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(11) |
EP 0 416 420 B1 |
| (12) |
EUROPEAN PATENT SPECIFICATION |
| (45) |
Mention of the grant of the patent: |
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14.12.1994 Bulletin 1994/50 |
| (22) |
Date of filing: 27.08.1990 |
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| (54) |
Magnesium oxide coating for electrical steels and the method of coating
Magnesiumoxyd-Beschichtung für Elektrobleche und Beschichtungsverfahren
Revêtement d'oxyde de magnésium pour aciers électriques et procédé pour former un
revêtement
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| (84) |
Designated Contracting States: |
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BE DE FR GB IT |
| (30) |
Priority: |
08.09.1989 US 404714
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| (43) |
Date of publication of application: |
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13.03.1991 Bulletin 1991/11 |
| (73) |
Proprietor: ARMCO INC. |
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Middletown,
Ohio 45044-3999 (US) |
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| (72) |
Inventors: |
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- Wright, Wade S.
Fairfield,
Ohio 45014 (US)
- Murphy, Robin A.
Franklin,
Ohio 45005 (US)
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| (74) |
Representative: Beetz & Partner
Patentanwälte |
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Steinsdorfstrasse 10 80538 München 80538 München (DE) |
| (56) |
References cited: :
EP-A- 0 305 966 US-A- 3 841 925 US-A- 4 032 366
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FR-A- 2 399 485 US-A- 3 956 029 US-A- 4 190 469
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| |
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- PATENT ABSTRACTS OF JAPAN, vol. 3, no. 68 (C-48), 13 June 1979; & JP-A-54 041 220
- PATENT ABSTRACTS OF JAPAN, vol. 3, no. 152 (C-67), 14 December 1979; & JP-A-54 128
928
- PATENT ABSTRACTS OF JAPAN, vol. 9, no. 237 (C-305)(1960), 24 September 1985; & JP-A-60
096 770
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| |
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| Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
BACKGROUND OF THE INVENTION
[0001] The present invention relates to a coating composition which provides good insulative
properties and acts as an annealing separator during the final high temperature anneal
for grain oriented electrical steels. Magnesia is used extensively as a separator
for high temperature annealing of electrical steels after cold rolling. The coating
is normally applied after decarburizing and forms a glass film during the final high
temperature anneal.
DESCRIPTION OF THE PRIOR ART
[0002] Magnesia coatings which are composed mainly of magnesium oxide and magnesium hydroxide,
are used extensively as a separator coating on electrical steel during the high temperature
anneal to prevent the coil laps from sticking. A glass film forms from a reaction
between the steel surface and the magnesia. A magnesia coating must possess certain
physical qualities and also improve the overall magnetic qualities of the electrical
steel. To provide all of these properties, the prior workers have done extensive modification
to the basic magnesia composition.
[0003] Magnesium oxides when present with water can hydrate to magnesium hydroxide in a
short period of time. The degree of hydration has a strong influence on the viscosity
of the magnesia slurry and the control of the process for applying the coating. The
amount of water in the coating can have an adverse effect on the glass film formation.
To control hydration, prior workers have changed the size and distribution of the
magnesia particles. They have adjusted the calcining temperatures for magnesia production.
U.S. Patent No. 4,168, 189 (Haselkorn) is representative of this work.
[0004] Far more work has been done with additives to the magnesia to improve the glass film
formation. A thin insulative glass film requires a reaction at elevated temperatures
between the magnesia and the oxide film on the surface of the silicon steel after
decarburization. Various silica and silicate compounds have been added to improve
the reactions. Oxides of titanium, chromium and manganese have been added to improve
the adherence and glass film. Phosphate additions have been taught to act as binders
in the coating and improve hygroscopicity. Various coating additives are used to improve
the appearance, thickness, oxidation resistance and other properties of the glass
film produced during the high temperature anneal.
[0005] Considerable work has also been done to improve the magnetic properties of the silicon
steel by adjusting the composition of the magnesia. The magnesia has a strong influence
on surface reactions relating to atmosphere interactions and grain size control. U.S.
Patent No. 3,627,594 adds titanium dioxide and manganese oxides. U.S. Patent No. 3,676,227
adds boron compounds to the magnesia.
[0006] Chlorides have been added to magnesias in the past but in combination with other
compounds. U.S. Patent No. 4,543,134 adds a chloride of Sb, Sr, Ti or Zr with an antimony
compound, such as Sb₂(SO₄)₃, to seal the strip surface and prevent the atmosphere
from reacting with the base metal. The chlorides are used to increase the silica formed
on the surface and reduce the FeO content. The sealing function of the magnesia coating
is attributed to the antimony compound which prevents the removal and absorption of
the inhibitor elements. The level of chlorine in the coating may range from 0.0025
to 0.4%.
[0007] U.S. Patent No. 3,841,925 adds a chlorine contributor and sodium metasilicate to
magnesia to resist hydration and form a nonporous insulative coating. The critical
balance between these additions results in a magnesia with sodium chloride and magnesium
silicate which delay hydration and provide a longer residence time for coating. The
magnesia has a high level of chlorine, typically about 0.22 to 3.4% based on the weight
of magnesia.
[0008] U.S. Patent No. 4,287,006 in Fig. 1 clearly shows the importance of eliminating chlorine
by requiring the temperature of calcining to be above 1300°C for the control of hydration
of magnesias. Column 7, line 27 of this patent states annealing separator should contain
no magnesium chloride or magnesium sulfate because they hinder the formation of the
glass film.
