WO2011142285A1 - 高強度鋼板とその製造方法 - Google Patents
高強度鋼板とその製造方法 Download PDFInfo
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- WO2011142285A1 WO2011142285A1 PCT/JP2011/060495 JP2011060495W WO2011142285A1 WO 2011142285 A1 WO2011142285 A1 WO 2011142285A1 JP 2011060495 W JP2011060495 W JP 2011060495W WO 2011142285 A1 WO2011142285 A1 WO 2011142285A1
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 85
- 239000010959 steel Substances 0.000 title claims abstract description 85
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 229910001566 austenite Inorganic materials 0.000 claims abstract description 15
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 229910052796 boron Inorganic materials 0.000 claims abstract description 6
- 238000009863 impact test Methods 0.000 claims abstract description 6
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 6
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 5
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 238000005096 rolling process Methods 0.000 claims description 57
- 230000001186 cumulative effect Effects 0.000 claims description 15
- 238000005098 hot rolling Methods 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 abstract description 2
- 239000002245 particle Substances 0.000 abstract 1
- 238000005452 bending Methods 0.000 description 64
- 238000010438 heat treatment Methods 0.000 description 26
- 239000010410 layer Substances 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 14
- 230000000694 effects Effects 0.000 description 12
- 238000001816 cooling Methods 0.000 description 11
- 238000005336 cracking Methods 0.000 description 10
- 229910000734 martensite Inorganic materials 0.000 description 10
- 239000002344 surface layer Substances 0.000 description 9
- 238000005496 tempering Methods 0.000 description 9
- 229910001563 bainite Inorganic materials 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- 230000000171 quenching effect Effects 0.000 description 8
- 238000009864 tensile test Methods 0.000 description 8
- 238000010276 construction Methods 0.000 description 7
- 238000005261 decarburization Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 238000005728 strengthening Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- 238000003303 reheating Methods 0.000 description 4
- 238000003466 welding Methods 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 229910001567 cementite Inorganic materials 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000010191 image analysis Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000007545 Vickers hardness test Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000013585 weight reducing agent Substances 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
- C21D3/00—Diffusion processes for extraction of non-metals; Furnaces therefor
- C21D3/02—Extraction of non-metals
- C21D3/04—Decarburising
-
- 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
- C21D1/62—Quenching devices
- C21D1/667—Quenching devices for spray quenching
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0226—Hot rolling
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—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
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—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
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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
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
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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
- 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
- C22C38/48—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
-
- 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
- B21B1/38—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 sheets of limited length, e.g. folded sheets, superimposed sheets, pack rolling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B3/00—Rolling materials of special alloys so far as the composition of the alloy requires or permits special rolling methods or sequences ; Rolling of aluminium, copper, zinc or other non-ferrous metals
-
- 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
- C21D2211/008—Martensite
Definitions
- the present invention relates to a high-strength steel plate having a yield strength of 885 MPa or more, a plate thickness of 6 mm or more and 32 mm or less, which is excellent in bending workability, weldability and toughness used for structural members of construction machines and industrial machines, and a method for producing the same.
- Construction machines such as cranes and concrete pump cars tend to become larger and larger with the recent rise in buildings.
- the need for weight reduction of structural members is increasing, and the demand for high-strength steel having a yield strength of 885 MPa or more or a tensile strength of 950 MPa or more is also increasing.
- severe bending is often performed, for example, 2.0 t (bending radius is 2.0 times the plate thickness and 180 ° bending can be performed without cracking). In many cases, bending with such a severe bending radius is required.
- Patent Document 1 discloses a high-strength steel sheet having a yield strength of 885 MPa class (approximately 950 MPa or more in tensile strength) as a high-strength steel sheet having a tensile strength of 950 MPa class.
- a thick steel plate is assumed, bending workability is not particularly taken into consideration, and a large amount of Ni is indispensable for securing toughness, which is not economical for construction machinery.
- Patent Document 2 relates to a method of manufacturing a steel sheet mainly for line pipes having a tensile strength of 950 MPa or more, but bending workability is not considered, and rolling in a two-phase region at a low temperature is essential. The low productivity is also a problem.
- Patent Document 3 discloses a thick steel plate having a tensile strength of 950 MPa or more which is excellent in strain aging resistance, but this steel plate also does not consider bending workability at all.
- Patent Document 4 also discloses a method for producing a steel sheet having a tensile strength of 980 MPa or more without being subjected to non-tempering.
- Mn and the like are included. Since the amount of the alloy must be high, it is not economical, and the bending workability is not considered.
- Patent Document 5 relates to a steel having a tensile strength of 980 MPa in which bending workability is also considered, but relies on refinement of the crystal grain size to improve the bending workability, and is offline in order to make the crystal grain size uniform and uniform. Since reheating and quenching is premised on, the productivity is low and it is not possible to sufficiently meet vigorous demand. Further, since the index of bending workability is only the elongation value, it is not clear whether bending work with a severe bending radius such as 2.0 t is possible.
