JPH06108190A - Rare earth permanent magnet alloy - Google Patents

Rare earth permanent magnet alloy

Info

Publication number
JPH06108190A
JPH06108190A JP4280829A JP28082992A JPH06108190A JP H06108190 A JPH06108190 A JP H06108190A JP 4280829 A JP4280829 A JP 4280829A JP 28082992 A JP28082992 A JP 28082992A JP H06108190 A JPH06108190 A JP H06108190A
Authority
JP
Japan
Prior art keywords
rare earth
permanent magnet
magnet alloy
earth permanent
phase
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
Application number
JP4280829A
Other languages
Japanese (ja)
Inventor
Kazuhiro Takaguchi
和博 高口
Kenji Yamamoto
健治 山本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP4280829A priority Critical patent/JPH06108190A/en
Publication of JPH06108190A publication Critical patent/JPH06108190A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/032Magnets 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
    • H01F1/04Magnets 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
    • H01F1/047Alloys characterised by their composition
    • H01F1/053Alloys characterised by their composition containing rare earth metals
    • H01F1/055Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
    • H01F1/0555Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together
    • H01F1/0557Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together sintered

Landscapes

  • 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

(57)【要約】 (修正有) 【構成】重量百分率で、24〜28%のR(Rは希土類元素
のうち1種以上)、10〜20%のFe、3〜6%のCu、2〜
4%のZr、残部Coからなり、かつR2Co17 相から成る微
細なセル状組織のセル内のCu量が1原子%以上3原子%
以下の範囲内であることを特徴とする希土類永久磁石合
金。 【効果】本発明によれば、保磁力が 20KOeを超えるよう
な高特性R2Co17系希土類永久磁石合金を製造することが
でき、産業上その利用価値は極めて高い。
(57) [Summary] (Modified) [Structure] Percentage by weight: 24-28% R (R is at least one of rare earth elements), 10-20% Fe, 3-6% Cu, 2 ~
The Cu content in the cell of the fine cellular structure composed of 4% Zr and the balance Co and the R 2 Co 17 phase is 1 atom% or more and 3 atom% or more.
A rare earth permanent magnet alloy characterized by being in the following range. [Effect] According to the present invention, it is possible to produce a high-performance R 2 Co 17 series rare earth permanent magnet alloy having a coercive force exceeding 20 KOe, and its industrial utility value is extremely high.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、R2Co17系希土類永久磁
石合金に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an R 2 Co 17 type rare earth permanent magnet alloy.

【0002】[0002]

