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JPH0262146B2 - - Google Patents
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JPH0262146B2 - - Google Patents

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Publication number
JPH0262146B2
JPH0262146B2 JP24743983A JP24743983A JPH0262146B2 JP H0262146 B2 JPH0262146 B2 JP H0262146B2 JP 24743983 A JP24743983 A JP 24743983A JP 24743983 A JP24743983 A JP 24743983A JP H0262146 B2 JPH0262146 B2 JP H0262146B2
Authority
JP
Japan
Prior art keywords
magnetic
magnetic powder
coupling agent
ferrite
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.)
Expired
Application number
JP24743983A
Other languages
Japanese (ja)
Other versions
JPS60139759A (en
Inventor
Akihiro Koga
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.)
Dainippon Plastics Co Ltd
Original Assignee
Dainippon Plastics 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 Dainippon Plastics Co Ltd filed Critical Dainippon Plastics Co Ltd
Priority to JP24743983A priority Critical patent/JPS60139759A/en
Publication of JPS60139759A publication Critical patent/JPS60139759A/en
Publication of JPH0262146B2 publication Critical patent/JPH0262146B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はプラスチツクマグネツト組成物に関す
るものである。特に本発明はすぐれた磁気特性を
有し、且つ成形性に於いてもすぐれている組成物
に関するものである。 従来の永久磁石は鋳造磁石としてアルニコ磁
石、酸化鉄を用いた焼結フエライト磁石が使われ
ており、特に焼結フエライト磁石は重電、家電、
電子機器に多く使われている。近年電子機器の小
型精密化、高性能信頼性が要求され高磁力のサマ
リウムコバルト合金磁石が伸びている。しかしこ
れらの磁石は脆いこと、切削、研磨などの二次加
工が必要である等の理由により用途拡大の障害と
なつている。 これらの問題点を改良するため、磁性材料と各
種合成樹脂との複合材料が実用化されてきてい
る。これらは主としてフエライトまたは希土類金
属を主体とする磁性粉体とポリアミド、ポリプロ
ピレン等のプラスチツクを複合させたものであり
従来の磁性材料では不可能であつた複雑な形状の
ものを効率よく成形することが出来る。しかしプ
ラスチツクの添加による磁力の低下や分散不良に
よる磁力のバラツキが生じ易く、且つ射出成形に
於いての流動性不良等の問題がある。これらの問
題点を改良する方法として、磁性粉体の表面処理
等が行なわれているが未だ充分でない。 本発明者は特に磁性粉体の表面処理につき鋭意
研究した結果、数あるカツプリング剤の中でもア
ルミニウム系カツプリング剤が表面処理剤として
特に優れている事実を見出した。 本発明で用いるアルミニウム系カツプリング剤
は、従来、充填剤や顔料等の分散剤として知られ
ているが、本発明者の知る限りプラスチツクマグ
ネツト組成物の磁性体粉末の処理に用いられるこ
とは知られていない。 かくしてこの発明によれば、磁性体粉末と合成
樹脂を主成分とするプラスチツクマグネツト組成
物において、磁性体粉末として、アルミニウム系
カツプリング剤で予め表面処理した磁性体粉末を
用いたことを特徴とするプラスチツクマグネツト
組成物が提供される。 本発明の表面処理は特に磁性粉体に潤滑性等を
付与し且つ分散及び成形加工性の向上により、磁
気特性のすぐれたものを得ることが出来るもので
ある。本発明の組成物は特に成形性がすぐれてお
り、また射出成形時磁場配向させることにより磁
気特性のすぐれたものが得られる。 本発明に使用するアルミニウム系カツプリング
剤としては、アセトアルコキシアルミニウムジエ
チレート、アセトアルコキシアルミニウムジイソ
プロピレート、アセトアルコキシアルミニウム−
ジ−n−ブチレート、アセトアルコキシアルミニ
ウムジエチルヘキシレート等のアセトアルコキシ
アルミニウムジアルキレート類が挙げられるが最
も好ましいのは、アセト低級アルコキシアルミニ
ウムジイソプロピレートである。その添加量につ
いては、磁性粉体に対して0.5部以上1.5部以下が
好ましい。0.5部以下ではカツプリング剤処理効
果が不充分であり1.5部以上では未反応カツプリ
ング剤が残つて悪影響を与えることが多い。 本発明に使用する磁性体粉末としては、バリウ
ムフエライト、ストロンチウムフエライト、カル
シウムフエライト、鉛フエライト、ナトリウム−
ランタンフエライト等のフエライト類やサマリウ
ムコバルト等の希土類の磁性粉末が挙げられ、こ
れらのうちマグネプラムバイト型の磁性粉末が好
適である。その粒子径は特に規制するものではな
いが、5ミクロン以下の比較的細かいものが好ま
しい。 本発明に使用する合成樹脂としては、各種の熱
可塑性樹脂及び熱硬化性樹脂が用いられ、例え
ば、ポリオレフイン系樹脂やポリアマイド系樹脂
が挙げられる。特にナイロン−6、ナイロン−12
等のポリアマイドは耐熱性、耐薬品性、耐衝撃
性、成形性等の点ですぐれている。 磁性体粉末と合成樹脂との全量中に占める磁性
粉体の割合は、特に規制するものではないが、80
重量%以上で95重量%以下が好ましい。80重量%
以下では成形性は良いが、磁気特性が不充分であ
る。また95重量%以上では成形困難となり脆いも
のとなる。 この発明において、磁性粉末の表面処理は、通
常アルミニウム系カツプリング剤は液状であるた
め、これらを所定割合で直接混合することにより
行なえばよいが、場合によつては揮発性溶剤の存
在下で行なつてもよく、少なくとも磁性体粉末と
アルミニウム系カツプリング剤が均一に接触しう
る条件下で行なえばよい。この際の表面処理は室
温ないしアルミニウム系カツプリング剤の分解温
度程度の高温下(ただし分解温度未満;例えば
320℃前後)で行うことができる。カツプリング
剤での表面処理は、一般に100℃未満で行なうこ
とが普通である。しかし、100℃以上でカツプリ
ング剤の分解温度程度迄の高温であつても有効で
あることが見出された。 具体的な表面処理法としては種々の方法が用い
られるが、例えば磁性粉体をヘンシエルミキサー
に仕込み撹拌しながら所定量のカツプリング剤を
滴下し、その後さらに撹拌を行なうのが適当であ
る。 本発明の組成物は、上記主成分以外必要に応じ
て滑剤、熱安定剤等を含有させることも出来る。 本発明の方法により製造したプラスチツクマグ
ネツト材料は磁場配向を行なうことにより磁気性
能のすぐれたものが出来る。 これらは、小型精密モーター、計器部品、小型
発電機等広汎な分野に使用される。 以下本発明を実施例により説明する。 実施例 1 平均粒径1.2μの異方性ストロンチユームフエラ
イト8.8Kgをヘンシエルミキサーに仕込み室温に
て撹拌しながらアセトメトキシアルミニウムジイ
ソプロピレート70gを滴下し、その後更に10分間
撹拌して表面処理されたストロンチウムフエライ
ト粉末を得る。これに60メツシユより細かいナイ
ロン−6粉末1.2Kgを添加し10分間撹拌混合を行
なつた。 この配合物を2軸の押出機にてペレツト成形を
行ないさらに射出成形による磁場成形を行なつ
た。この場合の成形条件は、磁界12000Oeにて6
秒間着磁を行なつたものであり、この成形品にて
各種物性等の測定を行なつた。その測定方法は下
記の通りである。 A 流動性 メルトインデクサーを用い、260℃で荷重10
Kgの場合で10分間の流出量を測定した(ノズル
