CN118574944A - Hot rolled high strength steel strip - Google Patents
Hot rolled high strength steel strip Download PDFInfo
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- CN118574944A CN118574944A CN202380017873.0A CN202380017873A CN118574944A CN 118574944 A CN118574944 A CN 118574944A CN 202380017873 A CN202380017873 A CN 202380017873A CN 118574944 A CN118574944 A CN 118574944A
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- steel strip
- hot rolled
- high strength
- hot
- strength steel
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 198
- 239000010959 steel Substances 0.000 title claims abstract description 198
- 229910000859 α-Fe Inorganic materials 0.000 claims abstract description 28
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 229910000734 martensite Inorganic materials 0.000 claims abstract description 21
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 20
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 15
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 13
- 239000012535 impurity Substances 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 11
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 10
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 10
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 9
- 229910052802 copper Inorganic materials 0.000 claims abstract description 8
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 8
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 8
- 229910052796 boron Inorganic materials 0.000 claims abstract description 6
- 238000009826 distribution Methods 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims description 35
- 238000000576 coating method Methods 0.000 claims description 25
- 229910045601 alloy Inorganic materials 0.000 claims description 23
- 239000000956 alloy Substances 0.000 claims description 23
- 238000005098 hot rolling Methods 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 20
- 238000005266 casting Methods 0.000 claims description 15
- 238000003303 reheating Methods 0.000 claims description 11
- 238000005096 rolling process Methods 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 238000005554 pickling Methods 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 238000007598 dipping method Methods 0.000 claims description 2
- 239000010936 titanium Substances 0.000 description 30
- 230000035945 sensitivity Effects 0.000 description 27
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- 239000010955 niobium Substances 0.000 description 20
- 229910001566 austenite Inorganic materials 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 238000005275 alloying Methods 0.000 description 13
- 239000002244 precipitate Substances 0.000 description 12
- 238000001556 precipitation Methods 0.000 description 12
- 238000001887 electron backscatter diffraction Methods 0.000 description 11
- 239000011701 zinc Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 229910001567 cementite Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 230000009466 transformation Effects 0.000 description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- 229910001297 Zn alloy Inorganic materials 0.000 description 7
- 229910052725 zinc Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 238000005728 strengthening Methods 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 230000006835 compression Effects 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 150000001247 metal acetylides Chemical class 0.000 description 5
- 238000009628 steelmaking Methods 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- 229910001563 bainite Inorganic materials 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 238000000265 homogenisation Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000013480 data collection Methods 0.000 description 3
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- 238000005246 galvanizing Methods 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- 239000011135 tin Substances 0.000 description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
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- 238000004881 precipitation hardening Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- INZDTEICWPZYJM-UHFFFAOYSA-N 1-(chloromethyl)-4-[4-(chloromethyl)phenyl]benzene Chemical compound C1=CC(CCl)=CC=C1C1=CC=C(CCl)C=C1 INZDTEICWPZYJM-UHFFFAOYSA-N 0.000 description 1
- 229910018134 Al-Mg Inorganic materials 0.000 description 1
- 229910021364 Al-Si alloy Inorganic materials 0.000 description 1
- 229910018137 Al-Zn Inorganic materials 0.000 description 1
- 229910018467 Al—Mg Inorganic materials 0.000 description 1
- 229910018573 Al—Zn Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- 229910003023 Mg-Al Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241001596784 Pegasus Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 229910009369 Zn Mg Inorganic materials 0.000 description 1
- 229910007570 Zn-Al Inorganic materials 0.000 description 1
- 229910007573 Zn-Mg Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- DXHPZXWIPWDXHJ-UHFFFAOYSA-N carbon monosulfide Chemical class [S+]#[C-] DXHPZXWIPWDXHJ-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 1
- 238000000445 field-emission scanning electron microscopy Methods 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009957 hemming Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
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- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0247—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
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/005—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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
Abstract
本发明涉及一种热轧高强度钢带材,其具有以重量%计由以下组成的组成:0.02‑0.13%C,1.20‑3.50%Mn;0.10‑1.00%Si;0.05‑1.0%Mo;0.02‑0.70%Al,0.04‑0.25%Ti,至多0.010%N,至多0.02%P,至多0.01%S,至多0.005%B,任选一种或多种选自以下的元素:(至多1.5%Cu,至多0.70%Cr,至多0.50%Ni,至多0.30%V,至多0.10%Nb),以及余量的Fe和不可避免的杂质;并且其中该钢带材具有至少95体积%的铁素体和最多5体积%的马氏体,和优选至少0.2体积%的马氏体的显微组织;具有在1/4厚度处至少0.65的取向差分布(MOD)指数;至多55%的面积分数,具有0‑1的内核平均取向差(KAM);至少45%的面积分数,具有1‑5的内核平均取向差(KAM);和至少1400mm‑1的总晶界长度(ΣGB[5°‑65°]);并且其中该钢带材至少具有以下机械性质:至少950MPa,优选至少960MPa的极限拉伸强度(Rm),至少10%的总伸长率(A50),和至少40%的扩孔率(λ)值。本发明还涉及制造此类热轧钢带材的方法,并涉及包含该热轧钢带材的汽车零件。
The present invention relates to a hot rolled high strength steel strip having a composition consisting of, in weight %, 0.02-0.13% C, 1.20-3.50% Mn; 0.10-1.00% Si; 0.05-1.0% Mo; 0.02-0.70% Al, 0.04-0.25% Ti, up to 0.010% N, up to 0.02% P, up to 0.01% S, up to 0.005% B, optionally one or more elements selected from the group consisting of: (up to 1.5% Cu, up to 0.70% Cr, up to 0.50% N i, up to 0.30% V, up to 0.10% Nb), and the balance Fe and unavoidable impurities; and wherein the steel strip has a microstructure of at least 95% by volume ferrite and at most 5% by volume martensite, and preferably at least 0.2% by volume martensite; having a misorientation distribution (MOD) index of at least 0.65 at 1/4 thickness; up to 55% area fraction with a core average misorientation (KAM) of 0-1; at least 45% area fraction with a core average misorientation (KAM) of 1-5; and a total grain boundary length (ΣGB[5°-65°]) of at least 1400 mm -1 ; and wherein the steel strip has at least the following mechanical properties: an ultimate tensile strength (Rm) of at least 950 MPa, preferably at least 960 MPa, a total elongation (A50) of at least 10%, and a hole expansion ratio (λ) value of at least 40%. The invention also relates to a method for producing such a hot rolled steel strip and to an automotive part comprising the hot rolled steel strip.
Description
技术领域Technical Field
本发明涉及一种热轧高强度钢带材,其特别适用于汽车部件。本发明还涉及制造此类热轧高强度钢带材的方法。此外,本发明涉及并入该热轧高强度钢带材的汽车零件。The present invention relates to a hot rolled high strength steel strip, which is particularly suitable for automotive components. The present invention also relates to a method for producing such a hot rolled high strength steel strip. Furthermore, the present invention relates to an automotive part incorporating the hot rolled high strength steel strip.
背景技术Background Art
公知的是,随着热轧(HR)钢带材强度的提高,可成形性降低。HR钢在运输和汽车应用中的主要应用领域是底盘和悬架(C&S)。其它领域包括卡车的车架纵梁、保险杠横梁或电动车辆的电池盒。用于这些应用的HR钢的典型厚度小于4.5mm。较厚规格的HR钢带材(例如高达12mm)可用于工程应用,如起重机吊臂,或用于重型卡车车架的运输应用。从减轻重量的角度来看,上述应用必须采用更高强度的钢,以便能够减小钢带材的规格。因此,具有通常超过950MPa的极限拉伸强度(Rm)的超高强度钢将可用于该目的。HR钢的这些应用需要难以协调的机械性质。除高强度外,钢带材还应具有良好的可成形性,用于经由例如冷成形来制造部件,因为与热成形相比冷成形是一种节能的制造路线。此外,对于如保险杠横梁、电池外壳、起重机吊臂或车架纵梁的应用,也需要良好的冲击和断裂韧性或能量吸收能力。为了组装该部件,还需要良好的可焊性。但是,随着钢的拉伸强度提高,可成形性参数降低。可成形性是钢板的通用术语,其被视为在若干机械操作(如拉伸、弯曲、拉拔和卷边)期间材料行为的组合。取决于部件几何形状,材料的两种或多种属性中的任一种或组合在金属板成形期间是重要的。It is well known that with the increase of the strength of hot rolled (HR) steel strip, the formability decreases. The main application areas of HR steel in transportation and automotive applications are chassis and suspension (C&S). Other areas include frame rails of trucks, bumper beams or battery boxes of electric vehicles. The typical thickness of HR steel used for these applications is less than 4.5mm. Thicker HR steel strips (e.g., up to 12mm) can be used for engineering applications, such as crane booms, or for transportation applications of heavy truck frames. From the perspective of weight reduction, the above applications must adopt higher strength steel so that the specifications of the steel strip can be reduced. Therefore, ultra-high strength steels with an ultimate tensile strength (Rm) of generally more than 950MPa will be used for this purpose. These applications of HR steel require mechanical properties that are difficult to coordinate. In addition to high strength, the steel strip should also have good formability for manufacturing components via, for example, cold forming, because cold forming is an energy-saving manufacturing route compared to hot forming. In addition, good impact and fracture toughness or energy absorption capacity is also required for applications such as bumper beams, battery housings, crane arms or frame rails. In order to assemble the component, good weldability is also required. However, as the tensile strength of the steel increases, the formability parameter decreases. Formability is a general term for steel sheets, which is considered to be a combination of the material's behavior during several mechanical operations such as stretching, bending, drawing and hemming. Depending on the component geometry, any one or a combination of two or more properties of the material are important during sheet metal forming.
为了减轻部件重量,常见的方法是应用高强度钢并减小用于减轻重量的钢带材的厚度。但是,这可能导致刚度损失,这对于汽车零件中的一些应用是不合意的。降低用于制造汽车部件的钢带材的厚度造成的固有刚度损失可以通过优化部件几何形状来重新获得,例如产生更深的凸缘或具有提高的拉伸或弯曲程度的凸缘。为了允许经由几何形状优化来提高部件刚度,高强度钢带材在拉伸伸长率和扩孔能力方面需要优异的可成形性。In order to reduce the weight of the component, a common approach is to apply high-strength steel and reduce the thickness of the steel strip used to reduce the weight. However, this may result in a loss of stiffness, which is undesirable for some applications in automotive parts. The inherent stiffness loss caused by reducing the thickness of the steel strip used to make automotive parts can be regained by optimizing the component geometry, such as creating deeper flanges or flanges with increased stretch or bending. In order to allow for increased component stiffness via geometry optimization, high-strength steel strips require excellent formability in terms of tensile elongation and hole expansion capability.
在两种可成形性模式均处于高水平的情况下摆脱了全局可成形性(例如拉伸伸长率)与局部可成形性(例如扩孔能力或HEC)之间的常规约束的单相析出强化铁素体高强度钢在某些条件下(例如在压缩下)可具有低断裂韧性值和提高的边缘裂纹敏感性,并且在剪切过程中易于具有提高的对不稳定脆性断裂行为和分层的敏感性,这损害了剪切边缘疲劳。Single-phase precipitation-hardened ferritic high-strength steels that break free from the conventional constraints between global formability (e.g., tensile elongation) and local formability (e.g., hole expansion capability or HEC) with both formability modes at high levels may have low fracture toughness values and increased edge crack sensitivity under certain conditions (e.g., under compression), and are prone to increased susceptibility to unstable brittle fracture behavior and delamination during shearing, which impairs shear edge fatigue.
