JPS60184661A - Material for permanent magnet - Google Patents
Material for permanent magnetInfo
- Publication number
- JPS60184661A JPS60184661A JP59039054A JP3905484A JPS60184661A JP S60184661 A JPS60184661 A JP S60184661A JP 59039054 A JP59039054 A JP 59039054A JP 3905484 A JP3905484 A JP 3905484A JP S60184661 A JPS60184661 A JP S60184661A
- Authority
- JP
- Japan
- Prior art keywords
- permanent magnet
- alloy
- rare earth
- earth element
- saturation magnetization
- 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
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は希土類元素を含有する新規な永久磁石用材料に
関するものである。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to a novel permanent magnet material containing rare earth elements.
これまでに希土類元素と遷移金属元素からなる合金系に
関して数多くの研究がなされてお勺、その中でも希土類
元素■とCo よりなる合金系が今日実用材料となって
いる。具体的にはRCOII系ならびにCu添加几IC
017系合金である。Many studies have been carried out on alloy systems consisting of rare earth elements and transition metal elements, and among these, alloy systems consisting of rare earth elements (1) and Co2 have become practical materials today. Specifically, RCOII system and Cu-added IC
It is a 017 series alloy.
一方遷移金属元素としてCOより資源的に豊富で安価な
Fe と希土類元素からなる化合物又は合金系について
は、これまでいくつかの研究がなされているが、得られ
た基本物性値からは磁石材料としての可能性が否定され
ていた。On the other hand, several studies have been conducted on compounds or alloys consisting of rare earth elements and Fe, which is more abundant and cheaper than CO as a transition metal element. possibility had been denied.
例えばRFC,〜几sF’eiy系合金において最高の
キューリ一点としても187℃(Gd* F’e17が
該当)しか示さず、又1軸結晶異方性として大きな値を
示す物質も見出されていす、従って実用永久磁石材料と
しての可能性はないとされていた。For example, the highest Curie point in the RFC, ~ sF'eiy series alloys is only 187°C (Gd*F'e17 corresponds), and some materials have also been found that exhibit large values for uniaxial crystal anisotropy. Therefore, it was considered that there was no possibility of it being used as a practical permanent magnet material.
ところが、近年R−re−X系においてXとしてボ四ン
0を添加することによって飽和磁化(4xIs )が高
くかつ異方性磁場(HA)およびキューリ一温度(Tc
)が改良されることが見出され磁石材料となりつつある
。However, in recent years, the addition of boron 0 as
) has been found to be improved and is becoming used as a magnetic material.
この几−Fe−B系磁石合金は、約10KG以上の高い
飽和磁化を有しかつ高い異方性磁場およびキューリ一温
度を有する。This Fe-B-based magnet alloy has a high saturation magnetization of about 10 KG or more, a high anisotropic magnetic field, and a Curie temperature.
父上配合−金系にCOを添加した場合にはTcをさらに
上昇し温度特性を改良しうる。Father blend - When CO is added to the gold system, the Tc can be further increased and the temperature characteristics improved.
本発明は永久磁石材料としての可能性を一層拡大するた
め、上述の合金系にさら[Agを添加することにより、
几−Fe−B系および几−Fe−Co−B系の改良を図
ったことを特徴とするものである。In order to further expand the possibilities as a permanent magnet material, the present invention further expands the possibilities as a permanent magnet material by adding [Ag] to the above-mentioned alloy system.
It is characterized by an improvement of the phosphorus-Fe-B system and the phosphorus-Fe-Co-B system.