[0009] U.S. Patent No. 3,956,029 states chlorine should be below 0.04% in magnesia coatings
because it forms a corrosive gas which attacks the base metal and causes a rough surface.
The irregular coating thickness which results causes a poor glass film with subsequent
peeling problems.
[0010] U.S. Patent No. 3,941,623 teaches the control of the moisture which remains from
the hydration of magnesium oxide during the final high temperature anneal. The patent
uses metal nitrides which are subsequently converted into oxides during the anneal
to consume water and lower the dew point. This reduces the steel oxides and provides
an improved glass film and grain growth control in the (110)[001] direction.
[0011] Magnesium oxides used for annealing separators in processing electrical steels during
the final anneal at temperatures between 1100°C and 1300°C have been modified in many
ways. The problems of hydration control, glass film-metal surface reactions, impurity
removal at the surface and excellent magnetic properties in the glass film and base
metal have been so complex that the solutions have been only partially successful.
The additions to magnesia in the past have also been very complex in nature due to
the interactions with other additives.
[0012] EP-A-0 305 966 discloses a method for coating a grain-oriented electrical steel sheet
with an annealing separator consisting of 100 parts by weight of magnesia blended
with 2 - 40 parts of one or more salts of alkali metal and alkaline-earth metal, e.g.
CaCl₂.
[0013] FR-A-2 399 485 discloses, for the same purpose, a magnesia slurry, containing magnesia
having a citric acid activity less than 200 s, and a decomposable phosphate compound,
such as calcium phosphate, in an amount of 0.5 to 25 wt.%, calculated as P₂O₅, of
the magnesia weight.
[0014] The present invention has provided magnesia additives used for annealing separators
which do not cause an unsafe environmental working condition and which are less expensive
to use. The interactions with the magnesia components are less complex but still provide
the desired benefits of a high quality glass film and excellent improvements to magnetic
quality. The additives are carefully controlled within critical limits to provide
the desired combination of properties.
SUMMARY OF THE INVENTION
[0015] The present invention has discovered that the addition of a metal chloride (selected
from the group of Mg, Na, K and Ca) to magnesia will provide improved orientation
and magnetic quality without the combined addition of sodium metasilicate or antimony
sulfate. The level of chlorine from the chloride addition within the range of 0.01
to 0.2% was found to produce excellent glass film quality and magnetic improvements
equivalent to prior art magnesias but without the environmental concerns of antimony.
The chloride addition of the present invention lowers the glass film formation temperature
to seal the surface at a lower temperature. The control of coating porosity using
chlorides without the need for another additive which reacts with the chlorine is
unexpected based on prior work with chlorides. The chloride addition provides an improved
control of final grain orientation and grain size by limiting the diffusion and surface
interactions. The use of Mg, Ca, Na and/or K to provide the source of chlorine is
also critical to the quality of the glass film and the magnetic properties of the
electrical steel strip. It is important to note that the total level of chlorine in
the magnesia must be considered to optimize the level of metal chloride being added.
The production of the magnesia may inherently have some level of chlorine which may
be adjusted in combination with the metal chloride addition.
[0016] The magnesias of the present invention may also contain additions of titanium dioxide
to stabilize the aqueous suspension and improve the glass film quality and the magnetic
properties of the steel strip. Boron, chromium, silica and calcium phosphate additions
are also optional with the present coating composition. The magnesias of the present
invention may also be modified to optimize the benefits for regular grain oriented
or high permeability grain oriented silicon steel.
[0017] The present invention also provides a process for coating silicon containing electrical
steel strip with an adherent electrically insulative coating prior to the final high
temperature anneal. The aqueous slurry of magnesia is conventionally applied to the
decarburized strip, heated to remove water and dry the coating and annealed above
about 1,000°C to form a glass film and develop the desired magnetic properties.
DETAILED DESCRIPTION OF THE INVENTION
[0018] The annealing separator of the present invention is a magnesia with a controlled
level of hydration to allow the aqueous slurry to be applied by conventional processing.
Magnesia slurries will have some degree of hydration which require the water of hydration
to be driven off during the high temperature anneal. The water remaining after drying
will cause porosity in the final glass. To provide a magnesia slurry with controlled
hydration, the majority of the particles should have a citric acid activity (CAA)
below 200 and preferably below 100. CAA is a measure of the activity of the magnesia
determined by the time required for a predetermined amount of hydroxyl ions to neutralize
a given weight of citric acid. The test is disclosed fully in U.S. Patent No. 3,841,925
at lines 22-46 of column 4. The magnesias of the present invention may also include
up to about 45% inactive magnesia which has a CAA above 200 and typically about 500-5,000.
The inactive magnesia tends to control hydration since it hydrates more slowly and
also is less expensive. The amount of inactive magnesia which can be effectively used
is related to the quality of the glass film and the control of porosity in the film.
[0019] The magnesia of the present invention requires a chlorine addition within the critical
range of 0.01 to 0.20 weight % to provide good glass film formation and improved magnetic
quality in the grain oriented electrical steel. The chlorine level required may be
partially provided by the magnesia production in combination with at least 0.01% metal
chloride. It is the total level of chlorine present which must be controlled within
the ranges of 0.01 to 0.20%.
