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JPH01150303A - Magnetic anisotropy type sintered magnet and manufacture thereof - Google Patents

Magnetic anisotropy type sintered magnet and manufacture thereof

Info

Publication number
JPH01150303A
JPH01150303A JP62308594A JP30859487A JPH01150303A JP H01150303 A JPH01150303 A JP H01150303A JP 62308594 A JP62308594 A JP 62308594A JP 30859487 A JP30859487 A JP 30859487A JP H01150303 A JPH01150303 A JP H01150303A
Authority
JP
Japan
Prior art keywords
weight
parts
sintered
sintered magnet
powder
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
JP62308594A
Other languages
Japanese (ja)
Inventor
Sakae Higano
栄 日向野
Kazunori Umo
羽毛 和記
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.)
Mitsubishi Steel Mfg Co Ltd
Original Assignee
Mitsubishi Steel Mfg Co 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 Mitsubishi Steel Mfg Co Ltd filed Critical Mitsubishi Steel Mfg Co Ltd
Priority to JP62308594A priority Critical patent/JPH01150303A/en
Publication of JPH01150303A publication Critical patent/JPH01150303A/en
Pending legal-status Critical Current

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/032Magnets 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
    • H01F1/04Magnets 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
    • H01F1/047Alloys characterised by their composition
    • H01F1/053Alloys characterised by their composition containing rare earth metals
    • H01F1/055Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
    • H01F1/057Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
    • H01F1/0571Alloys 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
    • H01F1/0575Alloys 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 pressed, sintered or bonded together
    • H01F1/0577Alloys 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 pressed, sintered or bonded together sintered

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  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Hard Magnetic Materials (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、複雑形状や複雑で微細構造を有する希土類系
異方性焼結磁石及びその製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an anisotropic rare earth sintered magnet having a complicated shape or a complicated fine structure, and a method for manufacturing the same.

〔従来の技術〕[Conventional technology]

従来の希土類磁石は、合金粉末を金型中(配向磁場の有
無を問わず)で3〜lot/cdの圧力で加圧成形後焼
結したり、ホットプレスに続くホットホーミングで焼結
体を作成している。
Conventional rare earth magnets are produced by press-forming alloy powder in a mold (with or without an orienting magnetic field) at a pressure of 3-lot/cd and then sintering it, or by hot pressing followed by hot homing to form a sintered body. Creating.

(例えば特願昭57−145072号参照)又、希土類
磁石合金粉末と結合剤からなる混合物を磁場押出成形法
により成形後焼結して焼結体を作成する方法もある。(
例えば特開昭61−27[1303号公報参照) 〔発明が解決しようとする問題点〕 上記従来技術の中、ホットプレスを用いる方法では、作
成できる焼結体が比較的単純な形状(円柱、リング、角
柱、板等)に限定され、複雑形状にしようとすれば、後
加工が必要であり、それでもなお限度があってしかもコ
ストアップを招く。
(For example, see Japanese Patent Application No. 57-145072.) There is also a method in which a mixture of rare earth magnet alloy powder and a binder is formed by magnetic extrusion and then sintered to produce a sintered body. (
For example, see JP-A-61-27 [1303] [Problems to be solved by the invention] Among the above-mentioned conventional techniques, in the method using hot press, the sintered body that can be produced has a relatively simple shape (cylindrical, (rings, prisms, plates, etc.), and if you try to create a complicated shape, post-processing is required, which still has its limits and increases costs.

さらに、押出成形によるものも、上記の°方法と同様に
比較的qt純形状の連続体しか得られず、しかも成形後
に所定の長さに切断する工程が必要で、これも又コスト
アップを招く。
Furthermore, as with the above-mentioned ° method, extrusion molding also yields only a continuum with a relatively pure shape, and furthermore, it requires a step of cutting into a predetermined length after molding, which also increases costs. .

そこで、本発明では、筐体状の磁石とか、磁石部分と非
磁性金属部分が同時成形で得られるような成形体又は円
柱に角穴を複数個あけ、部分々々により肉厚に偏りのあ
るような複雑形状の磁石体を得んとするものである。し
かも複雑で不定形状をとるにも拘らず、歪のない磁石を
得んとするものである。
Therefore, in the present invention, a plurality of square holes are drilled in a case-shaped magnet, a molded body or a cylinder in which a magnet part and a non-magnetic metal part are obtained by simultaneous molding, and the wall thickness is uneven depending on the part. The objective is to obtain a magnet body with such a complicated shape. Furthermore, the aim is to obtain a magnet free from distortion, even though it has a complex and irregular shape.

°〔問題点を解決するための手段〕 本発明の第1は主成分が20〜45重量%のR(Rは希
土類元素の少くとも1種)と、0.1〜3、Oi[t%
のBと、52〜79.9fff fi1%のFeまたは
Fe+Co (ただしCOはFeの1/2以下)の範囲
を有し、その平均粒径が1〜20μmを存する粉末10
0部と、バインダとしてワックス、レジンおよび滑剤の
6〜14部との混合物の焼結材で、焼結密度が90〜9
8%であることを特徴とする磁気異方性焼結磁石である
。又、第2は、主成分が20〜45重鑓%のR(Rは希
土類元素の少くとも1種)と、残部がFes Co5C
u及びZrよりなる合金で、その平均粒径が1〜20μ
mを有する粉末100部と、バインダとしてワックス、
レンジおよび滑剤の6〜14部との混合物の焼結材で、
焼結密度が90〜98%であることを特徴とする磁気異
方性焼結磁石である。さらに第3は、主成分が20〜4
5重量%のR(Rは希土類元素の少くとも1種)と、O
01〜3.0重−%のBと52〜79.9重量%のFe
またはFe+Co(ただし、CoはFeの1/2以下)
である合金を1〜20μmに粉砕し、その粉砕粉100
部に対し、バインダとしてワックス、レジンおよび滑剤
の6〜14部を添加混合してペレットにした後、磁石粉
末が異方的に配列するように設計された金型中にに射出
成形し、ついで得られた成形体を脱ワックス後、焼結密
度が90〜98%となるように焼結する磁気異方性焼結
磁石の製造方法。そして第4発明は主成分が20〜45
重量%のR(Rは希土類元素の少くとも1種)と、残部
がFe5Co、Cu及びZrである合金を1〜20μm
に粉砕し、その粉砕粉100部に対し、バインダとして
ワックス、レジンおよび滑剤の6〜14部を添加混合し
てペレットにした後、磁石粉末が異方的に配列するよう
に設計された金型中にに射出成形し、ついで得られた成
形体を脱ワックス後、焼結密度が90〜98%となるよ
うに焼結することを特徴とする磁気異方性焼結磁石の製
造方法である。
° [Means for solving the problem] The first aspect of the present invention is that the main components are 20 to 45% by weight of R (R is at least one kind of rare earth element), 0.1 to 3% by weight, Oi[t%]
B and 52 to 79.9 fff fi1% of Fe or Fe+Co (however, CO is 1/2 or less of Fe), and the average particle size is 1 to 20 μm.
0 parts and 6 to 14 parts of wax, resin and lubricant as binders, with a sintered density of 90 to 9.
This is a magnetically anisotropic sintered magnet characterized by a magnetic anisotropy of 8%. The second one is mainly composed of 20 to 45% R (R is at least one kind of rare earth element) and the balance is Fes Co5C.
An alloy consisting of u and Zr with an average grain size of 1 to 20μ
100 parts of a powder having m and wax as a binder,
in a range and a mixture of sintered material with 6 to 14 parts of lubricant,
This is a magnetically anisotropic sintered magnet characterized by a sintered density of 90 to 98%. Furthermore, the third one has a main component of 20 to 4
5% by weight of R (R is at least one rare earth element) and O
01-3.0 wt-% B and 52-79.9 wt-% Fe
or Fe+Co (however, Co is less than 1/2 of Fe)
The alloy is pulverized to 1 to 20 μm, and 100
6 to 14 parts of wax, resin, and lubricant as binders are added and mixed into pellets, which are then injection molded into a mold designed to arrange magnet powder anisotropically. A method for producing a magnetically anisotropic sintered magnet, in which the obtained compact is dewaxed and then sintered to a sintered density of 90 to 98%. And the fourth invention has a main component of 20 to 45
% by weight of R (R is at least one kind of rare earth element) and the balance is Fe5Co, Cu, and Zr.
100 parts of the pulverized powder is mixed with 6 to 14 parts of wax, resin, and lubricant as a binder to form pellets, and then a mold is designed so that the magnetic powder is arranged anisotropically. A method for producing a magnetically anisotropic sintered magnet, which is characterized by injection molding the molded body inside the magnet, dewaxing the obtained molded body, and then sintering it to a sintered density of 90 to 98%. .

すなわち、本発明は、R−Fe (Co) −B合金も
しくは、R[FG、 C0% Cus Zrl n系合
金の1(雑で精密な形状を有する磁気異方性焼結磁石を
得るために、■磁石粉末の特定範囲の設定、■精密金型
中に忠実に充填できる特定の組成にすること、■金型を
規定の異方性を付与できる磁界強度と向きに作成して射
出成形すること、■成形体を特定の圧力下で脱バインダ
し、続いて焼結処理すること、等の主要な要件を組合せ
ることによって所期の目的を達するものである。
That is, the present invention uses R-Fe (Co)-B alloy or R[FG, C0% Cus Zrl n-based alloy 1 (in order to obtain a magnetically anisotropic sintered magnet having a rough and precise shape, ■ Setting a specific range of magnetic powder, ■ Creating a specific composition that can be faithfully filled into a precision mold, ■ Creating a mold with a magnetic field strength and orientation that gives a specified anisotropy, and then performing injection molding. The desired objective is achieved by combining the following main requirements: (1) Debinding of the molded body under a specific pressure and subsequent sintering treatment.

本発明の合金組成において、RとしてはSc。In the alloy composition of the present invention, R is Sc.

Y1ランタニド、アクチニド系列の希土類から選択され
るが、とくにY1ランタニド系列の元素が好ましい。R
の童が20重置火より少ないと、高い保磁力が得られず
、45重置火よりも多いと、磁化の大きさが低下し、い
ずれも永久磁石には適さなくなる。
It is selected from rare earth elements of Y1 lanthanide and actinide series, and elements of Y1 lanthanide series are particularly preferred. R
If the number of magnets is less than 20, high coercive force cannot be obtained, and if it is more than 45, the magnitude of magnetization decreases, making both of them unsuitable for permanent magnets.

Coはキュリー温度を上昇させる目的でFeと置換する
ことが可能であるが、Fefaの1/2を越えて置換す
ると、磁化の大きさが低ドしてくるので、永久磁石には
適さなくなる。
Co can be substituted with Fe for the purpose of increasing the Curie temperature, but if more than half of Fefa is substituted, the magnitude of magnetization decreases, making it unsuitable for permanent magnets.

なお、第2発明におけるCuSZrを含む合金によく知
られている2−17系合金であるので、Cu、Zrの添
加理由も知られており、ここで詳細に述べることに省略
する。
Note that since the alloy is a 2-17 alloy which is well known as the alloy containing CuSZr in the second invention, the reason for adding Cu and Zr is also known, and will not be described in detail here.

又、第1発明、第2発明共に合金の保磁力を増加させる
目的で、Al5SiSTi、V。
Further, in both the first invention and the second invention, Al5SiSTi, V is used for the purpose of increasing the coercive force of the alloy.

Cr、Mn5Cu、Zn5GaSGe、Zr。Cr, Mn5Cu, Zn5GaSGe, Zr.

Nb、  MOS Sn、  Sb、  Hf  S 
Ta、W%Bi等(CuSZrは第2発明のみ)を必要
に応じて添加することも可能である。
Nb, MOS Sn, Sb, HfS
It is also possible to add Ta, W%Bi, etc. (CuSZr is only in the second invention) as necessary.

合金粉末の平均粒径が1〜20μmとしたのは、1μm
より小さくする場合は、粉砕に時間がかかり、かつ粉末
が酸化したり発火したりするおそれがあり、取り扱いが
むずかしくなる。また、粉末の平均粒径が20μmを越
えると、熱処理によっても充分大きな保磁力が得られな
くなり、かつ、磁場による配向性が低下する。
The average particle size of the alloy powder is 1 μm to 20 μm.
If the powder is made smaller, it will take more time to crush the powder, and there is a risk that the powder will oxidize or catch fire, making it difficult to handle. Furthermore, if the average particle size of the powder exceeds 20 μm, a sufficiently large coercive force cannot be obtained even by heat treatment, and the orientation caused by a magnetic field decreases.

バインダーとしてのワックス、レジン、滑剤は、加熱混
練性、流動性、脱ワックス性を基本にその添加量を考慮
すべきである。すなわち、ペレット化する際の加熱混練
性の観点から合金粉末とぬれ性のよい極性基を持つアク
リル系やEVA(酢酸ビニールアセテート)が、流動性
(−成形性)の観点からポリエチレン系やポリスチレン
系、さらには粉末の滑りをよくする意味での滑剤として
ステアリン酸アミド等が挙げられる。さらに正確な型を
保ったまま脱フックス効果を上げるためには、アクリル
系樹脂と一緒にパラフィン系や変性ワックスが推奨され
る。
The amount of wax, resin, and lubricant used as binders should be considered based on heat-kneading properties, fluidity, and dewaxing properties. In other words, acrylic and EVA (vinyl acetate), which have polar groups that have good wettability with alloy powder, are used from the viewpoint of heat kneading properties when pelletizing, while polyethylene and polystyrene are used from the viewpoint of fluidity (-formability). Furthermore, stearic acid amide and the like can be mentioned as a lubricant to improve the slippage of the powder. In order to increase the de-fuxing effect while maintaining a more accurate shape, paraffin-based or modified wax is recommended along with acrylic resin.

これらのワックス、レジン、滑剤の配合割合は、合金粉
末の種類、粒径および粒度分布によって異なるが、総量
として、合金粉末100部に対して6〜14部が適当で
ある。6部未満では射出成形の際、合金粉末が射出筒に
つまってしまうし、14部を越えると脱ワックス工程や
焼結工程で型部れや変形等の不良品を出してしまう。
The proportions of these waxes, resins, and lubricants vary depending on the type, particle size, and particle size distribution of the alloy powder, but the appropriate total amount is 6 to 14 parts per 100 parts of the alloy powder. If it is less than 6 parts, the alloy powder will clog the injection tube during injection molding, and if it exceeds 14 parts, defective products such as mold part warping or deformation will be produced in the dewaxing process or sintering process.

ワックス、レジン、滑剤のそれぞれの配合口は、合金粉
末100部に対して、ワックス1〜4部、レジン4.5
〜8部、滑剤0.5〜2部の範囲が好適である。
The mixing ratio of wax, resin, and lubricant is 1 to 4 parts of wax and 4.5 parts of resin to 100 parts of alloy powder.
-8 parts, lubricant 0.5-2 parts is suitable.

本発明焼結磁石の密度は90〜98%の範囲がよく、9
0%未満では磁石として不満足な特性しか得られず、9
8%を越えると割れの恐れが出る場合もあるので好まし
くない。
The density of the sintered magnet of the present invention is preferably in the range of 90 to 98%;
If it is less than 0%, only unsatisfactory characteristics as a magnet will be obtained, and 9
If it exceeds 8%, cracking may occur, which is not preferable.

製造方法の発明における射出成形工程は、90℃未満で
は混線物がスムーズに射出されないし、又、IH℃以上
になると熱分解の可能性が大きくなったり、過剰流動性
となり、ワックス分だけ先に射出されたりする。
In the injection molding process of the manufacturing method invention, if the temperature is lower than 90℃, the mixed material will not be injected smoothly, and if the temperature is higher than IH℃, there is a greater possibility of thermal decomposition or excessive fluidity, and the wax component will be injected first. It may be ejected.

又、射出成形特金型のキャビティ内の磁場強さは10k
Oe以上とするとよいが、IQkOc未満では、合金粉
末の配向が充分でない。
Also, the magnetic field strength inside the cavity of the special injection mold is 10k.
It is preferable to set it to Oe or more, but if it is less than IQkOc, the orientation of the alloy powder is not sufficient.

又、脱ワックス工程は、望ましくは1 kg / cd
以ドの圧力下で、3〜b 400℃まで昇温しで行なう。かかる条件下で脱ワック
スを行なうことにより、成形体の形状を健全に保ち、ワ
ックスの溶出を容易にし、かつ、とかく長時間に亘り易
い脱ワックス工程を短縮するのに効果的である。昇温速
度が3℃/hr未満では生産性からみて実用性がなく、
■5℃/11rを越えると、成形体の形状が崩れる場合
がある。
Also, the dewaxing process is preferably 1 kg/cd
The temperature is raised to 3-400°C under the following pressure. By dewaxing under such conditions, it is effective to maintain the shape of the molded body, to facilitate wax elution, and to shorten the dewaxing process, which tends to take a long time. If the heating rate is less than 3°C/hr, it is not practical in terms of productivity;
■If the temperature exceeds 5°C/11r, the shape of the molded product may collapse.

又、温度を400℃以上にすると脱ワックスにより成形
体が崩れて元の合金粉末に戻ってしまうことが多い。
Furthermore, if the temperature is increased to 400° C. or higher, the compact often collapses due to dewaxing and returns to the original alloy powder.

焼結はl kg / cd以上の不活性ガス圧下で1.
000〜1.2[10℃で行なうとよい。不活性ガスに
よる加圧は合金元素の蒸発を防止する。焼結温度は 1
.000℃未満では焼結体の密度が90%未満となり、
又1,200℃を越えると密度が9g%を越えてしまい
、ワレの発生等の出る場合があって不適当である。
Sintering is carried out under an inert gas pressure of 1 kg/cd or more.
000 to 1.2 (preferably carried out at 10°C). Pressurization with inert gas prevents evaporation of alloying elements. The sintering temperature is 1
.. At temperatures below 000°C, the density of the sintered body becomes less than 90%,
Moreover, if the temperature exceeds 1,200°C, the density will exceed 9 g%, which may cause cracking, etc., which is inappropriate.

〔実施例〕〔Example〕

以下、本発明を実施例によって詳細に説明する。 Hereinafter, the present invention will be explained in detail with reference to Examples.

実施例 1 25重量%S m S18重量%Fe、5重量%Cu 
s2.2重量%Z「、残COおよび不可避不純物よりな
る組成の合金を粉砕し、平均粒径を9μmとした。この
粉末100部に対し、アクリル樹脂粉末6部、パラフィ
ン2部、ステアリン酸アミド1部を添加し、加圧ニーダ
(N2ガス5kg/cd、  140℃xlhr)でペ
レットにした。
Example 1 25% by weight S m S 18% by weight Fe, 5% by weight Cu
An alloy with a composition consisting of s2.2 wt% 1 part was added and pelletized using a pressure kneader (N2 gas 5 kg/cd, 140°C x lhr).

第1図!1しびに第2図に示す複雑形状の磁石(放射状
配向磁界−IQkOc 、外径a−60鰭、歯先円内1
k b −40mm 、歯高c −5in、筒長d−2
0mm)を成形すべき金型を備えた射出成形機で、ノズ
ル温度130℃に調整し、520kg/c+Jの圧力で
射出し、グリーン成形体を得た。
Figure 1! 1. A complex-shaped magnet shown in Fig. 2 (radial orientation magnetic field - IQkOc, outer diameter a - 60 fin, tip circle 1
k b -40mm, tooth height c -5in, tube length d-2
Using an injection molding machine equipped with a mold for molding 0 mm), the nozzle temperature was adjusted to 130° C., and injection was performed at a pressure of 520 kg/c+J to obtain a green molded product.

グリーン成形体の各部位の寸法を測定後、脱ワックス炉
に入れ、Arガスを2 kg / c+Jに保ちつつ流
し、400℃まで5℃/hrで昇温し、400℃で1時
間保持後冷却した。この時点でバインダーの90%は除
去されており、外径で測定した収縮率はほとんど0であ
った。
After measuring the dimensions of each part of the green molded body, place it in a dewaxing furnace, flow Ar gas while maintaining it at 2 kg/c+J, raise the temperature to 400°C at a rate of 5°C/hr, hold it at 400°C for 1 hour, and then cool it. did. At this point, 90% of the binder had been removed and the shrinkage measured by the outer diameter was almost 0.

次にこれを焼結炉に入れ、5×104Torrに真空曵
き後、室温より 600℃までを2時間で昇温(Arガ
ス1kg/cl#)L、ここで1時間保持しくこの時点
でバインダーはほとんど除去された)、1.180℃ま
で1時間で昇温した。1,180℃で2時間保持後、室
温までArガスで冷却し、引続き800℃で2時間、次
いで400℃まで0.8℃/minで徐冷し、400℃
で4時間保持し、次いで炉冷という上程をとった。焼結
体についての各AJl定値は表1の通りであった。rと
は試料の磁場配向方向、2とはそれと直角方向(厚み方
向)に/lII定したことを示す。
Next, this was placed in a sintering furnace, and after being vacuumed to 5 x 104 Torr, the temperature was raised from room temperature to 600°C in 2 hours (Ar gas 1kg/cl#) and held there for 1 hour.At this point, the binder was removed. 1. The temperature was raised to 180° C. in 1 hour. After being held at 1,180°C for 2 hours, it was cooled to room temperature with Ar gas, then at 800°C for 2 hours, and then slowly cooled to 400°C at a rate of 0.8°C/min.
The mixture was held for 4 hours and then cooled in the furnace. Each AJl constant value for the sintered body was as shown in Table 1. r indicates the magnetic field alignment direction of the sample, and 2 indicates that /lII is set in the direction perpendicular to it (thickness direction).

表  1 実施例 2 28.5重量%Nd、  3.5重量%Dy、  1.
5重量%B、8重量%Co、残Feおよび不可避不純物
よりなる組成の合金を粉砕し、平均粒径3.8μmとし
た。一方、99.99%のCu粉(平均粒径lOμm)
を用意し、表2の諸元でペレット化し、2軸射出成形機
で、第3図並びに第4図に示す形状のものを一体成形し
た。すなわち、図中2は磁石部(放射状配向)、3はC
uよりなる磁石保持部である。
Table 1 Example 2 28.5% by weight Nd, 3.5% by weight Dy, 1.
An alloy having a composition of 5% by weight B, 8% by weight Co, residual Fe, and unavoidable impurities was ground to give an average particle size of 3.8 μm. On the other hand, 99.99% Cu powder (average particle size lOμm)
were prepared, pelletized according to the specifications in Table 2, and integrally molded into the shapes shown in FIGS. 3 and 4 using a two-screw injection molding machine. That is, in the figure, 2 is the magnet part (radial orientation), 3 is C
This is a magnet holding part made of u.

表  2 バインダーは全て合金粉、Cu粉それぞれ100部に対
しての割合である。
Table 2 All binders are in proportion to 100 parts of each of the alloy powder and Cu powder.

このグリーンシート成形体をA「ガス°1.5kg/ 
cdの加圧下、350℃までlO℃/hrで昇温し、3
50℃で1時間保持して、脱ワックスした。次いでこれ
を焼結炉に移し、4〜5×lO”’ Torrの真空度
で600℃まで2時間で昇温し、ここで1時間保持後、
1,075℃までAr2kg/c−の加圧下で1時間か
けて昇温し、3時間保持後ガス急冷した。
This green sheet molded body was
Under pressure of cd, the temperature was raised to 350°C at a rate of 10°C/hr, and
It was held at 50° C. for 1 hour to dewax. Next, this was transferred to a sintering furnace, and the temperature was raised to 600 °C in 2 hours at a vacuum level of 4 to 5 × 1O'' Torr, and after holding there for 1 hour,
The temperature was raised to 1,075°C over 1 hour under a pressure of 2 kg/c- of Ar, and after being maintained for 3 hours, it was rapidly cooled with gas.

焼結体を炉より取り出し、磁石部、磁石保持部のそれぞ
れを切り出して密度を測定した結果、95%、99%で
あり、収縮率は表3の通りであった。
The sintered body was taken out of the furnace, the magnet part and the magnet holding part were cut out, and the densities were measured, and the results were 95% and 99%, and the shrinkage percentages were as shown in Table 3.

表  3 さらに、焼結体より切り出した磁石部の半径方向(磁場
配向方向−「)、円周方向(−X)、高さh゛向(−z
)の磁性値は表4の通りであった。
Table 3 Furthermore, the radial direction (magnetic field orientation direction -'), circumferential direction (-X), and height h' direction (-z
) were as shown in Table 4.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、複雑で精密な形状で、しかも歪のない
焼結磁石が容易に得られる。
According to the present invention, a sintered magnet with a complicated and precise shape and without distortion can be easily obtained.

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

第1図は本発明の一実施例の磁石の正面図、第2図は第
1図の・1と面図、第3図は他の実施例の磁石の正面図
、第4図は第3図の平面図である。
Fig. 1 is a front view of a magnet according to one embodiment of the present invention, Fig. 2 is a side view of .1 in Fig. 1, Fig. 3 is a front view of a magnet of another embodiment, and Fig. 4 is a FIG.

Claims (8)

【特許請求の範囲】[Claims] (1)主成分が20〜45重量%のR(Rは希土類元素
の少くとも1種)と、0.1〜3.0重量%のBと、5
2〜79.9重量%のFeまたはFe+Co(ただしC
oはFeの1/2以下)の範囲を有し、その平均粒径が
1〜20μmを有する粉末100部と、バインダとして
ワックス、レジンおよび滑剤の6〜14部との混合物の
焼結材で、焼結密度が90〜98%であることを特徴と
する磁気異方性焼結磁石。
(1) The main components are 20-45% by weight of R (R is at least one rare earth element), 0.1-3.0% by weight of B, and 5% by weight of B.
2 to 79.9% by weight of Fe or Fe+Co (however, C
A sintered material of a mixture of 100 parts of powder having an average particle size of 1 to 20 μm and 6 to 14 parts of wax, resin, and lubricant as a binder. , a magnetically anisotropic sintered magnet characterized by having a sintered density of 90 to 98%.
(2)主成分が20〜45重量%のR(Rは希土類元素
の少くとも1種)と、残部がFe、Co、Cu及びZr
よりなる合金で、その平均粒径が1〜20μmを有する
粉末100部と、バインダとしてワックス、レンジおよ
び滑剤の6〜14部との混合物の焼結材で、焼結密度が
90〜98%であることを特徴とする磁気異方性焼結磁
石。
(2) The main component is 20 to 45% by weight of R (R is at least one rare earth element), and the balance is Fe, Co, Cu, and Zr.
A sintered material consisting of a mixture of 100 parts of powder having an average particle size of 1 to 20 μm and 6 to 14 parts of wax, range, and lubricant as binders, with a sintered density of 90 to 98%. A magnetically anisotropic sintered magnet characterized by:
(3)主成分が20〜45重量%のR(Rは希土類元素
の少くとも1種)と、0.1〜3.0重量%のBと52
〜79.9重量%のFeまたはFe+Co(ただし、C
oはFeの1/2以下)である合金を1〜20μmに粉
砕し、その粉砕粉100部に対し、バインダとしてワッ
クス、レジンおよび滑剤の6〜14部を添加混合してペ
レットにした後、磁石粉末が異方的に配列するように設
計された金型中にに射出成形し、ついで得られた成形体
を脱ワックス後、焼結密度が90〜98%となるように
焼結することを特徴とする磁気異方性焼結磁石の製造方
法。
(3) The main components are 20 to 45% by weight of R (R is at least one rare earth element), 0.1 to 3.0% by weight of B, and 52
~79.9% by weight of Fe or Fe+Co (however, C
(o is 1/2 or less of Fe) is pulverized to 1 to 20 μm, and to 100 parts of the pulverized powder, 6 to 14 parts of wax, resin, and lubricant are added as a binder and mixed to form pellets. Injection molding is carried out into a mold designed to arrange magnet powder anisotropically, and then the obtained molded body is dewaxed and sintered so that the sintered density is 90 to 98%. A method for manufacturing a magnetically anisotropic sintered magnet, characterized by:
(4)主成分が20〜45重m%のR(Rは希土類元素
の少くとも1種)と、残部がFe、Co、Cu及びZr
である合金を平均粒径1〜20μmに粉砕し、その粉砕
粉100部に対し、バインダとしてワックス、レジンお
よび滑剤の6〜14部を添加混合してペレットにした後
、磁石粉末が異方的に配列するように設計された金型中
にに射出成形し、ついで得られた成形体を脱ワックス後
、焼結密度が90〜98%となるように焼結することを
特徴とする磁気異方性焼結磁石の製造方法。
(4) The main component is 20 to 45% by weight of R (R is at least one rare earth element), and the balance is Fe, Co, Cu, and Zr.
The alloy is pulverized to an average particle size of 1 to 20 μm, and 6 to 14 parts of wax, resin, and lubricant are added as a binder to 100 parts of the pulverized powder to form pellets. A method of manufacturing a magnetic material that is characterized by injection molding into a mold designed to arrange the particles, and then dewaxing the obtained molded product and sintering it to a sintered density of 90 to 98%. A method for manufacturing a oriented sintered magnet.
(5)射出成形を90〜160℃、1kg/cm^2以
上の加圧下で行なう特許請求の範囲第(3)項又は第(
4)項記載の磁気異方性焼結磁石の製造方法。
(5) Injection molding is carried out at 90 to 160°C and under pressure of 1 kg/cm^2 or more.
4) A method for producing a magnetically anisotropic sintered magnet as described in item 4).
(6)射出成形金型中のキャビティ磁場強さが10kO
c以上で射出ノズル温度が100〜140℃とする特許
請求の範囲第(3)項又は第(4)項記載の磁気異方性
焼結磁石の製造方法。
(6) The cavity magnetic field strength in the injection mold is 10kO
The method for producing a magnetically anisotropic sintered magnet according to claim 3 or 4, wherein the injection nozzle temperature is 100 to 140° C.
(7)脱ワックスを1kg/cm^2以下の不活性ガス
加圧下で、3〜15℃/hrで400℃まで昇温するこ
とにより行なう特許請求の範囲第(3)項又は第(4)
項記載の磁気異方性焼結磁石の製造方法。
(7) Claim (3) or (4) wherein dewaxing is carried out by heating up to 400°C at a rate of 3 to 15°C/hr under an inert gas pressure of 1 kg/cm^2 or less
A method for producing a magnetically anisotropic sintered magnet as described in .
(8)焼結を1kg/cm^2以下の不活性ガス圧下で
1,000〜1,200℃で行なう特許請求の範囲第(
3)項又は第(4)項記載の磁気異方性焼結磁石の製造
方法。
(8) The sintering is carried out at 1,000 to 1,200°C under an inert gas pressure of 1 kg/cm^2 or less (
The method for manufacturing a magnetically anisotropic sintered magnet according to item 3) or item (4).
JP62308594A 1987-12-08 1987-12-08 Magnetic anisotropy type sintered magnet and manufacture thereof Pending JPH01150303A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62308594A JPH01150303A (en) 1987-12-08 1987-12-08 Magnetic anisotropy type sintered magnet and manufacture thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62308594A JPH01150303A (en) 1987-12-08 1987-12-08 Magnetic anisotropy type sintered magnet and manufacture thereof

Publications (1)

Publication Number Publication Date
JPH01150303A true JPH01150303A (en) 1989-06-13

Family

ID=17982920

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62308594A Pending JPH01150303A (en) 1987-12-08 1987-12-08 Magnetic anisotropy type sintered magnet and manufacture thereof

Country Status (1)

Country Link
JP (1) JPH01150303A (en)

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JPS60184605A (en) * 1984-07-09 1985-09-20 Sumitomo Special Metals Co Ltd Molding improver for alloy powder for permanent magnet
JPS6230847A (en) * 1985-08-01 1987-02-09 Sumitomo Special Metals Co Ltd Production of permanent magnet material
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