【従来の技術】希土類永久磁石合金としては、現在、R2
Co17系磁石合金と R2Fe14B系磁石合金とが一般に使用さ
れている。通常、R2Fe14B系磁石合金の方が最大エネルギ
ー積が大きいため幅広く利用されているが、R2Fe14B系磁
石合金はキュリー温度が約 300℃と低いため 100℃を超
えるような高温では磁気特性が極端に低下してしまい使
用に耐えない。反面、R2Co17系磁石合金はキュリー温度
が約 800℃と高いため、高温においては R2Fe14B系磁石
合金よりも磁気特性が高くなり、高温での使用ではR2Co
17系磁石合金が用いられており、用途が限定されつつも
さらなる高特性を目指して研究開発が進められている。
R2Co17系希土類永久磁石合金はその組織構造として微細
なセル状組織を有していることはよく知られている。こ
のセル状組織は、500〜5,000 Åのセル径をもつR2Co17
からなるセルと、幅50〜 200Åの境界相であるRCo5相と
からなっている。R2Co17系希土類永久磁石合金は、この
微細なセル状組織に磁壁がピンニングされることにより
保磁力が発生するピンニング型の磁石である。従って、
微細構造であるセル状組織と磁気特性は密接に関係して
おり、セル状組織を適切に制御することにより、磁気特
性を高めようという試みが従来からなされてきた。例え
ば、特開昭 56-156734号および特開昭 56-156735号で
は、セル状組織のセルとセルとの距離を適当な大きさに
制御することにより 15KOeを越えるような大きな保磁力
を得ている。
2. Description of the Related Art Currently, R 2 is a rare earth permanent magnet alloy.
Co 17 series magnet alloys and R 2 Fe 14 B series magnet alloys are generally used. Normally, the R 2 Fe 14 B-based magnet alloy is widely used because it has a larger maximum energy product. However, the R 2 Fe 14 B-based magnet alloy has a low Curie temperature of about 300 ° C, so it may exceed 100 ° C. At high temperatures, the magnetic properties deteriorate extremely and cannot be used. On the other hand, the Curie temperature of the R 2 Co 17- based magnet alloy is as high as about 800 ° C., so the magnetic properties are higher than those of the R 2 Fe 14 B-based magnet alloy at high temperatures, and the R 2 Co 17- based magnet alloy becomes R 2 Co when used at high temperatures.
A 17- based magnet alloy is used, and research and development is being pursued with the aim of achieving even higher properties while its application is limited.
It is well known that the R 2 Co 17 type rare earth permanent magnet alloy has a fine cellular structure as its structural structure. This cellular structure consists of cells consisting of R 2 Co 17 phase having a cell diameter of 500 to 5,000 Å and RCo 5 phase which is a boundary phase with a width of 50 to 200 Å. The R 2 Co 17 type rare earth permanent magnet alloy is a pinning type magnet in which a coercive force is generated by pinning a domain wall in this fine cellular structure. Therefore,
The cellular structure, which is a fine structure, is closely related to the magnetic properties, and attempts have been made to enhance the magnetic properties by appropriately controlling the cellular structure. For example, in JP-A-56-156734 and JP-A-56-156735, a large coercive force exceeding 15 KOe can be obtained by controlling the distance between cells having a cellular structure to an appropriate size. There is.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、セル状
組織の制御は未だ十分に行われているとは言えず、セル
状組織を十分に制御することによってR2Co17系希土類永
久磁石合金のさらなる高特性化が期待できる。
However, it cannot be said that the control of the cellular structure is still sufficiently performed, and the R 2 Co 17 type rare earth permanent magnet alloy is further improved by controlling the cellular structure sufficiently. Higher characteristics can be expected.

【0004】[0004]

【課題を解決するための手段】本発明者等は、微細なセ
ル状組織と磁気特性について鋭意研究を続けた結果、セ
ル内のCuの量が磁気特性、特に保磁力に大きな影響を及
ぼし、セル内のCu量を適切に制御することにより保磁力
が 20KOeを超えるような高特性なR2Co17系永久磁石を製
造することに成功し、本発明を完成した。本発明の要旨
は、重量百分率で、24〜28%のR(Rは希土類元素のう
ち1種以上)、10〜20%のFe、3〜6%のCu、2〜4%
のZr、残部Coからなり、かつR2Co17 相から成る微細な
セル状組織のセル内のCu量が1原子%以上3原子%以下
の範囲内であることを特徴とする希土類永久磁石合金で
ある。
Means for Solving the Problems The inventors of the present invention have conducted extensive studies on a fine cellular structure and magnetic characteristics, and as a result, the amount of Cu in the cells has a great influence on the magnetic characteristics, particularly the coercive force, By appropriately controlling the Cu content in the cell, we succeeded in producing a high-performance R 2 Co 17 system permanent magnet having a coercive force exceeding 20 KOe, and completed the present invention. The gist of the present invention is, by weight percentage, 24-28% R (R is one or more of rare earth elements), 10-20% Fe, 3-6% Cu, 2-4%.
Rare earth permanent magnet alloy, characterized in that the Cu content in the cells of the fine cellular structure consisting of Zr and the balance Co and consisting of the R 2 Co 17 phase is in the range of 1 atom% to 3 atom%. Is.

