JPH0547526A - Rare earth bonded magnet - Google Patents

Abstract

PURPOSE:To avoid the deformation of the title rare earth bonded magnet making the manufacture thereof impossible while pertinently maintaining the flexibility of the magnet. CONSTITUTION:Exceeding 5wt% of (Ce, La)-Fe-B base magnetic powder is added to Nd-Fe-B base magnetic powder so that the filler bulk density to the whole rare earth bonded magnet may be kept within the pertinent range to preserve the excellent characteristics such as the flexibility and rigidity of said magnet.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rare earth bonded magnet used by being incorporated in a rotating electric machine or the like.

[0002]

2. Description of the Related Art Conventionally, various bond magnets have been developed which are relatively inexpensive and have good magnetic characteristics. For example, Japanese Unexamined Patent Publication No. 59-2111549 proposes a bonded magnet obtained by solidifying rare earth-iron-boron magnetic powder with an adhesive, and Japanese Unexamined Patent Publication No. 61-17436.
Japanese Unexamined Patent Publication No. 4 (1994) proposes a plastic magnet obtained by mixing misch metal-transition metal-boron magnetic powder with a binder. Further, JP-A-63-274114 and JP-A-63-287003 propose a plastic magnet using a mixture of rare earth magnetic powder and ferrite magnetic powder, and JP-A-2-2280.
No. 3 gazette proposes a bonded magnet formed by mixing rare earth magnetic powders.

Each of the above-mentioned bonded magnets is one in which magnetic powder is kneaded to be dispersed in a resin binder, and the manufacturing method thereof is, for example, JP-A-60-16431.
No. 3 publication. According to the manufacturing method disclosed in this publication, the magnetic powder and the silane coupling agent are mixed little by little in the resin binder and kneading is performed using a mixing roll. The obtained kneaded product is once crushed and then rolled into a sheet. The sheet-shaped magnet material is subjected to heat treatment with, for example, steam to remove the strain generated in the rolling process or to be cured by vulcanization.

[0004]

In such a bonded magnet, when the present inventors obtain a flexible rare earth bonded magnet by dispersing the rare earth magnetic powder in a flexible resin binder. However, if the rare earth magnetic powder is mixed in an amount less than a certain amount due to, for example, the required magnetic force being set to a small value, the magnet may be deformed by the magnetic force or internal stress of the bond magnet itself when magnetized. I found it. It is considered that this is because the rare earth-transition metal-boron-based magnetic powder has high magnetic properties, so that the amount of the magnetic powder relative to the binder, that is, the filler filling rate tends to be low. When the filling rate of the filler is less than a certain value, the amount of the binder is relatively increased, and the flexibility of the binder makes the entire magnet easily expandable and contractable. If such a deformation of the magnet occurs in the motor, for example, the air gap between the core and the magnet may fluctuate, and the motor characteristics may change significantly, making it impossible to use the motor. On the other hand, if the rare earth magnetic powder is added in an excessive amount, it will be hardened so that it cannot be molded into a sheet, or its flexibility will be insufficient to make it impossible to incorporate it into a product. We have found a phenomenon in which the magnet collapses due to the magnetic force and internal stress of the bond magnet itself. It is considered that this is because when the filling rate of the rare earth magnetic powder becomes too high, the coercive force of the binder, that is, the rigidity of the magnet is lost to the magnetic force and the internal stress.

In order to solve such a problem, the inventors of the present invention added a non-magnetic powder as a reinforcing material to the rare earth magnetic powder, thereby preventing the filler filling rate from decreasing and increasing the rigidity of the bonded magnet. The invention is filed at the same time as the present application. However, particularly when Nd-Fe-B based magnetic powder is used, there is a circumstance that it is difficult to perform vulcanization by heating, and therefore the rigidity of the bonded magnet cannot be sufficiently obtained.

It is an object of the present invention to provide a flexible rare earth bonded magnet having high rigidity which does not cause deformation or collapse.

[0007]

In order to achieve the above object, a rare earth bonded magnet according to the present invention is a rare earth bonded magnet obtained by kneading Nd-Fe-B based magnetic powder in a flexible resin binder by kneading. In the above Nd-Fe-B system magnetic powder, (Ce, La) -Fe-B system magnetic powder is added so as to be 5% by weight or more of the total magnetic powder.

