JPH06333712A - Composition for resin bonded type magnet and resin-bonded type magnet - Google Patents
Composition for resin bonded type magnet and resin-bonded type magnetInfo
- Publication number
- JPH06333712A JPH06333712A JP5139245A JP13924593A JPH06333712A JP H06333712 A JPH06333712 A JP H06333712A JP 5139245 A JP5139245 A JP 5139245A JP 13924593 A JP13924593 A JP 13924593A JP H06333712 A JPH06333712 A JP H06333712A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- epoxy resin
- magnetic powder
- composition
- binder
- 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
- H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
- H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
- H01F1/0575—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together
- H01F1/0576—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together pressed, e.g. hot working
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、磁気特性及び圧環強度
に優れた樹脂結合型磁石を与える組成物、及びそれを用
いた樹脂結合型磁石に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition which gives a resin-bonded magnet excellent in magnetic properties and radial crushing strength, and a resin-bonded magnet using the composition.
【0002】[0002]
【従来の技術】希土類永久磁石はその優れた磁気特性か
ら、一般家電製品や通信・音響機器、医療機器、一般産
業機器に至る幅広い分野で応用されつつある。この希土
類永久磁石には、樹脂結合型と焼結型とがある。樹脂結
合型の磁石は、磁性粉末に樹脂バインダーを配合してプ
レス成形するものであるため、焼結型の磁石に比べて、
(1)寸法精度が高く複雑な形状に成形できる、(2)
品質、性能の均一性が高い、(3)歩留まりがよく、機
械加工性が良い、等の利点がある。しかし、樹脂バイン
ダーの配合比率を高めれば機械的強度が増し、組立時に
割れや欠けが生じなくなるが、その比率が増すにつれ磁
性粉末の比率が低下して磁石の磁気特性が低下するとい
う欠点がある。2. Description of the Related Art Due to their excellent magnetic properties, rare earth permanent magnets are being applied in a wide range of fields including general home appliances, communication / audio equipment, medical equipment, and general industrial equipment. This rare earth permanent magnet is classified into a resin-bonded type and a sintered type. Resin-bonded magnets are magnetic powders mixed with a resin binder and press-molded, so compared to sintered magnets,
(1) It has high dimensional accuracy and can be molded into complicated shapes. (2)
There are advantages such as high uniformity of quality and performance, (3) good yield and good machinability. However, if the compounding ratio of the resin binder is increased, the mechanical strength increases and cracks and chips do not occur during assembly, but as the ratio increases, the ratio of the magnetic powder decreases and the magnetic properties of the magnet deteriorate. .
【0003】一方、小型モーター、音響機器、OA機器
等に用いられる樹脂結合型磁石は、機器の小型化の要請
から、機械的強度、特にリング圧環強度に優れていると
共に磁気特性も高いものが要求されている。この磁気特
性の向上と機械的強度の向上という相反する要求を満た
すものとして、エポキシ樹脂をバインダーとした樹脂結
合型磁石が提案されている。エポキシ樹脂をバインダー
とすれば、リング圧環強度や耐熱性、成形性を著しく損
なわなくても高い磁気特性が得られる。On the other hand, resin-bonded magnets used in small motors, audio equipment, office automation equipment, etc., have excellent mechanical strength, especially ring radial crushing strength, and high magnetic characteristics because of the demand for downsizing of the equipment. Is required. A resin-bonded magnet using an epoxy resin as a binder has been proposed as a material satisfying the contradictory requirements of improving the magnetic properties and the mechanical strength. When an epoxy resin is used as a binder, high magnetic properties can be obtained without significantly impairing ring radial crushing strength, heat resistance, and moldability.
【0004】[0004]
【発明が解決しようとする課題】しかしながら単独のエ
ポキシ樹脂のみの使用では機械的強度の向上に限界があ
り、薄型成形品等では未だ機械的強度が十分ではない。
本発明は上記事情に鑑みてなされたものであり、その目
的は、バインダー樹脂の比率を低く抑えても、得られる
磁石の磁気特性や機械的強度が優れている樹脂結合型磁
石用組成物、及び該組成物により得られる樹脂結合型磁
石を提供することにある。However, there is a limit to the improvement of mechanical strength when only a single epoxy resin is used, and thin molded articles and the like still have insufficient mechanical strength.
