JP7267430B2 - Steel plate preparation method - Google Patents
Steel plate preparation method Download PDFInfo
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- JP7267430B2 JP7267430B2 JP2021538959A JP2021538959A JP7267430B2 JP 7267430 B2 JP7267430 B2 JP 7267430B2 JP 2021538959 A JP2021538959 A JP 2021538959A JP 2021538959 A JP2021538959 A JP 2021538959A JP 7267430 B2 JP7267430 B2 JP 7267430B2
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- 229910000831 Steel Inorganic materials 0.000 title claims description 137
- 239000010959 steel Substances 0.000 title claims description 137
- 238000002360 preparation method Methods 0.000 title description 5
- 229910001566 austenite Inorganic materials 0.000 claims description 39
- 238000001816 cooling Methods 0.000 claims description 36
- 238000005096 rolling process Methods 0.000 claims description 35
- 229910000734 martensite Inorganic materials 0.000 claims description 27
- 229910052748 manganese Inorganic materials 0.000 claims description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 23
- 238000005496 tempering Methods 0.000 claims description 21
- 238000002791 soaking Methods 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 238000010438 heat treatment Methods 0.000 claims description 15
- 229910052750 molybdenum Inorganic materials 0.000 claims description 15
- 229910052759 nickel Inorganic materials 0.000 claims description 15
- 238000010791 quenching Methods 0.000 claims description 15
- 230000000171 quenching effect Effects 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 229910052710 silicon Inorganic materials 0.000 claims description 13
- 239000012535 impurity Substances 0.000 claims description 12
- 229910052719 titanium Inorganic materials 0.000 claims description 10
- 238000005275 alloying Methods 0.000 claims description 9
- 238000007670 refining Methods 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 238000003723 Smelting Methods 0.000 claims description 7
- 238000006477 desulfuration reaction Methods 0.000 claims description 7
- 230000023556 desulfurization Effects 0.000 claims description 7
- 238000004512 die casting Methods 0.000 claims description 7
- 238000009863 impact test Methods 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 5
- 238000005266 casting Methods 0.000 claims description 4
- 238000012360 testing method Methods 0.000 claims description 4
- 238000012545 processing Methods 0.000 claims description 2
- 239000010409 thin film Substances 0.000 claims description 2
- 239000011572 manganese Substances 0.000 description 29
- 238000004519 manufacturing process Methods 0.000 description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 230000009286 beneficial effect Effects 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 238000005728 strengthening Methods 0.000 description 6
- 238000005204 segregation Methods 0.000 description 5
- 230000009466 transformation Effects 0.000 description 5
- 238000009749 continuous casting Methods 0.000 description 4
- 239000006104 solid solution Substances 0.000 description 4
- 238000013461 design Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005242 forging Methods 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 150000001247 metal acetylides Chemical class 0.000 description 3
- 230000008646 thermal stress Effects 0.000 description 3
- 238000003917 TEM image Methods 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- QFGIVKNKFPCKAW-UHFFFAOYSA-N [Mn].[C] Chemical compound [Mn].[C] QFGIVKNKFPCKAW-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003828 downregulation Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
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- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/004—Heat treatment of ferrous alloys containing Cr and Ni
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- 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
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/0081—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for slabs; for billets
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—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
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- 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
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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
- C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
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- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
- Treatment Of Steel In Its Molten State (AREA)
- Carbon Steel Or Casting Steel Manufacturing (AREA)
Description
本発明は、極厚鋼板およびその製造方法に関し、特に690MPaグレードの極厚鋼板およびその製造方法に関する。 TECHNICAL FIELD The present invention relates to an extra-thick steel plate and a method for producing the same, and more particularly to an extra-thick steel plate of 690 MPa grade and a method for producing the same.
国家海洋開発戦略の実施および石油ガス資源の採掘が徐々に陸地から深海および極地方向に展開することによって、海洋プラットフォームの性能および構造の安全性に対する要件がより高くなってきている。海洋プラットフォームの製造に必要な鋼材は、高強度かつ高靭性に向かって発展しており、降伏強度690MPaグレードの高強度・高靭性海洋プラットフォームのための厚板の需要量が大きくなってきている。従来の海洋工学のための690MPaグレードの極厚鋼板のコアの機械的特性は改善が難しい。鋼板の全体的な性能を均一に向上させるためには、通常、Ni、Mo、Cr、Cuなどの多数の元素が添加され、これらの元素の総量は4%以上もあるので、合金コストが高い。また、製造方法には、多数の焼き入れなどの工程が必要となり、製造困難が大きい。近年、海洋工学建設の改善を満たすために、高強度グレードの極厚鋼板の開発が広く懸念されている。 With the implementation of the national offshore development strategy and the gradual expansion of the exploration of oil and gas resources from land to deep water and polar directions, the requirements for the performance and structural safety of offshore platforms are becoming higher. The steel materials required for the manufacture of offshore platforms are evolving towards high strength and high toughness, and the demand for plate for high strength and high toughness offshore platforms with a yield strength grade of 690 MPa is increasing. The mechanical properties of the core of 690 MPa grade extra heavy steel for conventional marine engineering are difficult to improve. In order to uniformly improve the overall performance of the steel sheet, a large number of elements such as Ni, Mo, Cr, and Cu are usually added, and the total amount of these elements is 4% or more, so the alloy cost is high. . In addition, the production method requires a large number of steps such as quenching, making the production difficult. In recent years, the development of high-strength grade extra-thick steel plates has been widely concerned to meet the improvement of marine engineering construction.
特許番号201510125485.1である中国発明特許は、低温衝撃靭性に優れた低降伏比、高靭性、高強度の極厚鋼板およびその製造方法を開示しているが、その低降伏比、高靭性、高強度の極厚鋼板の化学組成にNiが3.6~5.5%含有されているので、コストが高い。 Chinese Invention Patent No. 201510125485.1 discloses a low yield ratio, high toughness and high strength extra thick steel plate with excellent low temperature impact toughness and a method for producing the same. Since 3.6 to 5.5% of Ni is contained in the chemical composition of the high-strength extra-thick steel plate, the cost is high.
特許番号201610026446.0である中国発明特許は、海洋工学用の高強度鋼板およびその製造方法を開示しているが、NbとVマイクロマイヤ化方法を使用しているにもかかわらず、Mnなどの焼入れ性は高くなり含有量が高くないので、鋼板の最大厚さは100mmを超えることができない。 A Chinese invention patent with patent number 201610026446.0 discloses a high-strength steel plate for marine engineering and a method for producing the same, but despite using Nb and V micromyerization methods, such as Mn Since the hardenability is high and the content is not high, the maximum thickness of the steel sheet cannot exceed 100 mm.
材料開発の現状から見れば、高性能の海洋工学用極厚鋼板の性能がまだ改善される必要がある。 In view of the current state of material development, the performance of high-performance marine engineering heavy steel plates still needs to be improved.
発明の目的:従来技術の欠点を克服するために、本発明は、海洋工学などの過酷な使用環境での高性能極厚鋼板の需要に対応できる、優れたコアの機械的特性を有する690MPaグレードの極厚鋼板を提供する。
本発明の他の目的は、上記の690MPaグレードの極厚鋼板を製造するための方法を提供することである。
Object of the Invention: In order to overcome the shortcomings of the prior art, the present invention provides a 690MPa grade with excellent core mechanical properties, which can meet the demand for high-performance extra-thick steel plates in harsh use environments such as marine engineering. provide extra heavy steel plates.
Another object of the present invention is to provide a method for producing the above 690 MPa grade extra heavy steel plate.
