JPH0441652A - Rare earth magnetic alloy - Google Patents

Rare earth magnetic alloy

Info

Publication number
JPH0441652A
JPH0441652A JP2147009A JP14700990A JPH0441652A JP H0441652 A JPH0441652 A JP H0441652A JP 2147009 A JP2147009 A JP 2147009A JP 14700990 A JP14700990 A JP 14700990A JP H0441652 A JPH0441652 A JP H0441652A
Authority
JP
Japan
Prior art keywords
rare earth
corrosion resistance
magnetic properties
alloy
magnetic alloy
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
JP2147009A
Other languages
Japanese (ja)
Inventor
Takaaki Daimon
大門 孝彰
Yoshio Inokoshi
良夫 猪越
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 Instruments Inc
Original Assignee
Seiko Instruments Inc
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 Instruments Inc filed Critical Seiko Instruments Inc
Priority to JP2147009A priority Critical patent/JPH0441652A/en
Publication of JPH0441652A publication Critical patent/JPH0441652A/en
Pending legal-status Critical Current

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  • Hard Magnetic Materials (AREA)

Abstract

PURPOSE:To improve corrosion resistance and to obtain a rare earth magnetic alloy excellent in magnetic properties by adding new light rare earth oxide to an alloy containing R2TM14B1 type tetragonal crystal as main phase. CONSTITUTION:Light rare earth oxide (La2O3, Ce2O3, Pr2O3, Nb2O3, Sm2O3)is incorporated by 0.1-1.0wt.% into a rare earth permanent magnet containing R2TM14B1, (R is Ce, Pr, Nd, Gd, Tb, or Dy and TM is Fe or Co) type tetragonal crystal as main phase, by which the rare earth permanent magnet alloy excellent in corrosion resistance and magnetic properties can be produced.

Description

【発明の詳細な説明】 [産業上の利用分野1 希土類磁石はフェライト磁石に比べ、優れた磁気特性を
有しており、高い磁気力を利用し、工業製品の小型化に
たいへん有利であり、を子式腕時計からコンピュータの
端末に到るまで幅広い分野に適用されている。本発明は
この希土類磁石に関するもので、詳しくはその耐食性の
向上に関する物である。
[Detailed Description of the Invention] [Industrial Application Field 1 Rare earth magnets have superior magnetic properties compared to ferrite magnets, and are very advantageous for downsizing industrial products by utilizing high magnetic force. It is applied in a wide range of fields, from child-type watches to computer terminals. The present invention relates to this rare earth magnet, and more specifically to improving its corrosion resistance.

[発明の概要] R2T1114 Bl  (R=Ce、Pr、Nd、G
d、TbあるいはD y 、 T y = F eある
いはCO)型正方晶を主相とする希土類永久磁石は、m
気モーメントの源となるFeあるいはCoの含有量が多
いため、飽和m化が高く現在市眼されている希土類磁石
の中で最大エネルギー積((BH)max)が最も高い
、しかしながら、SmCo系磁石をはじめとした他の希
土類永久磁石に比べ耐食性に劣り、特に体積の小さな磁
石では、メツキ等の表面処理を施しても表面保護層とi
1石との体積分率が大きくなることがら、最大エネルギ
ー積(BH)maxの低下が著しく、上記磁石の磁気特
性の面で、他の種類の磁石に対する(り値付が発揮でき
ない。
[Summary of the invention] R2T1114 Bl (R=Ce, Pr, Nd, G
d, Tb or D y , T y = Fe or CO) type tetragonal as the main phase, m
SmCo-based magnets have a high saturation rate and have the highest maximum energy product ((BH)max) among the rare earth magnets currently in the market due to their high content of Fe or Co, which is the source of the SmCo-based moment. Compared to other rare earth permanent magnets such as
Since the volume fraction with one stone becomes large, the maximum energy product (BH) max decreases significantly, and the above-mentioned magnet cannot exhibit a higher value than other types of magnets in terms of magnetic properties.

そこで1本発明では、係る耐食性の問題を表面処理によ
る方法ではなく、R2T、、4B、型正方晶を主相とす
る合金に新規な軽希土類酸化物を添加することにより、
耐食性を向上させかつ磁気特性の優れた希土類磁石合金
を見い出したものである。
Therefore, in the present invention, the problem of corrosion resistance is not solved by surface treatment, but by adding a new light rare earth oxide to an alloy whose main phase is R2T, 4B, type tetragonal.
We have discovered a rare earth magnet alloy that has improved corrosion resistance and excellent magnetic properties.

本合金は軽希土類酸化物の微量添加による磁石製品コス
トの上昇が微々たるものであることを考えると、その工
業的価値は極めて大きい。
Considering that the increase in the cost of magnet products due to the addition of a small amount of light rare earth oxide to this alloy is negligible, its industrial value is extremely large.

[従来の技術] 従来、希土類鉄系磁石の耐食化の方法としてはNdFe
B系焼結磁石の表面に気相めっきあるいはクロム酸皮膜
等を形成させるなど、表面処理の方法が行われている。
[Conventional technology] Conventionally, as a method for making rare earth iron magnets corrosion resistant, NdFe
Surface treatment methods such as vapor phase plating or forming a chromic acid film on the surface of B-based sintered magnets are used.

[発明が解決しようとする課I11 従来の表面処理による方法では、体積の比較的大きな磁
石の場合に限り、表面保護層による磁気特性(特に最大
エネルギー積(BH)max)の低下は相対的に小さく
なり特に問題はない、しかしながら、磁石の体積が小さ
(なるにつれて表面保護層による磁気特性に及ぼす影響
が大きくなり、例えば約5 X I O−’cm”の体
積をもつ腕時計用ステッピングモータ回転子用磁石では
、最大エネルギー積(BH)maxが約30%以上低下
してしまい実用上使用できないという欠点を有していた
[Issue to be solved by the invention I11 In the conventional surface treatment method, only in the case of a magnet with a relatively large volume, the decrease in magnetic properties (especially maximum energy product (BH) max) due to the surface protective layer is relatively small. However, as the volume of the magnet becomes smaller (the smaller the volume of the magnet, the greater the influence of the surface protective layer on the magnetic properties. For example, a stepping motor rotor for a wristwatch with a volume of approximately 5 The conventional magnet had a drawback that the maximum energy product (BH) max decreased by about 30% or more, making it unusable for practical use.

〔課題を解決するための手段1 上記課題を解決するために、本発明においては軽希土類
酸化物(Lag Os 、Cez Ox 、Pry O
s 、Ndt Os 、Sma Os )を0.1〜1
.0wt%含有することにより、耐食性及び磁気特性に
優れた希土類永久磁石合金を見い出したものである。
[Means for Solving the Problems 1 In order to solve the above problems, the present invention uses light rare earth oxides (Lag Os, Cez Ox, Pry O
s, NdtOs, SmaOs) from 0.1 to 1
.. By containing 0 wt%, a rare earth permanent magnet alloy has been found that has excellent corrosion resistance and magnetic properties.

[作用及び実施例] 実施例:1 Nd15at%、Fe77at%、Blat%3元合金
粉末(平均粒度3.2LLm)に軽希土類酸化物(La
g Ox 、Cez Ox 、Pry Os 。
[Function and Examples] Example: 1 Light rare earth oxide (La
gOx, CezOx, PryOs.

Ndx Os 、Sma Os )の粉末(平均粒度2
゜5μm)を0〜5.0wt%添加し、低エネルギー型
回転ボールミルにより有機溶剤中にて1時間混合した。
Ndx Os, Sma Os) powder (average particle size 2
5 μm) was added in an amount of 0 to 5.0 wt% and mixed for 1 hour in an organic solvent using a low energy rotary ball mill.

この混合粉末を15KOeの磁場を圧力方向に対し垂直
な方向に印加させなから10t / c m 2の圧力
で加圧形成を行った。得られた成形体を1070℃、1
時間焼結し、ついで室温まで冷却した後、600℃で2
時間時効処理を施し試料とした。
This mixed powder was formed under pressure at a pressure of 10 t/cm 2 while applying a magnetic field of 15 KOe in a direction perpendicular to the pressure direction. The obtained molded body was heated at 1070°C for 1
After sintering for an hour and then cooling to room temperature, the
A sample was subjected to time aging treatment.

なお、X線回折法により本焼結合金は多量のNd 2 
F 6148 +正方品、Nd−rich相および軽希
土類酸化物から成ることが確認できた。
Furthermore, X-ray diffraction analysis revealed that the sintered alloy contains a large amount of Nd2.
It was confirmed that the product consisted of an F 6148 + tetragonal product, an Nd-rich phase, and a light rare earth oxide.

作製された試料は、温度80℃、湿度95%の恒温環境
中に0〜1000時間放置し、試料の重量変化を測定し
、これを耐食性の評価とした。また磁気特性は直流式B
l(トレーサーを用いて測定した。
The prepared samples were left in a constant temperature environment of 80° C. and 95% humidity for 0 to 1000 hours, and changes in weight of the samples were measured, which was used as an evaluation of corrosion resistance. In addition, the magnetic characteristics are DC type B
l (measured using a tracer.

実施例、2 以下の表1に示す組成の合金をアーク溶解により溶製し
、粗粉砕後振動ボールミルにより平均粒度3,0μmに
微粉砕した。得られた微粉末にSm20.を0.5wt
添加混合した。その後の工程は実施例1と同一である。
Example 2 An alloy having the composition shown in Table 1 below was melted by arc melting, coarsely pulverized, and then finely pulverized using a vibrating ball mill to an average particle size of 3.0 μm. The obtained fine powder was coated with Sm20. 0.5wt
Add and mix. The subsequent steps are the same as in Example 1.

実施例2においても、いずれの合金もRtT−4B、型
正方晶、R−rich相(Rは希土類元素)相及びSm
t Osの混在相からなることをX線回折法により確認
できた。
In Example 2, all alloys were RtT-4B, tetragonal, R-rich phase (R is a rare earth element) phase, and Sm
It was confirmed by X-ray diffraction that it consisted of a mixed phase of tOs.

[発明の効果1 以上のような実施例から、本発明の効果として次のよう
なことがあげられる。
[Effects of the Invention 1 From the above examples, the following effects can be mentioned as effects of the present invention.

第1図はN d +@F eア?B83元合金における
軽希土類酸化物(Lag 03 、Ce20S 、Pr
201.Nd、Ox 、Sm20.)を0.5wt%添
加したときの恒温f4境への放置時間と重量変化の関係
を示す特性図であり、この結果がら重量の増加は腐食生
成物の増大を意味することがら、軽希土類酸化物の添加
により、耐食性が向上することが明らかとなった。
Figure 1 shows N d + @ F e a? Light rare earth oxides (Lag 03, Ce20S, Pr
201. Nd, Ox, Sm20. ) is a characteristic diagram showing the relationship between leaving time at a constant temperature F4 boundary and weight change when 0.5 wt% of It has become clear that corrosion resistance is improved by the addition of

第2図は放置時間500時間におけるS m 203添
加量と重量変化の関係を表わしている特性図で、これよ
りO,1wt%以上S m * Osを添加すると耐食
性が向上することが認められる。
FIG. 2 is a characteristic diagram showing the relationship between the amount of S m 203 added and the weight change after a standing time of 500 hours, and it is recognized from this that the corrosion resistance is improved when O, 1 wt % or more of S m *Os is added.

第3図にはS m 20 s添加量による減磁曲線およ
び最大エネルギー積(BH)maxへの影響を示す特性
図で、1.0wt%以下の添加量であれば、最大エネル
ギー積の減少が少ないことが認められる。これは他の酸
化物についても同様の傾向がみられる。
Figure 3 is a characteristic diagram showing the demagnetization curve and the effect on the maximum energy product (BH) max depending on the amount of S m 20 s added. It is recognized that there are few. A similar tendency is observed for other oxides as well.

以上の結果から、軽希土類酸化物添加により耐食性の向
上と、高い磁気特性が両立して得られる効果が詔められ
るものである。
The above results suggest that the addition of light rare earth oxides is effective in achieving both improved corrosion resistance and high magnetic properties.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の軽希土類酸化物を添加と重量変化を示
す特性図。 第2図は本発明の酸化サマリウム(SmmO3)の添加
と重量変化を示す特性図。 第3図(A)、(B)は本発明のSm、O,浜田願人 
セイコー電子工業株式会社 代理人 弁理士  林   敬 之 助m203 添加量(w t ’/J 第 図 抹置時閂(h) H(にOe)
FIG. 1 is a characteristic diagram showing the weight change with addition of the light rare earth oxide of the present invention. FIG. 2 is a characteristic diagram showing the addition of samarium oxide (SmmO3) and weight change according to the present invention. Figures 3 (A) and (B) are Sm, O, Ganto Hamada of the present invention.
Seiko Electronics Industries Co., Ltd. Representative Patent Attorney Keisuke Hayashi m203 Addition amount (w t '/J Figure Removal time bar (h) H (to Oe)

Claims (1)

【特許請求の範囲】[Claims]  R_2T_M_1_4B_1(RはCe、Pr、Nd
、Gd、TbあるいはDyのうち一種あるいは二種以上
の組み合せ、T_MはFeあるいはCoのうち一種ある
いは二種の組み合せ)型正方晶を主相とし、軽希土類酸
化物(La_2O_3、Ce_2O_3、Pr_2O_
3、Nd_2O_3、Sm_2O_3)を0.1〜1.
0wt%含有することを特徴とする希土類磁石合金。
R_2T_M_1_4B_1 (R is Ce, Pr, Nd
, a combination of one or more of Gd, Tb, or Dy; T_M is a combination of one or two of Fe or Co) type tetragonal crystal is the main phase, and light rare earth oxides (La_2O_3, Ce_2O_3, Pr_2O_
3, Nd_2O_3, Sm_2O_3) from 0.1 to 1.
A rare earth magnet alloy characterized by containing 0 wt%.
JP2147009A 1990-06-05 1990-06-05 Rare earth magnetic alloy Pending JPH0441652A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2147009A JPH0441652A (en) 1990-06-05 1990-06-05 Rare earth magnetic alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2147009A JPH0441652A (en) 1990-06-05 1990-06-05 Rare earth magnetic alloy

Publications (1)

Publication Number Publication Date
JPH0441652A true JPH0441652A (en) 1992-02-12

Family

ID=15420493

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2147009A Pending JPH0441652A (en) 1990-06-05 1990-06-05 Rare earth magnetic alloy

Country Status (1)

Country Link
JP (1) JPH0441652A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101499345B (en) 2008-10-23 2012-01-04 运城恒磁科技有限公司 Method for improving rare earth permanent magnet coercive force
CN103632787A (en) * 2013-12-11 2014-03-12 湖南航天工业总公司 Method for sintering and tempering rare-earth cobalt permanent magnetic material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101499345B (en) 2008-10-23 2012-01-04 运城恒磁科技有限公司 Method for improving rare earth permanent magnet coercive force
CN103632787A (en) * 2013-12-11 2014-03-12 湖南航天工业总公司 Method for sintering and tempering rare-earth cobalt permanent magnetic material
CN103632787B (en) * 2013-12-11 2015-11-25 湖南航天磁电有限责任公司 A kind of sintering of rare earth cobalt permanent magnets and tempering method

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