BACKGROUND OF THE INVENTION
[0001] The present invention relates to nanocrystalline alloy having an insulating coating
thereon, which is excellent in high-frequency characteristics and suitable for use
in various magnetic parts such as transformer, choke coil, etc., and further relates
to a magnetic core made of the nanocrystalline alloy and a method for forming the
insulating coating on the nanocrystalline alloy.
[0002] A nanocrystalline alloy, which contains fine crystal grains having an average grain
size of 50 nm or less in an area ratio of 50% or more of the alloy structure, has
been, because of its good soft magnetic properties, used for producing magnetic cores
of a common-mode choke coil, a high-frequency transformer, an electrical leak alarm,
pulse transformer, etc. Typical examples for such a nanocrystalline alloy are disclosed
in U.S. Patent No. 4,881,989 and JP-A-1-242755. The nanocrystalline alloy known in
the art has been generally produced by subjecting an amorphous alloy obtained by quenching
a molten or vaporized alloy to a heat treatment for forming fine crystals. A method
for quenching a molten alloy to produce an amorphous alloy may include a single roll
method, a twin roll method, a centrifugal quenching method, a rotation spinning method,
an atomization method, a cavitation method, etc. A method for quenching a vaporized
metal may include a sputtering method, a vapor deposition method, an ion plating method,
etc. The nanocrystalline alloy is produced by finely crystallizing an amorphous alloy
produced by the above method, and is known to have, contrary to amorphous alloys,
a good heat stability as well as a high saturation magnetic flux density, a low magnetostriction,
and a good soft magnetic property. The nanocrystalline alloy is also known to show
a little change with time in its properties and have a good temperature stability.
[0003] Conventionally, the magnetic core used in a noise filter, a pulse transformer, etc.
has been made of a highly permeable material having good high-frequency characteristics
such as ferrite, an amorphous alloy, etc. In a high-frequency transformer for an inverter,
a material low in the magnetic core loss has been used. Further, the Fe-based nanocrystalline
alloy disclosed in U.S. Patent No. 4,881,989 is described to have a high permeability
and a low magnetic core loss, and therefore, suitable for the use mentioned above.
[0004] However, it has been found by the inventor that a magnetic core for a common-mode
choke coil or a high-frequency magnetic core for an inverter transformer made of thin
ribbon of an Fe-based nanocrystalline alloy does not exhibit sufficient properties
when the surface of the thin ribbon is not smooth and the thin ribbons are not subjected
to layer insulation because the influence of eddy current on the properties comes
to remarkable with increasing width of the thin ribbon. As a method of layer insulation,
JP-A-63-302504 discloses to apply SiO₂ powder or MgO powder on a part of or complete
surface of a thin alloy ribbon or to coat a thin alloy ribbon with an alcohol solution
of a modified alkyl silicate added with an acid. JP-A-2-297903 discloses to form a
heat-resistant insulating layer of 0.5-5 µm thick by heating a coating comprising
a uniform mixture of 20-90 weight % (calculated in terms of SiO₂) of a silanol oligomer
and 80-10 weight % of a ceramic fine particle to allow the oligomers cross-linked
each other.
[0005] However, since an amorphous alloy contracts during the heat treatment for nanocrystallization,
an insulating layer on the alloy is cracked or separated from the surface of the alloy
due to the contraction stress. Also, sufficient magnetic properties cannot be attained
due to the internal stress of the alloy generated by contraction. Although the method
disclosed in JP-A-2-297903 solved these problems, the insulating layer formed by the
method has a poor affinity for a resin. Therefore, when a magnetic core, for example,
for an inverter transformer made of a thin alloy ribbon having such an insulating
layer is cut after impregnation with a resin, the resin exfoliates from the cut surface
and the thin alloy ribbons are not laminated each other. In the method wherein SiO₂
powder or MgO powder is applied on the surface of an alloy, the powder is likely to
be separated from the alloy surface during the production of the magnetic core to
lead to insufficient insulation.
