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EP2291547A1 - Method for manufacturing very high strength, cold-rolled, dual phase steel sheets, and sheets thus produced - Google Patents

Method for manufacturing very high strength, cold-rolled, dual phase steel sheets, and sheets thus produced

Info

Publication number
EP2291547A1
EP2291547A1 EP09761870A EP09761870A EP2291547A1 EP 2291547 A1 EP2291547 A1 EP 2291547A1 EP 09761870 A EP09761870 A EP 09761870A EP 09761870 A EP09761870 A EP 09761870A EP 2291547 A1 EP2291547 A1 EP 2291547A1
Authority
EP
European Patent Office
Prior art keywords
product
temperature
rolled
steel sheet
cold
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.)
Granted
Application number
EP09761870A
Other languages
German (de)
French (fr)
Other versions
EP2291547B1 (en
Inventor
Antoine Moulin
Véronique Sardoy
Catherine Vinci
Gloria Restrepo Garces
Tom Waterschoot
Mohamed Goune
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.)
ArcelorMittal Investigacion y Desarrollo SL
Original Assignee
ArcelorMittal Investigacion y Desarrollo SL
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 ArcelorMittal Investigacion y Desarrollo SL filed Critical ArcelorMittal Investigacion y Desarrollo SL
Priority to PL09761870T priority Critical patent/PL2291547T3/en
Priority to EP09761870A priority patent/EP2291547B1/en
Publication of EP2291547A1 publication Critical patent/EP2291547A1/en
Application granted granted Critical
Publication of EP2291547B1 publication Critical patent/EP2291547B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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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
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/001Continuous casting of metals, i.e. casting in indefinite lengths of specific alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D7/00Casting ingots, e.g. from ferrous metals
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/84Controlled slow cooling
    • 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
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/004Heat treatment of ferrous alloys containing Cr and Ni
    • 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
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
    • 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
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/008Heat treatment of ferrous alloys containing Si
    • 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 by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0205Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
    • 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 by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/021Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a particular fabrication or treatment of ingot or slab
    • 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 by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
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    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold rolling
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    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0263Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
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    • 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 by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
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    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0278Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a particular surface treatment
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    • 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
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    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
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    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
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    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/48Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/50Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/54Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/022Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
    • C23C2/0224Two or more thermal pretreatments
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    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
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    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
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    • C23C2/06Zinc or cadmium or alloys based thereon
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    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
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    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
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    • C23C2/40Plates; Strips
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    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/005Ferrite
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    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/008Martensite

