JP2000232026A - MANUFACTURE OF Fe-B-R PERMANENT MAGNET HAVING CORROSION-RESISTING COATING - Google Patents

Abstract

PROBLEM TO BE SOLVED: To realize a method for easily and inexpensively manufacturing an Fe-B-R permanent magnet, whose magnet surface has a corrosion resisting coating with superior adhesiveness with the magnet for developing stable high magnetic characteristics without deteriorating the magnetic characteristics, even when this magnet is left as it is for a long time at high temperature and high humidity condition of 80 deg.C temperature and relative humidity of 90%, without subjecting the magnet to plating treatment or treatment using hexavalent chromium. SOLUTION: An Fe-B-R permanent magnet and a metallic piece are placed in a treatment vessel, and vibration is applied to them in the treatment container, and/or they are stirred so that a metallic coating can be formed on the magnetic surface. Then, sol solution obtained through hydrolytic reaction and polymer reaction of a metallic compound being the material of a metallic oxide coating is applied on the metallic coating, and heat treatment is carried out so that the metallic oxide coating can be formed.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an Fe-BR-based permanent magnet having an excellent corrosion-resistant coating.
More specifically, it is simple, low-cost, has excellent adhesion to magnets, and does not require plating or treatment using hexavalent chromium. The present invention relates to a method for producing a Fe-BR-based permanent magnet having a corrosion-resistant coating on a magnet surface capable of exhibiting stable and high magnetic properties without deterioration of magnetic properties even when left for a long time.

[0002]

2. Description of the Related Art Fe--B--R permanent magnets, represented by Fe--B--Nd permanent magnets, are made of materials that are more abundant and inexpensive than Sm--Co permanent magnets, and Because of its high magnetic properties, it has been put to practical use in various applications. However, since the Fe-BR based permanent magnet contains highly reactive R and Fe, it is easily oxidized and corroded in the air, and when used without any surface treatment, a slight amount of acid or Corrosion progresses from the surface due to the presence of alkali, moisture, etc., and rust is generated, which leads to deterioration and variation in magnet characteristics. Furthermore, when the rusted magnet is incorporated into a device such as a magnetic circuit, the rust may scatter and contaminate peripheral components.

[0003]

SUMMARY OF THE INVENTION In view of the above, Fe
In order to improve the corrosion resistance of -BR type permanent magnets, magnets in which a metal plating film having corrosion resistance is formed on the magnet surface by a wet plating method such as an electroless plating method or an electroplating method have already been proposed (see, Japanese Patent Publication No. Hei 3-74012). However, in this method, an acidic solution or an alkaline solution used in the pretreatment of the plating treatment may remain in the magnet hole, and the magnet may corrode with time. Further, since the magnet has poor chemical resistance, the surface of the magnet may be corroded during plating. Furthermore, even if a metal plating film is formed on the magnet surface as described above, the temperature is 60 ° C.
X Corrosion resistance test under the condition of 90% relative humidity
After 00 hours, the magnetic properties may be degraded by 10% or more from the initial value.

A method of forming an oxidation-resistant chemical conversion film such as a phosphate film or a chromate film on the surface of an Fe-BR-based permanent magnet has also been proposed (Japanese Patent Publication No. 4-2200).
No. 8, the coating obtained by this method is excellent in adhesion to a magnet, but has a temperature of 60 ° C. and a relative humidity of 90.
%, The magnetic properties may deteriorate by 10% or more from the initial value after 300 hours.

Further, a method of forming an Al film by a vapor phase growth method and then performing a chromate treatment, that is, a so-called aluminum-chromate treatment method (proposed to improve the corrosion resistance of the Fe-BR based permanent magnet) ( Japanese Patent Publication No. 6-66173) significantly improves the corrosion resistance of the magnet. However, since the chromate treatment used in this method uses hexavalent chromium which is environmentally undesirable, the waste liquid treatment method is complicated. Further, since the film obtained by this method contains hexavalent chromium in a small amount, there is a concern that the effect on the human body when handling the magnet is also concerned.

On the other hand, a method has been proposed in which an underlayer mainly composed of a metal is formed on the surface of an Fe-BR-based permanent magnet, and a glass layer is formed on the surface of the underlayer (Japanese Patent Laid-Open No. 1-16).
If the underlayer is formed using a wet plating method, the magnet may corrode with time as described above. For example, if the underlayer is formed by using a vapor phase plating method such as a vacuum evaporation method, it is possible to provide a magnet having excellent corrosion resistance without such a problem. However, in order to perform the vapor phase plating process, a large-sized apparatus is required, and the apparatus is expensive. In addition, an extremely high degree of vacuum is required to perform a pretreatment, such as cleaning the magnet surface or forming an underlayer mainly composed of an easily oxidizable metal such as Al, Sn, and Zn. Therefore, it is undeniable that the manufacturing process is complicated and requires a long time, for example, a long-time evacuation process is required.

Therefore, in the present invention, it is possible to simply carry out plating treatment or treatment using hexavalent chromium without performing such treatment.
Low cost, excellent adhesion to magnets, stable and high magnetic properties without deterioration of magnetic properties even when left for a long time under high temperature and humidity conditions of 80 ° C x 90% relative humidity. With a corrosion resistant film on the magnet surface
An object of the present invention is to provide a method for producing a BR permanent magnet.