[0020] The chlorine in a metal compound selected from the group of Mg, Na, K and Ca may
be added to the magnesia in an amount of 0.01 to 0.20 weight % based on the weight
of MgO depending on the level of chlorine present in the magnesia initially. The metals
used with the chlorides are selected to provide improved magnetic quality without
any adverse effects on safety, cost and glass film and may be used alone or in combination.
The magnesia of the present invention will have a citric acid activity of less than
200 for the majority of the particles. The magnesia may also contain up to about 45%
inactive magnesia particles having a citric acid activity above 200 and typically
from above 500 to 5,000.
[0021] The magnesia coating of the present invention is applied to cold rolled strip of
electrical steel prior to the final high temperature anneal. The electrical steel
strip is typically grain oriented silicon steel containing up to 4 % silicon, up to
0.08 % carbon, and any of the well known grain growth inhibitors, such as AN, MnS,
MnSe, BN, and others. High permeability silicon steel is generally considered to possess
a permeability above 1880 at 796 A/m and has an aluminum nitride inhibitor system
as a result of adding about 0.01 to 0.065% aluminum. U.S. Patent No. 3,676,227 is
typical of this technology. Decarburization of the strip produces a carbon level below
about 0.003% and a surface oxide which reacts with the magnesia during the final high
temperature anneal to form the glass film of forsterite. The oxide film formed during
decarburizing is basically fayalite and SiO₂ with some iron oxide present.
[0022] The chloride addition of the present invention modifies the surface reactions and
the level must be carefully controlled. Total chlorine levels above 0.20% produce
a glass film with too high a level of iron to be acceptable quality. Excessive chlorine
levels also result in poor oxidation resistance and poor surface resistivity due to
the iron content on the surface. The interface between the glass film and the base
metal also becomes too rough with high levels of chlorine. Chlorine is preferably
added at levels below about 0.15% and more preferably below about 0.12%. To obtain
the magnetic improvement to the electrical steel, a minimum level of 0.01 % chlorine
must be present. A preferred minimum chlorine added as a metal chloride of the invention
is about 0.015% (and more preferably 0.02%) which provides an optimum balance between
improving the glass film and the magnetic properties of the base metal.
[0023] The chlorides of the present invention act to seal the surface during annealing to
control the grain growth inhibitors. This plays a major role in the stability of secondary
grain growth. In prior chloride additions to magnesia, such as U.S.Patent No. 3,841,925,
the formation of a nonporous coating was provided by the reaction with a compound
such as sodium metasilicate which was balanced stoichiometrically to the chlorides.
The reaction produced magnesium silicate and sodium chloride which formed the nonporous
coating and controlled hydration. Examples with magnesium chlorides within the ranges
of the present invention were shown to be unsuitable for coating (viscosity so low
that the slurry was too thin and resulted in excessive porosity). The work done in
this patent clearly shows a quantity of sodium silicate less than the stoichiometric
equivalent to react with magnesium chloride will produce a coating which is deficient
in insulative properties and is porous. The present invention has found that a critical
lower level of chlorine does not require the sodium silicate addition.
[0024] The other prior work of interest was the addition of Sb, Sr, Ti or Zr chloride with
antimony sulfate in U.S.Patent No. 4,543,134. The chlorine was selected in an amount
from 0.0025 to 0.4%. With less than 0.05% antimony sulfate, the patent taught magnetic
properties would not be improved. The present invention provides the same improvements
without the antimony sulfate addition which this patent taught was required. The present
invention also uses different metals to provide the addition of the chlorine.
[0025] In order to apply the magnesia of the present invention by conventional means, the
hydration of the magnesia must be controlled to provide a slurry having a viscosity
within a workable range and a stability sufficient to provide a reasonable range of
operation. This is accomplished by controlling the temperature of the magnesia slurry,
the particle size of the magnesia and the use of various additives.
[0026] The temperature of the magnesia is controlled to be above freezing and below about
75°F (25°C) and preferably between about 32-45°F (0-7°C). This eliminates the need
for additional additives for hydration control which may have an adverse influence
on glass film quality or the magnetic properties of the silicon steel. To maintain
the temperature range of the slurry, the magnesia is maintained in an insulated vessel
with refrigeration coils. The magnesia is mixed with cold water and never stored for
prolonged periods of time. By maintaining this cold condition of the magnesia, the
slurry does not hydrate to a significant degree which would interfere with the coating
thickness or uniformity of the glass film. The temperature of the magnesia has a general
relationship to the storage life before hydration adversely affects the application
of the coating. The higher the temperature, the more quickly it must be used.
[0027] The particle size and citric acid activity of the magnesia for high permeability
silicon steel plays an important role in the glass film quality. The majority of the
particles will have a CAA below 200 and preferably below 100. The magnesia may contain
up to about 45 % inactive magnesia which has a CAA above 200 and typically from 500
to 5,000. Regular grain oriented silicon steel may use a magnesia with larger particle
size and have more inactive magnesia. The bulk density or packing factor of the dried
magnesia coating is dependent on the particle size distribution and CAA to control
the interactions with the atmosphere and surface reactions on the steel. The degree
of hydration will also influence the magnesia particles during drying. The amount
of water of hydration will be reduced with larger particle sizes. Too coarse of particles
will tend to settle out of the slurry and not undergo reaction with the silica during
the final anneal. To avoid having a porous coating due to excess hydration and have
a magnesia which may be applied as an aqueous slurry by dipping, spraying or metering
rolls, all of these variables must be controlled. The magnesia coatings of the invention
will produce a good glass film under these conditions and will eliminate the need
for the sulfate and silicate additions required in prior coatings.