The present invention has been made in view of the above circumstances, and an object thereof is to provide a resin-bonded magnet composition having excellent magnetic properties and mechanical strength of the obtained magnet even if the ratio of the binder resin is suppressed to a low level, And to provide a resin-bonded magnet obtained by the composition.
【0005】[0005]
【課題を解決するための手段】本発明者らは上記課題を
達成するため、樹脂結合型磁石のバインダーに使用する
樹脂について種々の検討を行った結果、下記の構成によ
り目的とする樹脂結合型磁石用組成物が得られることを
見いだし、本発明を完成した。即ち本発明の樹脂結合型
磁石用組成物は、磁性粉末と樹脂バインダーからなる樹
脂結合型磁石用組成物において、上記磁性粉末は異方性
磁場が50kOe以上で、かつ、上記樹脂バインダー
は、主鎖にポリサルファイド骨格を有するエポキシ樹脂
とノボラック型エポキシ樹脂と、必要により芳香族アミ
ン系エポキシ樹脂硬化剤とを含有している点に特徴があ
る。また、本発明の樹脂結合型磁石は、上記樹脂結合型
磁石用組成物を、加圧成形後、加熱硬化して得られる点
に特徴がある。In order to achieve the above object, the inventors of the present invention have conducted various studies on resins used as binders of resin-bonded magnets, and as a result, have the following resin-bonded type It was found that a composition for magnets was obtained, and the present invention was completed. That is, the resin-bonded magnet composition of the present invention is a resin-bonded magnet composition comprising magnetic powder and a resin binder, wherein the magnetic powder has an anisotropic magnetic field of 50 kOe or more, and the resin binder is mainly It is characterized in that it contains an epoxy resin having a polysulfide skeleton in its chain, a novolac type epoxy resin, and, if necessary, an aromatic amine epoxy resin curing agent. Further, the resin-bonded magnet of the present invention is characterized in that it is obtained by pressure-molding the composition for a resin-bonded magnet described above, followed by heat curing.
【0006】本発明で使用する磁性粉末は、異方性磁場
(HA)が50kOe以上の磁性粉末であれば特に制約
なく使用できる。従って、この条件を満たす限り通常樹
脂結合型磁石に用いられている磁性粉末を使用でき、例
えば、Sm-Co5系、Sm2(CoFeZrV)17系等
の希土類コバルト系、Nd-Fe-Co-B系、Nd-Dy
-Fe-B系、Nd-Fe-B系等の希土類-鉄-ホウ素系、
Sm-Fe-N系、Nd-Fe-Ti-N系、Nd-Fe-V-
N系等の窒化物系磁性粉末等が挙げられる。いずれにお
いても磁性粉末の粒径は、通常、35メッシュ(JI
S)以下が好ましい。As the magnetic powder used in the present invention, any magnetic powder having an anisotropic magnetic field (H A ) of 50 kOe or more can be used without particular limitation. Therefore, as long as this condition is satisfied, magnetic powders that are usually used in resin-bonded magnets can be used. For example, rare-earth cobalt-based materials such as Sm-Co 5 series and Sm 2 (CoFeZrV) 17 series, Nd-Fe-Co- B system, Nd-Dy
-Fe-B type, Nd-Fe-B type rare earth-iron-boron type,
Sm-Fe-N system, Nd-Fe-Ti-N system, Nd-Fe-V-
N-based nitride-based magnetic powder and the like can be mentioned. In any case, the particle size of the magnetic powder is usually 35 mesh (JI
S) or less is preferable.
【0007】磁性粉末として上で例示した希土類-鉄-ホ
ウ素系の場合は、液体急冷法による合金粉末の使用が特
に好ましい。液体急冷法とは、所要組成の合金を高周波
誘導加熱等の方法によって溶解し、得られた溶湯を高速
回転する銅またはアルミニウム製のロールに吹き付けて
急冷し、厚さ数十ミクロンのリボンとし、このリボンに
適当な熱処理を施して、例えば平均結晶粒径を3000
A以下とした後に、スタンプミル、ボールミル等により
乾式あるいは湿式粉砕することにより磁性粉末を得る方
法である。In the case of the rare earth-iron-boron system exemplified above as the magnetic powder, it is particularly preferable to use the alloy powder by the liquid quenching method. Liquid quenching method, the alloy of the required composition is melted by a method such as high frequency induction heating, and the resulting molten metal is sprayed onto a high-speed rotating copper or aluminum roll to be rapidly cooled to form a ribbon having a thickness of several tens of microns. By subjecting this ribbon to an appropriate heat treatment, for example, the average crystal grain size is increased to 3000.
