JPS60113403A - Manufacture of rare earth resin magnet - Google Patents
Manufacture of rare earth resin magnetInfo
- Publication number
- JPS60113403A JPS60113403A JP58219359A JP21935983A JPS60113403A JP S60113403 A JPS60113403 A JP S60113403A JP 58219359 A JP58219359 A JP 58219359A JP 21935983 A JP21935983 A JP 21935983A JP S60113403 A JPS60113403 A JP S60113403A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- magnetic field
- temperature
- applying
- range
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
- H01F1/047—Alloys characterised by their composition
- H01F1/053—Alloys characterised by their composition containing rare earth metals
- H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
- H01F1/0555—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together
- H01F1/0558—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together bonded together
Abstract
Description
【発明の詳細な説明】
本発明は、希土類磁石粉末であるサマリウムとコバル1
に一主成分とする金属間化合物粉末とポリフェニレンサ
ルファイド樹脂t7tはポリエーテルエーテルクトン樹
脂からなる混合物を使用した異方性または等方性の永久
磁石の製造方法に関するものである〇
射出成形による樹脂磁石は焼結磁石に比べて(1)成形
性が良く、複雑な形状のものができる。DETAILED DESCRIPTION OF THE INVENTION The present invention utilizes samarium and cobal 1, which are rare earth magnet powders.
The main component of intermetallic compound powder and polyphenylene sulfide resin t7t relates to a method for manufacturing an anisotropic or isotropic permanent magnet using a mixture consisting of polyether ether lactone resin. 〇Resin magnet by injection molding Compared to sintered magnets, (1) it has better formability and can be made into complex shapes;
(2)成形品の寸法精度が良い。(2) Good dimensional accuracy of the molded product.
(3)量産性が良い。(3) Good mass productivity.
(4)機械的強度が向上する。(4) Mechanical strength is improved.
(5)磁気特性が安定する。(5) Magnetic properties are stabilized.
などの利点がある。しかし、この樹脂磁石の耐熱性は、
焼結磁石のそれに比べて著しく劣る。There are advantages such as However, the heat resistance of this resin magnet is
It is significantly inferior to that of sintered magnets.
そこで、従来耐熱性のより向上した樹脂磁石の製造方法
が試みられてきており、その中で、35容量チ以上のポ
リカーボネート樹脂と、残部がサマリウムとコバルトを
主成分とする公知の金属間化合物磁石粉末(比重8.2
〜8.6.以下これを磁石粉末という)とを温度260
℃程度で混練した後、得られた混合物を温度260℃程
度、圧力1300〜1500(偏程度で磁界を印加しf
cりしなかったりして射出成形して異方性または等方性
の耐熱性ある樹脂磁石を製造する方法は公知である。Therefore, attempts have been made to produce resin magnets with improved heat resistance, and among them, known intermetallic compound magnets whose main components are polycarbonate resin with a capacity of 35% or more, and the balance being samarium and cobalt. Powder (specific gravity 8.2
~8.6. (hereinafter referred to as magnet powder) at a temperature of 260°C.
After kneading at about ℃, the obtained mixture was kneaded at a temperature of about 260℃ and a pressure of 1,300 to 1,500 degrees (a magnetic field was applied with an uneven degree).
A method of manufacturing an anisotropic or isotropic heat-resistant resin magnet by injection molding without any heat-resistance is known.
しかしながら、このような方法によって製造された樹脂
磁石の耐熱性は、熱変形温度が約140℃(ASTMD
648による)で十分でなく、更に耐熱性の向上し素樹
脂磁石を製造する方法の開発が望まれていた。However, the heat resistance of resin magnets manufactured by such a method is limited to a heat distortion temperature of approximately 140°C (ASTMD
648) was not sufficient, and there was a desire to develop a method for manufacturing base resin magnets with further improved heat resistance.
本発明者等は、上記の観点に鑑み、熱可塑性樹脂と、残
部が磁石粉末との混合物から更に耐熱性の向上した樹脂
磁石の製造方法を提供すべく、鋭意研究した結果、前記
公知方法において250〜300℃程度の耐熱性を有す
る種々の熱可塑性樹脂の中からポリフェニレンサルファ
イド樹脂、ポリエーテルエーテルケトン樹脂を使用する
こと、そして磁石粉末をシランカップリング剤で表面処
理して使用することによって、前記目的が達成され得る
ことを見出し本発明に到達した。In view of the above-mentioned viewpoints, the present inventors conducted extensive research in order to provide a method for producing resin magnets with further improved heat resistance from a mixture of a thermoplastic resin and the remainder being magnet powder, and as a result, they found that By using polyphenylene sulfide resin and polyether ether ketone resin from among various thermoplastic resins having heat resistance of about 250 to 300 degrees Celsius, and by surface treating magnet powder with a silane coupling agent, The inventors have discovered that the above object can be achieved and have arrived at the present invention.
