JPH03248504A - Bond type permanent magnet - Google Patents
Bond type permanent magnetInfo
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- JPH03248504A JPH03248504A JP2046307A JP4630790A JPH03248504A JP H03248504 A JPH03248504 A JP H03248504A JP 2046307 A JP2046307 A JP 2046307A JP 4630790 A JP4630790 A JP 4630790A JP H03248504 A JPH03248504 A JP H03248504A
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Abstract
Description
【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明はボンド型永久磁石に関する。[Detailed description of the invention] [Purpose of the invention] (Industrial application field) The present invention relates to a bond type permanent magnet.
(従来の技術)
ボンド型永久磁石としては、フェライト系、SmCo系
、NdFeB系等が知られており、通常、これらの合金
の粉末を樹脂と混合したものを圧縮成型、射出成型等の
方法により製造されている。(Prior art) Ferrite-based, SmCo-based, NdFeB-based, etc. are known as bonded permanent magnets, and powders of these alloys are usually mixed with resin by compression molding, injection molding, etc. Manufactured.
しかしながら、同一の原料磁性粉を用いた場合でも、製
造プロセス等により得られる磁気特性にバラツキが生じ
、また、磁気特性、特に、最大エネルギー積の改善のた
めの異方性ボンド磁石を製造する場合には、磁性粉の配
向性にもバラツキが見られる。そのために、最終製品の
品質が一定しない。However, even when the same raw material magnetic powder is used, variations occur in the magnetic properties obtained due to the manufacturing process, etc., and when manufacturing anisotropic bonded magnets to improve magnetic properties, especially the maximum energy product. There are also variations in the orientation of the magnetic powder. As a result, the quality of the final product is inconsistent.
特に、NdFeB系ボンド磁石の場合、成型時の磁性粉
の割れや欠けが、保磁力や磁石のヒステリシス曲線の角
型性の大きな劣化を引き起こすために、最終製品の品質
管理上の大きな問題となっている。さらに、異方性ボン
ド磁石の製造に際しては、磁性粉に磁場を印加して異方
性化することが一般的な方法であるが、この際に磁性粉
同志が互いに機械的な相互作用を引き起こし、所期の配
向度が得られないという問題がある。In particular, in the case of NdFeB bonded magnets, cracks and chips in the magnetic powder during molding cause significant deterioration of the coercive force and squareness of the magnet's hysteresis curve, which poses a major problem in quality control of the final product. ing. Furthermore, when manufacturing anisotropic bonded magnets, a common method is to apply a magnetic field to magnetic powder to make it anisotropic, but at this time, the magnetic powder causes mechanical interaction with each other. , there is a problem that the desired degree of orientation cannot be obtained.
(発明が解決しようとする課題)
従来のボンド型永久磁石は、磁性粉の配向性にバラツキ
が生じ、安定した品質の磁石が得られないという問題が
ある。(Problems to be Solved by the Invention) Conventional bonded permanent magnets have a problem in that the orientation of magnetic powder varies, making it impossible to obtain magnets of stable quality.
本発明の目的は、成形時の磁気特性の劣化を軽減し、異
方性化する場合には良好な配向性が図られ、良好な磁気
特性を有するボンド型永久磁石を提供することにある。An object of the present invention is to provide a bonded permanent magnet that reduces deterioration of magnetic properties during molding, achieves good orientation when anisotropic, and has good magnetic properties.
[発明の構成]
(課題を解決するための手段および作用)本発明は、平
均のアスペクト比が2.5以下であり、かつ、粒径が4
0μm以上のものが重量比で90%以上である磁性粉か
らなることを特徴とするボンド型永久磁石である。ここ
で、アスペクト比とは、通常ボンド磁石に使用される磁
性粉の個々の形状は一定していないが、磁性粉の有する
最大幅、即ち、長軸方向の長さとこの長軸と直交する短
軸方向の最大幅および最小幅の幾何平均との比によって
定義されるものである。[Structure of the invention] (Means and effects for solving the problem) The present invention provides particles having an average aspect ratio of 2.5 or less and a particle size of 4.
This is a bond type permanent magnet characterized by being made of magnetic powder in which 90% or more by weight of magnetic powder has a particle size of 0 μm or more. Here, the aspect ratio refers to the maximum width of the magnetic powder, that is, the length in the major axis direction and the short width perpendicular to this major axis, although the individual shapes of the magnetic powders normally used in bonded magnets are not constant. It is defined by the ratio of the maximum width in the axial direction and the geometric mean of the minimum width.