Definitions

  • the invention relates to the manufacture of cold-rolled and annealed sheets of so-called "dual-phase" steels having a very high strength and a deformability for the manufacture of parts by shaping, in particular in the automotive industry.
  • the dual-phase steels whose structure includes martensite, possibly bainite, in a ferritic matrix, have developed a great deal because they combine high resistance with significant possibilities of deformation.
  • their yield strength is relatively low compared to their breaking strength, which gives them a very favorable ratio (yield strength / strength) during forming operations.
  • Their consolidation capacity is very large, which allows a good distribution of deformations in the case of a collision and obtaining a significantly higher yield strength on the part after forming.
  • EP0796928A1 also describes cold-rolled Dual Phase steels with a resistance greater than 550 MPa, with a composition of 0.05-0.3% C, 0.8-3% Mn, 0.4-2.5% AI. , 0.01-0.2% Si.
  • the ferritic matrix contains martensite, bainite and / or residual austenite.
  • the examples presented show that the resistance does not exceed 660 MPa, even for a high carbon content (0.20-0.21%)
  • JP11350038 describes dual phase steels with a resistance greater than 980 MPa, composition 0.10.
  • the object of the present invention is to provide a method of manufacturing dual-phase steel plates very high strength, cold rolled, bare or coated, not having the disadvantages mentioned above.
  • the invention aims to provide Dual Phase steel sheets with a mechanical strength of between 980 and 1100 MPa together with an elongation greater than 9% rupture and good formability, including folding
  • the invention also aims to provide a manufacturing method in which small variations in the parameters do not lead to significant changes in the microstructure or mechanical properties.
  • the invention also aims to provide a sheet of steel easily fabricated by cold rolling, that is to say whose hardness after the hot rolling step is limited so that the rolling forces remain moderate during of the cold rolling step.
  • the invention also aims to have a steel having good weldability by means of conventional assembly methods such as spot resistance welding.
  • the invention also aims to provide an economical manufacturing process by avoiding the addition of expensive alloying elements.
  • the subject of the invention is a dual-phase cold-rolled and annealed steel sheet having a strength of between 980 and 1100 MPa, an elongation at break of greater than 9%, the composition of which comprises the contents being expressed in terms of Weight: 0.055% ⁇ C ⁇ 0.095%, 2% ⁇ Mn ⁇ 2.6%, 0.005% ⁇ Si ⁇ 0.35%, S ⁇ 0.005%, P ⁇ 0.050%, 0.1 ⁇ AI ⁇ 0.3% , 0.05% ⁇ Mo ⁇ 0.25%, 0.2% ⁇ Cr ⁇ 0.5%, with the proviso that Cr + 2Mo ⁇ 0.6%, Ni ⁇ 0.1%, 0.01O ⁇ Nb ⁇ 0.040%, 0.01 O ⁇ Ti ⁇ 0.050%, 0.0005 ⁇ B ⁇ 0.0025%, 0.002% ⁇ N ⁇ 0.007%, the rest of the composition consisting of iron and unavoidable impurities resulting from the development.
  • the composition of the steel contains, the content being expressed by weight: 0.
  • the composition of the steel contains, the content being expressed by weight: 0.10% ⁇ Si ⁇ 0.30%.
  • the composition of the steel preferably contains: 0.15% ⁇ Si ⁇ 0.28%.
  • the composition contains: P ⁇ 0.015%.
  • the microstructure of the sheet preferably contains 35 to 50% of martensite in surface proportion.
  • the complement of the microstructure consists of 50 to 65% of ferrite in surface proportion.
  • the complement of the microstructure consists of 1 to 10% of bainite and 40 to 64% of ferrite in surface proportion.
  • the surface fraction of non-recrystallized ferrite relative to the entire ferritic phase is preferably less than or equal to 15%.
  • the steel sheet preferably has a ratio between its elastic limit R e and its resistance R m such that: 0.6 ⁇ Re / R m ⁇ 0.8.
  • the sheet is galvanized continuously.
  • the sheet has a galvannealed coating.
  • the subject of the invention is also a process for manufacturing a cold rolled and annealed dual phase steel sheet, characterized in that a composition steel is supplied according to any one of the above characteristics, and then
  • the semi-finished product is hot-rolled with an end-of-rolling temperature TFL ⁇ A ⁇ 3 in order to obtain a hot-rolled product, and then
  • the product is cooled to a temperature below the temperature M 5 with a speed V sufficient for the austenite to become totally martensite.
  • the subject of the invention is also a process for producing a cold rolled, annealed and galvanized dual phase steel sheet characterized in that supplying the heated and annealed product with a structure comprising austenite according to the above characteristic then,
  • the product heated and annealed is cooled with a speed V R sufficient to prevent the transformation of the austenite into ferrite, until it reaches a temperature close to the dip galvanizing temperature T Zn , then
  • the product is continuously galvanized by immersion in a bath of zinc or of Zn alloy at a temperature of 450 ° C. ⁇ Zn ⁇ 480 ° C. to obtain a galvanized product, and then
  • the galvanized product is cooled to room temperature with a speed VR greater than 4 ° C / s to obtain a cold rolled steel sheet, annealed and galvanized.
  • the subject of the invention is also a process for producing a cold-rolled and galvannealed dual phase steel sheet, characterized in that the heated and annealed product is supplied with a structure comprising austenite according to the characteristic above, then,
  • the product heated and annealed is cooled with a speed V R sufficient to prevent the transformation of said austenite into ferrite, until it reaches a temperature close to the dip galvanizing temperature T Zn , then
  • the galvanized product is heated at a temperature of between 490 and 550 ° C. for a period of between 10 and 40 seconds to obtain a galvannealed product, and then the galvannealed product is cooled to ambient temperature at a speed V "R greater than 4 ° C / s, to obtain a cold-rolled and galvannealed steel sheet.
  • the invention also relates to a manufacturing method according to one of the above characteristics, characterized in that the temperature T M is between 760 and 83O 0 C.
  • the cooling rate V R is greater than or equal to 15 ° C / s.
  • the invention also relates to the use of a steel sheet according to any one of the above characteristics, or manufactured by a process according to any one of the above characteristics, for the manufacture of structures or safety for motor vehicles.
  • FIG. 1 shows an example of microstructure of a steel sheet according to the invention.
  • FIGS. 2 and 3 show examples of microstructure of steel sheets not in accordance with the invention.
  • This element also plays an important role in the formation of the microstructure by preventing the precipitation of carbides and by promoting the formation of martensite which enters the structure of the Dual Phase steels. It plays an effective role beyond 0.005%.
  • An addition of silicon in an amount greater than 0.10%, preferably greater than 0.15%, makes it possible to achieve the highest levels of resistance to which the invention relates.
  • an increase in the silicon content degrades the dip coating ability by promoting the formation of adherent oxides on the surface of the products: its content must be limited to 0.35% by weight, and preferably 0.30% to obtain a good coating.
  • the silicon decreases the weldability: a content of less than 0.28% makes it possible simultaneously to ensure very good weldability as well as good coating.
  • the ductility is reduced due to the excessive presence of sulfides such as MnS which decrease the ability to deform, especially during hole expansion tests.
  • Phosphorus is an element that hardens in solid solution but decreases spot weldability and hot ductility, particularly because of its ability to segregate at grain boundaries or co-segregate with manganese. For these reasons, its content must be limited to 0.050%, and preferably to 0.015% in order to obtain a good spot welding ability.
  • Aluminum plays an important role in the invention by preventing the precipitation of carbides and promoting the formation of martensitic constituents upon cooling. These effects are obtained when the aluminum content is greater than 0.1%, and preferably when the aluminum content is greater than 0.12%.
  • AlN aluminum limits grain growth during annealing after cold rolling.
  • This element is also used for the deoxidation of the liquid steel in an amount usually less than about 0.050%. It is usually considered that higher levels increase the erosion of refractories and the risk of plugging the nozzles. In excessive amounts, aluminum reduces hot ductility and increases the risk of defects in continuous casting. It is also sought to limit inclusions of alumina, in particular in the form of clusters, in order to ensure sufficient elongation properties.
  • the inventors have demonstrated, in connection with the other elements of the composition, that an amount of aluminum up to 0.3% by weight could be added without adverse effect vis-à-vis other properties required particularly with respect to the deformability, and also provided the desired microstructural and mechanical properties.
  • molybdenum plays an effective role on quenchability and delays the enlargement of ferrite and the appearance of bainite.
  • a content greater than 0.25% excessively increases the cost of the additions.
  • chromium by its role on quenchability, also contributes to delay the formation of proeutectoid ferrite. Beyond 0.5%, the cost of the addition is too excessive.
  • chromium and molybdenum are taken into account in the invention according to their specific characteristics; according to the invention, the chromium and molybdenum contents are such that: Cr + (2 ⁇ Mo) ⁇ 0.6%.
  • the coefficients in this relation reflect the respective influence of these two elements on the quenchability in order to favor the obtaining of a fine ferritic structure.
  • Titanium and niobium are microalloy elements used together according to the invention:
  • titanium combines essentially with nitrogen and carbon to precipitate in the form of nitrides and / or carbonitrides. These precipitates are stable during reheating of the slabs at 1150-1250 ° C. before hot rolling, which makes it possible to control the size of the austenitic grain. Beyond a 0.050% titanium content, there is a risk of forming coarse titanium nitrides precipitated in the liquid state, which tend to reduce ductility.
  • niobium is very effective in forming Fine precipitates of Nb (CN) in the austenite or ferrite during hot rolling, or during annealing in a temperature range close to the intercritical transformation interval. It retards recrystallization during hot rolling and annealing and refines the microstructure.
  • an excessive amount of niobium decreasing weldability should be limited to 0.040%.
  • the titanium and niobium contents above make it possible to ensure that the nitrogen is completely trapped in the form of nitrides or carbonitrides, so that the boron is in free form and can play an effective role on the quenchability.
  • the effect of boron on quenchability is fundamental.
  • boron indeed makes it possible to control and limit the diffusive phase transformations (ferritic or pearlitic transformation during cooling) and to form hardening phases (bainite or martensite) necessary for obtaining high mechanical strength characteristics.
  • the addition of boron is therefore an important component of the present invention, it also makes it possible to limit the addition of quenching elements such as Mn, Mo, Cr and to reduce the analytical cost of the steel grade.
  • the minimum boron content to ensure effective quenchability is 0.0005%. Beyond 0.0025%, the effect on the quenchability is saturated and there is a detrimental effect on the coating and hot ductility.
  • a minimum content of 0.002% nitrogen is required. The nitrogen content is limited to 0.007% to avoid the formation of BN which would decrease the amount of free boron required for the hardening of the ferrite.
  • a steel of composition according to the invention is supplied
  • This casting can be carried out in ingots or continuously in the form of thick slabs of the order of 200mm. It is also possible to perform the casting in the form of slabs of a few tens of millimeters thick or thin strips between contra-rotating steel rolls.
  • the cast semifinished products are first brought to a temperature TR greater than 1150 ° C. to reach at any point a temperature favorable to the high deformations that the steel will undergo during rolling.
  • the austenitic grains increase undesirably.
  • the only precipitates likely to effectively control the size of the austenitic grain are titanium nitrides, and the reheating temperature should be limited to 1250 ° C. in order to maintain a fine austenitic grain at this stage.
  • the hot rolling step of these semi-products starting at more than 1150 ° C. can be done directly after casting so well. that an intermediate heating step is not necessary in this case.
  • the semi-finished product is hot-rolled in a temperature range where the structure of the steel is totally austenitic: if TFL is lower than the starting temperature of transformation from austenite to cooling A F3 , the ferrite grains are hardened by rolling and ductility is reduced.
  • a rolling end temperature of greater than 850 ° C. will be chosen.
  • the hot-rolled product is then rolled at a temperature T bO b of between 500 and 570 ° C.
  • T bO b This temperature range makes it possible to obtain a complete bainitic transformation during the quasi-isothermal maintenance associated with the winding.
  • This range leads to a morphology of Ti and Nb precipitates which are sufficiently fine in order to allow the exploitation of their hardening and quenching power during the subsequent steps of the manufacturing process.
  • a winding temperature greater than 57O 0 C leads to the formation of coarser precipitates, whose coalescence during continuous annealing significantly reduces the efficiency.
  • the hot-rolled product is then etched according to a process known per se, followed by cold rolling with a reduction ratio preferably comprised between 30 and 80%.
  • the cold-rolled product is then heated, preferably in a continuous annealing installation, with an average heating rate Vc of between 1 and 5 ° C./sec. In relation to the TM annealing temperature below, this heating rate range makes it possible to obtain a fraction of non-recrystallized ferrite less than or equal to 15%.
  • the heating is carried out up to an annealing temperature T M between the temperature A 0I (allotropic transformation start temperature at heating) + 40 ° C, and A ⁇ (end of allotropic transformation temperature at heating) - 30 ° C. C, that is to say in a particular temperature range of the intercritical range: when TM is less than (A c i + 40 ° C), the structure may also comprise non-recrystallized ferrite zones whose surface fraction may reach 15 %. This proportion of non-recrystallized ferrite is evaluated as follows: after having identified the ferritic phase within the microstructure, the surface percentage of non-recrystallized ferrite relative to the entire ferritic phase is quantified.
  • An annealing temperature T M makes it possible to obtain an amount of austenite sufficient to subsequently form the cooling of the martensite in an amount such that the desired characteristics are attained.
  • a temperature TM lower than (Ac 3 - 30 ° C.) also makes it possible to ensure that the carbon content of the austenite islands formed at the temperature T M indeed leads to a subsequent martensitic transformation: when the annealing temperature is too high, the carbon content of the austenite islands becomes too low, which leads to a subsequent transformation into bainite or unfavorable pearlite. In addition, too high a temperature leads to an increase in the size of niobium precipitates which lose some of their curing ability. The final mechanical strength is then decreased.
  • TM temperature between 760 0 C and 83O 0 C.
  • a minimum holding time t M of 30s at the temperature T M allows the dissolution of the carbides, a partial transformation into austenite is carried out. The effect is saturated beyond a duration of 300 s.
  • a holding time greater than 300s is also difficult to comply with the productivity requirements of continuous annealing equipment, in particular the speed of scrolling.
  • the holding time tM is between 30 and 300s.
  • cooling is carried out to a temperature below the temperature M s (martensite formation start temperature) with a cooling rate V sufficient for the austenite formed during annealing is totally transformed into martensite.
  • This cooling can be carried out from the temperature T M in one or several steps and may involve in the latter case different cooling modes such as cold or boiling water baths, jets of water or gas . These possible accelerated cooling modes can be combined to obtain a complete martensitic transformation of the austenite. After this martensitic transformation, the sheet is cooled to room temperature. The microstructure of the cooled bare sheet then consists of a ferritic matrix with islands of martensite whose surface proportion is between 35 and 50%, and is free of bainite.
  • the product is cooled to a temperature close to the temperature T Zn dip galvanizing, the speed of VR cooling is fast enough to avoid the transformation of austenite to ferrite.
  • the cooling rate V R is preferably greater than 15 0 CVs.
  • Galvanizing is carried out by immersion in a bath of zinc or alloy of zinc whose temperature Tz n is between 450 and 480 ° C. A partial transformation of austenite into bainite occurs at this stage, which leads to the formation of 1 to 10% of bainite, this value being expressed in surface proportion.
  • the maintenance in this temperature range must be less than 80s so as to limit the surface proportion of bainite to 10% and thus obtain a sufficient proportion of martensite.
  • the galvanized product is then cooled at a rate V ' R greater than 4 ° C./s up to room temperature in order to completely convert the remaining austenite fraction into martensite: in this way a sheet of aluminum is obtained.
  • the product is cooled at the end of the maintenance of annealing until reaching a temperature close to the dip galvanizing temperature T Zn , the cooling rate V R being fast enough to avoid the transformation of austenite to ferrite.
  • the cooling rate V R is preferably greater than 15 ° C / s.
  • Galvanizing is carried out by dipping by immersion in a bath of zinc or zinc alloy whose temperature T Zn is between 450 and 480 ° C.
  • a partial transformation of the austenite into bainite occurs at this stage, which leads to the formation of 1 to 10% of bainite, this value being expressed in surface proportion.
  • the maintenance in this temperature range must be less than 80s so as to limit the proportion of bainite to 10%.
  • the galvanized product is heated to a temperature T G of between 490 and 550 0 C for a period XQ of between 10 and 40s. This causes the interdiffusion of iron and the thin layer of zinc or zinc alloy deposited during the immersion, which allows to obtain a galvannealed product.
  • This product is cooled to room temperature with a speed V " R greater than 4 ° C./s: a galvannealed sheet of ferritic matrix steel is obtained in this way, containing 40-64% of ferrite in surface proportion, 35-50% of martensite and 1-10% of bainite Martensite is typically in the form of islands of average size less than 4 micrometers, or even two microns, these Islets presenting, for more than 50% of them, a massive morphology rather than an elongated morphology.
  • the morphology of a given island is characterized by the ratio between its maximum size L max and minimum L min .
  • a given island is considered to have a
  • Steels have been developed whose composition is shown in the table below, expressed as a percentage by weight. In addition to the steels IX to IZ used for the manufacture of sheets according to the invention, it was indicated for comparison the composition of a steel R used for the manufacture of reference sheets.
  • Cast half-products corresponding to the above compositions were heated to 123O 0 C and then hot rolled to a thickness of 2.8-4 mm in a field where the structure is entirely austenitic.
  • the manufacturing conditions of these hot-rolled products (rolling end temperature T F L, winding temperature T bO b) are shown in Table 2.
  • References 1X1, IX2 and IX3 denote for example three steel sheets manufactured under different conditions from the steel composition IX.
  • the sheets were galvanized by dipping in a zinc bath at a temperature T Zn of 460 ° C., others were further subjected to a galvannealing treatment.
  • Table 3 shows the manufacturing conditions for annealed sheet after cold rolling:
  • the mechanical tensile properties obtained (elastic limit Re, resistance Rm, elongation at break A were given in Table 4 below), the ratio Re / Rm was also indicated, and the microstructure of the steels was determined.
  • the matrix is ferritic
  • the surface fractions of bainite and martensite were quantified after Picral and LePera reagent etching respectively, followed by an image analysis using Aphelion TM software, and the non-recrystallized ferrite surface fraction was determined by to observations in optical microscopy and scanning electron where the ferritic phase has been identified, then quantified the recrystallized fraction within this ferritic phase
  • the non-recrystallized ferrite is generally in the form of islands elongated by rolling.
  • the folding ability was quantified as follows: sheets were folded in a block on themselves in several turns. In this way, the bending radius decreases each turn. The foldability is then evaluated by noting the presence of cracks on the surface of the folded block, the rating being expressed from 1 (low foldability) to 5 (very good ability). satisfactory.
  • the steel sheets according to the invention have a set of microstructural and mechanical characteristics enabling the advantageous manufacture of parts, in particular for structural applications: resistance of between 980 and 1100 MPa, ratio R e / R m of between 0.6 and 0.8, elongation at break of greater than 9%, good folding ability.
  • Figure 1 illustrates the morphology of the 1X1 steel sheet, where the ferrite is completely recrystallized.
  • the sheets according to the invention have good weldability, in particular resistance, the equivalent carbon being less than 0.25.
  • weldability range as defined by the standard I S018278-2, in spot welding is very wide, of the order of 3500A. It is increased relative to a reference grade of the same grade.
  • cross-tension or tensile-shear tests carried out on welded points of sheets according to the invention reveal that the resistance of these welded points is very high with regard to the mechanical characteristics.
  • the reference plates do not offer these same characteristics:
  • FIG. 2 illustrates the microstructure of the steel sheet IX3: there is the presence of non-recrystallized ferrite in the form of elongate islands (marked (A)) coexisting with recrystallized ferrite and martensite, the latter constituting appearing darker on micrography.
  • a scanning electron micrograph (FIG. 3) makes it possible to finely distinguish the zones of non-recrystallized ferrite (A) from those recrystallized (B).
  • Sheet IX5 is a galvannealed sheet annealed at a temperature T M too high: the carbon content of austenite at high temperature then becomes too low and the appearance of bainite is favored at the expense of the formation of martensite. Coalescence of niobium precipitates is also observed, which causes a loss of hardening. The resistance is then insufficient, the ratio Re / R m being too high.
  • the Galvannealed 1X7 sheet was cooled at a rate V R too slow after the annealing step: the transformation of the austenite formed into ferrite then occurs in this cooling step excessively, the steel sheet containing at the stage final a proportion of bainite too important and a proportion of martensite too low, which leads to insufficient resistance.
  • the composition of the steel sheet R does not correspond to the invention, its carbon content being too high, and its content of manganese, aluminum, niobium, titanium, boron being too low. As a result, the martensite fraction is too weak so that the mechanical strength is insufficient.
  • the steel sheets according to the invention will be used profitably for the manufacture of structural parts or safety in the automotive industry.

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Abstract

The invention relates to an annealed, cold-rolled, dual phase steel sheet having a strength of 980 to 1100 MPa and an elongation at break greater than 9%, comprising the following composition (as expressed in wt.-%): 0.055% = C = 0.095%, 2% = Mn = 2.6%, 0.005% = Si = 0.35%, S = 0.005%, P = 0.05%, 0.1 = Al = 0.3%, 0.05% = Mo = 0.25%, 0.2% = Cr = 0.5%, assuming that Cr+2Mo = 0.6%, Ni = 0.1%, 0.01 = Nb = 0.04%, 0.01 = Ti = 0.050%, 0.0005 = B = 0.0025%, 0.002% = N = 0.007%, the remainder of the composition consisting of iron and inevitable impurities resulting from production.

