JP7789205B2 - High-yield-ratio high-strength steel with excellent impact resistance after cold forming and its manufacturing method - Google Patents
High-yield-ratio high-strength steel with excellent impact resistance after cold forming and its manufacturing methodInfo
- Publication number
- JP7789205B2 JP7789205B2 JP2024527810A JP2024527810A JP7789205B2 JP 7789205 B2 JP7789205 B2 JP 7789205B2 JP 2024527810 A JP2024527810 A JP 2024527810A JP 2024527810 A JP2024527810 A JP 2024527810A JP 7789205 B2 JP7789205 B2 JP 7789205B2
- Authority
- JP
- Japan
- Prior art keywords
- steel
- less
- temperature
- thickness
- cooling
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- 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
- C21D1/02—Hardening articles or materials formed by forging or rolling, with no further heating beyond that required for the formation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21C—MANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES, PROFILES OR LIKE SEMI-MANUFACTURED PRODUCTS OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
- B21C47/00—Winding-up, coiling or winding-off metal wire, metal band or other flexible metal material characterised by features relevant to metal processing only
- B21C47/02—Winding-up or coiling
-
- 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
-
- 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0221—Modifying the physical properties of ferrous metals or ferrous alloys 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
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0247—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
-
- 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0247—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
- C21D8/0263—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following 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
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0294—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a localised treatment
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/001—Austenite
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/002—Bainite
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/005—Ferrite
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
-
- 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
- C21D2211/009—Pearlite
-
- 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
- C21D2221/00—Treating localised areas of an article
- C21D2221/02—Edge parts
-
- 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
- C21D2221/00—Treating localised areas of an article
- C21D2221/10—Differential treatment of inner with respect to outer regions, e.g. core and periphery, respectively
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
- Heat Treatment Of Sheet Steel (AREA)
Description
本発明は、高強度鋼及びその製造方法に関するものであり、より詳細には、冷間成形後の耐衝撃性に優れ、高降伏比を有する高強度鋼及びその製造方法に関するものである。 The present invention relates to high-strength steel and a manufacturing method thereof, and more specifically to high-strength steel having excellent impact resistance after cold forming and a high yield ratio, and a manufacturing method thereof.
従来の商用車シャーシ部品は、車両特性上、厚さ8mm以上の鋼材が主に適用され、メンバ類には引張強度が600MPaレベルの高強度熱延鋼板を、ホイールディスクには引張強度が440MPaレベルの熱延鋼板を用いている。しかし、最近の軽量化のために、メンバ類には引張強度が700MPa以上、ホイールディスクには引張強度が590MPa以上の高強度鋼板を適用し、鋼板の厚さを下向きにしたり、部品のデザインを変更している傾向にある。また、ホイールは従来、プレス成形工程で製造されたが、最近ではスピニング(Spinning)及びフローフォーミング(Flow forming)によって製造される傾向にある。このような成形工程は熱延鋼板により大きい変形量を与えるため、より優れた伸び率を有する熱延鋼板が要求され、成形された部品は使用中の耐久性及び耐衝撃性の確保が要求される。 Due to vehicle characteristics, conventional commercial vehicle chassis parts are typically made of steel with a thickness of 8 mm or more. High-strength hot-rolled steel sheets with a tensile strength of 600 MPa are used for members, and hot-rolled steel sheets with a tensile strength of 440 MPa are used for wheel discs. However, in recent years, in pursuit of weight reduction, high-strength steel sheets with a tensile strength of 700 MPa or more are being used for members and 590 MPa or more for wheel discs, with a trend toward reducing steel thickness and changing part designs. Additionally, while wheels were traditionally manufactured using a press forming process, they are now increasingly being manufactured using spinning and flow forming. Because these forming processes subject hot-rolled steel sheets to greater deformation, they require hot-rolled steel sheets with higher elongation rates, and the formed parts must ensure durability and impact resistance during use.
しかし、従来の高強度鋼は、上記のスピニング及びフローフォーミング工程に適用する際に、部品の耐久性が従来と同等以上でなければならないが、部品の成形時に、せん断面等で微細なクラックが発生したり、成形量の高い部位で耐久性が劣るなど適用に困難性を伴う。 However, when conventional high-strength steel is used in the spinning and flow forming processes described above, the durability of the resulting parts must be equal to or greater than conventional steels. However, this can be difficult to achieve due to the occurrence of fine cracks on shear surfaces and other areas where the forming volume is high, resulting in poor durability.
従来の高強度鋼は、特許文献1及び2のように、通常のオーステナイト域の熱間圧延を経た後、高温で巻き取ってフェライトを基地組織とし、析出物を微細に形成させており、特許文献3のように、粗大なパーライトが形成されないように巻き取り温度をベイナイト基地組織が形成される温度まで冷却した後、巻き取る技術を適用している。また、特許文献4のように、Ti、Nb等を活用して熱間圧延中の未再結晶域で40%以上に大圧下して、オーステナイト結晶粒を微細化させる技術も提案されている。最近では、特許文献5のように、鋼板の厚さ表層部と深層部との間の微細組織の均一性を向上させ、粗大な炭化物形成を抑制する技術が提案されており、特許文献6のように、耐久性に悪影響を及ぼすパーライトとMA相(Martensite and Austenite)及びマルテンサイトの形成を同時に抑制する技術が提案された。 Conventional high-strength steels, as disclosed in Patent Documents 1 and 2, undergo normal hot rolling in the austenite region, followed by coiling at high temperatures to form a ferrite matrix and fine precipitates. Patent Document 3 also employs a coiling technique in which the steel is cooled to a temperature at which a bainite matrix structure is formed, preventing the formation of coarse pearlite. Patent Document 4 also proposes a technique for refining austenite grains by using Ti, Nb, etc. to reduce the roll width by a large reduction of 40% or more in the unrecrystallized region during hot rolling. More recently, Patent Document 5 proposes a technique for improving the uniformity of the microstructure between the surface and deeper layers of the steel plate and suppressing the formation of coarse carbides. Patent Document 6 proposes a technique for simultaneously suppressing the formation of pearlite, MA (Martensite and Austenite) phases, and martensite, which adversely affect durability.
しかし、特許文献1~4は、高強度厚物材のせん断成形時に、せん断面及びその周辺にクラックが発生することを考慮できておらず、厚さ8mm以上の厚物材では製造時に、確保し難い冷却速度条件と大圧下条件で構成されている。厚物材の結晶粒を微細化すると同時に強度確保のためにTi、Nb、V等の析出物形成元素を活用する場合、析出物が形成されやすい500~700℃の高温で巻き取るとフェライトが過度に成長して、降伏強度が減少し、粗大なパーライトが形成されるという問題がある。また、ベイナイト基地組織を活用するために低い巻き取り温度で製造する場合にも、熱延後の冷却中の鋼板の幅方向の冷却速度を均一に制御しないと、熱延鋼板に不均一微細組織が形成されて、高い伸び率を有し難く、安定した高降伏比特性の確保が難しくなり、成形時に、せん断面の割れ発生などの成形クラックに対する敏感度も増加するようになる。さらに、このような技術は、乗用車用に用いられる厚さ5mm未満の熱延鋼板を対象としているため、必要な冷却速度が高すぎて厚物材製造に不適合である。また、未再結晶域で40%の大圧下を加えることは、圧延板の形状品質を劣化させ、設備に負荷をかけることがあるため、厚さ8mm以上の厚物材に適用し難い。特許文献5及び6は、厚物材を対象とした発明である。まず、特許文献5は厚物高強度鋼の耐久性の向上のために厚さ深層部(1/4t~1/2t)内の結晶粒形状が等軸晶であり、微細な結晶粒を有するようにし、MA相及びマルテンサイト形成を抑制するように製造する技術を提案した。特許文献6は、特定の成分に対して導出された関係式を介して熱延コイルを長さ方向に3等分し、Head、Mid、Tail部をそれぞれ互いに異なる冷却終了温度まで一定の冷却速度条件で冷却した後、巻き取って製造する技術が提案された。このような技術は、部品のせん断面の品質を考慮して特定の成分に対して導出された関係式を介して熱間圧延後の冷却速度を制御することにより微細組織を均一に製造する技術であり、パンチングホール(hole)を多数含み、荷重が加えられ続ける商用車ホイールの耐久性を向上させるのに効果的な側面はあるが、成形後の耐衝撃性が考慮されなかった。また、熱間圧延後の鋼板の冷却を全幅にわたって均一に制御し難く、厚さが8mm以上で熱延鋼板が厚い場合には実際の冷却速度で制御しにくいという問題がある。 However, Patent Documents 1 to 4 fail to consider the occurrence of cracks on and around the sheared surfaces during shear forming of high-strength thick steel sheets, and are configured with cooling rate and large reduction conditions that are difficult to achieve during the production of thick steel sheets with a thickness of 8 mm or more. When using precipitate-forming elements such as Ti, Nb, and V to refine the grain size of thick steel sheets while simultaneously ensuring strength, coiling at high temperatures of 500 to 700°C, where precipitates are likely to form, can lead to excessive ferrite growth, reduced yield strength, and the formation of coarse pearlite. Furthermore, even when manufacturing at a low coiling temperature to utilize a bainite matrix structure, if the cooling rate in the width direction of the steel sheet during cooling after hot rolling is not uniformly controlled, a non-uniform microstructure will form in the hot-rolled steel sheet, making it difficult to achieve high elongation and stable high yield ratio properties. This also increases sensitivity to forming cracks, such as cracks on the sheared surfaces, during forming. Furthermore, since this technique is intended for hot-rolled steel sheets with a thickness of less than 5 mm used in passenger cars, the required cooling rate is too high and is therefore unsuitable for manufacturing thick steel sheets. Furthermore, applying a large reduction of 40% in the unrecrystallized region can deteriorate the shape quality of the rolled sheet and place a strain on the equipment, making it difficult to apply to thick steel sheets with a thickness of 8 mm or more. Patent Documents 5 and 6 are inventions aimed at thick steel sheets. First, Patent Document 5 proposes a manufacturing technique for thick high-strength steel sheets, in which the crystal grain shape in the deep thickness portion (1/4t to 1/2t) is equiaxed and has fine crystal grains, thereby suppressing the formation of MA phases and martensite, in order to improve the durability of the thick high-strength steel sheets. Patent Document 6 proposes a manufacturing technique in which a hot-rolled coil is divided into three equal parts in the length direction using a relational expression derived for specific components, and the head, mid, and tail portions are cooled to different cooling end temperatures at constant cooling rates and then coiled. This technology produces a uniform microstructure by controlling the cooling rate after hot rolling through a relationship derived for specific components, taking into account the quality of the shear surface of the part. While this is effective in improving the durability of commercial vehicle wheels, which contain numerous punched holes and are subject to constant load, it does not take into account impact resistance after forming. Furthermore, it is difficult to uniformly control the cooling of the steel sheet after hot rolling across its entire width, and when the hot-rolled steel sheet is thick, with a thickness of 8 mm or more, it is difficult to control the actual cooling rate.