技術的解決策:本発明の690MPaグレードの極厚鋼板において、化学組成の質量百分率は、C:0.04~0.08%、Mn:5.2~6.0%、Si:0.1~0.4%、Mo:0.1~0.5%、Ni:0.2~0.6%、Cr:0.2~0.6%、Ti:0.01~0.05%、S:≦0.005%、P:≦0.010%、残部Feおよび不純物を含む。 Technical solution: In the 690MPa grade extra heavy steel plate of the present invention, the mass percentage of the chemical composition is C: 0.04-0.08%, Mn: 5.2-6.0%, Si: 0.1 ~0.4%, Mo: 0.1-0.5%, Ni: 0.2-0.6%, Cr: 0.2-0.6%, Ti: 0.01-0.05%, S: ≤ 0.005%, P: ≤ 0.010%, the balance containing Fe and impurities.
さらに、前記鋼板の厚さが80~150mmとなっている。 Further, the steel plate has a thickness of 80 to 150 mm.
さらに、前記鋼板の微細構造は、マルテンサイトとオーステナイトを有し、その中に、オーステナイトの体積分率は4~10%である。 Moreover, the microstructure of the steel sheet comprises martensite and austenite, in which the volume fraction of austenite is 4-10%.
さらに、前記鋼板のコアの機械的特性は、降伏強度が690MPa以上、引張強度が770MPa以上、破壊後の伸びは14%以上、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは80J以上である。 Furthermore, the mechanical properties of the core of the steel sheet are such that the yield strength is 690 MPa or more, the tensile strength is 770 MPa or more, the elongation after breaking is 14% or more, and the Charpy pendulum impact test of the V-shaped test piece at -60 ° C. is absorbed. energy is 80J or more.
さらに、前記鋼板の板厚方向の延びによる断面収縮率は50%以上である。 Further, the steel sheet has a cross-sectional shrinkage of 50% or more due to elongation in the thickness direction.
本発明に記載の690MPaグレードの極厚鋼板の製造方法は、以下のステップを含む技術的解決策を採用している。
(1)鉄水脱硫処理後、転炉製錬を行い、鋼水の中のS、P含有量をS≦0.005%、P≦0.010%に還元する。
(2)LF精錬によってC、Mn、Si、Mo、Ni、Ti元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度≦4mbar、加工時間≧20minにする。
(3)鋳造によってスラブを取得し、スラブの厚さと鋼板の厚さの比は4以上となっている。
(4)スラブの温度を1060~1140℃まで加熱し、均熱時間が40~90minとなっている。
(5)加熱されたスラブを圧延し、圧延開始温度≦1020℃、圧延終了温度≧930℃、通過変形量≧10%にする。
(6)圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の赤に戻る温度が≦360℃で、平均冷却速度が1~5℃/sとなっている。
(7)焼入れ熱処理を行い、鋼板を780~830℃までに再加熱し、均熱時間が5~15minで、鋼板表面の赤に戻る温度が≦110℃までに水冷し、平均冷却速度が2~8℃/sとなっている。
(8)焼戻し熱処理を行い、焼入れ後の鋼板を610~640℃までに加熱し、均熱時間が40~70minで、焼戻し後の鋼板が室温までに空冷される。
The method for producing 690MPa grade extra heavy steel plate according to the present invention adopts a technical solution including the following steps.
(1) After iron water desulfurization treatment, converter smelting is performed to reduce the S and P contents in the steel water to S≦0.005% and P≦0.010%.
(2) After completing the alloying of the required mass fractions of C, Mn, Si, Mo, Ni and Ti elements by LF refining, perform RH treatment to make the degree of vacuum ≦4 mbar and the working time ≧20 min.
(3) The slab is obtained by casting, and the ratio of the thickness of the slab to the thickness of the steel plate is 4 or more.
(4) The temperature of the slab is heated to 1060-1140° C., and the soaking time is 40-90 minutes.
(5) Roll the heated slab to a rolling start temperature ≤ 1020°C, a rolling end temperature ≥ 930°C, and a transit deformation amount ≥ 10%.
(6) The steel sheet after rolling is immediately water-cooled, and the temperature at which the surface of the steel sheet after cooling returns to red is ≤360°C, and the average cooling rate is 1 to 5°C/s.
(7) Perform quenching heat treatment, reheat the steel sheet to 780 ~ 830 ℃, soaking time is 5 ~ 15 minutes, water cooling until the temperature of the steel sheet surface returns to red is ≤ 110 ℃, average cooling rate is 2 ~8°C/s.
(8) Perform tempering heat treatment, heat the quenched steel sheet to 610 to 640° C., soak for 40 to 70 minutes, and air-cool the tempered steel sheet to room temperature.
有益な効果:本発明の鋼板は、マンガンを主な合金元素として使用し、極厚鋼板の製造時にニッケルなどの高価な元素の添加量を減らすことで、合金コストが削減している。特定の製造プロセスを使用することによって、製造された極厚鋼板に高強度、高塑性、高靭性の優れたコアの機械的特性、および抗層状引き裂き性能を備えさせ、海洋工学などの過酷な使用環境での高性能極厚鋼板に対する需要に対応することができる。 Beneficial effect: The steel sheet of the present invention uses manganese as the main alloying element, and reduces the addition amount of expensive elements such as nickel during the production of extra thick steel sheet, thereby reducing the alloying cost. By using a specific manufacturing process, the produced extra-thick steel plate has excellent core mechanical properties of high strength, high plasticity, high toughness, and anti-lamellar tearing performance, making it suitable for harsh uses such as marine engineering. It can meet the demand for high-performance extra-thick steel plates in the environment.
以下では、実施例に合わせて本発明の化学組成、製造工程、構成および性能を説明する。 In the following, the chemical composition, manufacturing process, configuration and performance of the present invention will be described in accordance with examples.
本発明の690MPaグレードの極厚鋼板の化学組成設計において、Cは、格子間固溶体強化により構造強度を大幅に高めることができ、重要な強化元素であり、重要なオーステナイト安定化元素でもあるが、低温衝撃靭性と溶接性を確保するために、その添加量を低レベルに制御する必要がある。Mnは、置換と固溶体強化によって構造の強度を高めると同時に、オーステナイトの安定性を大幅に向上させることができる。CとMnを適切に添加すると、焼入れ性が大幅に向上し、過冷却オーステナイトの相転移温度を下げ、高強度のマルテンサイト構造を取得することができる。一方、マルテンサイト焼戻しプロセスでは、CとMnの添加によって、一定量の逆変換オーステナイトを形成するのに必要な温度を下げた。CおよびMnは、逆変換オーステナイトに富んでいるため、低温でも安定した構造を維持することができ、本発明の可塑性および靭性を改善するための重要な構造となっている。本発明の焼戻し温度が600℃より低い場合、特に550℃の温度付近で焼戻しをする場合、Mn、Pなどの元素の粒界偏析を引き起こしやすく、靭性を減らすことがあるので、ご留意ください。発明者は、本発明におけるCおよびMn元素の作用機序を十分に検討し、Cが0.04~0.08%、Mnが5.2~6.0%と言う「低炭素中マンガン」組成設計を決定した。 In the chemical composition design of the 690 MPa grade extra heavy steel plate of the present invention, C can significantly increase the structural strength through interstitial solid solution strengthening, and is an important strengthening element and an important austenite stabilizing element. In order to ensure low temperature impact toughness and weldability, its addition should be controlled to a low level. Mn can greatly improve the stability of austenite at the same time as increasing the strength of the structure through substitution and solid solution strengthening. Appropriate addition of C and Mn can significantly improve hardenability, lower the phase transition temperature of supercooled austenite, and obtain a high-strength martensitic structure. On the other hand, in the martensite tempering process, the addition of C and Mn lowered the temperature required to form a certain amount of reverse-transformed austenite. Since C and Mn are rich in reverse-transformed austenite, they can maintain a stable structure even at low temperatures, making them important structures for improving the plasticity and toughness of the present invention. If the tempering temperature of the present invention is lower than 600°C, especially around 550°C, grain boundary segregation of elements such as Mn and P tends to occur, which may reduce toughness. The inventor fully studied the mechanism of action of the C and Mn elements in the present invention, and found that "low carbon manganese" with 0.04 to 0.08% C and 5.2 to 6.0% Mn A compositional design was decided.
