EP3867417A1 - Tôle d'acier laminée à chaud à ultra-haute résistance et ayant une aptitude au façonnage améliorée et son procédé de production - Google Patents

Tôle d'acier laminée à chaud à ultra-haute résistance et ayant une aptitude au façonnage améliorée et son procédé de production

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Publication number
EP3867417A1
EP3867417A1 EP19784114.1A EP19784114A EP3867417A1 EP 3867417 A1 EP3867417 A1 EP 3867417A1 EP 19784114 A EP19784114 A EP 19784114A EP 3867417 A1 EP3867417 A1 EP 3867417A1
Authority
EP
European Patent Office
Prior art keywords
steel sheet
high strength
hot rolled
strength steel
rolled high
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.)
Pending
Application number
EP19784114.1A
Other languages
German (de)
English (en)
Inventor
Shangping Chen
Richard MOSTERT
Radhakanta RANA
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.)
Tata Steel Nederland Technology BV
Original Assignee
Tata Steel Nederland Technology BV
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 Tata Steel Nederland Technology BV filed Critical Tata Steel Nederland Technology BV
Publication of EP3867417A1 publication Critical patent/EP3867417A1/fr
Pending legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • C—CHEMISTRY; METALLURGY
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    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/004—Heat treatment of ferrous alloys containing Cr and Ni
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/005—Heat treatment of ferrous alloys containing Mn
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/008—Heat treatment of ferrous alloys containing Si
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226—Hot rolling
    • C—CHEMISTRY; METALLURGY
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    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0263—Modifying 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
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/001—Ferrous alloys, e.g. steel alloys containing N
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/002—Ferrous 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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    • C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
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    • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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    • C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
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    • C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
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    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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    • C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/16—Ferrous alloys, e.g. steel alloys containing copper
    • C—CHEMISTRY; METALLURGY
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C—CHEMISTRY; METALLURGY
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    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
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    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
    • C—CHEMISTRY; METALLURGY
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/32—Ferrous alloys, e.g. steel alloys containing chromium with boron
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/34—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42—Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/48—Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/50—Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/54—Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/001—Austenite
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/002—Bainite
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/005—Ferrite
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/008—Martensite

Definitions

  • the invention relates to a hot rolled high strength steel sheet having improved formability and a method for producing such a steel sheet.
  • Advanced high strength steels such as dual phase (DP) steels and transformation induced plasticity (TRIP) steels are currently typical of high-ductility, high- strength steels used for automobiles.
  • DP steels the presence of martensite within a ferrite matrix enables to obtain a tensile strength greater than 450 MPa, combined with good cold formability.
  • TRIP Transformation Induced Plasticity steels have been developed to provide even higher tensile strength and elongation. These properties are associated with the structure of such steels, which consists of a ferritic matrix containing bainite/martensite and retained austenite.
  • the retained austenite is generally stabilized by an addition of silicon or aluminium to the steel composition, retarding the precipitation of carbides.
  • the presence of retained austenite brings high ductility in an undeformed steel sheet.
  • the retained austenite is progressively transformed to martensite, resulting in substantial hardening and delaying the occurrence of necking in the uniaxial tensile deformation, thus providing an excellent elongation.
  • US4472208 discloses a hot-rolled high tensile titanium steel plate and production thereof.
  • the steel plate has improved toughness and cold formability and is made of a killed steel which consists essentially of (in wt%): C: 0.05-0.20, Si : not more than 1.2, Mn: 0.5-2.0, Ti: 0.04-0.20, P: not more than 0.025, S: not more than 0.015, sol.
  • the steel has a composition containing (in wt%) C at 0.05 to 0.15, Si at 0.2 to 1.2, Mn at 1.0 to 2.0, P at not more than 0.04, S at not more than 0.005, Ti at 0.05 to 0.15, Al at 0.005 to 0.10 and N at not more than 0.007.
  • EP0997548 discloses a hot rolled high strength steel sheet having a satisfactory strength - elongation balance and an excellent formability, which contains (in wt%): C: 0.05 - 0.15, Si: 0.5 - 2.0, Mn: 0.5 - 2.0, P: 0.05 or less, S: 0.010 or less, Al : 0.005 - 0.10, and the balance of Fe and inevitable impurities, and in which the metal structure mainly comprises three phases of ferrite, retained austenite and bainite.
  • EP1790737 discloses a high strength steel sheet having a strength not lower than 780 MPa and exhibiting a high yield ratio, an excellent balance between the strength and the uniform elongation, and a good plating property in addition to a good balance between the strength and the stretch flangeability.
  • the invention provides a high strength steel, comprising 0.05 to 0.25% of C, less than 0.5% of Si, 0.5 to 3.0% of Mn, not more than 0.06% of P, not more than 0.01% of S, 0.50 to 3.0% of Sol. Al, not more than 0.02% of
  • the steel has a structure formed of at least three phases including a bainite phase, and a retained austenite phase in addition to a ferrite phase having a composite carbide containing Ti and Mo dispersed and precipitated therein, wherein the total volume of the ferrite phase and the bainite phase is not smaller than 80%, the volume of the bainite phase is 5% to 60%, and the volume of the retained austenite phase is 3 to 20%.