すなわち本発明は、几−Fe−B−Agおよび11.−
Fe−B−Co−Ag系に関するものであり、組成式で
表現すれば
ψ R(BxAgyFex −x−y)A二(イ旦し、
几はYを含む希土類元素La、、 Ce、 Pr、 N
d、 8mの1種又は2種以上の組合せ)Q、(1≦X
≦0.5.α01≦y≦0.3.4≦A≦16
■ R・(BxAg”yCOzF el−x−y−z
)A : (但し、itはYを含む希土類元素La1C
e+ P re Ndt Smの1種又は2種以上の組
合せ)0.01≦X≦0.3゜0.01≦y≦0.5,
0.01≦z(0,98,4≦A≦16なる組成を有す
ることを特徴とするものである。That is, the present invention provides 几-Fe-B-Ag and 11. −
It is related to the Fe-B-Co-Ag system, and if expressed as a composition formula, ψ R(BxAgyFex -x-y)A2(Itanshi,
几 is a rare earth element containing Y La, Ce, Pr, N
d, 8m (one type or combination of two or more types) Q, (1≦X
≦0.5. α01≦y≦0.3.4≦A≦16 ■ R・(BxAg”yCOzF el-x-y-z
)A: (However, it is a rare earth element La1C containing Y.
one type or combination of two or more types of e+ P re Ndt Sm) 0.01≦X≦0.3゜0.01≦y≦0.5,
It is characterized by having a composition of 0.01≦z (0,98, 4≦A≦16).
このようなAgの添加は異方性磁場および飽和磁化を改
良し、より充分な磁石材料となりえる事を見出したもの
である。これらの組成合金は、高周波溶解、アーク溶解
等で得た溶湯を金型等に鋳込んで作成したもので結晶質
の合金である。It has been discovered that such addition of Ag improves the anisotropic magnetic field and saturation magnetization, making it possible to provide a more satisfactory magnetic material. These compositional alloys are crystalline alloys made by casting molten metal obtained by high-frequency melting, arc melting, etc. into a mold or the like.
本発明において個々の成分および成分量範囲を限定した
理由は下記の通りである。すなわちB景(X)が0.0
1以下となると異方性磁界が小さくなる。又B量が0.
3以上になると飽和磁化の大きさが低下する。このため
、B量:は0.01≦X≦0.5となるが、好ましくは
0,02≦X≦α2#より好ましくは0.02≦x(0
,15となるとより良好な特性を示すようKなる。この
よりなりとしてはフェロボロンをもちいてもよい。又A
g1(Y)がα3以上となると飽和磁化の大きさが低下
する。又Ag1ftが0.01以下となると、磁気特性
に関し、添加効果がなくなる。このため、Ag量は[L
01≦y≦0,3となるが、好ましくはα01≦y≦(
L2゜よシ好ましくは0.01≦y≦[115となると
より良好な特性を示すようになる。COの添加は必ずし
も必要ではないが、COの添加によりキューリ一温度が
上昇する。COの添加駄(z)が0.1以上、好ましく
は0.05以上となるとより良好となる。又2が0.9
8以上となると飽和磁化の大きさが低下する。このため
2はα01≦z(0,98となるが好ましくは0.05
≦2≦0.95、より好ましくはα05(z(0,6と
なる。一方(13+Ag−1−Fe ) あるいは(B
+Ag+Fe+Co) hlとR(#、のモル比(Z)
について4≦2≦16とした理由は、モル比2が4以下
になると飽和磁化の強さが低下し、モル比2が16より
も大きくなると異方性磁界の大きさが低下してしまう。The reasons for limiting the individual components and component amount ranges in the present invention are as follows. In other words, B view (X) is 0.0
When it is less than 1, the anisotropic magnetic field becomes small. Also, the amount of B is 0.