Siは製鋼工程の脱酸素元素であり、適量のSiはMnとPの偏析を抑制し、靭性を向上させることができる。Siは固溶体強化も可能であるが、含有量が0.3%を超えると靭性が大幅に低下することがある。本発明では、Siを0.1~0.4%に制御されている。 Si is a deoxidizing element in the steelmaking process, and an appropriate amount of Si can suppress segregation of Mn and P and improve toughness. Solid solution strengthening is also possible with Si, but if the content exceeds 0.3%, the toughness may be significantly reduced. In the present invention, Si is controlled to 0.1 to 0.4%.
Moは焼戻し後のマルテンサイトの強度を高めることができ、特定の含有量範囲内で、Mnの粒界偏析を弱めて靭性を向上させることもできる。本発明において、Moの含有量を0.1~0.5%に制御されているため、Moの役割を果たしながら、コストを大幅に増加させることはない。 Mo can increase the strength of martensite after tempering, and within a specific content range, can also weaken grain boundary segregation of Mn to improve toughness. In the present invention, since the Mo content is controlled to 0.1 to 0.5%, Mo does not significantly increase the cost while fulfilling the role of Mo.
Niはオーステナイト相の安定化、焼入れ性の向上、延性-脆性転移温度の低下が可能で、低温靭性の向上に有効な元素であると同時に、溶接性の向上にも役立つ。但し、Niは高価であり、本発明は、Ni含有量を0.2~0.6%に制御し、コストを大幅に増加させることなく、Ni元素の有益な効果を十分に発揮している。 Ni stabilizes the austenite phase, improves hardenability, and lowers the ductility-brittle transition temperature. It is an element effective in improving low-temperature toughness and also helps improve weldability. However, Ni is expensive, and the present invention controls the Ni content to 0.2 to 0.6%, and fully exhibits the beneficial effects of the Ni element without significantly increasing the cost. .
Crは明らかな固溶体強化効果を生み出すことができ、強度の向上に有益で、耐食性の改善をすることができる。しかし、本発明において多数のMn元素を添加する場合では、Cr含有量が高すぎると、焼戻し時に粒界でCrおよびMnの炭化物が形成されやすくなり、亀裂成長に対する粒界の障壁を減らし、塑性および靭性を低下させることがある。本発明において、Crの含有量範囲は0.2~0.6%の適切な範囲内に制御されている。 Cr can produce a distinct solid-solution strengthening effect, which is beneficial for increasing strength and can improve corrosion resistance. However, in the case of adding a large number of Mn elements in the present invention, if the Cr content is too high, carbides of Cr and Mn are likely to be formed at the grain boundaries during tempering, which reduces the grain boundary barriers to crack growth and increases plasticity. and may reduce toughness. In the present invention, the Cr content range is controlled within an appropriate range of 0.2 to 0.6%.
本発明では、少量のTiが添加されているため、微細で分散した第2相析出形態を介した高温での粒界移動を妨げることができ、それにより結晶粒を微細化し、機械的特性を改善している。添加量は0.01~0.05%の範囲内に制御されている。 In the present invention, a small amount of Ti is added, which can prevent grain boundary migration at high temperature through a fine and dispersed second phase precipitation morphology, thereby refining grains and improving mechanical properties. Improving. The amount added is controlled within the range of 0.01 to 0.05%.
PおよびSの含有量を厳密に制御する必要があり、本発明において、中程度含有量のMn元素を添加した場合、Sは、MnとMnSを形成しやすく、可塑性を低下させることがある。Pは粒界に偏析する傾向があり、粒界の亀裂成長抵抗を低下させ、靭性が低下させる。本発明は、S≦0.005%およびP≦0.010%が必要となる。 It is necessary to strictly control the contents of P and S. In the present invention, when a medium content of Mn element is added, S easily forms Mn and MnS, which may reduce plasticity. P tends to segregate at grain boundaries, lowering crack growth resistance at grain boundaries and reducing toughness. The present invention requires S≤0.005% and P≤0.010%.
本発明の残りの部分はFeであるが、通常の製造工程では原材料または周囲の環境から不純物が混入することは避けらない。これらの不純物は当業者には明らかであるため、それらの名前および内容は、本明細書では具体的に記載されていない。 The remainder of the present invention is Fe, but the normal manufacturing process unavoidably introduces impurities from raw materials or the surrounding environment. Since these impurities are obvious to those skilled in the art, their names and contents are not specifically described herein.
本発明の製造方法において、鉄水脱硫処理後、転炉製錬を行うことによって、S、P含有量をS≦0.005%、P≦0.010%に還元し、十分高い真空度(真空度≦4mbar)、十分長い真空時間(処理時時間≧20min)のRH処理によってガス不純物元素の含有量を減らしているが、C、Mn、Si、Mo、Ni、Tiおよびその他の合金の添加はLF精錬によって完了するため、高純度の製錬効果が得られる。 In the production method of the present invention, the S and P contents are reduced to S ≤ 0.005% and P ≤ 0.010% by performing converter smelting after iron water desulfurization treatment, and a sufficiently high degree of vacuum ( The content of gas impurity elements is reduced by RH treatment with a vacuum degree ≤ 4 mbar) and a sufficiently long vacuum time (treatment time ≥ 20 min), but the addition of C, Mn, Si, Mo, Ni, Ti and other alloys is completed by LF refining, so a high-purity refining effect can be obtained.
スラブ鋳造は、連続鋳造または型鋳造+鍛造で、さまざまなサイズのスラブを得ることができる。スラブの厚さ≦320mmの場合は連続鋳造によって得られるため、生産効率が高い。それより厚いスラブ(>320mm)は、型鋳造+鍛造によって得られる。本発明で要求されるコアの機械的特性を達成するために、必要な条件として十分な圧延総変形量が必要となっている。本発明では、鋼板の厚さに対するスラブの厚さの比は4以上である必要があるので、圧延総変形量が75%以上であることを保証することができる。鋼板の厚さが80mmの場合、必要なスラブの厚さは320mm以上、鋼板の厚さが150mmの場合、必要なスラブの厚さは600mm以上である。得られたスラブは、圧延および熱処理プロセスを通じて必要な構造と特性を取得する。 Slab casting can be continuous casting or die casting + forging to obtain slabs of various sizes. When the thickness of the slab is ≦320 mm, the production efficiency is high because it is obtained by continuous casting. Thicker slabs (>320 mm) are obtained by die casting + forging. In order to achieve the mechanical properties of the core required in the present invention, a sufficient rolling total deformation amount is required as a necessary condition. In the present invention, since the ratio of the thickness of the slab to the thickness of the steel sheet must be 4 or more, it is possible to ensure that the total rolling deformation amount is 75% or more. If the steel plate thickness is 80 mm, the required slab thickness is 320 mm or more, and if the steel plate thickness is 150 mm, the required slab thickness is 600 mm or more. The resulting slab acquires the required structure and properties through rolling and heat treatment processes.
本発明の組成範囲内では、鋼のAc3温度が770℃以下である。スラブを1060~1140℃に加熱すると、高温のオーステナイト構造が形成されると同時に、C、Mnなどの合金元素が拡散により均質化される。スラブのコアの温度が表面温度に近く、保温が続く均熱中に、オーステナイトはスラブ全体で均質化され、40~90minの均熱時間は元素の均一な拡散を保証することができる。1140°C以下の温度では、Tiの第2相粒子が結晶粒の成長を妨げる役割を果たすことができる。ただし、温度が1060℃未満の場合、元素の拡散が遅くなり、オーステナイトの均質化効率が低くなることがある。 Within the composition range of the present invention, the Ac3 temperature of the steel is 770°C or less. When the slab is heated to 1060-1140° C., a high temperature austenitic structure is formed and at the same time the alloying elements such as C, Mn are homogenized by diffusion. During soaking when the temperature of the core of the slab is close to the surface temperature and the heat retention continues, the austenite is homogenized throughout the slab, and the soaking time of 40-90min can ensure the uniform diffusion of the elements. At temperatures below 1140° C., Ti second phase particles can play a role in hindering grain growth. However, if the temperature is less than 1060° C., the diffusion of the elements slows down and the austenite homogenization efficiency may decrease.