[0006] The influence of the contraction by the heat treatment is not necessary to be considered
when an amorphous alloy provided with an insulating coating is produced. However,
as described above, the contraction during the heat treatment causes defective insulation
due to cracking or peeling of the insulating coating or deterioration of magnetic
properties due to increased internal stress. Therefore, an insulating coating free
from the above problems and a method for forming such an insulating coating on a nanocrystalline
alloy has been demanded to be developed. Further, an insulating coating exhibiting
sufficient insulation properties even if the insulating coating is made thinner has
been required in the field of electronic circuitry which requires a small-sized magnetic
core.
OBJECT AND SUMMARY OF THE INVENTION
[0007] Accordingly, an object of the present invention is to provide a nanocrystalline alloy
excellent in insulating properties. Another object of the present invention is to
provide a magnetic core excellent in magnetic properties at high frequency, and still
another object of the present invention is to provide a method for forming an insulating
coating free from the conventional problems.
[0008] As a result of the intense research in view of the above objects, the inventor have
found that an insulating coating formed by heating a solution of at least one insulating
material selected from the group consisting of aluminum silicates, lithium silicates
and magnesium methylate is free from cracking and peeling during the heat treatment
for crystallization of an amorphous alloy, and a nanocrystalline alloy provided with
such an insulating coating is excellent in insulating properties and suitable as a
material for magnetic core used at high frequency. The present invention has been
accomplished based on the finding.
[0009] Thus, in a fist aspect of the present invention, there is provided a nanocrystalline
alloy having on at least one surface thereof an insulating coating, the nanocrystalline
alloy having a chemical composition represented by the following formula:
(Fe
1-aM
a)
100-x-y-z-bA
xM'
yM''
zX
b (by atomic %),
wherein M is at least one element selected from the group consisting of Co and Ni,
A is at least one element selected from the group consisting of Cu and Au, M' is at
least one element selected from the group consisting of Ti, V, Zr, Nb, Mo, Hf, Ta
and W, M'' is at least one element selected from the group consisting of Cr, Mn, Al,
Sn, Zn, Ag, In, platinum group elements, Mg, Ca, Sr, Y, rare earth elements, N, O
and S, X is at least one element selected from the group consisting of B, Si, C, Ge,
Ga and P, and each of a, x, y, z and b respectively satisfies 0≦ a≦ 0.5, 0≦ x≦ 10,
0. 1≦ y≦ 20, 0≦ z≦ 20 and 2≦ b≦ 30, and the insulating coating having an average thickness
of 2 µm or less and comprising at least one insulating material selected from the
group consisting of aluminum silicates, lithium silicate and magnesium oxide.
[0010] In a second aspect of the present invention, there is provided a magnetic core made
of the nanocrystalline alloy as defined above.
[0011] In a third aspect of the present invention, there is provided a method for forming
an insulating coating on a nanocrystalline alloy, which comprises (1) rapidly quenching
a molten alloy having a chemical composition represented by the following formula:
(Fe
1-aM
a)
100-x-y-z-bA
xM'
yM''
zX
b (by atomic %),
wherein M is at least one element selected from the group consisting of Co and Ni,
A is at least one element selected from the group consisting of Cu and Au, M' is at
least one element selected from the group consisting of Ti, V, Zr, Nb, Mo, Hf, Ta
and W, M'' is at least one element selected from the group consisting of Cr, Mn, Al,
Sn, Zn, Ag, In, platinum group elements, Mg, Ca, Sr, Y, rare earth elements, N, O
and S, X is at least one element selected from the group consisting of B, Si, C, Ge,
Ga and P, and each of a, x, y, z and b respectively satisfies 0≦ a≦ 0.5, 0≦ x≦ 10,
0. 1≦ y≦ 20, 0≦ z≦ 20 and 2≦ b≦ 30 to produce an amorphous alloy; (2) coating on at
least one surface of the amorphous alloy a solution containing at least one insulating
material selected from the group consisting of aluminum silicates, lithium silicate
and magnesium methylate; (3) drying the solution-coated amorphous alloy at a temperature
between 80°C and 350°C; and (4) heat-treating the dried amorphous alloy at a temperature
not lower than a crystallization temperature of said amorphous alloy so as to form
a fine crystal grain having a grain size of 30 nm or less in alloy structure while
forming said insulating coating having a thickness of 2 µm or less and comprising
at least one insulating material selected from the group consisting of aluminum silicates,
lithium silicate and magnesium oxide.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012]
Fig. 1 is a schematic representation illustrative of one embodiment of the method
of the present invention;
Fig. 2 is a schematic representation illustrative of another embodiment of the method
of the present invention;
Fig. 3 is a schematic representation illustrative of still another embodiment of the
method of the present invention; and
Fig. 4 is a schematic view showing a toroidal magnetic core of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
[0013] The nanocrystalline alloy of the present invention which has an insulating coating
on at least one surface thereof may be produce as described below.