【0005】以下、本発明を詳細に説明する。R2Co17
希土類永久磁石合金は、一般に、次のような工程により
製造される。先ず、所定量の原料金属を秤量して高周波
溶解炉またはアーク炉などの溶解炉で溶解しインゴット
を鋳造する。次いでこのインゴットをジョークラッシャ
ー、スタンプミル、ブラウンミル等を用いて粗粉砕し、
ジェットミル、ボールミル等により粒径1〜50μmにな
るように微粉砕を行う。次にこの微粉を磁場中で所望の
形に圧縮成形した後、1,100 〜1,250 ℃で燒結し、続い
て燒結温度よりも0〜50℃低い温度で溶体化する。燒
結、溶体化に要する時間は、0.5〜5時間が適当である。
最後に時効処理として、通常初段時効を 700〜 950℃で
一定時間保持し、その後、連続冷却または多段時効を行
う。上記の各工程は、R2Co17系合金が酸化されると特性
の劣化が著しいので、これを防止するため真空中または
非酸化性の雰囲気下で行われる。
The present invention will be described in detail below. The R 2 Co 17 type rare earth permanent magnet alloy is generally manufactured by the following steps. First, a predetermined amount of raw material metal is weighed and melted in a melting furnace such as a high frequency melting furnace or an arc furnace to cast an ingot. Then, this ingot is roughly crushed using a jaw crusher, a stamp mill, a brown mill, etc.,
It is finely pulverized by a jet mill, a ball mill or the like so that the particle diameter becomes 1 to 50 μm. Next, this fine powder is compression-molded into a desired shape in a magnetic field, then sintered at 1,100-1,250 ° C, and subsequently solution-treated at a temperature 0-50 ° C lower than the sintering temperature. The time required for sintering and solution treatment is 0.5 to 5 hours.
Finally, as the aging treatment, the first stage aging is usually maintained at 700 to 950 ° C for a certain period of time, and then continuous cooling or multi-stage aging is performed. The above-mentioned steps are carried out in a vacuum or in a non-oxidizing atmosphere in order to prevent the deterioration of the characteristics of the R 2 Co 17 alloy when it is oxidized.

【0006】溶体化処理終了直後のR2Co17系合金は TbC
u7型の結晶構造を示すが、次工程の時効処理により、R2
Co17相とRCo5相とに分離し、微細なセル状組織を形成す
る。セル状組織は初段時効時に形成され、そのセルの大
きさは、概ね初段時効の温度で決まる。その後の連続冷
却または多段時効により各構成元素が拡散し、セルを構
成するR2Co17相、境界を構成するRCo5相の組成は変化し
ていく。R、Cuは境界相へと拡散し、Co、Feはセル内へ
と拡散するがZrは殆ど拡散しない。R2Co17相とRCo5相の
組成が変化するにつれて、R2Co17系磁石合金の特性も変
化していく。
Immediately after completion of solution treatment, R 2 Co 17 alloy is TbC
Although it shows a u 7 type crystal structure, R 2
Separates into a Co 17 phase and a RCo 5 phase to form a fine cellular structure. The cellular structure is formed during the first-stage aging, and the size of the cell is determined by the temperature of the first-stage aging. Subsequent continuous cooling or multi-step aging causes each constituent element to diffuse, and the composition of the R 2 Co 17 phase forming the cell and the RCo 5 phase forming the boundary changes. R and Cu diffuse into the boundary phase, Co and Fe diffuse into the cell, but Zr hardly diffuses. As the composition of the R 2 Co 17 phase and the RCo 5 phase changes, the characteristics of the R 2 Co 17 system magnetic alloy also change.

【0007】本発明の最大の特徴は、これらの構成元素
の内、セル内に拡散するCuの量が保磁力に大きな影響を
及ぼすことを見出し、その量を制御したことにある。セ
ルを構成するR2Co17相に含まれるCu量が3原子%を超え
るとR2Co17系磁石合金の保磁力は小さくなってしまう
が、これはR2Co17相の結晶磁気異方性が小さくなるため
だと考えられる。従って、大きな保磁力を得るために、
セルのR2Co17相に含まれるCu量を3原子%以下となるよ
うに時効処理すればよいが、1原子%以下にするために
は長時間の時効処理を必要とし製造上不利であるので、
セルのR2Co17相に含まれるCu量は1原子%以上3原子%
以下の範囲内でに限定される。
The greatest feature of the present invention is that, of these constituent elements, the amount of Cu diffused in the cell was found to have a great effect on the coercive force, and the amount thereof was controlled. When the amount of Cu contained in the R 2 Co 17 phase constituting the cell exceeds 3 atomic%, the coercive force of the R 2 Co 17 system magnetic alloy becomes small, but this is due to the crystal magnetic anisotropy of the R 2 Co 17 phase. It is thought that this is because the sex becomes smaller. Therefore, in order to obtain a large coercive force,
The aging treatment may be performed so that the amount of Cu contained in the R 2 Co 17 phase of the cell is 3 atom% or less, but in order to reduce the amount of Cu to 1 atom% or less, a long aging treatment is required, which is disadvantageous in manufacturing. So
The amount of Cu contained in the R 2 Co 17 phase of the cell is 1 atom% or more and 3 atom% or more.
It is limited to the following range.

