US3671335A - Non-reactive refractory separating coatings for electrical steels - Google Patents

Non-reactive refractory separating coatings for electrical steels Download PDF

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US3671335A
US3671335A US22682A US3671335DA US3671335A US 3671335 A US3671335 A US 3671335A US 22682 A US22682 A US 22682A US 3671335D A US3671335D A US 3671335DA US 3671335 A US3671335 A US 3671335A
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/147Alloys characterised by their composition
    • H01F1/14766Fe-Si based alloys
    • H01F1/14775Fe-Si based alloys in the form of sheets
    • H01F1/14783Fe-Si based alloys in the form of sheets with insulating coating
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/68Temporary coatings or embedding materials applied before or during heat treatment
    • C21D1/70Temporary coatings or embedding materials applied before or during heat treatment while heating or quenching
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23DENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
    • C23D5/00Coating with enamels or vitreous layers
    • C23D5/10Coating with enamels or vitreous layers with refractory materials

Definitions

  • a refractory material is introduced between the adjacent sheets or convolutions to separate them from each other.
  • the problem of obtaining and maintaining this desired separation, and thus avoiding sticking, increases in difficulty with in creasing annealing temperatures.
  • the refractory separating medium in some instances, is required to be essentially inert and non-reactive with respect to the alloy sheet undergoing the annealing operation. Certain textures or orientations are obtained in alloys by surface energy mechanism. For this mechanism to operate successfully, the alloy surfaces must be mirror-bright and a reaction between the separating medium and the alloy is not permissible.
  • One material which has been successfully employed as a separating medium is a dry alumina (A1 0 powder which is sprinkled on the surface of the sheets prior to annealing.
  • the alumina powder should be applied in a form which would adhere to the steel sheet before and during annealing, but which would be easily removable after the annealing treatment.
  • a slurry containing alumina powder would appear to offer a solution, however, difiiculties involving the reactivity of the coating with the steel sheet during annealing have thus far prevented the successful application of the alumina in slurry form.
  • efforts to provide an inert slurry containing alpha phase alumina made by the Bayer process have been unsuccessful due to reactivity of the alumina with the steel sheet.
  • This invention is an improvement in the process of heat treating coiled or stacked electrical steel sheet at elevated temperatures which involves providing the steel sheet with an adherent non-reactive refractory separating coating which is readily removable after the heat treatment.
  • the coating of refractory material is applied in the form of a slurry containing fine A1 0 powder as a solid constituent suspended in an aqueous solution of polyvinyl alcohol and a cellulosic suspending agent such as hydroxyethyl cellulose.
  • a slurry containing fine A1 0 powder as a solid constituent suspended in an aqueous solution of polyvinyl alcohol and a cellulosic suspending agent such as hydroxyethyl cellulose.
  • the refractory slurry of this invention contains about a 30 to 70%, and preferably about 60% by weight of fine A1 0 powder suspended in an aqueous solution comprising, by weight, from about 0.5% to 4% polyvinyl alcohol and from about 0.3% to 1% hydroxyethyl cel-. lulose. All weights stated are based on the weight of water present. When the slurry is dried on the steel sheet the weight of the coating per unit area will be from about 0.3 gm./ft. to '3 gm./ft.
  • the slurry of this invention is composed of alumina powder, hydroxyethyl cellulose, polyvinyl alcohol and water.
  • Suitable alumina powder may be produced using hydrated.alumina (Al(OH) by the'following process::
  • Hydrated alumina powder is placed in ceramic trays or crucibles in a layer not over 4 inches deep.
  • the hydrated alumina powder is alpha phase alumina.
  • the trays or crucibles of hydrated alumina are placed in an oven at a temperature of about 100 C. and held approximately-2 hours. Thereafter the temperature is raised about 100 C. at a-time with holding periods of at least 3 hours at about 200 C. and about 300 ;C. The temperature of the oven is then increased to about 500 C. and a holding period at that temperature of; 12 hours is employed. The temperature of the oven is finally raised to about 1000 C. and a holding. period of 12 hours is employed.
  • the alumina processed as described was identified by X-ray diffraction means as being kappa (K) phase aluminum oxide.