[0028] The chloride addition has another important consideration which has not been addressed
in the prior art. Laser scribing for domain refinement has become a required practice
for high permeability grain oriented silicon steel. The nature of the surface film
has a considerable influence on the amount of energy from the laser which passes through
the glass film and the amount of damage caused to the glass film during domain refinement.
The present glass film developed by the chloride additions of the present invention
is controlled to provide a glass film which may be laser treated without surface damage.
A laser process such as taught in U.S. Patent No. 4,456,812 has been found to be very
beneficial in providing domain refinement without damage to the glass film.
[0029] To evaluate the properties of glass film produced from a magnesia having a chlorine
addition using a compound of the invention, a series of experiments were conducted.
Cold rolled strip of high permeability silicon steel having an AIN inhibitor system
was coated with a magnesia having MgCl₂ of various amounts. The results were compared
to a magnesia having an addition of antimony sulfate as described in U.S. Patent No.
4,543,134 and are shown in TABLE 1. The material was 0.23 mm in thickness, 76 mm in
width and 305 mm in length. The results are the average of 10 samples coated with
Tateho AI120 magnesia with 5% TiO₂. The samples were heated up to 1200°C in a 25%
nitrogen-75% hydrogen atmosphere with a 4°C dew point. The samples were soaked at
1200°C for 15 hours in 100% H₂. After the final anneal was completed, the samples
were scrubbed and stress relief annealed. The magnesia used had a chlorine level of
0.02 weight %.
TABLE 1
| ADDITIVE |
TOTAL %Cl WEIGHT % |
1.5 T (15 KG) WATTS/LB* CORE LOSS |
1.7 T (17 KG) WATTS/LB* CORE LOSS |
H-10 PERM |
| ---------------- |
0.02 |
.397 |
.566 |
1925 |
| Sb₂(SO₄)₃ +SbCl₃ |
0.035 |
.392 |
.549 |
1938 |
| " |
0.065 |
.389 |
.531 |
1939 |
| " |
0.095 |
.396 |
.561 |
1931 |
| ---------------- |
0.02 |
.397 |
.566 |
1925 |
| MgCl₂ |
0.035 |
.392 |
.548 |
1927 |
| " |
0.065 |
.398 |
.547 |
1940 |
| " |
0.095 |
.393 |
.533 |
1941 |
[0030] A comparison of the magnetic properties between the 2 additives to the magnesias
indicate the magnesium chloride addition which adds about 0.015 to 0.075 % chlorine
produces magnetic properties equal to or better than the same level of chloride addition
with the antimony sulfate within the range of about 0.03 to 0.10% total chlorine.
It is clearly suggested that levels of chlorine up to 0.20% should produce better
magnetic properties with the magnesium chloride addition of the present invention
based on the trend up to the 0.10% level. The higher the chlorine level, the more
the magnesium chloride is preferred over the Sb chloride additives.
[0031] As part of the investigation, other samples were also evaluated for glass film quality
using comparative evaluations on secondary coating adherence, oxidation resistance
and Franklin resistivity measurements on the glass film. These results are shown in
TABLE 2.
TABLE 2
| PHYSICAL GLASS FILM QUALITY |
| Total % Cl |
Oxidation Resistance |
% Secondary Coating Flaking |
Franklin Amps Glass Film |
| 0.011 |
Good |
Fair |
.506 |
| 0.031 |
Very Good |
Very Good |
.587 |
| 0.061 |
Fair |
Very Good |
.665 |
| 0.111 |
Poor |
Best |
.755 |
All chloride additions are MgCl₂, MgO has 0.011% Cl
All coating weights are about 6.4 g/m²/side
0.23mm High Permeability Silicon Steel |
[0032] A preferred level of total chlorine has been determined to be about 0.015 to about
0.15%. A more preferred total level of chlorine is about 0.015 to about 0.12%, which
provides a good balance of magnetic improvements with a glass film having good physical
properties. The optimum total chlorine level appears to be from 0.02 to 0.10%.
[0033] The resulting glass film must also permit laser scribing without coating damage.
The laser scribing process of U.S Patent No. 4,456,812 provides improved domain refinement
with the present glass films and avoids coating damage. The magnesia composition of
the present invention provides improved optical characteristics for laser treatments.
While any of the metals selected from the group of Mg, Ca, K or Na may be used alone
or in combination, the use of Mg and Na are preferred. The magnesia may include up
to 15 weight % TiO₂ and preferably about 5 to 10% when added. Colloidal silica may
also be added in amounts up to 10 weight %. For high permeability grain oriented silicon
steel, the level of silica is preferably about 3 to 7% and boron is preferably about
0.05 to 0.15%. Chromium is also an optional addition up to 15 weight %. Preferably
the level is restricted to about 2.5 to about 5% when added.
[0034] The magnesias of the present invention may also be used for insulative coatings for
regular grain oriented electrical steels. These magnesias may be varied slightly to
include up to about 20% phosphate additions with calcium phosphate additions preferred
within the range of 4-15%, up to 15% chromium additions with 2-10% preferred, up to
10% silica with about 3-7% preferred and up to 0.15% boron with a preferred maximum
of 0.10%.
[0035] The glass film formed from the magnesia may have an insulative coating applied over
the surface and the secondary coating will have good adherence.
