JPH0410602A - Isotropic permanent magnet and manufacture thereof - Google Patents
Isotropic permanent magnet and manufacture thereofInfo
- Publication number
- JPH0410602A JPH0410602A JP2113331A JP11333190A JPH0410602A JP H0410602 A JPH0410602 A JP H0410602A JP 2113331 A JP2113331 A JP 2113331A JP 11333190 A JP11333190 A JP 11333190A JP H0410602 A JPH0410602 A JP H0410602A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- magnet
- atomic
- magnets
- pair
- 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.)
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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
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- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Powder Metallurgy (AREA)
- Hard Magnetic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、モータに使用される希土類鉄系永久磁石に関
する。更に詳しくは、液体急冷法によって得られる希土
類鉄系薄片、または粉末を出発原料とし、結合剤を用い
ずに集合体化した熱安定性のよい磁気的に等方性である
永久磁石およびその製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to rare earth iron permanent magnets used in motors. More specifically, a thermally stable and magnetically isotropic permanent magnet made from rare earth iron flakes or powder obtained by a liquid quenching method as a starting material and aggregated without using a binder, and its production. It is about the method.
従来の技術
モータ用磁石は、イ史用されるモータによっては、単位
体積当たりの磁気特性の高いものが要求されたり、また
は、特性の低いものの方が適切であったり様々である。Conventional motor magnets vary depending on the motor used, with some requiring high magnetic properties per unit volume, and others with low properties being more appropriate.
この磁気特性は、体積当たりの磁性粉末の充填量、つま
り磁石の相対密度と見なせるので、同一磁性粉を用いた
広い範囲の相対密度の磁石の出現が望まれている。Since this magnetic property can be regarded as the amount of magnetic powder packed per volume, that is, the relative density of the magnet, it is desired to develop magnets with a wide range of relative densities using the same magnetic powder.
従来の希土類鉄系永久磁石の原料の一つとして特開昭5
9−64739号に示されているものとしては、液体急
冷法による等方性磁性粉が開示されており、樹脂磁石と
して広(実用化されている。As one of the raw materials for conventional rare earth iron permanent magnets,
No. 9-64739 discloses an isotropic magnetic powder produced by a liquid quenching method, which has been widely used as a resin magnet.
この磁性粉は、結合剤である樹脂とブレンドした後、射
出成形法や圧縮成形法で、集合体として具体的形状に成
形される。これらの樹脂磁石は、それぞれの成形法によ
り、磁性粉と樹脂の配合割合に限界があるため、その相
対密度にも限界があり、例えば圧縮成形法では82%程
度のものであった。This magnetic powder is blended with a resin as a binder and then molded into a specific shape as an aggregate by injection molding or compression molding. These resin magnets have a limit in the blending ratio of magnetic powder and resin depending on the respective molding method, so there is also a limit in their relative density; for example, in the compression molding method, it was about 82%.
さらにこの磁石は、合金組成が酸化しゃすいFeベース
となっているため、S m −Co系の磁石に比較して
錆びやす(、このためその表面に各種の防錆処理が施さ
れている。これらの防錆法は、大別すると金属の薄膜で
被覆する方法と、有機質または非金属の無機質を被覆す
る方法がある。金属の薄膜で被覆する方法は磁石との密
着性において不安定さがあり、一般には実用化されてお
らず、現在主として有機質を被覆する方法、具体的には
、エポキシ樹脂のスプレー塗装や電着塗装による防錆処
理が採用されている。Furthermore, since the alloy composition of this magnet is Fe-based, which is less susceptible to oxidation, it rusts more easily than S m -Co magnets (for this reason, its surface is subjected to various anti-corrosion treatments). These anti-corrosion methods can be roughly divided into methods of coating with a thin metal film and methods of coating with an organic or non-metallic inorganic material. However, it has not been put to practical use in general, and currently the main method used is to coat it with an organic substance, specifically, anti-corrosion treatment using epoxy resin spray coating or electrodeposition coating.