When it becomes 3 or more, the magnitude of saturation magnetization decreases. Therefore, the amount of B: is 0.01≦X≦0.5, preferably 0.02≦X≦α2#, more preferably 0.02≦x(0
, 15, K shows better characteristics. Ferroboron may be used as this material. Also A
When g1(Y) becomes α3 or more, the magnitude of saturation magnetization decreases. Further, when Ag1ft is less than 0.01, the addition effect disappears in terms of magnetic properties. Therefore, the amount of Ag is [L
01≦y≦0,3, but preferably α01≦y≦(
If L2° is preferably 0.01≦y≦[115, better characteristics will be exhibited. Although the addition of CO is not necessary, the addition of CO increases the Curie temperature. It will be better if the CO addition value (z) is 0.1 or more, preferably 0.05 or more. Also 2 is 0.9
When the value is 8 or more, the magnitude of saturation magnetization decreases. Therefore, 2 becomes α01≦z (0.98, but preferably 0.05
≦2≦0.95, more preferably α05(z(0,6. On the other hand, (13+Ag-1-Fe) or (B
+Ag+Fe+Co) molar ratio (Z) of hl and R(#)
The reason for setting 4≦2≦16 is that when the molar ratio 2 becomes 4 or less, the strength of saturation magnetization decreases, and when the molar ratio 2 exceeds 16, the magnitude of the anisotropic magnetic field decreases.
この場合、好ましくは5≦2≦14より好ましくは5≦
2≦12になると異方性磁場および飽和磁化の大きさと
してより高い値を得ることができる。In this case, preferably 5≦2≦14, more preferably 5≦
When 2≦12, higher values of the anisotropic magnetic field and saturation magnetization can be obtained.
以下実施例について示す。Examples will be shown below.
実施例j Nd (Bo、osAgoloFeo、52
)s の合金を作成し、物性値としてHAについて測定
した結果、約60KOeであった。1方比較例としてN
d (BonsFe o、oz)gおよびNdFea
合金を作成し同様に測定した。Nd (B o、os
P e O,92) s合金は50KOeであり、Nd
Fe5 合金はHAとしては殆んど1軸韮方性は示さな
かった。Example j Nd (Bo, osAgoloFeo, 52
)s alloy was prepared and the physical property value of HA was measured, and the result was about 60 KOe. As a comparison example, N
d(BonsFe o,oz)g and NdFea
An alloy was prepared and measured in the same manner. Nd (Bo, os
P e O,92)s alloy is 50KOe, Nd
Fe5 alloy showed almost no uniaxial chirotropy as HA.
又Agを添加した合金は無添加合金に比べて約7チの飽
和磁化の増加を示しだ。The alloy with added Ag also showed an increase in saturation magnetization of about 7 cm compared to the alloy without the addition of Ag.
この結果よりAgを含む合金は、R−Fe−BおよびI
L−Fe系と比べて良好な特性を有する事がわかる。From this result, alloys containing Ag are R-Fe-B and I
It can be seen that it has better characteristics compared to the L-Fe type.
実施例2 実施例1と同様にNd (Bo、osAgo
、oy■ゝe o、ss ) sおよびNd (Bo、
osAgo、x2Feo、sc+)s 合金を作成した
。実施例1とほぼ同様にAg添加効果が認められた。Example 2 As in Example 1, Nd (Bo, osAgo
,oy■ゝe o,ss)s and Nd(Bo,
osAgo, x2Feo, sc+)s alloys were created. Almost the same effect as in Example 1, the effect of adding Ag was observed.
実施例5 Nd(Bo、o<Ago、xoFeo、sJ
s の合金を作成し、物性値としてHAについて測定し
た結果、約52KOeであった。1方比較例としてNd
(B O,04F e o、ms ) aおよびN
d F e a合金を作成し同様に測定した。Nd (
Bo、osFe 0J2)+!金合金25KOeであり
、NdFe5合金はf(Aとしては殆んど1 itl+
異方性は示さなかった。Example 5 Nd(Bo, o<Ago, xoFeo, sJ
An alloy of s was prepared and HA was measured as a physical property value, and the result was about 52 KOe. As a comparative example, Nd
(BO,04F e o,ms) a and N
A dFe alloy was prepared and measured in the same manner. Nd (
Bo, osFe 0J2)+! The gold alloy is 25KOe, and the NdFe5 alloy is f (almost 1 itl+ as A).
It showed no anisotropy.
又Agを添加した合金は無添加合金に比べて約40チの
飽和磁化の上昇を示した。Furthermore, the alloy to which Ag was added showed an increase in saturation magnetization of about 40 mm compared to the alloy without the addition of Ag.