Description

PROCEDE DE FABRICATION DE TOLES D'ACIERS DUAL PHASE LAMINEES A FROID A TRES HAUTE RESISTANCE ET TOLES AINSI METHOD FOR MANUFACTURING COLD LAMINATED DUAL PHASE STEEL SHEETS WITH VERY HIGH RESISTANCE AND SHEETS THUS

PRODUITESGOODS

L'invention concerne la fabrication de tôles laminées à froid et recuites d'aciers dits « dual-phase » présentant une très haute résistance et une aptitude à la déformation pour la fabrication de pièces par mise en forme, en particulier dans l'industrie automobile. Les aciers dual-phase, dont la structure comprend de la martensite, éventuellement de la bainite, au sein d'une matrice ferritique, ont connu un grand développement car ils allient une résistance élevée à des possibilités importantes de déformation. A l'état de livraison, leur limite d'élasticité est relativement basse comparée à leur résistance à la rupture, ce qui leur confère un rapport (limite d'élasticité/résistance) très favorable lors des opérations de formage. Leur capacité de consolidation est très grande, ce qui permet une bonne répartition des déformations dans le cas d'une collision et l'obtention d'une limite d'élasticité nettement plus importante sur pièce après formage. On peut réaliser ainsi des pièces aussi complexes qu'avec des aciers conventionnels, mais avec des propriétés mécaniques plus élevées, ce qui autorise une diminution d'épaisseur pour tenir un cahier des charges fonctionnel identique. De la sorte, ces aciers sont une réponse efficace aux exigences d'allégement et de sécurité des véhicules. Dans le domaine des tôles laminées à chaud (d'épaisseur allant par exemple de 1 à 10mm) ou laminées à froid (épaisseur allant par exemple de 0,5 à 3 mm), ce type d'aciers trouve notamment des applications pour des pièces de structures et de sécurité pour les véhicules automobile, telles que les traverses, longerons, pièces de renfort, ou encore les voiles de roues.The invention relates to the manufacture of cold-rolled and annealed sheets of so-called "dual-phase" steels having a very high strength and a deformability for the manufacture of parts by shaping, in particular in the automotive industry. . The dual-phase steels, whose structure includes martensite, possibly bainite, in a ferritic matrix, have developed a great deal because they combine high resistance with significant possibilities of deformation. In the delivery state, their yield strength is relatively low compared to their breaking strength, which gives them a very favorable ratio (yield strength / strength) during forming operations. Their consolidation capacity is very large, which allows a good distribution of deformations in the case of a collision and obtaining a significantly higher yield strength on the part after forming. It is thus possible to produce parts as complex as with conventional steels, but with higher mechanical properties, which allows a reduction in thickness to maintain identical functional specifications. In this way, these steels are an effective response to the requirements of lightening and safety of vehicles. In the field of hot-rolled sheets (of thickness ranging for example from 1 to 10 mm) or cold-rolled (thickness ranging for example from 0.5 to 3 mm), this type of steel finds particular applications for parts. structures and safety for motor vehicles, such as sleepers, longitudinal members, reinforcement pieces, or wheel sails.

Les exigences récentes d'allégement et de réduction de la consommation d'énergie ont conduit à une demande accrue d'aciers dual-phase à très haute résistance, c'est à dire dont la résistance mécanique Rm est comprise entre 980 et 1100MPa. Outre ce niveau de résistance, ces aciers doivent présenter une bonne soudabilité et une bonne aptitude à la galvanisation en continu au trempé. Ces aciers doivent également présenter une bonne aptitude au pliage.The recent requirements for lightening and reducing energy consumption have led to an increased demand for very high strength dual-phase steels, that is to say whose mechanical strength R m is between 980 and 1100 MPa. In addition to this level of resistance, these steels must have good weldability and good continuous galvanizing ability at the same time. tempered. These steels must also have good folding ability.

La fabrication d'aciers Dual Phase à haute résistance est par exemple décrite dans le document EP1201780 A1 relatif à des aciers de composition : 0,01- 0,3%C, 0,01 -2%Si, 0,05-3%Mn, <0,1%P, <0,01%S, 0,005-1 %AI, dont la résistance mécanique est supérieure à 540MPa, qui présentent une bonne résistance à la fatigue et une aptitude à l'expansion de trou. Cependant, la plupart des exemples présentés dans ce document révèlent une résistance inférieure à 875 MPa. Les rares exemples dans ce document allant au delà de cette valeur sont relatifs à des aciers à forte teneur en carbone (0,25 ou 0,31%) pour lesquelles l'aptitude au soudage et à l'expansion de trou n'est pas suffisante.The manufacture of high strength dual phase steels is for example described in EP1201780 A1 relating to steels of composition: 0.01-0.3% C, 0.01 -2% Si, 0.05-3% Mn, <0.1% P, <0.01% S, 0.005-1% AI, with mechanical strength greater than 540 MPa, which exhibit good fatigue strength and hole expansion capability. However, most of the examples presented in this document disclose a resistance of less than 875 MPa. The rare examples in this document going beyond this value are relative to steels with a high carbon content (0.25 or 0.31%) for which the weldability and the expansion of the hole are not sufficient.

Le document EP0796928A1 décrit par ailleurs des aciers Dual Phase laminés à froid dont la résistance est supérieure à 550MPa, de composition 0,05- 0,3%C, 0,8-3%Mn, 0,4-2,5%AI, 0,01-0,2%Si. La matrice ferritique contient de la martensite, de la bainite et/ou de l'austénite résiduelle. Les exemples présentés montrent que la résistance ne dépasse pas 660MPa, même pour une teneur en carbone élevée (0,20-0,21%) Le document JP11350038 décrit des aciers Dual Phase dont la résistance est supérieure à 980MPa, de composition 0,10-0,15%C, 0,8-1 , 5%Si, 1 ,5- 2,0%Mn, 0,01-0,05%P, moins de 0,005%S, 0,01-0,07%AI en solution, moins de 0,01 %N, contenant en outre un ou plusieurs éléments : 0,001 -0,02%Nb, 0,001 -0,02%V, 0,001 -0,02%Ti. Cette résistance élevée est cependant obtenue au prix d'une addition importante de silicium qui permet certes la formation de martensite, mais peut néanmoins conduire à la formation d'oxydes superficiels qui détériorent la revêtabilité au trempé. Le but de la présente invention est de proposer un procédé de fabrication de tôles d'aciers dual-phase à très haute résistance, laminées à froid, nues ou revêtues, ne présentant pas les inconvénients mentionnés précédemment. Elle vise à mettre à disposition des tôles d'acier Dual Phase présentant une résistance mécanique comprise entre 980 et 1100 MPa conjointement avec un allongement à rupture supérieur à 9% et une bonne aptitude au formage, notamment au pliage L'invention vise également à mettre à disposition un procédé de fabrication dont de faibles variations des paramètres n'entraînent pas de modifications importantes de la microstructure ou des propriétés mécaniques. L'invention vise également à mettre à disposition une tôle d'acier aisément fabricable par laminage à froid, c'est à dire dont la dureté après l'étape de laminage à chaud est limitée de telle sorte que les efforts de laminage restent modérés lors de l'étape de laminage à froid.The document EP0796928A1 also describes cold-rolled Dual Phase steels with a resistance greater than 550 MPa, with a composition of 0.05-0.3% C, 0.8-3% Mn, 0.4-2.5% AI. , 0.01-0.2% Si. The ferritic matrix contains martensite, bainite and / or residual austenite. The examples presented show that the resistance does not exceed 660 MPa, even for a high carbon content (0.20-0.21%) JP11350038 describes dual phase steels with a resistance greater than 980 MPa, composition 0.10. -0.15% C, 0.8-1.5% Si, 1.5-2.0% Mn, 0.01-0.05% P, less than 0.005% S, 0.01-0.07 % AI in solution, less than 0.01% N, additionally containing one or more elements: 0.001-0.02% Nb, 0.001-0.02% V, 0.001-0.02% Ti. This high strength is, however, obtained at the cost of a significant addition of silicon which certainly allows the formation of martensite, but may nevertheless lead to the formation of surface oxides which deteriorate the coating on quenching. The object of the present invention is to provide a method of manufacturing dual-phase steel plates very high strength, cold rolled, bare or coated, not having the disadvantages mentioned above. It aims to provide Dual Phase steel sheets with a mechanical strength of between 980 and 1100 MPa together with an elongation greater than 9% rupture and good formability, including folding The invention also aims to provide a manufacturing method in which small variations in the parameters do not lead to significant changes in the microstructure or mechanical properties. The invention also aims to provide a sheet of steel easily fabricated by cold rolling, that is to say whose hardness after the hot rolling step is limited so that the rolling forces remain moderate during of the cold rolling step.

Elle vise également à disposer d'une tôle d'acier apte au dépôt d'un revêtement métallique, en particulier par galvanisation au trempé selon les procédés usuels.It also aims to have a steel sheet capable of depositing a metal coating, in particular by dip galvanizing according to the usual methods.

Elle vise encore à disposer d'un acier présentant une bonne aptitude au soudage au moyen des procédés d'assemblage usuels tels que le soudage par résistance par points. L'invention vise également à mettre à disposition un procédé de fabrication économique en évitant l'addition d'éléments d'alliage coûteux.It also aims to have a steel having good weldability by means of conventional assembly methods such as spot resistance welding. The invention also aims to provide an economical manufacturing process by avoiding the addition of expensive alloying elements.

A cet effet, l'invention a pour objet une tôle d'acier Dual Phase laminée à froid et recuite de résistance comprise entre 980 et 1100MPa, d'allongement à rupture supérieur à 9 %, dont la composition comprend, les teneurs étant exprimées en poids : 0,055% <C < 0,095%, 2% ≤Mn <2,6%, 0,005% < Si≤ 0,35%, S<0,005%, P <0,050%, 0,1 ≤AI < 0,3%, 0,05% ≤Mo <0,25%, 0,2%<Cr<0,5%, étant entendu que Cr+2Mo<0,6%, Ni≤ 0,1%, 0,01 O≤Nb <0,040%, 0,01 O≤Ti ≤0,050%, 0,0005 ≤B <0,0025%, 0,002%<N<0,007%, le reste de la composition étant constitué de fer et d'impuretés inévitables résultant de l'élaboration. Préférentiellement, la composition de l'acier contient, la teneur étant exprimée en poids : 0,12% <AI<0,25%.For this purpose, the subject of the invention is a dual-phase cold-rolled and annealed steel sheet having a strength of between 980 and 1100 MPa, an elongation at break of greater than 9%, the composition of which comprises the contents being expressed in terms of Weight: 0.055% <C <0.095%, 2% ≤Mn <2.6%, 0.005% <Si≤0.35%, S <0.005%, P <0.050%, 0.1 ≤AI <0.3% , 0.05% ≤Mo <0.25%, 0.2% <Cr <0.5%, with the proviso that Cr + 2Mo <0.6%, Ni≤0.1%, 0.01O≤Nb <0.040%, 0.01 O≤Ti ≤0.050%, 0.0005 ≤B <0.0025%, 0.002% <N <0.007%, the rest of the composition consisting of iron and unavoidable impurities resulting from the development. Preferably, the composition of the steel contains, the content being expressed by weight: 0.12% <Al <0.25%.

Selon un mode préféré, la composition de l'acier contient, la teneur étant exprimée en poids : 0,10% ≤ Si ≤ 0,30%. La composition de l'acier contient à titre préférentiel :0,15% ≤ Si ≤ 0,28%. Selon un mode préféré, la composition contient : P ≤0,015%.According to a preferred embodiment, the composition of the steel contains, the content being expressed by weight: 0.10% ≤ Si ≤ 0.30%. The composition of the steel preferably contains: 0.15% ≤ Si ≤ 0.28%. According to a preferred embodiment, the composition contains: P ≤ 0.015%.

La microstructure de la tôle contient préférentiellement 35 à 50% de martensite en proportion surfacique. Selon un mode particulier, le complément de la microstructure est constitué de 50 à 65% de ferrite en proportion surfacique.The microstructure of the sheet preferably contains 35 to 50% of martensite in surface proportion. According to one particular embodiment, the complement of the microstructure consists of 50 to 65% of ferrite in surface proportion.

Selon un autre mode particulier, le complément de la microstructure est constitué de 1 à 10% de bainite et de 40 à 64% de ferrite en proportion surfacique.According to another particular mode, the complement of the microstructure consists of 1 to 10% of bainite and 40 to 64% of ferrite in surface proportion.

La fraction surfacique de ferrite non recristallisée rapportée à la totalité de la phase ferritique est préférentiellement inférieure ou égale à 15%.The surface fraction of non-recrystallized ferrite relative to the entire ferritic phase is preferably less than or equal to 15%.

La tôle d'acier possède préférentiellement un rapport entre sa limite d'élasticité Re et sa résistance Rm tel que : 0,6<Re/Rm <0,8. Selon un mode particulier, la tôle est galvanisée en continu.The steel sheet preferably has a ratio between its elastic limit R e and its resistance R m such that: 0.6 <Re / R m <0.8. In a particular embodiment, the sheet is galvanized continuously.

