JPS60238448A - Permanent magnet containing rare earth element - Google Patents
Permanent magnet containing rare earth elementInfo
- Publication number
- JPS60238448A JPS60238448A JP59095971A JP9597184A JPS60238448A JP S60238448 A JPS60238448 A JP S60238448A JP 59095971 A JP59095971 A JP 59095971A JP 9597184 A JP9597184 A JP 9597184A JP S60238448 A JPS60238448 A JP S60238448A
- Authority
- JP
- Japan
- Prior art keywords
- rare earth
- permanent magnet
- alloy
- magnet
- composition
- 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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- Hard Magnetic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は希土類金属、遷移金属そして半金属もしくは半
導体元素からなる合金より製造される希土類永久磁石に
関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to rare earth permanent magnets manufactured from alloys of rare earth metals, transition metals, and semimetal or semiconductor elements.
現在工業化されている希土類磁石は、Sm0os。 The rare earth magnet currently being industrialized is Sm0os.
Sm(TM)ty (但し、TMは遷移金属を表わす)
、そしてN 6− F e −B糸等である。これらの
磁石に使われている希土類金属線、モナザイト、バスト
ネサイト等の鉱石からイオン交換法や溶媒抽出法を用い
て得られる分離箱出であるため、コストが高くなり、さ
らに多量に使用される分離箱出では供給量に不安を生じ
る等の問題かでてきた。このため一部では低コストの混
合箱金属(ミツシュメタル、以下MMと略す)を用いて
低コスト希土類磁石を開発することが試みられている。Sm(TM)ty (TM represents a transition metal)
, and N6-Fe-B yarn. The rare earth metal wires used in these magnets, monazite, bastnaesite, and other ores are separated and extracted using ion exchange and solvent extraction methods, which increases the cost and requires them to be used in large quantities. Problems have arisen in the separation of boxes, including concerns about the amount of supply. For this reason, some attempts have been made to develop low-cost rare earth magnets using low-cost mixed box metals (Mitsuhmetal, hereinafter abbreviated as MM).
このような希土類成分にMMを使用した磁石のの磁気性
能は、MMOo5で焼結磁石の場合、残留磁束密度(以
下1.i、 Bl rと略す)8100(G)、固有の
保磁力(以下、iHcと略す)9000(Oe)、最大
エネルギー積(以下(B H) maxと略す)14、
5 (M G Oe ) (H、Nagel、H,P、
に1einA工P Conf、Proc 24 695
(L974))等の報告がなされている。しかし、一般
に混合箱出を用いた永久砥石は、磁気性能が低いという
欠点があった。また、比較的高い磁気性能を有している
N d −F e −B糸の磁石はキュリ一点(Tc)
が350(’C)と低いため、実際の使用においてはか
なりの制限をうけている。The magnetic performance of a magnet using MM as the rare earth component is as follows: In the case of a sintered magnet with MMOo5, the residual magnetic flux density (hereinafter referred to as 1.i, abbreviated as Blr) is 8100 (G), and the intrinsic coercive force (hereinafter referred to as , iHc) 9000 (Oe), maximum energy product (hereinafter abbreviated as (B H) max) 14,
5 (M G Oe ) (H, Nagel, H, P,
ni1einA EngineeringP Conf, Proc 24 695
(L974)) etc. have been reported. However, permanent grindstones using a mixed grinder generally have a drawback of low magnetic performance. In addition, the magnet of N d -F e -B thread, which has relatively high magnetic performance, has a Curie point (Tc)
Since the temperature is as low as 350 ('C), there are considerable limitations in actual use.
本発明はこの様な問題点を解決するもので、その目的と
するところは、低コストかつ高性能な永久磁石を開発す
るところにある。The present invention is intended to solve these problems, and its purpose is to develop a low-cost, high-performance permanent magnet.
