CA1086194A - Silicon steel and processing therefore - Google Patents
Silicon steel and processing thereforeInfo
- Publication number
- CA1086194A CA1086194A CA280,688A CA280688A CA1086194A CA 1086194 A CA1086194 A CA 1086194A CA 280688 A CA280688 A CA 280688A CA 1086194 A CA1086194 A CA 1086194A
- Authority
- CA
- Canada
- Prior art keywords
- steel
- weight
- boron
- parts
- compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910000976 Electrical steel Inorganic materials 0.000 title claims abstract description 12
- 238000000576 coating method Methods 0.000 claims abstract description 30
- 239000011248 coating agent Substances 0.000 claims abstract description 29
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 28
- 229910052796 boron Inorganic materials 0.000 claims abstract description 28
- 239000010959 steel Substances 0.000 claims abstract description 28
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 14
- 230000035699 permeability Effects 0.000 claims abstract description 12
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 12
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 10
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 10
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 10
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 10
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- 239000010703 silicon Substances 0.000 claims abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000000137 annealing Methods 0.000 claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 6
- 238000005097 cold rolling Methods 0.000 claims abstract description 6
- 239000000155 melt Substances 0.000 claims abstract description 5
- 238000005266 casting Methods 0.000 claims abstract description 4
- 238000005098 hot rolling Methods 0.000 claims abstract description 4
- 239000000126 substance Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052711 selenium Inorganic materials 0.000 claims description 4
- 239000011669 selenium Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 150000001639 boron compounds Chemical class 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 150000004679 hydroxides Chemical class 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000011777 magnesium Substances 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229940065287 selenium compound Drugs 0.000 claims description 2
- 150000003343 selenium compounds Chemical class 0.000 claims description 2
- 150000003464 sulfur compounds Chemical class 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 2
- 229910017464 nitrogen compound Inorganic materials 0.000 claims 1
- 150000002830 nitrogen compounds Chemical class 0.000 claims 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BUCORZSTKDOEKQ-UHFFFAOYSA-N 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine Chemical compound C=12C=C(Cl)C=CC2=NC(=NC)CN(O)C=1C1=CC=CC=C1 BUCORZSTKDOEKQ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000161 steel melt Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
- C21D8/1277—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties involving a particular surface treatment
- C21D8/1283—Application of a separating or insulating coating
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23D—ENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
- C23D5/00—Coating with enamels or vitreous layers
- C23D5/10—Coating with enamels or vitreous layers with refractory materials
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets 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
- H01F1/14—Magnets 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets 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
- H01F1/14—Magnets 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
- H01F1/147—Alloys characterised by their composition
- H01F1/14766—Fe-Si based alloys
- H01F1/14775—Fe-Si based alloys in the form of sheets
- H01F1/14783—Fe-Si based alloys in the form of sheets with insulating coating
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
- C21D8/1244—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
- C21D8/1261—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest following hot rolling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Electromagnetism (AREA)
- Power Engineering (AREA)
- Dispersion Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Soft Magnetic Materials (AREA)
- Chemical Treatment Of Metals (AREA)
- Manufacturing Of Steel Electrode Plates (AREA)
- Coating With Molten Metal (AREA)
Abstract
SILICON STEEL AND PROCESSING THEREFORE
ABSTRACT OF THE DISCLOSURE
A process for producing electromagnetic silicon steel having a cube-on-edge orientation and a permeability of at least 1870 (G/Oe) at 10 oersteds, The process includes the steps of: preparing a melt of silicon steel containing from 0.02 to 0.06% carbon, from 0.0006 to 0.0080% boron, up to 0.0100% nitrogen, no more than 0.008% aluminum and from 2.5 to 4.0%
silicon; casting said steel; hot rolling said steel; cold rolling said steel;
decarburizing said steel; applying a refractory oxide coating containing both boron and SiO2; and final texture annealing said steel.
ABSTRACT OF THE DISCLOSURE
A process for producing electromagnetic silicon steel having a cube-on-edge orientation and a permeability of at least 1870 (G/Oe) at 10 oersteds, The process includes the steps of: preparing a melt of silicon steel containing from 0.02 to 0.06% carbon, from 0.0006 to 0.0080% boron, up to 0.0100% nitrogen, no more than 0.008% aluminum and from 2.5 to 4.0%
silicon; casting said steel; hot rolling said steel; cold rolling said steel;
decarburizing said steel; applying a refractory oxide coating containing both boron and SiO2; and final texture annealing said steel.