  • Hydroxyethyl cellulose is a non-ionic water-soluble polymer derived from cellulose, one type of which is sold under the trademark, Natrosol. In the slurry of this invention the hydroxyethyl cellulose performs the function of a suspending agent. Hydroxyethyl cellulose is a white free-flowing powder and one preferred aqueous solution of this material is prepared initially in the following manner: (1) A predetermined amount of water is heated to a temperature of 60 C. (2) Exactly 0.6% hydroxyethyl cellulose based on the amount of water is weighed out; (3) The heated water is stirred to form a vortex and the hydroxyethyl cellulose is slowly sifted into the vortex of vigorously agitated water.
  • the rate of addition of the hydroxyethyl cellulose should be slow. enough for the particles to separate in water without lump formation, but not so slow that the solution thickens appreciably before all of the solid is added. Agitation should be continued until all of the swollen or gelatinized particles are dissolved to yield a smooth solution; (4) The solution of hydroxyethyl cellulose is cooled to room temperature.
  • the hydroxyethyl cellulose is available in grades of high, medium and low molecular weights. Ingeneral, it is desired in the present invention to provide the required viscosity with as small an addition as possible, and for this purpose, the high molecular weight compounds are best. Those compounds which produce a solution viscosity of from 300 to 500 centipoises at 25 C., and preferably from 350 to 400 centipoises, with an addition of up to 1%, by weight, or less of the compound, are satisfactory.
  • the polyvinyl alcohol (PVA) is added to the slurry primarily to improve the adhesion of the coating to the sheet steel, but it also contributes secondarily as a suspending agent.
  • the preferred polyvinyl alcoholemployed is a high molecular weight type having a molecular weight in the range of 73 to 125. Such a product is sold under the trademark Elvanol.
  • a solution of polyvinyl alcohol is prepared in the following manner: (1) Water at a temperature of 75 F. or lower is stirred with a high speed agitator to produce a Vortex-(2) The polyvinyl alcohol powder is sifted directly into the vortex so that it is rapidly wet and dispersed and the slurry thus formed is stirred for 10 minutes.
  • the separately prepared hydroxyethyl cellulose solution and the poly-. vinyl alcohol solution are mixed together. Then, for ex? ample, about 60% by weight of finely divided A1 0 based on the weight of water to be used, which has had the water of hydration removed as described above, is added to the hydroxyethyl cellulose-polyvinyl alcohol solution while it is being vigorously stirred. The A1 0 is added slowly to the vortex to assure that all particles are suspended.
  • the typical slurry mix has the following constituents: e
  • these organic additives promote adhesion of the alumina particles to the alloy sheets.
  • these additives can be used only in relatively small quantities to avoid introducing excessive amounts of carbonaceous contaminants into the annealing process. Accordingly, continuous agitation of the slurryis desirable, and a mixing tank with suitable slurry pumps may be used to, aid in holding the slurry in suspension and to deliver it to the coating rolls.
  • the electrical sheet passes be tween the coating rolls and a slurry reservoir is provided to wet the bottom roll and a transfer pump from the mixing tank may be used to wet the top roll with the required amount of slurry.
  • the roll apparatus consists of two mated rubber or plastic rolls with a screwdown device to regulate the roll pressure.
  • the rolls are grooved .008 to .012 inch deep with about 36 threads per inch and good results are obtained when the durometer hardness of the rolls is about 50.
  • the length and diameter of 'the rolls is determined by the width and length of the electrical steel sheets, and the velocity of the sheet.
  • the sheet is passed through a drying oven to obtain a temperature in the electrical steel sheet of between to C.
  • the temperature is maintained in this range since higher temperatures may char the additives.
  • One satisfactory procedure to avoid scraping or rub bing the laminations prior to the transformation anneal is to stack a plurality of laminations between /2 inch thick plates of low carbon steel to eliminate individual handling of the laminations or sheets.
  • the stack height of the sheets may be 6 inches, for example; the sheets having a thickness of from 3 to mils.
  • the stack of plates and electrical sheet laminations can be banded tightly and stored in a dry condition prior to the transformation anneal.
  • Coils of electrical sheet steel can also be handed and stored under dry conditions prior to the transformation anneal.
  • the transformation anneal of the coated steel is carried out at about 1200 C. in a dry hydrogen atmosphere. Under these conditions the organic binding and suspension agents present in the alumina coating are completely removed. The alumina remains on the surface of the electrical steel sheet. It is inert and can be removed by dry brushing or wiping the surface with a cloth after the transformation anneal. A very clean surface on the electrical steel sheet is then exposed.