本発明の永久磁石はL a −Oe −D i (ジジ
ムび該合金中のBの1部をAt、Ga 、工n、Sn、
Pd、Bi、c、Ge、PISの元素群の中の1種また
は2種以上の元素で置換した合金を使用して、焼結法あ
るいは樹脂結合法で製造することを特徴とする。混合希
土金属L a −OB −D iは分離箱出を抽出する
過程で得られるものであり、コスト的には分離箱出にく
らべて非常に安くなり、またL a −Oe −D i
−F e −Co −B系の組成を規定することにより
高い磁気性能が得られ、さらにCOを添加したことによ
りTOの向上が見られた。The permanent magnet of the present invention is made of L a -Oe -D i (didymium and a part of B in the alloy are At, Ga, N, Sn,
It is characterized in that it is manufactured by a sintering method or a resin bonding method using an alloy substituted with one or more elements from the element group Pd, Bi, c, Ge, and PIS. Mixed rare earth metal L a -OB -D i is obtained in the process of extracting separated boxed metals, and the cost is much lower than that of separated boxed metals, and L a -Oe -D i
By specifying the composition of the -Fe-Co-B system, high magnetic performance was obtained, and by adding CO, an improvement in TO was observed.
以下本発明について実施例に基づき詳細に説明する。 The present invention will be described in detail below based on examples.
〈実施例1〉
第1表に示す組成の合金を低周波溶解炉を用いてArガ
ス中で溶解する。<Example 1> An alloy having the composition shown in Table 1 is melted in Ar gas using a low frequency melting furnace.
第1表
該合金は1170℃×10時間溶体化処理、800℃×
4時間時効処理を行ない、その後ボールミルで粉砕し粒
径が2μ濯〜80μ常の微粉末とする。この磁性粉末に
エポキシ樹脂を2.(:3重量%加え混練し、この混合
物を磁場中で圧縮成形する。この成形体を150℃×1
時間加熱して永久磁石を得る。得られた永久磁石の磁気
性能を第2表に示す。第2表より本発明磁石は混合箱出
を使用■ ナー sx シ 11丁tゴ40當「真しz
EH優性台し ル宥 1、て し)ることか判る。Table 1: The alloy was solution treated at 1170°C for 10 hours, and at 800°C.
The material is aged for 4 hours, and then ground in a ball mill to form a fine powder with a particle size of 2 to 80 microns. Add 2. epoxy resin to this magnetic powder. (: 3% by weight is added and kneaded, and this mixture is compression molded in a magnetic field. This molded body is
Get a permanent magnet by heating for a while. The magnetic performance of the obtained permanent magnet is shown in Table 2. From Table 2, the magnet of the present invention uses a mixed box.
It turns out that EH is dominant.
第 2 表
〈実施例2〉
組成式がaeo、asLao、o 6Pro、INdo
、s (Feo、s 9−No□0.41BN)56と
表される系においてNの値を変化させた糸について、実
施例1と同じ方法を用いて永久磁石を製造する。得られ
た永久磁石の磁気性能を第1図に示す。第1図よりnの
値は0.02≦N≦0.2の範囲が望ましいことが判る
。Table 2 <Example 2> Compositional formulas are aeo, asLao, o 6Pro, INdo
, s (Feo, s 9-No□0.41BN) 56, and a permanent magnet is produced using the same method as in Example 1 using yarns in which the value of N is changed. The magnetic performance of the obtained permanent magnet is shown in FIG. It can be seen from FIG. 1 that the value of n is preferably in the range of 0.02≦N≦0.2.
〈実施例6〉
組成式がOeo、35LaO,05Pro、lNa0.
5(?eOJ00oo41BO,Oc+)zと表される
系においてLの値を変化させた系について実施例1と同
じ方法を用いて永久磁石を製造する0この永久磁石の磁
気性能を第、2図に示す。<Example 6> The composition formula is Oeo, 35LaO, 05Pro, lNa0.
5. Manufacture a permanent magnet using the same method as in Example 1 for a system expressed as (?eOJ00oo41BO,Oc+)z in which the value of L is changed.0 The magnetic performance of this permanent magnet is shown in Figure 2. show.
Lの値は4.0≦L≦aOが望ましいと言える。It can be said that the value of L is preferably 4.0≦L≦aO.
〈実施例4〉
組成式がaeo、a 5Lao、o 5Pro、INd
o、s (Fe0.91−MCOMBo、09)56と
表される糸においてMの値を変えた合金のT cを第6
図に示す。COを添加することによりTcは向上してい
るが、M>0.8以上ではコスト的な曲で不利となるの
で、Mの値は0.1部M≦0゜8の範囲が望ましい。<Example 4> Composition formula is aeo, a5Lao, o5Pro, INd
o, s (Fe0.91-MCOMBo, 09) 56
As shown in the figure. Although Tc is improved by adding CO, if M>0.8 or more, it becomes disadvantageous in terms of cost, so the value of M is preferably in the range of 0.1 part M≦0°8.