【0008】次に、R2Co17系永久磁石合金の組成を重量
百分率で、24〜28%のR(Rは希土類元素のうち1種以
上)、10〜20%のFe、3〜6%のCu、2〜4%のZr、残
部Coと限定したのは、以下のような理由からである。R2
Co17系永久磁石合金中に含まれるRの量が、28重量%を
超えるとBrが低下すし、24重量%未満では角型が悪くな
る。ここにRは、Yを含む La,Ce,Pr,Nd,Pm,Sm,Eu,Gd,T
b,Dy,Ho,Er,Tm,YbおよびLuの内から選択される1種また
は2種以上の混合元素であり、好ましくはSmである。ま
た、R2Co17系永久磁石合金中に含まれるFe量が、10重量
%未満ではBrが低下してしまい、20重量%を超えると保
磁力が低下し、Zr量が2重量%未満では充分な保磁力が
得られず、4重量%より多くなると最大エネルギー積の
低下を引き起こす。更にCu量が3重量%未満では保磁力
が低くなってしまい、6重量%より多くなるとBrの低下
をもたらす。
Next, the composition of the R 2 Co 17 type permanent magnet alloy is expressed by weight percentage of 24-28% R (R is one or more of rare earth elements), 10-20% Fe, 3-6%. The reason for limiting Cu to 2%, Zr of 2 to 4%, and the balance Co is as follows. R 2
If the amount of R contained in the Co 17 type permanent magnet alloy exceeds 28% by weight, Br decreases, and if it is less than 24% by weight, the squareness deteriorates. Here, R is Y including La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, T
One or two or more kinds of mixed elements selected from b, Dy, Ho, Er, Tm, Yb and Lu, and preferably Sm. Further, if the Fe content in the R 2 Co 17 system permanent magnet alloy is less than 10% by weight, Br will decrease, and if it exceeds 20% by weight, the coercive force will decrease, and if the Zr content is less than 2% by weight. Sufficient coercive force cannot be obtained, and if it exceeds 4% by weight, the maximum energy product decreases. Further, if the Cu content is less than 3% by weight, the coercive force will be low, and if it exceeds 6% by weight, Br will be lowered.

【0009】[0009]

【実施例】以下、本発明の実施態様を実施例を挙げて具
体的に説明するが、本発明はこれらに限定されるもので
はない。 (実施例1)合金組成がSm25.5重量%、Fe14重量%、Cu
4.5重量%、Zr3重量%、残Coとなるように原料金属を
秤量をした後、これらを高周波溶解炉にて溶解し合金イ
ンゴットを作製した。得られた合金インゴットをブラウ
ンミルを用いて粗粉砕し、その後ジェットミルで微粉砕
を行った。微粉砕後の合金粉の平均粒径は約5μmであ
った。この合金粉を磁場中で成形を行い、得られた成形
体を1,200 ℃で燒結、1,180 ℃で溶体化した。次いで時
効処理はまず初段時効として 850℃で2時間保持した
後、5℃/min、1℃/min、0.2℃/min、のそれぞれの冷却
速度で 400℃まで連続冷却を行い、急冷した。得られた
永久磁石は、磁気特性を測定し、透過電子顕微鏡で微細
組織を観察し、エネルギー分散型X線分析装置で微細組
織のセル内の組成のCuの定量分析を行った。得られた結
果を表1に示す。
EXAMPLES The embodiments of the present invention will be specifically described below with reference to examples, but the present invention is not limited thereto. (Example 1) Alloy composition is Sm25.5% by weight, Fe14% by weight, Cu
The raw material metals were weighed so as to be 4.5% by weight, 3% by weight Zr, and the balance Co, and then melted in a high-frequency melting furnace to produce an alloy ingot. The obtained alloy ingot was coarsely pulverized using a brown mill, and then finely pulverized with a jet mill. The average particle size of the alloy powder after pulverization was about 5 μm. This alloy powder was molded in a magnetic field, and the obtained molded body was sintered at 1,200 ° C and solution-treated at 1,180 ° C. Next, the aging treatment was first holding as aging at 850 ° C. for 2 hours, followed by continuous cooling to 400 ° C. at 5 ° C./min, 1 ° C./min, 0.2 ° C./min, and then rapid cooling. The magnetic properties of the obtained permanent magnet were measured, the fine structure was observed with a transmission electron microscope, and Cu of the composition in the cell of the fine structure was quantitatively analyzed with an energy dispersive X-ray analyzer. The results obtained are shown in Table 1.