熱間圧延後の冷却工程は、通常、長さ100~120mのROT(Run-Out Table)から数十秒以内で行われるが、熱延鋼板の厚さ深層部の冷却速度が提案した範囲を満足しながら、冷却終了温度または巻き取り温度まで冷却して製造し難い。したがって、上記従来技術において厚さが8mm以上の熱延鋼板は、粗大な炭化物の形成が抑制される効果を得にくく、高いレベルの耐衝撃性を確保するにも不足するという問題点がある。 The cooling process after hot rolling is typically carried out within a few tens of seconds from a 100-120m long ROT (Run-Out Table), but it is difficult to produce hot-rolled steel sheets that are cooled to the cooling end temperature or coiling temperature while the cooling rate deep within the thickness range satisfies the proposed range. Therefore, with the above-mentioned conventional technology, it is difficult to achieve the effect of suppressing the formation of coarse carbides in hot-rolled steel sheets with a thickness of 8mm or more, and there are problems with not being able to ensure a high level of impact resistance.
本発明の一側面は、冷間成形後の耐衝撃性に優れ、高降伏比を有する高強度鋼及びその製造方法を提供することを課題とする。 One aspect of the present invention is to provide a high-strength steel that has excellent impact resistance after cold forming and a high yield ratio, and a method for manufacturing the same.
本発明の課題は、上述した内容に限定されない。通常の技術者であれば、本明細書の全体内容から本発明のさらなる課題を理解するのに何ら困難がない。 The objectives of the present invention are not limited to the above. A person of ordinary skill in the art would have no difficulty in understanding the further objectives of the present invention from the overall content of this specification.
本発明の一側面は、重量%で、C:0.05~0.15%、Si:0.01~0.5%、Mn:1.0~2.0%、Al:0.01~0.1%、Cr:0.001~1.0%、P:0.001~0.05%、S:0.001~0.01%、N:0.001~0.01%、Ti:0.03~0.08%、Nb:0.01~0.05%、残部Fe及びその他の不可避不純物を含み、NbとTiの合計が0.04~0.1%であり、
表面から厚さ50μm範囲の表層部の微細組織は、面積%で、等軸晶フェライトを95%以上、パーライトを3%以下含み、ベイニティックフェライト、ベイナイト、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種以上を合計で5%以下含み、
厚さ1/4~3/4範囲の中心部の微細組織は面積%で、ベイニティックフェライトを80~95%、ベイナイトを10%以下、パーライトを3%以下、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種または2種を合計で5~10%含み、残りは等軸晶フェライトを含む鋼板を提供することができる。
One aspect of the present invention is a steel sheet containing, by weight%, C: 0.05 to 0.15%, Si: 0.01 to 0.5%, Mn: 1.0 to 2.0%, Al: 0.01 to 0.1%, Cr: 0.001 to 1.0%, P: 0.001 to 0.05%, S: 0.001 to 0.01%, N: 0.001 to 0.01%, Ti: 0.03 to 0.08%, Nb: 0.01 to 0.05%, the balance being Fe and other inevitable impurities, with the sum of Nb and Ti being 0.04 to 0.1%;
The microstructure of the surface layer portion within a thickness range of 50 μm from the surface contains, in area%, 95% or more of equiaxed ferrite and 3% or less of pearlite, and contains 5% or less in total of one or more of bainitic ferrite, bainite, MA (Martensite-Austenite constituent) phase, and martensite,
It is possible to provide a steel sheet in which the microstructure in the center portion within the range of ¼ to ¾ of the thickness contains, in area %, 80 to 95% bainitic ferrite, 10% or less bainite, 3% or less pearlite, 5 to 10% in total of one or two of an MA (Martensite-Austenite constituent) phase and martensite, and the remainder contains equiaxed ferrite.
上記鋼板は厚さが8~25mmであることができる。 The steel plate can be 8 to 25 mm thick.
上記鋼板は、引張強度が590MPa以上であり、破壊伸び率が25%以上であり、降伏比が0.75~0.9であり、冷間成形後の-20℃での衝撃靭性が70J以上であることができる。 The above steel plate has a tensile strength of 590 MPa or more, a fracture elongation of 25% or more, a yield ratio of 0.75 to 0.9, and an impact toughness of 70 J or more at -20°C after cold forming.
上記鋼板は、冷間成形後の-20℃での衝撃靭性(E)と冷間成形前の降伏強度(YS)の比(E/YS)が0.15以上であることができる。 The above steel plate may have a ratio (E/YS) of impact toughness (E) at -20°C after cold forming to yield strength (YS) before cold forming of 0.15 or more.
上記鋼板は、幅方向を基準に、両端部で30%の領域に該当するエッジ部と両エッジ部を除いた領域に該当する中心40%領域の中央部を含み、上記エッジ部と中央部は引張強度の差が10MPa以下であり、破壊伸び率の差が8%以下であり、冷間成形後の-20℃での衝撃靭性の差が20J以下であることができる。 The steel plate includes edge portions corresponding to 30% of the width at both ends and a central portion of the central 40% region excluding both edge portions, and the difference in tensile strength between the edge portions and the central portion is 10 MPa or less, the difference in fracture elongation is 8% or less, and the difference in impact toughness at -20°C after cold forming is 20 J or less.
本発明の他の一側面は、重量%で、C:0.05~0.15%、Si:0.01~0.5%、Mn:1.0~2.0%、Al:0.01~0.1%、Cr:0.001~1.0%、P:0.001~0.05%、S:0.001~0.01%、N:0.001~0.01%、Ti:0.03~0.08%、Nb:0.01~0.05%、残部Fe及びその他の不可避不純物を含み、NbとTiの合計が0.04~0.1%の鋼スラブを再加熱する段階;
上記再加熱された鋼スラブを熱間圧延する段階;及び
上記熱間圧延された鋼板を500~650℃の温度範囲まで1~30℃/sの範囲内で下記関係式1で定義されるCR値以上である平均冷却速度で冷却及び巻き取る段階を含み、
上記冷却及び巻き取り段階において、コイル幅方向を基準に両端部で30%の領域に該当するエッジ部は550~650℃の温度(TE)で、幅方向に両エッジ部を除いた領域に該当する中心40%領域の中央部は500~550℃の温度(TC)で冷却し、
エッジ部と中央部の平均温度差は50~150℃の鋼板の製造方法を提供することができる。
[関係式1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(ここで、[C]、[Si]、[Mn]、[Cr]、[Ti]及び[Nb]は各元素の重量%であり、tは鋼板の厚さ(mm)である。)
Another aspect of the present invention is a method for producing a steel slab containing, by weight, 0.05-0.15% C, 0.01-0.5% Si, 1.0-2.0% Mn, 0.01-0.1% Al, 0.001-1.0% Cr, 0.001-0.05% P, 0.001-0.01% S, 0.001-0.01% N, 0.03-0.08% Ti, 0.01-0.05% Nb, the balance being Fe and other unavoidable impurities, the total of which is 0.04-0.1% Nb and Ti;
hot-rolling the reheated steel slab; and cooling the hot-rolled steel sheet to a temperature range of 500 to 650°C at an average cooling rate of 1 to 30°C/s, which is equal to or greater than the CR value defined by the following Relation 1, and coiling the steel sheet,
In the cooling and winding step, the edge portions corresponding to 30% of the area at both ends in the coil width direction are cooled at a temperature of 550 to 650 ° C. (TE), and the central portion of the central 40% area corresponding to the area excluding both edge portions in the width direction is cooled at a temperature of 500 to 550 ° C. (TC).
A method for manufacturing a steel plate in which the average temperature difference between the edge portion and the center portion is 50 to 150°C can be provided.
[Relationship 1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(Here, [C], [Si], [Mn], [Cr], [Ti] and [Nb] are the weight percentages of each element, and t is the thickness of the steel plate (mm).)
上記再加熱温度は1100~1350℃であり、
上記熱間圧延温度は800~1150℃であることができる。
The reheating temperature is 1100 to 1350°C,
The hot rolling temperature may be 800 to 1150°C.
上記巻き取られたコイルを200℃以下の温度範囲で空冷する段階をさらに含むことができる。 The method may further include air-cooling the wound coil at a temperature range of 200°C or less.
上記鋼板は厚さが8~25mmであることができる。 The steel plate can be 8 to 25 mm thick.
本発明の一側面によると、冷間成形後の耐衝撃性に優れ、高降伏比を有する高強度鋼及びその製造方法を提供することができる。 One aspect of the present invention provides high-strength steel that has excellent impact resistance after cold forming and a high yield ratio, as well as a manufacturing method thereof.
本発明の一側面によると、中大型商用車シャーシメンバ類及びホイール等に用いられる鋼材に適用できる高強度鋼及びその製造方法を提供することができる。 One aspect of the present invention provides high-strength steel that can be used for chassis members and wheels of medium- to large-sized commercial vehicles, and a manufacturing method thereof.
以下では、本発明の好ましい実施形態を説明する。本発明の実施形態は、様々な形に変形することができ、本発明の範囲が以下で説明される実施形態に限定されるものと解釈されてはいけない。本実施形態は、当該発明が属する技術分野における通常の知識を有する者に本発明をさらに詳細に説明するために提供されるものである。 The following describes preferred embodiments of the present invention. The embodiments of the present invention can be modified in various ways, and the scope of the present invention should not be construed as being limited to the embodiments described below. The present embodiments are provided to further explain the present invention to those skilled in the art to which the invention pertains.
