US20200340073A1 - Steel section having a thickness of at least 100mm and method of manufacturing the same - Google Patents

Steel section having a thickness of at least 100mm and method of manufacturing the same Download PDF

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US20200340073A1
US20200340073A1 US16/762,078 US201816762078A US2020340073A1 US 20200340073 A1 US20200340073 A1 US 20200340073A1 US 201816762078 A US201816762078 A US 201816762078A US 2020340073 A1 US2020340073 A1 US 2020340073A1
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steel section
precipitates
steel
vanadium
recited
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Christophe HOUYOUX
Valerie RINALDI
Boris Donnay
Liudmila WEBBER
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ArcelorMittal SA
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ArcelorMittal SA
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    • CCHEMISTRY; METALLURGY
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B1/00Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
    • B21B1/08Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling structural sections, i.e. work of special cross-section, e.g. angle steel
    • B21B1/088H- or I-sections
    • 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
    • C21D1/02Hardening articles or materials formed by forging or rolling, with no further heating beyond that required for the formation
    • 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
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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
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
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    • 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
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    • C21D7/00Modifying the physical properties of iron or steel by deformation
    • C21D7/13Modifying the physical properties of iron or steel by deformation by hot working
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    • 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
    • C21D8/005Modifying the physical properties by deformation combined with, or followed by, heat treatment of ferrous alloys
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    • 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
    • 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
    • C21D9/0068Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for particular articles not mentioned below
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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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    • C22CALLOYS
    • 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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    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
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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
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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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
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
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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
    • C22C38/38Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous 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
    • CCHEMISTRY; METALLURGY
    • 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
    • C22C38/46Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • CCHEMISTRY; METALLURGY
    • 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
    • CCHEMISTRY; METALLURGY
    • 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
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04CSTRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C3/00Structural elongated elements designed for load-supporting
    • E04C3/02Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces
    • E04C3/04Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces of metal
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/002Bainite
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/004Dispersions; Precipitations
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/005Ferrite
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/008Martensite
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/009Pearlite
    • 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
    • C21D2221/00Treating localised areas of an article
    • C21D2221/10Differential treatment of inner with respect to outer regions, e.g. core and periphery, respectively
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04CSTRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C3/00Structural elongated elements designed for load-supporting
    • E04C3/02Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces
    • E04C3/04Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces of metal
    • E04C2003/0404Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces of metal beams, girders, or joists characterised by cross-sectional aspects
    • E04C2003/0443Joists; Girders, trusses, or trusslike structures, e.g. prefabricated; Lintels; Transoms; Braces of metal beams, girders, or joists characterised by cross-sectional aspects characterised by substantial shape of the cross-section
    • E04C2003/0452H- or I-shaped

Definitions

  • the present invention deals with a steel section comprising a web central portion connected on each side to a flange portion having a thickness above 100 mm.
  • the steel section according to the invention is particularly well suited for the manufacture of columns for high-rise buildings, long span, transfer and belt trusses, outriggers and bridge girders.
  • Another object of the present invention is to provide a method of manufacturing of a steel section comprising the following steps:
  • FIG. 1 shows an electron micrograph illustrating randomly distributed precipitates in the core of the flange of the heavy section
  • FIG. 2 shows an electron micrograph illustrating precipitates, arranged in regularly spaced bands
  • FIG. 3 shows schematically the web portion and flanges of the steel section.
  • carbon plays an important role in the formation of the microstructure and reaching of the targeted mechanical properties. Its main role is to provide strengthening through hardening of the martensite/bainite phases but also through formation of carbides and/or carbo-nitrides of metallic elements of the steel.
  • the carbon content of the grade according to the invention is between 0.06 and 0.16% weight. Carbon content below 0.06% will not result in a sufficient level of mechanical resistance, leading to yield strengths value below 485 MPa. On the opposite, carbon contents above 0.16% would result in reducing ductility and the weldability of the steel.
  • the carbon content is between 0.08 and 0.14%, so as to obtain sufficient strength and weldability.
  • Manganese is an element which increases hardenability.
  • the manganese content of the grade according to the invention is between 1.10 and 2.00%. Manganese content below 1.10% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, manganese content above 2.00% would result in decreased weldability or would promote the formation of hard martensite-austenite constituents, also negatively impacting the toughness of the steel.
  • Silicon is a deoxidizing element and contributes to improving strength. Silicon content below 0.10% will not result in a sufficient level of mechanical resistance nor a good deoxidation. On the opposite side of the range, silicon contents above 0.40% would result in the formation of oxides, reducing welding properties of the steel.
  • Copper is an element contributing to improving the strength of the steel by hardenability improvement and precipitation strengthening. Copper content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, copper contents above 0.50% would result in increasing the carbon equivalent and thus deteriorating the weldability or impacting the hot shortness of the steel during hot deformation, caused by penetration of the Cu-enriched phase into grain boundaries.
  • Nickel is an element contributing to improving the strength and toughness of the steel. Nickel content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, nickel contents above 0.30% would lead to high alloying costs.