本発明において、加熱されたスラブは、結晶粒を微細化するために、930℃以上で再結晶化され、圧延される。圧延開始温度≦1020℃の場合は、再結晶後の結晶粒成長速度が速すぎるのを防ぐことができる。通過変形量が10%以上の場合は、再結晶の微細化効果を保証するために、オーステナイトを変形後に十分な歪みエネルギーの累積を持たせることができる。 In the present invention, the heated slab is recrystallized at 930° C. or higher and rolled to refine grains. When the rolling start temperature ≤ 1020°C, it is possible to prevent the crystal grain growth rate after recrystallization from becoming too fast. If the passing deformation amount is 10% or more, the austenite can have sufficient accumulated strain energy after deformation to ensure the refinement effect of recrystallization.
鋼板を圧延した後、圧延変形後に微細化された再結晶粒の過度の成長を避けるために、圧延後の鋼板を直ちに水冷する必要がある。水冷中にマルテンサイトの変換が発生することもある。本発明において十分な量のMn元素を添加することにより、マルテンサイト変換の臨界冷却速度は1℃/s未満であるが、冷却速度が低い場合でもマルテンサイト構造を得ることができる。鋼板の厚さが厚い場合、コアの冷却は通常、表面の冷却よりも大幅に遅くなるが、本発明の組成設計は、厚さ80~150mmの鋼板のコアにおいてもマルテンサイト変換が発生することを保証することができる。但し、冷却速度が速すぎると、鋼板の熱応力が高すぎになりやすく、鋼板にひび割れが生じることさえあり得るので、本発明は、平均冷却速度が5℃/sを超えないように制御されている。圧延後に冷却された鋼板の表面が赤に戻る温度は360℃以下に選択されているため、冷却中の明らかな元素偏析を防ぎ、粗大な炭化物の析出を抑えることができると同時に、この温度はまた、本発明の組成におけるマルテンサイト変換開始温度よりも低い。本発明で選択された圧延後の冷却プロセスは、その後の熱処理プロセスに適した前駆体構造を提供することができる。 After rolling the steel sheet, it is necessary to immediately water-cool the steel sheet after rolling in order to avoid excessive growth of recrystallized grains refined after rolling deformation. Martensite transformation may also occur during water cooling. By adding a sufficient amount of Mn element in the present invention, the critical cooling rate for martensitic conversion is less than 1° C./s, but a martensitic structure can be obtained even at low cooling rates. When the thickness of the steel plate is large, the cooling of the core is usually much slower than the cooling of the surface, but the compositional design of the present invention allows the martensite transformation to occur even in the core of the steel plate with a thickness of 80 to 150 mm. can be guaranteed. However, if the cooling rate is too fast, the thermal stress of the steel sheet tends to be too high, and cracks may even occur in the steel sheet. ing. The temperature at which the surface of the steel plate cooled after rolling returns to red is selected below 360°C, which can prevent obvious elemental segregation during cooling and suppress the precipitation of coarse carbides. In addition, it is lower than the martensite transformation start temperature in the composition of the present invention. The post-rolling cooling process selected in the present invention can provide a precursor structure suitable for subsequent heat treatment processes.
本発明は、鋼板に対して焼入れ+焼戻し熱処理を行う。780~830℃の焼入れ温度はAc3より高く、オーステナイト構造は均熱により得られる。鋼板は圧延後に水冷を行い、冷却中の元素の偏析や粗大な炭化物の生成が回避されたため、オーステナイト内の元素の均質化時間が大幅に短縮されている。本発明が選択された焼入れ加熱の均熱時間は5~15minで、オーステナイトの均質化を確保しながら、結晶粒径を効果的に微細化することもでき、鋼板の機械的特性の改善に有益である。焼入れ冷却速度の選択は、圧延後の冷却速度の選択と同じ理由で、2~8℃/sに制御されている。しかし、焼入れされた鋼板の表面が赤に戻る温度は110℃以下である必要があり、この温度は本発明の組成の下でのマルテンサイト変換終了温度よりも低く、鋼板全体が高強度の焼入れマルテンサイト構造を得ることが保証できる。 In the present invention, a steel sheet is subjected to quenching and tempering heat treatment. The quenching temperature of 780-830°C is higher than Ac3, and the austenitic structure is obtained by soaking. The steel sheet is water-cooled after rolling, which avoids the segregation of elements and the formation of coarse carbides during cooling, thus greatly shortening the homogenization time of the elements in the austenite. The soaking time for quenching heating selected in the present invention is 5 to 15 minutes, and it is possible to effectively refine the grain size while ensuring homogenization of austenite, which is beneficial for improving the mechanical properties of the steel plate. is. The selection of the cooling rate for quenching is controlled at 2-8° C./s for the same reason as the selection of the cooling rate after rolling. However, the temperature at which the surface of the quenched steel sheet returns to red must be 110°C or lower, which is lower than the martensite transformation end temperature under the composition of the present invention, and the entire steel sheet can be quenched with high strength. Obtaining a martensitic structure can be guaranteed.
焼入れ後の鋼板に対して焼戻し熱処理を行う。焼戻し温度が610~640℃、均熱時間が40~70minの焼戻し工程では、マルテンサイトの強度・靭性整合性の向上に加え、体積分率が4~10%の逆変換オーステナイトも得られ、これは主にフィルムの形をしており、マルテンサイトのスラットの間に分布されている。焼戻し中に、CやMnなどのオーステナイト安定化元素がオーステナイト内に富み、オーステナイトの安定性が向上させているだけでなく、焼戻し後室温までに空冷中、およびそれよりも温度が低い場合でも、オーステナイト依然として結晶構造の安定性を維持でき、マルテンサイト変換が起こらない。焼戻し後の鋼板への空冷が、極厚鋼板の熱応力を低減し、鋼板の品質を向上させることもできる。 Tempering heat treatment is performed on the steel plate after quenching. In the tempering process with a tempering temperature of 610 to 640 ° C. and a soaking time of 40 to 70 minutes, in addition to improving the strength and toughness consistency of martensite, reverse-transformed austenite with a volume fraction of 4 to 10% can be obtained. is mainly in the form of a film and is distributed between the martensite slats. During tempering, austenite stabilizing elements such as C and Mn are enriched in the austenite, which not only increases the stability of the austenite, but also during air cooling to room temperature after tempering and even at lower temperatures. Austenite can still maintain the stability of the crystal structure and no martensite transformation occurs. Air-cooling the steel plate after tempering can also reduce the thermal stress of the extra-thick steel plate and improve the quality of the steel plate.