〈実施例5〉
第6表に示す組成の合金を実施例1と同じ方法を用いて
永久磁石を製造する。この永久磁石の磁気性能を第4表
に示す。<Example 5> A permanent magnet is manufactured using the same method as in Example 1 using an alloy having the composition shown in Table 6. The magnetic performance of this permanent magnet is shown in Table 4.
第3表
第4表よりBの1部をAt、oa;工n、Sn、−Pd
、Bi、Si、C,Ge、P、Sの各元素で置換しても
良好な磁気性能を得ることが判る。From Table 3 and Table 4, a part of B is At, oa; Eng, Sn, -Pd
, Bi, Si, C, Ge, P, and S, good magnetic performance can be obtained.
第4表
〈実施例6〉
実施例1および5の中の試料N[L 1および7の組成
の合金について低周波醪解炉を用いてArガス中で溶解
する。該合金をボールミルで粒径2μ恒〜5μmの微粉
末にする。この粉末を磁場中で圧縮成形し、その成形体
を1200℃×1時間焼結後1170°CX2時間溶体
化処理を行ない急冷し、さらに800℃×4時間時効処
理して永久磁石を得る。この永久磁石の磁気性能を第5
表に示す本発朗磁石は焼結法で製造した場合、SmCO
5の焼結磁石に匹敵する磁気性能を有している。Table 4 (Example 6) Sample N[L in Examples 1 and 5 Alloys having compositions 1 and 7 are melted in Ar gas using a low frequency melting furnace. The alloy is made into a fine powder with a particle size of 2 μm to 5 μm using a ball mill. This powder is compression molded in a magnetic field, and the compact is sintered at 1200° C. for 1 hour, then solution treated at 1170° C. for 2 hours, rapidly cooled, and further aged at 800° C. for 4 hours to obtain a permanent magnet. The magnetic performance of this permanent magnet is the fifth
When the magnets shown in the table are produced by the sintering method, SmCO
It has magnetic performance comparable to No. 5 sintered magnet.
〈実施例7〉
試料Nα1,7の組成の合金について実施例1と同じ方
法で粒径2μm〜80μ情の粉末をつくる。この粉末を
樹脂と混練して押出成形機および射出成形機でにより磁
場中で成形する。第6表に成形条件、第7表に得られた
永久磁石の磁気性能を示す。<Example 7> Powder having a particle size of 2 μm to 80 μm is prepared using the same method as in Example 1 for alloys having the compositions of samples Nα1 and 7. This powder is kneaded with a resin and molded in a magnetic field using an extrusion molding machine and an injection molding machine. Table 6 shows the molding conditions, and Table 7 shows the magnetic performance of the obtained permanent magnets.
第6表
〔効果〕
以上述べてきたように本発明によれば、高性能希土類永
久磁石を廉価で供給することが可能となるため、産業界
に及ぼす効果は大きいと言える。Table 6 [Effects] As described above, according to the present invention, it is possible to supply high-performance rare earth permanent magnets at a low price, so it can be said that the present invention has a great effect on the industrial world.
第1図はBの量と磁気性能の関係を表すグラフ第2図は
Lの値を変えたときの磁石の磁気性能を表したグラフ。
第6図はCOの量とTcの増加値との関係を表すグラフ
。
以 上
出願人 株式会社諏訪精工舎
代理人 弁理士 最上 務
0 0.05 0.j O,150,2N Q→
第1図
Lイ直 →
第2図Figure 1 is a graph showing the relationship between the amount of B and magnetic performance. Figure 2 is a graph showing the magnetic performance of a magnet when the value of L is changed. FIG. 6 is a graph showing the relationship between the amount of CO and the increase in Tc. Applicant Suwa Seikosha Co., Ltd. Agent Patent Attorney Tsutomu Mogami 0 0.05 0. j O, 150, 2N Q → Figure 1 L straight → Figure 2
Claims (2)
z(Fet−M−NooMBN)L l (但しX、Y
、Z、L、M、Nはそれぞれ下記の範囲にある。) 0〈x≦o、 1 0.1≦Y≦0.5 0.1≦2≦0,85 40≦L≦a0 0.1部M≦0.8 002≦N≦0.2 ’ o(1−x−y−Z≦80 で表される組成の合金からなることを特徴とする希土類
永久磁石。(1) Atomic ratio eel-X-Y-Z LaxPryNd
z(Fet-M-NooMBN) L l (However, X, Y
, Z, L, M, and N are each in the following ranges. ) 0〈x≦o, 1 0.1≦Y≦0.5 0.1≦2≦0,85 40≦L≦a0 0.1 part M≦0.8 002≦N≦0.2 ' o( A rare earth permanent magnet characterized by being made of an alloy having a composition expressed as 1-x-y-Z≦80.
