JPS6336501A - Manufacture of compound magnet - Google Patents
Manufacture of compound magnetInfo
- Publication number
- JPS6336501A JPS6336501A JP61177816A JP17781686A JPS6336501A JP S6336501 A JPS6336501 A JP S6336501A JP 61177816 A JP61177816 A JP 61177816A JP 17781686 A JP17781686 A JP 17781686A JP S6336501 A JPS6336501 A JP S6336501A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- magnetic powder
- composite magnet
- present
- resin
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Hard Magnetic Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は磁気特性に優れた複合磁石の製造方法に関する
ものである。さらに詳しくは磁性粉末を樹脂と混練成形
してなる複合磁石の製造方法において予め前記磁性粉末
をラジカル重合可能なモノマーと緊密に接触させた状態
に維持し、酸性亜硫酸イオンの存在下で重合反応を行わ
せて前記粉末を、l IJママ−被覆する事により磁性
粉末の表面を改質せしめる事を%徴とする複合磁石の製
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 manufacturing a composite magnet with excellent magnetic properties. More specifically, in a method for producing a composite magnet in which magnetic powder is kneaded and molded with a resin, the magnetic powder is kept in close contact with a monomer capable of radical polymerization in advance, and the polymerization reaction is carried out in the presence of acidic sulfite ions. The present invention relates to a method for producing a composite magnet, the feature of which is to modify the surface of the magnetic powder by coating the powder with an IJ polymer.
磁性粉末とバインダーとを混合混練し、押出成形、圧縮
成形、あるいは射出成形によシ複合磁石を製造すること
は周知である。複合磁石は割れカケが生じにくい、二次
加工が不要で複雑な形状や薄肉の形状に適する。ラノア
ル異方性の製品が得られる等の特徴を持つことからi!
L近の磁気特性の改善も伴って例えば小父モータ、セン
サー、リレ−及びOA機器等らの利用が増加してきてい
る。It is well known to mix and knead magnetic powder and a binder and to produce a composite magnet by extrusion molding, compression molding, or injection molding. Composite magnets are less prone to cracking and do not require secondary processing, making them suitable for complex shapes and thin-walled shapes. i!
With improvements in magnetic properties near L, the use of small motors, sensors, relays, OA equipment, etc., is increasing.
一方、複合磁石の欠点としては、成分として非磁性のバ
インダー及び添加物が混入されるため。On the other hand, a drawback of composite magnets is that non-magnetic binders and additives are mixed in as components.
その体積分だけ磁気特性が低下する事が挙げられ”る。One example is that the magnetic properties deteriorate by the volume.
この欠点を改善する方法としては磁性粉末の充填量を増
すこと及び磁性粉末の配向度を高める事が必要である。In order to improve this drawback, it is necessary to increase the amount of magnetic powder packed and to increase the degree of orientation of the magnetic powder.
しかし、一般に磁性粉末の混入量を多くすると成形時に
流れが悪くなシ、成形性が悪くなったり、あるいは製品
が得られなくなる。However, in general, when the amount of magnetic powder mixed in is increased, flow during molding becomes poor, moldability deteriorates, or a product cannot be obtained.
又かろうじて形状を作ったとしても磁性粉末の配向度が
低下し、満足な磁気特性は得られない。Moreover, even if the shape is barely formed, the degree of orientation of the magnetic powder decreases, making it impossible to obtain satisfactory magnetic properties.
このような不具合を改善する方法の一つと七で磁性粉末
を各種カップリング剤で表面処理する事によシ充填率及
び機械強度向上を図る方法が提晶されてきた。この方法
は磁性粉末の表面を親水性から親油性に変え、バインダ
ーとのl−11じみを良く鉛
する効果があり、従って充填率、配方性2機械強度の改
善が出来る。このような方法により従来の方法に比べて
特に磁気特性は向上せしめる事が出来るが、特にOA機
器用としてのモーター用マグネットなどについては軽薄
短少化指向が強く、一層の磁気特性の向上が望まれてい
る。One of the methods to improve such problems is to surface-treat magnetic powder with various coupling agents to improve the filling rate and mechanical strength. This method has the effect of changing the surface of the magnetic powder from hydrophilic to oleophilic, effectively preventing l-11 from forming with the binder, and thus improving the filling rate, orientation, and mechanical strength. Although this method can particularly improve magnetic properties compared to conventional methods, there is a strong desire to make magnets lighter, thinner, and shorter, especially for motor magnets used in office automation equipment, and further improvements in magnetic properties are desired. ing.
