JPH0458681B2 - - Google Patents
Info
- Publication number
- JPH0458681B2 JPH0458681B2 JP58040198A JP4019883A JPH0458681B2 JP H0458681 B2 JPH0458681 B2 JP H0458681B2 JP 58040198 A JP58040198 A JP 58040198A JP 4019883 A JP4019883 A JP 4019883A JP H0458681 B2 JPH0458681 B2 JP H0458681B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- magnet
- magnetic
- ferrite powder
- resin magnet
- 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 - Lifetime
Links
- 239000011347 resin Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 18
- 229910000859 α-Fe Inorganic materials 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 229920006122 polyamide resin Polymers 0.000 claims description 5
- 230000005294 ferromagnetic effect Effects 0.000 claims description 3
- 230000005291 magnetic effect Effects 0.000 description 22
- 238000001125 extrusion Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000004907 flux Effects 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000010137 moulding (plastic) Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- AJCDFVKYMIUXCR-UHFFFAOYSA-N oxobarium;oxo(oxoferriooxy)iron Chemical compound [Ba]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O AJCDFVKYMIUXCR-UHFFFAOYSA-N 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
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
- H01F1/10—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 non-metallic substances, e.g. ferrites, e.g. [(Ba,Sr)O(Fe2O3)6] ferrites with hexagonal structure
- H01F1/11—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 non-metallic substances, e.g. ferrites, e.g. [(Ba,Sr)O(Fe2O3)6] ferrites with hexagonal structure in the form of particles
- H01F1/113—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 non-metallic substances, e.g. ferrites, e.g. [(Ba,Sr)O(Fe2O3)6] ferrites with hexagonal structure in the form of particles in a bonding agent
Description
産業上の利用分野
この発明は、複写機、フアクシミリ等に用いら
れるマグネツトロールに使用する樹脂マグネツト
組成物に関するものである。
従来例の構成とその問題点
複写機、フアクシミリ等における現像方式は、
磁性粉体からなる磁性トナー(一成分現像剤)や
非磁性トナーと磁性粉キヤリアからなる現像剤
(二成分現像剤)を、図面に示すように複数の磁