  • US5470529 discloses a high tensile strength, hot or cold rolled steel sheet having improved ductility and hole expandability consisting essentially, on a weight basis, of: C:
  • the steel sheet has a structure comprising at least 5% by volume of retained austenite in ferrite or in ferrite and bainite.
  • a hot rolled steel sheet is produced by hot rolling with a finish rolling end temperature in the range of 780-840 °C, cooling to a coiling temperature in the range of 300 - 450 °C.
  • a cold rolled steel sheet is produced by hot rolling, cooling to a coiling temperature in the range of 300 - 720 °C, descaling, cold rolling with a reduction of 30 - 80%, and annealing. Annealing is performed by heating between the Acl point and the Ac3 point and cooling such that the temperature is either kept for at least 30 seconds in the range of 550 to 350 °C or slowly decreased at a rate of 400 °C/min or less in that temperature range.
  • US20090107588 relates to a hot-rolled steel sheet having a tensile strength of greater than 1200 MPa, an Re/Rm ratio of less than 0.75 and an elongation at break of greater than 10%, the composition of which contains, the contents being expressed by weight: 0.10% ⁇ C ⁇ 0.25%; 1% ⁇ Mn ⁇ 3%; Al > 0.015%; Si ⁇ 1.985%; Mo ⁇ 0.30%; Cr ⁇ 1.5%; S ⁇ 0.015%; P ⁇ 0.1%; Co ⁇ 1.5%; B ⁇ 0.005%; it being understood that 1% ⁇ Si + Al ⁇ 2%; Cr + (3 x Mo) > 0.3%, the balance of the composition consisting of iron and inevitable impurities resulting from the smelting, the microstructure of the steel consisting of at least 75% bainite, retained austenite in an amount equal to or greater than 5% and martensite in an amount equal to or greater than 2%.
  • US20080202645 relates to a steel sheet excellent in both a balance between strength and elongation and a balance between strength and hole expandability, in other words, a multi-phase steel sheet having an excellent balance between strength and hole expandability.
  • the invention is a multi-phase steel sheet excellent in hole expandability characterized in that: the steel sheet contains, as chemical components in mass, C: 0.03 to 0.15%, P: not more than 0.010%, S: not more than 0.003%, and either one or both of Si and Al in a total amount of 0.5 to 4%, and one or more of Mn, Ni, Cr, Mo and Cu in a total amount of 0.5 to 4%, with the balance consisting of Fe and unavoidable impurities; the microstructure at a section of the steel sheet is composed of either one or both of retained austenite and martensite which account(s) for 3 to 30% in total in area percentage and the balance consisting of either one or both of ferrite and bainite; the maximum length of the crystal grains in the microstructure
  • EP2714947 relates to a bainite steel consisting of the following elements in weight %: C: 0.25 - 0.55, Si: 0.5 - 1.8, Mn : 0.8 - 3.8, Cr: 0.2 - 2.0, Ti: 0.0 - 0.1, Cu: 0.0 - 1.2, V: 0.0 - 0.5, Nb: 0.0 - 0.06, Al: 0.0 - 2.75, N: ⁇ 0.004, P: ⁇ 0.025, S: ⁇ 0.025 and a method for manufacturing a bainite steel strip that comprises the step of cooling the coiled strip of such composition to ambient temperature, during which the bainite transformation takes place.
  • An object of the invention is to provide a hot rolled high strength steel sheet having improved formability, suitable for structural or high strength components to be shaped by press forming or flange forming in automobiles, industrial machinery and equipment.
  • a further object of the invention is to provide a hot rolled high strength steel sheet having improved formability including increased ductility, improved hole expandability and bendability.
  • a further object of the invention is to provide a method of manufacturing a hot rolled high strength steel sheet according to the objects described hereinabove.
  • a hot rolled high strength steel sheet having a tensile strength of at least 950 MPa consisting of the following elements in weight %:
  • hot rolled high strength steel sheet has a complex phase microstructure comprising in vol.%:
  • microstructure comprises less than 3% carbides
  • the invention provides a hot rolled high strength steel sheet having an excellent improved formability including increased ductility, improved hole expandability and bendability.
  • This excellent combination is derived from a good balance in the strength and ductility of the carbide-free bainitic ferrite/tempered martensite matrix and the TRIP effect of the retained austenite.
  • Bainitic ferrite refers to plate-shaped ferrite having higher density of dislocations (which may have a lath-shaped substructure or a granular substructure), and is different from pro-eutectoid ferrite that has a low density of dislocations.
  • Tempered martensite has a similar substructure as bainitic ferrite albeit with a finer size substructure.