一方、上記磁性粉と同一磁性粉を使用して、結合剤を使
用せず、熱間て圧縮成形された、フル密度の等方性磁石
が特開昭60−100402号に開示されている。この
磁石は、相対密度が、95%を越えるものであり、その
分前述の樹脂磁石より高性能である。この等方性フル密
度磁石では、結合剤を使用しないので、結合剤の耐熱性
による使用温度の限界はなく、磁石自身の熱減磁特性か
らのみ使用温度は制限される。またこの磁石は、樹脂磁
石と異なり、集合体のすべてが磁性粉であり、樹脂磁石
のように、磁石の表面が樹脂と磁性粉、つまり金属と樹
脂の混在状態ではないので、密着性上樹脂磁石では採用
出来なかった無機質系の防錆処理、例えば、水ガラスな
どが防錆処理として採用されている。On the other hand, JP-A-60-100402 discloses a full-density isotropic magnet that is hot compression molded using the same magnetic powder as the above-mentioned magnetic powder without using a binder. This magnet has a relative density of over 95%, and has a higher performance than the resin magnet described above. Since this isotropic full density magnet does not use a binder, there is no limit to the operating temperature due to the heat resistance of the binder, and the operating temperature is limited only by the thermal demagnetization characteristics of the magnet itself. Also, unlike resin magnets, the entire aggregate of this magnet is magnetic powder, and unlike resin magnets, the surface of the magnet is not a mixture of resin and magnetic powder, that is, metal and resin. Inorganic anti-rust treatments that cannot be used with magnets, such as water glass, have been adopted as anti-rust treatments.
発明が解決しようとする課題
上記従来の製造方法によりえられる樹脂磁石は相対密度
が82%以下となり等方性フル密度磁石では、95%以
上の相対密度のものしが製造できないので、磁石が使用
されるモータの特性にあった両者間のもの、つまり、相
対密度が82%を越え、95%以下の磁石を得ることが
不可能であった。Problems to be Solved by the Invention The resin magnet obtained by the above conventional manufacturing method has a relative density of 82% or less, and isotropic full-density magnets cannot produce a measuring stick with a relative density of 95% or more, so magnets are used. It has been impossible to obtain a magnet with a relative density of more than 82% and less than 95%, which matches the characteristics of the motor to be used.
また、樹脂磁石では、結合剤として使用する樹脂の耐熱
性により、磁石の使用温度が制限されるため、この点か
らも採用できない場合があった。Furthermore, in the case of resin magnets, the temperature at which they can be used is limited by the heat resistance of the resin used as a binder, so there are cases where resin magnets cannot be used.
さらに、エポキシ樹脂のスプレー塗装は、低コストであ
るが、塗膜の信頼性を確保するためには、25ミクロン
以上の膜厚が必要であり、かつ、円筒形の磁石では、そ
の内径側の塗膜の信頼性を保証することが困難である。Furthermore, spray painting with epoxy resin is low cost, but in order to ensure the reliability of the paint film, a film thickness of 25 microns or more is required, and for cylindrical magnets, the inner diameter side It is difficult to guarantee the reliability of the coating.
他方、電着塗装は、10ミクロンで塗膜の信頼性を保証
することができ、かつ形状の自由度もあるが、処理コス
トが高価であるという欠点がある。On the other hand, electrodeposition coating can guarantee the reliability of the coating film at a thickness of 10 microns and has a degree of freedom in shape, but has the drawback of high processing costs.
本発明は上記課題に鑑み、使用されるモータに適切な磁
気特性を有する磁石を選択するために樹脂磁石や等方性
フル密度磁石の製造方法では得られない任意な相対密度
を有し、結合剤の耐熱性に左右される事なく使用でき、
更に、低コストの水ガラス系防錆処理が可能な等方性永
久磁石およびその製造方法を提供することを目的とする
ものである。In view of the above-mentioned problems, the present invention aims to select a magnet having magnetic properties suitable for the motor to be used. It can be used without being affected by the heat resistance of the agent.
A further object of the present invention is to provide an isotropic permanent magnet that can be subjected to low-cost water glass rust prevention treatment and a method for manufacturing the same.
課題を解決するための手段
上記従来の課題を解決するために本発明は、液体急冷法
で得られた磁性粉を熱間て圧縮成形する方法により、7
0%以上の任意の密度の磁石を提供するものである。Means for Solving the Problems In order to solve the above-mentioned conventional problems, the present invention provides a method of hot compression molding magnetic powder obtained by a liquid quenching method.
The present invention provides magnets with arbitrary density of 0% or more.
更に詳しくは、R−Fe−Co−Bを基本組成とする。More specifically, the basic composition is R-Fe-Co-B.
合金を、メルトスピニング法により、微細結晶構造を有
する磁気的に等方性である薄片状粉末を得、この粉末を
成形キャビティーに納め、1O−1)−ル以上の真空中
で放電を起こさせ、更に直接電流を加え、同時に所定の
寸法に圧縮するものである。A magnetically isotropic flaky powder having a microcrystalline structure is obtained by melt spinning the alloy, and this powder is placed in a molding cavity to cause an electric discharge in a vacuum of 10-1)-1 or more. This method compresses the material to a predetermined size at the same time by applying a direct current to the material.