- Patent Document 6 relates to a hot-rolled steel sheet having a tensile strength of 950 MPa or more in consideration of bending workability and weldability.
- a large amount of Ti is necessary, and when applied to a thick plate, the weldability is low. It seems to be reduced, and there is also a problem in economic efficiency because addition of Ni is essential in order to compensate for a decrease in toughness due to addition of high Ti.
- the object of the present invention is to solve the above-mentioned conventional problems, yield strength of 885 MPa or more excellent in bending workability, weldability and toughness used for structural members of construction machinery and industrial machinery, tensile strength of 950 to 1200 MPa, plate It is to provide a high-strength steel sheet having a thickness of 6 mm or more and 32 mm or less and a method for producing the same.
- the inventors diligently studied a method for greatly improving the bending workability of high-strength steel having a yield strength of 885 MPa or higher and a tensile strength of 950 to 1200 MPa. As a result, it became clear that the influence of the hardness on the outermost surface of the steel sheet is extremely large. In other words, even if the strength of the majority of the steel sheet is high, if the surface layer has a softened layer with a certain thickness, it is possible to suppress the occurrence of cracks on the surface during bending, greatly improving bending workability. can do.
- the upper limit of yield strength and tensile strength shall be 1200 MPa. If necessary, the upper limit of yield strength or tensile strength may be limited to 1150 MPa or 1100 MPa. As the plate thickness increases, it becomes difficult to improve bending workability, strength, and weldability. Therefore, the upper limit of the plate thickness may be limited to 25 mm, 20 mm, or 16 mm. If the plate thickness becomes small, it becomes difficult to ensure the cooling start temperature, so the lower limit of the plate thickness may be limited to 8 mm or 10 mm.
- the structure of the steel sheet is also important, and it has been found that there is a good correlation between the degree of elongation of prior austenite grains (hereinafter referred to as aspect ratio) in the direction parallel to the bending direction and bending workability.
- aspect ratio degree of elongation of prior austenite grains
- from the surface side of the steel plate where deformation due to bending increases specifically from the surface to a depth of 1/4 of the plate thickness (hereinafter referred to as “surface side from the plate thickness of 1/4 t”), 3 /
- the aspect ratio from the depth of 4 to the back side (hereinafter referred to as “the back side from the plate thickness 3 / 4t”) is important.
- the bending workability of high-strength steel can be greatly improved. Specifically, in order for a steel plate having a yield strength of 885 MPa or more and a thickness of 32 mm or less to satisfy bending workability at a severe bending radius of 2.0 t, the following control is necessary.
- FIG. 1 is an example of a graph showing the relationship between hardness and elongation in a tensile test of various strength steel materials having almost uniform hardness. From this, it can be seen that the elongation of the steel material depends greatly on the hardness.
- the 13B tensile test piece prescribed in JIS Z 2241 was used as the test piece.
- Hv (Vickers hardness) of high strength steel having a yield strength of 885 MPa or more is about 300 or more, but when Hv is 300 to 250 or less, the elongation is improved by about 2% or more.
- the softening layer of Hv 250 or less is 50 ⁇ m or more on the surface layer of the plate thickness, the elongation of the surface layer is improved and the occurrence of cracks during bending can be considerably suppressed, and the bending workability of the entire steel plate Can be greatly improved.
- the thickness of the softened layer is too large, the average hardness of the entire thickness, that is, the strength of the tensile test is lowered.
- the aspect ratio of the surface side from the plate thickness 1 / 4t and the back side from the plate thickness 3 / 4t are important, but the aspect ratio at the plate thickness 1 / 4t may be used as an index. .
- 1 / 4t and 3 / 4t have substantially the same aspect ratio, and the aspect ratio is larger on the front side than 1 / 4t and on the back side than 3 / 4t. Accordingly, the aspect ratio from the front surface side to 1 / 4t and the back surface side from 3 / 4t can be considered to be equal to or higher than the aspect ratio of 1 / 4t.
- FIG. 2 examined the relationship between the softened layer thickness and aspect ratio and bending workability in various high-strength steel sheets having a thickness of 12 mm or more and 32 mm or less, a yield strength of 885 MPa or more, and a tensile strength of 950 to 1200 MPa. It is a graph which shows a result.
- the bending workability was evaluated in accordance with the method specified in JIS Z 2248 in the direction parallel to the final rolling direction (hereinafter referred to as “L”) using a No. 1 test piece with a bending radius (2.0 t) of 2.0 times the plate thickness.
- the aspect ratio is a section parallel to the final rolling direction (hereinafter referred to as “L section”) in the case of bending in the L direction, and a section perpendicular to the final rolling direction (hereinafter referred to as “T section”) in the case of bending in the T direction. )),
- L section a section parallel to the final rolling direction
- T section a section perpendicular to the final rolling direction
- the prior austenite grain boundary at the position of the thickness 1/4 t was revealed by picric acid corrosion, and 5 fields of 200 ⁇ m ⁇ 200 ⁇ m were measured and calculated by image analysis.