[0014] First, an amorphous alloy is produced by rapidly quenching a molten alloy having
a chemical composition represented by the following formula:
(Fe
1-aM
a)
100-x-y-z-bA
xM'
yM''
zX
b (by atomic %),
wherein M is at least one element selected from the group consisting of Co and Ni,
A is at least one element selected from the group consisting of Cu and Au, M' is at
least one element selected from the group consisting of Ti, V, Zr, Nb, Mo, Hf, Ta
and W, M'' is at least one element selected from the group consisting of Cr, Mn, Al,
Sn, Zn, Ag, In, platinum group elements, Mg, Ca, Sr, Y, rare earth elements, N, O
and S, X is at least one element selected from the group consisting of B, Si, C, Ge,
Ga and P, and each of a, x, y, z and b respectively satisfies 0≦ a≦ 0.5, 0≦ x≦ 10,
0. 1≦ y≦ 20, 0≦ z≦ 20 and 2≦ b≦ 30. A single-roll method, a twin-roll method, etc.
may be employed to rapidly quenching the molten alloy.
[0015] A chemical composition out side the above range fails to give a sufficient effect
attained by the present invention due to a remarkable reduction in specific permeability
or a remarkable increasing in magnetic core lose, thereby making it unable to obtain
a nanocrystalline alloy of practical characteristics.
[0016] Then, a solution of at least one insulating material is applied on at least one surface
of the amorphous alloy thus produced. The insulating material is selected from the
group consisting of aluminum silicates, modified aluminum silicates, lithium silicates
and magnesium methylate. The solution may include oxide powder, nitride powder, etc.
which is known to be used for insulating coating. The concentration of the insulating
material in the solution is preferably 5 to 50 % by weight. The solution thus prepared
may be mixed with a solution of colloidal silica. The solution may be applied on an
amorphous alloy after subjecting the amorphous alloy to anodizing treatment which
improves the insulating properties and corrosion resistance of the resulting nanocrystalline
alloy. The amount of the solution being applied on the amorphous alloy is regulated
so that the thickness of the resulting insulating coating may be 2 µm or less.
[0017] The amorphous alloy applied with the solution is then dried at a temperature of 80-350°C,
preferably for 5 seconds to 10 minutes. The drying may be effected by blowing the
applied solution with air or another gas such as argon, nitrogen, helium, etc. maintained
at 80-350°C to rapidly dry the solution. This makes the insulating coating uniform
in its thickness.
[0018] Before subjected to the subsequent heat treatment, the amorphous alloy thus dried
is usually made into a form of magnetic core by winding the thin ribbon of amorphous
alloy or laminating cut sheets or punched sheets of the amorphous alloy. The winding
or laminating step may be carried out after heat treatment when the heat-treated alloy
ribbon is sufficiently flexible.
[0019] The heat treatment for crystallization is carried out at a temperature not lower
than the crystallization temperature of the amorphous alloy, usually at 450-700°C,
for 1 minute to 24 hours in an inert gas atmosphere such as nitrogen gas atmosphere,
argon gas atmosphere, etc. or an oxidizing atmosphere such as air. By this heat treatment,
fine crystal grains are formed in the alloy structure, and simultaneously, the insulating
coating is formed on the surface of the resulting nanocrystalline alloy. During the
heat treatment, the magnesium methylate is oxidized to provide an insulating coating
comprising magnesium oxide.