【0010】[0010]

【表1】 [Table 1]

【0011】(実施例2)実施例1と同様な条件で燒結
体を作成し、その後次のような時効処理を施した。すな
わち、初段時効として 870℃で1、2、5、10時間保持
した後、1℃/minの冷却速度で 400℃まで連続冷却し急
冷した。得られた永久磁石は、磁気特性を測定し、透過
電子顕微鏡で微細組織を観察し、エネルギー分散型X線
分析装置で微細組織のセル内の組成のCuの定量分析を行
った。得られた結果を表2に示す。
Example 2 A sintered body was prepared under the same conditions as in Example 1 and then subjected to the following aging treatment. That is, as the first stage aging, it was held at 870 ° C for 1, 2, 5 and 10 hours, and then continuously cooled to 400 ° C at a cooling rate of 1 ° C / min and rapidly cooled. The magnetic properties of the obtained permanent magnet were measured, the microstructure was observed with a transmission electron microscope, and Cu of the composition in the cell of the microstructure was quantitatively analyzed with an energy dispersive X-ray analyzer. The obtained results are shown in Table 2.

【0012】[0012]

【表2】 [Table 2]

【0013】(実施例3)実施例1と同様な条件で燒結
体を作製し、その後次のような時効処理を施した。すな
わち、初段時効としてそれぞれ 800℃、850℃、900℃で10
時間保持した後、700℃で1時間、600℃で2時間、500℃
で5時間、400℃で10時間の多段時効を行った。得られた
永久磁石は、磁気特性を測定し、透過電子顕微鏡で微細
組織を観察し、エネルギー分散型X線分析装置で微細組
織のセル内の組成のCuの定量分析を行った。得られた結
果を表3に示す。
(Example 3) A sintered body was produced under the same conditions as in Example 1, and then subjected to the following aging treatment. That is, the first-stage aging is 10 ° C at 800 ° C, 850 ° C, and 900 ° C, respectively.
Hold for 700 hours, 700 ℃ for 1 hour, 600 ℃ for 2 hours, 500 ℃
It was aged for 5 hours at 400 ° C for 10 hours at 400 ° C. The magnetic properties of the obtained permanent magnet were measured, the fine structure was observed with a transmission electron microscope, and Cu of the composition in the cell of the fine structure was quantitatively analyzed with an energy dispersive X-ray analyzer. The results obtained are shown in Table 3.

【0014】[0014]

【表3】 [Table 3]

【0015】[0015]

【発明の効果】本発明によれば、保磁力が 20KOeを超え
るような高特性R2Co17系希土類永久磁石合金を製造する
ことができ、産業上その利用価値は極めて高い。
According to the present invention, it is possible to produce a high-performance R 2 Co 17 type rare earth permanent magnet alloy having a coercive force exceeding 20 KOe, and its industrial utility value is extremely high.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // H01F 7/02 Z ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location // H01F 7/02 Z

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】重量百分率で、24〜28%のR(Rは希土類
元素のうち1種以上)、10〜20%のFe、3〜6%のCu、
2〜4%のZr、残部Coからなり、かつR2Co17相から成
る微細なセル状組織のセル内のCu量が1原子%以上3原
子%以下の範囲内であることを特徴とする希土類永久磁
石合金。
1. In weight percentage, 24-28% R (R is at least one of rare earth elements), 10-20% Fe, 3-6% Cu,
It is characterized in that the Cu content in the cell of the fine cellular structure composed of 2 to 4% of Zr and the balance of Co and of the R 2 Co 17 phase is in the range of 1 atom% or more and 3 atom% or less. Rare earth permanent magnet alloy.
JP4280829A 1992-09-25 1992-09-25 Rare earth permanent magnet alloy Pending JPH06108190A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4280829A JPH06108190A (en) 1992-09-25 1992-09-25 Rare earth permanent magnet alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4280829A JPH06108190A (en) 1992-09-25 1992-09-25 Rare earth permanent magnet alloy

Publications (1)

Publication Number Publication Date
JPH06108190A true JPH06108190A (en) 1994-04-19

Family

ID=17630570

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4280829A Pending JPH06108190A (en) 1992-09-25 1992-09-25 Rare earth permanent magnet alloy

Country Status (1)

Country Link
JP (1) JPH06108190A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003058648A1 (en) * 2001-12-28 2003-07-17 Shin-Etsu Chemical Co., Ltd. Rare earth element sintered magnet and method for producing rare earth element sintered magnet
CN107430915A (en) * 2015-09-15 2017-12-01 株式会社东芝 Permanent magnet and electric rotating machine

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61260610A (en) * 1985-05-15 1986-11-18 Seiko Instr & Electronics Ltd Manufacture of permanent magnet
JPH02104632A (en) * 1988-10-12 1990-04-17 Hitachi Metals Ltd Manufacture of permanent magnetic alloy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61260610A (en) * 1985-05-15 1986-11-18 Seiko Instr & Electronics Ltd Manufacture of permanent magnet
JPH02104632A (en) * 1988-10-12 1990-04-17 Hitachi Metals Ltd Manufacture of permanent magnetic alloy

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003058648A1 (en) * 2001-12-28 2003-07-17 Shin-Etsu Chemical Co., Ltd. Rare earth element sintered magnet and method for producing rare earth element sintered magnet
KR100746897B1 (en) * 2001-12-28 2007-08-07 신에쓰 가가꾸 고교 가부시끼가이샤 Manufacturing method of rare earth sintered magnet and rare earth sintered magnet
KR100788330B1 (en) * 2001-12-28 2007-12-27 신에쓰 가가꾸 고교 가부시끼가이샤 Rare earth element sintered magnet and method for producing rare earth element sintered magnet
US7438768B2 (en) 2001-12-28 2008-10-21 Shin-Etsu Chemical Co., Ltd. Rare earth element sintered magnet and method for producing rare earth element sintered magnet
CN107430915A (en) * 2015-09-15 2017-12-01 株式会社东芝 Permanent magnet and electric rotating machine
EP3352181A4 (en) * 2015-09-15 2019-05-08 Kabushiki Kaisha Toshiba PERMANENT MAGNET, AND ROTATING ELECTRIC MACHINE
US11081264B2 (en) 2015-09-15 2021-08-03 Kabushiki Kaisha Toshiba Permanent magnet and rotary electrical machine

Similar Documents

Publication Publication Date Title
US5110377A (en) Process for producing permanent magnets and products thereof
JP3143156B2 (en) Manufacturing method of rare earth permanent magnet
JP2904667B2 (en) Rare earth permanent magnet alloy
JPH01219143A (en) Sintered permanent magnet material and its production
JPH04245403A (en) Rare earth-fe-co-b-based anisotropic magnet
JPH03129702A (en) Rare-earth-fe-b-based permanent magnet powder and bonded magnet excellent in magnetic anisotropy and corrosion resistance
JP3368295B2 (en) Method for producing anisotropic rare earth alloy powder for permanent magnet
JPS60204862A (en) Rare earth element-iron type permanent magnet alloy
JPS59217304A (en) Permanent magnet material and manufacture thereof
JP3303044B2 (en) Permanent magnet and its manufacturing method
JPH0354805A (en) Rare earth permanent magnet and its manufacturing method
JPH0776708A (en) Production of anisotropic rare earth alloy powder for permanent magnet
JP3126199B2 (en) Manufacturing method of rare earth permanent magnet
JPH06108190A (en) Rare earth permanent magnet alloy
JPH0146575B2 (en)
JP3151265B2 (en) Manufacturing method of rare earth permanent magnet
JPS61264133A (en) Permanent magnet alloy and its manufacture
JP2951491B2 (en) Rare earth permanent magnet alloy
JPH0146574B2 (en)
JPH045739B2 (en)
JPS62181403A (en) Permanent magnet
JPH06124812A (en) Nitride magnet powder and its synthesizing method
JPH045737B2 (en)
JPH06112019A (en) Nitride magnetic material
JPS6119084B2 (en)