JPS6024339A - Permanent magnet alloy - Google Patents

Permanent magnet alloy

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Publication number
JPS6024339A
JPS6024339A JP58131196A JP13119683A JPS6024339A JP S6024339 A JPS6024339 A JP S6024339A JP 58131196 A JP58131196 A JP 58131196A JP 13119683 A JP13119683 A JP 13119683A JP S6024339 A JPS6024339 A JP S6024339A
Authority
JP
Japan
Prior art keywords
permanent magnet
alloy
magnet alloy
same
page
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
JP58131196A
Other languages
Japanese (ja)
Inventor
Masaaki Tokunaga
徳永 雅亮
Chitoshi Hagi
萩 千敏
Noriaki Meguro
目黒 訓昭
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.)
Proterial Ltd
Original Assignee
Hitachi Metals 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 Hitachi Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP58131196A priority Critical patent/JPS6024339A/en
Publication of JPS6024339A publication Critical patent/JPS6024339A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a very useful novel permanent magnet having further improved characteristics by adding Mn and Al to a conventional permanent magnet alloy. CONSTITUTION:This permanent magnet alloy has a composition represented by the formula, wherein R is one or more kinds of rare earth elements, M is one or more among Zr, Hf, Ti, Nb, Ta and Si, and 0.01<=x<=0.7, 0.001<=y<=0.25, 0.001<=z <=0.15, 0.01<=alpha<=0.3, 0.01<=beta<=0.4, and 5<=A<=12.

Description

【発明の詳細な説明】 本発明は希土類金属とCOからなる金属間化合物、特に
希土類成分の低いCu添加型R2’C0cr系永久磁石
合金の改良に関するものである。3m。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an intermetallic compound consisting of a rare earth metal and CO, particularly to the improvement of a Cu-added R2'C0cr permanent magnet alloy with a low rare earth component. 3m.

Ceを中心とした希土類元素の1種又は2種以上の組み
あわぜからなる希土類元素(以下Rと記す)と、co、
Fe、Cu、添加物Mを含有するR(Go 4−X−y
−Z F e4 qu、M7’)A (ここでM:Z 
r、 ト1f、Ti、Nb、Ta、Si、Mo、Vの1
種又は2種以上の組合せ、0501≦×≦0.40.0
.02≦y≦0.25 、 0.001≦2≦0.15
 。
A rare earth element (hereinafter referred to as R) consisting of one type or a combination of two or more rare earth elements centered on Ce, co,
R(Go 4-X-y
-Z F e4 qu, M7')A (where M:Z
r, 1f, Ti, Nb, Ta, Si, Mo, V
species or combination of two or more species, 0501≦×≦0.40.0
.. 02≦y≦0.25, 0.001≦2≦0.15
.

6.5≦A≦8.3)で表わされる永久磁石合金は、残
留磁束密度(j3r)、保磁力(zhlc 、B+−1
c’ )の優れた永久磁石材わ1として知られている。
6.5≦A≦8.3), the permanent magnetic alloy has a residual magnetic flux density (j3r), a coercive force (zhlc, B+-1
c') is known as an excellent permanent magnet material.

(例えば特開昭53−8662G号公報、特開昭51−
4729G。
(For example, JP-A No. 53-8662G, JP-A No. 51-Sho.
4729G.

特開昭53−106326) 上記合金はすでに30M G Oeにも達するエネルギ
ー梢(’ (Bl−l ) max )および5〜30
KOeの、l−I Cが1がられている。しかしながら
/1・、 +−+r 、 r+ 。
JP-A-53-106326) The above alloy already has an energy peak (' (Bl-l) max) reaching as much as 30M G Oe and a
KOe's l-IC is set to 1. However, /1・, +−+r, r+.

Nb、Ta、Si 、MO,V等の添加物を用いてもさ
らに高Br化をはかるために必要な高F’e。
Even if additives such as Nb, Ta, Si, MO, V, etc. are used, high F'e is necessary to further increase Br.

低Cu化に限界があった。There was a limit to lowering Cu.

