EP0750049A1 - Ferritic steel and its manufacture and use - Google Patents
Ferritic steel and its manufacture and use Download PDFInfo
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- EP0750049A1 EP0750049A1 EP96107884A EP96107884A EP0750049A1 EP 0750049 A1 EP0750049 A1 EP 0750049A1 EP 96107884 A EP96107884 A EP 96107884A EP 96107884 A EP96107884 A EP 96107884A EP 0750049 A1 EP0750049 A1 EP 0750049A1
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 50
- 239000010959 steel Substances 0.000 title claims abstract description 50
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 25
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 15
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 10
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 8
- 229910000859 α-Fe Inorganic materials 0.000 claims abstract description 8
- 229910000734 martensite Inorganic materials 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 6
- 229910001566 austenite Inorganic materials 0.000 claims abstract description 4
- 229910001563 bainite Inorganic materials 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- 239000011572 manganese Substances 0.000 claims description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 12
- 238000005098 hot rolling Methods 0.000 claims description 12
- 238000001816 cooling Methods 0.000 claims description 11
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000011651 chromium Substances 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 230000005496 eutectics Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 description 10
- 229910001562 pearlite Inorganic materials 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910001568 polygonal ferrite Inorganic materials 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000282983 Capreolus capreolus Species 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 241000219307 Atriplex rosea Species 0.000 description 1
- 229910001035 Soft ferrite Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- OSMSIOKMMFKNIL-UHFFFAOYSA-N calcium;silicon Chemical compound [Ca]=[Si] OSMSIOKMMFKNIL-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- VCTOKJRTAUILIH-UHFFFAOYSA-N manganese(2+);sulfide Chemical class [S-2].[Mn+2] VCTOKJRTAUILIH-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 210000002105 tongue Anatomy 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Images
Classifications
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- 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
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- 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
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0226—Hot rolling
-
- 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
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/001—Austenite
-
- 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/002—Bainite
-
- 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/005—Ferrite
-
- 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
Definitions
- the invention relates to a ferritic steel, a method for producing this steel with a predominantly polygonal-ferritic structure and one or more carbon-enriched second phases, and a preferred use of this steel.
- the steel should have high strength and good formability as well as improved surface quality after hot forming in the last production stage.
- Dual-phase steels which have a structure, e.g. B. from up to 80 vol .-% of polygonal relatively soft ferrite and the rest of carbon-rich martensite.
- the carbon-rich second phase which is present in smaller quantities, is embedded in the island in the pre-eutectoid ferritic phase.
- Such a steel has good mechanical properties and favorable cold formability.
- Known steels with predominantly polygonal ferrite in the structure and martensite embedded therein consist of (in mass%) 0.03 to 0.12% C, up to 0.8% Si and 0.8 to 1.7% Mn (DE 29 24 340 C2) or 0.02 to 0.2% C, 0.05 to 2.0% Si, 0.5 to 2% Mn, 0.3 to 1.5% Cr and up to 1% Cu, Ni and Mo (EP 0 072 867 B1). Both steels are calmed with aluminum and contain soluble residual contents of less than 0.1% Al. Silicon in these steels promotes ferrite transformation. In combination with manganese and if necessary, chromium is suppressed to form pearlite.
- a steel with (in mass%) 0.05 to 0.3% carbon 0.8 to 3.0% manganese 0.4 to 2.5% aluminum 0.01 to 0.2% silicon less than 0.08% phosphorus less than 0.05% sulfur Balance iron including unavoidable impurities proposed with a structure consisting predominantly of polygonal ferrite and smaller proportions of martensite and / or bainite and / or residual austenite, which with a carbon equivalent (C eq. ) of greater than 0.1 to 0.325 C.
- equ. % C + 1/20% Mn + 1/20% Cr + 1/15% Mo
- the desired conversion to bainite or martensite in a previously formed ferrite matrix results in a favorable residual stress state of the structure with a positive influence on the cold forming ability.
- the level of tensile strength is increased compared to a ferritic-pearlitic structure, as is the case in the known hot-rolled structural steels (St 37 to St 52).
- the higher strength offers the possibility of reducing the thickness and thus saving weight.
- Such a steel not only achieves the good strength level of known silicon-alloyed dual-phase steels, but also has improved surface quality after the hot forming, as is e.g. for wheel disks of motor vehicles, which are produced by cold forming the hot-rolled steel.
- the following additional elements can be added to the steel up to the specified amounts (in mass%): up to 0.05% titanium up to 0.8% chromium up to 0.5% molybdenum up to 0.8% copper up to 0.5% nickel.
- Characteristic of the steel according to the invention is the aluminum content, which is considerably increased compared to known steels with 0.4-2.5%.
- the silicon content was limited to less than 0.2% according to the invention.
- known steels of this type mostly had silicon contents of over 1%.
- the steels alloyed with aluminum according to the invention have the desired pearlite-free two- or multi-phase structure and have excellent strength properties. Above all, the surface quality of the thermoformed product is much better than that of previously known silicon alloyed steels.