この結果よりAgを含む合金は、几−Fe−Hおよび几
−Fe系と比べて良好な特性を有する事がわかる。This result shows that the alloy containing Ag has better characteristics than the phosphor-Fe-H and phosphor-Fe systems.
実施例4 実施例5と同様にNd (B o、oa A
g o、oaP e o、so ) aおよびNd (
Bo、04 Ago、os Fe ons) s合金を
作成した。実施例1とはげ同様にAg添加効果が認めら
れた。Example 4 Similar to Example 5, Nd (B o, oa A
go, oaP eo, so) a and Nd (
Bo, 04 Ago, os Fe ons) s alloys were created. Similar to Example 1 and baldness, the effect of adding Ag was observed.
実施例5 Nd(Bo、osAgo、toCOo、ts
Feo、gy)s、sの合金を作成し、物性値としてH
Aについて測定した結果、約65KOeであった。Example 5 Nd(Bo, osAgo, toCOo, ts
An alloy of Feo, gy)s, s was created, and the physical properties were H
The measurement result for A was approximately 65 KOe.
1方比較例として、Nd (Bo、osCoo、tsF
e 0.77)11.5の合金を作成し同様に測定した
。Nd (B o、osco o、ssF e o、y
y ) s、sの合金はHA = 52 KOeであっ
た。As a comparative example, Nd (Bo, osCoo, tsF
e 0.77) An alloy of 11.5 was prepared and measured in the same manner. Nd (B o, osco o, ssF e o, y
y) s,s alloy had HA = 52 KOe.
この結果からもわかるようにAgの効果は明らかである
。As can be seen from this result, the effect of Ag is clear.
なお希土類元素RとしてYr La、 Ce+ Pro
Smの1棟又は2種以上の組合わせおよびNd との
組合せを用いても同様に有効なAg添加の効果を示す。In addition, as the rare earth element R, Yr La, Ce+ Pro
A similar effect of Ag addition is also shown when using one type of Sm or a combination of two or more types of Sm and a combination with Nd.
特許出願人
手 続 補 正 書
昭和599年3月メツ
特許庁長官殿
昭和59年3月1日提出の特許願(2)2、発明の名称
永久磁石用材料
&補正をする者
小作との関係 特許出願人
住所 東京都中央区日本橋−丁目13蚤1号氏名 (3
06)ティーディーケイ株式会社5、袖正により増加す
る発明のB。Patent Applicant Procedures Amendment Document March 1982 To the Commissioner of the Patent Office, Patent Application (2) 2, filed on March 1, 1980, Name of invention Material for permanent magnet & Relationship with tenancy of person making amendments Patent Applicant address No. 1, Nihonbashi-chome-13, Chuo-ku, Tokyo Name (3)
06) TDC Co., Ltd. 5, B of the invention increased by Sode Masa.
五補正の対象
明細書の特W1・請求の軛曲の41ft+及び発明の詳
細な説明の楠
l補正の内容
(1) 特許請求の範囲を別紙のとおシ補正する。5. Contents of amendments to Feature W1 of the specification to be amended, 41 ft+ of claims, and Kusunoki I of the detailed description of the invention (1) The scope of the claims will be amended as a separate sheet.
(2) 明細書第6頁17行目c) 「La、 Ce、
Pr。(2) Page 6, line 17 c) “La, Ce,
Pr.
Nd、 8m Jの文を削除する。Nd, 8m Delete the sentence J.
(3)明細書第4頁1行目の「La、 Ce、 Pr、
Nd。(3) “La, Ce, Pr,” on page 4, line 1 of the specification
Nd.
SmJの文を削除する。Delete the sentence SmJ.
(4) 明all 15第8負1行目f) 「Y、 L
a、 Ce、 Pr。(4) Clear all 15th 8th negative 1st line f) “Y, L
a, Ce, Pr.
SmJの文の次に以下の文を挿入する。Insert the following sentence after the SmJ sentence.