、?I′なわらr e ff1A = 0.3. Cu
 fa B = 0.05が限界Hであり、A > 0
.3. B < 0.0!1なる組成領域においては添
加物の量を増加しても良好な磁気特性が得られなかった
,? I'nawara r e ff1A = 0.3. Cu
fa B = 0.05 is the limit H, and A > 0
.. 3. In the composition range of B < 0.0!1, good magnetic properties could not be obtained even if the amount of additives was increased.

本発明は上記従来技術の欠点を改良し、さらに特性の高
い極めて有用な、新規な永久磁石を提供することを目的
とする。
It is an object of the present invention to improve the above-mentioned drawbacks of the prior art and to provide a novel permanent magnet that has excellent characteristics and is extremely useful.

上記目的を達成するため、本発明はざらにMn。In order to achieve the above object, the present invention mainly focuses on Mn.

A1を添加することにより、Feff1の増加をはかる
ことを特徴とするものである。
It is characterized in that Feff1 is increased by adding A1.

発明者等は種々の実験の結果、Mn、AIを合金元素と
してあらたに加えることにより、高81・化に必要なF
ewの増加が可能であることを見出した。すなわちMn
、AIの添加によりFeff1の増加を行なっても永久
磁石として充分なzHcの得られることを見出した。
As a result of various experiments, the inventors found that by newly adding Mn and AI as alloying elements, the F required for increasing the temperature to 81.
It has been found that it is possible to increase ew. That is, Mn
It was found that sufficient zHc for a permanent magnet can be obtained even if Feff1 is increased by adding AI.

Mn、AIの添加によって、一般的にキューリ一点、B
rは低下するが、IHCの確保に重要である。CU置換
型R2GO竹系磁石の保磁力は析出物による磁壁のビン
止めによって説明されており、従来技術におりてはFe
lの増加により析出物の形状、大きさ2組成が変化し、
充分なビン止めが実現できなかった。しかしながら本発
明によるMn。
By adding Mn and AI, generally one cucumber, B
Although r decreases, it is important for ensuring IHC. The coercive force of the CU-substituted R2GO bamboo magnet is explained by the binding of the domain wall by precipitates, and in the prior art, Fe
As l increases, the shape, size, and composition of the precipitates change,
A sufficient bottle stop could not be achieved. However, Mn according to the present invention.

A1を添加することにより、析出物中のMn、へ濃度が
増加し、高Feff1組成領域においても高工1−IC
が得られるのである。
By adding A1, the concentration of Mn in the precipitates increases, and even in the high Feff1 composition region, the concentration of Mn in the precipitates increases.
is obtained.

本発明において、Mnの添加が0.01より少ない場合
はFe量の増加が行なえず、0.3を越える場合はキュ
ーリ一点の低下、3rの低下が大きく永久磁石材料とし
て好ましくない。又A1の添加が0.01以下の場合は
Fe量の増加が行なえず、0.4以上の場合はキューリ
一点の低下、I3rの低下が大きい。したがってA1と
Mnの量はFeeとのかねあいで決まり、高Fe吊組成
の場合、A1とM nの量は増加する傾向にある。Mで
表わされる2r、1−If 、Ti 、Nb 、Ta 
、Siの1種又は2種以上の組みあわせはその添加量が
o、ooi以下の場合は充分な止lcが得られず、0.
15を越えさぜるが、zl−1cの低下をまねく。特に
本発明によるMn、AIを用いた場合は3rの増加に有
用であるFeff1を増加しても保磁力の低下が少ない
ため、Mn、AIを用いない場合よりもFeflを多く
できる。「0置換聞が0.01以下の場合は[3rの増
加に効果が少なく、又0.7以上の場合は保磁力の低下
をまねく。Cuff1が0.001以下の場合は本発明
によるMn、AIを用いても充分な保磁力が得られない
。CUtが0.25を越える場合はB。
In the present invention, if the addition of Mn is less than 0.01, the amount of Fe cannot be increased, and if it exceeds 0.3, the Curie point decreases and the 3r decreases significantly, which is not preferable as a permanent magnet material. Further, if the addition of A1 is less than 0.01, the amount of Fe cannot be increased, and if it is more than 0.4, the Curie point decreases and the I3r decreases significantly. Therefore, the amounts of A1 and Mn are determined by the balance with Fee, and in the case of a high Fe suspension composition, the amounts of A1 and Mn tend to increase. 2r, 1-If, Ti, Nb, Ta represented by M
, Si, or a combination of two or more types, if the amount added is less than o, ooi, sufficient stopping lc will not be obtained;
15, but it causes a decrease in zl-1c. In particular, when Mn and AI according to the present invention are used, coercive force decreases little even if Feff1, which is useful for increasing 3r, is increased, so Fefl can be increased more than when Mn and AI are not used. "If the zero displacement is less than 0.01, it will have little effect on increasing [3r, and if it is more than 0.7, it will cause a decrease in coercive force. If Cuff1 is less than 0.001, the Mn according to the present invention, Even if AI is used, sufficient coercive force cannot be obtained.B if CUt exceeds 0.25.