  • the matrix of bainitic ferrite and/or tempered martensite is carbide-free and is different from the conventional bainite that contains carbides. Without wishing to be bound by theory it is believed that the matrix of bainitic ferrite and/or tempered martensite provides high strength due to a high dislocation density and a supersaturated carbon content. The matrix also provides high global elongation and stretch flangeability since it is carbide-free and the fine retained austenite grains can be present on the boundary of lath-shaped bainitic ferrite and/or tempered martensite. It is controlled so that the bainitic ferrite and/or tempered martensite matrix occupies at least 65 % in terms of a volume fraction to the entire structure. Retained austenite enhances ductility partly through the TRIP effect, which manifests itself in an increase in uniform elongation.
  • the hardness difference between the bainitic ferrite and/or tempered martensite matrix and retained austenite is minimal, thereby improving the local ductility at a late stage of deformation in press forming and preventing related issues such as premature edge cracking during stretch flanging, resulting in improved hole expandability and bendability.
  • the local ductility is improved even further by ensuring the absence of carbides in the bainitic ferrite and/or tempered martensite matrix.
  • the steel according to the invention can be obtained without the need of various expensive alloying elements, only requiring the presence of carbon, manganese, silicon and aluminium. This is beneficial for cost reasons as well as for simplifying the process, as thermomechanical manufacturing systems are not necessary.
  • alloying elements for the present invention is as follows. All amounts of elements in compositions are given in weight %, unless specified otherwise. Compulsory elements
  • Carbon (C) is controlled to a value between 0.13 and 0.35. Carbon serves to strengthen the steel and to stabilize the austenite.
  • a bainite transformation takes place and bainitic ferrite laths are initially formed within a still predominantly austenitic matrix.
  • C becomes concentrated in an untransformed austenite phase as bainitic transformation proceeds in the course of coil cooling (austempering) after hot rolling, thereby stabilizing the austenite phase.
  • the retained austenite provides TRIP effect.
  • C should be 0.13 or more, preferably 0.15 or more, more preferably 0.17 or more, most preferably 0.20 or more.
  • the C content is limited to 0.35 less, preferably to 0.32 or less, more preferably 0.30 or less, most preferably 0.26 or less.
  • Manganese (Mn) is controlled to a value between 0.80 and 3.50. Mn promotes the formation of the g-phase and stabilizes the austenite by lowering the transformation temperature Ar3. The addition of manganese also contributes to effective solid-solution hardening and to achieving a higher tensile strength. In order to obtain sufficient hardenability, Mn should be 0.80 or more, preferably 1.20 or more, more preferably 1.40 or more, most preferably 1.60 or more. A Mn content in excess of 3.50 will result in a decrease of the ductility and hampers the formation of acicular ferrite in a sufficient amount during cooling after hot rolling or annealing, thereby affecting the stability of the austenite phase. The risk of forming deleterious banded microstructures is also increased. Therefore, the Mn content is limited to 3.50 or less, preferably to 3.00 or less, more preferably to 2.60 or less, most preferably to 2.40 or less.
  • Silicon (Si) is controlled to a value between 0.01 and 2.50 and has the main function to prevent carbon from precipitating in the form of iron carbides, most commonly cementite and to suppress decomposition of retained austenite.
  • Si is a ferrite stabilizer and is known to be quite effective for the retention of austenite during cooling after hot rolling.
  • a minimal amount of 0.50 Si is needed to effectively suppress the carbide formation, when no substantial amount of Al is present.
  • the lower limit of the Si content is not critical as Al also suppresses the formation of carbides, and a minimal Si content of 0.01 is present.
  • Si in excess of 2.50 is undesirable, as this results in the formation of coarse bainite grains or hard martensite, thereby deteriorating the hole expandability and also causes Si-rich scales inherent in Si-containing steels to form in an appreciable amount, thereby deteriorating the surface appearance and surface processability by alloyed galvanizing. Therefore, the Si content is limited to 2.50 or less and preferably to 2.00 or less, more preferably to 1.50 or less.
  • Aluminium (Al) is controlled to a value between 0.02 to 1.00. A primary function of Al is deoxidising the liquid steel before casting, therefore at least 0.02 is needed for this function.
  • Al is a ferrite stabilizer like Si and assists in retention of austenite during cooling after hot rolling by accelerating the formation of acicular ferrite, facilitating the enrichment of C in the untransformed austenite phase, and retarding the precipitation of carbides.
  • the lower limit of the Al content is not critical as Al also suppresses the formation of carbides. Addition of Al in excess of 1.00 increases the Ac3 temperature of the steels significantly, which may introduce too much ferrite in the microstructure, thereby adversely affecting the strength and ductility. Therefore, the Al content is limited to 1.00 or less, preferably 0.80 or less, more preferably 0.60 or less.
  • the total amount of the Si and the Al content (Si + Al) is controlled at a value between 0.52 and 2.50, thereby achieving the desired microstructures to be formed while maintaining satisfactory usage properties.
  • the total amount of Si + Al is controlled to a value between 0.80 and 2.00, more preferably between 1.00 and 1.60.