It is a method of obtaining a magnetic powder by dry- or wet-milling with a stamp mill, a ball mill or the like after adjusting to A or less.
【0008】樹脂バインダーのエポキシ樹脂主剤は、少
なくとも主鎖にポリサルファイド骨格を有するエポキシ
樹脂とノボラック型エポキシ樹脂の2種類のエポキシ樹
脂を成分とする。エポキシ樹脂の第1の成分は主鎖にポ
リサルファイド骨格を有するエポキシ樹脂であれば、特
に分子量、分子量分布、側鎖や官能基等の制約なく使用
することができる。エポキシ樹脂の第2の成分はノボラ
ック型エポキシ樹脂であれば、クレゾールノボラック型
でもフェノールノボラック型でもよく、また、特に分子
量、分子量分布、側鎖や官能基等の制約なく使用するこ
とができる。The epoxy resin main component of the resin binder contains at least two kinds of epoxy resins, an epoxy resin having a polysulfide skeleton in the main chain and a novolac type epoxy resin. If the first component of the epoxy resin is an epoxy resin having a polysulfide skeleton in the main chain, it can be used without any restriction on the molecular weight, the molecular weight distribution, the side chain, the functional group and the like. The second component of the epoxy resin may be a cresol novolac type or a phenol novolac type as long as it is a novolac type epoxy resin, and it can be used without any particular restrictions on the molecular weight, the molecular weight distribution, the side chain, the functional group and the like.
【0009】また、これらのエポキシ樹脂以外にも、第
3成分以上として、例えばグリジルエーテル型エポキシ
樹脂、グリジルエステル型エポキシ樹脂、グリジルアミ
ン型エポキシ樹脂、線状脂肪族エポキサイド型エポキシ
樹脂、脂肪族エポキサイド型エポキシ樹脂等を、単独ま
たは2種類以上の組み合わせで追加混合使用してもよ
い。In addition to these epoxy resins, as the third component or more, for example, glycidyl ether type epoxy resin, glycidyl ester type epoxy resin, glycidyl amine type epoxy resin, linear aliphatic epoxide type epoxy resin, aliphatic The epoxide type epoxy resin or the like may be used alone or in a combination of two or more, and additionally mixed and used.
【0010】樹脂バインダー中の各成分の配合は、主鎖
にポリサルファイド骨格を有するエポキシ樹脂100重
量部に対し、ノボラック型エポキシ樹脂の量が5重量部
以上950重量部以下、好ましくは10重量部以上90
0重量部以下である。ノボラック型エポキシ樹脂の量が
5重量部より少ない場合、950重量部より多い場合の
いずれにおいても、充分なリング圧環強度が得難い。本
発明の組成物に於けるバインダー樹脂の配合量は、磁性
粉末100重量部当り0.5〜5重量部が好ましく、さ
らには1.0〜3.0重量部がより好ましい。The amount of the novolac type epoxy resin is 5 parts by weight or more and 950 parts by weight or less, preferably 10 parts by weight or more based on 100 parts by weight of the epoxy resin having a polysulfide skeleton in the main chain. 90
It is 0 parts by weight or less. When the amount of the novolac type epoxy resin is less than 5 parts by weight or more than 950 parts by weight, it is difficult to obtain sufficient ring radial crushing strength. The content of the binder resin in the composition of the present invention is preferably 0.5 to 5 parts by weight, and more preferably 1.0 to 3.0 parts by weight, based on 100 parts by weight of the magnetic powder.
