[0001] This invention relates to a method of producing permalloy (high permeability Ni-Fe
alloy) cores.
[0002] High permeability Ni-Fe magnetic alloys are widely used to form magnetic cores for
light electrical equipment applications. The cores are produced by slitting wide permalloy
strip to a final width and winding the strip to form wound cores, or by the steps
of punching, bending and drawing core plates to a final shape. After annealing at
1000 to 1300
*C to remove internal stresses and impurities, the material is assembled into the device
concerned.
[0003] The processed core pieces are stacked in the furnace for the annealing operation.
The high temperature can cause the core pieces to seize together or to be burned at
points of contact with the metal vessel. To prevent this, taking wound cores as an
example, after being slit to the prescribed final width the core strips are degreased,
immersed in a slurry consisting of water and alumina or magnesia, dried, wound to
the prescribed diameter, and then are annealed.
[0004] When manufacturing E and I magnetic cores, after the cores have been punched out
the punching fluid is removed and the cores are then coated with finely powdered alumina
or magnesia to prepare them for the annealing. Magnetic shielding materials are first
degreased, bent and drawn to the prescribed shape, and are then coated with an annealing
separator at specified points to prepare for the annealing process.
[0005] Thus, in the prior art the core pieces, for example core strips for wound cores,
are slit to the final width, degreased, coated, dried and wound, a series of steps
that has to be carried out core by core, which is extremely time-consuming and inefficient.
Moreover, the thickness of the coating can vary from core to core or place to place,
which can easily lead to non-uniform pressure during the winding operation and degrade
the magnetic properties of the end product. Also in the case of E and I cores and
magnetic shielding material, usually after the small cores have been formed they are
individually degreased, coated and dried, which in practice is a highly complex and
inefficient task.
[0006] An object of the present invention is to provide a method of efficiently manufacturing
permalloy wound cores, E cores, I cores and other such magnetic cores with highly
stable magnetic properties.
[0007] The basic feature of the present invention that distinguishes it from the conventional
methods is that the annealing separator is applied at a different time. Specifically,
the method of producing permalloy cores according to the present invention comprises
the step of applying an annealing separator coating 0.1 to 50 /1.m thick to at least
one surface of wide permalloy strip, and subsequent steps for which there are the
two modes of application described below.
[0008] A first method, comprising the steps of slitting the wide permalloy strip to final
width followed by winding or punching, applying additional annealing separator as
required to cut surface portions following any bending or drawing that is required,
and annealing at a temperature range of from 1000 ° to 1300 C.
[0009] The method of producing permalloy cores according to the present invention makes
it possible to efficiently manufacture wound cores, E cores, I cores and other such
cores in addition to which the products have highly stabilized magnetic properties,
and as such has high commercial value.
[0010] In the prior art the annealing separator is applied after the core material has been
slit to the final width. The feature of the first method of the present invention,
however, is that by the time the strips are slit to the final width they have already
been coated with the annealing separator, an arrangement that was found to give rise
to a number of advantages.
[0011] For the purposes of this first method of the invention the permalloy may be any Ni-Fe
alloy. However, for manufacturing high permeability magnetic cores and magnetic shielding
materials, it is preferable to use a Ni-Fe alloy having a nickel content within the
range of 40 to 90%. Elements such as molybdenum, copper, cobalt, chromium, manganese,
boron, vanadium, niobium, and titanium may be added. There is no specific limitation
on the thickness of the permalloy strip, which usually ranges from around 0.01 mm
to 5.0 mm. Similarly, there is no specific limitation on the width of the strip, other
than that it should be of a width that enables it to be slit into a multiplicity of
strips of the final width. In practice there is a wide range of widths, from around
10 mm to 1200 mm, but most commonly widths range from 50 mm to 700 mm.
[0012] For convenience, the starting coil strip will be referred to as wide coil strip.
The annealing separation coating is applied to one or both surfaces of the strip.
[0013] The thickness of the coating is limited to 0.1 to 50 /1.m because is it is thinner
than 0.1 µm the coating will not provide sufficient separation, while a thickness
that exceeds 50 µm will produce a marked decrease in the space factor. There is no
specific limitation on the main constituent components of the annealing separator
coating; a conventional composition may be used. The wide coil strip is immersed in
a solution that is a suspension of water and a fine powder of one or more substances
selected from among alumina, magnesia, magnesium hydroxide, calcium oxide, calcium
hydroxide and titanium oxide, for example, after which the moisture is evaporated.
