EP2775007B1 - Verfahren zur Herstellung eines kornorientierten elektrischen Stahls - Google Patents

Verfahren zur Herstellung eines kornorientierten elektrischen Stahls Download PDF

Info

Publication number
EP2775007B1
EP2775007B1 EP13158409.6A EP13158409A EP2775007B1 EP 2775007 B1 EP2775007 B1 EP 2775007B1 EP 13158409 A EP13158409 A EP 13158409A EP 2775007 B1 EP2775007 B1 EP 2775007B1
Authority
EP
European Patent Office
Prior art keywords
strip
annealing
temperature
process according
hot rolled
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.)
Not-in-force
Application number
EP13158409.6A
Other languages
English (en)
French (fr)
Other versions
EP2775007A1 (de
Inventor
Herbert Kreuzer
Stefano Cicalé
Luciano Albini
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Voestalpine Stahl GmbH
Original Assignee
Voestalpine Stahl GmbH
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Voestalpine Stahl GmbH filed Critical Voestalpine Stahl GmbH
Priority to EP13158409.6A priority Critical patent/EP2775007B1/de
Publication of EP2775007A1 publication Critical patent/EP2775007A1/de
Application granted granted Critical
Publication of EP2775007B1 publication Critical patent/EP2775007B1/de
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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
    • C21D8/00Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • 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
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/004Very low carbon steels, i.e. having a carbon content of less than 0,01%
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/008Ferrous alloys, e.g. steel alloys containing tin
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/16Ferrous alloys, e.g. steel alloys containing copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/60Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur

Definitions

  • the present invention relates to a process for the production of grain oriented electrical steel, particularly grain oriented steel strips to be used for cores in transformers and other electrical machines.
  • JP2009228118 discloses a method for manufacturing a grain-oriented electrical steel sheet with secondary-recrystallization annealing performed after primary-recrystallization annealing process takes place, followed by continuous-type finish annealing.
  • the "low heating rate" "high soaking temperature” batch annealing during which secondary recrystallization is performed constitutes a high time-consumption and high cost in the known CRGO production process.
  • the final product in which the steel strips manufactured according to the process of the invention are intended to be employed as core material has a maximum core loss at 1.7 T and 50 Hz (P 17/50 ) of ⁇ 2 W/kg and/or a magnetic polarization at 800 A/m (J 800 ) of > 1.7 T.
  • the thickness of such strips is typically in the range of 0.23 - 0.35 mm.
  • a process for the manufacturing of a grain oriented electrical steel strip comprising the steps of: a) providing a hot rolled strip comprising in weight %: C ⁇ 0.006 preferably ⁇ 0.003 Si 3.0 - 3.5 preferably 3.1-3.3 Mn 0.4 - 2.0 preferably 0.45 - 0.65 Als 0.005-0.03 preferably 0.01-0.02 N 0.004 - 0.009 preferably 0.005 - 0.008 S ⁇ 0.008 preferably ⁇ 0.005 Ti ⁇ 0.006 preferably ⁇ 0.004 optionally one or more of Cu 0.05 - 0.3 Sn 0.04-0.15 Ni ⁇ 0.1 preferably ⁇ 0.05 Cr ⁇ 0.2 preferably ⁇ 0.05 P ⁇ 0.02 preferably ⁇ 0.01 B ⁇ 0.01 preferably 0.001 - 0.005 Te ⁇ 0.01 preferably ⁇ 0.005 Cd ⁇ 0.01 preferably ⁇ 0.005 Zn ⁇ 0.01 preferably ⁇ 0.005 As ⁇ 0.01
  • the new and efficient process results in a final product typically having a maximum core loss at 1.7 T at a strip thickness of 0.30 mm and 50 Hz (P 17/50 ) of ⁇ 2 W/kg and a magnetic polarization at 800 A/m (J 800 ) of > 1.7 T.
  • Key features of the inventive process includes the provision of a hot rolled strip having a carefully balance composition, in particular a very low carbon content.
  • a decarburization annealing need not be performed during the transformation process of the hot rolled strip down to finished product.
  • a further key feature is that the final annealing during which the secondary recrystallization happens is divided in two steps:
  • This two step annealing allows the possibility of finalizing the recrystallization annealing in the continuous annealing line if not already completed during the batch annealing.
  • the drawing schematically illustrates a process line for the manufacturing of a grain oriented electrical steel strip according to the invention.
  • the steel composition of the hot rolled band is defined in claim 1.
  • the carbon level is closely reflected in the carbon level of the secondary recrystallized strip since the process dispenses with any deliberate intermediate decarburization annealing. For this reason it is of the utmost importance to control the carbon content during steelmaking such that the carbon content is less than 30 ppm (0.003 wt. %) in the melt to be cast.
  • the inhibition to control the secondary recrystallization is mainly based on the precipitation of AlN. Accordingly, the content of Al and N should be controlled such that AlN is dissolved during slab reheating, precipitation is minimized or avoided during hot rolling but occur during the annealing of the strip performed at intermediate thickness. For best result the contents of Als (acid soluble Al) and N are controlled such that the ratio Als/N is stoichiometric. However, from a practical point of view ⁇ 35 % of the stoichiometric ratio or preferably within ⁇ 15 % of the stoichiometric ratio can be tolerated.
  • the sulfur content should be maintained at a low level in order to avoid undue precipitation of MnS.
  • the content should be less than 30 ppm, preferably less than 20 ppm and most preferred less than 10 ppm.
  • the manganese content is maintained at 0.4 - 2 % in order to increase the resistivity of the alloy and thereby decreasing the core loss.
  • the content of titanium should also be closely controlled since Ti is a strong nitride former. Ti enters the steel melt from the raw materials used in iron- and steelmaking. Accordingly, the ladle slag is normally to be skimmed after tapping and FeSi having a low Ti-content should be used.
  • the content of Ti should be less than 0.006 % , preferably less than 0.004% or even less than 0.0020% (20 ppm).
  • AlN In addition to AlN other inhibitors may be used to assist the control.
  • Other possible elements that may be present are defined in claim 1. It may be noted that in some cases these elements are present as impurities. Cu and Sn may be added, typical in an amount of 0.1 %. As, Pb, P and Zn may be added as defined in claim 1. However, preferably, the total amount of these elements is less than 0.2%, in particular less than 0.05%. B, Ni, Cr, Te and Cd may be present as defined in claim 1. However, in most cases it is preferred that the total amount of these elements is restricted to 0.30%. Bismuth, when used, need to be present in an amount of at least 5 ppm in order to provide an effect. However, if the content is higher than 20 ppm brittleness problems may occur.
  • reference numeral I represents a section for the provision of a steel alloy having the adequate chemical composition prepared for cold rolling, and of a hot rolled strip of the steel alloy according to a) and b) in the foregoing while reference numeral II represents a section for cold rolling of the hot rolled steel strip and for heat treatment of the strip in connection therewith according to c), d) and e) in the foregoing.
  • molten steel is manufactured in a mode, which principles may be conventional per se, by means a complex of iron and steel manufacturing facilities which also may be conventional such as a number of the following ones: blast furnace, LD converter, electric arc furnace, VOD, RH degasser and others.
  • blast furnace LD converter
  • electric arc furnace VOD
  • RH degasser any chosen combination of apparatuses for making molten steel is symbolically represented by complex 1.
  • the continuously cast strand 4 is successively cut to slabs 5 which are reheated in a walking beam furnace 6 to a temperature of between 1220 and 1300 °C, suitably to a temperature of about 1260 °C.
  • a series of induction heating devices locally reheat the slabs eliminating any skid mark effect.
  • each reheated slab 5 is subjected to roughing at > 1200 °C in a roughing facility 7 in order to produce a plate or bar having a thickness of 20 - 80 mm.
  • the plate or bar is hot rolled in a hot rolling mill 8 to form a strip 9 with a thickness of 1.5 - 4 mm, preferably 2 - 3 mm or 2 - 2.5 mm.
  • the starting temperature of the hot rolling in the hot rolling mill 8 is > 920 °C, preferably 950 - 1200 °C, and most preferable 970 - 1150 °C, while the finish rolling temperature is > 850 °C.
  • the hot rolled steel strip is cooled at a rate of 5 - 100 °C/s down to a coiling temperature ⁇ 600 °C and coiled at that temperature.
  • the hot rolled strip is passed through a scale breaker (not shown), pickled in the pickling unit 10 and optionally annealed (not shown).
  • pickling may be performed in sulphuric acid at a concentration of 235-245 g/l, which is regenerated by crystallization and centrifugation.
  • the pickling time can be varied in the range 20 - 60 seconds. After pickling, the strip is trimmed and recoiled.
  • the hot rolled strip is cold rolled in a cold rolling mill 12 to an intermediate thickness of 0.38 - 1.2 mm, preferably to 0.5 - 1.0 mm. Then, the cold rolled strip having said intermediate thickness is subjected to continuous intermediate annealing in a continuous type annealing furnace 13 at a temperature of 850 - 1000 °C, preferably at 880 - 930 °C, such that the cold rolled strip material is recrystallized.
  • the atmosphere in the annealing furnace may be 100 % hydrogen or a mixture of hydrogen and nitrogen.
  • the recrystallized strip is cooled and then cold rolled a second time in cold rolling mill 12, now with a reduction rate of 40 - 70 % to a final thickness of 0.23 - 0.35 mm.
  • the temperature of the strip is maintained in the range of 80 - 400 °C, preferably in the range of 100 - 200 °C.
  • the cold rolled strip is now prepared to be annealed to provoke secondary recrystallization.
  • the annealing is performed in two steps according to the invention.
  • the final microstructure is obtained by secondary recrystallization annealing, which is incubated at low temperature in the batch annealing furnace and may subsequently be completed by the continuous annealing at high temperature, if not already completely recrystallized after batch annealing.
  • the cold rolled and coiled strip 15 having said final thickness is batch annealed in a batch annealing furnace 16 by heating the strip at a rate of less than 200 °C/h to a holding temperature of 860 - 950 °C and holding the strip at that temperature for a period of time of 2 - 20 hours.
  • the batch annealing is preferably performed in an atmosphere of dry hydrogen.
  • an annealing separator in particular a MgO powder layer is built on the strip surface before entering the batch annealing furnace in order to prevent sticking.
  • the atmosphere of the continuous intermediate annealing performed in a continuous type annealing furnace 13 contains water so that the water partial pressure and hydrogen partial pressure is in the range 0.1-0.7. Due to this presence of water an oxide layer, which is composed of Silica, Fayalite and Iron Oxide, adherent to the strip surface is built on the strip surface.
  • the cold rolled and batch annealed strip 17 is continuously annealed at a temperature of 800-1200 °C for 30 - 600 seconds in a continuous annealing furnace 18 in an atmosphere preferably consisting of dry hydrogen or dry hydrogen/nitrogen mixture.
  • the continuous annealing mainly effects thermo-flattening and the temperature may be in the range of 800-950 °C.
  • the secondary recrystallization is to be completed during this step, then it is better to perform the continuous annealing in the range of 950-1200 °C, preferably 1050-1150 °C.
  • the process further includes coating the continuously annealed strip 19 with an organic or inorganic coating as an annealing separator, optionally with tensioning properties and curing the strip for more than 20 seconds at a temperature exceeding 150 °C in a continuous curing furnace 20 before coiling. Due to the invention as described in this patent specification and claims, the final product will have a maximum core loss at 1.7 T and 50 Hz (P 17/50 ) of ⁇ 2 W/kg and/or a magnetic polarization at 800 A/m (J 800 ) of > 1.7 T.
  • the final annealing temperature may be optimized according to the starting rolling temperature.
  • the starting finishing rolling temperature is ⁇ 1050°C then the final annealing as specified in point g) of claim 1 can be performed with a soaking temperature laying in the lower part of said range.
  • the temperature could be in the range of 800-950 °C, preferably 860-950° because an annealing temperature above 950°C does not improve the final characteristics of the material but it increases the consumption of energy necessary to perform the annealing.
  • the starting finishing rolling temperature is higher than 1050°C then the final annealing temperature specified in point g) of claim 1 should be the upper part of said.
  • the temperature should in this case be in the range of 950°C-1200°C, preferably in the range of 1050°C-1150°C.
  • the final annealing optimal temperature range varies depending on the starting rolling temperature is not completely clear but it would appear that when the starting rolling temperature is below 1050°C then the secondary recrystallization is virtually completed during the low temperature batch annealing. In this case, the final annealing is necessary only for performing thermo-flattening of the steel strip when the batch annealing is performed with the strip wound in a coil.
  • a steel with a chemical composition as reported in Table 1 has been cast to form a slab, slab has been reheated at 1260 °C temperature, and hot rolled.
  • a steel with a chemical composition as reported in Table 3 has been cast, slab have been treated at 1250 °C slab reheating temperature and hot rolled.
  • - Samples after hot rolling have been cold rolled down to 0,70 mm intermediate thickness.
  • - Samples at intermediate thickness have been annealed at 900°C for 100 sec.
  • - Annealed samples have been cold rolled down to final thickness of 0,30 mm.
  • - Cold rolled samples at final thickness have been subjected to batch annealing with the following cycle: Heating from 25°C to 900 °C in 12 h; holding at 900 °C for 10 h; cooling from 900 °C to 25 °C in 18 h.
  • a steel with a chemical composition as reported in Table 5 has been cast in 3 different slabs: a, b, c. Cast slabs have been reheated at A:1210 °C, B:1240 °C and C:1260 °C, and hot rolled.
  • a steel with a chemical composition as reported in Table 9 has been cast in 2 different slabs: a, b. Cast slabs have been reheated at 1240 °C and hot rolled, after roughing, with two different starting finishing rolling temperature:
  • Samples after hot rolling have been cold rolled down to 0,70 mm intermediate thickness. Samples at intermediate thickness have been annealed at 900°C for 100 sec.
  • Annealed samples have been cold rolled down to final thickness of 0,30 mm and have been undergone to batch annealing with following cycle: heating from 25°C to 900°C in 6 h ; holding at 900°C for 10 h; cooling from 900°C to 25°C in 18 h.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Electromagnetism (AREA)
  • Manufacturing & Machinery (AREA)
  • Manufacturing Of Steel Electrode Plates (AREA)

Claims (15)

  1. Prozess für die Herstellung eines kornorientierten elektrischen Stahlbandes, der die folgenden Schritte umfasst:
    a) Bereitstellen eines warmgewalzten Bandes, das in Gewichtsprozent enthält: C < 0, 006 vorzugsweise < 0,003 Si 3, 0 - 3,5 vorzugsweise 3,1 - 3,3 Mn 0,4 - 2, 0 vorzugsweise 0,45 - 0,65 Als 0,005 - 0,03 vorzugsweise 0,01 - 0,02 N 0,004 - 0,009 vorzugsweise 0,005 - 0,008 S < 0,008 vorzugsweise <0,005 Ti < 0,006 vorzugsweise <0,004
    optional eine oder mehrere von folgenden Cu 0,05 - 0,3 Sn 0,04 - 0,15 Ni < 0,1 vorzugsweise < 0,05 Cr < 0,2 vorzugsweise < 0,05 P < 0,02 vorzugsweise < 0,01 B < 0,01 vorzugsweise 0,001 - 0,005 Te < 0,01 vorzugsweise < 0,005 Cd < 0,01 vorzugsweise < 0,005 Zn < 0,01 vorzugsweise < 0,005 As < 0,01 vorzugsweise < 0,005 Pb < 0,01 vorzugsweise < 0,005 Bi < 0,002 vorzugsweise 0,0005 - 0,002
    Abgleichen von Fe mit Verunreinigungen, wobei Als säurelösliches Aluminium ist,
    b) optional Tempern und/oder Beizen des warmgewalzten Streifens,
    c) Kaltwalzen des warmgewalzten Streifens auf eine Zwischendicke,
    d) Tempern des kaltgewalzten Streifens, um den kaltgewalzten Streifen zu rekristallisieren,
    e) Kaltwalzen des rekristallisierten Streifens auf eine endgültige Dicke,
    f) Haubenglühen des kaltgewalzten Streifens, der die Enddicke hat, vorzugsweise durch Erwärmen des Streifens mit einer Rate von ≤ 200 °C/h auf eine Haltetemperatur innerhalb des Bereichs von 860 - 950 °C und Halten des Streifens auf solch einer Temperatur für 2 - 20 h,
    g) kontinuierliches Tempern des stapelgetemperten Streifens bei einer Temperatur von 800 - 1200 °C über eine Zeit von 30 - 600 s.
  2. Prozess nach Anspruch 1, wobei die Zwischendicke des Streifens in Schritt c) 0,38 - 1,2 mm, vorzugsweise 0,5 - 1,0 mm beträgt.
  3. Prozess nach Anspruch 1 oder 2, wobei der Streifen in Schritt e) mit einer Reduktionsrate von 40 - 70 % bis zu einer Enddicke von 0,23 - 0,35 mm kaltgewalzt wird.
  4. Prozess nach einem der vorherigen Ansprüche, wobei die Temper-Temperatur in Schritt d) 850 - 1000 °C, vorzugsweise 880 - 930 °C beträgt.
  5. Prozess nach einem der vorherigen Ansprüche, wobei die Zusammensetzung des warmgewalzten Streifens zumindest eine der folgenden Anforderungen erfüllt: C < 0,003 vorzugsweise < 0,002 Si 3,0 - 3,5 vorzugsweise 3,1 - 3,3 Mn 0,4 - 1,0 vorzugsweise 0,45 - 0,65 Als 0,012 - 0,017 vorzugsweise 0,014 - 0,016 N 0,005 - 0,008 vorzugsweise 0,006 - 0,007 S < 0,003 vorzugsweise < 0,002 Ti < 0,004 vorzugsweise < 0,002
    optional eine oder mehrere von folgenden Cu 0,08 - 0,12 Sn 0,08 - 0,12 Ni < 0,04 vorzugsweise < 0,01 Cr < 0,04 vorzugsweise < 0,01 P < 0,015 vorzugsweise < 0,01 B < 0,005 vorzugsweise 0,001 - 0,002 Te < 0,01 vorzugsweise < 0,005 Cd < 0,01 vorzugsweise < 0,005 Zn < 0.01 vorzugsweise < 0,005 As < 0,01 vorzugsweise < 0,005 Pb < 0,01 vorzugsweise < 0,005 Bi < 0,002 vorzugsweise 0,0005 - 0,002
  6. Prozess nach einem der vorherigen Ansprüche, wobei die Temperatur des Streifens während eines oder beider Schritte aus den Kaltwalzschritten c) bzw. e) im Bereich von 80 - 400 °C, vorzugsweise 100 - 200 °C gehalten wird.
  7. Prozess nach einem der vorherigen Ansprüche, wobei der Schritt des Bereitstellens des warmgewalzten Streifens einen der Schritte Gießen von Blöcken, kontinuierliches Brammengießen, Dünnbrammengießen oder Bandgießen umfasst.
  8. Prozess nach einem der vorherigen Ansprüche, wobei der Schritt a) des Bereitstellens eines warmgewalzten Streifens einen oder mehrere der Schritte kontinuierliches Gießen einer Bramme, Wiedererwärmen der Bramme auf T > 1220 °C, Schruppen der Bramme bei > 1100 °C, um eine Stange zu erzeugen, die eine Dicke von 20 - 80 mm hat, und Warmwalzen der Stange umfasst, um den warmgewalzten Streifen herzustellen.
  9. Prozess nach Anspruch 8, wobei die Anfangstemperatur des Warmwalzens > 920 °C, vorzugsweise 950 - 1200 °C, vorzugsweise 970 °C - 1150 °C beträgt, und wobei die Fertigwalztemperatur > 850 C ist.
  10. Prozess nach Anspruch 9, wobei die Anfangstemperatur des Warmwalzens niedriger als 1050 °C ist und/oder das kontinuierliche Tempern, das in Punkt g) von Anspruch 1 definiert wurde, bei einer Temperatur im Bereich 800 - 950 °C ausgeführt wird.
  11. Prozess nach Anspruch 9, wobei die Anfangstemperatur des Warmwalzens höher als 1050 °C ist und/oder das kontinuierliche Tempern, das in Punkt g) von Anspruch 1 definiert wurde, im Bereich 950 - 1200 °C und vorzugsweise im Bereich 1050 - 1150 °C liegt.
  12. Prozess nach einem der Ansprüche 8, 9, 10 oder 11, wobei das warmgewalzte Stahlband mit einer Rate von 5 - 100 °C/s bis auf eine Wickeltemperatur von < 600 °C abgekühlt und bei dieser Temperatur aufgewickelt wird.
  13. Prozess nach einem der vorherigen Ansprüche, wobei das warmgewalzte Band eine Dicke von 1,5 - 4 mm, vorzugsweise 2 - 3 mm hat.
  14. Prozess nach einem der vorherigen Ansprüche, wobei der Gehalt an Als und N so gesteuert wird, dass das Verhältnis Als/N innerhalb von ± 35 % des stöchiometrischen Verhältnisses, vorzugsweise innerhalb von ± 15 % des stöchiometrischen Verhältnisses ist.
  15. Prozess nach einem der vorherigen Ansprüche, wobei der Prozess ferner mindestens einen der folgenden Schritte umfasst: Beschichten des kontinuierlich getemperten Bandes, das in Schritt g) erhalten wurde, mit einer organischen oder anorganischen Beschichtung als Glühseparator, optional mit Spanneigenschaften und Härtung bei > 150 °C über > 20 s.
EP13158409.6A 2013-03-08 2013-03-08 Verfahren zur Herstellung eines kornorientierten elektrischen Stahls Not-in-force EP2775007B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP13158409.6A EP2775007B1 (de) 2013-03-08 2013-03-08 Verfahren zur Herstellung eines kornorientierten elektrischen Stahls

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP13158409.6A EP2775007B1 (de) 2013-03-08 2013-03-08 Verfahren zur Herstellung eines kornorientierten elektrischen Stahls

Publications (2)

Publication Number Publication Date
EP2775007A1 EP2775007A1 (de) 2014-09-10
EP2775007B1 true EP2775007B1 (de) 2018-12-05

Family

ID=47843143

Family Applications (1)

Application Number Title Priority Date Filing Date
EP13158409.6A Not-in-force EP2775007B1 (de) 2013-03-08 2013-03-08 Verfahren zur Herstellung eines kornorientierten elektrischen Stahls

Country Status (1)

Country Link
EP (1) EP2775007B1 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6337967B2 (ja) 2014-09-01 2018-06-06 新日鐵住金株式会社 方向性電磁鋼板
RU2695736C1 (ru) * 2015-10-26 2019-07-25 Ниппон Стил Корпорейшн Электротехнический стальной лист с ориентированной зеренной структурой и обезуглероженный стальной лист, используемый для его производства
KR101675318B1 (ko) * 2015-12-21 2016-11-11 주식회사 포스코 방향성 전기강판 및 이의 제조방법
CN106298221B (zh) * 2016-08-30 2018-01-30 河南中岳非晶新型材料股份有限公司 非晶体抗直流铁芯及其热处理方法
CN108277429B (zh) * 2017-01-05 2020-01-07 鞍钢股份有限公司 一种高硅电工钢的生产方法
JP6911596B2 (ja) * 2017-07-13 2021-07-28 日本製鉄株式会社 皮膜密着性に優れる一方向性電磁鋼板及びその製造方法
JP6911597B2 (ja) * 2017-07-13 2021-07-28 日本製鉄株式会社 皮膜密着性に優れる一方向性珪素鋼板及びその製造方法
KR102410519B1 (ko) * 2017-07-25 2022-06-17 현대자동차주식회사 연속 소둔 설비

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2287467A (en) 1940-01-03 1942-06-23 American Rolling Mill Co Process of producing silicon steel
JPH08134542A (ja) * 1994-11-08 1996-05-28 Sumitomo Metal Ind Ltd 打抜き性に優れた方向性電磁鋼板の製造方法
DE69515892T3 (de) * 1994-11-16 2005-10-20 Nippon Steel Corp. Verfahren zur herstellung eines elektrisch direktionalen bleches mit guter glasbeschichtbarkeit und hervorragenden magnetischen eigenschaften
BR9800978A (pt) 1997-03-26 2000-05-16 Kawasaki Steel Co Chapas elétricas de aço com grão orientado tendo perda de ferro muito baixa e o processo de produção da mesma
JPH10273725A (ja) * 1997-03-31 1998-10-13 Sumitomo Metal Ind Ltd 方向性電磁鋼板の製造方法
US6309473B1 (en) * 1998-10-09 2001-10-30 Kawasaki Steel Corporation Method of making grain-oriented magnetic steel sheet having low iron loss
EP0997540B1 (de) * 1998-10-27 2004-04-28 JFE Steel Corporation Elektrostahlblech und dessen Herstellungsverfahren
JP4123653B2 (ja) * 1999-10-12 2008-07-23 Jfeスチール株式会社 方向性電磁鋼板の製造方法
EP1279747B1 (de) * 2001-07-24 2013-11-27 JFE Steel Corporation Verfahren zur Herstellung von kornorientierten Elektrostahlblechen
JP4258349B2 (ja) 2002-10-29 2009-04-30 Jfeスチール株式会社 方向性電磁鋼板の製造方法
JP5194927B2 (ja) * 2008-03-25 2013-05-08 Jfeスチール株式会社 方向性電磁鋼板の製造方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
EP2775007A1 (de) 2014-09-10

Similar Documents

Publication Publication Date Title
EP2775007B1 (de) Verfahren zur Herstellung eines kornorientierten elektrischen Stahls
US5643370A (en) Grain oriented electrical steel having high volume resistivity and method for producing same
EP2470679B1 (de) Verfahren zur herstellung eines kornorientierten elektrischen stahlstreifen
JP6844125B2 (ja) 方向性電磁鋼板の製造方法
EP2876173B1 (de) Verfahren zur herstellung kornorientierter elektrobleche
EP2880190B1 (de) Verfahren zur herstellung von kornorientiertem siliciumstahlblech, kornorientiertem elektrostahlblech und verwendung davon
RU2391416C1 (ru) Способ производства листа текстурированной электротехнической стали с высокой плотностью магнитного потока
CN105274427A (zh) 一种高磁感取向硅钢及生产方法
JP7312249B2 (ja) 二方向性電磁鋼板およびその製造方法
JPH0686631B2 (ja) 磁束密度の高い一方向性電磁鋼板の製造方法
JP2883226B2 (ja) 磁気特性の極めて優れた薄方向性けい素鋼板の製造方法
JP2023507437A (ja) 二方向性電磁鋼板およびその製造方法
KR20150073802A (ko) 방향성 전기강판 및 그 제조방법
KR20200035755A (ko) 방향성 전기강판 및 그의 제조방법
US5425820A (en) Oriented magnetic steel sheets and manufacturing process therefor
US4371405A (en) Process for producing grain-oriented silicon steel strip
KR950009760B1 (ko) 방향성 규소강판의 제조방법
JPH0949023A (ja) 鉄損が優れた一方向性電磁鋼板の製造方法
JP2023508294A (ja) 無方向性電磁鋼板およびその製造方法
JPH0419297B2 (de)
JP3921807B2 (ja) 方向性珪素鋼板の製造方法
JPH08279408A (ja) 磁気特性が優れた一方向性電磁鋼板の製造方法
KR950014313B1 (ko) 소량의 보론첨가로 입자-방향성 규소강을 제조하는 방법
KR102319831B1 (ko) 방향성 전기강판의 제조방법
JP4261633B2 (ja) 一方向性電磁鋼板の製造方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20130308

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

R17P Request for examination filed (corrected)

Effective date: 20141209

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

17Q First examination report despatched

Effective date: 20150202

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602013047671

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C22C0038020000

Ipc: C22C0038000000

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: C22C 38/06 20060101ALI20180628BHEP

Ipc: C22C 38/02 20060101ALI20180628BHEP

Ipc: C21D 8/12 20060101ALI20180628BHEP

Ipc: C22C 38/00 20060101AFI20180628BHEP

Ipc: C21D 9/46 20060101ALI20180628BHEP

Ipc: C22C 38/16 20060101ALI20180628BHEP

Ipc: C22C 38/04 20060101ALI20180628BHEP

INTG Intention to grant announced

Effective date: 20180725

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1073149

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181215

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602013047671

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1073149

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181205

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190305

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190305

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190306

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190405

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190405

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602013047671

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

26N No opposition filed

Effective date: 20190906

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190308

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190331

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190331

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190308

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20200327

Year of fee payment: 8

Ref country code: SE

Payment date: 20200327

Year of fee payment: 8

Ref country code: FI

Payment date: 20200327

Year of fee payment: 8

Ref country code: DE

Payment date: 20200327

Year of fee payment: 8

Ref country code: NL

Payment date: 20200326

Year of fee payment: 8

Ref country code: IT

Payment date: 20200323

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190308

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20200325

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20130308

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602013047671

Country of ref document: DE

REG Reference to a national code

Ref country code: FI

Ref legal event code: MAE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210308

REG Reference to a national code

Ref country code: NL

Ref legal event code: MM

Effective date: 20210401

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20210308

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20211001

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210309

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210331

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210308

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210401

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210308

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205