- the steel of the present invention has a tempered martensite or bainite main structure, and the aspect ratio here is the average aspect ratio of the prior austenite grain boundaries.
- the plate thickness surface layer has a softening layer of Hv 250 or less and a thickness of 50 ⁇ m or more. If the average aspect ratio of the prior austenite grains in the cross section is 1.6 or more, it can be bent without cracking even in the bending radius condition of 2.0t in both the L-direction bending and the T-direction bending. It turns out that it becomes.
- FIG. 3 shows the relationship between the cumulative rolling reduction in the final rolling direction and the vertical direction and the average aspect ratio of the T-section structure in the temperature range of 1000 ° C. or less (non-recrystallization temperature range) in Nb-added steel. Is the relationship between the cumulative rolling reduction in the final rolling direction and the average aspect ratio of the L cross-sectional structure in the temperature range of 1000 ° C. or less. The aspect ratio is measured at a thickness of 1/4 t.
- the component ranges of the test steel plates are C: 0.11 to 0.16%, Si: 0.27 to 0.33%, Mn: 0.95 to 1.31%, P : 0.001 to 0.004%, S: 0.001 to 0.002%, Mo: 0.16 to 0.35%, Al: 0.03 to 0.04%, Nb: 0.016 to 0 0.033%, Ti: 0.012 to 0.019%, B: 0.0009 to 0.0019%, N: 0.0033 to 0.0049%, Pcm: 0.24 to 0.29%, The thickness of the test steel plate was 6 mm to 32 mm.
- the average aspect ratio is 1.6 or more when the cumulative rolling reduction in the temperature range of 1000 ° C. or less is 25% or more. Therefore, as a specific rolling method, after rolling out so that the cumulative reduction ratio in the temperature range of 1000 ° C. or less is 25% or more, the rolling direction is rotated by 90 °, and the cumulative reduction ratio is 25%. Rolling is performed in the final rolling direction so as to achieve the above. In order to obtain an appropriate aspect ratio by this method, it is essential to add Nb which has an effect of expanding the non-recrystallization temperature range.
- the inventor conducted a y-type weld crack test specified in JIS Z3158 on various steel plates having a thickness of 25 mm to 32 mm, a yield strength of 885 MPa or more, and a tensile strength of 950 to 1200 MPa. The relationship with temperature was investigated. The result is shown in FIG.
- the preheating temperature is as low as possible.
- the target thickness was 25 to 32 mm and the preheating temperature at which the crack stop preheating temperature, that is, the root cracking rate becomes 0, was 50 ° C. or less.
- FIG. 5 shows that the Pcm for the root crack rate to be completely 0 at a preheating temperature of 50 ° C. is 0.29% or less, and this is taken as a guideline for the upper limit of the alloy addition amount.
- the average of the absorbed energy value of the impact test at ⁇ 40 ° C. of the JIS Z 2242 V notch test piece is 33 J / cm 2 or more which is considered to be sufficient as a structural member. This is achieved by regulating the upper limit of the amount of alloying elements to be inhibited and selecting an appropriate tempering temperature.
- the gist of the present invention is as follows. (1) In mass%, C: 0.10% or more, 0.18% or less, Si: more than 0.20%, 0.80% or less, Mn: 0.20% or more, 1.60% or less, Mo: 0.10% or more, 0.60% or less, Nb: 0.010% or more, 0.050% or less, Ti: 0.005% or more, 0.030% or less, Al: 0.01% or more, 0.10% or less, B: 0.0003% or more, 0.0030% or less, P: 0.012% or less, S: 0.005% or less, N: 0.0060% or less, with the balance being Fe and inevitable impurities, and having a component composition satisfying that Pcm defined by the following (Formula 1) is 0.29% or less.
- It has a softening layer of Hv250 or less, having a thickness of 50 ⁇ m or more and not exceeding 3% of the plate thickness of the steel plate, and is parallel to the final rolling direction at a position at a depth of 1/4 of the plate thickness from the surface.
- the average aspect ratio of the prior austenite grains in the cross section and the cross section perpendicular to the final rolling direction is 1.6 or more, the yield strength is 885 MPa or more, and the average absorbed energy value in the impact test at ⁇ 40 ° C. is 33 J / cm 2 or more.
- a high-strength steel sheet characterized by being.
- a steel plate having a thickness of 6 mm or more and 32 mm or less is obtained by hot rolling. After rolling in the direction perpendicular to the final rolling direction so as to be not less than 90%, the rolling direction is rotated by 90 °, and the final rolling is performed so that the cumulative rolling reduction is not less than 25%.
- the method for producing a high-strength steel sheet is characterized in that it is water-cooled to a temperature of 300 ° C. or lower and then tempered at a temperature of 400 ° C. or higher.
- a high-strength steel sheet having an average of 33 J / cm 2 or more and a thickness of 6 mm or more and 32 mm or less can be economically provided.
