US20180230570A1 - High strength hot dip galvanised steel strip - Google Patents
High strength hot dip galvanised steel strip Download PDFInfo
- Publication number
- US20180230570A1 US20180230570A1 US15/580,776 US201615580776A US2018230570A1 US 20180230570 A1 US20180230570 A1 US 20180230570A1 US 201615580776 A US201615580776 A US 201615580776A US 2018230570 A1 US2018230570 A1 US 2018230570A1
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- United States
- Prior art keywords
- steel strip
- temperature
- strip
- hot dip
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- 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.)
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 68
- 239000010959 steel Substances 0.000 title claims abstract description 68
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 19
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 16
- 229910052796 boron Inorganic materials 0.000 claims abstract description 15
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 11
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 11
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 9
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 5
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims abstract description 3
- 229910000734 martensite Inorganic materials 0.000 claims description 19
- 229910001566 austenite Inorganic materials 0.000 claims description 17
- 229910001563 bainite Inorganic materials 0.000 claims description 17
- 229910000859 α-Fe Inorganic materials 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 229910000885 Dual-phase steel Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 230000000717 retained effect Effects 0.000 claims description 8
- 229910001567 cementite Inorganic materials 0.000 claims description 7
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910001208 Crucible steel Inorganic materials 0.000 claims description 4
- 229910001562 pearlite Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 description 14
- 238000000137 annealing Methods 0.000 description 13
- 239000011572 manganese Substances 0.000 description 13
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 12
- 239000004411 aluminium Substances 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 11
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
- 238000005246 galvanizing Methods 0.000 description 9
- 239000010703 silicon Substances 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000009466 transformation Effects 0.000 description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
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- 239000002436 steel type Substances 0.000 description 6
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- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
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- 150000001247 metal acetylides Chemical class 0.000 description 4
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
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- 239000011248 coating agent Substances 0.000 description 2
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- 235000019362 perlite Nutrition 0.000 description 2
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- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 2
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- 239000002893 slag Substances 0.000 description 2
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- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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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
- 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
-
- 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
- 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
- C21D8/0247—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
- 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
- C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
- C21D8/0273—Final recrystallisation annealing
-
- 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
Definitions
- the invention relates to a high strength hot dip galvanised steel strip having improved formability, such as used in the automotive industry.
- the invention also relates to a method for producing such steel strip.
- Formability is not the only requirement for a TRIP assisted dual phase steel strip.
- the alloying elements should be low in amount to make the cost of the steel. as low as possible, and it should be as easy as possible to produce the steel strip at a is broader width both in the hot rolling mill and in the cold rolling mill.
- the steel strip should be easy to coat with a zinc based coating, the steel strip has to have high strength and a good weldability, and should also exhibit a good surface quality.
- the balance being Fe and inevitable impurities.
- the inventors have found that by a careful selection of the amounts of the main constituting elements of the steel, being carbon, manganese, silicon, aluminium, chromium and boron, a high strength hot dip galvanised steel strip can be produced that has the required formability, homogeneity, processability, strength and elongation, while at the same time providing a sufficient weldability, coatability and surface quality.
- the inventors have especially found that it is advantageous to add boron to the composition of the steel.
- the hot rolled steel can be cooled fast enough on the run-out table to get a coiling temperature that provides a suitable microstructure for further processing.
- the inventors due to the addition of boron, the inventors have found that the properties of the end product have a high degree of homogeneity.
- the steel strip can be produced in a width that is commercially interesting.
- TRIP assisted steel grades can be made by intercritically annealing of the cold rolled strip so that ferrite nucleation is not required.
- adding boron improves the hardenability of the steel, resulting in the possibility to use less of the other alloying elements. This results in an improved dimensional window for the steel strip, meaning a higher width to thickness ratio while the mechanical properties of the steel over the width of the strip remain suitable.
- C 0.10-0.21 mass %.
- Carbon has to be present in an amount that is high enough to ensure hardenability and the formation of martensite at the cooling rates available in a conventional annealing/galvanising line, Martensite is required to deliver adequate strength. Free carbon also enables stabilisation of austenite which delivers improved work hardening potential and good formability for the resulting strength level. A lower limit of 0,10 mass % is needed for these reasons. A maximum level of 0.21 mass % a has been found to be essential to ensure good weldability.
- Mn 1.75-2.50 mass %.
