comparative Example 1] was added, and after 20 hour pulverization, heat treatment was performed at 900° in the air for 0.2 hours. Obtained I: 12% by weight of nylon 12 was mixed with magnetic powder, and the mixture was kneaded with a twin-screw presser to form pellets. After that, magnetic field molding was performed using an injection molding machine, and the magnetic properties were measured using a DC magnetometer.

第1表から判るようにM型フェライト(比較例2)に比
べて最大エネルギー積が大きくなっている。
As can be seen from Table 1, the maximum energy product is larger than that of M-type ferrite (Comparative Example 2).

(発明の効果) 本発明により得られたW型7エライトを使用した永久磁
石はM型フェライトを使用した永久磁石より高磁力を有
する優れた磁気特性を持つため、永久磁石を必要とする
OA機器、FA機器のモーターなどの性能を向上させる
ことができる。
(Effects of the Invention) Permanent magnets using W type 7 ferrite obtained by the present invention have superior magnetic properties with higher magnetic force than permanent magnets using M type ferrite, so they can be used in OA equipment that requires permanent magnets. , the performance of motors in FA equipment can be improved.

Claims (1)

【特許請求の範囲】[Claims] (1)SrCO_3、ZnO、Li_2CO_3、Fe
_2O_3の各粉末を原料とし、試料組成 Sr[Zn(LiFe)_0_._5]Fe_1_6O
_2_7となるように混合して、大気中で1100〜1
600℃、5〜9時間仮焼し、その後粒径1mm以下に
粉砕し、弗化物を1〜3重量%添加し湿式粉砕し、再び
大気中で600〜1400℃の温度で1〜6時間熱処理
したW型フェライトに熱可塑性樹脂を5〜50重量%添
加し混練することを特徴とする永久磁石用磁性材料の製
造方法。
(1) SrCO_3, ZnO, Li_2CO_3, Fe
Each powder of _2O_3 was used as a raw material, and the sample composition was Sr[Zn(LiFe)_0_. _5]Fe_1_6O
Mix to give _2_7 and mix in the air to
Calcined at 600°C for 5-9 hours, then crushed to a particle size of 1 mm or less, added 1-3% by weight of fluoride, wet-milled, and heat-treated again in the air at a temperature of 600-1400°C for 1-6 hours. A method for producing a magnetic material for permanent magnets, which comprises adding 5 to 50% by weight of a thermoplastic resin to W-type ferrite and kneading the mixture.
JP63254944A 1988-10-12 1988-10-12 Manufacture of magnetic material for permanent magnet Pending JPH02102506A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63254944A JPH02102506A (en) 1988-10-12 1988-10-12 Manufacture of magnetic material for permanent magnet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63254944A JPH02102506A (en) 1988-10-12 1988-10-12 Manufacture of magnetic material for permanent magnet

Publications (1)

Publication Number Publication Date
JPH02102506A true JPH02102506A (en) 1990-04-16

Family

ID=17272027

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63254944A Pending JPH02102506A (en) 1988-10-12 1988-10-12 Manufacture of magnetic material for permanent magnet

Country Status (1)

Country Link
JP (1) JPH02102506A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1598835A1 (en) * 2003-02-25 2005-11-23 TDK Corporation Ferrite magnet powder, sintered magnet, bond magnet and magnetic recording medium

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1598835A1 (en) * 2003-02-25 2005-11-23 TDK Corporation Ferrite magnet powder, sintered magnet, bond magnet and magnetic recording medium
EP1598835A4 (en) * 2003-02-25 2008-06-25 Tdk Corp Ferrite magnet powder, sintered magnet, bond magnet and magnetic recording medium
US7879469B2 (en) 2003-02-25 2011-02-01 Tdk Corporation Ferrite magnet powder, sintered magnet, bond magnet, and magnetic recording medium

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