JPS60218445A - Resin bonded rare earth element-cobalt magnet - Google Patents

Resin bonded rare earth element-cobalt magnet

Info

Publication number
JPS60218445A
JPS60218445A JP59073999A JP7399984A JPS60218445A JP S60218445 A JPS60218445 A JP S60218445A JP 59073999 A JP59073999 A JP 59073999A JP 7399984 A JP7399984 A JP 7399984A JP S60218445 A JPS60218445 A JP S60218445A
Authority
JP
Japan
Prior art keywords
rare earth
earth element
magnet
cobalt magnet
resin bonded
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
Application number
JP59073999A
Other languages
Japanese (ja)
Other versions
JPH0621307B2 (en
Inventor
Koji Akioka
宏治 秋岡
Tatsuya Shimoda
達也 下田
Ryuichi Ozaki
隆一 尾崎
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.)
Seiko Epson Corp
Suwa Seikosha KK
Original Assignee
Seiko Epson Corp
Suwa Seikosha KK
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 Seiko Epson Corp, Suwa Seikosha KK filed Critical Seiko Epson Corp
Priority to JP59073999A priority Critical patent/JPH0621307B2/en
Publication of JPS60218445A publication Critical patent/JPS60218445A/en
Publication of JPH0621307B2 publication Critical patent/JPH0621307B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an Sm-saving los-cost resin bonded rare earth element-Co magnet having high performance by substituting a rare earth element other than Sm for part of Sm in a 2-17 type rare earth element-Co magnet contg. Sm. CONSTITUTION:A rare earth element other than Sm is substituted for part of Sm in a 2-17 type rare earth element-Co magnet contg. Sm to obtain a resin bonded rare earth element-Co magnet having a composition represented by a formula Sm1-aRaTMz. In the formula, R is one or more among Y, Pr and Nd, TM is Co-base transition metals, z is the ratio of TM to rare earth elements, and a=0.2-0.5.

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、Smを用いる2−17系希土類コバルト磁石
において1.EImの一部を他の希土類元素で置換した
高性能かつ省Sm−低コストの希土類コバルト磁石に関
する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention provides a 2-17 rare earth cobalt magnet using Sm. The present invention relates to a high-performance, Sm-saving and low-cost rare earth cobalt magnet in which a part of EIm is replaced with another rare earth element.

〔従来技術〕[Prior art]

希土類コバルト磁石の高性能化のためにSmを置換する
方法は、1−5系ではかなり行なわれており、一部実用
化もなされている。ところが2−17系では、1−5系
に比して、保磁力1Hcを得にくいため研究例も少な(
(K e n Oha 8 h i :EFFI!;C
TS OF PRASEODYM工UM 5UBST工
TU−T工ON ON PRF:q’IP工TATIO
N HARDENEDRARE EARTHMAGNE
TS:5th R−Co WORK−f3HOP P4
95〜501 :1981) がある程度である。そし
て、この文献によれば、Smを20atチ以上置換する
と、焼結が完全に行なわれず密度が上がらない。また、
保磁力iHc も急激に減少し、置換量は20atチ程
度が限界とされていた。
The method of replacing Sm in order to improve the performance of rare earth cobalt magnets has been widely used in the 1-5 series, and has even been put to practical use in some cases. However, in the 2-17 series, compared to the 1-5 series, it is difficult to obtain a coercive force of 1Hc, so there are few research examples (
(K e n Oha 8 h i :EFFI!;C
TS OF PRASEODYM UM 5UBST TU-T ON ON PRF: q'IP TATIO
N HARDENEDRARE EARTH MAGNE
TS:5th R-Co WORK-f3HOP P4
95-501:1981) to some extent. According to this document, if 20 at or more of Sm is substituted, sintering will not be completed and the density will not increase. Also,
The coercive force iHc also decreased rapidly, and the amount of substitution was considered to be limited to about 20 at.

〔目 的〕〔the purpose〕

本発明の目的は、樹脂結合法を用いることにより、Sm
置換量を大幅に増加させ、焼結法では不可能であった組
成を実現し、よシ高性能・省Sm・低コストの希土類コ
バルト磁石を得ることにある。
The purpose of the present invention is to achieve Sm by using resin bonding method.
The objective is to significantly increase the amount of substitution, realize a composition that was impossible with the sintering method, and obtain a rare earth cobalt magnet with higher performance, less Sm, and lower cost.

〔概 要〕〔overview〕

R,Go、、化合物(Rは希土類)のうちでSmよりも
飽和磁化4π工8の高い元素にはY、Pr。
Among R, Go, and compounds (R is a rare earth element), elements with higher saturation magnetization 4π-8 than Sm include Y and Pr.

N(1の3種類がある。またこの6種の元素は希土類鉱
石中での含有量がSmよシも数倍〜数十倍も高く、資源
的に見ても非常に有利な元素である。
There are three types of N (1). Also, the content of these six elements in rare earth ores is several to several tens of times higher than Sm, making them very advantageous elements from a resource perspective. .