Selon un autre mode particulier, la tôle comporte un revêtement galvannealed.In another particular embodiment, the sheet has a galvannealed coating.

L 'invention a également pour objet un procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid et recuite caractérisé en ce qu'on approvisionne un acier de composition selon l'une quelconque des caractéristiques ci-dessus, puisThe subject of the invention is also a process for manufacturing a cold rolled and annealed dual phase steel sheet, characterized in that a composition steel is supplied according to any one of the above characteristics, and then

- on coule l'acier sous forme de demi-produit, puis- the steel is cast as a semi-finished product, then

- on porte le demi-produit à une température 1150°C<TR<1250oC, puis- one carries the semi-finished product at a temperature 1150 ° C <T R <1250 ° C, then

- on lamine à chaud le demi-produit avec une température de fin de laminage TFL ≥AΓ3 pour obtenir un produit laminé à chaud, puisthe semi-finished product is hot-rolled with an end-of-rolling temperature TFL ≥AΓ3 in order to obtain a hot-rolled product, and then

- on bobine le produit laminé à chaud à une température 5000C ≤TbOb≤ 5700C, puis on décape le produit laminé à chaud, puis on effectue un laminage à froid avec un taux de réduction compris entre 30 et 80% pour obtenir un produit laminé à froid, puis - on chauffe le produit laminé à froid à une vitesse 1 °C/s<Vc≤5oC/s jusqu'à une température de recuit TM telle que : Ad +40°C<TM≤Ac3-30oC où l'on effectue un maintien pendant une durée : 30s≤tM ≤300s de façon à obtenir un produit chauffé et recuit avec une structure comprenant de l'austénite, puis- one coil the hot rolled product at a temperature of 500 0 C ≤ T bO b≤ 570 0 C., then pickled hot-rolled, followed by cold rolling with a reduction rate between 30 and 80% to obtain a cold-rolled product, and then - the cold-rolled is heated at a rate 1 ° C / s <V c ≤5 ° C / s down to a temperature T M annealing as: Ad + 40 ° C <T M ≤Ac3-30 o C where a maintenance is carried out for a duration: 30s≤t M ≤300s so as to obtain a heated and annealed product with a structure comprising austenite, then

- on refroidit le produit jusqu'à une température inférieure à la température M5 avec une vitesse V suffisante pour que l'austénite se transforme totalement en martensite.the product is cooled to a temperature below the temperature M 5 with a speed V sufficient for the austenite to become totally martensite.

L'invention a également pour objet un procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid, recuite et galvanisée caractérisé en ce qu'on approvisionne le produit chauffé et recuit avec une structure comprenant de l'austénite selon la caractéristique ci-dessus puis,The subject of the invention is also a process for producing a cold rolled, annealed and galvanized dual phase steel sheet characterized in that supplying the heated and annealed product with a structure comprising austenite according to the above characteristic then,

- on refroidit le produit chauffé et recuit avec une vitesse VR suffisante pour éviter la transformation de l'austénite en ferrite, jusqu'à atteindre une température proche de la température TZn de galvanisation au trempé, puisthe product heated and annealed is cooled with a speed V R sufficient to prevent the transformation of the austenite into ferrite, until it reaches a temperature close to the dip galvanizing temperature T Zn , then

- on galvanise en continu le produit par immersion dans un bain de zinc ou d'alliage de Zn à une température 450°C≤Tzn≤480°C pour obtenir un produit galvanisé, puisthe product is continuously galvanized by immersion in a bath of zinc or of Zn alloy at a temperature of 450 ° C.≤Zn≤480 ° C. to obtain a galvanized product, and then

- on refroidit le produit galvanisé jusqu'à la température ambiante avec une vitesse VR supérieure à 4°C/s pour obtenir une tôle d'acier laminée à froid, recuite et galvanisée.- The galvanized product is cooled to room temperature with a speed VR greater than 4 ° C / s to obtain a cold rolled steel sheet, annealed and galvanized.

L'invention a également pour objet un procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid et galvannealed, caractérisé en ce qu'on approvisionne le produit chauffé et recuit avec une structure comprenant de l'austénite selon la caractéristique ci-dessus, puis,The subject of the invention is also a process for producing a cold-rolled and galvannealed dual phase steel sheet, characterized in that the heated and annealed product is supplied with a structure comprising austenite according to the characteristic above, then,

- on refroidit le produit chauffé et recuit avec une vitesse VR suffisante pour éviter la transformation de ladite austénite en ferrite, jusqu'à atteindre une température proche de la température TZn de galvanisation au trempé, puisthe product heated and annealed is cooled with a speed V R sufficient to prevent the transformation of said austenite into ferrite, until it reaches a temperature close to the dip galvanizing temperature T Zn , then

- on galvanise en continu le produit par immersion dans un bain de zinc ou d'alliage de Zn à une température 450oC≤TZn≤480°C pour obtenir un produit galvanisé, puis- is continuously galvanized product by immersion in a bath of zinc or Zn alloy at a temperature of 450 o C≤T Zn ≤480 ° C to obtain a galvanized product, then

- on chauffe le produit galvanisé à une température TG comprise entre 490 et 550°C pendant une durée to comprise entre 10 et 40 s pour obtenir un produit galvannealed, puis - on refroidit le produit galvannealed jusqu'à la température ambiante à une vitesse V"R supérieure à 4°C/s, pour obtenir une tôle d'acier laminée à froid et galvannealed.the galvanized product is heated at a temperature of between 490 and 550 ° C. for a period of between 10 and 40 seconds to obtain a galvannealed product, and then the galvannealed product is cooled to ambient temperature at a speed V "R greater than 4 ° C / s, to obtain a cold-rolled and galvannealed steel sheet.

L'invention a également pour objet un procédé de fabrication selon l'une des caractéristiques ci-dessus, caractérisé en ce que la température TM est comprise entre 760 et 83O0C.The invention also relates to a manufacturing method according to one of the above characteristics, characterized in that the temperature T M is between 760 and 83O 0 C.

Selon un mode particulier, la vitesse de refroidissement VR est supérieure ou égale à 15°C/s. L'invention a également pour objet l'utilisation d'une tôle d'acier selon l'une quelconque des caractéristiques ci-dessus, ou fabriquée par un procédé selon l'une quelconque des caractéristiques ci-dessus, pour la fabrication de pièces de structures ou de sécurité pour véhicules automobiles. D'autres caractéristiques et avantages de l'invention apparaîtront au cours de la description ci-dessous, donnée à titre d'exemple et faite en référence aux figures annexées ci-jointes selon lesquelles :According to a particular mode, the cooling rate V R is greater than or equal to 15 ° C / s. The invention also relates to the use of a steel sheet according to any one of the above characteristics, or manufactured by a process according to any one of the above characteristics, for the manufacture of structures or safety for motor vehicles. Other features and advantages of the invention will become apparent from the description below, given by way of example and with reference to the appended accompanying figures in which:

- La figure 1 présente un exemple de microstructure d'une tôle d'acier selon l'invention - Les figures 2 et 3 présentent des exemples de microstructure de tôles d'acier non conforme à l'invention.FIG. 1 shows an example of microstructure of a steel sheet according to the invention. FIGS. 2 and 3 show examples of microstructure of steel sheets not in accordance with the invention.

L'invention va maintenant être décrite de façon plus précise, mais non limitative, en considérant ses différents éléments caractéristiques : En ce qui concerne la composition chimique de l'acier, le carbone joue un rôle important sur la formation de la microstructure et sur les propriétés mécaniques : au-dessous de 0,055% en poids, la résistance devient insuffisante. Au-delà de 0,095%, un allongement de 9% ne peut plus être garanti. La soudabilité est également réduite. Outre un effet durcissant par solution solide, le manganèse est un élément qui augmente la trempabilité et réduit la précipitation de carbures. Une teneur minimale de 2% en poids est nécessaire pour obtenir les propriétés mécaniques désirées. Cependant, au-delà de 2,6%, son caractère gammagène conduit à la formation d'une structure en bandes trop marquée. Le silicium est un élément participant à la désoxydation de l'acier liquide et au durcissement en solution solide. Cet élément joue en outre un rôle important dans la formation de la microstructure en empêchant la précipitation des carbures et en favorisant la formation de martensite qui entre dans la structure des aciers Dual Phase. Il joue un rôle effectif au-delà de 0,005%. Une addition de silicium en quantité supérieure à 0,10%, préférentiellement supérieure à 0,15%, permet d'atteindre les plus hauts niveaux de résistance visés par l'invention. Cependant, une augmentation de la teneur en silicium dégrade l'aptitude au revêtement au trempé en favorisant la formation d'oxydes adhérents à la surface des produits : sa teneur doit être limitée à 0,35% en poids, et préférentiellement à 0,30% pour obtenir une bonne revêtabilité. En outre, le silicium diminue la soudabilité : une teneur inférieure à 0,28% permet d'assurer simultanément une très bonne aptitude au soudage ainsi qu'une bonne revêtabilité. Au-delà d'une teneur en soufre de 0,005%, la ductilité est réduite en raison de la présence excessive de sulfures tels que MnS qui diminuent l'aptitude à la déformation, en particulier lors d'essais d'expansion de trou. Le phosphore est un élément qui durcit en solution solide mais qui diminue la soudabilité par points et la ductilité à chaud, particulièrement en raison de son aptitude à la ségrégation aux joints de grains ou à la co-ségrégation avec le manganèse. Pour ces raisons, sa teneur doit être limitée à 0,050%, et préférentiellement à 0,015% afin d'obtenir une bonne aptitude au soudage par points. L'aluminium joue un rôle important dans l'invention en empêchant la précipitation des carbures et en favorisant la formation des constituants martensitiques au refroidissement. Ces effet sont obtenus lorsque la teneur en aluminium est supérieure à 0,1%, et préférentiellement lorsque la teneur en aluminium est supérieure à 0,12%. Sous forme d'AIN, l'aluminium limite la croissance du grain lors du recuit après laminage à froid. Cet élément est aussi utilisé pour la désoxydation de l'acier liquide en quantité usuellement inférieure à environ 0,050%. On considère en effet habituellement que des teneurs plus importantes accroissent l'érosion des réfractaires et le risque de bouchage des busettes. En quantité excessive, l'aluminium diminue la ductilité à chaud et augmente le risque d'apparition de défauts en coulée continue. On cherche également à limiter les inclusions d'alumine, en particulier sous forme d'amas, dans le but de garantir des propriétés d'allongement suffisantes. Or les inventeurs ont mis en évidence, en liaison avec les autres éléments de la composition, qu'une quantité d'aluminium allant jusqu'à 0,3% en poids pouvait être ajoutée sans effet néfaste vis-à-vis des autres propriétés requises, en particulier vis- à-vis de l'aptitude à la déformation, et permettait également d'obtenir les propriétés microstructurales et mécaniques visées. Au delà de 0,3%, il existe un risque d'interaction entre le métal liquide et le laitier lors de la coulée continue, qui conduit à l'apparition éventuelle de défauts. Une teneur en aluminium allant jusqu'à 0,25% en poids permet d'assurer la formation d'une microstructure fine sans îlots martensitiques de grande taille qui joueraient un rôle néfaste sur la ductilité. Les inventeurs ont montré que, d'une manière surprenante, il était possible d'obtenir un niveau de résistance élevé, compris entre 980 et 1100MPa, même en dépit de la limitation des additions d'aluminium et de silicium. Ceci est obtenu par la combinaison particulière des éléments d'alliage ou de microalliage selon l'invention en particulier grâce aux additions de Mo, Cr, Nb1Ti, B.The invention will now be described in a more precise but nonlimiting manner, considering its various characteristic elements: With regard to the chemical composition of steel, carbon plays an important role in the formation of the microstructure and in the mechanical properties: below 0.055% by weight, the resistance becomes insufficient. Beyond 0.095%, a lengthening of 9% can no longer be guaranteed. The weldability is also reduced. In addition to a solid solution hardening effect, manganese is an element that increases quenchability and reduces carbide precipitation. A minimum content of 2% by weight is necessary to obtain the desired mechanical properties. However, beyond 2.6%, its gammagenic character leads to the formation of a band structure too marked. Silicon is a component involved in the deoxidation of liquid steel and hardening in solid solution. This element also plays an important role in the formation of the microstructure by preventing the precipitation of carbides and by promoting the formation of martensite which enters the structure of the Dual Phase steels. It plays an effective role beyond 0.005%. An addition of silicon in an amount greater than 0.10%, preferably greater than 0.15%, makes it possible to achieve the highest levels of resistance to which the invention relates. However, an increase in the silicon content degrades the dip coating ability by promoting the formation of adherent oxides on the surface of the products: its content must be limited to 0.35% by weight, and preferably 0.30% to obtain a good coating. In addition, the silicon decreases the weldability: a content of less than 0.28% makes it possible simultaneously to ensure very good weldability as well as good coating. Beyond a sulfur content of 0.005%, the ductility is reduced due to the excessive presence of sulfides such as MnS which decrease the ability to deform, especially during hole expansion tests. Phosphorus is an element that hardens in solid solution but decreases spot weldability and hot ductility, particularly because of its ability to segregate at grain boundaries or co-segregate with manganese. For these reasons, its content must be limited to 0.050%, and preferably to 0.015% in order to obtain a good spot welding ability. Aluminum plays an important role in the invention by preventing the precipitation of carbides and promoting the formation of martensitic constituents upon cooling. These effects are obtained when the aluminum content is greater than 0.1%, and preferably when the aluminum content is greater than 0.12%. In the form of AlN, aluminum limits grain growth during annealing after cold rolling. This element is also used for the deoxidation of the liquid steel in an amount usually less than about 0.050%. It is usually considered that higher levels increase the erosion of refractories and the risk of plugging the nozzles. In excessive amounts, aluminum reduces hot ductility and increases the risk of defects in continuous casting. It is also sought to limit inclusions of alumina, in particular in the form of clusters, in order to ensure sufficient elongation properties. However, the inventors have demonstrated, in connection with the other elements of the composition, that an amount of aluminum up to 0.3% by weight could be added without adverse effect vis-à-vis other properties required particularly with respect to the deformability, and also provided the desired microstructural and mechanical properties. Beyond 0.3%, there is a risk of interaction between the liquid metal and the slag during casting continuous, which leads to the possible appearance of defects. An aluminum content of up to 0.25% by weight makes it possible to ensure the formation of a fine microstructure without large martensitic islands which would play a detrimental role on the ductility. The inventors have shown that, surprisingly, it was possible to obtain a high level of resistance, between 980 and 1100 MPa, even in spite of the limitation of additions of aluminum and silicon. This is achieved by the particular combination of the alloying or microalloying elements according to the invention in particular by virtue of the additions of Mo, Cr, Nb 1 Ti, B.