半径1.0mm)。 B 磁気特性 直流磁化特性自動記録装置により、ヒステリ
シス曲線を測定しこれにより、残留磁束密度
(Br)、保磁力(BHc)、固有保磁力(IHc)及
びこれらより最大エネルギー積(B.Hmax)の
磁気特性を評価した。尚、測定材料は直径20
mm、高さ10mmの円筒形のものである。
TECHNICAL FIELD This invention relates to plastic magnet compositions. In particular, the present invention relates to a composition having excellent magnetic properties and excellent moldability. Conventional permanent magnets include Alnico magnets as cast magnets, and sintered ferrite magnets using iron oxide.In particular, sintered ferrite magnets are used in heavy electrical appliances, home appliances,
Used in many electronic devices. In recent years, demand for high-magnetic samarium-cobalt alloy magnets has increased due to the demand for smaller, more precise electronic equipment and higher performance and reliability. However, these magnets are an obstacle to expanding their use because they are brittle and require secondary processing such as cutting and polishing. In order to improve these problems, composite materials of magnetic materials and various synthetic resins have been put into practical use. These are composites of magnetic powder mainly made of ferrite or rare earth metals and plastics such as polyamide and polypropylene, and can be efficiently molded into complex shapes that were impossible with conventional magnetic materials. I can do it. However, there are problems such as a decrease in magnetic force due to the addition of plastic and variations in magnetic force due to poor dispersion, as well as poor fluidity during injection molding. As a method to improve these problems, surface treatment of magnetic powder has been carried out, but it is still not sufficient. As a result of extensive research into the surface treatment of magnetic powders, the inventors of the present invention have discovered that among many coupling agents, aluminum-based coupling agents are particularly excellent as surface treatment agents. The aluminum coupling agent used in the present invention has been conventionally known as a dispersant for fillers, pigments, etc., but as far as the inventors know, it is not known to be used for treating magnetic powder in plastic magnet compositions. It has not been done. Thus, according to the present invention, in a plastic magnet composition containing magnetic powder and synthetic resin as main components, magnetic powder whose surface has been previously treated with an aluminum-based coupling agent is used as the magnetic powder. A plastic magnet composition is provided. In particular, the surface treatment of the present invention imparts lubricity to the magnetic powder and improves dispersion and moldability, thereby making it possible to obtain excellent magnetic properties. The composition of the present invention has particularly excellent moldability, and can have excellent magnetic properties by orienting it in a magnetic field during injection molding. Examples of the aluminum coupling agent used in the present invention include acetalkoxyaluminum diethylate, acetalkoxyaluminum diisopropylate, acetalkoxyaluminum diisopropylate, and acetalkoxyaluminum diisopropylate.
Examples include acetoalkoxyaluminum dialkylates such as di-n-butyrate and acetoalkoxyaluminum diethylhexylate, but the most preferred is acetolower alkoxyaluminum diisopropylate. The amount added is preferably 0.5 parts or more and 1.5 parts or less based on the magnetic powder. If the amount is less than 0.5 part, the coupling agent treatment effect will be insufficient, and if it is more than 1.5 parts, unreacted coupling agent will remain and often have an adverse effect. The magnetic powder used in the present invention includes barium ferrite, strontium ferrite, calcium ferrite, lead ferrite, and sodium ferrite.