「、 Eu、 Gd、 Tb、 Dy、 Ho、 Er
、 Tm、 Yb、 Lu J特許請求の範囲
(1)■も(BxAgyFel−x−y )A (ただ
し0.01≦X≦0.3,0.01≦y≦0.5.4≦
A≦16)なる組成式で表わされ、上記組成式において
Rは、Yを含む希土類元素の1種又は2種以上の組合せ
であることを特徴とする永久磁石用材料。", Eu, Gd, Tb, Dy, Ho, Er
, Tm, Yb, Lu J Claim (1)■also(BxAgyFel-x-y)A (However, 0.01≦X≦0.3, 0.01≦y≦0.5.4≦
A material for a permanent magnet, characterized in that it is represented by the compositional formula A≦16), and in the compositional formula, R is one type or a combination of two or more types of rare earth elements including Y.
(2)lも(B xA g y COz p el−x
、 、 )人<たたし001≦X≦0.5,0.01≦
y≦0.3,0.01≦z(0,98,4≦A≦16)
なる組成式で表わされ、上記組成式において九は、Yを
含む希土類元素の1種又は2種以上の組合せでおること
を特徴とする永久磁石用材料。(2) l too (B xA g y COz p el-x
, , ) person<Tatashi001≦X≦0.5,0.01≦
y≦0.3, 0.01≦z (0,98, 4≦A≦16)
1. A permanent magnet material represented by the following compositional formula, wherein 9 is one or a combination of two or more rare earth elements including Y.
Claims (2)
し0口1≦X≦0.3,0.01≦y≦0.3.4≦A
≦16)なる組成式で表わされ、上記組成式において几
は、Yを含む希土類元素Lap Ce+ P rt N
cL Smの1種又は2 $fii以上の組合せである
ことを特徴とする永久磁石用材料。(1) 几(HxAgyFex -X-y) A (However, 0 mouth 1≦X≦0.3, 0.01≦y≦0.3.4≦A
≦16), and in the above composition formula, 几 is a rare earth element containing Y.
A material for a permanent magnet, characterized in that it is one type or a combination of two or more of cL Sm.
A(ただしくL01≦X≦0.3,0.01≦y≦o、
s、o、oi≦z (Q、 98 。 4≦A≦16)なる組成式で表わされ、上記組成式にお
いてR4j、Yを含む希土類元素LH+Ce、 Pr、
Nd、 Smの1種又は2種以上の組合せであること
を特徴とする永久磁石用材料。(2) , JBxAgyCozFex-x-y-z)
A (provided that L01≦X≦0.3, 0.01≦y≦o,
It is represented by the composition formula s, o, oi≦z (Q, 98. 4≦A≦16), and in the above composition formula, rare earth elements LH+Ce, Pr, containing R4j, Y,
A permanent magnet material comprising one or a combination of two or more of Nd and Sm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59039054A JPS60184661A (en) | 1984-03-01 | 1984-03-01 | Material for permanent magnet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59039054A JPS60184661A (en) | 1984-03-01 | 1984-03-01 | Material for permanent magnet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60184661A true JPS60184661A (en) | 1985-09-20 |
JPH0549741B2 JPH0549741B2 (en) | 1993-07-27 |
Family
ID=12542411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59039054A Granted JPS60184661A (en) | 1984-03-01 | 1984-03-01 | Material for permanent magnet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60184661A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH023206A (en) * | 1988-06-20 | 1990-01-08 | Seiko Epson Corp | Rare earth-iron system permanent magnet |
US9551052B2 (en) | 2005-07-15 | 2017-01-24 | Hitachi Metals, Ltd. | Rare earth sintered magnet and method for production thereof |
-
1984
- 1984-03-01 JP JP59039054A patent/JPS60184661A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH023206A (en) * | 1988-06-20 | 1990-01-08 | Seiko Epson Corp | Rare earth-iron system permanent magnet |
US9551052B2 (en) | 2005-07-15 | 2017-01-24 | Hitachi Metals, Ltd. | Rare earth sintered magnet and method for production thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0549741B2 (en) | 1993-07-27 |
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