JP2625767B2 - Rare earth magnet surface treatment method - Google Patents
Rare earth magnet surface treatment methodInfo
- Publication number
- JP2625767B2 JP2625767B2 JP25930187A JP25930187A JP2625767B2 JP 2625767 B2 JP2625767 B2 JP 2625767B2 JP 25930187 A JP25930187 A JP 25930187A JP 25930187 A JP25930187 A JP 25930187A JP 2625767 B2 JP2625767 B2 JP 2625767B2
- Authority
- JP
- Japan
- Prior art keywords
- magnet
- rare earth
- earth magnet
- surface treatment
- treatment method
- 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
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- Chemical Treatment Of Metals (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、モータ用などに使われる希土類磁石の表面
処理方法に関する。Description: TECHNICAL FIELD The present invention relates to a surface treatment method for a rare earth magnet used for a motor or the like.
(従来の技術) 近年、電気機器やモータ等に使用される永久磁石は、
その保磁力、最大エネルギ積等の磁気特性が極めて高性
能なものになってきている。(Prior Art) In recent years, permanent magnets used for electric devices, motors, etc.
Magnetic properties such as coercive force and maximum energy product have become extremely high performance.
その永久磁石の代表的なものとして希土類磁石がよく
知られているが、この希土類磁石は耐食性が劣り、特に
Nd−Fe−B系の磁石は、焼結磁石、プラスチック磁石の
いずれについても、ほとんど磁石表面にコーティング層
を施して使用している。Rare earth magnets are well known as a representative of the permanent magnets, but these rare earth magnets have poor corrosion resistance, and
Nd-Fe-B-based magnets, both sintered magnets and plastic magnets, are used by applying a coating layer on the magnet surface.
従来の磁石の表面コーティング方法としては、電着塗
装や吹き付けによる有機樹脂コーティング法ならびにメ
ッキ法等が知られている。これらの表面処理法により希
土類磁石の表面の耐食性を向上させている。As a conventional magnet surface coating method, an organic resin coating method by electrodeposition coating or spraying and a plating method are known. With these surface treatment methods, the corrosion resistance of the surface of the rare earth magnet is improved.
(発明が解決しようとする問題点) しかしながら、このような従来の希土類磁石の表面処
理方法にあっては、具体的には、有機樹脂コーティング
法の場合、有機樹脂の膜厚が10μm以上必要とされ、し
かも膜厚精度が悪く、またコーティング作業が煩雑にな
るという問題がある。(Problems to be solved by the invention) However, in such a conventional surface treatment method for a rare earth magnet, specifically, in the case of an organic resin coating method, the film thickness of the organic resin is required to be 10 μm or more. In addition, there is a problem that the film thickness accuracy is poor and the coating operation is complicated.
メッキ法の場合には、磁石内部の気孔にメッキ液が浸
透しやすいので、気孔に残存するメッキ液により磁石内
部から錆が発生するという問題がある。In the case of the plating method, since the plating solution easily penetrates into the pores inside the magnet, there is a problem that the plating solution remaining in the pores generates rust from inside the magnet.
さらに、鋼材の表面処理法として知られている化成被
膜処理法により、例えばリン酸亜鉛被膜処理を磁石に施
すと、リン酸酸性液が磁石表面に浸されるだけで、この
酸性液から磁石を取り出したときには磁石表面に被膜形
成が十分になされないという問題がある。Furthermore, when a magnet is subjected to, for example, a zinc phosphate coating treatment by a chemical conversion coating method known as a surface treatment method for steel materials, a phosphoric acid acid solution is merely immersed in the magnet surface, and the magnet is formed from the acid solution. There is a problem that the film is not sufficiently formed on the magnet surface when it is taken out.
本発明はこのような問題点を解決するためになされた
もので、希土類元素を含有する所定の化学成分のアルカ
リ性水溶液に希土類磁石を浸すことにより、簡単な操作
で磁石表面に密着性の高い耐食性被膜を形成することを
目的とする。The present invention has been made in order to solve such a problem, and by dipping a rare earth magnet in an alkaline aqueous solution of a predetermined chemical component containing a rare earth element, a high corrosion resistance with high adhesion to the magnet surface with a simple operation. The purpose is to form a coating.
(問題点を解決するための手段) そのために、本発明による希土類磁石の表面処理方法
は、Al・K・NaおよびSiのうちの少なくとも1種以上の
元素ならびに希土類元素のうちの少なくとも1種以上の
元素を含有するアルカリ性水溶液に希土類磁石を濡ら
し、その後この希土類磁石を乾燥し、この希土類磁石表
面に耐食性被膜を形成したことを特徴とする。(Means for Solving the Problems) For that purpose, the method for treating the surface of a rare earth magnet according to the present invention comprises at least one or more elements of Al, K, Na and Si, and at least one or more of rare earth elements. Characterized in that the rare earth magnet is wetted with an alkaline aqueous solution containing the element described above, and then the rare earth magnet is dried to form a corrosion resistant film on the surface of the rare earth magnet.
この場合、コーティング方法としては、アルカリ性水
溶液中に希土類磁石を浸漬するのが作業性の面で望まし
いが、吹き付けコーティングでもよい。さらに真空状態
でアルカリ性水溶液に希土類磁石を浸漬すると、磁石内
部の気孔への溶液の含浸効果が高められ、耐食性はさら
に向上する。このことは、磁石内部の気孔に希土類元素
が侵入することにより、この希土類元素が磁石表面層に
緻密な化合物を形成するためと考えられる。In this case, as a coating method, it is desirable to immerse the rare earth magnet in an alkaline aqueous solution from the viewpoint of workability, but spray coating may be used. Further, when the rare earth magnet is immersed in an alkaline aqueous solution in a vacuum state, the effect of impregnating the pores inside the magnet with the solution is enhanced, and the corrosion resistance is further improved. This is presumably because the rare earth element penetrates the pores inside the magnet and forms a dense compound in the magnet surface layer.
(発明の効果) 本発明によれば、アルカリ性水溶液に希土類磁石を浸
すという極めて簡単な操作により、希土類磁石の表面に
密着性の高い被膜形成を行なうことができるので、磁石
の耐食性が一層向上するという効果がある。(Effects of the Invention) According to the present invention, a coating with high adhesion can be formed on the surface of a rare-earth magnet by a very simple operation of immersing the rare-earth magnet in an alkaline aqueous solution, so that the corrosion resistance of the magnet is further improved. This has the effect.
(実施例) 本発明の実施例について述べる。(Example) An example of the present invention will be described.
本発明の実施例で用いた希土類磁石は、 :Nd(32wt%)−Fe−B(1wt%)焼結磁石 :Nd(30wt%)−Fe−B(0.7wt%)プラスチック磁石 である。この場合、のNd−Fe−Bプラスチック磁石の
プラスチック材として用いた樹脂はエポキシ樹脂(含有
率2%)であり、このプラスチック磁石はプレス成形に
より成形した。およびの磁石は、ともに円盤状のも
ので、直径10mm、高さ5mmとした。The rare earth magnet used in the embodiment of the present invention is: Nd (32 wt%)-Fe-B (1 wt%) sintered magnet: Nd (30 wt%)-Fe-B (0.7 wt%) plastic magnet. In this case, the resin used as the plastic material of the Nd-Fe-B plastic magnet was an epoxy resin (content 2%), and this plastic magnet was formed by press molding. The magnets and were both disk-shaped, having a diameter of 10 mm and a height of 5 mm.
およびの磁石を浸漬した化成液は、 A: Al 6.0wt% K 2.0wt% Na 2.0wt% Si 1.0wt% 希土類元素 0.2wt% を含有するアルカリ性水溶液(PH=11.7、比重1.04
1)、 B: Al 6.0wt% K 2.0wt% Na 2.0wt% Si 1.0wt% を含有するアルカリ性水溶液(PH=11.7、比重1.041) の2種のアルカリ性水溶液を用いた。ここに、希土類元
素は、Y、La、Ce、Pr、Lu等である。The chemical solution in which the magnets were immersed was A: Al 6.0 wt% K 2.0 wt% Na 2.0 wt% Si 1.0 wt% An alkaline aqueous solution containing a rare earth element 0.2 wt% (PH = 11.7, specific gravity 1.04
1), B: Two kinds of alkaline aqueous solutions containing 6.0% by weight of Al, 2.0% by weight of K, 2.0% by weight of Na, and 1.0% by weight of Si (pH = 11.7, specific gravity 1.041) were used. Here, the rare earth element is Y, La, Ce, Pr, Lu or the like.
前記AおよびBの化成液に前記およびの磁石を浸
漬した。具体的には、第2図(A)に示すように、試料
としての磁石10を入れた容器7を真空ポンプ8により真
空にし、次いで、バルブ9を開け、第2図(B)に示す
ように、容器11中のアルカリ性水溶液を通路12を介して
容器7に移動し、アルカリ性水溶液で磁石10を浸漬状態
にする。アルカリ性水溶液の温度は70℃、浸漬時間は2
分とした。その後、AおよびBの化成液からおよび
の磁石を取り出し、水切りし乾燥した。乾燥温度は130
℃であり、乾燥時間は3分とした。The above magnets were immersed in the chemical conversion solutions A and B. Specifically, as shown in FIG. 2 (A), the container 7 containing the magnet 10 as a sample is evacuated by the vacuum pump 8, then the valve 9 is opened, and as shown in FIG. 2 (B). Next, the alkaline aqueous solution in the container 11 is moved to the container 7 via the passage 12, and the magnet 10 is immersed in the alkaline aqueous solution. The temperature of the alkaline aqueous solution is 70 ° C and the immersion time is 2
Minutes. Thereafter, the magnets were removed from the chemical solutions of A and B, drained and dried. Drying temperature is 130
° C and the drying time was 3 minutes.
この結果、およびの磁石表面に形成された被膜の
厚さは、それぞれ2.1μmであった。As a result, the thicknesses of the films formed on the magnet surfaces were 2.1 μm, respectively.
被膜形成された各磁石について耐食性試験を行なっ
た。耐食性試験は、温度60℃、相対湿度95%で錆の発生
の有無によって行なった。錆発生テストの結果は第1表
に示すとおりであった。A corrosion resistance test was performed on each of the magnets on which a film was formed. The corrosion resistance test was performed at a temperature of 60 ° C. and a relative humidity of 95% based on the presence or absence of rust. The results of the rust generation test were as shown in Table 1.
第1表から明らかなように、化成液に磁石を浸さなか
った比較例2においては、錆が発生し、錆の発生量は試
験時間が長いほど錆発生率が高く、割れが発生したもの
もあった。、の磁石を化成液Bに浸した比較例1に
おいては、化成液に浸さなかった比較例に比べ、錆の発
生率は低いが、それでもかなりの錆発生率の値を示し
た。これに対し、本発明の場合のように、、の磁石
を化成液Aに浸したものにおいては、比較的短い時間で
あれば錆発生が生じなかった。また長時間の試験時間の
場合にも、錆発生率はかなり低かった。本発明のよう
に、錆発生がほとんど生じなかったのは、化成液中に希
土類磁石の含有元素である希土類元素が含まれており、
この化成液中の希土類元素が磁石中の希土類元素と強固
に結合し、磁石表面に密着性の高い被膜形成を行なうこ
とができたためと考えられる。 As is clear from Table 1, in Comparative Example 2 in which the magnet was not immersed in the chemical conversion solution, rust was generated, and the amount of rust was higher as the test time was longer. there were. In Comparative Example 1 in which the magnet was immersed in the chemical conversion liquid B, the rust generation rate was lower than that of the comparative example in which the magnet was not immersed in the chemical conversion liquid, but the value was still considerable. On the other hand, when the magnet was immersed in the chemical conversion solution A as in the case of the present invention, no rust was generated in a relatively short time. Also, the rust generation rate was quite low even for long test times. As in the present invention, the occurrence of rust hardly occurred because the chemical conversion solution contains a rare earth element that is a contained element of the rare earth magnet,
It is considered that the rare earth element in the chemical conversion solution was strongly bonded to the rare earth element in the magnet, and a film having high adhesion was formed on the magnet surface.
次に、Nd−Fe−Bプラスチック磁石について、磁石表
面への被膜の密着試験を行なった。密着試験は、密着性
テストとして行なった。すなわち、第1図に示すよう
に、希土類磁石1の表面に被膜層2が形成され、この被
膜層2に接着剤層4を挟んで鉄片4を接合したものにつ
いて、希土類磁石1と鉄片4とにそれぞれチャック5と
6を噛み合わせ、図示矢印方向に引張り力を加えた。接
着剤層3の接着面積は0.2cm2、鉄片4は鋼種SS41、接着
剤には2液性エポキシ樹脂を用いた。Next, for the Nd-Fe-B plastic magnet, an adhesion test of the coating on the magnet surface was performed. The adhesion test was performed as an adhesion test. That is, as shown in FIG. 1, a coating layer 2 is formed on the surface of a rare earth magnet 1 and an iron piece 4 is bonded to the coating layer 2 with an adhesive layer 4 interposed therebetween. The chucks 5 and 6 were respectively engaged with each other, and a tensile force was applied in the direction of the arrow shown in the figure. The adhesive area of the adhesive layer 3 was 0.2 cm 2 , the iron piece 4 was steel type SS41, and the adhesive was a two-component epoxy resin.
密着性テストの結果は、第2表に示すとおりであっ
た。The results of the adhesion test were as shown in Table 2.
希土類元素を含まない化成液Bに磁石を浸漬した比
較例3においては、磁石と接着剤層の境界面すなわち被
膜層の部分で剥離し、しかもそのときの接着強度は12kg
/cm2と低い値であった。これに対し、本発明のように希
土類元素を含む化成液Aに磁石を浸したものにおいて
は、被膜層で剥離することなく、鉄片と接着剤層の境界
面で剥離し、しかも接着強度は29kg/cm2と高い値であっ
た。 In Comparative Example 3 in which the magnet was immersed in the chemical solution B containing no rare earth element, the magnet was peeled off at the interface between the magnet and the adhesive layer, that is, the coating layer, and the adhesive strength at that time was 12 kg.
/ cm 2 , a low value. On the other hand, when the magnet is immersed in the chemical conversion solution A containing a rare earth element as in the present invention, the magnet peels off at the interface between the iron piece and the adhesive layer without peeling off at the coating layer, and has an adhesive strength of 29 kg. / cm 2 was a high value.
本発明のアルカリ性水溶液中に含有する希土類元素の
量は、溶液中に0.001〜1wt%の範囲にするのが望まし
い。これは、0.001wt%未満であると、磁石表面に十分
な膜厚の被膜が形成できないからであり、1wt%をこえ
ると、表面処理コストが高くなる時の理由による。The amount of the rare earth element contained in the alkaline aqueous solution of the present invention is desirably in the range of 0.001 to 1 wt% in the solution. This is because if the content is less than 0.001 wt%, a film having a sufficient thickness cannot be formed on the magnet surface, and if it exceeds 1 wt%, the surface treatment cost becomes high.
第1図は密着性テストを行なったときの引張り試験装置
の概略構成を示す断面図であり、第2図(A)、(B)
は化成液に磁石を浸漬するための作業工程を示す図であ
る。 1……希土類磁石、 2……被膜層、 3……接着剤層、 4……鉄片、 5、6……チャック。FIG. 1 is a cross-sectional view showing a schematic configuration of a tensile test apparatus when an adhesion test is performed, and FIGS. 2 (A) and 2 (B).
FIG. 3 is a view showing an operation process for immersing a magnet in a chemical conversion solution. 1 ... Rare earth magnet, 2 ... Coating layer, 3 ... Adhesive layer, 4 ... Iron piece, 5, 6 ... Chuck.
Claims (1)
種以上の元素ならびに希土類元素のうちの少なくとも1
種以上の元素を含有するアルカリ性水溶液に希土類磁石
を濡らし、その後この希土類磁石を乾燥し、この希土類
磁石表面に耐食性被膜を形成したことを特徴とする希土
類磁石の表面処理方法。At least one of Al, K, Na and Si
At least one of more than one element and rare earth element
A rare earth magnet surface treatment method comprising: wetting a rare earth magnet in an alkaline aqueous solution containing at least one kind of element; drying the rare earth magnet; and forming a corrosion-resistant coating on the rare earth magnet surface.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25930187A JP2625767B2 (en) | 1987-10-14 | 1987-10-14 | Rare earth magnet surface treatment method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25930187A JP2625767B2 (en) | 1987-10-14 | 1987-10-14 | Rare earth magnet surface treatment method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01104784A JPH01104784A (en) | 1989-04-21 |
| JP2625767B2 true JP2625767B2 (en) | 1997-07-02 |
Family
ID=17332176
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25930187A Expired - Lifetime JP2625767B2 (en) | 1987-10-14 | 1987-10-14 | Rare earth magnet surface treatment method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2625767B2 (en) |
-
1987
- 1987-10-14 JP JP25930187A patent/JP2625767B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01104784A (en) | 1989-04-21 |
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