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JPH0444402B2 - - Google Patents
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JPH0444402B2 - - Google Patents

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Publication number
JPH0444402B2
JPH0444402B2 JP62146513A JP14651387A JPH0444402B2 JP H0444402 B2 JPH0444402 B2 JP H0444402B2 JP 62146513 A JP62146513 A JP 62146513A JP 14651387 A JP14651387 A JP 14651387A JP H0444402 B2 JPH0444402 B2 JP H0444402B2
Authority
JP
Japan
Prior art keywords
resin
coercive force
magnetic field
aging treatment
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.)
Expired - Lifetime
Application number
JP62146513A
Other languages
Japanese (ja)
Other versions
JPS63308902A (en
Inventor
Hirofumi Nakano
Masakuni Kamya
Yoshio Matsuo
Kazuo Matsui
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.)
FDK Corp
Original Assignee
FDK Corp
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 FDK Corp filed Critical FDK Corp
Priority to JP62146513A priority Critical patent/JPS63308902A/en
Publication of JPS63308902A publication Critical patent/JPS63308902A/en
Publication of JPH0444402B2 publication Critical patent/JPH0444402B2/ja
Granted legal-status Critical Current

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  • Hard Magnetic Materials (AREA)
  • Manufacturing Cores, Coils, And Magnets (AREA)

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、樹脂結合剤を用いて磁石粉体を結合
した永久磁石の製造方法に関し、更に詳しくは、
2−17系希土類磁石粉体を時効処理前の低保磁力
状態において磁場中成形を行い、その後に時効処
理を施し、特定性状の高分子樹脂を含浸固化させ
ることによつて磁気特性に優れ且つ機械的強度の
高い樹脂結合型永久磁石を製造できる方法に関す
るものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for manufacturing a permanent magnet in which magnetic powder is bonded using a resin binder, and more specifically,
2-17 rare earth magnet powder is molded in a magnetic field in a low coercive force state before aging treatment, and then subjected to aging treatment and impregnated and solidified with a polymer resin with specific properties, resulting in excellent magnetic properties and The present invention relates to a method for manufacturing resin-bonded permanent magnets with high mechanical strength.

[従来の技術] 従来、樹脂結合型の希土類永久磁石を製造する
方法としては、先ず原料である希土類磁石合金を
粉砕し成形して焼結した後、そのまま時効処理を
行い、次にそれを粉砕した後、その時効処理後の
粉体と有機結合剤とを混練し、磁場中で形成した
後、内部に含まれている有機結合剤を固化処理す
る方法が一般的である。ここで有機結合剤として
は、熱可塑性樹脂または熱硬化性樹脂が用いられ
る。
[Prior Art] Conventionally, the method for manufacturing resin-bonded rare earth permanent magnets is to first crush, shape and sinter the raw material rare earth magnet alloy, then subject it to an aging treatment, and then crush it. After that, the aging-treated powder and an organic binder are kneaded and formed in a magnetic field, and then the organic binder contained therein is generally solidified. Here, as the organic binder, a thermoplastic resin or a thermosetting resin is used.

このような樹脂結合型の希土類磁石は、磁気特
性が比較的高く、量産性に優れ寸法精度が出し易
く、また形状の自由度が大きい等の利点があり、
近年、急速に種々な用途で使用されつつある。
Such resin-bonded rare earth magnets have relatively high magnetic properties, are easy to mass-produce, can easily achieve dimensional accuracy, and have a large degree of freedom in shape.
In recent years, it is rapidly being used for various purposes.

[発明が解決しようとする問題点] 磁場中で成形を行う時に磁石粉体を十分に配向
させるためには、印加する磁場の強さは素材であ
る磁石粉体の保磁力の4〜5倍以上が必要である
と言われている。このため従来技術において、例
えばSm2Co17系の樹脂結合型永久磁石の場合に
は、成形時に40〜50kOe以上の強い磁場を印加し
なければならない。
[Problems to be solved by the invention] In order to sufficiently orient the magnetic powder when molding is performed in a magnetic field, the strength of the applied magnetic field must be 4 to 5 times the coercive force of the magnetic powder that is the material. It is said that more than that is necessary. For this reason, in the prior art, for example, in the case of Sm 2 Co 17 based resin-bonded permanent magnets, a strong magnetic field of 40 to 50 kOe or more must be applied during molding.