En quantité supérieure à 0,05% en poids, le molybdène joue un rôle efficace sur la trempabilité et retarde le grossissement de la ferrite et l'apparition de la bainite. Cependant, une teneur supérieure à 0,25% accroît excessivement le coût des additions. En quantité supérieure à 0,2%, le chrome, par son rôle sur la trempabilité, contribue également à retarder la formation de ferrite proeutectoïde. Au delà de 0,5%, le coût de l'addition est là aussi excessif.In an amount greater than 0.05% by weight, molybdenum plays an effective role on quenchability and delays the enlargement of ferrite and the appearance of bainite. However, a content greater than 0.25% excessively increases the cost of the additions. In an amount greater than 0.2%, chromium, by its role on quenchability, also contributes to delay the formation of proeutectoid ferrite. Beyond 0.5%, the cost of the addition is too excessive.

Les effets conjoints du chrome et du molybdène sur la trempabilité sont pris en compte dans l'invention selon leurs caractéristiques propres ; selon l'invention, les teneurs en chrome et en molybdène sont telles que : Cr+(2 x Mo) <0,6%. Les coefficients dans cette relation traduisent l'influence respective de ces deux éléments sur la trempabilité en vue de favoriser l'obtention d'une structure ferritique fine. Le titane et le niobium sont des éléments de microalliage utilisés conjointement selon l'invention :The joint effects of chromium and molybdenum on quenchability are taken into account in the invention according to their specific characteristics; according to the invention, the chromium and molybdenum contents are such that: Cr + (2 × Mo) <0.6%. The coefficients in this relation reflect the respective influence of these two elements on the quenchability in order to favor the obtaining of a fine ferritic structure. Titanium and niobium are microalloy elements used together according to the invention:

- En quantité comprise entre 0,010 et 0,050%, le titane se combine essentiellement à l'azote et au carbone pour précipiter sous forme de nitrures et/ou de carbonitrures. Ces précipités sont stables lors d'un réchauffage des brames à 1150-12500C avant le laminage à chaud, ce qui permet de contrôler la taille du grain austénitique. Au delà d'une teneur en titane de 0,050%, il existe un risque de former des nitrures de titane grossiers précipités dès l'état liquide, qui tendent à réduire la ductilité.In an amount of between 0.010 and 0.050%, titanium combines essentially with nitrogen and carbon to precipitate in the form of nitrides and / or carbonitrides. These precipitates are stable during reheating of the slabs at 1150-1250 ° C. before hot rolling, which makes it possible to control the size of the austenitic grain. Beyond a 0.050% titanium content, there is a risk of forming coarse titanium nitrides precipitated in the liquid state, which tend to reduce ductility.

- En quantité supérieure à 0,010%, le niobium est très efficace pour former de fins précipités de Nb(CN) dans l'austénite ou dans la ferrite lors du laminage à chaud, ou encore lors du recuit dans une gamme de température voisine de l'intervalle de transformation intercritique. Il retarde la recristallisation lors du laminage à chaud et lors du recuit et affine la microstructure. Cependant, une quantité excessive en niobium diminuant la soudabilité, il convient de limiter celle-ci à 0,040%.- In an amount greater than 0.010%, niobium is very effective in forming Fine precipitates of Nb (CN) in the austenite or ferrite during hot rolling, or during annealing in a temperature range close to the intercritical transformation interval. It retards recrystallization during hot rolling and annealing and refines the microstructure. However, an excessive amount of niobium decreasing weldability should be limited to 0.040%.

Les teneurs en titane et en niobium ci-dessus permettent de faire en sorte que l'azote soit entièrement piégé sous forme de nitrures ou de carbonitrures, si bien que le bore se trouve sous forme libre et peut jouer un rôle efficace sur la trempabilité. L'effet du bore sur la trempabilité est fondamental. En limitant l'activité du carbone, le bore permet en effet de contrôler et de limiter les transformations de phase diffusives (transformation ferritique ou perlitique lors du refroidissement) et de former des phases durcissantes (bainite ou martensite) nécessaires à l'obtention de hautes caractéristiques de résistance mécanique. L'ajout de bore est donc une composante importante de la présente invention, il permet de limiter par ailleurs l'addition d'éléments trempants tels que Mn, Mo, Cr et de réduire le coût analytique de la nuance d'acier. La teneur minimale en bore pour assurer une trempabilité efficace est de 0,0005%. Au delà de 0,0025%, l'effet sur la trempabilité est saturé et on constate un effet néfaste sur la revêtabilité et sur la ductilité à chaud. Afin de former une quantité suffisante de nitrures et de carbonitrures, une teneur minimale de 0,002% en azote est requise. La teneur en azote est limitée à 0,007% pour éviter la formation de BN qui diminuerait la quantité de bore libre nécessaire au durcissement de la ferrite.The titanium and niobium contents above make it possible to ensure that the nitrogen is completely trapped in the form of nitrides or carbonitrides, so that the boron is in free form and can play an effective role on the quenchability. The effect of boron on quenchability is fundamental. By limiting the activity of carbon, boron indeed makes it possible to control and limit the diffusive phase transformations (ferritic or pearlitic transformation during cooling) and to form hardening phases (bainite or martensite) necessary for obtaining high mechanical strength characteristics. The addition of boron is therefore an important component of the present invention, it also makes it possible to limit the addition of quenching elements such as Mn, Mo, Cr and to reduce the analytical cost of the steel grade. The minimum boron content to ensure effective quenchability is 0.0005%. Beyond 0.0025%, the effect on the quenchability is saturated and there is a detrimental effect on the coating and hot ductility. In order to form a sufficient amount of nitrides and carbonitrides, a minimum content of 0.002% nitrogen is required. The nitrogen content is limited to 0.007% to avoid the formation of BN which would decrease the amount of free boron required for the hardening of the ferrite.

Une addition optionnelle de nickel peut être réalisée de façon à obtenir un durcissement supplémentaire de la ferrite. Cette addition est cependant limitée à 0,1% pour des raisons de coût. La mise en œuvre du procédé de fabrication d'une tôle laminée selon l'invention comporte les étapes successives suivantes :Optional addition of nickel may be performed to provide additional hardening of the ferrite. This addition is, however, limited to 0.1% for cost reasons. The implementation of the method of manufacturing a rolled sheet according to the invention comprises the following successive steps:

- On approvisionne un acier de composition selon l'inventionA steel of composition according to the invention is supplied

- On procède à la coulée d'un demi-produit à partir de cet acier. Cette coulée peut être réalisée en lingots ou en continu sous forme de brames d'épaisseur de l'ordre de 200mm. On peut également effectuer la coulée sous forme de brames minces de quelques dizaines de millimètres d'épaisseur ou de bandes minces entre cylindres d'acier contra-rotatifs.- It proceeds to the casting of a half-product from this steel. This casting can be carried out in ingots or continuously in the form of thick slabs of the order of 200mm. It is also possible to perform the casting in the form of slabs of a few tens of millimeters thick or thin strips between contra-rotating steel rolls.

Les demi-produits coulés sont tout d'abord portés à une température TR supérieure à 1150 0C pour atteindre en tout point une température favorable aux déformations élevées que va subir l'acier lors du laminage.The cast semifinished products are first brought to a temperature TR greater than 1150 ° C. to reach at any point a temperature favorable to the high deformations that the steel will undergo during rolling.

Cependant, si la température TR est trop importante, les grains austénitiques croissent de façon indésirable. Dans ce domaine de température, les seuls précipités susceptibles de contrôler efficacement la taille du grain austénitique sont les nitrures de titane, et il convient de limiter la température de réchauffage à 12500C afin de maintenir un grain austénitique fin à ce stade.However, if the temperature T R is too high, the austenitic grains increase undesirably. In this temperature range, the only precipitates likely to effectively control the size of the austenitic grain are titanium nitrides, and the reheating temperature should be limited to 1250 ° C. in order to maintain a fine austenitic grain at this stage.

Naturellement, dans le cas d'une coulée directe de brames minces ou de bandes minces entre cylindres contra-rotatifs, l'étape de laminage à chaud de ces demi-produits débutant à plus de 11500C peut se faire directement après coulée si bien qu'une étape de réchauffage intermédiaire n'est pas nécessaire dans ce cas.Naturally, in the case of a direct casting of thin slabs or thin strips between contra-rotating rolls, the hot rolling step of these semi-products starting at more than 1150 ° C. can be done directly after casting so well. that an intermediate heating step is not necessary in this case.

On lamine à chaud le demi-produit dans un domaine de température où la structure de l'acier est totalement austénitique : si TFL est inférieure à la température de début de transformation de l'austénite au refroidissement AF3, les grains de ferrite sont écrouis par le laminage et la ductilité est réduite.The semi-finished product is hot-rolled in a temperature range where the structure of the steel is totally austenitic: if TFL is lower than the starting temperature of transformation from austenite to cooling A F3 , the ferrite grains are hardened by rolling and ductility is reduced.

Préférentiellement, on choisira une température de fin de laminage supérieure à 850°C.Preferably, a rolling end temperature of greater than 850 ° C. will be chosen.

On bobine ensuite le produit laminé à chaud à une température TbOb comprise entre 500 et 5700C : cette gamme de température permet d'obtenir une transformation bainitique complète pendant le maintien quasi-isotherme associé au bobinage. Cette gamme conduit à une morphologie de précipités de Ti et Nb suffisamment fine afin de permettre l'exploitation de leur pouvoir durcissant et trempant lors des étapes ultérieures du procédé de fabrication. Une température de bobinage supérieure à 57O0C conduit à la formation de précipités plus grossiers, dont la coalescence lors du recuit continu diminue significativement l'efficacité.The hot-rolled product is then rolled at a temperature T bO b of between 500 and 570 ° C. This temperature range makes it possible to obtain a complete bainitic transformation during the quasi-isothermal maintenance associated with the winding. This range leads to a morphology of Ti and Nb precipitates which are sufficiently fine in order to allow the exploitation of their hardening and quenching power during the subsequent steps of the manufacturing process. A winding temperature greater than 57O 0 C leads to the formation of coarser precipitates, whose coalescence during continuous annealing significantly reduces the efficiency.