Examples include magnetic powders of ferrites such as lanthanum ferrite and rare earths such as samarium cobalt, and among these, magnetoplumite magnetic powders are preferred. The particle size is not particularly limited, but relatively fine particles of 5 microns or less are preferred. As the synthetic resin used in the present invention, various thermoplastic resins and thermosetting resins are used, such as polyolefin resins and polyamide resins. Especially nylon-6, nylon-12
These polyamides have excellent heat resistance, chemical resistance, impact resistance, moldability, etc. The proportion of magnetic powder in the total amount of magnetic powder and synthetic resin is not particularly regulated, but it is 80%
It is preferably at least 95% by weight. 80% by weight
Below, the moldability is good, but the magnetic properties are insufficient. Moreover, if it exceeds 95% by weight, it becomes difficult to mold and becomes brittle. In this invention, the surface treatment of the magnetic powder can be carried out by directly mixing aluminum coupling agents in a predetermined ratio since they are usually liquid, but in some cases it may be carried out in the presence of a volatile solvent. The process may be carried out under conditions where at least the magnetic powder and the aluminum-based coupling agent can come into uniform contact with each other. In this case, the surface treatment is carried out at room temperature or at a high temperature around the decomposition temperature of the aluminum coupling agent (but below the decomposition temperature; e.g.
It can be carried out at a temperature of around 320℃). Surface treatment with a coupling agent is generally carried out at a temperature below 100°C. However, it has been found that it is effective even at high temperatures of 100°C or higher, which is about the decomposition temperature of the coupling agent. Various methods can be used as specific surface treatment methods, but for example, it is appropriate to charge the magnetic powder into a Henschel mixer, drop a predetermined amount of the coupling agent while stirring, and then further stir. The composition of the present invention can also contain a lubricant, a heat stabilizer, etc., if necessary, in addition to the above-mentioned main components. The plastic magnet material produced by the method of the present invention can have excellent magnetic properties by being oriented in a magnetic field. These are used in a wide range of fields such as small precision motors, instrument parts, and small generators. The present invention will be explained below with reference to Examples. Example 1 8.8 kg of anisotropic strontium ferrite with an average particle size of 1.2 μ was placed in a Henschel mixer, and 70 g of acetomethoxyaluminum diisopropylate was added dropwise while stirring at room temperature, followed by further stirring for 10 minutes for surface treatment. Obtain strontium ferrite powder. To this was added 1.2 kg of nylon-6 powder finer than 60 mesh, and the mixture was stirred and mixed for 10 minutes. This mixture was formed into pellets using a twin-screw extruder, and further subjected to magnetic field molding by injection molding. The molding conditions in this case are 6 in a magnetic field of 12000 Oe.
The molded product was magnetized for seconds, and various physical properties were measured on this molded product. The measurement method is as follows. A Fluidity Using a melt indexer, load 10 at 260℃
The outflow amount for 10 minutes was measured in the case of Kg (nozzle radius 1.0 mm). B Magnetic properties The hysteresis curve is measured using a DC magnetization property automatic recording device, and from this the residual magnetic flux density (Br), coercive force (BHc), intrinsic coercive force (IHc), and the maximum energy product (B.Hmax) are calculated from these. The magnetic properties were evaluated. In addition, the measuring material is 20 mm in diameter.
It is cylindrical with a height of 10 mm and a height of 10 mm.