[0036] The addition of the metal chloride in the present invention does not require a precipitation
reaction with a solution of a silicate salt as claimed in U.S. Patent No. 3,941,622.
A magnesia-silica complex is not applied in the process of the present invention.
TABLE 3 below shows the influence of the metal chloride addition within the ranges
of the invention for magnesium, calcium and sodium. The permeability and core losses
are dramatically improved by adding these levels of chlorides. The results also indicate
that increasing calcium to the more preferred level for magnesium and sodium does
not provide any additional benefit and, in fact, may cause a slight degradation in
properties. While no data is provided for potassium, it is expected to behave similar
to sodium in the levels required to obtain similar benefits. Both sodium and potassium
tend to smooth the metal interface. Magnesium tends to be more neutral in this regard.
Calcium appears to improve adherence of the glass film. All of the metal chloride
additives of the invention provide a level of chlorine which roughen the strip surface.
As stated previously, the chlorine also lowers the temperature of glass film formation.
It is important to note that magnesias may have an inherent level of chlorine, such
as 0.011% in the first example of TABLE 3. This chlorine level must be considered
as contributing to the total level of chlorine reacting in the system. The minimum
metal chloride addition to provide 0.01% chlorine must be adhered to regardless of
the chlorine content of the magnesia. Part of the preferred higher chlorine contents
may include chlorine from the magnesia in combination with the metal chlorides.
TABLE 3
| CHLORIDE ADDITIVES |
| Additive |
Total % Cl |
Stress Relief Annealed |
Laser Scribed |
| |
|
W15/60 (w/kg) |
W17/60 (w/kg) |
B8 (T) |
W15/60 (w/kg) |
W17/60 (w/kg) |
| -------- |
0.011 |
.901 |
1.258 |
1.914 |
.835 |
1.141 |
| MgCl₂ |
0.041 |
.881 |
1.231 |
1.925 |
.802 |
1.081 |
| MgCl₂ |
0.071 |
.872 |
1.218 |
1.927 |
.793 |
1.070 |
| NaCl |
0.041 |
.874 |
1.225 |
1.923 |
.800 |
1.084 |
| NaCl |
0.071 |
.874 |
1.203 |
1.932 |
.786 |
1.048 |
| CaCl₂ |
0.041 |
.881 |
1.231 |
1.923 |
.802 |
1.084 |
| CaCl₂ |
0.071 |
.894 |
1.242 |
1.927 |
.804 |
1.079 |
| Stress relief anneal at 830°C (1525°F), 2 hours, in 95%N₂-5%H₂ |
[0037] The levels of the metal chloride required to improve glass film and magnetic properties
appear to vary slightly depending on the metal selected. The preferred maximum level
of chlorine with calcium chloride appears to be lower than with magnesium, sodium
or potassium chloride additions. While the reason for this difference is not completely
understood, the improved properties occur with a preferred calcium addition of about
0.015-0.07%. The preferred levels with the other metal chloride additions of the invention
is about 0.015-0.10%. These addition levels may be adjusted to compensate for the
level of chlorine present in the source of magnesia.
1. A magnesia slurry for coating cold rolled oriented silicon steels prior to a final
high temperature anneal, said slurry being maintained below 25°C and consisting essentially
of:
a) magnesia with a majority of the particles having a citric acid activity less than
200;
b) a total chlorine level in said magnesia of 0.01 to 0.20 weight % based on the weight
of said magnesia with at least 0.01 weight % chlorine being from a metal chloride
selected from the group of Mg,Ca,Na and/or K;
c) up to 15% TiO₂;
d) up to 10% SiO₂;
e) up to 15% Cr;
f) up to 0.3% B; and
g) up to 20% phosphate.
2. The magnesia slurry according to claim 1, wherein 5 to 10 weight % TiO₂ have been
added.
3. The magnesia slurry according to claim 1, wherein said magnesia slurry is maintained
between 0 to 15°C.
4. The magnesia slurry according to claim 1, wherein said total chlorine level is from
0.015 to 0.15%.
5. The magnesia slurry according to claim 1, wherein said metal chloride has been added
in an amount to produce a chlorine level of 0.015 to 0.12%.
6. The magnesia slurry according to claim 1, wherein said metal chloride has been added
in an amount to produce a chlorine level of 0.02 to 0.10%.
7. The magnesia slurry according to claim 1, wherein said metal chloride is selected
from the group of Mg, Na and/or K and has been added in an amount to produce a total
chlorine level of 0.015 to 0.10%.
8. The magnesia slurry according to claim 1, wherein said metal chloride is Ca and has
been added in an amount to produce a total chlorine level of 0.015 to 0.07%.
9. The magnesia slurry according to claim 1, wherein 3 to 7 % SiO₂ and 0.05 to 0.15%
boron have been added to said magnesia.
10. The magnesia slurry according to claim 1, wherein 2.5 to 5% Cr have been added.
11. The magnesia slurry according to claim 1, which includes up to 0.15% boron.
12. The magnesia slurry according to claims 1 and 11, wherein said phosphate addition
is calcium phosphate in an amount of 4-15%, said SiO₂ content is 3-7%, said Cr content
is 2-10% and said boron content is up to 0.10%.