[0020] When an amorphous alloy applied with the solution is directly subjected to heat treatment
without being dried, the heat-treatment atmosphere comes to contain a large amount
of moisture evaporated form the solution. This leads to a preferential crystallization
of the surface of the alloy. As a result, a nanocrystalline alloy of a uniform and
fine structure cannot be obtained. Also, cracking and peeling of the insulating coating
are likely to occur. Therefore, the drying step prior to the heat treatment of crystallization
is indispensable.
[0021] The production method of the present invention will be further described while referring
to the drawings.
[0022] In Fig. 1, a thin ribbon 1 of amorphous alloy, which is unwound in the direction
indicated by the arrow from a winding reel 2, is allowed to pass through a solution
4 stored in a vessel 3 to apply the solution 4 on both the surface of the thin ribbon
1 of amorphous alloy. After passing through a scraper 5, the thin ribbon 1 of amorphous
alloy is introduced into a drying furnace 6 kept at 80- 350°C. The dried thin ribbon
1 of amorphous alloy is then wound on a winding reel 7 and subjected to the subsequent
heat treatment of crystallization.
[0023] In Fig. 2, a thin ribbon 1 of amorphous alloy, which is unwound in the direction
indicated by the arrow from a winding reel 2, is allowed to pass through a roll coater
8. A transfer roll 10 is partially immersed in a solution 4 stored in a vessel 3 to
apply the solution 4 on the lower surface of the thin ribbon 1 of amorphous alloy,
which is then introduced into a drying furnace 6 kept at 80 - 350°C. The dried thin
ribbon 1 of amorphous alloy is then wound on a winding reel 7 and subjected to the
subsequent heat treatment of crystallization.
[0024] In Fig. 3, the upper surface of a thin ribbon 1 of amorphous alloy, which is unwound
in the direction indicated by the arrow from a winding reel 2, is sprayed with a solution
4 from a spray 9. The thin ribbon 1 of amorphous alloy is then introduced into a drying
furnace 6 kept at 80-350°C. The dried thin ribbon 1 of amorphous alloy is then wound
on a winding reel 7 and subjected to the subsequent heat treatment of crystallization.
[0025] The nanocrystalline alloy produced by the method described above has preferably a
thickness of 2 to 50 µm and contains fine crystals having an average grain size of
30 nm or less, preferably in an area ratio of 50 % or more. The fine crystals mainly
comprise bcc Fe-phase (body centered cubic lattice phase) containing Si, and may contain
an ordered lattice phase or are constituted of ordered lattice. Alloying elements
other than Si, i.e., B, Al, Ge, Zr, etc. may be contained as a solid solution component
in the bcc Fe-phase. The remaining part other than the crystal phase mainly comprises
amorphous phase. However, a nanocrystalline alloy substantially comprising only crystal
phase is also embraced within the scope of the present invention. A compound phase
may also be formed in a part of the alloy structure.
[0026] The average thickness of the insulating coating is 2 µm or less, preferably 0.01
to 1 µm. An average thickness of 0.5 µm or less is particularly preferred because
the size of magnetic core can be reduced while maintaining its excellent insulating
properties.
[0027] A solution of aluminum silicate (Al₂O₃·SiO₂) provides the surface of nanocrystalline
alloy with an insulating coating having a uniform thickness and a high resistance
to peeling because internal stress is hardly generated in the alloy during the crystallization
process. Therefore, the insulating properties can be improved. A nanocrystalline alloy
having such an insulating coating exhibits a high permeability and a low magnetic
core loss at low and high frequency range.
[0028] A solution of lithium silicate (Li₂O·SiO₂) produces the same effect as above because
internal stress is hardly generated in the alloy during the crystallization process.
[0029] Since a solution of magnesium methylate can be dried rapidly, a thin, uniform and
hard insulating coating comprising magnesium oxide, which exhibits improved insulating
properties, is formed on the nanocrystalline alloy.
[0030] The magnetic core made by laminating or winding the nanocrystalline alloy described
above is excellent in layer insulation and has little internal stress, and therefore,
suitable for magnetic core used in a high-frequency range. In addition, since the
nanocrystalline alloy has a good affinity for a resin such as an epoxy-type resin,
a cut core having a high interlaminar strength can be obtained.
[0031] The present invention will be further described while referring to the following
Examples which should be considered to illustrate various preferred embodiments of
the present invention.