しかし現在広く用いられている磁場プレス装置
で得られる磁場の強さは上記の値を満足できない
(一般に製造ラインで印加可能な磁場は15kOe程
度である)ため、実際に行われている磁場中成形
では素材原料粉体を十分に配向できない。
However, the strength of the magnetic field obtained with the currently widely used magnetic press equipment cannot satisfy the above values (generally, the magnetic field that can be applied on the production line is about 15 kOe), so In this case, the raw material powder cannot be sufficiently oriented.

このような問題を解決するため、本発明者等は
先に時効処理する以前の保磁力が6kOe以下の磁
石粉体を先に磁場中成形し、その後に時効処理を
施す方法を提案した。この方法は成形時に低磁場
でも磁石粉体の十分な配向ができることから、容
易に高い磁気特性を有する樹脂結合型永久磁石を
製造できる利点がある。
In order to solve such problems, the present inventors proposed a method in which magnet powder with a coercive force of 6 kOe or less before being subjected to aging treatment is first formed in a magnetic field, and then subjected to aging treatment. This method has the advantage that a resin-bonded permanent magnet with high magnetic properties can be easily produced because magnet powder can be sufficiently oriented even in a low magnetic field during molding.

しかしこの製造方法では、時効処理後に高分子
樹脂を含浸させ固化処理する必要があり、得られ
る樹脂結合型磁石は、使用する高分子樹脂の条件
(性状)によつては磁石粉体と高分子樹脂とを均
一に分布させた状態で固着することが難しく、そ
のため、ややもすると機械的強度の低下を招く場
合があつた。
However, with this manufacturing method, it is necessary to impregnate and solidify a polymer resin after aging treatment, and the resulting resin-bonded magnet may contain magnet powder and polymer resin depending on the conditions (properties) of the polymer resin used. It is difficult to adhere to the resin in a uniformly distributed state, which may lead to a decrease in mechanical strength.

本発明の目的は、本発明者等が先に提案した時
効処理する以前の保磁力が6kOe以下の磁石粉体
を用いて磁場中成形を行つた後に時効処理を施す
方法を更に発展させて、従来技術に比べてより一
層磁気特性を向上させることができるのは無論の
こと、磁石粉体と高分子樹脂とを均一に分布させ
て固着させ、機械的強度の優れた樹脂結合型永久
磁石を製造できる方法を提供することにある。
The purpose of the present invention is to further develop the method previously proposed by the present inventors in which magnet powder with a coercive force of 6 kOe or less before aging is subjected to forming in a magnetic field and then subjected to aging treatment. It goes without saying that the magnetic properties can be further improved compared to conventional technology, but the magnet powder and polymer resin are evenly distributed and bonded together, resulting in resin-bonded permanent magnets with excellent mechanical strength. The purpose is to provide a method for manufacturing.

[問題点を解決するための手段] 上記のような目的を達成することのできる本発
明は、2−17系希土類磁石粉体を、時効処理する
以前の保磁力が6kOe以下の時に磁場中成形し、
その後、得られた成形体を時効処理し、次いで粘
度が20〜3000cp(センチポアズ)の高分子樹脂を
含浸させ固化処理する樹脂結合型永久磁石の製造
方法である。
[Means for Solving the Problems] The present invention, which can achieve the above objects, forms 2-17 rare earth magnet powder in a magnetic field when its coercive force is 6 kOe or less before aging treatment. death,
Thereafter, the obtained molded body is subjected to an aging treatment, and then impregnated with a polymer resin having a viscosity of 20 to 3000 cp (centipoise) and solidified.

原料となる2−17系の希土類石粉体は、
R2TM17(但し、RはYを含むSm、Ce、Pr、Nd
等の希土類元素の1種又は2種以上、TMはFe、
Co、Ni等の遷移金属元素の1種又は2種以上)
で表される組成を主成分とするものである。この
ような原料は通常、所定の組成を有する合金を粉
砕した後、一定の形状に成形し焼結し、また必要
があればそれを所定の条件で溶体化処理すること
によつて得られる。
The raw material is 2-17 rare earth stone powder.
R 2 TM 17 (However, R is Sm, Ce, Pr, Nd including Y
One or more rare earth elements such as TM is Fe,
One or more transition metal elements such as Co, Ni, etc.)
The main component is the composition represented by: Such raw materials are usually obtained by pulverizing an alloy having a predetermined composition, shaping it into a predetermined shape, sintering it, and, if necessary, subjecting it to solution treatment under predetermined conditions.