そこでこれらの元素をSmに置換し・で用いることがで
きれば、高性能・省Sm−低コストの2−17系コバル
ト磁石を得る可能性がある。ところが、R’、j!o、
、化合物(RはY、Pr、Nd)は異方性磁界Hムが1
0〜20KOe程度とSn+、0Q17の約100KO
eに比して非常に小さく、SmをこれらのR元素で置換
すれば、保磁力iHcの低下は否めない。さらに現在、
量産されている焼結2−17系コバルト磁石のiHcは
6〜10KOθ程度とあまシ大きくないことと、前記し
た大橋氏の文献による、Pr、Y等の8m置換時には、
焼結性が低下し密度が充分に上がらない。そのため(B
H)max も高くならず、焼結法によっては、20a
t%以上のSm[換は実現していない。ところが樹脂結
合法を用いれば、Sm[換を行っても、磁石粉末の充填
率は無置換のものと同じレベルを維持できるので、成分
椰成の性質を充分に引き出せる。また置換量に応じて熱
処理を適当に変更することにより、約50at%までの
Sm置換が可能となった。
Therefore, if these elements can be replaced with Sm and used, it is possible to obtain a high-performance, Sm-saving, and low-cost 2-17 cobalt magnet. However, R',j! o,
, the compound (R is Y, Pr, Nd) has an anisotropic magnetic field H of 1
Approximately 0-20KOe and Sn+, approximately 100KO of 0Q17
If Sm is replaced with these R elements, the coercive force iHc will inevitably decrease. Furthermore, currently
The iHc of mass-produced sintered 2-17 cobalt magnets is not very large, about 6 to 10 KOθ, and according to the above-mentioned paper by Mr. Ohashi, when replacing 8m of Pr, Y, etc.,
The sinterability deteriorates and the density does not increase sufficiently. Therefore (B
H) max is not high, depending on the sintering method, it may be 20a
Sm [conversion of t% or more has not been realized. However, if the resin bonding method is used, even if Sm is replaced, the filling rate of the magnet powder can be maintained at the same level as that without replacement, so the properties of the component composition can be fully brought out. Furthermore, by appropriately changing the heat treatment depending on the amount of substitution, Sm substitution of up to about 50 at % became possible.

〔実施例〕〔Example〕

以下、本発明について実施例に基づき詳細に説明する。 Hereinafter, the present invention will be described in detail based on examples.

実施例1゜ 一般式でSmI−a Ra (’!Oo、svy au
ll、0?ll F’eO,tlzro、oys )s
、1 (RはY、Pr、Nd、aは0.1゜0.3,0
.5の3種類)なる合金を低周波溶解炉で溶解し合金イ
ンゴットを作成した。このインゴットを1100〜12
00℃の種々の温度範囲で8時間の溶体化処理を行ない
、続いて850℃×6時間の時効処理を行ない、樹脂結
合法によシ異方性磁石を作成し、特性比較を行った。な
お比較例は、5ftl(OOo、ayy ’!uo、。
Example 1゜The general formula is SmI-a Ra ('!Oo, svy au
ll, 0? ll F'eO, tlzro, oys )s
, 1 (R is Y, Pr, Nd, a is 0.1°0.3,0
.. Three types of alloys (5) were melted in a low frequency melting furnace to create alloy ingots. This ingot is 1100~12
Solution treatment was performed for 8 hours at various temperature ranges of 00°C, followed by aging treatment at 850°C for 6 hours, and anisotropic magnets were produced by a resin bonding method, and characteristics were compared. Note that the comparative example is 5ftl(OOo, ayy'!uo,.

71 F’eo、、t zro、ots )11.1 
で溶体化処理は1190℃×8時間、時効処理は850
℃×6時間であった。
71 F'eo,, tzro, ots)11.1
Solution treatment at 1190℃ x 8 hours, aging treatment at 850℃
℃ x 6 hours.

以下に特性評価結果を示す。Characteristic evaluation results are shown below.

第 1 表 (SSTは溶体化処理を意味する。)第1
表に示すように、本発明によシ1.’Br。
Table 1 (SST means solution treatment)
As shown in the table, according to the present invention, 1. 'Br.

(BH)max が大きく増加していることがわかる1
、また置換量を示すa値が増しても、溶体化処理温度を
適当な温度に設定すれば、a=Q、5までは、はぼ実用
上問題のない6KOe以上のiHcが得られている。
It can be seen that (BH)max has increased significantly1
, and even if the a value indicating the amount of substitution increases, if the solution treatment temperature is set to an appropriate temperature, an iHc of 6 KOe or more, which is practically acceptable up to a = Q, 5, can be obtained. .