すなわち、本発明は、20〜40容量チのポリフェニレ
ンサルファイド樹脂(比重1.6〜2.01以下、PP
S樹脂という)マタはポリエーテルエーテルケトン樹脂
(比重1.2〜1.3、以下、PEEK樹脂という)と
残部が7ランカツプリング剤で表面処理した磁石粉末と
を、前記樹脂の融点と分解温度との間の温度範囲で混練
した後、得られた混合物を前記温度範囲および1000
〜2000 Kg、夕の圧力範囲で、磁界を印加しなが
らまたは磁界を印加することなく射出成形することを特
徴とするものである。That is, the present invention uses polyphenylene sulfide resin (specific gravity 1.6 to 2.01 or less, PP
Mata uses polyetheretherketone resin (specific gravity 1.2 to 1.3, hereinafter referred to as PEEK resin) and magnet powder whose surface has been treated with a 7-run coupling agent to determine the melting point and decomposition of the resin. After kneading in a temperature range between 1000 and 1000
It is characterized by injection molding in the pressure range of ~2000 Kg, with or without applying a magnetic field.
以下、本発明について詳細に説明する。The present invention will be explained in detail below.
本発明において、熱可塑性樹脂として、PPS樹脂また
はPEEK樹脂を使用する。そして、その使用量は、2
0〜40容量優にすることが必要である。In the present invention, PPS resin or PEEK resin is used as the thermoplastic resin. And the usage amount is 2
It is necessary to have a capacity of 0 to 40.
20容量チ未満では射出による成形加工が極めて困難に
なり、40容量96を超えると磁気特性が従来品より低
下する。If the capacity is less than 20, molding by injection becomes extremely difficult, and if the capacity exceeds 40, the magnetic properties will be lower than that of conventional products.
また、磁石粉末は、シランカップリング剤で表面処理し
たものを使用することが必要である。シランカップリン
グ剤としては、例えば、r−メルカプト−プロピル−ト
リメトキシシラン、2−スチリル−エチル−トリメトキ
シシラン、N−β−(アミノエチル)r−アミノ−プロ
ピル−トリメトキシシラン、β−(3、4−エポキシシ
クロ−ヘキシル〕エチルートリメトキシシラン、r−ア
ミノ−プロピル−トリメトキシシラン、γ−グリシドキ
シープロビルトリメトキシシラン、フェニルトリメトキ
シシラン、メチルジメトキシシランなどの単体およびこ
れらの混合物が使用できる。Furthermore, it is necessary to use magnet powder that has been surface-treated with a silane coupling agent. Examples of the silane coupling agent include r-mercapto-propyl-trimethoxysilane, 2-styryl-ethyl-trimethoxysilane, N-β-(aminoethyl)r-amino-propyl-trimethoxysilane, β-( Single substances such as 3,4-epoxycyclohexyl]ethyltrimethoxysilane, r-amino-propyl-trimethoxysilane, γ-glycidoxyprobyltrimethoxysilane, phenyltrimethoxysilane, methyldimethoxysilane, and mixtures thereof can be used.
前記表面処理は、磁石粉末を5〜20容量チのシランカ
ップリング剤のアルコールなどの溶液で湿潤させた後、
室温以上、好ましくは120〜150℃で乾燥すること
により行なえばよい。このようなカップリング剤による
表面処理により、磁石粉末に撥水性や潤滑性が付与され
、得られる樹脂磁石の主として機械的強度を向上させる
。The surface treatment is performed by moistening the magnet powder with a solution of 5 to 20 volumes of a silane coupling agent such as alcohol, and then
This may be carried out by drying at room temperature or higher, preferably at 120 to 150°C. Surface treatment with such a coupling agent imparts water repellency and lubricity to the magnet powder, and improves mainly the mechanical strength of the resulting resin magnet.