本発明者らは、ボンド型永久磁石の製造工程、特に、成
型工程において原料となる磁性粉のアスペクト比および
粒径が得られる磁石との間に密接な関係があることを見
出した。The present inventors have discovered that there is a close relationship between the aspect ratio and particle size of the magnetic powder used as a raw material in the manufacturing process of a bonded permanent magnet, particularly in the molding process, and the magnet obtained.
まず、アスペクト比が2.5を超える場合は以下の問題
が生じる。First, when the aspect ratio exceeds 2.5, the following problems occur.
(1)目的とする製品が等方性ボンド磁石か異方性ボン
ド磁石かに拘らず、成型時に加圧等に起因する磁性粉の
割れや欠けが多くなり、磁気特性が大きく劣化する。(1) Regardless of whether the target product is an isotropic bonded magnet or an anisotropic bonded magnet, the magnetic powder is often cracked or chipped due to pressure during molding, and the magnetic properties are significantly deteriorated.
(2)目的とする製品が異方性ボンド磁石の場合、磁性
粉が磁場の印加等によって十分に配向せず、初期の磁気
特性が得られない。(2) When the intended product is an anisotropic bonded magnet, the magnetic powder is not sufficiently oriented by the application of a magnetic field, etc., and initial magnetic properties cannot be obtained.
これらの問題点は、原料の磁性粉の平均アスペクト比を
制御することにより改善することができる。この場合、
磁性粉の平均アスペクト比は、2.5以下、好ましくは
2以下とすることが望ましい。These problems can be improved by controlling the average aspect ratio of the raw magnetic powder. in this case,
The average aspect ratio of the magnetic powder is desirably 2.5 or less, preferably 2 or less.
また、原料の磁性粉の粉末粒径が40μmを下回る場合
、磁気特性の改善効果は小さくなる。特に、原料の磁性
粉が、例えば、NdFeB系である場合、粉末粒径が小
さくなると、保磁力、磁石のヒステリシス曲線の角型性
の劣化も見られ、さらに、耐蝕性の面からも問題が生じ
る。従って、磁性粉の粉末粒径は40μm以上であるこ
とが望ましい。Furthermore, if the powder particle size of the raw material magnetic powder is less than 40 μm, the effect of improving magnetic properties becomes small. In particular, when the raw material magnetic powder is, for example, NdFeB-based, as the powder particle size becomes smaller, the coercive force and the squareness of the hysteresis curve of the magnet deteriorate, and furthermore, there are problems in terms of corrosion resistance. arise. Therefore, it is desirable that the particle size of the magnetic powder is 40 μm or more.
特に、粒径が40μmを下回る磁性粉が重量比で10%
を超えた場合は、ボンド型永久磁石の特性劣化を生じる
。従って、重量比で90%以上の磁性粉の粒径は40μ
m以上であることが望ましい。In particular, magnetic powder with a particle size of less than 40 μm accounts for 10% by weight.
If it exceeds this, the characteristics of the bonded permanent magnet will deteriorate. Therefore, the particle size of 90% or more of the magnetic powder by weight is 40μ
It is desirable that it is more than m.
上述の選択された磁性粉による効果は、原料となる磁性
粉の種類によって、その程度が異なる。The effect of the above-mentioned selected magnetic powder varies depending on the type of magnetic powder used as the raw material.
特に、原料の磁性粉がNdFeB系である場合、割れや
欠けによる表面層の劣化が直ちに保磁力や角型性の劣化
に直結する素材であるために、磁性粉の平均アスペクト
比の制御はボンド磁石の磁気特性の改善に極めて有効で
ある。また、NdFeB系異方性ボンド磁石の製造に際
しても、磁性粉の平均アスペクト比の制御により、磁性
粉の配向性を大きく改善することができる。In particular, when the raw material magnetic powder is NdFeB-based, the deterioration of the surface layer due to cracking or chipping is directly linked to the deterioration of the coercive force and squareness, so controlling the average aspect ratio of the magnetic powder is It is extremely effective in improving the magnetic properties of magnets. Furthermore, in the production of NdFeB-based anisotropic bonded magnets, the orientation of the magnetic powder can be greatly improved by controlling the average aspect ratio of the magnetic powder.
本発明のボンド型永久磁石の製造方法について、NdF
eB系焼結合金を出発原料とした場合を例にとって、説
明する。Regarding the method for manufacturing a bonded permanent magnet of the present invention, NdF
An example will be explained in which an eB-based sintered alloy is used as a starting material.