For narrow strip, the method disclosed by JP-A-63-121670 may be used comprising immersing
the strip in a solution constituted of at least one substance selected from among
organo-metallic compounds and decomposition products thereof, then drying the strip.
[0014] One application of permalloy strip is wound cores, which are formed by slitting the
permalloy into strips of the final service width ranging from several millimeters
to several tens of millimeters, coating the strips with a slurry of fine alumina powder,
drying the coating, winding the strips into coils of specified diameter ranging from
several millimeters to several hundred millimeters and annealing these coils.
[0015] Coating the wide strip starting material with the annealing separator in accordance
with this first method of the invention reduces the time needed to manufacture wound
cores, the reason being that while coating and drying limited the winding speed of
the conventional method, with the present invention the strips can be wound at high
speed to form the cores after the strips have been slit to the final width. This speeds
up the operation, while among other advantages are that it results in a uniform coating
thickness and winding pressure that make it easier to achieve more stable magnetic
properties, and there is little variation in the space factor.
[0016] Another application of permalloy strip is E and I cores for use in small transformers.
To form these, the permalloy is slit into strips of the final service width ranging
from several millimeters to several tens of millimeters, the E and I core pieces are
punched, then coated with a fine powder of A1
20
3 or the like as the annealing separator, and the cores are then annealed.
[0017] Producing E and I cores from permalloy strip that has been coated with the annealing
separator eliminates the type of difficult, time-consuming operation of the prior
art method which involved individually applying the A1
20
3 powder to each of the small punched-out core pieces. Instead, with the first method
of the present invention, the punching and mechanical stacking of the core pieces
for annealing can be implemented on a continuous basis, greatly enhancing operating
efficiency.
[0018] The first method of the present invention basically eliminates the need to apply
the annealing separator immediately prior to annealing. However, optionally additional
annealing separator may be applied when burning of the cut or punched edges may be
a problem. Compared to the prior art procedure, this additional application of the
annealing separator involves far less work.
[0019] In this method of the present invention, the reason for specifying a lower limit
of 1000°C for the annealing temperature is that at a lower temperature stress release
and elimination of impurities will be inadequate, while temperatures above 13000 C
soften the permalloy, making it unable to retain its strength. Therefore a range of
1000 - 13000 C has been specified for the annealing temperature. The annealing time
will normally be 1 - 3 hours, but at high temperatures may be a matter of a few minutes.
[0020] The magnesium hydroxide (Mg(OH)
2) specified as the main component of the annealing separator of this first method
of the invention enhances the effect of the method. The reason for specifying Mg(OH)
2 as the main component of the annealing separator is that hydrolysis during the annealing
heating produces MgO, which has good annealing separation properties, while the film
formed by Mg(OH)
2 has better adherence to the permalloy than other separators such as alumina (AI
20
3). The most important reason for using Mg(OH)
2 is that it possesses a good solid-lubricant effect, so that during slitting, punching,
bending and drawing operations, rather than having the adverse abrasive effect of
the A1
20
3 that is generally used, its lubricating effect extends the service life of the machine
tools and lessens or eliminates the need for the usual slitting and punching lubricating
fluides. What this means is that in some cases the step of washing off lubricating
fluids is no longer required, the effect of which is considerable.
[0021] The coating consisting mainly of Mg(OH)
2 may be applied in the form of a slurry of water and Mg(OH)
2. A small amount of a finely powdered ceramics substance such as, for example, MgO,
A1
20
3, CaC0
3 may be added. Optionally, one or more selected from a binder, a thickening agent
and a defoaming agent may be added to the slurry to improve permalloy adhesion, spreadability
and other such properties. It is particularly useful to improve adhesion in cases
where slitting, punching, bending and drawing operations exert a frictional force
on the surface of the permalloy strip that causes peeling of the coating.
[0022] Preferably the binder should be one developed for ceramics applications, with as
few organic components as possible, and only the minimum amount required should be
used. Adding a large amount of binder increases the viscosity, decreasing the spreadability,
and in the annealing process organic components present in the Ni-Fe become included
as impurities, degrading the magnetic properties.
[0023] There is no specific limitation on the composition of the binder. Any substance that
provides the requisite function may be used as the main constituent, such as a water-soluble
emulsion type acrylic ester copolymer resin or ethylene-vinyl acetate copolymer resin.
