JPH04293206A - Pare earth elements-fe-b based anisotropic permanent magnet - Google Patents
Pare earth elements-fe-b based anisotropic permanent magnetInfo
- Publication number
- JPH04293206A JPH04293206A JP3081876A JP8187691A JPH04293206A JP H04293206 A JPH04293206 A JP H04293206A JP 3081876 A JP3081876 A JP 3081876A JP 8187691 A JP8187691 A JP 8187691A JP H04293206 A JPH04293206 A JP H04293206A
- Authority
- JP
- Japan
- Prior art keywords
- rare earth
- permanent magnet
- magnet
- earth elements
- atomic
- 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.)
- Withdrawn
Links
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 27
- 239000013078 crystal Substances 0.000 claims abstract description 14
- 150000002910 rare earth metals Chemical class 0.000 claims abstract description 12
- 229910052737 gold Inorganic materials 0.000 claims abstract description 8
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 8
- 229910052709 silver Inorganic materials 0.000 claims abstract description 7
- 229910052718 tin Inorganic materials 0.000 claims abstract description 7
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000012535 impurity Substances 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 description 16
- 229910045601 alloy Inorganic materials 0.000 description 10
- 239000000956 alloy Substances 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
- 239000012071 phase Substances 0.000 description 9
- 230000007423 decrease Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 238000005245 sintering Methods 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002775 capsule Substances 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 238000005098 hot rolling Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- -1 Until now Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- 229910052689 Holmium Inorganic materials 0.000 description 1
- 229910000583 Nd alloy Inorganic materials 0.000 description 1
- 229910017495 Nd—F Inorganic materials 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910000828 alnico Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
- H01F1/047—Alloys characterised by their composition
- H01F1/053—Alloys characterised by their composition containing rare earth metals
- H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
- H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
- H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Hard Magnetic Materials (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は希土類元素−Fe−B系
異方性化永久磁石に関し、詳細には薄肉でありながら高
性能であり、例えばボイスコイルモータ用として最適な
特性を発揮する希土類元素−Fe−B系異方性化永久磁
石に関するものである。[Industrial Application Field] The present invention relates to rare earth element-Fe-B anisotropic permanent magnets, and more specifically, rare earth element magnets that are thin-walled yet high-performance, and that exhibit optimal characteristics for use in, for example, voice coil motors. The present invention relates to an anisotropic permanent magnet based on element-Fe-B.
【0002】0002
【従来の技術】磁性材料は、永久磁石を始めとして、一
般家庭用の各種電気製品から大型コンピュータの周辺末
端機器に至るまで幅広い分野で使用されており、重要な
電気,電子材料である。最近では、モータ等の小型化,
高性能化が進められ、永久磁石においても、より薄肉,
高性能であることが要求されている。特に、磁気ヘッド
を磁気ディスク上の任意の情報トラックに位置決めする
為のヘッドアクチュエータ機構で用いられるボイスコイ
ルモータには、より薄肉,高性能の永久磁石が要求され
ている。2. Description of the Related Art Magnetic materials, including permanent magnets, are used in a wide range of fields, from various household appliances to peripheral end devices for large computers, and are important electrical and electronic materials. Recently, the miniaturization of motors, etc.
As performance continues to improve, permanent magnets are becoming thinner and thinner.
High performance is required. In particular, thinner, higher-performance permanent magnets are required for voice coil motors used in head actuator mechanisms for positioning magnetic heads on arbitrary information tracks on magnetic disks.
【0003】近年、フェライト磁石およびアルニコ磁石
に次ぐ第3の永久磁石として、希土類磁石が注目を集め
ている。この希土類磁石は電気製品や精密機器類の小型
化および高精度化に寄与し得る優れた磁気的性質を発揮
するものと期待され、物性研究面および生産技術面共に
活発な進展を見せている。中でも近年特に期待されてい
るのは、希土類元素−遷移元素−B系、例えばNd−F
e−BやPr−Fe−B等の永久磁石である。本発明の
永久磁石組成は希土類元素−Fe−Bを基本成分とする
他、Ag,Au,Pt,SnおよびZnよりなる群から
選択される1種以上の元素を必須成分として含むもので
あって、その評価については追って詳述するが、以下の
説明においては便宜上、希土類元素−Fe−B系(以下
R−Fe−B系磁石と略称することがある)の3元系磁
石を代表的に取り上げて述べることとする。[0003] In recent years, rare earth magnets have attracted attention as the third type of permanent magnet after ferrite magnets and alnico magnets. This rare earth magnet is expected to exhibit excellent magnetic properties that can contribute to the miniaturization and higher precision of electrical products and precision instruments, and active progress is being made in both physical property research and production technology. Among them, the rare earth element-transition element-B system, such as Nd-F, has been particularly expected in recent years.
It is a permanent magnet such as e-B or Pr-Fe-B. The permanent magnet composition of the present invention has a rare earth element -Fe-B as a basic component, and also contains one or more elements selected from the group consisting of Ag, Au, Pt, Sn and Zn as an essential component. Although the evaluation will be explained in detail later, in the following explanation, for convenience, we will use a rare earth element-Fe-B system (hereinafter sometimes abbreviated as R-Fe-B system magnet) ternary system magnet as a representative. I would like to discuss this topic.
【0004】ところでR−Fe−B系磁石の製造方法と
しては、当初次の2方法が検討された。第1の方法は例
えば特開昭59−46008号に見られる様な粉末冶金
に基づく焼結法であるが、■焼結工程に先立って合金の
粉末化処理が必要であること、■粉末状となって酸化を
受け易くなり、焼結中に持込まれる酸素が磁気的性能に
悪影響を与えること、■焼結時に添加される成形助剤に
基づく炭素分の混入によって磁気的性能が低下すること
、■焼結前の生成形体(グリーン体)は低強度であり、
ハンドリング性が悪いこと、等といった幾つかの欠点が
ある為、R−Fe−B系磁石に期待されている特性が十
分に発揮されるには至っていない。By the way, the following two methods were initially considered as methods for manufacturing R--Fe--B magnets. The first method is a sintering method based on powder metallurgy as seen in, for example, JP-A No. 59-46008; (2) Oxygen brought in during sintering has a negative effect on magnetic performance. (2) Magnetic performance may be degraded due to carbon content from forming aids added during sintering. , ■ The formed body (green body) before sintering has low strength,
Due to several drawbacks such as poor handling, the characteristics expected of R-Fe-B magnets have not been fully demonstrated.
【0005】第2の方法は急冷薄片を作った後熱可塑性
樹脂等を用いてボンド磁石とする方法であり、上記欠点
を伴なわない代り、■生産性が低い、■原理的に等方性
磁石しか得られず、従って残留磁束密度(Br)と保磁
力(iHc)の積で示される最大エネルギー積[以下(
BH)maxで表わすことがある]が低く、角形性も良
くない、といった欠点が生じる。そこで積極的に異方性
化するための手段として、急冷薄片を2段階ホットプレ
ス処理(機械的配向処理)に付すことも考えられた(例
えば特開昭59−211549 号,同60−1004
02 号等)。しかしながら生産性が更に低いものとな
るため、量産の必要性を考えると現実的な方法ではない
。The second method is to make a quenched flake and then use a thermoplastic resin or the like to make a bonded magnet.It does not have the above drawbacks, but has the following disadvantages: (1) low productivity, and (2) isotropic in principle. Only magnets can be obtained, and therefore the maximum energy product [hereinafter (
BH) max] is low, and the squareness is also poor. Therefore, as a means to actively make the anisotropy, it has been considered to subject the rapidly cooled flakes to a two-step hot press treatment (mechanical orientation treatment) (for example, Japanese Patent Application Laid-open Nos. 59-211549 and 60-1004).
No. 02, etc.). However, this is not a realistic method considering the need for mass production since the productivity is even lower.
【0006】そこで第3の方法として、例えば特開昭6
2−276803 号に見られる様に、鋳造合金に熱間
圧延を加え、結晶粒の微細化を達成して保磁力の増大を
実現すると共に、結晶軸を特定の方向に並べて磁気的な
異方性化を図るという手段が開発された。しかしながら
通常の圧延方法では板幅方向両側からの拘束が無いため
、圧下された鋳塊の中央部は板幅方向に展延されるが、
板幅端側では十分な密度が得られず、また結晶軸の配向
が不完成となる。従ってこの方法を採用したからといっ
て、直ちに板幅方向全体に亘って磁気的異方性が得られ
る訳ではない。しかも上記の様な通常の熱間圧延条件に
よって板幅全体に所望程度までの軸配向を形成しようと
すれば、相当の強加工を行なわなければならず、従って
これに対応し得る加工性を備えた素材が要求されること
となって希土類磁石の合金組成が大きく制限されるとい
う問題もあった。[0006] Therefore, as a third method, for example,
As seen in No. 2-276803, hot rolling is applied to cast alloys to refine the grains and increase the coercive force. A means of sexualization was developed. However, in the normal rolling method, there is no restraint from both sides in the plate width direction, so the central part of the rolled ingot is rolled out in the plate width direction.
Sufficient density cannot be obtained on the edge side of the plate width, and the orientation of the crystal axes is incomplete. Therefore, even if this method is adopted, it does not mean that magnetic anisotropy can be immediately obtained over the entire width direction of the plate. Moreover, in order to form the desired degree of axial orientation across the entire width of the sheet under the normal hot rolling conditions described above, it is necessary to carry out considerably strong working, and therefore it is necessary to have sufficient workability to cope with this. There was also a problem in that the alloy composition of rare earth magnets was greatly restricted due to the requirement for materials with a high degree of compatibility.
【0007】そこで本発明者らは、上記第3の方法によ
る欠点を解消し得る方法として、合金鋳塊を金属カプセ
ルに封入し、該金属カプセルに対して幅方向から拘束を
加えつつ熱間塑性加工(圧延,鋳造)し、また必要によ
り熱間加工後に熱処理する一連の方法を提案し、先に出
願している(特開平2−250918〜23)。上記技
術の開発によって、加工上の理由に基づく素材面での制
約から解放され、しかも比較的簡単に磁気特性の優れた
異方性化永久磁石が得られる様になった。[0007] The present inventors therefore proposed a method that can overcome the drawbacks of the third method described above, by enclosing an alloy ingot in a metal capsule and applying hot plasticity to the metal capsule while constraining it from the width direction. We have proposed a series of methods for processing (rolling, casting) and, if necessary, heat treatment after hot working, and have previously filed an application (Japanese Patent Laid-Open No. 2-250918-23). With the development of the above-mentioned technology, it has become possible to obtain anisotropic permanent magnets with excellent magnetic properties relatively easily and freed from restrictions in terms of materials due to processing reasons.
【0008】[0008]
【発明が解決しようとする課題】上述した如く、ボイス
コイルモータの様に小型化,高性能化が特に要求される
製品には、用いられる永久磁石に対して、薄肉化と高性
能化という両特性を満足することが必要となる。しかし
ながら一般的に、磁石を薄肉化する程性能は低下する傾
向にあり、この相反する両特性をいかにして満足させる
かが重要なポイントとなる。[Problems to be Solved by the Invention] As mentioned above, for products such as voice coil motors that require particularly small size and high performance, the permanent magnets used must be thinner and have higher performance. It is necessary to satisfy the characteristics. However, in general, the thinner the magnet, the lower its performance tends to be, and the important point is how to satisfy both of these contradictory characteristics.
【0009】例えば1mm以下の薄肉の永久磁石は、ボ
ンド磁石では製造可能であるが、上述した如く磁気特性
の点で難があり、まして薄肉化および高性能が要求され
るボイスコイルモータ用永久磁石としては使用に耐えな
い。一方焼結法においては薄肉のままの焼結が困難であ
り、例えば3mm以下の薄肉の磁石を得ようとすれば、
大きなブロックから削り出すことになるが、薄肉化によ
る性能低下が起こり、後記実施例に示す様に1mm程度
になると希望する磁気特性は得られなくなる。尚薄肉の
異方性磁石に関しては、例えば特開昭62−19256
6 号に示される様に、磁石を機械的に研磨して薄肉化
する方法が提案されている。しかし生産性の低下は免か
れない。For example, thin-walled permanent magnets of 1 mm or less can be manufactured using bonded magnets, but as mentioned above, there are difficulties in terms of magnetic properties, and even more so for permanent magnets for voice coil motors, which require thinner walls and higher performance. It is not usable as such. On the other hand, in the sintering method, it is difficult to sinter the thin wall. For example, if you want to obtain a thin magnet of 3 mm or less,
Although it is machined from a large block, the performance decreases due to thinning, and as shown in Examples below, when the thickness is about 1 mm, the desired magnetic properties cannot be obtained. Regarding thin-walled anisotropic magnets, for example, JP-A-62-19256
As shown in No. 6, a method of mechanically polishing a magnet to make it thinner has been proposed. However, a decline in productivity cannot be avoided.
【0010】本発明は上記の様な技術的課題を解決する
為になされたものであって、その目的は、薄肉でしかも
高性能という両特性を備えた、焼結磁石以上の磁気特性
を有する希土類元素−Fe−B系磁石を提供することに
ある。[0010] The present invention was made to solve the above-mentioned technical problems, and its purpose is to provide a thin-walled magnet with magnetic properties superior to those of a sintered magnet, which also has the characteristics of high performance. An object of the present invention is to provide a rare earth element-Fe-B magnet.
【0011】[0011]
【課題を解決するための手段】上記目的を達成し得た本
発明とは、下記(A)〜(D) の組成を有する平均粒
径30μm 以下の柱状晶組織を熱間塑性加工および熱
処理して異方性化したものであり、30μm 以下の平
均粒径を有する希土類元素−Fe−B系磁石である。
(A) Yを含む希土類元素の2種以上(但しその50
重量%以上がPrである):12〜18原子%(B)
B:4〜6原子%
(C) Ag,Au,Pt,SnおよびZnよりなる群
から選択される1種以上の元素:0.2 〜2原子%(
D) 残部:Feおよび不可避不純物[Means for Solving the Problems] The present invention, which has achieved the above object, is a method in which a columnar crystal structure having an average grain size of 30 μm or less and having the following compositions (A) to (D) is subjected to hot plastic working and heat treatment. It is a rare earth element-Fe-B magnet having an average grain size of 30 μm or less. (A) Two or more rare earth elements including Y (however, 50
% by weight or more is Pr): 12 to 18 atomic % (B)
B: 4 to 6 atomic% (C) One or more elements selected from the group consisting of Ag, Au, Pt, Sn and Zn: 0.2 to 2 atomic% (
D) Remainder: Fe and inevitable impurities
【0012】0012
【作用】本発明者らは、先に提案開示した製造方法に従
って磁石を製造し、薄肉で且つ高性能という両特性を具
備する永久磁石について様々な角度から検討した。その
結果R−Fe−B系磁石の高性能化には、図1に示す如
く、原料となる鋳塊段階での柱状晶組織の平均粒径(鋳
塊粒径)を微細化することが有効であることが分かった
。上記微細化の為には、鋳造時の抜熱量を大きくするこ
とである程度は達成可能であるが、設備が大がかりとな
って生産性の低下を招く。そこで本発明者らは、添加元
素による微細化について検討を重ねたところ、R−Fe
−B系に対する第4の元素として、Ag,Au,Pt,
Sn,Zn等が有効であり、これらを1種または2種以
上組合わせて添加すれば、磁石合金の結晶粒の微細化が
達成されることを見出した。更に、上記添加元素は合金
の粒界相に存在し、加工に伴なう表面劣化層の生成をも
抑制し、0.5mm 程度の薄肉にした場合においても
、焼結磁石を凌駕する磁気特性[(BH)max=35
MGOe以上,iHc =14KOe 以上]が得られ
ることを見出し、本発明を完成した。[Operation] The present inventors manufactured a magnet according to the manufacturing method proposed and disclosed above, and studied from various angles a permanent magnet that has both characteristics of being thin and having high performance. As a result, in order to improve the performance of R-Fe-B magnets, it is effective to refine the average grain size of the columnar crystal structure (ingot grain size) at the ingot stage, which is the raw material, as shown in Figure 1. It turned out to be. Although the above-mentioned refinement can be achieved to some extent by increasing the amount of heat removed during casting, the equipment becomes large-scale, leading to a decrease in productivity. Therefore, the inventors of the present invention repeatedly investigated the refinement using additive elements, and found that R-Fe
-As the fourth element for the B system, Ag, Au, Pt,
It has been found that Sn, Zn, etc. are effective, and by adding one or more of them in combination, the crystal grains of the magnetic alloy can be made finer. Furthermore, the above additive elements exist in the grain boundary phase of the alloy, suppressing the formation of a surface deterioration layer due to processing, and even when the thickness is made as thin as 0.5 mm, the magnetic properties surpass those of sintered magnets. [(BH)max=35
MGOe or more, iHc = 14KOe or more], and completed the present invention.
【0013】次に本発明のR−Fe−B系磁石を構成す
る合金組成について説明する。まず希土元素としては、
これまでもYを含むランタノイド系希土類元素が汎用さ
れてきたが、本発明ではこれらのうち特にPrを半分以
上含む2種以上の希土類元素で構成することが有用であ
るとの結論を得た。Prに併用される希土類元素の種類
は特に限定されないが、中でもNd,Ce,La,Tb
,Dy,Ho,Y等を使用するのが特に好ましい。本発
明の磁石で用いる希土類元素のうち、50重量%以上を
Prとしたのは、Prがもっとも優れた磁気特性を示す
からである。Pr以外については、上記希土類元素のう
ちPr以外のものから、1種または2種以上を組合わせ
て用いればよいが、実用的にはPr−Nd合金がもっと
も有利に用いられる。尚本発明の磁石中の希土類元素に
は、上記以外の希土類元素が少量含まれてもよいが、1
重量%以下に抑えるべきである。Next, the alloy composition constituting the R-Fe-B magnet of the present invention will be explained. First of all, as a rare earth element,
Until now, lanthanoid rare earth elements containing Y have been widely used, but in the present invention, it has been concluded that it is useful to use two or more rare earth elements containing at least half of Pr. The type of rare earth element used in combination with Pr is not particularly limited, but among them Nd, Ce, La, Tb
, Dy, Ho, Y, etc. are particularly preferred. The reason why 50% by weight or more of the rare earth elements used in the magnet of the present invention is Pr is because Pr exhibits the most excellent magnetic properties. Regarding rare earth elements other than Pr, one type or a combination of two or more of the rare earth elements other than Pr may be used, but Pr--Nd alloy is most advantageously used practically. Note that the rare earth elements in the magnet of the present invention may contain a small amount of rare earth elements other than the above, but 1
It should be kept below % by weight.
【0014】本発明のR−Fe−B系磁石において、R
が少な過ぎると主相R2−Fe14−B (原子比、例
えばPr2Fe14B)を形成することができず、熱間
加工時の異方性化に必要とする十分な液相量(主相量)
が得られず、磁石の高性能化は達成されない。こうした
観点からして、希土類元素の割合は12原子%以上とす
る必要がある。一方上限については18原子%を超える
と、非磁性相であるRリッチ相の過剰を招き、これが磁
束密度の低下等となって現われ、良好な磁気特性を発揮
することはできない。In the R-Fe-B magnet of the present invention, R
If it is too small, the main phase R2-Fe14-B (atomic ratio, e.g. Pr2Fe14B) cannot be formed, and the amount of liquid phase (main phase amount) necessary for anisotropy during hot working cannot be formed.
cannot be obtained, and the high performance of the magnet cannot be achieved. From this point of view, the proportion of rare earth elements needs to be 12 atomic % or more. On the other hand, if the upper limit exceeds 18 at %, the R-rich phase, which is a non-magnetic phase, will be excessive, and this will appear as a decrease in magnetic flux density, making it impossible to exhibit good magnetic properties.
【0015】Bは4〜6原子%とする必要があり、4原
子%未満では主相体積率の不足が生じ、磁束密度の低下
を招く。他方上限については、磁気特性を有しないR2
Fe4B4相の出現によるiHc の低下を防止すると
いう観点から6原子%以下とする必要がある。B must be contained in an amount of 4 to 6 atomic %; if it is less than 4 atomic %, the volume fraction of the main phase will be insufficient, leading to a decrease in magnetic flux density. On the other hand, regarding the upper limit, R2 does not have magnetic properties.
From the viewpoint of preventing a decrease in iHc due to the appearance of the Fe4B4 phase, it is necessary to keep it at 6 atomic % or less.
【0016】Ag,Au,Pt,SnおよびZn等の添
加元素は、上述の如く柱状組織の微細化、および研削加
工に伴なう表面劣化層の生成抑制等を達成し、これによ
って薄肉であっても高い性能を発揮させる為のものであ
る。上記効果を達成するためには、単独または合計で0
.2 原子%とする必要があるが、あまり多くすると非
磁性の粒界相が増加し、特性の低下を招くので2原子%
以下とすべきである。Additive elements such as Ag, Au, Pt, Sn, and Zn achieve the refinement of the columnar structure and the suppression of the formation of a surface deterioration layer that accompanies the grinding process, as described above, thereby making it possible to achieve thin walls. It is designed to achieve high performance even when In order to achieve the above effect, it is necessary to use 0 individually or in total.
.. It is necessary to set it to 2 at%, but if it is too large, the non-magnetic grain boundary phase will increase and the properties will deteriorate, so it should be set at 2 at%.
It should be:
【0017】本発明の磁石は、上記必須成分の他、残部
は基本的にはFeおよび不可避不純物からなる。Feは
磁性相形成にとって必須の元素であるが、その一部(例
えば20重量%程度)をCoで置換してもよい。In addition to the above-mentioned essential components, the magnet of the present invention basically consists of Fe and inevitable impurities. Although Fe is an essential element for forming a magnetic phase, a portion (for example, about 20% by weight) of Fe may be replaced with Co.
【0018】本発明の磁石においては、柱状晶組織およ
び異方性化した後の結晶組織のいずれにおいても、その
結晶平均粒径を30μm 以下に規定したものであるが
、その理由は下記の通りである。まず図1に示した如く
、焼結磁石と同等以上の特性を得る為には鋳造後におけ
る柱状晶組織の平均粒径を30μm 以下とする必要が
ある。また鋳塊に対して熱間塑性加工および熱処理を施
すと保磁力が向上するが、過剰な熱処理を行なうと結晶
粒が粗大化してかえって保磁力の低下を招くので、熱処
理して異性化した後の結晶においても平均粒径を30μ
m 以下にする必要がある。In the magnet of the present invention, the average grain size of both the columnar crystal structure and the crystal structure after anisotropy is specified to be 30 μm or less, and the reason for this is as follows. It is. First, as shown in FIG. 1, in order to obtain properties equivalent to or better than those of a sintered magnet, the average grain size of the columnar crystal structure after casting must be 30 μm or less. In addition, hot plastic working and heat treatment of the ingot improves the coercive force, but excessive heat treatment will coarsen the crystal grains and cause a decrease in the coercive force. Even in crystals, the average grain size is 30μ
It must be less than m.
【0019】以下本発明を実施例によって更に詳細に説
明するが、下記実施例は本発明を限定する性質のもので
はなく、前・後記の趣旨に徴して設計変更することはい
ずれも本発明の技術的範囲に含まれるものである。[0019] The present invention will be explained in more detail with reference to examples below, but the following examples are not intended to limit the present invention, and any design changes in accordance with the spirit of the preceding and following descriptions are within the scope of the present invention. It is included in the technical scope.
【0020】[0020]
【実施例】表1に示す組成の合金鋳塊(No. 1 〜
20) を高周波溶解によって製造した。尚このときの
出発原料は、Feとしては純度99.9重量%の電解鉄
,Bはフェロボロン合金,希土類元素およびその他の添
加元素は純度99.9重量%のものを夫々用いた。そし
て銅鋳型によって鋳造し、平均粒径30μm 以下の微
細な柱状晶を形成した。[Example] Alloy ingots having the compositions shown in Table 1 (No. 1 to
20) was produced by high frequency melting. The starting materials at this time were electrolytic iron with a purity of 99.9% by weight for Fe, ferroboron alloy for B, and 99.9% by weight of rare earth elements and other additive elements. Then, it was cast using a copper mold to form fine columnar crystals with an average grain size of 30 μm or less.
【0021】[0021]
【表1】[Table 1]
【0022】次に、合金鋳塊を切断後鉄製カプセルに封
入し、幅方向から拘束を加えつつ950 ℃にて全圧下
率76%の熱間圧延を行なった。引き続き、1000℃
×6時間(1段目)および480 ℃×2時間(2段目
)の熱処理を行い、得られた磁石合金の磁気特性および
平均粒径を調査した。その結果を表2に示すが、Ag,
Au,Pt,Sn,Zn等を添加したものは、結晶を微
細化することができ良好な磁気特性が得られていること
が分かる。Next, the alloy ingot was cut and sealed in an iron capsule, and hot rolled at 950° C. with a total reduction of 76% while being restrained from the width direction. Continue to 1000℃
Heat treatment was performed at 480°C for 6 hours (first stage) and at 480°C for 2 hours (second stage), and the magnetic properties and average grain size of the obtained magnet alloy were investigated. The results are shown in Table 2.Ag,
It can be seen that those to which Au, Pt, Sn, Zn, etc. are added can make the crystals finer and obtain good magnetic properties.
【0023】[0023]
【表2】[Table 2]
【0024】次に、Nd13Dy1Fe79B7の組成
(原子比)で、且つ平均粒径が3μm からなる合金粉
末を、10KOe 磁界中で1.5ton/cm2の圧
力で加圧成形した後、99.999%純度のArガス中
(250Torr)で1070℃×2時間焼結し、更に
530 ℃×1時間の時効熱処理を行なって焼結磁石を
得た。得られた焼結磁石と、表2に示したNo. 11
,14,17,19,20の磁石を夫々用い、厚みが3
,1 ,0.5 ,0.3 ,1.0 ,0.05(
mm)となる様に研削し、それぞれの磁気特性を調査し
た。その結果を表3に示すが、本発明のものは、0.5
mm の薄肉でも例えばボイスコイルモータ用の永久磁
石として十分使用に耐え得る良好な磁気特性を示してい
ることがわかる。Next, an alloy powder having a composition (atomic ratio) of Nd13Dy1Fe79B7 and an average particle size of 3 μm was pressure-molded in a 10 KOe magnetic field at a pressure of 1.5 ton/cm2, and then the powder had a purity of 99.999%. The magnet was sintered in Ar gas (250 Torr) at 1070°C for 2 hours, and further subjected to aging heat treatment at 530°C for 1 hour to obtain a sintered magnet. The obtained sintered magnet and No. 1 shown in Table 2. 11
, 14, 17, 19, and 20 magnets with a thickness of 3
,1 ,0.5 ,0.3 ,1.0 ,0.05(
mm), and the magnetic properties of each were investigated. The results are shown in Table 3, and the one of the present invention is 0.5
It can be seen that even with a thickness as thin as mm 2 , it exhibits good magnetic properties that can be used as a permanent magnet for a voice coil motor, for example.
【0025】[0025]
【表3】[Table 3]
【0026】[0026]
【発明の効果】以上述べた如く本発明によれば、希土類
元素−Fe−B系に第4の元素としてAg,Au,Pt
,Sn,Zn等を添加することによって結晶粒の微細化
が達成され、3μm 以下の薄肉であっても良好な磁気
特性を発揮することのできる永久磁石が得られた。また
本発明に係る永久磁石は、その特性からしてボイスコイ
ルモータ用の永久磁石として最適である。Effects of the Invention As described above, according to the present invention, Ag, Au, and Pt are added as the fourth element to the rare earth element-Fe-B system.
By adding . Further, the permanent magnet according to the present invention is most suitable as a permanent magnet for a voice coil motor due to its characteristics.
【図1】鋳塊粒径と磁気特性の関係を示すグラフである
。FIG. 1 is a graph showing the relationship between ingot particle size and magnetic properties.
Claims (2)
すると共に、平均粒径30μm 以下の柱状晶組織を熱
間塑性加工および熱処理して異方性化したものであり、
30μm 以下の平均粒径を有するものであることを特
徴とする希土類元素−Fe−B系異方性化永久磁石。 (A) Yを含む希土類元素の2種以上(但しその50
重量%以上がPrである):12〜18原子%(B)
B:4〜6原子% (C) Ag,Au,Pt,SnおよびZnよりなる群
から選択される1種以上の元素:0.2 〜2原子%(
D) 残部:Feおよび不可避不純物[Claim 1] Containing the following components (A) to (D), a columnar crystal structure with an average grain size of 30 μm or less is made anisotropic by hot plastic working and heat treatment,
A rare earth element-Fe-B anisotropic permanent magnet having an average particle size of 30 μm or less. (A) Two or more rare earth elements including Y (however, 50
% by weight or more is Pr): 12 to 18 atomic % (B)
B: 4 to 6 atomic% (C) One or more elements selected from the group consisting of Ag, Au, Pt, Sn and Zn: 0.2 to 2 atomic% (
D) Remainder: Fe and inevitable impurities
異方性化方向の厚みが0.5 〜3mmであり、最大エ
ネルギー積が35MGOe以上,保磁力が14KOe
以上である請求項1に記載の異方性化永久磁石。[Claim 2]
The thickness in the anisotropy direction is 0.5 to 3 mm, the maximum energy product is 35 MGOe or more, and the coercive force is 14 KOe.
The anisotropic permanent magnet according to claim 1, which is the above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3081876A JPH04293206A (en) | 1991-03-20 | 1991-03-20 | Pare earth elements-fe-b based anisotropic permanent magnet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3081876A JPH04293206A (en) | 1991-03-20 | 1991-03-20 | Pare earth elements-fe-b based anisotropic permanent magnet |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04293206A true JPH04293206A (en) | 1992-10-16 |
Family
ID=13758662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3081876A Withdrawn JPH04293206A (en) | 1991-03-20 | 1991-03-20 | Pare earth elements-fe-b based anisotropic permanent magnet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04293206A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007010860A1 (en) * | 2005-07-15 | 2007-01-25 | Neomax Co., Ltd. | Rare earth sintered magnet and method for production thereof |
| JP2007027428A (en) * | 2005-07-15 | 2007-02-01 | Neomax Co Ltd | Rare earth sintered magnet and manufacturing method thereof |
| JP2007134417A (en) * | 2005-11-08 | 2007-05-31 | Neomax Co Ltd | Manufacturing method of rare earth sintered magnet |
| JP2007154241A (en) * | 2005-12-02 | 2007-06-21 | Neomax Co Ltd | Rare earth sintered magnet and manufacturing method thereof |
| JP2007220885A (en) * | 2006-02-16 | 2007-08-30 | Hitachi Metals Ltd | Rare earth sintered magnet, and its manufacturing method |
-
1991
- 1991-03-20 JP JP3081876A patent/JPH04293206A/en not_active Withdrawn
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007010860A1 (en) * | 2005-07-15 | 2007-01-25 | Neomax Co., Ltd. | Rare earth sintered magnet and method for production thereof |
| JP2007027428A (en) * | 2005-07-15 | 2007-02-01 | Neomax Co Ltd | Rare earth sintered magnet and manufacturing method thereof |
| US9551052B2 (en) | 2005-07-15 | 2017-01-24 | Hitachi Metals, Ltd. | Rare earth sintered magnet and method for production thereof |
| DE112006000070B4 (en) | 2005-07-15 | 2024-12-05 | Hitachi, Ltd. | Rare earth metal sintered magnet and method for its production |
| JP2007134417A (en) * | 2005-11-08 | 2007-05-31 | Neomax Co Ltd | Manufacturing method of rare earth sintered magnet |
| JP2007154241A (en) * | 2005-12-02 | 2007-06-21 | Neomax Co Ltd | Rare earth sintered magnet and manufacturing method thereof |
| JP2007220885A (en) * | 2006-02-16 | 2007-08-30 | Hitachi Metals Ltd | Rare earth sintered magnet, and its manufacturing method |
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