本発明者は、上述した従来の問題点を解決し、優れた成形性及び耐衝撃性を確保するために、鋼板の微細組織特徴による冷間成形後の耐衝撃性の変化を研究した。これにより、合金組成及び製造条件を最適化して鋼板の厚さ及び幅方向に応じた微細組織を制御することにより目的とする物性を確保することができることを確認し、本発明を完成するに至った。 In order to solve the above-mentioned conventional problems and ensure excellent formability and impact resistance, the inventors studied the changes in impact resistance after cold forming depending on the microstructural characteristics of the steel sheet. As a result, they confirmed that the desired physical properties can be achieved by optimizing the alloy composition and manufacturing conditions and controlling the microstructural characteristics according to the thickness and width directions of the steel sheet, leading to the completion of the present invention.
通常コイルの形態で製造される熱延鋼板において、粗大な炭化物及びパーライトは、約500~700℃の高温域で長時間維持されるときに形成されやすい。特に、熱間圧延終了後の冷却過程で開始されるフェライト相変態がゆっくり進行する場合、未変態相には炭素の高容量が増加するため、粗大な炭化物やパーライトが形成しやすい条件となる。さらに、コイル幅の中央部はエッジ部に比べて冷却速度が遅くて、このような組織がさらに発達するようになる。したがって、コイル幅の中央部でこのような粗大な炭化物とパーライト形成を抑制するためには、巻き取られたコイルを水冷などの強制冷却により常温まで冷却することが必要であるが、この場合には冷却速度の速いエッジ部は、マルテンサイトやMA(Martensite and Austenite)相が過度に形成されて微細組織が不均一になり、高い伸び率を確保することが難しくなり、せん断面の割れも増加するため、好ましくない。したがって、本発明では、コイルを強制冷却せずとも粗大な炭化物及びパーライトの形成を抑制することができる方案を提案する。 In hot-rolled steel sheets typically manufactured in coil form, coarse carbides and pearlite are likely to form when maintained at high temperatures of approximately 500-700°C for long periods of time. In particular, if the ferrite phase transformation that begins during the cooling process after hot rolling proceeds slowly, the untransformed phases tend to contain a high amount of carbon, creating conditions favorable for the formation of coarse carbides and pearlite. Furthermore, the cooling rate is slower in the center of the coil than in the edge regions, further promoting the development of these structures. Therefore, to prevent the formation of coarse carbides and pearlite in the center of the coil, the wound coil must be cooled to room temperature by forced cooling, such as by water cooling. However, this is undesirable because the edge regions, where the cooling rate is faster, experience excessive formation of martensite and MA (Martensite and Austenite) phases, resulting in a non-uniform microstructure. This makes it difficult to achieve high elongation and increases cracking on the shear surface. Therefore, this invention proposes a method that can suppress the formation of coarse carbides and pearlite without forcibly cooling the coil.
以下、本発明について詳細に説明する。 The present invention is described in detail below.
以下では、本発明の鋼組成について詳細に説明する。 The steel composition of the present invention is described in detail below.
本発明において特に断りのない限り、各元素の含有量を表す%は重量を基準とする。 Unless otherwise specified, the percentages representing the content of each element in this invention are based on weight.
本発明の一側面に係る鋼は、重量%で、C:0.05~0.15%、Si:0.01~0.5%、Mn:1.0~2.0%、Al:0.01~0.1%、Cr:0.001~1.0%、P:0.001~0.05%、S:0.001~0.01%、N:0.001~0.01%、Ti:0.03~0.08%、Nb:0.01~0.05%、残部Fe及びその他の不可避不純物を含み、TiとNbの合計が0.04~0.1%であることができる。 The steel according to one aspect of the present invention contains, by weight, C: 0.05-0.15%, Si: 0.01-0.5%, Mn: 1.0-2.0%, Al: 0.01-0.1%, Cr: 0.001-1.0%, P: 0.001-0.05%, S: 0.001-0.01%, N: 0.001-0.01%, Ti: 0.03-0.08%, Nb: 0.01-0.05%, the balance being Fe and other unavoidable impurities, and the sum of Ti and Nb can be 0.04-0.1%.
炭素(C):0.05~0.15%
炭素(C)は、鋼を強化させるのに最も経済的且つ効果的な元素であり、添加量が増加すると析出強化効果またはベイナイト相分率が増加して強度確保が容易であることができる。しかし、熱延鋼板の厚さが増加すると、熱間圧延後の冷却中の厚さ中心部の冷却速度が遅くなって、炭素(C)の含有量が大きい場合に粗大な炭化物やパーライト(Pearlite)が形成されやすい。したがって、炭素(C)含有量が0.05%未満であると、十分な強化効果が得られにくく、その含有量が0.15%を超過すると、厚さ中心部にパーライトや粗大な炭化物の形成により耐衝撃性が低下するという問題点があり、溶接性も劣化するおそれがある。好ましい下限は0.055%であることができ、より好ましい上限は0.12%であることができる。
Carbon (C): 0.05-0.15%
Carbon (C) is the most economical and effective element for strengthening steel, and increasing its content increases the precipitation strengthening effect or the bainite phase fraction, making it easier to ensure strength. However, as the thickness of a hot-rolled steel sheet increases, the cooling rate at the center of the thickness during cooling after hot rolling slows, and a high carbon (C) content can easily lead to the formation of coarse carbides and pearlite. Therefore, if the carbon (C) content is less than 0.05%, it is difficult to achieve sufficient strengthening effects. If the carbon (C) content exceeds 0.15%, there are problems such as reduced impact resistance due to the formation of pearlite and coarse carbides at the center of the thickness, and weldability may also be deteriorated. The preferred lower limit is 0.055%, and the more preferred upper limit is 0.12%.
シリコン(Si):0.01~0.5%
シリコン(Si)は、溶鋼脱酸及び鋼を固溶強化させるのに効果的であり、粗大な炭化物形成を遅らせて成形性向上にも効果的な元素である。しかし、その含有量が0.01%未満であると、固溶強化及び炭化物形成を遅らせる効果を極大化することができず、その含有量が0.5%を超過すると、熱間圧延時に鋼板表面に赤色スケールが形成されて品質が非常に劣るだけでなく、延性や溶接性も低下するという問題点がある。好ましくは0.05%以上含むことができ、より好ましくは0.3%以下含むことができる。
Silicon (Si): 0.01 to 0.5%
Silicon (Si) is an element that is effective in deoxidizing molten steel and solid-solution strengthening steel, and also in delaying the formation of coarse carbides to improve formability. However, if its content is less than 0.01%, the effects of solid-solution strengthening and delaying carbide formation cannot be maximized, while if its content exceeds 0.5%, red scale is formed on the steel sheet surface during hot rolling, resulting in significantly inferior quality, as well as reduced ductility and weldability. Preferably, Si may be contained in an amount of 0.05% or more, and more preferably 0.3% or less.
マンガン(Mn):1.0~2.0%
マンガン(Mn)は、Siと同様に鋼を固溶強化させるのに効果的な元素であり、鋼の硬化能を増加させて熱間圧延後に冷却中のベイナイトの形成を容易にすることができる。しかし、その含有量が1.0%未満であると、添加による上記効果が得られず、2.0%を超過すると、硬化能が大きく増加してマルテンサイト相変態が起こりやすく、連鋳工程でスラブ鋳造時の厚さ中心部から偏析部が大きく発達するおそれがある。好ましくは1.3%以上含むことができ、より好ましくは1.8%以下含むことができる。
Manganese (Mn): 1.0 to 2.0%
Manganese (Mn), like Si, is an effective element for solid-solution strengthening of steel, increasing the hardening ability of steel and facilitating the formation of bainite during cooling after hot rolling. However, if the Mn content is less than 1.0%, the above-mentioned effect of addition cannot be obtained, and if the Mn content exceeds 2.0%, the hardening ability increases significantly, making martensitic phase transformation more likely to occur, and there is a risk of large segregation developing from the thickness center during slab casting in the continuous casting process. Preferably, Mn can be contained in an amount of 1.3% or more, and more preferably 1.8% or less.
アルミニウム(Al):0.01~0.1%
アルミニウム(Al)は、主に脱酸のために添加する成分であり、その含有量が0.01%未満であると、その添加効果が不足することがある。一方、その含有量が0.1%を超過すると、窒素と結合してAlNが形成されて連続鋳造時にスラブにコーナークラックが発生しやすく、介在物形成による欠陥が発生しやすい。好ましくは0.015%以上、より好ましくは0.06%以下含むことができる。
Aluminum (Al): 0.01 to 0.1%
Aluminum (Al) is a component added primarily for deoxidation, and if its content is less than 0.01%, its effect may be insufficient. On the other hand, if its content exceeds 0.1%, it combines with nitrogen to form AlN, which is likely to cause corner cracks in the slab during continuous casting and defects due to the formation of inclusions. Aluminum may be added preferably at 0.015% or more, more preferably at 0.06% or less.
クロム(Cr):0.001~1.0%
クロム(Cr)は、Mnと類似に鋼を固溶強化させ、冷却時のフェライト相変態を遅らせてベイナイト形成を助ける役割を果たす。しかし、その含有量が0.001%未満であると、添加による上記効果が得られず、1.0%を超過すると、フェライト相変態を過度に遅らせて過度のマルテンサイト形成により伸び率が劣化することがある。また、過度のCr添加は厚さ中心部での偏析部が大きく発達し、厚さ方向の微細組織を不均一にして耐衝撃性を劣化させる。好ましい下限は0.01%であることができ、より好ましい上限は0.5%であることができる。
Chromium (Cr): 0.001 to 1.0%
Chromium (Cr), like Mn, strengthens steel through solid solution and retards the ferrite phase transformation during cooling, promoting the formation of bainite. However, if its content is less than 0.001%, the above effects cannot be achieved. If its content exceeds 1.0%, the ferrite phase transformation may be excessively retarded, resulting in excessive martensite formation and reduced elongation. Furthermore, excessive Cr addition can lead to the development of large segregations in the center of the steel, resulting in uneven microstructures across the thickness and reduced impact resistance. The preferred lower limit is 0.01%, and the more preferred upper limit is 0.5%.