[0024] Generally, in a slurry consisting of water and Mg(OH)
2, or of water, Mg(OH)
2 and MgO, with the addition of a small amount of binder, solids in the slurry such
as the Mg(OH)
2 and MgO settle, degrading the spreadability. To a considerable extent this can be
remedied by adding a small amount of a thickening agent to enable the slurry to maintain
the right viscosity. Adding too much thickening agent can cause gelling, markedly
decreasing the spreadability. Such a thickening agent may be constituted of a substance
having a smectitic structure that is composed mainly of Si0
2; this is not limitative, however, and any substance having the above effect may be
used.
[0025] The addition of a binder tends to produce foaming in the separator solution, reducing
the spreadability. In most cases this can be solved by adding minute amounts of a
commercial defoaming agent.
[0026] During fabrication of wound cores, for example, after the permalloy strip has been
slit to the final width the separator is coated and dried on the strip, but this immersion
method does not always produce a coating having the uniform prescribed thickness.
A roll coater or bar coater can be used to apply a coating of a thickness in the range
0.1 - 50 /1.m, more preferably 0.5 - 10 /1.m. Roll or bar coater application is a
known method of applying a uniform coating to thin sheet materials, and is also well
suited to the object of this first method of the invention. Roll coaters are suitable
for sheet thicknesses of 0.1 - 5 mm and bar coaters for thicknesses of 0.01 - 0.1
mm.
[0027] The applied slurry is dried until the water content evaporates and it is not sticky
to the touch. Drying takes a short time at 100°C and is usually done on a continuous
basis. The thickness of the coating is controlled according to the thickness of the
permalloy strip and the intended application, but applied with a roll coater or bar
coater can be in the range 0.1 - 50 µm, a 50 µm coating being for thick sheet and
a 0.1 µm coating for very thin sheet. In practice the thickness will usually be 0.5
- 10 µm.
[0028] As the coating comprised mainly of Mg(OH)
2 has lubricating properties, as mentioned, the amount of lubricating fluid generally
used for slitting, punching, bending and drawing operations can be reduced or omitted.
This also means that the task of washing off the conventional lubricating fluid is
shortened or eliminated, showing one of the invention's major effects.
[0029] When a very thin coating is used, all or part of the annealing separator can be utilized
as interlaminar insulation, as the annealing does not result in any large loss of
adhesion.
[0030] The production of permalloy cores according to the first method of the present invention
markedly improves production efficiency and provides magnetic cores with excellent
magnetic properties and space factors.
[0031] The above is a description of first method of the present invention.
[0032] The second method of this invention will now be described, with specific reference
to the manufacture of wound cores from wide permalloy strip that has been coated with
an annealing separator. In accordance with this second method of the invention, the
wound cores are formed by winding unslit permalloy strip, that is permalloy strip
in its wide state, that has been coated with an annealing separator into coils having
a prescribed inner diameter and thickness. A further improvement in efficiency can
be realized by arranging this winding operation on the same production line used to
apply and dry the coating. It is also possible to apply and dry the coating and wind
the strip into large starting coils, then afterwards uncoil the strip and rewind it
to form wound cores having the prescribed inner diameter and thickness.
[0033] The wide coils thus formed are slit to the final width of the wound cores. Compared
to the conventional method in which the strip for each wound core is individually
coated, dried and wound, there is far less variation among finished wound cores obtained
in accordance with the second method of this invention, comprising uniformly coating
an entire coil of wide-strip material, winding the wide strip at a constant pressure,
and then slitting the wound strip into sections to form the individual wound cores.
Slitting methods vary according to the diameter of the core and the intended application,
but include high-speed rotary fine-tooth slitters, saws, and laser-beam cutters. Care
should be taken not to cut strip where it sags. The lubricating properties of the
main constituent of the coating, Mg(OH)
2, come in useful when a saw is used. The wound cores in their final form are then
annealed. At this point, annealing separator may optionally be applied where metallic
surface luster portions are exposed at the edge of the cut portions. This additional
application is very easy, compared to the conventional arrangement. Annealing takes
place at a temperature of 1000 - 13000 C for a period of 1 - 3 hours.