  • Chromium is an element contributing to improving the strength of the steel by improving hardenability through solution hardening but also through precipitation hardening. Chromium content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, chromium contents above 0.50% would result in generating coarse chromium carbides or carbo-nitrides that may deteriorate the toughness of the steel
  • Molybdenum is an element contributing to improving the strength of the steel by improving hardenability. Molybdenum content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, molybdenum contents above 0.20% would result in reducing the toughness of the steel.
  • Vanadium is an important element that is used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides but also through grain refining.
  • the formation of vanadium precipitation limits the austenite grain coarsening, by resulting in ferrite grain decrease and improved strength by precipitation in ferrite phase.
  • Vanadium would also prevent the chromium and manganese migration in the cementite, resulting in their application in small precipitation formation.
  • Vanadium content below 0.06% will not result in a sufficient level of mechanical resistance.
  • vanadium contents above 0.12% would result in a risk that an excessive precipitation may cause a reduction in toughness, which has to be avoided.
  • vanadium addition is limited to 0.09% to improve further the toughness of the steel.
  • Nitrogen is an important element to form nitrides and carbo-nitrides of metallic elements like vanadium, niobium aluminum and titanium. Their size, distribution density and stability have a significant effect to mechanical strengthening. Nitrogen content below 0.0050% will not result in a sufficient level precipitation and grain size control. To further improve those properties, a minimum level of 0.0060%, or even of 0.0070% or even better of 0.0080% is preferred. On the opposite side of the range, nitrogen contents above 0.0200% would result in the presence of free nitrogen in the steel, which is known as having a negative impact on toughness in the Heat Affected Zone after welding.
  • the precipitation strengthening can be enhanced by optimizing the vanadium to nitrogen ratio in the steels section to approach the stoichiometric ratio of 4:1.
  • the ratio of V to N is comprised between 2.5 and 7, and even comprised between 3 and 5.
  • Aluminium can be added in the steel for deoxidizing effect and removing of the oxygen from the steel. If other deoxidizing elements are added in the steel, the aluminum content is 0.005% and lower. Otherwise, the aluminum content is between 0.005% and 0.040%. If the aluminum content is too high, the formation of AlN will occur in preference to VN, and AlN being bigger in size than VN, it will be not as efficient for pinning of austenite grain boundaries as VN.
  • Sulfur and phosphorus are impurities that embrittle the grain boundaries and lead to the formation of center and micro-segregation. Their respective contents must not exceed 0.030 and 0.040% so as to maintain sufficient hot ductility and to avoid deterioration in welding properties.
  • Niobium is an element that may optionally be used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides. It suppresses the growth of austenite grains during rolling, by refining them, thus resulting in improvement of strength and low-temperature toughness. However, when its amount is above 0.05%, could deteriorate toughness in the Heat Affected Zone due to martensite hardening. On the other hand, when niobium amount is 0.05% and higher, it will pin to available nitrogen and thus impairing nitrogen from forming vanadium precipitates that assures the strengthening of the ductile core of the section.
  • Titanium is an element that may optionally be used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides. However, when its amount is above or equal to 0.005%, there is a risk of TiN formation rather than VN. Moreover, TiN being cuboids particles may react as stress concentrators thus negatively impacting the toughness and fatigue properties of the steel. In a preferred embodiment, the maximum amount of titanium is set to 0.003% and even to 0.001%.
  • the carbon, manganese, chromium, molybdenum, vanadium, nickel and copper contents of the grade are such that
  • Respecting these values ensures that the hardenability of the steel section will be in suitable ranges through sufficient formation of bainite, while maintaining a good weldability of the steel sections.
  • the reduced carbon equivalent allows avoiding weld processing steps such as preheating (when acceptable) and also results in reduction of fabrication costs.
  • CEV ⁇ 0.5%.
  • the steel section comprises a web central portion 100 connected on each side to a flange portion 102 , 104 , as shown schematically in FIG. 3 .
  • the thickness of the flange of the steel section according to the invention is set above 100 mm, allowing the use of such beam for high-rise building structures, notably. Its thickness is preferably below 140 mm as a sufficient cooling rate to ensure the requested tensile and toughness properties is difficult to obtain.
  • the web and the flanges of the heavy section are composed of a hardened zone, resulting from the water cooling of the surface and a non-hardened zone, in the core of the product.
  • Each zone of the steel section can have a specific microstructure that can include one or more phases among tempered martensite, bainite, ferrite and pearlite. Ferrite can be present under the form of acicular ferrite or of regular ferrite.
  • microstructure of each zone depends on the steel section thickness and on the thermal path it is subjected to.
  • the microstructure of the flanges portions include, from surface to core, a first zone comprising tempered martensite and possibly bainite and a second zone comprising ferrite and pearlite.
  • the first zone can, for example, extend up to 10 mm under the surface of the flange portion.