- Aluminum ensures an extensive formation of globular ferrite with a content in the range of 0.4 to 2.5%. The formation of pearlite is delayed more than that of silicon-alloyed steels and can be safely avoided if the claimed process parameters are observed.
- the carbon content of 0.05 to 0.3% is within the normal range for generic steels.
- Manganese is added in an amount of 0.8 to 3.0% in order to avoid the formation of pearlite and to enrich the austenite in addition to carbon. Manganese has a solidifying effect and increases the strength level. The contents of carbon and manganese are interchangeable under the aspects of pearlite avoidance and effects on ferrite formation within the framework set by the carbon equivalent.
- Carbon equivalence values higher than 0.1% result in higher aluminum contents.
- the intersection of the carbon equivalent value and the corresponding aluminum value should lie in the shaded area in FIG. 1 in order to ensure a ferrite content of over 70% and suppression of pearlite formation under large-scale production conditions.
- the carbon equivalent value should ensure a max. 0.325 can be limited.
- titanium up to 0.05% ensures nitrogen removal and prevents the formation of elongated manganese sulfides.
- Chromium in an amount of up to 0.8% can be added to improve the martensite resistance and to prevent pearlite formation.
- molybdenum increases the range of successful cooling rates.
- Copper and nickel in an amount of up to 0.5% each can help lower the transition temperature and prevent pearlite.
- the hot rolling end temperature ET should be in the range of Ar3 - 50 ° C ⁇ ET ⁇ Ar3 + 100 ° C lie.
- the cooling of the hot rolling end temperature to the reel temperature between room temperature and 500 ° C is accelerated with a cooling rate of 15 to 70 K / s.
- the process according to the invention can further promote the formation of ferrite in the range from Ar3 to Ar3 - 200 ° C. by taking a cooling break of 2 to 30 s, in which the cooling rate is below 15 K / s.
- Fig. 2 shows a schematic representation of the production of hot strip coupled with the cooling process of the steel according to the invention during and after hot rolling.
- a steel A according to the invention with the values according to Table 1 was hot-rolled to a final strip thickness of 3.7 mm with a hot-rolling end temperature of 875 ° C.
- the cooling from this temperature was carried out at 30 K / s to the reel temperatures (HT) given in Table 2.
- the properties of this steel A according to the invention were determined on flat tensile specimens in accordance with DIN EN 10002.
- the reel temperature was varied between 80 ° C and 350 ° C.
- the strength values determined in each case make it clear that the steel according to the invention has very good properties in the entire reel area, which at least correspond to those of the known silicon-alloyed comparison steel B.
- Table 2 also shows the mechanical properties of a steel C according to the invention of the composition according to Table 1.
- the results were determined on a round tensile specimen with a diameter of 4 mm.
- the hot rolling was simulated by a flat compression test.
- the values were measured in the longitudinal direction (material flow direction).
- the reel temperature was 200 ° C for the first sample and 400 ° C for the second sample.
- This steel also has the favorable range of mechanical properties; but also better surface quality than steel B.
- Table 2 The results reported in Table 2 make it clear that the yield ratio in the entire range of the reel temperature is below 0.8.
- Table 1 (Chemical composition) stole C% Mn% Si% P% Al% Cr% N% S% C equ A 0.076 1.45 0.053 0.019 1.23 0.35 0.002 ⁇ 0.001 0.16 B * 0.090 0.38 0.71 0.013 0.025 0.62 0.006 0.009 0.14 C. 0.090 1.51 0.03 ⁇ 0.005 1.19 0.50 0.005 0.004 0.19 D 0.20 1.49 0.04 ⁇ 0.005 1.99 0.02 0.005 0.004 0.27 *) Comparative steel
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
Description
Die Erfindung betrifft einen ferritischen Stahl, ein Verfahren zur Herstellung dieses Stahls mit überwiegend polygonal-ferritischem Gefüge und einer oder mehreren kohlenstoffangereicherten Zweitphasen sowie eine bevorzugte Verwendung dieses Stahls. Der Stahl soll hohe Festigkeit und gute Umformbarkeit sowie verbesserte Oberflächenqualität nach einer Warmverformung in der letzten Erzeugungsstufe besitzen.The invention relates to a ferritic steel, a method for producing this steel with a predominantly polygonal-ferritic structure and one or more carbon-enriched second phases, and a preferred use of this steel. The steel should have high strength and good formability as well as improved surface quality after hot forming in the last production stage.
Bekannt sind Dualphasenstähle, die ein Gefüge, z. B. aus bis zu 80 Vol.-% aus polygonalem relativ weichen Ferrit und Rest aus kohlenstoffreichem Martensit haben. Die in kleinerer Menge vorliegende kohlenstoffreiche zweite Phase ist inselförmig in der voreutektoiden ferritischen Phase eingelagert. Ein derartiger Stahl hat gute mechanische Eigenschaften und günstige Kaltumformbarkeit.Dual-phase steels are known which have a structure, e.g. B. from up to 80 vol .-% of polygonal relatively soft ferrite and the rest of carbon-rich martensite. The carbon-rich second phase, which is present in smaller quantities, is embedded in the island in the pre-eutectoid ferritic phase. Such a steel has good mechanical properties and favorable cold formability.
Bekannte Stähle mit überwiegend polygonalem Ferrit im Gefüge sowie darin eingelagertem Martensit bestehen aus (in Masse-%) 0,03 bis 0,12 % C, bis 0,8 % Si und 0,8 bis 1,7 % Mn (DE 29 24 340 C2) oder 0,02 bis 0,2 % C, 0,05 bis 2,0 % Si, 0,5 bis 2 % Mn, 0,3 bis 1,5 % Cr sowie bis 1 % Cu, Ni und Mo (EP 0 072 867 B1). Beide Stähle sind aluminiumberuhigt und enthalten lösliche Restgehalte von weniger als 0,1 % Al. Silizium in diesen Stählen fördert die Ferritumwandlung. In Kombination mit Mangan und gegebenenfalls Chrom wird die Perlitbildung unterdrückt. Dadurch wird die ausreichende Anreicherung von Kohlenstoff in der zweiten Phase sichergestellt und die Bildung von polygonalem Ferrit im überwiegenden Verhältnis zur zweiten Phase erreicht. Diese bekannten Legierungen haben jedoch den Nachteil, daß sich beim Warmwalzen eine inhomogene Oberflächenstruktur ausbildet, die durch Zungen von rotem Zunder sichtbar wird. Nach dem Beizen verbleiben Unebenheiten auf der Oberfläche. Für viele Anwendungsfälle ist derartiges Material nicht verkaufsfähig. Bisher ist es nicht gelungen, die Oberflächenqualität dieser warmgewalzten Stähle zu verbessern. Im übrigen besteht ein Bedarf nach Stählen, die sowohl hohe Festigkeit als auch gutes Kaltumformungsvermögen aufweisen. Diese Anforderungen können duch das Produkt aus Zugfestigkeit und Dehnung Rm · A5 charakterisiert werden. Dieses sollte über 16.000 N/mm2 · % sowohl in Walzlängs- als auch in Querrichtung liegen.Known steels with predominantly polygonal ferrite in the structure and martensite embedded therein consist of (in mass%) 0.03 to 0.12% C, up to 0.8% Si and 0.8 to 1.7% Mn (DE 29 24 340 C2) or 0.02 to 0.2% C, 0.05 to 2.0% Si, 0.5 to 2% Mn, 0.3 to 1.5% Cr and up to 1% Cu, Ni and Mo (EP 0 072 867 B1). Both steels are calmed with aluminum and contain soluble residual contents of less than 0.1% Al. Silicon in these steels promotes ferrite transformation. In combination with manganese and if necessary, chromium is suppressed to form pearlite. This ensures sufficient accumulation of carbon in the second phase and the formation of polygonal ferrite in predominant relation to the second phase. However, these known alloys have the disadvantage that an inhomogeneous surface structure is formed during hot rolling, which is visible through tongues of red scale. After pickling, bumps remain on the surface. For many applications, such material is not salable. So far, it has not been possible to improve the surface quality of these hot-rolled steels. There is also a need for steels which have both high strength and good cold forming properties. These requirements can be characterized by the product of tensile strength and elongation Rm · A5. This should be over 16,000 N / mm 2 ·% in both the longitudinal and transverse directions.
Daraus leitet sich die Aufgabe ab, einen Stahl mit überwiegend polygonalem ferritischen Gefüge zu entwickeln, der das hervorragende Spektrum der mechanischen Eigenschaften bekannter Stähle zumindestens in gleicher Größe aufweist, mit Zugfestigkeitswerten Rm > 500 N/mm2 und Dehnungswerten A5 > 16000/Rm in % ebenso gut kaltumformbar ist wie die bekannten Stähle, jedoch nach der Erzeugung durch Warmumformung in der letzten Erzeugnisstufe eine bessere Oberflächen-struktur aufweist als die bekannten Stähle.This leads to the task of developing a steel with a predominantly polygonal ferritic structure, which has the outstanding range of mechanical properties of known steels at least in the same size, with tensile strength values Rm> 500 N / mm 2 and elongation values A5> 16000 / Rm in% is just as good cold formable as the known steels, but has a better surface structure than the known steels after the production by hot forming in the last product stage.
Zur Lösung dieser Aufgabe wird ein Stahl mit (in Masse-%)
0,05 bis 0,3 % Kohlenstoff
0,8 bis 3,0 % Mangan
0,4 bis 2,5 % Aluminium
0,01 bis 0,2 % Silizium
weniger als 0,08 % Phosphor
weniger als 0,05 % Schwefel
Rest Eisen einschließlich unvermeidbarer Verunreinigungen
mit einem überwiegend aus polygonalem Ferrit und kleineren Anteilen an Martensit und/oder Bainit und/oder Restaustenit bestehenden Gefüge vorgeschlagen, der bei einem Kohlenstoffäquivalent (Cäqu.) von größer als 0,1 bis 0,325 mit
0.05 to 0.3% carbon
0.8 to 3.0% manganese
0.4 to 2.5% aluminum
0.01 to 0.2% silicon
less than 0.08% phosphorus
less than 0.05% sulfur
Balance iron including unavoidable impurities
proposed with a structure consisting predominantly of polygonal ferrite and smaller proportions of martensite and / or bainite and / or residual austenite, which with a carbon equivalent (C eq. ) of greater than 0.1 to 0.325
Aluminium in einer Menge von in Masse-%
Die angestrebte Umwandlung zu Bainit oder Martensit in einer zuvor gebildeten Ferritmatrix bewirkt einen günstigen Eigenspannungszustand des Gefüges mit einem positiven Einfluß auf das Kaltumformvermögen. Gleichzeitig wird das Zugfestigkeitsniveau gegenüber einem ferritisch-perlitischen Gefüge, wie es in den bekannten warmgewalzten Baustählen (St 37 bis St 52) vorliegt, angehoben. Bei ähnlich guter Eignung wie bei den bekannten Baustählen für eine Direktverarbeitung zu geometrisch anspruchsvoll umgeformten Endprodukten, bietet die höhere Festigkeit die Möglichkeit zur Dickenreduktion und damit zur Gewichtseinsparung.The desired conversion to bainite or martensite in a previously formed ferrite matrix results in a favorable residual stress state of the structure with a positive influence on the cold forming ability. At the same time, the level of tensile strength is increased compared to a ferritic-pearlitic structure, as is the case in the known hot-rolled structural steels (St 37 to St 52). With similar suitability as the known structural steels for direct processing into geometrically sophisticated formed end products, the higher strength offers the possibility of reducing the thickness and thus saving weight.
Ein solcher Stahl erreicht nicht nur das gute Festigkeitsniveau bekannter siliziumlegierter Dualphasenstähle sondern weist nach Abschluß der Warmumformung verbesserte Oberflächenqualität auf, wie sie z.B. für Radscheiben von Kraftfahrzeugen gefordert wird, die durch Kaltumformung des warmgewalzten Stahls erzeugt werden.Such a steel not only achieves the good strength level of known silicon-alloyed dual-phase steels, but also has improved surface quality after the hot forming, as is e.g. for wheel disks of motor vehicles, which are produced by cold forming the hot-rolled steel.
Zusätzlich können dem Stahl folgende weitere Elemente bis zu den angegebenen Mengen (in Masse-%) zulegiert werden:
bis 0,05 % Titan
bis 0,8 % Chrom
bis 0,5 % Molybdän
bis 0,8 % Kupfer
bis 0,5 % Nickel.In addition, the following additional elements can be added to the steel up to the specified amounts (in mass%):
up to 0.05% titanium
up to 0.8% chromium
up to 0.5% molybdenum
up to 0.8% copper
up to 0.5% nickel.
Ein derartiger anstelle von Silizium mit Aluminium legierter Stahl erreicht eine Bruchdehnung A5 > 34 % bei einem Zugfestigkeitswert Rm = 500 N/mm2 und eine Bruchdehnung A5 > 24 % bei einem Zugfestigkeitswert von 700 N/mm2, d.h. das Produkt Rm · A5 liegt sicher über 16.000 N/mm2 · % sowohl in Walzquerrichtung als auch in Walzlängsrichtung.Such a steel alloyed with aluminum instead of silicon achieves an elongation at break A 5 > 34% with a tensile strength value R m = 500 N / mm 2 and an elongation at break A 5 > 24% with a tensile strength value of 700 N / mm 2 , ie the product Rm · A5 is certainly over 16,000 N / mm 2 ·% in both the transverse direction and in the longitudinal direction.
Kennzeichen des erfindungsgemäßen Stahls ist der gegenüber bekannten Stählen mit 0,4 - 2,5 % erheblich erhöhte Gehalt an Aluminium. Dafür wurde erfindungsgemäß der Gehalt an Silizium auf weniger als 0,2 % begrenzt.Characteristic of the steel according to the invention is the aluminum content, which is considerably increased compared to known steels with 0.4-2.5%. For this purpose, the silicon content was limited to less than 0.2% according to the invention.
Bekannte Stähle dieses Typs hatten dagegen meist Siliziumgehalte über 1 %. Die erfindungsgemäß mit Aluminium legierten Stähle weisen die erwünschte perlitfreie Zwei- oder Mehrphasen-Gefügestruktur auf und haben hervorragende Festigkeitseigenschaften. Vor allem ist die Oberflächenqualität des warmverformten Erzeugnisses wesentlich besser, als man dies von siliziumlegierten Stählen bisher kannte. Aluminium stellt bei einem Gehalt im Bereich von 0,4 bis 2,5 % eine umfangreiche Bildung von globularem Ferrit sicher. Die Perlitbildung wird gegenüber siliziumlegierten Stählen stärker verzögert und kann bei Einhaltung der beanspruchten Verfahrensparameter sicher vermieden werden.In contrast, known steels of this type mostly had silicon contents of over 1%. The steels alloyed with aluminum according to the invention have the desired pearlite-free two- or multi-phase structure and have excellent strength properties. Above all, the surface quality of the thermoformed product is much better than that of previously known silicon alloyed steels. Aluminum ensures an extensive formation of globular ferrite with a content in the range of 0.4 to 2.5%. The formation of pearlite is delayed more than that of silicon-alloyed steels and can be safely avoided if the claimed process parameters are observed.
Der Kohlenstoffgehalt liegt mit 0,05 bis 0,3 % in dem für gattungsgemäße Stähle üblichen Rahmen.The carbon content of 0.05 to 0.3% is within the normal range for generic steels.
Mangan wird in einer Menge von 0,8 bis 3,0 % zugegeben, um die Perlitbildung zu vermeiden und um neben Kohlenstoff den Austenit anzureichern. Mangan wirkt mischkristallverfestigend und hebt das Festigkeitsniveau. Die Gehalte an Kohlenstoff und Mangan sind unter den Aspekten der Perlitvermeidung und Wirkung auf die Ferritbildung innerhalb des durch das Kohlenstoffäquivalent gesteckten Rahmens austauschbar. Das Kohlenstoffäquivalent wird ermittelt zu:
Höhere Kohlenstoffäquivalenzwerte als 0,1 % bedingen höhere Aluminiumgehalte. Der Schnittpunkt des Kohlenstoffäquivalenzwertes und des dazu passenden Aluminiumwertes soll erfindungsgemäß in dem schraffierten Bereich in der Fig. 1 liegen, um unter großtechnischen Produktionsbedingungen einen Ferritanteil über 70 % und Unterdrückung der Perlitbildung sicherzustellen. Der Kohlenstoffäquivalenzwert sollte zur Sicherstellung der Schweißeignung auf max. 0,325 begrenzt werden.Carbon equivalence values higher than 0.1% result in higher aluminum contents. According to the invention, the intersection of the carbon equivalent value and the corresponding aluminum value should lie in the shaded area in FIG. 1 in order to ensure a ferrite content of over 70% and suppression of pearlite formation under large-scale production conditions. The carbon equivalent value should ensure a max. 0.325 can be limited.
Ein Zusatz von Titan bis 0,05 % sichert die Stickstoffabbindung und vermeidet die Ausbildung gestreckter Mangansulfide.An addition of titanium of up to 0.05% ensures nitrogen removal and prevents the formation of elongated manganese sulfides.
Chrom in einer Menge bis 0,8 % kann zur Verbesserung der Martensitanlaßbeständigkeit und zur Vermeidung von Perlitbildung zugesetzt werden.Chromium in an amount of up to 0.8% can be added to improve the martensite resistance and to prevent pearlite formation.
Molybdän vergrößert in einer Menge bis 0,5 % die Spannbreite erfolgreicher Abkühlraten.In an amount of up to 0.5%, molybdenum increases the range of successful cooling rates.
Kupfer und Nickel in einer Menge bis jeweils 0,5 % können zur Absenkung der Umwandlungstemperatur und zur Vermeidung von Perlit beitragen.Copper and nickel in an amount of up to 0.5% each can help lower the transition temperature and prevent pearlite.
Zur Beeinflussung der Einformung von Sulfiden ist eine Behandlung der Metallschmelze mit Kalzium-Silizium sinnvoll.To influence the formation of sulfides, treatment of the molten metal with calcium silicon is advisable.
Die Warmwalzendtemperatur ET sollte im Bereich von
Die Ar3-Temperatur, die im Bereich von 750 bis 950 °C liegen soll, errechnet sich für Al-Gehalte bis 1 % zu
Bei Aluminiumgehalten über 1 bis 2,5 % gilt:
Beim Erzeugen von Warmband aus dem erfindungsgemäßen Stahl sind erhöhte Warmwalzendtemperaturen gegenüber bisher überwiegend nur bis 850 °C zulässig. Das Walzen bei höheren Walzendtemperaturen bewirkt einen positiven Einfluß auf das Warmbandprofil. Das Walzen kann mit geringeren Kräften erfolgen, und die Walzgeschwindigkeit kann erhöht werden. Ein Pendeln des Vorbandes zur Abkühlung vor der Fertigstaffel kann entfallen. Insgesamt ergibt sich hieraus ein Produktivitätsgewinn.When hot strip is produced from the steel according to the invention, elevated hot rolling end temperatures are predominantly only permissible up to 850 ° C. Rolling at higher final roll temperatures has a positive influence on the hot strip profile. Rolling can be done with less force, and the rolling speed can be increased. There is no need to swing the supporting strip to cool down before the finishing relay. Overall, this results in a productivity gain.
Die Abkühlung von Warmwalzendtemperatur auf die zwischen Raumtemperatur und 500 °C liegende Haspeltemperatur erfolgt beschleunigt mit einer Abkühlungsgeschwindigkeit von 15 bis 70 K/s.The cooling of the hot rolling end temperature to the reel temperature between room temperature and 500 ° C is accelerated with a cooling rate of 15 to 70 K / s.
Bei der Abkühlung von Warmwalzendtemperatur kann man bei dem erfindungsgemäßen Verfahren im Bereich von Ar3 bis Ar3 - 200 °C durch Einlegen einer Kühlpause von 2 bis 30 s, in der die Abkühlrate unter 15 K/s liegt, die Ferritbildung weiter fördern.When cooling the hot rolling end temperature, the process according to the invention can further promote the formation of ferrite in the range from Ar3 to Ar3 - 200 ° C. by taking a cooling break of 2 to 30 s, in which the cooling rate is below 15 K / s.
Fig. 2 zeigt eine schematische Darstellung der Erzeugung von Warmband gekoppelt mit dem Abkühlungsverlauf des erfindungsgemäßen Stahls beim und nach dem Warmwalzen.Fig. 2 shows a schematic representation of the production of hot strip coupled with the cooling process of the steel according to the invention during and after hot rolling.
Daraus ist erkennbar, daß der unerwünschte Eintritt in das Perlitgebiet sicher vermieden werden kann, wenn die angegebenen Bedingungen für die Warmwalzendtemperatur, die Abkühlungsgeschwindigkeit und die Haspeltemperatur eingehalten werden.From this it can be seen that the undesired entry into the pearlite area can be reliably avoided if the specified conditions for the hot rolling end temperature, the cooling rate and the reel temperature are observed.
Ein erfindungsgemäßer Stahl A mit den Werten nach Tabelle 1 wurde auf eine Endbanddicke von 3,7 mm warmgewalzt mit einer Warmwalzendtemperatur von 875 °C. Die Abkühlung von dieser Temperatur erfolgte mit 30 K/s auf die in Tabelle 2 angegebenen Haspeltemperaturen (HT). Die Eigenschaften dieses erfindungsgemäßen Stahls A wurden nach DIN EN 10002 an Flachzugproben ermittelt.A steel A according to the invention with the values according to Table 1 was hot-rolled to a final strip thickness of 3.7 mm with a hot-rolling end temperature of 875 ° C. The cooling from this temperature was carried out at 30 K / s to the reel temperatures (HT) given in Table 2. The properties of this steel A according to the invention were determined on flat tensile specimens in accordance with DIN EN 10002.
Die Werte für die Streckgrenze, Zugfestigkeit, Dehnung und das Streckgrenzenverhältnis für die Lagen längs und quer zur Walzrichtung sind in Tabelle 2 mitgeteilt.The values for the yield strength, tensile strength, elongation and the yield ratio for the layers along and across the rolling direction are given in Table 2.
Eine A-Probe wurde bei höherer Temperatur gehaspelt (HT = 685 °C). Diese war nicht perlitfrei und erreichte nicht die geforderten Eigenschaften.A sample was coiled at higher temperature (HT = 685 ° C). This was not pearlite-free and did not achieve the required properties.
Zum Vergleich wurde in Tabelle 2 auch die entsprechenden Festigkeitseigenschaften eines aus der DE 34 40 752 C2 bekannten Stahls B mit der Zusammensetzung nach Tabelle 1 eingetragen.For comparison, the corresponding strength properties of a steel B known from DE 34 40 752 C2 with the composition according to table 1 were also entered in table 2.
Für den erfindungsgemäßen Stahl A wurde die Haspeltemperatur zwischen 80 °C und 350 °C variiert. Die dafür jeweils ermittelten Festigkeitskennwerte machen deutlich, daß der erfindungsgemäße Stahl in dem gesamten Haspelbereich sehr gute Eigenschaften hat, die denen des bekannten siliziumlegierten Vergleichsstahls B mindestens entsprechen.For steel A according to the invention, the reel temperature was varied between 80 ° C and 350 ° C. The strength values determined in each case make it clear that the steel according to the invention has very good properties in the entire reel area, which at least correspond to those of the known silicon-alloyed comparison steel B.
In Tabelle 2 sind auch die mechanischen Eigenschaften eines erfindungsgemäßen Stahls C der Zusammensetzung gemäß Tabelle 1 mitgeteilt. Die Ergebnisse wurden an einer Rundzugprobe von 4 mm Durchmesser ermittelt. Das Warmwalzen wurde durch einen Flachstauchversuch simuliert. Die Werte wurden in Längsrichtung (Materialflußrichtung) gemessen. Die Haspeltemperatur lag bei der ersten Probe bei 200 °C und bei der zweiten Probe bei 400 °C. Auch dieser Stahl hat das günstige mechanische Eigenschaftsspektrum; dazu aber noch bessere Oberflächenqualität als der Stahl B.Table 2 also shows the mechanical properties of a steel C according to the invention of the composition according to Table 1. The results were determined on a round tensile specimen with a diameter of 4 mm. The hot rolling was simulated by a flat compression test. The values were measured in the longitudinal direction (material flow direction). The reel temperature was 200 ° C for the first sample and 400 ° C for the second sample. This steel also has the favorable range of mechanical properties; but also better surface quality than steel B.
Die in Tabelle 2 mitgeteilten Ergebnisse machen deutlich, daß das Streckgrenzenverhältnis im gesamten Bereich der Haspeltemperatur unter 0,8 liegt.
*)VergleichsstahlExplanation of table 2
*) Comparative steel
HT: Haspeltemperatur
Rp0.2: 0,02 %-Dehngrenze
Rm: Zugfestigkeit
A5:Bruchdehnung
L: Längs /
Q: Quer**) Outside the stressed range (HT> 500 ° C) Determination of the properties according to DIN EN 10002 on flat tensile samples
HT: reel temperature
Rp 0.2 : 0.02% proof stress
R m : tensile strength
A 5 : Elongation at break
L: longitudinal /
Q: Cross
Claims (5)
0,05 bis 0,3 % Kohlenstoff
0,8 bis 3,0 % Mangan
0,4 bis 2,5 % Aluminium
weniger als 0,2 % Silizium
weniger als 0,08 % Phosphor
weniger als 0,05 % Schwefel
Rest Eisen einschließlich unvermeidbarer
Verunreinigungen,
der bei einem Kohlenstoffäquivalent von größer als 0,1 bis 0,325 mit
0.05 to 0.3% carbon
0.8 to 3.0% manganese
0.4 to 2.5% aluminum
less than 0.2% silicon
less than 0.08% phosphorus
less than 0.05% sulfur
Rest of iron including unavoidable
Impurities,
with a carbon equivalent of greater than 0.1 to 0.325
dadurch gekennzeichnet, daß der Stahl zusätzlich mit (in Masse-%)
bis 0,05 % Titan
bis 0,8 % Chrom
bis 0,5 % Molybdän
bis 0,5 % Kupfer
bis 0,8 % Nickel
einzeln oder zu mehreren legiert wird.Method according to claim 2,
characterized in that the steel additionally with (in mass%)
up to 0.05% titanium
up to 0.8% chromium
up to 0.5% molybdenum
up to 0.5% copper
up to 0.8% nickel
is alloyed individually or in groups.
dadurch gekennzeichnet, daß im Temperaturbereich zwischen Ar3 und Ar3 -200 °C für die Dauer von 2 bis 30 s eine Kühlpause eingelegt wird, in der die Abkühlungsgeschwindigkeit kleiner als 15 K/s ist.Method according to claim 2,
characterized in that in the temperature range between Ar3 and Ar3 -200 ° C there is a cooling break for a period of 2 to 30 s during which the cooling rate is less than 15 K / s.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19521836 | 1995-06-16 | ||
| DE19521836 | 1995-06-16 | ||
| DE19605696 | 1996-02-16 | ||
| DE19605696A DE19605696C2 (en) | 1995-06-16 | 1996-02-16 | Ferritic steel and process for its manufacture and use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0750049A1 true EP0750049A1 (en) | 1996-12-27 |
Family
ID=26016011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP96107884A Withdrawn EP0750049A1 (en) | 1995-06-16 | 1996-05-17 | Ferritic steel and its manufacture and use |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0750049A1 (en) |
| CN (1) | CN1190997A (en) |
| AR (1) | AR002501A1 (en) |
| BR (1) | BR9608672A (en) |
| CA (1) | CA2224817A1 (en) |
| CZ (1) | CZ402497A3 (en) |
| HU (1) | HUP9801908A3 (en) |
| PL (1) | PL324555A1 (en) |
| TR (1) | TR199701720T1 (en) |
| WO (1) | WO1997000332A1 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL1007739C2 (en) * | 1997-12-08 | 1999-06-09 | Hoogovens Staal Bv | Method and device for manufacturing a high strength steel strip. |
| AU756917B2 (en) * | 1996-06-07 | 2003-01-30 | Corus Staal B.V. | Process and device for producing a high-strength steel strip |
| US6616778B1 (en) | 1997-12-08 | 2003-09-09 | Corus Staal Bv | Process and device for producing a ferritically rolled steel strip |
| EP1642990A4 (en) * | 2003-06-19 | 2006-11-29 | Nippon Steel Corp | HIGH STRENGTH STEEL PLATE WITH EXCELLENT FORMABILITY AND CORRESPONDING PRODUCTION PROCESS |
| RU2346061C2 (en) * | 2003-06-18 | 2009-02-10 | Смс Демаг Акциенгезелльшафт | Method and plant for manufacturing of hot-rolled strip with duplex structure |
| CN110551878A (en) * | 2019-10-12 | 2019-12-10 | 东北大学 | A kind of ultra-high-strength ultra-high toughness low-density dual-phase layered steel plate and preparation method thereof |
| AT525283A4 (en) * | 2021-10-29 | 2023-02-15 | Primetals Technologies Austria GmbH | Method for producing a dual-phase steel strip in a combined casting and rolling plant, a dual-phase steel strip produced using the method and a combined casting and rolling facility |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE506596C2 (en) | 1996-05-17 | 1998-01-19 | Nobel Biocare Ab | Self-tapping anchoring elements for tooth screw ice |
| JP4259347B2 (en) * | 2004-02-19 | 2009-04-30 | 住友金属工業株式会社 | Manufacturing method of high strength non-tempered seamless steel pipe |
| EP1832667A1 (en) * | 2006-03-07 | 2007-09-12 | ARCELOR France | Method of producing steel sheets having high strength, ductility and toughness and thus produced sheets. |
| CN109266956B (en) * | 2018-09-14 | 2019-08-06 | 东北大学 | A kind of automobile B-pillar reinforcement plate steel and preparation method thereof |
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- 1996-06-01 CN CN96195583A patent/CN1190997A/en active Pending
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Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU756917B2 (en) * | 1996-06-07 | 2003-01-30 | Corus Staal B.V. | Process and device for producing a high-strength steel strip |
| CZ298363B6 (en) * | 1997-12-08 | 2007-09-05 | Corus Staal B. V. | Process for producing high-strength steel strip and apparatus for making the same |
| US6616778B1 (en) | 1997-12-08 | 2003-09-09 | Corus Staal Bv | Process and device for producing a ferritically rolled steel strip |
| US6773522B1 (en) | 1997-12-08 | 2004-08-10 | Corus Staal Bv | Process and device for producing a high-strength steel strip |
| WO1999029444A1 (en) * | 1997-12-08 | 1999-06-17 | Corus Staal Bv | Process and device for producing a high-strength steel strip |
| NL1007739C2 (en) * | 1997-12-08 | 1999-06-09 | Hoogovens Staal Bv | Method and device for manufacturing a high strength steel strip. |
| DE10327383C5 (en) * | 2003-06-18 | 2013-10-17 | Aceria Compacta De Bizkaia S.A. | Plant for the production of hot strip with dual phase structure |
| RU2346061C2 (en) * | 2003-06-18 | 2009-02-10 | Смс Демаг Акциенгезелльшафт | Method and plant for manufacturing of hot-rolled strip with duplex structure |
| EP1633894B1 (en) | 2003-06-18 | 2017-04-26 | SMS group GmbH | Method and installation for the production of hot-rolled strip having a dual-phase structure |
| EP1642990A4 (en) * | 2003-06-19 | 2006-11-29 | Nippon Steel Corp | HIGH STRENGTH STEEL PLATE WITH EXCELLENT FORMABILITY AND CORRESPONDING PRODUCTION PROCESS |
| US8262818B2 (en) | 2003-06-19 | 2012-09-11 | Nippon Steel Corporation | Method for producing high strength steel sheet excellent in formability |
| US7922835B2 (en) | 2003-06-19 | 2011-04-12 | Nippon Steel Corporation | High strength steel sheet excellent in formability |
| CN110551878A (en) * | 2019-10-12 | 2019-12-10 | 东北大学 | A kind of ultra-high-strength ultra-high toughness low-density dual-phase layered steel plate and preparation method thereof |
| AT525283A4 (en) * | 2021-10-29 | 2023-02-15 | Primetals Technologies Austria GmbH | Method for producing a dual-phase steel strip in a combined casting and rolling plant, a dual-phase steel strip produced using the method and a combined casting and rolling facility |
| AT525283B1 (en) * | 2021-10-29 | 2023-02-15 | Primetals Technologies Austria GmbH | Method for producing a dual-phase steel strip in a combined casting and rolling plant, a dual-phase steel strip produced using the method and a combined casting and rolling facility |
Also Published As
| Publication number | Publication date |
|---|---|
| HUP9801908A2 (en) | 1998-11-30 |
| CZ402497A3 (en) | 1998-06-17 |
| AR002501A1 (en) | 1998-03-25 |
| HUP9801908A3 (en) | 1998-12-28 |
| CN1190997A (en) | 1998-08-19 |
| BR9608672A (en) | 1999-05-04 |
| TR199701720T1 (en) | 1998-05-21 |
| MX9710230A (en) | 1998-03-29 |
| CA2224817A1 (en) | 1997-01-03 |
| WO1997000332A1 (en) | 1997-01-03 |
| PL324555A1 (en) | 1998-06-08 |
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