作用
薄片状粉末は、・放電により発生するプラズマにより、
その表面に付着している酸化物やガスが取り除かれ、活
性化される。更に、直接通電により、ジュール熱で発熱
し、所定の温度まで昇温すると同時に、軟化し、付加さ
れた一軸の圧力により、所定の寸法に圧縮され、粉末間
に原子の拡散が起こり、前記粉末は原子的結合が成され
る。これによって所定の形状の磁気的に等方性である集
合体が得られる。EffectThe flaky powder is caused by plasma generated by electric discharge.
Oxides and gases adhering to the surface are removed and activated. Furthermore, by direct energization, Joule heat is generated, the temperature rises to a predetermined temperature, and at the same time, the powder is softened and compressed to a predetermined size by the applied uniaxial pressure, causing diffusion of atoms between the powders. are formed into an atomic bond. This results in a magnetically isotropic aggregate of a predetermined shape.
本発明の磁石では、熱間圧縮以前に、プラズマにより粉
末を活性化させであるため、従来不可能であった95%
以下の低密度でも粉末間で原子の拡散が起こり、十分な
結合強度が発現されるので、特別の結合手段、例えば接
着剤、なとが不要である。しかしながら、磁石の相対密
度が70%以下では、結合強度が不十分であり着磁行為
により破損する場合もあり、実用的磁石とならない。ま
た、基本組成は、磁石の磁気特性を決定すると同時に、
特にCoは、合金のキューリー温度を上昇させ、残留磁
束密度の温度特性を改善するものであり、熱安定性の良
い磁石を提供する本発明の目的を達成するための重要要
素である。さらに、本発明の磁石では、粉末を集合固化
せしめる工程において、直接通電法を加熱手段とするの
で、短時間にて処理できるので、磁性粉の微細結晶粒の
粗大化が阻止できるので、磁石の保磁力の温度特性の低
下が起こらない。In the magnet of the present invention, the powder is activated by plasma before hot compaction, so the powder can be reduced by 95%, which was previously impossible.
Even at low densities below, atomic diffusion occurs between powders and sufficient bonding strength is developed, so special bonding means such as adhesives are not required. However, if the relative density of the magnet is less than 70%, the bonding strength is insufficient and the magnet may be damaged by the act of magnetization, so that it cannot be used as a practical magnet. In addition, the basic composition determines the magnetic properties of the magnet, and at the same time
In particular, Co increases the Curie temperature of the alloy and improves the temperature characteristics of residual magnetic flux density, and is an important element for achieving the object of the present invention, which is to provide a magnet with good thermal stability. Furthermore, in the magnet of the present invention, since the direct energization method is used as the heating means in the process of agglomerating and solidifying the powder, the process can be completed in a short time, and coarsening of the fine crystal grains of the magnetic powder can be prevented. No reduction in temperature characteristics of coercive force occurs.
実施例 以下に、本発明の詳細を一実施例を基に説明する。Example The details of the present invention will be explained below based on one embodiment.
第1図は本発明の製造方法に係わるキャビティーと電極
ポンチの構成を示す図である。Ndまたは/およびPr
が13原子%、COが15=原子%、Bが6原子%、F
e残部からなる合金を、メルトスピニング法により急冷
固化せしめ、厚さ20〜30ミクロンの薄片状粉末とし
た。この粉末を、第1図に示す内径20mmの非導電性
セラミックス性キャビティー1と一対の導電性セラミッ
クス性電極ポンチ2で構成された空間3に納め、一対の
電極ポンチに250 kg f / cn?の圧力を加
え、更に10−1〜10 ’ トールの真空雰囲気とし
、パルス幅40m5ecで20Vの直流電圧を60se
c印加し、しかるのち、1 、5 k Aの直流電流を
直接一対の電極間に40〜60sec流し、一対の電極
ポンチをあらかじめ設定した所定の位置まで加圧移動さ
せた。最終的に、キャビティー内粉末の温度は?、 O
0〜750℃に達した。これを冷却して、外径20 m
mパーミアンス1で、相対密度の異なる種々の磁石を得
た。第2図に相対密度85%の磁石の室温における磁気
特性を示す。曲線10が本発明の実施例の磁石の圧縮方
向を、曲線12は圧縮方向に直角方向に推定した値であ
り、曲線14は使用した磁性粉の特性である。曲線10
の残留磁束密度Jは、曲線14のJの相対密度(85%
)を若干上回る。また、曲線10と12では若干の差異
があり、これはわずかながら磁石が異方化していること
を示しているが、このぐらいの差異では、本質的には等
方性の磁石とすべきである。一方探磁力においては、本
発明の磁石のほうが原料である粉末より約2 k Oe
高い。これは、本発明の磁石の特徴であり、プラズマに
よる活性化により、粉末がクリーニングされるため保磁
力Hcjか上昇したものである。第3図に相対密度の異
なる各磁石に磁気特性を示す。各磁石は相対密度に比例
した残留磁束密度を有し、一方探磁力はおおむね一定で
ある。FIG. 1 is a diagram showing the structure of a cavity and an electrode punch related to the manufacturing method of the present invention. Nd or/and Pr
is 13 at%, CO is 15 at%, B is 6 at%, F
The alloy consisting of the remainder e was rapidly solidified by melt spinning to form flaky powder with a thickness of 20 to 30 microns. This powder was placed in a space 3 consisting of a non-conductive ceramic cavity 1 with an inner diameter of 20 mm and a pair of conductive ceramic electrode punches 2 shown in Fig. 1, and 250 kg f/cn? , a vacuum atmosphere of 10-1 to 10' Torr was applied, and a DC voltage of 20 V was applied for 60 sec with a pulse width of 40 m5 ec.
