EP4279626A1 - 400 mpa-grade corrosion-resistant steel bar and production method therefor - Google Patents

400 mpa-grade corrosion-resistant steel bar and production method therefor Download PDF

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Publication number
EP4279626A1
EP4279626A1 EP21918802.6A EP21918802A EP4279626A1 EP 4279626 A1 EP4279626 A1 EP 4279626A1 EP 21918802 A EP21918802 A EP 21918802A EP 4279626 A1 EP4279626 A1 EP 4279626A1
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EP
European Patent Office
Prior art keywords
working procedure
steel
steel bar
corrosion
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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EP21918802.6A
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German (de)
English (en)
French (fr)
Inventor
Han Ma
Yun ZHOU
Jiaqi ZHAO
Yu Zhang
Huande CHEN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Institute Of Research Of Iron And Steel Jiangsu Province/sha Steel Co Ltd Cn
Jiangsu Shagang Group Co Ltd
Original Assignee
Institute Of Research Of Iron And Steel Jiangsu Province/sha Steel Co Ltd Cn
Jiangsu Shagang Group Co Ltd
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Application filed by Institute Of Research Of Iron And Steel Jiangsu Province/sha Steel Co Ltd Cn, Jiangsu Shagang Group Co Ltd filed Critical Institute Of Research Of Iron And Steel Jiangsu Province/sha Steel Co Ltd Cn
Publication of EP4279626A1 publication Critical patent/EP4279626A1/en
Pending legal-status Critical Current

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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
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • 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
    • C21D9/08—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for tubular bodies or pipes
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21B—ROLLING OF METAL
    • B21B1/00—Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
    • B21B1/16—Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling wire rods, bars, merchant bars, rounds wire or material of like small cross-section
    • B21B1/18—Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling wire rods, bars, merchant bars, rounds wire or material of like small cross-section in a continuous process
    • 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
    • C21C7/0006—Adding metallic additives
    • 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
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/84—Controlled slow cooling
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/002—Heat treatment of ferrous alloys containing Cr
    • C—CHEMISTRY; METALLURGY
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    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/004—Heat treatment of ferrous alloys containing Cr and Ni
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    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/005—Heat treatment of ferrous alloys containing Mn
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C21D6/008—Heat treatment of ferrous alloys containing Si
    • 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
    • C21D8/005—Modifying the physical properties by deformation combined with, or followed by, heat treatment of ferrous alloys
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    • 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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    • C21—METALLURGY OF IRON
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    • 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
    • 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
    • C21D8/10—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of tubular bodies
    • C21D8/105—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of tubular bodies of ferrous alloys
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/0075—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for rods of limited length
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C33/00—Making ferrous alloys
    • C22C33/04—Making ferrous alloys by melting
    • C22C33/06—Making ferrous alloys by melting using master alloys
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/001—Ferrous alloys, e.g. steel alloys containing N
    • 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
    • C—CHEMISTRY; METALLURGY
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/20—Ferrous alloys, e.g. steel alloys containing chromium with copper
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
    • C—CHEMISTRY; METALLURGY
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    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42—Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • 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
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    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • C—CHEMISTRY; METALLURGY
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    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/48—Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
    • 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
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/50—Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/54—Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/002—Bainite
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00—Microstructure comprising significant phases
    • C21D2211/005—Ferrite
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/50—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for welded joints

Definitions

  • the present invention belongs to the technical field of metallurgy, and relates to a 400 MPa corrosion-resistant steel bar and a production method of the 400 MPa corrosion-resistant steel bar.
  • Reinforced concrete structures are the most widely used structure form in infrastructure construction.
  • the theoretical service life of the reinforced concrete structures is long, but there are many cases of premature failure of reinforced concrete in practical engineering, which not only increases the maintenance cost, but also causes great waste of energy and resources.
  • the coastal reinforced concrete structures are affected by high chloride ion and sulfate contents and harsh environments such as high temperature and high humidity, so after they are put in use for 10-15 years, serious corrosion damage may generally occur, and they are far from achieving the designed theoretical service life.
  • Concrete in the reinforced concrete structures belongs to a strong alkaline environment.
  • the surfaces of steel bars will be passivated to form a layer of stable metal oxide passivation film.
  • the dissolution and repair of the passivation film are theoretically in a nearly balanced state, so that the potential of various positions on the surface of the steel bars is basically consistent, thus ensuring that the steel bars are difficult to corrode or the corrosion rate is very low.
  • stainless-steel bars are a common type of steel bars with good corrosion-resistant performance.
  • alloy elements such as Cr, Ni and Mo
  • the corrosion-resistant performance of the stainless-steel bars may be greatly improved through being compared with that of common carbon-steel bars, and the corrosion-resistant performance is excellent.
  • the present invention is directed to provide a 400 MPa corrosion-resistant steel bar which has excellent corrosion-resistant performance, comprehensive mechanical performance and welding performance, can be prepared at lower material cost and process cost and is suitable to be widely used in ocean engineering.
  • the present invention provides a 400 MPa corrosion-resistant steel bar.