まず、原子分率で、8〜30%のR(RはYを含む希土
類元素の内から選択された少なくとも1種の元素)、2
〜28%のB、0.1〜13%のM (MはAgまたは
Gaの少なくとも1種の元素)、残部が実質的にFeま
たはCoの一種以上からなる永久磁石合金を製造する。First, in terms of atomic fraction, 8 to 30% R (R is at least one element selected from rare earth elements including Y), 2
A permanent magnet alloy is produced which consists of ~28% B, 0.1~13% M (M is at least one element of Ag or Ga), and the balance essentially consists of one or more of Fe or Co.
次に、ボールミル等の粉砕手段を用いて永久磁石合金を
粉砕する。この際、後工程の成型と焼結を容易にし、か
つ磁気特性を良好にするために、粉末の平均粒径が2〜
10μmとなるように微粉砕することが望ましい。この
粒径が10μmを超えると保磁力(iHc)の低下をも
たらし、一方、2μm未満となると残留磁束密度(Br
)等の磁気特性の低下を招く。Next, the permanent magnet alloy is crushed using a crushing means such as a ball mill. At this time, in order to facilitate molding and sintering in the post-process and to improve magnetic properties, the average particle size of the powder should be 2 to 2.
It is desirable that the powder be finely pulverized to a particle size of 10 μm. When this particle size exceeds 10 μm, the coercive force (iHc) decreases, while when it becomes less than 2 μm, the residual magnetic flux density (Br
), etc., resulting in a decrease in magnetic properties.
微粉砕された永久磁石合金粉末を所望の形状にプレス成
型する。成型の際には、無磁場でも良いし、通常の焼結
磁石を製造する場合と同様に、例えば、15koe程度
の磁場を印加し、配向処理行う。引き続いて、例えば、
1000〜1140℃で、0.5〜5時間程度の条件で
成形体を焼結する。この焼結は合金中の酸素濃度を増加
させないように、Arガス等の不活性ガス雰囲気中、も
しくは、真空中で行うことが望ましい。この場合、酸素
分圧は、1torr以下とすることが望ましい。Finely pulverized permanent magnet alloy powder is press-molded into a desired shape. At the time of molding, no magnetic field may be used, or a magnetic field of, for example, about 15 koe is applied to perform the orientation treatment, as in the case of producing a normal sintered magnet. Subsequently, for example,
The molded body is sintered at 1000 to 1140°C for about 0.5 to 5 hours. This sintering is desirably performed in an inert gas atmosphere such as Ar gas or in vacuum so as not to increase the oxygen concentration in the alloy. In this case, it is desirable that the oxygen partial pressure be 1 torr or less.
こうして得られた焼結体を粉砕し、粉末粒径が40μm
以上の磁性粉とする。この場合、粒径が40μmを下回
る粒径の磁性粉のある程度の混入は差し支えない。得ら
れた磁性粉は、不活性ガス気流または有機溶剤の液流に
より球状化処理を行い、平均アスペクト比を2.5以下
、好ましくは、2.0以下に調整する。球状化処理を施
された粉末は、分級等の方法により、粒径が40μm以
上とする。The sintered body thus obtained was crushed to a powder particle size of 40 μm.
or more magnetic powder. In this case, a certain amount of magnetic powder having a particle size of less than 40 μm may be mixed in. The obtained magnetic powder is subjected to a spheroidization treatment using an inert gas stream or an organic solvent liquid stream to adjust the average aspect ratio to 2.5 or less, preferably 2.0 or less. The powder subjected to the spheroidization treatment is made to have a particle size of 40 μm or more by a method such as classification.
この場合、40μmを下回る粒径の粉末の量は重量比で
10%未満とする。In this case, the amount of powder with a particle size below 40 μm is less than 10% by weight.
こうして得られた粉末に500〜800℃の温度範囲で
、0.1〜10時間程時間時効処理を行う。この時効処
理の温度が500℃未満または800℃を超えると、保
磁力の減少または角型性の劣化を招き、磁気特性は大幅
に低下する。従って、この時効処理の温度は、500〜
800℃の範囲が好ましい。The powder thus obtained is subjected to aging treatment at a temperature range of 500 to 800° C. for about 0.1 to 10 hours. If the temperature of this aging treatment is lower than 500°C or higher than 800°C, the coercive force will decrease or the squareness will deteriorate, and the magnetic properties will deteriorate significantly. Therefore, the temperature of this aging treatment is 500~
A range of 800°C is preferred.
この時効処理の前に、550〜1150℃の第1段階の
時効処理を施すことにより、より大きな保磁力を持つ粉
末が得られる。この第1段階の時効処理は、550℃未
満または1150℃を超える場合は、顕著な効果が得ら
れない。By performing a first stage aging treatment at 550 to 1150° C. before this aging treatment, a powder having a larger coercive force can be obtained. This first stage aging treatment will not produce any significant effect if the temperature is lower than 550°C or higher than 1150°C.