リン(P):0.001~0.05%
リン(P)は、Siと同様に固溶強化及びフェライト相変態促進効果を同時に有している。しかし、リン(P)の含有量を0.001%未満にして製造するためには、製造費用が多くかかって経済的に不利であり、強度を得るにも不十分である。一方、その含有量が0.05%を超過すると、粒界偏析による脆性が発生し、成形時に微細な割れが発生しやすくて、耐衝撃性を大きく悪化させることができる。
Phosphorus (P): 0.001 to 0.05%
Like Si, phosphorus (P) simultaneously strengthens the solid solution and promotes ferrite phase transformation. However, manufacturing with a phosphorus (P) content of less than 0.001% is economically disadvantageous due to the high manufacturing costs and is insufficient to obtain sufficient strength. On the other hand, if the P content exceeds 0.05%, embrittlement occurs due to grain boundary segregation, which easily causes microcracks during molding and significantly reduces impact resistance.
硫黄(S):0.001~0.01%
上記Sは、鋼中に存在する不純物であり、その含有量が0.01%を超過すると、Mn等と結合して非金属介在物を形成し、これにより、成形時に微細な割れが発生しやすくて、耐衝撃性を大きく低下させるという問題点がある。但し、その含有量を0.001%未満にして製造するためには、製鋼操業時に時間が多くかかって、生産性が劣るようになる。
Sulfur (S): 0.001 to 0.01%
S is an impurity present in steel, and if its content exceeds 0.01%, it combines with Mn and other elements to form non-metallic inclusions, which can cause microcracks during forming and significantly reduce impact resistance. However, reducing the content to less than 0.001% requires a long time during steelmaking operations, resulting in poor productivity.
窒素(N):0.001~0.01%
窒素(N)は、Cと共に代表的な固溶強化元素であり、Ti、Alなどと共に粗大な析出物を形成する。一般的に、窒素(N)の固溶強化効果はCより優れるが、鋼中の窒素(N)の量が増加するほど靭性が大きく低下するという問題点がある。したがって、その含有量の上限を0.01%に制限することができる。一方、その含有量を0.001%未満にして製造するためには、製鋼操業時に時間が多くかかって、生産性が劣るようになる。
Nitrogen (N): 0.001 to 0.01%
Nitrogen (N), along with carbon, is a representative solid solution strengthening element and forms coarse precipitates with titanium, aluminum, and other elements. While nitrogen (N) generally has a stronger solid solution strengthening effect than carbon, the toughness of steel decreases significantly as the nitrogen (N) content increases. Therefore, the upper limit of nitrogen (N) content can be limited to 0.01%. However, reducing the nitrogen content to less than 0.001% can result in a longer steelmaking operation time and reduced productivity.
チタン(Ti):0.03~0.08%
チタン(Ti)は、代表的な析出強化元素であり、Nとの強い親和力で鋼中に粗大なTiNを形成する。TiNは、熱間圧延のための加熱過程で結晶粒が成長することを抑制する効果がある。また、Nと反応して残ったチタン(Ti)が鋼中に固溶してCと結合することで形成されるTiC析出物は、鋼の強度を向上させるのに有用な成分である。チタン(Ti)の含有量が0.03%未満であると、上記効果が得られず、その含有量が0.08%を超過すると、粗大なTiNの発生及び析出物の粗大化により成形時に耐衝突特性を劣化させるという問題点がある。好ましくは0.04%以上含むことができ、より好ましくは0.075%以下含むことができる。
Titanium (Ti): 0.03 to 0.08%
Titanium (Ti) is a typical precipitation strengthening element and forms coarse TiN in steel due to its strong affinity with N. TiN has the effect of suppressing grain growth during the heating process for hot rolling. Furthermore, TiC precipitates, formed when the remaining titanium (Ti) reacts with N and dissolves in the steel and combines with C, are a useful component for improving the strength of steel. If the titanium (Ti) content is less than 0.03%, the above effect cannot be achieved. However, if the titanium (Ti) content exceeds 0.08%, the generation of coarse TiN and the coarsening of the precipitates can lead to problems such as degraded impact resistance during forming. Preferably, the titanium content is 0.04% or more, and more preferably 0.075% or less.
ニオブ(Nb):0.01~0.05%
ニオブ(Nb)は、Tiと共に代表的な析出強化元素であり、熱間圧延中に析出して再結晶遅延による結晶粒微細化効果によって鋼の強度と衝撃靭性の向上に効果的である。ニオブ(Nb)の含有量が0.01%未満であると、上記効果が得られず、その含有量が0.05%を超過すると、熱間圧延中に過度の再結晶遅延で延伸した結晶粒形成及び粗大な複合析出物の形成により成形性を劣化させるという問題点がある。好ましい下限は0.015%であることができ、より好ましい上限は0.04%であることができる。
Niobium (Nb): 0.01 to 0.05%
Niobium (Nb), along with Ti, is a representative precipitation strengthening element that precipitates during hot rolling and effectively improves the strength and impact toughness of steel by refining grains through delayed recrystallization. If the niobium (Nb) content is less than 0.01%, the above effect cannot be obtained, while if the Nb content exceeds 0.05%, excessive delayed recrystallization during hot rolling can lead to the formation of elongated grains and coarse complex precipitates, deteriorating formability. The preferred lower limit is 0.015%, and the more preferred upper limit is 0.04%.
本発明の鋼は、上述した組成以外に、残りの鉄(Fe)及び不可避不純物を含むことができる。不可避不純物は、通常の製造工程で意図せずに混入される可能性があるため、これを排除することはできない。このような不純物は、通常の鉄鋼製造分野の技術者であれば誰でも分かることであるため、そのすべての内容を特に本明細書では言及しない。 In addition to the above-mentioned composition, the steel of the present invention may contain the remaining iron (Fe) and unavoidable impurities. Unavoidable impurities cannot be excluded because they may be unintentionally mixed in during normal manufacturing processes. Since such impurities are known to any engineer in the field of normal steel manufacturing, their full content will not be specifically mentioned in this specification.
本発明の一側面による鋼は、ニオブ(Nb)とチタン(Ti)の合計が0.04~0.1%であることができる。 The steel according to one aspect of the present invention may have a total of niobium (Nb) and titanium (Ti) of 0.04 to 0.1%.
ニオブ(Nb)とチタン(Ti)は、(Ti、Nb)(C、N)系複合析出物として析出し、熱間圧延中に析出すると再結晶遅延による結晶粒微細化効果が大きく増加する。しかし、複合析出物の形成が過度であると、粗大な複合析出物が増加して強度向上効果は少なく、成形性は劣化するという問題点がある。ニオブ(Nb)とチタン(Ti)の合計が0.04%未満であると、結晶粒微細化及び強度向上効果が小さいことがある。一方、その合計が0.1%を超過すると、成形性が劣化するようになり、経済的にも不利である。好ましい下限は0.045%であることができ、より好ましい上限は0.09%であることができる。 Niobium (Nb) and titanium (Ti) precipitate as (Ti, Nb) (C, N) composite precipitates, and when they precipitate during hot rolling, they significantly enhance the grain refinement effect by delaying recrystallization. However, excessive formation of these composite precipitates results in an increase in coarse composite precipitates, resulting in little strength improvement and poor formability. If the total content of niobium (Nb) and titanium (Ti) is less than 0.04%, the grain refinement and strength improvement effects may be limited. On the other hand, if the total content exceeds 0.1%, formability will deteriorate and this is economically disadvantageous. The preferred lower limit is 0.045%, and the more preferred upper limit is 0.09%.
以下では、本発明の鋼微細組織について詳細に説明する。 The steel microstructure of the present invention is described in detail below.
本発明で特に断りのない限り、微細組織の分率を表示する%は、面積を基準とする。 Unless otherwise specified in this invention, the percentages indicating the fraction of microstructures are based on area.
本発明の一側面に係る鋼は、表面から厚さ50μm範囲の表層部の微細組織は面積%で、等軸晶フェライトを95%以上、パーライトを3%以下含み、ベイニティックフェライト、ベイナイト、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種以上を合計で5%以下含み、厚さ1/4~3/4の範囲の中心部の微細組織は面積%で、ベイニティックフェライトを80~95%、ベイナイトを10%以下、パーライトを3%以下、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種または2種を合計で5~10%含み、残りは等軸晶フェライトを含むことができる。 In one aspect of the steel of the present invention, the microstructure of the surface layer within a 50 μm thick range from the surface contains, by area percentage, 95% or more equiaxed ferrite, 3% or less pearlite, and a total of 5% or less of one or more of bainitic ferrite, bainite, MA (Martensite-Austenite constituent) phase, and martensite; the microstructure of the center portion within a 1/4 to 3/4 thickness range contains, by area percentage, 80 to 95% bainitic ferrite, 10% or less bainite, 3% or less pearlite, and a total of 5 to 10% of one or two of the MA (Martensite-Austenite constituent) phase and martensite, with the remainder being equiaxed ferrite.
本発明では、表層部で等軸晶フェライトが95%未満であると、商用車ホイール製造時に、適用するスピニング及びフローフォーミング成形時に、延性が不足し、表層部での加工硬化が激しくなって成形中に微細なクラックが発生するおそれがある。特に、脆性の強いパーライトが3%以上形成されるか、硬度の高いベイニティックフェライト、ベイナイト、MA相及びマルテンサイトのうち1種以上が5%を超過して含まれると、基地相との界面に沿ってクラックが容易に伝播するという問題点がある。したがって、成形中に表層部で形成される微細なクラックの発生を抑制し、クラックの伝播を防止するためにベイニティックフェライト、ベイナイト、MA相及びマルテンサイトのうち1種以上を合計で5%以下含むことが好ましい。本発明では、表層部の微細組織で等軸晶フェライトが100%であることができ、パーライト、ベイニティックフェライト、ベイナイト、MA相及びマルテンサイトの合計が0%であることができる。 In the present invention, if the surface layer contains less than 95% equiaxed ferrite, the ductility may be insufficient during spinning and flow forming, which are used in the manufacture of commercial vehicle wheels. This may result in severe work hardening in the surface layer, leading to the risk of fine cracks occurring during forming. In particular, if more than 3% of highly brittle pearlite is formed, or if more than 5% of one or more of the highly hard bainitic ferrite, bainite, MA phase, and martensite is included, cracks may easily propagate along the interface with the base phase. Therefore, to suppress the formation of fine cracks in the surface layer during forming and prevent crack propagation, it is preferable to include a total of 5% or less of one or more of bainitic ferrite, bainite, MA phase, and martensite. In the present invention, the microstructure in the surface layer may be 100% equiaxed ferrite, and the total of pearlite, bainitic ferrite, bainite, MA phase, and martensite may be 0%.