  • the upper value should not exceed 2.50 because the beneficial effects of Si and Al saturate and the steel processing becomes difficult.
  • the lower value should be at least 0.52 to effectively supress carbide formation and deoxidize the liquid steel before casting.
  • the ratio of Si : Al is preferably higher than 2: 1, more preferably 3 : 1 when they are used together.
  • composition according to the invention may comprise one or more of the following elements. These elements can be present as alloying elements or residual elements.
  • Residual elements are defined as elements which are not added on purpose to steel and which cannot be removed by simple metallurgical processes. Some of the elements can be present as residual element, like chromium, but chromium can also be added to the steel during steelmaking, in which case it would no longer be a residual element or inevitable impurity, but an alloying element. In many cases it cannot be determined in the finished steel product whether (e.g.) chromium was added as an alloying element, or whether it was present as a residual element.
  • the composition according to the invention may contain one or two elements selected from Ca and a rare earth metal (REM), in an amount consistent with a treatment for MnS inclusion control.
  • the rare earth element include scandium, yttrium, and lanthanide.
  • Ca and/or a rare earth metal (REM) is added to the steel composition to modify the shape of the sulfides.
  • Ca is controlled between 0.0002 and 0.0030 and REM is controlled to a value between 0.0004 and 0.0100.
  • Ca and/or REM combines with sulfur and oxygen, thus creating oxysulfides that do not exert a detrimental effect on ductility, as in the case of elongated manganese sulfides which would form if no Ca or REM is present.
  • the amount of Ca, if present, is controlled to a value below 0.0030, more preferably below 0.0020.
  • the lower limit of Ca, if present, is controlled at 0.0002, preferably 0.0005.
  • the lower limit of REM, if present, is controlled at 0.0004, preferably 0.0005.
  • Chromium (Cr) is an optional element for the present invention and can contribute to the prevention of pro-eutectoid ferrite formation and to the hardening and refinement of the bainitic microstructure. However, in combination with the other elements of the composition that also increase hardenability, a Cr addition is not necessary but can be present as a residual element.
  • the allowable level of Cr as a residual element is 0.04. If it is present as an alloying element, the Cr content is controlled between 0.10 and 1.50. In order to obtain a hardening effect of the bainitic microstructure by Cr, a lower limit of 0.10 is needed, preferably 0.15 and more preferably 0.20. Cr should not exceed 1.50 because it will significantly slow down the bainite transformation kinetics and increases the cost of the steel. Preferably the level of Cr is 1.00 or less, more preferably 0.50 or less.
  • Molybdenum (Mo) is another optional element which, if present, is controlled between 0.05 and 0.50.
  • the allowable level of Mo as a residual element is 0.02.
  • Mo can retard the bainite transformation, may contribute to solid-solution hardening and can also refine the size of the bainite laths formed.
  • a lower limit of 0.05 is needed, preferably 0.10, more preferably 0.15.
  • Mo should be 0.50 or less, preferably 0.30 or less, more preferably 0.20 or less.
  • Boron (B) is another optional element which, if present, is controlled between 0.0005 and 0.0050.
  • An addition of boron increases the quench hardenability and contributes to the elimination of pro-eutectoid ferrite and also helps to increase the tensile strength levels, to obtain these effects of B, a lower limit of 0.0005 is needed, preferably 0.0007, more preferably 0.0010. However, when too much B is added, the effect is saturated.
  • B should be controlled to be 0.0050 or less, preferably 0.0040 or less, more preferably 0.0030 or less, because when B is present in excess, the advantages of this element may be saturated.
  • Copper (Cu) is another optional element which if present, is controlled between 0.10 and 1.00.
  • the allowable level of Cu as a residual element is 0.04.
  • Cu serves to facilitate the removal of high-Si scales formed in the hot rolling stage which is mainly beneficial for subsequent cold rolled product.
  • Cu can improve the corrosion resistance when the cold rolled steel sheet is used as such without surface treatment or improve the wettability by molten zinc or the alloy forming ability when it is subjected to galvanizing or alloyed galvanizing in a continuous galvanizing line. To obtain these effects, Cu should preferably be present in 0.10 or more, preferably 0.15 or more.
  • the Cu content should be controlled to be 1.00 or less, preferably 0.80 or less, more preferably 0.50 or less, when Cu is added.
  • Nickel (Ni) is another optional element which if present, is controlled between 0.10 and 1.00.
  • the allowable level of Ni as a residual element is 0.04.
  • Ni serves to minimize the formation of the surface defects caused by Cu by increasing the melting point of the alloy phase. This effect of Ni is appreciable when the Ni content is > [Cu(%)/3].
  • the sum of Cr+Ni+Cu+Mo should not exceed 1.50, preferably 1.00 for cost reasons.
  • Niobium (Nb), titanium (Ti) and vanadium (V) all precipitate as a carbo-nitride in a ferrite matrix, thereby contributing to a further increase in tensile strength of the steel sheet and are also optional elements for the steel according to the invention.
  • the lower limit for any of these elements should be controlled at 0.010 or more, preferably 0.030 or more.
  • the allowable levels of Nb, Ti and V as a residual element is 0.005 for each.
  • the effect becomes saturated when the content exceeds 0.100 for Nb and Ti or 0.200 for V. Therefore, when these elements are added, the Nb content and Ti content are controlled between 0.010 and 0.100 and the V content between 0.020 and 0.200.
  • the upper limit is 0.050 or less for Nb and Ti and 0.100 or less for V, because when these are added excessively, too much carbo-nitride is precipitated which result in deteriorating the workability.
  • Ti+Nb+V should not exceed 0.250, preferably 0.100 for workability and cost.
  • no additional Ti and/or Nb and/or V and/or Ni and/or Cu and/or B and/or Mo and/or Cr are added as alloying elements in order to reduce the cost of the final product while still obtaining a hot rolled high strength steel sheet having an excellent improved formability including increased ductility, improved hole expandability and bendability.
  • N Nitrogen
  • the steel according to the invention preferably has a minimized N content.
  • the maximum acceptable N content is 0.0100 since a greater N content significantly increases the amount of Al consumed as AIN, thereby not only diminishing the above-described favorable effects of Al but also causing a prominent deterioration in ductility.
  • the N content is 0.0050 or less, more preferably 0.0040 or less.
  • Phosphorus (P) is another incidental impurity and adversely affects weldability and ductility.
  • P is limited to 0.100 or less.
  • the P content is 0.050 or less, more preferably 0.020 or less.
  • S Sulphur
  • S is also an incidental impurity, which adversely affects ductility and press formability by the formation of sulfide inclusions.
  • S is limited to 0.050 or less.
  • the S content be 0.010 or less, even more preferably 0.005 or less.
  • phase transformation temperatures of steels are dependent on the alloy compositions and are defined as follows, as well known to a person skilled in the art.
  • Ar3 the temperature at which austenite begins to transform to ferrite during cooling.
  • Arl the temperature at which austenite transforms to ferrite during cooling ends.
  • Bs the temperature at which, during cooling, transformation of the austenite into bainite starts.
  • Ms the temperature at which, during cooling, transformation of the austenite into martensite starts.
  • Mf the temperature at which, during cooling, transformation of the austenite into martensite ends.
  • Mf the temperature at which, during cooling, transformation of the austenite into martensite ends.
  • critical phase transformation temperatures can be determined by dilatometer experiments.
  • the Bs and Ms points can be calculated beforehand, according to the standard practice.
  • the steel according to the invention has a complex phase microstructure, comprising in vol.% 65% or more of a matrix of carbide free bainitic ferrite (BF) and/or tempered martensite (TM) and 5 to 25% of retained austenite (RA).
  • BF carbide free bainitic ferrite
  • TM tempered martensite
  • RA retained austenite
  • the matrix of a mixture of carbide free bainitic ferrite (BF) and/or tempered martensite (TM) ensures a good balance in the strength and ductility of the steel, while the retained austenite contributes to the TRIP effect.
  • a matrix of BF may be obtained during austempering when the quenching stop temperature and the coiling temperature are in the temperature range between Ms and Bs-50 °C.
  • the BF in these steels is generally present in the form of plates with an ultrafine grain size (typically ⁇ 5 pm long and ⁇ 200 nm thick).
  • the TM can be obtained during quenching and partitioning when the quenching stop temperature is between Ms and Mf and the coiling is conducted in the temperature range between Ms and Bs.
  • the TM has a similar substructure to BF but a finer size of substructure.
  • the precipitation of carbides between the ferritic laths which is known to be detrimental to ductility, is suppressed by alloying with Si and/or Al.
  • Such carbide free BF and/or TM microstructures are expected to provide high strength and good elongation due to the intermediate hard bainitic ferrite structure and to achieve good stretch-flangeability due to their uniform fine lath structure.
  • the BF and/or TM should be the matrix of the steel in a volume fraction of 65% or more, more preferably 70% or more. While the upper limit of the proportion depends on the balance between the bainitic ferrite structure and other structures, it is recommended to set the upper limit at about 95%, or preferably at 90%. Below the lower limit, the high strength cannot be guaranteed. Above the upper limit, insufficient retained austenite will be present, and thus elongation will be too low.
  • Retained austenite enhances ductility partly through the TRIP effect, which manifests itself in an increase in uniform elongation.
  • the volume fraction of retained austenite is controlled to be 5% or higher, preferably 8% or higher. Below 5% the desired level of ductility and uniform elongation will not be achieved.
  • the upper limit is set by the composition of the steel and processing parameters in a production line. For a given composition, the C content in the retained austenite becomes too low if the amount of the retained austenite is too high. The retained austenite is not stable enough and the stretch flangeability will deteriorate. Therefore, it is recommended that the volume fraction of retained austenite is within an upper limit of 25%, preferably less than 20%, more preferably less than 15%.
  • the matrix of the steel consists of carbide free BF only, and no TM is present.
  • Such a hot rolled high strength steel is expected to provide a good balance of strength and ductility.
  • the concentration of C in the retained austenite has great influence on the TRIP (strain- induced transformation processing) characteristics.
  • the retained austenite is effective in improving the elongation property when the carbon concentration is 0.90% or higher, preferably 0.95% or higher, and more preferably 1.00% or higher.
  • the upper limit of carbon in the retained austenite is 1.60% or lower, preferably 1.50% or lower, more preferably 1.40% or lower to ensure the TRIP effect.
  • the complex phase steel may further comprise amounts of other types of microstructures such as pro-eutectoid ferrite and fresh martensite, which volumes are dependent on both the alloying composition as well as the process settings.
  • the presence of some pro-eutectoid ferrite other than BF has a remarkable effect on the tensile properties and formability.
  • the pro-eutectoid ferrite includes the polygonal ferrite (PF), typically formed in the hot rolling temperature range (above Arl) and the acicular ferrite (AF), typically formed during cooling stage to the coiling temperature.
  • PF polygonal ferrite
  • AF acicular ferrite
  • Pro-eutectoid ferrite in general decreases yield strength and increases total elongation.
  • Acicular ferrite, formed at lower temperatures during the fast cooling stage has an acicular shape, is similar to bainitic ferrite in morphology and has some dislocations.
  • the hot rolled high strength steel sheet has a microstructure wherein the matrix further comprises acicular ferrite, and wherein the total volume of bainitic ferrite + tempered martensite + acicular ferrite is between 70 to 95 %.
  • the microstructure comprises less than 20% acicular ferrite, preferably less than 15%.
  • the presence of a small amount of acicular ferrite may increase global ductility significantly without sacrificing local ductility too much. Therefore, if present, the microstructure of the hot rolled high strength steel sheet comprises 3% or more acicular ferrite, preferably 5% or more.
  • the formation of acicular ferrite allows more carbon to partition to the remaining austenite, which is beneficial for the stability of the retained austenite.
  • the amount of acicular ferrite should not be too high for the local ductility of the steel.
  • the microstructure comprises less than 5% polygonal ferrite, preferably less than 3%, more preferably less than 1%.
  • the microstructure is free from polygonal ferrite (PF).
  • PF polygonal ferrite
  • the PF is very soft and is detrimental to local ductility and leads to insufficient HEC. Therefore, the formation of PF is preferably controlled at lower levels.
  • the overall microstructure comprises less than 3% carbides, either present as separate phase or in the form of pearlite, preferably less than 2%, more preferably less than 1%. Most preferably, the microstructure is free from carbides as the formation of carbides is detrimental to strength and ductility.
  • the microstructure also comprises fresh martensite.
  • the amount of fresh martensite is preferably less than 15%, more preferably less than 10%, most preferably less than 5%.
  • the presence of some fresh martensite can have a beneficial effect on work hardening rate. However over 15% it will negatively influence the hole expansion capacity.
  • the microstructure of the steel can be determined by optical microscopy, scanning electronic microscopy, x-ray measurement and dilatation test analysis, as well known in the art. Specific reference is made to chapter 3 of Micro-structural Quantification of Multi-Phase Steels (Micro-Quant the article Aarnts, M.P.; Rijkenberg, R.A. et al.).
  • the steel according to the invention will have good balanced properties of improved formability including increased ductility, improved hole expandability and bendability in combination with high strength as illustrated by the examples below.
  • the hot rolled steel has a yield strength (YS) of at least 600 MPa, more preferably at least 700 MPa, most preferably at least 800 MPa.
  • the yield strength is determined according to NEN-EN10002-1 :2001. Steels with these higher yield strength are particularly suitable for automotive applications, as frame, wheel and other parts in cars. They can also be applied to structural materials for architecture, bridge, ship and rolling stock body.
  • the hot rolled steel has a tensile strength (TS) of at least 950 MPa, more preferably at least 1050 MPa, most preferably 1150 MPa.
  • TS tensile strength
  • the tensile strength is determined via NEN-EN10002-1 :2001. Steels with these higher yield strength are particularly suitable for automotive applications, as frame, wheel and other parts in heavy trucks. They can also be applied to structural materials for architecture, bridge, ship and rolling stock body to reduce weight.
  • the hot rolled steel has a total elongation (TE) of at least 10%, preferably at least 13%, more preferably at least 15%.
  • TE total elongation
  • the hot rolled steel has a hole expansion capacity (HEC) of at least 20%, preferably at least 30%, more preferably at least 40%.
  • HEC hole expansion capacity
  • the HEC is measured according to the stretch flangeability evaluation test, in accordance with The Japan Iron and Steel Federation Standards JFS T 1001.
  • the hot rolled steel has a bending angle (BA) of 50° or more, preferably 60° or more, more preferably 70° or more. With increasing bending angle, the formability becomes better.
  • the bending angle is determined via a three-point bending test according to the VDA 238-100 standard.
  • a method for producing the hot rolled high strength steel sheet according to the first aspect of the invention comprising the steps of:
  • the method according to the invention provides a manufacturing process of the hot rolled steel sheet, in which small variations in the parameters do not cause substantial modifications to the microstructure and to the mechanical properties.
  • the hot-rolling is carried out as well known in the art.
  • the finish rolling temperature, cooling rate, stop temperature and coiling temperature are important to obtain a steel sheet with the desired properties.
  • the manufacturing process is carried out as follows: a steel of the composition as described above is made and the slab is casted using conventional methods such as ingot casting or continuous casting.
  • the cast slab is reheated to a temperature above the Ac3 point and preferably above 1150 °C to completely dissolve the added alloying elements in the austenite phase to form a solid solution prior to hot rolling.
  • the optimum reheating temperature depends on the alloying elements. However, the inventors found that a suitable range is above the Ac3, preferably between 1150 °C and 1250 °C to obtain homogeneous microstructures.
  • the slab is hot-rolled in a temperature range in which the structure of the steel is entirely austenitic.
  • a suitable temperature for hot rolling is between 1150 °C and 1250 °C. Standard hot rolling processes can be applied.
  • the final sheet thickness is normally based on the final application of the steel sheet.
  • Hot rolling is completed by finishing hot rolling at a temperature being above the Ar3 point of the steel, preferably in the range of 800-950 °C, whereby the austenite phase is refined into fine grains.
  • finish rolling temperature is too low, premature formation of ferrite may occur during hot rolling to form polygonal ferrite, thereby deteriorating the press formability of the resulting hot rolled steel sheet.
  • finish rolling temperature is above 950 °C, the austenite grain size may become too large, which affect the formation of the pro-eutectoid ferrite in the following cooling step and the formation of the bainitic ferrite during coiling, thereby deteriorating the strength and ductility.
  • the strip is then cooled at a cooling rate (Vcool) of 20 to 100 °C/s to a temperature Tstop below Bs - 25 and above Mf + 25 °C, preferably below Bs - 50 °C and above Mf + 50 °C.
  • Vcool a cooling rate of 20 to 100 °C/s to a temperature Tstop below Bs - 25 and above Mf + 25 °C, preferably below Bs - 50 °C and above Mf + 50 °C.
  • Vcool cooling rate after hot rolling
  • pro-eutectoid ferrite may form in an excess amount and/or pearlite may form during cooling.
  • the presence of too much amount of the ferrite can increase the elongation but significantly reduce the strength and HEC value.
  • Vcool is higher than 100 °C/s acicular ferrite will not be formed in an amount sufficient to enable the retention of a substantial amount of austenite.
  • the Vcool is preferably in the range of 25 to 80 °C/s, more preferably 30 to 60 °C/s.
  • the Tstop temperature should be below Bs - 25 °C, more preferably Bs - 50 °C. If the temperature Tstop is too high, proeutectoid polygonal ferrite or pearlite may form in an excess amount during cooling, which will significantly reduce the yield strength and HEC value.
  • the Tstop should be above Mf + 25 °C, more preferably above Mf + 50 °C to ensure the presence of a sufficient amount of the retained austenite, which is necessary to obtain the TRIP effect.
  • Coiling is then carried out at a temperature Tcoil below Bs - 80 °C and above Ms, preferably below Bs - 100 °C and above Ms, to obtain a microstructure of at least 65% of a matrix of carbide-free bainitic ferrite and tempered martensite. If Tcoil is too high, the bainitic ferrite becomes too coarse and carbides might be formed along the original austenite grain boundaries or in the form of the pearlite microstructure. As a consequence, the required amount of the BF and the retained austenite will not be obtained. If Tcoil is too low, bainite transformation may be not complete and the carbon enrichment of the austenite may be insufficient.
  • the cooling rate during coil cooling(Vcoil) is preferably less than 0.05 °C/s, more preferably 0.03 °C/s to allow bainitic transformation to complete before the strip temperature reaches 300 °C.
  • the Tstop temperature is below Bs - 25 °C and above Ms, preferably below Bs - 50°C and above Ms, and the Tcoil is below Bs - 80 °C and above Ms.
  • This process results in a steel sheet with a carbide-free bainitic ferrite (BF) base microstructure.
  • the hot rolled strip is cooled down to the Tcoil in the run-out table, preferably with a cooling rate (Vrot) not lower than 1 °C/s to avoid the formation of carbides. The natural cooling in the air is sufficient for this purpose.
  • the matrix of BF can be obtained during austempering when the quenching stop temperature (Tstop) and the coiling temperature (Tcoil) are in the temperature range of above Ms and below Bs - 25 °C, as shown in Figure 1 which depicts a schematic temperature (vertical) vs. time (horizontal) diagram for austempering steel to obtain a BF base microstructure.