  • An essential characteristic of the invention is the presence, in the steel section microstructure, of at least one kind of vanadium precipitates possibly comprising also one or more metal chosen among chromium, manganese and iron, said precipitates being chosen among nitrides, carbides, carbo-nitrides or any combination of them, more than 70% of such precipitates and preferably more than 80%, having a mean diameter below 6 nm.
  • the mean diameter determination was done in the following way: the surface of each detected precipitate was measured and applied to the corresponding circle, from which the diameter was extracted, giving then the mean diameter size for all detected precipitates.
  • the mean density of those precipitates is of at least 500 precipitates per mm 2 , preferably of at least 1000 precipitates per mm 2 .
  • Those precipitates have a beneficial effect on strength, known as being increased with precipitates size decrease and precipitates content increase.
  • Such precipitates are preferably present in the core zone of the flange of the section, mainly in the ferrite phase. At least 70% of such precipitates and preferably at least 80%, have a mean diameter below 6 nm. The reduced size of such precipitates increases their hardening effect and hence the tensile strength of the steel section.
  • two types of precipitates are preferably present in the core of the flange of the steel section:
  • the randomly distributed precipitated are bigger than the one arranged in regularly spaced bands.
  • such regularly spaced precipitates include at least vanadium and chromium.
  • more than 80% of the randomly distributed precipitates have a mean diameter between 3.5 and 6 nm.
  • Such precipitates preferably include at least vanadium, chromium and iron.
  • the steel section according to the invention can be produced by any appropriate manufacturing method and one of skill in the art can define one. It is however advisable to use a process ending by an accelerated cooling, in that case quenching and self-tempering of the surface layer after hot-rolling step.
  • the method according to the invention comprises the following steps:
  • the steel sections according to the present invention are preferably produced through a method in which a semi product made of a steel according to the present invention having the composition described above, is cast, the cast input stock is heated to a temperature above 1000° C., preferably above 1050° C. and more preferably above 1100° C. or 1150° C. or used directly at such a temperature after casting, without intermediate cooling. Such temperatures allow full dissolution of vanadium carbonitrides, which will further participate in precipitation strengthening mechanism.
  • the final hot-rolling step is performed at a temperature above 850° C.
  • the end-of-rolling temperature is above or equal to 850° C. in order to assure the austenite grains refining and thus the formation of a thinner microstructure after transformation, which is known to enhance the toughness and strength properties.
  • the aim is to create fine grained microstructure by grain refinement during the subsequent recristallization during rolling.
  • the hot-rolled product obtained by the process described above is then cooled using preferably a quenching and self-tempering process.
  • the so-called quenching and self-tempering process consists in subjecting a hot rolled steel section emerging from the finishing stand of the rolling mill to cooling by means of a fluid so as to produce martensitic and/or bainitic quenching of the surface layer of all or part of the product. Moreover, at the outlet of the fluid cooling zone, the non-quenched portion of the rolled product is at a temperature high enough to permit, during subsequent air cooling, tempering of the surface layer of martensite and/or bainite to take place.
  • the cooling fluid employed for carrying out the quenching and self tempering step is usually water with or without conventional additives, or aqueous of mineral salts, for example.
  • the fluid may be a mist, for example obtained by suspending water in a gas, or it may be a gas, such as steam.
  • desired cooling of the rolled products depends on the cooling devices used, and on suitable choice of the length and the flow rate characteristics of the cooling means.
  • the dimensions of the product are known as well as the composition of the steel, and thus its continuous cooling transformation diagram, making it possible to determine the conditions to apply for an adequate treatment of the steel section, among which, the temperature at which martensite is formed and the maximum time available for performing surface quenching to the desired depth.
  • the amount of heat to be removed can be as well as the characteristics of the cooling devices and the flow rates of the fluid applied by the cooling devices.
  • the evolutions of the skin temperature of the steel section starting from the end of the martensitic and/or bainitic quenching are being measured. After quenching, the skin temperature rises while the temperature at the core continuously decreases after the section has emerged from the last stand of the rolling mill.
  • the skin temperature and the core temperature in a given cross-section converge towards a time from where the two curves continue substantially parallel to one another. The skin temperature at this point is called the “equalization temperature”.
  • Trial 1 is a comparative example and trial 2 is an example according to the invention.
  • phase percentages of the microstructures of the obtained steel section were determined:
  • section no 1 The phase percentages in both zones, especially in the core zone, of section no 1 are quite similar to section no 2, showing that the impact of the vanadium precipitation strengthening is observed at smaller microstructural scale.
  • Precipitation analysis done by TEM examination of carbon extraction replicas taken from the core zone of the flange thickness of the section, showed the presence of vanadium precipitates. Fine precipitates analysis was performed through TEM thin foil method, which allowed quantifying the mean size and the density of the precipitates.
  • FIG. 1 shows the vanadium precipitates mostly having spherical shape, with bigger or smaller size.
  • the bigger size precipitates typically size about 6 nm in diameter
  • the fine precipitates typically size about 3 nm in diameter
  • FIG. 2 shows the microstructure consists of parallel sheets densely populated with vanadium particles. The sheets appear with a regular spacing.
