JPS6036633A - Production of magnet consisting of rare earth cobalt - Google Patents
Production of magnet consisting of rare earth cobaltInfo
- Publication number
- JPS6036633A JPS6036633A JP58144581A JP14458183A JPS6036633A JP S6036633 A JPS6036633 A JP S6036633A JP 58144581 A JP58144581 A JP 58144581A JP 14458183 A JP14458183 A JP 14458183A JP S6036633 A JPS6036633 A JP S6036633A
- Authority
- JP
- Japan
- Prior art keywords
- rare earth
- less
- production
- cooling rate
- earth cobalt
- 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.)
- Granted
Links
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- Powder Metallurgy (AREA)
- Hard Magnetic Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は希土類コバルト磁石の製造方法、特にR2T1
7系磁石合金を粉末冶金法によって製造する時の磁石特
性の改善に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing rare earth cobalt magnets, particularly R2T1
This invention relates to improvement of magnetic properties when manufacturing a 7-series magnetic alloy by powder metallurgy.
本発明は高性能磁気特性を有する永久磁石材料が容易に
得られる新規かつ改良された希−L類コバルト磁石の製
造方法に関するもので、これはR2Tj7系磁石合金を
粉末冶金法により製造するにあたって、Rを22.5〜
27.5wt%、 Feを15.0〜23.Owt%、
Cuを3.3〜5゜3wt%、 Zrを1.5〜3.
5wt%、 Coを残部とする合金を成形し1170℃
以上で焼結した後、降温速度150℃/H以下で113
0℃〜1200℃まで降温し、溶体化処理を行なった後
、600〜950℃で02〜60時間保持した後、30
0℃/H以下の冷却速度で500℃以下まで冷却するこ
とを特徴とするものである。The present invention relates to a new and improved method for manufacturing rare-L class cobalt magnets that allows permanent magnet materials with high performance magnetic properties to be easily obtained. R from 22.5
27.5 wt%, Fe 15.0 to 23. Owt%,
Cu: 3.3-5°3wt%, Zr: 1.5-3.
An alloy containing 5 wt% and Co as the balance was formed and heated to 1170°C.
After sintering with the above, 113
After lowering the temperature to 0°C to 1200°C and performing solution treatment, it was held at 600 to 950°C for 02 to 60 hours, and then
It is characterized by cooling to 500°C or less at a cooling rate of 0°C/H or less.
これを説明すると1本発明は希土類コバルト磁石につい
て、よりすぐれた磁気特性を有する永久磁石を得るため
に種々研究の結果、上記した様な限定された製造条件、
特には特定された熱処理条件を採用することに、J−っ
て、従来不可能とされていた高性能永久磁石が得られる
ことを見出し本発明を完成するに至ったのであり。To explain this, the present invention is based on various researches on rare earth cobalt magnets in order to obtain permanent magnets with better magnetic properties.
In particular, they discovered that by employing specified heat treatment conditions, a high-performance permanent magnet, which was previously considered impossible, could be obtained, leading to the completion of the present invention.
事実」−記した本発明の方法によれば29.5MGOe
に達する最大エイ・ルギー積を有する永久磁石が容易に
得られるというすぐれた効果が与えられる。Fact” - According to the method of the invention described, 29.5 MGOe
The advantageous effect is that permanent magnets with a maximum A-Lugie product reaching .
これをさらに詳細に説明すると、まず熱処理条件、特に
その温度は厳密に制御する必要がある。To explain this in more detail, first, the heat treatment conditions, especially the temperature, need to be strictly controlled.
まず焼結工程であるが、これは1170℃以上。First is the sintering process, which is over 1170°C.
好ましくは1170℃〜1230℃の範囲内で行なう必
要があり、焼結温度がこれよりも低いときは残留磁化が
低1;シ、高いときは残留磁化が大きくなるが保磁力お
よび履歴曲線の角型性が低下するなどの欠点を生じる。It is necessary to perform the sintering preferably within the range of 1170°C to 1230°C, and when the sintering temperature is lower than this, the residual magnetization is low (1); when it is high, the residual magnetization is large, but the coercive force and the angle of the hysteresis curve are This results in disadvantages such as reduced moldability.