  • the coated sheets are stacked and annealed in a furnace at a temperature of 1200 C. for a period of 24 hours in an atmosphere of dry hydrogen (dew point of 60 C.) into which is introduced 35 p.p.m. of hydrogen sulfide.
  • the alloy sheets are thereafter removed from the furnace and cooled to room temperature. No sticking is observed between sheets and the alumina is readily removed by light brushing. Transformation of the alloy sheets to cube texture by the described annealing treatment is accomplished to the extent of 98% (100) [001] texture by volume.
  • the slurry of the invention has also been employed in the annealing of 50% nickel-50% iron alloy.
  • the alloy strip is coated on one side with the slurry and stainless steel wiper bars are used to obtain a uniform coating.
  • the coating is dried by passing the strip through a bank of heat lamps before the strip is wound into cores.
  • the wound cores are then annealed and it is found that the coating is nonreactive at the annealing temperature, typically 1066 C.
  • a slurry for providing an adherent separating coating on electrical steel prior to annealing consisting essentially of from 30% to 70% by weight of finely divided kappa phase A1 0 powder suspended in an aqueous solution containing from 0.5% to 4% by weight of polyvinyl alcohol and from 0.3% to 1% by weight of at least one suspending agent selected from the group consisting of high molecular weight hydroxyethyl cellulose and carboxymethyl cellulose suflicient to produce a solution viscosity in the range between 300 and 500 centipoises at 25 0., all weights based upon the amount of water present.

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Abstract

AN AQUEOUS SLSURRY COMPRISING ABOUT 60% BY WEIGHT OF AL2O3, BASED ON THE WEIGHT OF THE WATER, AND SMALL AMOUNTS OF POLYVINYL ALCOHOL AND AN ORGANIC SUSPENDING AGENT (MORE PARTICULARLY, A CELLULOSIC SUSPENDING AGENT), IS APPLIED TO ELECTRICAL SHEET STEEL AND DRIED THEREON TO PROVIDE A RELATIVELY THIN AND UNIFORM SEPARATING COATING. A PLURALITY OF SUCH COATED SHEETS MAY BE STACKED OR A SINGLE SUCH SHEET MAY BE COILED FOR FINAL ANNEALING AT ELEVATED TEMPERATURE.

Description

United States Patent Ofice 3,671,335 Patented June 20, 1972 3,671,335 NON-REACTIVE REFRACTORY SEPARATING COATINGS FOR ELECTRICAL STEELS Norman M. Pavlik, Pittsburgh, Pa., assignor to Westinghouse Electric Corporation, Pittsburgh, Pa.
No Drawing. Original application Nov. 6, 1967, Ser. No. 681,026, now Patent No. 3,523,837. Divided and this application Mar. 25, 1970, Ser. No. 22,682
Int. Cl. H01f 1/18 US. Cl. 14828 3 Claims ABSTRACT OF THE DISCLOSURE An aqueous slurry comprising about 60% by weight of A1 based on the 'weight of the Water, and small amounts of polyvinyl alcohol and an organic suspending agent (more particularly, a cellulosic suspending agent), is applied to electrical sheet steel and dried thereon to provide a relatively thin and uniform separating coating. A plurality of such coated sheets may be stacked or a single such sheet may be coiled for final annealing at elevated temperature.
CROSS REFERENCE TO RELATED APPLICATION The present application is filed as a divisional application of Ser. No. 681,026 filed Nov. 6, 1967, now Patent No. 3,523,837. See also application Ser. No. 22,683 filed Mar. 25, 1970.
BACKGROUND OF THE INVENTION It is common practice in annealing electrical sheet steel to stack a plurality of sheets or to coil a single sheet so that lots weighing several hundreds of pounds may be annealed at a time in a furnace of suitable size. In order to prevent adjacent sheets of the stack or the adjacent convolutions of a coil fiom sticking together, a refractory material is introduced between the adjacent sheets or convolutions to separate them from each other. The problem of obtaining and maintaining this desired separation, and thus avoiding sticking, increases in difficulty with in creasing annealing temperatures. The refractory separating medium, in some instances, is required to be essentially inert and non-reactive with respect to the alloy sheet undergoing the annealing operation. Certain textures or orientations are obtained in alloys by surface energy mechanism. For this mechanism to operate successfully, the alloy surfaces must be mirror-bright and a reaction between the separating medium and the alloy is not permissible.
This problem of reactivity is particularly important in the annealing of iron-silicon electrical sheet steels having; the (100) [001] grain orientation. A process for making iron-silicon alloy sheets having this orientation is set forth in US. Pat. No. 3,240,638, issued Mar. 15, 1966 to G. W. Wiener et al. In this so-called cube textured sheet steel, the desired orientation is obtained by means of surface energy phenomena and it is imperative that the surface of the iron-silicon alloy sheet steel be extremely clean with a mirror-bright surface. A coating which reacts with the surface of the alloy sheet steel will defeat the necessary surface energy phenomena and the desired grain orientation will not be obtained.
Another group of materials in which surface energy phenomena is important in obtaining a desired orientation, and therefore, in which a non-reactive separating medium is necessary, are the alloys disclosed in application Ser. No. 372,693, filed June 4, 1964 and entitled Process for Producing Magnetic Sheets With Cube-On-Face Grain Texture by Robert G. Aspden.
One material which has been successfully employed as a separating medium is a dry alumina (A1 0 powder which is sprinkled on the surface of the sheets prior to annealing.
The problem of an even distribution of powder materials of this type, and the further problem of maintaining an even distribution once it is achieved, are readily apparent. Further, it has been found that individual steel sheets in stacks employing dry alumina powder tend to shift and slide, due to the ball-bearing action of the alumina powder, and it is difiicult to maintain the stack alignment. The problem of maintaining a uniform distribution of dry alumina powder in a coil of electrical steel has not been solved and further, a phenomenon known as telescoping is frequently observed in such coils as the inner turns of the coil telescope outwardly on the low friction surface provided by the alumina powder.
Ideally then, the alumina powder should be applied in a form which would adhere to the steel sheet before and during annealing, but which would be easily removable after the annealing treatment. A slurry containing alumina powder would appear to offer a solution, however, difiiculties involving the reactivity of the coating with the steel sheet during annealing have thus far prevented the successful application of the alumina in slurry form. In particular, efforts to provide an inert slurry containing alpha phase alumina made by the Bayer process have been unsuccessful due to reactivity of the alumina with the steel sheet.
SUMMARY OF THE INVENTION This invention is an improvement in the process of heat treating coiled or stacked electrical steel sheet at elevated temperatures which involves providing the steel sheet with an adherent non-reactive refractory separating coating which is readily removable after the heat treatment.
More specifically, the coating of refractory material is applied in the form of a slurry containing fine A1 0 powder as a solid constituent suspended in an aqueous solution of polyvinyl alcohol and a cellulosic suspending agent such as hydroxyethyl cellulose. When the slurry is dried it provides a thin coating on the electrical steel sheet of adherent A1 0 powder associated with certain organic residues.
The refractory slurry of this invention contains about a 30 to 70%, and preferably about 60% by weight of fine A1 0 powder suspended in an aqueous solution comprising, by weight, from about 0.5% to 4% polyvinyl alcohol and from about 0.3% to 1% hydroxyethyl cel-. lulose. All weights stated are based on the weight of water present. When the slurry is dried on the steel sheet the weight of the coating per unit area will be from about 0.3 gm./ft. to '3 gm./ft.
It is an object of this invention to provide an adherent non-reactive refractory coating for use in the annealing of silicon-iron and other alloys annealed at high temperatures, and which coating is readily removable after annealing.
It is another object of this invention to provide a nonreactive refractory and adherent coating as a separating medium during the high temperature annealing of siliconiron alloy sheet which promotes the development of a in part, be obvious and will, in part, appear hereinafter.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The slurry of this invention is composed of alumina powder, hydroxyethyl cellulose, polyvinyl alcohol and water.
Suitable alumina powder may be produced using hydrated.alumina (Al(OH) by the'following process::
(1) Hydrated alumina powder is placed in ceramic trays or crucibles in a layer not over 4 inches deep. The hydrated alumina powder is alpha phase alumina. (2) The trays or crucibles of hydrated alumina are placed in an oven at a temperature of about 100 C. and held approximately-2 hours. Thereafter the temperature is raised about 100 C. at a-time with holding periods of at least 3 hours at about 200 C. and about 300 ;C. The temperature of the oven is then increased to about 500 C. and a holding period at that temperature of; 12 hours is employed. The temperature of the oven is finally raised to about 1000 C. and a holding. period of 12 hours is employed. This curing schedule has provensatisfactory, but other schedules may clearly be used, the temperature rise at each step is limited only to prevent excessively violent boiling ofi? of the water inthe alumina, with consequent loss of powder. Approximately 35% by weight of the hydrated alumina, namely the water of hydration must be removed.