[0034] The production of the coils wound to a specified diameter and thickness for cutting
into sections will now be described. There are two methods. In the first method the
cores are wound on the same line used to apply the coating, and in the second method
the strip is rolled into large-diameter starting coils, and is then uncoiled and wound
into cores. The coating used for the second method has to have a stronger adhesion
than the coating used for the first method. This can be achieved by adding a small
amount of binder. It is preferable to use a binder that has a very low organic content
the major part of which will be eliminated in the course of the annealing heating
process. A binder developed for ceramics application may be used such as one constituted
mainly of a water-soluble emulsion type acrylic ester copolymer resin or ethylene-vinyl
acetate copolymer resin, but this not limitative as any substance having the above-described
requisite effect may be used.
[0035] With a slurry of finely powdered ceramics, spreadability may be adversely affected
by settling of the solids in the slurry. This can be prevented by adding a small amount
of a thickening agent. The thickening agent may be constituted of a substance with
a smectitic structure that is composed mainly of Si0
2. However, this is not limitative, and any substance having the above effect may be
used. The addition of a binder tends to produce foaming in the separator solution,
reducing the spreadability. In most cases this can be solved by adding small amounts
of a commercial defoaming agent.
[0036] The production of permalloy cores according to this second method of the invention
improves productivity and provides permalloy wound cores of excellent quality.
[0037] The efficacy of the first and second methods according to the present invention will
now be described with reference to the following examples.
Example 1
[0038] PC grade permalloy consisting of 77.0% Ni, 3.6% Cu, 4.3% Mo, 0.007% C, 0.4% Si, 0.6%
Mn and the balance of Fe and unavoidable impurities was cold-rolled to form coils
of wide permalloy sheet 350 mm wide and 0.1 mm thick. These coils were divided into
types (1) and (2). Type (1) are coils with a final width of 10 mm obtained by slitting
the wide permalloy strip, in accordance with the conventional method. After degreasing
with trichlene the narrow strip coil (1) and wide strip coil (2) were immersed in
a slurry of distilled water and alumina powder with an average particle size of 0.2
µm and are then dried by being passed through a furnace at 150°C. At this point, in
both cases the thickness of the applied coating was about 5 µm but in the case of
the narrow coils (1) there was variation in thickness in the widthwise direction,
with the thickness at the center portion being 4.5 - 5.5 µm while the thickness at
the edges was 5 - 15 µm. In the case of the wide strip coil (2), while the thickness
right at the edges was 5 - 15 µm, the thickness at most of the center portion was
4.5 - 5.5 µm. The narrow coils (1) formed a total of 30 wound cores, each 50 turns
thick and having an inside diameter of 40 mm, and these cores were subjected to annealing.
A slitter was used to cut the wide strip coil (2) material into strips 10 mm wide
which used to form 30 wound cores, each 50 turns thick and having an inside diameter
of 40 mm, and these cores were subjected to annealing. The wound cores obtained from
the narrow coils (1) and the wide strip coil (2) were annealed for 30 minutes at 11500
C in a stream of dry hydrogen. The magnetic properties and outside diameter (which
has a bearing on the space factor) were measured and are listed in Table 1.
[0039] From the results listed in Table 1 it can be seen that wound cores produced by the
method of the present invention exhibit highly stable magnetic properties and an excellent
space factor.
Example 2
[0040] PCS grade permalloy consisting of 79.3% Ni, 5.1% Mo, 0.003% C, 0.33% Si, 0.9% Mn,
0.0004% S, 0.002% P, 0.0007% N and the balance of Fe and unavoidable impurities was
cold-rolled to form wide permalloy strip coil 250 mm wide and 0.01 mm thick. After
degreasing with trichlene, a coating 3 µm thick consisting mainly of magnesium hydroxide
was applied to each surface of the strip sheet by the following method. 150 g of highly
active magnesium hydroxide with an average particle size of 0.1 µm was mixed into
5 liters of distilled water and the mixture was stirred vigorously for 30 minutes
at room temperature. Then, a small amount of a binder consisting of water-soluble
emulsion type acrylic ester copolymer resin developed for ceramics applications was
added to the mixture, together with a small amount of a smectitic thickening agent
composed mainly of Si0
2, and the mixture was stirred for a further 30 minutes. The resultant slurry was then
applied to the sheet with a rubber bar-coater and then furnace-dried at 150 ° C to
form permalloy sheet with an annealing separator coating consisting mainly of Mg(OH)
2 and featuring high adhesion. The sheet was then slit into strips 15 mm wide, the
final width, and a high-speed automatic coiling machine was then used to wind the
strips into wound cores 100 turns thick and having an inside diameter of 50 mm. Finely
powdered A1
20
3 was sprinkled over the cut edges of the cores, which were then vacuum-annealed for
2 hours at 1100°C. The ten wound cores thus obtained had an average effective relative
permeability at 1 kHz of 47,500.