13. A method for producing an electrically insulative coating on oriented silicon steel,
said method comprising the steps of :
a) cold rolling said silicon steel into strip;
b) providing a decarburizing anneal to reduce the carbon level of said strip to a
level below 0.003%;
c) maintaining a magnesia slurry at a temperature from above freezing to 25°C;
d) applying a magnesia coating having 0.01 to 0.20 weight % total chlorine with at
least 0.01% being from a metal chloride addition selected from the group of Mg, Ca,
Na and/or K and a majority of magnesia particles having a citric acid activity less
than 200;
e) drying said magnesia to remove excess water; and
f) providing a final high temperature anneal to form a glass film and develop improved
magnetic properties.
14. The method of claim 13, wherein a laser domain refinement step is used after said
final anneal.
15. The method of claim 13, wherein 0.015 to 0.15% of the chlorine is added as a metal
chloride selected from the group of Mg, Na, Ca and/or K.
16. The method of claim 13, wherein said magnesia slurry is maintained between 0 and 15°C
prior to coating on said steel strip.
17. The method of claim 13, wherein said magnesia slurry has up to 45% inactive magnesia
particles with a citric acid activity above 200.
18. The method of claim 13, wherein said magnesia slurry has up to 45% of the particles
with a citric acid activity of 500 to 5,000.
19. The method of claim 13, wherein said metal chloride in combination with a chlorine
level present in said magnesia slurry provides a total chlorine level of 0.015 to
0.12% chlorine.
20. The method of claim 13, wherein said metal chloride in combination with a chlorine
level present in said magnesia slurry provides a total chlorine level of 0.02 to 0.10%
chlorine.
21. The method of claim 13, wherein said total chlorine is from 0.015 to 0.10% and said
metal chloride is selected from the group of Mg, Na and/or K.
22. The method of claim 13, wherein said metal chloride is Ca and is added in an amount
to produce a chlorine level of 0.015 to 0.07%.
23. The method of claim 13, wherein said magnesia slurry includes:
a) up to 15% TiO₂;
b) up to 10% SiO₂;
c) up to 15% Cr;
d) up to 0.3% B; and
e) up to 20% phosphate.
24. The method of claim 23, wherein said steel is regular grain oriented silicon steel
and said magnesia slurry includes up to 20% phosphate and up to 0.15% B.
25. The method of claim 24, wherein said magnesia slurry includes 4-15% calcium phosphate,
2-10% Cr, up to 0.10% B and 3-7% SiO₂.
26. The method of claim 23, wherein said steel is high permeability grain oriented silicon
steel and said magnesia slurry includes 5-10% TiO₂, 3-7% SiO₂, 2.5-5 % Cr and 0.05-0.15%
B.
1. Magnesiumoxidaufschlämmung zum Beschichten kaltgewalzter ausgerichteter Siliziumstähle
vor einem Hochtemperaturschlußanlassen, welche Aufschlämmung unter 25 °C gehalten
wird und im wesentlichen aus
a) Magnesiumoxid mit einer Mehrzahl der Teilchen mit einer Zitronensäureaktivität
unter 200;
b) einem Gesamtchlorniveau im Magnesiumoxid von 0,01 bis 0,20 Gew.% auf Basis des
Gewichts des Magnesiumoxids, wobei wenigstens 0,01 Gew.% Chlor aus einem Metallchlorid
stammt, das aus der Gruppe von Mg, Ca, Na und/oder K gewählt ist;
c) bis zu 15 % TiO₂;
d) bis zu 10 % SiO₂;
e) bis zu 15 % Cr;
f) bis zu 0,3 % B; und
g) bis zu 20 % Phosphat besteht.
2. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei 5 bis 10 Gew.% TiO₂ zugesetzt wurden.
3. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei die Magnesiumoxidaufschlämmung zwischen
0 und 15 °C gehalten wird.
4. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei das Gesamtchlorniveau 0,015 bis
0,15 % ist.
5. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei das Metallchlorid in einer Menge
zugesetzt wurde, um ein Chlorniveau von 0,015 bis 0,12 % zu erzeugen.
6. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei das Metallchlorid in einer Menge
zugesetzt wurde, um ein Chlorniveau von 0,02 bis 0,10 % zu erzeugen.
7. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei das Metallchlorid aus der Gruppe
von Mg, Na und/oder K gewählt ist und in einer Menge zugesetzt wurde, um ein Gesamtchlorniveau
von 0,015 bis 0,10 % zu erzeugen.
8. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei das Metallchlorid Ca ist und in
einer Menge zugesetzt wurde, um ein Gesamtchlorniveau von 0,015 bis 0,07 % zu erzeugen.
9. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei 3 bis 7 % SiO₂ und 0,05 bis 0,15
% B dem Magnesiumoxid zugesetzt wurden.
10. Magnesiumoxidaufschlämmung nach Anspruch 1, wobei 2,5 bis 5 % Cr zugesetzt wurden.
11. Magnesiumoxidaufschlämmung nach Anspruch 1, die bis zu 0,15 % Bor enthält.
12. Magnesiumoxidaufschlämmung nach den Ansprüchen 1 und 11, wobei der Phosphatzusatz
Calciumphosphat in einer Menge von 4 - 15 % ist, der SiO₂-Gehalt 3 - 7 % ist, der
Cr-Gehalt 2 - 10 % ist und der Borgehalt bis zu 0,10 % ist.