Using nominal 325 mesh aluminum trihydrate, the
particle size distribution of alumina produced by this method was analyzed as follows:
+100 mesh- 0.70%
-100 to +200 mesh-10.38% 200 to +325 mesh-42.59% 325 mesh 46.31%
The alumina processed as described was identified by X-ray diffraction means as being kappa (K) phase aluminum oxide.
Hydroxyethyl cellulose is a non-ionic water-soluble polymer derived from cellulose, one type of which is sold under the trademark, Natrosol. In the slurry of this invention the hydroxyethyl cellulose performs the function of a suspending agent. Hydroxyethyl cellulose is a white free-flowing powder and one preferred aqueous solution of this material is prepared initially in the following manner: (1) A predetermined amount of water is heated to a temperature of 60 C. (2) Exactly 0.6% hydroxyethyl cellulose based on the amount of water is weighed out; (3) The heated water is stirred to form a vortex and the hydroxyethyl cellulose is slowly sifted into the vortex of vigorously agitated water. The rate of addition of the hydroxyethyl cellulose should be slow. enough for the particles to separate in water without lump formation, but not so slow that the solution thickens appreciably before all of the solid is added. Agitation should be continued until all of the swollen or gelatinized particles are dissolved to yield a smooth solution; (4) The solution of hydroxyethyl cellulose is cooled to room temperature.
The hydroxyethyl cellulose is available in grades of high, medium and low molecular weights. Ingeneral, it is desired in the present invention to provide the required viscosity with as small an addition as possible, and for this purpose, the high molecular weight compounds are best. Those compounds which produce a solution viscosity of from 300 to 500 centipoises at 25 C., and preferably from 350 to 400 centipoises, with an addition of up to 1%, by weight, or less of the compound, are satisfactory.
Somewhat less satisfactory as suspending ,agents, although still useful, are the high molecular weight com pounds of carboxymethyl cellulose.
The polyvinyl alcohol (PVA) is added to the slurry primarily to improve the adhesion of the coating to the sheet steel, but it also contributes secondarily as a suspending agent. The preferred polyvinyl alcoholemployed is a high molecular weight type having a molecular weight in the range of 73 to 125. Such a product is sold under the trademark Elvanol. A solution of polyvinyl alcohol is prepared in the following manner: (1) Water at a temperature of 75 F. or lower is stirred with a high speed agitator to produce a Vortex-(2) The polyvinyl alcohol powder is sifted directly into the vortex so that it is rapidly wet and dispersed and the slurry thus formed is stirred for 10 minutes. (3) The polyvinyl alcohol slurry is heated to 195 F. or higher and agitated at this temperature until solution is complete, which usually takes from 30 to 60 minutes. The suggested maximum concentrations for solutions prepared with ordinary high speed mixers is from 10 to 15% by weight of polyvinyl alcohol having a molecular weight of 73 to 125. (4)The .poly vinyl alcohol, solution is reduced to about 1% by weight of PVA by the addition of water. v p While polyvinyl alcohols (PVA) of high molecular weight are preferred, polyvinyl alcohols of intermediate l. and low molecular weight may be used, but larger additions of up to 4% must be employed to obtain the same result accomplished by smaller additions'of high molecular weight PVA. I a
' In the preparation of the coating slurry, the separately prepared hydroxyethyl cellulose solution and the poly-. vinyl alcohol solution are mixed together. Then, for ex? ample, about 60% by weight of finely divided A1 0 based on the weight of water to be used, which has had the water of hydration removed as described above, is added to the hydroxyethyl cellulose-polyvinyl alcohol solution while it is being vigorously stirred. The A1 0 is added slowly to the vortex to assure that all particles are suspended. The typical slurry mix has the following constituents: e
1000 parts by weight H 0 6 parts by weight hydroxyethyl cellulose 10 parts by weight polyvinyl alcohol 600 parts by weight A1 0 (average particle size mesh and finer) described above, aid in achieving a viscosity in this range,
an d so help maintain the solids in suspension and further, these organic additives promote adhesion of the alumina particles to the alloy sheets. However, these additives can be used only in relatively small quantities to avoid introducing excessive amounts of carbonaceous contaminants into the annealing process. Accordingly, continuous agitation of the slurryis desirable, and a mixing tank with suitable slurry pumps may be used to, aid in holding the slurry in suspension and to deliver it to the coating rolls. The electrical sheet, of course, passes be tween the coating rolls and a slurry reservoir is provided to wet the bottom roll and a transfer pump from the mixing tank may be used to wet the top roll with the required amount of slurry.