- C is an important element that greatly affects the strength of the steel of the present invention mainly composed of a tempered martensite structure or a tempered bainite structure.
- a yield strength of 885 MPa or more In order to obtain a yield strength of 885 MPa or more, addition of 0.10% or more is necessary. However, if it exceeds 0.18%, bending workability deteriorates, so the upper limit is made 0.18%.
- the lower limit of C may be set to 0.11% or 0.12%. In order to improve weldability, the upper limit of C may be 0.17%, 0.16%, or 0.15%.
- Si has the effect of suppressing the cementite coarsening and improving the strength-toughness balance when the martensite structure is tempered.
- Si is 0.2% or less, cementite of the martensite structure is likely to be coarsened, so the Si addition amount is set to exceed 0.2%.
- Si is 0.25% or more.
- the upper limit is made 0.80%. In order to improve toughness, the upper limit of Si may be limited to 0.55%, 0.40%, or 0.34%.
- Mn is an element effective for improving hardenability and improving strength, and 0.20% or more is added. However, if it exceeds 1.60%, segregation is promoted and coarse MnS may be formed to inhibit bending workability, so 1.60% is made the upper limit of addition.
- the amount of Mn added is desirably 1.40% or less.
- the lower limit of Mn may be limited to 0.45%, 0.70%, 0.85%, or 0.95%.
- the upper limit of Mn may be limited to 1.40%, 1.30% or 1.25%.
- Mo improves hardenability with a relatively small amount of addition, and is very effective for improving the strength of the tempered martensite structure or tempered bainite structure by precipitation strengthening, so addition of 0.10% or more is essential. . However, if a large amount is added, weldability may be impaired, and it is also an expensive element, so the addition is made 0.60% or less.
- the lower limit of Mo may be limited to 0.17%, 0.25%, or 0.30%.
- the upper limit of Mo may be limited to 0.55%, 0.50%, or 0.45%.
- Nb is an essential element for generating fine carbides during rolling to widen the non-recrystallization temperature range to enhance the control rolling effect and to increase the aspect ratio of austenite.
- the precipitation strengthening effect is effective in improving the strength of the tempered martensite structure or tempered bainite structure.
- Nb is added by 0.010% or more. However, if added excessively, weldability may be hindered, so the added amount is made 0.050% or less.
- the lower limit of Nb may be set to 0.014% or 0.018% for strength improvement and fine graining. In order to improve weldability, the lower limit of Nb may be 0.040%, 0.035%, or 0.031%.
- B is used to obtain sufficient hardenability, but it is necessary to secure free B during direct quenching heat treatment.
- N is added for the purpose of fixing N as TiN.
- Ti is added in an amount of 0.005% or more for this purpose, but excessive addition may reduce weldability, so the upper limit is made 0.030%.
- the lower limit of Ti may be 0.008%, 0.010%, or 0.012%.
- the upper limit of Ti may be 0.026% or 0.020%.
- Al is added in an amount of 0.01% or more as a deoxidizer, but excessive addition may reduce toughness, so the upper limit is 0.10%.
- the lower limit of Al may be set to 0.02% or 0.03%.
- the upper limit of Al may be 0.07% or 0.05%.
- B is required to be 0.0003% or more in order to exert the effect of improving hardenability and ensure the strength, but if added over 0.0030%, weldability and toughness may be lowered.
- the content of is 0.0003% or more and 0.0030% or less.
- the lower limit of B may be 0.0005%, 0.0008%, or 0.0010%.
- the upper limit of B may be 0.0025%, 0.0022%, or 0.0019%.
- P is a harmful element that reduces toughness as an inevitable impurity. Therefore, the content is suppressed to 0.012% or less. In order to improve toughness, it may be 0.010% or less, 0.008% or 0.005% or less.
- S is an unavoidable impurity and is a harmful element that reduces the bending workability by forming MnS, so it is desirable to reduce it as much as possible. Therefore, the content is suppressed to 0.005% or less. In order to improve bending workability, it may be 0.004% or less, 0.003% or 0.002% or less.
- the upper limit of N may be set to 0.0050% or 0.0041%. Since N is mixed as an unavoidable impurity during the production of steel, no lower limit is particularly provided.
- Cu is an element that can improve strength without reducing toughness by solid solution strengthening, and may be added in an amount of 0.01% or more for that purpose. However, even if added in a large amount, the effect of improving the strength is limited, and the weldability may be impaired due to the excessive addition, so the addition is made 1.00% or less. In order to improve economy, the upper limit of Cu may be limited to 0.55%, 0.35%, or 0.25%.
- Ni has the effect of improving hardenability and toughness, so 0.01% or more may be added.
- Ni is an expensive element, and if a large amount of Ni is added, the decarburization reaction may be suppressed and the softening layer necessary for the present invention may not be obtained appropriately, so the addition is 0.25% or less. To do. As needed, it is good also as 0.20% or less and 0.15% or less.