カップリング剤で表面処理された磁石粉末は、次に樹脂
と混練して混合物を得るが、この際の混線は、磁石粉末
の分散を良好にする友めに樹脂の融点以上で、かつ樹脂
が分解しないように、樹脂の分解温度未満の温度範囲す
なわち、PPS樹脂を使用した場合は290〜400℃
、 PEEK樹脂を使用した場合は330〜560℃で
行なう必要がある。The magnet powder that has been surface-treated with a coupling agent is then kneaded with a resin to obtain a mixture. To avoid decomposition, the temperature range is below the decomposition temperature of the resin, i.e. 290-400°C when using PPS resin.
, When PEEK resin is used, it is necessary to carry out the process at 330 to 560°C.
混練して得られた混合物は、更に金型で射出成形するが
、この際の温度は、混線の際の温度範囲と同様の範囲に
、また圧力は1000〜2000 Iveriの5−
範囲にする必要がある。温度範囲をこのようにするのは
、混練の際と同様の理由によるものでhv、また、圧力
を上記のようにするのは、良好な成形加工性を維持する
ためであp、具体的には、1000V−未満では、混合
物の流れが悪くなって、寸法精度の優れた成形品が得ら
れ難くなり、2000 Kg/cdを超えると、成形品
にひびわれなどが生じ易くなる。The mixture obtained by kneading is further injection molded in a mold, but the temperature at this time needs to be in the same range as the temperature range during mixing, and the pressure needs to be in the 5-5 range of 1000 to 2000 Iveri. There is. The temperature range is set in this way for the same reason as during kneading (hv), and the pressure is set as above in order to maintain good molding processability.Specifically, If it is less than 1000 V-, the flow of the mixture will be poor and it will be difficult to obtain a molded product with excellent dimensional accuracy, and if it exceeds 2000 Kg/cd, cracks will easily occur in the molded product.
射出成型を磁界を印加しながら行なうことによって磁石
粉末を一定方向に配向させた異方性樹脂磁石を製造する
ことができ、また、磁界を印加しないで行なうことによ
ってあらゆる方向に着磁することが可能な等方性樹脂磁
石を製造することができる。By performing injection molding while applying a magnetic field, it is possible to manufacture an anisotropic resin magnet in which the magnet powder is oriented in a certain direction, and by performing injection molding without applying a magnetic field, it is possible to magnetize in any direction. isotropic resin magnets can be manufactured.
このようにして製造された樹脂磁石は、磁気特性および
機械的強度は従来品差みであるが、耐熱性が従来品のそ
れに比べて著しく向上している。The magnetic properties and mechanical strength of the resin magnet manufactured in this manner are on a par with conventional products, but the heat resistance is significantly improved compared to that of conventional products.
以下、実施例により本発明を更に説明する。The present invention will be further explained below with reference to Examples.
実施例
シランカップリング剤で表面処理したSmCo56一
(SmCoB系)およびSm (Coqe* F’6[
120Cu((16Zrqol ) z4(Sm2 C
ol□系)磁石粉末(平均粒径は夫々5μm。Example SmCo56 (SmCoB system) and Sm (Coqe* F'6[
120Cu((16Zrqol)z4(Sm2C
ol□ series) magnet powder (average particle size is 5 μm each.
35μm)とpps樹脂(保土谷化学社製、商品名ライ
ドン) 、PEEK樹脂(三井東圧化学社製、商品名P
EEKナチョナル)またはポリカーボネート樹脂(エン
ジニアリングプラスチック社製、商品名クラスチック皿
、後掲表中ではPC樹脂という)とを混練した後、射出
成形して、種々の異方性(印加磁界1.2〜1,6万ガ
ウス)および等方性樹脂磁石を製造した。この際、磁石
粉末の表面処理は、磁石粉末を7容量チのシランカップ
リング剤のアルコール溶液中で攪拌した後、濾過し、次
いで表面に付着している溶液を120℃オーブン中で乾
燥することによフ行なった。その他、これらの樹脂磁石
の製造条件を第1表および第2表に示す。35 μm), pps resin (manufactured by Hodogaya Chemical Co., Ltd., trade name Rydon), PEEK resin (manufactured by Mitsui Toatsu Chemical Co., Ltd., trade name P
EEK National) or polycarbonate resin (manufactured by Engineering Plastics Co., Ltd., trade name: Clastic Dish, referred to as PC resin in the table below), injection molding is performed, and various anisotropies (applied magnetic field of 1.2 to 1 , 60,000 Gauss) and isotropic resin magnets. At this time, the surface treatment of the magnet powder is carried out by stirring the magnet powder in a 7-volume alcoholic solution of a silane coupling agent, filtering it, and then drying the solution adhering to the surface in an oven at 120°C. I went to Yofu. Other manufacturing conditions for these resin magnets are shown in Tables 1 and 2.
得られた樹脂磁石の熱変形温度、磁気特性および抗折力
を測定しく熱変形温度はASTM D 648 。The heat distortion temperature, magnetic properties, and transverse rupture strength of the obtained resin magnet were measured according to ASTM D 648.
抗折力はASTM D 790の試験法によっ7′l:
、) 、その結果を、やはり第1表および第2表に示し
た。Transverse rupture strength is 7'l according to ASTM D 790 test method:
), the results are also shown in Tables 1 and 2.
第1表および第2表より、本発明方法によって製造され
た樹脂磁石は、従来方法によって製造された樹脂磁石に
比べて、磁気特性および抗折力は同等程度であるが、耐
熱性が著しく向上していることが判る。From Tables 1 and 2, the resin magnets manufactured by the method of the present invention have comparable magnetic properties and transverse rupture strength, but have significantly improved heat resistance compared to resin magnets manufactured by the conventional method. I can see that you are doing it.
Claims (1)
たはポリエーテルエーテルクトン樹脂と。 残部がシランカップリング剤で表面処理したサマリウム
とコバルトを主成分とする金属間化合物磁石粉末とを、
前記樹脂の融点と分解温度との間の温度範囲で混練した
後、得られた混合物を前記温度範囲および1000〜2
00015dlの圧力範囲で、磁界を印加しながらまた
は磁界を印加することなく射出成形することを特徴とす
る希土類樹脂磁石の製造方法。[Claims] 20 to 40 volumes of polyphenylene sulfide resin or polyether ether lactone resin. Intermetallic compound magnet powder whose main components are samarium and cobalt, the remainder of which has been surface-treated with a silane coupling agent,
After kneading in a temperature range between the melting point and the decomposition temperature of the resin, the resulting mixture is
A method for producing a rare earth resin magnet, characterized by injection molding in a pressure range of 00015 dl while applying a magnetic field or without applying a magnetic field.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58219359A JPS60113403A (en) | 1983-11-24 | 1983-11-24 | Manufacture of rare earth resin magnet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58219359A JPS60113403A (en) | 1983-11-24 | 1983-11-24 | Manufacture of rare earth resin magnet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60113403A true JPS60113403A (en) | 1985-06-19 |
Family
ID=16734192
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58219359A Pending JPS60113403A (en) | 1983-11-24 | 1983-11-24 | Manufacture of rare earth resin magnet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60113403A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6190401A (en) * | 1984-10-09 | 1986-05-08 | Shin Etsu Chem Co Ltd | Composition of plastic magnet |
JPS61279106A (en) * | 1985-06-04 | 1986-12-09 | Seiko Epson Corp | Resin-bonded type permanent magnet |
JPS62242317A (en) * | 1986-04-14 | 1987-10-22 | Kanegafuchi Chem Ind Co Ltd | Flame resistive resin magnet |
JPH01128503A (en) * | 1987-11-13 | 1989-05-22 | Tokin Corp | Composite magnet composition and preparation thereof |
EP0350781A2 (en) * | 1988-07-12 | 1990-01-17 | Idemitsu Kosan Company Limited | Magnetic powder material and resin-bonded type magnet |
-
1983
- 1983-11-24 JP JP58219359A patent/JPS60113403A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6190401A (en) * | 1984-10-09 | 1986-05-08 | Shin Etsu Chem Co Ltd | Composition of plastic magnet |
JPS61279106A (en) * | 1985-06-04 | 1986-12-09 | Seiko Epson Corp | Resin-bonded type permanent magnet |
JPS62242317A (en) * | 1986-04-14 | 1987-10-22 | Kanegafuchi Chem Ind Co Ltd | Flame resistive resin magnet |
JPH01128503A (en) * | 1987-11-13 | 1989-05-22 | Tokin Corp | Composite magnet composition and preparation thereof |
EP0350781A2 (en) * | 1988-07-12 | 1990-01-17 | Idemitsu Kosan Company Limited | Magnetic powder material and resin-bonded type magnet |
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