本発明は熱処理後に、鋼板の厚さ方向全体、特に鋼板のコア部分にマルテンサイト+オーステナイト構造が得られた。引張変形中に、マルテンサイトマトリックスは690MPa以上の降伏強度を提供し、焼き戻し後のマルテンサイトの塑性も改善されている。オーステナイトは、変形の初期段階と中期段階で局所的な応力集中を緩和するための軟質相として機能するが、変形の後期段階でマルテンサイトが発生し、強化の役割を果たすことができる。したがって、オーステナイトの存在は、亀裂の発生と伝播を遅らせ、引張強度と破壊後の伸び率を改善する重要な役割を果たしている。衝撃変形中に、オーステナイトの存在は亀裂伝播を妨げ、亀裂伝播抵抗を向上させることによって、衝撃靭性が改善された。本発明におけるオーステナイトは十分な安定性を有するので、-60℃の場合でも衝撃靭性に有益な効果を発揮することができる。本発明におけるオーステナイト構造の有益な効果は、その体積分率および元素濃縮度と密接に関連されており、製造方法のプロセスパラメータ、特に焼戻し熱処理のプロセスパラメータの選択は、最も直接的にオーステナイト構造の性質を決定されている。 In the present invention, after heat treatment, a martensite+austenite structure was obtained in the entire thickness direction of the steel sheet, particularly in the core portion of the steel sheet. During tensile deformation, the martensite matrix provides a yield strength of over 690 MPa, and the plasticity of martensite after tempering is also improved. Austenite acts as a soft phase to relieve local stress concentrations during the early and middle stages of deformation, whereas martensite occurs during the later stages of deformation and can play a strengthening role. Therefore, the presence of austenite plays an important role in retarding crack initiation and propagation and improving tensile strength and post-break elongation. During impact deformation, the presence of austenite improved impact toughness by impeding crack propagation and increasing crack propagation resistance. The austenite in the present invention has sufficient stability to exert beneficial effects on impact toughness even at -60°C. The beneficial effect of the austenitic structure in the present invention is closely related to its volume fraction and elemental enrichment, and the selection of process parameters of the manufacturing method, especially the tempering heat treatment, is most directly related to the austenitic structure. nature is determined.
具体的には、本発明の鋼板のコアの機械的特性は、降伏強度が690MPa以上、引張強度が770MPa以上、破壊後の伸び率が14%以上、および、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは80J以上である。 Specifically, the mechanical properties of the core of the steel sheet of the present invention are a yield strength of 690 MPa or more, a tensile strength of 770 MPa or more, an elongation after breakage of 14% or more, and a V-shaped test piece at -60 ° C. The energy absorbed in the Charpy pendulum impact test is 80 J or more.
本発明における機械的特性の定義は、規格GB/T228.1、GB/T229およびGB/T5313に従っているが、これらの技術的指標の定義は当業者には明らかであるため、この明細書では詳しく説明をしない。 The definition of mechanical properties in the present invention follows standards GB/T228.1, GB/T229 and GB/T5313. No explanation.
特に、本発明は優れた鋼板のコアの機械的特性を達成すると同時に、鋼板の厚さの他の位置の機械的特性もコアの機械的特性に達している。本発明は、極厚鋼板の各位置の構成および性能を効果的に制御されているため、鋼板は、高い厚さ方向の断面収縮率を有し、板厚方向の延びによる断面収縮率は50%以上で、その抗層状引き裂き性能は非常に優れている。 In particular, the present invention achieves excellent core mechanical properties of the steel sheet, while the mechanical properties of other positions in the thickness of the steel sheet also reach the core mechanical properties. Since the present invention effectively controls the structure and performance of each position of the extra thick steel plate, the steel plate has a high cross-sectional shrinkage in the thickness direction, and the cross-sectional shrinkage due to elongation in the thickness direction is 50%. % and above, its anti-lamellar tear performance is very good.
以下は、具体的に実施例によって、上記鋼板およびその製造方法の詳細について説明する。 The details of the steel sheet and the method for producing the steel sheet will be described below by way of specific examples.
実施例1:80mmの厚さ、および0.06%のC、5.7%のMn、0.22%のSi、0.35%のMo、0.2%のNi、0.31%のCr、0.02%のTi、S≦0.005%、P≦0.010%、残りのFeおよびその他の回避できない不純物元素を含む化学組成(含有量は質量百分率で表す)を備えたコアの機械的特性が優れている690MPaグレードの極厚鋼板。 Example 1: 80 mm thick and 0.06% C, 5.7% Mn, 0.22% Si, 0.35% Mo, 0.2% Ni, 0.31% A core with a chemical composition containing Cr, 0.02% Ti, S≤0.005%, P≤0.010%, the balance Fe and other unavoidable impurity elements (content expressed in mass percentage) 690 MPa grade extra heavy steel plate with excellent mechanical properties.
上記鋼板の製造方法は以下のとおりとなっている。
鉄水脱硫処理後、転炉製錬を行い、鋼水の中のS、P含有量をS≦0.005%、P≦0.010%に還元する。LF精錬によってC、Mn、Si、Mo、Ni、Tiなどの元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度が3mbar、処理時間が23minにして、鋼水中のガス不純物元素の含有量を減らす。連続鋳造によってスラブを取得し、厚さ320mmのスラブを取得する。スラブの温度を1140℃まで加熱し、均熱時間が60minである。加熱されたスラブを圧延し、圧延開始温度が1005℃で、圧延終了温度が952℃であり、圧延機の押下規程は320mm-280mm -240mm-200mm-165mm-135mm-110mm-90mm-80mmとなっている。圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の赤に戻る温度が350℃で、平均冷却速度が3.1℃/sとなっている。鋼板に対して焼入れし+焼き戻しの熱処理を行う。焼入れ温度は810℃、均熱時間は10minで、鋼板の表面が赤に戻る温度77℃までに水冷し、平均冷却速度は2.9℃/s、焼戻し温度は626℃、均熱時間は55minで、焼き戻し後の鋼板を室温までに空冷する。
The manufacturing method of the steel plate is as follows.
After iron water desulfurization treatment, converter smelting is performed to reduce the S and P contents in the steel water to S≦0.005% and P≦0.010%. After completing the alloying of the required mass fraction of elements such as C, Mn, Si, Mo, Ni, Ti by LF refining, RH treatment is performed, the vacuum degree is 3 mbar, the treatment time is 23 minutes, and the reduce the content of gas impurity elements in A slab is obtained by continuous casting to obtain a slab with a thickness of 320 mm. The temperature of the slab is heated up to 1140° C. and the soaking time is 60 min. The heated slab is rolled, the rolling start temperature is 1005 ° C., the rolling end temperature is 952 ° C., and the pressing regulation of the rolling mill is 320 mm - 280 mm - 240 mm - 200 mm - 165 mm - 135 mm - 110 mm - 90 mm - 80 mm. ing. The steel sheet after rolling is immediately water-cooled, the temperature at which the surface of the steel sheet after cooling returns to red is 350°C, and the average cooling rate is 3.1°C/s. The steel plate is quenched and tempered. The quenching temperature is 810°C, the soaking time is 10 minutes, and the surface of the steel sheet is water-cooled to a temperature of 77°C at which the surface returns to red. The average cooling rate is 2.9°C/s, the tempering temperature is 626°C, and the soaking time is 55 minutes. Then, the tempered steel sheet is air-cooled to room temperature.
得られた鋼板構造はマルテンサイトとオーステナイトを含み、オーステナイトの体積分率は6.5%となっている。図1に鋼板のコア構造の透過型電子顕微鏡写真を示し、マルテンサイトとオーステナイトが間隔を置いて分布していることが写真で観察でき、その中で、明るいコントラストのスラット状構造はマルテンサイトで、暗いコントラストのフィルム状構造はオーステナイトである。鋼板のコアの降伏強度は758MPa、引張強度は842MPa、破壊後の伸び率は16%、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは135Jである。鋼板の厚さ方向の断面収縮率は63%である。 The resulting steel plate structure contains martensite and austenite, with the austenite volume fraction being 6.5%. Figure 1 shows a transmission electron micrograph of the core structure of the steel sheet. It can be observed in the photograph that martensite and austenite are distributed at intervals, among which the slat-like structure with bright contrast is martensite. , the dark-contrast film-like structure is austenite. The core of the steel sheet has a yield strength of 758 MPa, a tensile strength of 842 MPa, an elongation after breaking of 16%, and an energy absorbed of 135 J in a Charpy pendulum impact test of a V-shaped specimen at -60°C. The cross-sectional shrinkage in the thickness direction of the steel sheet is 63%.