Example 1
[0032] An amorphous alloy ribbon having a width of 25.4 mm and a thickness of 18 µm was
produced by quenching a molten alloy of F
bal.Cu
0.9Nb
2.8Si
15.5B
6.2(atomic %) by using a single roll method. After being passed through a solution containing
each insulating material listed in Table 1, the amorphous alloy ribbon was dried in
a hot-gas furnace kept at 200°C. The dried amorphous alloy ribbon was then wound to
form a toroidal shape of 100 mm outer diameter and 80 mm inner diameter, and then
heated to 570°C in a furnace at a heating rate of 1 .5°C/min and maintained there
for 15 minutes to be subjected to heat treatment in a nitrogen atmosphere. The heat-treated
product was cooled to room temperature to obtain each magnetic core. The most part
of the alloy structure of the resulting nanocrystalline alloy was occupied with extremely
fine grains comprising bcc-phase of an average grain size of about 12 nm.
[0033] For comparison, a toroidal magnetic core having no insulating coating was produced
in the same manner as above (Sample No. 9).
[0034] The specific permeability (µ
r) at 10 MHz, the magnetic core loss (Pc) at 500 kHz and 0.05 T, the average thickness
of the insulating coating and the resistance (R) between the innermost part and the
surface of the magnetic core are shown in Table 1.
Table 1
Sample No. |
Insulating Material |
µr |
Pc (kW/m³) |
R (Ω) |
Thickness (µm) |
Invention |
|
|
|
|
|
1 |
modified aluminum silicate |
640 |
220 |
135 |
0.8 |
2 |
lithium silicate |
650 |
220 |
138 |
0.7 |
3 |
magnesium methylate |
590 |
240 |
128 |
0.2 |
4 |
lithium silicate |
710 |
210 |
142 |
1.2 |
5 |
magnesium methylate |
620 |
260 |
121 |
0.1 |
Comparison |
|
|
|
|
|
6 |
alumina sol |
410 |
360 |
27 |
1.1 |
7 |
alkyl silicate |
490 |
310 |
35 |
1.2 |
8 |
colloidal silica |
480 |
330 |
29 |
0.2 |
9 |
- |
120 |
590 |
1.1 |
- |
[0035] As seen from Table 1, the nanocrystalline alloy having the insulating coating of
the present invention had a large value of R, which means a high interlaminar insulating
resistance. This results in high magnetic properties of a high µ
r and a low Pc.
Example 2
[0036] An amorphous alloy ribbon having a width of 20 mm and a thickness of 18 µm was produced
by quenching a molten alloy having each chemical composition shown in Table 2 by using
a single roll method. After being passed through a solution dissolving each insulating
material listed in Table 2, the amorphous alloy ribbon was dried in a hot-gas furnace
kept at 200°C. The dried amorphous alloy ribbon was then wound to form a toroidal
shape of 100 mm outer diameter and 80 mm inner diameter, and then heated to 570°C
in a furnace at a heating rate of 1 . 5°C/min and maintained there for 15 minutes
to be subjected to heat treatment in a nitrogen atmosphere. The heat-treated product
was cooled to room temperature to obtain each magnetic core. The most part of the
alloy structure of the resulting nanocrystalline alloy was occupied with extremely
fine grains comprising bcc-phase of an average grain size of about 12 nm.
[0037] The specific permeability (µ
r) at 10 MHz, the magnetic core loss (Pc) at 500 kHz and 0.05 T, the average thickness
of the insulating coating and the resistance (R) between the innermost part the surface
of the magnetic core are shown in Table 2.

From Table 2, the magnetic core of the present invention is found to be excellent
because of its high permeability (µ
r) and low magnetic core loss (Pc).