- Manganese is added to increase hardenability thus making the formation of hard phases like martensite or bainite easier within the cooling rate capability of a conventional continuous annealing/galvanising line.
- Manganese also contributes to the solid solution strengthening which increases the tensile strength and strengthens the ferrite phase, and also helps to stabilise retained austenite, Manganese lowers the transformation temperature range of the dual phase steel, thus lowering the required annealing temperature to levels that can be readily attained in a conventional continuous annealing/galvanising line.
- a lower limit of 1.75 mass % is needed for the above reasons. This lower limit is possible in view of the addition of other elements, such as boron.
- a maximum level of 2.50 mass % is imposed to ensure acceptable rolling forces in the hot mill and to ensure acceptable rolling forces in the cold mill by ensuring sufficient transformation of the dual phase steel to soft transformation products (fenite and pearlite). This maximum level is also given in view of the stronger segregation during casting and the forming of a band of martensite in the strip at higher values.
- the amount of manganese is between 1.9 and 2.3 mass %, more preferably between 2.0 and 2.2 mass %.
- Si 0.04-0.60 mass %.
- Silicon provides solid solution strengthening thus enabling the attainment of high strength, and the stabilisation of austenite via strengthening of the ferrite matrix. Silicon very effectively retards the formation of carbides during overaging, thus keeping carbon in solution for stabilisation of austenite. For these reasons a lower limit of 0.04 mass % is needed. A maximum level of 0.60 mass % is imposed in view of the coatability of the steel strip, since high levels of silicon lead to unacceptable coating quality due to reduced adherence.
- Al 0.20-1.40 mass %. Aluminium is added to liquid steel for the purpose of de-oxidation. In the right quantity it also provides an acceleration of the bainite transformation, thus enabling bainite formation within the time constraints imposed by the annealing section of a conventional continuous annealing/galvanising line. Aluminium also retards the formation of carbides thus keeping carbon in solution, thus causing partitioning to austenite during overaging, and promoting the stabilisation of austenite. A lower level of 0.20 mass % is required for the above reasons. A maximum level of 1.40 mass % is imposed for castability, since high aluminium contents lead to poisoning of the casting mould slag and consequently an increase in mould slag viscosity, leading to incorrect heat transfer and lubrication during casting.
- Cr max 0.50 mass %. Chrome is added to increase hardenability. Chrome promotes formation of ferrite. A maximum level of 0.50 mass % is imposed to ensure that not too much martensite forms at the cost or retained austenite. It is also possible to add no chrome. Preferably, the amount of Cr is between 0.01 and 0.40 mass %, more preferably between 0.02 and 0.25 mass %.
- Titanium max 0.20%. Titanium is mainly added to strengthen the steel, A maximum level of 0.20 is imposed to limit the cost of the steel. It is also possible to add no Ti,
- Ca max 0.004 mass %.
- the addition of calcium modifies the morphology of manganese sulphide inclusions. When calcium is added the inclusions get a globular rather than an elongated shape. Elongated inclusions, also called stringers, may act as planes of weakness along Which lamellar tearing and delamination fracture can occur. The avoidance of stringers is beneficial for forming processes of steel sheets which entail the expansion of holes or the stretching of flanges and promotes isotropic forming behaviour.
- Calcium treatment also prevents the formation of hard, angular, abrasive alumina inclusions in aluminium deoxidised steel types, forming instead calcium aluminate inclusions which are softer and globular at rolling temperatures, thereby improving the material's processing characteristics.
- some inclusions occurring in molten steel have a tendency to block the nozzle, resulting in lost output and increased costs.
- Calcium treatment reduces the propensity for blockage by promoting the formation of low melting point species which will not clog the caster nozzles. It is also possible to add no calcium when the sulphur content is very low.
- the amount of Ca is between 0.0005 and 0.003 mass %.
- P 0.001-0.025 mass %.
- Phosphorus interferes with the formation of carbides, and therefore some phosphorus in the steel is advantageous.
- phosphorus can make steel brittle upon welding, so the amount of phosphorus should he carefully controlled during steelmaking, especially in combination with other embrittling elements such as sulphur and nitrogen.
- embrittling elements such as sulphur and nitrogen.
- boron it is possible to have more phosphorus in the steel then usual.
- the content of Nitrogen is limited to max 0.015 wt % as is typical for continuous casting plants. Usually, the amount of N is between 0.001 and 0.010 wt %.
- the ranges for aluminium, boron, silicon, chromium and manganese are chosen such that a correct balance is found to deliver a transformation that is as homogeneous as possible on the run-out table and during coil cooling, to ensure a steel strip that can be cold rolled, and to provide a starting structure enabling rapid dissolution of carbon in the annealing line to promote hardenability and correct ferritic/bainitic transformation behaviour.
- aluminium accelerates and chromium decelerates the bainitic transformation the right balance between aluminium and chromium has to be present to produce the right quantity of bainite within the timescales permitted by a conventional hot dip galvanising line with a restricted overage section. In practice, this means that the content of aluminium should be higher than the content of chromium.
- the amounts of Al and Si are chosen such that 0.60% ⁇ Al+Si ⁇ 1.40%
- the amounts of Mn and Cr are chosen such that Mn+Cr>2.00%.
- the amounts of Al and Si are chosen such that Si ⁇ Al.
- Aluminium and silicon together should be maintained between 0.60 and 1.40 mass % to ensure suppression of carbides in the end product and stabilisation of a sufficient amount of austenite, with the correct composition, to provide a desirable extension of formability.
- Manganese and chromium together should be above 2.00 mass % to ensure sufficient hardenability for formation of martensite and/or bainite and thus achievement of strength in a conventional continuous annealing line and hot dip galvanising line.
- Mn aids to stabilise retained austenite.
- Mn+Cr should be above 2.10 mass %, especially when the amount of Si is low.
- Al should preferably be present in an amount equal to or higher then Si in view of a good zinc coatability.
- element C is present in an amount of 0.13-0.18%. In this range the hardenability of the steel is optimal while the weldability of the steel is enhanced, also by the presence of boron. More preferably element C is present in an amount of 0.14-0.17%. This amount of C has been found to work well in practice.
- element Si is present in an amount of 0.05-0.50%, more preferably 0.05-0.40%.
- a amount of silicon lower then 0.50% improves the coatability of the steel strip, even more so when the amount of silicon is below 0.40%.
- element Al is present in an amount of 0.30-1.20%, preferably an amount of 0.40-1.00%.
- a raised lower level of aluminium has the same effect as a higher amount of silicon, but hardly increases the strength of the steel.
- a lower upper limit of aluminium improves the castability of the steel.
- the amount of element B is preferably between 0.0011 and 0.0040%, more preferably between 0.0013 and 0.0030%. to provide the desired hardenability and hence bring sufficient strength.
- the amount of Ti is preferably max 0.10% so as to limit the cost of the steel and keep the dimensional window as large as possible. More preferably, the amount of Ti is between 0.005 and 0.05%.
- the hot dip galvanised steel strip has an ultimate tensile strength Rill above 750 MPa and/or a 0.2% proof strength Rp of 430-700 MPa, preferably the difference between the middle and the edges of the steel strip being less then 75 MPa for both Rp and/or Rm, more preferably this difference being less then 60 MPa.
- Rill ultimate tensile strength
- Rp 0.2% proof strength
- the hot dip galvanised steel strip has a microstructure, consisting of 20-50 volume % ferrite, 10-25 volume % retained austenite+martensite, of which 5-12% retained austenite, the remainder being tempered martensite, bainite and cementite.
- a method for producing a high strength hot dip galvanised steel strip as defined above, wherein the cast steel is hot rolled to a thickness of 2.0-4.0 mm and coiled at a Coiling Temperature CT below Bs ⁇ 20° C. temperature and above Ms+60° C. temperature, the strip is cold rolled with a reduction of 40% or more, after which the strip is intercritically annealed at a temperature between Ac1 and Ac3 temperature, and the strip is averaged at a temperature below Bs temperature to form bainite and/or tempered martensite, after which the strip is hot dip galvanised.
- the hot rolled coil has a microstructure consisting of 50-70 volume % ferrite, 20-50 volume % pearlite and/or bainite, and less then 10% cementite.
- the coil has the right properties for further processing, especially for the annealing step, and can be cold rolled in a wide dimensional window.
- the hot dip galvanised strip is tension rolled with a reduction of 0.2-0.8%. This percentage of tension rolling can provide the right mechanical properties to the strip, such as the tight strength level, while the other properties remain inside the desired window.
- a method for producing a high strength hot dip galvanised complex phase steel strip wherein the cast steel is hot rolled to a thickness of 2.0-4.0 mm and coiled at a Coiling Temperature CT below Bs ⁇ 20° C. temperature and above Ms+60° C. temperature, the strip is cold rolled with a reduction of 40% or more, after which the strip is annealed at a temperature above Ad temperature plus 50° C., and the strip is overaged at a temperature below Bs temperature to form bainite and/or tempered martensite, after which the strip is hot dip galvanised.
- This complex phase steel strip can be made due to the precise Coiling Temperature and the prescribed annealing and overaging temperatures.
- this hot dip galvanised complex phase steel strip is tension rolled with a reduction of 0.4-2.0%, preferably with a reduction of 0.4-1.2%.
- This percentage of tension rolling can provide the right mechanical properties to the strip, such as the right strength level, while the other properties remain inside the desired window.
- FIG. 1 shows measurement of the ultimate tensile strength Rm and 0.2% proof strength Rp after annealing.
- compositions of line trialled materials Unless indicated different, the compositions are defined in mill-wt %. Bs and Ms values were calculated from 1 . Al ⁇ Cast C Mn P Si Cr B ppm zo Ti N ppm Al + Si Mn + Cr Bs ⁇ 20° C. Ms +60° C.
- the material was hot and subsequently cold rolled to a typical gauge in the range 0.8-2.0 mm.
- microstructure and phase fractions defined is provided in FIG. 2 .
- the microstructure over different sampling positions over the coil is provided in Table 2.
- the microstructure is given for the head, middle and tail of a coil.
- M indicates the middle of the strip, R the right hand side.
- a Dual Phase steel strip was produced.
- the hot roll finishing temperature was approximately 875° C. for all casts but for cast 4 , as indicated above.
- the coiling temperature was between 500-520° C., well between Bs ⁇ 20° C. and Ms+60° C., Subsequently, the material was cold rolled and intercritically annealed at around 800° C., and the overage temperature was 400° C. After hot dip galvanising, the strip was temper rolled with a reduction of around 0.3%,
- a Complex Phase steel strip was produced.
- the hot roll finishing temperature was approximately 875° C.
- the coiling temperature was 550° C.
- the material was cold rolled and intercritically annealed at around 840° C., and the overage temperature was 400° C. After hot dip galvanising, the strip was temper rolled with a reduction of 1.0%.
- FIG. 2 shows typical microstructures (Nital etched) obtained at the middle of the hot rolled strip product, after coiling and cooling down. Used is the composition of cast 1 .
- the coiling temperature CT was 500° C.
- the right-hand picture shows the same material but after a coiling temperature of 550° C.
- the dark phase is perlite/bainite and the light phase is ferrite; black dots are cementite.
- perlite/bainite is present in 25-35%, ferrite 60-70% and cementite less than 10%.
- perlitelbainite is present in 20-30%, ferrite 65-75% and cementite less than 10%.
- FIG. 3 shows the variation in Rm and Rp over the width of the strip.
- FIG. 3 a shows this variation for a strip composition that is not according to the invention, having a composition of 0.15 C, 2.05 Mn, 0.2 Cr, 0.7 Al, 0.07 Si, 0.015 Nb and 0.004 N (in wt %).
- the difference in Rrn between middle and edge of the strip is approximately 100 MPa, the difference in Rp is approximately 50 MPa.
- FIG. 3 b shows the variation in Rm and Rp for a strip with the composition of cast 1 .
- This figure shows that it is possible to get a variation between the middle and the edge of the strip that is less than 20 MPa for both Rm and Rp.
- FIG. 3 c shows in fact the same for a strip with the composition of cast 3 .
- the strip shown in FIGS. 3 b and 3 c has been manufactured in accordance with the method of the invention.
- FIG. 4 shows three different ways of graphically indicating the microstructures of the casts after using the method of the invention. These are the well known Picral, Nital and LePera representations. In the Picral graphs black represents bainite or tempered martensite. In the Nital graph the white spots indicate ferrite. In contrast, in the LePera graph white indicates (tempered) martensite+retained austenite. The differences between DP800 on the left-hand side and CP800 on the right-hand side are clearly visible.
- the length indications in FIGS. 2 and 4 all indicate a length of 10 ⁇ m.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Coating With Molten Metal (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15020109 | 2015-07-01 | ||
| EPEP15020109.3 | 2015-07-01 | ||
| PCT/EP2016/064704 WO2017001303A1 (en) | 2015-07-01 | 2016-06-24 | High strength hot dip galvanized steel strip |
Publications (1)
| Publication Number | Publication Date |
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| US20180230570A1 true US20180230570A1 (en) | 2018-08-16 |
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| US15/580,776 Abandoned US20180230570A1 (en) | 2015-07-01 | 2016-06-24 | High strength hot dip galvanised steel strip |
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| Country | Link |
|---|---|
| US (1) | US20180230570A1 (enExample) |
| JP (1) | JP2018524471A (enExample) |
| KR (1) | KR20180025852A (enExample) |
| CN (1) | CN107787375A (enExample) |
| BR (1) | BR112017023814A2 (enExample) |
| CA (1) | CA2989710A1 (enExample) |
| MX (1) | MX2017016843A (enExample) |
| WO (1) | WO2017001303A1 (enExample) |
| ZA (1) | ZA201707294B (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020245627A1 (en) * | 2019-06-03 | 2020-12-10 | Arcelormittal | Cold rolled and coated steel sheet and a method of manufacturing thereof |
| US10927429B2 (en) | 2015-12-15 | 2021-02-23 | Tata Steel Ijmuiden B.V. | High strength hot dip galvanised steel strip |
| CN116815062A (zh) * | 2023-07-10 | 2023-09-29 | 攀钢集团攀枝花钢铁研究院有限公司 | 一种低成本600MPa级热镀锌用增强塑性双相钢及其制造方法 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020058330A1 (de) * | 2018-09-19 | 2020-03-26 | Sms Group Gmbh | Hochfester mehrphasenstahl, stahlband aus diesem stahl sowie verfahren zur herstellung eines stahlbandes |
| WO2020221628A1 (en) * | 2019-04-30 | 2020-11-05 | Tata Steel Ijmuiden B.V. | Process for producing batch annealed tailor rolled strip |
| WO2020245626A1 (en) * | 2019-06-03 | 2020-12-10 | Arcelormittal | Cold rolled and coated steel sheet and a method of manufacturing thereof |
| DE102020110319A1 (de) | 2020-04-15 | 2021-10-21 | Salzgitter Flachstahl Gmbh | Verfahren zur Herstellung eines Stahlbandes mit einem Mehrphasengefüge und Stahlband hinzu |
| CN113355604B (zh) * | 2021-06-25 | 2022-05-24 | 攀钢集团攀枝花钢铁研究院有限公司 | 低成本700MPa级热镀锌复相钢板及其制备方法 |
| CN117802400A (zh) * | 2022-09-23 | 2024-04-02 | 宝山钢铁股份有限公司 | 一种低点焊裂纹敏感性的带镀层超高强钢及其制造方法 |
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- 2016-06-24 JP JP2017567681A patent/JP2018524471A/ja active Pending
- 2016-06-24 US US15/580,776 patent/US20180230570A1/en not_active Abandoned
- 2016-06-24 CA CA2989710A patent/CA2989710A1/en not_active Abandoned
- 2016-06-24 KR KR1020177034172A patent/KR20180025852A/ko not_active Ceased
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- 2016-06-24 MX MX2017016843A patent/MX2017016843A/es unknown
- 2016-06-24 WO PCT/EP2016/064704 patent/WO2017001303A1/en not_active Ceased
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| US20180363082A1 (en) * | 2015-12-15 | 2018-12-20 | Tata Steel Ijmuiden B.V. | High strength hot dip galvanised steel strip |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10927429B2 (en) | 2015-12-15 | 2021-02-23 | Tata Steel Ijmuiden B.V. | High strength hot dip galvanised steel strip |
| WO2020245627A1 (en) * | 2019-06-03 | 2020-12-10 | Arcelormittal | Cold rolled and coated steel sheet and a method of manufacturing thereof |
| CN116815062A (zh) * | 2023-07-10 | 2023-09-29 | 攀钢集团攀枝花钢铁研究院有限公司 | 一种低成本600MPa级热镀锌用增强塑性双相钢及其制造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201707294B (en) | 2019-02-27 |
| WO2017001303A1 (en) | 2017-01-05 |
| BR112017023814A2 (pt) | 2018-07-31 |
| CA2989710A1 (en) | 2017-01-05 |
| CN107787375A (zh) | 2018-03-09 |
| MX2017016843A (es) | 2018-04-24 |
| JP2018524471A (ja) | 2018-08-30 |
| KR20180025852A (ko) | 2018-03-09 |
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