の低下をまねき本発明が生かされない。The present invention cannot be utilized as a result.

Aの値が5以下の場合、[3rの低下をまねき本発明が
生かされない。12以上の場合は、l−I Cの低下が
見られ永久磁石材料として好ましくない。
If the value of A is 5 or less, the value of [3r] decreases and the present invention cannot be utilized. If it is 12 or more, a decrease in l-I C is observed and it is not preferable as a permanent magnet material.

以下、実施例によって本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 S m 、(CohoIF eo、40M no、og
、A Io4o Cuo、oss P、a7Zrθ、0
. )7 なる合金を高周波溶解し、ショークラッシャ
ー、ブラウンミルを用いて粗粉砕後、ジェット・ミルに
よる微粉砕を行なった。粉砕媒体はN2ガスであり、微
粉末粒度は40μmである。本粉砕粉を30KOeの磁
粉中で配向後2tOn/Cm2の圧力で静水圧プレスを
用いて圧縮成形した。得られた成形体を1150℃で2
時間真空中焼結した。焼結後1120℃× 1時間溶体
化し、水中に急冷、した。さらに800℃×2時間時効
し、1℃/minの冷却速度で200℃まで冷却した。
Example 1 S m , (CohoIF eo, 40M no, og
, A Io4o Cuo, oss P, a7Zrθ, 0
.. ) 7 was melted by high frequency, coarsely pulverized using a Shaw crusher and a Brown mill, and then finely pulverized using a jet mill. The grinding media is N2 gas and the fine powder particle size is 40 μm. This pulverized powder was oriented in 30 KOe magnetic powder and compression molded using a hydrostatic press at a pressure of 2 tOn/Cm2. The obtained molded body was heated at 1150°C for 2
Sintered in vacuum for an hour. After sintering, it was solution-treated at 1120°C for 1 hour, and then rapidly cooled in water. It was further aged at 800°C for 2 hours and cooled to 200°C at a cooling rate of 1°C/min.

得られた磁気特性は、B r 〜10330G BHC〜70000゜ s@ C〜76000e (B H> max 〜25.9MGOeであった。The obtained magnetic properties are B r ~ 10330G BHC~70000° s@C~76000e (BH>max~25.9MGOe.

実施例2 S mOJ P ro、、5” ’(C0baJL F
 e6..3(、M I)、)1,7A+、、09 C
u6,0.5Sio、ol Hf(、,01)7なる合
金を実施例1と同様の方法で溶解、粉砕、成形した。得
られた成形体を1150℃で2時間、水中焼結した。焼
結後1120℃× 1時間溶体化し、水中に急冷した。
Example 2 S mOJ Pro, 5''' (C0baJL F
e6. .. 3(,M I),)1,7A+,,09C
An alloy u6,0.5Sio,ol Hf(,,01)7 was melted, crushed, and molded in the same manner as in Example 1. The obtained molded body was sintered in water at 1150°C for 2 hours. After sintering, it was solution-treated at 1120°C for 1 hour and rapidly cooled in water.