なお、焼結工程(以後の熱処理工程も同様であるが)は
真空中もしくはアルゴンなどの不活性ガス雰囲気中で行
うことが必要であることばいうまでもないことである。It goes without saying that the sintering process (the same applies to the subsequent heat treatment process) must be performed in a vacuum or in an inert gas atmosphere such as argon.
焼結工程を終った成型物は9次に冷却工程に入るが2本
発明においてはこの冷却速度も又正確に制御されるべき
重要なファクターであって。After the sintering process, the molded product enters the ninth cooling process, and in the present invention, the cooling rate is also an important factor that must be accurately controlled.
降温速度150℃/H以下で1130℃〜1200℃ま
で降温し、溶体化処理を行なった後、600〜950℃
で0.2〜60時間保持した後、300℃/H以下の冷
却速度で500℃以下まで冷却する。冷却速度が上記よ
りも速くなると保磁力および残留磁束密度さらには最大
エネルギー積が低下する。The temperature is lowered to 1130°C to 1200°C at a cooling rate of 150°C/H or less, and after solution treatment, the temperature is reduced to 600°C to 950°C.
After holding for 0.2 to 60 hours, the temperature is cooled to 500°C or less at a cooling rate of 300°C/H or less. When the cooling rate is faster than the above, the coercive force and residual magnetic flux density as well as the maximum energy product decrease.
次に5本発明の実施例を挙げるが、これは本発明を限定
するものではない。Next, five examples of the present invention will be listed, but these are not intended to limit the present invention.
〈実施例1〉
Smが22.0〜28.0 wt%、Feが15.0〜
24.0wt%、 Cuが3.0〜5.0 wt%、
Zrが1.5〜3.5wt%、残部coとなる様に、ア
ルゴン雰囲気中で。<Example 1> Sm is 22.0-28.0 wt%, Fe is 15.0-28.0 wt%
24.0 wt%, Cu 3.0 to 5.0 wt%,
In an argon atmosphere such that Zr was 1.5 to 3.5 wt% and the balance was co.
高周波加熱によりR2Tj7系合金を溶解した。The R2Tj7 alloy was melted by high frequency heating.
この合金を粗粉砕した後、ボールミルを用いて、平均粒
径約47zmに微粉砕した。この粉末な 3−
ト
10KOeの磁界中1pan/caの圧力で成形した。This alloy was coarsely ground and then finely ground to an average particle size of about 47 zm using a ball mill. This powder was molded at a pressure of 1 pan/ca in a magnetic field of 10 KOe.
成形物をAr雰囲気中、1j70℃〜1260℃で焼結
した後、1130℃〜1200℃で溶体化処理を行なっ
た。After sintering the molded product at 1j70°C to 1260°C in an Ar atmosphere, solution treatment was performed at 1130°C to 1200°C.
次にこの試料を600〜950℃で0,2〜50時間保
持した後、5℃/min以下の冷却速度で500℃以下
まで冷却した。Next, this sample was held at 600 to 950°C for 0.2 to 50 hours, and then cooled to 500°C or less at a cooling rate of 5°C/min or less.
この試料の組成と磁気特性を第1図、第2図。Figures 1 and 2 show the composition and magnetic properties of this sample.
第5図、第4図に示す。第1図はSm22.0〜28.
0wt%、Fe19.0wt%、Cu4.5wt%、
Zr 2.6wt%、残部coである。第2図はSm2
6.0wt%。It is shown in FIGS. 5 and 4. Figure 1 shows Sm22.0-28.
0wt%, Fe19.0wt%, Cu4.5wt%,
Zr: 2.6 wt%, balance: co. Figure 2 shows Sm2
6.0wt%.
Fe 15.0〜24.Owt 、 Ou 4.8 w
t%、Zr2゜4wt%。Fe 15.0-24. Owt, Ou 4.8w
t%, Zr2゜4wt%.