Lorsque la température de bobinage est trop basse, la dureté du produit est augmentée, ce qui augmente les efforts nécessaires lors du laminage à froid à froid ultérieur.When the winding temperature is too low, the hardness of the product is increased, which increases the efforts required during cold rolling at a later time.

On décape ensuite le produit laminé à chaud selon un procédé connu en lui- même, puis on effectue un laminage à froid avec un taux de réduction compris préférentiellement entre 30 et 80%.The hot-rolled product is then etched according to a process known per se, followed by cold rolling with a reduction ratio preferably comprised between 30 and 80%.

On chauffe ensuite le produit laminé à froid, préférentiellement au sein d'une installation de recuit continu, avec une vitesse moyenne de chauffage Vc comprise entre 1 et 5°C/s. En relation avec la température de recuit TM ci- dessous, cette gamme de vitesse de chauffage permet d'obtenir une fraction de ferrite non recristallisée inférieure ou égale à 15%.The cold-rolled product is then heated, preferably in a continuous annealing installation, with an average heating rate Vc of between 1 and 5 ° C./sec. In relation to the TM annealing temperature below, this heating rate range makes it possible to obtain a fraction of non-recrystallized ferrite less than or equal to 15%.

Le chauffage est effectué jusqu'à une température de recuit TM comprise entre la température A0I (température de début de transformation allotropique au chauffage)+40°C, et A^ (température de fin de transformation allotropique au chauffage) - 3O0C, c'est à dire dans une gamme de température particulière du domaine intercritique : lorsque TM est inférieure à (Aci+40°C), la structure peut comporter encore des zones de ferrite non recristallisées dont la fraction surfacique peut atteindre 15%. Cette proportion de ferrite non recristallisée est évaluée de la façon suivante : après avoir identifié la phase ferritique au sein de la microstructure, on quantifie le pourcentage surfacique de ferrite non recristallisée rapportée à la totalité de la phase ferritique. Les inventeurs ont mis en évidence que ces zones non recristallisées jouent un rôle néfaste sur la ductilité et ne permettent pas d'obtenir les caractéristiques visées par l'invention. Une température de recuit TM selon l'invention permet d'obtenir une quantité d'austénite suffisante pour former ultérieurement au refroidissement de la martensite en quantité telle que les caractéristiques désirées soient atteintes. Une température TM inférieure à (Ac3 - 3O0C) permet également d'assurer que la teneur en carbone des îlots d'austénite formés à la température TM conduit bien à une transformation martensitique ultérieure : lorsque la température de recuit est trop élevée, la teneur en carbone des îlots d'austénite devient trop faible, ce qui conduit à une transformation ultérieure en bainite ou en perlite non favorable. De plus, une température trop élevée conduit à un accroissement de la taille des précipités de niobium qui perdent une partie de leur capacité de durcissement. La résistance mécanique finale est alors diminuée.The heating is carried out up to an annealing temperature T M between the temperature A 0I (allotropic transformation start temperature at heating) + 40 ° C, and A ^ (end of allotropic transformation temperature at heating) - 30 ° C. C, that is to say in a particular temperature range of the intercritical range: when TM is less than (A c i + 40 ° C), the structure may also comprise non-recrystallized ferrite zones whose surface fraction may reach 15 %. This proportion of non-recrystallized ferrite is evaluated as follows: after having identified the ferritic phase within the microstructure, the surface percentage of non-recrystallized ferrite relative to the entire ferritic phase is quantified. The inventors have demonstrated that these non-recrystallized zones play a detrimental role on the ductility and do not make it possible to obtain the characteristics targeted by the invention. An annealing temperature T M according to the invention makes it possible to obtain an amount of austenite sufficient to subsequently form the cooling of the martensite in an amount such that the desired characteristics are attained. A temperature TM lower than (Ac 3 - 30 ° C.) also makes it possible to ensure that the carbon content of the austenite islands formed at the temperature T M indeed leads to a subsequent martensitic transformation: when the annealing temperature is too high, the carbon content of the austenite islands becomes too low, which leads to a subsequent transformation into bainite or unfavorable pearlite. In addition, too high a temperature leads to an increase in the size of niobium precipitates which lose some of their curing ability. The final mechanical strength is then decreased.

On choisira préférentiellement à cet effet une température TM comprise entre 7600C et 83O0C.Preferably will be chosen for this purpose a TM temperature between 760 0 C and 83O 0 C.

Une durée de maintien minimale tM de 30s à la température TM permet la dissolution des carbures, une transformation partielle en austénite est réalisée. L'effet est saturé au delà d'une durée de 300 s. Un temps de maintien supérieur à 300s est également difficilement compatible avec les exigences de productivité des installations de recuit continu, en particulier la vitesse de défilement. La durée de maintien tM est comprise entre 30 et 300s. Les étapes suivantes du procédé diffèrent selon que l'on fabrique une tôle d'acier non revêtue, ou galvanisée en continu au trempé, ou galvannealed :A minimum holding time t M of 30s at the temperature T M allows the dissolution of the carbides, a partial transformation into austenite is carried out. The effect is saturated beyond a duration of 300 s. A holding time greater than 300s is also difficult to comply with the productivity requirements of continuous annealing equipment, in particular the speed of scrolling. The holding time tM is between 30 and 300s. The following process steps differ depending on whether an uncoated, or continuously galvanized, or galvannealed steel sheet is manufactured:

- Dans le premier cas, à la fin du maintien de recuit, on effectue un refroidissement jusqu'à une température inférieure à la température Ms (température de début de formation de la martensite) avec une vitesse de refroidissement V suffisante pour que l'austénite formée lors du recuit se transforme totalement en martensite.In the first case, at the end of the maintenance of annealing, cooling is carried out to a temperature below the temperature M s (martensite formation start temperature) with a cooling rate V sufficient for the austenite formed during annealing is totally transformed into martensite.

Ce refroidissement peut être effectué à partir de la température TM en une seule ou en plusieurs étapes et peut faire intervenir dans ce dernier cas différents modes de refroidissement tels que des bains d'eau froide ou bouillante, des jets d'eau ou de gaz. Ces éventuels modes de refroidissement accéléré peuvent être combinés de façon à obtenir une transformation martensitique complète de l'austénite. Après cette transformation martensitique, le tôle est refroidie jusqu'à la température ambiante. La microstructure de la tôle nue refroidie est alors constituée d'une matrice ferritique avec des îlots de martensite dont la proportion surfacique est comprise entre 35 et 50%, et est exempte de bainite.This cooling can be carried out from the temperature T M in one or several steps and may involve in the latter case different cooling modes such as cold or boiling water baths, jets of water or gas . These possible accelerated cooling modes can be combined to obtain a complete martensitic transformation of the austenite. After this martensitic transformation, the sheet is cooled to room temperature. The microstructure of the cooled bare sheet then consists of a ferritic matrix with islands of martensite whose surface proportion is between 35 and 50%, and is free of bainite.

- Dans le cas où l'on souhaite fabriquer une tôle galvanisée en continu au trempé, à la fin du maintien de recuit, on refroidit le produit jusqu'à atteindre une température proche de la température TZn de galvanisation au trempé, la vitesse de refroidissement VR étant suffisamment rapide pour éviter la transformation de l'austénite en ferrite. A cet effet, la vitesse de refroidissement VR est préférentiellement supérieure à 150CVs. On effectue la galvanisation au trempé par immersion dans un bain de zinc ou d'alliage de zinc dont la température Tzn est comprise entre 450 et 4800C. Une transformation partielle de l'austénite en bainite intervient à ce stade, qui conduit à la formation de 1 à 10% de bainite, cette valeur étant exprimée en proportion surfacique. Le maintien dans cette gamme de température doit être inférieur à 80s de façon à limiter la proportion surfacique de bainite à 10% et obtenir ainsi une proportion suffisante de martensite. On refroidit ensuite le produit galvanisé à une vitesse comprise V'R supérieure à 4°C/s jusqu'à la température ambiante dans le but de transformer complètement la fraction d'austénite restante en martensite : on obtient de la sorte une tôle d'acier laminée à froid, recuite et galvanisée contenant en proportion surfacique 40-64% de ferrite, 35-50% de martensite et 1-10% de bainite. - Dans le cas où l'on souhaite fabriquer une tôle d'acier Dual Phase laminée à froid et « galvannealed », c'est à dire galvanisée-alliée, on refroidit le produit à la fin du maintien de recuit jusqu'à atteindre une température proche de la température TZn de galvanisation au trempé, la vitesse de refroidissement VR étant suffisamment rapide pour éviter la transformation de l'austénite en ferrite. A cet effet, la vitesse de refroidissement VR est préférentiellement supérieure à 15°C/s. On effectue la galvanisation au trempé par immersion dans un bain de zinc ou d'alliage de zinc dont la température TZn est comprise entre 450 et 4800C. Une transformation partielle de l'austénite en bainite intervient à ce stade, qui conduit à la formation de 1 à 10% de bainite, cette valeur étant exprimée en proportion surfacique. Le maintien dans cette gamme de température doit être inférieur à 80s de façon à limiter la proportion de bainite à 10%. Après la sortie du bain de zinc, on chauffe le produit galvanisé à une température TG comprise entre 490 et 5500C pendant une durée XQ comprise entre 10 et 40s. On provoque ainsi l'interdiffusion du fer et de la fine couche de zinc ou d'alliage de zinc déposée lors de l'immersion, ce qui permet d'obtenir un produit galvannealed. On refroidit ce produit jusqu'à la température ambiante avec une vitesse V"R supérieure à 4°C/s: on obtient de la sorte une tôle d'acier galvannealed à matrice ferritique, contenant en proportion surfacique 40-64% de ferrite, 35-50% de martensite et 1-10% de bainite. La martensite se trouve typiquement sous forme d'îlots de taille moyenne inférieure à 4 micromètres, voire deux micromètres, ces îlots présentant majoritairement, pour plus de 50% d'entre eux, une morphologie massive plutôt qu'une morphologie allongée. La morphologie d'un îlot donné est caractérisée par le rapport entre sa taille maximale Lmax et minimale Lmin. Un îlot donné est considéré comme possédant une- In the case where it is desired to manufacture a galvanized sheet continuously quenched, at the end of the maintenance of annealing, the product is cooled to a temperature close to the temperature T Zn dip galvanizing, the speed of VR cooling is fast enough to avoid the transformation of austenite to ferrite. For this purpose, the cooling rate V R is preferably greater than 15 0 CVs. Galvanizing is carried out by immersion in a bath of zinc or alloy of zinc whose temperature Tz n is between 450 and 480 ° C. A partial transformation of austenite into bainite occurs at this stage, which leads to the formation of 1 to 10% of bainite, this value being expressed in surface proportion. The maintenance in this temperature range must be less than 80s so as to limit the surface proportion of bainite to 10% and thus obtain a sufficient proportion of martensite. The galvanized product is then cooled at a rate V ' R greater than 4 ° C./s up to room temperature in order to completely convert the remaining austenite fraction into martensite: in this way a sheet of aluminum is obtained. Cold-rolled, annealed and galvanized steel containing 40-64% ferrite, 35-50% martensite and 1-10% bainite in surface proportion. - In the case where it is desired to manufacture a cold-rolled and "galvannealed" dual-phase steel sheet, that is to say galvanized-alloyed, the product is cooled at the end of the maintenance of annealing until reaching a temperature close to the dip galvanizing temperature T Zn , the cooling rate V R being fast enough to avoid the transformation of austenite to ferrite. For this purpose, the cooling rate V R is preferably greater than 15 ° C / s. Galvanizing is carried out by dipping by immersion in a bath of zinc or zinc alloy whose temperature T Zn is between 450 and 480 ° C. A partial transformation of the austenite into bainite occurs at this stage, which leads to the formation of 1 to 10% of bainite, this value being expressed in surface proportion. The maintenance in this temperature range must be less than 80s so as to limit the proportion of bainite to 10%. After leaving the zinc bath, the galvanized product is heated to a temperature T G of between 490 and 550 0 C for a period XQ of between 10 and 40s. This causes the interdiffusion of iron and the thin layer of zinc or zinc alloy deposited during the immersion, which allows to obtain a galvannealed product. This product is cooled to room temperature with a speed V " R greater than 4 ° C./s: a galvannealed sheet of ferritic matrix steel is obtained in this way, containing 40-64% of ferrite in surface proportion, 35-50% of martensite and 1-10% of bainite Martensite is typically in the form of islands of average size less than 4 micrometers, or even two microns, these Islets presenting, for more than 50% of them, a massive morphology rather than an elongated morphology. The morphology of a given island is characterized by the ratio between its maximum size L max and minimum L min . A given island is considered to have a

5 morphologie massive lorsque son rapport est inférieur ou égal à 2. 5 massive morphology when its ratio is less than or equal to 2.