【0011】樹脂バインダーのエポキシ系樹脂硬化剤に
は、芳香族アミン系エポキシ樹脂硬化剤を使用すること
ができる。エポキシ系樹脂硬化剤としては、芳香族アミ
ン型であれば、特に分子量、分子量分布、側鎖、官能基
等の制約なく使用することができる。樹脂バインダー中
のエポキシ樹脂硬化剤の配合は、エポキシ樹脂主剤総量
100重量部に対して、1〜40重量部が好ましく、さ
らには、10〜30重量部がより好ましい。エポキシ系
樹脂やエポキシ系樹脂硬化剤は、そのまま、あるいは例
えばアセトン、メチルエチルケトン、などの有機溶剤に
溶かした状態で使用できる。An aromatic amine epoxy resin curing agent can be used as the epoxy resin curing agent of the resin binder. As the epoxy resin curing agent, if it is an aromatic amine type, it can be used without particular restrictions on molecular weight, molecular weight distribution, side chains, functional groups and the like. The content of the epoxy resin curing agent in the resin binder is preferably 1 to 40 parts by weight, more preferably 10 to 30 parts by weight, based on 100 parts by weight of the total amount of the epoxy resin main agent. The epoxy resin or the epoxy resin curing agent can be used as it is or in a state of being dissolved in an organic solvent such as acetone or methyl ethyl ketone.
【0012】芳香族アミン系硬化剤としては、例えば、
m−フェニレンジアミン、 p,p’-ジアミノジフェニ
ルメタン、 p,p’-ジアミノジフェニルスルフォン、
メタキシレンジアミン、 キシレンジアミン、 1,3-
ビス(アミノメチル)シクロヘキサン等、一般的に芳香
族ポリアミンまたは芳香族アミンと称されている硬化剤
であれば使用することができ、これらの変性品等も無論
使用することができる。上述した芳香族アミン系硬化剤
は、構成されるエポキシ樹脂の種類や芳香族アミン系硬
化剤の種類によってエポキシ当量、活性水素当量が異な
るため適正量を規定することは困難であるが、一般的に
は、前記磁性粉末100重量部当たり0.01〜10重
量部、特に、0.1〜5重量部の量で使用されることが
好適である。5重量部よりも多量に使用しても、0.1
よりも少量使用であっても樹脂結合型磁石の機械的強度
が損なわれる。Examples of the aromatic amine curing agent include, for example,
m-phenylenediamine, p, p'-diaminodiphenylmethane, p, p'-diaminodiphenylsulfone,
Metaxylenediamine, xylenediamine, 1,3-
Any curing agent generally called aromatic polyamine or aromatic amine such as bis (aminomethyl) cyclohexane can be used, and of course, modified products thereof can also be used. It is difficult to specify an appropriate amount of the above-mentioned aromatic amine-based curing agent because the epoxy equivalent and active hydrogen equivalent differ depending on the type of epoxy resin and the type of aromatic amine-based curing agent that are configured, In particular, it is preferable to use 0.01 to 10 parts by weight, particularly 0.1 to 5 parts by weight, per 100 parts by weight of the magnetic powder. Even if used more than 5 parts by weight, 0.1
Even if used in a smaller amount, the mechanical strength of the resin-bonded magnet is impaired.
【0013】また、その他の樹脂硬化剤、硬化促進剤を
使用しても良い。例えば樹脂硬化剤としては、単一ポリ
アミン型硬化剤、変性ポリアミン型硬化剤、酸無水物型
硬化剤、ポリフェノール型硬化剤、ポリメルカプタン型
硬化剤、アニオン重合硬化剤、カチオン重合型硬化剤等
が挙げられる。また硬化促進剤としては、第三級アミン
類、イミダゾール類、有機金属塩類、塩化物類、有機過
酸化物類等が挙げられる。これら、樹脂硬化剤、硬化促
進剤は必要に応じて2種類以上を組み合わせて使用して
も良い。Other resin curing agents and curing accelerators may also be used. For example, as the resin curing agent, a single polyamine type curing agent, a modified polyamine type curing agent, an acid anhydride type curing agent, a polyphenol type curing agent, a polymercaptan type curing agent, an anionic polymerization curing agent, a cationic polymerization type curing agent, etc. Can be mentioned. Examples of the curing accelerator include tertiary amines, imidazoles, organic metal salts, chlorides, organic peroxides and the like. These resin curing agents and curing accelerators may be used in combination of two or more, if necessary.