また、中心部でベイニティックフェライトが80%未満であると、ホイール製造時に、パンチング及びせん断成形過程でせん断面にクラックが容易に発生するという問題点があり、成形後に、耐衝撃性も劣るという問題がある。また、鋼板を製造する際に熱間圧延後の鋼板の冷却過程において、圧延板の厚さ中心部は基地組織であるベイニティックフェライトが形成された後、未変態されたオーステナイトには高い濃度の残留Cが残存するため、パーライトを形成しやすくすることができる。このとき、パーライトが3%を超過して形成されると、成形過程においてせん断面でクラック発生がひどくなり、成形後の耐衝撃性も劣る。パーライト分率が3%以下であるとき、せん断等成形による割れ発生がなく、低温での耐衝撃性に優れることができる。本発明では、直径1μm以上の炭化物及び窒化物をパーライトで含むことができる。 Furthermore, if the bainitic ferrite content in the center is less than 80%, cracks easily occur on the sheared surfaces during punching and shear forming during wheel manufacturing, resulting in poor impact resistance after forming. Furthermore, during the cooling process of a steel plate after hot rolling, bainitic ferrite, the matrix structure, is formed in the center of the thickness of the rolled plate. A high concentration of residual carbon remains in the untransformed austenite, facilitating the formation of pearlite. However, if the pearlite content exceeds 3%, severe cracking occurs on the sheared surfaces during forming, resulting in poor impact resistance after forming. When the pearlite fraction is 3% or less, cracks do not occur during forming, such as shearing, and excellent impact resistance at low temperatures can be achieved. In the present invention, pearlite can contain carbides and nitrides with a diameter of 1 μm or more.
これに対して、MA相またはマルテンサイトを5~10%含む場合、クラック発生に影響を及ぼすことなく、成形後の耐衝撃性及び高い強度を確保するのに有利であることができる。MA相は周辺に電位密度を形成して高強度を確保するのに有利な側面があり、フェライト及びベイナイトで構成された基地組織とともに形成されたとき、冷間成形後に電位密度が増加しても耐衝撃性に優れることができる。しかし、MA相またはマルテンサイトが5%未満であると降伏強度及び引張強度が不足し、10%を超過して含まれると、延性が不足して成形性が劣るという問題がある。ベイナイトも10%を超過する場合、延性が不足するという問題点がある可能性がある。 In contrast, containing 5-10% MA phase or martensite can be advantageous for ensuring impact resistance and high strength after forming without affecting crack generation. The MA phase is advantageous for creating potential density around it to ensure high strength, and when formed together with a matrix structure composed of ferrite and bainite, it can provide excellent impact resistance even when the potential density increases after cold forming. However, if the MA phase or martensite is less than 5%, the yield strength and tensile strength will be insufficient, and if it is contained in excess of 10%, there will be problems with insufficient ductility and poor formability. Bainite, too, may also be problematic in that it lacks ductility if it exceeds 10%.
本発明では、中心部の微細組織でベイナイト、パーライトはそれぞれ0%であることができ、ベイニティックフェライト、ベイナイト、パーライト、MA相及びマルテンサイトの他に、不可避に等軸晶フェライトを含むことができる。 In the present invention, the microstructure in the center can contain 0% bainite and 0% pearlite, and in addition to bainitic ferrite, bainite, pearlite, MA phase, and martensite, equiaxed ferrite can be unavoidably included.
本発明では、微細組織の面積分率を光学顕微鏡及び走査電子顕微鏡(SEM、Scanning Electron Microscope)を用いて分析することができ、圧延断面の厚さ中心部に該当する位置で3,000倍率で観察したイメージからの相の面積分率を測定することができる。 In the present invention, the area fraction of the microstructure can be analyzed using an optical microscope and a scanning electron microscope (SEM), and the area fraction of the phases can be measured from an image observed at 3,000x magnification at a position corresponding to the center of the thickness of the rolled cross section.
以下では、本発明の鋼製造方法について詳細に説明する。 The steel manufacturing method of the present invention is described in detail below.
本発明の一側面に係る鋼は、上述した合金組成を満足する鋼スラブを再加熱、圧延、冷却及び巻き取って製造されることができる。 Steel according to one aspect of the present invention can be produced by reheating, rolling, cooling, and coiling a steel slab that satisfies the alloy composition described above.
再加熱
本発明の合金組成を満たす鋼スラブを1100~1350℃の温度範囲で再加熱することができる。
Reheating Steel slabs meeting the alloy composition of the present invention can be reheated at temperatures ranging from 1100 to 1350°C.
再加熱温度が1100℃未満であると析出物が十分に再固溶されず、熱間圧延後の工程で析出物の形成が減少することがあり、粗大なTiNが残存することができる。一方、その温度が1350℃を超過するとオーステナイト結晶粒の異常粒成長によって強度が低下することがある。 If the reheating temperature is below 1100°C, the precipitates will not be fully redissolved, which may result in reduced precipitate formation in processes after hot rolling, leaving coarse TiN remaining. On the other hand, if the temperature exceeds 1350°C, abnormal grain growth of austenite grains may result in a decrease in strength.
熱間圧延
上記再加熱された鋼スラブを800~1150℃の温度範囲で熱間圧延を行うことができる。
Hot Rolling The reheated steel slab can be hot rolled in the temperature range of 800 to 1150°C.
熱間圧延温度が1150℃を超過すると、熱延鋼板の温度が高くなり、結晶粒径が粗大になり、熱延鋼板の表面品質が劣化することがある。一方、その温度が800℃未満であると、再結晶遅延により延伸した結晶粒が発達して、異方性がひどくなって成形性が悪くなることがあり、オーステナイト温度域以下の温度で圧延すると、不均一な微細組織がさらにひどく発達することがある。 If the hot rolling temperature exceeds 1150°C, the temperature of the hot-rolled steel sheet will become too high, the grain size will become coarse, and the surface quality of the hot-rolled steel sheet may deteriorate. On the other hand, if the temperature is below 800°C, recrystallization will be delayed, causing elongated grains to develop, which may result in severe anisotropy and poor formability. Rolling at a temperature below the austenite temperature range may further worsen the development of a non-uniform microstructure.
冷却及び巻き取り
上記熱間圧延された鋼板を500~650℃の温度範囲まで1~30℃/sの範囲内で下記関係式1で定義されるCR値以上である平均冷却速度で冷却及び巻き取ることができる。上記冷却時に、コイル幅方向に両端部で30%のエッジ部は550~650℃の温度(TE)で、幅方向に両エッジ部を除いた中心40%の中央部は500~550℃の温度(TC)で冷却することができる。このとき、エッジ部と中央部の平均温度差は50~150℃であることができる。
Cooling and Coiling The hot-rolled steel sheet may be cooled to a temperature range of 500 to 650°C at an average cooling rate within a range of 1 to 30°C/s, which is equal to or greater than the CR value defined by the following Relation 1, and then coiled. During the cooling, the edge portions of 30% of the coil at both ends in the width direction may be cooled to a temperature of 550 to 650°C (TE), and the central portion of the central 40% of the coil excluding both edges in the width direction may be cooled to a temperature of 500 to 550°C (TC). At this time, the average temperature difference between the edge portions and the central portion may be 50 to 150°C.
本発明では、鋼板冷却時に、適正レベルのフェライト相変態を誘発し、微細且つ均一なMA相を形成させ、過度のパーライト形成を抑制するために、関係式1を導出した。冷却速度が関係式1のCR値未満の場合、厚さ中心部のフェライトが粗大になり、パーライトが過度に形成されてせん断面のクラック発生がひどくなり、成形後の耐衝撃特性が劣化することがある。また、冷却速度が30℃/sを超過する場合、ベイナイト、MA相及びマルテンサイトが過度に形成されて延性が不足し、せん断面品質も劣るという問題点がある。
[関係式1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(ここで、[C]、[Si]、[Mn]、[Cr]、[Ti]及び[Nb]は各元素の重量%であり、tは鋼板の厚さ(mm)である。)
In the present invention, Relational Formula 1 was derived to induce an appropriate level of ferrite phase transformation during cooling of a steel sheet, form a fine and uniform MA phase, and suppress excessive pearlite formation. If the cooling rate is less than the CR value of Relational Formula 1, ferrite in the center of the thickness becomes coarse and pearlite is excessively formed, resulting in severe cracking on the shear surface and deterioration of impact resistance after forming. In addition, if the cooling rate exceeds 30°C/s, bainite, MA phase, and martensite are excessively formed, resulting in insufficient ductility and poor shear surface quality.
[Relationship 1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(Here, [C], [Si], [Mn], [Cr], [Ti] and [Nb] are the weight percentages of each element, and t is the thickness of the steel plate (mm).)
過度の炭化物とパーライト形成を抑制するためには、熱間圧延後の冷却時に、冷却終了温度を下回る必要があるが、過度のベイナイト形成によるフェライト減少またはMA相及びマルテンサイトの過度の形成により目標とする伸び率確保が難しいおそれがある。 In order to prevent excessive carbide and pearlite formation, the cooling temperature after hot rolling must be below the end of cooling temperature. However, excessive bainite formation can result in a reduction in ferrite or excessive formation of MA phases and martensite, making it difficult to achieve the target elongation.
したがって、本発明では、コイルの幅方向の中央部での冷却速度を高め、巻き取り後のコイルが高温で維持される時間を減少させるために、熱間圧延後の冷却時に、幅方向の中央部とエッジ部の冷却終了温度を異ならせて設定することができる。但し、このとき、エッジ部と中央部の平均温度差は50~150℃であることができる。平均温度差が50℃未満であると、上記効果が得られ難いことがある。一方、その温度が150℃を超過すると、上記の効果はこれ以上増加しないが、コイルの区間別温度を制御することが困難になることがある。 Therefore, in the present invention, in order to increase the cooling rate at the center of the coil width direction and reduce the time the coil is maintained at high temperature after coiling, the cooling end temperatures at the center and edge portions of the coil width direction can be set differently during cooling after hot rolling. However, in this case, the average temperature difference between the edge and center portions can be 50 to 150°C. If the average temperature difference is less than 50°C, it may be difficult to achieve the above effect. On the other hand, if the temperature exceeds 150°C, the above effect will not be further increased, but it may be difficult to control the temperature of each section of the coil.