[0008]

Means for Solving the Problems The present inventors have conducted various studies in view of the above points, and as a result, put a Fe-BR-based permanent magnet and a metal piece into a processing vessel, and When vibration is applied to both and / or both are stirred, fine metal powder generated from a metal piece adheres to the surface of the magnet, and forms a metal film on the surface of the magnet using the fine metal powder as a constituent source. That sol-
When a metal oxide film is formed by a gel film forming method, the metal oxide film is firmly adhered to the magnet and the corrosion resistance of the magnet is improved. It has been found that the effect on the environment can be significantly reduced, and that the production method is very simple.

The present invention has been made based on this finding. The method for producing a permanent magnet having a metal oxide film on a magnet surface via a metal film according to the present invention is based on Fe-B. Placing the R-based permanent magnet and the metal piece in a processing container, applying vibration to both in the processing container, and / or
Alternatively, by stirring both, a metal film is formed on the magnet surface, and a sol liquid obtained by a hydrolysis reaction and a polymerization reaction of a metal compound serving as a raw material of a metal oxide film is applied on the metal film. And heat-treating to form a metal oxide film. Further, the manufacturing method according to claim 2 is the manufacturing method according to claim 1, wherein the Al, S
It is characterized by using a metal piece for forming a metal film made of at least one metal component selected from n and Zn. A manufacturing method according to a third aspect is characterized in that, in the manufacturing method according to the first aspect, a needle-shaped or cylindrical metal piece having a size (major axis) of 0.05 mm to 10 mm is used. Further, the manufacturing method according to claim 4 is the manufacturing method according to claim 1, wherein the thickness of the metal film is 0.0
It is 1 μm to 1 μm. The manufacturing method according to claim 5 is the manufacturing method according to claim 1, wherein the metal oxide comprises at least one metal oxide component selected from an Al oxide, a Si oxide, a Zr oxide, and a Ti oxide. It is characterized by using a sol liquid for forming a film. The manufacturing method according to claim 6 is characterized in that, in the manufacturing method according to claim 1, a sol liquid for forming a metal oxide film containing the same metal component as the metal component of the metal film is used. . A manufacturing method according to a seventh aspect is characterized in that, in the manufacturing method according to the first aspect, the metal oxide film has a thickness of 0.01 μm to 10 μm. Further, the manufacturing method according to claim 8 is a method according to claim 1.
The method according to claim 1, wherein the metal oxide film contains C
Is in the range of 50 ppm to 1000 ppm. A manufacturing method according to a ninth aspect is characterized in that, in the manufacturing method according to the first aspect, the metal oxide film is made of a metal oxide mainly composed of amorphous.

[0010]

BEST MODE FOR CARRYING OUT THE INVENTION First, a Fe-BR based permanent magnet and a metal piece are placed in a processing vessel, and both are vibrated and / or agitated in the processing vessel. A method for forming a metal film on the magnet surface will be described.

As the metal piece, one corresponding to the metal component of the desired metal film may be used, for example, Al, Sn, Z
Examples include a metal piece made of at least one metal component selected from n, Cu, Fe, Ni, Co, and Ti. Among these, Al, Sn, and Zn are metal components that can efficiently form a metal film on the sintered magnet. The metal piece may be made of a single metal or may be made of an alloy. Further, a metal film composed of a plurality of metal components may be formed by using a plurality of metal pieces having different metal components. Various shapes such as needles (wires), cylinders, and blocks can be used as the metal pieces. However, from the viewpoint of efficiently generating fine metal powder as a constituent source of the metal film, the ends are sharp. It is desirable to use a simple needle-like or columnar one. The size (major axis) of the metal piece is preferably 0.05 mm to 10 mm from the viewpoint of efficiently generating metal fine powder serving as a constituent source of the metal film,
More preferably, it is 0.3 mm to 5 mm, and further preferably, it is 0.5 mm to 3 mm. Metal pieces have the same shape
Those having the same size may be used, or those having different shapes and different sizes may be mixed and used.

[0012] Vibration and / or agitation on the magnet and the metal piece take into account that both are easily oxidized and corroded.
It is desirable to carry out the treatment in a dry manner, and the treatment can be carried out in an air atmosphere at room temperature. The processing vessel that can be used in the present invention does not require a complicated apparatus, and may be, for example, a processing chamber of a barrel apparatus. As the barrel device, a known device such as a rotary type, a vibration type, and a centrifugal type can be used. In the case of a rotary type, it is desirable that the number of rotations be 20 rpm to 50 rpm. In case of vibration type, the frequency is 50H
It is desirable that z to 100 Hz and the vibration amplitude be 0.3 mm to 10 mm. In the case of centrifugal type, the rotation speed is 70r
It is desirable to set it to pm to 200 rpm. The amount of magnets and metal pieces to be put in the processing vessel is 20 v
ol% to 90 vol% is desirable. If it is less than 20 vol%, the amount of treatment is too small to be practical, and if it exceeds 90 vol%, the metal film may not be formed efficiently. Further, the ratio of the magnet and the metal piece put in the processing container is desirably 3 or less in terms of volume ratio (magnet / metal piece). If the volume ratio exceeds 3, it takes a long time to form the metal film, which may not be practical. The processing time also depends on the processing amount, but usually,
1 hour to 10 hours.