- Cr improves the hardenability and is effective in improving the strength, so 0.01% or more may be added. However, if excessively added, the weldability may be lowered, so the addition is made 2.00% or less. In order to improve economy, the upper limit of Cr may be limited to 1.00%, 0.55%, or 0.35%.
- V also improves hardenability, has a precipitation strengthening effect in the tempered martensite structure or tempered bainite structure, and is effective in improving the strength. Therefore, V may be added in an amount of 0.005% or more. However, since a large amount of addition may impair weldability and is an expensive element, the addition is made 0.080% or less. In order to improve economy, the upper limit of V may be limited to 0.07%, 0.04%, or 0.03%.
- Ca has the effect of reducing the influence of MnS, which is harmful to bending workability, by spheroidizing the sulfide of the steel sheet, and 0.0001% or more may be added for this purpose.
- the upper limit of addition is made 0.0030% or less.
- the upper limit of Ca may be limited to 0.0020%, 0.0015%, or 0.0010%.
- the component composition in order to ensure weldability and strength, is limited so that Pcm defined by the following (Formula 1) is 0.29% or less. To do. In order to improve weldability, the upper limit of Pcm may be limited to 0.28%, 0.27%, or 0.26%. In order to improve the strength, the lower limit of Pcm may be limited to 0.22%, 0.23%, or 0.24%.
- Pcm [C] + [Si] / 30 + [Mn] / 20 + [Cu] / 20 + [Ni] / 60 + [Cr] / 20 + [Mo] / 15 + [V] / 10 + 5 [B] ...
- (Formula 1) it is preferable to limit the component composition so that Ceq defined by the following (formula 2) is 0.38 to 0.60.
- the upper limit of Ceq may be limited to 0.55%, 0.52, or 0.49%.
- the lower limit of Ceq may be limited to 0.40%, 0.42%, or 0.44%.
- the slab having the above steel component composition is heated for 3 hours or more at a temperature of 1250 ° C. or more and 1350 ° C. or less in an atmosphere having an oxygen concentration of 3% or more. This is to form a relatively thick decarburized layer on the surface of the slab in order to form a softened layer on the surface layer of the steel plate, and when the steel plate finally has a plate thickness of 32 mm or less by hot rolling, it is 50 ⁇ m on the surface of the steel plate.
- the purpose is to leave the above decarburized layer.
- the heating temperature is less than 1250 ° C.
- a sufficient decarburized layer thickness of 50 ⁇ m or more cannot be obtained. If the heating temperature exceeds 1350 ° C., the decarburized layer becomes too thick and the average hardness of the entire thickness or the strength of the tensile test may be lowered. Therefore, the upper limit of the heating temperature is 1350 ° C.
- the thickness of the slab is large, the thickness of the decarburized layer of the rolled steel sheet becomes relatively thin. Therefore, it is desirable that the thickness of the slab to be heated does not exceed 350 mm.
- the thickness of the slab may be 300 mm or less or 250 mm or less. It is good also considering the thickness of a slab as 50 mm or more, 80 mm or more, or 100 mm or more so that the ratio of the decarburization layer in a steel plate may not become large. Even if the heating time is excessively long, the decarburized layer may be too thick, which may reduce the average hardness of the entire thickness or the strength of the tensile test. Therefore, it is desirable that the heating time does not exceed 30 hours.
- the slab after heating may be cooled once as it is depending on the timing of input to the next step, or may be subsequently input to the next step of reheating to 1100 ° C. or higher.
- the conditions for cooling are not particularly limited in terms of the material, but may be cooled after preliminary hot rolling or forging to an appropriate thickness according to the final steel plate thickness.
- the slab is reheated to 1100 ° C. or higher so that Nb is sufficiently dissolved, and is hot rolled to obtain a steel plate having a thickness of 6 mm to 32 mm.
- the rolling direction After rolling so that the cumulative reduction ratio in the temperature range of 1000 ° C. or lower is 25% or more, the rolling direction is rotated by 90 °, and further rolling is performed so that the cumulative reduction ratio is 25% or more. If necessary, the rolling direction may be rotated 90 ° thereafter.
- the average aspect ratio of both the T cross-sectional structure and the L cross-sectional structure is 1.6 or more, and by having a softened layer of 50 ⁇ m or more on the plate thickness surface layer, a high strength of 32 mm or less and a yield strength of 885 MPa or more is obtained.
- the steel plate In both the L-direction bending and the T-direction bending, the steel plate can be bent without being broken even by bending at a bending radius of a steel plate thickness of 2.0 t.
- the cumulative reduction ratio in each direction or both directions may be 30% or more or 35% or more.
- On-line water cooling is to perform water cooling subsequent to hot rolling by water cooling equipment arranged on the same line as the rolling mill, and so-called direct quenching.
- the purpose of direct quenching is also to make the structure martensite or bainite to obtain high strength.
- direct quenching that does not require off-line quenching, that is, quenching after reheating is advantageous.
- the water cooling start temperature is high. If the temperature is Ar3 or higher, it may be 750 ° C or higher, 780 ° C or higher, or 800 ° C or higher.
- the yield stress is much lower than the tensile strength.
- a tempering heat treatment is performed at a temperature of 400 ° C. or higher to obtain a tempered martensite or tempered bainite structure, whereby a high strength of a yield strength of 885 MPa or more can be obtained and an excellent toughness can be obtained.
- the reason why the tempering temperature is set to 400 ° C. or higher is to avoid a brittle region of 300 ° C. to 400 ° C. and to obtain sufficient precipitation strengthening by fine carbides such as Mo.
- the time for the tempering heat treatment may be about 15 minutes or more.
- the upper limit of the tempering temperature may be 600 ° C, 575 ° C, or 550 ° C.
- the lower limit of the tempering temperature may be 425 ° C, 450 ° C, or 475 ° C.
- high-temperature long-time heating to form a decarburized layer is also possible by heating at the time of hot rolling of the steel sheet, but in that case, the austenite coarsening by high-temperature long-time heating is the coarsening of the austenite grain size after rolling Therefore, it is preferable to use a soaking heat treatment of the slab for the purpose of reducing segregation.
- Steel pieces obtained by melting steels of A to AI having the composition shown in Table 1 are manufactured according to the production conditions of Examples 1 to 18 of the present invention and Comparative Examples of 19 to 49 shown in Table 2, respectively. Steel plates having a thickness of 6 to 32 mm were produced.
- Decarburization treatment in Table 2
- all cooling was performed once.
- reheating to 1100 ° C. or higher (“Hot rolling and accelerated cooling / rolling heating temperature” in Table 2) was performed.
- Ar3 is an actual measurement value measured by detecting thermal expansion when a sample collected from a steel sheet is heated to 1100 ° C. and then cooled at 2.5 ° C./min.
- the thickness of the softening layer of Hv 250 or less on the steel sheet surface layer and the aspect ratio of the austenite grains in the L direction and the T direction are measured, and the yield strength, tensile strength, weld cracking property, bending workability, and toughness are measured. evaluated.
- the thickness of the softening layer of Hv250 or less in the steel sheet surface layer was measured by carrying out the micro Vickers hardness test (Hv0.1) defined in JIS Z 2244 at a pitch of 10 ⁇ m, and the ratio of the surface softening layer to the plate thickness was determined. .
- the aspect ratio of the prior austenite grains in the L direction and the T direction was calculated by image analysis by measuring the prior austenite grain boundary at the plate thickness 1 / 4t position by picric acid corrosion and measuring 5 fields of 200 ⁇ m ⁇ 200 ⁇ m. .
- the yield strength and the tensile strength were measured by taking the No. 1A tensile test piece specified in JIS Z 2241 and measured by the tensile test specified in JIS Z 2241, and the yield strength passed 885 MPa or more.
- the evaluation of bending workability was performed by 180 degree bending in the L direction and the T direction with a bending radius (2.0 t) of 2.0 times the plate thickness with the No. 1 test piece according to the method specified in JIS Z 2248. In any direction, the test was accepted if no cracks or other defects occurred outside the curved portion after the bending test.
- the weld cracking property was evaluated in a y-type weld cracking test specified in JIS Z 3158.
- the welding conditions are CO2 welding with a heat input of 15 kJ / cm, and the steel plate thickness used for the evaluation is 25 mm and 32 mm.
- the root cracking rate was 0 at a preheating temperature of 50 ° C., it was evaluated as acceptable.
- the weldability is considered to be the same as that of Examples 2, 5, and 9 of the same component, so the y-type weld cracking test was omitted. .
- the toughness was obtained by taking a JIS Z 2242 V notch test piece from the center of the plate thickness at right angles to the rolling direction, and evaluating it with the average value of the three absorbed energy values of the impact test at ⁇ 40 ° C., with a target of 33 J / cm 2 or more. Value.
- board thickness is 6 mm, it was set as the target value that it was set as the Charpy test piece of 5 mm subsize, and the absorbed energy value was 33 J / cm ⁇ 2 > or more.
- Comparative Examples 19 to 37 in which the chemical components indicated by the underline in the table deviate from the scope limited by the present invention, the yield strength and the bending work were obtained even though the production method was the method of the present invention.
- One or more of the properties, weld cracking properties, and toughness is less than the target value.
- Comparative Example 38 in which the Pcm value deviates from the range of the present invention has a poor weld cracking property.
- Comparative Example 39 having a low heating temperature for decarburization heat treatment
- Comparative Example 41 having a short heating time for decarburization heat treatment
- furnace oxygen concentration during decarburization heat treatment In Comparative Examples 42 having a low thickness, the thickness of the surface softening layer is small, so that the bending workability is unacceptable.
- Comparative Example 40 where the heating temperature of the decarburization heat treatment is too high, the yield ratio is low because the thickness ratio of the surface softening layer is too large.
- Comparative Example 43 having a low rolling heating temperature, since Nb does not dissolve, austenite is not sufficiently refined and bending workability is unacceptable.
- Comparative Example 44 having a low cumulative rolling reduction in the final rolling direction and perpendicular direction at 1000 ° C. or lower, and Comparative Example 45 having a low cumulative rolling reduction in the final rolling direction at 1000 ° C. or lower have aspect ratios in the T direction and L direction, respectively. Is low and bending workability is unacceptable.
- the comparative example 46 having a low water cooling start temperature and the comparative example 47 having a high water cooling end temperature have low yield strength because a necessary quenched structure cannot be obtained.
- Comparative Example 48 without tempering heat treatment has low yield strength, and Comparative Example 49 with low tempering heat treatment temperature has low toughness.
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Abstract
Description
(1)質量%で、
C:0.10%以上、0.18%以下、
Si:0.20%超、0.80%以下、
Mn:0.20%以上、1.60%以下、
Mo:0.10%以上、0.60%以下、
Nb:0.010%以上、0.050%以下、
Ti:0.005%以上、0.030%以下、
Al:0.01%以上、0.10%以下、
B:0.0003%以上、0.0030%以下、
P:0.012%以下、
S:0.005%以下、
N:0.0060%以下
を含み、残部がFe及び不可避的不純物からなり、下記(式1)で定義されるPcmが0.29%以下であることを満たす成分組成を有し、鋼板表層に50μm以上で、かつ鋼板の板厚の3%を超えない厚さの、Hv250以下の軟化層を有し、さらに表面から板厚の1/4の深さの位置において、最終圧延方向に平行な断面および最終圧延方向に垂直な断面における旧オーステナイト粒の平均アスペクト比がそれぞれ1.6以上であり、降伏強度885MPa以上、−40℃における衝撃試験の吸収エネルギー値の平均が33J/cm2以上であることを特徴とする高強度鋼板。
Pcm=〔C〕+〔Si〕/30+〔Mn〕/20+〔Cu〕/20+〔Ni〕/60+〔Cr〕/20+〔Mo〕/15+〔V〕/10+5〔B〕
・・・(式1)
ここで、〔C〕、〔Si〕、〔Mn〕、〔Cu〕、〔Ni〕、〔Cr〕、〔Mo〕、〔V〕〔B〕は、それぞれC、Si、Mn、Cu、Ni、Cr、Mo、V、Bの質量%で表した含有量を意味する。
(2)さらに、
Cu:0.01%以上、1.00%以下、
Ni:0.01%以上、0.25%以下、
Cr:0.01%以上、2.00%以下、
V:0.005%以上、0.080%以下、
Ca:0.0001%以上、0.0030%以下
のうち1種類以上含有することを特徴とする(1)に記載の高強度鋼板。
(3)板厚が6mm以上、32mm以下であり、引張強さが950MPa以上、1200MPa以下であることを特徴とする(1)又は(2)に記載の高強度鋼板。
(4)(1)又は(2)に記載の化学組成を有するスラブを、酸素濃度3%以上の雰囲気下で1250℃以上、1350℃以下の温度で3時間以上加熱した後に、一旦冷却後、あるいは引き続き、該スラブを1100℃以上に再加熱後、熱間圧延により板厚6mm以上、32mm以下の鋼板となし、その熱間圧延に際しては、1000℃以下の温度範囲での累積圧下率が25%以上となるように最終圧延方向と垂直方向に圧延した後、圧延方向を90°回転し、さらに累積圧下率が25%以上となるように最終圧延を行い、熱間圧延後Ar3以上の温度から、300℃以下の温度まで水冷し、その後400℃以上の温度で焼戻し熱処理することを特徴とする、高強度鋼板の製造方法。
まず、本発明の鋼成分の限定理由を述べる。
Cは、焼戻しマルテンサイト組織または焼戻しベイナイト組織を主体とする本発明鋼の強度に大きく影響する重要な元素である。885MPa以上の降伏強度を得るために0.10%以上の添加が必要であるが、0.18%超では曲げ加工性が低下するため、上限を0.18%とする。強度を安定して確保するために、Cの下限を0.11%又は0.12%としてもよい。溶接性の改善のため、Cの上限を0.17%、0.16%又は0.15%としてもよい。
Pcm=[C]+[Si]/30+[Mn]/20+[Cu]/20+[Ni]/60+[Cr]/20+[Mo]/15+[V]/10+5[B]
・・・(式1)
また、下記(式2)で定義されるCeqが0.38~0.60となるように成分組成を限定することが好ましい。溶接性の改善のため、Ceqの上限を0.55%、0.52又は0.49%に制限してもよい。強度向上のために、Ceqの下限を0.40%、0.42%又は0.44%に制限してもよい。
Ceq=[Si]/24+[Mn]/6+[Ni]/40+[Cr]/5+