  • Steel sections according to the present invention show excellent values of high strength, toughness and good weldability, which is nowadays not easily achievable.
  • design and construction teams involved in large-scale construction projects can benefit from more efficient structural solutions.
  • the steel section's higher yield strength enables weight savings and lower transportation and fabrication costs than other commonly-used structural steel grades. And thus, the present invention makes an extremely significant contribution to construction industry.

Abstract

A steel section has a web central portion connected on each side to a flange portion having a thickness of at least 100 mm. The steel section microstructure includes at least one kind of vanadium precipitates possibly comprising also one or more metal chosen among chromium, manganese and iron, the precipitates being chosen among nitrides, carbides, carbo-nitrides or any combination of them, more than 70% of such precipitates having a mean diameter below 6 nm. It also deals with a manufacturing method thereof.

Description

  • The present invention deals with a steel section comprising a web central portion connected on each side to a flange portion having a thickness above 100 mm. The steel section according to the invention is particularly well suited for the manufacture of columns for high-rise buildings, long span, transfer and belt trusses, outriggers and bridge girders.
  • BACKGROUND
  • The development of new modern structural steel grades is always driven by the users' requirements towards higher mechanical properties such as yield strength and toughness, as well as excellent technological properties, ensuring an efficient fabrication technology at workshop and on site.
  • SUMMARY OF THE INVENTION
  • It is an object of the invention to provide a steel heavy section reaching a high yield strength of at least 485 MPa and a high tensile strength of at least 580 MPa with excellent weldability.
  • In the practice of structural steel manufacturing, it is known that in order to improve strength and toughness it is preferable to refine the structure through hot rolling at lower temperatures or to add some alloying elements for austenite grain refining. Both solutions are not sufficient for heavy structural steel manufacturing, because in case of lower hot rolling temperatures the overheating of the rolls is inevitable. At the same time, when the alloyed elements are added in high amounts, the weldability of the steel deteriorates.
  • It is an object of the present invention to provide a steel section, comprising a web central portion connected on each side to a flange portion having a thickness of at least 100 mm, such steel section having a composition comprising, in weight percentage:
      • C: 0.06-0.16%
      • Mn: 1.10-2.00%
      • Si: 0.10-0.40%
      • Cu: 0.001-0.50%
      • Ni: 0.001-0.30%
      • Cr: 0.001-0.50%
      • Mo: 0.001-0.20%
      • V: 0.06-0.12%
      • N: 0.0050%-0.0200%
      • Al≤0.040%
      • P≤0.040%
      • S≤0.030%
      • and comprising optionally one or more of the following elements, in weight percentage:
      • Ti<0.005%
      • Nb≤0.05%
      • the reminder being iron and impurities resulting from elaboration, and said steel section microstructure including at least one kind of vanadium precipitates possibly comprising also one or more metal chosen among chromium, manganese and iron, said precipitates being chosen among nitrides, carbides, carbo-nitrides or any combination of them, more than 70% of such precipitates having a mean diameter below 6 nm.
  • Another object of the present invention is to provide a method of manufacturing of a steel section comprising the following steps:
      • feeding a steel semi-product which composition is according to claims 1 to 3,
      • reheating such steel semi-product at a temperature above 1000° C. and hot rolling it with a final rolling temperature of at least 850° C., to obtain a hot rolled steel section,
      • cooling the hot rolled steel section so as to produce martensitic and/or bainitic quenching of the surface layer of all or part of the product, the non-quenched portion of the rolled product remaining at a temperature high enough to make it possible to cause a self-tempering of the quenched surface layer of martensite and/or bainite and to transform the austenite into ferrite and carbides in the core part of the section during the subsequent cooling, the maximum temperature of the tempered surface of the product after quenching being 450 to 650° C.
    BRIEF DESCRIPTION OF THE DRAWINGS
  • Other characteristics and advantages of the invention will become apparent from the following detailed description of the invention and the drawings:
  • FIG. 1: shows an electron micrograph illustrating randomly distributed precipitates in the core of the flange of the heavy section,
  • FIG. 2: shows an electron micrograph illustrating precipitates, arranged in regularly spaced bands, and
  • FIG. 3: shows schematically the web portion and flanges of the steel section.
  • DETAILED DESCRIPTION
  • All compositional percentages are given in weight percent (wt. %), unless indicated otherwise. Regarding the chemical composition of the steel, carbon plays an important role in the formation of the microstructure and reaching of the targeted mechanical properties. Its main role is to provide strengthening through hardening of the martensite/bainite phases but also through formation of carbides and/or carbo-nitrides of metallic elements of the steel. The carbon content of the grade according to the invention is between 0.06 and 0.16% weight. Carbon content below 0.06% will not result in a sufficient level of mechanical resistance, leading to yield strengths value below 485 MPa. On the opposite, carbon contents above 0.16% would result in reducing ductility and the weldability of the steel. Preferably, the carbon content is between 0.08 and 0.14%, so as to obtain sufficient strength and weldability.
  • Manganese is an element which increases hardenability. The manganese content of the grade according to the invention is between 1.10 and 2.00%. Manganese content below 1.10% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, manganese content above 2.00% would result in decreased weldability or would promote the formation of hard martensite-austenite constituents, also negatively impacting the toughness of the steel.
  • Silicon is a deoxidizing element and contributes to improving strength. Silicon content below 0.10% will not result in a sufficient level of mechanical resistance nor a good deoxidation. On the opposite side of the range, silicon contents above 0.40% would result in the formation of oxides, reducing welding properties of the steel.
  • Copper is an element contributing to improving the strength of the steel by hardenability improvement and precipitation strengthening. Copper content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, copper contents above 0.50% would result in increasing the carbon equivalent and thus deteriorating the weldability or impacting the hot shortness of the steel during hot deformation, caused by penetration of the Cu-enriched phase into grain boundaries.
  • Nickel is an element contributing to improving the strength and toughness of the steel. Nickel content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, nickel contents above 0.30% would lead to high alloying costs.
  • Chromium is an element contributing to improving the strength of the steel by improving hardenability through solution hardening but also through precipitation hardening. Chromium content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, chromium contents above 0.50% would result in generating coarse chromium carbides or carbo-nitrides that may deteriorate the toughness of the steel
  • Molybdenum is an element contributing to improving the strength of the steel by improving hardenability. Molybdenum content below 0.001% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, molybdenum contents above 0.20% would result in reducing the toughness of the steel.
  • Vanadium is an important element that is used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides but also through grain refining. The formation of vanadium precipitation limits the austenite grain coarsening, by resulting in ferrite grain decrease and improved strength by precipitation in ferrite phase. Vanadium would also prevent the chromium and manganese migration in the cementite, resulting in their application in small precipitation formation. Vanadium content below 0.06% will not result in a sufficient level of mechanical resistance. On the opposite side of the range, vanadium contents above 0.12% would result in a risk that an excessive precipitation may cause a reduction in toughness, which has to be avoided. In a preferred embodiment, vanadium addition is limited to 0.09% to improve further the toughness of the steel.
  • Nitrogen is an important element to form nitrides and carbo-nitrides of metallic elements like vanadium, niobium aluminum and titanium. Their size, distribution density and stability have a significant effect to mechanical strengthening. Nitrogen content below 0.0050% will not result in a sufficient level precipitation and grain size control. To further improve those properties, a minimum level of 0.0060%, or even of 0.0070% or even better of 0.0080% is preferred. On the opposite side of the range, nitrogen contents above 0.0200% would result in the presence of free nitrogen in the steel, which is known as having a negative impact on toughness in the Heat Affected Zone after welding.
  • During hot rolling, part of the vanadium will combine with nitrogen in order to form VN particles for austenite grain boundaries pinning. The remaining vanadium, in solution, will then precipitate in form of fine precipitates during cooling of the steel, thus making an important contribution to final strength. The inventors have found that the precipitation strengthening can be enhanced by optimizing the vanadium to nitrogen ratio in the steels section to approach the stoichiometric ratio of 4:1. In a preferred embodiment, the ratio of V to N is comprised between 2.5 and 7, and even comprised between 3 and 5.
  • Aluminium can be added in the steel for deoxidizing effect and removing of the oxygen from the steel. If other deoxidizing elements are added in the steel, the aluminum content is 0.005% and lower. Otherwise, the aluminum content is between 0.005% and 0.040%. If the aluminum content is too high, the formation of AlN will occur in preference to VN, and AlN being bigger in size than VN, it will be not as efficient for pinning of austenite grain boundaries as VN.
  • Sulfur and phosphorus are impurities that embrittle the grain boundaries and lead to the formation of center and micro-segregation. Their respective contents must not exceed 0.030 and 0.040% so as to maintain sufficient hot ductility and to avoid deterioration in welding properties.
  • Niobium is an element that may optionally be used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides. It suppresses the growth of austenite grains during rolling, by refining them, thus resulting in improvement of strength and low-temperature toughness. However, when its amount is above 0.05%, could deteriorate toughness in the Heat Affected Zone due to martensite hardening. On the other hand, when niobium amount is 0.05% and higher, it will pin to available nitrogen and thus impairing nitrogen from forming vanadium precipitates that assures the strengthening of the ductile core of the section.
  • Titanium is an element that may optionally be used to achieve hardening and strengthening by precipitation of nitrides, carbo-nitrides or carbides. However, when its amount is above or equal to 0.005%, there is a risk of TiN formation rather than VN. Moreover, TiN being cuboids particles may react as stress concentrators thus negatively impacting the toughness and fatigue properties of the steel. In a preferred embodiment, the maximum amount of titanium is set to 0.003% and even to 0.001%.
  • In a preferred embodiment, the carbon, manganese, chromium, molybdenum, vanadium, nickel and copper contents of the grade are such that

  • 0.4≤CEV≤0.6 with CEV=C+Mn/6+(Cr+Mo+V)/5+(Ni+Cu)/15
  • Respecting these values ensures that the hardenability of the steel section will be in suitable ranges through sufficient formation of bainite, while maintaining a good weldability of the steel sections. The reduced carbon equivalent allows avoiding weld processing steps such as preheating (when acceptable) and also results in reduction of fabrication costs. In a preferred embodiment, CEV≤0.5%.
  • The steel section comprises a web central portion 100 connected on each side to a flange portion 102, 104, as shown schematically in FIG. 3.
  • The thickness of the flange of the steel section according to the invention is set above 100 mm, allowing the use of such beam for high-rise building structures, notably. Its thickness is preferably below 140 mm as a sufficient cooling rate to ensure the requested tensile and toughness properties is difficult to obtain.
  • According to the invention, the web and the flanges of the heavy section are composed of a hardened zone, resulting from the water cooling of the surface and a non-hardened zone, in the core of the product. Each zone of the steel section can have a specific microstructure that can include one or more phases among tempered martensite, bainite, ferrite and pearlite. Ferrite can be present under the form of acicular ferrite or of regular ferrite.
  • The microstructure of each zone depends on the steel section thickness and on the thermal path it is subjected to.
  • In a preferred embodiment, the microstructure of the flanges portions include, from surface to core, a first zone comprising tempered martensite and possibly bainite and a second zone comprising ferrite and pearlite.
  • The first zone can, for example, extend up to 10 mm under the surface of the flange portion.
  • An essential characteristic of the invention is the presence, in the steel section microstructure, of at least one kind of vanadium precipitates possibly comprising also one or more metal chosen among chromium, manganese and iron, said precipitates being chosen among nitrides, carbides, carbo-nitrides or any combination of them, more than 70% of such precipitates and preferably more than 80%, having a mean diameter below 6 nm. The mean diameter determination was done in the following way: the surface of each detected precipitate was measured and applied to the corresponding circle, from which the diameter was extracted, giving then the mean diameter size for all detected precipitates.
  • In a preferred embodiment, the mean density of those precipitates is of at least 500 precipitates per mm2, preferably of at least 1000 precipitates per mm2. Those precipitates have a beneficial effect on strength, known as being increased with precipitates size decrease and precipitates content increase.
  • Such precipitates are preferably present in the core zone of the flange of the section, mainly in the ferrite phase. At least 70% of such precipitates and preferably at least 80%, have a mean diameter below 6 nm. The reduced size of such precipitates increases their hardening effect and hence the tensile strength of the steel section.
  • In a preferred embodiment, two types of precipitates are preferably present in the core of the flange of the steel section:
      • precipitates randomly distributed inside ferrite and
      • precipitates arranged in regularly spaced bands, forming thus parallel sheets densely populated with particles.
  • The randomly distributed precipitated are bigger than the one arranged in regularly spaced bands.
  • In a preferred embodiment, such regularly spaced precipitates include at least vanadium and chromium.
  • In another preferred embodiment more than 80% of the randomly distributed precipitates have a mean diameter between 3.5 and 6 nm. Such precipitates preferably include at least vanadium, chromium and iron.
  • The steel section according to the invention can be produced by any appropriate manufacturing method and one of skill in the art can define one. It is however advisable to use a process ending by an accelerated cooling, in that case quenching and self-tempering of the surface layer after hot-rolling step.
  • The method according to the invention comprises the following steps:
      • feeding a semi-product which composition is according to the invention
      • reheating such semi-product at a temperature above 1000° C. and hot rolling it with a final rolling temperature of at least 900° C., to obtain a hot rolled steel section,
      • cooling the hot rolled steel section so as to produce martensitic and/or bainitic quenching of the surface layer of all or part of the product, the non-quenched portion of the rolled product remaining at a temperature high enough to make it possible to cause a self-tempering of the quenched surface layer of martensite and/or bainite and to transform the austenite into ferrite and carbides in the core part of the section during the subsequent cooling, the maximum temperature of the tempered surface of the product after quenching being 450 to 650° C. and even 550-650° C.
  • The steel sections according to the present invention are preferably produced through a method in which a semi product made of a steel according to the present invention having the composition described above, is cast, the cast input stock is heated to a temperature above 1000° C., preferably above 1050° C. and more preferably above 1100° C. or 1150° C. or used directly at such a temperature after casting, without intermediate cooling. Such temperatures allow full dissolution of vanadium carbonitrides, which will further participate in precipitation strengthening mechanism.
  • The final hot-rolling step is performed at a temperature above 850° C. The end-of-rolling temperature is above or equal to 850° C. in order to assure the austenite grains refining and thus the formation of a thinner microstructure after transformation, which is known to enhance the toughness and strength properties.
  • During hot-rolling, it is preferable to use managed combination of rolling steps and controlling the rolling temperature. The aim is to create fine grained microstructure by grain refinement during the subsequent recristallization during rolling.
  • The hot-rolled product obtained by the process described above is then cooled using preferably a quenching and self-tempering process.
  • The so-called quenching and self-tempering process (QST) consists in subjecting a hot rolled steel section emerging from the finishing stand of the rolling mill to cooling by means of a fluid so as to produce martensitic and/or bainitic quenching of the surface layer of all or part of the product. Moreover, at the outlet of the fluid cooling zone, the non-quenched portion of the rolled product is at a temperature high enough to permit, during subsequent air cooling, tempering of the surface layer of martensite and/or bainite to take place.
  • The cooling fluid employed for carrying out the quenching and self tempering step is usually water with or without conventional additives, or aqueous of mineral salts, for example. The fluid may be a mist, for example obtained by suspending water in a gas, or it may be a gas, such as steam.
  • From a practical view point, desired cooling of the rolled products depends on the cooling devices used, and on suitable choice of the length and the flow rate characteristics of the cooling means.
  • The dimensions of the product are known as well as the composition of the steel, and thus its continuous cooling transformation diagram, making it possible to determine the conditions to apply for an adequate treatment of the steel section, among which, the temperature at which martensite is formed and the maximum time available for performing surface quenching to the desired depth.
  • Based on curves of the temperature gradients in the core and the skin of the rolled steel section, the amount of heat to be removed can be as well as the characteristics of the cooling devices and the flow rates of the fluid applied by the cooling devices.
  • To monitor the formation of the desired microstructures in the different zones of the steel section, the evolutions of the skin temperature of the steel section starting from the end of the martensitic and/or bainitic quenching are being measured. After quenching, the skin temperature rises while the temperature at the core continuously decreases after the section has emerged from the last stand of the rolling mill. The skin temperature and the core temperature in a given cross-section converge towards a time from where the two curves continue substantially parallel to one another. The skin temperature at this point is called the “equalization temperature”.
  • EXAMPLES
  • Two grades, which compositions are gathered in table 1, were cast in semi-products and processed into steel sections following the process parameters gathered in table 2, going through heating, controlled hot rolling and subsequent water cooling, achieved by quenching and self-tempering.
  • TABLE 1
    Compositions
    Trial C Mn Si Cu Ni Cr Mo V N Ti Nb Al P S CEV
    1 82 1059 171 170 162 129 49 34 9.6 1 1 3 13 23 0.32
    2 98 1559 191 193 117 122 35 74 16.2 1 1 13 17 29 0.43
  • The tested compositions are gathered in the following table wherein the element content are expressed in thousands of weight percent:
  • Trial 1 is a comparative example and trial 2 is an example according to the invention.
  • TABLE 2
    Process parameters
    Hot rolling Quenching and self-tempering
    Hot Self-
    Flange rolling Specific tempering
    thickness Reheating finish T water flow Temperature
    Trial (mm) T (° C.) (° C.) (l/m2/s) (° C.)
    1  80 1150 868 46 640
    2 125 1170 893 46 600
  • Steel semi-products, as cast, were processed under the following conditions:
  • The resulting samples were then analyzed and the corresponding microstructure elements and mechanical properties were respectively gathered in table 3 and 4.
  • TABLE 3
    Microstructure and precipitates
    Hardened zone Core zone
    Tempered Regular Acicular Pearlite +
    Trial martensite Bainite Ferrite ferrite Bainite
    1 33.4% 66.6% 76.7% 5.5% 17.7%
    2 56.7% 43.3% 72.4% 0.4% 27.2%
  • The phase percentages of the microstructures of the obtained steel section were determined:
  • The phase percentages in both zones, especially in the core zone, of section no 1 are quite similar to section no 2, showing that the impact of the vanadium precipitation strengthening is observed at smaller microstructural scale.
  • Precipitation analysis done by TEM examination of carbon extraction replicas taken from the core zone of the flange thickness of the section, showed the presence of vanadium precipitates. Fine precipitates analysis was performed through TEM thin foil method, which allowed quantifying the mean size and the density of the precipitates.
  • It was found that precipitates participating in mechanical strengthening of the section were located in the core zone of the steel sections, in particular inside the ferrite phase.
  • FIG. 1 shows the vanadium precipitates mostly having spherical shape, with bigger or smaller size. The bigger size precipitates (typical size about 6 nm in diameter) were mostly randomly distributed. But the fine precipitates (typical size about 3 nm in diameter) were arranged in regularly spaced bands. It can be seen on FIG. 2 that the microstructure consists of parallel sheets densely populated with vanadium particles. The sheets appear with a regular spacing.
  • Regularly Spaced Precipitates
  • Precipitates characteristics
    % of precipitates with a Mean density in Mean diameter
    Trial mean diameter below 6 nm ferrite (per mm2) (nm)
    1 0% ≤100
    2 98%   1213 3.2
  • Randomly Distributed Precipitates
  • TABLE 4
    Mechanical properties
    Precipitates characteristics
    % of precipitates with Mean density in Mean Repartition of metallic
    a mean diameter ferrite diameter elements in precipitates, %
    Trial below 6 nm (per mm2) (nm) V Cr Mn Fe
    1 0% <100
    2 70%   880 5.7 66.6 21.9 4.2 9.3
  • Mechanical properties of the tested steel were determined and gathered in the following table:
  • Yield Strength Tensile strength
    Trial (MPa) (MPa) CEV (%)
    1 398 450 0.32
    2 495 653 0.43
  • The examples show that the steel sections according to the invention are the only one to show all the targeted properties thanks to their specific composition and microstructures.
  • Steel sections according to the present invention show excellent values of high strength, toughness and good weldability, which is nowadays not easily achievable. With the steel grade as per the invention, design and construction teams involved in large-scale construction projects can benefit from more efficient structural solutions. The steel section's higher yield strength enables weight savings and lower transportation and fabrication costs than other commonly-used structural steel grades. And thus, the present invention makes an extremely significant contribution to construction industry.

Claims (15)

1-14. (canceled)
15. A steel section comprising a web central portion connected on each side to flange portions having a thickness of at least 100 mm, the steel section having a composition comprising, in weight percentage:
C: 0.06-0.16%
Mn: 1.10-2.00%
Si: 0.10-0.40%
Cu: 0.001-0.50%
Ni: 0.001-0.30%
Cr: 0.001-0.50%
Mo: 0.001-0.20%
V: 0.06-0.12%
N: 0.0050%-0.0200%
Al≤0.040%
P≤0.040%
S≤0.030%
and optionally including at least one of the following elements, in weight percentage:
Ti<0.005%
Nb≤0.05%
a reminder being iron and impurities resulting from processing;
a microstructure of the steel structure including vanadium precipitates, the vanadium precipitates optionally including at least one metal chosen from the group consisting of chromium, manganese and iron, the vanadium precipitates being chosen among nitrides, carbides, carbo-nitrides or any combination of them, more than 70% of the vanadium precipitates having a mean diameter below 6 nm.
16. The steel section as recited in claim 15 wherein such section composition is such that the following relationship is fulfilled:

0.4≤CEV≤0.6 with CEV=C+Mn/6+(Cr+Mo+V)/5+(Ni+Cu)/15
17. The steel section as recited in claim 15 wherein the ratio of vanadium to nitrogen amounts is between 2.5 and 7.
18. The steel section as recited in claim 15 wherein the microstructure of the flanges portions includes, from surface to core, a hardened zone including tempered martensite and optionally bainite and a core zone including ferrite and pearlite.
19. The steel section as recited in claim 15 wherein such steel section includes portions having a mean density of the vanadium precipitates of at least 500 precipitates per mm2.
20. The steel section as recited in claim 15 wherein at least part of the vanadium precipitates is arranged in regularly spaced bands.
21. The steel section as recited in claim 20 wherein more than 80% of such regularly spaced precipitates have a mean diameter below 3 nm.
22. The steel section as recited in claim 21 wherein such regularly spaced precipitates include at least vanadium and chromium.
23. The steel section as recited in claim 15 wherein at least part of such precipitates is randomly distributed in a ferrite phase located in a core zone of the steel section.
24. The steel section as recited in claim 23 wherein more than 80% of the randomly distributed vanadium precipitates have a mean diameter between 3.5 and 6 nm.
25. The steel section as recited in claim 24 wherein the randomly distributed vanadium precipitates include at least vanadium, chromium and iron.
26. The steel section as recited in claim 15 wherein the vanadium precipitates are located in a core zone of the steel section.
27. The steel section as recited in claim 15 wherein the flange portions have a thickness of at most 140 mm.
28. A method of manufacturing of a steel section comprising the following steps:
feeding a steel semi-product comprising, in weight percentage:
C: 0.06-0.16%
Mn: 1.10-2.00%
Si: 0.10-0.40%
Cu: 0.001-0.50%
Ni: 0.001-0.30%
Cr: 0.001-0.50%
Mo: 0.001-0.20%
V: 0.06-0.12%
N: 0.0050%-0.0200%
Al≤0.040%
P≤0.040%
S≤0.030%
 and optionally including at least one of the following elements, in weight percentage:
Ti≤0.005%
Nb≤0.05%
 a reminder being iron and impurities resulting from processing;
reheating the steel semi-product at a temperature above 1000° C. and hot rolling the steel semi-product with a final rolling temperature of at least 850° C., to obtain a hot rolled steel section; and
cooling the hot rolled steel section so as to produce martensitic or bainitic quenching of the surface layer of all or part of the product, a non-quenched portion of the rolled product remaining at a temperature high enough to enable a self-tempering of the quenched surface layer of martensite or bainite and to transform the austenite into ferrite and carbides in a core part of the section during the subsequent cooling, a maximum temperature of the tempered surface of the product after quenching being 450 to 650° C.
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