According to the above method, metal fine powder generated from a metal piece is applied to the surface of the magnet to form a metal film. The phenomenon that the metal fine powder adheres to the magnet surface is considered to be a kind of mechanochemical reaction, and the metal fine powder adheres firmly to the magnet surface, and the resulting metal film exhibits excellent corrosion resistance. From the viewpoint of ensuring sufficient corrosion resistance, the film thickness is desirably 0.01 μm or more. Although the upper limit of the film thickness is not particularly limited, since it takes time to form a metal film having a film thickness exceeding 1 μm, this method is suitable as a method for forming a metal film having a film thickness of 1 μm or less. I have.

After the metal film is formed on the magnet surface by the above-described method, heat treatment can be performed to increase the adhesion between the magnet surface and the metal film. The heat treatment may be performed at this stage, but the same effect can be obtained by a heat treatment for forming a metal oxide film described later. If the temperature of the heat treatment exceeds 500 ° C., the magnetic properties of the magnet may be degraded or the metal film may be dissolved.

Next, a method of applying a sol solution obtained by a hydrolysis reaction and a polymerization reaction of a metal compound as a raw material of a metal oxide film on the formed metal film and heat-treating the sol solution to form a metal oxide film. Will be described.

The metal oxide film may be a film composed of a single metal oxide component or a composite film composed of a plurality of metal oxide components. Examples of the metal oxide component include at least one metal oxide component selected from Al oxide, Si oxide, Zr oxide, and Ti oxide. Among the films composed of a single metal oxide component, a Si oxide film (SiO _x film: 0 <x ≦
2) is that the sol liquid for forming the film is more stable than the sol liquid for forming other metal oxide films,
Since it can be formed at a lower temperature than in the case of forming a film composed of another metal oxide component, it is convenient in that the influence on the magnetic properties of the magnet can be reduced. Zr
An oxide film (ZrO _x film: 0 <x ≦ 2) is advantageous in that it has excellent alkali resistance in addition to corrosion resistance. Further, a metal oxide film containing the same metal component as the metal component of the metal film serving as the underlayer (for example, Al
An Al oxide film (Al ₂ O _x film: 0 <x ≦
When 3) is formed), it is convenient in that the adhesion at the interface between the metal film and the metal oxide film becomes stronger. As a composite film composed of a plurality of metal oxide components, a Si—Al composite oxide film (SiO _x .Al ₂ O _y)
Coating: 0 <x ≦ 2.0 <y ≦ 3) or Si-Zr composite oxide coating (SiO _x / ZrO _y coating: 0 <x ≦ 2.0 <
y ≦ 2) or a Si—Ti composite oxide film (SiO _x · T
iO _y film: 0 <x ≦ 2.0 <y ≦ 2). The composite coating containing the Si oxide component is advantageous in that the sol solution is relatively stable and that it can be formed at a relatively low temperature, so that the influence on the magnetic properties of the magnet can be reduced. The composite coating containing the Zr oxide component is advantageous in that it has excellent alkali resistance. Further, if it is a composite film containing the same metal component as the metal component of the metal film to be the underlayer (for example, S
When an i-Al composite oxide film is formed or when a Si-Ti composite oxide film is formed on a Ti film), the adhesion at the interface between the metal film and the composite film becomes stronger. Is convenient.

The sol liquid used in the sol-gel film forming method is prepared by adjusting a metal compound, a catalyst, a stabilizer, water, etc., which are constituent sources of the metal oxide film, in an organic solvent, and performing a hydrolysis reaction of the metal compound. This is a solution in which a colloid obtained by a polymerization reaction or the like is dispersed.

Examples of the metal compound serving as a constituent source of the metal oxide film include metal alkoxides such as methoxide, ethoxide, propoxide, and butoxide (some of the alkoxyl groups are alkyl groups such as methyl group and ethyl group, phenyl group, etc.) Carboxylate such as metal oxalate, acetate, octylate, stearate, chelate compound of metal with acetylacetonate, etc., and metal nitrate And inorganic salts typified by chlorides. Considering the stability and cost of the sol solution, for example, in the case of an Al compound used for forming an Al oxide film or a Zr compound used for forming a Zr oxide film, the propoxy of Al or Zr is used. It is desirable to use an alkoxide having an alkoxyl group having 3 to 4 carbon atoms, such as butoxide or butoxide, or a carboxylate such as a metal acetate or octylate. In the case of a Si compound used when forming a Si oxide film, it is desirable to use an alkoxide having an alkoxyl group having 1 to 3 carbon atoms, such as methoxide, ethoxide, and propoxide of Si. In the case of a Ti compound used for forming a Ti oxide film, the compound having 2 to 4 carbon atoms such as ethoxide, propoxide and butoxide of Ti is used.
It is desirable to use an alkoxide having an alkoxyl group.

When forming a composite oxide film, a plurality of
Metal compounds can be mixed and used, and metal composites
Metal complex compounds such as alkoxides alone or
It can also be used as a mixture with a genus compound. For example, S
When forming the i-Al composite oxide film, Si-O-
An alkoxyl group having 1 to 4 carbon atoms having an Al bond
Part of the alkoxyl group is an alkyl such as methyl or ethyl
May be substituted with a phenyl group or a phenyl group.
Si) such as Si-Al composite alkoxide having
An Al composite compound can be used. Such a compound
As the object, specifically, (H₃CO)₃-Si-O-
Al- (OCH₃)₂And (H₅C₂O) ₃-Si-O
-Al- (OC₂H₅)₂And the like.

When a composite oxide film is formed using a plurality of metal compounds, the mixing ratio of each metal compound is not particularly limited, and may be determined according to the desired component ratio of the composite oxide film. . For example, when forming a Si-Al composite oxide film on an Al film,
-The number of moles of Al (Al / Si + Al) with respect to the total number of moles of Si and Al contained in the Al composite oxide film is 0.1%.
001 or more (molar ratio) so that the Si compound and the Al
It is desirable to use a mixture of the compounds or a mixture of the Si compound and the Si-Al composite compound. By setting the mixing ratio as described above, the excellent characteristics of the Si oxide film (the sol liquid is relatively stable,
(The ability to form a film at a relatively low temperature) while improving the reactivity at the interface with the Al film. In addition, when the heat treatment after applying the sol liquid on the metal film surface is performed at 150 ° C. or less, the above molar ratio is desirably 0.5 or less, and when the heat treatment is performed at 100 ° C. or less, the above molar ratio is described later. Is desirably 0.2 or less. This is because the heat treatment temperature needs to be increased as the mixing ratio of Al increases.

The mixing ratio of the metal compound to the sol solution is as follows:
0.1 wt% to 20 wt% (in terms of metal oxide (for example, in the case of Si compound, in terms of SiO ₂ , Si compound + A
In the case of 1 compound, the range of SiO ₂ + Al ₂ O ₃ ) is desirable. If the compounding ratio is less than 0.1 wt%, an excessive number of film forming steps may be required to obtain a film having a sufficient film thickness. On the other hand, if the content exceeds 20 wt%, the viscosity of the sol liquid may increase, which may make it difficult to form a film.

As the catalyst, acids such as acetic acid, nitric acid and hydrochloric acid can be used alone or as a mixture. The appropriate addition amount is defined by the hydrogen ion concentration of the sol solution to be prepared, and it is desirable to add the sol solution to have a pH of 2 to 5. If the pH is less than 2 or more than 5, there is a possibility that a hydrolysis reaction or a polymerization reaction in preparing a sol liquid suitable for forming a film may not be controlled.

The stabilizer used as necessary for stabilizing the sol solution is appropriately selected depending on the chemical stability of the metal compound used. Compounds that form chelates with metals, such as β-keto acid esters such as diketones and ethyl acetoacetate, are desirable. When β-diketone is used, for example, the amount of the stabilizer is desirably 2 or less in terms of molar ratio (stabilizer / metal compound). If the molar ratio exceeds 2, the hydrolysis reaction or the polymerization reaction during the preparation of the sol solution may be inhibited.

The water contained in the sol solution may be supplied directly, for example, by a chemical reaction such as utilizing water generated by an esterification reaction with a carboxylic acid when an alcohol is used as a solvent. The method may be an indirect supply using a gas, or a method of utilizing water vapor in the atmosphere. When water is supplied directly or indirectly into the sol, the molar ratio of water / metal compound is desirably 100 or less. If the molar ratio exceeds 100, the stability of the sol may be affected.

The organic solvent is not limited as long as it can uniformly dissolve the metal compound, the catalyst, the stabilizing agent, and the water, which are the components of the sol, and uniformly disperse the obtained colloid. For example, lower alcohols typified by ethanol, hydrocarbon ether alcohols typified by ethylene glycol monoalkyl ether, acetate esters of hydrocarbon ether alcohols typified by ethylene glycol monoalkyl ether acetate, typified by ethoxyethyl acetate Acetates of lower alcohols, such as acetates of lower alcohols and ethyl acetate, and ketones of acetone, etc. can be used, but from the viewpoint of safety and cost during treatment, lower alcohols such as ethanol, isopropyl alcohol, and butanol can be used. Alcohol alone Or it is preferable to use a mixture.

Although the viscosity of the sol depends on the combination of various components contained in the sol, it is generally desirable that the viscosity be less than 20 cP. If it exceeds 20 cP, it becomes difficult to form a uniform film, and cracks may occur during heat treatment.

The time and temperature for adjusting the sol liquid depend on the combination of various components contained in the sol liquid.
Adjustment time is 1 minute to 72 hours, adjustment temperature is 0 ° C to 100 ° C
It is.

As a method for applying the sol solution to the surface of the metal film, a dip coating method, a spray method, a spin coating method or the like can be used.

After applying the sol solution to the surface of the metal film, heat treatment is performed. The temperature of the treatment must be at least enough to evaporate the organic solvent. For example, when ethanol is used as the organic solvent, its boiling point is 80 ° C.
is necessary. On the other hand, in the case of a sintered magnet, the heat treatment temperature is 5
If the temperature exceeds 00 ° C., the magnetic properties of the magnet may be deteriorated, or the metal film may be dissolved. Therefore, the heat treatment temperature is preferably from 80 ° C. to 500 ° C., but is more preferably from 80 ° C. to 250 ° C. from the viewpoint of minimizing the occurrence of cracks during cooling after the heat treatment. In the case of a bonded magnet, the temperature condition of the heat treatment must be set in consideration of the heat resistant temperature of the resin used. For example, in the case of a bonded magnet using an epoxy resin or a polyamide resin, the heat treatment temperature is desirably set to 80 ° C. to 200 ° C. in consideration of the heat resistance temperature of these resins.
Note that the heat treatment time is usually 1 minute to 1 hour.

According to the above method, a metal oxide film mainly composed of an amorphous material having excellent corrosion resistance can be obtained. For example, in the case of a Si—Al composite oxide film, its structure is such that in the case of a film rich in Si components, the structure is Si—O—Si
When the bond contains many bonds and Si—O—Al bonds and the Al component is abundant, it contains many Al—O—Al bonds and Si—O—Al bonds. The proportion of both components in the coating is determined by the proportion of the metal compound.

According to the above method, the metal oxide film contains C originating from the metal compound and the stabilizer. C
, It is easy to obtain a metal oxide film mainly composed of an amorphous material having excellent corrosion resistance, but its content is desirably 50 ppm to 1000 ppm (wt / wt). If the content of C is less than 50 ppm, cracks may be formed in the film, and the content of C may be 1000 pp.
If it exceeds m, the densification of the film may not be sufficiently caused.

The metal oxide film obtained by the above method has excellent corrosion resistance if the film thickness is 0.01 μm or more. The upper limit of the thickness of the film that can be formed by the above method is not limited, but it is required to reduce the size of the magnet itself or to be durable when incorporated into a component having a large temperature change such as an automobile motor. From the viewpoint of ensuring the properties, it is suitable for forming a film having a thickness of 10 μm or less, preferably 5 μm or less, more preferably 1 μm or less. It goes without saying that the application of the sol liquid to the surface of the metal film and the subsequent heat treatment may be repeated a plurality of times, if necessary.

Forming a metal oxide film on a metal film
As a pre-process, shot peening (hard particles are
Surface modification method)
No. Metal film by shot peening
Metal acid that has excellent corrosion resistance even in thin films
It is possible to easily form a nitride film. Shotpi
The powder used for cleaning is the hardness of the formed metal film.
It is desirable that the hardness is equal to or higher than
Mohs hardness of 3 such as ball or glass beads
The above-mentioned spherical hard powder is mentioned. The average particle size of the powder is
If it is less than 30 μm, the pressing force on the metal film is small and
It takes time to understand. On the other hand, if it exceeds 3000 μm,
Roughness may be so rough that the finished surface may be uneven
There is. Therefore, the average particle size of the powder is 30 μm to 3 μm.
000 μm is preferable, and 40 μm to 2000 μm is more preferable.
desirable. Injection pressure in shot peening is 1.0
kg / cm²~ 5.0kg / cm ²Is desirable. Injection pressure
Is 1.0kg / cm²If less than the pressing force on the metal film
Is small and takes a long time to process, and the injection pressure is 5.0 kg / c
m²Beyond the limit, the pressing force against the metal film becomes uneven.
This may cause deterioration of the surface roughness. Show
Injection time in hot peening is 1 minute to 1 hour
New If the spraying time is less than 1 minute, a uniform treatment
Surface roughness after 1 hour.
This is because there is a risk of causing deterioration of the image quality.

The rare earth element (R) in the Fe—BR permanent magnet used in the present invention is Nd, Pr, D
at least one of y, Ho, Tb, and Sm, or La, Ce, Gd, Er, Eu, Tm, Yb,
A material containing at least one of Lu and Y is desirable.
In general, one kind of R is sufficient, but in practice, a mixture of two or more kinds (such as misch metal and dymium) can be used for convenience and other reasons. F
The content of R in the eBR type permanent magnet is 10 atomic%.
If it is less than 3, the crystal structure becomes a cubic structure having the same structure as α-Fe, so that high magnetic properties, particularly high coercive force (iHc) cannot be obtained. Increases, the residual magnetic flux density (Br) decreases, and a permanent magnet having excellent characteristics cannot be obtained.
Desirably, it is 0 to 30 atomic%.

If the content of Fe is less than 65 at%, Br decreases, and if it exceeds 80 at%, high iHc cannot be obtained. Therefore, the content of 65 to 80 at% is desirable. Further, by replacing part of Fe with Co, the temperature characteristics can be improved without impairing the magnetic characteristics of the obtained magnet. However, when the amount of Co exceeds 20% of Fe, the magnetic characteristics become poor. It is not desirable because it deteriorates. When the amount of Co substitution is 5 atomic% to 15 atomic%, Br increases in comparison with the case where no substitution is made, and thus it is desirable to obtain a high magnetic flux density.

If the B content is less than 2 atomic%, the rhombohedral structure becomes the main phase, and high iHc cannot be obtained. If the B content exceeds 28 atomic%, the B-rich non-magnetic phase increases, and Br decreases, resulting in excellent Br. 2% by atom to 2%
A content of 8 atomic% is desirable. Further, in order to improve the manufacturability of the magnet and to reduce the price, 2.0 wt% or less of P, 2.0 w
At least one of S of t% or less, a total amount of 2.0
wt% or less may be contained. Further, by replacing a part of B with 30 wt% or less of C, the corrosion resistance of the magnet can be improved.

Further, Al, Ti, V, Cr, Mn, B
i, Nb, Ta, Mo, W, Sb, Ge, Sn, Zr,
Addition of at least one of Ni, Si, Zn, Hf, and Ga is effective in improving the coercive force and the squareness of the demagnetization curve, improving the manufacturability, and reducing the cost. In order to make the maximum energy product (BH) max equal to or more than 20 MGOe, at least 9 kG of Br is required. Therefore, it is preferable to add Br in a range that satisfies the above condition. It should be noted that the Fe-BR-based permanent magnet may contain impurities inevitable in industrial production in addition to R, Fe, and B.

Further, Fe-B used in the present invention
The -R permanent magnet has a main phase of a compound having a tetragonal crystal structure having an average crystal grain size in a range of 1 µm to 80 µm, and a nonmagnetic phase (oxide phase of 1% to 50% by volume ratio). Excluding). The magnet has iHc ≧ 1k
Oe, Br> 4 kG, (BH) max ≧ 10 MGOe, and the maximum value of (BH) max reaches 25 MGOe or more.

Incidentally, another film may be laminated on the metal oxide film of the present invention. By adopting such a configuration, the characteristics of the metal oxide film can be enhanced or supplemented, and further functionality can be imparted.

[0040]

For example, as described in U.S. Pat. No. 4,770,723, 17Nd-1Pr obtained by pulverizing a well-known casting ingot, performing pulverization, forming, sintering, heat treatment and surface processing. -75Fe-7
The following experiment was performed using a sintered magnet having a B composition and a size of 23 mm × 10 mm × 6 mm (hereinafter referred to as “magnet test piece”). In the following experiments, the film thickness of the metal film was measured using a fluorescent X-ray film thickness meter. The thickness of the metal oxide film was measured by observing the fracture surface with an electron microscope. The C content in the metal oxide film was measured using a glow discharge mass spectrometer. The structure of the metal oxide film was analyzed using an X-ray diffractometer. The present invention is not limited to application to Fe-BR-based sintered magnets, but can also be applied to Fe-BR-based bonded magnets.

Experimental Example 1: 150 magnet test pieces (appearance capacity 0.5 l, weight 1.6 kg) and diameter 0.8 mm,
A short cylindrical Al piece (approximate capacity 20 l, weight 100 kg) having a length of 1 mm is charged into a processing chamber of a vibration barrel apparatus having a volume of 50 l (total charging amount is 40 vol% of the processing chamber volume).
Dry treatment was performed for 5 hours under the conditions of a vibration frequency of 60 Hz and a vibration amplitude of 1.8 mm to form an Al film on the magnet surface.
The thickness of the obtained Al film was 0.05 μm. The sol solution was adjusted with the components, viscosities, and pHs shown in Table 2 using the Al compounds, catalysts, stabilizers, organic solvents, and water shown in Table 1 by dip coating. The coating was applied to a magnet having an Al film at a pulling rate, and heat treatment was performed to form an Al oxide film on the Al film.
The film thickness of the obtained film (Al ₂ O _x film: 0 <x ≦ 3) was 1 μm. The C content in the film was 450 ppm. The structure of the coating was amorphous. The magnet having the Al oxide film formed on the magnet surface via the Al film obtained by the above method is left for 300 hours under a high-temperature and high-humidity condition of a temperature of 80 ° C and a relative humidity of 90% to accelerate the corrosion resistance. The test was performed. Table 4 shows the magnetic properties before and after the test and the appearance change after the test. As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance without substantially deteriorating in magnetic properties and appearance even when left under a high temperature and high humidity condition for a long time. In another experiment, a modified acrylate-based adhesive (product number, Hard Rock G-5) was used.
5: manufactured by Denki Kagaku Kogyo Co., Ltd.), the resulting magnet was bonded to a cast iron jig, and after standing for 24 hours, a compression shear test was performed with an Amsler tester to determine the shear adhesive strength of the obtained magnet. It was measured and showed an excellent value of 331kg weight / cm ^2.

Experimental Example 2: Each component of the Si compound, catalyst, stabilizer, organic solvent and water shown in Table 1 was applied to the magnet having a 0.05 μm Al film on the magnet surface obtained in Experimental Example 1. Then, the sol solution having the composition, viscosity and pH shown in Table 2 was adjusted, and the sol solution was applied by a dip coating method at the pulling rate shown in Table 3 and heat-treated to form S on the Al film.
An i-oxide film was formed. The film thickness of the obtained film (SiO _x film: 0 <x ≦ 2) was 0.8 μm. The C content in the film was 450 ppm. The structure of the coating was amorphous. The accelerated corrosion resistance test under the same conditions as in Experimental Example 1 was performed on the magnet having the Si oxide film via the Al film on the magnet surface obtained by the above method. Table 4 shows the results. As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance. Further, as another experiment, a compression shear test under the same conditions as in Example 1 was performed, and the shear adhesion strength of the obtained magnet was measured. As a result, an excellent value of 274 kgf / cm ² was shown.

Experimental Example 3: Each component of the Zr compound, catalyst, stabilizer, organic solvent and water shown in Table 1 was applied to the magnet having a 0.05 μm Al film on the magnet surface obtained in Experimental Example 1. Then, the sol solution having the composition, viscosity and pH shown in Table 2 was adjusted, applied by a dip coating method at a pulling rate shown in Table 3, and heat-treated to form a Z on the Al film.
An oxide film was formed. The film thickness of the obtained film (ZrO _x film: 0 <x ≦ 2) was 1 μm. C in the film
The amount was 450 ppm. The structure of the coating was amorphous. Experimental Example 1 was applied to a magnet having a Zr oxide film via an Al film on the magnet surface obtained by the above method.
An accelerated corrosion resistance test was performed under the same conditions. Table 4 shows the results.
Shown in As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance.

Experimental Example 4 Each component of the Ti compound, catalyst, stabilizer, organic solvent and water shown in Table 1 was applied to the magnet having a 0.05 μm Al film on the magnet surface obtained in Experimental Example 1. Then, the sol solution having the composition, viscosity and pH shown in Table 2 was adjusted, applied by a dip coating method at a pulling rate shown in Table 3, and subjected to heat treatment to form a T on the Al film.
An i-oxide film was formed. The thickness of the obtained film (TiO _x film: 0 <x ≦ 2) was 1 μm. C in the film
The amount was 320 ppm. The structure of the coating was amorphous. Experimental Example 1 was applied to a magnet having a Ti oxide film via an Al film on the magnet surface obtained by the above method.
An accelerated corrosion resistance test was performed under the same conditions. Table 4 shows the results.
Shown in As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance.

[0045]

[Table 1]

[0046]

[Table 2]

[0047]

[Table 3]

[0048]

[Table 4]

Comparative Example 1: Magnet test piece was degreased and pickled.
It was immersed in a treatment solution consisting of 4.6 g / l of zinc and 17.8 g / l of a phosphate at a bath temperature of 70 ° C. to form a 1 μm-thick phosphate film on the surface of the magnet. The obtained magnet was subjected to a corrosion resistance acceleration test under the same conditions as in Experimental Example 1. Table 4 shows the results. As a result, the obtained magnet was deteriorated in magnetic properties and rusted.

Comparative Example 2: A test piece for magnet body was subjected to an accelerated corrosion resistance test under the same conditions as in Experimental Example 1. Table 4 shows the results. As a result, the magnet body test piece caused deterioration of magnetic properties and rust.

Experimental Example 5: The magnet having the 0.05 μm Al film on the magnet surface obtained in Experimental Example 1 was subjected to Si compound, Al compound, catalyst, stabilizer, organic solvent and water shown in Table 5. For each of the components, a sol solution having the composition, viscosity, and pH shown in Table 6 was adjusted, and the dip coating method was used.
It was applied at the pulling speed shown in Table 7 and heat-treated to give Al
An Si-Al composite oxide film was formed on the film. Obtained film (SiO _x .Al ₂ O _y film: 0 <x ≦ 2.0)
The film thickness of <y ≦ 3) was 0.9 μm. The C content in the film was 290 ppm. The structure of the coating was amorphous. The accelerated corrosion resistance test under the same conditions as in Experimental Example 1 was performed on the magnet having the Si-Al composite oxide film on the magnet surface via the Al film obtained by the above method. Table 8 shows the results. As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance.
Further, as another experiment, a compression shear test under the same conditions as in Example 1 was performed, and the shear adhesive strength of the obtained magnet was measured. As a result, an excellent value of 323 kgf / cm ² was shown.

[0052]

[Table 5]

[0053]

[Table 6]

[0054]

[Table 7]

[0055]

[Table 8]

Experimental Example 6: 30 magnet body test pieces (0.1 l in apparent capacity, 0.32 kg in weight) and 0.8 mm in diameter,
1 mm long short cylindrical Sn piece (apparent capacity 2 l, weight 1
1 kg) is charged into a processing chamber of a 3.5-liter vibration barrel device (total charging amount is 60 vol% of the volume of the processing chamber), and dry processing is performed for 5 hours under conditions of a vibration frequency of 60 Hz and a vibration amplitude of 1.5 mm. Then, a Sn film was formed on the magnet surface. The thickness of the obtained Sn film was 0.4 μm. The sol solution was adjusted with the components, viscosities and pHs shown in Table 10 using the Si compounds, catalysts, stabilizers, organic solvents and water shown in Table 9 by dip coating. It was applied to a magnet having a Sn film at a pulling rate, and heat treatment was performed to form a Si oxide film on the Sn film. The film thickness of the obtained film (SiO _x film: 0 <x ≦ 2) was 0.3 μm. The C content in the film was 350 ppm. The structure of the coating was amorphous. A corrosion resistance acceleration test under the same conditions as in Experimental Example 1 was performed on the magnet having the Si oxide film on the magnet surface via the Sn film obtained by the above method. Table 12 shows the results. As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance.

Experimental Example 7: 150 magnet body test pieces (apparent capacity 0.5 l, weight 1.6 kg) and short cylindrical Zn pieces 1 mm in diameter and 1 mm long (apparent capacity 20 l, weight 10
0 kg) into a processing chamber of a 50-liter vibration barrel device (total charging amount is 40 vol% of the processing chamber volume), and dry-processed for 5 hours under conditions of a vibration frequency of 60 Hz and a vibration amplitude of 1.8 mm. A Zn film was formed on the magnet surface. The thickness of the obtained Zn film was 0.2 μm. Sol solution,
Composition, viscosity and pH shown in Table 10 were obtained for each of the components of the Si compound, catalyst, stabilizer, organic solvent and water shown in Table 9.
, And applied to a magnet having a Zn film at a pulling rate shown in Table 11 by a dip coating method, followed by heat treatment to form a Si oxide film on the Zn film. The film thickness of the obtained film (SiO _x film: 0 <x ≦ 2) is 0.
It was 7 μm. The C content in the film was 450 ppm. The structure of the coating was amorphous. A corrosion resistance acceleration test under the same conditions as in Experimental Example 1 was performed on the magnet having a Si oxide film on the magnet surface via a Zn film obtained by the above method. Table 12 shows the results. as a result,
It was found that the obtained magnet sufficiently satisfied the required corrosion resistance.

Experimental Example 8: Each component of the Zr compound, catalyst, stabilizer, organic solvent and water shown in Table 9 was applied to the magnet having a Zn coating of 0.2 μm on the magnet surface obtained in Experimental Example 7. Then, a sol solution having the composition, viscosity and pH shown in Table 10 was adjusted, applied by a dip coating method at a pulling rate shown in Table 11, and subjected to heat treatment to form a Zr oxide film on the Zn film. did. The film thickness of the obtained film (ZrO _x film: 0 <x ≦ 2) was 0.6 μm. The C content in the film was 140 ppm. The structure of the coating was amorphous. A corrosion resistance acceleration test under the same conditions as in Experimental Example 1 was performed on the magnet having a Zr oxide film via a Zn film on the magnet surface obtained by the above method. Table 12 shows the results. As a result, it was found that the obtained magnet sufficiently satisfied the required corrosion resistance.

[0059]

[Table 9]

[0060]

[Table 10]

[0061]

[Table 11]

[0062]

[Table 12]

[0063]

According to the present invention, Fe-B having a corrosion-resistant film is provided.
According to the method for producing an R-based permanent magnet, it is simple, low-cost, has excellent adhesion to a magnet, and has a temperature of 80 ° C. and a relative humidity of 90% without performing a plating process or a process using hexavalent chromium. It is possible to form a corrosion-resistant coating on the magnet surface that can exhibit stable and high magnetic properties without deteriorating the magnetic properties even if left for a long time under high temperature and high humidity conditions. An Fe-BR-based permanent magnet can be provided.

 ──────────────────────────────────────────────────続 き Continued on the front page (31) Priority claim number Japanese Patent Application No. 10-303731 (32) Priority date October 26, 1998 (1998. 10.26) (33) Priority claim country Japan (JP) (31) Priority claim number Japanese Patent Application No. 10-349915 (32) Priority date December 9, 1998 (12.9 December 1998) (33) Country claiming priority Japan (JP) (72) Inventor Fumi Kikui Autumn 2-15-17 Egawa, Shimamoto-cho, Mishima-gun, Osaka Prefecture F-term in Yamazaki Works, Sumitomo Special Metals Co., Ltd. 4K018 AA27 FA23 FA24 FA27 KA45 KA58 5E040 AA04 AA20 BC01 CA01 HB14 HB15 NN05 5E062 CD04 CE01 CG07

Claims (9)

[Claims] 1. A method of placing an Fe—BR—R permanent magnet and a metal piece in a processing vessel and applying vibration to and / or agitating the two in the processing vessel to form a metal on the magnet surface. After forming a film, a sol solution obtained by a hydrolysis reaction and a polymerization reaction of a metal compound as a raw material of the metal oxide film is applied on the metal film, and a heat treatment is performed to form a metal oxide film. A method for producing a permanent magnet having a metal oxide film on a magnet surface via a metal film. 2. The method according to claim 1, wherein a metal piece for forming a metal film made of at least one metal component selected from Al, Sn and Zn is used. 3. Needle-shaped or column-shaped, size (long diameter)
The method according to claim 1, wherein a metal piece of 0.05 mm to 10 mm is used. 4. The metal film has a thickness of 0.01 μm to 1 μm.
The method according to claim 1, wherein 5. An Al oxide, a Si oxide, a Zr oxide,
2. The method according to claim 1, wherein a sol solution for forming a metal oxide film comprising at least one metal oxide component selected from Ti oxides is used. 6. The method according to claim 1, wherein a sol solution for forming a metal oxide film containing the same metal component as the metal component of the metal film is used. 7. The metal oxide film having a thickness of 0.01 μm or more.
The method according to claim 1, wherein the thickness is 10 μm. 8. The content of C contained in the metal oxide film is 5
The production method according to claim 1, wherein the content is 0 ppm to 1000 ppm. 9. The method according to claim 1, wherein the metal oxide film comprises a metal oxide mainly composed of amorphous.