专利文献EP1616970-A1公开了一种用于制造高强度热轧钢板的方法,其包括以下步骤:在1150℃至1300℃的温度范围内再加热钢板坯,所述钢板坯以重量%计由0.04至0.15质量%的C、1.5质量%或更少的Si、0.5至1.6质量%的Mn、0.04质量%或更少的P、0.005质量%或更少的S、0.04质量%或更少的Al、0.03至0.15质量%的Ti、0.03至0.5质量%的Mo以及余量的Fe和不可避免的杂质组成;在Ar3转变温度或更高的终轧温度下将再加热的钢板坯热轧成热轧钢板;以20℃/秒或更高的平均冷却速率在700至850℃的温度范围内对热轧钢板进行初次冷却;将初次冷却的钢板在680℃或更高的温度下保持超过1秒;并在550℃或更低的温度下以30℃/秒或更高的平均冷却速率二次冷却该钢板,接着卷取该钢板。优选地,不仅将热轧钢板初次冷却到700至850℃的温度范围,而且将其初次冷却到(SRT/3+300)至(SRT/8+700)℃的温度范围,其中SRT表示钢板坯的再加热温度。在EP1616970-A1的实施例中,这在实践中导致初次保持温度为667至860℃。该加工条件使得获得由含有铁素体的析出物、贝氏体和/或马氏体的第二相、以及其它相组成的显微组织,其中含有铁素体的析出物的百分比为40至95%,并且其它相的百分比为5%或更低。Patent document EP1616970-A1 discloses a method for manufacturing a high-strength hot-rolled steel plate, comprising the following steps: reheating a steel slab at a temperature range of 1150°C to 1300°C, wherein the steel slab is composed of, in terms of weight %, 0.04 to 0.15 mass % C, 1.5 mass % or less Si, 0.5 to 1.6 mass % Mn, 0.04 mass % or less P, 0.005 mass % or less S, 0.04 mass % or less Al, 0.03 to 0.15 mass % Ti, 0.03 to 0.5 mass % Mo and the balance Fe and inevitable impurities; hot rolling the reheated steel slab into a hot rolled steel sheet at a finishing temperature of Ar3 transformation temperature or higher; primary cooling the hot rolled steel sheet at an average cooling rate of 20°C/second or higher in a temperature range of 700 to 850°C; holding the primary cooled steel sheet at a temperature of 680°C or higher for more than 1 second; and secondary cooling the steel sheet at a temperature of 550°C or lower at an average cooling rate of 30°C/second or higher, followed by coiling the steel sheet. Preferably, the hot rolled steel sheet is not only primary cooled to a temperature range of 700 to 850°C, but also primary cooled to a temperature range of (SRT/3+300) to (SRT/8+700)°C, where SRT represents the reheating temperature of the steel slab. In the embodiment of EP1616970-A1, this results in a primary holding temperature of 667 to 860°C in practice. The processing conditions are such that a microstructure consisting of precipitates containing ferrite, a second phase of bainite and/or martensite, and other phases is obtained, wherein the percentage of precipitates containing ferrite is 40 to 95% and the percentage of other phases is 5% or less.
专利文献EP1338665-A1公开了一种用于制造高强度热轧钢板的方法,其包括以下步骤:生产钢板坯,该钢板坯以重量%计基本上由0.06%或更少的C、0.5%或更少的Si、0.5至2.0%的Mn、0.06%或更少的P、0.005%或更少的S、0.1%或更少的Al、0.006%或更少的N、0.05至0.6%的Mo、0.02至0.10%的Ti和余量的Fe组成,并满足方程0.8≤(C/12)/[(Ti/48)+(Mo/96)]≤1.3;通过在Ar3转变点或更高的温度下热轧所述钢板坯来生产热轧钢板;和在550至700℃的温度下卷取所述热轧钢板。该加工条件使得获得基本上由铁素体结构单相的基质和作为分散在所述基质中的晶粒尺寸小于10nm的含有Ti和Mo的复合碳化物的微细析出物组成的显微组织,其中所述微细析出物以5×104/μm3或更高的每单位体积的数量分散。Patent document EP1338665-A1 discloses a method for manufacturing high-strength hot-rolled steel plates, which includes the following steps: producing a steel slab, which is basically composed of 0.06% or less C, 0.5% or less Si, 0.5 to 2.0% Mn, 0.06% or less P, 0.005% or less S, 0.1% or less Al, 0.006% or less N, 0.05 to 0.6% Mo, 0.02 to 0.10% Ti and the balance Fe, in terms of weight %, and satisfies the equation 0.8≤(C/12)/[(Ti/48)+(Mo/96)]≤1.3; producing a hot-rolled steel plate by hot rolling the steel slab at a temperature of Ar3 transformation point or higher; and coiling the hot-rolled steel plate at a temperature of 550 to 700°C. The processing conditions provide a microstructure consisting essentially of a matrix of a ferrite structure single phase and fine precipitates as composite carbides containing Ti and Mo dispersed in the matrix having a grain size of less than 10 nm, wherein the fine precipitates are dispersed in an amount of 5×10 4 /μm 3 or more per unit volume.
需要具有高可成形性特性并具有降低的裂纹敏感性的热轧高强度钢带材。There is a need for hot rolled high strength steel strip having high formability characteristics and with reduced crack sensitivity.
发明详述DETAILED DESCRIPTION OF THE INVENTION
如本文中理解的那样,对于合金组成或优选的合金组成的任何描述,所有提及的百分比均按重量百分比计,除非另行说明。As understood herein, with respect to any description of alloy compositions or preferred alloy compositions, all references to percentages are by weight unless otherwise stated.
当用于描述合金添加的组成范围或量时,本文中使用的术语“约”是指合金添加的实际量可能因诸如本领域技术人员理解的标准加工变化的因素而与标称预期量不同。As used herein, the term "about" when used to describe a compositional range or amount of an alloying addition means that the actual amount of the alloying addition may vary from the nominal intended amount due to factors such as standard processing variations understood by those skilled in the art.
本文中使用的术语“至多”和“至多约”明确地包括但不限于其所指的特定合金组分的零重量百分比的可能性。例如,至多0.03%的Cr可以包括不具有Cr的钢带材组成。As used herein, the terms "up to" and "up to about" expressly include, but are not limited to, the possibility of zero weight percent of the particular alloying component to which they refer. For example, up to 0.03% Cr may include a steel strip composition having no Cr.
本发明的一个目的是提供一种热轧高强度钢带材,其具有高的总伸长率(A50或A80)以及高的扩孔能力。An object of the present invention is to provide a hot rolled high strength steel strip having a high total elongation (A50 or A80) and a high hole expansion capability.
本发明的一个目的是提供一种热轧高强度钢带材,其具有高的总伸长率(A50或A80)以及高的扩孔能力,并具有降低的裂纹敏感性(特别是降低的边缘裂纹敏感性)。An object of the present invention is to provide a hot rolled high strength steel strip having a high total elongation (A50 or A80) and a high hole expansion capability and having reduced crack sensitivity (in particular reduced edge crack sensitivity).
本发明的另一目的是提供一种制造此类热轧高强度钢带材的方法,所述热轧高强度钢带材具有改善的总伸长率、扩孔能力与降低的裂纹敏感性(特别是降低的边缘裂纹敏感性)的平衡。Another object of the present invention is to provide a method for producing such hot rolled high strength steel strip having an improved balance of total elongation, hole expansion capability and reduced crack sensitivity, in particular reduced edge crack sensitivity.
本发明满足了这些和其它目的以及进一步的优点,本发明提供了一种热轧高强度钢带材,其具有以重量%计由以下组成的组成:These and other objects and further advantages are met by the present invention, which provides a hot rolled high strength steel strip having a composition, in weight %, consisting of:
0.02–0.13重量%的C;0.02–0.13 wt% C;
1.20–3.50重量%的Mn;1.20–3.50 wt% Mn;
0.10–1.0重量%的Si;0.10–1.0 wt% Si;
0.05-1.0重量%的Mo;0.05-1.0 wt% Mo;
0.02–0.70重量%的Al;0.02–0.70 wt% Al;
0.04–0.25重量%的Ti;0.04–0.25 wt% Ti;
至多0.010重量%的N(100ppm),优选至多0.0065重量%的N(65ppm);Up to 0.010 wt. % N (100 ppm), preferably up to 0.0065 wt. % N (65 ppm);
至多0.02重量%的P,优选至多0.015重量%的P;Up to 0.02 wt. % P, preferably up to 0.015 wt. % P;
至多0.01重量%的S,优选至多0.0025重量%的S(25ppm);Up to 0.01 wt. % S, preferably up to 0.0025 wt. % S (25 ppm);
至多0.0050重量%的B(50ppm),优选至多0.0030重量%的B(30ppm);Up to 0.0050 wt. % B (50 ppm), preferably up to 0.0030 wt. % B (30 ppm);
任选一种或多种选自以下的元素:One or more elements selected from the following:
(至多1.5重量%的Cu,优选至多0.6重量%的Cu,和更优选至多0.10重量%的Cu,(up to 1.5 wt. % Cu, preferably up to 0.6 wt. % Cu, and more preferably up to 0.10 wt. % Cu,
至多0.70重量%的Cr,优选至多0.40重量%的Cr,和更优选至多0.25重量%的Cr,at most 0.70 wt. % Cr, preferably at most 0.40 wt. % Cr, and more preferably at most 0.25 wt. % Cr,
至多0.50重量%的Ni,优选至多0.3重量%的Ni,和更优选至多0.10重量%的Ni,at most 0.50 wt. % Ni, preferably at most 0.3 wt. % Ni, and more preferably at most 0.10 wt. % Ni,
至多0.30重量%的V,优选至多0.20重量%的V,up to 0.30 wt. % V, preferably up to 0.20 wt. % V,
至多0.10重量%的Nb,优选至多0.03重量%的Nb),up to 0.10 wt. % Nb, preferably up to 0.03 wt. % Nb),
余量为Fe和由炼铁和炼钢工艺产生的不可避免的杂质;且The balance is Fe and unavoidable impurities arising from the iron and steel making processes; and
-其中该钢带材具有至少95体积%的铁素体和最多5体积%的马氏体,和优选至少0.2体积%的马氏体的显微组织;- wherein the steel strip has a microstructure of at least 95% by volume of ferrite and at most 5% by volume of martensite, and preferably at least 0.2% by volume of martensite;
-具有在1/4厚度处至少0.65的取向差分布(MisOrientation Distribution)(MOD)指数;- having a MisOrientation Distribution (MOD) index of at least 0.65 at 1/4 thickness;
-至多55%的面积分数,具有0-1的内核(Kernel)平均取向差(KAM);- up to 55% area fraction with a kernel average misorientation (KAM) of 0-1;
-至少45%的面积分数,具有1-5的内核平均取向差(KAM);- an area fraction of at least 45% with a kernel average misorientation (KAM) of 1 to 5;
-和至少1400 1/mm的总晶界长度(ΣGB[5°-65°]);- and a total grain boundary length (ΣGB[5°-65°]) of at least 1400 1/mm;
并且其中该钢带材至少具有以下机械性质:And wherein the steel strip has at least the following mechanical properties:
至少950MPa,优选至少960MPa,和更优选至少980MPa的极限拉伸强度(Rm);An ultimate tensile strength (Rm) of at least 950 MPa, preferably at least 960 MPa, and more preferably at least 980 MPa;
至少10%,和优选至少14%的总伸长率(A50);和A total elongation (A50) of at least 10%, and preferably at least 14%; and
至少40%的扩孔率(λ)值。A hole expansion ratio (λ) value of at least 40%.
根据本发明,已经发现,具有与显微组织结合的这些窄合金组成范围的热轧钢带材提供了改善的高强度(Rm)、总伸长率(A50)与扩孔率的平衡。本发明的另一个重要发现在于,该钢带材的显微组织导致成形操作中降低的边缘裂纹敏感性。降低的裂纹敏感性,特别是降低的边缘裂纹敏感性,可以根据本文中描述的测量方法客观表示为平均总裂纹长度(ATCL)。在一个优选实施方案中,根据本发明的钢带材具有小于45mm,并且在最佳实例中小于40mm的ATCL。According to the present invention, it has been found that hot rolled steel strips having these narrow alloy composition ranges in combination with a microstructure provide an improved balance of high strength (Rm), total elongation (A50) and hole expansion. Another important finding of the present invention is that the microstructure of the steel strip results in reduced edge crack sensitivity during forming operations. Reduced crack sensitivity, in particular reduced edge crack sensitivity, can be objectively expressed as an average total crack length (ATCL) according to the measurement method described herein. In a preferred embodiment, the steel strip according to the present invention has an ATCL of less than 45 mm, and in the best example less than 40 mm.
在该钢带材的一个实施方案中,其屈服强度(Rp)为至少800MPa,优选至少850MPa。在该钢带材的一个实施方案中,其屈服强度(Rp)为最大960MPa,优选最大950MPa。In one embodiment of the steel strip, its yield strength (Rp) is at least 800 MPa, preferably at least 850 MPa. In one embodiment of the steel strip, its yield strength (Rp) is at most 960 MPa, preferably at most 950 MPa.
该钢带材具有至少950MPa的极限拉伸强度(Rm)。在该钢带材的一个实施方案中,其具有至少960MPa和优选至少980MPa的极限拉伸强度。The steel strip has an ultimate tensile strength (Rm) of at least 950 MPa. In one embodiment of the steel strip, it has an ultimate tensile strength of at least 960 MPa and preferably at least 980 MPa.
该钢带材具有至少10%和优选至少14%的总伸长率(A50)。The steel strip has a total elongation (A50) of at least 10% and preferably at least 14%.
该钢带材所需的显微组织通过窄的组成范围和通过制造过程的仔细控制、钢带材在输出辊道(ROT)上的加速冷却和特别是卷取温度(CT)的窄操作窗口来实现。The desired microstructure of the steel strip is achieved by a narrow composition range and by careful control of the manufacturing process, accelerated cooling of the steel strip on the run-out table (ROT) and in particular a narrow operating window of the coiling temperature (CT).
根据本发明的钢带材的显微组织由以下组成:至少95体积%的铁素体,并且其用钛和钼、任选用钒和/或铌的碳化物析出物进行析出强化;和至多5体积%的马氏体,余量是不可避免的量的夹杂物,并且总和合计为100体积%。在一个实施方案中,该显微组织具有至少98体积%,更优选至少99体积%的铁素体。根据本发明,认为一些马氏体的存在有利于钝化任何裂纹尖端并减少裂纹扩展。在实践中,马氏体可能含有一些痕量的残留奥氏体,但优选不存在残留奥氏体。该钢带材的显微组织优选具有至少0.2体积%,和更优选至少0.3体积%的马氏体。在一个优选实施方案中,该钢带材具有至多3体积%,和更优选至多2体积%的马氏体。The microstructure of the steel strip according to the invention consists of at least 95% by volume of ferrite, which is precipitation strengthened with carbide precipitates of titanium and molybdenum, optionally with vanadium and/or niobium; and at most 5% by volume of martensite, the remainder being inclusions in an unavoidable amount, and the sum totaling 100% by volume. In one embodiment, the microstructure has at least 98% by volume, more preferably at least 99% by volume of ferrite. According to the invention, it is believed that the presence of some martensite is beneficial for blunting any crack tips and reducing crack propagation. In practice, the martensite may contain some traces of retained austenite, but preferably no retained austenite is present. The microstructure of the steel strip preferably has at least 0.2% by volume, and more preferably at least 0.3% by volume of martensite. In a preferred embodiment, the steel strip has at most 3% by volume, and more preferably at most 2% by volume of martensite.
该钢带材的整体显微组织的织构进一步通过至少0.65,优选至少0.80,更优选至少0.83,和在最佳实例中为至少0.90的足够高的取向差分布(MOD)指数来表征。MOD指数在钢带材的四分之一厚度处测得。The overall microstructural texture of the steel strip is further characterized by a sufficiently high misorientation distribution (MOD) index of at least 0.65, preferably at least 0.80, more preferably at least 0.83, and in the best case at least 0.90. The MOD index is measured at one quarter of the thickness of the steel strip.
该钢带材的整体显微组织的织构进一步通过至多55%、更优选至多52%的内核平均取向差(KAM)为0-1的面积分数和至少45%、更优选至少48%的内核平均取向差(KAM)为1-5的面积分数来表征。The texture of the overall microstructure of the steel strip is further characterized by an area fraction of at most 55%, more preferably at most 52%, having a core average misorientation (KAM) of 0-1 and an area fraction of at least 45%, more preferably at least 48%, having a core average misorientation (KAM) of 1-5.
该钢带材的整体显微组织进一步通过至少1400/mm/mm2或1/mm、优选至少1500 1/mm的(5°至65°)晶界长度(ΣGB)来表征。较高的ΣGB表示较高程度的晶粒细化,导致所需降低的裂纹敏感性并抑制或阻止裂纹扩展,获得了有利的较短的ATCL,例如在压缩下时。The overall microstructure of the steel strip is further characterized by a (5° to 65°) grain boundary length (ΣGB) of at least 1400/mm/mm 2 or 1/mm, preferably at least 1500 1/mm. A higher ΣGB indicates a higher degree of grain refinement, resulting in the desired reduced crack sensitivity and inhibiting or preventing crack propagation, resulting in an advantageously shorter ATCL, for example when under compression.
碳以0.02至0.13重量%的量存在。为了获得足够的强度,合适的最小C含量为0.04重量%,并且在一个优选实施方案中为至少0.070重量%。在一个优选实施方案中,C含量为至多0.12重量%,并且有利于抑制冷却速率依赖性对最终显微组织的均匀性的影响并促进高的扩孔能力。此外,C是与形成碳化物的微合金元素如钛、铌(如果添加的话)或钒(如果添加的话)组合实现析出强化以及清除C以抑制最终显微组织中的渗碳体形成的必要元素。通过优化其它合金元素,包括Ti、Nb和/或V,可以获得基本没有渗碳体的几乎均匀的铁素体或贝氏体-铁素体显微组织。Carbon exists with the amount of 0.02 to 0.13 % by weight.In order to obtain enough intensity, suitable minimum C content is 0.04 % by weight, and is at least 0.070 % by weight in a preferred embodiment.In a preferred embodiment, C content is at most 0.12 % by weight, and is conducive to suppressing the influence of cooling rate dependency on the uniformity of final microstructure and promoting high hole expansion ability.In addition, C is to realize precipitation strengthening and remove C to suppress the necessary element that cementite in the final microstructure forms with the microalloying element such as titanium, niobium (if adding) or vanadium (if adding) that forms carbide.By optimizing other alloying elements, including Ti, Nb and/or V, it is possible to obtain almost uniform ferrite or bainite-ferrite microstructure without cementite substantially.
该钢带材具有1.20重量%至3.50重量%的Mn以实现足够的淬透性和晶粒细化。在一个实施方案中,Mn含量为1.40重量%至2.40重量%,以改善强度、耐腐蚀性、断裂韧性和边缘裂纹敏感性的平衡。优选地,Mn含量为至少1.50重量%以获得足够的晶粒细化,改善断裂韧性并降低裂纹敏感性。在一个实施方案中,Mn含量最大为2.20重量%,更优选最大为2.0重量%。过高的Mn含量可能导致铸造过程中的偏析,这不利地影响所需的性质平衡。The steel strip has 1.20 wt% to 3.50 wt% Mn to achieve sufficient hardenability and grain refinement. In one embodiment, the Mn content is 1.40 wt% to 2.40 wt% to improve the balance of strength, corrosion resistance, fracture toughness and edge crack sensitivity. Preferably, the Mn content is at least 1.50 wt% to obtain sufficient grain refinement, improve fracture toughness and reduce crack sensitivity. In one embodiment, the Mn content is a maximum of 2.20 wt%, more preferably a maximum of 2.0 wt%. Too high a Mn content may lead to segregation during casting, which adversely affects the desired property balance.
硅以0.10至1.0重量%的量存在以便通过铁晶格的置换固溶体强化来改善钢的强度。此外,Si有利于抑制碳化物析出(渗碳体和其它碳化物)。但是,当使用较高量的Si时,钢的可焊性和可涂覆性劣化,因此Si的量优选为至多0.95重量%,并且在一个优选的实施方案中为至多0.70重量%,更优选至多0.60重量%。Silicon is present in an amount of 0.10 to 1.0 wt % to improve the strength of the steel by substitutional solid solution strengthening of the iron lattice. In addition, Si helps to inhibit carbide precipitation (cementite and other carbides). However, when higher amounts of Si are used, the weldability and coatability of the steel deteriorate, so the amount of Si is preferably at most 0.95 wt %, and in a preferred embodiment at most 0.70 wt %, more preferably at most 0.60 wt %.
在根据本发明的钢中,铝的表现与Si相当。铝减慢碳化物析出动力学并抑制渗碳体的形成。当Al小于0.02重量%时,抑制碳化物形成的效果可忽略不计。低于0.02重量%的铝的值被认为是来自炼钢过程中脱氧步骤的残余物,因此约0.02重量%的最小值是优选的。另一方面,当Al高于0.70重量%时,在钢的热机械加工(板坯再加热、热轧、卷取等)过程中可能存在过量的氧化物形成。此外,Al提高了铁素体向奥氏体的转变温度,要求在更高温度下热轧该钢以完成奥氏体相中的热轧,因为在较低温度下出现临界区(intercritical)铁素体。在更高的温度下可能发生更高量的氧化。这些氧化物鳞皮对热轧、酸洗、涂覆和整体表面外观有害。此外,当Al超过0.70重量%时,热轧过程中的轧制力提高,与Si的存在组合使得钢非常脆且更难以热轧。因此,Al在本发明中以0.02至0.70重量%、优选0.02至0.60重量%和更优选0.030-0.50重量%的量存在。In the steel according to the invention, the performance of aluminum is comparable to that of Si. Aluminum slows down the carbide precipitation kinetics and inhibits the formation of cementite. When Al is less than 0.02 wt%, the effect of inhibiting carbide formation is negligible. Values of aluminum below 0.02 wt% are considered to be residues from the deoxidation step during steelmaking, so a minimum value of about 0.02 wt% is preferred. On the other hand, when Al is above 0.70 wt%, there may be excessive oxide formation during the thermomechanical processing of steel (slab reheating, hot rolling, coiling, etc.). In addition, Al increases the transition temperature from ferrite to austenite, requiring hot rolling of the steel at higher temperatures to complete hot rolling in the austenite phase because intercritical ferrite appears at lower temperatures. Higher amounts of oxidation may occur at higher temperatures. These oxide scales are harmful to hot rolling, pickling, coating and overall surface appearance. In addition, when Al exceeds 0.70 wt%, the rolling force during hot rolling increases, which, combined with the presence of Si, makes the steel very brittle and more difficult to hot roll. Therefore, Al is present in the present invention in an amount of 0.02 to 0.70 wt%, preferably 0.02 to 0.60 wt%, and more preferably 0.030-0.50 wt%.
钛是另一种必需的合金元素,并以0.04重量%至0.25重量%的量存在,因为其提供淬透性并充当碳化物形成元素,抑制渗碳体的形成,同时经由形成小的Ti基碳化物提供析出强化。但是,Ti也与N、S和C结合以形成氮化物和碳硫化物,取决于钢的具体化学组成。因此,存在至少0.04重量%的Ti以结合钢中基本所有的N和S,并具有足够过量的Ti以便与钢中的C结合。当存在超过0.25重量%的Ti时,可能形成粗大的Ti氮化物、碳氮化物和碳化物,其在热轧之前的板坯再加热过程中难以溶解。此外,这些粗大的Ti氮化物、碳氮化物和碳化物导致钢的扩孔能力的劣化。优选存在0.07至0.22重量%的Ti。在一个实施方案中,Ti含量不超过0.20重量%,优选不超过0.15重量%,更优选不超过0.13重量%。Titanium is another essential alloying element and is present in an amount of 0.04 wt % to 0.25 wt % because it provides hardenability and acts as a carbide forming element, inhibiting the formation of cementite while providing precipitation strengthening via the formation of small Ti-based carbides. However, Ti also combines with N, S and C to form nitrides and carbon sulfides, depending on the specific chemical composition of the steel. Therefore, there is at least 0.04 wt % Ti to combine substantially all N and S in the steel, and there is enough excess Ti to combine with C in the steel. When there is more than 0.25 wt % Ti, coarse Ti nitrides, carbonitrides and carbides may be formed, which are difficult to dissolve during the slab reheating process before hot rolling. In addition, these coarse Ti nitrides, carbonitrides and carbides cause the deterioration of the hole expansion ability of the steel. Preferably, there is 0.07 to 0.22 wt % Ti. In one embodiment, the Ti content is no more than 0.20 wt %, preferably no more than 0.15 wt %, and more preferably no more than 0.13 wt %.
该钢带材具有Mo作为目的合金元素,其以约0.05重量%至1.0重量%存在以实现淬透性。在一个实施方案中,Mo含量为至少约0.10重量%,优选至少约0.20重量%,更优选至少0.25重量%,最优选至少0.30重量%。在一个实施方案中,Mo含量不超过约0.80重量%,优选不超过约0.55重量%,更优选不超过0.40重量%。Mo的存在还可以改善钢带材的可焊性。The steel strip has Mo as the alloying element of interest, which is present in an amount of about 0.05 wt % to 1.0 wt % to achieve hardenability. In one embodiment, the Mo content is at least about 0.10 wt %, preferably at least about 0.20 wt %, more preferably at least 0.25 wt %, and most preferably at least 0.30 wt %. In one embodiment, the Mo content does not exceed about 0.80 wt %, preferably does not exceed about 0.55 wt %, and more preferably does not exceed 0.40 wt %. The presence of Mo can also improve the weldability of the steel strip.
优选将由以下等式以重量%表示的Mo相对于微合金元素Nb、Ti和V的总量的原子比:The atomic ratio of Mo relative to the total amount of microalloying elements Nb, Ti and V is preferably expressed in weight % by the following equation:
保持在0.75至1.25的范围内,以提高碳化物析出物的热稳定性,导致减少来自例如在该钢的卷材冷却或任何后续热处理过程中(例如在涂覆或焊接过程中)的热时效引起的析出粗化的析出强化损失。Maintained in the range of 0.75 to 1.25 to improve thermal stability of carbide precipitates, resulting in reduced precipitation strengthening losses from precipitation coarsening caused by, for example, thermal aging during coil cooling or any subsequent heat treatment of the steel, such as during coating or welding.
氮、硫和磷是由于炼钢和精炼过程而存在于钢中的残留元素。它们的量被限制为至多0.01重量%的S、至多0.02重量%的P和至多0.010重量%的N。高于这些的量对机械性质、可成形性、韧性和可焊接性是有害的。在一个实施方案中,P仅以至多0.015重量%存在。在一个实施方案中,S仅以至多0.005重量%,更优选仅以至多0.0025重量%存在。N与Ti形成氮化钛,其在再加热过程中充当用于奥氏体晶粒尺寸控制的弥散体(dispersoids)。但是,过高的N可能导致过多的粗TiN颗粒,这可损害扩孔能力。优选地,N含量为至多0.0065重量%(65ppm)。合适的最小N含量为0.0010重量%(10ppm)。Nitrogen, sulfur and phosphorus are residual elements present in steel due to steelmaking and refining processes. Their amounts are limited to at most 0.01% by weight of S, at most 0.02% by weight of P and at most 0.010% by weight of N. Amounts above these are harmful to mechanical properties, formability, toughness and weldability. In one embodiment, P is present only at most 0.015% by weight. In one embodiment, S is present only at most 0.005% by weight, more preferably at most 0.0025% by weight. N forms titanium nitride with Ti, which acts as a dispersoid for austenite grain size control during reheating. However, too high N may result in too much coarse TiN particles, which may impair hole expansion capability. Preferably, N content is at most 0.0065% by weight (65ppm). Suitable minimum N content is 0.0010% by weight (10ppm).
不需要硼来获得钢带材的所需性能平衡,但硼可以以至多0.005重量%(由此至多50ppm)和优选至多0.0030重量%(30ppm)存在。B对于提高钢的淬透性非常有效,这意味着可以在输出辊道上使用低碳含量和/或更低的冷却速率,同时不形成或仅形成极少的先共晶铁素体。B也是非常适于提高屈服强度的合金元素。Boron is not required to obtain the desired balance of properties of the steel strip, but may be present in an amount of up to 0.005 wt. % (therefore up to 50 ppm) and preferably up to 0.0030 wt. % (30 ppm). B is very effective in increasing the hardenability of the steel, which means that low carbon contents and/or lower cooling rates can be used on the run-out table with no or only minimal formation of proeutectic ferrite. B is also an alloying element very suitable for increasing yield strength.
Cr可以以至多约0.70重量%、优选至多0.25重量%的量添加到钢带材中,并提高钢的淬透性。在一个优选实施方案中,该钢带材具有Cr作为可容许的杂质元素。实际上,这意味着其可以以至多0.10%、优选至多0.050%、和更优选至多0.03%存在,因为其可以损害未涂覆的钢带材基材的腐蚀性能。Cr can be added to the steel strip in an amount of up to about 0.70 wt. %, preferably up to 0.25 wt. %, and improves the hardenability of the steel. In a preferred embodiment, the steel strip has Cr as a tolerable impurity element. In practice, this means that it can be present in an amount of up to 0.10%, preferably up to 0.050%, and more preferably up to 0.03%, as it can impair the corrosion properties of the uncoated steel strip substrate.
铜在以至多1.5重量%存在时通过固溶强化以及通过铜析出物的析出硬化来提高钢的强度。在一个实施方案中,Cu含量不超过0.6重量%。在一个实施方案中,Cu不作为目的合金元素添加,并且可以以至多0.10重量%、和更优选至多0.05重量%存在。至多约0.50重量%和优选至多0.30重量%的镍提高了冲击韧性,并抵消了由于铜的存在而在钢带材的热加工过程中可能发生的任何热脆性。在一个实施方案中,Ni不作为目的合金元素添加,并且可以以至多0.3重量%、优选至多0.10重量%、和更优选至多0.050重量%存在。Copper improves the strength of steel by solution strengthening and precipitation hardening by copper precipitates when present at most 1.5 wt %. In one embodiment, the Cu content is no more than 0.6 wt %. In one embodiment, Cu is not added as a target alloying element and may be present at most 0.10 wt %, and more preferably at most 0.05 wt %. Up to about 0.50 wt % and preferably at most 0.30 wt % nickel improves impact toughness and offsets any hot brittleness that may occur during hot working of steel strip due to the presence of copper. In one embodiment, Ni is not added as a target alloying element and may be present at most 0.3 wt %, preferably at most 0.10 wt %, and more preferably at most 0.050 wt %.
钒可以以至多约0.30重量%、优选至多约0.20重量%和更优选至多0.17重量%存在于钢中。但是,V是相对昂贵的合金元素,其主要用于替代Ti的析出强化效果,并通过形成碳化钒来避免渗碳体形成。在一个优选实施方案中,V以至少0.05重量%、更优选至少0.08重量%的量有目的地添加。Ti和V的组合添加是有利的,因为Ti为V析出提供催化效果,使得V析出更有效。Vanadium can be present in steel with about 0.30 % by weight at the most, preferably about 0.20 % by weight at the most and more preferably 0.17 % by weight at the most. But V is a relatively expensive alloying element, which is mainly used to replace the precipitation strengthening effect of Ti, and avoids cementite formation by forming vanadium carbide. In a preferred embodiment, V is purposefully added with at least 0.05 % by weight, more preferably at least 0.08 % by weight. It is favourable for the combination of Ti and V to add, because Ti is for V to separate out and provide catalytic effect, so that V is separated out more effectively.
铌可以以至多0.10重量%存在于钢中。Nb部分地通过析出硬化改善钢的强度,但最重要的是通过晶粒细化来改善钢的强度。但是,对于大量的Nb,这些效果是饱和的。因此,优选存在至多0.08重量%的Nb,且更优选至多0.060重量%,因为Nb是相当昂贵的合金元素,在一个实施方案中,Nb并非有目的地添加的并作为杂质元素存在,且不超过0.03重量%,并且优选其不超过0.02重量%,并且更优选其不超过0.0050重量%。在最优选的实施方案中,Nb是由炼铁和炼钢工艺产生的不可避免的杂质。已经发现,通过将Ti保持在足够高的水平,可以克服Nb的使用,同时仍然达到可成形性、机械性质与改善的断裂或边缘开裂特性的目标平衡。此外,由于中心线偏析,Nb具有很高的偏析和形成粗大的NbC粒子的倾向,由此避免使用Nb导致了改善的扩孔能力和提高的剪切边缘品质。Niobium can be present in the steel at up to 0.10 wt%. Nb improves the strength of the steel partly by precipitation hardening, but most importantly by grain refinement. However, for large amounts of Nb, these effects are saturated. Therefore, it is preferred that up to 0.08 wt% Nb is present, and more preferably up to 0.060 wt%, because Nb is a relatively expensive alloying element, in one embodiment, Nb is not purposefully added and is present as an impurity element, and does not exceed 0.03 wt%, and preferably it does not exceed 0.02 wt%, and more preferably it does not exceed 0.0050 wt%. In the most preferred embodiment, Nb is an unavoidable impurity resulting from the ironmaking and steelmaking processes. It has been found that by keeping Ti at a sufficiently high level, the use of Nb can be overcome while still achieving the target balance of formability, mechanical properties and improved fracture or edge cracking characteristics. In addition, due to centerline segregation, Nb has a high tendency to segregate and form coarse NbC particles, thereby avoiding the use of Nb leads to improved hole expansion ability and improved shear edge quality.
此外,已经发现,如果以重量%表示的碳化物形成元素Ti、Nb、V和Mo的量满足以下等式,则可以抑制渗碳体形成,并且可以更好地控制显微组织中一小部分马氏体加残留奥氏体的有利形成:Furthermore, it has been found that cementite formation can be suppressed and the favorable formation of a small portion of martensite plus retained austenite in the microstructure can be better controlled if the amounts of carbide-forming elements Ti, Nb, V and Mo expressed in weight % satisfy the following equation:
其中Ti_sol定义为溶体中游离Ti的量并表示为:where Ti_sol is defined as the amount of free Ti in the solution and is expressed as:
其中Ti和N的量以重量%表示。优选地,该等式的下限为0.75,更优选为0.80。在一个实施方案中,上限优选为1.8,更优选为1.5,以进一步抑制渗碳体的存在和/或控制马氏体的量。在一个优选实施方案中,该式在0.9至1.1的范围内。Wherein the amount of Ti and N is expressed in weight %. Preferably, the lower limit of the equation is 0.75, more preferably 0.80. In one embodiment, the upper limit is preferably 1.8, more preferably 1.5, to further suppress the presence of cementite and/or control the amount of martensite. In a preferred embodiment, the formula is in the range of 0.9 to 1.1.
在一个实施方案中,该钢带材具有由以下组成的组成:0.02至0.13重量%的C,1.20至2.0重量%的Mn,0.10至0.60重量%的Si,0.01至0.70重量%的Al,0.04至0.25重量%的Ti,0.05至0.80重量%的Mo,至多0.10%的Cr,优选至多0.050%的Cr,至多0.010重量%的N,至多0.02重量%的P,优选至多0.015重量%的P,至多0.01重量%的S,优选至多0.0025重量%的S,至多0.0050重量%的B,任选一种或多种选自以下的元素:(至多0.10%的Cu,至多0.10%的Ni,至多0.30%的V,至多0.10重量%的Nb,优选至多0.03%的Nb),和余量的Fe以及由炼铁和炼钢工艺产生的不可避免的杂质,并且更优选的范围如本文中描述和要求保护的那样。In one embodiment, the steel strip has a composition consisting of: 0.02 to 0.13 wt. % C, 1.20 to 2.0 wt. % Mn, 0.10 to 0.60 wt. % Si, 0.01 to 0.70 wt. % Al, 0.04 to 0.25 wt. % Ti, 0.05 to 0.80 wt. % Mo, up to 0.10 wt. % Cr, preferably up to 0.050 wt. % Cr, up to 0.010 wt. % N, up to 0.02 wt. % P, preferably up to 0.0 15 wt.% P, up to 0.01 wt.% S, preferably up to 0.0025 wt.% S, up to 0.0050 wt.% B, optionally one or more elements selected from the following: (up to 0.10% Cu, up to 0.10% Ni, up to 0.30% V, up to 0.10 wt.% Nb, preferably up to 0.03% Nb), and the balance Fe and inevitable impurities generated by ironmaking and steelmaking processes, and the more preferred ranges are as described and claimed herein.
根据EN 10002-1/150 6892-1,采用平行于轧制方向的拉伸测试,用A50试样几何形状在室温下由准静态(应变速率3×10-4s-1)拉伸测试测定0.2%偏移保证强度或屈服强度(Rp)、极限拉伸强度(Rm)、均匀伸长率(Ag)和拉伸伸长率(A50)。该拉伸试样的几何形状包括在轧制方向上50mm标距长度、12.5mm宽度和取决于最终规格的厚度。测量钢在0.2%偏移应变下的强度作为屈服强度(Rp或YS)。屈服强度对极限拉伸强度的比率(Rp/Rm)表示为屈服比。The 0.2% offset proof strength or yield strength (Rp), ultimate tensile strength (Rm), uniform elongation (Ag) and tensile elongation (A50) are determined by quasi-static (strain rate 3×10 -4 s -1 ) tensile testing at room temperature with an A50 specimen geometry according to EN 10002-1/150 6892-1 using a tensile test parallel to the rolling direction. The geometry of the tensile specimen comprises a 50 mm gauge length in the rolling direction, a 12.5 mm width and a thickness depending on the final specification. The strength of the steel at a 0.2% offset strain is measured as the yield strength (Rp or YS). The ratio of the yield strength to the ultimate tensile strength (Rp/Rm) is denoted as the yield ratio.
通过扩孔试验确定钢带材的延伸凸缘性能或扩孔能力(HEC)。从卷取的钢切割出尺寸为90mm×90mm×带材最终厚度的试样。在试样的中间冲压10mm直径的孔,并根据ISO/TS16630:2003(E)标准进行扩孔试验。采用上部去毛刺进行样品的扩孔测试。从下方向上推60°的锥形冲头,并在形成穿透裂纹时测量孔直径df。使用下式计算扩孔率λ,其中do=10mm:The extended flange properties or hole expansion capacity (HEC) of steel strips are determined by hole expansion tests. Specimens with dimensions of 90 mm x 90 mm x final thickness of the strip are cut from the coiled steel. A hole with a diameter of 10 mm is punched in the middle of the specimen and the hole expansion test is carried out according to ISO/TS16630:2003(E) standard. The hole expansion test of the specimen is carried out with upper deburring. A 60° conical punch is pushed upward from below and the hole diameter d f is measured when a through crack is formed. The hole expansion ratio λ is calculated using the following formula, where d o =10 mm:
对于所有上述机械试验,对每种条件测试至少三个试样,并在本文中报告平均值。For all the above mechanical tests, at least three specimens were tested for each condition and the average values are reported herein.
平均总裂纹长度(ATCL)用于评估类似于工业应用的情况下裂纹形成的敏感性。ATCL参数在常见的实验室圆柱形深冲试验中使用冲头、拉模和坯料夹住器(blank holder)来测定。在该程序中,冲头的直径为50mm,冲头半径为7mm。模具具有62mm的内径和8mm的半径。该设置示意性显示在图1B中。内径足够大以允许形成的杯的边缘自由移动。间隙(即冲头壁与模具壁之间的距离)为6mm。坯料夹住器的力设定为50kN。该坯料为正方形,实测90×90mm。如图1A所示,正方形的四个角沿两条对角线的方向切割10mm。在圆柱形深冲试验的初始阶段过程中,由于冲压过程中的高局部压缩应力,坯料边缘处的四个区域塑性变形。这导致边缘的局部起皱。在试验结束时并且在释放坯料夹住器的力时,四个压缩区域由于回弹而受到反向载荷,因为成形的圆柱形杯的这些区域开始失去与坯料夹住器的接触。由于回弹引起的这种反向载荷可导致冲压杯的四个压缩和起皱区域中的成核和裂纹生长(参见例如图1E)。裂纹可以穿过钢带材的整个厚度并且在冲压杯的两侧(即内和外)可见,或者仅在该杯的两侧之一处可见。使用配备有比例网格的10×放大镜测量深冲杯的四个压缩边缘(如图1D所示)的内侧和外侧上的所有可见裂纹的长度。对四个冲压杯中的三个将杯壁内侧和外侧上的所有可观察的裂纹的长度之和取平均值并报告为平均总裂纹长度(ATCL),以mm表示。The average total crack length (ATCL) is used to evaluate the sensitivity of crack formation in situations similar to industrial applications. The ATCL parameter is determined in a common laboratory cylindrical deep drawing test using a punch, a die and a blank holder. In this procedure, the punch has a diameter of 50 mm and a punch radius of 7 mm. The die has an inner diameter of 62 mm and a radius of 8 mm. The setup is schematically shown in Figure 1B. The inner diameter is large enough to allow the edge of the formed cup to move freely. The gap (i.e., the distance between the punch wall and the die wall) is 6 mm. The force of the blank holder is set to 50 kN. The blank is square and measures 90×90 mm. As shown in Figure 1A, the four corners of the square are cut 10 mm in the direction of the two diagonals. During the initial stage of the cylindrical deep drawing test, four areas at the edge of the blank are plastically deformed due to the high local compressive stresses during the stamping process. This results in local wrinkling of the edge. At the end of the test and when the force of the blank gripper is released, the four compression areas are subjected to reverse loading due to springback as these areas of the formed cylindrical cup begin to lose contact with the blank gripper. This reverse loading due to springback can lead to nucleation and crack growth in the four compression and wrinkling areas of the punched cup (see, for example, Figure 1E). The cracks can pass through the entire thickness of the steel strip and be visible on both sides of the punched cup (i.e., inside and outside), or only on one of the two sides of the cup. The lengths of all visible cracks on the inside and outside of the four compression edges of the deep punched cup (as shown in Figure 1D) were measured using a 10× magnifying glass equipped with a proportional grid. The sum of the lengths of all observable cracks on the inside and outside of the cup wall was averaged for three of the four punched cups and reported as the average total crack length (ATCL) in mm.
通过本领域中公知的技术——电子背散射衍射(EBSD)分析钢带材的显微组织,该技术又允许定量各种组分的面积或体积分数。在安装在导电树脂中并机械抛光至1μm的平行于轧制方向的横截面(RD-ND平面)上进行EBSD测量。为了获得完全无变形的表面,用胶体二氧化硅(OPS)进行最终抛光步骤。The microstructure of the steel strips was analyzed by electron backscatter diffraction (EBSD), a technique well known in the art, which in turn allows the quantification of the area or volume fractions of the various components. EBSD measurements were performed on cross sections parallel to the rolling direction (RD-ND plane) mounted in a conductive resin and mechanically polished to 1 μm. In order to obtain a completely deformation-free surface, a final polishing step was performed with colloidal silica (OPS).
用于EBSD测量的扫描电子显微镜(SEM)是配备有场发射枪和EDAX PEGASUS XM4HIKARI EBSD系统的Zeiss Ultra 55机器(FEG-SEM)。在四分之一厚度处的板材的RD-ND平面上收集EBSD扫描。将样品在70°角下放置在SEM中。加速电压为15kV,高电流选项接通。使用120μm光圈,并且在扫描过程中通常的工作距离为17mm。为了补偿样品的高倾斜角,在扫描过程中使用动态聚焦校正。The scanning electron microscope (SEM) used for EBSD measurements was a Zeiss Ultra 55 machine (FEG-SEM) equipped with a field emission gun and an EDAX PEGASUS XM4HIKARI EBSD system. EBSD scans were collected on the RD-ND plane of the plate at one-quarter thickness. The sample was placed in the SEM at a 70° angle. The accelerating voltage was 15 kV and the high current option was turned on. A 120 μm aperture was used and the usual working distance during scanning was 17 mm. To compensate for the high tilt angle of the sample, dynamic focus correction was used during scanning.
使用TexSEM Laboratories(TSL)软件:“Orientation Imaging Microscopy(OIM)Data Collection version 7.2”来捕获EBSD扫描。通常,使用以下数据收集设置:与背景减除(标准模式)组合的5×5像素合并的Hikari相机。在所有情况下,扫描区域均位于样品厚度的1/4的位置处,并且尽可能仔细地避免在该扫描区域中包括非金属夹杂物。EBSD扫描尺寸在所有情况下为100×100μm,步长为0.1μm,扫描速率为约100帧/秒。使用Fe(α)和Fe(γ)来标引Kikuchi图样。在数据收集过程中使用的Hough设置为:约96的像素合并图样尺寸;θ集尺寸为1;约90的rho分数;最大峰计数为10;最小峰值计数为5;Hough类型设置为典型;Hough分辨率设置为低;蝶式卷积掩模为9×9;峰对称性为0.5;最小峰幅度为10;最大峰距离为20。EBSD scans were captured using TexSEM Laboratories (TSL) software: "Orientation Imaging Microscopy (OIM) Data Collection version 7.2". Typically, the following data collection settings were used: a 5×5 pixel binned Hikari camera combined with background subtraction (standard mode). In all cases, the scan area was located at 1/4 of the sample thickness, and care was taken to avoid including non-metallic inclusions in the scan area as much as possible. The EBSD scan size was 100×100 μm in all cases, with a step size of 0.1 μm and a scan rate of approximately 100 frames/second. Fe(α) and Fe(γ) were used to index the Kikuchi patterns. The Hough settings used during data collection were: binning pattern size of approximately 96; theta set size of 1; rho score of approximately 90; maximum peak count of 10; minimum peak count of 5; Hough type set to typical; Hough resolution set to low; butterfly convolution mask of 9 × 9; peak symmetry of 0.5; minimum peak amplitude of 10; and maximum peak distance of 20.
用TSL OIM分析软件版本“8.0x64[12-14-16]”评估EBSD扫描。通常,数据集在RD轴上旋转90°以获得相对于测量取向处于适当取向的扫描。进行标准晶粒膨胀清除(颗粒公差角(GTA)为5°,最小晶粒尺寸为5个像素,使用的标准是晶粒必须包含多个行,用于单一膨胀迭代清除)。接下来,应用伪对称清除(GTA 5,轴角度30°@111)。EBSD scans were evaluated using TSL OIM Analysis Software Version 8.0x64 [12-14-16]. Typically, the data set was rotated 90° in the RD axis to obtain a scan in the proper orientation relative to the measured orientation. Standard grain expansion cleaning was performed (grain tolerance angle (GTA) of 5°, minimum grain size of 5 pixels, and the criterion used was that the grains must contain multiple rows for a single expansion iteration to clean). Next, pseudo-symmetric cleaning was applied (GTA 5, axis angle 30°@111).
使用EBSD图像品质(IQ)图来确定马氏体的量。具有低IQ的区域鉴定为MS区域。对于给定的实验条件,通常低IQ阈值为≈0.4的IQ直方图中的峰-最大值位置。但是,对每次扫描手动检查低IQ阈值以防止在马氏体面积分数中包括来自粒状贝氏体或上贝氏体区域的晶界。The amount of martensite is determined using the EBSD image quality (IQ) map. Regions with low IQ are identified as MS regions. For given experimental conditions, the low IQ threshold is typically the peak-maximum position in the IQ histogram of ≈0.4. However, the low IQ threshold is manually checked for each scan to prevent grain boundaries from granular bainite or upper bainite regions from being included in the martensite area fraction.
为了计算EBSD内核平均取向差(KAM)图,使用第五个最接近的相邻区域,最大取向差为5°(内核中的所有点用于KAM计算)。内核平均取向差被认为是铁素体类型的特征,因为内核平均取向差是内部位错密度的量度。具有相对低的内部位错密度的区域将主要对应于KAM值在0和1°之间的区域。具有相对高的内部位错密度的区域将主要对应于KAM值在1-5°之间的区域。To calculate the EBSD kernel average misorientation (KAM) map, the fifth nearest neighbor is used with a maximum misorientation of 5° (all points in the kernel are used for the KAM calculation). The kernel average misorientation is considered characteristic of the ferrite type because the kernel average misorientation is a measure of the internal dislocation density. Regions with relatively low internal dislocation density will mainly correspond to regions with KAM values between 0 and 1°. Regions with relatively high internal dislocation density will mainly correspond to regions with KAM values between 1-5°.
由在1/4厚度处在RD-ND平面上在100×100μm面积(0.01mm2)上的EBSD扫描,也已经测量了取向差角为5°至15°(ΣGB5-15)和15°至65°(ΣGB15-65)的晶界的总晶界长度(以mm计)之和(ΣGB)。ΣGB的值以mm-1表示,并且是大角度晶界密度的量度。大角度晶界对阻止裂纹扩展是有效的。因此,提高的ΣGB值将有益于提高的断裂韧性和降低的裂纹敏感性。The sum of the total grain boundary lengths (in mm ) of grain boundaries with misorientation angles of 5° to 15° (ΣGB 5-15 ) and 15° to 65° (ΣGB 15-65 ) has also been measured (ΣGB) from EBSD scans over a 100×100 μm area (0.01 mm 2 ) in the RD-ND plane at ¼ thickness. The value of ΣGB is expressed in mm −1 and is a measure of the density of high-angle grain boundaries. High-angle grain boundaries are effective in arresting crack propagation. Therefore, increased ΣGB values will benefit from increased fracture toughness and reduced crack sensitivity.
在本发明的一个方面,其涉及一种制造如本文中描述和要求保护的钢带材的方法,该方法按该顺序包括以下步骤:In one aspect of the invention it relates to a method of manufacturing a steel strip as described and claimed herein, the method comprising the following steps in this order:
-铸造板坯,接着是将凝固的板坯再加热到1050℃至1260℃的温度,优选持续30分钟或更长时间,更优选60分钟或更长时间的步骤,并热轧所述板坯,或者铸造板坯或带材,接着是热轧所述板坯或带材的步骤;- casting a slab followed by a step of reheating the solidified slab to a temperature of 1050° C. to 1260° C., preferably for 30 minutes or more, more preferably for 60 minutes or more, and hot rolling said slab, or casting a slab or strip followed by a step of hot rolling said slab or strip;
-热轧该钢板坯或带材,并在820℃至940℃、优选850℃至940℃、最优选850℃至920℃且高于钢的Ar3温度的终轧温度下完成所述热轧。终轧温度(FRT)高于钢的Ar3温度,其中Ar3是在冷却过程中奥氏体开始转变为铁素体时的温度。如本领域已知的那样,可以根据以下等式计算Ar3温度:- hot rolling the steel slab or strip and completing the hot rolling at a finishing temperature of 820°C to 940°C, preferably 850°C to 940°C, most preferably 850°C to 920°C and above the Ar3 temperature of the steel. The finishing temperature (FRT) is above the Ar3 temperature of the steel, where Ar3 is the temperature at which austenite begins to transform into ferrite during cooling. As known in the art, the Ar3 temperature can be calculated according to the following equation:
Ar3=910℃-203×[C]1/2+44.7×[Si]-30×[Mn]+31.5×[Mo];Ar3=910℃-203×[C] 1/2 +44.7×[Si]-30×[Mn]+31.5×[Mo];
-以20至250℃/秒、优选40至200℃/秒的输出辊道冷却速率将热轧钢带材加速冷却到560℃至620℃的输出辊道上的温度;- accelerated cooling of the hot rolled steel strip to a temperature on the run-out roller table of 560° C. to 620° C. at a run-out roller table cooling rate of 20 to 250° C./s, preferably 40 to 200° C./s;
-在550℃至600℃、优选550℃至595℃、和更优选550℃至590℃的温度下卷取该热轧并冷却的带材;- coiling the hot rolled and cooled strip at a temperature of 550°C to 600°C, preferably 550°C to 595°C, and more preferably 550°C to 590°C;
-使卷取的热轧钢带材进一步冷却至环境温度;并- further cooling the coiled hot rolled steel strip to ambient temperature; and
-酸洗该热轧钢带材,- pickling the hot rolled steel strip,
-任选为该热轧钢带材提供金属性涂层,所述金属性涂层优选选自:Zn层、Zn基合金层、Al基合金层,以便在使用中提供改善的耐腐蚀性。该金属性涂层优选通过热涂覆或热浸涂来施加。- Optionally providing the hot rolled steel strip with a metallic coating, preferably selected from: a Zn layer, a Zn-based alloy layer, an Al-based alloy layer, in order to provide improved corrosion resistance in use. The metallic coating is preferably applied by hot coating or hot dipping.
本文中描述和要求保护的制造方法产生所需的显微组织,其提供改善的可成形性、机械性质和断裂特性的目标平衡。本发明还体现为通过本文中描述和要求保护的方法制造的一种钢带材,其具有所述显微组织和改善的可成形性、机械性质与断裂特性的平衡。The manufacturing method described and claimed herein produces a desired microstructure that provides a targeted balance of improved formability, mechanical properties, and fracture characteristics. The invention is also embodied in a steel strip produced by the method described and claimed herein having the microstructure and the improved balance of formability, mechanical properties, and fracture characteristics.
本发明不受铸造方法的限制。钢可以在直接带材工厂中铸造为具有150mm至350mm、且通常为225mm至250mm的铸造厚度的常规厚板坯,以及具有50mm至150mm的铸造厚度的薄板坯。在图2A和2B中分别显示了涉及常规热带材轧机和薄板坯铸造/无锭轧机的工艺的示意性实例。对于常规的厚板坯铸造,板坯的再加热是必要的,以便从环境温度再加热板坯(通常,在板坯堆场中,厚铸造板坯已经从铸造温度冷却至环境温度)并使板坯的组成均匀化,因此再加热温度应高于约1050℃以便在存在微合金元素时溶解任何析出物,并使板坯达到使得精轧机中的最终热轧仍可在FRT>Ar3下进行的温度。这通常需要1050℃至约1260℃的(板坯)再加热温度。对于薄板坯铸造,在铸造该薄板坯之后立即在均化炉中对铸造板坯施以均化处理,其中该均化温度应高于约1050℃,并且通常为约1100至1160℃。当存在微合金元素(如果有的话)时,这也将防止形成任何析出物,并且还使薄板坯达到使得精轧机中的最终热轧仍可在FRT>Ar3下进行的温度。根据本发明,薄板坯铸造路线的再加热或均化时间优选为30分钟或更久。The present invention is not limited by the casting method. Steel can be cast in a direct strip mill as a conventional thick slab with a casting thickness of 150mm to 350mm, and typically 225mm to 250mm, and a thin slab with a casting thickness of 50mm to 150mm. Schematic examples of processes involving conventional hot strip mills and thin slab casting/ingot mills are shown in Figures 2A and 2B, respectively. For conventional thick slab casting, the reheating of the slab is necessary to reheat the slab from ambient temperature (typically, in the slab yard, the thick cast slab has been cooled from the casting temperature to ambient temperature) and to homogenize the composition of the slab, so the reheating temperature should be higher than about 1050°C to dissolve any precipitates when there are microalloying elements, and to make the slab reach a temperature that allows the final hot rolling in the finishing mill to still be carried out under FRT>Ar3. This generally requires a (slab) reheating temperature of 1050°C to about 1260°C. For thin slab casting, the cast slab is subjected to a homogenization treatment in a homogenization furnace immediately after casting the thin slab, wherein the homogenization temperature should be above about 1050° C., and is typically about 1100 to 1160° C. This will also prevent the formation of any precipitates when microalloying elements are present (if any), and also bring the thin slab to a temperature such that the final hot rolling in the finishing mill can still be carried out at FRT>Ar3. According to the present invention, the reheating or homogenization time for the thin slab casting route is preferably 30 minutes or more.
钢的热轧必须在奥氏体相中进行以控制最终显微组织。在工业规模的轧制上,FRT应保持高于Ar3温度。在一个优选实施方案中,FRT高于(Ar3+30℃),例如通常高于850℃,以避免在带材的较冷边缘或尾部处局部热轧低于Ar3。在奥氏体区域中,FRT不应过高,因为较低的FRT将促进更多的奥氏体变形,并因此有助于提高的晶粒细化和提高的ΣGB。高于950℃的FRT将会导致提高的边缘裂纹敏感性。此外,不太高的FRT还将促进最终显微组织中有益于韧性的织构(例如{332}<113>)并抑制有害的那些织构(例如{001}<110>旋转立方体)。因此,FRT不应超过约940℃,优选地,FRT不超过约920℃,更优选地,FRT不超过约910℃。Hot rolling of steel must be carried out in the austenite phase to control the final microstructure. In industrial-scale rolling, FRT should be kept above Ar3 temperature. In a preferred embodiment, FRT is higher than (Ar3+30°C), for example, usually higher than 850°C, to avoid local hot rolling below Ar3 at the cooler edge or tail of the strip. In the austenite region, FRT should not be too high, because lower FRT will promote more austenite deformation, and thus contribute to improved grain refinement and improved ΣGB. FRT higher than 950°C will lead to increased edge crack sensitivity. In addition, not too high FRT will also promote textures that are beneficial to toughness in the final microstructure (e.g., {332}<113>) and suppress those harmful textures (e.g., {001}<110> rotated cube). Therefore, FRT should not exceed about 940°C, preferably, FRT does not exceed about 920°C, and more preferably, FRT does not exceed about 910°C.
在热轧后,将钢带材在输出辊道(ROT)上加速冷却到560℃至620℃的温度。为了促进最终显微组织的晶粒细化和提高的ΣGB,需要加速的冷却速率来抑制奥氏体中内部储存能量的恢复和损失。该冷却速率应当足够高以避免在提高的温度下奥氏体向铁素体的相变,并优选在输出辊道上在约560至630℃的相对低的温度下促进奥氏体向铁素体的相变。提高的冷却速度将会促进晶粒细化、提高的ΣGB,并因此促进提高的断裂韧性和降低的裂纹敏感性。提高的冷却速率还将抑制织构随机化,并因此抑制由促进韧性的变形奥氏体发展的那些织构(例如{332}<113>)的强度损失。从显微组织的观点来看,只要本文中提到的冷却速率超过钢带材的穿透厚度,就不存在临界输出辊道冷却速率(ROT-CR)。但是,不必要的高ROT-CR可影响冷却后带材的平坦度,并导致在正确的冷却停止温度下停止的控制问题,因此合适的最大ROT-CR为约250℃/秒、优选约200℃/秒、更优选约150℃/秒。实际的ROT-CR范围为约20至100℃/秒,更优选约40至100℃/秒,因为这可以根据钢带材的厚度通过风冷、层流冷却或水射流冷却来实现。出于实际原因,输出辊道冷却速率(ROT-CR)被定义为钢带材表面的平均冷却速率。After hot rolling, the steel strip is accelerated cooled on the run-out table (ROT) to a temperature of 560°C to 620°C. In order to promote grain refinement and improved ΣGB of the final microstructure, an accelerated cooling rate is required to suppress the recovery and loss of internal stored energy in austenite. The cooling rate should be high enough to avoid the phase transformation of austenite to ferrite at an elevated temperature, and preferably promotes the phase transformation of austenite to ferrite at a relatively low temperature of about 560 to 630°C on the run-out table. The increased cooling rate will promote grain refinement, improved ΣGB, and therefore promote improved fracture toughness and reduced crack sensitivity. The increased cooling rate will also suppress texture randomization and therefore suppress the strength loss of those textures (e.g., {332}<113>) developed by the deformed austenite that promotes toughness. From a microstructural point of view, there is no critical run-out table cooling rate (ROT-CR) as long as the cooling rate mentioned herein exceeds the penetration thickness of the steel strip. However, an unnecessarily high ROT-CR can affect the flatness of the strip after cooling and cause control problems in stopping at the correct cooling stop temperature, so a suitable maximum ROT-CR is about 250°C/sec, preferably about 200°C/sec, and more preferably about 150°C/sec. A practical ROT-CR range is about 20 to 100°C/sec, more preferably about 40 to 100°C/sec, as this can be achieved by air cooling, laminar cooling, or water jet cooling, depending on the thickness of the steel strip. For practical reasons, the run-out roller cooling rate (ROT-CR) is defined as the average cooling rate of the steel strip surface.
接下来,在550℃至600℃、优选550℃至600℃、更优选约560℃至600℃的温度下卷取该热轧钢带材。在一个实施方案中,热轧带材在不超过595℃、更优选不超过590℃的温度下卷取。钢带材的卷取温度是达到钢带材所需显微组织的关键工艺参数,所述显微组织提供了如本文中描述的改善的机械性质的平衡。Next, the hot rolled steel strip is coiled at a temperature of 550° C. to 600° C., preferably 550° C. to 600° C., more preferably about 560° C. to 600° C. In one embodiment, the hot rolled strip is coiled at a temperature not exceeding 595° C., more preferably not exceeding 590° C. The coiling temperature of the steel strip is a key process parameter to achieve the desired microstructure of the steel strip that provides a balance of improved mechanical properties as described herein.
当卷取温度太低时,析出的动力学不足,因此将实现低强度水平。当卷取温度过高时,晶粒细化不足,导致降低的断裂韧性和提高的边缘裂纹敏感性。过高的卷取温度也不会促进任何马氏体作为最终显微组织中的第二相成分。过高的卷取温度还将降低MOD指数,分数KAM 0-1将增加,且分数KAM 1-5将过低。在卷材冷却过程中,可能发生一些进一步的析出,以及一些进一步的相变。不合意的是,析出物一旦形成可能在卷材冷却过程中粗化。合金组成与要求保护的卷取温度组合抑制了这种现象。这种卷取温度将有助于促进在卷取或卷材冷却过程中形成的铁素体的小晶粒,抑制强化铁素体基质的析出物的粗化,并且还促进少量马氏体的形成。When the coiling temperature is too low, the kinetics of precipitation are insufficient, so a low strength level will be achieved. When the coiling temperature is too high, the grain refinement is insufficient, resulting in reduced fracture toughness and increased edge crack sensitivity. Too high a coiling temperature will not promote any martensite as a second phase component in the final microstructure. Too high a coiling temperature will also reduce the MOD index, the fraction KAM 0-1 will increase, and the fraction KAM 1-5 will be too low. During coil cooling, some further precipitation may occur, as well as some further phase transformations. Undesirably, the precipitates once formed may coarsen during coil cooling. The alloy composition combined with the claimed coiling temperature suppresses this phenomenon. This coiling temperature will help promote small grains of ferrite formed during coiling or coil cooling, suppress the coarsening of precipitates that strengthen the ferrite matrix, and also promote the formation of a small amount of martensite.
在专利文献EP1616970-A1中,公开了低于680℃的保持温度导致铁素体转变的驱动力不足,随后导致过低分数的含有铁素体的析出物。对于本发明,奥氏体向铁素体的相变在低于680℃的温度下进行,以便获得提高的晶粒细化和提高的ΣGB,用于改善的断裂韧性和降低的裂纹敏感性,同时仍具有足够的析出动力学。此外,专利文献EP1616970-A1公开了在680℃或更高的温度下保持该钢带材超过1秒之后,需要以30℃/秒或更高、优选50℃/秒或更高的平均冷却速率施加二次冷却至550℃或更低、优选450℃或更低、更优选350℃或更低的卷取温度,并进行卷取以形成贝氏体和/或马氏体的二次相并将其它相的形成抑制在5体积%或更少。对于本发明,卷取温度相当高,其值为550℃至600℃、优选550℃至595℃、更优选550℃至590℃,以便允许奥氏体向铁素体的相变在相对低的温度下持续进行以促进细晶粒铁素体,其用包含Ti和Mo以及任选的Nb和/或V的碳化物析出物进行析出强化。晶粒细化和提高的ΣGB提供了改善的断裂韧性和降低的(边缘)裂纹敏感性。低于550℃的卷取将导致铁素体形成不足和析出损失。此外,其可导致过高的马氏体分数。In the patent document EP1616970-A1, it is disclosed that a holding temperature below 680°C results in insufficient driving force for ferrite transformation, which subsequently results in too low a fraction of ferrite-containing precipitates. For the present invention, the phase transformation from austenite to ferrite is carried out at a temperature below 680°C in order to obtain improved grain refinement and improved ΣGB for improved fracture toughness and reduced crack sensitivity while still having sufficient precipitation kinetics. In addition, the patent document EP1616970-A1 discloses that after holding the steel strip at a temperature of 680°C or higher for more than 1 second, it is necessary to apply secondary cooling to a coiling temperature of 550°C or lower, preferably 450°C or lower, more preferably 350°C or lower at an average cooling rate of 30°C/second or higher, preferably 50°C/second or higher, and to coil to form a secondary phase of bainite and/or martensite and suppress the formation of other phases to 5 volume % or less. For the present invention, the coiling temperature is relatively high, with a value of 550°C to 600°C, preferably 550°C to 595°C, more preferably 550°C to 590°C, in order to allow the phase transformation from austenite to ferrite to continue at a relatively low temperature to promote fine-grained ferrite, which is precipitation-strengthened with carbide precipitates containing Ti and Mo and optionally Nb and/or V. Grain refinement and increased ΣGB provide improved fracture toughness and reduced (edge) crack sensitivity. Coiling below 550°C will result in insufficient ferrite formation and precipitation losses. In addition, it may result in too high a martensite fraction.
尽管专利文献EP1338665-A1公开了550℃至700℃的卷取温度,但制得的具有至少950MPa的拉伸强度和至少40%的扩孔能力的钢均以超过600℃的卷取温度生产。所有这些钢的终轧温度为880至930℃。根据本发明,已经发现,过高的卷取温度尤其导致提高的裂纹敏感性,特别是边缘裂纹敏感性,并且还导致降低的断裂韧性。Although patent document EP1338665-A1 discloses coiling temperatures of 550° C. to 700° C., steels having a tensile strength of at least 950 MPa and a hole expansion capacity of at least 40% are produced at coiling temperatures exceeding 600° C. The final rolling temperature of all these steels is 880 to 930° C. According to the invention, it has been found that excessively high coiling temperatures lead in particular to increased crack sensitivity, in particular edge crack sensitivity, and also to reduced fracture toughness.
在钢带材冷却至室温后,通过在温热温度(80-120℃)下在酸溶液(例如HCl)中酸洗或通过酸洗与带材表面的机械刷洗的组合来去除热轧钢带材上的氧化物(鳞皮)。当任选需要耐腐蚀性时,该步骤对于使钢带材表面适于直接用作未涂覆的热轧钢或使其适合于涂覆过程是必要的。After the steel strip has cooled to room temperature, the oxides (scale) on the hot rolled steel strip are removed by pickling in an acid solution (e.g. HCl) at warm temperature (80-120° C.) or by a combination of pickling and mechanical brushing of the strip surface. This step is necessary to make the steel strip surface suitable for direct use as uncoated hot rolled steel or to make it suitable for coating processes, when corrosion resistance is optionally required.
在一个实施方案中,该热轧钢带材的厚度为约1.5mm至8mm,更优选为约1.8mm至6mm,且最优选为约1.8mm至4mm。In one embodiment, the hot rolled steel strip has a thickness of about 1.5 mm to 8 mm, more preferably about 1.8 mm to 6 mm, and most preferably about 1.8 mm to 4 mm.
该热轧钢带材产品可以是裸产品或未涂覆的产品,或者它可以在其一个或两个主表面上提供薄金属性涂层,通常钢带材每侧至多约100g/m2,优选每侧至多约50g/m2。金属性涂层优选选自铝合金涂层(例如Al-Si合金或Al-Zn合金)、锌涂层和锌合金涂层(例如Zn-Al合金、Zn-Mg合金、Zn-Fe合金、Zn-Al-Mg合金或Zn-Mg-Al合金)。The hot rolled steel strip product may be a bare or uncoated product, or it may be provided with a thin metallic coating on one or both major surfaces thereof, typically up to about 100 g/ m2 per side of the steel strip, preferably up to about 50 g/ m2 per side. The metallic coating is preferably selected from aluminium alloy coatings (e.g. Al-Si alloys or Al-Zn alloys), zinc coatings and zinc alloy coatings (e.g. Zn-Al alloys, Zn-Mg alloys, Zn-Fe alloys, Zn-Al-Mg alloys or Zn-Mg-Al alloys).
锌或锌合金涂层的组成没有限制。尽管涂层可以以各种方式施加,但优选使用标准GI涂覆浴进行热浸镀锌。Zn基涂层可以包含含有Al作为合金元素的Zn合金。优选的锌浴组合物含有约0.10-0.35重量%的Al,其余为锌和不可避免的杂质。The composition of the zinc or zinc alloy coating is not limited. Although the coating can be applied in various ways, hot-dip galvanizing using a standard GI coating bath is preferred. The Zn-based coating may comprise a Zn alloy containing Al as an alloying element. The preferred zinc bath composition contains about 0.10-0.35 wt. % Al, the remainder being zinc and unavoidable impurities.
也可以施加其他锌涂层。一个实例包括根据经此引用并入本文的专利文献WO2008/102009-A1的锌合金涂层,特别是由0.3至4.0重量%的Mg和0.05%至6.0重量%的Al、优选0.1至5.0重量%的Al,以及任选至多0.2重量%的一种或多种附加元素以及不可避免的杂质(其余为锌)组成的锌合金涂层。包含Mg和Al作为主要合金元素的优选Zn浴具有以下组成:0.5至3.8重量%的Al、0.5至3.0重量%的Mg、任选至多0.2重量%的一种或多种附加元素;余量为锌和不可避免的杂质。通常以小于0.2重量%的少量添加的附加元素可以选自Pb、Sb、Ti、Ca、Mn、Sn、La、Ce、Cr、Ni、Zr和Bi。通常添加Pb、Sn、Bi和Sb以形成锌花(spangles)。优选地,锌合金中附加元素的总量为至多0.2重量%,更优选至多0.1重量%。对于通常的应用,这些少量的附加元素不会在任何显著程度上改变涂层或浴的性质。优选地,当涂层中存在一种或多种附加元素时,每种元素以至多0.02重量%的量存在,优选每种元素以至多0.01重量%的量存在。通常仅添加附加元素以防止在用于热浸镀锌的具有熔融锌合金的浴中形成浮渣,或添加附加元素以便在涂覆层中形成锌花。Other zinc coatings may also be applied. One example includes a zinc alloy coating according to patent document WO2008/102009-A1, which is incorporated herein by reference, in particular a zinc alloy coating consisting of 0.3 to 4.0 wt. % Mg and 0.05 to 6.0 wt. % Al, preferably 0.1 to 5.0 wt. % Al, and optionally up to 0.2 wt. % of one or more additional elements and unavoidable impurities (the remainder is zinc). A preferred Zn bath comprising Mg and Al as main alloying elements has the following composition: 0.5 to 3.8 wt. % Al, 0.5 to 3.0 wt. % Mg, optionally up to 0.2 wt. % of one or more additional elements; the balance is zinc and unavoidable impurities. The additional elements, which are usually added in small amounts of less than 0.2 wt. %, may be selected from Pb, Sb, Ti, Ca, Mn, Sn, La, Ce, Cr, Ni, Zr and Bi. Pb, Sn, Bi and Sb are usually added to form spangles. Preferably, the total amount of additional elements in the zinc alloy is at most 0.2 wt.%, more preferably at most 0.1 wt.%. For typical applications, these small amounts of additional elements do not modify the properties of the coating or bath to any significant extent. Preferably, when one or more additional elements are present in the coating, each element is present in an amount of at most 0.02 wt.%, preferably each element is present in an amount of at most 0.01 wt.%. The additional elements are usually only added to prevent the formation of dross in a bath with molten zinc alloy for hot dip galvanizing, or to form spangles in the coating layer.
在另一实施方案中,金属性涂层包含(商业上纯的)铝层或铝合金层。用于热浸涂此类铝层的典型金属浴包含与硅合金化的铝合金,例如与约8至11重量%的硅和至多4重量%的铁、任选至多0.2重量%的一种或多种附加元素(如钙)、不可避免的杂质合金化的铝合金(余量为铝)。存在硅以便防止形成降低粘附性和可成形性的厚的铁-金属性金属间化合物层。铁优选以1至4重量%、更优选至少2重量%的量存在。In another embodiment, metallic coating comprises (commercially pure) aluminum layer or aluminum alloy layer.The typical metal bath for hot-dip coating of this type of aluminum layer comprises aluminum alloy alloyed with silicon, for example with about 8 to 11 % by weight of silicon and 4 % by weight of iron at the most, optionally 0.2 % by weight of one or more additional elements (such as calcium), inevitable impurity alloyed aluminum alloy (surplus is aluminum) at the most.There is silicon to prevent the formation of the thick iron-metallic intermetallic compound layer that reduces adhesion and formability.Iron preferably exists with 1 to 4 % by weight, more preferably at least 2 % by weight.
在本发明的一个方面,其涉及通过热浸镀锌根据本发明的热轧高强度钢带材获得的镀锌钢带材。In one aspect of the present invention, it relates to a galvanized steel strip obtained by hot-dip galvanizing a hot rolled high strength steel strip according to the present invention.
在本发明的一个方面,其涉及一种汽车部件,特别是汽车底盘部件,其包含根据本发明的热轧高强度钢带材或由根据本发明的热轧高强度钢带材制得,并且尤其受益于改善的强度、可成形性和改善的断裂韧性与降低的(边缘)裂纹敏感性的平衡。该钢带材可以在本领域已知的冷成形操作、温成形和热成形操作中成型为汽车部件。汽车部件包括悬架臂、加强构件、白车身框架构件、侧构件、座椅框架、座椅导轨、保险杠横梁、用于电动车辆的电池盒,所有这些都具有复杂的形状。通过使用该热轧高强度钢带材,可以以高质量、成本有效和高产率制造这些部件。根据本发明的高强度热轧钢产品也可用于工程应用。In one aspect of the present invention, it relates to an automotive component, in particular an automotive chassis component, which comprises a hot-rolled high-strength steel strip according to the present invention or is made from a hot-rolled high-strength steel strip according to the present invention, and in particular benefits from improved strength, formability and a balance of improved fracture toughness and reduced (edge) crack sensitivity. The steel strip can be formed into automotive components in cold forming operations, warm forming and hot forming operations known in the art. Automotive components include suspension arms, reinforcement members, body-in-white frame members, side members, seat frames, seat rails, bumper beams, battery boxes for electric vehicles, all of which have complex shapes. By using the hot-rolled high-strength steel strip, these components can be manufactured with high quality, cost-effectiveness and high yield. The high-strength hot-rolled steel product according to the present invention can also be used in engineering applications.
附图说明BRIEF DESCRIPTION OF THE DRAWINGS
现在将通过以下非限制性附图解释本发明。The invention will now be explained by means of the following non-limiting drawings.
图1A至图1E显示了使用用于冲压杯的常见圆柱形深冲试验来测定钢带材产品的平均总裂纹长度(ATCL)的方法的若干特征。1A-1E illustrate several features of a method for determining the average total crack length (ATCL) of a steel strip product using a common cylindrical deep draw test for a punched cup.
用于加工厚铸钢板坯的热轧机的示意图显示在图2A中,并且具有无锭轧机的薄板坯铸造设施显示在图2B中。A schematic diagram of a hot rolling mill for processing thick cast steel slabs is shown in FIG. 2A , and a thin slab casting facility with an ingot mill is shown in FIG. 2B .
现在将参考根据本发明的非限制性比较例和实施例来说明本发明。The invention will now be illustrated with reference to non-limiting comparative examples and examples according to the invention.
实施例Example
通过在真空感应炉中熔融装料来铸造尺寸为320×100×100mm的五种本发明(Inv.)化学组成A-E和对比(Comp.)钢F的钢锭。这些钢的化学组成在表1中给出。在表1中,还列出了以下两个比率A和B:Ingots of five inventive (Inv.) chemical compositions A-E and comparative (Comp.) steel F having dimensions of 320×100×100 mm were cast by melting the charge in a vacuum induction furnace. The chemical compositions of these steels are given in Table 1. In Table 1, the following two ratios A and B are also listed:
将所有铸锭在1240℃下再加热1小时,并粗轧至35mm厚度。随后,将带材再次再加热至1220℃下40分钟,并在高于870℃且低于910℃的FRT(其处于所有这些钢的奥氏体相区域中)的情况下在5个轧制道次中热轧至其约3.2至3.6mm的最终厚度。在最终轧制道次之后,将热轧钢转移到输出辊道,其中输出辊道的起始温度(TSTART)为840℃至880℃,并用水和空气的混合物以30℃/秒至70℃/秒的冷却速率从奥氏体相区域主动冷却至565℃至615℃的输出辊道处的铁素体相区域中的最终温度(TEND)。接着,将钢转移到炉中以重复缓慢的卷材冷却。这是在540、580℃和610℃的炉温(CT—卷取温度)下进行的(参见表2)。All ingots were reheated at 1240°C for 1 hour and rough rolled to a thickness of 35 mm. Subsequently, the strip was reheated again to 1220°C for 40 minutes and hot rolled to its final thickness of about 3.2 to 3.6 mm in 5 rolling passes at a FRT above 870°C and below 910°C (which is in the austenite phase region of all these steels). After the final rolling pass, the hot rolled steel was transferred to a run-out table, where the start temperature (T START ) of the run-out table was 840°C to 880°C, and actively cooled from the austenite phase region to the final temperature (T END ) in the ferrite phase region at the run-out table at 565°C to 615°C with a mixture of water and air at a cooling rate of 30°C/sec to 70°C/ sec . Next, the steel was transferred to a furnace to repeat the slow coil cooling. This was carried out at furnace temperatures (CT—coiling temperature) of 540, 580°C and 610°C (see Table 2).
在根据本文中描述的方法测试机械性质、扩孔能力和平均总裂纹长度之前,对热轧板喷砂以除去氧化物层。根据本文中描述的方法用EBSG测定热轧带材的显微组织。随采用的加工参数而变的这些试验的结果列举在表2中。Before testing mechanical properties, hole expansion capability and average total crack length according to the methods described herein, the hot rolled plates were sandblasted to remove the oxide layer. The microstructure of the hot rolled strip was determined with EBSG according to the methods described herein. The results of these tests as a function of the processing parameters employed are listed in Table 2.
表1.以重量%计的钢的化学组成。“Inv.”是根据本发明的实施例,且“Comp.”是对比例。Table 1. Chemical composition of steels in wt. %. "Inv." is an example according to the invention and "Comp." is a comparative example.
从表2的结果可以看出,具有在要求保护的范围之外的组成并根据本发明(CT 580℃)加工的钢17具有太低的Rm。提高卷取温度(CT 610℃)提供了提高的Rm,但钢16的边缘裂纹敏感性显著降低。这种降低可能是由于具有过低的MOD指数和如ΣGB所反映的不充分的晶粒细化程度的显微组织。钢18的过低的卷取温度(CT 540℃)导致与钢17相比甚至更低的Rm。From the results of Table 2, it can be seen that Steel 17, which has a composition outside the claimed range and is processed according to the invention (CT 580°C), has too low an Rm. Increasing the coiling temperature (CT 610°C) provides an increased Rm, but the edge crack sensitivity of Steel 16 is significantly reduced. This reduction is probably due to a microstructure with a too low MOD index and an insufficient degree of grain refinement as reflected by ΣGB. The too low coiling temperature of Steel 18 (CT 540°C) results in an even lower Rm compared to Steel 17.
钢1-3(合金A)具有所有根据本发明的组成,并且其中钢2已经根据本发明加工(CT580℃)。钢2提供了高强度(Rm 1011MPa)、高伸长率(A50 15.8%)、良好的扩孔率(HEC42%)和非常好的抗边缘开裂性(ATCL 28.9mm)的非常好的平衡。这是由于组成、加工和显微组织。该显微组织的特征在于非常高的晶粒细化度(ΣGB 18541/mm)和高MOD指数(1.20)。对钢1,将CT提高至610℃仍获得高Rm,但边缘裂纹敏感性降低到不可接受的水平(ATCL 49.3mm)。这是显微组织变化的结果,尤其如由过低的MOD指数(0.52)、过高的KAM 0-1和低的KAM 1-5以及过少的晶粒细化(如过低的ΣGB所反映)所反映的那样。将钢3的CT降低至540℃导致Rp和Rm的显著降低。Steels 1-3 (alloy A) have all compositions according to the invention, and of these Steel 2 has been processed according to the invention (CT 580°C). Steel 2 provides a very good balance of high strength (Rm 1011 MPa), high elongation (A50 15.8%), good hole expansion (HEC 42%) and very good edge cracking resistance (ATCL 28.9 mm). This is due to composition, processing and microstructure. The microstructure is characterized by very high grain refinement (ΣGB 18541/mm) and a high MOD index (1.20). For Steel 1, increasing the CT to 610°C still results in a high Rm, but the edge crack sensitivity is reduced to an unacceptable level (ATCL 49.3 mm). This is a result of microstructural changes, especially as reflected by too low MOD index (0.52), too high KAM 0-1 and low KAM 1-5, and too little grain refinement (as reflected by too low ΣGB). Lowering the CT of Steel 3 to 540°C resulted in a significant decrease in Rp and Rm.
与钢1-3(合金A)类似的趋势可以在钢4-6(合金B)中看到。A similar trend to that of Steels 1-3 (Alloy A) can be seen in Steels 4-6 (Alloy B).
钢7-9(合金C)具有所有根据本发明的组成,并有目的地添加V。钢8已经根据本发明以CT 580℃加工,并提供高强度(Rm 1005MPa)、高伸长率(A50 14.7%)、良好的扩孔率和非常好的抗边缘开裂性(ATCL为34.8mm)的非常好的平衡。这是由于组成、加工和显微组织。该显微组织的特征在于非常高的晶粒细化度。该显微组织具有约2.6体积%的马氏体,并且据信这有助于由34.8mm的ATCL所表示的良好的抗边缘开裂性。将钢7的CT提高至610℃略微提高了Rm和Rp,但钢7的边缘裂纹敏感性显著降低。这种降低可能是由于MOD指数和KAM值所反映的显微组织变化以及由ΣGB(ΣGB 1134 1/mm)所反映的不足的晶粒细化度。钢9过低的卷取温度(CT 540℃)导致与钢8相比较低的Rm和显著较低的Rp以及过低的扩孔率。Steels 7-9 (alloy C) have all compositions according to the invention with purposeful additions of V. Steel 8 has been processed according to the invention at CT 580°C and provides a very good balance of high strength (Rm 1005 MPa), high elongation (A50 14.7%), good hole expansion and very good edge cracking resistance (ATCL of 34.8 mm). This is due to composition, processing and microstructure. The microstructure is characterized by very high grain refinement. The microstructure has about 2.6 volume % martensite and it is believed that this contributes to the good edge cracking resistance indicated by the ATCL of 34.8 mm. Increasing the CT of Steel 7 to 610°C slightly increases Rm and Rp, but the edge cracking sensitivity of Steel 7 is significantly reduced. This reduction is probably due to the microstructural changes reflected by the MOD index and KAM value and the insufficient grain refinement reflected by ΣGB (ΣGB 1134 1/mm). The too low coiling temperature (CT 540° C.) of Steel 9 resulted in a lower Rm and a significantly lower Rp as compared to Steel 8, as well as a too low hole expansion ratio.
与合金B(钢4-6)相比,合金D(钢10-12)具有提高的Al含量。钢5和11(均根据本发明加工)的比较显示,添加Al将获得提高的强度(Rm)。钢11还显示出如MOD指数、KAM值所示的有利的显微组织和如ΣGB所示的足够的晶粒细化度,并因此提供了所需的性质平衡。Alloy D (steels 10-12) has an increased Al content compared to alloy B (steels 4-6). Comparison of steels 5 and 11 (both processed according to the present invention) shows that the addition of Al results in an increased strength (Rm). Steel 11 also shows a favorable microstructure as shown by the MOD index, KAM value and sufficient grain refinement as shown by ΣGB, and thus provides the desired balance of properties.
与合金D(钢10-12)相比,合金E(钢13-15)有目的地添加V。与钢11相比,钢14提供了进一步降低的边缘裂纹敏感性。钢14与钢15的比较显示了较低的卷取温度(CT 540℃)尤其导致显著降低的Rp。并且钢13与钢14的比较显示了将钢13的CT提高至610℃仍然得到高的Rm和Rp,但是边缘裂纹敏感性降低到不可接受的水平(ATCL 56.3mm)。这尤其由过低的MOD指数、过高的KAM 0-1和低KAM 1-5以及低ΣGB来反映。Compared to alloy D (steels 10-12), alloy E (steels 13-15) has a purposeful addition of V. Compared to steel 11, steel 14 provides a further reduction in edge crack sensitivity. Comparison of steel 14 with steel 15 shows that the lower coiling temperature (CT 540°C) leads in particular to a significantly reduced Rp. And comparison of steel 13 with steel 14 shows that increasing the CT of steel 13 to 610°C still results in high Rm and Rp, but the edge crack sensitivity is reduced to an unacceptable level (ATCL 56.3 mm). This is reflected in particular by the too low MOD index, the too high KAM 0-1 and the low KAM 1-5, and the low ΣGB.
现在已经充分描述了本发明,对于本领域普通技术人员显而易见的是,在不脱离本文中描述的本发明的精神或范围的情况下,可以进行许多改变和修改。The invention now being fully described, it will be apparent to those skilled in the art that numerous changes and modifications can be made without departing from the spirit or scope of the invention described herein.
表2.采用的工艺参数以及所得的可成形性特性、机械性质、显微组织和显微组织的织构组分Table 2. Process parameters employed and resulting formability characteristics, mechanical properties, microstructure and textural components of the microstructure
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