さらに780℃×2時間時効し、1℃7’ m i n
の冷却速度で200℃まで冷却した。得られた磁気特性
は、 B r 〜11500G Bll C□” 79000e zHC〜85000a (3トl ) max 〜31’、8M G Oeであ
った。
It was further aged at 780°C for 2 hours and aged at 1°C7'min.
It was cooled to 200°C at a cooling rate of . The obtained magnetic properties were B r ~11500G Bll C□''79000e zHC ~85000a (3 Tor) max ~31', and 8M G Oe.

実施例3 N d (c obni F eo、q M 11o、
o乙 A 16.07 CU6,6g S p)、ol
Hf O,Q/ )7.)なる合金を実施例1と同様の
方法で溶解、粉砕、焼結した。焼結後1100℃×2時
間溶体化処理した。800℃× 1時間の加熱のあと2
0000sの磁界中で500℃まで冷却した。冷却速度
は1°C/ minである。500℃で磁場印加を止め
、さらに500℃×2時間+400℃×5時間の時効を
加えた。
Example 3 N d (c obni F eo, q M 11o,
o Otsu A 16.07 CU6,6g S p), ol
Hf O,Q/ )7. ) was melted, crushed, and sintered in the same manner as in Example 1. After sintering, solution treatment was performed at 1100°C for 2 hours. 2 after heating at 800°C for 1 hour
It was cooled to 500° C. in a magnetic field of 0,000 s. The cooling rate is 1°C/min. At 500°C, the application of the magnetic field was stopped, and further aging was performed at 500°C for 2 hours + 400°C for 5 hours.

なお、磁場の印加方向は先に行なった磁場中配向の方向
と同一である。得られた磁気特性は、B r 〜11’
900G 8I−IC−81000゜ 工HO〜125000e (B H) max 〜34.IM GO8であった。
Note that the direction of application of the magnetic field is the same as the direction of orientation in the magnetic field performed previously. The obtained magnetic properties are B r ~11'
900G 8I-IC-81000゜engineering HO~125000e (B H) max ~34. It was IM GO8.

実施例4 第1表に示す組成を有する合金を実施例2と同様の方法
で溶解、粉砕、焼結、熱処理した。得ら第1表 第2表 手続補正書 事件の表示 昭和58年 特許願 第131196@発明の名称 永
久磁石合金 補圧をする者 事件どの関係 特許出願人 住所 東京都千代田区丸ノ内二丁目1番2号名称 (5
08)日立金属株式会社 明■1書の「発明の詳細な説明」の欄。
Example 4 An alloy having the composition shown in Table 1 was melted, crushed, sintered, and heat treated in the same manner as in Example 2. Obtained Table 1 Table 2 Procedural Amendment Case 1982 Patent Application No. 131196 @ Title of Invention Permanent Magnet Alloy Compensator Case Relationship Patent Applicant Address 2-1-2 Marunouchi, Chiyoda-ku, Tokyo Issue name (5
08) "Detailed description of the invention" column of Hitachi Metals Co., Ltd. Mei ■ 1 book.

補正の内容 明細内箱6頁第9行の「水中焼結」を1水素特許庁長官
殿 事件の表示 昭和58年 特請願 第131196号発明の名称 永
久磁石合金 補正をりる者 事件との関係 特許出願人− 住所 東京都千代田区丸ノ内二丁目1番25:3名称 
(508)日立金属株式会社 代表者 河 野 典 夫 代理人 居所 東京都千代田区丸の内二丁目1番2号11 3′
/ 金 属 株 式 会 ネ1 内1、明細書第2頁第
10行の「得られている。しかしながら」を「得られて
いるが、B rは11000G′/J<イの最大値であ
った。このためJに訂正する。
1. Indication of "underwater sintering" on page 6, line 9 of the details box of the amendment. 1. Indication of the case of the Commissioner of the Hydrogen Patent Office. 1981. Special petition No. 131196. Name of the invention. Relationship with the case of the person who removed the permanent magnet alloy amendment. Patent applicant - Address 2-1-25:3 Marunouchi, Chiyoda-ku, Tokyo Name
(508) Hitachi Metals Co., Ltd. Representative Nori Kono Husband Agent Residence 2-1-2 Marunouchi, Chiyoda-ku, Tokyo 11-3'
/Metal Co., Ltd. 1, page 2, line 10 of the specification, "obtained. However,""obtained, but Br is the maximum value of 11000G'/J<a. Therefore, it is corrected to J.