極を有する円柱状マグネツトロール1内蔵の円筒
状非磁性スリーブ2上に保持し、マグネツトロー
ル1を回転させるか、あるいはマグネツトロール
1を固定してスリーブ2を回転させるか、両方と
も回転させたスリーブ2上の現像剤を感光体潜像
面まで搬送し顕像化する磁気ブラシ現像法が主流
をなしている。
マグネツトロール材料としては、従来より焼結
フエライトが使用されていたが、その加工性の悪
さ、重いこと、脆いことなどの欠点を有してい
た。これらの欠点を改善する目的で樹脂あるいは
ゴム等をベースとした樹脂マグネツトが使用され
るようになつた。樹脂マグネツトは、小型軽量で
自由な形に成形でき、さらに低コストで後仕上げ
が容易なことから、ロール状、シート状、棒状な
どさまざまな形状のものが使用されている。従つ
て、その製造方法も圧延成形法、射出成形法、カ
レンダー成形法、押出成形法と多様である。
シヤフト3の周囲に樹脂マグネツトを被覆する
マグネツトロール1の製造方法は、磁性フエライ
ト、結着剤および添加剤を加温状態の加圧ニーダ
で混練し、混練物を冷却後、1〜2mmに粗粉砕し
て圧延ローラにてシーテイングしながらフエライ
ト粉末を機械的に配向させシート状の樹脂マグネ
ツトを得、これを棒状シヤフト3に巻き付け、所
定の寸法にあわせて着磁を行ないマグネツトロー
ル1にする圧延成形法が最も一般的である。さら
に、配向効率を高めるために上記圧延樹脂マグネ
ツトシートを数枚重ねて扇形に加圧成形して分離
した扇形ピースをシヤフト3に接着剤を用いて固
定するなどの工夫がなされていた。
また、射出成形法や加圧成形法を用いて加熱可
塑状態の樹脂マグネツト組成物を金型中で配向磁
場を与えてフエライトを配向させ、所定形状のピ
ースに成形してシヤフト3に接着剤で固定する方
法があつた。ところが、これらはいずれもバツチ
生産であるため生産性に劣るものであつた。
これらの方法のほかに、生産性の優れた押出成
形法があるが、シヤフト3周囲に樹脂マグネツト
を連続的に被覆して押し出すため十分な磁力が得
られないため実用するには至つていない。
発明の目的
この発明は生産性の高い押出成形法によつて十
分な磁力を得ることができる樹脂マグネツト組成
物を提供することを目的とする。
発明の構成
この発明の樹脂マグネツト組成物は、180℃に
おける溶融粘度が100ポイズ以下で一般式HO−
[CO−R2−CO・NH−R3−NH・CO−R1−
CO・NH−R3−NH]oHで示される重合脂肪酸系
のポリアミド樹脂(以下ポリアミド樹脂と称す
る。)と、強磁性フエライト粉末とを含むもので
あつて、押出機において配向磁場を与えながら冷
却する部分を設け、シヤフトの周囲に樹脂マグネ
ツトを円筒状に連続的に被覆して押出すことがで
きる。
180℃における溶融粘度100ボイスを越えるポリ
アミド樹脂は押出機中の可塑化状態での溶融粘度
が高いために、与えられた磁場に対してフエライ
ト粉末の配向が困難となり、磁気特性が低くな
る。
前記フエライト粉末の含有量は総重量に対して
70〜92重量%であるのが好ましく、92重量%を越
えるときは混練や押出成形が極めて困難となり、
またその含有量が70重量%未満のときは、与えら
れた配向磁場に対してフエライト粉末の配向は高
くなるが、量的に不十分で磁気特性が低くなる。
強磁性フエライト粉末は、バリウムフエライ
ト、ストロンチウムフエライト等の市販のフエラ
イトが使用できる。
また、押出成形時の成形性を改善するために、
一般のプラスチツク成形と同様にステアリン酸カ
ルシウム、ステアリン酸バリウム等の脂肪酸金属
塩やステアリン酸、パルチミン酸等の高級脂肪
酸、さらにワツクス類の滑剤を用いることができ
る。
実施例の説明
実施例 1〜8
第1表に示す各組成物を150〜180℃に加温した
加圧ニーダで混練を行ない、冷却した後、粗粉砕
機により2〜5mmの粗粉砕物を得た。各組成物を
配向磁場を与えながら冷却する部分を設けた押出
成形機に投入し、シヤフトに樹脂マグネシウムを
被覆させて連続押出成形し、マグネツトロールを
得た。このものの外径は20mmになるように設定し
押出中に与えた磁束密度は10000ガウスで押出ス
ピードは7.5mm/秒で行なつた。
INDUSTRIAL APPLICATION FIELD This invention relates to a resin magnet composition used in magnet rolls used in copying machines, facsimile machines, and the like. Conventional structure and its problems The developing method used in copiers, facsimile machines, etc.