本発明では、巻き取り時に、エッジ部と中央部の冷却終了温度を異ならせて制御する方法を特に限定しないが、一例としては熱間圧延された鋼板を冷却する際に、エッジ部に注水される冷却水が鋼板に到達する前に遮断するか、または注水される冷却水量を異ならせて調節する方法を適用することができる。あるいは、2つの方法を並行して用いることもできる。 The present invention does not particularly limit the method for controlling the end cooling temperatures of the edge and center during coiling. As an example, when cooling a hot-rolled steel sheet, a method can be applied in which the cooling water injected into the edge is stopped before it reaches the steel sheet, or the amount of cooling water injected is adjusted by varying the amount. Alternatively, the two methods can be used in parallel.
本発明では、目的とする強度、成形性及び耐衝撃性を確保するために、上記関係式1と冷却終了温度の条件を全て満たすことが好ましい。上記冷却条件を全て満たす場合、厚さ方向の中心部にはベイニティックフェライトを基地組織として均一且つ微細な微細組織を有するようにし、冷却速度が遅いコイルの内巻部及び厚さ中心部で粗大な炭化物やパーライトが減少するようになって、熱延鋼板の不均一組織が解消されることができる。また、冷却速度が比較的速いコイルの外巻部とエッジ部では、MA相の不均一な形成と粗大なマルテンサイトの形成を抑制することができる。 In the present invention, in order to ensure the desired strength, formability, and impact resistance, it is preferable to satisfy all of the conditions for the above relational expression 1 and the cooling end temperature. When all of the above cooling conditions are satisfied, the center in the thickness direction has a uniform and fine microstructure with bainitic ferrite as the base structure, and coarse carbides and pearlite are reduced in the inner winding part of the coil and the center in the thickness direction, where the cooling rate is slow, thereby eliminating the non-uniform structure of the hot-rolled steel sheet. Furthermore, the non-uniform formation of MA phases and the formation of coarse martensite can be suppressed in the outer winding part and edge part of the coil, where the cooling rate is relatively fast.
冷却
上記巻き取られたコイルを200℃以下の温度範囲で空冷することができる。
Cooling The wound coil can be air cooled to a temperature range up to 200°C.
本発明では、巻き取られたコイルを200℃以下の温度範囲で空冷することができる。コイルの空冷は、冷却速度0.001~10℃/hで常温の大気中に冷却することを意味する。このとき、冷却速度が10℃/hを超過するとコイルの外巻部には鋼中の一部未変態された相がMA相に変態しやすくなって、鋼のせん断成形性及びパンチング成形性と耐久性が劣ることがある。一方、冷却速度を0.001℃/h未満に制御するためには、別途の加熱及び保熱設備等が必要であるため、経済的に不利になることがある。好ましい下限は0.01℃/hであることができ、より好ましい上限は1℃/hであることができる。 In the present invention, the wound coil can be air-cooled at a temperature range of 200°C or less. Air-cooling the coil means cooling it in air at room temperature at a cooling rate of 0.001 to 10°C/h. If the cooling rate exceeds 10°C/h, some untransformed phases in the steel at the outer winding portion of the coil are likely to transform into the MA phase, which may result in poor shear formability, punching formability, and durability of the steel. On the other hand, controlling the cooling rate to less than 0.001°C/h requires separate heating and heat retention equipment, which can be economically disadvantageous. A preferred lower limit is 0.01°C/h, and a more preferred upper limit is 1°C/h.
このように製造された本発明の鋼は、厚さが8~25mmであり、引張強度が590MPa以上であり、破壊伸び率が25%以上であり、降伏比が0.75~0.9であり、冷間成形後の-20℃での衝撃靭性が70J以上であり、冷間成形後の衝撃靭性と冷間成形前の降伏強度との比が0.15以上であり、高降伏比を有しつつ、衝撃靭性に優れた特性を備えることができる。また、上記鋼は幅方向を基準として、両端部で30%の領域に該当するエッジ部と、両エッジ部を除いた領域に該当する中心40%領域の中央部を含み、上記エッジ部と中央部は、引張強度の差が10MPa以下であり、破壊伸び率の差が8%以下であり、冷間成形後の-20℃での衝撃靭性の差が20J以下であることができる。 The steel of the present invention manufactured in this manner has a thickness of 8 to 25 mm, a tensile strength of 590 MPa or more, a fracture elongation of 25% or more, a yield ratio of 0.75 to 0.9, an impact toughness at -20°C after cold forming of 70 J or more, and a ratio of the impact toughness after cold forming to the yield strength before cold forming of 0.15 or more, thereby providing excellent impact toughness properties while maintaining a high yield ratio. Furthermore, the steel includes edge portions corresponding to 30% of the width at both ends and a central portion of the central 40% region corresponding to the region excluding both edge portions, and the difference in tensile strength between the edge portions and the central portion may be 10 MPa or less, the difference in fracture elongation of 8% or less, and the difference in impact toughness at -20°C after cold forming of 20 J or less.
以下、実施例を介して本発明をより具体的に説明する。但し、以下の実施例は、本発明を例示してより詳細に説明するためのものであり、本発明の権利範囲を制限するものではないことに留意する必要がある。 The present invention will now be described in more detail through examples. However, it should be noted that the following examples are intended to illustrate and explain the present invention in more detail, and are not intended to limit the scope of the present invention.
(実施例)
下記表1の合金組成を有する鋼スラブを下記表2の条件で熱延鋼板を製造した。このとき、鋼スラブは1100~1350℃の温度で再加熱した後に熱間圧延を行った。表2には製造時に適用された冷却速度、関係式1のCR値を示しており、冷却終了温度は幅方向の中央部の40%範囲の温度(TC)、幅方向の両端部のそれぞれ30%範囲の温度(TE)をそれぞれ示した。また、中央部の温度とエッジ部の温度の差を示した。
(Example)
Hot-rolled steel sheets were manufactured from steel slabs having the alloy compositions shown in Table 1 below under the conditions shown in Table 2 below. The steel slabs were reheated at temperatures of 1100 to 1350°C and then hot-rolled. Table 2 shows the cooling rates applied during manufacturing and the CR values of Relation 1. The cooling end temperatures are the temperature (TC) within 40% of the width at the center and the temperature (TE) within 30% of the width at both ends. The difference between the temperature at the center and the temperature at the edge is also shown.
(ここで、[C]、[Si]、[Mn]、[Cr]、[Ti]及び[Nb]は各元素の重量%であり、tは鋼板の厚さ(mm)である。)
(Here, [C], [Si], [Mn], [Cr], [Ti] and [Nb] are the weight percentages of each element, and t is the thickness of the steel plate (mm).)
下記表3には、製造された鋼板の微細組織を測定して記載した。微細組織は厚さ方向の表層部と中心部をそれぞれ測定し、幅方向のエッジ部と中央部もそれぞれ分率を測定して示した。表層部は表面から厚さ50μmまでの部分の微細組織を観察し、中心部は鋼板表面から厚さ方向に1/4~3/4t(25~75%区間、tは厚さ(mm))部分について観察した。また、エッジ部は幅方向の両端で30%に該当する部分の微細組織を観察し、中央部はエッジ部を除いた中央40%に該当する部分を基準に観察した。MA相とマルテンサイトの面積分率の測定は、Leperaエッチング法でエッチングした後、光学顕微鏡とImage分析器を用い、1,000倍率で分析した結果である。その他、等軸晶フェライト(PF)、ベイニティックフェライト(BF)、ベイナイト(B)及びパーライト(P)の分率は、走査電子顕微鏡(SEM)を用いて3,000倍と5,000倍率で分析した結果から測定した。ここで、PFは等軸晶形状を有するPolygonal Ferriteであり、BFは、針状型フェライト、ベイニティックフェライトなどの低温域で観察されるフェライトを含むことができる。また、Pはパーライトと直径1μm以上の粗大な炭化物及び窒化物を含む。 Table 3 below lists the microstructure measurements of the manufactured steel sheets. The microstructure was measured at the surface and center in the thickness direction, and the fractions were also measured at the edge and center in the width direction. For the surface, the microstructure was observed from the surface to a thickness of 50 μm, while for the center, the microstructure was observed from the surface to 1/4 to 3/4 of the thickness (25-75% interval, where t is thickness (mm)) in the thickness direction. For the edge, the microstructure was observed in the 30% region at both ends in the width direction, while for the center, the microstructure was observed based on the central 40% region excluding the edge. The area fractions of the MA phase and martensite were measured using an optical microscope and an image analyzer at 1,000x magnification after etching using the Lepera etching method. Additionally, the fractions of equiaxed ferrite (PF), bainitic ferrite (BF), bainite (B), and pearlite (P) were measured using a scanning electron microscope (SEM) at 3,000x and 5,000x magnifications. Here, PF represents polygonal ferrite with an equiaxed crystal shape, and BF includes ferrites observed in low-temperature regions, such as acicular ferrite and bainitic ferrite. Furthermore, P includes pearlite and coarse carbides and nitrides with diameters of 1 μm or more.
下記表4には、製造された各試験片に対する物性値を幅方向の中央部とエッジ部に対して測定して示した。降伏強度(YS)、引張強度(TS)、降伏比(YR)、破壊伸び率(T-El)は、JIS5号規格試験片を圧延方向に直角方向に試験片を採取して引張試験を行って評価された。また、冷間成形後の-20℃での衝撃吸収エネルギー(E)を測定し、冷間成形後の-20℃での衝撃吸収エネルギーと降伏強度の比(E/YS)を示した。衝撃吸収エネルギーはASTM規格(ASTM A370)に基づいて製作されたシャルピーV-ノッチ試験片を用い、圧延方向に垂直な方向に採取して試験した。 Table 4 below shows the physical properties of each manufactured test piece, measured at the center and edge in the width direction. Yield strength (YS), tensile strength (TS), yield ratio (YR), and fracture elongation (T-El) were evaluated by conducting tensile tests on JIS No. 5 standard test pieces taken perpendicular to the rolling direction. In addition, the impact absorption energy (E) at -20°C after cold forming was measured, and the ratio of impact absorption energy to yield strength (E/YS) at -20°C after cold forming is shown. Impact absorption energy was measured using Charpy V-notch test pieces manufactured in accordance with ASTM standards (ASTM A370) taken perpendicular to the rolling direction.
表3及び4に示されたように、本発明の合金組成及び製造条件を満足する発明例の場合、本発明で提案する微細組織特徴を満足し、本発明で目的とする物性を確保した。図1は、本発明の一側面に係る発明例2の熱延鋼板の微細組織を走査電子顕微鏡(×3,000)で観察して示した写真である。 As shown in Tables 3 and 4, inventive examples that satisfy the alloy composition and manufacturing conditions of the present invention, the microstructural characteristics proposed in the present invention were satisfied and the physical properties targeted by the present invention were secured. Figure 1 is a photograph showing the microstructure of the hot-rolled steel sheet of invention example 2 according to one aspect of the present invention, observed with a scanning electron microscope (x3,000).
一方、比較例1は、Ti及びNb含有量の合計が本発明の範囲を超過した場合であり、フェライト粒内に過度の析出物による粗大な析出物とTiN形成によって耐衝撃性が劣化した。 On the other hand, in Comparative Example 1, the total Ti and Nb content exceeded the range specified by the present invention, and impact resistance deteriorated due to the formation of coarse precipitates and TiN caused by excessive precipitates within the ferrite grains.
比較例2は、冷却速度が関係式1で提案した冷却速度の基準に達しなかった場合で、図2に示されたように、微細組織内に過度のパーライトが形成された。 In Comparative Example 2, the cooling rate did not meet the cooling rate standard suggested by Relation 1, resulting in excessive pearlite formation within the microstructure, as shown in Figure 2.
図2に示されたように、これにより強度は大きく低下しなかったが、目標とする耐衝撃特性を確保することができなかった。 As shown in Figure 2, this did not significantly reduce strength, but it did not ensure the desired impact resistance properties.
比較例3は、幅方向の中央部の巻き取り温度が本発明で提案する範囲を超過した場合であり、特に、中央部とエッジ部の全てにおいて厚さ方向の中心部で過度のパーライトが形成され、目標とする耐衝撃特性を確保することができなかった。 In Comparative Example 3, the winding temperature in the widthwise center portion exceeded the range proposed by the present invention. In particular, excessive pearlite formed in the thicknesswise center portion in both the center and edge portions, making it impossible to achieve the target impact resistance properties.
比較例4は、幅方向のエッジ部の巻き取り温度が本発明で提案する範囲を超過した場合である。そこで、エッジ部の厚さ方向の中心部で過度のパーライトの形成により、耐衝撃性が劣化することが示された。これは、エッジ部温度が高くて、巻き取りコイルの熱伝達がエッジ部でゆっくり進行されたためである。 In Comparative Example 4, the winding temperature of the widthwise edge portion exceeded the range proposed by the present invention. As a result, it was shown that impact resistance deteriorated due to excessive pearlite formation in the center of the thickness direction of the edge portion. This was because the edge portion temperature was high, and heat transfer from the winding coil proceeded slowly at the edge portion.
比較例5は、幅方向の中央部の巻き取り温度が本発明の範囲に未達する場合であり、中央部の厚さ方向の中心部でベイナイトが過度に形成され、表層部にはパーライト、MA相及びマルテンサイト等が本発明で提案した水準以上に過度に形成されて伸び率が劣化した。一方、エッジ部は巻き取り温度の範囲を満足して伸び率と耐衝撃特性が比較的良好であったが、表層部でのフェライトが本発明で提案する範囲に未達した。これは、幅方向の中央部の低い冷却終了温度によって巻き取り後のコイルのエッジ部の温度も急速に減少したためであると判断される。 In Comparative Example 5, the coiling temperature in the widthwise center portion did not reach the range of the present invention. As a result, excessive bainite was formed in the center portion of the thickness direction of the center portion, and pearlite, MA phase, martensite, etc. were formed in the surface layer portion in excess of the levels proposed by the present invention, resulting in a deterioration in elongation. Meanwhile, the edge portion satisfied the coiling temperature range and had relatively good elongation and impact resistance properties, but ferrite in the surface layer portion did not reach the range proposed by the present invention. This is believed to be due to the fact that the low cooling end temperature in the widthwise center portion caused the temperature at the edge portion of the coil to rapidly decrease after coiling.
比較例6は、幅方向のエッジ部の巻き取り温度が本発明の範囲に未達する場合、厚さ方向の中心部でベイナイトが過度に形成されて伸び率が劣化することを確認することができた。また、中央部の表層部は、フェライトが不足し、中央部ではベイニティックフェライトが不足し、これにより耐衝撃特性と降伏強度の比が本発明で提案するレベルを満たさなかった。 In Comparative Example 6, it was confirmed that when the coiling temperature of the widthwise edge portion did not reach the range of the present invention, excessive bainite was formed in the center portion in the thickness direction, resulting in a deterioration in elongation. Furthermore, there was a lack of ferrite in the surface layer of the center portion, and there was a lack of bainitic ferrite in the center portion, which resulted in the ratio of impact resistance to yield strength not meeting the level proposed by the present invention.
比較例7は、鋼の厚さが8mmに満たない場合であり、与えられた鋼成分において冷却速度が過度に適用されるため、表層部ではフェライトが不足し、厚さ方向の中心部にベイニティックフェライトが減少すると同時にパーライトが過度に形成された。これは、初期冷却過程で未変態した相が増加して、比較的Cの含有量が高い部位でパーライトが形成されたものと判断される。その結果、目的とするレベルの伸び率を確保することができなかった。 In Comparative Example 7, the steel thickness was less than 8 mm. Due to the excessive cooling rate applied for the given steel composition, ferrite was insufficient in the surface layer, bainitic ferrite decreased in the center of the thickness direction, and excessive pearlite formed. This is believed to be due to an increase in untransformed phases during the initial cooling process, resulting in the formation of pearlite in areas with a relatively high C content. As a result, the desired level of elongation could not be achieved.
比較例8は、Ti及びNb含有量の合計が本発明の範囲に未達する場合であり、各位置別に測定された微細組織のそれぞれの相分率は、本発明の提案する範囲を満足したが、熱間圧延中の析出物の減少により、微細組織が粗大になり、冷却及び巻き取り後の微細析出物も減少して強度が不足し、耐衝撃性も大きく減少した。 Comparative Example 8 is a case in which the total Ti and Nb content did not reach the range of the present invention. The phase fractions of the microstructure measured at each position satisfied the range proposed by the present invention, but the microstructure became coarse due to the reduction in precipitates during hot rolling, and the fine precipitates also decreased after cooling and coiling, resulting in insufficient strength and a significant decrease in impact resistance.
比較例9は、冷却速度が関係式1のCR値以上であり、本発明で提案する範囲を満足したが、30℃/sを超過した場合である。その結果、表層部のポリゴナルフェライトが不足し、厚さ方向の中心部にベイナイトが過度に形成されて、目的とするレベルの伸び率を確保することができなかった。 In Comparative Example 9, the cooling rate was equal to or greater than the CR value in Relational Formula 1, satisfying the range proposed by the present invention, but exceeding 30°C/s. As a result, there was a shortage of polygonal ferrite in the surface layer, and excessive bainite was formed in the center of the thickness direction, making it impossible to achieve the desired level of elongation.
以上、実施例を介して本発明を詳細に説明したが、これと異なる形態の実施例も可能である。よって、以下に記載された特許請求の範囲の技術的思想及び範囲は実施例に限定されない。 The present invention has been described in detail above through examples, but other embodiments are possible. Therefore, the technical spirit and scope of the claims set forth below are not limited to the examples.
Claims (9)
表面から厚さ50μm範囲の表層部の微細組織は、面積%で、等軸晶フェライトを95%以上、パーライトを3%以下含み、ベイニティックフェライト、ベイナイト、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種以上を合計で5%以下含み、
厚さ1/4~3/4の範囲の中心部の微細組織は、面積%で、ベイニティックフェライトを80~95%、ベイナイトを10%以下、パーライトを3%以下、MA(Martensite-Austenite constituent)相及びマルテンサイトのうち1種または2種を合計で5~10%含み、残りは等軸晶フェライトを含む、鋼板。 The alloy contains, by weight, C: 0.05 to 0.15%, Si: 0.01 to 0.5%, Mn: 1.0 to 2.0%, Al: 0.01 to 0.1%, Cr: 0.001 to 1.0%, P: 0.001 to 0.05%, S: 0.001 to 0.01%, N: 0.001 to 0.01%, Ti: 0.03 to 0.08%, and Nb: 0.01 to 0.05%, with the balance being Fe and other unavoidable impurities, and the total of Nb and Ti being 0.04 to 0.1%;
The microstructure of the surface layer portion within a thickness range of 50 μm from the surface contains, in area%, 95% or more of equiaxed ferrite and 3% or less of pearlite, and contains 5% or less in total of one or more of bainitic ferrite, bainite, MA (Martensite-Austenite constituent) phase, and martensite,
The microstructure of the center portion within the range of 1/4 to 3/4 of the thickness contains, in area percentages, 80 to 95% bainitic ferrite, 10% or less bainite, 3% or less pearlite, 5 to 10% in total of one or two of an MA (Martensite-Austenite constituent) phase and martensite, and the remainder containing equiaxed ferrite.
前記エッジ部と中央部は、引張強度の差が10MPa以下であり、破壊伸び率の差が8%以下であり、冷間成形後の-20℃での衝撃靭性の差が20J以下である、請求項1に記載の鋼板。 The steel sheet includes edge portions corresponding to 30% regions at both ends in the width direction and a central portion of a central 40% region corresponding to a region excluding both edge portions,
The difference in tensile strength between the edge portion and the center portion is 10 MPa or less, the difference in fracture elongation is 8% or less, and the difference in impact toughness at −20 ° C. after cold forming is 20 J or less. Steel plate according to claim 1.