【表】 表中の比較例1はカツプリング剤処理を行な
わなかつたものである。比較例2はイソプロプ
ルトリ(N−アミノエチルアミノエステル)チ
タネートで室温にて処理したものであり、実施
例1と比較した場合流動性及び磁気特性共に劣
る。 実施例 2 実施例1でカツプリング剤の処理温度を140℃
とした以外は同様にして実験を行なつた。結果を
下表に示す。
[Table] Comparative Example 1 in the table was not treated with a coupling agent. Comparative Example 2 was treated with isopropyltri(N-aminoethylaminoester) titanate at room temperature, and when compared with Example 1, both fluidity and magnetic properties were inferior. Example 2 The processing temperature of the coupling agent in Example 1 was changed to 140°C.
The experiment was conducted in the same manner except for the following. The results are shown in the table below.

【表】 比較例3はイソプロプルトリ(N−アミノエチ
ルアミノエステル)チタネートで140℃の処理を
行なつたものである。 実施例 3 実施例1でカツプリング剤として、アセトメト
キシアルミニウムジエチルヘキシレートを使用し
た以外は、全く同様にして実験を行なつた。結果
を下記に示す。
[Table] Comparative Example 3 was treated with isopropylene tri(N-aminoethylaminoester) titanate at 140°C. Example 3 An experiment was carried out in exactly the same manner as in Example 1, except that acetomethoxyaluminum diethylhexylate was used as the coupling agent. The results are shown below.

【表】 実施例 4 合成樹脂として、120メツシユ通過のナイロン
−12粉末1.1Kgを用いる以外、実施例1と同様に
して実験を行なつた。結果を下表に示す。
[Table] Example 4 An experiment was conducted in the same manner as in Example 1 except that 1.1 kg of nylon-12 powder passing through 120 mesh was used as the synthetic resin. The results are shown in the table below.

【表】 実施例 5 合成樹脂として、100メツシユ通過のポリプロ
ピレン粉末1.2Kgを用いた以外は、実施例1と同
様にして配合物を作製しその諸性能を測定した。
その結果を下表に示す。
[Table] Example 5 A blend was prepared in the same manner as in Example 1, except that 1.2 kg of polypropylene powder that passed through 100 meshes was used as the synthetic resin, and its various performances were measured.
The results are shown in the table below.

【表】【table】

Claims (1)

【特許請求の範囲】 1 磁性体粉末と合成樹脂を主成分とするプラス
チツクマグネツト組成物において、 磁性体粉末として、アルミニウム系カツプリン
グ剤で予め表面処理した磁性体粉末を用いたこと
を特徴とするプラスチツクマグネツト組成物。
[Scope of Claims] 1. A plastic magnet composition containing magnetic powder and synthetic resin as main components, characterized in that magnetic powder whose surface has been previously treated with an aluminum-based coupling agent is used as the magnetic powder. Plastic magnet composition.
JP24743983A 1983-12-27 1983-12-27 Plastic magnet composition Granted JPS60139759A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24743983A JPS60139759A (en) 1983-12-27 1983-12-27 Plastic magnet composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24743983A JPS60139759A (en) 1983-12-27 1983-12-27 Plastic magnet composition

Publications (2)

Publication Number Publication Date
JPS60139759A JPS60139759A (en) 1985-07-24
JPH0262146B2 true JPH0262146B2 (en) 1990-12-25

Family

ID=17163451

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24743983A Granted JPS60139759A (en) 1983-12-27 1983-12-27 Plastic magnet composition

Country Status (1)

Country Link
JP (1) JPS60139759A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63225657A (en) * 1986-10-28 1988-09-20 Calp Corp Composite polymer composition

Also Published As

Publication number Publication date
JPS60139759A (en) 1985-07-24

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