Then, a direct current of 1.5 kA was applied directly between the pair of electrodes for 40 to 60 seconds, and the pair of electrode punches were moved under pressure to a predetermined position. Finally, what is the temperature of the powder inside the cavity? , O
The temperature reached 0-750°C. After cooling this, the outer diameter was 20 m.
Various magnets with different relative densities were obtained with m permeance of 1. FIG. 2 shows the magnetic properties of a magnet with a relative density of 85% at room temperature. Curve 10 is the compression direction of the magnet of the example of the present invention, curve 12 is the estimated value in the direction perpendicular to the compression direction, and curve 14 is the characteristic of the magnetic powder used. curve 10
The residual magnetic flux density J of curve 14 is the relative density of J (85%
). Also, there is a slight difference between curves 10 and 12, which indicates that the magnet is slightly anisotropic, but with such a difference, the magnet should essentially be isotropic. be. On the other hand, in terms of magnetic exploration force, the magnet of the present invention has a higher magnetic force of about 2 k Oe than the raw material powder.
expensive. This is a feature of the magnet of the present invention, and the coercive force Hcj increases because the powder is cleaned by activation by plasma. Figure 3 shows the magnetic properties of magnets with different relative densities. Each magnet has a residual magnetic flux density that is proportional to its relative density, while the retrieval force is approximately constant.
上記本発明の磁石およびそれと同一磁性粉にて圧縮成形
法で製造された樹脂磁石とをそれぞれ電着塗装および水
ガラスによるコーティングを施し、600C,90RH
%の環境下で防錆力の評価を実施した。その結果を第1
表に示す。The above-mentioned magnet of the present invention and a resin magnet manufactured by compression molding using the same magnetic powder were each subjected to electrodeposition coating and coating with water glass, and were heated to 600C, 90RH.
The rust prevention ability was evaluated in an environment of The result is the first
Shown in the table.
以下余白
第1表
電着塗装の場合は、いずれの磁石でも十分な防錆力を発
揮するが、低コストである水ガラスでは、樹脂磁石は1
00時間以内で皮膜が浮いてしまうが、本発明の磁石で
は、その表面がすへて金属であるため密着性が良(十分
な防錆力を有している。In the case of electrodeposition coating on the first surface of the margin below, any magnet will exhibit sufficient rust prevention power, but for water glass, which is low cost, resin magnets
Although the film will peel off within 0.00 hours, the magnet of the present invention has good adhesion (sufficient rust prevention) because its surface is entirely metal.
尚、水ガラスのコーティング厚さは2〜3ミクロンであ
り、電着塗装の1/2以下の厚みで同様の防錆力を発揮
している。The coating thickness of water glass is 2 to 3 microns, which is less than 1/2 the thickness of electrodeposition coating and exhibits the same anti-corrosion ability.