【0014】更に、上記の磁性粉末、樹脂バインダーの
他に、必要に応じて公知のSi系、Ti系またはAl系
の化学結合型表面処理剤、硬化触媒等を、一種単独また
は複数組み合わせて添加することができる。Si系、T
i系及びAl系の化学結合型表面処理剤(カップリング
剤)としては、例えば、ビニルトリエトキシシラン、γ
-アミノプロピルトリエトキシシラン、 N-(β-アミノ
エチル)-γ-アミノプロピルトリメトキシシラン、 N-
(β-アミノエチル)-γ- アミノプロピルメチルジメト
キシシラン、 γ-メルカプトプロピルトリメトキシシラ
ン、 γ-グリシドキシプロピルトリメトキシシラン、
γ-グリシドキシプロピルメチルジメトキシシラン、 γ
-メタクリロキシプロピルトリメトキシシラン、 γ-メ
タクリロキシプロピルメチルジメトキシシラン、 イソ
プロピルトリイソステアロイルチタネート、 イソプロ
ピルトリス(ジオクチルパイロホスフェート)チタネー
ト、 イソプロピルトリ(N-アミノエチル-アミノエチ
ル)チタネート、 テトラオクチルビス(ジトリデシル
ホスファイト)チタネート、 イソプロピルトリオクタ
ノイルチタネート、 イソプロピルジメタクリルイソス
テアロイルチタネート、 イソプロピルトリデシルベン
ゼンスルフォニルチタネート、 アセトアルコキシアル
ミニウムジイソプロピレート等が代表的なものとして挙
げられる。これらは、例えば乾式法、湿式法、インテグ
ラルブレンド法等により組成物に混合することができ、
磁石粉末と樹脂バインダーとの密着性を向上させる。Furthermore, in addition to the above magnetic powder and resin binder, known Si-based, Ti-based or Al-based chemically-bonded surface-treating agents, curing catalysts, etc. may be added alone or in combination. can do. Si-based, T
Examples of the i-type and Al-type chemically-bonded surface treatment agents (coupling agents) include vinyltriethoxysilane and γ.
-Aminopropyltriethoxysilane, N- (β-aminoethyl) -γ-aminopropyltrimethoxysilane, N-
(Β-aminoethyl) -γ-aminopropylmethyldimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane,
γ-glycidoxypropylmethyldimethoxysilane, γ
-Methacryloxypropyltrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, isopropyltriisostearoyl titanate, isopropyltris (dioctylpyrophosphate) titanate, isopropyltri (N-aminoethyl-aminoethyl) titanate, tetraoctylbis (ditrityl) Typical examples are decyl phosphite) titanate, isopropyl trioctanoyl titanate, isopropyl dimethacryl isostearoyl titanate, isopropyl tridecyl benzene sulfonyl titanate, and acetoalkoxyaluminum diisopropylate. These can be mixed into the composition by, for example, a dry method, a wet method, an integral blend method, or the like,
Improves the adhesion between the magnet powder and the resin binder.
【0015】樹脂結合型磁石用組成物は、各所要成分を
混合することにより得られるが、混合方法は特に限定さ
れず、例えば、メチルエチルケトン等の有機溶剤に有機
成分を溶解し、磁性粉末と混合した後、乾燥し組成物を
得る湿式法、例えばリボンブレンダー、タンブラー、ナ
ウターミキサー、ヘンシェルミキサー、スーパーミキサ
ー、ハイスピードミキサー等の混合器中で所要成分を一
括混合する乾式法等のいずれでもよい。こうして得られ
る組成物は粉末状である。The resin-bonded magnet composition can be obtained by mixing the required components, but the mixing method is not particularly limited. For example, the organic component is dissolved in an organic solvent such as methyl ethyl ketone and mixed with the magnetic powder. After that, a wet method for obtaining a composition by drying, for example, a dry method of collectively mixing required components in a mixer such as a ribbon blender, a tumbler, a Nauter mixer, a Henschel mixer, a super mixer, or a high speed mixer may be used. . The composition thus obtained is in powder form.
【0016】上記組成物を用いた樹脂結合型磁石は、上
記組成物を各種の圧縮成形装置によりプレス成形した
後、加熱処理を施してバインダー樹脂を硬化させ、その
後磁場中で着磁することにより得られる。組成物のプレ
ス成形は、通常4〜8t/cm2の圧力下で行い、バイ
ンダー樹脂の硬化は、芳香族アミン系エポキシ樹脂硬化
剤を用いる場合は150〜200℃の温度で0.5〜4
時間程度、用いない場合は常温〜200℃の温度で0.