En outre, les inventeurs ont constaté que de faibles variations des paramètres de fabrication au sein des conditions définies selon l'invention, n'entraînent pas de modifications importantes de la microstructure ou des propriétés mécaniques, ce qui est un avantage pour la stabilité des 0 caractéristiques des produits industriels fabriqués.In addition, the inventors have found that small variations in the manufacturing parameters within the conditions defined according to the invention do not lead to significant modifications of the microstructure or the mechanical properties, which is an advantage for the stability of the characteristics of manufactured industrial products.

La présente invention va être maintenant illustrée à partir des exemples suivants donnés à titre non limitatif :The present invention will now be illustrated on the basis of the following nonlimiting examples:

Exemple:Example:

On a élaboré des aciers dont la composition figure au tableau ci-dessous, 5 exprimée en pourcentage pondéral. Outre les aciers IX à IZ ayant servi à la fabrication de tôles selon l'invention, on a indiqué à titre de comparaison la composition d'un acier R ayant servi à la fabrication de tôles de référence.Steels have been developed whose composition is shown in the table below, expressed as a percentage by weight. In addition to the steels IX to IZ used for the manufacture of sheets according to the invention, it was indicated for comparison the composition of a steel R used for the manufacture of reference sheets.

Tableau 1 Compositions d'aciers (% poids). R= Référence Valeurs soulignées : Non conformes à l'invention. 0Table 1 Compositions of steel (% by weight). R = Reference Underlined values: Not in accordance with the invention. 0

Des demi-produits coulés correspondant aux compositions ci-dessus ont été réchauffés à 123O0C puis laminés à chaud jusqu'à une épaisseur de 2,8- 4 mm dans un domaine où la structure est entièrement austénitique. Les conditions de fabrication de ces produits laminés à chaud (température de fin 5 de laminage TFL, température de bobinage TbOb) sont indiquées au tableau 2. Cast half-products corresponding to the above compositions were heated to 123O 0 C and then hot rolled to a thickness of 2.8-4 mm in a field where the structure is entirely austenitic. The manufacturing conditions of these hot-rolled products (rolling end temperature T F L, winding temperature T bO b) are shown in Table 2.

Tableau 2 Conditions de fabrication des produits laminés à chaudTable 2 Manufacturing conditions for hot-rolled products

Les produits laminés à chaud ont été ensuite décapés puis laminés à froid jusqu'à une épaisseur de 1 ,4 à 2 mm soit un taux de réduction de 50%. A partir d'une même composition, certains aciers ont fait l'objet de différentes conditions de fabrication. Les références 1X1 , IX2 et IX3 désignent par exemple trois tôles d'aciers fabriquées selon des conditions différentes à partir de la composition d'acier IX. Les tôles ont été galvanisées au trempé dans un bain de zinc à une température TZn de 4600C, d'autres ont fait en outre l'objet d'un traitement de galvannealing. Le tableau 3 indique les conditions de fabrication des tôles recuites après laminage à froid :The hot-rolled products were then pickled and then cold-rolled to a thickness of 1.4 to 2 mm, a reduction rate of 50%. From the same composition, some steels have been subject to different manufacturing conditions. References 1X1, IX2 and IX3 denote for example three steel sheets manufactured under different conditions from the steel composition IX. The sheets were galvanized by dipping in a zinc bath at a temperature T Zn of 460 ° C., others were further subjected to a galvannealing treatment. Table 3 shows the manufacturing conditions for annealed sheet after cold rolling:

. Vitesse de chauffage Vc . Heating speed V c

- Température de recuit TM.- Annealing temperature T M.

- Temps de maintien au recuit tM - Vitesse de refroidissement après recuit VR - Annealing hold time t M - Cooling speed after annealing V R

- Vitesse de refroidissement après galvanisation VR- Cooling rate after galvanizing VR

- Température de galvannealing TG - Galvannealing temperature T G

- Durée de galvannealing {Q- Duration of galvannealing {Q

- Vitesse de refroidissement V"R après traitement de galvannealing Les températures de transformation A01 et Ac3 ont été également portées au tableau 3. - Cooling rate V "R after galvannealing treatment The transformation temperatures A 01 and Ac 3 were also reported in Table 3.

Tableau 3 Conditions de fabrications des tôles laminées à froid et recuites Valeurs soulignées : non conformes à l'inventionTable 3 Manufacturing conditions for cold-rolled and annealed sheets Underlined values: not in accordance with the invention

Les propriétés mécaniques de traction obtenues (limite d'élasticité Re, résistance Rm, allongement à rupture A ont été portées au tableau 4 ci- dessous. Le rapport Re/Rm a été également indiqué. On a également déterminé la microstructure des aciers, dont la matrice est ferritique. Les fractions surfaciques de bainite et de martensite ont été quantifiées après attaque aux réactifs Picral et LePera respectivement, suivies par une analyse d'image grâce au logiciel Aphelion™. On a également déterminé la fraction surfacique de ferrite non recristallisée grâce à des observations en microscopie optique et électronique à balayage où l'on a identifié la phase ferritique, puis quantifié la fraction recristallisée au sein de cette phase ferritique. La ferrite non recristallisée se présente en général sous forme d'îlots allongés par le laminage. L'aptitude au pliage a été quantifiée de la façon suivante : des tôles ont été pliées à bloc sur elles-mêmes en plusieurs tours. De la sorte, le rayon de pliage diminue à chaque tour. L'aptitude au pliage est ensuite évaluée en relevant la présence de fissures à la surface du bloc plié, la cotation étant exprimée de 1 (faible aptitude au pliage) à 5 (très bonne aptitude) Des résultats cotés 1-2 sont considérés comme non satisfaisants.The mechanical tensile properties obtained (elastic limit Re, resistance Rm, elongation at break A were given in Table 4 below), the ratio Re / Rm was also indicated, and the microstructure of the steels was determined. the matrix is ferritic The surface fractions of bainite and martensite were quantified after Picral and LePera reagent etching respectively, followed by an image analysis using Aphelion ™ software, and the non-recrystallized ferrite surface fraction was determined by to observations in optical microscopy and scanning electron where the ferritic phase has been identified, then quantified the recrystallized fraction within this ferritic phase The non-recrystallized ferrite is generally in the form of islands elongated by rolling. The folding ability was quantified as follows: sheets were folded in a block on themselves in several turns. In this way, the bending radius decreases each turn. The foldability is then evaluated by noting the presence of cracks on the surface of the folded block, the rating being expressed from 1 (low foldability) to 5 (very good ability). satisfactory.

Tableau 4 Résultats obtenus sur les tôles laminées à froid et recuites Valeurs soulignées : non conformes à l'inventionTable 4 Results obtained on cold-rolled and annealed sheets Underlined values: not in accordance with the invention

Les tôles d'aciers selon l'invention présentent un ensemble de caractéristiques microstructurales et mécaniques permettant la fabrication avantageuse de pièces, notamment pour des applications structurales : résistance comprise entre 980 et 1100 MPa, rapport Re/Rm compris entre 0,6 et 0,8, allongement à rupture supérieur à 9%, bonne aptitude au pliage. La figure 1 illustre la morphologie de la tôle d'acier 1X1 , où la ferrite est totalement recristallisée.The steel sheets according to the invention have a set of microstructural and mechanical characteristics enabling the advantageous manufacture of parts, in particular for structural applications: resistance of between 980 and 1100 MPa, ratio R e / R m of between 0.6 and 0.8, elongation at break of greater than 9%, good folding ability. Figure 1 illustrates the morphology of the 1X1 steel sheet, where the ferrite is completely recrystallized.

Les tôles selon l'invention présentent une bonne aptitude au soudage, notamment par résistance, le carbone équivalent étant inférieur à 0,25. En particulier, le domaine de soudabilité tel que défini par la norme I S018278-2, en soudage par points est très large, de l'ordre de 3500A. Il est augmenté par rapport à une nuance de référence de même grade. En outre, des essais de traction en croix ou de traction-cisaillement effectués sur des points soudés de tôles selon l'invention révèlent que la résistance de ces points soudés est très élevée au regard des caractéristiques mécaniques. Par comparaison, les tôles de référence n'offrent pas ces mêmes caractéristiques :The sheets according to the invention have good weldability, in particular resistance, the equivalent carbon being less than 0.25. In particular, the weldability range as defined by the standard I S018278-2, in spot welding is very wide, of the order of 3500A. It is increased relative to a reference grade of the same grade. In addition, cross-tension or tensile-shear tests carried out on welded points of sheets according to the invention reveal that the resistance of these welded points is very high with regard to the mechanical characteristics. By comparison, the reference plates do not offer these same characteristics:

Les tôles d'acier IX3 (galvanisée) et IX6 (galvannealed) ont été recuites à une température TM trop faible : en conséquence, la fraction de ferrite non recristallisée est excessive ainsi que la fraction de martensite. Ces caractéristiques microstructurales sont associées à une diminution de l'allongement et de l'aptitude au pliage. La figure 2 illustre la microstructure de la tôle d'acier IX3 : on note la présence de ferrite non recristallisée sous forme d'îlots allongés (repérés (A)) coexistant avec la ferrite recristallisée et la martensite, ce dernier constituant apparaissant plus foncé sur la micrographie. Une micrographie en Microscopie Electronique à Balayage (figure 3) permet de distinguer finement les zones de ferrite non recristallisée (A) de celles recristallisées (B).The steel plates IX3 (galvanized) and IX6 (galvannealed) were annealed at a temperature T M too low: consequently, the fraction of non-recrystallized ferrite is excessive as well as the martensite fraction. These microstructural features are associated with a decrease in elongation and foldability. FIG. 2 illustrates the microstructure of the steel sheet IX3: there is the presence of non-recrystallized ferrite in the form of elongate islands (marked (A)) coexisting with recrystallized ferrite and martensite, the latter constituting appearing darker on micrography. A scanning electron micrograph (FIG. 3) makes it possible to finely distinguish the zones of non-recrystallized ferrite (A) from those recrystallized (B).

La tôle IX5 est une tôle galvannealed recuite à une température TM trop élevée : la teneur en carbone de l'austénite à haute température devient alors trop faible et l'apparition de la bainite est favorisée au détriment de la formation de martensite. On assiste également à une coalescence des précipités de niobium, ce qui provoque une perte de durcissement. La résistance est alors insuffisante, le rapport Re/Rm étant trop élevé. La tôle 1X7 galvannealed a été refroidie à une vitesse VR trop lente après l'étape de recuit : la transformation de l'austénite formée en ferrite se produit alors dans cette étape de refroidissement de façon excessive, la tôle d'acier contenant au stade final une proportion de bainite trop importante et une proportion de martensite trop faible, ce qui conduit à une résistance insuffisante.Sheet IX5 is a galvannealed sheet annealed at a temperature T M too high: the carbon content of austenite at high temperature then becomes too low and the appearance of bainite is favored at the expense of the formation of martensite. Coalescence of niobium precipitates is also observed, which causes a loss of hardening. The resistance is then insufficient, the ratio Re / R m being too high. The Galvannealed 1X7 sheet was cooled at a rate V R too slow after the annealing step: the transformation of the austenite formed into ferrite then occurs in this cooling step excessively, the steel sheet containing at the stage final a proportion of bainite too important and a proportion of martensite too low, which leads to insufficient resistance.

La composition de la tôle d'acier R ne correspond pas à l'invention, sa teneur en carbone étant trop importante, et sa teneur en manganèse, aluminium, niobium, titane, bore étant trop faibles. En conséquence, la fraction de martensite est trop faible si bien que la résistance mécanique est insuffisante. Les tôles d'aciers selon l'invention seront utilisées avec profit pour la fabrication de pièces de structures ou de sécurité dans l'industrie automobile. The composition of the steel sheet R does not correspond to the invention, its carbon content being too high, and its content of manganese, aluminum, niobium, titanium, boron being too low. As a result, the martensite fraction is too weak so that the mechanical strength is insufficient. The steel sheets according to the invention will be used profitably for the manufacture of structural parts or safety in the automotive industry.