発明の効果
以上述べた如く、本発明の磁石は、特別の結合剤を使用
しないで、熱間で圧縮成形することにより
る原子的結合のみにより実用的で、かつ相対密度70%
以上の任意の密度の磁石を提供することができる。これ
により、結合剤の耐熱性が理由による使用温度の限界が
取り除かれる。さらに本発明の磁石は、樹脂等の結合剤
を使用しないので、樹脂磁石では、密着性が悪く実用不
可能であった水ガラス系の防錆処理の採用が可能であり
、この防錆処理法では、コーティング厚さが2〜3ミク
ロンと、有機質のコーティングの1/2以下で十分な性
能を発揮するので、磁石を電気機器に組み込んだとき、
その磁気回路中に発生する磁気的空間の発生を減少せし
めるもので、磁石のパーミアンスを高くすることが可能
となり、電気機器の小型化に有効である。さらに、この
防錆処理は、無機質であるので使用温度の限界が十分高
く、磁石の使用範囲に限界を発生させないなとのすぐれ
た高価を恭するものである、。Effects of the Invention As mentioned above, the magnet of the present invention is practical due to only atomic bonding achieved by hot compression molding without using any special binder, and has a relative density of 70%.
Magnets of any density above can be provided. This eliminates the use temperature limitations due to the heat resistance of the binder. Furthermore, since the magnet of the present invention does not use a binder such as a resin, it is possible to use a water glass-based rust prevention treatment, which is impractical due to poor adhesion with resin magnets. Since the coating thickness is 2 to 3 microns, which is less than half of that of organic coatings, it exhibits sufficient performance, so when magnets are incorporated into electrical equipment,
This reduces the generation of magnetic spaces in the magnetic circuit, making it possible to increase the permeance of the magnet, which is effective in downsizing electrical equipment. Furthermore, since this anti-corrosion treatment is inorganic, it has a sufficiently high operating temperature limit and does not limit the usable range of the magnet, which is a very expensive treatment.
第1図は本発明の製造方法係わる一実施例のキャビティ
ーと電極ポンチの構成を示す図、第2図は本発明の磁石
の実施例て、相対密度が85%の磁石の磁気特性を示す
グラフ、第3図は本発明の相対密度の異なる磁石の磁気
特性を示す図である。
代理人の氏名 弁理士 粟野重孝 ほか1名第2図
第1図
Hcノ/koeFig. 1 is a diagram showing the structure of a cavity and an electrode punch in an embodiment of the manufacturing method of the present invention, and Fig. 2 is an embodiment of the magnet of the present invention, showing the magnetic properties of a magnet with a relative density of 85%. The graph in FIG. 3 is a diagram showing the magnetic properties of magnets of the present invention having different relative densities. Name of agent: Patent attorney Shigetaka Awano and one other person Figure 2 Figure 1 Hc/koe
Claims (2)
Ndを含む一種または二種以上の希土類)を急冷固化さ
せて得られた薄片状または粉末を出発原料とする等方性
永久磁石であって、薄片または粉末間か原子的に結合し
、かつ、相対密度が70%以上であることを特徴とする
等方性永久磁石。(1) Alloy whose basic component is R-Fe-Co-B (R:
An isotropic permanent magnet that uses flakes or powder as a starting material obtained by rapidly cooling and solidifying one or more rare earths (including Nd), in which the flakes or powders are atomically bonded, and An isotropic permanent magnet characterized by a relative density of 70% or more.
10^−^1トール以上の真空中で放電を起こさせ、さ
らに直流電流を加え、加熱すると同時に圧縮成形する等
方性永久磁石の製造方法。(2) Putting the raw material according to claim 1 into a molding cavity,
A method for producing an isotropic permanent magnet, in which a discharge is caused in a vacuum of 10^-^1 Torr or more, a direct current is applied, heating is performed, and compression molding is performed at the same time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11333190A JP3164811B2 (en) | 1990-04-27 | 1990-04-27 | Manufacturing method of isotropic permanent magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11333190A JP3164811B2 (en) | 1990-04-27 | 1990-04-27 | Manufacturing method of isotropic permanent magnet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0410602A true JPH0410602A (en) | 1992-01-14 |
| JP3164811B2 JP3164811B2 (en) | 2001-05-14 |
Family
ID=14609533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11333190A Expired - Fee Related JP3164811B2 (en) | 1990-04-27 | 1990-04-27 | Manufacturing method of isotropic permanent magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3164811B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997012435A1 (en) * | 1995-09-28 | 1997-04-03 | Yoshiaki Takahashi | Generator/motor |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01319909A (en) * | 1988-06-21 | 1989-12-26 | Matsushita Electric Ind Co Ltd | Manufacturing method of Fe-BR permanent magnet |
-
1990
- 1990-04-27 JP JP11333190A patent/JP3164811B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01319909A (en) * | 1988-06-21 | 1989-12-26 | Matsushita Electric Ind Co Ltd | Manufacturing method of Fe-BR permanent magnet |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997012435A1 (en) * | 1995-09-28 | 1997-04-03 | Yoshiaki Takahashi | Generator/motor |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3164811B2 (en) | 2001-05-14 |
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