2−17系希土類磁石は、時効処理により析出硬
化が起こり高保磁力が出現する。本発明はこの現
象を有効に利用している。
2-17 rare earth magnets undergo precipitation hardening due to aging treatment and develop a high coercive force. The present invention effectively utilizes this phenomenon.

本発明では上記のような原料焼結体を先ず粉砕
する。これにより得られた磁石粉体は時効処理前
であり6kOe以下の低保持力状態である。このよ
うな低保持力の磁石粉体を使用するのは、本発明
者等が磁場成形前の磁石粉体の保磁力と時効後の
樹脂結合型永久磁石の磁気特性の関係について
種々の実験を行つた結果、保磁力が6kOe以下の
磁石粉体を用いて樹脂結合型永久磁石を作製すれ
ば、従来法により得られた同じ保磁力を有する樹
脂結合型永久磁石に比べて極めて磁気特性、特に
Brと(BH)maxが良好になることを見出したこ
とによる。
In the present invention, the raw material sintered body as described above is first pulverized. The magnet powder thus obtained has a low coercive force of 6 kOe or less before aging treatment. The reason for using such low coercive force magnet powder is that the present inventors conducted various experiments on the relationship between the coercive force of magnet powder before magnetic field forming and the magnetic properties of resin-bonded permanent magnets after aging. As a result, we found that if a resin-bonded permanent magnet is made using magnet powder with a coercive force of 6 kOe or less, the magnetic properties are significantly higher than that of a resin-bonded permanent magnet with the same coercive force obtained by conventional methods.
This is due to the discovery that Br and (BH)max are improved.

そして前記磁石粉体を磁場中で成形し、成形さ
れた形状を保持したまま時効処理を行つて高い保
磁力を出現させる。その後、粘度が20〜3000cp
の高分子樹脂を含浸させ固化処理する。
Then, the magnet powder is molded in a magnetic field and subjected to an aging treatment while maintaining the molded shape to develop a high coercive force. Then the viscosity is 20~3000cp
Impregnated with polymer resin and solidified.

本発明の特徴は、上記のように磁石粉体を低保
磁力の状態で磁場中成形し、時効処理を行つた
後、20〜3000cpの粘度範囲を高分子樹脂を含浸
させ固化する点にある。
The feature of the present invention is that, as described above, magnet powder is molded in a magnetic field with a low coercive force, and after aging treatment, it is impregnated with a polymer resin with a viscosity in the range of 20 to 3000 cp and solidified. .

ここで使用する高分子樹脂としては、エポキシ
樹脂、フエノール樹脂、アクリル樹脂、嫌気性樹
脂等、その粘度が20〜3000cpの範囲にあれば如
何なる種類の樹脂でも使用可能である。本発明に
おいて高分子樹脂の粘度を20〜3000cpとしたの
は実験結果から導き出された次のような理由によ
る。つまり20cp未満では含浸後あるいは硬化中
に樹脂の流れ出し現象がみられ、また3000cpを
超えると高粘度となりすぎ含浸が十分行えず中心
部に含浸残りが発生し易くなり、いずれにせよ第
1図に示すように機械的強度が極端に低下してし
まうからである。
As the polymer resin used here, any type of resin can be used as long as its viscosity is in the range of 20 to 3000 cp, such as epoxy resin, phenolic resin, acrylic resin, and anaerobic resin. The reason why the viscosity of the polymer resin is set to 20 to 3000 cp in the present invention is as follows, which was derived from experimental results. In other words, if it is less than 20 cp, the resin will flow out after impregnation or during curing, and if it exceeds 3,000 cp, the viscosity will become too high and impregnation will not be able to be carried out sufficiently, leaving a residue of impregnation in the center. This is because, as shown, the mechanical strength is extremely reduced.

なお特に残留磁束密度を向上し成形性を高くす
るため、成形時にPVA、PVB、CMC、PEG、
パラフイン等の成形助剤を添加し、時効処理前あ
るいは時効処理中にそれら成形助剤を加熱飛散さ
せてもよい。
In particular, in order to improve residual magnetic flux density and enhance moldability, PVA, PVB, CMC, PEG,
A molding aid such as paraffin may be added and the molding aid may be blown off by heating before or during the aging treatment.