[0008]

In the means having such a structure, Nd-Fe-
In addition to the Nd-Fe-B magnetic powder (Ce,
By adding La) -Fe-B system magnetic powder,
The filler filling rate, which tends to be insufficient in the Nd-Fe-B system magnetic powder, is complemented by the (Ce, La) -Fe-B system magnetic powder, and thus the amount of the binder is maintained so as not to be excessive. Vulcanization by heating the magnet is promoted, and the required magnet rigidity is sufficiently obtained.

A more specific structure of the above means will be described. First, a rare earth-transition metal magnetic powder is obtained by the ultraquenching method. The jet casting method is an example of the ultra-quenching method. In this jet casting method, an ingot-shaped magnetic alloy is housed in a pan and the alloy is melted by a high frequency wave or the like in an inert environment. The magnetic alloy in a molten state is poured into a pool of water with a nozzle and dropped through a nozzle onto a rotating wheel. The rotating wheel is cooled by water, where rapid cooling takes place. The rapidly cooled magnetic alloy is solidified into ribbon-shaped magnetic powder, drops downward, and is collected in a container.

When the rare earth-transition metal magnetic powder is used, one or more kinds of lanthanoids are used as the rare earth, and the transition metals are Fe, Co, and
One or more of Ni are used. The rare earth-transition metal magnetic powder can contain boron to form a rare earth-transition metal-boron (RTB) magnetic powder. Specifically, Nd-Fe-B based magnetic powders are Nd-Fe-B, Nd-Fe-Co-B, (Nd, Pr).
-Fe-B, (Nd, Pr) -Fe-Co-B and the like are used, and (Ce, La) -Fe-B magnetic powder is (Ce, L).
a) -Fe-B, (Ce, La) -Fe-Co-B, MM-Fe-
B, MM-Fe-Co-B, etc., and Sm-Co
Examples of magnetic powders include Sm-Co, Sm-Co-Fe, Sm-
Co-Mn or the like is used.

Next, as shown in FIG. 1, the rare earth-transition metal-boron magnetic powder is weighed so as to be 92 to 96 wt% with respect to the entire magnet. The magnetic powder content is set to 96% by weight or less with respect to the entire magnet because when the ratio of the magnetic powder is higher than 96% by weight, the amount of the binder with respect to the magnetic powder becomes insufficient and the magnetic force of the magnet itself. The binder strength is lost to the internal stress and causes the magnet to collapse, or the magnet becomes too hard to be molded into a sheet, or lacks flexibility and cannot be incorporated into products. Because it becomes. On the other hand, the magnetic powder is set to 92% by weight or more with respect to the entire magnet, because if the ratio of the magnetic powder is less than 92% by weight, the filling rate of the magnetic powder becomes too low and the magnet is easily deformed. Is.

At this time, the rare earth-transition metal-boron system (R
In the case of using -TB) magnetic powder, it is preferable to pulverize the magnetic powder to a fine powder having a median diameter of 78 µm or less, for example, 42 µm, in order to obtain the filling rate. The magnetic powder is adjusted by using a ball mill, a roll or the like.

Further, since the magnetic properties of the rare earth magnetic powder are good, especially when the required magnetic force of the magnet is set to be small, the amount of the magnetic powder charged is too small to reach the predetermined filling rate. There is. In that case, non-magnetic powder such as white carbon may be added as a reinforcing material in a binder (described later) together with the magnetic powder. By using such a mixed filler, it is possible to increase the so-called filler filling rate in the magnet to a required value, thereby improving the deformability of the magnet and increasing the rigidity of the magnet. At this time, the filling rate of the filler in which the magnetic powder and the non-magnetic powder are added is appropriately in the range of 50 to 73% in terms of volume percentage, of which the rare earth-transition metal-boron system (RT)
-B) The magnetic powder is 13 to 71% by volume, and the mixed filler is 2 to 60% by volume. This is to prevent the amount of the binder with respect to the magnetic powder (filler) from being excessive or insufficient and preventing the magnet from collapsing or over-curing as described above.

As the non-magnetic mixed filler, chemically or physically stable powder such as talc, carbon black, carbon fiber or ferrite powder can be used in addition to the white carbon described above. The particle size of the mixed filler is 78 μm or less in terms of median diameter.

Further, when Nd-Fe-B is used as the magnetic powder, a rare earth-transition metal-other than the Nd-Fe-B type magnetic powder is used instead of the above-mentioned non-magnetic mixed filler.
It is preferable to use a boron (R-T-B) magnetic powder. This is because the magnet using the Nd-Fe-B system magnetic powder is difficult to vulcanize (described later) and it is difficult to obtain the required rigidity. Rare earth mixed in this case-Transition metal-
As the boron-based (RTB) magnetic powder, (Ce, La)
-Fe-B, disim (Nd, Pr) -Fe-B, misch metal-Fe-B and the like can be adopted. In particular, if the (Ce, La) -Fe-B based magnetic powder that is easy to vulcanize is mixed, the vulcanization is promoted to the inside of the magnet, the rigidity of the magnet is enhanced, and the deformation of the magnet can be prevented.

The mixing ratio of the magnetic powders may be any ratio as long as the residual magnetic flux density Br is 2,500 G or more and 6300 G or less. If the residual magnetic flux density Br after magnetization exceeds 6300 G, the binder strength is lost to the magnetic force and internal stress of the magnet itself, causing the magnet to collapse, or the magnet becomes too hard to be formed into a sheet. On the other hand, when the residual magnetic flux density Br after magnetization is less than 2500 G, the magnetic flux density becomes too small and the rare earth-transition metal-boron system (RT-
B) The usefulness of using magnetic powder is lost.

Particularly, Nd-Fe-B system magnetic powder and (Ce, La)
When mixed with -Fe-B based magnetic powder, (Ce, L
If a) -Fe-B based magnetic powder is mixed in an amount of 5% by weight or more based on the whole magnetic powder, it is possible to obtain a predetermined rigidity. FIG. 2 shows the thermal deformation in the case of incorporating a ring-shaped magnet into the rotor of the motor, that is, the relationship between the magnetic powder filling rate (horizontal axis) and the roundness change amount (vertical axis). .. The heating conditions at this time are 10 cycles of repeated heating in which the temperature is kept at −40 ° C. and 70 ° C. for 1 hour. As is clear from this figure, (Ce, La) -Fe-
When the addition ratio of the B-based magnetic powder is less than 5% by weight, the roundness change amount exceeds 40 μ which is a limit value as a product.

It is also possible to add the above-mentioned reinforcing material to a mixture of such magnetic powders so as to increase the filler filling rate to a required value. By doing so, the filler filling rate is complemented while suppressing an increase in magnetic force, whereby the deformability of the magnet can be improved and the magnet rigidity can be improved.

Next, a predetermined amount of a rust preventive agent and an epoxy main agent are mixed with the magnetic powder as described above to form an oxide film, an epoxy resin film and a rust preventive film (film forming step). That is, first, an inert gas is injected into the mixing device, and the air in the mixing device is gas-substituted so that the oxygen concentration becomes 0.08 to 3%. A ball mill, a V type blender, a double cone type blender or the like is used as the mixing device. Argon gas is used as the inert gas.
(Ar), nitrogen gas (N ₂ ), carbon dioxide gas (CO ₂ ) and the like are used.

The rare earth-transition metal magnetic powder, the epoxy main agent and the rust preventive agent are charged into the mixing device thus gas-replaced, and the mixing is carried out for about 2 hours. In the mixing, first, a small amount of oxygen remaining in the mixing device forms an oxide film on the surface of the magnetic powder, and further an epoxy resin film and a rust preventive film are formed thereon. The oxygen concentration is set to 0.08% to 3% because if the oxygen concentration is less than 0.08%, the oxide film cannot be formed or the formed oxide film is extremely thin. This is because if the concentration exceeds 3%, there is a danger of ignition due to oxygen.

As the epoxy main agent, one or more of bisphenol-based, phenoxy-based, novolac-based, polyphenol-based, polyhydroxybenzene-based and derivatives thereof are used, and rust inhibitor sorbitan monooleate. And a mixture of mineral oil or synthetic oil.