Example 3
[0038] An amorphous alloy ribbon having a width of 20 mm and a thickness of 12 µm was produced
by quenching a molten alloy of Fe
bal.Cu₁Nb₃Si₁₆B
6.5Cr
0.5Sn
0.05 (atomic %) by using a single roll method. After being passed through a solution of
lithium silicate, the amorphous alloy ribbon was dried in a hot-gas furnace kept at
each temperature listed in Table 3. The dried amorphous alloy ribbon having a coating
of about 1 µm thick was then wound to form a toroidal shape of 60 mm outer diameter
and 50 mm inner diameter, and then heated to 570°C in a furnace at a heating rate
of 1 .2°C/min and maintained there for 15 minutes to be subjected to heat treatment
in a nitrogen atmosphere. The heat-treated product was cooled to room temperature
to obtain each magnetic core. The most part of the alloy structure of the resulting
nanocrystalline alloy was occupied with extremely fine grains comprising bcc-phase
of an average grain size of about 12 nm.
[0039] The specific permeability (µ
r) at 1 kHz of each magnetic core is shown in Table 3.
[0040] Further, the brittleness of each nanocrystalline alloy was evaluated by whether brittle
fracture occurred when the alloy was bent.
Table 3
Sample No. |
Drying Temperature (°C) |
µr |
Brittle Fracture |
Invention |
|
|
|
25 |
80 |
91200 |
None |
26 |
100 |
93200 |
None |
27 |
150 |
94500 |
None |
28 |
200 |
96800 |
None |
29 |
250 |
96700 |
None |
30 |
300 |
95800 |
None |
31 |
350 |
96100 |
None |
Comparison |
|
|
|
32 |
40 |
73200 |
None |
33 |
60 |
85900 |
None |
34 |
380 |
- |
Observed |
35 |
400 |
- |
Observed |
[0041] When the drying temperature was lower than 80°C (Sample Nos. 32 and 33), the alloy
ribbons after heat treatment for crystallization were stuck each other because of
insufficient drying to result in reduced magnetic properties. On the other hand, when
the dried temperature was higher than 350°C (Sample Nos. 34 and 35), the alloy ribbons
were embrittled and easily broken. This made the production of the magnetic core very
difficult, and therefore, the permeability (µ
r) was unable to be determined.
Example 4
[0042] An amorphous alloy ribbon having a width of 25 mm and a thickness of 12 µm was produced
by quenching a molten alloy of Fe
bal.Nb₃Ga₄Si₁₄B₇ (atomic %) by using a single roll method. After being passed through
a solution containing each insulating material listed in Table 4, the amorphous alloy
ribbon was dried in a hot-gas furnace kept at 200°C. The dried amorphous alloy ribbon
was then wound to form a toroidal shape shown in Fig. 4, and then heated to 550°C
in a furnace at a heating rate of 1. 2°C/min and maintained there for 15 minutes to
be subjected to heat treatment in a nitrogen atmosphere. The heat-treated product
was cooled to room temperature to obtain each magnetic core. The most part of the
alloy structure of the resulting nanocrystalline alloy was occupied with extremely
fine grains comprising bcc-phase of an average grain size of about 14 nm. Each magnetic
core was impregnated with an epoxy-type resin and made into a cut core by cutting
after the impregnated resin was hardened. The average thickness of the insulating
coating, the magnetic core loss (Pc) at 20 kHz and 0.2 T, the resistance (R) between
the innermost part and the surface and the appearance of the cut surface of each magnetic
core are shown in Table 4.
Table 4
Sample No. |
Insulating Material |
Thickness (µm) |
Pc (kW/m³) |
R (Ω) |
Appearance of cut surface |
Invention |
|
|
|
|
|
36 |
aluminum silicate |
0.8 |
42 |
83 |
+ |
37 |
lithium silicate |
0.2 |
38 |
95 |
+ |
38 |
magnesium methylate |
0.05 |
42 |
81 |
+ |
39 |
lithium silicate |
0. 1 |
41 |
80 |
+ |
40 |
magnesium methylate |
0.1 |
41 |
88 |
+ |
Comparison |
|
|
|
|
|
41 |
alumina sol |
1.2 |
68 |
32 |
- |
42 |
alkyl silicate |
1.8 |
62 |
41 |
- |
43 |
- |
0 |
120 |
0.9 |
+ |
Note: "+" means that no exfoliation of the resin and no interlaminar separation were
observed at the cut surface, while "-" means that such were observed. |
[0043] As seen from Table 4, no exfoliation of the resin and no interlaminar separation
were observed at the cut surface in the magnetic cores of the present invention, this
resulting in a low magnetic core loss. Further, the higher values of R show that the
magnetic cores of the present invention are provided with sufficient layer insulation.