13. Verfahren zur Herstellung eines elektrisch isolierenden Überzugs auf ausgerichtetem
Siliziumstahl, das die Schritte aufweist:
a) Kaltwalzen des Siliziumstahls zu Band;
b) Vorsehen eines entkohlenden Anlassens zur Verringerung des Kohlenstoffniveaus des
Bandes auf ein Niveau unter 0,003 %;
c) Halten einer Magnesiumoxidaufschlämmung bei einer Temperatur von über dem Erstarren
bis 25 °C;
d) Aufbringen eines Magnesiumoxidüberzugs mit 0,01 bis 0,20 Gew.% Gesamtchlor, wobei
wengistens 0,01 % von einem Metallchloridzusatz ist, der von der Gruppe Mg, Ca, Na
und/oder K gewählt ist, und wobei eine Mehrzahl der Magnesiumoxidteilchen eine Zitronensäureaktivität
unter 200 hat;
e) Trocknen des Magnesiumoxids zur Entfernung von Überschußwasser; und
f) Vorsehen eines Hochtemperatur-Schlußanlassens zur Bildung eines Glasfilms und Entwicklung
verbesserter magnetischer Eigenschaften.
14. Verfahren nach Anspruch 13,
bei dem ein Laserdomänenverfeinerungsschritt nach dem Schlußanlassen verwendet wird.
15. Verfahren nach Anspruch 13,
bei dem 0,015 bis 0,15 % des Chlors als Metallchlorid zugesetzt werden, das aus der
Gruppe Mg, Na, Ca und/oder K gewählt wird.
16. Verfahren nach Anspruch 13,
bei dem die Magnesiumoxidaufschlämmung vor dem Aufbringen auf das Stahlband zwischen
0 und 15 °C gehalten wird.
17. Verfahren nach Anspruch 13,
bei dem die Magnesiumoxidaufschlämmung bis zu 45 % inaktive Magnesiumoxidteilchen
mit einer Zitronensäureaktivität über 200 hat.
18. Verfahren nach Anspruch 13,
bei dem die Magnesiumoxidaufschlämmung bis zu 45 % der Teilchen mit einer Zitronensäureaktivität
von 500 bis 5000 hat.
19. Verfahren nach Anspruch 13,
bei dem das Metallchlorid in Kombination mit einem in der Magnesiumoxidaufschlämmung
vorhandenen Chlorniveau ein Gesamtchlorniveau von 0,015 bis 0,12 % Chlor ergibt.
20. Verfahren nach Anspruch 13,
bei dem das Metallchlorid in Kombination mit einem in der Magnesiumoxidaufschlämmung
vorhandenen Chlorniveau ein Gesamtchlorniveau von 0,02 bis 0,10 % Chlor ergibt.
21. Verfahren nach Anspruch 13,
bei dem das Gesamtchlor von 0,015 bis 0,10 % ist und das Metallchlorid aus der Gruppe
von Mg, Na und/oder K gewählt wird.
22. Verfahren nach Anspruch 13,
bei dem das Metallchlorid das von Ca ist und in einer Menge zur Erzeugung eines Chlorniveaus
von 0,015 bis 0,07 % zugesetzt wird.
23. Verfahren nach Anspruch 13,
bei dem die Magnesiumoxidaufschlämmung enthält:
a) bis zu 15 % TiO₂;
b) bis zu 10 % SiO₂;
c) bis zu 15 % Cr;
d) bis zu 0,3 % B; und
e) bis zu 20 % Phosphat.
24. Verfahren nach Anspruch 23,
bei dem der Stahl regulärer kornorientierter Siliziumstahl ist und die Magnesiumoxidaufschlämmung
bis zu 20 % Phosphat und bis zu 0,15 % Bor enthält.
25. Verfahren nach Anspruch 24,
bei dem die Magnesiumoxidaufschlämmung 4 - 15 % Calciumphosphat, 2 - 10 % Cr, bis
zu 0,10 % B und 3 - 7 % SiO₂ enthält.
26. Verfahren nach Anspruch 23,
bei dem der Stahl kornorientierter Hochpermeabilitäts-Siliziumstahl ist und die Magnesiumoxidaufschlämmung
5 - 10 % TiO₂, 3 - 7 % SiO₂, 2,5 - 5 % Cr und 0,05 - 0,15 % B enthält.
1. Suspension de magnésie destinée au revêtement d'aciers au silicium orientés laminés
à froid avant un recuit final à haute température, cette suspension étant maintenue
au-dessous de 25°C et comprenant essentiellement :
a) de la magnésie avec une majorité de particules ayant une activité en acide citrique
inférieure à 200 ;
b) une teneur totale en chlore de cette magnésie de 0,01 à 0,20 % en poids sur la
base du poids de la magnésie, au moins 0,01 % en poids du chlore provenant d'un chlorure
métallique choisi dans le groupe des métaux Mg, Ca, Na et/ou K ;
c) jusqu'à 15 % de TiO₂ ;
d) jusqu'à 10 % de Si0₂ ;
e) jusqu'à 15 % de Cr ;
f) jusqu'à 0,3 % de B ; et
g) jusqu'à 20 % de phosphate.
2. Suspension de magnésie suivant la revendication 1, dans laquelle ont été ajoutés 5
à 10 % en poids de TiO₂.
3. Suspension de magnésie suivant la revendication 1, cette suspension de magnésie étant
maintenue entre 0 et 15°C.
4. Suspension de magnésie suivant la revendication 1, dont la teneur totale en chlore
va de 0,015 à 0,15 %.