[Mo]/4+[V]/14 ・・・(式2)
ここで、[C]、[Si]、[Mn]、[Cu]、[Ni]、[Cr]、[Mo]、[V]、[B]はそれぞれ、C、Si、Mn、Cu、Ni、Cr、Mo、V、Bの質量%である。
加熱時間が過剰に長くても、やはり脱炭層が厚くなりすぎて全厚の平均硬さあるいは引張試験の強度を低下させることがあるので、加熱時間は30時間を超えないことが望ましい。
これらの鋼板について、鋼板表層におけるHv250以下の軟化層の厚さ、およびL方向およびT方向のオーステナイト粒のアスペクト比を測定し、降伏強度、引張強さ、溶接割れ性、曲げ加工性、靭性を評価した。
L方向およびT方向の旧オーステナイト粒のアスペクト比は、ピクリン酸腐食により板厚1/4t位置における旧オーステナイト粒界を現出させて、200μm×200μmを5視野測定して、画像解析により算出した。
鋼成分組成は本発明範囲内であるが、Pcm値が本発明範囲を逸脱している比較例38は、溶接割れ性が不合格である。
Claims (4)
- 質量%で、
C:0.10%以上、0.18%以下、
Si:0.20%超、0.80%以下、
Mn:0.20%以上、1.60%以下、
Mo:0.10%以上、0.60%以下、
Nb:0.010%以上、0.050%以下、
Ti:0.005%以上、0.030%以下、
Al:0.01%以上、0.10%以下、
B:0.0003%以上、0.0030%以下、
P:0.012%以下、
S:0.005%以下、
N:0.0060%以下
を含み、残部がFe及び不可避的不純物からなり、下記(式1)で定義されるPcmが0.29%以下であることを満たす成分組成を有し、鋼板表層に50μm以上で、かつ鋼板の板厚の3%を超えない厚さの、Hv250以下の軟化層を有し、さらに表面から板厚の1/4の深さの位置において、最終圧延方向に平行な断面および最終圧延方向に垂直な断面における旧オーステナイト粒の平均アスペクト比がそれぞれ1.6以上であり、降伏強度885MPa以上、−40℃における衝撃試験の吸収エネルギー値の平均が33J/cm2以上であることを特徴とする高強度鋼板。
Pcm=〔C〕+〔Si〕/30+〔Mn〕/20+〔Cu〕/20+〔Ni〕/60+〔Cr〕/20+〔Mo〕/15+〔V〕/10+5〔B〕
・・・(式1)
ここで、〔C〕、〔Si〕、〔Mn〕、〔Cu〕、〔Ni〕、〔Cr〕、〔Mo〕、〔V〕〔B〕は、それぞれC、Si、Mn、Cu、Ni、Cr、Mo、V、Bの質量%で表した含有量を意味する。 - さらに、
Cu:0.01%以上、1.00%以下、
Ni:0.01%以上、0.25%以下、
Cr:0.01%以上、2.00%以下、
V:0.005%以上、0.080%以下、
Ca:0.0001%以上、0.0030%以下
のうち1種類以上含有することを特徴とする請求項1に記載の高強度鋼板。 - 板厚が6mm以上、32mm以下であり、引張強さが950MPa以上、1200MPa以下であることを特徴とする請求項1又は請求項2記載の高強度鋼板。
- 請求項1又は2に記載の化学組成を有するスラブを、酸素濃度3%以上の雰囲気下で1250℃以上、1350℃以下の温度で3時間以上加熱した後に、一旦冷却後、あるいは引き続き、該スラブを1100℃以上に再加熱後、熱間圧延により板厚6mm以上、32mm以下の鋼板となし、その熱間圧延に際しては、1000℃以下の温度範囲での累積圧下率が25%以上となるように最終圧延方向と垂直方向に圧延した後、圧延方向を90°回転し、さらに累積圧下率が25%以上となるように最終圧延を行い、熱間圧延後Ar3以上の温度から、300℃以下の温度まで水冷し、その後400℃以上の温度で焼戻し熱処理することを特徴とする、高強度鋼板の製造方法。
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CN102605253A (zh) * | 2012-04-18 | 2012-07-25 | 江苏省沙钢钢铁研究院有限公司 | 低成本高强度高韧性钢板及其生产工艺 |
CN103725985A (zh) * | 2013-12-28 | 2014-04-16 | 首钢总公司 | 一种超高强度钢板及其生产方法 |
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JP2016079424A (ja) * | 2014-10-10 | 2016-05-16 | 新日鐵住金株式会社 | 靭性に優れた鋼板およびその製造方法 |
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JP7032537B2 (ja) | 2017-12-22 | 2022-03-08 | ポスコ | 曲げ性及び低温靭性に優れた高強度熱延鋼板及びその製造方法 |
US11732339B2 (en) | 2017-12-22 | 2023-08-22 | Posco Co., Ltd | High-strength hot-rolled steel sheet having excellent bendability and low-temperature and method for manufacturing same |
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JPWO2011142285A1 (ja) | 2013-07-22 |
CN102712972A (zh) | 2012-10-03 |
JP4897125B2 (ja) | 2012-03-14 |
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