  • the steel bar includes the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.5% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, and the balance of Fe and unavoidable impurities.
  • Cr+Mo+0.5Mn+0.35Ni+0.25Cu is 11.1-12.2%
  • C+N+0.3Si+Mn+1.8Nb is 0.4-0.8%.
  • the steel bar further includes the following chemical ingredients in percentage by mass: any one or more of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B.
  • a micro-structure of the steel bar is ferrite and bainite, and the ferrite accounts for 28%-40%.
  • an A-type inclusion, B-type inclusion, C-type inclusion and D-type inclusion of the steel bar at the standard of GB/T10561 are all less than or equal to 1.0 level.
  • a yield strength of the steel bar is greater than or equal to 420 MPa
  • a tensile strength is greater than or equal to 540 MPa
  • a percentage elongation after fracture is greater than or equal to 18%
  • a maximum force total elongation percentage is greater than or equal to 7.5%.
  • a nominal diameter of the steel bar is 6-32 mm.
  • the steel bar when the nominal diameter of the steel bar is 6-10 mm, the steel bar is made into a coiled steel bar; and when the nominal diameter of the steel bar is 12-32 mm, the steel bar is made into a straight steel bar.
  • an average weight loss corrosion rate of the steel bar is 0.05-0.1 g/(m 2 ⁇ h); in a salt mist corrosion test, an average weight loss corrosion rate of the steel bar is 0.01-0.04 g/(m 2 ⁇ h); and in simulated concrete pore fluid with the chloride ion concentration greater than or equal to 3 mol/L, a self-corrosion potential of the steel bar is -0.1 V to -0.15 V, a polarization resistance is 2500-3000 k ⁇ /cm 2 , and a self-corrosion current density is less than or equal to 0.13 ⁇ A/cm 2 .
  • the steel bar is able to be prepared by a process route I and a process route II.
  • the process route I includes a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an AOD furnace refining working procedure, an LF furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure and a temperature-controlled cooling working procedure which are performed in sequence.
  • the process route II includes a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure, an RH furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure and a temperature-controlled cooling working procedure which are performed in sequence.
  • a tapping temperature of the converter smelting working procedure is 1600-1660°C; in the AOD furnace refining working procedure, high-carbon ferro-chrome alloy and ferro-molybdenum alloy are added into molten steel to realize preliminary alloying on the molten steel, slagging-off is performed after reduction, then, manganese alloy is added, before tapping, a steel ladle for tapping is purged by argon gas for 5 min or a longer time, 20 kg of aluminum ingots are added into the molten steel in the tapping process, a tapping temperature is 1630-1670°C, and a tapping C content is less than or equal to 0.01%; in the LF furnace refining working procedure, after the molten steel reaches the steel ladle of an LF furnace, slag regulation is performed according to a scheme of adding 13-15 kg of lime and 4.0-6.5 kg of fluorite into per ton of molten steel, a white slag maintaining time is greater than
  • micro-carbon ferro-chrome alloy is added into molten steel in the tapping process to realize preliminary alloying on the molten steel, and a tapping temperature is 1700-1750°C;
  • a steel ladle in an LF furnace is subjected to whole-process bottom blowing at an argon gas flow rate of 80-160 L/min, and a tapping temperature is 1560-1600°C;
  • the RH furnace refining working procedure after vacuum pumping on an RH furnace for 3 min, oxygen is started to be blown into the RH furnace, a total oxygen blowing amount is 500-700 Nm 3 , then, micro-carbon ferro-chrome alloy is added into molten steel to realize alloying on the molten steel, clean circulation treatment is performed for 5 min or a longer time when a vacuum degree is less than 2 mbar, a tapping temperature is 1560-1600°C, and a tapping C content is less
  • the process route I and the process route II in the hot continuous rolling working procedure, continuous-casting billets are heated in heating furnaces, a heating temperature is 1080-1130°C, an in-furnace time is 60-120 min, then, the billets are rolled into coiled thread steel bars with a diameter of 6-10 mm, an initial rolling temperature is 980-1030°C, a finish rolling temperature is 850-950°C, and a spinning temperature is 830-920°C.
  • both the process route I and the process route II include an on-line acid pickling working procedure and a packing working procedure which are performed in sequence after the temperature-controlled cooling working procedure; and in the on-line acid pickling working procedure, the steel bars sequentially pass through an acid pickling tank, a passivation tank and a drying device, and gas jet holes of the acid pickling tank are distributed around a center line of the acid pickling tank.
  • the present invention has the following beneficial effects:
  • the present invention is directed to provide a production method of a 400 MPa corrosion-resistant steel bar.
  • the steel bar prepared by the production method has excellent corrosion-resistant performance, comprehensive mechanical performance and welding performance, has lower material cost and process cost and is suitable to be widely used in ocean engineering.
  • the present invention provides a production method of a 400 MPa corrosion-resistant steel bar.
  • the production method includes the following steps:
  • the steel billets further include the following chemical ingredients in percentage by mass: any one or more of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B.
  • Step (1) if a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an AOD furnace refining working procedure and an LF furnace refining working procedure are sequentially used for molten steel melting, a tapping temperature of the converter smelting working procedure is 1600-1660°C; in the AOD furnace refining working procedure, high-carbon ferro-chrome alloy and ferro-molybdenum alloy are added into molten steel to realize preliminary alloying on the molten steel, slagging-off is performed after reduction, then, manganese alloy is added, before tapping, a steel ladle for tapping is purged by argon gas for 5 min or a longer time, 20 kg of aluminum ingots are added into the molten steel in the tapping process, a tapping temperature is 1630-1670°C, and a tapping C content is less than or equal to 0.01%; in the LF furnace refining working procedure, after the molten steel reaches the steel ladle
  • a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure and an RH furnace refining working procedure are sequentially used for molten steel melting
  • micro-carbon ferro-chrome alloy is added into molten steel in the tapping process to realize preliminary alloying on the molten steel, and a tapping temperature is 1700-1750°C
  • a steel ladle in an LF furnace is subjected to whole-process bottom blowing at an argon gas flow rate of 80-160 L/min, and a tapping temperature is 1560-1600°C
  • the RH furnace refining working procedure after vacuum pumping on an RH furnace for 3 min, oxygen is started to be blown into the RH furnace, a total oxygen blowing amount is 500-700 Nm 3 , then, micro-carbon ferro-chrome alloy is added into molten steel to realize alloying on the molten steel,
  • the production method further includes Step (3) on-line acid pickling: sequentially passing the steel bars obtained in Step (2) through an acid pickling tank, a passivation tank and a drying device for on-line acid pickling, where gas jet holes of the acid pickling tank are distributed around a center line of the acid pickling tank; and packing the steel bars after the steel bars leave away from the drying device.
  • a micro-structure of the steel bar prepared by the production method is ferrite and bainite, and the ferrite accounts for 28%-40%.
  • an A-type inclusion, B-type inclusion, C-type inclusion and D-type inclusion of the steel bar prepared by the production method at the standard of GB/T10561 are all less than or equal to 1.0 level.
  • a yield strength of the steel bar prepared by the production method is greater than or equal to 420 MPa, a tensile strength is greater than or equal to 540 MPa, a percentage elongation after fracture is greater than or equal to 18%, and a maximum force total elongation percentage is greater than or equal to 7.5%.
  • an average weight loss corrosion rate of the steel bar prepared by the production method is 0.05-0.1 g/(m 2 ⁇ h); in a salt mist corrosion test, an average weight loss corrosion rate of the steel bar is 0.01-0.04 g/(m 2 ⁇ h); and in simulated concrete pore fluid with the chloride ion concentration greater than or equal to 3 mol/L, a self-corrosion potential of the steel bar is -0.1 V to -0.15 V, a polarization resistance is 2500-3000 k ⁇ /cm 2 , and a self-corrosion current density is less than or equal to 0.13 ⁇ A/cm 2 .
  • the present invention has the following beneficial effects:
  • a corrosion-resistant steel bar particularly a hot rolled ribbed steel bar.
  • the steel bar included the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, and the balance of Fe and unavoidable impurities.
  • the mass percentage of Cr, Mo, Mn, Ni and Cu in the chemical ingredients of the steel bar also met: 11.1% ⁇ Cr+Mo+0.5Mn+0.35Ni+0.25Cu ⁇ 12.2%, and the mass percentage of C, N, Si, Mn and Nb further met: 0.4% ⁇ C+N+0.3Si+Mn+1.8Nb ⁇ 0.8%.
  • each chemical ingredient in the steel bar is as follows: Cr: it is an important corrosion-resistant element, and capable of forming an oxide passivation film on the surfaces of steel bars to thus effectively prevent the steel bar oxidization and improve the corrosion-resistant capability of matrixes of the steel bars; it can give more excellent corrosion-resistant performance to the steel bars and prevent occurrence of pitting corrosion under the condition of co-existence with elements such as Mo and Ni; and additionally, the element Cr can also improve the hardenability of the steel bars.
  • the Cr content was controlled to be 9.5-10.4%.
  • Mo it is an important corrosion-resistant element. No matter in a reducing acid environment or a strong oxidizing salt solution environment, by adding the element Mo, the surfaces of the steel bars may be passivated, and the occurrence of pitting corrosion of the steel bars in a chloride solution can be prevented, so that the corrosion-resistant performance of the steel bars in various environments can be integrally improved. Additionally, the inhibition effect of the element Mo on the pearlite conversion is very obvious, and at the same time, in combination with a carbide forming element Cr, the generation of bainite may be promoted; and in addition, the element Mo can promote grain refinement and improve the hardenability and heat resistance of the steel bars. However, when the Mo content is too high, the oxidization resistance of the steel bar may deteriorate. In the chemical ingredient design of the present invention, the Mo content was controlled to be 1.0-1.2%.
  • Mn it is a solid solution strengthening element, can improve the strength of a wire rod, can be combined with a harmful element S to reduce the hot shortness of the steel bars, and is also an important deoxidizing agent, desulfurizing agent and austenite forming element at the same time.
  • the Mn content was controlled to be 0.3-0.6%.
  • Ni it is an important corrosion-resistant element, enables the steel bars to achieve higher corrosion-resistant capability to acidic and alkaline environments, and enables the steel bars to achieve higher anti-rust capability and heat-resistant capability at a high temperature; and at the same time, the element Ni is an austenite forming element, and capable of enabling the steel to have uniform austenite tissues to improve the corrosion-resistant performance.
  • the Ni content was controlled to be 0.01-1.00%.
  • the Cu it is an important corrosion-resistant element, and is favorable for improving the corrosion-resistant performance of the steel bars, however, when the Cu content is too high, the plasticity reduction of the steel may be caused, and hot rolling cracking may be caused.
  • the Cu content was controlled to be 0.01-0.50%.
  • the C content was controlled to be 0.014% or less.
  • N it is an austenite forming element. If the N content is too high, the plasticity of the steel bars may be reduced, and the too high N content may be unfavorable for the proportion control of ferrite to bainite in steel bar tissues. In the chemical ingredient design of the present invention, the N content was controlled to be 0.004% or less.
  • Nb it is a micro-alloy strengthening element, and can achieve precipitation strengthening and refined crystalline strengthening effects in a rolling process (such as a hot continuous rolling working procedure as mentioned below); and however, too high Nb content may cause plasticity reduction and cost increase of the steel bars.
  • the Nb content was controlled to be 0.01-0.05%.
  • Si it is a solid solution strengthening element, can achieve solid solution into ferrite, can inhibit the diffusion of the element C in the austenite and delay the phase change of ferrite and pearlite, and can improve the yield strength and tensile strength of the steel bars; and however, too high Si content may reduce the plasticity of the steel and deteriorate the welding performance of the steel bars.
  • the Si content was controlled to be 0.2-0.6%.
  • P it can improve the strength and corrosion-resistant performance of the steel bars, but may easily generate segregation in steel, and additionally, too high P content may cause poor mechanical performance at a low temperature.
  • the P content was controlled to be 0.01-0.03%.
  • an oxidation film on the surfaces of the steel bars has the sufficient compactness, the corrosion-resistant repair capability of the matrixes of the steel bars is improved, and the corrosion-resistant performance of the oxidation film of the steel bars and the matrixes of the steel bars is ensured.
  • too low proportion of the ferrite in the steel bar tissues is avoided, the microscopic structure and the proportion of the steel bars are favorably controlled to improve the plasticity of the steel bars, and the percentage elongation after fracture and the maximum force total elongation percentage are increased.
  • C+N+0.3Si+Mn+1.8Nb it is very important on the comprehensive control of mechanical performance of strength, plasticity, etc. of the steel bars.
  • the alloy element is enabled to sufficiently achieve the respective effects of solid solution strengthening, precipitation strengthening, tissue strengthening, etc. to improve the strength of the steel bars.
  • lower proportion of the ferrite in the steel bar tissues is avoided, higher proportion of the bainite in the steel bar tissues is avoided, the respective proportions of the ferrite and bainite in the steel bar tissues are optimized, the plasticity of the steel bars is improved, and the percentage elongation after fracture and the maximum force total elongation percentage are increased.
  • C+N+0.3Si+Mn+1.8Nb met 0.4-0.8%.
  • the present invention had the advantages that in the chemical ingredient design of the present invention: (1) on the premise of an ultra-low carbon design, the respective contents and association relationships of Cr, Mo, Mn, Ni and Cu were properly designed, at the same time, the respective contents and association relationships of C, N, Si, Mn and Nb were properly designed, so that the steel bar had a micro-structure of ferrite and bainite, the proportion of the ferrite was 28%-40%, the proportion of the bainite was 60%-72%, additionally, the steel bar had the excellent corrosion-resistant performance, comprehensive mechanical performance and welding performance, the overall comprehensive performance of the steel bar was excellent, and the steel bar met the use requirements of ocean engineering; and (2) under the condition of a design scheme of the chemical ingredients, the excellent corrosion-resistant performance, comprehensive mechanical performance and welding performance can be realized, in addition, the cost of alloy elements was low, the energy was saved, the consumption was reduced, the 400 MPa corrosion-resistant steel bar can be prepared through a plurality of process routes, the cost of
  • the micro-structure of the steel bar was ferrite and bainite, the ferrite accounted for 28%-40%, and the bainite accounted for 60%-72%. Therefore, the influence of the micro-structure and the proportions of the ferrite and bainite of the micro-structure on the steel bar was further embodied in two aspects: the first aspect was the mechanical performance, the proper yield strength and good percentage elongation including the percentage elongation after fracture and the maximum force total elongation percentage can be ensured through the proportion control of the ferrite and bainite in this embodiment, and the good comprehensive mechanical performance was ensured.
  • the other aspect was the corrosion-resistant performance, and the corrosion-resistant performance of the steel bar can be improved by ensuring a certain bainite tissue proportion.
  • the steel bar was a 400 MPa or greater steel bar with a yield strength greater than or equal to 420 MPa, a tensile strength greater than or equal to 540 MPa, a percentage elongation after fracture greater than or equal to 18%, and a maximum force total elongation percentage greater than or equal to 7.5%.
  • the steel bar was well controlled in an aspect of inclusions. Specifically, An A-type inclusion, B-type inclusion, C-type inclusion and D-type inclusion of the steel bar at the standard of GB/T10561 were all less than or equal to 1.0 level. Therefore, the toughness of the steel bar under the low-temperature condition can be improved, and the mechanical performance of the steel bar was favorably ensured.
  • the corrosion-resistant performance in a periodic infiltration corrosion test and a salt mist corrosion test, the corrosion-resistant performance was improved by 45 times or greater through being compared with that of ordinary HRB400.
  • an average weight loss corrosion rate of the steel bar was 0.05-0.1 g/(m 2 ⁇ h); and in the salt mist corrosion test, an average weight loss corrosion rate of the steel bar was 0.01-0.04 g/(m 2 ⁇ h); and in simulated concrete pore fluid with the chloride ion concentration greater than or equal to 3 mol/L, a self-corrosion potential of the steel bar was -0.1 V to -0.15 V, a polarization resistance was 2500-3000 k ⁇ /cm 2 , and a self-corrosion current density was less than or equal to 0.13 ⁇ A/cm 2 .
  • a specific method of the used periodic infiltration corrosion test was as follows: a treated sample was put into a periodic infiltration test tank, the test was performed according to a corrosion test method of a YB/T4367 steel bar in a chloride ion environment, a solution was 2.0 ⁇ 0.05(wt%) NaCl, a pH value was 6.5-7.2, a temperature of the solution was 45°C ⁇ 2°C, a drying temperature was 70°C ⁇ 10°C, the test was continuously performed, and an average weight loss corrosion rate at 168 h was obtained.
  • a specific method of the used salt mist corrosion test was as follows: a treated sample was put into a salt mist test tank, the test was performed according to a GB/T10125 artificial atmosphere corrosion test-salt mist corrosion test, a solution was 2.0 ⁇ 0.05(wt%) NaCl, a pH value was 6.5-7.2, a temperature of the solution was 35°C ⁇ 2°C, the test was continuously performed, and an average weight loss corrosion rate at 168 h was obtained.
  • a specific method of the used electrochemical corrosion test was as follows: the electrochemical corrosion test was performed according to GB/T24196-2009 "Corrosion of metals and alloys-Electrochemical test methods-Guidelines for conducting potentiostatic and potentiodynamic polarization measurements", a three-electrode system was used, a reference electrode was a saturated calomel electrode, an auxiliary electrode was a Pt sheet, and a test solution was a simulated concrete pore fluid with the chloride ion concentration greater than or equal to 3 mol/L; a polarization curve test scanning range was -300 mV to 600 mV relative to the sample self-corrosion potential, and a scanning frequency was 1 mV/s; and an electrochemical impedance test scanning frequency range was 10 -2 -10 5 Hz, and an alternating current excitation signal amplitude value was ⁇ 5 mV.
  • the steel bar had excellent corrosion-resistant performance, and under the condition of performing the corrosion performance test in a simulated sea water solution, each index was much better than that of an ordinary thread steel bar of the same level.
  • the steel bar was easy to weld.
  • a welding point structure was firm, breaking cannot easily occur, a breaking point of the welded sample in a tensile test was formed in a base material position of the two steel bars instead of a welding point position.
  • a nominal diameter of the steel bar was 6-32 mm.
  • the steel bar When the nominal diameter of the steel bar was 6-10 mm, the steel bar was made into a coiled steel bar; and when the nominal diameter of the steel bar was 12-32 mm, the steel bar was made into a straight steel bar. Therefore, the requirement of ocean engineering on the steel bar can be met. Additionally, through the design of the diameter, the comprehensive mechanical performance and corrosion-resistant performance of the steel bar structure can be improved.
  • a corrosion-resistant steel bar was provided, and was particularly a hot rolled ribbed steel bar suitable for ocean engineering.
  • the corrosion-resistant steel bar mainly differed from the first embodiment in that: any one or more of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B were further added to chemical ingredients to further improve the performance of the steel bar.
  • the steel bar included the following ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, any one of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B, and the balance of Fe and unavoidable impurities.
  • the mass percentage of Cr, Mo, Mn, Ni and Cu in the chemical ingredients of the steel bar also met: 11.1% ⁇ Cr+Mo+0.5Mn+0.35Ni+0.25Cu ⁇ 12.2%, and the mass percentage of C, N, Si, Mn and Nb further met: 0.4% ⁇ C+N+0.3Si+Mn+1.8Nb ⁇ 0.8%.
  • V it is a microalloy strengthening element, can achieve precipitation of V (C, N) compounds in a rolling process (such as a hot continuous rolling working procedure as mentioned below), has a certain precipitation strengthening effect, can prevent austenite and ferrite crystalline grains from growing, and has a refined crystalline strengthening effect; and however, too high V content may cause plasticity reduction and cost increase of the steel bar.
  • the V content was controlled to be 0.1-0.15%.
  • Ti it has higher affinity than Cr, so that the occurrence of grain boundary chromium depletion due to chromium carbide precipitation can be avoided, so that the inter-crystalline corrosion is effectively prevented; in addition, by adding a proper amount of Ti, fine TiO x and TiN in dispersed distribution can be formed in a steel plate; and however, too high Ti content may increase the viscosity of the molten steel, is unfavorable for the melting of the molten steel, and may also cause the course size of the formed TiO x and deteriorate the toughness of the steel plate at the same time. In the chemical ingredient design of the present invention, the Ti content was controlled to be 0.01-0.05%.
  • Al it is a common deoxidizing agent, and can improve the electrode potential of the matrix of the steel bar, improve the corrosion-resistant performance and prevent austenite crystalline grains from growing to improve the strength of the steel bar; however, too high Al content may cause increase of oxides in the steel, and is unfavorable for the welding performance of the steel bar.
  • the Al content was controlled to be 0.01-0.03%.
  • B it is a strengthening element, has a significant effect on improving the strength of the steel bar, but too high B content is unfavorable for the improvement of the inter-crystalline corrosion-resistant performance.
  • the B content was controlled to be 0.0005-0.0020%.
  • the performance of the steel bar may be further improved based on the first embodiment, the steel bar had the excellent corrosion-resistant performance, mechanical performance, plasticity and welding performance, the engineering construction was convenient, and the steel bar may achieve a longer theoretical service life when being used in ocean engineering.
  • a production method of a corrosion-resistant steel bar was provided.
  • the production method may be used for producing and preparing the corrosion-resistant steel bar according to the first embodiment, and may be used for producing and preparing the corrosion-resistant steel bar according to the second embodiment.
  • a process route of the production method included a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an AOD furnace refining working procedure, an LF furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure, a temperature-controlled cooling working procedure and a packing working procedure which were performed in sequence.
  • the production method will be described below in detail according to the step sequence.
  • a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an AOD furnace refining working procedure and an LF furnace refining working procedure were sequentially adopted for molten steel melting, and the obtained molten steel was continuously cast into steel billets through the square billet continuous casting working procedure.
  • the chemical ingredients of the steel billets obtained in this step were the same as the chemical ingredients of the steel bar according to the first embodiment. That was, the steel billets included the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, and the balance of Fe and unavoidable impurities, and in addition, Cr+Mo+0.5Mn+0.35Ni+0.25Cu was 11.1-12.2%, and C+N+0.3Si+Mn+1.8Nb was 0.4-0.8.
  • the chemical ingredients of the steel billets in the step were the same as the chemical ingredients of the steel bar according to the second embodiment. That was, the steel billets included the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, any one or more of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B, and the balance of Fe and unavoidable impurities, and in addition, Cr+Mo+0.5Mn+0.35Ni+0.25Cu was 11.1-12.2%, and
  • a tapping temperature of the converter smelting working procedure was 1600-1660°C, the decarburization and dephosphorization effects were ensured, and the subsequent alloying was facilitated.
  • a tapping temperature was 1630-1670°C
  • a tapping C content was less than or equal to 0.01%, and a molten steel decarburization effect and a production rhythm were ensured.
  • slag regulation was performed according to a scheme of adding 13-15 kg of lime and 4.0-6.5 kg of fluorite into per ton of molten steel, a white slag maintaining time was greater than or equal to 8 min, a soft stirring time was 8-15 min, a tapping temperature was 1600-1620°C, and the molten steel deoxidization and desulfuration were completed step by step.
  • Step (1) the steel billets obtained in Step (1) were rolled into steel bars with a nominal diameter of 6-32 mm through a hot continuous rolling working procedure, and then, a temperature-controlled cooling working procedure was performed. According to different nominal diameters of the steel bars, the specific process schemes of this step were different.
  • the steel billets obtained in Step (1) were heated in a heating furnace at a heating temperature of 1100-1200°C for an in-furnace time of 60-120 min, alloy elements were sufficiently redissolved, and the strengthening effects of the alloy elements were facilitated. Then, the steel billets were rolled into straight thread steel bars with a diameter of 12-32 mm at an initial rolling temperature of 1000-1100°C and a finish rolling temperature of 850-950°C, so that austenite crystalline grains were maintained at a certain size. Then, in the temperature-controlled cooling working procedure, the rolled straight thread steel bars were naturally cooled on a cooling bed at a temperature on the cooling bed of 860-920°C, and the subsequent ferrite and pearlite size and proportion control were ensured.
  • the steel billets obtained in Step (1) were heated in a heating furnace at a heating temperature of 1080-1130°C, sufficient redissolution of alloy elements was facilitated, and the in-furnace time was 60-120 min. Then, the steel billets were rolled into coiled thread steel bars with a diameter of 6-10 mm at an initial rolling temperature of 980-1030°C, a finish rolling temperature of 850-950°C and a spinning temperature of 830-920°C, so that austenite crystalline grains were maintained at a certain size.
  • Step (2) The steel bars cooled in Step (2) were packed to be transported and put into engineering application.
  • a production method of a corrosion-resistant steel bar was provided.
  • the production method may be used for producing and preparing the corrosion-resistant steel bar according to the first embodiment, and may be used for producing and preparing the corrosion-resistant steel bar according to the second embodiment.
  • the process route of the production method included a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure, an RH furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure, a temperature-controlled cooling working procedure and a packing working procedure which were performed in sequence. That was, this embodiment mainly differed from the third embodiment in: the molten iron pre-desulfuration working procedure, the converter smelting working procedure, the LF furnace refining working procedure, the RH furnace refining working procedure and the square billet continuous casting working procedure, i.e., the steel making steps.
  • the production method according to this embodiment will be described in detail hereafter only in aspects of the steel making steps.
  • a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure and an RH furnace refining working procedure were sequentially adopted for molten steel melting, and the obtained molten steel was continuously cast into steel billets through the square billet continuous casting working procedure.
  • the chemical ingredients of the steel billets obtained in this step were the same as the chemical ingredients of the steel bar according to the first embodiment. That was, the steel billets included the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, and the balance of Fe and unavoidable impurities, and in addition, Cr+Mo+0.5Mn+0.35Ni+0.25Cu was 11.1-12.2%, and C+N+0.3Si+Mn+1.8Nb was 0.4-0.8.
  • the chemical ingredients of the steel billets in the step were the same as the chemical ingredients of the steel bar according to the second embodiment. That was, the steel billets included the following chemical ingredients in percentage by mass: 9.5-10.4% of Cr, 1.0-1.2% of Mo, 0.3-0.6% of Mn, 0.01-1.00% of Ni, 0.01-0.50% of Cu, at most 0.014% of C, at most 0.004% of N, 0.01-0.05% of Nb, 0.2-0.6% of Si, at most 0.004% of S, at most 0.003% of O, at most 0.01% of As, 0.01-0.03% of P, any one or more of 0.1-0.15% of V, 0.01-0.05% of Ti, 0.01-0.03% of Al and 0.0005-0.0020% of B, and the balance of Fe and unavoidable impurities, and in addition, Cr+Mo+0.5Mn+0.35Ni+0.25Cu was 11.1-12.2%, and
  • micro-carbon ferro-chrome alloy was added into molten steel in a tapping process to realize preliminary alloying on the molten steel, the C content in the molten steel was possibly controlled from an alloy adding perspective, the efficiency was improved, a tapping temperature was 1700-1750°C, a dephosphorization effect was ensured, and good preparation was prepared for subsequent melting.
  • a steel ladle in an LF furnace was subjected to whole-process bottom blowing at an argon gas flow rate of 80-160 L/min, and a tapping temperature was 1560-1600°C. The dissolution and homogenization of alloy in the steel ladle were ensured, and a production rhythm was facilitated.
  • a production method of a corrosion-resistant steel bar was provided.
  • a process route of the production method included a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure, an RH furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure, a temperature-controlled cooling working procedure, an on-line acid pickling working procedure and a packing working procedure which are performed in sequence.
  • the above-mentioned third embodiment can be adopted, and the above-mentioned fourth embodiment can also be adopted, that was, according to this embodiment, based on the above-mentioned third embodiment or fourth embodiment, the on-line acid pickling working procedure was added before the packing working procedure. Only the on-line acid pickling working procedure will be described below, and other details are not described again.
  • the steel bar sequentially passed through an acid pickling tank, a passivation tank and a drying device to realize on-line acid pickling of the steel bar.
  • Gas jet holes of the acid pickling tank were distributed around a center line of the acid pickling tank to enhance the acid pickling effect.
  • each of Examples 1-16 and Comparative examples 1-4 provided a steel bar, and chemical ingredients of the steel bar were as shown in Table 1.
  • Example 12 was implemented according to the first embodiment of the present invention.
  • Other Examples were implemented according to the second embodiment of the present invention.
  • Comparative examples 1-4 did not meet any embodiment of the present invention.
  • Example 1 Chemical ingredients in percentage by mass (wt, %) Cr Mo Mn Ni Cu C N Nb Si S O As P V Ti Al B
  • Example 2 9.53 1.02 0.44 0.92 0.08 0.013 0.0039 0.017 0.59 0.002 0.003 0.006 0.015 0.15 0.05 0.03 0.0020
  • Example 2 9.52 1.02 0.32 0.06 0.29 0.014 0.0020 0.014 0.20 0.004 0.001 0.005 0.012 0.13 0.01 0.04 0.0005
  • Example 3 9.50 1.20 0.36 0.97 0.13 0.014 0.0020 0.010 0.42 0.002 0.001 0.005 0.017 0.15 - 0.03 -
  • Example 4 9.61 1.19 0.38 0.74 0.19 0.013 0.0033 0.017 0.24 0.003 0.003 0.008 0.010 0.14 0.02 0.03 0.0017
  • Example 5 10.17 1.00 0.33 0.75 0.09 0.010 0.0035 0.050 0.55 0.002 0.003 0.008 0.024 0.
  • the production method according to Examples 1-8 adopted a process route of sequentially performing a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an AOD furnace refining working procedure, an LF furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure, a temperature-controlled cooling working procedure and an on-line acid pickling working procedure.
  • Each working procedure will be described hereafter.
  • the production method according to Examples 9-16 adopted a process route of sequentially performing a molten iron pre-desulfuration working procedure, a converter smelting working procedure, an LF furnace refining working procedure, an RH furnace refining working procedure, a square billet continuous casting working procedure, a hot continuous rolling working procedure, a temperature-controlled cooling working procedure and an on-line acid pickling working procedure.
  • a molten iron pre-desulfuration working procedure a converter smelting working procedure
  • an LF furnace refining working procedure an RH furnace refining working procedure
  • a square billet continuous casting working procedure a hot continuous rolling working procedure
  • a temperature-controlled cooling working procedure a temperature-controlled cooling working procedure and an on-line acid pickling working procedure.
  • the production method adopted by Comparative examples 1-4 was conventional process route of converter smelting, square billet continuous casting, hot continuous rolling and cooling bed cooling.
  • a heating temperature in the heating furnace was 1210-1290°C
  • an initial rolling temperature was 1090-1170°C
  • a temperature on a cooling bed was greater than or equal to 1100°C
  • natural cooling was performed on the cooling bed.
  • Examples 1-16 were obviously superior to Comparative examples 1-4 in aspects of the mechanical performance, they met 400 MPa aseismic steel bar requirements, in addition, the yield strength was greater than or equal to 420 MPa, the tensile strength was greater than or equal to 540 MPa, the percentage elongation after fracture was greater than or equal to 18%, and the maximum force total elongation percentage was greater than or equal to 7.5%.
  • the steel bars according to Examples 1-16 and Comparative examples 1-4 were subjected to a periodic infiltration corrosion test, a salt mist corrosion test and an electrochemical corrosion test according to the same method, and the test results were as shown in Table 3.
  • a specific method of the used periodic infiltration corrosion test was as follows: a treated sample was put into a periodic infiltration test tank, the test was performed according to a corrosion test method of a YB/T4367 steel bar in a chloride ion environment, a solution was 2.0 ⁇ 0.05(wt%) NaCl, a pH value was 6.5-7.2, a temperature of the solution was 45°C ⁇ 2°C, a drying temperature was 70°C ⁇ 10°C, the test was continuously performed, and an average weight loss corrosion rate at 168 h was obtained.
  • a specific method of the used salt mist corrosion test was as follows: a treated sample was put into a salt mist test tank, the test was performed according to a GB/T10125 artificial atmosphere corrosion test-salt mist corrosion test, a solution was 2.0 ⁇ 0.05(wt%) NaCl, a pH value was 6.5-7.2, a temperature of the solution was 35°C ⁇ 2°C, the test was continuously performed, and an average weight loss corrosion rate at 168 h was obtained.
  • a specific method of the used electrochemical corrosion test was as follows: the electrochemical corrosion test was performed according to GB/T24196-2009 "Corrosion of metals and alloys-Electrochemical test methods-Guidelines for conducting potentiostatic and potentiodynamic polarization measurements", a three-electrode system was used, a reference electrode was a saturated calomel electrode, an auxiliary electrode was a Pt sheet, and a test solution was a simulated concrete pore fluid with the chloride ion concentration greater than or equal to 3 mol/L; a polarization curve test scanning range was -300 mV to 600 mV relative to the sample self-corrosion potential, and a scanning frequency was 1 mV/s; and an electrochemical impedance test scanning frequency range was 10 -2 -10 5 Hz, and an alternating current excitation signal amplitude value was ⁇ 5 mV.
  • Examples 1-16 were much more superior to Comparative examples 1-4 in an aspect of the corrosion-resistant performance.
  • the average weight loss corrosion rate of the steel bar was 0.05-0.1 g/(m 2 ⁇ h)
  • the average weight loss corrosion rate of the steel bar was 0.01-0.04 g/(m 2 ⁇ h)
  • the anti-corrosion performance was improved by more than 45 times through being compared with that of ordinary HRB400.
  • inclusion detection and micro-structure detection were performed through sampling.
  • An A-type inclusion, B-type inclusion, C-type inclusion and D-type inclusion at the standard of GB/T10561 were all less than or equal to 1.0 level.
  • the micro-structure was ferrite and bainite, the ferrite accounted for 28%-40%, and the bainite accounted for 60%-72%.
EP21918802.6A 2021-01-15 2021-04-12 400 mpa-grade corrosion-resistant steel bar and production method therefor Pending EP4279626A1 (en)

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