Example 5
[0044] An amorphous alloy ribbon having a width of 20 mm and a thickness of 15 µm was produced
by quenching a molten alloy of Fe
bal.Cu₁Ta₃Si₁₆B₆ (atomic %) by using a single roll method. After coating on the surface
of the amorphous alloy a solution of each insulating material listed in Table 5 by
using a roll coater, the amorphous alloy ribbon was dried in a hot-gas furnace kept
at 20 °C. The dried amorphous alloy ribbon was then wound to form a toroidal shape
of 35 mm outer diameter and 30 mm inner diameter, and then heated to 550°C in a furnace
at a heating rate of 1 . 5°C/min and maintained there for 15 minutes to be subjected
to heat treatment in a nitrogen atmosphere. The heat-treated product was cooled to
room temperature to obtain each magnetic core. The most part of the alloy structure
of the resulting nanocrystalline alloy was occupied with extremely fine grains comprising
bcc-phase of an average grain size of about 12 nm.
[0045] The specific permeability (µ
r) at 10 MHz, the magnetic core loss (Pc) at 500 kHz and 0.05 T, the average thickness
of the insulating coating and the resistance (R) between the innermost part and the
surface of the magnetic core are shown in Table 5.
Table 5
Sample No. |
Insulating Material |
µr |
Pc (kW/m³) |
R (Ω) |
Thickness (µm) |
Invention |
|
|
|
|
|
44 |
aluminum silicate |
640 |
230 |
28.0 |
0.2 |
45 |
lithium silicate |
650 |
220 |
29.1 |
0.1 |
46 |
magnesium methylate |
650 |
210 |
29.2 |
0.01 |
47 |
lithium silicate |
610 |
240 |
27.6 |
0.05 |
48 |
magnesium methylate |
630 |
220 |
28.7 |
0.05 |
Comparison |
|
|
|
|
|
49 |
alumina sol |
380 |
350 |
6.2 |
0.8 |
50 |
alkyl silicate |
460 |
320 |
7.1 |
1.1 |
[0046] As seen from Table 5, the magnetic cores of the present invention were superior to
the comparative magnetic cores because of their high permeabilities, low magnetic
core losses and high insulating resistances.
Example 6
[0047] An amorphous alloy ribbon having a width of 25 mm and a thickness of 15 µm was produced
by quenching a molten alloy of F
bal.Cu₁Zr₃Si
14.5B
6.5 (atomic %) by using a single roll method. After spraying on the surface of the amorphous
alloy a solution of each insulating material listed in Table 6, the amorphous alloy
ribbon was dried in a hot-gas furnace kept at 200°C. The dried amorphous alloy ribbon
was then wound to form a toroidal shape of 50 mm outer diameter and 30 mm inner diameter,
and then heated to 550°C in a furnace at a heating rate of 1 . 5°C/min and maintained
there for 15 minutes to be subjected to heat treatment in a nitrogen atmosphere. The
heat-treated product was cooled to room temperature to obtain each magnetic core.
The most part of the alloy structure of the resulting nanocrystalline alloy was occupied
with extremely fine grains comprising bcc-phase of an average grain size of about
12 nm.
[0048] The specific permeability (µ
r) at 10 MHz, the magnetic core loss (Pc) at 500 kHz and 0.05 T, the average thickness
of the insulating coating and the resistance (R) between the innermost part and the
surface of the magnetic core are shown in Table 6.
Table 6
Sample No. |
Insulating Material |
µr |
Pc (kW/m³) |
R (Ω) |
Thickness (µm) |
Invention |
|
|
|
|
|
51 |
aluminum silicate |
610 |
240 |
90.5 |
0.8 |
52 |
lithium silicate |
650 |
220 |
91.3 |
0.3 |
53 |
magnesium methylate |
640 |
230 |
89.5 |
0.1 |
54 |
lithium silicate |
560 |
250 |
87.6 |
0.2 |
55 |
magnesium methylate |
550 |
260 |
86.6 |
0.06 |
Comparison |
|
|
|
|
|
56 |
alumina sol |
340 |
360 |
21.1 |
1.3 |
57 |
alkyl silicate |
390 |
330 |
23.1 |
1.1 |
[0049] As seen from Table 6, the magnetic cores of the present invention were superior to
the comparative magnetic cores because of their high permeabilities, low magnetic
core losses and high insulating resistances.