5〜24時間程度で反応させればよい。The resin-bonded magnet using the above composition is obtained by press-molding the above-mentioned composition by various compression molding devices, heat-treating it to cure the binder resin, and then magnetizing it in a magnetic field. can get. Press molding of the composition is usually performed under a pressure of 4 to 8 t / cm 2 , and curing of the binder resin is 0.5 to 4 at a temperature of 150 to 200 ° C. when an aromatic amine-based epoxy resin curing agent is used.
If not used for about an hour, at room temperature to 200 ° C.
The reaction may be performed for about 5 to 24 hours.
【0017】[0017]
【作用】本発明の組成物では、バインダー樹脂として、
主鎖にポリサルファイド骨格を有するエポキシ樹脂とノ
ボラック樹脂との混合物が使用されるため、これら樹脂
のそれぞれが単独で使用された場合に比べて硬化させた
ときにより高い重合率が得られるとともに、磁性粉末と
樹脂層の接着強度が著しく増すため、優れた機械的強度
が得られるものと考えられる。In the composition of the present invention, as the binder resin,
Since a mixture of an epoxy resin having a polysulfide skeleton in the main chain and a novolac resin is used, a higher polymerization rate is obtained when cured than when each of these resins is used alone, and the magnetic powder It is considered that the excellent mechanical strength can be obtained because the adhesive strength of the resin layer is significantly increased.
【0018】[0018]
【実施例】以下の材料及び方法で樹脂結合型磁石用組成
物及び磁石を製造し、評価した。用いた材料を下記に示
す。EXAMPLE A resin-bonded magnet composition and a magnet were manufactured and evaluated by the following materials and methods. The materials used are shown below.
【0019】A 磁性粉末 ・磁性粉末1:Nd-Fe-B系磁石粉末 (商品名:MQP−B、米国ゼネラルモーターズ社製) 異方性磁場:70.4kOe ・磁性粉末2:Sm-Co5 系磁性粉末 (商品名:RCo5 合金、住友金属鉱山(株)製) 異方性磁場:246kOe、平均粒径10μmA Magnetic powder-Magnetic powder 1: Nd-Fe-B magnet powder (trade name: MQP-B, manufactured by General Motors of the United States) Anisotropic magnetic field: 70.4 kOe-Magnetic powder 2: Sm-Co 5 Magnetic powder (trade name: RCo 5 alloy, manufactured by Sumitomo Metal Mining Co., Ltd.) Anisotropic magnetic field: 246 kOe, average particle size 10 μm
【0020】B エポキシ樹脂 I ・エポキシ樹脂 :主鎖にポリサルファイド骨格を有
するエポキシ樹脂 (商品名:フレップ60、東レチオコール(株)製) ・エポキシ樹脂 II:クレゾールノボラック型エポキシ
樹脂 (商品名:EOCN−1025、日本化薬(株)製)B Epoxy resin I Epoxy resin: Epoxy resin having a polysulfide skeleton in the main chain (trade name: Flep 60, manufactured by Toray Thiokol Co., Ltd.) Epoxy resin II: cresol novolac type epoxy resin (trade name: EOCN- 1025, manufactured by Nippon Kayaku Co., Ltd.
【0021】C 硬化剤 ・硬化剤 i:芳香族アミン系エポキシ樹脂硬化剤 (商品名:HT972、日本チバ・ガイギー(株)製) ・硬化剤 ii:ジシアンジアミドC Curing agent-Curing agent i: Aromatic amine-based epoxy resin curing agent (trade name: HT972, manufactured by Ciba-Geigy Co., Ltd.)-Curing agent ii: Dicyandiamide
【0022】各実施例、比較例の組成を表1〜表5に示
す。組成物の調整は、表1〜表5に示す樹脂及び硬化剤
の量を配合してメチルエチルケトンで10倍に希釈し、
磁性粉末100重量部に添加した。表1、表2に示す実
施例1〜実施例5、及び、比較例1〜比較例3では、硬
化剤にジシアンジアミドを総樹脂量に対して10重量%
用いた。磁性粉末と樹脂等を希釈した溶液との混合物を
撹拌した後、30℃、10-1Torrの減圧下でメチル
エチルケトンを完全に揮散させ、各組成物を得た。The compositions of Examples and Comparative Examples are shown in Tables 1-5. The composition was adjusted by blending the amounts of the resin and the curing agent shown in Tables 1 to 5 and diluting 10 times with methyl ethyl ketone.