Magnetic toner (single-component developer) made of magnetic powder and developer made of non-magnetic toner and magnetic powder carrier (two-component developer) are stored in a built-in cylindrical magnet roll 1 with multiple magnetic poles as shown in the drawing. The developer on the rotated sleeve 2 is exposed to light, either by holding it on a cylindrical non-magnetic sleeve 2 and rotating the magnet roll 1, or by fixing the magnet roll 1 and rotating the sleeve 2. The mainstream is a magnetic brush development method in which the image is conveyed to the latent image surface and visualized. Sintered ferrite has conventionally been used as a magnet roll material, but it has drawbacks such as poor workability, heavy weight, and brittleness. In order to overcome these drawbacks, resin magnets based on resin or rubber have come into use. Resin magnets are small, lightweight, can be molded into any shape, are low cost, and can be easily finished, so they are used in a variety of shapes, including rolls, sheets, and rods. Therefore, there are various manufacturing methods such as rolling molding, injection molding, calendar molding, and extrusion molding. The manufacturing method of the magnet roll 1, which coats the shaft 3 with a resin magnet, is to knead magnetic ferrite, a binder, and additives in a heated pressure kneader, cool the kneaded material, and then knead it to a thickness of 1 to 2 mm. The ferrite powder is coarsely pulverized and mechanically oriented while being sheeted with a rolling roller to obtain a sheet-like resin magnet, which is wound around a rod-shaped shaft 3, magnetized to a predetermined size, and placed on a magnet roll 1. The most common method is rolling. Further, in order to improve the orientation efficiency, some measures have been taken, such as stacking several sheets of the above-mentioned rolled resin magnet sheets and press-molding them into a fan shape, and then fixing the separated fan-shaped pieces to the shaft 3 using an adhesive. In addition, using an injection molding method or a pressure molding method, an orienting magnetic field is applied to the thermoplasticized resin magnet composition in a mold to orient the ferrite, and the piece is molded into a predetermined shape and attached to the shaft 3 with an adhesive. I found a way to fix it. However, these were all produced in batches and were therefore inferior in productivity. In addition to these methods, there is an extrusion molding method that has excellent productivity, but it has not been put to practical use because sufficient magnetic force cannot be obtained because the resin magnet is continuously coated around the shaft 3 and extruded. . OBJECTS OF THE INVENTION An object of the present invention is to provide a resin magnet composition that can obtain sufficient magnetic force by extrusion molding with high productivity. Structure of the Invention The resin magnet composition of the present invention has a melt viscosity of 100 poise or less at 180°C and has a general formula HO-
[CO−R 2 −CO・NH−R 3 −NH・CO−R 1 −
CO・NH−R 3 −NH] o It contains a polymerized fatty acid-based polyamide resin (hereinafter referred to as polyamide resin) represented by H and ferromagnetic ferrite powder. A cooling part is provided, and a resin magnet can be continuously coated around the shaft in a cylindrical shape and then extruded. Polyamide resins with a melt viscosity exceeding 100 voices at 180°C have a high melt viscosity in the plasticized state in an extruder, making it difficult to orient the ferrite powder in response to an applied magnetic field, resulting in poor magnetic properties. The content of the ferrite powder is based on the total weight
The content is preferably 70 to 92% by weight; when it exceeds 92% by weight, kneading and extrusion molding become extremely difficult.
If the content is less than 70% by weight, the orientation of the ferrite powder will be high with respect to the applied orientation magnetic field, but the amount will be insufficient and the magnetic properties will deteriorate. As the ferromagnetic ferrite powder, commercially available ferrites such as barium ferrite and strontium ferrite can be used. In addition, in order to improve the moldability during extrusion molding,
As in general plastic molding, fatty acid metal salts such as calcium stearate and barium stearate, higher fatty acids such as stearic acid and palmitic acid, and lubricants such as waxes can be used. Description of Examples Examples 1 to 8 Each composition shown in Table 1 was kneaded in a pressure kneader heated to 150 to 180°C, and after cooling, coarsely pulverized products of 2 to 5 mm were crushed by a coarse pulverizer. Obtained. Each composition was put into an extrusion molding machine equipped with a cooling part while applying an orienting magnetic field, and the shaft was coated with resin magnesium and continuously extruded to obtain a magnet roll. The outer diameter of this material was set to 20 mm, the magnetic flux density applied during extrusion was 10,000 Gauss, and the extrusion speed was 7.5 mm/sec.
【表】
成形したマグネツトロールをさらに着磁器を用
いて着磁を行ない、表面磁束密度を電子磁器工業
(株)製のガウスメータによりマグネツトロール表面
に接触させて測定した。その結果を第2表に示
す。
比較例 1〜3
下記に示す各組成物を用いて、実施例と同様に
してマグネツトロールを作製し、その表面磁束密
度を測定した。その結果を第3表に示す。
比較例 1
(成分) (重量%)
GP−825(前出) 91
塩素化ポリエチレン(溶融せず)(昭和電工(株)製)
8.73
ステアリン酸カルシウム(堺化学工業(株)製) 0.27
比較例 2
(成分) (重量%)
GP−825(前出) 64
トーマイド#1310(前出):180℃で溶融粘度が48
ポイズ 35
アーモワクツスEBS(ライオン・アクゾ(株)製) 1
比較例 3
(成分) (重量%)
GP−825(前出) 85
EBR(高粘度)(日本合成ゴム(株)製) 15[Table] The molded magnet roll is further magnetized using a magnetizer, and the surface magnetic flux density is determined by Denshi Porcelain Industry.
Measurements were made using a Gaussmeter manufactured by Co., Ltd. by contacting the surface of the magnet roll. The results are shown in Table 2. Comparative Examples 1 to 3 Magnet rolls were produced in the same manner as in Examples using each of the compositions shown below, and their surface magnetic flux densities were measured. The results are shown in Table 3. Comparative Example 1 (Ingredients) (Weight %) GP-825 (mentioned above) 91 Chlorinated polyethylene (not melted) (manufactured by Showa Denko K.K.)
8.73 Calcium stearate (manufactured by Sakai Chemical Industry Co., Ltd.) 0.27 Comparative example 2 (components) (wt%) GP-825 (mentioned above) 64 Tomide #1310 (mentioned above): Melt viscosity at 180°C is 48
Poise 35 Armowactus EBS (manufactured by Lion Akzo Co., Ltd.) 1 Comparative example 3 (Components) (% by weight) GP-825 (mentioned above) 85 EBR (high viscosity) (manufactured by Japan Synthetic Rubber Co., Ltd.) 15
【表】【table】
【表】
第2表および第3表から明らかなように、実施
例1〜8で得たマグネツトロールはいずれも表面
が滑らかで、表面磁束密度が1000G以上であるの
に対し、比較例1〜3で得たマグネツトロールは
1000G以下の低い値であつた。
発明の効果
この発明によれば、フエライト粉末の結着剤と
して180℃で100ポイズ以下の溶融粘度を有する一
般式HO−[CO−R2−CO・NH−R3−NH・CO
−R1−CO・NH−R3−NH]oHで示される重合
脂肪酸系のポリアミド樹脂を使用することによ
り、溶融粘度が低いため配向時の粘性抵抗が少な
く高磁力のものが得られる。また、高磁力の磁石
が得られるため、従来の機械的配向によるマグネ
ツトの製造方法としてバツチ生産だけではなく押
出連続生産が可能となり、さらに押出生産で軸方
向の磁力を安定することができる。その結果、従
来の樹脂マグネツト組成物ではなし得なかつた押
出成形法による磁気特性の優れたマグネツトロー
ルを製造することができるという効果がある。[Table] As is clear from Tables 2 and 3, the magnet rolls obtained in Examples 1 to 8 all had smooth surfaces and surface magnetic flux densities of 1000 G or more, whereas Comparative Example 1 ~The magnet roll obtained in 3 is
The value was low, less than 1000G. Effects of the Invention According to the present invention, as a binder for ferrite powder, the general formula HO-[CO- R2 -CO・NH- R3 -NH・CO having a melt viscosity of 100 poise or less at 180°C
-R 1 -CO.NH-R 3 -NH] o By using a polymerized fatty acid-based polyamide resin represented by H, a resin with low melt viscosity and low viscous resistance during orientation and high magnetic force can be obtained. Furthermore, since a magnet with high magnetic force can be obtained, continuous extrusion production is possible in addition to batch production, which is the conventional manufacturing method for magnets by mechanical orientation, and furthermore, extrusion production can stabilize the magnetic force in the axial direction. As a result, it is possible to produce a magnet roll with excellent magnetic properties by extrusion molding, which has not been possible with conventional resin magnet compositions.
図面は通常のマグネツトロールの断面図であ
る。
1……マグネツトロール、2……非磁性スリー
ブ、3……シヤフト。
The drawing is a cross-sectional view of an ordinary magnet roll. 1...Magnetic roll, 2...Nonmagnetic sleeve, 3...Shaft.