実施例2:80mmの厚さ、および0.04%のC、5.2%のMn、0.4%のSi、0.1%のMo、0.6%のNi、0.6%のCr、0.01%のTi、S≦0.005%、P≦0.010%、残りのFeおよびその他の回避できない不純物元素を含む化学組成(含有量は質量百分率で表す)を備えたコアの機械的特性が優れている690MPaグレードの極厚鋼板。 Example 2: 80 mm thick and 0.04% C, 5.2% Mn, 0.4% Si, 0.1% Mo, 0.6% Ni, 0.6% A core with a chemical composition containing Cr, 0.01% Ti, S≤0.005%, P≤0.010%, the balance Fe and other unavoidable impurity elements (content expressed in mass percentage) 690 MPa grade extra heavy steel plate with excellent mechanical properties.
上記鋼板の製造方法は以下のとおりとなっている。
鉄水脱硫処理後、転炉製錬を行い、鋼水の中のS、P含有量をS≦0.005%、P≦0.010%に還元する。LF精錬によってC、Mn、Si、Mo、Ni、Tiなどの元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度が3mbar、処理時間が20minにして、鋼水中のガス不純物元素の含有量を減らす。連続鋳造によってスラブを取得し、厚さ320mmのスラブを取得する。スラブの温度を1105℃まで加熱し、均熱時間が40minである。加熱されたスラブを圧延し、圧延開始温度が1001℃で、圧延終了温度が930℃であり、圧延機の押下規程は320mm-280mm-240mm-200mm-165mm-135mm-110mm-90mm-80mmとなっている。圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の赤に戻る温度が271℃で、平均冷却速度が4.7℃/sとなっている。鋼板に対して焼入れし+焼き戻しの熱処理を行う。焼入れ温度は830℃、均熱時間は5minで、鋼板の表面が赤に戻る温度51℃までに水冷し、平均冷却速度は4.2℃/s、焼戻し温度は640℃、均熱時間は40minで、焼き戻し後の鋼板を室温までに空冷する。
The manufacturing method of the steel plate is as follows.
After iron water desulfurization treatment, converter smelting is performed to reduce the S and P contents in the steel water to S≦0.005% and P≦0.010%. After completing the alloying of the required mass fraction of elements such as C, Mn, Si, Mo, Ni, and Ti by LF refining, RH treatment is performed, the vacuum degree is 3 mbar, the treatment time is 20 min, and the reduce the content of gas impurity elements in A slab is obtained by continuous casting to obtain a slab with a thickness of 320 mm. The temperature of the slab is heated up to 1105°C and the soaking time is 40min. The heated slab is rolled, the rolling start temperature is 1001°C, the rolling end temperature is 930°C, and the press down regulation of the rolling mill is 320mm-280mm-240mm-200mm-165mm-135mm-110mm-90mm-80mm. ing. The steel sheet after rolling is immediately water-cooled, the temperature at which the surface of the steel sheet after cooling returns to red is 271°C, and the average cooling rate is 4.7°C/s. The steel plate is quenched and tempered. The quenching temperature is 830°C, the soaking time is 5 minutes, and the surface of the steel sheet is water-cooled to a temperature of 51°C at which the surface returns to red. The average cooling rate is 4.2°C/s, the tempering temperature is 640°C, and the soaking time is 40 minutes. Then, the tempered steel sheet is air-cooled to room temperature.
得られた鋼板構造はマルテンサイトとオーステナイトを含み、オーステナイトの体積分率は10%となっている。鋼板のコアの降伏強度は741MPa、引張強度は821MPa、破壊後の伸び率は17.5%、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは165Jである。 鋼板の厚さ方向の断面収縮率は71%である。 The resulting steel plate structure contains martensite and austenite, with the austenite volume fraction being 10%. The core of the steel sheet has a yield strength of 741 MPa, a tensile strength of 821 MPa, an elongation after fracture of 17.5%, and an energy absorbed of 165 J in a Charpy pendulum impact test of a V-shaped specimen at -60°C. The cross-sectional shrinkage in the thickness direction of the steel plate is 71%.
実施例3:150mmの厚さ、および0.08%のC、6.0%のMn、0.1%のSi、0.5%のMo、0.5%のNi、0.2%のCr、0.05%のTi、S≦0.005%、P≦0.010%、残りのFeおよびその他の回避できない不純物元素を含む化学組成(含有量は質量百分率で表す)を備えたコアの機械的特性が優れている690MPaグレードの極厚鋼板。 Example 3: 150 mm thick and 0.08% C, 6.0% Mn, 0.1% Si, 0.5% Mo, 0.5% Ni, 0.2% A core with a chemical composition containing Cr, 0.05% Ti, S≤0.005%, P≤0.010%, the balance Fe and other unavoidable impurity elements (content expressed in mass percentage) 690 MPa grade extra heavy steel plate with excellent mechanical properties.
上記鋼板の製造方法は以下のとおりとなっている。
鉄水脱硫処理後、転炉製錬を行い、鋼水の中のS、P含有量をS≦0.005%、P≦0.010%に還元する。LF精錬によってC、Mn、Si、Mo、Ni、Tiなどの元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度が3mbar、処理時間が26minにして、鋼水中のガス不純物元素の含有量を減らす。型鋳造後の鍛造によってスラブを取得し、厚さ610mmのスラブを取得する。スラブの温度を1060℃まで加熱し、均熱時間が90minである。加熱されたスラブを圧延し、圧延開始温度が1015℃で、圧延終了温度が942℃であり、圧延機の押下規程は610mm-540mm-470mm-400mm-340mm-290mm-245mm-215mm-190mm-170mm-150mmとなっている。圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の赤に戻る温度が327℃で、平均冷却速度が1.5℃/sとなっている。鋼板に対して焼入れし+焼き戻しの熱処理を行う。焼入れ温度は780℃、均熱時間は15minで、鋼板の表面が赤に戻る温度102℃までに水冷し、平均冷却速度は1.2℃/s、焼戻し温度は610℃、均熱時間は70minで、焼き戻し後の鋼板を室温までに空冷する。
The manufacturing method of the steel plate is as follows.
After iron water desulfurization treatment, converter smelting is performed to reduce the S and P contents in the steel water to S≦0.005% and P≦0.010%. After completing the alloying of the required mass fraction of elements such as C, Mn, Si, Mo, Ni, and Ti by LF refining, RH treatment is performed, the degree of vacuum is 3 mbar, the treatment time is 26 min, and the reduce the content of gas impurity elements in A slab with a thickness of 610 mm is obtained by forging after die casting. The temperature of the slab is heated up to 1060°C and the soaking time is 90min. The heated slab is rolled, the rolling start temperature is 1015°C, the rolling end temperature is 942°C, and the pressing range of the rolling mill is 610mm-540mm-470mm-400mm-340mm-290mm-245mm-215mm-190mm-170mm. -150 mm. The steel sheet after rolling is immediately water-cooled, the temperature at which the surface of the steel sheet after cooling returns to red is 327°C, and the average cooling rate is 1.5°C/s. The steel plate is quenched and tempered. The quenching temperature is 780°C, the soaking time is 15 minutes, and the surface of the steel sheet is water-cooled to 102°C, the temperature at which the surface returns to red, the average cooling rate is 1.2°C/s, the tempering temperature is 610°C, and the soaking time is 70 minutes. Then, the tempered steel sheet is air-cooled to room temperature.
得られた鋼板構造はマルテンサイトとオーステナイトを含み、オーステナイトの体積分率は4%となっている。鋼板のコアの降伏強度は745MPa、引張強度は819MPa、破壊後の伸び率は15%、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは106Jである。鋼板の厚さ方向の断面収縮率は57%である。 The resulting steel plate structure contains martensite and austenite, with the volume fraction of austenite being 4%. The core of the steel sheet has a yield strength of 745 MPa, a tensile strength of 819 MPa, an elongation after fracture of 15%, and an energy absorbed of 106 J in a Charpy pendulum impact test of a V-shaped specimen at -60°C. The cross-sectional shrinkage in the thickness direction of the steel sheet is 57%.
実施例4:4組の平行実験を設計し、詳細は以下の表1に示すように、構成要素の含有量および調製方法は、圧延開始温度を除いて、基本的に実施例1のものと同じであった。 Example 4: Four sets of parallel experiments were designed, the details of which are shown in Table 1 below. was the same.
表1から分かるように、グループ1~2は本発明の範囲内の圧延開始温度であるが、グループ3~4は本発明の範囲外の圧延開始温度であり、それによって調製された鋼板の破断後の伸び、低温衝撃エネルギーおよび板厚方向の断面収縮率などの性能が低下している。 As can be seen from Table 1, groups 1 and 2 have rolling start temperatures within the range of the present invention, but groups 3 and 4 have rolling start temperatures outside the range of the present invention, whereby the steel sheets prepared thereby break. Performance such as post-elongation, low-temperature impact energy, and cross-sectional shrinkage in the plate thickness direction are degraded.
実施例5:3組の平行実験を設計し、詳細は以下の表2に示すように、構成要素の含有量および調製方法は、焼入れ後の冷却速度を除いて、基本的に実施例2のものと同じであった。 Example 5: Three sets of parallel experiments were designed, the details of which are shown in Table 2 below. was the same as
表2から分かるように、グループ1は本発明の範囲内の焼入れ後の水冷の平均冷却速度であるが、グループ2~3は本発明の範囲外の平均冷却速度であり、グループ2の鋼板の降伏強度と低温衝撃エネルギーの性能が低下している。グループ3の鋼板の低温衝撃エネルギーの性能が低下し、熱応力による亀裂が鋼板に現れている。 As can be seen from Table 2, Group 1 is the average cooling rate of water cooling after quenching within the range of the present invention, but Groups 2 and 3 are average cooling rates outside the range of the present invention. Yield strength and low temperature impact energy performance are degraded. The low temperature impact energy performance of the Group 3 steel sheets is degraded and cracks due to thermal stress appear in the steel sheets.
(付記)
(付記1)
化学組成の質量百分率はC:0.04~0.08%、Mn:5.2~6.0%、Si:0.1~0.4%、Mo:0.1~0.5%、Ni:0.2~0.6%、Cr:0.2~0.6%、Ti:0.01~0.05%、S:≦0.005%、P:≦0.010%、残部Feおよび不純物を含む、
ことを特徴とする690MPaグレードの極厚鋼板。
(Appendix)
(Appendix 1)
The mass percentage of the chemical composition is C: 0.04 to 0.08%, Mn: 5.2 to 6.0%, Si: 0.1 to 0.4%, Mo: 0.1 to 0.5%, Ni: 0.2 to 0.6%, Cr: 0.2 to 0.6%, Ti: 0.01 to 0.05%, S: ≤0.005%, P: ≤0.010%, balance containing Fe and impurities,
A 690 MPa grade extra-thick steel plate characterized by:
(付記2)
前記鋼板の厚さが80~150mmである、
ことを特徴とする付記1に記載の690MPaグレードの極厚鋼板。
(Appendix 2)
The steel plate has a thickness of 80 to 150 mm,
A 690 MPa grade extra-thick steel plate according to appendix 1, characterized in that:
(付記3)
前記鋼板の微細構造がマルテンサイトおよびオーステナイトを有し、その中に、オーステナイトの体積分率が4~10%である、
ことを特徴とする付記1に記載の690MPaグレードの極厚鋼板。
(Appendix 3)
The microstructure of the steel sheet has martensite and austenite, in which the volume fraction of austenite is 4-10%.
A 690 MPa grade extra-thick steel plate according to appendix 1, characterized in that:
(付記4)
前記オーステナイトが薄膜の形態であり、オーステナイトがマルテンサイトスラット間に分布している、
ことを特徴とする付記3に記載の690MPaグレードの極厚鋼板。
(Appendix 4)
wherein the austenite is in the form of a thin film and the austenite is distributed between the martensitic slats;
A 690 MPa grade extra-thick steel plate according to appendix 3, characterized in that:
(付記5)
前記鋼板のコアの機械的特性は、降伏強度が690MPa以上、引張強度が770MPa以上、破壊後の伸びは14%以上、-60℃でのV型試験片のシャルピー振り子衝撃試験で吸収されるエネルギーは80J以上である、
ことを特徴とする付記1に記載の690MPaグレードの極厚鋼板。
(Appendix 5)
The mechanical properties of the core of the steel plate are yield strength of 690 MPa or more, tensile strength of 770 MPa or more, elongation after breakage of 14% or more, and energy absorbed in a Charpy pendulum impact test of a V-shaped test piece at -60 ° C. is greater than or equal to 80 J,
A 690 MPa grade extra-thick steel plate according to appendix 1, characterized in that:
(付記6)
前記鋼板の板厚方向の延びによる断面収縮率は50%以上である、
ことを特徴とする付記1に記載の690MPaグレードの極厚鋼板。
(Appendix 6)
The cross-sectional shrinkage rate due to elongation in the thickness direction of the steel sheet is 50% or more.
A 690 MPa grade extra-thick steel plate according to appendix 1, characterized in that:
(付記7)
下記ステップを含むことを特徴とする付記1~6のいずれか1つに記載の690MPaグレードの極厚鋼板の調製方法であって、
(1)鉄水脱硫処理後、転炉製錬を行い、鋼水の中のS、P含有量をS≦0.005%、P≦0.010%に還元し、
(2)LF精錬によってC、Mn、Si、Mo、Ni、Ti元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度≦4mbar、加工時間≧20minにし、
(3)鋳造によってスラブを取得し、スラブの厚さと鋼板の厚さの比は4以上となり、
(4)スラブの温度を1060~1140℃まで加熱し、
(5)加熱されたスラブを圧延し、圧延開始温度≦1020℃、圧延終了温度≧930℃、通過変形量≧10%にし、
(6)圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の赤に戻る温度が≦360℃で、平均冷却速度が1~5℃/sとなり、
(7)焼入れ熱処理を行い、鋼板を780~830℃までに再加熱し、均熱時間が5~15minで、鋼板表面の赤に戻る温度が≦110℃までに水冷し、平均冷却速度が2~8℃/sとなり、
(8)焼戻し熱処理を行い、焼入れ後の鋼板を610~640℃までに加熱し、均熱時間が40~70minで、焼戻し後の鋼板が室温までに空冷される、
調製方法。
(Appendix 7)
A method for preparing a 690 MPa grade extra heavy steel plate according to any one of appendices 1 to 6, characterized in that it comprises the steps of:
(1) After the iron water desulfurization treatment, converter smelting is performed to reduce the S and P contents in the steel water to S ≤ 0.005% and P ≤ 0.010%,
(2) After completing the alloying of the required mass fractions of C, Mn, Si, Mo, Ni, and Ti elements by LF refining, perform RH treatment to make the degree of vacuum ≤ 4 mbar and the processing time ≥ 20 min,
(3) A slab is obtained by casting, and the ratio of the thickness of the slab to the thickness of the steel plate is 4 or more,
(4) heating the slab to a temperature of 1060-1140°C;
(5) Roll the heated slab to a rolling start temperature ≤ 1020°C, a rolling end temperature ≥ 930°C, and a passing deformation amount ≥ 10%;
(6) The steel sheet after rolling is immediately water-cooled, the temperature at which the surface of the steel sheet returns to red after cooling is ≦360° C., and the average cooling rate is 1 to 5° C./s,
(7) Perform quenching heat treatment, reheat the steel sheet to 780 ~ 830 ℃, soaking time is 5 ~ 15 minutes, water cooling until the temperature of the steel sheet surface returns to red is ≤ 110 ℃, average cooling rate is 2 ~8°C/s,
(8) Perform tempering heat treatment, heat the steel plate after quenching to 610 to 640 ° C., soak for 40 to 70 minutes, and air cool the steel plate after tempering to room temperature.