このように処理された粉末を、エポキシ、ナイロン等の
樹脂と混練して所望の形状に成型して、ボンド型永久磁
石が得られる。成型の際、磁場を印加することにより、
異方性化することができる。The thus treated powder is kneaded with a resin such as epoxy or nylon and molded into a desired shape to obtain a bonded permanent magnet. By applying a magnetic field during molding,
It can be made anisotropic.
また、上記の例では焼結合金を永久磁石合金として用い
たが、等方性磁石を得る場合は、磁場配向、焼結を省略
し、インゴットを用いても良い。Further, in the above example, a sintered alloy was used as the permanent magnet alloy, but when obtaining an isotropic magnet, magnetic field orientation and sintering may be omitted and an ingot may be used.
(実施例) 以下、本発明の実施例について説明する。(Example) Examples of the present invention will be described below.
(実施例1)
まず、原子分率で、14.5%のNd、17%のCos
1%のGas 5−5%の81残部がFeとなる
ように配合し、Ar雰囲気中で水冷銅ボートを用いてア
ーク溶解した。得られた合金をAr雰囲気中で粗粉砕し
、さらに、ジェットミルにより平均粒径的3.0μmま
で、微粉砕した。(Example 1) First, in terms of atomic fraction, 14.5% Nd, 17% Cos
A mixture of 1% Gas, 5% to 5% 81% Fe, and arc melting was performed using a water-cooled copper boat in an Ar atmosphere. The obtained alloy was coarsely ground in an Ar atmosphere, and further finely ground to an average particle size of 3.0 μm using a jet mill.
この微粉末を所定の押型に充填して20kOeの磁界を
印加しつつ、2 ton/c−の圧力で圧縮成型した。This fine powder was filled into a predetermined mold and compression molded at a pressure of 2 ton/c- while applying a magnetic field of 20 kOe.
この成形体をAr雰囲気中で、1600℃で1時間焼結
し、平均粒径400μmまで粉砕した後、Ar気流下で
、球状化処理を行い粉末の平均アスペクト比を1.6に
調整した。球状化処理が施された粉末は、ふるいにより
分級し、粉末粒径が40μm未満の粉末を除去した後、
900℃、1時間の時効処理を施した。この粉末を室温
まで急冷した後、さらに、600°C,3時間の時効処
理を行った。This compact was sintered at 1600° C. for 1 hour in an Ar atmosphere, pulverized to an average particle size of 400 μm, and then subjected to spheroidization treatment under an Ar flow to adjust the average aspect ratio of the powder to 1.6. The powder that has been subjected to the spheroidization treatment is classified using a sieve, and after removing powder with a powder particle size of less than 40 μm,
Aging treatment was performed at 900°C for 1 hour. After this powder was rapidly cooled to room temperature, it was further aged at 600°C for 3 hours.
得られた磁性粉を液状エポキシ樹脂(3wt%)と混練
し、18koeの磁界を印加しつつ、磁界方向と直角方
向に4 ton/cJの圧力で圧縮成型した。The obtained magnetic powder was kneaded with liquid epoxy resin (3 wt%), and compression molded at a pressure of 4 ton/cJ in a direction perpendicular to the direction of the magnetic field while applying a magnetic field of 18 koe.
得られた磁石について残留磁束密度(Br)、保磁力(
iHC)、最大エネルギー積(BHmax)を測定した
。その結果、Br−94kG% 1Hc=11.2kO
e、BH+++ax −17,9MGOeであった。ま
た、配向方向と直角方向の残留磁束密度(Br=)を測
定し、以下の(1)式により配向度を評価したところ、
A−89%と、良好な値が得られた。The residual magnetic flux density (Br) and coercive force (
iHC), and the maximum energy product (BHmax) was measured. As a result, Br-94kG% 1Hc=11.2kO
e, BH+++ax -17,9MGOe. In addition, the residual magnetic flux density (Br=) in the direction perpendicular to the orientation direction was measured, and the degree of orientation was evaluated using the following equation (1).
A good value of A-89% was obtained.
A(%) −B r/ (B r +B r −) X
100 ・(L)(比較例1)
原料の磁性粉の平均アスペクト比が3.1であることを
除いて、実施例1と同様な方法でボンド型永久磁石を製
造した。得られた磁石の磁気特性および配向度を測定し
た。その結果、Br−8,6kGSiHc−8,8kO
e、BHmax =LLIMGOeであった。また、配
向度は、A−75%であった。これらの結果は、いずれ
も実施例1に比べて、劣っていることが分かる。A (%) −Br/ (Br +Br −) X
100.(L) (Comparative Example 1) A bonded permanent magnet was manufactured in the same manner as in Example 1, except that the average aspect ratio of the raw material magnetic powder was 3.1. The magnetic properties and degree of orientation of the obtained magnet were measured. As a result, Br-8,6kGSiHc-8,8kO
e, BHmax = LLIMGOe. Moreover, the degree of orientation was A-75%. It can be seen that these results are all inferior to Example 1.