[0041] In the case of the prior art method in which the annealing separator is applied and
dried on strips that have already been slit to the final width, non-uniformity of
the coating thickness makes it impossible to use a high-speed automatic winder to
wind the strip. With the method of the present invention, however, as there is no
such problem the winding proceeds smoothly.
Example 3
[0042] PC grade permalloy consisting of 77.5% Ni, 3.4% Cu, 4.4% Mo, 0.008% C, 0.2% Si, 0.5%
Mn and the balance of Fe and unavoidable impurities was cold-rolled to form wide permalloy
strip coil 400 mm wide and 0.25 mm thick. These wide strip coils were divided into
types (3) and (4). The type (3) strip was slit into strips having a final width of
20 mm, in accordance with the conventional method. E and I core pieces were punched
from these strips, degreased with trichlene and coated with alumina powder having
an average particle size of 0.3 µm. The wide type (4) strip was degreased with trichlene,
immersed in a tank of 5 weight-percent butyl acetate solution of Zr(OC4 H2)4 and then
passed through the drying furnace. This cycle of operations was repeated a number
of times to form a surface coating 3 µm thick. The strip was then slit into 20-mm
widths from which E and I core pieces were punched.
[0043] 100 kg of cores thus obtained from each of the types (3) and (4) were then annealed
for 1 hour at 11200 C in a stream of dry hydrogen. Table 2 lists the time required
to produce the cores (comparative time required from wide strip to annealing) and
the magnetic properties (measurements were conducted on sets of four hollow-square-shaped
specimens punched from each final-width strip; the specimens measured 20 mm by 20
mm, thereby including the strip edge portions, and had a center hole measuring 12
mm by 12 mm.). As shown by Table 2, with the method of this invention it takes less
time to produce the cores compared to the time required by the conventional method,
and there was less variation among the cores.
Example 4
[0044] PCS grade permalloy consisting of 79.5% Ni, 5.0% Mo, 0.004% C, 0.24% Si, 0.8% Mn,
0.0003% S, 0.001% P, 0.0005% N and the balance of Fe and unavoidable impurities was
cold-rolled to form wide permalloy strip coil sheet 250 mm wide and 0.35 mm thick.
This wide strip coil was divided into types (5) and (6). Type (5) material corresponds
to strip prepared by the prior art method, and was used to prepare annealed samples
by the same method applied to the type (3) strip of Example 3. The type (6) wide strip
coil was degreased with trichlene and a coating about 2
/1.m thick consisting mainly of magnesium hydroxide was applied to each surface of the
strip by the following method. 150 g of highly active magnesium hydroxide with an
average particle size of 0.1 µm was mixed into 5 liters of distilled water and the
mixture was stirred vigorously for 20 minutes at room temperature. A small amount
of a binder consisting of water-soluble emulsion type acrylic ester copolymer resin
developed for ceramics applications was then added to the mixture, together with a
small amount of a smectitic thickening agent composed mainly of Si0
2, and the mixture was stirred for a further 30 minutes. The resultant slurry was then
applied to the sheet with a rubber roll-coater and then furnace-dried at 250 ° C to
form permalloy sheet with an annealing separator coating consisting mainly of Mg(OH)
2 and featuring high adhesion. A round-tooth slitter was then used to cut the wide
strip thus prepared into strips 20 mm wide, the final width, and E and I cores were
punched from these strips. Slitting or punching fluid is not required, so the following
degreasing process can be omitted. 100 kg of E and I cores thus obtained from each
of the types (5) and (6) were then vacuum-annealed for 3 hours at 1100°C. In the case
of cores obtained from the type (6) strip, even after the annealing the coating had
some adhesion so the cores could be installed as they were; thus the coating can function
as interlaminar insulation.
[0045] Table 3 shows measured values obtained by the same method used in Example 3.