Description
~86~4 1 The present invention relates to an improvement in the ~ ~.
manufacture of grain-oriented silicon steel.
United States Patent Nos. 3,873,381, 3,905,842, 3,905,843 and 3,957,546 describe processing for producing boron-inhibited grain oriented electromagnetic silic~n steel. Described therein are processes for producing steel of high magnetic quality from boron-bearing silicon steel melts. Through this invention, I now provide a process which improves upon those of f the cited patents~ Speaking broadly, I provide a process which improves llpon those of said patents by incorporating controlled amounts of both boron and SiO2 in the base coating, which is applied prior to the final texture anneal.
- It is accordingly an object of the present invention to provide an improvement in the manufacture of grain-oriented :. silicon steels.
. In accordance with the present invention a melt of silicon steel containing from 0.02 to 0.06~ carbon, from 0.0006 :.
to 0.0080~ boron, up to 0.0100% nitrogen, no more than 0.008%
: aluminum and from 2.5 to 4.0% silicon is subjected to the con-.~ 20 ventional steps of casting, hot rolling, one or more cold ;` rollings, an intermediate normalize when two or more cold rollings are employed, decarburizing, application of a refractory oxide coating and final texture annealing; and to the improvement comprising the steps o~ coating the surface of the steel with a refractory oxide coating consisting essentially of:
~a) 100 parts, by weight, of at least one substance from the group consisting o~ oxides, hydroxides, carbonates ; . and boron compounds of magnesium, calcium~ aluminum and ! .
:~ . titanium;
. 30 (b) up to 100 parts, by weight, of at least one other -- 1 .
.~ . .
r~
. . .
'"' . ' ' , , '; , ' ~ , : . . : , 6~9~
1 substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight of boron;
(c) from 0.5 to A0 parts, by weiyht, of SiO2;
~d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents;
and final texture annealing said steel with said coating thereon.
.
For purposes of definition, "one part" equals the total weight lO of (a~ hereinabove, divided by 100. -~
Specific processing as to the convention steps, is not critical and can be in accordance with that specified in any - number of publications including United States Patent No.
manufacture of grain-oriented silicon steel.
United States Patent Nos. 3,873,381, 3,905,842, 3,905,843 and 3,957,546 describe processing for producing boron-inhibited grain oriented electromagnetic silic~n steel. Described therein are processes for producing steel of high magnetic quality from boron-bearing silicon steel melts. Through this invention, I now provide a process which improves upon those of f the cited patents~ Speaking broadly, I provide a process which improves llpon those of said patents by incorporating controlled amounts of both boron and SiO2 in the base coating, which is applied prior to the final texture anneal.
- It is accordingly an object of the present invention to provide an improvement in the manufacture of grain-oriented :. silicon steels.
. In accordance with the present invention a melt of silicon steel containing from 0.02 to 0.06~ carbon, from 0.0006 :.
to 0.0080~ boron, up to 0.0100% nitrogen, no more than 0.008%
: aluminum and from 2.5 to 4.0% silicon is subjected to the con-.~ 20 ventional steps of casting, hot rolling, one or more cold ;` rollings, an intermediate normalize when two or more cold rollings are employed, decarburizing, application of a refractory oxide coating and final texture annealing; and to the improvement comprising the steps o~ coating the surface of the steel with a refractory oxide coating consisting essentially of:
~a) 100 parts, by weight, of at least one substance from the group consisting o~ oxides, hydroxides, carbonates ; . and boron compounds of magnesium, calcium~ aluminum and ! .
:~ . titanium;
. 30 (b) up to 100 parts, by weight, of at least one other -- 1 .
.~ . .
r~
. . .
'"' . ' ' , , '; , ' ~ , : . . : , 6~9~
1 substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight of boron;
(c) from 0.5 to A0 parts, by weiyht, of SiO2;
~d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents;
and final texture annealing said steel with said coating thereon.
.
For purposes of definition, "one part" equals the total weight lO of (a~ hereinabove, divided by 100. -~
Specific processing as to the convention steps, is not critical and can be in accordance with that specified in any - number of publications including United States Patent No.