2、同書同頁第12行の「もさらに」を1さらに」に訂
正する。
2. In the 12th line of the same page of the same book, ``Momore'' is corrected to ``Momore''.

3、同書同頁同行「はかるために」を[はかることも試
みられているが、]に訂正する。
3. On the same page of the same book, ``To measure'' is corrected to ``Although attempts have been made to measure.''

4、同■同頁第14行〜第17行を次の通り訂正する。4. Correct the following lines 14 to 17 on the same page.

1−リ′41つちFO量0.3. CLI笛0.0!i
が限界量であり、X > 0.3.1/ < 0.05
なる組成領域にJ、jいては添加物の吊を増加しても良
好な特性が得られなかった。」 5、同町同頁第18〜20行を次の通り訂正する。
1-Li'41 FO amount 0.3. CLI whistle 0.0! i
is the critical amount, X > 0.3.1/ < 0.05
In the composition range J, j, even if the amount of additives was increased, good characteristics could not be obtained. 5. Lines 18-20 of the same page for the same town are corrected as follows.

r本発明は従来限界とされていた組成領域にJ3い(,
1”な4つI3高Fc、低Cu組成においてさらにBr
 、(Bl−1)maxの高い有用な、新規な永久磁石
を提供することを目的とする。」 6、同書箱3貝第1・〜3行を次の通り訂正する。
rThe present invention extends to the composition range that was conventionally considered to be the limit (,
1" four I3 high Fc, low Cu composition further Br
, (Bl-1)max, and to provide a new and useful permanent magnet. ” 6. Correct the following lines 1-3 of box 3 of the same book.

系にざらに〜1n、AIを添加することにJミリ「Cm
の増加を実現し、磁気Q’J M、、待にBr 、(B
l−1)maxの向上をはかることを特徴どりるもので
ある。。
By roughly adding ~1n and AI to the system, J milli "Cm"
By realizing an increase in magnetic Q'J M,, finally Br, (B
l-1) It is characterized by improving max. .

7、同書回頁第10〜12行ノF Mll 、 A l
 町−重要である。Jを「〜1n、AIの添加にょ−)
て、一般的にキューリ一点、Bl゛は低下することは公
知。であるが、r l−1cの確保に重要であることが
判明した。Jに訂正する。
7. Same book, page 10-12, F Mll, A l
Town - important. J is ``~1n, addition of AI~)
It is well known that BL generally decreases by one point. However, it was found to be important for securing r l-1c. Correct to J.

8、同書第6頁第4行と第5行の間に次の文を挿入する
8. Insert the following sentence between lines 4 and 5 on page 6 of the same book.

「 1旧・7にS n+ (Cab、I F eo、4o(
’、 uo、o5S io、01 ”0,0/ )yな
る合金を評価し、以下の磁気特性を得I(。
"1 old, 7, S n+ (Cab, IF eo, 4o(
', uo, o5S io, 01 ``0,0/ )y alloy was evaluated and the following magnetic properties were obtained I(.