Claims

REVENDICATIONS 1. Tôle d'acier Dual Phase laminée à froid et recuite de résistance comprise entre 980 et 1100MPa, d'allongement à rupture supérieur à 9 %, dont la composition comprend, les teneurs étant exprimées en poids :1. Cold-rolled, annealed, double-strength steel sheet having a strength of between 980 and 1100 MPa, elongation at break greater than 9%, the composition of which includes the contents being expressed by weight: 0,055% ≤C < 0,095%0.055% ≤C <0.095% 2% ≤Mn <2,6% 0,005% < Si≤ 0,35%2% ≤Mn <2.6% 0.005% <Si≤ 0.35% S<0,005% P <0,050%S <0.005% P <0.050% 0,1 <AI < 0,3% 0,05%<Mo <0,25%0.1 <AI <0.3% 0.05% <Mo <0.25% 0,2%<Cr≤0,5% étant entendu que Cr+2Mo<0,6% Ni≤ 0,1%0.2% <Cr≤0.5% with the proviso that Cr + 2Mo <0.6% Ni ≤ 0.1% 0,010<Nb <0,040%0.010 <Nb <0.040% 0,010<Ti <0,050%0.010 <Ti <0.050% 0,0005 ≤B <0,0025%0.0005 ≤B <0.0025% 0,002%≤N<0,007% le reste de la composition étant constitué de fer et d'impuretés inévitables résultant de l'élaboration0.002% ≤N <0.007%, the balance of the composition consisting of iron and unavoidable impurities resulting from the elaboration 2. Tôle d'acier selon la revendication 1 , caractérisée en ce que la composition dudit acier contient, la teneur étant exprimée en poids : 0,12% <AI≤0,25%2. Steel sheet according to claim 1, characterized in that the composition of said steel contains, the content being expressed by weight: 0.12% <AI 0 0.25% 3. Tôle d'acier selon la revendication 1 ou 2, caractérisée en ce que la composition dudit acier contient, la teneur étant exprimée en poids :3. Sheet steel according to claim 1 or 2, characterized in that the composition of said steel contains, the content being expressed by weight: 0,10% < Si ≤ 0,30% 4 Tôle d'acier selon la revendication 1 ou 2, caractérisée en ce que la composition dudit acier contient, la teneur étant exprimée en poids :0.10% <If ≤ 0.30% 4 steel sheet according to claim 1 or 2, characterized in that the composition of said steel contains, the content being expressed by weight: 0,15% < Si < 0,28%0.15% <If <0.28% 5 Tôle d'acier selon l'une quelconque des revendications 1 à 4, caractérisée en ce que la composition dudit acier contient, la teneur étant exprimée en poids :Steel sheet according to any one of claims 1 to 4, characterized in that the composition of said steel contains, the content being expressed by weight: P <0,015%P <0.015% 6 Tôle d'acier selon l'une quelconque des revendications 1 à 5, caractérisée en ce que sa microstructure contient 35 à 50% de martensite en proportion surfacique6 steel sheet according to any one of claims 1 to 5, characterized in that its microstructure contains 35 to 50% of martensite in surface proportion 7 Tôle d'acier selon la revendication 6, caractérisée en ce que le complément de ladite microstructure est constitué de 50 à 65% de ferrite en proportion surfacique7 steel sheet according to claim 6, characterized in that the complement of said microstructure consists of 50 to 65% of ferrite in surface proportion 8 Tôle d'acier selon la revendication 6, caractérisée en ce que le complément de ladite microstructure est constitué de 1 à 10% de bainite et de 40 à 64% de ferrite en proportion surfacique8 steel sheet according to claim 6, characterized in that the complement of said microstructure consists of 1 to 10% of bainite and 40 to 64% of ferrite in surface proportion 9 Tôle d'acier selon l'une quelconque des revendications 1 à 8 caractérisée en ce que sa fraction surfacique de ferrite non recristallisée rapportée à la totalité de la phase ferritique, est inférieure ou égale à 15%9 steel sheet according to any one of claims 1 to 8 characterized in that its surface fraction of non-recrystallized ferrite relative to the entire ferritic phase, is less than or equal to 15% 10 Tôle d'acier selon l'une quelconque des revendications 1 à 9 caractérisée en ce que le rapport entre sa limite d'élasticité Re et sa résistance Rm est tel que : 0,6<Re/Rm <0,810 steel sheet according to any one of claims 1 to 9 characterized in that the ratio between its elastic limit R e and its resistance R m is such that: 0.6 <Re / R m <0.8 11 Tôle d'acier selon l'une quelconque des revendications 1 à 6 ou 8 à 10, caractérisée qu'elle est galvanisée en continu 12 Tôle d'acier selon l'une quelconque des revendications 1 à 6 ou 8 à 10, caractérisée qu'elle comporte un revêtement galvannealed11 Steel sheet according to any one of claims 1 to 6 or 8 to 10, characterized in that it is continuously galvanized Steel sheet according to one of Claims 1 to 6 or 8 to 10, characterized in that it comprises a galvannealed coating 13 Procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid et recuite caractérisé en ce qu'on approvisionne un acier de composition selon l'une quelconque des revendications 1 à 5, puis13 Process for manufacturing a cold rolled and annealed dual phase steel sheet, characterized in that a composition steel is supplied according to any one of Claims 1 to 5, and then - on coule ledit acier sous forme de demi-produit, puis on porte ledit demi-produit à une température 1150°C≤TR<1250°C, puis on lamine à chaud ledit demi-produit avec une température de fin de laminage TFL ≥Ar3 pour obtenir un produit laminé à chaud, puis on bobine ledit produit laminé à chaud à une température Tbob telle que :said steel is cast in the form of a semi-finished product, then said semi-finished product is brought to a temperature of 1150 ° C./TR <1250 ° C., and said semi-finished product is then hot-rolled with an end-of-rolling temperature T F L ≥ Ar3 to obtain a hot rolled product, then said hot rolled product is rolled at a temperature Tbob such that: 5000C <Tbob≤ 5700C, puis on décape ledit produit laminé à chaud, puis on effectue un laminage à froid avec un taux de réduction compris entre 30 et 80% pour obtenir un produit laminé à froid, puis500 0 C <T b ob 57 570 0 C, then said hot-rolled product is scraped off, then cold rolling is carried out with a reduction ratio of between 30 and 80% to obtain a cold-rolled product, then - on chauffe ledit produit laminé à froid à une vitesse 1 °C/s<Vc≤5°C/s jusqu'à une température de recuit TM telle que : Ad +40°C≤TM≤AC3-30°C où l'on effectue un maintien pendant une durée : 30s≤tM ≤300s de façon à obtenir un produit chauffé et recuit avec une structure comprenant de l'austénite, puissaid cold-rolled product is heated at a rate of 1 ° C./s <Vc≤5 ° C./s up to an annealing temperature T M such that: Ad + 40 ° C≤TM≤AC3-30 ° C where a maintenance is carried out for a period: 30s≤tM ≤300s so as to obtain a heated and annealed product with a structure comprising austenite, then - on refroidit ledit produit jusqu'à une température inférieure à la température M5 avec une vitesse V suffisante pour que ladite austénite se transforme totalement en martensitesaid product is cooled to a temperature below the temperature M 5 with a speed V sufficient for said austenite to be totally transformed into martensite 14 Procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid, recuite et galvanisée caractérisé en ce qu'on approvisionne ledit produit chauffé et recuit avec une structure comprenant de l'austénite selon la revendication 13 puis,Process for producing a cold-rolled, annealed and galvanized Dual Phase steel sheet characterized in that said heated and annealed product is supplied with a structure comprising austenite according to claim 13 and then - on refroidit ledit produit chauffé et recuit avec une vitesse VR suffisante pour éviter la transformation de ladite austénite en ferrite, jusqu'à atteindre une température proche de la température Tzn de galvanisation au trempé, puis - on galvanise en continu ledit produit par immersion dans un bain de zinc ou d'alliage de Zn à une température 450°C<TZn≤480oC pour obtenir un produit galvanisé, puissaid heated and annealed product is cooled with a sufficient speed VR in order to avoid the transformation of said austenite into ferrite, until it reaches a temperature close to the dip galvanization temperature Tz n , then - Continuously galvanizing said product by immersion in a bath of zinc or Zn alloy at a temperature 450 ° C <T Z n≤480 o C to obtain a galvanized product, then - on refroidit ledit produit galvanisé jusqu'à la température ambiante avec une vitesse V'R supérieure à 4°C/s pour obtenir une tôle d'acier laminée à froid, recuite et galvaniséesaid galvanized product is cooled to ambient temperature with a speed V ' R greater than 4 ° C./s to obtain a cold-rolled, annealed and galvanized steel sheet 15 Procédé de fabrication d'une tôle d'acier Dual Phase laminée à froid et galvannealed, caractérisé en ce qu'on approvisionne ledit produit chauffé et recuit avec une structure comprenant de l'austénite selon la revendication 13 puis,A process for producing a cold-rolled and galvannealed dual phase steel sheet, characterized in that said heated and annealed product is supplied with a structure comprising austenite according to claim 13 and then - on refroidit ledit produit chauffé et recuit avec une vitesse VR suffisante pour éviter la transformation de ladite austénite en ferrite, jusqu'à atteindre une température proche de la température TZn de galvanisation au trempé, puissaid heated and annealed product is cooled with a speed V R sufficient to prevent the transformation of said austenite into ferrite, until it reaches a temperature close to the dip galvanizing temperature T Zn , then - on galvanise en continu ledit produit par immersion dans un bain de zinc ou d'alliage de Zn à une température 450°C<TZn≤480oC pour obtenir un produit galvanisé, puis- Continuously galvanizing said product by immersion in a bath of zinc or Zn alloy at a temperature of 450 ° C <T Zn ≤480 o C to obtain a galvanized product, then - on chauffe ledit produit galvanisé à une température TQ comprise entre 490 et 5500C pendant une durée XQ comprise entre 10 et 40 s pour obtenir un produit galvannealed, puissaid galvanized product is heated at a temperature TQ of between 490 and 550 ° C. for a period XQ of between 10 and 40 s to obtain a galvannealed product, then - on refroidit ledit produit galvannealed jusqu'à la température ambiante à une vitesse V"R supérieure à 4°C/s, pour obtenir une tôle d'acier laminée à froid et galvannealedsaid galvannealed product is cooled to ambient temperature at a speed V "R greater than 4 ° C./s, to obtain a cold rolled steel sheet and galvannealed 16 Procédé de fabrication selon l'une quelconque des revendications 13 à 15, caractérisé en ce que ladite température TM est comprise entre 760 et 8300CManufacturing method according to any one of claims 13 to 15, characterized in that said temperature TM is between 760 and 830 0 C 17 Procédé de fabrication selon la revendication 14 ou 15, caractérisé en ce que ladite vitesse de refroidissement VR est supérieure ou égale à 15°C/s 18 Utilisation d'une tôle d'acier selon l'une quelconque des revendications 1 à 12, ou fabriquée par un procédé selon l'une quelconque des revendications 13 à 17, pour la fabrication de pièces de structures ou de sécurité pour véhicules automobiles Manufacturing method according to claim 14 or 15, characterized in that said cooling rate VR is greater than or equal to 15 ° C / sec. 18 Use of a steel sheet according to any one of claims 1 to 12, or manufactured by a method according to any one of claims 13 to 17, for the manufacture of structural parts or safety for motor vehicles
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CA2725290C (en) 2015-10-13
MA32294B1 (en) 2011-05-02
CN102046827A (en) 2011-05-04
BRPI0912879A2 (en) 2017-05-16
KR101328768B1 (en) 2013-11-13
EP2123786A1 (en) 2009-11-25
US20160222486A1 (en) 2016-08-04
KR20110013490A (en) 2011-02-09
WO2009150319A1 (en) 2009-12-17
JP5425896B2 (en) 2014-02-26
PL2291547T3 (en) 2012-09-28
BRPI0912879B1 (en) 2018-06-26
CA2725290A1 (en) 2009-12-17
US10190187B2 (en) 2019-01-29
UA100056C2 (en) 2012-11-12
CN102046827B (en) 2013-03-06
MX2010012584A (en) 2011-04-05
ES2386701T3 (en) 2012-08-27
US20190106765A1 (en) 2019-04-11
JP2011523440A (en) 2011-08-11
EP2291547B1 (en) 2012-04-25
ZA201007964B (en) 2011-07-27
ATE555225T1 (en) 2012-05-15
RU2010152214A (en) 2012-06-27
RU2470087C2 (en) 2012-12-20

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