(実施例2)
原料合金の組成が原子分率で14%のNd、16%のC
o、2%のAΩ、5.5%の81残部が実質的にFeか
らなること、圧縮成型を無磁場下で行うことを除いては
、実施例1と同様な方法でボンド型永久磁石を製造した
。得られた磁石の磁気特性を測定した。その結果、B
r = 6.3k G。(Example 2) The composition of the raw material alloy is 14% Nd and 16% C in atomic fraction.
A bonded permanent magnet was produced in the same manner as in Example 1, except that the remaining part of 81 was essentially Fe, and the compression molding was carried out in the absence of a magnetic field. Manufactured. The magnetic properties of the obtained magnet were measured. As a result, B
r = 6.3kG.
i Hc =10.8k Oe、 B Hmax −8
,2MGOeであった。i Hc =10.8k Oe, B Hmax -8
, 2MGOe.
(比較例2)
原料の磁性粉の平均アスペクト比が3.0であることを
除いて実施例2と同様な方法でボンド型永久磁石を製造
した。得られた磁石の磁気特性を測定した。その結果、
Br−5,8kGS 1Hc−8,1kOe、BHma
x −5,5MGOeであり、角型性も実施例2に比較
して劣化している。(Comparative Example 2) A bonded permanent magnet was manufactured in the same manner as in Example 2, except that the average aspect ratio of the raw material magnetic powder was 3.0. The magnetic properties of the obtained magnet were measured. the result,
Br-5,8kGS 1Hc-8,1kOe, BHma
x −5,5MGOe, and the squareness is also deteriorated compared to Example 2.
(比較例3)
原料の磁性粉として、粒径が40μmのものの割合が重
量比40%である以外は、実施例1と同様な方法でボン
ド型永久磁石を製造した。得られた磁石の磁気特性を測
定した。その結果、Br−7,6kG、、i Hc −
6,5koe、 BHa+ax −7,8M G Oe
であった。この磁石は、実施例1の磁石に比較して、角
型性も大幅に劣化し、磁気特性も大幅に低下している。(Comparative Example 3) A bonded permanent magnet was manufactured in the same manner as in Example 1, except that the raw material magnetic powder had a particle size of 40 μm at a weight ratio of 40%. The magnetic properties of the obtained magnet were measured. As a result, Br-7,6kG, i Hc −
6,5koe, BHa+ax -7,8M G Oe
Met. Compared to the magnet of Example 1, this magnet has significantly deteriorated squareness and greatly deteriorated magnetic properties.
[発明の効果]
以上の様に、本発明によれば、成形時の磁気特性の劣化
を軽減し、異方性化する場合には良好な配向性が図られ
、良好な磁気特性を有するボンド型永久磁石を提供する
ことができる。[Effects of the Invention] As described above, according to the present invention, deterioration of magnetic properties during molding is reduced, good orientation is achieved when anisotropy is made, and a bond having good magnetic properties is produced. type permanent magnet can be provided.
Claims (1)
が40μm以上のものが重量比で90%以上である磁性
粉からなることを特徴とするボンド型永久磁石。A bonded permanent magnet comprising magnetic powder having an average aspect ratio of 2.5 or less and a weight ratio of 90% or more of the particles having a particle size of 40 μm or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2046307A JP3057664B2 (en) | 1990-02-27 | 1990-02-27 | Bonded permanent magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2046307A JP3057664B2 (en) | 1990-02-27 | 1990-02-27 | Bonded permanent magnet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03248504A true JPH03248504A (en) | 1991-11-06 |
| JP3057664B2 JP3057664B2 (en) | 2000-07-04 |
Family
ID=12743536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2046307A Expired - Fee Related JP3057664B2 (en) | 1990-02-27 | 1990-02-27 | Bonded permanent magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3057664B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01162702A (en) * | 1987-12-17 | 1989-06-27 | Kobe Steel Ltd | Rare earth series magnetic powder for resin combined-type magnet |
-
1990
- 1990-02-27 JP JP2046307A patent/JP3057664B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01162702A (en) * | 1987-12-17 | 1989-06-27 | Kobe Steel Ltd | Rare earth series magnetic powder for resin combined-type magnet |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3057664B2 (en) | 2000-07-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |