EP3159424A1 - Rebar and preparation method thereof - Google Patents
Rebar and preparation method thereof Download PDFInfo
- Publication number
- EP3159424A1 EP3159424A1 EP14895253.4A EP14895253A EP3159424A1 EP 3159424 A1 EP3159424 A1 EP 3159424A1 EP 14895253 A EP14895253 A EP 14895253A EP 3159424 A1 EP3159424 A1 EP 3159424A1
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- EP
- European Patent Office
- Prior art keywords
- steel
- temperature
- less
- rolling
- rebar
- Prior art date
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- 238000002360 preparation method Methods 0.000 title 1
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 424
- 239000010959 steel Substances 0.000 claims abstract description 424
- 238000005260 corrosion Methods 0.000 claims abstract description 88
- 230000007797 corrosion Effects 0.000 claims abstract description 87
- 239000004615 ingredient Substances 0.000 claims abstract description 53
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 44
- 239000012535 impurity Substances 0.000 claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 claims abstract description 28
- 238000005096 rolling process Methods 0.000 claims description 131
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 118
- 238000000034 method Methods 0.000 claims description 71
- 238000006477 desulfuration reaction Methods 0.000 claims description 64
- 230000023556 desulfurization Effects 0.000 claims description 64
- 238000001816 cooling Methods 0.000 claims description 62
- 238000010079 rubber tapping Methods 0.000 claims description 61
- 238000009749 continuous casting Methods 0.000 claims description 57
- 238000006392 deoxygenation reaction Methods 0.000 claims description 56
- 229910052717 sulfur Inorganic materials 0.000 claims description 56
- 229910052742 iron Inorganic materials 0.000 claims description 54
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 51
- 229910052799 carbon Inorganic materials 0.000 claims description 50
- 238000007670 refining Methods 0.000 claims description 50
- 238000005275 alloying Methods 0.000 claims description 47
- 229910052748 manganese Inorganic materials 0.000 claims description 47
- 239000002893 slag Substances 0.000 claims description 44
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 43
- 239000011593 sulfur Substances 0.000 claims description 43
- 230000008569 process Effects 0.000 claims description 37
- 229910052710 silicon Inorganic materials 0.000 claims description 34
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 33
- 229910052760 oxygen Inorganic materials 0.000 claims description 33
- 239000001301 oxygen Substances 0.000 claims description 33
- 229910052804 chromium Inorganic materials 0.000 claims description 31
- 238000010438 heat treatment Methods 0.000 claims description 31
- 238000007664 blowing Methods 0.000 claims description 30
- 238000005266 casting Methods 0.000 claims description 29
- 238000005261 decarburization Methods 0.000 claims description 28
- 238000003756 stirring Methods 0.000 claims description 28
- 229910052750 molybdenum Inorganic materials 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 229910052698 phosphorus Inorganic materials 0.000 claims description 26
- 230000001681 protective effect Effects 0.000 claims description 26
- 229910052718 tin Inorganic materials 0.000 claims description 26
- 229910000859 α-Fe Inorganic materials 0.000 claims description 24
- 238000012360 testing method Methods 0.000 claims description 19
- 229910001563 bainite Inorganic materials 0.000 claims description 18
- 229910045601 alloy Inorganic materials 0.000 claims description 16
- 239000000956 alloy Substances 0.000 claims description 16
- 238000003723 Smelting Methods 0.000 claims description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 13
- 229910000805 Pig iron Inorganic materials 0.000 claims description 13
- 239000011261 inert gas Substances 0.000 claims description 13
- 239000011574 phosphorus Substances 0.000 claims description 13
- 150000002910 rare earth metals Chemical class 0.000 claims description 13
- 239000007789 gas Substances 0.000 claims description 12
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 238000007654 immersion Methods 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 230000001965 increasing effect Effects 0.000 abstract description 14
- 239000011150 reinforced concrete Substances 0.000 abstract description 8
- 239000013535 sea water Substances 0.000 abstract description 6
- 239000011651 chromium Substances 0.000 description 58
- 239000010936 titanium Substances 0.000 description 22
- 238000007667 floating Methods 0.000 description 21
- 238000012545 processing Methods 0.000 description 13
- 230000002829 reductive effect Effects 0.000 description 13
- 238000005728 strengthening Methods 0.000 description 12
- 238000004925 denaturation Methods 0.000 description 11
- 230000036425 denaturation Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 10
- 229910000640 Fe alloy Inorganic materials 0.000 description 10
- 241000209094 Oryza Species 0.000 description 10
- 235000007164 Oryza sativa Nutrition 0.000 description 10
- 235000011941 Tilia x europaea Nutrition 0.000 description 10
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 10
- 239000010436 fluorite Substances 0.000 description 10
- 239000010903 husk Substances 0.000 description 10
- 239000004571 lime Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- 235000009566 rice Nutrition 0.000 description 10
- 229910052720 vanadium Inorganic materials 0.000 description 9
- 239000006104 solid solution Substances 0.000 description 7
- 229910052719 titanium Inorganic materials 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 229910000975 Carbon steel Inorganic materials 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000010962 carbon steel Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000004567 concrete Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910001566 austenite Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
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- 230000001590 oxidative effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- 229910017888 Cu—P Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- CYKMNKXPYXUVPR-UHFFFAOYSA-N [C].[Ti] Chemical class [C].[Ti] CYKMNKXPYXUVPR-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- GVEHJMMRQRRJPM-UHFFFAOYSA-N chromium(2+);methanidylidynechromium Chemical compound [Cr+2].[Cr]#[C-].[Cr]#[C-] GVEHJMMRQRRJPM-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910003470 tongbaite Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
Images
Classifications
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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
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/525—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length for wire, for rods
-
- 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
- C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D11/00—Continuous casting of metals, i.e. casting in indefinite lengths
- B22D11/001—Continuous casting of metals, i.e. casting in indefinite lengths of specific alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C1/00—Refining of pig-iron; Cast iron
- C21C1/02—Dephosphorising or desulfurising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
- C21C5/30—Regulating or controlling the blowing
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/04—Removing impurities by adding a treating agent
- C21C7/06—Deoxidising, e.g. killing
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/04—Removing impurities by adding a treating agent
- C21C7/064—Dephosphorising; Desulfurising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/04—Removing impurities by adding a treating agent
- C21C7/068—Decarburising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/10—Handling in a vacuum
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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
- C21D8/06—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires
- C21D8/065—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires 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
- C21D8/06—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires
- C21D8/08—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires for concrete reinforcement
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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
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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- 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
- C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
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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
- C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
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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
- C22C38/008—Ferrous alloys, e.g. steel alloys containing tin
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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
- C22C38/18—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
- C22C38/28—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
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
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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
- C21D2211/005—Ferrite
Definitions
- the present invention relates to a steel rebar and a production method thereof, which pertains to the field of alloy steel.
- the first way is applying organic or inorganic coatings onto carbon steel rebar
- the second way is alloying or various processing techniques to obtain steel rebar materials with excellent corrosion resistance performance.
- coated corrosion resistant steel rebar products epoxy coated steel rebar is researched earliest and used most widely, however, epoxy coated steel rebar has essential disadvantages reflected as: the coating has high brittleness, and is easily damaged and shed off during transporting and processing; defects in the coating might cause concentrated corrosion which leads to severe local corrosion; the bond stress between epoxy coated steel rebar and concrete is reduced as compared to ordinary steel rebar, etc.
- Citri patent literature CN102605255A disclosed a 400MPa level corrosion resistant steel rebar comprising element ingredients of: 0.1%-0.25% of C, 0.5%-0.90% of Si, 0.7%-1.5% of Mn, 0.04%-0.09% of P, 0.015% or less of S, 0.3%-0.6% of Cu, 0.1%-0.4% of Ni, 0.1% of Cr, and 0.03% ⁇ 0.08% of V. Its corrosion resistance performance is increased by 2 times compared to ordinary steel rebar, but the increment is still too limited to meet the service life requirement of 50-100 years for oceanic reinforced concrete structures.
- a technical problem to be solved by the present invention is to overcome the technical defects in prior art that steel rebar has poor corrosion resistance performance in ocean environment and cannot meet the designed service life of reinforced concrete structures, by providing a steel rebar with excellent corrosion resistance performance and comprehensive mechanical properties as well as a production method thereof.
- the present invention provides a steel rebar comprising the following ingredients calculated in weight percentage:
- a steel rebar with a 400MPa level yield strength comprising the following ingredients calculated in weight percentage:
- a steel rebar with a 500MPa level yield strength comprising the following ingredients calculated in weight percentage:
- a steel rebar with a 600MPa level yield strength comprising the following ingredients calculated in weight percentage:
- the steel rebar has a microscopic structure composed of ferrite and bainite, with the ferrite accounting for a percentage of 50%-70%.
- the steel rebar has a ratio of tensile strength to yield strength at greater than 1.25, a maximum stress total elongation percentage greater than 9%, an after-fracture elongation percentage greater than 18%, a corrosion rate by cyclic immersion corrosion test at less than 0.45m 2 h, and a corrosion rate by salt spray corrosion test at less than 0.45m 2 h.
- the present invention also provides a production method of steel rebar comprising the following steps:
- Step S2 the steel for steel tapping has a temperature no higher than 1690°C.
- Step S4 the decarburization by blowing oxygen is performed at a temperature no lower than 1605°C during refining in the RH vacuum refining furnace, the deoxygenation is performed at a temperature no lower than 1575°C during refining in the LF furnace to control the oxygen content at 0.002%-0.005%, the soft stirring is performed for a duration no less than 5min, and the temperature of the molten steel is raised to 1570-1600°C.
- Step S6 the continuous casting slab is heated to 1100-1200°C in the heating furnace, the temperature when the rolled steel is initially placed onto the cooling bed is 900-960°C, the start rolling temperature before the rough rolling is 1030-1100°C, and the temperature during the precision rolling is 950-1050°C.
- C is an important strengthening element mainly existing in the form of carbide to provide functions of precipitation hardening and crystal grain refining.
- C has a strong affinity with Cr, and may form a series of complicated carbides with Cr. The formation of such carbides would reduce corrosion resistance of steel at the same time of increasing hardness of steel. Furthermore, too much content of C would reduce plasticity and toughness of steel, thus deteriorating welding performance of steel.
- Si is an important reducing agent and deoxidizing agent, and when added into steel, Si can significantly increase elastic limit, yield point and tensile strength of steel. When Si is combined with Mo, W, Cr, etc., it has certain function to increase corrosion resistance and oxidation resistance. But increasing the content of Si would reducing welding performance of steel.
- Mn is a good deoxidizing agent and desulfurizing agent, provides a function of solid solution strengthening in steel, is an important strengthening element, and at the same time is an austenite forming element.
- too much content of Mn would significantly increase hardenability of steel, thus reducing plasticity and weldability of steel.
- the function of Mn is not notable.
- S and P are harmful impurity elements during steelmaking process, because they easily form harmful inclusions in steel, which reduces toughness and plasticity of steel.
- Some weathering resistant steel adopts an ingredient design of Cu-P system. but the increment of its corrosion resistance is limited, while P easily forms segregation at grain boundaries which increases brittleness of steel. Therefore, the present invention adopts very low contents of S and P within a range no more than 0.01%.
- Cr is an important element which increases oxidation resistance and corrosion resistance, and by forming a stable passive film on the steel surface under suitable environmental conditions, Cr can increase corrosion resistance performance of steel.
- the function of Cr in a non-oxidative medium is not as notable as Mo or Ni. Solely adding Cr element cannot greatly enhance sea water corrosion resistance performance of steel, but instead would increase susceptibility to pitting corrosion tendency.
- Mo may generally increase corrosion resistance performance of steel, by causing passivation of the steel surface in both reductive acids and strong oxidative salt solutions, and Mo can also prevent steel from pitting corrosion in chloride solutions.
- Mo When the content of Mo is relatively high (>3%), oxidation resistance of steel deteriorates.
- Mo In the aspect of structure property, Mo can promote crystal grain refining and increase hardenability and heat resistance of steel.
- Sn is a corrosion resistant metal which does not oxidize in air at normal temperature and, when heated intensely, stabilizes by forming stannic oxide protective film on its surface. In addition, Sn is stable towards water, can slowly dissolve in a dilute acid, and quickly dissolves in a concentrated acid. Sn is mainly used for manufacturing alloy and producing tin plates. When added as an alloying element to form a solid solution in a matrix, Sn can increase the electrode potential of the matrix, reduce the driving force of electrochemical corrosion of steel itself, lower the corrosion rate, and also cause an increasing tendency of strength and hardness of steel. When Sn interacts with Cr and Mo, they can significantly increase corrosion resistance performance of steel.
- Rare Earth element may notably increase the overall corrosion resistance performance of steel when added into steel at a proper amount.
- the important materialogy reasons for improvement on corrosion resistance performance of steel includes the functions of Rare Earth element in purifying molten steel, metamorphic inclusions, and improving microstructure conditions and grain boundary conditions. Solid solutions of Rare Earth element in steel can increase the polarization resistance and self-corrosion potential of steel matrix, which is beneficial for increasing corrosion resistance performance of steel matrix.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- the present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- Table 2 shows the effects about mechanical properties of Embodiment 1-10 and comparison examples 1-3.
- Table 3 shows the effects about corrosion resistance performance of Embodiment 1-10 and comparison examples 1-3.
- Table 2 Effects about mechanical properties R 0.2 /MPa R m /MPa A/% R m / R 0.2 A gt /% Embodiment 1 432 627 24.5 1.45 11.8 Embodiment 2 408 613 25.3 1.50 12.6 Embodiment 3 482 696 24.5 1.44 11.1 Embodiment 4 561 728 18.9 1.30 10.8 Embodiment 5 611 793 19.6 1.29 10.5 Embodiment 6 554 755 20.8 1.36 10.3 Embodiment 7 524 716 21.2 1.37 10.7 Embodiment 8 523 743 25.0 1.42 11.3 Embodiment 9 536 729 21.0 1.36 10.7 Embodiment 10 621 795 18.0 1.28 9.5 Comparison Example 1 435 632 22.0 1.45 12.0 Comparison Example 2 486
- V and/or Ti elements are added into steel rebar, and it can be seen from Table 2, the adding of V and/or Ti elements improves the yield strength and tensile strength of steel rebar, and at the same time, the after-fracture elongation percentage is greater than 18%, the ratio of tensile strength to yield strength is greater than 1.25, and the maximum stress total elongation percentage is greater than 9%, thereby endowing the steel product with good anti-knock performance.
- the steel rebar of the present invention by reasonably designing the ingredients and accurately controlling the element ingredients and temperature during the smelting process, in combination with the technique of controlled rolling and controlled cooling, the steel rebar is made to obtain a microstructure of bainite plus ferrite (with the ferrite accounting for a percentage of 50%-70%) as shown in FIG. 1 , thereby endowing the steel rebar with excellent comprehensive mechanical properties as well as excellent corrosion resistance performance which is increased by more than 6 times compared to ordinary steel rebar, so that the service life requirement of reinforced concrete structures in oceanographic engineering can be fulfilled.
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Abstract
Description
- The present invention relates to a steel rebar and a production method thereof, which pertains to the field of alloy steel.
- Along with consciousness enhancing of ocean strategy of various countries and development of modern ocean science and technology, constructions of infrastructure such as huge cross-river or cross-sea bridges, seaport wharfs, and offshore buildings are entering into a peak season. Meanwhile, the durability problem of steel rebar used as a main structural material becomes increasingly prominent. The ocean environment is a relatively harsh corrosion environment in the nature, with its special conditions of high temperature, high humidity, and high salinity easily causing corrosion of steel. Severe corrosion usually occurs in the reinforced concrete structures along the coast of China after 10-15 years on service, which results in damage to the structures, rendering the structures unable to meet their designed service life of 50 years.
- There are two major ways to increase the corrosion resistance performance of steel rebar in a concrete structure: the first way is applying organic or inorganic coatings onto carbon steel rebar, while the second way is alloying or various processing techniques to obtain steel rebar materials with excellent corrosion resistance performance. Among coated corrosion resistant steel rebar products, epoxy coated steel rebar is researched earliest and used most widely, however, epoxy coated steel rebar has essential disadvantages reflected as: the coating has high brittleness, and is easily damaged and shed off during transporting and processing; defects in the coating might cause concentrated corrosion which leads to severe local corrosion; the bond stress between epoxy coated steel rebar and concrete is reduced as compared to ordinary steel rebar, etc. In European and American countries, in order to allow the service life of structures to reach the design requirement of 100 years, stainless steel rebar is developed, and because the critical concentration causing its corrosion is increased a lot compared to ordinary steel rebar, the durability of concrete structures is greatly increased. But its cost is expensive, at about 6-10 times that of ordinary carbon steel rebar, therefore, it cannot be used for large scale application in engineering, and is normally used only at key positions of structures or in relatively harsh environments. Furthermore, macro cell corrosion easily occurs when stainless steel rebar is overlapped with ordinary steel rebar, which also adversely affect the service life of structures.
- Research and development of non-rebar low alloy corrosion resistant steel is relatively mature both at home and abroad. Marine Steel is developed in U. S. in 1950s, APS20A Steel is developed in France in 1960s, and sea water corrosion resistant 10CrMoAl steel is developed in China in 1970s. Corrosion resistance performances of these steels are enhanced to a great extent compared to ordinary carbon steel, but they still cannot meet the prolonged service life required in reinforced concrete structures. Therefore, all of these types of steels cannot be used in oceanic reinforced concrete structures.
- Chinese patent literature
CN102605255A disclosed a 400MPa level corrosion resistant steel rebar comprising element ingredients of: 0.1%-0.25% of C, 0.5%-0.90% of Si, 0.7%-1.5% of Mn, 0.04%-0.09% of P, 0.015% or less of S, 0.3%-0.6% of Cu, 0.1%-0.4% of Ni, 0.1% of Cr, and 0.03%∼0.08% of V. Its corrosion resistance performance is increased by 2 times compared to ordinary steel rebar, but the increment is still too limited to meet the service life requirement of 50-100 years for oceanic reinforced concrete structures. - Therefore, a technical problem to be solved by the present invention is to overcome the technical defects in prior art that steel rebar has poor corrosion resistance performance in ocean environment and cannot meet the designed service life of reinforced concrete structures, by providing a steel rebar with excellent corrosion resistance performance and comprehensive mechanical properties as well as a production method thereof.
- In order to solve the above-mentioned technical problem, the present invention provides a steel rebar comprising the following ingredients calculated in weight percentage:
- 0.005%-0.030% of C,
- 0.3%-0.6% of Si,
- 1.2%-2.5% of Mn,
- 0.01% or less of P,
- 0.01% or less of S,
- 8.0%-10.0% of Cr,
- 1.0%-3.0% of Mo,
- 0.2%-0.4% of Sn,
- 0.01%-0.05% of Rare Earth element, and
- the remainder being Fe and unavoidable impurities.
- Preferably, there is provided a steel rebar with a 400MPa level yield strength comprising the following ingredients calculated in weight percentage:
- 0.005%-0.030% of C,
- 0.3%-0.6% of Si,
- 1.2%-1.8% of Mn,
- 0.01% or less of P,
- 0.01% or less of S,
- 8.0%-10.0% of Cr,
- 1.0%-1.6% of Mo,
- 0.2%-0.4% of Sn,
- 0.01%-0.05% of Rare Earth element, and
- the remainder being Fe and unavoidable impurities.
- There is provided a steel rebar comprising the following ingredients calculated in weight percentage:
- 0.005%-0.030% of C,
- 0.3%-0.6% of Si,
- 1.2%-2.5% of Mn,
- 0.01% or less of P,
- 0.01% or less of S,
- 8.0%-10.0% of Cr,
- 1.0%-3.0% of Mo,
- 0.2%-0.4% of Sn,
- 0.01%-0.05% of Rare Earth element,
- 0.04%-0.18% of V and/or 0.010%-0.030% of Ti,
- and the remainder being Fe and unavoidable impurities.
- Preferably, there is provided a steel rebar with a 500MPa level yield strength comprising the following ingredients calculated in weight percentage:
- 0.005%-0.030% of C,
- 0.3%-0.6% of Si,
- 1.7%-2.5% of Mn,
- 0.01% or less of P,
- 0.01% or less of S,
- 8.0%-10.0% of Cr,
- 1.5%-2.0% of Mo,
- 0.2%-0.4% of Sn,
- 0.01%-0.05% of Rare Earth element,
- 0.04%-0.08% of V, and
- the remainder being Fe and unavoidable impurities.
- More preferably, there is provided a steel rebar with a 600MPa level yield strength comprising the following ingredients calculated in weight percentage:
- 0.005%-0.030% of C,
- 0.3%-0.6% of Si,
- 1.7%-2.5% of Mn,
- 0.01% or less of P,
- 0.01% or less of S,
- 8.0%-10.0% of Cr,
- 1.8%-3.0% of Mo,
- 0.2%-0.4% of Sn,
- 0.01%-0.05% of Rare Earth element,
- 0.10%-0.18% of V,
- 0.010%-0.030% of Ti, and
- the remainder being Fe and unavoidable impurities.
- The steel rebar has a microscopic structure composed of ferrite and bainite, with the ferrite accounting for a percentage of 50%-70%.
the steel rebar has a ratio of tensile strength to yield strength at greater than 1.25, a maximum stress total elongation percentage greater than 9%, an after-fracture elongation percentage greater than 18%, a corrosion rate by cyclic immersion corrosion test at less than 0.45m2h, and a corrosion rate by salt spray corrosion test at less than 0.45m2h. - Moreover, the present invention also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron to control the sulfur content at no more than 0.01%;
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping;
- S3: performing steel tapping, during the process of which, alloying elements of Si and Mn are added for deoxygenation and carbon powder and slag former are also added;
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen in an RH vacuum refining furnace so as to control the Cr and C contents within the required range; performing deoxygenation with an LF furnace, adding the required alloying elements of Mn, Mo, Sn, Rare Earth, as well as V and/or Ti, into the steel after deoxygenation, and then adding calcium-ferrum alloy under soft stirring by blowing inert gas, so as to control contents of these elements within the required range; raising the temperature of the molten steel and adding a cover agent;
- S5: performing continuous casting, by casting the molten steel under protective casting with a continuous casting machine to form a continuous casting slab;
- S6: performing rolling, by heating the continuous casting slab to a temperature higher than its austenitization temperature in a heating furnace, rough rolling, moderate rolling, precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling, so as to produce a finished product of steel rebar with the required ingredients.
- In Step S2, the steel for steel tapping has a temperature no higher than 1690°C.
- In Step S4, the decarburization by blowing oxygen is performed at a temperature no lower than 1605°C during refining in the RH vacuum refining furnace, the deoxygenation is performed at a temperature no lower than 1575°C during refining in the LF furnace to control the oxygen content at 0.002%-0.005%, the soft stirring is performed for a duration no less than 5min, and the temperature of the molten steel is raised to 1570-1600°C.
- In Step S6, the continuous casting slab is heated to 1100-1200°C in the heating furnace, the temperature when the rolled steel is initially placed onto the cooling bed is 900-960°C, the start rolling temperature before the rough rolling is 1030-1100°C, and the temperature during the precision rolling is 950-1050°C.
- In the steel, C is an important strengthening element mainly existing in the form of carbide to provide functions of precipitation hardening and crystal grain refining. However, C has a strong affinity with Cr, and may form a series of complicated carbides with Cr. The formation of such carbides would reduce corrosion resistance of steel at the same time of increasing hardness of steel. Furthermore, too much content of C would reduce plasticity and toughness of steel, thus deteriorating welding performance of steel.
- Si is an important reducing agent and deoxidizing agent, and when added into steel, Si can significantly increase elastic limit, yield point and tensile strength of steel. When Si is combined with Mo, W, Cr, etc., it has certain function to increase corrosion resistance and oxidation resistance. But increasing the content of Si would reducing welding performance of steel.
- Mn is a good deoxidizing agent and desulfurizing agent, provides a function of solid solution strengthening in steel, is an important strengthening element, and at the same time is an austenite forming element. However, too much content of Mn would significantly increase hardenability of steel, thus reducing plasticity and weldability of steel. In the aspect of corrosion resistance performance, the function of Mn is not notable.
- S and P are harmful impurity elements during steelmaking process, because they easily form harmful inclusions in steel, which reduces toughness and plasticity of steel. Some weathering resistant steel adopts an ingredient design of Cu-P system. but the increment of its corrosion resistance is limited, while P easily forms segregation at grain boundaries which increases brittleness of steel. Therefore, the present invention adopts very low contents of S and P within a range no more than 0.01%.
- Cr is an important element which increases oxidation resistance and corrosion resistance, and by forming a stable passive film on the steel surface under suitable environmental conditions, Cr can increase corrosion resistance performance of steel. However, the function of Cr in a non-oxidative medium is not as notable as Mo or Ni. Solely adding Cr element cannot greatly enhance sea water corrosion resistance performance of steel, but instead would increase susceptibility to pitting corrosion tendency.
- Mo may generally increase corrosion resistance performance of steel, by causing passivation of the steel surface in both reductive acids and strong oxidative salt solutions, and Mo can also prevent steel from pitting corrosion in chloride solutions. When the content of Mo is relatively high (>3%), oxidation resistance of steel deteriorates. In the aspect of structure property, Mo can promote crystal grain refining and increase hardenability and heat resistance of steel.
- Sn is a corrosion resistant metal which does not oxidize in air at normal temperature and, when heated intensely, stabilizes by forming stannic oxide protective film on its surface. In addition, Sn is stable towards water, can slowly dissolve in a dilute acid, and quickly dissolves in a concentrated acid. Sn is mainly used for manufacturing alloy and producing tin plates. When added as an alloying element to form a solid solution in a matrix, Sn can increase the electrode potential of the matrix, reduce the driving force of electrochemical corrosion of steel itself, lower the corrosion rate, and also cause an increasing tendency of strength and hardness of steel. When Sn interacts with Cr and Mo, they can significantly increase corrosion resistance performance of steel.
- Rare Earth element may notably increase the overall corrosion resistance performance of steel when added into steel at a proper amount. The important materialogy reasons for improvement on corrosion resistance performance of steel includes the functions of Rare Earth element in purifying molten steel, metamorphic inclusions, and improving microstructure conditions and grain boundary conditions. Solid solutions of Rare Earth element in steel can increase the polarization resistance and self-corrosion potential of steel matrix, which is beneficial for increasing corrosion resistance performance of steel matrix.
- Compared to prior art, the aforementioned technical solution of the present invention has the following advantages:
- (1) In the steel rebar of the present invention, the content of C is controlled at 0.005%-0.030%, the content of Si is controlled at 0.3%-0.6%, the content of Mn is controlled at 1.2%-2.5%, the contents of impurity elements S and P are both controlled at no more than 0.001%, and 8.0%-10.0% of Cr, 1.0%-3.0% of Mo, 0.01%-0.05% of Rare Earth element are added, accompanied by adding 0.2%-0.4% of Sn. By providing a reasonable ratio of element ingredients, as well as interaction between Cr and Sn, the corrosion resistance performance of the steel product is significantly increased, and the added Mo and Rare Earth element improve pitting corrosion resistance and inter-granular corrosion resistance of the steel product, thereby greatly improving the sea water corrosion resistance performance of the steel rebar and increasing the service life of the steel rebar in sea water.
- (2) In the steel rebar of the present invention, there contains 0.005-0.030% of C, 0.3%-0.6% of Si, 1.2%-1.8% of Mn, 0.01 % or less of P, 0.01 % or less of S, 8.0%-10.0% of Cr, 1.0%-1.6% of Mo, 0.2%-0.4% of Sn, 0.01%-0.05% of Rare Earth element, and the remainder being Fe and unavoidable impurities. By providing a reasonable ingredient design, a 400MPa level corrosion resistant steel rebar is produced, so as to obtain a steel rebar which is low-cost, able to meet requirements of basic mechanical properties, and resistant to sea water corrosion.
- (3) In the steel rebar of the present invention, there contains 0.005%-0.030% of C, 0.3%-0.6% of Si, 1.2%-2.5% of Mn, 0.01 % or less of P, 0.01 % or less of S, 8.0%-10.0% of Cr, 1.0%-3.0% of Mo, 0.2%-0.4% of Sn, 0.01%-0.05% of Rare Earth element, 0.04%-0.18% of V and/or 0.010%-0.030% of Ti, and the remainder being Fe and unavoidable impurities. Micro-alloying elements V and/or Ti are further added into steel. V is a micro-alloying element that can cause a V(C,N) compound to precipitate out during the rolling process, which prevents austenite and ferrite form growing and has relatively strong effects of precipitation strengthening and refined crystalline strengthening as well as certain effect of solid solution strengthening, thereby significantly increase the strength of steel and thus compensating for the defect of insufficient strength due to low carbon content. Ti is a strong forming element of carbonitride with effects of refining crystal grain structure and precipitation strengthening. Meanwhile, because carbon preferentially reacts with Ti to produce carbon titanium compounds, the precipitation of chromium carbide in chromium-containing steel which causes chromium depletion at grain boundaries is avoided, thereby effectively preventing inter-granular corrosion. By solid solution strengthening, refined crystalline strengthening, and precipitation strengthening as V(C,N) and/or Ti(C,N) are produced, the micro-alloying elements V and/or Ti increase the strength of steel and endow the steel rebar with excellent mechanical properties.
- (4) In the steel rebar of the present invention, by controlling the element contents in steel, especially the contents of micro-alloying elements V and/or Ti, steel products that meet various strength requirements are produced. For instance, in a steel rebar with a 500MPa level yield strength, there contains 0.005%-0.030% of C, 0.3%-0.6% of Si, 1.7%-2.5% of Mn, 0.01 % or less of P, 0.01 % or less of S, 8.0%-10.0% of Cr, 1.5%-2.0% of Mo, 0.2%-0.4% of Sn, 0.01%-0.05% of Rare Earth element, 0.04%-0.08% of V, and the remainder being Fe and unavoidable impurities; for another instance, in a steel rebar with a 600MPa level yield strength, there contains 0.005%-0.030% of C, 0.3%-0.6% of Si, 1.7%-2.5% of Mn, 0.01 % or less of P, 0.01 % or less of S, 8.0%-10.0% of Cr, 1.8%-3.0% of Mo, 0.2%-0.4% of Sn, 0.01%-0.05% of Rare Earth element, 0.10%-0.18% of V, 0.010%-0.030% of Ti, and the remainder being Fe and unavoidable impurities.
- (5) In the steel rebar of the present invention, the percentage of ferrite is 50%-70%. While bainite has good strength and toughness, ferrite has better plasticity. By reasonably controlling a ratio of the two phases, the steel rebar can be endowed with excellent comprehensive mechanical properties, wherein, on the basis of obtaining the required yield strength and tensile strength, the after-fracture elongation percentage is greater than 18%, the ratio of tensile strength to yield strength is greater than 1.25, and the maximum stress total elongation percentage is greater than 9%, thereby endowing the steel product with good anti-knock performance.
- (6) The production method of steel rebar of the present invention controls the content of S by a KR desulfurization method, controls the content of P in a convertor, adds alloying elements of Si and Mn during the steel tapping process for deoxygenation and meanwhile adds carbon powder and slag former to create a reductive atmosphere for the refining furnace, carries out decarburization by blowing oxygen in an RH vacuum refining furnace so as to control the contents of carbon and chromium elements, carries out deoxygenation in an LF furnace while adding the remaining alloying elements into steel so as to control the contents of oxygen and various alloying elements, as well as adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, carries out soft stirring to make the ingredients uniformly distributed and remove inclusions, provides protective casting during the continuous casting process so as to control the gas content in steel, to prevent oxidization or secondary inclusions, heats the casting slab to 1100-1200°C before rolling in a heating furnace to ensure austenization and cause the elements therein to sufficiently enter a solid solution state, adopts rough rolling, moderate rolling and precision rolling during rolling can strictly control the deformation amount of the steel when rolled, while the precipitation strengthening effect of micro-alloying elements V(C,N) and/or Ti(C,N) can be brought into full play by controlling the rolling parameters, and places the rolled steel onto a cooling bed for air cooling so as to render the final microstructure of the steel product being bainite and ferrite.
- (7) The production method of steel rebar of the present invention, by controlling the temperature of the steel for steel tapping at no higher than 1690°C, reduces the oxygen content in the steel, increases the element yield, reduces inclusions in the steel, increases the service life of the convertor, increases the quality of steel, and reduces production cost of steel.
- (8) In the production method of steel rebar of the present invention, by controlling the temperature of decarburization by blowing oxygen during refining in the RH vacuum refining furnace to be no lower than 1605°C, the decarburization effect in the RH furnace can be increased, and it also facilitates controlling the contents of carbon and chromium elements in the steel. By controlling the temperature of deoxygenation during refining in the LF furnace, the refinement effect of deoxygenation in the LF furnace can be increased, which facilitates controlling the oxygen content within a predetermined range. And by controlling the oxygen content at 0.002%-0.005% through deoxygenation in the LF furnace, inclusions in the steel can be effectively controlled, and the quality of the steel in improved. By controlling the duration of soft stirring at no less than 5min, the ingredients and temperature of steel can be made more uniformly distributed, and it also facilitates removing the inclusions by floating. By raising the temperature of the molten steel to 1570-1600°C before continuous casting, smooth operation of the continuous casting is ensured.
- (9) In the production method of steel rebar of the present invention, by heating the casting slab to 1100-1200°C in the heating furnace, the steel is heated to a temperature higher than its austenitization temperature, and a solid solution state of the alloying elements in the steel is ensured. By controlling the start rolling temperature at 1030-1100°C and controlling the temperature during the precision rolling at 950-1050°C, precipitation of a strengthening phase can be induced by deformation, so as to increase the strength of the steel. By controlling the temperature when the steel product is initially placed onto the cooling bed, the required microstructure of bainite plus ferrite can be obtained.
- (10) The production method of steel rebar of the present invention, by accurately controlling the element contents and temperature of the molten steel during each procedure, greatly reduces the amount of harmful elements and inclusions in the steel, and improves the quality, mechanical properties and corrosion resistance performance of the steel.
- (11) The steel rebar manufactured by using the steel rebar production method of the present invention, by means of reasonable processing steps, has a microscopic structure composed of ferrite and bainite, with the ferrite accounting for a percentage of 50%-70%. While bainite has good strength and toughness, ferrite has better plasticity. By reasonably controlling a ratio of the two phases, the steel rebar can be endowed with excellent comprehensive mechanical properties, wherein, on the basis of obtaining the required yield strength and tensile strength, the after-fracture elongation percentage is greater than 18%, the ratio of tensile strength to yield strength is greater than 1.25, and the maximum stress total elongation percentage is greater than 9%, thereby endowing the steel product with good anti-knock performance
- In order to make the present invention easy and clear to understand, hereinafter, the present invention will be further described in detail according to specific embodiments of the present invention and with reference to the appended drawings, wherein:
-
FIG. 1 is a microstructure view of a steel rebar of the present invention. -
Table 1 Steel rebar ingredients of Embodiments 1-10 as well as comparison examples 1-3 (wt.%) C Si Mn Cr Mo RE Sn V Ti P S Embodiment 1 0.005 0.60 2.5 9.0 1.0 0.05 0.20 - - <0.01 <0.01 Embodiment 2 0.030 0.45 1.2 10.0 3.0 0.01 0.40 - - <0.01 <0.01 Embodiment 3 0.015 0.30 1.8 8.0 1.6 0.03 0.30 - - <0.01 <0.01 Embodiment 4 0.020 0.5 2.3 8.5 2.2 0.02 0.25 0.04 - <0.01 <0.01 Embodiment 5 0.025 0.55 1.7 8.2 2.3 0.02 0.35 0.18 0.01 <0.01 <0.01 Embodiment 6 0.009 0.35 1.8 8.5 2.5 0.04 0.36 0.1 0.03 <0.01 <0.01 Embodiment 7 0.012 0.40 2.2 9.5 1.5 0.03 0.28 - 0.02 <0.01 <0.01 Embodiment 8 0.012 0.57 1.8 9.7 2.0 0.03 0.21 0.08 - <0.01 <0.01 Embodiment 9 0.018 0.50 1.9 9.0 1.7 0.02 0.30 0.06 - <0.01 <0.01 Embodiment 10 0.026 0.50 2.3 8.1 1.8 0.05 0.40 0.15 0.02 <0.01 <0.01 Comparison Example 1 0.23 0.54 1.5 - - - - - - <0.01 <0.01 Comparison Example 2 0.015 0.48 1.9 9.1 1.8 0.02 0.60 - - <0.01 <0.01 Comparison Example 3 0.024 0.52 2.0 9.8 2.0 0.02 - - - <0.01 <0.01 - The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping step with a steel tapping temperature of 1680°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1605°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1575°C until the oxygen content in the molten steel reaches 40ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 5min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 1 in Table 1; raising the temperature of the molten steel to 1580°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1100°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1030°C and the precision rolling temperature at 950°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 900°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1690°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1625°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1600°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 6min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 2 in Table 1; raising the temperature of the molten steel to 1600°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1200°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1100°C and the precision rolling temperature at 1050°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 960°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1685°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1610°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1585°C until the oxygen content in the molten steel reaches 30ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 6min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 3 in Table 1; raising the temperature of the molten steel to 1570°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1120°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1050°C and the precision rolling temperature at 960°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 910°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1690°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, performed by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1620°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1590°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 6min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 4 in Table 1; raising the temperature of the molten steel to 1585°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1180°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1040°C and the precision rolling temperature at 990°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 950°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1675°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1615°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1580°C until the oxygen content in the molten steel reaches 25ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V, Ti into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 5 in Table 1; raising the temperature of the molten steel to 1580°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1190°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1095°C and the precision rolling temperature at 1030°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 950°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1670°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1610°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1580°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V, Ti into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 6 in Table 1; raising the temperature of the molten steel to 1590°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1185°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1085°C and the precision rolling temperature at 1035°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 955°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1685°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1615°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1580°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, Ti into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 7 in Table 1; raising the temperature of the molten steel to 1585°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1180°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1080°C and the precision rolling temperature at 1020°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 940°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1680°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1610°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1585°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 8 in Table 1; raising the temperature of the molten steel to 1590°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1150°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1065°C and the precision rolling temperature at 1025°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 965°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1675°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1605°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1575°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 9 in Table 1; raising the temperature of the molten steel to 1580°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1105°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1045°C and the precision rolling temperature at 1005°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 945°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- The present embodiment provides a steel rebar, comprising the following elements: C, Si, Mn, P, S, Cr, Mo, Sn, Rare Earth element, V, Ti, Fe and unavoidable impurities, wherein, the weight percentages of the ingredients are as shown in Table 1, the mechanical properties are as shown in Table 2, and the corrosion resistance performance is as shown in Table 3.
- The present embodiment also provides a production method of steel rebar comprising the following steps:
- S1: performing preliminary desulfurization of molten iron by using a KR method to control the sulfur content at no more than 0.01%. Because sulfur element as an impurity element would reduce mechanical properties and corrosion resistance performance of steel and normally cannot be removed in a convertor, therefore, in order to reduce the sulfur content in steel, preliminary desulfurization treatment needs to be performed in molten iron. Before performing desulfurization, the blast furnace slag needs to be removed in order to increase the desulfurization efficiency. A mixture of lime powder and fluorite mixed at a mass ratio of 9:1 is adopted as the desulfurization agent. After still standing of the desulfurated molten iron, the desulfurization residue is removed to prevent it from entering the convertor and causing convertor resulfurization. Thereby, the sulfur content in the steel is ensured to be controlled at less than 0.01%.
- S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping. The convertor is a top and bottom combined blown converter.
- S3: performing steel tapping with a steel tapping temperature of 1685°C. During the steel tapping process, alloying elements of Si and Mn are added for deoxygenation, and carbon powder and slag former are also added. During the operation process of steel tapping, a protective gas is blown into the molten steel for stirring the molten steel at a pressure of 0.5MPa. The fluidity of the molten steel is utilized to make the deoxygenation of the added Si and Mn elements more thoroughly and to facilitate the removal of inclusions by floating. The carbon powder and slag former are added to increase the carbon content of steel and to produce reduced slag, so as to prepare for the subsequent refining procedure outside the convertor.
- S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen at 1620°C in an RH vacuum refining furnace, so that C element is partially removed by the decarburization process, thereby controlling the contents of Cr and C elements within the required range; performing deoxygenation with an LF furnace at 1585°C until the oxygen content in the molten steel reaches 20ppm, and adding the required alloying elements of Mn, Mo, Sn, Rare Earth, V, Ti into the steel after deoxygenation, wherein, while the added alloying elements may be a pure metallic element, normally they are added in the form of iron alloy; and then adding calcium-ferrum alloy to perform denaturation treatment on the inclusions, performing soft stirring by blowing inert gas for 7min to make the ingredients and temperature of the steel uniformly distributed and to facilitate the removal of inclusions by floating, so that the contents of the ingredients are controlled within the ranges as shown in data of Embodiment 10 in Table 1; raising the temperature of the molten steel to 1595°C during a later period of processing with the LF furnace, in order to ensure smooth operation of continuous casting, and then adding a cover agent which usually is carbonized rice husk.
- S5: continuous casting, by casting the molten steel under protective casting with a continuous casting machine to produce small square billets of 150mm×150mm.
- S6: performing rolling, by heating the continuous casting slab to 1195°C in a heating furnace, performing rough rolling, moderate rolling and precision rolling by using a continuous rod and wire rolling machine with the start rolling temperature at 1095°C and the precision rolling temperature at 1045°C, without passing water cooling after precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling until room temperature, thereby producing a finished product of steel rebar as shown in Table 1, wherein, the temperature when the rolled steel is initially placed onto the cooling bed is 955°C. By means of the technique of controlled rolling and controlled cooling, the microstructure of bainite plus ferrite is finally obtained.
- In order to prove the technical effects of the present invention, the following experiments are performed on the steel rebar produced by Embodiment 1-10 and comparison examples 1-3:
- 1. Experimental methods
- 1.1 mechanical property tests: performed according to "GB1499.2-2007, steel used in reinforced concrete, Part II: hot-rolled ribbed rebar". The yield strength (R0.2), tensile strength (Rm), and after-fracture elongation percentage (A) are tested.
- 1.2 corrosion resistance performance tests:
- 1.2.1 cyclic immersion corrosion test: performed according to "corrosion test methods of steel rebar in a chloride ion environment, a draft for consultation" proposed by Steel Industry Association of China and drafted by institutes of Iron and Steel Research Institute and Metallurgical Industry Information Standardization Research Institute.
The test sample is a cylinder of ∮13mm×50mm;
The test solution is a solution of sodium chloride with an initial concentration of (0.34±0.009)mol•L-1 (an initial mass percentage of 2.0%±0.05%). And the specific test conditions are as follows:- Temperature: 45°C±2°C
- Humidity: 70%±10% RH
- PH value of solution: 6.5-7.2
- Test time: 360h
- Each cyclic period: 60 min±5min, with an immersion time of 12 min±2min Highest temperature of test sample surface after baking: 70°C±10°C
- 1.2.2 salt spray corrosion test: performed according to "GBT10125-1997, corrosion tests in an artificial atmosphere, salt spray test".
The test sample is a test plate of 3mm×15mm×40mm;
The test solution is a solution of sodium chloride with a concentration of (50±5)g•L-1 (a mass percentage of 5.0%±0.5%). And the specific test conditions are as follows: Temperature: 35°C±2°C
PH value of solution: 6.5-7.2
Test time: 360h - 2. Experimental results
- Table 2 shows the effects about mechanical properties of Embodiment 1-10 and comparison examples 1-3. Table 3 shows the effects about corrosion resistance performance of Embodiment 1-10 and comparison examples 1-3.
Table 2 Effects about mechanical properties R0.2/MPa Rm/MPa A/% Rm/ R0.2 Agt/% Embodiment 1 432 627 24.5 1.45 11.8 Embodiment 2 408 613 25.3 1.50 12.6 Embodiment 3 482 696 24.5 1.44 11.1 Embodiment 4 561 728 18.9 1.30 10.8 Embodiment 5 611 793 19.6 1.29 10.5 Embodiment 6 554 755 20.8 1.36 10.3 Embodiment 7 524 716 21.2 1.37 10.7 Embodiment 8 523 743 25.0 1.42 11.3 Embodiment 9 536 729 21.0 1.36 10.7 Embodiment 10 621 795 18.0 1.28 9.5 Comparison Example 1 435 632 22.0 1.45 12.0 Comparison Example 2 486 586 13.4 1.21 6.2 Comparison Example 3 477 687 24.8 1.44 11.0 Table 3 Effects about corrosion resistance performance cyclic immersion test salt spray test Corrosion rate (g/m2·h) Relative corrosion rate Increase of corrosion resistance performance (%) Corrosion rate (g/m2·h) Relative corrosion rate Increase of corrosion resistance performance (%) Embodiment 1 0.415 0.127 690 0.411 0.130 666 Embodiment 2 0.191 0.058 1616 0.205 0.065 1437 Embodiment 3 0.419 0.128 682 0.432 0.137 629 Embodiment 4 0.356 0.109 821 0.367 0.117 758 Embodiment 5 0.441 0.135 643 0.445 0.141 608 Embodiment 6 0.349 0.106 839 0.360 0.114 775 Embodiment 7 0.386 0.118 749 0.395 0.125 697 Embodiment 8 0.272 0.083 1105 0.288 0.091 994 Embodiment 9 0.370 0.113 786 0.381 0.121 727 Embodiment 10 0.433 0.132 657 0.435 0.138 624 Comparison Example 1 3.278 1 - 3.150 1 - Comparison Example 2 0.365 0.111 798 0.377 0.120 736 Comparison Example 3 0.456 0.151 561 0.463 0.160 526 (The relative corrosion rates in Table 3 are all compared with Comparison Example 1, by setting the relative corrosion rate of Comparison Example 1 to be 1.000) - As known from Table 3, in Embodiment 1-10, because Cr, Sn, Mo, Rare Earth elements are added, the corrosion resistance performance of steel rebar is increased by more than 600% compared with Comparison Example 1. As can be seen from the corrosion resistance performance data of Comparison Example 3, the increment of the corrosion resistance performance of steel rebar which does not contain Sn element is not as great as that of steel rebar which contains Sn element. By comparing Embodiment 1, 2, 3 and Comparison Example 2, it can be concluded that, when the Sn content is within the range of 0.02-0.04%, along with the increase of the Sn content, the corrosion resistance performance of steel rebar increases, but its yield strength and tensile strength decrease. And when the Sn content surpasses 0.04%, the corrosion resistance performance of steel rebar presents no more notable increment, but the mechanical properties are adversely affected, especially the after-fracture elongation percentage and the maximum stress total elongation percentage decrease significantly, while the ratio of tensile strength to yield strength also considerably decreases. In Embodiments 4-10, V and/or Ti elements are added into steel rebar, and it can be seen from Table 2, the adding of V and/or Ti elements improves the yield strength and tensile strength of steel rebar, and at the same time, the after-fracture elongation percentage is greater than 18%, the ratio of tensile strength to yield strength is greater than 1.25, and the maximum stress total elongation percentage is greater than 9%, thereby endowing the steel product with good anti-knock performance.
- In the steel rebar of the present invention, by reasonably designing the ingredients and accurately controlling the element ingredients and temperature during the smelting process, in combination with the technique of controlled rolling and controlled cooling, the steel rebar is made to obtain a microstructure of bainite plus ferrite (with the ferrite accounting for a percentage of 50%-70%) as shown in
FIG. 1 , thereby endowing the steel rebar with excellent comprehensive mechanical properties as well as excellent corrosion resistance performance which is increased by more than 6 times compared to ordinary steel rebar, so that the service life requirement of reinforced concrete structures in oceanographic engineering can be fulfilled. - Apparently, the aforementioned embodiments are merely examples illustrated for clearly describing the present invention, rather than limiting the implementation ways thereof. For those skilled in the art, various changes and modifications in other different forms can be made on the basis of the aforementioned description. It is unnecessary and impossible to exhaustively list all the implementation ways herein. However, any obvious changes or modifications derived from the aforementioned description are intended to be embraced within the protection scope of the present invention.
Claims (13)
- A steel rebar, characterized in comprising the following ingredients calculated in weight percentage:0.005%-0.030% of C,0.3%-0.6% of Si,1.2%-2.5% of Mn,0.01% or less of P,0.01% or less of S,8.0%-10.0% of Cr,1.0%-3.0% of Mo,0.2%-0.4% of Sn,0.01%-0.05% of Rare Earth element, andthe remainder being Fe and unavoidable impurities.
- The steel rebar in accordance with Claim 1, characterized in comprising the following ingredients calculated in weight percentage:0.005%-0.030% of C,0.3%-0.6% of Si,1.2%-1.8% of Mn,0.01% or less of P,0.01% or less of S,8.0%-10.0% of Cr,1.0%-1.6% of Mo,0.2%-0.4% of Sn,0.01%-0.05% of Rare Earth element, andthe remainder being Fe and unavoidable impurities.
- A steel rebar, characterized in comprising the following ingredients calculated in weight percentage:0.005%-0.030% of C,0.3%-0.6% of Si,1.2%-2.5% of Mn,0.01% or less of P,0.01% or less of S,8.0%-10.0% of Cr,1.0%-3.0% of Mo,0.2%-0.4% of Sn,0.01%-0.05% of Rare Earth element, 0.04%-0.18% of V and/or 0.010%-0.030% of Ti, and the remainder being Fe and unavoidable impurities.
- The steel rebar in accordance with Claim 3, characterized in comprising the following ingredients calculated in weight percentage:0.005%-0.030% of C,0.3%-0.6% of Si,1.7%-2.5% of Mn,0.01% or less of P,0.01% or less of S,8.0%-10.0% of Cr,1.5%-2.0% of Mo,0.2%-0.4% of Sn,0.01%-0.05% of Rare Earth element,0.04%-0.08% of V, andthe remainder being Fe and unavoidable impurities.
- The steel rebar in accordance with Claim 3, characterized in comprising the following ingredients calculated in weight percentage:0.005%-0.030% of C,0.3%-0.6% of Si,1.7%-2.5% of Mn,0.01% or less of P,0.01% or less of S,8.0%-10.0% of Cr,1.8%-3.0% of Mo,0.2%-0.4% of Sn,0.01%-0.05% of Rare Earth element,0.10%-0.18% of V,0.010%-0.030% of Ti, andthe remainder being Fe and unavoidable impurities.
- The steel rebar in accordance with any one of Claims 1-5, characterized in that, the steel rebar has a microscopic structure composed of ferrite and bainite, with the ferrite accounting for a percentage of 50%-70%.
- The steel rebar in accordance with any one of Claims 1-6, characterized in that, the steel rebar has a ratio of tensile strength to yield strength at greater than 1.25, a maximum stress total elongation percentage greater than 9%, an after-fracture elongation percentage greater than 18%, a corrosion rate by cyclic immersion corrosion test at less than 0.45m2h, and a corrosion rate by salt spray corrosion test at less than 0.45m2h.
- A production method of steel rebar, characterized in comprising the following steps:S1: performing preliminary desulfurization of molten iron to control the sulfur content at no more than 0.01%;S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping;S3: performing steel tapping, during the process of which, alloying elements of Si and Mn are added for deoxygenation and carbon powder and slag former are also added;S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen in an RH vacuum refining furnace so as to control the Cr and C contents within the range in accordance with Claim 1 or 2; carrying out deoxygenation with an LF furnace, adding the required alloying elements of Mn, Mo, Sn and Rare Earth into the steel after deoxygenation, and then adding calcium-ferrum alloy under soft stirring by blowing inert gas, so as to control contents of these elements within the range in accordance with Claim 1 or 2; raising the temperature of the molten steel and adding a cover agent;S5: performing continuous casting, by casting the molten steel under protective casting with a continuous casting machine to form a continuous casting slab;S6: performing rolling, by heating the continuous casting slab to a temperature higher than its austenitization temperature in a heating furnace, rough rolling, moderate rolling, precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling, so as to produce a finished product of steel rebar with ingredients in accordance with Claim 1 or 2.
- A production method of steel rebar, characterized in comprising the following steps:S1: performing preliminary desulfurization of molten iron to control the sulfur content at no more than 0.01%;S2: performing smelting in a convertor, by feeding the molten iron processed by Step S1 together with steel scrap and/or pig iron into a convertor to be smelted, thus obtaining steel with a carbon content less than 0.05% and a phosphorus content less than 0.01% for steel tapping;S3: performing steel tapping, during the process of which, alloying elements of Si and Mn are added for deoxygenation and carbon powder and slag former are also added;S4: performing refining outside the convertor, by adding Cr element and meanwhile performing decarburization by blowing oxygen in an RH vacuum refining furnace so as to control the Cr and C contents within the range in accordance with Claim 3 or 4 or 5 or 6; carrying out deoxygenation with an LF furnace, adding the required alloying elements of Mn, Mo, Sn, Rare Earth, as well as V and/or Ti, into the steel after deoxygenation, and then adding calcium-ferrum alloy under soft stirring by blowing inert gas, so as to control contents of these elements within the range in accordance with Claim 3 or 4 or 5 or 6; raising the temperature of the molten steel and adding a cover agent;S5: performing continuous casting, by casting the molten steel under protective casting with a continuous casting machine to form a continuous casting slab;S6: performing rolling, by heating the continuous casting slab to a temperature higher than its austenitization temperature in a heating furnace, rough rolling, moderate rolling, precision rolling, and placing the rolled steel after precision rolling onto a cooling bed for air cooling, so as to produce a finished product of steel rebar with ingredients in accordance with Claim 3 or 4 or 5 or 6.
- The production method in accordance with Claim 8 or 9, characterized in that, in Step S2, the steel for steel tapping has a temperature no higher than 1690°C.
- The production method in accordance with Claim 8 or 9 or 10, characterized in that, in Step S3, a protective gas is blown into the molten steel for stirring during the process of steel tapping.
- The production method in accordance with any one of Claims 8-11, characterized in that, in Step S4, the decarburization by blowing oxygen is performed at a temperature no lower than 1605°C during refining in the RH vacuum refining furnace, the deoxygenation is performed at a temperature no lower than 1575°C during refining in the LF furnace to control the oxygen content at no more than 50ppm, the soft stirring is performed for a duration no less than 5min, and the temperature of the molten steel is raised to 1570-1600°C.
- The production method in accordance with any one of Claims 8-12, characterized in that, in Step S6, the continuous casting slab is heated to 1100-1200°C in the heating furnace, the start rolling temperature before the rough rolling is 1030-1100°C, the temperature during the precision rolling is 950-1050°C, and the temperature when the rolled steel is initially placed onto the cooling bed is 900-960°C.
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2014
- 2014-06-18 CN CN201410273604.3A patent/CN104018091B/en active Active
- 2014-06-27 EP EP14895253.4A patent/EP3159424B1/en active Active
- 2014-06-27 KR KR1020167011662A patent/KR101828856B1/en active IP Right Grant
- 2014-06-27 WO PCT/CN2014/080994 patent/WO2015192391A1/en active Application Filing
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CN111945079A (en) * | 2020-07-31 | 2020-11-17 | 阳春新钢铁有限责任公司 | Ultra-high pulling speed niobium-containing HRB500E deformed steel bar and production process thereof |
CN113737081A (en) * | 2021-08-31 | 2021-12-03 | 中国科学院上海应用物理研究所 | Stainless steel smelting method, stainless steel modification method and stainless steel |
CN113737081B (en) * | 2021-08-31 | 2022-04-01 | 中国科学院上海应用物理研究所 | Stainless steel smelting method, stainless steel modification method and stainless steel |
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Publication number | Publication date |
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CN104018091B (en) | 2016-11-23 |
WO2015192391A1 (en) | 2015-12-23 |
CN104018091A (en) | 2014-09-03 |
KR101828856B1 (en) | 2018-02-13 |
EP3159424A4 (en) | 2017-11-15 |
US20170029919A1 (en) | 2017-02-02 |
KR20160065192A (en) | 2016-06-08 |
EP3159424B1 (en) | 2019-04-24 |
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