2,867,557 and the other patents cited hereinabove. Moreover, the term casting is intended to include continuous casting processes. A hot rolled band heat treatment is also includable :, , within the scope of the present invention. It is howeyer, preferred to cold roll the steel to a thickness no greater than 0.020 inch, without an intermediate anneal between cold rolling passes; from a hot rolled band having a thickness of from about 0.050 to about 0.120 inch. Melts consisting essen~ially of, by weight, 0.02 to 0.06% carbon, 0.015 to 0.15% ~anganese, 0 01 to ! 0-05% of material from the group consisting o sul~ur and ~elenium, 0.0006 to 0.0080~ boron, up ~o 0.0100% nitrogen, ~.5 to 4.0% silicon, up to 1.0% copper, no more than 0.008% aluminum, balance iron, have proven to be particularly adaptable to ~he subject invention. Boron levels are usually in excess of 0.0008%.
Steel produced in accordance with the present invention has a permeability of at least 1870 tG/Oe) at 10 oersteds. Preferably, ' 30 the steel has a permeability of at least 1900 (G/Oe) at 10 ~;
i :' ' - ~.
'' ~ 619~
1 oersteds and a core loss o~ no more than 0.700 watts per pound at 17 kilogauss. ~ ~ ;
The specific mode of applying the coating of the subject invention is not critical thereto. It is just as much within the scope of the subject invention to mix the coating with water and apply it as a slurry, as it is to apply it electrolytically. Like-wise, the constituents which make up the coating can be applied together or as individual layers. It is, however, preferred to ;~
have at laast 0.2%, by weight, of boron and/or at least 3 parts, by weight, of SiO2, in the coating. Boron levels usually do not exceed 15%. They are generally, however, below 5%. Silica levels ' are generally not in excess of 20 parts by weight. The additional inhibiting substances includable with the coating are usually ~ from the group consisting of sulfur, sulfur compounds, nitrogen Z~ compounds, selenium and selenium compounds. Typical sources of Z~ boron are boric acid, fused boric acid (B203), ammonium penta-' ~ -borate and sodium borate. Typical fluxing agents include lithium Zl oxide, sodium oxide and other oxides known to those skilled in the art. Those skllled in the art are, of course, aware o various ways of adding silica. Colloidal silica is, however, preferred.
Also includable as part of the subject invention is the steel in its primary recrystallized state with the coating of the .. i, .
! subject invention adhered thereto. The primary recrystalliæed steel has a thickness no greater than 0.020 inch and is, in accordance with the present invention, suitable for processing into grain oriented silicon steel having a permeability of at least 1870 ~G/Oe) at 10 oersteds. Primary recrystallization takes Z~ place during the final normalize.
'~ ~ 30 The following examples are illustrative of several ., .
!~ aspects of the invention.
Steel produced in accordance with the present invention has a permeability of at least 1870 tG/Oe) at 10 oersteds. Preferably, ' 30 the steel has a permeability of at least 1900 (G/Oe) at 10 ~;
i :' ' - ~.
'' ~ 619~
1 oersteds and a core loss o~ no more than 0.700 watts per pound at 17 kilogauss. ~ ~ ;
The specific mode of applying the coating of the subject invention is not critical thereto. It is just as much within the scope of the subject invention to mix the coating with water and apply it as a slurry, as it is to apply it electrolytically. Like-wise, the constituents which make up the coating can be applied together or as individual layers. It is, however, preferred to ;~
have at laast 0.2%, by weight, of boron and/or at least 3 parts, by weight, of SiO2, in the coating. Boron levels usually do not exceed 15%. They are generally, however, below 5%. Silica levels ' are generally not in excess of 20 parts by weight. The additional inhibiting substances includable with the coating are usually ~ from the group consisting of sulfur, sulfur compounds, nitrogen Z~ compounds, selenium and selenium compounds. Typical sources of Z~ boron are boric acid, fused boric acid (B203), ammonium penta-' ~ -borate and sodium borate. Typical fluxing agents include lithium Zl oxide, sodium oxide and other oxides known to those skilled in the art. Those skllled in the art are, of course, aware o various ways of adding silica. Colloidal silica is, however, preferred.
Also includable as part of the subject invention is the steel in its primary recrystallized state with the coating of the .. i, .
! subject invention adhered thereto. The primary recrystalliæed steel has a thickness no greater than 0.020 inch and is, in accordance with the present invention, suitable for processing into grain oriented silicon steel having a permeability of at least 1870 ~G/Oe) at 10 oersteds. Primary recrystallization takes Z~ place during the final normalize.
'~ ~ 30 The following examples are illustrative of several ., .
!~ aspects of the invention.
3 -. , .
"'` ~ ' ' ~ , .:
;` ~ : . . .. ,, , , . , :
, ~6~9~
Example _I
Samples from ~hree heats (Healts A, B and C) of silicon steel were cast and processed into silicon steel having a cube-on-edge orientation. The chemistry of the heats appears hereinbelow in Table I.
TABLE I
Com osition (wt. %) P
Heat C Mn S B N Si Cu Al Fe A0.031 0.0320.020 0.0011 0.0047 3.15 0.32 0.004 Bal.
lO B0.032 0.036 0.020 0.0013 0.0043 3.15 0.35 0.004 Bal.
C0.030 0.0350.020 0.0013 0.0046 3.15 0.34 0.004 Bal.
Processing for the samples involved soaking at an elevated temperature for several hours, hot rolling to a nominal gage o~ 0.080 inch, hot roll band normalizing at a temperature o approximately 1740F, cold rolling to final gage, decarburizing, coating as described hereinbelow in Table II, and final ~exture annealing at a maximum temperature of 2150F in hydrogen. As for Table II, and in particular the sample identification, the letter referes to the heat and the number -to the sample from that 20 heat. For example, Al refers to Heat A, Sample 1.
TABI,E II
MgO H3BO3 Sample ~Parts, by wt.) (Parts, by wt.) A~, Bl Cl ~ 100 o A2 B2 C2 L00 2.3 (o.496 B) A3 B3 C3 100 4.6 (0.8% B) The samples were tested Eor permeabllity and core loss.
The results of the tests appear hereinbelow in Table III.
:, :
, 30 '~ ' ' ~: ,' : _ _ :
:~ ~
___ _ Permeability Core Loss ( P at 17 KB) Al 1882 0.736 A 1892 0.725 A32 1921 0.668 Bl 1903 0.708 B2 1902 0.708 B3 1927 0.677 Cl 1558 1.27 C2 1891 0.697 C3 1908 0.677 The benefit of boron in the coating is clearly evident j 10 from Table III. Improvement in both permeability and core loss can be attributed thereto. Moreover, Samples A3, B3 and C3, with more than 0.5% boron in the coating, each attained a permeability in excess of 1900 (G/Oe) at 10 oersteds and a core loss below 0.700 watts per pound at 17 kilogauss.
Example II
- Additional groups of samples ~Group 4 through 8) were processed as were Group 1 through 3 samples, with the exception of the coating. The coatings applied to the Group 4 through 8 samples appear hereinbelow in Table IV, along with that applied to the Group 2 and 3 samples.
., .
TABLE IV
I MgO H3BO3 SiO2 ; Sample (Parts, by wt.) (Parts, by wt .L (Parts, by wt.) A2 B2 C2 100 2.3 ~0.4~ B) 0 A4 B4 C4 100 2.3 1.8 A5 B5 C5 100 2.3 3.6 A3 B3 C3 100 4.6 (0.8% B) 0 ~6 B6 C6 100 4.6 1.8 A7 B7 C7 100 4.6 3.6 A8 B8 C8 100 4.6 7.3 The samples were tested for permeability and core loss.
The results of the tests appear hereinbelow in Table V.
, :- .
Permeability Core Loss Sample (at 10 O ) (WPP at 17 KB) e A~ 1892 0.725 .
A4 1899 Q.705 A5 1901 0.702 B2 1902 0.708 : B4 1909 0.706 B5 1923 0.690 C2 1891 0.697 A3 1921 0.668 A6 1933 0.654 A7 1929 0.645 A8 1925 0.654 B3 1927 0.677 B6 1936 0.651 B7 1934 0.655 B8 1928 0.653 C3 1908 0.677 C 191~ 0.660 6 1901 0.649 C781908 0.655 :'', ' ~ 20 ., , ,~ .
1 ' ' :, .
.: :, : . '' , , :
:, .` ' ' :, , , ,~' , .
: . :, , . : .,: , . ,: -61~9~
From Table V, a further improvement in magne',:ic properties i9 attributable to the additlon of SiO~ to the base coating~ SiOz increases permeabilities and decreases core losses. Moreover, as notable from Table VI, hereinbelow SiO2 improves the insulating characteristic of the subject base coating, Table VI lists the Franklin values at 900 psi for the C2, C4 and Cs and C3, C6, C7 and C8 samples; and as known to those skilled in the art, a perfect insulator has a Fr~klin value of 0~ whereas a perfect conductor has a Franklin value of 1 ampere.
' :; . TABLE VI
. Franklin Value - Sample .(at 900 psi) C2 . 0,97 C4 0,96 , . C~ 0, 90 1 5 . , (::3 ~ 93 ~i C6 0,95 C7 0, 90 C8 0,88 `, ~ ` , ` ., .
Note how the Franklin values decrease with increasing SiO2 addition~. Most favorable results were obtained when the coating contained mor e than 3, O parts SiC)~, .1 .
~j It will be apparent to tho9e 9killed in tha art that the novel principles of the invention disclosed hereis~ in connection wîth specific , . ~
examples thereof will suggest variou9 other modification9 and applications of the same, It is accordingly desired th~t in construing the breadth of the ~j appended claims they shall not be limited to the specific examples of the " .
invention described herein, .
1 ` - ?-
"'` ~ ' ' ~ , .:
;` ~ : . . .. ,, , , . , :
, ~6~9~
Example _I
Samples from ~hree heats (Healts A, B and C) of silicon steel were cast and processed into silicon steel having a cube-on-edge orientation. The chemistry of the heats appears hereinbelow in Table I.
TABLE I
Com osition (wt. %) P
Heat C Mn S B N Si Cu Al Fe A0.031 0.0320.020 0.0011 0.0047 3.15 0.32 0.004 Bal.
lO B0.032 0.036 0.020 0.0013 0.0043 3.15 0.35 0.004 Bal.
C0.030 0.0350.020 0.0013 0.0046 3.15 0.34 0.004 Bal.
Processing for the samples involved soaking at an elevated temperature for several hours, hot rolling to a nominal gage o~ 0.080 inch, hot roll band normalizing at a temperature o approximately 1740F, cold rolling to final gage, decarburizing, coating as described hereinbelow in Table II, and final ~exture annealing at a maximum temperature of 2150F in hydrogen. As for Table II, and in particular the sample identification, the letter referes to the heat and the number -to the sample from that 20 heat. For example, Al refers to Heat A, Sample 1.
TABI,E II
MgO H3BO3 Sample ~Parts, by wt.) (Parts, by wt.) A~, Bl Cl ~ 100 o A2 B2 C2 L00 2.3 (o.496 B) A3 B3 C3 100 4.6 (0.8% B) The samples were tested Eor permeabllity and core loss.
The results of the tests appear hereinbelow in Table III.
:, :
, 30 '~ ' ' ~: ,' : _ _ :
:~ ~
___ _ Permeability Core Loss ( P at 17 KB) Al 1882 0.736 A 1892 0.725 A32 1921 0.668 Bl 1903 0.708 B2 1902 0.708 B3 1927 0.677 Cl 1558 1.27 C2 1891 0.697 C3 1908 0.677 The benefit of boron in the coating is clearly evident j 10 from Table III. Improvement in both permeability and core loss can be attributed thereto. Moreover, Samples A3, B3 and C3, with more than 0.5% boron in the coating, each attained a permeability in excess of 1900 (G/Oe) at 10 oersteds and a core loss below 0.700 watts per pound at 17 kilogauss.
Example II
- Additional groups of samples ~Group 4 through 8) were processed as were Group 1 through 3 samples, with the exception of the coating. The coatings applied to the Group 4 through 8 samples appear hereinbelow in Table IV, along with that applied to the Group 2 and 3 samples.
., .
TABLE IV
I MgO H3BO3 SiO2 ; Sample (Parts, by wt.) (Parts, by wt .L (Parts, by wt.) A2 B2 C2 100 2.3 ~0.4~ B) 0 A4 B4 C4 100 2.3 1.8 A5 B5 C5 100 2.3 3.6 A3 B3 C3 100 4.6 (0.8% B) 0 ~6 B6 C6 100 4.6 1.8 A7 B7 C7 100 4.6 3.6 A8 B8 C8 100 4.6 7.3 The samples were tested for permeability and core loss.
The results of the tests appear hereinbelow in Table V.
, :- .
Permeability Core Loss Sample (at 10 O ) (WPP at 17 KB) e A~ 1892 0.725 .
A4 1899 Q.705 A5 1901 0.702 B2 1902 0.708 : B4 1909 0.706 B5 1923 0.690 C2 1891 0.697 A3 1921 0.668 A6 1933 0.654 A7 1929 0.645 A8 1925 0.654 B3 1927 0.677 B6 1936 0.651 B7 1934 0.655 B8 1928 0.653 C3 1908 0.677 C 191~ 0.660 6 1901 0.649 C781908 0.655 :'', ' ~ 20 ., , ,~ .
1 ' ' :, .
.: :, : . '' , , :
:, .` ' ' :, , , ,~' , .
: . :, , . : .,: , . ,: -61~9~
From Table V, a further improvement in magne',:ic properties i9 attributable to the additlon of SiO~ to the base coating~ SiOz increases permeabilities and decreases core losses. Moreover, as notable from Table VI, hereinbelow SiO2 improves the insulating characteristic of the subject base coating, Table VI lists the Franklin values at 900 psi for the C2, C4 and Cs and C3, C6, C7 and C8 samples; and as known to those skilled in the art, a perfect insulator has a Fr~klin value of 0~ whereas a perfect conductor has a Franklin value of 1 ampere.
' :; . TABLE VI
. Franklin Value - Sample .(at 900 psi) C2 . 0,97 C4 0,96 , . C~ 0, 90 1 5 . , (::3 ~ 93 ~i C6 0,95 C7 0, 90 C8 0,88 `, ~ ` , ` ., .
Note how the Franklin values decrease with increasing SiO2 addition~. Most favorable results were obtained when the coating contained mor e than 3, O parts SiC)~, .1 .
~j It will be apparent to tho9e 9killed in tha art that the novel principles of the invention disclosed hereis~ in connection wîth specific , . ~
examples thereof will suggest variou9 other modification9 and applications of the same, It is accordingly desired th~t in construing the breadth of the ~j appended claims they shall not be limited to the specific examples of the " .
invention described herein, .
1 ` - ?-
Claims (11)
1. In a process for producing electromagnetic silicon steel having a cube-on-edge orientation and a permeability of at least 1870 (G/Oe) at 10 oersteds, which process includes the steps of: preparing a melt of silicon steel containing from 0.02 to 0.06% carbon, from 0.0006 to 0.0080% boron, up to 0.0100%
nitrogen, no more than 0.008% aluminum and from 2.5 to 4.0%
silicon; casting said steel; hot rolling said steel; cold rolling said steel; decarburizing said steel; applying a refractory oxide coating to said steel; and final texture annealing said steel; the improvement comprising the steps of coating the surface of said steel with a refractory oxide coating con-sisting essentially of;
(a) 100 parts, by weight, of at least one substance from the group consisting of oxides, hydroxides, carbonates and boron compounds of magnesium, calcium, aluminum and titanium;
(b) up to 100 parts, by weight, of at least one other substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight, of boron;
(c) from 0.5 to 40 parts, by weight, of SiO2;
(d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents;
and final texture annealing said steel with said coating thereon.
nitrogen, no more than 0.008% aluminum and from 2.5 to 4.0%
silicon; casting said steel; hot rolling said steel; cold rolling said steel; decarburizing said steel; applying a refractory oxide coating to said steel; and final texture annealing said steel; the improvement comprising the steps of coating the surface of said steel with a refractory oxide coating con-sisting essentially of;
(a) 100 parts, by weight, of at least one substance from the group consisting of oxides, hydroxides, carbonates and boron compounds of magnesium, calcium, aluminum and titanium;
(b) up to 100 parts, by weight, of at least one other substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight, of boron;
(c) from 0.5 to 40 parts, by weight, of SiO2;
(d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents;
and final texture annealing said steel with said coating thereon.
2. A process according to claim 1, wherein said melt has at least 0.0008% boron.
3. A process according to claim 2, wherein said coating has at least 0 2% by weight, of boron.
4. A process according to claim 2, wherein said coating has at least 3 parts, by weight, of SiO2.
5. A process according to claim 2, wherein said inhibiting substances or compounds thereof are from the group consisting of sulfur, sulfur compounds, nitrogen compounds, selenium and selenium compounds.
6. A process according to claim 2, wherein said hot rolled steel has a thickness of from 0.050 at about 0.120 inch and wherein said hot rolled steel is cold rolled to a thickness of no more than 0.020 inch without an intermediate anneal between cold rolling passes.
7. A process according to claim 1, wherein said melt con-sists essentially of, by weight, 0.02 to 0.06% carbon, 0.015 to 0.15% manganese, 0.01 to 0.05% of material from the group con-sisting of sulfur and selenium, 0.0006 to 0.0080% boron, up to 0.0100% nitrogen, 2.5 to 4.0% silicon, up to 1.0% copper, no more than 0.008% aluminum, balance iron.
8. A process according to claim 7, wherein said melt has at least 0.0008% boron.
9. A process according to claim 1, wherein said steel has a permeability of at least 1900 (G/Oe) at 10 oersteds and a core loss of no more than 0.700 watts per pound at 17 kilogauss.
10. Primary recrystallized steel from a melt consisting essentially of, by weight, 0.02 to 0.06% carbon, 0.015 to 0.15%
manganese, 0.01 to 0.05% of material from the group consisting of sulfur and selenium, 0.0006 to 0.0080% boron, up to 0.0100%
nitrogen, 2.5 to 4.0% silicon, up to 1.0% copper, no more than 0.008% aluminum, balance iron; and having adhered thereto, a coating consisting essentially of:
10. Primary recrystallized steel from a melt consisting essentially of, by weight, 0.02 to 0.06% carbon, 0.015 to 0.15%
manganese, 0.01 to 0.05% of material from the group consisting of sulfur and selenium, 0.0006 to 0.0080% boron, up to 0.0100%
nitrogen, 2.5 to 4.0% silicon, up to 1.0% copper, no more than 0.008% aluminum, balance iron; and having adhered thereto, a coating consisting essentially of:
Claim 10 continued...
(a) 100 parts, by weight, of at least one substance from the group consisting of oxides, hydroxides, carbonates and boron compounds of magnesium, calcium, aluminum and titanium;
(b) up to 100 parts, by weight, of at least one other substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight, of boron;
(c) from 0.5 to 40 parts, by weight, of SiO2;
(d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents.
(a) 100 parts, by weight, of at least one substance from the group consisting of oxides, hydroxides, carbonates and boron compounds of magnesium, calcium, aluminum and titanium;
(b) up to 100 parts, by weight, of at least one other substance from the group consisting of boron and compounds thereof, said coating containing at least 0.1%, by weight, of boron;
(c) from 0.5 to 40 parts, by weight, of SiO2;
(d) up to 20 parts, by weight, of inhibiting substances or compounds thereof; and (e) up to 10 parts, by weight, of fluxing agents.
11. Primary recrystallized steel according to claim 10, having at least 0.0008% boron.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69696576A | 1976-06-17 | 1976-06-17 | |
| US696,965 | 1976-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1086194A true CA1086194A (en) | 1980-09-23 |
Family
ID=24799233
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA280,688A Expired CA1086194A (en) | 1976-06-17 | 1977-06-16 | Silicon steel and processing therefore |
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| Country | Link |
|---|---|
| JP (1) | JPS52153825A (en) |
| AR (1) | AR217648A1 (en) |
| AT (1) | AT363975B (en) |
| AU (1) | AU511231B2 (en) |
| BE (1) | BE855834A (en) |
| BR (1) | BR7703865A (en) |
| CA (1) | CA1086194A (en) |
| CS (1) | CS218567B2 (en) |
| DE (1) | DE2726013A1 (en) |
| ES (1) | ES459890A1 (en) |
| FR (1) | FR2355087A1 (en) |
| GB (1) | GB1565474A (en) |
| HU (1) | HU179103B (en) |
| IN (1) | IN146549B (en) |
| IT (1) | IT1078912B (en) |
| MX (1) | MX4371E (en) |
| PL (1) | PL114605B1 (en) |
| RO (1) | RO71136A (en) |
| SE (1) | SE7707029L (en) |
| YU (1) | YU151477A (en) |
| ZA (1) | ZA773084B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0717959B2 (en) * | 1989-03-30 | 1995-03-01 | 新日本製鐵株式会社 | Method for manufacturing unidirectional high magnetic flux density electrical steel sheet |
| ZA9110113B (en) * | 1990-12-27 | 1993-01-27 | Stone Container Corp | Shipping platform apparatus |
| GB2307917B (en) * | 1995-12-08 | 1999-03-17 | Hitachi Powdered Metals | Manufacturing process of sintered iron alloy improved in machinability,mixed powder for manufacturing modification of iron alloy and iron alloy product |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2809137A (en) * | 1954-12-02 | 1957-10-08 | Gen Electric | Insulating coating for magnetic sheet material and method of making the same |
| DE1954773C3 (en) * | 1968-11-01 | 1974-02-28 | Yawata Iron & Steel Co., Ltd., Tokio | Process for the production of single grain oriented silicon steel sheets with high magnetic induction and low iron loss |
| BE754777A (en) * | 1969-08-18 | 1971-02-12 | Morton Int Inc | COMPOSITION OF COATING BASED ON MAGNESIUM OXIDE AND PROCEDURE FOR USING THIS COMPOSITION |
| US3873381A (en) * | 1973-03-01 | 1975-03-25 | Armco Steel Corp | High permeability cube-on-edge oriented silicon steel and method of making it |
| US3945862A (en) * | 1973-06-26 | 1976-03-23 | Merck & Co., Inc. | Coated ferrous substrates comprising an amorphous magnesia-silica complex |
| SE7703456L (en) * | 1976-04-15 | 1977-10-16 | Gen Electric | THILE PLATE OF IRON IRON WITH ADDITIONAL ADDITION AND PROCEDURE FOR MANUFACTURE THEREOF |
-
1977
- 1977-05-23 ZA ZA00773084A patent/ZA773084B/en unknown
- 1977-05-25 IN IN789/CAL/77A patent/IN146549B/en unknown
- 1977-05-26 AU AU25523/77A patent/AU511231B2/en not_active Expired
- 1977-06-08 DE DE19772726013 patent/DE2726013A1/en not_active Withdrawn
- 1977-06-14 GB GB24711/77A patent/GB1565474A/en not_active Expired
- 1977-06-14 AT AT0419877A patent/AT363975B/en active
- 1977-06-15 PL PL1977198882A patent/PL114605B1/en unknown
- 1977-06-15 BR BR7703865A patent/BR7703865A/en unknown
- 1977-06-15 IT IT49833/77A patent/IT1078912B/en active
- 1977-06-15 HU HU77AE495A patent/HU179103B/en unknown
- 1977-06-16 SE SE7707029A patent/SE7707029L/en unknown
- 1977-06-16 FR FR7718531A patent/FR2355087A1/en active Granted
- 1977-06-16 MX MX775816U patent/MX4371E/en unknown
- 1977-06-16 CA CA280,688A patent/CA1086194A/en not_active Expired
- 1977-06-17 ES ES459890A patent/ES459890A1/en not_active Expired
- 1977-06-17 RO RO7790738A patent/RO71136A/en unknown
- 1977-06-17 BE BE178559A patent/BE855834A/en not_active IP Right Cessation
- 1977-06-17 AR AR268108A patent/AR217648A1/en active
- 1977-06-17 YU YU01514/77A patent/YU151477A/en unknown
- 1977-06-17 JP JP7197677A patent/JPS52153825A/en active Pending
- 1977-06-17 CS CS774018A patent/CS218567B2/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL114605B1 (en) | 1981-02-28 |
| BE855834A (en) | 1977-12-19 |
| JPS52153825A (en) | 1977-12-21 |
| MX4371E (en) | 1982-04-19 |
| HU179103B (en) | 1982-08-28 |
| FR2355087A1 (en) | 1978-01-13 |
| RO71136A (en) | 1982-02-01 |
| SE7707029L (en) | 1977-12-18 |
| CS218567B2 (en) | 1983-02-25 |
| ZA773084B (en) | 1978-04-26 |
| ATA419877A (en) | 1981-02-15 |
| PL198882A1 (en) | 1978-02-13 |
| BR7703865A (en) | 1978-05-02 |
| FR2355087B1 (en) | 1982-07-16 |
| ES459890A1 (en) | 1978-11-16 |
| YU151477A (en) | 1982-08-31 |
| AT363975B (en) | 1981-09-10 |
| DE2726013A1 (en) | 1977-12-29 |
| AU2552377A (en) | 1978-11-30 |
| GB1565474A (en) | 1980-04-23 |
| AR217648A1 (en) | 1980-04-15 |
| AU511231B2 (en) | 1980-08-07 |
| IN146549B (en) | 1979-07-14 |
| IT1078912B (en) | 1985-05-08 |
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