Method of preparation.
(付記8)
前記ステップ(3)の中のスラブが連続鋳造スラブまたは型鋳造後の鍛造スラブを採用する、
ことを特徴とする付記6に記載の調製方法。
(Appendix 8)
The slab in step (3) adopts a continuous cast slab or a forged slab after die casting.
The preparation method according to appendix 6, characterized in that:
(付記9)
スラブの厚さが320mm以下の場合、連続鋳造スラブを採用し、スラブの厚さが320mmを超えた場合、型鋳造後の鍛造スラブを採用する、
ことを特徴とする付記7に記載の調製方法。
(Appendix 9)
If the thickness of the slab is 320 mm or less, adopt the continuous cast slab, if the thickness of the slab exceeds 320 mm, adopt the forged slab after die casting.
The preparation method according to appendix 7, characterized in that
(付記10)
前記ステップ(4)において、スラブの均熱時間が40~90minとなっている、
ことを特徴とする付記6に記載の調製方法。
(Appendix 10)
In the step (4), the soaking time of the slab is 40 to 90 minutes,
The preparation method according to appendix 6, characterized in that:
Claims (6)
鋼板のコア部分の微細構造が、マルテンサイトおよびオーステナイトからなり、オーステナイトの体積分率が4~10%であり、前記オーステナイトが薄膜の形態であり、オーステナイトがマルテンサイトの薄板間に分布している、
鋼板の調製方法であって、
(1)溶鉄の脱硫処理後、転炉製錬を行い、溶鉄の中のS、P含有量をS≦0.005%、P≦0.010%に還元し、
(2)LF精錬によってC、Mn、Si、Mo、Ni、Ti元素に必要な質量分率の合金化を完了した後、RH処理を行い、真空度≦4mbar、加工時間≧20minにし、
(3)鋳造によってスラブを取得し、スラブの厚さと鋼板の厚さの比は4以上となり、
(4)スラブの温度を1060~1140℃まで加熱し、
(5)加熱されたスラブを圧延し、圧延開始温度≦1020℃、圧延終了温度≧930℃、1パス当たりの通過変形量≧10%にし、
(6)圧延後の鋼板に対して即時に水冷を行い、冷却後の鋼板表面の温度が≦360℃で、平均冷却速度が1~5℃/sとなり、
(7)焼入れ熱処理を行い、鋼板を780~830℃までに再加熱し、均熱時間が5~15minで、鋼板表面の温度が≦110℃までに水冷し、平均冷却速度が2~8℃/sとなり、
(8)焼戻し熱処理を行い、焼入れ後の鋼板を610~640℃までに加熱し、均熱時間が40~70minで、焼戻し後の鋼板が室温までに空冷される、
ステップを含むことを特徴とする鋼板の調製方法。 The mass percentage of the chemical composition is C: 0.04 to 0.08%, Mn: 5.2 to 6.0%, Si: 0.1 to 0.4%, Mo: 0.1 to 0.5%, Ni: 0.2 to 0.6%, Cr: 0.2 to 0.6%, Ti: 0.01 to 0.05%, S: ≤0.005%, P: ≤0.010%, balance consists of Fe and impurities,
The microstructure of the core part of the steel sheet consists of martensite and austenite, the volume fraction of austenite is 4-10%, the austenite is in the form of a thin film, and the austenite is distributed between the martensite thin plates. ,
A method for preparing a steel plate, comprising:
(1) After the desulfurization treatment of the molten iron, converter smelting is performed to reduce the S and P contents in the molten iron to S ≤ 0.005% and P ≤ 0.010%,
(2) After completing the alloying of the required mass fractions of C, Mn, Si, Mo, Ni, and Ti elements by LF refining, perform RH treatment to make the degree of vacuum ≤ 4 mbar and the processing time ≥ 20 min,
(3) A slab is obtained by casting, and the ratio of the thickness of the slab to the thickness of the steel plate is 4 or more,
(4) heating the slab to a temperature of 1060-1140°C;
(5) Rolling the heated slab to a rolling start temperature ≤ 1020 ° C, a rolling end temperature ≥ 930 ° C, a passing deformation per pass ≥ 10%,
(6) The steel sheet after rolling is immediately water-cooled, the surface temperature of the steel sheet after cooling is ≦360° C., and the average cooling rate is 1 to 5° C./s,
(7) Perform quenching heat treatment, reheat the steel plate to 780-830°C, soak for 5-15 minutes, water-cool the steel plate surface temperature to ≤110°C, and average cooling rate is 2-8°C. /s,
(8) Perform tempering heat treatment, heat the steel plate after quenching to 610 to 640 ° C., soak for 40 to 70 minutes, and air cool the steel plate after tempering to room temperature.
A method for preparing a steel sheet, comprising the steps of :
ことを特徴とする請求項1に記載の鋼板の調製方法。 The steel plate has a thickness of 80 to 150 mm,
The method for preparing a steel sheet according to claim 1, characterized in that:
ことを特徴とする請求項1に記載の鋼板の調製方法。 The mechanical properties of the core of the steel sheet are that the yield strength is 690 MPa or more, the tensile strength is 770 MPa or more , and the energy absorbed in the Charpy pendulum impact test of the V-shaped test piece at -60 ° C. is 80 J or more.
The method for preparing a steel sheet according to claim 1, characterized in that:
ことを特徴とする請求項1に記載の鋼板の調製方法。 The slab in step (3) adopts a continuous cast slab or a forged slab after die casting.
The method for preparing a steel sheet according to claim 1 , characterized in that:
ことを特徴とする請求項1に記載の鋼板の調製方法。 If the thickness of the slab is 320 mm or less, adopt the continuous cast slab, if the thickness of the slab exceeds 320 mm, adopt the forged slab after die casting.
The method for preparing a steel sheet according to claim 1 , characterized in that:
ことを特徴とする請求項1に記載の鋼板の調製方法。 In the step (4), the soaking time of the slab is 40 to 90 minutes,
The method for preparing a steel sheet according to claim 1 , characterized in that:
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| CN111778450A (en) * | 2020-06-24 | 2020-10-16 | 南京钢铁股份有限公司 | Medium-manganese medium-thickness steel for 800MPa engineering machinery and manufacturing method thereof |
| CN112359289B (en) * | 2020-11-23 | 2021-12-21 | 马鞍山钢铁股份有限公司 | Super-thick Q355-grade hot-rolled H-shaped steel with good low-temperature toughness and production method thereof |
| CN112899584A (en) * | 2021-01-15 | 2021-06-04 | 南京钢铁股份有限公司 | Ultralow temperature L-shaped steel and manufacturing method thereof |
| CN112705582A (en) * | 2021-01-28 | 2021-04-27 | 李艳峰 | Lead foil forming method |
| CN115323251B (en) * | 2022-08-24 | 2023-06-27 | 东北大学 | Super-thick steel plate for super-thick high-strength high-homogeneity hydropower and manufacturing method thereof |
| CN115582426A (en) * | 2022-09-05 | 2023-01-10 | 舞阳钢铁有限责任公司 | A Method for Improving the Shape of High Alloy Medium Plate After Quenching and Tempering |
| CN117926124A (en) * | 2023-12-29 | 2024-04-26 | 首钢集团有限公司 | Self-hardening crushing blade steel for straw returning and preparation method thereof |
| CN117626138B (en) * | 2023-12-29 | 2025-11-18 | 南京钢铁股份有限公司 | Low-temperature steel and its heat treatment methods and applications |
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