残部COである。第6図はSm26.3wt%、Fe2
O,5wt%、 Ou 3.0〜5.Owt%、 Zr
2.5wt%、残部COである。第4図はSm26.2
wt%、Fej9.5wt%。The remainder is CO. Figure 6 shows Sm26.3wt%, Fe2
O, 5wt%, Ou 3.0-5. Owt%, Zr
2.5 wt%, balance CO. Figure 4 shows Sm26.2
wt%, Fej9.5wt%.
Cu 4.9 wt%、 Zr 1.5−3.5wt%
、残部coである。Cu 4.9 wt%, Zr 1.5-3.5 wt%
, the remainder is co.
第1図に関しては希土類金属のRとしてSmを使用した
場合、その量が28%以上ではBrおよびHeが低下し
、従って(BH)maxも低下する。Regarding FIG. 1, when Sm is used as the rare earth metal R, if the amount is 28% or more, Br and He decrease, and therefore (BH)max also decreases.
第2図に関してはFe含有量が23%よりも多= 4−
くなると保磁力が低下しくBH)maxも急激に低下す
る。Regarding FIG. 2, when the Fe content becomes more than 23% = 4-, the coercive force decreases and BH)max also decreases rapidly.
第6図に関してはCu量は6.3%以下ではHeが低下
し5%以上とするとBrが低下してしまう。Regarding FIG. 6, if the Cu amount is less than 6.3%, He will decrease, and if it is more than 5%, Br will decrease.
第4図に関してはZrの含有量が1.5〜3.5wt%
の範囲を越えるどBrおよびエネルギー積(BH)ma
xが低下してしまう。Regarding Figure 4, the Zr content is 1.5 to 3.5 wt%.
Br and energy product (BH)ma exceeds the range of
x will decrease.
〈実施例2〉
Smが26.0wt%、 Feが19.2wt%、Cu
が4.7wt%、 Zrが2.4wt%、 Co残部な
る合金を実施例1と同様にして溶解、粉砕、磁場成形し
た。<Example 2> Sm is 26.0 wt%, Fe is 19.2 wt%, Cu
An alloy consisting of 4.7 wt% Zr, 2.4 wt% Zr, and the balance Co was melted, pulverized, and magnetically formed in the same manner as in Example 1.
この成形体をAr雰囲気中、1215℃で1時間焼結し
た後、降温速度50〜200℃/Hで1180℃まで冷
却し溶体化処理した。溶体化処理の終了は、焼結温度か
らの降温開始より1時間後とした。This molded body was sintered at 1215° C. for 1 hour in an Ar atmosphere, and then cooled to 1180° C. at a cooling rate of 50 to 200° C./H to undergo solution treatment. The solution treatment was completed one hour after the temperature started to decrease from the sintering temperature.
この試料を850℃で5時間保持した後、300℃/H
以下の冷却速度で500℃以下まで冷却した。After holding this sample at 850℃ for 5 hours, 300℃/H
It was cooled to 500°C or less at the following cooling rate.
その磁気特性を第5図に示す。Its magnetic properties are shown in FIG.
降温速度は第5図に示す通り150℃/Hr以上となる
と保磁力及び最大エネルギー積(BH)maxが低下し
てしまう。As shown in FIG. 5, when the temperature decreasing rate is 150° C./Hr or more, the coercive force and the maximum energy product (BH) max decrease.
以上の如く本発明はR2T17系磁石合金(ここでRは
イツトリウム及び精工類元素、Tは遷移金属を表わす。As described above, the present invention relates to an R2T17-based magnet alloy (where R represents yttrium and a refined element, and T represents a transition metal).
)を粉末冶金法により製造するにあたって、Rを22.
5〜27.5wt%、Feを15,0〜23.Owt%
+ 011を3.3〜5.[] wt%、 Zrを1.