i、Si、O,Ge、P、Sの元素群のうちの1種また
は2種以上の元素で置換したことを特徴とする特許請求
の範囲第1項記載の希土類永久磁石。(2) Part of B is At, Ga, N, Sm, Pd, B
2. The rare earth permanent magnet according to claim 1, wherein the rare earth permanent magnet is substituted with one or more elements from the element group consisting of i, Si, O, Ge, P, and S.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59095971A JPH066776B2 (en) | 1984-05-14 | 1984-05-14 | Rare earth permanent magnet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59095971A JPH066776B2 (en) | 1984-05-14 | 1984-05-14 | Rare earth permanent magnet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60238448A true JPS60238448A (en) | 1985-11-27 |
JPH066776B2 JPH066776B2 (en) | 1994-01-26 |
Family
ID=14152067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59095971A Expired - Lifetime JPH066776B2 (en) | 1984-05-14 | 1984-05-14 | Rare earth permanent magnet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH066776B2 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61159709A (en) * | 1985-09-17 | 1986-07-19 | Kaneo Mori | Permanent magnet |
JPS61159708A (en) * | 1984-12-31 | 1986-07-19 | Kaneo Mori | Permanent magnet |
JPS61174364A (en) * | 1985-09-17 | 1986-08-06 | Mori Kaneo | Permanent magnet |
US4935075A (en) * | 1986-06-12 | 1990-06-19 | Kabushiki Kaisha Toshiba | Permanent magnet |
US4954186A (en) * | 1986-05-30 | 1990-09-04 | Union Oil Company Of California | Rear earth-iron-boron permanent magnets containing aluminum |
JPH0722227A (en) * | 1993-11-08 | 1995-01-24 | Toshiba Corp | Production of permanent magnet |
USRE34838E (en) * | 1984-12-31 | 1995-01-31 | Tdk Corporation | Permanent magnet and method for producing same |
EP3324417A1 (en) * | 2016-11-17 | 2018-05-23 | Toyota Jidosha Kabushiki Kaisha | Rare earth magnet |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6361089B2 (en) | 2013-04-22 | 2018-07-25 | Tdk株式会社 | R-T-B sintered magnet |
JP5370609B1 (en) | 2013-04-25 | 2013-12-18 | Tdk株式会社 | R-T-B permanent magnet |
JP5565497B1 (en) | 2013-04-25 | 2014-08-06 | Tdk株式会社 | R-T-B permanent magnet |
JP5565498B1 (en) | 2013-04-25 | 2014-08-06 | Tdk株式会社 | R-T-B permanent magnet |
JP5565499B1 (en) | 2013-04-25 | 2014-08-06 | Tdk株式会社 | R-T-B permanent magnet |
-
1984
- 1984-05-14 JP JP59095971A patent/JPH066776B2/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61159708A (en) * | 1984-12-31 | 1986-07-19 | Kaneo Mori | Permanent magnet |
USRE34838E (en) * | 1984-12-31 | 1995-01-31 | Tdk Corporation | Permanent magnet and method for producing same |
JPS61159709A (en) * | 1985-09-17 | 1986-07-19 | Kaneo Mori | Permanent magnet |
JPS61174364A (en) * | 1985-09-17 | 1986-08-06 | Mori Kaneo | Permanent magnet |
US4954186A (en) * | 1986-05-30 | 1990-09-04 | Union Oil Company Of California | Rear earth-iron-boron permanent magnets containing aluminum |
US4935075A (en) * | 1986-06-12 | 1990-06-19 | Kabushiki Kaisha Toshiba | Permanent magnet |
JPH0722227A (en) * | 1993-11-08 | 1995-01-24 | Toshiba Corp | Production of permanent magnet |
EP3324417A1 (en) * | 2016-11-17 | 2018-05-23 | Toyota Jidosha Kabushiki Kaisha | Rare earth magnet |
Also Published As
Publication number | Publication date |
---|---|
JPH066776B2 (en) | 1994-01-26 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |