JPS63152111A - Permanent magnet manufacturing method - Google Patents

Permanent magnet manufacturing method

Info

Publication number
JPS63152111A
JPS63152111A JP61298697A JP29869786A JPS63152111A JP S63152111 A JPS63152111 A JP S63152111A JP 61298697 A JP61298697 A JP 61298697A JP 29869786 A JP29869786 A JP 29869786A JP S63152111 A JPS63152111 A JP S63152111A
Authority
JP
Japan
Prior art keywords
coupling
permanent magnet
silane
treated
coupling agent
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
JP61298697A
Other languages
Japanese (ja)
Inventor
Takashi Furuya
古谷 嵩司
Norio Yoshikawa
紀夫 吉川
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.)
Daido Steel Co Ltd
Original Assignee
Daido Steel 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 Daido Steel Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP61298697A priority Critical patent/JPS63152111A/en
Publication of JPS63152111A publication Critical patent/JPS63152111A/en
Pending legal-status Critical Current

Links

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
    • H01F1/0572Alloys 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 with a protective layer

Landscapes

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

Abstract

PURPOSE:To manufacture the permanent magnet having both excellent magnetic characteristics and corrosion-resisting property by a method wherein rareearth- iron magnetic powder is coupling-treated using silane or titanate coupling agent, and it is molded after mixing with resin. CONSTITUTION:The rareearth-iron magnetic powder manufactured by performing a superquenching treatment is coupling-treated using a titanate coupling agent. In this case, when the coupling treatment is going to be performed, various kinds of silane coupling agents and titanate coupling agents are properly diluted using the solvent such as alcohol, toluene and the like, and it is dried up. After the above-mentioned material has been dried up, the coupling-treated magnetic powder is mixed with thermosetting resin and thermoplastic resin, and the molded body of the prescribed shape is formed by performing a compression molding or an injection molding operation. Then, a curing treatment is performed on the molded body as occasion demands. As the material magnetic powder is coupling-treated using a silane or titanate coupling agent, the obtained permanent magnet has excellent corrosion-resisting property, and the deterioration in magnetic characteristics caused by the generation of corrosion can be prevented.

Description

【発明の詳細な説明】 [発明の目的〕 (産業上の利用分野) この発明は、家庭電化製品、音響製品、ff′?計部品
、自動車部品、精密機器等々の永久磁石を用いる広範囲
な用途に使用することができる永久磁石を製造するのに
利用される永久磁石の製造方法に関するものである。
[Detailed Description of the Invention] [Object of the Invention] (Industrial Application Field) This invention is applicable to home appliances, audio products, ff'? The present invention relates to a method for manufacturing permanent magnets that can be used in a wide range of applications using permanent magnets, such as instrument parts, automobile parts, and precision instruments.

〔従来の技術〕[Conventional technology]

近年、従来のアルニコ磁石や希土類−コバルト系磁石よ
りもさらに磁気特性に優れている磁石として、希土類−
鉄系の永久磁石が注目を集めるようになっている。
In recent years, rare earth magnets have been developed as magnets with even better magnetic properties than conventional alnico magnets and rare earth cobalt magnets.
Iron-based permanent magnets are attracting attention.

(発明が解決しようとする問題点) この冷土類−鉄系の永久磁石の代表的なものとしては、
Nd−Fe−B系の永久磁石がある。このNd−Fe−
B系の永久磁石は磁気特性には著しく優れているものの
、#食性があまり良くないという欠点を有している。
(Problems to be solved by the invention) Representative examples of this cold earth-iron permanent magnet include:
There are permanent magnets based on Nd-Fe-B. This Nd-Fe-
Although B-based permanent magnets have extremely excellent magnetic properties, they have the drawback of not having very good eating properties.

そして、例えば焼結法により製造したNb−Fe−B系
永久磁石の耐食性はあまりよくないほか、超急冷Nd−
Fe−B粉末を使用し、樹脂と混合して圧縮成形あるい
は射出成形した永久磁石においても、激しい腐食環境に
おいては必ずしも耐食性が良好であるとはいえないとい
う問題点があった。
For example, the corrosion resistance of Nb-Fe-B permanent magnets manufactured by the sintering method is not very good, and the ultra-quenched Nd-
Even in permanent magnets that are compression molded or injection molded using Fe-B powder and mixed with resin, there is a problem in that corrosion resistance is not necessarily good in a severely corrosive environment.

(発明の目的) この発明は、上述した従来の問題点に着目してなされた
もので、磁気特性が良好であるとともに耐食性にも優れ
ている永久磁石を製造することが可能である永久磁石の
製造方法を提供することを目的としているものである。
(Objective of the Invention) This invention was made by focusing on the above-mentioned conventional problems, and it is possible to produce a permanent magnet that has good magnetic properties and excellent corrosion resistance. The purpose is to provide a manufacturing method.

[発明の構成] この発明による永久磁石の製造方法は、希土類−鉄系の
磁石粉末をシラン系、チタネート系のカップリング剤で
カップリング処理し、次いで樹脂と混合して成形するよ
うにし、磁気特性が良好であるほか、耐食性を改善でき
るようにしたことを特徴としているものである。
[Structure of the Invention] The method for producing a permanent magnet according to the present invention involves coupling rare earth-iron magnet powder with a silane-based or titanate-based coupling agent, and then mixing it with a resin and molding it. In addition to having good properties, it is characterized by improved corrosion resistance.

この発明が適用される希土類−鉄系の磁石粉末としては
、超急冷法により製造した磁石粉末を用いることが磁気
特性および耐食性向上の観点からとくに望ましい。
As the rare earth-iron magnet powder to which this invention is applied, it is particularly desirable to use magnet powder produced by an ultra-quenching method from the viewpoint of improving magnetic properties and corrosion resistance.

また、希土類−鉄系の磁石粉末としては、R1−ct−
β−アFecxxβMyで表わされ、Rが希土類元素の
1種または2種以上、Feが鉄、XがB、C,N、Si
、Pの1種または2種以上、MがTi、Zr、Hf、V
、Nb、Ta。
In addition, as rare earth-iron magnet powder, R1-ct-
β-A is represented by FecxxβMy, R is one or more rare earth elements, Fe is iron, and X is B, C, N, Si.
, one or more types of P, M is Ti, Zr, Hf, V
, Nb, Ta.

Cr 、Mo 、W、All 、Znの1種または2種
以上であり。
One or more of Cr, Mo, W, All, and Zn.

0.60≦α≦0.85゜ 0<β≦0.15、 O≦γ≦o、oi 、 であるものに適用することが望ましく、なかでもNd−
Fe−B系の磁石粉末に適用することが磁気特性の優れ
た永久磁石の耐食性を改善できるようになることから望
ましい。
It is desirable to apply it to those where 0.60≦α≦0.85゜0<β≦0.15, O≦γ≦o, oi, among others, Nd-
It is desirable to apply this method to Fe-B-based magnet powder because it can improve the corrosion resistance of permanent magnets with excellent magnetic properties.

そして、上記式で定められる磁石粉末を用いる場合に、
0.60≦α≦0.85とすることによって良好な最大
エネルギ′u!L((BH)max)を得ることができ
、Fe中の0.10以下をN i 、 M n 、 C
oの1種または2種以上で置換することができ、N i
 、 M nによる保磁力(BHC、IHC)の向上、
Coによるキュリ一点の上昇を期待することができる。
When using the magnetic powder defined by the above formula,
By setting 0.60≦α≦0.85, a good maximum energy 'u! L((BH)max) can be obtained, and 0.10 or less in Fe can be obtained by combining N i , M n , C
o can be substituted with one or more types of N i
, improvement of coercive force (BHC, IHC) by Mn,
We can expect a one point increase due to Co.

また、O<β≦0.15の範囲とすることによって、保
磁力(BHC、IHC)の向上および残留磁束密度(B
r)の温度係数の向上に効果があり、γ≦0.01の範
囲とすることによってこれらM元素の硼化物、炭化物、
窒化物、珪化物。
In addition, by setting the range of O<β≦0.15, coercive force (BHC, IHC) and residual magnetic flux density (B
It is effective in improving the temperature coefficient of r), and by setting γ≦0.01, borides, carbides, and
Nitride, silicide.

燐化物等を形成させ、磁気特性を向上できるようになる
By forming phosphides, etc., magnetic properties can be improved.

そこで、この発明においては、より望ましくは超急冷法
により製造した上記希土類−鉄系の磁石粉末をシラン系
、チタネート系のカップリング剤でカップリング処理す
る。
Therefore, in the present invention, more preferably, the rare earth-iron magnet powder produced by the ultra-quenching method is coupled with a silane-based or titanate-based coupling agent.

この場合のカップリング処理に際しては、各種のシラン
系カップリング剤やチタネート系カップリング剤を適宜
アルコール、トルエン、蒸留水などの溶剤で稀釈し、そ
の後乾燥する。
In the coupling treatment in this case, various silane coupling agents and titanate coupling agents are appropriately diluted with a solvent such as alcohol, toluene, or distilled water, and then dried.

そして、前記乾燥後のカップリング処理した磁石粉末を
熱硬化性樹脂や熱可塑性樹脂などの樹脂と混合し、圧縮
成形や射出成形などによって所定形状の成形体とする。
Then, the magnet powder subjected to the coupling treatment after drying is mixed with a resin such as a thermosetting resin or a thermoplastic resin, and formed into a molded body of a predetermined shape by compression molding, injection molding, or the like.

その後、必要に応じて前記成形体に対してキュア処理を
施す。
Thereafter, the molded body is subjected to a curing treatment, if necessary.

このようにして製造された永久磁石は、原料となる磁石
粉末がシラン系やチタネート系のカップリング剤でカッ
プリング処理されているため、耐食性に優れたものとな
っており、錆発生による磁気特性の低下を防止できるよ
うになる。
Permanent magnets manufactured in this way have excellent corrosion resistance because the raw material magnet powder is coupled with a silane-based or titanate-based coupling agent. This makes it possible to prevent a decline in

(実施例1) 超急冷法により製造した3ONd−IB−Fe゛ の微
粉末(粒径:200pm以下)に対して、シランカップ
リング剤(日本ユニカー(株)製A−1100)を噴霧
状にして添加しながらカップリング処理した。このとき
、シランカップリング剤の添加量は、シランカップリン
グ剤:50重量部、エチルアルコール:135重量部、
蒸留水:15重量部の割合で混合した溶液を、磁石微粉
末に対して、シランカップリング剤が2重量%となるよ
うに調整した。
(Example 1) A silane coupling agent (A-1100 manufactured by Nippon Unicar Co., Ltd.) was sprayed onto fine powder (particle size: 200 pm or less) of 3ONd-IB-Fe produced by an ultra-quenching method. Coupling treatment was carried out while adding. At this time, the amount of silane coupling agent added was 50 parts by weight of silane coupling agent, 135 parts by weight of ethyl alcohol,
Distilled water: A mixed solution of 15 parts by weight was adjusted so that the amount of the silane coupling agent was 2% by weight based on the fine magnet powder.

次に、上記シランカップリング剤でカップリング処理し
た磁石粉末を100’Oで3時間加熱して乾燥したのち
、エポキシ樹脂を2重量%添加して混合し、7ton/
Cmノの圧力で直径11mm、高さ10mmの円柱体に
圧縮成形し、得られた成形体に対して150℃で1時間
加熱するキュア処理を施した。
Next, the magnet powder coupled with the above silane coupling agent was dried by heating at 100'O for 3 hours, and then 2% by weight of epoxy resin was added and mixed.
It was compression molded into a cylindrical body with a diameter of 11 mm and a height of 10 mm at a pressure of cm, and the resulting molded body was subjected to a curing treatment by heating at 150° C. for 1 hour.

一方、比較のために、同じ磁石粉末を用いてカップリン
グ処理を施さずに上記と同様の工程で成形体を得た。
On the other hand, for comparison, a molded body was obtained in the same process as above using the same magnet powder but without coupling treatment.

そして、上記2種類の成形体に対して、温度:50 ’
C、湿度=99%2時間96Hrの温州試験を実施した
ところ、第1表に示す結果であった。
Then, for the above two types of molded bodies, temperature: 50'
C. A Wenzhou test was carried out at 99% humidity for 2 hours and 96 hours, and the results are shown in Table 1.

(実施例2) 超急冷法により製造した3ONd−IB−Feの微粉末
(粒径:200Bm以下)に対して、チタネートカップ
リング剤(味の素(株)製T 1−KRTTS)を用い
てカップリング処理を行った。このとき、チタネートカ
ップリング剤:100重量部と、トルエン;100重量
部とを混合した溶液中に前記磁石粉末を浸漬してカップ
リング処理を行った。
(Example 2) Coupling was performed using a titanate coupling agent (T1-KRTTS manufactured by Ajinomoto Co., Inc.) to a fine powder of 3ONd-IB-Fe (particle size: 200 Bm or less) produced by an ultra-quenching method. processed. At this time, the magnet powder was immersed in a solution containing 100 parts by weight of a titanate coupling agent and 100 parts by weight of toluene to perform a coupling treatment.

次いで、前記磁石粉末を浸漬してカップリング処理を行
ったのち残った溶液を除去し、100°Cで3時間加熱
して乾燥したのち、エポキシ樹脂を2重量%添加して混
合し、7ton/cm2の圧力で直径11mm、高さ1
01mの円柱体を圧縮成形し、得られた成形体に対して
150°Cで1時間加熱するキュア処理を施した。
Next, after performing a coupling treatment by immersing the magnet powder, the remaining solution was removed, and after drying by heating at 100°C for 3 hours, 2% by weight of epoxy resin was added and mixed. Diameter 11mm, height 1 with cm2 pressure
A cylindrical body having a length of 0.01 m was compression molded, and the resulting molded body was subjected to a curing treatment by heating at 150°C for 1 hour.

一方、比較のために、同じ磁石粉末を用いてカップリン
グ処理を行わずに上記と同様の工程で成形体を得た。
On the other hand, for comparison, a molded body was obtained in the same process as above using the same magnet powder without performing the coupling treatment.

そして、上記2種類の成形体に対して96時間の塩水噴
霧試験を実施したところ、第2表に示す結果であった。
Then, a 96-hour salt water spray test was conducted on the two types of molded bodies, and the results are shown in Table 2.

[発明の効果] 以上説明してきたように、この発明による永久磁石の製
造方法によれば、希土類−鉄系の磁石粉末をシラン系、
チタネート系のカップリング剤でカップリング処理し、
次いで、樹脂と混合したのち成形するようにしたから、
磁気特性が良好であるとともに耐食性にも優れており、
錆の発生による磁気特性の低下をできるだけ防止するこ
とが可能であろ永久磁石を製造することができるように
なるという非常に優れた効果がもたらされる。
[Effects of the Invention] As explained above, according to the method for producing a permanent magnet according to the present invention, rare earth-iron based magnet powder is mixed with silane-based,
Coupling treatment with titanate coupling agent,
Next, it was mixed with resin and then molded, so
It has good magnetic properties and excellent corrosion resistance.
A very excellent effect is brought about in that permanent magnets can be manufactured by preventing deterioration of magnetic properties due to the occurrence of rust as much as possible.

Claims (1)

【特許請求の範囲】 (1)希土類−鉄系の磁石粉末をシラン系、チタネート
系のカップリング剤でカップリング処理し、次いで樹脂
と混合したのち成形することを特徴とする永久磁石の製
造方法。 (2)希土類−鉄系の磁石粉末が、 R_1_−_α_−_β_−_γFe_αX_βM_γ
で表わされ、Rが希土類元素の1種または2種以上、F
eが鉄、XがB、C、N、Si、Pの1種または2種以
上、MがTi、Zr、Hf、V、Nb、Ta、Cr、M
o、W、Al、Znの1種または2種以上であり、 0.60≦α≦0.85、 0<β≦0.15、 0≦γ≦0.01、 であることを特徴とする特許請求の範囲第(1)項に記
載の永久磁石の製造方法。 (3)Fe中の0.10以下をNi、Mn、Coの1種
または2種以上で置換したことを特徴とする特許請求の
範囲第(2)項に記載の永久磁石の製造方法。 (4)成形後にキュア処理を施すようにしたことを特徴
とする特許請求の範囲第(1)項ないし第(3)項のい
ずれかに記載の永久磁石の製造方法。
[Scope of Claims] (1) A method for producing a permanent magnet, characterized in that rare earth-iron magnet powder is subjected to a coupling treatment with a silane-based or titanate-based coupling agent, and then mixed with a resin and then molded. . (2) Rare earth-iron magnet powder is R_1_-_α_-_β_-_γFe_αX_βM_γ
, R is one or more rare earth elements, F
e is iron, X is one or more of B, C, N, Si, P, M is Ti, Zr, Hf, V, Nb, Ta, Cr, M
o, W, Al, and Zn, and is characterized by: 0.60≦α≦0.85, 0<β≦0.15, 0≦γ≦0.01. A method for manufacturing a permanent magnet according to claim (1). (3) The method for producing a permanent magnet according to claim (2), wherein 0.10 or less of Fe is replaced with one or more of Ni, Mn, and Co. (4) A method for manufacturing a permanent magnet according to any one of claims (1) to (3), characterized in that a curing treatment is performed after molding.
JP61298697A 1986-12-17 1986-12-17 Permanent magnet manufacturing method Pending JPS63152111A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61298697A JPS63152111A (en) 1986-12-17 1986-12-17 Permanent magnet manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61298697A JPS63152111A (en) 1986-12-17 1986-12-17 Permanent magnet manufacturing method

Publications (1)

Publication Number Publication Date
JPS63152111A true JPS63152111A (en) 1988-06-24

Family

ID=17863109

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61298697A Pending JPS63152111A (en) 1986-12-17 1986-12-17 Permanent magnet manufacturing method

Country Status (1)

Country Link
JP (1) JPS63152111A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0374810A (en) * 1989-08-16 1991-03-29 Hitachi Metals Ltd Resin bond magnet
JPH04129203A (en) * 1990-09-20 1992-04-30 Mitsubishi Steel Mfg Co Ltd permanent magnet powder

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5994406A (en) * 1982-11-19 1984-05-31 Dainippon Plastics Co Ltd Composition of plastic magnet
JPS60223102A (en) * 1984-04-19 1985-11-07 Seiko Epson Corp Manufacturing method of magnet powder
JPS60254708A (en) * 1984-05-31 1985-12-16 Daido Steel Co Ltd Manufacture of permanent magnet
JPS61174364A (en) * 1985-09-17 1986-08-06 Mori Kaneo permanent magnet
JPS61284906A (en) * 1985-06-10 1986-12-15 Seiko Epson Corp Resin bond magnet raw material
JPS62276803A (en) * 1985-08-13 1987-12-01 Seiko Epson Corp Rare earth-iron permanent magnet

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5994406A (en) * 1982-11-19 1984-05-31 Dainippon Plastics Co Ltd Composition of plastic magnet
JPS60223102A (en) * 1984-04-19 1985-11-07 Seiko Epson Corp Manufacturing method of magnet powder
JPS60254708A (en) * 1984-05-31 1985-12-16 Daido Steel Co Ltd Manufacture of permanent magnet
JPS61284906A (en) * 1985-06-10 1986-12-15 Seiko Epson Corp Resin bond magnet raw material
JPS62276803A (en) * 1985-08-13 1987-12-01 Seiko Epson Corp Rare earth-iron permanent magnet
JPS61174364A (en) * 1985-09-17 1986-08-06 Mori Kaneo permanent magnet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0374810A (en) * 1989-08-16 1991-03-29 Hitachi Metals Ltd Resin bond magnet
JPH04129203A (en) * 1990-09-20 1992-04-30 Mitsubishi Steel Mfg Co Ltd permanent magnet powder

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