EP4267777A1 - Coiling temperature influenced cold rolled strip or steel - Google Patents
Coiling temperature influenced cold rolled strip or steelInfo
- Publication number
- EP4267777A1 EP4267777A1 EP21848255.2A EP21848255A EP4267777A1 EP 4267777 A1 EP4267777 A1 EP 4267777A1 EP 21848255 A EP21848255 A EP 21848255A EP 4267777 A1 EP4267777 A1 EP 4267777A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- strip
- mpa
- rpo
- steel
- sheet according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 108
- 239000010959 steel Substances 0.000 title claims abstract description 108
- 239000012535 impurity Substances 0.000 claims abstract description 20
- 229910001566 austenite Inorganic materials 0.000 claims description 29
- 229910000734 martensite Inorganic materials 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 19
- 230000000717 retained effect Effects 0.000 claims description 17
- 238000002791 soaking Methods 0.000 claims description 16
- 238000000137 annealing Methods 0.000 claims description 13
- 229910001563 bainite Inorganic materials 0.000 claims description 13
- 230000008569 process Effects 0.000 claims description 13
- 229910001568 polygonal ferrite Inorganic materials 0.000 claims description 12
- 238000005097 cold rolling Methods 0.000 claims description 8
- 239000010960 cold rolled steel Substances 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- 238000005246 galvanizing Methods 0.000 claims description 5
- 238000005098 hot rolling Methods 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 238000003303 reheating Methods 0.000 claims description 2
- 238000005096 rolling process Methods 0.000 claims description 2
- GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000011651 chromium Substances 0.000 description 25
- 238000005452 bending Methods 0.000 description 21
- 239000011572 manganese Substances 0.000 description 21
- 238000005272 metallurgy Methods 0.000 description 10
- 229910000859 α-Fe Inorganic materials 0.000 description 10
- 238000007792 addition Methods 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910000794 TRIP steel Inorganic materials 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 238000005275 alloying Methods 0.000 description 4
- 229910001567 cementite Inorganic materials 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 4
- 229910001338 liquidmetal Inorganic materials 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 238000005266 casting Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000013074 reference sample Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 229910001562 pearlite Inorganic materials 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
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- 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
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/26—Methods of annealing
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/84—Controlled slow cooling
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/002—Heat treatment of ferrous alloys containing Cr
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0226—Hot rolling
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0236—Cold rolling
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- 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
- C21D8/0278—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a particular surface treatment
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- 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
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
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- 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
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/34—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/34—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
- C23C2/36—Elongated material
- C23C2/40—Plates; Strips
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/001—Austenite
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/002—Bainite
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
Definitions
- the present invention relates to high strength steel strips and sheets suitable for applications in automobiles.
- Automotive body parts are often stamped out of sheet steels, forming complex structural members of thin sheet.
- such parts cannot be produced from conventional high strength steels, because of a too low formability of the complex structural parts.
- multi-phase Transformation Induced Plasticity aided steels TRIP steels
- TRIP steels have gained considerable interest in the last years, in particular for use in auto body structural parts and as seat frame materials.
- TRIP steels possess a multi-phase microstructure, which includes a meta-stable retained austenite phase, which is capable of producing the TRIP effect.
- austenite transforms into martensite, which results in remarkable work hardening.
- This hardening effect acts to resist necking in the material and postpones failure in sheet forming operations.
- the microstructure of a TRIP steel can greatly alter its mechanical properties.
- TRIP steels have been known for long and attracted a lot of interest, mainly because the matrix allows an excellent stretch flangability. Moreover, the TRIP effect ensured by the strain-induced transformation of metastable retained austenite islands into martensite, remarkably improves their drawability.
- a slab is initially provided.
- the slab is hot rolled in austenitic temperature range to a hot rolled strip.
- the hot rolled strip is thereafter coiled.
- the coiling resistance is reduced with increasing temperature. Commonly a coiling temperature of 600 °C is employed.
- the coiled strip is thereafter batch annealed, followed by cold rolling.
- the cold rolled strip is thereafter continuously annealed.
- WO 2019/122963 Al and WO2019123043 Al both discloses a TRIP steel with improved phosphatation coverage. A good phosphatation coverage is enabled. The improved phosphatation coverage was achieved by controlling the alloying elements and the process parameters of which one is to have a low coiling temperature. All inventive examples have a coiling temperature of 450 °C. Reference examples with higher coiling temperatures did not provide sufficient phosphatation coverage. A low coiling temperature increases cold rolling forces.
- EP 2707514 Bl disclose a TRIP steel having a microstructure comprising of 5-20% polygonal ferrite, 10-15% residual austenite, 5-15 % martensite and balance bainite. According to the document the presence of polygonal ferrite between 5 and 20% makes it possible to exceed a V-bending angle of 90° without the occurrence of cracking.
- WO2018116155 disclose a TRIP steel.
- the inventive examples disclose a lower coiling temperature of 450 °C in combination with a higher batch annealing temperature of 620 °C respectively 650 °C, and a higher coiling temperature of 560 °C in combination with a lower batch annealing temperature of 460 °C.
- EP 3 653 738 Al discloses a TRIP steel having a microstructure comprising of 3-15% residual austenite, at least 30% tempered martensite, at most 5% fresh martensite, at most 35 % bainite, 5-15 % martensite, 5-35 % ferrite.
- the present invention is directed to cold rolled steels having a tensile strength of at least 950 MPa and an excellent formability, wherein it should be possible to produce the steel sheets/strips on an industrial scale in a Continuous Annealing Line (CAL) and in a Hot Dip Galvanizing Line (HDGL).
- the invention aims at providing a steel having a composition and microstructure that can be processed to complicated high strength structural members, where the bending properties are of importance.
- the careful selection of alloying elements and process parameters reduces grain boundary oxidation.
- the reduced grain boundary oxidation improves bendability and reduces the risk of liquid metal embrittlement and susceptibility to hydrogen embrittlement. It further facilitates good phospahtability.
- Fig. 1 shows a graph with the inventive samples within a within the dotted lines.
- Fig. 2a shows no an inventive sample with no grain boundary oxidation.
- Fig, 2b shows the surface of the inventive sample of Fig. 2a.
- Fig. 3a shows the grain boundary oxidation of a reference sample.
- Fig. 3b is a zoom in on the grain boundary of Fig. 3a.
- Fig. 3c shows the surface of the reference sample of Fig. 3a-3b.
- Fig. 4 shows the phosphatation coverage of the inventive sample Fig 2a- 2b.
- Fig. 5 shows the phosphatation coverage of the reference sample of Fig 3a-3c.
- the steel sheet has a composition consisting of the following alloying elements (in wt. %):
- C stabilizes the austenite and is important for obtaining sufficient carbon within the retained austenite phase.
- C is also important for obtaining the desired strength level. Generally, an increase of the tensile strength in the order of 100 MPa per 0.1 % C can be expected. When C is lower than 0.08 % it is difficult to attain a tensile strength of 950 MPa. If C exceeds 0.28 %, then the weldability is impaired.
- the upper limit may thus be 0.26, 0.24, 0.22, 0.20 or 0.18 %.
- the lower limit may be 0.10, 0.12, 0.14, or 0.16 %.
- Manganese is a solid solution strengthening element, which stabilises the austenite by lowering the M s temperature and prevents ferrite and pearlite to be formed during cooling.
- Mn lowers the Acs temperature and is important for the austenite stability.
- a tensile strength of 950 MPa and the austenitizing temperature might be too high for conventional industrial annealing lines.
- at lower contents it may be difficult to avoid the formation of polygonal ferrite.
- the upper limit may therefore be 4.2, 4.0, 3.8, 3.6, 3.4, 3.2, 3.0, 2.8, 2.6, or 2.4 %.
- the lower limit may be 1.5, 1.7, 1.9, 2.1, 2.3, or 2.5%.
- Cr is effective in increasing the strength of the steel sheet. Cr is an element that forms ferrite and retards the formation of pearlite and bainite. The A C 3 temperature and the M s temperature are only slightly lowered with increasing Cr content. Cr results in an increased amount of stabilized retained austenite. When above 0.5% it may impair surface finish of the steel, and therefore the amount of Cr is limited to 0.5 %.
- the upper limit may be 0.45 or 0.40, 0.35, 0.30 or 0.25 %.
- the lower limit may be 0.01, 0.03, 0.05, 0.07, 0.10, 0.15, 0,20 or 0.25 %.
- a deliberate addition of Cr is not conducted according to the present invention.
- Si acts as a solid solution strengthening element and is important for securing the strength of the thin steel strip. Si suppresses the cementite precipitation and is essential for austenite stabilization. However, if the content is too high, then too much silicon oxides will form on the strip surface, which may lead to cladding on the rolls in the CAL and, as a result there of, to surface defects on subsequently produced steel sheets.
- the upper limit is therefore 2.5 % and may be restricted to 2.4, 2.2, 2.0, 1.8 or 1.6 %.
- the lower limit may be 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.60, 0.80 or 1.0 %.
- Al 0.01 - 0.6 %
- Al promotes ferrite formation and is also commonly used as a deoxidizer.
- Al like Si, is not soluble in the cementite and therefore it considerably delays the cementite formation during bainite formation.
- galvanization and reduced susceptibility to Liquid metal embrittlement can be improved.
- Additions of Al result in a remarkable increase in the carbon content in the retained austenite.
- a main disadvantage of Al is its segregation behaviour during casting. During casting Mn is enriched in the middle of the slabs and the Al-content is decreased. Therefore, in the middle of the slab a significant austenite stabilized region or band may be formed. This results at the end of the processing in martensite banding and that low strain internal cracks are formed in the martensite band.
- the upper level may be 0.6, 0.5, 0.4, 0.3, 0.2, 0.1%.
- the lower limit may be set to 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, or 0.1 %. If Al is used for deoxidation only then the upper level may then be 0.09, 0.08, 0.07 or 0.06 %. For securing a certain effect the lower level may set to 0.03 or 0.04 %.
- Si and Al suppress the cementite precipitation during bainite formation. Their combined content is therefore preferably at least 0.1%.
- the upper limit may be 2 %.
- a certain amount of these elements is beneficial for the formation of austenite. Their combined content should therefore be at least > 0.4 %.
- the lower limit can be 0.5, 0.6 or 0.7%.
- Manganese and Chromium affects the hardenability of the steel. Their combined content is preferably within the range of 1.7 - 5.0 %.
- Molybdenum is a powerful hardenability agent. It may further enhance the benefits of NbC precipitates by reducing the carbide coarsening kinetics.
- the steel may therefore contain Mo in an amount up to 0.5 %.
- the upper limit may be restricted to 0.4, 0.3, 0.2, or 0.1 %. A deliberate addition of Mo is not necessary according to the present invention. The upper limit may therefore be restricted to ⁇ 0.01 %.
- Nb is commonly used in low alloyed steels for improving strength and toughness, because of its influence on the grain size. Nb increases the strength elongation balance by refining the matrix microstructure and the retained austenite phase due to precipitation of NbC.
- the steel may contain Nb in an amount of ⁇ 0.1%.
- the upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %. A deliberate addition of Nb is not necessary according to the present invention. The upper limit may therefore be restricted to ⁇ 0.004 %.
- V is similar to that of Nb in that it contributes to precipitation hardening and grain refinement.
- the steel may contain V in an amount of ⁇ 0.1 %.
- the upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %.
- a deliberate addition of V is not necessary according to the present invention.
- the upper limit may therefore be restricted to ⁇ 0.01 %.
- Ti is commonly used in low alloyed steels for improving strength and toughness, because of its influence on the grain size by forming carbides, nitrides or carbonitrides.
- Ti is a strong nitride former and can be used to bind the nitrogen in the steel.
- the upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %.
- a deliberate addition of Ti is not necessary according to the present invention. The upper limit may therefore be restricted to ⁇ 0.005%.
- Ca may be used for the modification of the non-metallic inclusions.
- the upper limit is 0.05% and may be set to 0.04, 0.03, 0.01 %.
- a deliberate addition of Ca is not necessary according to the present invention.
- the upper limit may therefore be restricted to ⁇ 0.005%.
- Cu is an undesired impurity element that is restricted to ⁇ 0.06 % by careful selection of the scrap used.
- Ni is also an undesired impurity element that is restricted to ⁇ 0.08 % by careful selection of the scrap used.
- B is an undesired impurity element that is restricted to ⁇ 0.0006 % by careful selection of the scrap used. B increases hardness but may come at a cost of reduced bendability and is therefore not desirable in the present suggested steel. B may further make scrap recycling more difficult and an addition of B may also deteriorate workability. A deliberate addition of B is therefore not desired according to the present invention.
- impurity elements may be comprised in the steel in normal occurring amounts. However, it is preferred to limit the amounts of P, S, As, Zr, Sn to the following optional maximum contents:
- N ⁇ 0.015 %, preferably 0.003 - 0.008 %
- Oxygen and hydrogen can further be limited to
- microstructural constituents are in the following expressed in volume % (vol. %).
- the cold rolled steel sheets of the present invention have a microstructure comprising at least 50% tempered martensite (TM) and bainite (B).
- TM tempered martensite
- B bainite
- the lower limit may restrict to at least 60, 70%, 75%, or 80 %.
- the upper limit may be restricted 8 % or 5 %. Small amounts of fresh martensite may improve edge flangeability and local ductility.
- the lower limit may be restricted 1% or 2%.
- These un-tempered martensite particles are often in close contact with the retained austenite particles and they are therefore often referred to as martensite-austenite (MA) particles.
- Retained austenite is a prerequisite for obtaining the desired TRIP effect.
- the amount of retained austenite should therefore be in the range of 2 - 20 %, preferably 5 - 15 %. The amount of retained austenite was measured by means of the saturation magnetization method described in detail in Proc. Int. Conf, on TRIP-aided high strength ferrous alloys (2002), Ghent, Belgium, p. 61-64.
- Polygonal ferrite is susceptible to Hydrogen Embrittlement and is therefore not a desired microstructural constituent. Polygonal ferrite in combination with martensite is bad for the bending properties. Furthermore, the presence of ferrite may impart the steel with formability and elongation and also to a certain degree resistance to fatigue failure. It may also have negative impacts due to the fact that ferrite increases the gap in hardness with hard phases such as martensite and bainite and reduces local ductility, resulting in lower hole expansion ratio. Polygonal ferrite (PF) is therefore limited to ⁇ 10 %, preferably ⁇ 5%, ⁇ 3 % or ⁇ l %. Most preferably, the steel is free from PF. The steel does not contain other kind of ferrite since the bending properties are affected negatively. Furthermore, the yield ratio is affected negatively by ferrite which is bad for bending properties.
- the R m , Rpo.2 values are derived according to the European norm EN 10002 Part 1, wherein the samples are taken in the longitudinal direction of the strip.
- the total elongation (A50) is derived in accordance with the Japanese Industrial Standard JIS Z 2241: 2011, wherein the samples are taken in the transversal direction of the strip.
- the bendability is evaluated by the ratio of the limiting bending radius (Ri), which is defined as the minimum bending radius with no occurrence of cracks, and the sheet thickness, (t).
- a 90° V-shaped block is used to bend the steel sheet in accordance with JIS Z2248.
- the value obtained by dividing the limit bending radius with the thickness (Ri/t) should be less than 5, preferably less than 4.
- Ri(t) may be further limited to 3, 2.5 or 2.
- a yield ratio YR is defined by dividing the yield strength YS with the tensile strength TS.
- Lower limit for YR can be 0.70, 0.75, 0.76, 0.77, or 0.78.
- the steel should further be within the area defined by the coordinates A, B, C, D of Fig. 1, where Ri/T (y-axle) is plotted vs TS/YR (x-axle), and where A is [1200, 2), B is [2000, 4], C is [2000, 3], and D is [1200, 1].
- the TS/YR value can further be limited such that TS/YR is within 1000-2000 (MPa).
- the lower limit may be 1100, 1200, 1300, 1400, 1500, 1600, 1700, or 1800.
- the upper limit may be 1900, 1800, 1700, 1600, 1500, or 1400.
- a preferred range can be 1200-1400.
- Other ranges can e.g. be 1400-1600, or 1600-1800, or 1800-2000.
- the hole expansion ratio (X) [HER] is preferably > 20 %.
- the hole expanding ratio (X) is determined by the hole expanding test according to ISO/WD 16630:2009 (E). In this test a conical punch having an apex of 60 ° is forced into a 10 mm diameter punched hole made in a steel sheet having the size of 100 x 100 mm 2 . The test is stopped as soon as the first crack is determined, and the hole diameter is measured in two directions orthogonal to each other. The arithmetic mean value is used for the calculation.
- the cold rolled heat treated steel sheet of the present invention may optionally be coated with zinc or zinc alloys, or with aluminum or aluminum alloys to improve its corrosion resistance.
- the suggested steel can be produced by making steel slabs of the conventional metallurgy by converter melting and secondary metallurgy with the composition suggested above.
- the slabs are hot rolled in austenitic range to a hot rolled strip.
- the hot rolled strip is coiled at a coiling temperature in the range of 500 - 540 °C.
- a scale removal process such as pickling.
- the coiled strip is thereafter batch annealed at a temperature in the range of 500 -650 °C, preferably 550-650 °C, for a duration of 5-30h. Thereafter cold rolling the annealed steel strip with a reduction rate between 35 and 90%, preferably around 40-60% reduction. Further treating the cold rolled steel strip in a Continuously Annealing Line (CAL) or in a Hot Dip Galvanizing Line (HDGL), in which the microstructure is fine tuned.
- CAL Continuously Annealing Line
- HDGL Hot Dip Galvanizing Line
- Both lines include subjecting the steel to a soaking temperature of 800 -1000 °C, preferably 830-900 °C, preferably followed by a rapid slow jet and rapid jet cooling to a holding temperature of 200-500 °C, preferably 350 - 450 °C, for a time of 150 to 1000 s, before cooling to room temperature.
- the soaking temperature is above A c3 to avoid formation of inter critical ferrite.
- a c3 as defined by the formula A c3 910-203*C 1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
- the soaking temperature is at least A c3 +20 °C, more preferably A c3 +30 °C.
- the soaking temperature and time is controlled to allow for 100 % austenite and no ferrite before cooling.
- the soaking time could e.g. be 40 s to 180 s.
- the holding temperature can be above or below Ms.
- the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
- the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
- V ⁇ 0.1 balance Fe apart from impurities and b) fulfil at least one of the following conditions:
- the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
- V ⁇ 0.1 balance Fe apart from impurities and b) fulfil at least one of the following conditions:
- TS tensile strength 1100- 1300 MPa YS yield strength (Rpo.2) 900- 1100 MPa YR yield ratio (Rpo.2/ Rm) >0.70 bendability (Ri/t) ⁇ 3 HER >20.
- the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
- V ⁇ 0.1 balance Fe apart from impurities and b) fulfil at least one of the following conditions:
- Fig. 1 the limiting bending radiuses (Ri) divided by the cold rolling thickness has been plotted against the tensile strengths divided by the yield ratios, TS/ YR, for the steels in Example 1-4.
- the inventive steels came within an area defined by the coordinates A, B, C, D when Ri/t (y-axle) is plotted vs TS/YR (x-axle), where A is [1200, 2), B is [2000, 4], C is [2000, 3], and D is [1200, 1],
- Steels 11-16, and reference steels R1 and R2 were produced by conventional metallurgy by converter melting and secondary metallurgy.
- the compositions are shown in table 1, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition.
- the steels were continuously cast and cut into slabs.
- the slabs were reheated and hot rolled in austenitic range to a thickness of about 2.8 mm.
- the hot rolling finishing temperature was about 900 °C.
- the hot rolled steel strips where thereafter coiled, steel 11-16 at a coiling temperature of 530 °C and the reference steels RI and R2 at about 630 °C.
- the coiled hot rolled strips were pickled and batch annealed at about 624 °C for 10 hours in order to reduce the tensile strength of the hot rolled strip and thereby reducing the cold rolling forces.
- the strips were thereafter cold rolled in a five stand cold rolling mill to a final thickness of about 1.41 mm and finally subjected to continuous annealing in a Continuous Annealing Line (CAL).
- CAL Continuous Annealing Line
- the strips were heated to a soaking temp of about 850 °C and held there for about 120s.
- the strips were slow jet cooled to about 750 °C (SJC), and then rapid jet cooled to a holding temperature of about 400 °C (RJC).
- SJC slow jet cooled to about 750 °C
- RJC rapid jet cooled to a holding temperature of about 400 °C
- the strips were hold at about 180 s and then cooled to room temperature.
- Yield strength YS and tensile strength TS were derived according to the European norm EN 10002 Part 1. The samples were taken in the longitudinal direction of the strip.
- Fig. 2a and 2b show an examination of inventive steel 16 coiled at 530 °C and Fig. 3a-3c show an examination of a reference steel R1 coiled at 630 °C.
- the reference steel R1 showed grain boundary oxidation whereas the inventive steel 16 showed no grain boundary oxidation.
- Fig. 3c shows visible cracks on the sample surface of the reference steel Rl. These comes from breakouts after pickling and cold rolling. Especially the grain boundary oxides lead to outbreaks around the present grains, which could lead to full grain breakouts. The cracks/outbreaks are decremental for the bending ratio.
- Fig. 2b show no visible cracks on the sample surface of the inventive steel.
- the lack of grain boundary oxides and no visible cracks of the inventive steel improves the bending ratio and reduces the risk of liquid metal embrittlement. It further facilitates good phosphatability.
- Fig. 4 show the phosphatation coverage for 16
- the microstructure of 16 was determined to:
- Steel 17 and reference steel R3 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 4, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition.
- the steels 17 and R3 having higher Cr and C contents and lower Si and Mn contents than the steels of example 1. This provides a steel having a higher yield strength and a higher tensile strength.
- Example 2 The steels were treated in the same process as Example 1, in which steel 17 was coiled at a coiling temperature of 532 °C and the reference steel R3 at 626 °C.
- the strips were heated to a soaking temp of about 850 °C and held there for about 120s. After annealing, the strips were slow jet cooled to about 700 °C (SJC), and then rapid jet cooled to a holding temperature of about 250 °C (RJC). The strips were hold at about 180 s and then cooled to room temperature. All other process parameters were about the same as those of Example 1.
- a c3 910-203*C 1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
- the limiting bending radius (Ri) of the steel 17 that was coiled at 532 °C was less than that of the steel R3 that was coiled at 626 °C.
- the microstructure of 17 was determined to:
- Bainite+ Tempered martensite about 95% retained austenite about 5 %
- Steel 18 and reference steel R4 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 7, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition. The steels 18 and R4 having higher Si and C contents and lower Cr content than the steels of example 1. This results in a steel having a slightly higher tensile strength than that of example 1.
- Example 1 The steels were treated in the same process as Example 1, in which steel 18 was coiled at a coiling temperature of 535 °C and the reference steel R4 at 633 °C. All other process parameters were about the same as those of Example 1.
- a C 3 910-203 *C 1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
- the limiting bending radius (Ri) of the steel 18 that was coiled at 535 °C was less than that of the steel R4 that was coiled at 633 °C.
- the microstructure of 19 was determined to:
- Steel 19 and reference steel R5 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 10, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition. The steels 19 and R5 having slightly higher C content and slightly lower Mn and Si content than the steels of example 1.
- Example 4 the CAL line weas replaced by a Hot Dip Galvanizing Line. Prior to the Hot Dip Galvanizing Line the steels were treated in a similar process as Example 1, in which steel 19 was coiled at a coiling temperature of 520 °C and the reference steel R5 at 630 °C. The batch annealing temperature was 570 °C.
- the limiting bending radius (Ri) of the steel 19 that was coiled at 520 °C was less than that of the steel R5 that was coiled at 630 °C.
- the microstructure of 19 was determined to:
- Bainite+ Tempered Martensite about 85 %
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Abstract
The invention relates to a cold roll strip or sheet comprising in (wt%) C 0.08 - 0.28; Mn 1.4 - 4.5; Cr 0.01 - 0.5; Si 0.01 - 2.5; Al 0.01 - 0.6; Si + Al ≥ 0.1; Si + Al + Cr ≥ 0.4; Nb ≤ 0.008; Ti ≤ 0.02; Mo ≤ 0.08; Ca ≤ 0.005; V ≤ 0.02; balance Fe apart from impurities. The steel being within the area defined by the coordinates A, B, C, D, where Ri/t (y-axle) is plotted vs TS(MPa)/YR (x-axle), and where A is [1200, 2), B is [2000, 4], C is [2000, 3], and D is [1200, 1].
Description
COILING TEMPERATURE INFLUENCED COLD ROLLED STRIP OR STEEL
TECHNICAL FIELD
The present invention relates to high strength steel strips and sheets suitable for applications in automobiles.
BACKGROUND ART
For a great variety of applications increased strength levels are a pre-requisite for light-weight constructions in particular in the automotive industry, since car body mass reduction results in reduced fuel consumption.
Automotive body parts are often stamped out of sheet steels, forming complex structural members of thin sheet. However, such parts cannot be produced from conventional high strength steels, because of a too low formability of the complex structural parts. For this reason, multi-phase Transformation Induced Plasticity aided steels (TRIP steels) have gained considerable interest in the last years, in particular for use in auto body structural parts and as seat frame materials.
TRIP steels possess a multi-phase microstructure, which includes a meta-stable retained austenite phase, which is capable of producing the TRIP effect. When the steel is deformed, the austenite transforms into martensite, which results in remarkable work hardening. This hardening effect acts to resist necking in the material and postpones failure in sheet forming operations. The microstructure of a TRIP steel can greatly alter its mechanical properties.
TRIP steels have been known for long and attracted a lot of interest, mainly because the matrix allows an excellent stretch flangability. Moreover, the TRIP effect ensured by the strain-induced transformation of metastable retained austenite islands into martensite, remarkably improves their drawability.
When producing cold rolled TRIP steel sheets a slab is initially provided. The slab is hot rolled in austenitic temperature range to a hot rolled strip. The hot rolled strip is thereafter coiled. The coiling resistance is reduced with increasing temperature. Commonly a coiling temperature of 600 °C is employed. The coiled strip is thereafter batch annealed, followed by cold rolling. The cold rolled strip is thereafter continuously annealed.
WO 2019/122963 Al and WO2019123043 Al both discloses a TRIP steel with improved phosphatation coverage. A good phosphatation coverage is enabled. The improved phosphatation coverage was achieved by controlling the alloying elements and the process parameters of which one
is to have a low coiling temperature. All inventive examples have a coiling temperature of 450 °C. Reference examples with higher coiling temperatures did not provide sufficient phosphatation coverage. A low coiling temperature increases cold rolling forces.
EP 2707514 Bl disclose a TRIP steel having a microstructure comprising of 5-20% polygonal ferrite, 10-15% residual austenite, 5-15 % martensite and balance bainite. According to the document the presence of polygonal ferrite between 5 and 20% makes it possible to exceed a V-bending angle of 90° without the occurrence of cracking.
WO2018116155 disclose a TRIP steel. The inventive examples disclose a lower coiling temperature of 450 °C in combination with a higher batch annealing temperature of 620 °C respectively 650 °C, and a higher coiling temperature of 560 °C in combination with a lower batch annealing temperature of 460 °C.
EP 3 653 738 Al discloses a TRIP steel having a microstructure comprising of 3-15% residual austenite, at least 30% tempered martensite, at most 5% fresh martensite, at most 35 % bainite, 5-15 % martensite, 5-35 % ferrite.
Although these steels disclose several attractive properties there is demand for >950 MPa steel sheet or strip having an improved property profile with respect to advanced forming operations, in particular bending properties. In particular bending property in relation to strength and toughness. Further desirable properties are: reduced grain-boundary oxidation, reduced susceptibility to Liquid metal embrittlement, reduced susceptibility to hydrogen embrittlement, and a good phosphatability.
DISCLOSURE OF THE INVENTION
The present invention is directed to cold rolled steels having a tensile strength of at least 950 MPa and an excellent formability, wherein it should be possible to produce the steel sheets/strips on an industrial scale in a Continuous Annealing Line (CAL) and in a Hot Dip Galvanizing Line (HDGL). The invention aims at providing a steel having a composition and microstructure that can be processed to complicated high strength structural members, where the bending properties are of importance.
The careful selection of alloying elements and process parameters reduces grain boundary oxidation. The reduced grain boundary oxidation improves bendability and reduces the risk of liquid metal embrittlement and susceptibility to hydrogen embrittlement. It further facilitates good phospahtability.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 shows a graph with the inventive samples within a within the dotted lines.
Fig. 2a shows no an inventive sample with no grain boundary oxidation.
Fig, 2b shows the surface of the inventive sample of Fig. 2a.
Fig. 3a shows the grain boundary oxidation of a reference sample.
Fig. 3b is a zoom in on the grain boundary of Fig. 3a.
Fig. 3c shows the surface of the reference sample of Fig. 3a-3b.
Fig. 4 shows the phosphatation coverage of the inventive sample Fig 2a- 2b.
Fig. 5 shows the phosphatation coverage of the reference sample of Fig 3a-3c.
DETAILED DESCRIPTION
The invention is described in the claims.
The steel sheet has a composition consisting of the following alloying elements (in wt. %):
C 0.08 - 0.28
Mn 1.4 - 4.5
Cr 0.01 - 0.5
Si 0.01 - 2.5
Al 0.01 - 0.6
Si + Al > 0.1
Si+Al+ Cr > 0.4
Nb < 0.1
Ti < 0.1
Mo < 0.5
Ca < 0.05
V < 0.1 balance Fe apart from impurities.
The importance of the separate elements and their interaction with each other as well as the limitations of the chemical ingredients of the claimed alloy are briefly explained in the following. All percentages for the chemical composition of the steel are given in weight % (wt. %) throughout the description. Upper and lower limits of the individual elements can be freely combined within the limits set out in the claims. The arithmetic precision of the numerical values can be increased by one or two digits for all values given in the present application. Hence, a value of given as e.g. 0.1 % can also be expressed as 0.10 or 0.100 %. The amounts of the microstructural constituents are given in volume % (vol. %).
C: 0.08 - 0.28 %
C stabilizes the austenite and is important for obtaining sufficient carbon within the retained austenite phase. C is also important for obtaining the desired strength level. Generally, an increase of the tensile strength in the order of 100 MPa per 0.1 % C can be expected. When C is lower than 0.08 % it is difficult to attain a tensile strength of 950 MPa. If C exceeds 0.28 %, then the weldability is impaired. The upper limit may thus be 0.26, 0.24, 0.22, 0.20 or 0.18 %. The lower limit may be 0.10, 0.12, 0.14, or 0.16 %.
Mn: 1.4 - 4.5 %
Manganese is a solid solution strengthening element, which stabilises the austenite by lowering the Ms temperature and prevents ferrite and pearlite to be formed during cooling. In addition, Mn lowers the Acs temperature and is important for the austenite stability. At a content of less than 1.5 % it might be difficult to obtain the desired amount of retained austenite, a tensile strength of 950 MPa and the austenitizing temperature might be too high for conventional industrial annealing lines. In addition, at lower contents it may be difficult to avoid the formation of polygonal ferrite. However, if the amount of Mn is higher than 4.5 %, problems with segregation may occur because Mn accumulates in the liquid phase and causes banding, resulting in a potentially deteriorated workability. The upper limit may therefore be 4.2, 4.0, 3.8, 3.6, 3.4, 3.2, 3.0, 2.8, 2.6, or 2.4 %. The lower limit may be 1.5, 1.7, 1.9, 2.1, 2.3, or 2.5%.
Cr: 0.01- 0.5 %
Cr is effective in increasing the strength of the steel sheet. Cr is an element that forms ferrite and retards the formation of pearlite and bainite. The AC3 temperature and the Ms temperature are only slightly lowered with increasing Cr content. Cr results in an increased amount of stabilized retained austenite. When above 0.5% it may impair surface finish of the steel, and therefore the amount of Cr is limited to 0.5 %. The upper limit may be 0.45 or 0.40, 0.35, 0.30 or 0.25 %. The lower limit may be 0.01, 0.03, 0.05, 0.07, 0.10, 0.15, 0,20 or 0.25 %. Preferably, a deliberate addition of Cr is not conducted according to the present invention.
Si: 0.01 - 2.5 %
Si acts as a solid solution strengthening element and is important for securing the strength of the thin steel strip. Si suppresses the cementite precipitation and is essential for austenite stabilization. However, if the content is too high, then too much silicon oxides will form on the strip surface, which may lead to cladding on the rolls in the CAL and, as a result there of, to surface defects on subsequently produced steel sheets. The upper limit is therefore 2.5 % and may be restricted to 2.4, 2.2, 2.0, 1.8 or 1.6 %. The lower limit may be 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.60, 0.80 or 1.0 %.
Al: 0.01 - 0.6 %
Al promotes ferrite formation and is also commonly used as a deoxidizer. Al, like Si, is not soluble in the cementite and therefore it considerably delays the cementite formation during bainite formation. In addition, galvanization and reduced susceptibility to Liquid metal embrittlement can be improved. Additions of Al result in a remarkable increase in the carbon content in the retained austenite. A main disadvantage of Al is its segregation behaviour during casting. During casting Mn is enriched in the middle of the slabs and the Al-content is decreased. Therefore, in the middle of the slab a significant austenite stabilized region or band may be formed. This results at the end of the processing in martensite banding and that low strain internal cracks are formed in the martensite band. On the other hand, Si and Cr are also enriched during casting. Hence, the propensity for martensite banding may be reduced by alloying with Si and Cr, since the austenite stabilization due to the Mn enrichment is counteracted by these elements. For these reasons the Al content is preferably limited. The upper level may be 0.6, 0.5, 0.4, 0.3, 0.2, 0.1%. The lower limit may be set to 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, or 0.1 %. If Al is used for deoxidation only then the upper level may then be 0.09, 0.08, 0.07 or 0.06 %. For securing a certain effect the lower level may set to 0.03 or 0.04 %.
Si + Al > 0.1 %
Si and Al suppress the cementite precipitation during bainite formation. Their combined content is therefore preferably at least 0.1%. The upper limit may be 2 %.
Si + Al + Cr > 0.4 %
A certain amount of these elements is beneficial for the formation of austenite. Their combined content should therefore be at least > 0.4 %. The lower limit can be 0.5, 0.6 or 0.7%.
Mn + Cr 1.7 - 5.0 %
Manganese and Chromium affects the hardenability of the steel. Their combined content is preferably within the range of 1.7 - 5.0 %.
Optional elements Mo < 0.5%
Molybdenum is a powerful hardenability agent. It may further enhance the benefits of NbC precipitates by reducing the carbide coarsening kinetics. The steel may therefore contain Mo in an amount up to 0.5 %. The upper limit may be restricted to 0.4, 0.3, 0.2, or 0.1 %. A deliberate addition of Mo is not necessary according to the present invention. The upper limit may therefore be restricted to < 0.01 %.
Nb: < 0.1%
Nb is commonly used in low alloyed steels for improving strength and toughness, because of its influence on the grain size. Nb increases the strength elongation balance by refining the matrix microstructure and the retained austenite phase due to precipitation of NbC. The steel may contain Nb in an amount of < 0.1%. The upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %. A deliberate addition of Nb is not necessary according to the present invention. The upper limit may therefore be restricted to < 0.004 %.
V: < 0.1%
The function of V is similar to that of Nb in that it contributes to precipitation hardening and grain refinement. The steel may contain V in an amount of < 0.1 %. The upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %. A deliberate addition of V is not necessary according to the present invention. The upper limit may therefore be restricted to < 0.01 %.
Ti: < 0.1%
Ti is commonly used in low alloyed steels for improving strength and toughness, because of its influence on the grain size by forming carbides, nitrides or carbonitrides. In particular, Ti is a strong nitride former and can be used to bind the nitrogen in the steel. However, the effect tends to be saturated above 0.1 %. The upper limit may be restricted to 0.09, 0.07, 0.05, 0.03, or 0.01 %. A deliberate addition of Ti is not necessary according to the present invention. The upper limit may therefore be restricted to < 0.005%.
Ca < 0.05
Ca may be used for the modification of the non-metallic inclusions. The upper limit is 0.05% and may be set to 0.04, 0.03, 0.01 %. A deliberate addition of Ca is not necessary according to the present invention. The upper limit may therefore be restricted to < 0.005%.
Cu: < 0.06 %
Cu is an undesired impurity element that is restricted to < 0.06 % by careful selection of the scrap used.
Ni: < 0.08 %
Ni is also an undesired impurity element that is restricted to < 0.08 % by careful selection of the scrap used.
B: < 0.0006%
B is an undesired impurity element that is restricted to < 0.0006 % by careful selection of the scrap used. B increases hardness but may come at a cost of reduced bendability and is therefore not desirable in the present suggested steel. B may further make scrap recycling more difficult and an addition of B may also deteriorate workability. A deliberate addition of B is therefore not desired according to the present invention.
Other impurity elements may be comprised in the steel in normal occurring amounts. However, it is preferred to limit the amounts of P, S, As, Zr, Sn to the following optional maximum contents:
P: < 0.02 %
S: < 0.005 %
As < 0.010%
Zr < 0.006%
Sn < 0.015%
It is also preferred to control the nitrogen content to the range:
N: < 0.015 %, preferably 0.003 - 0.008 %
In this range a stable fixation of the nitrogen can be achieved.
Oxygen and hydrogen can further be limited to
O: < 0.0003
H: < 0.0020
The microstructural constituents are in the following expressed in volume % (vol. %).
The cold rolled steel sheets of the present invention have a microstructure comprising at least 50% tempered martensite (TM) and bainite (B). The lower limit may restrict to at least 60, 70%, 75%, or 80 %.
And further, at most 10 % fresh martensite (FM). The upper limit may be restricted 8 % or 5 %. Small amounts of fresh martensite may improve edge flangeability and local ductility. The lower limit may be restricted 1% or 2%. These un-tempered martensite particles are often in close contact with the retained austenite particles and they are therefore often referred to as martensite-austenite (MA) particles.
Retained austenite is a prerequisite for obtaining the desired TRIP effect. The amount of retained austenite should therefore be in the range of 2 - 20 %, preferably 5 - 15 %. The amount of retained austenite was measured by means of the saturation magnetization method described in detail in Proc. Int. Conf, on TRIP-aided high strength ferrous alloys (2002), Ghent, Belgium, p. 61-64.
Polygonal ferrite (PF) is susceptible to Hydrogen Embrittlement and is therefore not a desired microstructural constituent. Polygonal ferrite in combination with martensite is bad for the bending properties. Furthermore, the presence of ferrite may impart the steel with formability and elongation and also to a certain degree resistance to fatigue failure. It may also have negative impacts due to the fact that ferrite increases the gap in hardness with hard phases such as martensite and bainite and reduces local ductility, resulting in lower hole expansion ratio. Polygonal ferrite (PF) is therefore limited to < 10 %, preferably < 5%, < 3 % or < l %. Most preferably, the steel is free from PF. The steel does not contain other kind of ferrite since the bending properties are affected negatively. Furthermore, the yield ratio is affected negatively by ferrite which is bad for bending properties.
The mechanical properties of the claimed steel are important, and the following requirements should be fulfilled:
TS tensile strength (Rm) 950 - 1550 MPa YS yield strength (Rp0.2) 550 - 1400 MPa YR yield ratio (Rpo.2/ Rm) > 0.50, preferably > 0.7 bendability (Ri/t) < 5
The Rm, Rpo.2 values are derived according to the European norm EN 10002 Part 1, wherein the samples are taken in the longitudinal direction of the strip. The total elongation (A50) is derived in accordance with the Japanese Industrial Standard JIS Z 2241: 2011, wherein the samples are taken in the transversal direction of the strip.
The bendability is evaluated by the ratio of the limiting bending radius (Ri), which is defined as the minimum bending radius with no occurrence of cracks, and the sheet thickness, (t). For this purpose, a 90° V-shaped block is used to bend the steel sheet in accordance with JIS Z2248. The value obtained by dividing the limit bending radius with the thickness (Ri/t) should be less than 5, preferably less than 4. Ri(t) may be further limited to 3, 2.5 or 2.
A yield ratio YR is defined by dividing the yield strength YS with the tensile strength TS. Lower limit for YR can be 0.70, 0.75, 0.76, 0.77, or 0.78.
The steel should further be within the area defined by the coordinates A, B, C, D of Fig. 1, where Ri/T (y-axle) is plotted vs TS/YR (x-axle), and where A is [1200, 2), B is [2000, 4], C is [2000, 3], and D is [1200, 1]. The upper dotted line can be mathematically expressed as y= 0.0025 *x -1 and the lower dotted line can be expressed as y=0.0025*x -2. This provides a criteria 1< 0.0025*TS/YR - Ri/t < 2. Steels fulfilling the criteria has been found out to have a good balance between strength and bendability. The lower limit may be 1.1, 1.2 or 1.3 and the upper limit may be 1.9 or 1.8.
The TS/YR value can further be limited such that TS/YR is within 1000-2000 (MPa). The lower limit may be 1100, 1200, 1300, 1400, 1500, 1600, 1700, or 1800. The upper limit may be 1900, 1800, 1700, 1600, 1500, or 1400. A preferred range can be 1200-1400. Other ranges can e.g. be 1400-1600, or 1600-1800, or 1800-2000.
The hole expansion ratio (X) [HER] is preferably > 20 %. The hole expanding ratio (X) is determined by the hole expanding test according to ISO/WD 16630:2009 (E). In this test a conical punch having an apex of 60 ° is forced into a 10 mm diameter punched hole made in a steel sheet having the size of 100 x 100 mm2. The test is stopped as soon as the first crack is determined, and the hole diameter is measured in two directions orthogonal to each other. The arithmetic mean value is used for the calculation.
The hole expanding ratio (X) in % is calculated as follows: = (Dh - Do)/Do x 100 wherein Do is the diameter of the hole at the beginning (10 mm) and Dh is the diameter of the hole after the test.
The cold rolled heat treated steel sheet of the present invention may optionally be coated with zinc or zinc alloys, or with aluminum or aluminum alloys to improve its corrosion resistance.
The suggested steel can be produced by making steel slabs of the conventional metallurgy by converter melting and secondary metallurgy with the composition suggested above. The slabs are hot rolled in austenitic range to a hot rolled strip. Preferably by reheating the slab to a temperature between 1000 °C and 1280 °C, rolling the slab completely in the austenitic range wherein the hot rolling finishing temperature is greater than or equal to 850 °C to obtain the hot rolled steel strip. Thereafter the hot rolled strip is coiled at a coiling temperature in the range of 500 - 540 °C. Optionally subjecting the coiled strip to a scale removal process, such as pickling. The coiled strip is thereafter batch annealed at a temperature in the range of 500 -650 °C, preferably 550-650 °C, for a duration of 5-30h. Thereafter cold rolling the annealed steel strip with a reduction rate between 35 and
90%, preferably around 40-60% reduction. Further treating the cold rolled steel strip in a Continuously Annealing Line (CAL) or in a Hot Dip Galvanizing Line (HDGL), in which the microstructure is fine tuned. Both lines include subjecting the steel to a soaking temperature of 800 -1000 °C, preferably 830-900 °C, preferably followed by a rapid slow jet and rapid jet cooling to a holding temperature of 200-500 °C, preferably 350 - 450 °C, for a time of 150 to 1000 s, before cooling to room temperature. The soaking temperature is above Ac3 to avoid formation of inter critical ferrite. Ac3 as defined by the formula Ac3= 910-203*C1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W. Preferably the soaking temperature is at least Ac3+20 °C, more preferably Ac3 +30 °C. Preferably the soaking temperature and time is controlled to allow for 100 % austenite and no ferrite before cooling. The soaking time could e.g. be 40 s to 180 s.
Ms can be defined by the formula: Ms=692-502*(C+0.68N)°5-37*Mn-14*Si+20*Al-l l*Cr.
The holding temperature can be above or below Ms.
In an embodiment the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
C 0.08 - 0.16
Mn 2.0 - 3.0
Cr 0.1 - 0.5
Si 0.5 - 1.2
Al 0.01 - 0.5
Si + Al > 0.1
Si + Al + Cr > 0.4
Nb < 0.1
Ti < 0.1
Mo < 0.5
Ca < 0.05
V < 0.1 balance Fe apart from impurities; and b) fulfil at least one of the following conditions:
TS tensile strength (Rm) 950 - 1150 MPa YS yield strength (Rpo.2) 750 - 1000 MPa YR yield ratio (Rpo.2/ Rm) > 0.70 bendability (Ri/t) < 2
HER > 20.
In another embodiment the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
C 0.15-0.25
Mn 1.0 -2.0
Cr 0.1 -0.5
Si 0.1 -0.5
Al 0.01-0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and b) fulfil at least one of the following conditions:
TS tensile strength (Rm) 1300 - 1550 MPa YS yield strength (Rpo.2) 1000 - 1300 MPa YR yield ratio (Rpo.2/ Rm) >0.70 bendability (Ri/t) <4
HER >20.
In another embodiment the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
C 0.15-0.25
Mn 2.0 - 3.0
Cr 0.1 -0.5
Si 1-2.0
Al 0.01-0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and b) fulfil at least one of the following conditions:
TS tensile strength (Rm) 1100- 1300 MPa YS yield strength (Rpo.2) 900- 1100 MPa YR yield ratio (Rpo.2/ Rm) >0.70 bendability (Ri/t) <3 HER >20.
In another embodiment the cold roll strip or sheet; a) have a composition comprising of (in wt. %):
C 0.10-0.20
Mn 2.0 - 3.0
Cr 0.1 -0.5
Si 0.2 -0.9
Al 0.01 -0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and b) fulfil at least one of the following conditions:
TS tensile strength (Rm) 900- 1100 MPa YS yield strength (Rpo.2) 600 - 800 MPa YR yield ratio (Rpo.2/ Rm) >0.65 bendability (Ri/t) <2.5
HER >20.
EXAMPLES
In Fig. 1 the limiting bending radiuses (Ri) divided by the cold rolling thickness has been plotted against the tensile strengths divided by the yield ratios, TS/ YR, for the steels in Example 1-4. The
inventive steels came within an area defined by the coordinates A, B, C, D when Ri/t (y-axle) is plotted vs TS/YR (x-axle), where A is [1200, 2), B is [2000, 4], C is [2000, 3], and D is [1200, 1], The upper dotted line can be mathematically expressed as y= 0.0025 *x -1 and the lower dotted line can be expressed as y=0.0025*x -2.
Hence, the reference steels that were coiled at a higher temperature are all above the upper dotted line mathematically defined by: y = 0.0025 *x -1, where y is Ri/t and x is TS (MPa)/YR.
The inventive steels of example 1-5 are all below the upper line.
The lower dotted line is defined by y = 0.0025 *x -2, where y is Ri/t and x is TS (MPa)/YR.
The inventive steels of example 1-5 are all above the lower line.
Within these borders a good bending property in relation to strength and toughness is achieved.
EXAMPLE 1
Steels 11-16, and reference steels R1 and R2 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 1, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition.
Table 1
The steels were continuously cast and cut into slabs.
The slabs were reheated and hot rolled in austenitic range to a thickness of about 2.8 mm. The hot rolling finishing temperature was about 900 °C.
The hot rolled steel strips where thereafter coiled, steel 11-16 at a coiling temperature of 530 °C and the reference steels RI and R2 at about 630 °C.
The coiled hot rolled strips were pickled and batch annealed at about 624 °C for 10 hours in order to reduce the tensile strength of the hot rolled strip and thereby reducing the cold rolling forces.
The strips were thereafter cold rolled in a five stand cold rolling mill to a final thickness of about 1.41 mm and finally subjected to continuous annealing in a Continuous Annealing Line (CAL). In the CAL the strips were heated to a soaking temp of about 850 °C and held there for about 120s. After annealing, the strips were slow jet cooled to about 750 °C (SJC), and then rapid jet cooled to a holding temperature of about 400 °C (RJC). The strips were hold at about 180 s and then cooled to room temperature.
AC3 was around 800 °C for all steels and the soaking was therefore performed well above Aca as defined by the formula Ac3= 910-203*C!/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
The process parameters are shown in table 2.
Table 2
Yield strength YS and tensile strength TS were derived according to the European norm EN 10002 Part 1. The samples were taken in the longitudinal direction of the strip.
Samples of the produced strips were subjected to V bend test in accordance with JIS Z2248 to find out the limiting bending radius (Ri). The samples were examined both by eye and under optical microscope with 25 times magnification in order to investigate the occurrence of cracks. Ri/t was determined by dividing the limiting bending radius (Ri) with the thickness of the cold rolled strip (t). Ri is the largest radius in which the material shows no cracks after three bending tests.
The limiting bending radius (Ri) of the steels II - 16 that were coiled at 530 °C were less than those Rl, R2 that were coiled at 630 °C.
Steel II - 16 all fulfilled the condition 1 < 0.0025*TS/YR - Ri/t < 2, whereas Rl and R2 fell short.
The mechanical properties are shown in table 3.
Table 3
Fig. 2a and 2b show an examination of inventive steel 16 coiled at 530 °C and Fig. 3a-3c show an examination of a reference steel R1 coiled at 630 °C. The reference steel R1 showed grain boundary oxidation whereas the inventive steel 16 showed no grain boundary oxidation.
Fig. 3c shows visible cracks on the sample surface of the reference steel Rl. These comes from breakouts after pickling and cold rolling. Especially the grain boundary oxides lead to outbreaks around the present grains, which could lead to full grain breakouts. The cracks/outbreaks are decremental for the bending ratio.
Fig. 2b show no visible cracks on the sample surface of the inventive steel. The lack of grain boundary oxides and no visible cracks of the inventive steel improves the bending ratio and reduces the risk of liquid metal embrittlement. It further facilitates good phosphatability.
Fig. 4 show the phosphatation coverage for 16
The microstructure of 16 was determined to:
Bainite + Tempered Martensite > 85%
Fresh martensite about 5% retained austenite about 5 %
EXAMPLE 2
Steel 17 and reference steel R3 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 4, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition. The steels 17 and R3 having higher Cr and C contents and lower Si and Mn contents than the steels of example 1. This provides a steel having a higher yield strength and a higher tensile strength.
Table 4
The steels were treated in the same process as Example 1, in which steel 17 was coiled at a coiling temperature of 532 °C and the reference steel R3 at 626 °C.
In the CAL the strips were heated to a soaking temp of about 850 °C and held there for about 120s. After annealing, the strips were slow jet cooled to about 700 °C (SJC), and then rapid jet cooled to a holding temperature of about 250 °C (RJC). The strips were hold at about 180 s and then cooled to room temperature. All other process parameters were about the same as those of Example 1.
Acs was around 780 °C for all steels and the soaking was therefore performed well above Ac3 as defined by the formula Ac3= 910-203*C1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
The process parameters are shown in table 5.
Table 5
Samples of the produced strips were the subjected to the same tests as those of Example 1.
The limiting bending radius (Ri) of the steel 17 that was coiled at 532 °C was less than that of the steel R3 that was coiled at 626 °C.
Steel 17 fulfilled the condition 1 < 0.0025 *TS/YR - Ri/t < 2, whereas R3 fell short.
The mechanical properties are shown in table 6.
Table 6
The microstructure of 17 was determined to:
Bainite+ Tempered martensite about 95% retained austenite about 5 %
EXAMPLE 3
Steel 18 and reference steel R4 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 7, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition. The steels 18 and R4 having higher Si and C contents and lower Cr content than the steels of example 1. This results in a steel having a slightly higher tensile strength than that of example 1.
Table 7
The steels were treated in the same process as Example 1, in which steel 18 was coiled at a coiling temperature of 535 °C and the reference steel R4 at 633 °C. All other process parameters were about the same as those of Example 1.
Acs was around 810-815 °C for the steels and the soaking was therefore performed well above AC3 as defined by the formula Ac3= 910-203 *C 1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
The process parameters are shown in table 8.
Table 8
Samples of the produced strips were the subjected to the same tests as those of Example 1.
The limiting bending radius (Ri) of the steel 18 that was coiled at 535 °C was less than that of the steel R4 that was coiled at 633 °C.
Steel 18 fulfilled the condition 1 < 0.0025*TS/YR - Ri/t < 2, whereas R4 fell short.
The mechanical properties are shown in table 9.
Table 9
The microstructure of 19 was determined to:
Bainite+ Tempered Martensite > 70 %
Fresh martensite < 15 % retained austenite < 15 %
EXAMPLE 4
Steel 19 and reference steel R5 were produced by conventional metallurgy by converter melting and secondary metallurgy. The compositions are shown in table 10, further elements were present only as impurities, and below the lowest levels specified in the present description. All steels having about the same composition. The steels 19 and R5 having slightly higher C content and slightly lower Mn and Si content than the steels of example 1.
Table 10
In example 4 the CAL line weas replaced by a Hot Dip Galvanizing Line. Prior to the Hot Dip Galvanizing Line the steels were treated in a similar process as Example 1, in which steel 19 was coiled at a coiling temperature of 520 °C and the reference steel R5 at 630 °C. The batch annealing temperature was 570 °C.
AC3 was around 780 °C for the steels and the soaking was therefore performed well above Ac3as defined by the formula Ac3= 910-203 *C 1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
The process parameters are shown in table 11.
Table 11
Samples of the produced strips were the subjected to the same tests as those of Example 1.
The limiting bending radius (Ri) of the steel 19 that was coiled at 520 °C was less than that of the steel R5 that was coiled at 630 °C.
Steel 19 fulfilled the condition 1 < 0.0025 *TS/YR - Ri/t < 2, whereas R5 fell short.
The mechanical properties are shown in table 12.
Table 12
The microstructure of 19 was determined to:
Bainite+ Tempered Martensite about 85 %
Fresh martensite about 5 % retained austenite about 10 %
Claims
1. A cold rolled steel strip or sheet a) having a composition consisting of (in wt. %):
C 0.08 - 0.28
Mn 1.4 -4.5
Cr 0.01-0.5
Si 0.01-2.5
Al 0.01-0.6
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities, b) fulfilling the following conditions: TS tensile strength (Rm) 950 - 1550 MPa YS yield strength (Rpo.2) 550 - 1400 MPa
YR yield ratio (Rpo.2/ Rm) > 0.50 bendability (Ri/t)
c) being within the area defined by the coordinates A, B, C, D, where Ri/t (y-axle) is plotted vs TS(MPa)/YR (x-axle), and where A is [1200, 2), B is [2000, 4], C is [2000, 3], and Dis [1200, 1]; d) having a multiphase microstructure comprising (in vol%) tempered martensite + bainite >50 fresh martensite < 10 retained austenite 2-20 polygonal ferrite < 10.
2. The cold roll strip or sheet according to claim 1 , wherein the composition comprising (in wt%):
C 0.1 - 0.25
Mn 1.4 - 3
Cr 0.01 - 0.5
Si 0.1 - 1
Al 0.01 - 0.1
Si + Al > 0.1
Si + Al + Cr > 0.4
Nb < 0.008
Ti < 0.02
Mo < 0.08
Ca < 0.005
V < 0.02 balance Fe apart from impurities.
3. The cold roll strip or sheet according to claim 1 or 2 wherein the polygonal ferrite is < 5, preferably < 1.
4. The cold roll strip or sheet according to any one of the preceding claims wherein the composition fulfilling at least one of the following requirements:
Si > 0.4
Si+Al > 0.8
Al < 0.1
Mn + Cr 1.7 - 5.0.
5. The cold roll strip or sheet according to claim 4 fulfilling all of the requirements of claim 4.
6. The cold roll strip or sheet according to any one of the preceding claims wherein the microstructure fulfils at least one of the following requirements: tempered martensite + bainite > 60 fresh martensite 1-10
retained austenite 5-15 polygonal ferrite
7. The cold roll strip or sheet according to any one of the preceding claims, wherein the yield ratio is > 0.70.
8. The cold roll strip or sheet according to claim 1, a) having a composition comprising of (in wt. %):
C 0.08-0.16
Mn 2.0 - 3.0
Cr 0.1 -0.5
Si 0.5 - 1.2
Al 0.01-0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and a) fulfilling at least one of the following conditions:
TS tensile strength (Rm) 950- 1150 MPa YS yield strength (Rpo.2) 750 - 1000 MPa YR yield ratio (Rpo.2/ Rm) >0.70 bendability (Ri/t) <2
HER >20.
9. The cold roll strip or sheet according to claim 1 , c) having a composition comprising of (in wt. %):
C 0.15-0.25
Mn 1.0 -2.0
Cr 0.1 -0.5
Si 0.1 -0.5
Al 0.01-0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and d) fulfilling at least one of the following conditions:
TS tensile strength (Rm) 1300 - 1550 MPa
YS yield strength (Rpo.2) 1000 - 1300 MPa
YR yield ratio (Rpo.2/ Rm) > 0.70 bendability (Ri/t) < 4
HER > 20.
10. The cold roll strip or sheet according to claim 1, a) having a composition comprising of (in wt. %):
C 0.15-0.25
Mn 2.0 - 3.0
Cr 0.1 -0.5
Si 1-2.0
Al 0.01-0.5
Si + Al >0.1
Si + Al + Cr >0.4
Nb <0.1
Ti <0.1
Mo <0.5
Ca <0.05
V <0.1 balance Fe apart from impurities; and b) fulfilling at least one of the following conditions:
TS tensile strength (Rm) 1100 - 1300 MPa
YS yield strength (Rpo.2) 900 - 1100 MPa
YR yield ratio (Rpo.2/ Rm) > 0.70
bendability (Ri/t)
HER > 20.
11. The cold roll strip or sheet according to claim 1 , a) having a composition comprising of (in wt. %):
C 0.10 - 0.20
Mn 2.0 - 3.0
Cr 0.1 - 0.5
Si 0.2 - 0.9
Al 0.01 - 0.5
Si + Al > 0.1
Si + Al + Cr > 0.4
Nb < 0.1
Ti < 0.1
Mo < 0.5
Ca < 0.05
V < 0.1 balance Fe apart from impurities; and b) fulfilling at least one of the following conditions:
TS tensile strength (Rm) 900 - 1100 MPa
YS yield strength (Rpo.2) 600 - 800 MPa
YR yield ratio (Rpo.2/ Rm) > 0.65 bendability (Ri/t) < 2.5
HER
12. The cold roll strip or sheet according to any one of the preceding claims, wherein
Al < 0.1.
13. A method of manufacturing of a cold rolled steel strip or sheet according to any one of claims 1-12, comprising the following steps: a) providing a steel slab having a composition according to anyone of the preceding claims b) hot rolling the slab in the austenitic range to a hot rolled strip; c) coiling the hot rolled strip at a coiling temperature in the range of 500 - 540 °C; d) optionally performing scale removal process on the coiled steel strip;
e) batch annealing the coiled strip at a temperature in the range of 500 -650 °C for a duration of 5-30h; f) cold rolling the annealed steel strip with a reduction rate between 35 and 90%; g) further treating the cold rolled steel strip in a Continuously Annealing Line or in a Hot Dip Galvanizing Line, in which the soaking temperature is 800-1000 °C; and h) further cooling the steel strip down to room temperature.
14. The method according to claim 13, fulfilling at least one of the following conditions:
- in step b) reheating the slab to a temperature between 1000 °C and 1280 °C, rolling the slab completely in the austenitic range wherein the hot rolling finishing temperature is greater than or equal to 850 °C to obtain the hot rolled steel strip;
- in step e) batch annealing in the range of 550-650 °C; and
- in step g) a holding temperature is 200-500 °C, preferably 350 - 450°C, for a time of 150 to 1000 s.
15. The method according to claim 13 or 14, wherein the soaking temperature in step g) is in the range of 830-900 °C.
16. The method according to any one of claim 13-15, wherein the soaking temperature in step g) is above AC3 as defined by: AC3= 910-203*C1/2 - 15.2 Ni - 30 Mn + 44.7 Si +104 V +31.5 Mo + 13.1 W.
17. The method according claim 16, wherein the soaking temperature in step g) is above AC3 +20 °C.
18. The method according claim 16, wherein the soaking temperature in step g) is above AC3 +30 °C.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE2051557A SE545210C2 (en) | 2020-12-23 | 2020-12-23 | Coiling temperature influenced cold rolled strip or steel |
PCT/EP2021/087596 WO2022136683A1 (en) | 2020-12-23 | 2021-12-23 | Coiling temperature influenced cold rolled strip or steel |
Publications (1)
Publication Number | Publication Date |
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EP4267777A1 true EP4267777A1 (en) | 2023-11-01 |
Family
ID=80050623
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Application Number | Title | Priority Date | Filing Date |
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EP21848255.2A Pending EP4267777A1 (en) | 2020-12-23 | 2021-12-23 | Coiling temperature influenced cold rolled strip or steel |
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US (1) | US20240229183A9 (en) |
EP (1) | EP4267777A1 (en) |
KR (1) | KR20230129178A (en) |
CN (1) | CN116867923A (en) |
SE (1) | SE545210C2 (en) |
WO (1) | WO2022136683A1 (en) |
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FR2833617B1 (en) * | 2001-12-14 | 2004-08-20 | Usinor | METHOD FOR MANUFACTURING VERY HIGH STRENGTH COLD ROLLED SHEET OF MICRO-ALLOY DUAL STEEL |
UA112771C2 (en) | 2011-05-10 | 2016-10-25 | Арселормітталь Інвестігасьон І Десароло Сл | STEEL SHEET WITH HIGH MECHANICAL STRENGTH, PLASTICITY AND FORMATION, METHOD OF MANUFACTURING AND APPLICATION OF SUCH SHEETS |
EP3128023B1 (en) * | 2014-03-31 | 2018-12-26 | JFE Steel Corporation | High-yield-ratio high-strength cold rolled steel sheet and production method therefor |
CA2947382C (en) * | 2014-04-15 | 2022-07-12 | Thyssenkrupp Steel Europe Ag | Method for producing a cold-rolled flat steel product with high yield strength and flat cold-rolled steel product |
WO2017109541A1 (en) * | 2015-12-21 | 2017-06-29 | Arcelormittal | Method for producing a high strength coated steel sheet having improved ductility and formability, and obtained coated steel sheet |
WO2017109540A1 (en) * | 2015-12-21 | 2017-06-29 | Arcelormittal | Method for producing a high strength steel sheet having improved ductility and formability, and obtained steel sheet |
JP6384623B2 (en) * | 2016-08-10 | 2018-09-05 | Jfeスチール株式会社 | High strength steel plate and manufacturing method thereof |
BR112019001901A2 (en) * | 2016-08-16 | 2019-05-07 | Nippon Steel & Sumitomo Metal Corporation | hot formed part |
WO2018115933A1 (en) * | 2016-12-21 | 2018-06-28 | Arcelormittal | High-strength cold rolled steel sheet having high formability and a method of manufacturing thereof |
WO2019122963A1 (en) | 2017-12-19 | 2019-06-27 | Arcelormittal | Cold rolled and heat treated steel sheet and a method of manufacturing thereof |
MX2020009652A (en) * | 2018-03-19 | 2020-10-08 | Nippon Steel Corp | High-strength cold-rolled steel sheet and manufacturing method therefor. |
US11753693B2 (en) * | 2018-09-28 | 2023-09-12 | Posco Co., Ltd | High-strength cold rolled steel sheet having high hole expansion ratio, highstrength hot-dip galvanized steel sheet, and manufacturing methods therefor |
US20220112575A1 (en) * | 2019-01-22 | 2022-04-14 | Voestalpine Stahl Gmbh | A high strength high ductility complex phase cold rolled steel strip or sheet |
ES2889200T3 (en) * | 2019-01-22 | 2022-01-11 | Voestalpine Stahl Gmbh | High strength and high ductility cold rolled complex phase steel strip or sheet |
-
2020
- 2020-12-23 SE SE2051557A patent/SE545210C2/en unknown
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2021
- 2021-12-23 CN CN202180093344.XA patent/CN116867923A/en active Pending
- 2021-12-23 WO PCT/EP2021/087596 patent/WO2022136683A1/en active Application Filing
- 2021-12-23 EP EP21848255.2A patent/EP4267777A1/en active Pending
- 2021-12-23 KR KR1020237025167A patent/KR20230129178A/en unknown
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CN116867923A (en) | 2023-10-10 |
US20240132989A1 (en) | 2024-04-25 |
SE545210C2 (en) | 2023-05-23 |
SE2051557A1 (en) | 2022-06-24 |
KR20230129178A (en) | 2023-09-06 |
WO2022136683A1 (en) | 2022-06-30 |
US20240229183A9 (en) | 2024-07-11 |
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