1. A nanocrystalline alloy having on at least one surface thereof an insulating coating,
said nanocrystalline alloy having a chemical composition represented by the following
formula:
(Fe1-aMa)100-x-y-z-bAxM'yM''zXb (by atomic %),
wherein M is at least one element selected from the group consisting of Co and Ni,
A is at least one element selected from the group consisting of Cu and Au, M' is at
least one element selected from the group consisting of Ti, V, Zr, Nb, Mo, Hf, Ta
and W, M'' is at least one element selected from the group consisting of Cr, Mn, Al,
Sn, Zn, Ag, In, platinum group elements, Mg, Ca, Sr, Y, rare earth elements, N, O
and S, X is at least one element selected from the group consisting of B, Si, C, Ge,
Ga and P, and each of a, x, y, z and b respectively satisfies 0≦ a≦ 0.5, 0≦ x≦ 10,
0. 1≦ y≦ 20, 0≦ z≦ 20 and 2≦ b≦ 30, and said insulating coating having an average
thickness of 2 µm or less and comprising at least one insulating material selected
from the group consisting of aluminum silicates, lithium silicate and magnesium oxide.
2. The nanocrystalline alloy according to claim 1, wherein the average thickness of said
insulating coating is 0.2 µm or less.
3. A magnetic core produced by laminating or winding said nanocrystalline alloy according
to claim 1 or 2.
4. The magnetic core according to claim 3, which is impregnated with an epoxy-type resin.
5. A method for forming an insulating coating on a nanocrystalline alloy, which comprises:
rapidly quenching a molten alloy having a chemical composition represented by the
following formula:
(Fe1-aMa)100-x-y-z-bAxM'yM''zXb (by atomic %),
wherein M is at least one element selected from the group consisting of Co and Ni,
A is at least one element selected from the group consisting of Cu and Au, M' is at
least one element selected from the group consisting of Ti, V, Zr, Nb, Mo, Hf, Ta
and W, M'' is at least one element selected from the group consisting of Cr, Mn, Al,
Sn, Zn, Ag, In, platinum group elements, Mg, Ca, Sr, Y, rare earth elements, N, O
and S, X is at least one element selected from the group consisting of B, Si, C, Ge,
Ga and P, and each of a, x, y, z and b respectively satisfies 0≦ a≦ 0.5, 0≦ x≦ 10,
0. 1≦ y≦ 20, 0≦ z≦ 20 and 2≦ b≦ 30, to produce an amorphous alloy;
coating on at least one surface of said amorphous alloy a solution containing at
least one insulating material selected from the group consisting of aluminum silicates,
lithium silicate and magnesium methylate;
drying the solution-coated amorphous alloy at a temperature between 80°C and 350°C;
and
heat-treating the dried amorphous alloy at a temperature not lower than a crystallization
temperature of said amorphous alloy so as to form a fine crystal grain having a grain
size of 30 nm or less in alloy structure while forming said insulating coating having
a thickness of 2 µm or less and comprising at least one insulating material selected
from the group consisting of aluminum silicates, lithium silicate and magnesium oxide.
6. The method according to claim 5, wherein said solution is coated on said amorphous
alloy by passing said amorphous alloy though said solution.
7. The method according to claim 5, wherein said solution is coated on said amorphous
alloy by passing said amorphous alloy though a roll coater.
8. The method according to claim 5, wherein said solution is coated on said amorphous
alloy by spraying said solution on the surface of said amorphous alloy.
9. The method according to any one of claims 5 to 8, wherein said amorphous alloy is
coated with said solution after the surface of said amorphous alloy is subjected to
anodizing treatment.
10. The method according to any one of claims 5 to 9, wherein said amorphous alloy coated
with said solution is dried by blowing a hot air, argon gas, nitrogen gas or helium
gas onto the surface of said amorphous alloy.