It was added to 100 parts by weight of magnetic powder. In Examples 1 to 5 and Comparative Examples 1 to 3 shown in Table 1 and Table 2, dicyandiamide was used as a curing agent in an amount of 10% by weight based on the total amount of resin.
Using. After stirring the mixture of the magnetic powder and the solution obtained by diluting the resin and the like, methyl ethyl ketone was completely volatilized under reduced pressure of 30 ° C. and 10 −1 Torr to obtain each composition.
【0023】[0023]
【表1】 [Table 1]
【0024】[0024]
【表2】 [Table 2]
【0025】[0025]
【表3】 [Table 3]
【0026】[0026]
【表4】 [Table 4]
【0027】[0027]
【表5】 [Table 5]
【0028】次に、得られた各実施例、各比較例の組成
物をプレス金型中に供給し、成形面圧5.7t/cm2
でプレス成形した。実施例5、比較例3、実施例10、
及び比較例6のSm-Co5 磁性粉末を使用した場合の
み磁場中成形を行った。得られた成形体は、縦10m
m、横15mm、厚さ5mmの直方体形状であった。こ
の成形体試料を1時間熱処理して試料中のバインダー樹
脂を硬化させ、樹脂結合型磁石試料を得た。熱処理温度
は、実施例1〜実施例5、及び、比較例1〜比較例3で
は185℃、実施例6〜実施例13、及び、比較例4〜
比較例6では145℃とした。次にこれらの試料の磁気
特性を、チオフィー型自記磁束計にて常温で測定した。
磁気特性のうち(BH)max(最大磁気エネルギー積)
の結果を表1〜表5に示す。Next, the obtained compositions of Examples and Comparative Examples were fed into a press die, and the molding surface pressure was 5.7 t / cm 2.
It was press molded with. Example 5, Comparative Example 3, Example 10,
Also, the molding was performed in the magnetic field only when the Sm-Co 5 magnetic powder of Comparative Example 6 was used. The obtained molded product has a length of 10 m.
It had a rectangular parallelepiped shape with m, width 15 mm, and thickness 5 mm. This molded sample was heat-treated for 1 hour to cure the binder resin in the sample and obtain a resin-bonded magnet sample. The heat treatment temperature is 185 ° C. in Examples 1 to 5 and Comparative Examples 1 to 3, and Examples 6 to 13 and Comparative Examples 4 to
In Comparative Example 6, the temperature was 145 ° C. Next, the magnetic characteristics of these samples were measured at room temperature with a Thiophie type self-recording magnetometer.
(BH) max (maximum magnetic energy product) of magnetic characteristics
The results are shown in Tables 1 to 5.
【0029】次に、上記と同じ組成物をリング金型中に
供給し、成形面圧5t/cm2 でプレス成形し、外径3
4mm、内径32mm、高さ8mmの円筒形状の成形体
を得た。これら成形体をそれぞれ大気圧中で1時間熱処
理し、試料中のバインダー樹脂を硬化させ、リング圧環
強度測定用試料を得た。熱処理温度は、実施例1〜実施
例5、及び、比較例1〜比較例3では185℃、実施例
6〜実施例13、及び、比較例4〜比較例6では145
℃とした。試料のリング圧環強度は、島津製作所(株)
製オートグラフを用いて、ヘッドスピード1mm/分と
し、常温下で求めた。結果を表1〜表5に示す。Next, the same composition as described above was fed into a ring mold and press-molded at a molding surface pressure of 5 t / cm 2 to give an outer diameter of 3
A cylindrical molded body having a diameter of 4 mm, an inner diameter of 32 mm and a height of 8 mm was obtained. Each of these molded bodies was heat-treated at atmospheric pressure for 1 hour to cure the binder resin in the sample and obtain a sample for ring radial crushing strength measurement. The heat treatment temperature is 185 ° C. in Examples 1 to 5 and Comparative Examples 1 to 3, and 145 in Examples 6 to 13 and Comparative Examples 4 to 6.
℃ was made. The ring radial crushing strength of the sample is Shimadzu Corporation.
Using an Autograph manufactured by K.K., the head speed was set to 1 mm / min and the temperature was determined at room temperature. The results are shown in Tables 1 to 5.