  • Tstop quenching stop temperature
  • Tcoil coiling temperature
  • This process results in a steel sheet with a matrix of a mixture of carbide-free bainitic ferrite and tempered martensite.
  • some amount of martensite is formed at Tstop temperature and then is tempered during coiling. In general, the lower the Tstop temperature is, the more the amount of tempered martensite is.
  • the Tstop should be above Mf + 25 °C, preferably above Mf + 50 °C to ensure the presence of a sufficient amount of the retained austenite.
  • the hot rolled strip is heated in the run-out table to the Tcoil temperature for coiling. The heating can be realized by adding an induction heating unit in the run-out table.
  • the heating time between Tstop and Tcoil is preferably between 1 second and 1 hour.
  • the TM can be obtained during quenching and partitioning when the quenching stop temperature (Tstop) is between Ms and Mf + 25 °C and the coiling is conducted in the temperature range between Ms and Bs - 80 °C, as shown in Figure 2, which depicts a schematic temperature (vertical) vs. time (horizontal) diagram for quenching and partitioning the steel to obtain a TM+BF base microstructure.
  • the steel according to the invention can be further processed according to common procedures known in the art, such as pickling and surface treatment.
  • Examples are performed using laboratory cast ingots.
  • Room temperature tensile tests were performed in a Schenk TREBEL testing machine following NEN-EN10002-1 :2001 standard to determine tensile properties (yield strength YS (MPa), ultimate tensile strength UTS (MPa), total elongation TE (%)). For each condition, three tensile tests were performed and the average values of mechanical properties are reported.
  • Bending test - Bending specimens (40 mm x 30 mm) from parallel and transverse to rolling directions were prepared from each of the conditions and tested by three-point bending test according to the VDA 238-100 standard. The experiments were stopped at different bending angles and the bent surface of the specimen was inspected for identification of failure in order to determine the bending angle (BA). The bending angles of the samples with bending axis parallel to the rolling direction are lower than those of the samples with bending axis perpendicular to the rolling direction. For each type of tests, three samples were tested and the average values from three tests are presented for each condition.
  • the tensile properties, the HEC and minimal BA value (the bending axis parallel to the rolling direction) are given in Table 2.
  • the amount of retained austenite (RA) and the carbon content in the retained austenite were determined using X-ray measurement (XRD) and subsequent Rietveld analysis. Reference is made to Onink M et.al, "The lattice parameters of austenite and ferrite in Fe-C alloys as functions of carbon concentration and temperature". Scr. Metal. Mater. 29: 1011-1016 (1993).
  • the microstructures were evaluated by optical microscopy and scanning electronic microscopy. The volume fractions were obtained from dilatation tests in combination with microstructural analysis. The volume fractions of microstructure are given in Table 3.
  • a steel according to the invention has excellent balanced properties both in terms of strength and ductility. From the steels that aren't according to the invention, the properties and/or the microstructures that do not meet the requirements are underlined.
  • the microstructure of examples A3, A4, E3 and F3 for example comprise carbides along the original grain boundaries and/or pearlite microstructure and a low amount of the retained austenite, resulting in low tensile strength.
  • A3 & A4 show a mediocre performance in the HEC test, whereas A1 & A2, which are according to the invention, show excellent properties on all tests.
  • Table 3 Corresponding microstructures of the alloys of table 2.

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Abstract

La présente invention concerne une tôle d'acier laminée à chaud à haute résistance ayant une aptitude au façonnage améliorée, constituée des éléments suivants en % massiques : 0,13-0,35 de C; 0,80-3,50 de Mn; 0,01-2,50 de Si; 0,02-1,00 d'Al; la somme de Si et d'Al allant de 0,52 à 2,50; et facultativement un ou plusieurs éléments choisis parmi : 0,0002-0,0030 de Ca; 0,0004-0,0100 de REM; 0,10-1,00 de Cu; 0,10-1,50 de Cr; 0,10-1,00 de Ni; 0,05-0,50 de Mo; 0,0005-0,0050 % de B; 0 010-0,100 de Nb; 0 010-0,100 de Ti; 0 020-0,200 de V; la somme de Nb + Ti + V étant de 0 à 0,250 et la somme de Cr + Ni + Cu + Mo allant de 0 à 1,50, et au plus 0,100 de P; au plus 0,050 de S; au plus 0,0100 de N; le reste étant constitué des inévitables impuretés et de Fe. La tôle d'acier à haute résistance laminée à chaud possède une microstructure de phase complexe comprenant, en % volumiques : 65 % ou plus d'une matrice d'un mélange de ferrite bainitique exempte de carbure (BF) et/ou de martensite revenue (TM), et de 5 à 25 % d'austénite résiduelle (RA).
EP19784114.1A 2018-10-19 2019-10-16 Tôle d'acier laminée à chaud à ultra-haute résistance et ayant une aptitude au façonnage améliorée et son procédé de production Pending EP3867417A1 (fr)

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