前記再加熱された鋼スラブを熱間圧延する段階;及び
前記熱間圧延された鋼板を500~650℃の温度範囲まで1~30℃/sの範囲内で下記関係式1で定義されるCR(℃/s)値以上である平均冷却速度で冷却及び巻き取る段階を含み、
前記冷却及び巻き取り段階において、コイル幅方向を基準に両端部で30%の領域に該当するエッジ部は550~650℃の温度(TE)で、幅方向に両エッジ部を除いた領域に該当する中心40%領域の中央部は500~550℃の温度(TC)で冷却し、
エッジ部と中央部の平均温度差は50~150℃である、請求項1に記載の鋼板を製造する、鋼板の製造方法。
[関係式1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(ここで、[C]、[Si]、[Mn]、[Cr]、[Ti]及び[Nb]は各元素の重量%であり、tは鋼板の厚さ(mm)である。) reheating a steel slab containing, by weight, C: 0.05 to 0.15%, Si: 0.01 to 0.5%, Mn: 1.0 to 2.0%, Al: 0.01 to 0.1%, Cr: 0.001 to 1.0%, P: 0.001 to 0.05%, S: 0.001 to 0.01%, N: 0.001 to 0.01%, Ti: 0.03 to 0.08%, and Nb: 0.01 to 0.05%, with the balance being Fe and other unavoidable impurities, and the sum of Nb and Ti being 0.04 to 0.1%;
hot-rolling the reheated steel slab; and cooling the hot-rolled steel sheet to a temperature range of 500 to 650°C at an average cooling rate of 1 to 30°C/s, the average cooling rate being equal to or greater than the CR (°C/s) value defined by the following Relation 1, and coiling the steel sheet,
In the cooling and winding step, the edge portions corresponding to 30% of the area at both ends in the coil width direction are cooled at a temperature of 550 to 650 ° C. (TE), and the central portion of the central 40% area corresponding to the area excluding both edge portions in the width direction is cooled at a temperature of 500 to 550 ° C. (TC),
The method for producing a steel plate according to claim 1 , wherein the average temperature difference between the edge portion and the center portion is 50 to 150°C.
[Relationship 1]
CR=45-16.3×[C]-5.6×[Si]-16.3×[Mn]-2.9×[Cr]+15×[Ti]+23×[Nb]-0.9×(t-8)
(Here, [C], [Si], [Mn], [Cr], [Ti] and [Nb] are the weight percentages of each element, and t is the thickness of the steel plate (mm).)
前記熱間圧延温度は800~1150℃である、請求項6に記載の鋼板の製造方法。 The reheating temperature is 1100 to 1350°C,
The method for producing a steel sheet according to claim 6, wherein the hot rolling temperature is 800 to 1150°C.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020210158366A KR20230072050A (en) | 2021-11-17 | 2021-11-17 | High strength steel plate having excellent impact toughness after cold forming and high yield ratio and method for manufacturing the same |
| KR10-2021-0158366 | 2021-11-17 | ||
| PCT/KR2022/017540 WO2023090751A1 (en) | 2021-11-17 | 2022-11-09 | High-yield ratio high-strength steel plate having excellent impact resistance after cold forming and manufacturing method therefor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2024543074A JP2024543074A (en) | 2024-11-19 |
| JP7789205B2 true JP7789205B2 (en) | 2025-12-19 |
Family
ID=86397427
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024527810A Active JP7789205B2 (en) | 2021-11-17 | 2022-11-09 | High-yield-ratio high-strength steel with excellent impact resistance after cold forming and its manufacturing method |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20250320590A1 (en) |
| EP (1) | EP4435135A4 (en) |
| JP (1) | JP7789205B2 (en) |
| KR (1) | KR20230072050A (en) |
| CN (1) | CN118265808A (en) |
| MX (1) | MX2024005901A (en) |
| WO (1) | WO2023090751A1 (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016108648A (en) | 2014-11-28 | 2016-06-20 | Jfeスチール株式会社 | Steel plate for linepipe, steel pipe for linepipe, and production method therefor |
| KR102236851B1 (en) | 2019-11-04 | 2021-04-06 | 주식회사 포스코 | High strength steel having high yield ratio and excellent durability, and method for producing same |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3477955B2 (en) | 1995-11-17 | 2003-12-10 | Jfeスチール株式会社 | Method for producing high-strength hot-rolled steel sheet having ultrafine structure |
| JP3885314B2 (en) * | 1997-09-29 | 2007-02-21 | Jfeスチール株式会社 | Method for producing high-strength hot-rolled steel sheet having excellent shape and workability |
| JP4528276B2 (en) | 2006-03-28 | 2010-08-18 | 新日本製鐵株式会社 | High strength steel plate with excellent stretch flangeability |
| JP5326403B2 (en) | 2007-07-31 | 2013-10-30 | Jfeスチール株式会社 | High strength steel plate |
| CN102301026B (en) * | 2009-01-30 | 2014-11-05 | 杰富意钢铁株式会社 | Thick-walled high-strength hot-rolled steel sheet excellent in low-temperature toughness and manufacturing method thereof |
| JP5246036B2 (en) * | 2009-05-25 | 2013-07-24 | Jfeスチール株式会社 | Manufacturing method of hot-rolled steel sheet |
| KR101304859B1 (en) * | 2009-12-04 | 2013-09-05 | 주식회사 포스코 | Ultra high strength steel plate for pipeline with high resistance to surface cracking and manufacturing metod of the same |
| JP5724267B2 (en) | 2010-09-17 | 2015-05-27 | Jfeスチール株式会社 | High-strength hot-rolled steel sheet excellent in punching workability and manufacturing method thereof |
| WO2013018740A1 (en) * | 2011-07-29 | 2013-02-07 | 新日鐵住金株式会社 | High-strength steel sheet having superior impact resistance, method for producing same, high-strength galvanized steel sheet, and method for producing same |
| BR112014002875B1 (en) * | 2011-08-09 | 2018-10-23 | Nippon Steel & Sumitomo Metal Corporation | hot-rolled steel sheets, and methods for producing them |
| JP6294197B2 (en) * | 2014-09-19 | 2018-03-14 | 株式会社神戸製鋼所 | Hot rolled steel sheet and manufacturing method thereof |
| KR102010081B1 (en) * | 2017-12-26 | 2019-08-12 | 주식회사 포스코 | Hot-rolled steel sheet having high-strength and high-toughness and method for producing the same |
| KR102131527B1 (en) | 2018-11-26 | 2020-07-08 | 주식회사 포스코 | High-strength steel sheet with excellent durability and method for manufacturing thereof |
| KR102307928B1 (en) | 2019-12-02 | 2021-09-30 | 주식회사 포스코 | High strength multiphase steel sheet with excellent durability and manufacturing method thereof |
-
2021
- 2021-11-17 KR KR1020210158366A patent/KR20230072050A/en active Pending
-
2022
- 2022-11-09 MX MX2024005901A patent/MX2024005901A/en unknown
- 2022-11-09 US US18/708,115 patent/US20250320590A1/en active Pending
- 2022-11-09 CN CN202280076717.7A patent/CN118265808A/en active Pending
- 2022-11-09 WO PCT/KR2022/017540 patent/WO2023090751A1/en not_active Ceased
- 2022-11-09 EP EP22895958.1A patent/EP4435135A4/en active Pending
- 2022-11-09 JP JP2024527810A patent/JP7789205B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016108648A (en) | 2014-11-28 | 2016-06-20 | Jfeスチール株式会社 | Steel plate for linepipe, steel pipe for linepipe, and production method therefor |
| KR102236851B1 (en) | 2019-11-04 | 2021-04-06 | 주식회사 포스코 | High strength steel having high yield ratio and excellent durability, and method for producing same |
Also Published As
| Publication number | Publication date |
|---|---|
| MX2024005901A (en) | 2024-05-30 |
| CN118265808A (en) | 2024-06-28 |
| EP4435135A1 (en) | 2024-09-25 |
| US20250320590A1 (en) | 2025-10-16 |
| EP4435135A4 (en) | 2025-04-30 |
| JP2024543074A (en) | 2024-11-19 |
| KR20230072050A (en) | 2023-05-24 |
| WO2023090751A1 (en) | 2023-05-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101883875B (en) | High-strength steel sheet with excellent low temperature toughness and manufacturing method thereof | |
| JP7244723B2 (en) | High-strength steel material with excellent durability and its manufacturing method | |
| JP7569928B2 (en) | High strength thick hot rolled steel sheet with excellent elongation ratio and its manufacturing method | |
| US12049687B2 (en) | High-strength steel having high yield ratio and excellent durability, and method for manufacturing same | |
| JP7508469B2 (en) | Ultra-high strength steel plate with excellent shear workability and its manufacturing method | |
| KR20200011742A (en) | High-strength steel sheet having excellent impact resistant property and method for manufacturing thereof | |
| JP2023507528A (en) | LOW-CARBON LOW-COST ULTRA-HIGH-STRENGTH MULTI-PHASE STEEL STEEL/STRIP AND METHOD FOR MANUFACTURING SAME | |
| JP7431325B2 (en) | Thick composite structure steel with excellent durability and its manufacturing method | |
| CN108913998A (en) | A kind of cold-rolled biphase steel and preparation method thereof | |
| JP7167159B2 (en) | Hot-rolled steel sheet for electric resistance welded steel pipe, manufacturing method thereof, and electric resistance welded steel pipe | |
| CN111511935B (en) | Hot-rolled steel sheet having excellent durability and method for producing same | |
| KR101560948B1 (en) | High strength multi-matrix hot rolled steel sheet having excellent impact resistance and formability of edge part and method for manufacturing the same | |
| JP7373576B2 (en) | High-strength hot-rolled steel sheet with excellent punchability and material uniformity and its manufacturing method | |
| JP3539545B2 (en) | High-tensile steel sheet excellent in burring property and method for producing the same | |
| JP2002363685A (en) | Low yield ratio high strength cold rolled steel sheet | |
| CN116368253B (en) | High-strength steel sheet with excellent thermal stability and method for manufacturing the same | |
| JP7789205B2 (en) | High-yield-ratio high-strength steel with excellent impact resistance after cold forming and its manufacturing method | |
| JP7588717B2 (en) | High-strength thick steel plate with excellent formability and its manufacturing method | |
| JP2024542247A (en) | HOT-ROLLED STEEL SHEET AND ITS MANUFACTURING METHOD | |
| JP2003193186A (en) | High-strength steel sheet and high-strength electroplated steel sheet excellent in ductility, stretch flangeability and shock absorption properties, and methods for producing them | |
| JP2025131727A (en) | Steel plate and its manufacturing method | |
| CN120476223A (en) | Hot rolled steel sheet and method for manufacturing the same | |
| CN118355143A (en) | High-strength and high-formability steel sheet with excellent spot weldability and method for producing the same | |
| JP2023554299A (en) | High strength steel plate with excellent ductility and its manufacturing method | |
| KR20210063135A (en) | High strength dp steel sheet of which the durability and flexibility are outstanding and a production metfod therefor |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20240513 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20250528 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20250610 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20250909 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20251111 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20251209 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 7789205 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |