[0001] This invention relates to a rare-earth bonded magnet used widely for industrial products
such as automobiles, business machines, domestic electrification machines and sounder
machines, to material, a material for such a magnet and a method suitable for manufacturing
the rare-earth bonded magnet.
[0002] Heretofore, there has been widely used Alnico magnets and Ferrite magnets as permanent
magnets. However, rare-earth magnets have been developed, which have excellent magnetic
properties as compared with the aforementioned magnets, and the application and demand
of the rare-earth magnets has increased remarkably in recent years.
[0003] The rare-earth magnets contain active metals and are easily oxidized. Therefore,
the rare-earth magnets of this kind are inferior in their corrosion resistance and
heat-resisting properties, especially in an atmosphere at a temperature higher than
room temperature.
[0004] Among the rare-earth magnets, R-Fe-B magnets and R-Fe-N magnets have Fe(iron) for
their main element in addition to R(rare-earth metals), and are oxidized more remarkably
as compared with Sm-Co magnets. Accordingly, the R-Fe rare-earth magnets have excellent
magnetic properties. However, they have serious problems from the view point of their
oxidation resistance, their corrosion resistance and their temperature characteristics
and heat resistance at a temperature higher than room temperature.
[0005] Among the rare-earth magnets, the sintered magnet is densified by sintering. Therefore,
it is possible to improve the heat resistance of the sintered magnet considerably
by coating the surface of the magnet with, for example, Ni, or resin at the final
stage of the magnet manufacturing process. Among the bonded magnets, especially in
a magnet manufactured by injection molding using thermoplastic resin such as polyamide
resin, it is possible to improve its heat resistance by coating the surface of the
magnet in a manner similar to that described above in relation to the sintered magnet
because the surface of magnetic powder is covered completely with the resin.
[0006] For bonded magnets, in a magnet manufactured by compression molding using a binder
such as thermosetting resin (for example, epoxy resin), metals or the like, a large
number of vacancies exist between the powdered magnetic material and the binder. Therefore,
it is not possible to prevent the magnet from oxidizing owing to the internal vacancies
even if the surface of the magnet is coated completely, and it is unavoidable to oxidize
the magnetic material through the coating layer and the internal vacancies. Consequently,
there is a problem in that secular change of the magnetic properties at room temperature
and a temperature higher than room temperature becomes large and the heat resistance
of the magnet is degraded with the passage of time.
[0007] This invention is made in view of the aforementioned problems of the prior art, it
is an aim to provide a rare-earth bonded magnet with improved heat-resistance characteristics
by preventing the oxidation of the rare-earth magnetic material as much as possible
and decreasing the secular change of the magnetic properties at room temperature and
at higher temperatures.
[0008] The material for the rare-earth bonded magnet according to this invention is characterized
by comprising rare-earth magnetic powder coated with heat resisting addition polymerized
thermosetting resin consisting mainly of triazine resin, optionally together with
binder if necessary.
[0009] The rare-earth bonded magnet according to this invention is characterized in that
rare-earth magnetic powder coated, optionally by using binder if necessary, with heat
resisting addition polymerized thermosetting resin consisting mainly of triazine resin
is agglomerated together with the optional binder.
[0010] The method of manufacturing a rare-earth bonded magnet according to this invention
is characterized by comprising steps of coating a surface of rare-earth magnetic powder
with heat resisting addition polymerized thermosetting resin consisting mainly of
triazine resin by adding the thermosetting resin into the rare-earth magnetic powder
almost at the same time as addition of binder, subsequently molding a compact by pressing
the rare-earth magnetic powder coated with the thermosetting resin together with the
binder and curing the thermosetting resin in the compact. The rare-earth magnetic
powder may by added with organometallic salt as a metallic catalyser together with
the binder and the heat resisting addition polymerized thermosetting resin in a preferred
aspect, and the curing of the thermosetting resin may be carried out at a temperature
of not lower than 150°C in a vacuum or in an atmosphere of argon in the other preferred
aspects.
[0011] The present invention will now be described in greater detail below.
[0012] In the present invention, magnetic powder containing rare-earth metals such as R-Fe,
R-Fe-B, R-Fe-N and the like are used as rare-earth magnetic powder.
[0013] As resin to be coated on the surface of the rare-earth magnetic powder of this kind,
heat resisting addition polymerized thermosetting resin is used which has triazine
resin (polymer having unsuturated triple bonds ( cyanato group -R-O-C≡N)) for its
main component.
[0014] The material for the rare-earth bonded magnet according to this invention comprises
rare-earth magnetic powder coated with heat resisting addition polymerized thermosetting
resin consisting mainly of triazine resin, together with binder if need require. In
case of coating, various methods may be applied, such as a method of coating the rare-earth
magnetic powder by dipping it into a solution (for example, methyl ethyl ketone is
used as a solvent) containing the heat resisting addition polymerized thermosetting
resin consisting mainly of triazine resin, a method of mixing the rare-earth magnetic
powder after adding the heat resisting addition polymerized thermosetting resin consisting
mainly of triazine resin in it, and a method of coating the rare-earth magnetic powder
by vaporizing the thermosetting resin and depositting it on the surface of the magnetic
powder, for example.
[0015] The rare-earth bonded magnet according to this invention is formed by agglomerating
rare-earth magnetic powder using binder, which magnetic powder is coated with heat
resisting addition polymerized thermosetting resin together with binder if need require.
In this case, thermosetting resin such as epoxy resin is used similarly as the binder,
and the magnetic powder is molded (agglomarated) into a compact having desired shape
by forming methods such as compression molding and so on.
[0016] After molding the compact, it is preferable to cure the thermosetting resin added
as the binder and the thermosetting resin consisting mainly of triazine resin at a
temperature of not lower than 150°C in a non-oxidative atmosphere or in a vacuum.
In the curing treatment, the thermosetting resin is hardened, while triazine resin
of the thermosetting resin is hardened by heating and triazine rings are formed therein.
The triazine ring is remarkably stable to thermal energy, so that the heat resistance
of the resin is improved.
[0017] In order to coat the thermosetting resin consisting mainly of triazine resin on surfaces
of the respective particles of the rare-earth magnetic powder more uniformly, it is
desirable to perform the curing at a temperature of not lower than 150°C in a vacuum
because the triazine resin is vapourized temporarily and hardened after depositting
on the surface of the rare-earth magnetic powder very uniformly.
[0018] In a case of manufacturing the rare- earth bonded magnet in such a manner, it is
advisable according to demand to add organometallic salt such as zinc octylate, iron
acetylacetonate or the like as a metallic catalyser together with the binder and the
heat resisting addition polymerized thermosetting resin. Namely, it is possible to
further reduce the secular change of the magnetic properties because adhesiveness
between the rare-earth magnetic powder and the thermosetting resin consisting mainly
of triazine resin is improved by addition of the organometallic salt as the metallic
catalyser, and a firm coating film having heat resistance can be obtained.
[0019] In the rare-earth bonded magnet, the material and the method for manufacturing the
rare-earth bonded magnet, the rare-earth magnetic powder is coated with the heat resisting
addition polymerized thermosetting resin consisting mainly of triazine resin on the
surface thereof and the coated magnetic powder is used. Therefore it is possible to
retard or prevent the oxidation of the magnetic material. The heat resistance of the
magnet is improved and the secular change of the rare-earth bonded magnet at room
temperature and at a temperature higher than room temperature is reduced remarkably.
[0020] The present invention is illustrated below with reference to the following non-limiting
Examples.
EXAMPLE 1
[0021] At first, by spraying rare-earth molten magnetic alloy consisting essentially of
28wt% of Nd - 0.9wt% of B - 5.0wt% of Co - Fe (remainder) on the surface of a copper
roll rotating at the peripheral speed of 25m/sec, a ribbon of about 30µm in thickness
was obtained, and rare-earth magnetic powder was obtained by comminuting the ribbon
into the size smaller than 200µm. Subsequently, the rare-earth magnetic powder was
annealed for 10 minutes at 550°C.
[0022] Next, epoxy resin which is a thermosetting resin was added into the annealed rare-earth
magnetic powder as much as 2wt% as binder, and triazine resin which is the heat resisting
addition polymerized thermosetting resin was added into the magnetic powder as much
as amount shown in Table 1, respectively. Then, these were mixed uniformly. And, zinc
octylate was further added in some of samples as a metallic catalyser as much as 0.0006wt%
of the triazine resin content, respectively.
[0023] Then, each of the mixed powders was compressed into a compact of 10mm in diameter
and 7mm in height, and cured for 1 hour at 170°C in an atmosphere of argon.
[0024] Furthermore, rare-earth bonded magnets were obtained by polarizing the cured compacts
in a pulse magnetic field of 50kOe, and open flux values of the polarized magnet were
measured, respectively. The open flux values were measured again at room temperature
after holding them for 1000 hours at 180°C, whereby the rates of decrease of the open
flux values, that is irreversible demagnetizing factors were obtained. The results
of measurement of the irreversible demagnetizing factors are shown in Table 1 together
with the triazine resin contents.
Table 1
| Sample Number |
Triazine resin content (wt%) |
Irreversible demagnetizing factor (%) |
| |
|
Without zinc octylate |
Addition of zinc octylate |
| Conventional example 1 |
0 |
55.0 |
55.0 |
| 2 |
0.01 |
38.0 |
32.5 |
| 3 |
0.05 |
27.5 |
20.6 |
| 4 |
0.10 |
10.8 |
9.9 |
| Inventive example 5 |
0.20 |
9.4 |
8.4 |
| 6 |
0.30 |
8.5 |
7.3 |
| 7 |
0.50 |
8.2 |
7.3 |
| 8 |
1.00 |
8.9 |
8.2 |
[0025] As shown in Table 1, in the case of the conventional example No.1 which is not coated
with triazine resin on the surface of the rare-earth magnetic powder, the irreversible
demagnetizing factor after holding it for 1000 hours at 180°C was considerably large.
As compared with above, in the cases of the examples Nos. 2-8 according to this invention
which are coated with triazine resin, it was confirmed that the irreversible demagnetizing
factor becomes considerably smaller when triazine resin is coated more than some degree.
However it is desirable to coat triazine resin not more than 2wt% since the magnetic
properties are degraded if the triazine resin is coated in excess. In addition, it
was confirmed that the irreversible demagnetizing factor becomes smaller when an organometallic
salt is added.
Example 2
[0026] By spraying molton rare-earth magnetic alloy consisting essentially of 28wt% of Nd
- 0.9wt% of B - 5.0wt% of Co - Fe (remainder) on the surface of the copper roll rotating
at the peripheral speed of 25m/sec, a ribbon of about 30µm in thickness was obtained,
and rare-earth magnetic powder was obtained by comminuting the ribbon into the size
of smaller than 200µm. rare-earth magnetic powder was annealed for 10 minutes at 550°C.
[0027] Secondly, epoxy resin of 2wt% which is the thermosetting resin was added into the
annealed rare-earth magnetic resin powder as binder, and triazine resin which is the
heat resisting addition polymerized thermosetting resin was added into the magnetic
powder as much as amount shown in Table 2, respectively. Then, these were mixed uniformly
similar to the case of Example 1. Furthermore, zinc octylate was also added in some
of samples as a metallic catalyser as much as 0.0006wt% of the triazine resin content,
respectively.
[0028] Then, each of the mixed powders was compressed into a compact of 10mm in diameter
and 7mm in height, and the compact was cured for 1 hour at 170°C in a vacuum.
[0029] Then, the cured compacts were polarized in a pulse magnetic field of 50 kOe, and
open flux values of the polarized magnets were measured, respectively. The open flux
values were measured again at room temperature after holding them for 1000 hour at
180°C, whereby the rates of decrease of the open flux values, that is irreversible
demagnetizing factors were obtained. The results of measurement of the irreversible
demagnetizing factors are shown in Table 2.
Table 2
| Sample Number |
Triazine resin content (wt%) |
Irreversible demagnetizing factor (%) |
| |
|
Without zinc octylate |
Addition of zinc octylate |
| Conventional example 9 |
0 |
53.5 |
53.5 |
| 10 |
0.01 |
13.6 |
11.5 |
| 11 |
0.05 |
10.8 |
9.1 |
| 12 |
0.10 |
9.3 |
8.8 |
| Inventive example 13 |
0.20 |
8.5 |
8.4 |
| 14 |
0.30 |
8.2 |
7.7 |
| 15 |
0.50 |
7.9 |
7.5 |
| 16 |
1.00 |
8.0 |
7.8 |
[0030] As shown in Table 2, in the case of performing the curing in a vacuum, it was confirmed
that the irreversible demagnatizing factor after holding for 1000 hours at 180°C becomes
smaller and the heat resistance of the magnet is further improved since the triazine
resin is coated more uniformly on the respective surface of the magnetic powder.
Example 3
[0031] After obtaining rare-earth magnetic powder consisting essentially of 31.1wt% of Nd
- 1.0wt% of B - Fe (remainder) in the same manner as Example 1, 2.0wt% of epoxy resin
being the thermosetting resin as binder and 0.3wt% of triazine resin being the heat
resisting addition polymerized thermosetting resin were added into the annealed rare-
earth magnetic powder, and they were mixed uniformly. In some of samples, zinc octylate
was further added as a metallic catalyser as much as 0.0006wt% of the triazine resin
content.
[0032] Next, each of the mixed powders was compressed into a compact of 10mm in diameter
and 7mm in height, and the compacts were cured for 1 hour at 170°C, in the air as
to a part of compacts, in an atmosphere of argon as to another part of compacts and
in a vacuum as to the remaining part of compacts, respectively.
[0033] Then, the cured compacts were polarized in a pulse magnetic field of 50kOe, and open
flux values of the polarized magnets were measured, respectively. The rates of decrease
of the open flux values, that is inneversible demagnetizing factors were obtained
by measuring the open flux values at room temperature after holding them for 1000
hours at 180°C. The measured results are shown in Table 3.
Table 3
| Sample Number |
Triazine resin content (wt%) |
Zinc octylate |
Curing |
Irreversible demagnetizing factor (%) |
| Conventional example 17 |
0 |
None |
in Air |
32.5 |
| 18 |
0 |
None |
in Argon |
41.5 |
| 19 |
0 |
None |
in Vacuum |
49.0 |
| Inventive 20 example |
0.3 |
None |
in Air |
4.9 |
| 21 |
0.3 |
None |
in Argon |
5.1 |
| 22 |
0.3 |
None |
in Vacuum |
3.5 |
| 23 |
0.3 |
Addition |
in Air |
4.4 |
| 24 |
0.3 |
Addition |
in Argon |
4.6 |
| 25 |
0.3 |
Addition |
in Vacuum |
3.0 |
[0034] As is obvious from Table 3, the conventional examples Nos.17-19 which do not include
triazine resin nor an organometallic salt showed large irreversible demagnetizing
factors after holding them for 1000 hours at 180°C. As compared with above, in the
examples Nos.20-22 which include triazine resin but do not include an organometallic
salt and the examples Nos.23-25 which include both the triazine resin and organometallic
salt, they showed considerably smaller irreversible demagnetizing factors after holding
them for 1000 hours at 180° C. It was confirmed that the irreversible demagnetizing
factor of the magnet cured in a vacuum is smaller than that of magnet cured in the
air and an atmosphere of argon and it is effective to cure in the vacuum for further
improving the heat resistance of the magnet. Furthermore, it became clear that it
is possible to further decrease the irreversible demagnetizing factor by adding an
organometallic salt as a metallic catalyser.
Example 4
[0035] An ingot having a composition represented by Sm2Fe17 was subjected to a homogenizing
treatment by heating it for 24 hours at a temperature of 1100° C, and grinded mechanically
into powder of the size passing 120 mesh. Then the powder was subjected to nitriding
by heating for 5 hours at a temperature of 550°C in an atmosphere of nitrogen.
[0036] Secondly, fine rare-earth magnetic powder was obtained by comminuting the nitrided
powder into particles of 3µm in mean diameter. Subsequently, the rare-earth magnetic
powder was added with epoxy resin of 2wt% as binder, and added with triazine resin
of 0.3wt% as the heat resisting addition polymerized thermosetting resin. In some
of samples, iron acetylacetone was further added as a metallic catalyser as much as
0.0015wt% of the triazine resin.
[0037] Then, each of the mixed powders was compressed into a compact of 10mm in diameter
and 7mm in height in a vertical magnetic field of 15kOe, and the compacts were cured
for 1 hour at 170° C, in an atmosphere of argon as to a part of compacts and in a
vacuum as to the other part of compacts, respectively.
[0038] The results shown in Table 4 were obtained by measuring the irreversible demagnetizing
factors after holding for 1000 hours at 180°C in the same manner as Example 1.
[0039] The following were typical magnetic properties of these rare-earth bonded magnets;
Br (residual magnetic flux density) : 8.0KG, iHc (coercive force) : 8.5kOe, (BH)max
(maximum energy product) : 11.8MGOe.
Table 4
| Sample Number |
Triazine resin content (wt%) |
Iron acetylacetonate |
Curing |
Irreversible demagnetizing factor (%) |
| Conventional example 26 |
0 |
None |
in Argon |
13.5 |
| Inventive 27 example |
0.3 |
None |
in Argon |
4.3 |
| 28 |
0.3 |
None |
in Vacuum |
2.5 |
| 29 |
0.3 |
Addition |
in Argon |
3.1 |
| 30 |
0.3 |
Addition |
in Vacuum |
2.0 |
[0040] As shown in Table 4, the conventional example No.26 which does not include triazine
resin nor an organometallic salt exhibited a large irreversible demagnetizing factor
after holding it for 1000 hours at 180° C. As compared with above, the inventive examples
Nos 27, 28 which include triazine resin but not an organometallic salt, and the inventive
examples No. 29, 30 which include both the triazine resin and an organometallic salt
exhibited considerably smaller irreversible demagnetizing factors after holding them
for 1000 hours at 180° C. It was confirmed that the irreversible demagnetizing factor
becomes smaller in the case of performing the curing in a vacuum and it is effective
to carry out the curing in a vacuum for further improving the heat resistance of the
magnet. Additionally, it was also confirmed that it is possible to further decrease
the irreversible demagnetizing factor by adding an organometallic salt as a metallic
catalyser.
[0041] As mentioned above, the rare-earth bonded magnet, the material and the method for
manufacturing the rare-earth bonded magnet according to this invention, it is possible
to prevent the oxidation of the rare-earth magnetic powder which is easily oxidized
and the secular change of the magnetic properties of the rare-earth bonded magnet
at room temperature and at a temperature higher than room temperature becomes smaller.
Accordingly, an excellent effect can be obtained since it is possible to provide the
rare-earth bonded magnet having improved heat resistance.
[0042] In this specification the phrase "almost at the same time" means that the thermosetting
resin is added into the rare-earth magnetic powder at the same time as addition of
the binder, or before or after the addtiion of the binder.
1. Material for a rare-earth bonded magnet comprising rare-earth magnetic powder coated
with heat resisting addition polymerized thermosetting resin consisting mainly of
triazine resin.
2. A rare-earth bonded magnet characterized by agglomerating rare-earth magnetic powder
coated with heat resisting addition polymerized thermosetting resin consisting mainly
of triazine resin, optionally, together with binder.
3. A method for manufacturing a rare-earth bonded magnet by compacting rare-earth magnetic
powder together with binder which comprises coating a surface of said rare-earth magnetic
powder with heat resisting addition polymerized thermosetting resin consisting mainly
of triazine resin by adding said thermosetting resin into the rare-earth magnetic
powder almost at the same time as addition of the binder, subsequently molding a compact
by pressing the rare-earth magnetic powder coated with the thermosetting resin and
curing the thermosetting resin in said compact.
4. A method for manufacturing a rare-earth bonded magnet as claimed in claim 3, wherein
said rare-earth magnetic powder is added with organometallic salt as a metallic catalyser
together with the binder and the heat resisting addition polymer-type thermosetting
resin.
5. A method for manufacturing a rare-earth bonded magnet as claimed in claim 3 or claim
4, wherein said curing of the thermosetting resin is carried out at a temperature
of not lower than 150°C in an atmosphere of argon.
6. A method for manufacturing a rare-earth bonded magnet as claimed in claim 3 or claim
4, wherein said curing of the thermosetting resin is carried out at a temperature
of not lower than 150°C in a vacuum.