The roll apparatus consists of two mated rubber or plastic rolls with a screwdown device to regulate the roll pressure. The rolls are grooved .008 to .012 inch deep with about 36 threads per inch and good results are obtained when the durometer hardness of the rolls is about 50. The length and diameter of 'the rolls is determined by the width and length of the electrical steel sheets, and the velocity of the sheet.
Following the coating step, the sheet is passed through a drying oven to obtain a temperature in the electrical steel sheet of between to C. The temperature is maintained in this range since higher temperatures may char the additives. I v
-It-is essential that an extremely uniformcoating be.
obtained .on the electrical steel sheet with no trailing edges. It has been found that--the amount of dried slurry present as a coating on each side of the electrical steel sheet should fall within the limits prescribed below:
GmJft. Minimum 0.3 Maximum 3.0
Excellent results have been obtained when the amount of dried slurry present on the electrical steel sheet was approximately 0.4 gm./ft. of the total surface area. While the dried alumina coating is reasonably adherent to the electrical sheet steel, care must be exercised in handling and in stacking the dried sheets. The sheets or laminations should not be rubbed or scraped in stacking or coiling because any bare sheet surfaces exposed by such scraping may result in welding together of the sheets or coil convolutions.
One satisfactory procedure to avoid scraping or rub bing the laminations prior to the transformation anneal is to stack a plurality of laminations between /2 inch thick plates of low carbon steel to eliminate individual handling of the laminations or sheets. The stack height of the sheets may be 6 inches, for example; the sheets having a thickness of from 3 to mils. The stack of plates and electrical sheet laminations can be banded tightly and stored in a dry condition prior to the transformation anneal.
Coils of electrical sheet steel can also be handed and stored under dry conditions prior to the transformation anneal.
The transformation anneal of the coated steel is carried out at about 1200 C. in a dry hydrogen atmosphere. Under these conditions the organic binding and suspension agents present in the alumina coating are completely removed. The alumina remains on the surface of the electrical steel sheet. It is inert and can be removed by dry brushing or wiping the surface with a cloth after the transformation anneal. A very clean surface on the electrical steel sheet is then exposed.
EXAMPLE Cold rolled sheets of 3.2% silicon-iron alloy having a thickness of 0.012 inch and a sheet size of 9" x 12", are coated with a slurry, applied by rolls. The aqueous slurry has a solution viscosity of about 400 centipoises and contains the following solid and dissolved constituents, by weight, based on the weight of the water present:
Percent Alumina 60 Hydroxyethyl cellulose 0.6 Polyvinyl alcohol 1 The sheets coated with this slurry are placed on a conveyor belt which carries them through a gas fired oven. In the oven, the sheets attain a temperature of about 150 C. which thoroughly dries the coating. The dried coating adheres well to the alloy sheets and is present on the sheets in the amount of 0.35 gm./ft. on each side of a sheet.
The coated sheets are stacked and annealed in a furnace at a temperature of 1200 C. for a period of 24 hours in an atmosphere of dry hydrogen (dew point of 60 C.) into which is introduced 35 p.p.m. of hydrogen sulfide. The alloy sheets are thereafter removed from the furnace and cooled to room temperature. No sticking is observed between sheets and the alumina is readily removed by light brushing. Transformation of the alloy sheets to cube texture by the described annealing treatment is accomplished to the extent of 98% (100) [001] texture by volume.
The success achieved with the process described above is in striking contrast to the many efforts previously made to anneal this electrical sheet steel with Bayer process alphaphase alumina applied as a slurry. In these previous efforts, reaction of the alumina with the sheet was sufficient to inhibit transformation to cube texture.
The slurry of the invention has also been employed in the annealing of 50% nickel-50% iron alloy. The alloy strip is coated on one side with the slurry and stainless steel wiper bars are used to obtain a uniform coating. The coating is dried by passing the strip through a bank of heat lamps before the strip is wound into cores. The wound cores are then annealed and it is found that the coating is nonreactive at the annealing temperature, typically 1066 C.