Claims (1)
般式HO−[CO−R2−CO・NH−R3−NH・CO
−R1−CO・NH−R3−NH]oHで示される重合
脂肪酸系のポリアミド樹脂と、強磁性フエライト
粉末とを含む樹脂マグネツト組成物。 2 前記フエライト粉末が総重量に対して70〜92
重量%の割合で含有される特許請求の範囲第1項
記載の樹脂マグネツト組成物。[Claims] 1. Melt viscosity at 180°C is 100 poise or less and the general formula HO-[CO-R 2 -CO・NH-R 3 -NH・CO
-R 1 -CO.NH-R 3 -NH] o A resin magnet composition containing a polymerized fatty acid-based polyamide resin represented by H and ferromagnetic ferrite powder. 2 The ferrite powder is 70 to 92% of the total weight
The resin magnet composition according to claim 1, wherein the resin magnet composition is contained in a proportion of % by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4019883A JPS59165403A (en) | 1983-03-10 | 1983-03-10 | Resin magnet composition substance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4019883A JPS59165403A (en) | 1983-03-10 | 1983-03-10 | Resin magnet composition substance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59165403A JPS59165403A (en) | 1984-09-18 |
JPH0458681B2 true JPH0458681B2 (en) | 1992-09-18 |
Family
ID=12574080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4019883A Granted JPS59165403A (en) | 1983-03-10 | 1983-03-10 | Resin magnet composition substance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59165403A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63299207A (en) * | 1987-05-29 | 1988-12-06 | Daiseru Hiyurusu Kk | Permanent magnet |
EP0691996A4 (en) * | 1993-03-29 | 1997-06-18 | Du Pont | Polyamide resin composition |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54109199A (en) * | 1978-02-16 | 1979-08-27 | Matsushita Electric Ind Co Ltd | Method of fabricating permanent magnets |
JPS54152198A (en) * | 1978-05-19 | 1979-11-30 | Matsushita Electric Ind Co Ltd | Manufacture of permanent magnet |
JPS5591803A (en) * | 1978-12-28 | 1980-07-11 | Matsushita Electric Ind Co Ltd | Permanent magnet |
JPS5593202A (en) * | 1979-01-02 | 1980-07-15 | Minnesota Mining & Mfg | Matrix coupled permanent magnet having highly aligned magnetic particles |
JPS55154707A (en) * | 1979-05-22 | 1980-12-02 | Daido Steel Co Ltd | Anisotropic resin magnet and manufacture thereof |
JPS56851A (en) * | 1979-06-18 | 1981-01-07 | Matsushita Electric Ind Co Ltd | Plastic magnet composition |
JPS58125803A (en) * | 1982-01-22 | 1983-07-27 | Seiko Epson Corp | Manufacture of rare-earth powder magnet |
-
1983
- 1983-03-10 JP JP4019883A patent/JPS59165403A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54109199A (en) * | 1978-02-16 | 1979-08-27 | Matsushita Electric Ind Co Ltd | Method of fabricating permanent magnets |
JPS54152198A (en) * | 1978-05-19 | 1979-11-30 | Matsushita Electric Ind Co Ltd | Manufacture of permanent magnet |
JPS5591803A (en) * | 1978-12-28 | 1980-07-11 | Matsushita Electric Ind Co Ltd | Permanent magnet |
JPS5593202A (en) * | 1979-01-02 | 1980-07-15 | Minnesota Mining & Mfg | Matrix coupled permanent magnet having highly aligned magnetic particles |
JPS55154707A (en) * | 1979-05-22 | 1980-12-02 | Daido Steel Co Ltd | Anisotropic resin magnet and manufacture thereof |
JPS56851A (en) * | 1979-06-18 | 1981-01-07 | Matsushita Electric Ind Co Ltd | Plastic magnet composition |
JPS58125803A (en) * | 1982-01-22 | 1983-07-27 | Seiko Epson Corp | Manufacture of rare-earth powder magnet |
Also Published As
Publication number | Publication date |
---|---|
JPS59165403A (en) | 1984-09-18 |
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