[作用] 本発明では時効処理前の低保磁力状態の磁石粉
末を用いて磁場中成形を行うから、一般の製造ラ
インで用いられているような磁場プレス装置を用
いても十分配向がなされる。そしてその状態のま
ま時効処理が行われるから、時効処理後の磁石粉
体の保磁力が大きくなつても良好な配向状態はそ
のまま保持され、高い磁気特性を発生させること
ができる。
[Function] In the present invention, since magnetic field compaction is performed using magnet powder in a low coercive force state before aging treatment, sufficient orientation can be achieved even if a magnetic field press device such as that used in a general production line is used. . Since the aging treatment is performed in this state, even if the coercive force of the magnet powder increases after the aging treatment, the good orientation state is maintained as it is, and high magnetic properties can be generated.

そして20〜3000cpの粘度の高分子樹脂を含浸
させるので、成形体の全体にわたつて磁石粉体が
均一に分布し樹脂を固化することによつて機械的
強度の優れた樹脂結合型永久磁石が製造できる。
Then, since it is impregnated with a polymer resin with a viscosity of 20 to 3000 cp, the magnet powder is evenly distributed throughout the molded body and the resin is solidified, creating a resin-bonded permanent magnet with excellent mechanical strength. Can be manufactured.

[実施例] 原料としてSm(Co0.68Fe0.20Cu0.10Zr0.027.75で示
される低保磁力状態のサマリウム−コバルト合金
をジエツトミルで粉砕し、磁場中成形した後、焼
結したものを用いた。
[Example] As a raw material, a samarium-cobalt alloy in a low coercive force state represented by Sm (Co 0.68 Fe 0.20 Cu 0.10 Zr 0.02 ) 7.75 was ground in a jet mill, formed in a magnetic field, and then sintered.

この原料焼結体をジヨークラツシヤーで粉砕し
篩別して平均粒径250μmの磁石粉体を得た。次
に成形助剤を使用せずに、この磁石粉体を10mm×
10mm×20mm(配向方向)の寸法に11kOeの磁場中
で3ton/cm2で圧縮成形した。
This raw material sintered body was crushed with a geocrusher and sieved to obtain magnet powder with an average particle size of 250 μm. Next, without using a forming aid, this magnetic powder was
Compression molding was performed at 3 tons/cm 2 in a magnetic field of 11 kOe to a size of 10 mm x 20 mm (orientation direction).

そしてこの成形体について真空中800℃、1時
間の時効処理を行い高保磁力化した。その後、
種々の粘度のエポキシ樹脂を含浸して固化し樹脂
結合型希土類磁石を製造した。ここで含浸固化の
処理条件は次の通りである。まず成形体を真空度
1×10-3Torrの真空槽中で脱気処理し、同槽に
あるエポキシ樹脂液中に浸漬し30分間保持後、そ
のまま別の槽の中に移し5気圧加圧した状態で30
分間保持し含浸させた。そして含浸後、120℃で
2時間の加熱硬化処理を行つた。
This compact was then aged in vacuum at 800°C for 1 hour to increase its coercive force. after that,
Epoxy resins of various viscosities were impregnated and solidified to produce resin-bonded rare earth magnets. Here, the treatment conditions for impregnation and solidification are as follows. First, the molded body is degassed in a vacuum tank with a vacuum level of 1 × 10 -3 Torr, immersed in an epoxy resin solution in the same tank, held for 30 minutes, and then transferred to another tank and pressurized to 5 atmospheres. 30 with
It was held for a minute to allow impregnation. After impregnation, heat curing treatment was performed at 120°C for 2 hours.

得られた樹脂結合型希土類磁石の磁気特性並び
に機械的強度特性を第1図に示す。この実験結果
から次のことが判る。まず最大エネルギー積
(BH)maxや残留磁束密度Brといつた磁気特性
は使用するエポキシ樹脂の粘度ηによらずほぼ一
定である。しかし曲げ強度は粘度ηが20cp未満
の場合や3000cpを超えると極端に低下してしま
う。その理由は、粘度が20cp未満だと固化の際
に高分子樹脂が流れ出してしまい、逆に3000cp
を超えると高粘度のための内部まで十分含浸でき
ず未結合の部分が残存し、いずれにせよ樹脂によ
る十分な結合が行われ難いためであると考えられ
る。
The magnetic properties and mechanical strength properties of the resin-bonded rare earth magnet obtained are shown in FIG. The following is clear from the results of this experiment. First, magnetic properties such as maximum energy product (BH) max and residual magnetic flux density Br are almost constant regardless of the viscosity η of the epoxy resin used. However, the bending strength is extremely reduced when the viscosity η is less than 20 cp or exceeds 3000 cp. The reason for this is that if the viscosity is less than 20cp, the polymer resin will flow out during solidification;
This is thought to be because if the resin exceeds 100%, the resin cannot be sufficiently impregnated into the interior due to its high viscosity, and unbonded parts remain, making it difficult for the resin to bond sufficiently.

なお比較のため従来方法に基づき上記と同様の
素材と条件で樹脂結合型希土類磁石を製造してみ
たが、本発明方法は従来法よりも磁気特性並びに
機械的強度特性の全ての面で優れていることが確
認された。
For comparison, a resin-bonded rare earth magnet was manufactured using the same materials and conditions as above based on the conventional method, and it was found that the method of the present invention is superior to the conventional method in all aspects of magnetic properties and mechanical strength characteristics. It was confirmed that there is.

[発明の効果] 本発明は上記のように時効処理により析出硬化
する磁石粉体を析出硬化前の低保磁力状態の時に
磁場中成形し、その後その形状を保持したまま析
出硬化させ高保磁力を出現させる方法であるた
め、従来技術に比べてより一層磁気特性を向上さ
せることができる効果がある。
[Effects of the Invention] As described above, the present invention forms magnet powder that undergoes precipitation hardening through aging treatment in a magnetic field when it is in a low coercive force state before precipitation hardening, and then precipitation hardens it while maintaining its shape to obtain a high coercive force. Since this is a method of making magnetic particles appear, it has the effect of further improving magnetic properties compared to conventional techniques.

また本発明では、磁石粉体を結合させるため含
浸固化する樹脂として20〜3000cpという特定粘
度範囲の高分子樹脂を使用しているから、磁石粉
体と高分子樹脂とを均一に分布させた状態で固着
させることができ、機械的強度も優れた樹脂結合
型永久磁石を製造できるすぐれた効果がある。
Furthermore, in the present invention, a polymer resin with a specific viscosity range of 20 to 3000 cp is used as the resin to be impregnated and solidified to bond the magnet powder, so that the magnet powder and the polymer resin are uniformly distributed. It has the excellent effect of producing a resin-bonded permanent magnet that can be fixed with a resin bond and has excellent mechanical strength.

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

第1図は本発明方法で使用する高分子樹脂の粘
度ηと作製した樹脂結合型希土類磁石の磁気特性
並びに曲げ強度の関係を示すグラフである。
FIG. 1 is a graph showing the relationship between the viscosity η of the polymer resin used in the method of the present invention and the magnetic properties and bending strength of the prepared resin-bonded rare earth magnet.

Claims (1)

【特許請求の範囲】[Claims] 1 2−17系希土類磁石粉体を、時効処理する以
前の保磁力が6kOe以下の時に磁場中成形し、そ
の後、得られた成形体を時効処理し、次いで粘度
が20〜3000センチポアズの高分子樹脂を含浸させ
固化処理することを特徴とする樹脂結合型永久磁
石の製造方法。
1 2-17 rare earth magnet powder is molded in a magnetic field when its coercive force is 6 kOe or less before aging treatment, and then the obtained molded body is aged, and then a polymer with a viscosity of 20 to 3000 centipoise is formed. A method for manufacturing a resin-bonded permanent magnet, characterized by impregnating it with a resin and solidifying it.
JP62146513A 1987-06-11 1987-06-11 Manufacture of resin bond type permanent magnet Granted JPS63308902A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62146513A JPS63308902A (en) 1987-06-11 1987-06-11 Manufacture of resin bond type permanent magnet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62146513A JPS63308902A (en) 1987-06-11 1987-06-11 Manufacture of resin bond type permanent magnet

Publications (2)

Publication Number Publication Date
JPS63308902A JPS63308902A (en) 1988-12-16
JPH0444402B2 true JPH0444402B2 (en) 1992-07-21

Family

ID=15409339

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62146513A Granted JPS63308902A (en) 1987-06-11 1987-06-11 Manufacture of resin bond type permanent magnet

Country Status (1)

Country Link
JP (1) JPS63308902A (en)

Also Published As

Publication number Publication date
JPS63308902A (en) 1988-12-16

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