[3r 〜11500G a Hc −−3000e r l−l c 〜 5000e (B H)’ max ・” 1.1t’vI G 0
eAI’、Mllを添加することにより、8 F O組
成領域においても高r t」q 、高(B l−1> 
maxの1!11うれることがわがる。J 9、同用周頁第17行と18行の間に次の文を挿入する
[3r ~11500G a Hc --3000e r l-l c ~ 5000e (B H)' max ・"1.1t'vI G 0
By adding eAI' and Mll, high r t'q and high (B l-1>
I know I'll be happy about max's 1!11. J 9. Insert the following sentence between lines 17 and 18 on the same page.

r同口4にS Ill。、、P r。、5.(Cob、
 F co、35 G ”6.05.S ’0.07H
ro、o、 >7 なる合金を評価し、以下の磁気特性
を1−1〕こ。
r Same mouth 4 S Ill. ,,Pr. ,5. (Cob,
F co, 35 G"6.05.S '0.07H
An alloy with ro, o, >7 was evaluated and the following magnetic properties were determined in 1-1].

131゛ −〜 11200G aI−1c〜4000e Ihlc・−fioOQ6 (B t−l ) 1IlaX 〜 1.3 M13 
QeJlo、同書第7頁第12行と13行の間に次の文
を挿入する。
131゛ - ~ 11200G aI-1c ~ 4000e Ihlc・-fioOQ6 (B t-l) 1IlaX ~ 1.3 M13
QeJlo, page 7 of the same book, insert the following sentence between lines 12 and 13.

1同時に木d(CO−r c。、、/5Cuo、oy 
S ’o、、11/ l−1%、ot )72なる合金
を評価し、以下の磁気特性を1がた。
1 Simultaneously tree d(CO-r c.,, /5Cuo,oy
An alloy named S'o,, 11/l-1%, ot) 72 was evaluated, and the following magnetic properties were determined.

1:3 r 〜114(1(IG s Hc ’= 1000e r l−l c 〜150Q6 (B H) n1ax +HO,,7M G Oe j
以上
1:3 r ~114 (1(IG s Hc '= 1000e r l-l c ~150Q6 (B H) n1ax +HO,,7M G Oe j
that's all

Claims (1)

【特許請求の範囲】 R(CO1−X−”J−Z−d−/j l二 eg C
Uy 、tvl’z M n、7AI、)A(ここでR
:希土類元素の1種又は2種以上の組みあわせ、M:Z
r 、 l−1f 、 Ti 、 Nb 。 Ta、Siの1種又は2種以上の組みあわせ、0.01
≦X≦0.7. 0.001≦y≦0.25 、 0.
001≦7≦0.t5 、 0.01≦α≦0.3. 
0.01≦β≦0.4,5≦A≦12)なる組成からな
ることを特徴とする永久磁石合金。
[Claims] R(CO1-X-"J-Z-d-/j l2 eg C
Uy, tvl'z M n, 7AI,)A (where R
: One type or combination of two or more rare earth elements, M:Z
r, l-1f, Ti, Nb. One or more combinations of Ta and Si, 0.01
≦X≦0.7. 0.001≦y≦0.25, 0.
001≦7≦0. t5, 0.01≦α≦0.3.
A permanent magnet alloy having a composition of 0.01≦β≦0.4, 5≦A≦12).
JP58131196A 1983-07-19 1983-07-19 Permanent magnet alloy Pending JPS6024339A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58131196A JPS6024339A (en) 1983-07-19 1983-07-19 Permanent magnet alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58131196A JPS6024339A (en) 1983-07-19 1983-07-19 Permanent magnet alloy

Publications (1)

Publication Number Publication Date
JPS6024339A true JPS6024339A (en) 1985-02-07

Family

ID=15052270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58131196A Pending JPS6024339A (en) 1983-07-19 1983-07-19 Permanent magnet alloy

Country Status (1)

Country Link
JP (1) JPS6024339A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03244106A (en) * 1990-02-22 1991-10-30 Toshiba Corp Permanent magnet
US5840133A (en) * 1995-06-08 1998-11-24 Takahashi; Yoshiaki Permanent magnet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03244106A (en) * 1990-02-22 1991-10-30 Toshiba Corp Permanent magnet
US5840133A (en) * 1995-06-08 1998-11-24 Takahashi; Yoshiaki Permanent magnet

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