Example 5
[0046] PB grade permalloy consisting of 45% Ni, 0.013% C, 0.3% Si, 0.5% Mn, 0.0005% S and
the balance of Fe and unavoidable impurities was cold-rolled to form wide permalloy
strip coil 250 mm wide and 0.1 mm thick. These wide strip coils were divided into
types (7) to (10). Type (7) was slit to form final width strips 8 mm wide, in accordance
with the conventional method, and after degreasing with trichlene the strips were
immersed in a slurry consisting of distilled water and alumina powder with an average
particle size of 0.5 µm, thoroughly mixed by means of a high-speed stirrer, and then
dried by being passed through a furnace at 180°C, forming a coating 3 µm thick. Twenty
conventional wound cores were then produced by winding these strips twenty times around
a bobbin 30 mm in diameter.
[0047] The wide strip coils (8), (9) and (10), produced by the method of this invention,
were degreased, immersed in their original widths in the same alumina slurry used
for type (7), and after the drying step, thereby forming a 3 µm coating, were each
wound twenty times around a long bobbin 30 mm in diameter. The wound coils were then
each cut into sections 8 mm long, using a high-speed cutter in the case of (8), a
fine-tooth saw in the case of (9) and a laser-beam cutter in the case of (10), thereby
producing 20 wound cores per coil, and these cores were annealed for 3 hours at 1100
° C in a stream of dry hydrogen. Table 4 lists the time required up to the annealing,
and the magnetic properties, in respect of each type. As shown by Table 4, with the
method of this invention it takes about half the time to produce the cores compared
to the time required by the conventional method, and the cores were better quality,
with less variation.
Example 6
[0048] PC grade permalloy consisting of 77.5% Ni, 3.4% Cu, 4.4% Mo, 0.008% C, 0.2% Si, 0.5%
Mn and the balance of Fe and unavoidable impurities was cold-rolled to form wide permalloy
strip coils (11) and (12), each 400 mm wide and 0.1 mm thick. Type (11) was slit to
form final width strips 20 mm wide. After degreasing with trichlene the narrow strip
coil (11) and wide strip coil (12) were immersed in a tank of 5 weight-percent butyl
acetate solution of Zr(OC4H2)4, and then dried in a furnace. This cycle of operations
was repeated a number of times to form a surface coating 2.5 µm thick.
[0049] The (11) strips were then wound to form 15 wound cores each 8 mm thick and having
an inside diameter of 50 mm. The (12) strip was wound in its full width state to an
inside diameter of 50 mm and a thickness of 8 mm, and was then cut into sections 20
mm long, using a high-speed cutter, thereby producing 15 finished wound cores. A1
20
3 powder was sprinkled over the cut edges of the cores which were then, together with
the (11) cores, annealed for 2 hours at 1150°C in a stream of hydrogen. Table 5 lists
the time required up to the annealing, and the magnetic properties. The results listed
in Table 5 show that the method of the present invention enables the efficient manufacture
of cores possessing good magnetic properties.
Example 7
[0050] PCS grade permalloy consisting of 79.5% Ni, 5.0% Mo, 0.004% C, 0.24% Si, 0.8% Mn,
0.0003% S, 0.001% P, 0.0005% N and the balance of Fe and unavoidable impurities was
cold-rolled to form wide permalloy strip coil 300 mm wide and 0.05 mm thick. In its
original wide state the strip was degreased with trichlene and a coating about 2 µm
thick consisting mainly of magnesium hydroxide was applied to each surface of the
strip by the following method. 150 g of highly active magnesium hydroxide with an
average particle size of 0.1 µm was mixed into 5 liters of distilled water and the
mixture was stirred vigorously for 20 minutes at room temperature. A small amount
of a binder consisting of water-soluble emulsion type acrylic ester copolymer resin
developed for ceramics applications was then added to the mixture, together with a
small amount of a smectitic thickening agent composed mainly of Si0
2, and the mixture was stirred for a further 30 minutes. The resultant slurry was then
applied to the sheet with a rubber roll-coater and then furnace-dried at 200 ° C to
form large-diameter permalloy coils with an annealing separator coating consisting
mainly of Mg(OH)
2 and featuring high adhesion. The coils were then rewound onto bobbins to form two
rolls, one with a diameter of 300 mm and a thickness of 3 mm, and the other with a
diameter of 100 mm and a thickness of 3 mm. A laser-beam cutter was then used to cut
the coils into sections 8 mm wide. A1
20
3 powder was sprinkled over the cut edges of the cores which were then vacuum-annealed
for 1 hour at 1150°C. The wound cores thus obtained had an average effective relative
permeability at 1 kHz of 48,000 - 52,000, exceeding the JIS standard (40,000 or more).