There has thus been presented means for obtaining a substantially completely inert slurry coating on siliconiron electrical sheet steel as a separating medium during the transformation anneal of such electrical steel sheets to obtain a cube texture. The slurry coating described herein provides substantial processing advantages over dry dusting or dusting over a wet surface.
It will be understood by those skilled in the art that although the invention has been described in connection with preferred embodiments, modification and variations in composition and in processing schedule and in other aspects, the invention may be employed without departing from the underlying spirit and scope of the invention.
What is claimed is:
1. A slurry for providing an adherent separating coating on electrical steel prior to annealing consisting essentially of from 30% to 70% by weight of finely divided kappa phase A1 0 powder suspended in an aqueous solution containing from 0.5% to 4% by weight of polyvinyl alcohol and from 0.3% to 1% by weight of at least one suspending agent selected from the group consisting of high molecular weight hydroxyethyl cellulose and carboxymethyl cellulose suflicient to produce a solution viscosity in the range between 300 and 500 centipoises at 25 0., all weights based upon the amount of water present.
2. The slurry of claim 1 wherein the polyvinyl alcohol is present in an amount of about 1% by weight of the solution and the cellulosic suspending agent is hydroxyethyl cellulose present in an amount of from 0.3% to 1% by weight.
3. The slurry of claim 2 wherein the A1 0 powder is present in an amount of about 60%, by weight, and the hydroxyethyl cellulose is present in an amount of about 0.6%, by weight.
References Cited UNITED STATES PATENTS 3,282,747 11/ 1966 Foster et al. 148-113 2,641,556 6/ 1953 Robinson 117-127 X 2,985,855 5/1961 Stone 148-113 X 3,189,483 6/1965 Trigg et al. 148-122 X 3,389,006 6/1968 Kohler 148-113 X 2,871,143 1/1959 Getting, Jr. 117-127 OTHER REFERENCES Paist, W. D., Cellulosics, N.Y., Reinhold, 1958, p. 201.
L. DEWAYNE RUTLEDGE, Primary Examiner G. K. WHITE, Assistant Examiner US. Cl. X.R.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3956028A (en) * 1972-09-25 1976-05-11 United States Steel Corporation Temporary scale retardant coatings
US3959028A (en) * 1972-11-20 1976-05-25 The International Nickel Company, Inc. Process of working metals coated with a protective coating
US4209366A (en) * 1977-07-01 1980-06-24 Centre De Recherches Metallurgiques Centrum Voor Research In De Metallurgie Process for improving the surface cleanliness of sheet steel
US4243439A (en) * 1976-10-19 1981-01-06 Societe De Vente De L'aluminium Pechiney Process of quenching metal pieces and product produced
FR2467242A1 (en) * 1979-10-15 1981-04-17 Allegheny Ludlum Steel PROCESS FOR PREPARING ELECTROMAGNETIC SILICON STEEL WITH ORIENTED GRAIN AND STEEL OBTAINED BY THIS PROCESS
WO1987004730A1 (en) * 1986-02-07 1987-08-13 Aluminum Company Of America Method of heat treatment

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3956028A (en) * 1972-09-25 1976-05-11 United States Steel Corporation Temporary scale retardant coatings
US3959028A (en) * 1972-11-20 1976-05-25 The International Nickel Company, Inc. Process of working metals coated with a protective coating
US4243439A (en) * 1976-10-19 1981-01-06 Societe De Vente De L'aluminium Pechiney Process of quenching metal pieces and product produced
US4209366A (en) * 1977-07-01 1980-06-24 Centre De Recherches Metallurgiques Centrum Voor Research In De Metallurgie Process for improving the surface cleanliness of sheet steel
FR2467242A1 (en) * 1979-10-15 1981-04-17 Allegheny Ludlum Steel PROCESS FOR PREPARING ELECTROMAGNETIC SILICON STEEL WITH ORIENTED GRAIN AND STEEL OBTAINED BY THIS PROCESS
WO1987004730A1 (en) * 1986-02-07 1987-08-13 Aluminum Company Of America Method of heat treatment
US4818302A (en) * 1986-02-07 1989-04-04 Aluminum Company Of America Method of heat treatment

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