US2528216A - Selective grain growth of silicon steel - Google Patents

Selective grain growth of silicon steel Download PDF

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US2528216A
US2528216A US9015A US901548A US2528216A US 2528216 A US2528216 A US 2528216A US 9015 A US9015 A US 9015A US 901548 A US901548 A US 901548A US 2528216 A US2528216 A US 2528216A
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grain growth
areas
copper
grains
silicon steel
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US9015A
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Cecil G Dunn
Jr Birger L Johnson
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General Electric Co
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General Electric Co
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    • 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
    • C21D1/78Combined heat-treatments not provided for above

Definitions

  • This invention relates to a process of effecting selective grain growth in siliconsteel and to the products of such process.
  • a protective coating such as an electroplated coating of copper
  • the process also makes possible the production of material for technical uses in which advantage is taken of its controlled heterogeneous character; For example, an air gap effect may be realized in a single, integral, structurally strong piece of material by developing therein two regions of large grains having excellent magnetic characteristics separated by a finite and precise region" of small grains having very poor magnetic qualities.
  • the preferred starting material is 3%4% silicon steel which has been cold rolled with or without intermediate heat treatment to the final thickness. Since the difference in size of grains in selected areas depends upon the introduction of certain impurities or-inhibitors before final heat treatment intojall parts .of. the material excepttho'se areas in which largegrains are desired, the latter areas must bepro- Application February 17, 1948, Serial No. 9,015
  • Thisprotective coating or mask may take the formof metal electroplate, cement, paint or any other material which will withstand the inhibiting treatment.
  • a copper electroplate at least 0.5 mil thick has been found to be very satisfactory and easily applied.
  • a copper coating may first be applied to the. entire piece employing a suitable plating bath after which the design or pattern desired is laid out on the plated surface.
  • the copper is then removed from all areas except the design by any suitable method.
  • the copper to be removed can be converted to copper sulfide and the sulfideremoved in, a cyanide bath, the design areasbeing protected from copper removal by painter other resistant material.
  • a solution of 4', ounces of liver of sulfur to each liter of water can be ,usedto convert a 0.5 mil thick copper plate to the sulfide in about 5 minutes at room temperature.
  • a further treatment at room temperature in a solution containing about 4- ounces of sodium cyanide per liter of water removes the copper sulfide in about 5 minutes. It will be understood, of course, that the concentrations of the above solutions may be varied if different times of reaction are desired. After the copper plate has been removed from the desired areas, the protective or masking coating is removed by mechanical or solvent means.
  • the copper plate may initially be applied only to certain areas of the steel by covering the remaining areas with a wax or other suitable material which will prevent deposition of copper during'the plating process.
  • the protective material may then be removed as by use of a solvent I before subjecting the steel to the inhibiting treatment. 7
  • the inhibiting treatment or process which forms grain-growth retarding'impurities in all areas except those covered by the copper plate, may be accomplished by carburizing, or nitriding the unprotected areas at temperatures below that at which large grains start to grow.
  • the inhibiting material in the case of the carburizing process probably is essentially iron carbide formed by example, the pack, gas, or salt bath processes.
  • carburizing stop-off paints or other masking material known in the carburizing art may be employed in lieu of the copperplate used herein.
  • a combination of carburizing and nitriding may also be employed, such as is accomplished by the known salt bath cyaniding o gas carbo-nitriding treatments.
  • the final anneal or grain growth heat treatment may be carried out in air, it is preferably carried out in a non-oxidizing atmosphere such as pure dry hydrogen, a neutral atmosphere such as argon, or in a vacuum, in order to obviate any possible oxidation or other undesired chemical reaction in or on the surface of the Steel.
  • a non-oxidizing atmosphere such as pure dry hydrogen, a neutral atmosphere such as argon, or in a vacuum, in order to obviate any possible oxidation or other undesired chemical reaction in or on the surface of the Steel.
  • a temperature from about 950 C. to about 1150 C. affords the desired grain growth in the uninhibited areas, the higher temperatures giving 'a more rapid development. stopped at any point after the desired grain growth has been obtained, and th strip etched with a suitable macroetching solution tobring out a visible contrast in grain size if such is desired.
  • the following is given as a specific example of he application of the preferred process of the present invention in depicting on a piece of silicon steel strip .01 inch thick the figure 0.
  • the piece is first plated with copper to a thickness of at least 0.5 mil. This is accomplished in about 30 minutes at room temperature with a current density of 0.1 ampere per square inch using a plating bath of the following composition:
  • the figure is next painted in the desired position on the strip with an acid resistant paint.
  • the copper plate is removed from all parts of the piece except the painted-over design by immersing the piece in a solution of four ounces of liver of Sulfur per liter of water for about 10 minutes at room temperature which converts the copper to the sulfide. This is followed by an immersion for about minutes in a water solution of about 4 ounces of sodium cyanide at room temperature which removes the copper sulfide.
  • the acid resistant paint which protects the copper plate design during the copper removal process is removed with any suitable solvent. 7
  • the resultant product having a copper 0 on the surface thereof is immersed in asalt bath containing the following ingredients, which, when operating at from 1500 F. to 1600 R, will car burize .01 thick strip sufficiently in 10 minutes:
  • the copper mask plate is removed as above described, to expose the uninhibited pattern, and the piece subjected to a heat treatment in a nonoxidizing atmosphere andpreferably. in; pure dry hydrogen at from 950 C. to 1150 0. ;As the grains in the design areas grow normally under The process ma be such heat treatment while the inhibited grains do not, there results a differential in size of grains as between the figure 0 design area with its large grains and other areas, the growth process being stopped at any stage simply b removing the piece from the high temperature. The piece is then macro-etched with a nitric acid solution to make the contrast grain size visible. The process may also be reversed, causing the figure 0 to be fine-grained in a large grain matrix.
  • Material of any convenient thickness may be treated by the present process although with thicker sheets the inhibiting process may tend to undercut the masked area and render an indistinct or less sharp border line between inhibited and uninhibited areas.
  • a carburizing salt bath of the above composition the following approximate case depths may be obtained either on one or both sides of the plate.
  • nitriding salt bath which may be used Inasmuch as nitriding generally has a less effective depth than carburizing, the latter method is recommended when it is desired to have the grain growth inhibition penetrate to a depth of more than 0.01 inch.
  • silicon steel treated as set forth herein is susceptible of both decorative and technical uses.
  • the contrast in grain size which is made visible thru macroetching may be used to give a pleasing and novel effect in jewelry, signs, nameplates and the like by growing the desireddesign in a single piece of material instead of having to make up the design by using separate contrasting parts.
  • the large grains may be developed to have a preferred crystal orientation, and therefore, magnetic characteristics superior to those of the small grains whose growth was inhibited, there may be obtained in an integral single piece of material regions of varying magnetic qualities.
  • an effect equivalent to an air gap can be realized by separating two areas of large selectively grown grains with extremely good magnetic characteristics by a region of controlled size consisting of small grains with very poor magnetic characteristics.
  • the product is an integral article, is stronger than one fabricated from separate pieces.
  • a cold rolled and heat treated silicon steel sheet containing 3 to 4% silicon characterized by a surface comprising selected areas of grains which are generally smaller than the grains of the remaining areas of said sheet, the said selected areas having a higher content of an element selected from the class consisting of carbon and nitrogen than the remaining areas of said sheet.

Description

?atented Oct. 31 1950 UNITEDSTATIES PATENT OFFICE SELECTIVE GRAIN GROWTH OF SILICON STEEL Cecil G. Dunn, Pittsfield, Mass., and Birger L. Johnson, Jr., Scotch Plains, N. J., assignors to General Electric Company, a corporation of New York No Drawing.
, l This invention relates to a process of effecting selective grain growth in siliconsteel and to the products of such process.
It is an object of this invention to provide a method for the selective control of grain growth in silicon steel.
It is another object of this invention to provide a method of selectively controlling the grain growth of silicon steel to produce any desired pattern or design therein.
It has been found that the above objects may be accomplished by the formation of impurities in certain parts of the material which inhibit normal grain growth.
More particularly it has been found that grain growth in silicon steel may be selectively con-= trolled by masking that part of the material in which normal growth of grainsis desired with a protective coating such as an electroplated coating of copper, subjecting the material to a car burizing or nitridingtreatment whichforms normal grain growth inhibiting impurities in that part of the material not protected by the coating, removing the protective coating or mask, and
heat treating the article at a temperature of about 950 C. to 1150 C., such heat treatment or anneal effecting the growth of large grains in the formerly protected or uninhibited portion of v the article. This process may be used to produce visual differences in a single piece of material, such differences or contrasts being in the metal itself and brought about by the presence of clearly defined areas comprising large grains and other areas containing only small grains. Such a contrast may be used in creating new and pleasing decorative effects in jewelry, signs, nameplates and similar articles. The process also makes possible the production of material for technical uses in which advantage is taken of its controlled heterogeneous character; For example, an air gap effect may be realized in a single, integral, structurally strong piece of material by developing therein two regions of large grains having excellent magnetic characteristics separated by a finite and precise region" of small grains having very poor magnetic qualities.
While any steel which lends itself to grain growth may be employed, the preferred starting material is 3%4% silicon steel which has been cold rolled with or without intermediate heat treatment to the final thickness. Since the difference in size of grains in selected areas depends upon the introduction of certain impurities or-inhibitors before final heat treatment intojall parts .of. the material excepttho'se areas in which largegrains are desired, the latter areas must bepro- Application February 17, 1948, Serial No. 9,015
10 Claims. (01.1 3 14) tectd or masked during such inhibiting treatment. Thisprotective coating or mask may take the formof metal electroplate, cement, paint or any other material which will withstand the inhibiting treatment.
- For the purpose of this invention a copper electroplate at least 0.5 mil thick has been found to be very satisfactory and easily applied. For example, a copper coating may first be applied to the. entire piece employing a suitable plating bath after which the design or pattern desired is laid out on the plated surface. The copper is then removed from all areas except the design by any suitable method. For example the copper to be removed can be converted to copper sulfide and the sulfideremoved in, a cyanide bath, the design areasbeing protected from copper removal by painter other resistant material. A solution of 4', ounces of liver of sulfur to each liter of water can be ,usedto convert a 0.5 mil thick copper plate to the sulfide in about 5 minutes at room temperature. A further treatment at room temperature in a solution containing about 4- ounces of sodium cyanide per liter of water removes the copper sulfide in about 5 minutes. It will be understood, of course, that the concentrations of the above solutions may be varied if different times of reaction are desired. After the copper plate has been removed from the desired areas, the protective or masking coating is removed by mechanical or solvent means.
If desired the copper plate may initially be applied only to certain areas of the steel by covering the remaining areas with a wax or other suitable material which will prevent deposition of copper during'the plating process. The protective material may then be removed as by use of a solvent I before subjecting the steel to the inhibiting treatment. 7
The inhibiting treatment or process, which forms grain-growth retarding'impurities in all areas except those covered by the copper plate, may be accomplished by carburizing, or nitriding the unprotected areas at temperatures below that at which large grains start to grow. The inhibiting material in the case of the carburizing process probably is essentially iron carbide formed by example, the pack, gas, or salt bath processes. If desired, carburizing stop-off paints or other masking material known in the carburizing art may be employed in lieu of the copperplate used herein. A combination of carburizing and nitriding may also be employed, such as is accomplished by the known salt bath cyaniding o gas carbo-nitriding treatments.
While the final anneal or grain growth heat treatment may be carried out in air, it is preferably carried out in a non-oxidizing atmosphere such as pure dry hydrogen, a neutral atmosphere such as argon, or in a vacuum, in order to obviate any possible oxidation or other undesired chemical reaction in or on the surface of the Steel. A temperature from about 950 C. to about 1150 C. affords the desired grain growth in the uninhibited areas, the higher temperatures giving 'a more rapid development. stopped at any point after the desired grain growth has been obtained, and th strip etched with a suitable macroetching solution tobring out a visible contrast in grain size if such is desired.
The following is given as a specific example of he application of the preferred process of the present invention in depicting on a piece of silicon steel strip .01 inch thick the figure 0. The piece is first plated with copper to a thickness of at least 0.5 mil. This is accomplished in about 30 minutes at room temperature with a current density of 0.1 ampere per square inch using a plating bath of the following composition:
Copper cyanide pounds 0.25 Sodium cyanide do 3.7 Sodium carbonate do 1.7 Sodium thiosulfate grains 5 Water "liters" 5.
The figure is next painted in the desired position on the strip with an acid resistant paint. When the paint is dry, the copper plate is removed from all parts of the piece except the painted-over design by immersing the piece in a solution of four ounces of liver of Sulfur per liter of water for about 10 minutes at room temperature which converts the copper to the sulfide. This is followed by an immersion for about minutes in a water solution of about 4 ounces of sodium cyanide at room temperature which removes the copper sulfide. The acid resistant paint which protects the copper plate design during the copper removal process is removed with any suitable solvent. 7
The resultant product having a copper 0 on the surface thereof is immersed in asalt bath containing the following ingredients, which, when operating at from 1500 F. to 1600 R, will car burize .01 thick strip sufficiently in 10 minutes:
After the introduction of normal grain growth inhibiting iron carbide into all parts of the strip except that coveredby the copper mask design,
the copper mask plate is removed as above described, to expose the uninhibited pattern, and the piece subjected to a heat treatment in a nonoxidizing atmosphere andpreferably. in; pure dry hydrogen at from 950 C. to 1150 0. ;As the grains in the design areas grow normally under The process ma be such heat treatment while the inhibited grains do not, there results a differential in size of grains as between the figure 0 design area with its large grains and other areas, the growth process being stopped at any stage simply b removing the piece from the high temperature. The piece is then macro-etched with a nitric acid solution to make the contrast grain size visible. The process may also be reversed, causing the figure 0 to be fine-grained in a large grain matrix.
It has been found that thin strip, about 0.01 inch and under, need have the design masked on one side only provided the other side is fully masked since the inhibiting process will penetrate thru to the opposite side. With thicker sheets of metal it is advisable to mask the design area on both faces to insure penetration of the inhibiting effect. However, if the design is to be superficial and on one side only it need usually be masked on only one side.
Material of any convenient thickness ma be treated by the present process although with thicker sheets the inhibiting process may tend to undercut the masked area and render an indistinct or less sharp border line between inhibited and uninhibited areas. Using a carburizing salt bath of the above composition the following approximate case depths may be obtained either on one or both sides of the plate.
1500 F 1550 F. 1000 F.
Inches Inches Inches If thicker case depths are desired resort may be had to gas or pack carburizing.
-A typical nitriding salt bath which may be used Inasmuch as nitriding generally has a less effective depth than carburizing, the latter method is recommended when it is desired to have the grain growth inhibition penetrate to a depth of more than 0.01 inch.
A pointed out above, silicon steel treated as set forth herein is susceptible of both decorative and technical uses. The contrast in grain size which is made visible thru macroetching may be used to give a pleasing and novel effect in jewelry, signs, nameplates and the like by growing the desireddesign in a single piece of material instead of having to make up the design by using separate contrasting parts. From the technical aspect, since the large grains may be developed to have a preferred crystal orientation, and therefore, magnetic characteristics superior to those of the small grains whose growth was inhibited, there may be obtained in an integral single piece of material regions of varying magnetic qualities. Thus an effect equivalent to an air gap can be realized by separating two areas of large selectively grown grains with extremely good magnetic characteristics by a region of controlled size consisting of small grains with very poor magnetic characteristics. The product is an integral article, is stronger than one fabricated from separate pieces.
What we claim as new and desire to secure by Letters Patent of the United States is:
1. The process of producing large grains in any desired area of a cold rolled steel sheet containing about 3%-4% silicon which comprises in hibiting all other areas against normal grain growth by carburizing followed by a heat treatment at about 950 to 1150 C. to produce the growth of large grains in the uninhibited area.
2. The process of producing large grains in any desired area of a cold rolled steel sheet containing about 3% to 4% silicon and about 115% aluminum which comprises inhibiting all other areas by nitriding followed by a heat treatment at about 950 C. to 1150 C. to produce the growth of large grains in the uninhibited area.
3. The process of producing large grains in any desired area of a cold rolled steel sheet containing about 3% to 4% silicon and about .05% chromium which comprises inhibiting all other areas by nitriding followed by a heat treatment at about 950 C. to 1150" C. to produce the growth of large grains in the uninhibited area.
4. The process of producing large grains in any desired area of a cold rolled steel sheet containing about 3% to 4% silicon and about .05% aluminum and chromium which comprises inhibiting all other areas b nitriding followed by a heat treatment at about 950 C. to 1150 C. to produce the growth of large grains in the uninhibited area.
5. The process of producing large grain growth in any desired area of a cold rolled silicon steel sheet which comprises inhibiting all other areas against normal grain growth by the introduction of an element selected from the class consisting of carbon and nitrogen followed by a heat treatment to produce large grains in the uninhibited areas.
6. The process of producing large grain growth in any desired area of cold rolled silicon steel which comprises copper plating the area of desired large grain growth, carburizing the material to inhibit normal grain growth in all areas except that protected by the copper followed by removal of the copper and heat treatment to produce large grains in the uninhibited area.
7. The process of producing large grain growth in any desired area of cold rolled silicon steel which comprises copper plating the area of desired large grain growth, nitriding the material to inhibit normal grain growth in all areas except that protected by the copper followed by removal of the copper and heat treatment to produce large grains in the uninhibited area,
8. The process of producing large grains in any desired area of cold rolled silicon steel strip which comprises masking the area of desired larg grain growth, carburizing the material to inhibit normal grain growth in all areas except that masked followed by removal of the masking and heat treatment to produce large grains in the uninhibited area.
9. The process of producing large grains in any desired area of cold rolled silicon steel sheet which comprises masking the area of desired large grain growth, nitriding the material to inhibit normal grain growth in all areas except that masked followed by removal of the masking and heat treatment to produce large grains in the uninhibited area.
10. A cold rolled and heat treated silicon steel sheet containing 3 to 4% silicon characterized by a surface comprising selected areas of grains which are generally smaller than the grains of the remaining areas of said sheet, the said selected areas having a higher content of an element selected from the class consisting of carbon and nitrogen than the remaining areas of said sheet.
CECIL G. DUNN. BIRGER L. JOHNSON, JR.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,966,130 Norton July 10, 1934 2,067,076 Craighead Jan. 5, 1937 2,237,061 Scharschu Apr. 1, 1941 2,242,234 Carpenter May 20, 1941 2,327,256 Fowle et a1 Aug. 17, 1943 2,336,617 Johnston Dec. 14, 1943

Claims (1)

  1. 5. THE PROCESS OF PRODUCING LARGE GRAIN GROWTH IN ANY DESIRED AREA OF A COLD ROLLED SILICON STEEL SHEET WHICH COMPRISES INHIBITING ALL OTHER AREAS AGAINST NORMAL GRAIN GROWTH BY THE INTRODUCTION OF AN ELEMENT SELECTED FROM THE CLASS CONSISTING OF CARBON AND NITROGEN FOLLOWED BY A HEAT TREATMENT TO PRODUCE LARGE GRAINS IN THE UNINHIBITED AREAS.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014823A (en) * 1956-08-29 1961-12-26 Int Nickel Co Production of hollow turbine blades
US3063816A (en) * 1959-06-08 1962-11-13 American Can Co Method of controlling crystal growth
US3932236A (en) * 1973-01-22 1976-01-13 Nippon Steel Corporation Method for producing a super low watt loss grain oriented electrical steel sheet
US3941623A (en) * 1973-08-28 1976-03-02 Nippon Steel Corporation Method for producing a grain-oriented electrical steel sheet using separators comprising metal nitrides

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1966130A (en) * 1930-10-18 1934-07-10 Bendix Brake Co Brake drum
US2067076A (en) * 1934-02-14 1937-01-05 Aluminum Co Of America Method of controlling grain structure in alloys and articles produced thereby
US2237061A (en) * 1936-10-07 1941-04-01 Allegheny Ludlum Steel Method of annealing magnetic material
US2242234A (en) * 1936-01-22 1941-05-20 American Rolling Mill Co Producing silicon steel sheets or strips
US2327256A (en) * 1941-08-02 1943-08-17 Frank F Fowle Carbon-steel alternating-current conductor
US2336617A (en) * 1943-04-05 1943-12-14 Us Steel Corp Of Delaware Heat treating electrical silicon steel

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1966130A (en) * 1930-10-18 1934-07-10 Bendix Brake Co Brake drum
US2067076A (en) * 1934-02-14 1937-01-05 Aluminum Co Of America Method of controlling grain structure in alloys and articles produced thereby
US2242234A (en) * 1936-01-22 1941-05-20 American Rolling Mill Co Producing silicon steel sheets or strips
US2237061A (en) * 1936-10-07 1941-04-01 Allegheny Ludlum Steel Method of annealing magnetic material
US2327256A (en) * 1941-08-02 1943-08-17 Frank F Fowle Carbon-steel alternating-current conductor
US2336617A (en) * 1943-04-05 1943-12-14 Us Steel Corp Of Delaware Heat treating electrical silicon steel

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3014823A (en) * 1956-08-29 1961-12-26 Int Nickel Co Production of hollow turbine blades
US3063816A (en) * 1959-06-08 1962-11-13 American Can Co Method of controlling crystal growth
US3932236A (en) * 1973-01-22 1976-01-13 Nippon Steel Corporation Method for producing a super low watt loss grain oriented electrical steel sheet
US3941623A (en) * 1973-08-28 1976-03-02 Nippon Steel Corporation Method for producing a grain-oriented electrical steel sheet using separators comprising metal nitrides

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