実施例2゜ 一般式でSm1−、−1.R1,R,b(OOo、e*
sワuo、oa F’i’O,11゜Hf0.01! 
)y、e (R+ e RtはY、 Pr、 N(1,
a+b=α3)なる合金を低周波溶解炉で溶解し合金イ
ンゴットを作成した。このインゴットf1070 ・〜
1170℃の種々の温度範囲で24時間の溶体化処理を
行ない、続いて850℃×20時間の時効処理を行ない
、樹脂結合法によシ異方性磁石を作成し特性比較を行っ
た。なお比較例は、Sm(000,6HI Cu、、。
Example 2゜The general formula is Sm1-, -1. R1, R, b(OOo, e*
swao, oa F'i'O, 11°Hf0.01!
)y, e (R+ e Rt is Y, Pr, N(1,
A+b=α3) was melted in a low frequency melting furnace to create an alloy ingot. This ingot f1070...
Solution treatment was carried out for 24 hours at various temperature ranges of 1170°C, followed by aging treatment at 850°C for 20 hours, and anisotropic magnets were produced by a resin bonding method and their characteristics were compared. Note that the comparative example is Sm(000,6HI Cu, .

6 FEB、S。Hfo、。tt)’r、eで溶体化処
理は1160℃×24時間、時効処理は850℃×20
時間であった。
6 FEB, S. Hfo,. tt) 'r, e, solution treatment at 1160℃ x 24 hours, aging treatment at 850℃ x 20
It was time.

以下に特性結果を示す。Characteristic results are shown below.

以下次ページにつづく 第 2 表 第2表に示すように、本発明によF)、Y、Pr。Continued on next page Table 2 As shown in Table 2, according to the present invention F), Y, Pr.

N(lを2種以上、合わせてSmとl!排しても第1表
に示したと同様、Br、(BH)maxの大幅な増加が
見られる。このことは、希土類の原鉱石の組成に合わせ
て置換が可能であることを示し、希土類相互の分離工程
が削減が可能となるので、省8m・高性能のみならず、
低コストな磁石の製造が可能であることをも示す。
Even if two or more types of N(l are excluded, including Sm and l!), a significant increase in Br and (BH)max is seen, as shown in Table 1. This indicates that the composition of rare earth ore This shows that it is possible to replace the rare earth elements according to
It also shows that it is possible to manufacture low-cost magnets.

〔効 果〕〔effect〕

以上、述べたように本発明によれば、磁気性能特に、エ
ネルギー積、残留磁束密度の向上と、省Sm・低コスト
の希土類コバルト磁石の製造が可能という効果を有する
As described above, according to the present invention, it is possible to improve the magnetic performance, particularly the energy product and the residual magnetic flux density, and to manufacture a rare earth cobalt magnet with reduced Sm and low cost.

以上 出願人 株式会社職訪精工合that's all Applicant: Shoboseikogo Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 組成式がSm1−aR,TM、 (Rは、Y、、Pr、
Ndのうちの少なくとも18i以上の元素、TMはコバ
ルトを主体とする遷移金属で、2け希土類元素とTMの
比を示す。)で表わされる、いわゆる2−17系希土類
コバルト磁石で、a値が0.2〜0.5の範囲であるこ
とを特徴とする、((4脂結合型希土類コバルト磁石、
The composition formula is Sm1-aR,TM, (R is Y, Pr,
Element of at least 18i or more of Nd, TM is a transition metal mainly composed of cobalt, and shows the ratio of 2 digit rare earth elements to TM. ) is a so-called 2-17 series rare earth cobalt magnet, characterized by an a value in the range of 0.2 to 0.5 ((4-lipid bonded rare earth cobalt magnet,
JP59073999A 1984-04-13 1984-04-13 Resin-bonded rare earth cobalt magnet Expired - Lifetime JPH0621307B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59073999A JPH0621307B2 (en) 1984-04-13 1984-04-13 Resin-bonded rare earth cobalt magnet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59073999A JPH0621307B2 (en) 1984-04-13 1984-04-13 Resin-bonded rare earth cobalt magnet

Publications (2)

Publication Number Publication Date
JPS60218445A true JPS60218445A (en) 1985-11-01
JPH0621307B2 JPH0621307B2 (en) 1994-03-23

Family

ID=13534336

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59073999A Expired - Lifetime JPH0621307B2 (en) 1984-04-13 1984-04-13 Resin-bonded rare earth cobalt magnet

Country Status (1)

Country Link
JP (1) JPH0621307B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5647886A (en) * 1993-11-11 1997-07-15 Seiko Epson Corporation Magnetic powder, permanent magnet produced therefrom and process for producing them
US6139765A (en) * 1993-11-11 2000-10-31 Seiko Epson Corporation Magnetic powder, permanent magnet produced therefrom and process for producing them
US8211246B2 (en) 2010-09-24 2012-07-03 Kabushiki Kaisha Toshiba Permanent magnet and motor and generator using the same

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5973996A (en) * 1982-10-22 1984-04-26 Nec Corp Optical recording medium

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5973996A (en) * 1982-10-22 1984-04-26 Nec Corp Optical recording medium

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5647886A (en) * 1993-11-11 1997-07-15 Seiko Epson Corporation Magnetic powder, permanent magnet produced therefrom and process for producing them
US6139765A (en) * 1993-11-11 2000-10-31 Seiko Epson Corporation Magnetic powder, permanent magnet produced therefrom and process for producing them
US8211246B2 (en) 2010-09-24 2012-07-03 Kabushiki Kaisha Toshiba Permanent magnet and motor and generator using the same

Also Published As

Publication number Publication date
JPH0621307B2 (en) 1994-03-23

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