本発明はこれらの情況に鑑みさらに磁気特性を向上せし
めるための製造方法を提供する事を目的とするものであ
る。In view of these circumstances, it is an object of the present invention to provide a manufacturing method for further improving magnetic properties.
即ち本発明は磁−性粉末を樹脂と混練成形してなる複合
磁石の製造方法において、予め前記磁性粉末をラジカル
重合可能なモノマーと緊密に接触させた状態に維持し、
酸性亜硫酸イオンの存在下で重合反応を行わせて前記粉
末ポリマーで被覆する事によシ表面改質を行わしめる事
を特徴とするものであり、さらにこの磁性粉末をポリア
ミド系の樹脂と混練し、複合化させることにより顕著な
効果が認められる事を見出し2本発明を完成するに至っ
た1ものである。That is, the present invention provides a method for manufacturing a composite magnet formed by kneading and molding magnetic powder with a resin, in which the magnetic powder is maintained in advance in close contact with a monomer capable of radical polymerization,
The magnetic powder is characterized in that the surface is modified by carrying out a polymerization reaction in the presence of acidic sulfite ions and coating it with the powdered polymer, and further, by kneading this magnetic powder with a polyamide resin. It was discovered that a remarkable effect can be obtained by combining the two, and this led to the completion of the present invention.
本発明に従えば、磁性粉末は一般式MO,6Fe2Q3
(但しMはCa” 、 Ba” r Sr” 、及びP
b++などの二価の金属イオンである)で衣わされるマ
グネトブランバイト型結晶を有するフェライト粉末が用
いられる。According to the invention, the magnetic powder has the general formula MO, 6Fe2Q3
(However, M is Ca", Ba" r Sr", and P
A ferrite powder having magnetobrambite-type crystals coated with divalent metal ions such as b++ is used.
又、樹脂はポリエチレン、ポリプロピレンなどのポリオ
レフィン系樹脂、ナイロン−6、ナイロン−12tナイ
ロ・ン610.ナイロン11.ナイロン66などのポリ
アミド系樹脂、ポリエチレンテレフタレート、ポリブチ
レンテレフタレートなどのポリエステル系樹脂、エチレ
ン−酢酸ビニル共重合体、エチレン−エチルアクリレー
ト共重合体、ポリフェニレンサルファイド、ポリエーテ
ルエーテルケトン、デリエーテルサルフォン及びこれら
の変性タイプの樹脂などが好適であるが、特にポリアミ
ド系樹脂が本発明による表面処理の効果を著しく発揮出
来る。In addition, resins include polyolefin resins such as polyethylene and polypropylene, nylon-6, nylon-12t nylon 610. Nylon 11. Polyamide resins such as nylon 66, polyester resins such as polyethylene terephthalate and polybutylene terephthalate, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer, polyphenylene sulfide, polyether ether ketone, deriether sulfone, and these Modified type resins such as these are suitable, but polyamide resins in particular can significantly exhibit the effect of the surface treatment according to the present invention.
又2本発明においてフェライト粉末をポリマーで被覆さ
せる場合、用いるラジカル重合又はラジカル共重合可能
なモノマーとして、アクリル酸。In addition, in the case of coating the ferrite powder with a polymer in the present invention, the radical polymerizable or radical copolymerizable monomer used is acrylic acid.
メタクリル酸及びアクリル酸メチル、アクリル酸ブチル
、メタクリル酸メチル、メタクリル酸エチル、などのア
クリル酸エステル類やメタクリル酸チルスチレンなどの
芳香族ビニル化合物類、ブタジェン、イソグレン、クロ
ロプレンなどのツエン類及びアクリロニトリルなどを挙
げる事が出来る。Acrylic acid esters such as methacrylic acid and methyl acrylate, butyl acrylate, methyl methacrylate, and ethyl methacrylate; aromatic vinyl compounds such as thylstyrene methacrylate; tzenes such as butadiene, isogrene, and chloroprene; and acrylonitrile. I can list many.
本発明の方法においては上記ラジカル重合又はラジカル
共重合可能なモノマー類から選ばれた1種あるいは2種
以上のモノマーが用いられる。In the method of the present invention, one or more monomers selected from the above radical polymerizable or radical copolymerizable monomers are used.
本発明で用いるモノマーの量は余りに多過ぎると機械強
度及び耐熱性の低下をもたらし、又余シに少な過ぎると
フェライト粉末を完全に被覆出来なく表面処理の効果が
発揮出来なくフェライト粉末に対して重量で0.1〜1
0%、好ましくは0.5チ〜7%の範囲にある。If the amount of monomer used in the present invention is too large, it will cause a decrease in mechanical strength and heat resistance, and if it is too small, it will not be possible to completely cover the ferrite powder and the surface treatment effect will not be exerted. 0.1-1 by weight
0%, preferably in the range of 0.5% to 7%.
又本発明で用いる散性亜硫酸イオンを供与する物質とし
て亜硫酸水、亜硫酸ガス、亜硫酸塩水溶液、酸性亜硫酸
塩水溶液などが使用される。この亜硫酸イオンの量は亜
硫酸換算でモノマー100重量部当90.1〜50重量
部、好ましくは05〜30重量部の範囲にある。In addition, sulfite water, sulfite gas, sulfite aqueous solution, acidic sulfite aqueous solution, etc. are used as the substance that provides the dispersible sulfite ions used in the present invention. The amount of sulfite ion is in the range of 90.1 to 50 parts by weight, preferably 05 to 30 parts by weight, based on 100 parts by weight of the monomer, in terms of sulfite.
本発明の被覆処理条件としては次のように行う事が出来
る。フェライト粉末1重量部を1〜10重量部の水に懸
濁させ、液性を中性(pH6〜8)に調整した後モノマ
ー及び亜硫酸イオンを供与する重合開始剤を加え10℃
〜100℃、好ましくは20〜70℃の範囲の温度で被
覆処理を行う。The coating treatment conditions of the present invention can be carried out as follows. 1 part by weight of ferrite powder was suspended in 1 to 10 parts by weight of water, and after adjusting the liquid to neutrality (pH 6 to 8), a monomer and a polymerization initiator for donating sulfite ions were added and the mixture was heated at 10°C.
The coating process is carried out at a temperature in the range from ~100<0>C, preferably from 20 to 70<0>C.
処理時間は1〜4時間でモノマーはほぼ100%ポリマ
ーに転化する。次いで得られた被覆処理済粉末の懸濁液
を中和処理し脱水、乾燥を行う。The treatment time is 1 to 4 hours and almost 100% of the monomer is converted to polymer. Next, the resulting suspension of coated powder is neutralized, dehydrated, and dried.
本発明による処理を施した磁性粉末は次に樹脂と混合混
練し、その後被レットとする。混練は加熱ニーダ−1−
軸又は二軸の押出機で行う事が出来る。もちろん表面処
理磁性粉を圧縮成形に供してもかまわない。The magnetic powder treated according to the present invention is then mixed and kneaded with a resin, and then made into pellets. Kneading is done using heating kneader-1-
It can be carried out using a screw or twin screw extruder. Of course, the surface-treated magnetic powder may be subjected to compression molding.
以下本発明の実施例について更に具体的に説明するが2
本発明がこれらの実施例に限定されるものではないこと
はもちろんである。Examples of the present invention will be explained in more detail below.
It goes without saying that the present invention is not limited to these examples.
実施例−1
攪拌機、温度計術の反応釜にストロンチウムフェライト
粉末(平均粒子径1μ)5kgと水507を加えて50
℃で30分激しくかき混ぜた。この時のp)Iは11で
あった。この液をIN塩酸でpH3に調整した後アクリ
ル酸メチルモノマー200.9と亜硫酸水素ナトリウム
52!jを加え50℃で2時間攪拌下に反応を行った。Example-1 Add 5 kg of strontium ferrite powder (average particle size 1 μm) and 50 ml of water to a reaction vessel equipped with a stirrer and a thermometer.
Stir vigorously for 30 minutes at °C. p)I at this time was 11. After adjusting this solution to pH 3 with IN hydrochloric acid, methyl acrylate monomer was 200.9 and sodium hydrogen sulfite was 52! j was added thereto, and the reaction was carried out at 50° C. for 2 hours with stirring.
反応終了後反応液を冷却しINNカー−−ダ水溶液でp
H7,5とした。After the reaction is completed, the reaction solution is cooled and purified with an aqueous INN card solution.
It was set as H7.5.
このものを脱水、乾燥し、被覆量を測定したところ12
5gであった。This material was dehydrated and dried, and the amount of coverage was measured: 12
It was 5g.
このようにし°C得られた被覆処理されたフェライト粉
末5kgにナイロン−6粉末543gを混合し二軸押出
機で混練した後被レフト化し成形用コンノクウンl″を
得た。このものを磁場15KOe下で射出成形を行った
。結果を表−1に示した。543 g of nylon-6 powder was mixed with 5 kg of coated ferrite powder obtained in this manner and kneaded in a twin-screw extruder, and then left to obtain a molding material. Injection molding was performed.The results are shown in Table-1.
比較例−1
実施例−1においてフェライト粉末を表面処理せずに用
いた以外は全〈実施例−1と同様にして行った。結果を
表−1に示した。Comparative Example-1 The same procedure as in Example-1 was carried out except that the ferrite powder was used without surface treatment. The results are shown in Table-1.
比較例−2
ストロンチウムフェライト(平均粒子径1μ)5 kg
をスーハーミキサーに投入し、120℃に加熱した後ン
ランカップリング剤(γ−アミノプロピルトリエトキシ
シラン)50Iを添加し、さらに120℃で30分間攪
拌を続けて表面処理を行った・このフェライ)・粉末を
実施例−1と同様の方法でペレット化し、射出成形に供
した。結果を衣−1に示した。Comparative example-2 Strontium ferrite (average particle size 1μ) 5 kg
was placed in a Suhar mixer, heated to 120°C, 50I of a Nran coupling agent (γ-aminopropyltriethoxysilane) was added, and the mixture was further stirred at 120°C for 30 minutes to perform surface treatment. - The powder was pelletized in the same manner as in Example-1 and subjected to injection molding. The results are shown in Cloth-1.
臥下宗臼
実施例2〜6
表−2に示した樹脂を用い、フェライト粉末の体積比を
60チとした以外は実施例−1と全く同様の方法で行っ
た。結果を宍−2に示した。Examples 2 to 6 Examples 2 to 6 of Examples 2 to 6 were carried out in exactly the same manner as in Example 1, except that the resin shown in Table 2 was used and the volume ratio of ferrite powder was changed to 60 inches. The results are shown in Shishi-2.
以下争臼
実施例7〜10
表−3に示したモノマー及び触媒を用いた以外は全〈実
施例−1と同様の方法で行った。結果を表−3に示した
。The following Examples 7 to 10 were carried out in the same manner as in Example 1 except that the monomers and catalysts shown in Table 3 were used. The results are shown in Table-3.
臥−ト弦β
又2本発明による表面処理を行った場合(ただし実施例
−1の場合)とシランカップリング法と未処理の場合と
の複合磁石におけるフェライト粉を
未含有率と磁気特性との関係歇第1図に示した。In addition, the ratio of ferrite powder free content and magnetic properties in composite magnets with surface treatment according to the present invention (in the case of Example 1), silane coupling method, and untreated case are also shown. The relationship is shown in Figure 1.
以上述べたごとく本発明によれば、非常に効果的な表面
処理法を見出した事により、磁気特性を大幅に向上した
複合磁石を得る事が出来たばかシか、成形性にも優れた
特徴を持たせる事が出来た。As described above, according to the present invention, by discovering a very effective surface treatment method, we were able to obtain a composite magnet with significantly improved magnetic properties, and also with excellent formability. I was able to have it.
従ってその工業的価値は大である。Therefore, its industrial value is great.
第1図は2本発明による表面処理を行った場合と、シラ
ンカップリング法と、未処理の場合の複合磁石における
フェライト粉末含有率と磁気特性との関係を示した図で
ある。
ン・シ・′
第1図
a78Ft 8’? QO91フエライト
粉末 (1,Z)
手続補正書C自発)
昭和62年?月29日FIG. 1 is a diagram showing the relationship between ferrite powder content and magnetic properties in composite magnets in which the surface treatment according to the present invention is performed, the silane coupling method, and the untreated case. Figure 1 a78Ft 8'? QO91 ferrite powder (1, Z) Procedural amendment C spontaneous) 1986? 29th of the month
Claims (1)
方法において、前記磁性粉末を予めラジカル重合可能な
モノマーと緊密に接触させた状態に維持し、酸性亜硫酸
イオンの存在下で重合反応を行わせて前記粉末をポリマ
ーで被覆する事を特徴とする複合磁石の製造方法。 2、前記磁性粉末が一般式MO.6Fe_2O_5(但
しMはCa^+^+、Ba^+^+、Sr^+^+及び
Pb^+^+などの二価の金属イオンである)で表わさ
れるマグネトプランバイト型結晶構造を有するフェライ
ト粉末であることを特徴とする特許請求の範囲第1項記
載の複合磁石の製造方法。 3、前記樹脂がポリアミド系樹脂である事を特徴とする
特許請求の範囲第1項記載の複合磁石の製造方法。[Claims] 1. A method for producing a composite magnet by kneading and molding magnetic powder with a resin, in which the magnetic powder is maintained in advance in close contact with a monomer capable of radical polymerization, and acidic sulfite ions are 1. A method for producing a composite magnet, which comprises coating the powder with a polymer by carrying out a polymerization reaction in the presence of a polymer. 2. The magnetic powder has the general formula MO. Ferrite having a magnetoplumbite crystal structure represented by 6Fe_2O_5 (where M is a divalent metal ion such as Ca^+^+, Ba^+^+, Sr^+^+, and Pb^+^+) The method for manufacturing a composite magnet according to claim 1, wherein the composite magnet is a powder. 3. The method for manufacturing a composite magnet according to claim 1, wherein the resin is a polyamide resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61177816A JPH0673329B2 (en) | 1986-07-30 | 1986-07-30 | Manufacturing method of composite magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61177816A JPH0673329B2 (en) | 1986-07-30 | 1986-07-30 | Manufacturing method of composite magnet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6336501A true JPS6336501A (en) | 1988-02-17 |
| JPH0673329B2 JPH0673329B2 (en) | 1994-09-14 |
Family
ID=16037595
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61177816A Expired - Lifetime JPH0673329B2 (en) | 1986-07-30 | 1986-07-30 | Manufacturing method of composite magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0673329B2 (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4888496A (en) * | 1972-02-24 | 1973-11-20 | ||
| JPS516289A (en) * | 1974-07-08 | 1976-01-19 | Sumitomo Bakelite Co | |
| JPS517092A (en) * | 1974-07-08 | 1976-01-21 | Sumitomo Bakelite Co | Anteiseio kairyoshita jiseizairyokeigurafutojugofukugotai |
| JPS517046A (en) * | 1974-07-08 | 1976-01-21 | Sumitomo Bakelite Co |
-
1986
- 1986-07-30 JP JP61177816A patent/JPH0673329B2/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4888496A (en) * | 1972-02-24 | 1973-11-20 | ||
| JPS516289A (en) * | 1974-07-08 | 1976-01-19 | Sumitomo Bakelite Co | |
| JPS517092A (en) * | 1974-07-08 | 1976-01-21 | Sumitomo Bakelite Co | Anteiseio kairyoshita jiseizairyokeigurafutojugofukugotai |
| JPS517046A (en) * | 1974-07-08 | 1976-01-21 | Sumitomo Bakelite Co |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0673329B2 (en) | 1994-09-14 |
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