5. Suspension de magnésie suivant la revendication 1, dans laquelle le chlorure métallique
a été ajouté en une quantité créant une teneur en chlore de 0,015 à 0,12 %.
6. Suspension de magnésie suivant la revendication 1, dans laquelle le chlorure métallique
a été ajouté en une quantité créant une teneur en chlore de 0,02 à 0,10 %.
7. Suspension de magnésie suivant la revendication 1, dans laquelle le chlorure métallique
est choisi dans le groupe des métaux Mg, Na et/ou K et a été ajouté en une quantité
créant une teneur totale en chlore de 0,015 à 0,10 %.
8. Suspension de magnésie suivant la revendication 1, dans laquelle le chlorure métallique
est du chlorure de calcium qui a été ajouté en une quantité créant une teneur totale
en chlore de 0,015 à 0,07 %.
9. Suspension de magnésie suivant la revendication 1, dans laquelle 3 à 7 % de SiO₂ et
0,05 à 0,15 % de bore ont été ajoutés à la magnésie.
10. Suspension de magnésie suivant la revendication 1, dans laquelle ont été ajoutés 2,5
à 5 % de chrome.
11. Suspension de magnésie suivant la revendication 1, qui contient jusqu'à O,15 % de
bore.
12. Suspension de magnésie suivant les revendications 1 et 11, dans laquelle le phosphate
ajouté est du phosphate de calcium en une quantité de 4 à 15 %, la teneur en Si0₂
va de 3 à 7 %, la teneur en chrome va de 2 à 10 % et la teneur en bore va jusqu'à
0,10 %.
13. Procédé de production d'un revêtement isolant électrique sur de l'acier au silicium
orienté, comprenant les étapes qui consistent :
a) à former un feuillard par laminage à froid de cet acier au silicium ;
b) à conduire un recuit de décarburation pour réduire la teneur en carbone du feuillard
à un niveau inférieur à 0,003 % ;
c) à maintenir une suspension de magnésie à une température allant d'une valeur supérieure
au point de congélation à 25°C ;
d) à appliquer un revêtement de magnésie ayant une teneur totale en chlore de 0,01
à 0,20 % en poids dont une proportion d'au moins 0,01 % est constituée d'une addition
de chlorure métallique choisi dans le groupe des métaux Mg, Ca, Na et/ou K et dont
une majorité des particules de magnésie ont une activité en acide citrique inférieure
à 200 ;
e) à sécher cette magnésie pour en éliminer l'eau en excès ; et
f) à conduire un recuit final à haute température pour former un film vitreux et pour
développer de meilleures propriétés magnétiques.
14. Procédé suivant la revendication 13, dans lequel une étape d'affinage par domaines
au laser est utilisée après le recuit final.
15. Procédé suivant la revendication 13, dans lequel une proportion de 0,015 à 0,15 %
du chlore est ajoutée sous forme d'un chlorure métallique choisi dans le groupe de
métaux Mg, Na, Ca, et/ou K.
16. Procédé suivant la revendication 13, dans lequel la suspension de magnésie est maintenue
entre 0 et 15° C avant son application sur le feuillard d'acier.
17. Procédé suivant la revendication 13, dans lequel la suspension de magnésie contient
jusqu'à 45 % de particules de magnésie inactives avec une activité en acide citrique
supérieure à 200.
18. Procédé suivant la revendication 13, dans lequel la suspension de magnésie contient
jusqu'à 45 % de particules ayant une activité en acide citrique de 500 à 5000.
19. Procédé suivant la revendication 13, dans lequel le chlorure métallique crée, en association
avec le chlore contenu dans la suspension de magnésie, une teneur totale en chlore
de 0,015 à 0,12 %.
20. Procédé suivant la revendication 13, dans lequel le chlorure métallique crée, en association
avec le chlore présent dans la suspension de magnésie, une teneur totale en chlore
de 0,02 à 0,10 %.
21. Procédé suivant la revendication 13, dans lequel le chlore total va de 0,015 à 0,10
% et le chlorure métallique est choisi dans le groupe des métaux Mg, Na et/ou K.
22. Procédé suivant la revendication 13, dans lequel le chlorure métallique est du chlorure
de calcium qui est ajouté en une quantité créant une teneur en chlore de 0,015 à 0,07
%.
23. Procédé suivant la revendication 13, dans lequel la suspension de magnésie contient
:
a) jusqu'à 15 % de TiO₂ ;
b) jusqu'à 10 % de SiO₂ ;
c) jusqu'à 15 % de Cr ;
d) jusqu'à 0,3 % de B ; et
e) jusqu'à 20 % de phosphate.
24. Procédé suivant la revendication 23, dans lequel l'acier est un acier au silicium
orienté à grain régulier et la suspension de magnésie contient jusqu'à 20 % de phosphate
et jusqu'à 0,15 % de bore.
25. Procédé suivant la revendication 24, dans lequel la suspension de magnésie contient
4 à 15 % de phosphate de calcium, 2 à 10 % de chrome, jusqu'à 0,10 % de bore et 3
à 7 % de SiO₂.
26. Procédé suivant la revendication 23, dans lequel l'acier est un acier au silicium
orienté à grain de haute perméabilité et la suspension de magnésie contient 5 à 10
% de TiO₂, 3 à 7 % de SiO₂, 2,5 à 5 % de chrome et 0,05 à 0,15 % de bore.