5〜3.5wt%、 Coを残部とする合金を成形し1
170℃以」二で焼結した後、降温速度150℃/H以
下で1160℃〜1200℃まで降温し、溶体化処理を
行なった後、600〜950℃で0.2〜30時間保持
した後、300℃/H以下の冷却速度で500℃以下ま
で冷却することにより高い保磁力を得ることができ、そ
の結果高エネルギー積が得られるという優れた効果を有
している。) by powder metallurgy, R is 22.
5-27.5 wt%, Fe 15.0-23. Owt%
+011 from 3.3 to 5. []wt%, Zr 1.
An alloy containing 5 to 3.5 wt% Co as the balance was formed into 1
After sintering at 170°C or higher, the temperature was lowered to 1160°C to 1200°C at a cooling rate of 150°C/H or lower, and solution treatment was performed, followed by holding at 600°C to 950°C for 0.2 to 30 hours. By cooling to 500°C or less at a cooling rate of 300°C/H or less, a high coercive force can be obtained, and as a result, it has the excellent effect of obtaining a high energy product.
第1図から第4図は、実施例1における異なる組成の磁
石特性をそれぞれ示す図、第5図は。
実施例2の磁石特性を示す図である。
第1図
第2図
Fe (wt、%)
第3図
Cμ(wt′yo)
第4図
Zy(wt%)
降温 迷 度 (0C/Hr)1 to 4 are diagrams showing the characteristics of magnets with different compositions in Example 1, and FIG. 5 is a diagram showing the characteristics of magnets of different compositions in Example 1. 3 is a diagram showing magnet characteristics of Example 2. FIG. Fig. 1 Fig. 2 Fe (wt, %) Fig. 3 Cμ (wt'yo) Fig. 4 Zy (wt%) Temperature fall Stray degree (0C/Hr)
Claims (1)
及び希土類元素、Tは遷移金属を表わす。)を粉末冶金
法により製造するにあたって、Rを22.5〜27.5
wt%、 Feを15.0〜23.0 wt%。 Ouを3.3〜5.Owt%、 Zrを1.5〜3.5
wt%、 C。 を残部とする合金粉末を成形し、1170℃以上で焼結
した後、降温速度150℃/H以下で1130℃〜12
00℃まで降温し、溶体化処理を行なった後、600〜
950℃で0.2〜30時間保持した後、600℃/H
以下の冷却速度で500℃以下まで冷却することを特徴
とする希土類コバルト磁石の製造方法。 以下余白[Claims] 1. In producing an R2T17-based magnetic alloy (where R represents yttrium and a rare earth element, and T represents a transition metal) by a powder metallurgy method, R is set to 22.5 to 27.5.
wt%, Fe from 15.0 to 23.0 wt%. Ou from 3.3 to 5. Owt%, Zr 1.5-3.5
wt%, C. After molding the alloy powder with the remainder as
After cooling down to 00℃ and performing solution treatment,
After holding at 950℃ for 0.2 to 30 hours, 600℃/H
A method for producing a rare earth cobalt magnet, characterized by cooling to 500°C or less at the following cooling rate. Margin below
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58144581A JPS6036633A (en) | 1983-08-08 | 1983-08-08 | Production of magnet consisting of rare earth cobalt |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58144581A JPS6036633A (en) | 1983-08-08 | 1983-08-08 | Production of magnet consisting of rare earth cobalt |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6036633A true JPS6036633A (en) | 1985-02-25 |
| JPS6358898B2 JPS6358898B2 (en) | 1988-11-17 |
Family
ID=15365460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58144581A Granted JPS6036633A (en) | 1983-08-08 | 1983-08-08 | Production of magnet consisting of rare earth cobalt |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6036633A (en) |
-
1983
- 1983-08-08 JP JP58144581A patent/JPS6036633A/en active Granted
Non-Patent Citations (2)
| Title |
|---|
| IEEE TRANSACTIONS ON MAGNETICS=1977 * |
| MICROSTRUCTURE AND PROPERTIES OF STEP AGED RARE EARTH ALLOY MAGNETS=1981 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6358898B2 (en) | 1988-11-17 |
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