The magnetic powder on which the oxide film, the epoxy resin film and the rust preventive film are formed is taken out and weighed.
It is kneaded with a flexible resin binder for several minutes by a pressure kneader or the like (kneading step). At this time, a curing agent and a curing accelerator for the epoxy resin are added. The curing agent and the curing accelerator are added at this stage in order to prevent the magnetic powder from being hardened immediately after the mixture of the magnetic powders is taken out. By such a kneading step, the rare earth-transition metal magnetic powder is almost uniformly dispersed in the flexible resin binder.

As the flexible resin binder at this time, natural rubber (NR) and isoprene rubber (I
R), budadiene rubber (BR), styrene-butadiene rubber (SBR), butyl rubber (IIR), ethylene-propylene rubber (EPR), ethylene-vinyl acetate rubber (EV)
A), nitrile rubber (NBR), acrylic rubber (A
R), urethane rubber (UR) and the like are used alone or in combination of two or more. That is, these resin binders are so-called ternary rubbers and have a non-polar rubber component (eg IIR) and a highly polar rubber component (eg NB).
R) is a rubber component containing halogen (for example, CR)
Are mixed well through. A rubber component having no polarity has difficulty in oil resistance and weather resistance, and a rubber component having a strong polarity is extremely hard and requires addition of an extender oil or a plasticizer. Therefore, if both rubber components are mixed through a halogen-containing rubber component, the rubber components that make up the difficulties of the respective rubber components are easily mixed, and the oil resistance and weather resistance are improved. is there.

As the rubber component containing halogen, chloroprene rubber (CR), hypalon (CSM),
Those containing chlorine such as chlorinated polyethylene are used alone or in combination of two or more. In this case, the halogen-containing rubber component should be set to 15% by weight or less, preferably 6.2% by weight or less, based on the total weight of the resin binder. If the rubber component containing halogen exceeds 15% by weight of the total weight of the resin binder, chlorine gas (Cl ₂ ) or hydrochloric acid gas (HCl) will be generated. For example, in the case of a motor, a commutator This is because it causes corrosion, rust of magnets and core rust. Also, the rubber component containing halogen is 6.2 of the total weight of the resin binder.
If the content exceeds 5% by weight, the magnet becomes too hard and becomes brittle, so that it cannot be molded into a sheet, or lack of flexibility, making it impossible to incorporate it in products. Moreover, it is easily destroyed by an external force or its own magnetic force.

Examples of the curing agent include polyamines such as aliphatic polyamines and aromatic polyamines, acid anhydrides such as phthalic anhydride, polyamide resins, polysulfide resins, amine complexes such as boron trifluoride, and synthetic resins such as phenolic resins. One kind or two or more kinds of the initial condensate or derivatives thereof are used. As the curing accelerator, amines such as trisdimethylaminomethylphenol, imidazoles such as 1-isobutyl-2-methylimidazole, and one or more of these derivatives are used.

In this kneading step, the pressure kneader is cooled, and kneading is carried out at a temperature of 95 ° C. or lower, preferably 50 to 60 ° C. With this temperature setting,
The risk of ignition in the kneading process is avoided. That is, if kneading is carried out at a temperature higher than 95 ° C, there is a danger of ignition due to heat generation, and at 40 ° C or lower, rubber is not plasticized sufficiently and sufficient kneading cannot be carried out.

The magnet material as a kneaded material obtained by the above kneading step is taken out from the pressure kneader and immediately divided into small lots of 10 kg or less. Each of these subdivided magnet materials is enclosed and stored in an airtight container, and is left as it is until the temperature of the magnet material drops to room temperature (preservation step). The heat release during this storage step avoids the risk of ignition.

The magnet material as a kneaded material, which has been sufficiently radiated by the above-mentioned storage step, is taken out and has a particle size of 5 mm.
It is crushed into the following sizes (crushing process). This crushing process is performed using argon gas (Ar), nitrogen gas (N ₂ ), carbon dioxide gas (CO
₂ ) is performed under cooling by the flow of an inert gas such as
The temperature condition is set to 95 ° C. or lower. A rotary blade or the like is used for crushing. That is, in this crushing step, air cooling with an inert gas is performed, and crushing can be performed in the atmosphere.

Then, the pulverized material obtained in the pulverizing step is rolled by a roll or the like to obtain a sheet-shaped bond magnet (sheet forming step). At this time, the surface temperature of the rolling roll is maintained at 20 to 80 ° C., whereby the tensile strength of the sheet-shaped magnet material is favorably maintained in the rollable range and the oxidation of the magnetic powder is suppressed. The deterioration of magnetic characteristics is prevented.

Rare earth-transition metal-boron system (R-T-
B) In the magnet using the magnetic powder, it is necessary to adjust the filling rate of the filler such as the magnetic powder so that the density after rolling becomes 4.9 to 5.8. This is because if the density of the magnet is smaller than 4.9, the rigidity of the magnet will be insufficient and it will be easily deformed, making it impossible to incorporate it in the product. If it exceeds, brittleness of the magnet becomes large and cracks and the like are likely to occur, which causes a problem such as the magnet collapsing due to magnetization.

Further, the sheet-shaped magnet material obtained by the above rolling step is preheated and then heat-treated. This is because the preheating step causes the moisture, gas, and the like that are unavoidably contained in the sheet-shaped magnet material to diffuse to the outside.
The temperature condition and time condition in this preheating step are 30 ° C.
It is set to ˜70 ° C. and 6 hours or more. At this time, entrapment of air in the sheet-shaped magnet material is suppressed as much as possible in advance.

On the other hand, the temperature condition and time condition in the heat treatment process after preheating are 125 ° C. to 180 ° C. and 60 minutes or more.
It is set within 80 minutes, and the sheet-shaped magnet material is left for 60 to 180 minutes in, for example, a heating device formed by stacking iron plates in upper and lower three stages, or a constant temperature bath including a steam can. When vulcanization is performed by this, a predetermined tensile strength is imparted. Also at this time, the entrainment of air in the sheet-shaped magnet material is suppressed in advance as much as possible. In the case of performing such high temperature heating, water and gas in the sheet-shaped magnet material have been diffused in advance by the above-described preheating step, so that the sheet-shaped magnet material may have problems such as air foaming during the heating step. It never happens.

During this heating, the heating temperature is 180 ° C.
If the temperature exceeds 125 ° C, the oxidation of the magnetic powder becomes remarkable and the magnetic properties deteriorate, and if the heating temperature is 125 ° C or lower, the vulcanization does not proceed and the required tensile strength cannot be obtained. For the same reason, heating time is 60 minutes or more 180
It takes minutes.

The sheet-shaped magnet material which has been subjected to the heat treatment is cut into a suitable size to obtain a sheet-shaped magnet. After cutting, the sheet-shaped magnet material is cut at 100 to 180 ° C. and 20 to 18 ° C. in a constant temperature bath.
The heat treatment is performed again under the condition of 0 minutes. The re-heat treatment after cutting accelerates vulcanization not only from the original surface but also from the cut surface, so that the rigidity of the magnet is enhanced. In this reheat treatment step, the inside of the thermostatic chamber is made to be an inert atmosphere such as an N ₂ gas atmosphere, so that oxidation of the sheet-shaped magnet material is prevented. When the inside of the constant temperature bath is not made an inert atmosphere, a means such as wrapping the periphery with aluminum foil is provided so that the surface of the sheet-shaped magnet material is not exposed to the atmosphere as much as possible.

The above rare earth-transition metal-boron system (R-T
-B) The sheet-shaped magnet material using the magnetic powder has a Shore hardness D of 45 ° or more after reheat treatment, and
Tensile strength is more than 4.5Kg / mm ² . Also, the amount of bending is within 60 mm. The amount of deflection here means that the base side 50 mm of a test piece molded into a dimension and shape with a cross-sectional dimension of 2.55 mm × 2.45 mm and a length dimension of 205.5 mm is fixed on a horizontal table, and this test is performed. The amount that the free end of the piece bends by its own weight after 15 seconds is defined as the amount measured at an ambient temperature of 15 to 25 ° C. If it is not within the range of heating temperature conditions as described above, it may cause deterioration of magnetic properties (when it exceeds the temperature range), or vulcanization does not proceed (when it falls below the temperature range), decrease of hardness, tensile strength. It causes a decrease in strength and an increase in the amount of bending.

The sheet magnet using the rare earth-transition metal-boron (R-T-B) magnetic powder obtained as described above is magnetized in a predetermined direction. At this time, when the rolled surface of the magnet is magnetized, the surface magnetic flux density is set to 350 G to 1400 G, and
When the magnet is magnetized on the surface orthogonal to the rolled surface, the range of the surface magnetic flux density is 40G to 1400G. When the rolled surface is magnetized, for example, it is performed as a main magnetization for driving a motor, and when the magnetized surface is orthogonal to the rolled surface, for example, for motor rotation detection. This is the case where the FG magnetization is performed.

When the surface magnetic flux density exceeds 1400 G and is magnetized, the binder in the magnet overcomes the magnetic force and cannot fix the magnetic powder, and the magnet collapses. On the other hand, when the main surface magnetization for driving a motor is performed on the rolled surface, if the surface magnetic flux density is 350 G or less, the magnetic flux density becomes too small and the rare earth-transition metal-boron system (RT- B) The utility of using magnetic powder is lost. This is because it is sufficient for the magnet having a magnetic flux density of 350 G or less to use the ferrite-based magnetic powder, which has a low production cost. Further, in the case where FG magnetization for motor rotation detection is performed on the plane orthogonal to the rolled surface, if the surface magnetic flux density is 40 G or less, the magnetic flux density becomes too small to obtain the required FG waveform.

[0038]

EXAMPLES Examples of the present invention will be described in detail below. Example 1 As the magnetic powder, Nd-Fe- whose particle size was adjusted by previously pulverizing MQP manufactured by General Motors Co., Ltd. with a wet ball mill
B magnetic powder and _{MM 14 (Fe 0. 9 Co} 0. 1) 79 to B ₇ made of alloy composition, and rapidly quenched ribbon by a single roll method, MM-Fe-Co, previously pulverized particle size control by a wet ball mill
-B magnetic powder was used. Since these magnetic powders are magnetic powders having a particle size of 2 mm or less as they are formed by the ultra-quenching method, they were pulverized to have a particle size of 78 μm or less. As a rust preventive agent, Leodol SP-O1 manufactured by Kao Corporation
0 was used, and Epicoat 828 manufactured by Yuka Shell Co., Ltd. was used as the epoxy main agent.

Then, in a ball mill container, magnetic powder,
Epoxy main agent, rust preventive agent and alumina balls were added, and the air in the container was replaced with N ₂ gas so that the oxygen concentration was 1.2%, and then mixed for 1 hour to oxidize the surface of the magnetic powder. A film, an epoxy resin film and an anticorrosive film were formed.

Next, the mixture thus obtained and the rubber binder were kneaded together with a curing agent and a curing accelerator in a pressure kneader for 7 minutes. As the above-mentioned hardening agent and hardening accelerator, YH-30 manufactured by Yuka Shell Co., Ltd.
2 and IBMI-12 were used.

Further, the obtained kneaded product was subdivided into small lots of 4 kg each, put in a vinyl bag, immediately tied at the mouth, and then stored in a closed container. Then, leave it for an appropriate time, take out the kneaded product from the closed container, and use a pulverizer to obtain a particle size of about 2.6 m.
It was crushed to about m. For the crusher, Urai 140 made by Horai Iron Works
A rotary blade type was used.

Rolling was performed while maintaining the surface temperature of the rolling roll used to obtain the sheet at about 50 ° C. to obtain a sheet-shaped magnet material. Then, after preheating the sheet magnet material under a temperature condition of about 50 ° C. for about 8 hours,
The rubber binder was vulcanized by heating to about 170 ° C.
Then, it was cut into a predetermined size to obtain a flexible sheet magnet.

The formulations in this example are shown in Table 1 below.

[Table 1] In Table 1 above, the MM-Fe-B magnetic powder was added at 20% by weight of the total magnetic powder. Also, in Table 2 below, M
A reference example when no M-Fe-B magnetic powder is added will be shown.

[Table 2] The Nd-Fe-B magnetic powder in Table 2 above is 100% by weight based on the whole magnetic powder.

First, according to the formulation examples shown in Table 1 above, the deformation of the magnet is suppressed to the extent that the dimensional accuracy required for the motor can be realized, and the reference formulation examples shown in Table 2 above are obtained. According to this, it was confirmed that the circularity change amount as the deformation of the magnet exceeds the product limit value of 40 μ. The result is shown in FIG. 2 described above. That is, FIG. 2 shows the thermal deformation of the magnet when the magnet is annularly incorporated in the rotor of the motor, and the heating conditions at this time are to leave at −40 ° C. and 70 ° C. for 1 hour each. Repeated heating is to be performed 10 cycles.

In addition, in the kneading step of this example, it was confirmed that according to such a compounding example, the magnet could not be collapsed due to the magnetic force, and a sufficient magnetic force necessary for, for example, a motor could be obtained. In the kneading step of this example, it was confirmed that the activity of the surface of the magnetic powder was lowered by the rust preventive coating formed in advance, and that air entrapment into the material hardly occurred. Furthermore, it was confirmed that the kneaded product was crushed into a predetermined small particle size under the flow of an inert gas in the crushing process, and thus air entrapment hardly occurred in the subsequent rolling process.

In the rolling process, since the surface of the rolling roll was maintained at a predetermined temperature, the tensile strength of the sheet-shaped magnet was maintained well within a rollable range, and the oxidation of the magnetic powder was suppressed, resulting in magnetic characteristics. It did not deteriorate.

It was further confirmed that in the subsequent high-temperature heating, defects such as air bubbling did not occur in the sheet-shaped magnet material. If the heating temperature exceeds 180 ° C,
Oxidation of the magnetic powder became remarkable and the magnetic properties were deteriorated. When the heating temperature was 125 ° C. or lower, the vulcanization did not proceed and the predetermined tensile strength could not be obtained.

Further, in this example, since the epoxy resin was charged and mixed in the mixing step, and the epoxy resin film was formed on the magnetic powder there, air entrapment was further reduced. Similar effects and advantages were obtained by adding the epoxy resin in the kneading step.

The magnetic characteristics of the magnet obtained in this example are as follows: Br = 5.3 [KG], iHc = 9.3 [kOe], bHc = 4.2 [k]
Oe] and (BH) max = 5.6 [MGOe]. Further, when the obtained magnet was left in an atmosphere of 60 ° C. and 90% RH for 80 hours, no rust was observed on the surface. Further with brush D
When used as a driving magnet for a C motor, 60 ° C, 2
No corrosion occurred in the brush material (Ag-Pd) and the commutator material (Ag-Cd) even after continuous rotation for 00 hours.

As described above, it was confirmed that the sheet-shaped flexible bonded magnet according to the present invention is preferably attached to a rotating electric machine and used. If a metal powder having a high magnetic permeability such as iron powder or an iron alloy is used instead of the permanent magnet powder, a flexible high magnetic permeability material can be formed.

[0052]

As described above, in the rare earth bonded magnet according to the present invention, Nd-Fe-B based magnetic powder is used in comparison with Nd-
By adding 5% by weight or more of (Ce, La) -Fe-B based magnetic powder other than Fe-B magnetic powder, it is possible to prevent insufficient filling rate of the filler with respect to the entire magnet and accelerate vulcanization. Therefore, it is possible to prevent the magnet from being deformed, which makes it impossible to commercialize it, while appropriately maintaining the flexibility of the magnet, and it is possible to obtain a very useful rare earth bonded magnet.

[Brief description of drawings]

FIG. 1 is a flow chart showing a manufacturing process of a rare earth bonded magnet according to the present invention.

FIG. 2 is a diagram showing the relationship between the compounding ratio of (Ce, La) -Fe-B based magnetic powder to the entire magnet and the deformation of the magnet.

Claims (1)

[Claims] 1. A rare earth bonded magnet comprising Nd-Fe-B based magnetic powder dispersed in a flexible resin binder by kneading, wherein the Nd-Fe-B based magnetic powder contains (Ce, La). -Fe-B
A rare earth bonded magnet, wherein the magnetic powder is added so as to be 5% by weight or more of the total magnetic powder.