【0030】磁石の(BH)max(最大磁気エネルギー
積)は、8MGOe以上あれば十分である。またリング
圧環強度は、3gf以上あれば機械的強度が十分であ
る。上記示したように、本発明の樹脂結合型磁石は、磁
気特性、機械的強度とも優れていることがわかる。It is sufficient for the (BH) max (maximum magnetic energy product) of the magnet to be 8 MGOe or more. Further, if the ring radial crushing strength is 3 gf or more, the mechanical strength is sufficient. As shown above, it can be seen that the resin-bonded magnet of the present invention has excellent magnetic properties and mechanical strength.
【0031】[0031]
【発明の効果】本発明の樹脂結合型磁石用組成物は、得
られる磁石の磁気特性と機械的強度がともに優れている
ため、一般家電製品、通信・音響機器、医療機器、一般
産業機器にいたる幅広い分野で、性能の向上、その利用
範囲の拡大が期待される。Industrial Applicability The resin-bonded magnet composition of the present invention is excellent in both magnetic properties and mechanical strength of the obtained magnet, and is therefore suitable for general household appliances, communication / audio equipment, medical equipment, and general industrial equipment. It is expected that performance will be improved and its range of use will be expanded in a wide range of fields.
Claims (4)
結合型磁石用組成物において、上記磁性粉末は異方性磁
場が50kOe以上であり、上記樹脂バインダーは、主
鎖にポリサルファイド骨格を有するエポキシ樹脂とノボ
ラック型エポキシ樹脂とを含有していることを特徴とす
る樹脂結合型磁石用組成物。1. A resin-bonded magnet composition comprising magnetic powder and a resin binder, wherein the magnetic powder has an anisotropic magnetic field of 50 kOe or more, and the resin binder is an epoxy resin having a polysulfide skeleton in the main chain. A resin-bonded magnet composition comprising a novolac type epoxy resin.
結合型磁石用組成物において、上記磁性粉末は異方性磁
場が50kOe以上であり、上記樹脂バインダーは、主
鎖にポリサルファイド骨格を有するエポキシ樹脂とノボ
ラック型エポキシ樹脂と芳香族アミン系エポキシ樹脂硬
化剤とを含有していることを特徴とする樹脂結合型磁石
用組成物。2. A resin-bonded magnet composition comprising a magnetic powder and a resin binder, wherein the magnetic powder has an anisotropic magnetic field of 50 kOe or more, and the resin binder is an epoxy resin having a polysulfide skeleton in its main chain. A resin-bonded magnet composition comprising a novolac type epoxy resin and an aromatic amine type epoxy resin curing agent.
と、主鎖にポリサルファイド骨格を有するエポキシ樹脂
と、ノボラック型エポキシ樹脂とを含有する樹脂結合型
磁石用組成物を、加圧成形後、加熱硬化して得られる樹
脂結合型磁石。3. A resin-bonded magnet composition containing a magnetic powder having an anisotropic magnetic field of 50 kOe or more, an epoxy resin having a polysulfide skeleton in the main chain, and a novolac type epoxy resin, after pressure molding, Resin-bonded magnet obtained by heating and curing.
と、主鎖にポリサルファイド骨格を有するエポキシ樹脂
と、ノボラック型エポキシ樹脂と、芳香族アミン系エポ
キシ樹脂硬化剤とを含有する樹脂結合型磁石用組成物
を、加圧成形後、加熱硬化して得られる樹脂結合型磁
石。4. A resin-bonded magnet containing magnetic powder having an anisotropic magnetic field of 50 kOe or more, an epoxy resin having a polysulfide skeleton in its main chain, a novolac type epoxy resin, and an aromatic amine type epoxy resin curing agent. A resin-bonded magnet obtained by press-molding a composition for pressurization and then heat-curing the composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5139245A JPH06333712A (en) | 1993-05-19 | 1993-05-19 | Composition for resin bonded type magnet and resin-bonded type magnet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5139245A JPH06333712A (en) | 1993-05-19 | 1993-05-19 | Composition for resin bonded type magnet and resin-bonded type magnet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06333712A true JPH06333712A (en) | 1994-12-02 |
Family
ID=15240838
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5139245A Pending JPH06333712A (en) | 1993-05-19 | 1993-05-19 | Composition for resin bonded type magnet and resin-bonded type magnet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06333712A (en) |
-
1993
- 1993-05-19 JP JP5139245A patent/JPH06333712A/en active Pending
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