TW201137130A - High-strength hot-dip galvanized steel sheet with excellent processability and impact resistance and process for producing same - Google Patents
High-strength hot-dip galvanized steel sheet with excellent processability and impact resistance and process for producing same Download PDFInfo
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- TW201137130A TW201137130A TW100102078A TW100102078A TW201137130A TW 201137130 A TW201137130 A TW 201137130A TW 100102078 A TW100102078 A TW 100102078A TW 100102078 A TW100102078 A TW 100102078A TW 201137130 A TW201137130 A TW 201137130A
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- iron
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- steel sheet
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- 229910001335 Galvanized steel Inorganic materials 0.000 title claims abstract description 13
- 239000008397 galvanized steel Substances 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 217
- 229910052742 iron Inorganic materials 0.000 claims abstract description 107
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 95
- 239000010959 steel Substances 0.000 claims abstract description 95
- 229910000859 α-Fe Inorganic materials 0.000 claims abstract description 43
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 239000012535 impurity Substances 0.000 claims abstract description 6
- 238000000137 annealing Methods 0.000 claims description 21
- 239000011324 bead Substances 0.000 claims description 19
- 238000005098 hot rolling Methods 0.000 claims description 15
- 238000011282 treatment Methods 0.000 claims description 13
- 238000005275 alloying Methods 0.000 claims description 9
- 229910052758 niobium Inorganic materials 0.000 claims description 8
- 238000012545 processing Methods 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 7
- 238000005246 galvanizing Methods 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- QNDQILQPPKQROV-UHFFFAOYSA-N dizinc Chemical compound [Zn]=[Zn] QNDQILQPPKQROV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 239000003337 fertilizer Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000011159 matrix material Substances 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 abstract description 4
- 229910000734 martensite Inorganic materials 0.000 abstract 2
- 229910001562 pearlite Inorganic materials 0.000 abstract 2
- 238000005096 rolling process Methods 0.000 description 28
- 239000010955 niobium Substances 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 13
- 238000007747 plating Methods 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 230000007423 decrease Effects 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 7
- 210000001161 mammalian embryo Anatomy 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 238000005097 cold rolling Methods 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000005121 nitriding Methods 0.000 description 5
- 238000005728 strengthening Methods 0.000 description 5
- 229910052719 titanium Inorganic materials 0.000 description 5
- 238000003723 Smelting Methods 0.000 description 4
- 238000005266 casting Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 239000010960 cold rolled steel Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000032683 aging Effects 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009749 continuous casting Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 150000001247 metal acetylides Chemical class 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229910001035 Soft ferrite Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 238000005261 decarburization Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 230000029052 metamorphosis Effects 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- -1 nitrogen carbides Chemical class 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000009628 steelmaking Methods 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 240000006413 Prunus persica var. persica Species 0.000 description 1
- 206010040844 Skin exfoliation Diseases 0.000 description 1
- 229910000746 Structural steel Inorganic materials 0.000 description 1
- 229910000794 TRIP steel Inorganic materials 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000010977 jade Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
-
- 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
- C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
- C21D8/0421—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the working steps
- C21D8/0426—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 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
- C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
- C21D8/0421—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the working steps
- C21D8/0436—Cold 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 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
- C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
- C21D8/0447—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the heat treatment
- C21D8/0473—Final recrystallisation annealing
-
- 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
- C22C38/02—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
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/34—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of 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
- C22C38/18—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
- C23C2/28—Thermal after-treatment, e.g. treatment in oil bath
-
- 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
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Thermal Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Coating With Molten Metal (AREA)
Abstract
Description
201137130 六、發明說明: 【發明所屬之技術領域】 用鋼板用途的耐衝擊特性 本發明係關於使用於作為汽車 優異之高強度炼融錢鋅鋼板。 【先前技術】 近年’就從地球環境保護的觀點,汽車的燃油效率提升已 成重要課題。因而,有利用車體材料的高強度化而達薄板 化,俾使車體本身變輕量化的動向正活躍中。“,鋼板的 高強度化料致軋延性降_卩絲加工⑽低),因而期待 合併具有W度與高加I性的材料開發。又因為汽車碰撞 時’各部位所承受到的應變速度係達心程度,因而在此 種高速度域下的_擊特性便屬特別重要。且,最近亦追加 提高對汽車_錄提升要求,便有錄断㈣行炼融鍵 鋅的高張力鋼板開發。且’為能確保沖祕、雜接性及塗 料密接性,大多使用經鍍敷後再施行熱處理,俾使鋼板的 Fe擴散於鍍敷層中的合金化熔融鍍鋅鋼板。 針對此種要求,加工性與耐衝擊吸收特性均優異的高強度 鋼板,代表性係有如專利文獻1所揭示,由肥粒鐵與麻田散 鐵的複合組織所構成之雙相組織鋼板(pp鋼板)。但是,原 本降伏強度較低的DP鋼板之所以呈現高衝擊吸收能力的理 由’係利用沖壓加工施行的加工硬化較大,以及若有加工應 變進入’在後續的烤漆步驟便會產生應變時效導致降伏強度 100102078 3 201137130 大幅提升’會有彎曲加工等心量較小的零件未必能發 夠衝擊吸收能力的問題。玉^ ^ ^ 疋 古麻轡敁巾u ’ DP鋼具有在10〜30%程度的 冋缝域中’衝擊吸收能力量較高,_擊特性優異 徵,雖適用於前碰料轉在鋪時會出現隸度變 吸收碰^里的部位,但從如側面碰撞部位確保駕駛員空 的觀點,對小應變域雹I古π 曰 〜支域而要巧吸收能量的部位,難謂充分 特性。 疋 Α再者’專利文獻2雖有揭示:制用殘留γ的塑性誘發變 態之TRIP鋼,使耐衝擊特性提升的技術,但具有與上述 DP鋼同樣的問題。 [先行技術文獻] [專利文獻] [專利文獻1]日本專利特開2003_213369號公報 [專利文獻2]日本專利特開2〇〇1_335891號公報 【發明内容】 (發明所欲解決之問題) 本發明目的在於提案:具有高強度(達590MPa以上的拉 伸強度TS) ’加工性優異,且即便沒有因沖壓加工而導入應 變’直到5%程度之低應變域的吸收能量仍較大,耐碰撞特 性優異的炫融鑛鋅鋼板及其製造方法。 (解決問題之手段) 本發明者等為能達成上述課題,製造加工性及耐衝擊特性 100102078 4 201137130 均優異的高強魏融輯鋼板,便從鋼板組成及微觀組織的 觀點進行深人鑽研。結果得知藉由主相為肥粒鐵,第二相含 有變勤肥粒鐵、麻田散鐵及珠粒鐵的組織,並滿足麻田散鐵 面積率/(_肥粒鐵面積率+珠粒鐵面積率 0.6,且將肥粒 鐵相中的Μη漢度與第二相中的Mn濃度比設為〇·7〇以上, 便可獲付較向的加工性與耐衝擊特性。 加工性的提升係藉由Si的活用便可利用屬於主相的肥 粒鐵之加卫硬化能力提升而提升軋延性,以及藉由變勃肥粒 鐵、珠粒鐵的活用’便可湘軟質肥粒鐵與硬質麻田散鐵的 硬度差緩和而提升擴孔性。 再者,通常已知Μη在熱軋時與退火時會濃化於第二相, 導致鋼中出現分佈,但藉由將熱軋時的捲取溫度設為低溫, 且將退火時的均熱時間設為適當,而將鋼中的Μη分佈呈均 勻,並藉由將肥粒鐵相中的Μη濃度與第二相中的Μη濃度 比設為0.70以上,即便沒有因沖壓加工而導入應變,直到 5%程度的低應變域中之吸收能量仍大,可提升耐碰撞特性。 本發明係以上述發現為基礎而構成。 即,本發明係如下述。 (1)一種加工性和耐衝擊特性優異之高強度熔融鍍鋅鋼 板,係成分組成為依質量%計含有:C : 0.04%以上且0 13% 以下、Si : 0.7%以上且2.3%以下、Μη : 0.8%以上且2.0% 以下、Ρ : 0.1%以下、S : 0.01%以下、Ai: 0 01%以上且〇1% 100102078 201137130 以下,其餘為鐵及不<避免的雜質構成;其中,組織係依面 積率計具有:75%以上的肥粒鐵相、與1<J/Q以上的變韌肥粒 鐵相、及1%以上且1〇°/°以下的珠粒鐵相,且麻田散鐵相的 面積率係10%以下;真 滿足麻田散鐵面積率/(變韌肥粒鐵面積率+珠粒鐵面積 率)S 0.6 ’且肥粒鐵相中的Μη >辰度與第二相中的濃度 比係0.70以上。 (2) 如(1)所記載之加工性和耐衝擊特性優異之高強度熔融 鑛鋅鋼板,其中,更進一步,成分組成係依質量%計,含有 從Cr : 0.05%以上且1.0%以下、V : 〇 〇〇5%以上且〇 5%以 下、Mo : 0.005%以上且0.5%以下中選擇至少ι種的元素。 (3) 如(1)或(2)所記載之加工性和耐衝搫特性優異之高強 度溶融鍵辞鋼板,其中,成分組成係依*旦。 貝夏/〇計’含有從 上且G.胸下、Nb :⑽%以上且以下、 B :⑽嶋以上且議㈣以下、Ni : 〇桃以上且i 〇%以 下、Cu : 0.05%以上且〖·〇%以下中選擇至少ι種的元素。 傷^如·^⑺項中任—賴記載之h性和耐衝擊特性 優異之尚強度炫融鍍鋅鋼板,盆中, " 又進一步,成分組成係 依貝罝树,含有從⑽賴以上且〇〇〇5%以下 議%以上且0.魏町中選擇至少丨種的元素。. (5)如⑴至(4)項巾任—項所記載之加 耐 優異之高猶融料喃,其中,更進—步,成== 100102078 6 201137130 依質量%計’含有從Ta: 〇.001%以上且〇 〇1〇%以下、§η: 0.002%以上且0.2%以下中選擇之至少i種的元素。 ⑹如⑴至(5)項中任-項所記載之加工性和耐衝擊特性 優異之高強度熔融鍍鋅鋼板,其中,更進一步,成分組成係 依質夏%§十’含有Sb : 0.002%以上且〇 2%以下。 ⑺-種加工性和耐衝擊特性優異之高強度炫融鑛鋅鋼板 之製造方法’係將具有⑴〜⑹項中任一項記載成分組成的鋼 胚’施行熱軋後,再依300。(:以上且57〇。〇以下的溫度進行 捲取而製得的熱軋板,予以酸洗、或更進一步施行冷軋,然 後,在750〜900°C之溫度域,依t:保持時間(8),滿足下式 的條件施行退火後, 15 ^ 47.6xlO",0/exp(-27〇16/(T+273)) T :退火溫度(°C) 經冷卻,依450〜550°C之溫度域保持10〜200s,接著施行 熔融鍍辞、或更進一步在500〜600。(:之溫度域中,依Tave : 平均保持溫度(°C)與th:保持時間(5)滿足下式的條件施行鍍 鋅的合金化處理; 0.45 ^ exp[200/(400-Tave)]xln(th)^ 1.0 。 (發明效果) 根據本發明’可獲得加工性優異、且即便沒有因沖壓加工 而導入應變,直到5%程度之低應變域的吸收能量仍大,耐 衝擊特性優異的高強度熔融鍍鋅鋼板,可兼顧汽車輕量化與f 100102078 7 201137130 碰撞安全性提升’達對汽車車體的高性能化具大幅貢獻的優 異效果。 【實施方式] 以下’針對本發明進行具體說明。 首先’針對將本發明的鋼成分組成限定於上述範圍的理由 進行说明。另外,相關成分的「%」表示,在無特別聲明的 前提下係指「質量%」。 C · 〇·04%以上且0.13%以下 C係使沃斯田鐵安定化的元素,因為容易生成肥粒鐵以外 的相’因而屬於鋼板強度上升的必要元素。若c量未滿 貝J即便達製造條件最佳化,仍較難確保所需的強 度反之,若C量超過0.13%,則肥粒鐵相會減少,鋼板的 加工J·生降低,且熔接部與熱影響部的硬化明顯,熔接部的機 械特陡劣化。就從此觀點,將C量設為〇·〇4。/。以上且〇.13% 以下。 8^〇^%以上且2.3%以下201137130 VI. Description of the Invention: [Technical Field of the Invention] Impact Resistance Characteristics for Steel Sheet Use The present invention relates to a high-strength smelting zinc steel sheet which is excellent as an automobile. [Prior Art] In recent years, from the perspective of global environmental protection, the improvement of fuel efficiency of automobiles has become an important issue. Therefore, there is a tendency to use a high strength of the vehicle body material to achieve a thin plate, and the movement of the vehicle body itself is becoming lighter. “The high-strength material of the steel sheet causes the rolling ductility to decrease—the silk processing (10) is low. Therefore, it is expected to combine the material development with W degree and high I. And because of the strain rate of each part when the car collides. The degree of reaching the heart is therefore particularly important in the high-speed range. Moreover, the recent development of the high-tension steel plate for the smelting of the zinc is recorded. In order to ensure the sharpness, the miscibility, and the adhesion of the coating, the alloyed hot-dip galvanized steel sheet which is subjected to heat treatment after plating and which diffuses Fe of the steel sheet into the plating layer is often used. A high-strength steel sheet excellent in both workability and impact absorption resistance is a two-phase structural steel sheet (pp steel sheet) composed of a composite structure of ferrite iron and granulated iron as disclosed in Patent Document 1. However, the original The reason why the DP steel sheet with low drop strength exhibits high impact absorption capacity is that the work hardening by stamping processing is large, and if the processing strain enters, it will be generated in the subsequent baking step. Variable aging results in the strength of the fall 100102078 3 201137130 Significantly improved 'There will be problems such as bending processing and other parts with small heart volume may not be able to absorb enough impact. Jade ^ ^ ^ 疋古麻辔敁 towel u 'DP steel has 10~ In the 30% degree quilting domain, the impact energy absorption capacity is high, and the _ hit characteristic is excellent. Although it is suitable for the part where the front touch material turns into the paving, the part of the absorbing force will be absorbed, but from the side collision site. It is difficult to say that it is sufficient to ensure that the driver is empty. It is difficult to say that it is sufficient to absorb energy in the small strain domain 古I ancient π 曰 支 支 疋Α 专利 专利 ' 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利In the case of the TRIP steel, which has been subjected to the change of the impact resistance characteristics, it has the same problem as the above-mentioned DP steel. [Prior Art Document] [Patent Document] [Patent Document 1] Japanese Patent Laid-Open Publication No. 2003-213369 [Patent Document 2] SUMMARY OF THE INVENTION PROBLEMS TO BE SOLVED BY THE INVENTION The object of the present invention is to provide a high strength (tensile strength TS of 590 MPa or more), which is excellent in workability and even In the present invention, the present inventors have been able to introduce a strain in the low strain range up to 5% by press working, and to have a large impact energy resistance, and a method for producing the same. In order to achieve the above-mentioned problems, the high-strength Wei Rong series steel plates, which are excellent in both workability and impact resistance, are well studied. From the viewpoint of steel plate composition and microstructure, it is found that the main phase is the ferrite iron. The two phases contain the structure of the fertile iron, the granulated iron and the granulated iron, and satisfy the area ratio of the granulated iron in the granules/(_the area of the iron granules + the area ratio of the granules of the granules of 0.6), and the iron content in the ferrite When the ratio of Mn concentration in Μη 汉度 to the second phase is set to 〇·7〇 or more, the comparative workability and impact resistance characteristics can be obtained. The improvement of the processability can improve the rolling ductility by utilizing the strengthening of the hardening iron of the fat iron which belongs to the main phase, and the use of the ferrite iron and the bead iron. The hardness difference between the ferrite iron and the hard hemp field is relaxed and the hole expandability is improved. Further, it is generally known that Μη is concentrated in the second phase during hot rolling and annealing, resulting in distribution in the steel, but by setting the coiling temperature during hot rolling to a low temperature, and soaking during annealing When the time is set to be appropriate, the Μη distribution in the steel is made uniform, and the ratio of the Μη concentration in the ferrite-grained iron phase to the Μn concentration ratio in the second phase is set to 0.70 or more, even if no strain is introduced by press working. Up to 5% of the low strain domain, the absorbed energy is still large, which improves the collision resistance. The present invention is constructed on the basis of the above findings. That is, the present invention is as follows. (1) A high-strength hot-dip galvanized steel sheet having excellent workability and impact resistance, and has a composition of: C: 0.04% or more and 0% or less, and Si: 0.7% or more and 2.3% or less, in terms of % by mass, Μη : 0.8% or more and 2.0% or less, Ρ: 0.1% or less, S: 0.01% or less, Ai: 0 01% or more, 〇1% 100102078, 201137130 or less, and the rest are iron and not < impurities to be avoided; The tissue system has an iron content of a ferrite grain of 75% or more, a ferro-grain iron phase of 1<J/Q or more, and a bead iron phase of 1% or more and 1〇°/° or less, depending on the area ratio, and The area ratio of the loose iron phase of Ma Tian is less than 10%; it really satisfies the area ratio of the loose iron in the field / (the area ratio of the iron toughened ferrite + the area of the iron of the bead) S 0.6 ' and the Μ η in the ferrite phase The concentration ratio in the second phase is 0.70 or more. (2) The high-strength molten zinc-zinc steel sheet which is excellent in workability and impact resistance as described in (1), and further, the component composition contains Cr: 0.05% or more and 1.0% or less in terms of % by mass. V : 〇〇〇 5% or more and 〇 5% or less, and Mo: 0.005% or more and 0.5% or less of at least one element selected. (3) A high-strength melting bond steel sheet excellent in workability and impact resistance as described in (1) or (2), wherein the component composition is based on the denier. Bezia/〇计' contains from the top and G. under the chest, Nb: (10)% or more, B: (10) 嶋 or more, and (4) or less, Ni: 〇 peach or more and i 〇% or less, Cu: 0.05% or more Select at least ι elements from 〇% below. Injury ^如·^(7) 任任 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖 赖In addition, 5% or less of the above-mentioned percentages and 0. Weicho chooses at least the elements of the species. (5) As in (1) to (4), the towel is a high-resistance sufficiency, which is more advanced, and further ==100102078 6 201137130 by mass %' containing from Ta: 〇. 001% or more and 〇〇1〇% or less, §η: 0.002% or more and 0.2% or less of at least one element selected. (6) The high-strength hot-dip galvanized steel sheet excellent in workability and impact resistance as described in any one of items (1) to (5), wherein, further, the component composition is based on the summer %§10' containing Sb: 0.002% Above and below 2%. (7) A method for producing a high-strength smelting zinc-zinc steel sheet having excellent workability and impact resistance characteristics, wherein the steel preform having the composition of any one of the items (1) to (6) is subjected to hot rolling, and then 300. (: The above and 57 〇. The hot-rolled sheet obtained by coiling at the following temperature is pickled, or further cold-rolled, and then, in the temperature range of 750 to 900 ° C, according to t: holding time (8), after the conditions of the following formula are applied, 15 ^ 47.6xlO", 0/exp(-27〇16/(T+273)) T: annealing temperature (°C), after cooling, according to 450~550° The temperature domain of C is maintained for 10 to 200 s, followed by a molten plating, or further in the range of 500 to 600. (In the temperature range, according to Tave: average holding temperature (°C) and th: holding time (5)) The alloying treatment of galvanizing is carried out under the conditions of the formula; 0.45 ^ exp [200 / (400 - Tave)] xln (th) ^ 1.0. (Effect of the invention) According to the present invention, excellent workability can be obtained, and even if it is not subjected to press working The strain is introduced until the absorption energy of the low strain range of 5% is still large, and the high-strength hot-dip galvanized steel sheet with excellent impact resistance can take into consideration the light weight of the automobile and the collision safety improvement of the f 100102078 7 201137130 The high performance of the high performance is greatly enhanced. [Embodiment] The following 'specification of the present invention First, the reason for limiting the steel component composition of the present invention to the above range will be described. The "%" of the relevant component means "% by mass" unless otherwise stated. C · 〇·04 % or more and 0.13% or less C is an element that stabilizes the Worthite iron because it is easy to form a phase other than the ferrite iron. Therefore, it is an essential element for the increase in the strength of the steel sheet. However, it is still difficult to ensure the required strength. Conversely, if the amount of C exceeds 0.13%, the iron phase of the ferrite is reduced, the processing of the steel sheet is reduced, and the hardening of the welded portion and the heat-affected portion is marked. From this point of view, the amount of C is set to 〇·〇4. /. or more and 〇.13% or less. 8^〇^% or more and 2.3% or less
Sl係肥粒鐵生成元素,且亦屬於對固溶強化具有效的元 素而為能改善強度與軋延性的均衡、及確保肥粒鐵的硬 度,必需添如達〇.7%以上。然而,若超過2 3%的&過剩添 會因發生諸如紅色鐵銹等而導致表面性狀劣化、引發 鍍敷附著•密接性劣化。故,㈣設為〇 7%以上且2 3%以 T。較佳係U%以上丑1.8%以下。 100102078 201137130 Μη : 0.8〇/〇以上且2.〇〇/。以下 皿11係_化的有效元素。且屬於使沃心鐵安定化的元 素,對第二相的分率調整屬於必要元素。因而,Mn必需添 加達〇.8〇/。以上。反之,若超過2 〇%的過剩添加,第二相中 的麻田散鐵面積率會增加,拉伸凸緣性降低。故,Mn係設 為0.8%以上且2.0%以下。較佳係! 〇%以上且以下。 p :0.1%以下 0 P係鋼強化的有效元素,若超過0.1%的過剩添加,便會 因晶界偏析而引發脆化,導致耐衝擊性劣化。又,若超過 〇.1% ’則會使合金化速度大幅延遲。故,P係設為〇 1%以 下。 s : 0.01%以下 ^會成為諸如Mns料雜物,導致成為耐衝擊性劣化、 2接部金屬流出現斷裂的肇因,因而最好盡量降低,就從 W造成本的觀點,s係設為0.01%以下。 A1 · 0.01%以上且〇1%以下 係具脫氧劑的仙,屬於對鋼的潔淨度具有效元素, 瑕好在脫氧步驟中添加。此處,若A1量未滿讀%,此項 添加效果便會變差,因而將下限設為G.G1%。然而,A1的 D剩添加會使製鋼時的扁胚品質劣化。所以,Μ餘為〇1% 以下。 本發明㈣強聽祕鋅鋼板細上述齡組成為基本 _02078 201137130 成分,其餘則由鐵及不可避免的雜質構成,但配合所需特性, 尚可適當含有從以下所述元素中選擇之至少丨種的元素。Sl is a ferrite-based iron-forming element and is also an element that is effective for solid solution strengthening. In order to improve the balance between strength and rolling ductility, and to ensure the hardness of ferrite, it is necessary to add more than 7%. However, if more than 2% of the excess is caused by red rust, etc., the surface properties are deteriorated, and plating adhesion and adhesion are deteriorated. Therefore, (4) is set to 〇 7% or more and 2 3% to T. Preferably, it is U% or more and less than 1.8%. 100102078 201137130 Μη : 0.8〇/〇 and above 2.2/. The following dishes 11 are effective elements of _. And it belongs to the element that makes the iron core stable, and the adjustment of the fraction of the second phase is an essential element. Therefore, Mn must be added up to 〇.8〇/. the above. On the other hand, if excessive addition exceeds 2%, the area ratio of the granulated iron in the second phase increases, and the stretch flangeability decreases. Therefore, the Mn system is set to be 0.8% or more and 2.0% or less. Better! 〇% or more and below. p : 0.1% or less 0 If the effective element of the P-based steel is excessively added, if it is excessively added in excess of 0.1%, embrittlement is caused by segregation at the grain boundary, and the impact resistance is deteriorated. Further, if it exceeds 〇.1%', the alloying speed is greatly delayed. Therefore, the P system is set to 〇 1% or less. s : 0.01% or less ^ will become a material such as Mns, which will cause deterioration of impact resistance and breakage of the metal flow in the joint. Therefore, it is preferable to reduce it as much as possible. 0.01% or less. A1 · 0.01% or more and 〇 1% or less The deodorizer is an effective element for the cleanliness of steel, and it is added in the deoxidation step. Here, if the A1 amount is less than the read %, the addition effect will be deteriorated, so the lower limit is set to G.G1%. However, the addition of D in A1 deteriorates the quality of the flat embryo at the time of steel making. Therefore, the surplus is less than 1%. According to the invention, the composition of the above-mentioned age is the basic composition of _02078 201137130, and the rest is composed of iron and unavoidable impurities, but it may be appropriately selected from the following elements in combination with the desired characteristics. Kind of elements.
Cr.0.05%以上且1.0%以下、V:0.005%以上且〇 5%以下、 Mo : 0.005%以上且0.5%以下 因為Cr、V、Mo係屬於提升淬火性、鋼強化的有效元素。 此項效果係依Cr: 0.05%以上、V : 〇·〇〇5%以上、Mo : 0.005% 以上才能獲得。然而’若分別超過Cr : i.〇〇/0、V : 0.5%、 Mo : 0.5%的過剩添加,則第二相的分率便會變為過大,會 有加工性降低的顧慮。所以,當添加該等元素時,其量分別 設為Cr : 0.05%以上且1.〇〇/0以下、v : 〇 〇〇5%以上且〇 5% 以下、Mo : 0.005%以上且〇.5〇/0以下。 更可含有從下述Ti、Nb、B、Ni、Cu中選擇1種以上的 元素。Cr. 0.05% or more and 1.0% or less, V: 0.005% or more and 〇 5% or less, and Mo: 0.005% or more and 0.5% or less. Cr, V, and Mo are effective elements for improving hardenability and steel strengthening. This effect is obtained by Cr: 0.05% or more, V: 〇·〇〇 5% or more, and Mo: 0.005% or more. However, if excessive addition exceeds Cr: i.〇〇/0, V: 0.5%, and Mo: 0.5%, the fraction of the second phase may become excessively large, which may cause a decrease in workability. Therefore, when these elements are added, the amounts are respectively set to be Cr: 0.05% or more and 1. 〇〇/0 or less, v: 〇〇〇5% or more and 〇5% or less, and Mo: 0.005% or more and 〇. 5〇/0 or less. Further, one or more elements selected from the group consisting of Ti, Nb, B, Ni, and Cu described below may be contained.
Ti: 0.01%以上且ο.ρ/。以下、Nb: 〇〇1%以上且〇 1%以下 Ti、Nb係對鋼的析出強化具有效,此項效果分別係依 0.01%以上才能獲得’若在本發明所規定範圍内亦無妨使用 於鋼的強化。但是’若分別超過〇1%,則加工性會降低。 所以’當添加Ti、Nb時,其添加量係就Ή設為〇〇1%以上 且0.1%以下’就Nb設為0.01%以上且〇1%以下。 B : 0.0003%以上且〇 〇〇5〇%以下 B係具有抑制從沃斯田鐵晶界的肥粒鐵生成/成長之作 用’因而視需要可添加。此項效果係達〇〇〇〇3%以上才能獲 100102078 201137130 得。但是’若超過0.0050% ’則加工性會降低。故,當添加 B時,便設為0.0003%以上且0.0050%以下。Ti: 0.01% or more and ο.ρ/. Hereinafter, Nb: 〇〇1% or more and 〇1% or less Ti and Nb are effective for precipitation strengthening of steel, and the effect is 0.01% or more, respectively, to obtain 'if it is within the scope of the present invention, it may be used for Steel reinforcement. However, if it exceeds 〇1%, the workability will decrease. Therefore, when Ti and Nb are added, the amount of addition is 〇〇1% or more and 0.1% or less', and Nb is set to 0.01% or more and 〇1% or less. B: 0.0003% or more and 〇 〇〇 5〇% or less The B system has a function of suppressing the formation/growth of the ferrite iron from the Worthfield iron grain boundary, and thus can be added as needed. This effect is more than 3% to get 100102078 201137130. However, if it exceeds 0.0050%, the workability will decrease. Therefore, when B is added, it is set to 0.0003% or more and 0.0050% or less.
Ni : 0.05%以上且1.0%以下、Cu : 0.05%以上且1.0%以下Ni: 0.05% or more and 1.0% or less, Cu: 0.05% or more and 1.0% or less
Ni、Cu係鋼強化的有效元素,若在本發明所規定範圍内 亦無妨使用於鋼的強化。為能獲得該等效果分別必需達 0.05%以上。另一方面,若Ni、Cu均添加超過1.0%,便會 使鋼板的加工性降低。所以,當添加Ni、Cu的情況,其添 加量分別設為0.05%以上且1.0%以下。 更可含有從下述Ca、REM中選擇1種以上的元素。The effective elements strengthened by Ni and Cu-based steels may be used for reinforcement of steel in the range specified by the present invention. In order to obtain these effects, it is necessary to achieve 0.05% or more. On the other hand, when both Ni and Cu are added in excess of 1.0%, the workability of the steel sheet is lowered. Therefore, when Ni or Cu is added, the amount of addition is set to 0.05% or more and 1.0% or less, respectively. Further, one or more elements selected from the following Ca and REM may be contained.
Ca : 0.001%以上且 0.005%以下、reM : 0.001%以上且 0.005%以下Ca : 0.001% or more and 0.005% or less, reM : 0.001% or more and 0.005% or less
Ca及REM係屬於為將硫化物的形狀予以球狀化,俾改善 硫化物對擴孔性造成不良影響的有效元素。為能獲得此項效 果分別必需達0.001%以上。然而,超過〇 005%的過剩添加 便會引發夾雜物等的增加’導致引發表面及内部缺陷等情況 發生。所以’當添加Ca、的情況,其添加量分別設為 0.001%以上且0·005%以下。 更可含有從下述Ta、Sn中選擇1種以上的元素。Ca and REM are effective elements for spheroidizing the shape of sulfides and improving the adverse effects of sulfides on hole expandability. In order to achieve this effect, it must be 0.001% or more. However, an excess of more than 00 5% will cause an increase in inclusions, etc., resulting in surface and internal defects. Therefore, when Ca is added, the amount of addition is 0.001% or more and 0. 005% or less. Further, one or more elements selected from the following Ta and Sn may be contained.
Ta : 0.001 〜0.010%、Sn : 0.002〜0.2%Ta : 0.001 to 0.010%, Sn: 0.002 to 0.2%
Ta係與Ti、Nb同樣的,會形成合金碳化物、合金氮碳化 物’不僅對高強度化具貢獻,且藉由其中一部分固溶於Nb 碳化物、Nb氮碳化物中,而形成諸如(Nb,Ta)(C,N)之類的複 s 100102078 201137130 合析出物’明顯抑制析出物的粗大化,判斷具有能使利用析 出強化而對強度的貢獻呈安定化之效果。因而,當添加仏 I 〃3有$最好設為0.001%以上。但是,當過剩添 加不僅上述析出物安定化效果已達飽和,且合金成本亦 會提高,因而當添加Ta的情況,其含有量最好設為0 0 以下。 2係就從抑制鋼板表面的氮化、氧化、或抑制因氧化所 k 鋼板表層數姆m區域的脫碳情形之觀點,係可添 ::::制此種氮化、氧化,便可防止鋼板表面的麻田散 、俾使疲勞特性與抗老化性獲改善。就從抑制 oD減的她,#添加Sn的情況,其含有量最好設為 =上’右超過G.2°摘會導致祕降低,因而最好將 其含有量設在〇.2%以下。 更可含有下述Sb。The Ta-based alloys, like Ti and Nb, form alloy carbides and alloyed nitrogen carbides, which not only contribute to high-strength, but also form a solid solution in Nb carbides and Nb-nitrogen carbides, such as Complex s 100102078, 201137130, Nb, Ta) (C, N) The precipitated product 'significantly inhibits the coarsening of the precipitate, and has an effect of making the contribution to the strength stable by precipitation strengthening. Therefore, when 仏 I 〃 3 is added, it is preferable to set it to 0.001% or more. However, when the excess is added, not only the above-mentioned precipitate stabilization effect is saturated, but also the alloy cost is increased. Therefore, when Ta is added, the content thereof is preferably set to 0 or less. From the viewpoint of suppressing the nitriding, oxidation, or decarburization of the surface of the steel sheet by the oxidation of the steel sheet, the 2 series can be added:::: This kind of nitriding and oxidation can be prevented. The diarrhea and enamel on the surface of the steel sheet improve fatigue characteristics and aging resistance. In the case of adding Sn from the inhibition of oD, the content of Sn is preferably set to = upper 'right than G. 2 °, which will result in a decrease in the secret. Therefore, it is preferable to set the content below 〇.2%. . It may further contain the following Sb.
Sb : 0.002-0.2% 亦讀Sn同樣的,就從抑制鋼板表面的氮化 =制Γ化所造成距鋼板表層數1⑽區域的脫碳情形之 ,點係、可添加。藉由抑制此種氮化、氧化, 善勞特性與抗老化性獲改 ,抑制氮化、氧化的觀點,當添加Sb的情況,其含 低,因上’若超過_彳會導致祕降 敢好將其含有量設在G.2%以下 100102078 12 201137130 其次,針對鋼組織進行說明。 肥粒鐵相之面積率:75%以上 為月t確保良好的軋延性,肥粒鐵相依面積率必需達75% 以上。 變韌肥粒鐵相之面積率:1〇/。以上 為月b確保良好的擴孔性,即為能緩和軟質肥粒鐵與硬質 麻田政鐵間之硬度差,變韌肥粒鐵相的面積率必需達1%以 上。 珠粒鐵相之面積率:1%以上且1〇%以下 為能確保良好的擴孔性,珠粒鐵相的面積率係設為1%以 上。若珠粒鐵相之面積率超過10%,軋延性(TSXEL)會降低。 所以’珠粒鐵相之面積率係設為1%以上且10%以下。 麻田散鐵相之面積率:10%以下 右麻田散鐵相之面積率超過10%’拉伸凸緣性降低會趨於 明顯。所以,麻田散鐵相之面積率係設為10%以下。 麻田散鐵面積率/(變韌肥粒鐵面積率+珠粒鐵面積 率)S0.6 ' 麻田散鐵係與肥粒鐵間之強度差較大,會使拉伸凸緣性降 低’但藉由使與變韌肥粒鐵及珠粒鐵共存,並設為麻田散鐵 面積率/(變韌肥粒鐵面積率+珠粒鐵面積率)S 0.6,便可抑制 因麻田散鐵所造成的擴孔性降低情形。故,設為麻田散鐵面 積率/(變韌肥粒鐵面積率+珠粒鐵面積率)$0.6。 100102078 13 201137130 另外,除肥粒鐵、變韌肥粒鐵、珠粒鐵、麻田散鐵之外, 尚有會生成殘留沃斯田鐵、回火麻田散鐵、碳化鐵體等碳化 物的情況’但若滿足上述肥粒鐵、變韋刀肥粒鐵、珠粒鐵、麻 田政鐵的面積率,便可達成本發明目的。 再者,本發明中所謂「肥粒鐵、變韌肥粒鐵、珠粒鐵、麻 田政鐵的面積率」,係指在觀察面積中所佔的各相面積比例。 微觀組織係針對鋼板在軋延方向剖面的板厚1/4部,施行 研磨後,使用3%Nital施行腐蝕,然後使用掃描式電子顯微 鏡依倍率5000倍的視野進行觀察,並使用Media cybemedcs 公司的Image-Pro求取各相之面積率。 此時,因為麻田散鐵與殘留沃斯田鐵的區分較為困難,因 而對所獲得熔融鍍鋅鋼板依20(rc施行2小時的回火處理, 然後,朝鋼板的軋延方向依照上述方法觀察平行板厚剖面的 、、气並將依上述方法所求得回火麻田散鐵相的面積率視為 「麻田散鐵相之面積率」。 再者’殘留沃斯田鐵相的含有量係將鋼板研磨至板厚方向 的1/4面,再利用該板厚1/4面的繞射χ射線強度便可求得。 此時’入射X射線係使用CoKa線,並針對殘留沃斯田鐵 相的{111}、{200}、{220}、{311}面、與肥粒鐵相的{11〇}、 {200}、{211}面之尖峰積分強度全部組合,求取強度比,並 將該等的平均值視為「殘留沃斯田鐵相之含有量」,且將該 含有量視同「殘留沃斯田鐵之面積率」。 100102078 】4 201137130 肥粒鐵相中的Μη濃度、與第二相中的Μη濃度比(肥粒鐵 相中的Mn濃度/第二相中的Μη濃度)達0.70以上 藉由將鋼中的Μη分佈形成均勻,即便沒有因沖壓加工而 導入應變,直到5%程度的低應變域中之吸收能量仍較大, 可提升耐碰撞特性,藉由將肥粒鐵相中的Μη濃度、與第二 相中的Μη濃度比設為〇.7〇以上,便可獲得此項效果。故, 將肥粒鐵相中的Μη濃度、與第二相中的Μη濃度比設為 0.70以上〇 其次,針對製造條件進行說明 將經调整為上述成分組成的鋼利用轉爐等進行熔製,再依 連續鑄造法等形成扁胚。對該鋼胚施行熱軋而形成熱軋鋼 板,再將該熱軋鋼板施行酸洗、或更進一步施行冷軋而形成 冷軋鋼板。對經酸洗過的熱軋鋼板或冷軋鋼板施行連續退火 後,再施行熔融鍍鋅處理、或更進一步施行鍍鋅的合金化處 理。針對各步驟的限定理由進行說明。 [熱軋條件] 捲取溫度:300°C以上且570。(:以下 若熱軋後的捲取溫度超過570。(:,在捲取後便會促進Mn 朝第二相的分’導致就最終組織將肥粒鐵相中的.濃度 與第二相中的Μη濃度比設為〇.7〇以上之事趨於困難。又, 若捲取溫度未滿30(TC,則熱軋板的形狀會惡化、或熱軋板 強度過度上升’導致冷軋較為困難。&,捲取溫度係設為 100102078 15 201137130 300°C以上且570°C以下。 [連續退火條件] 乂 在750〜900°C溫度域中,依滿足下式的條件施行退火。 15 ^ t ^ 47.6x 1 〇-10/exp(-27016/(T+273)) t :保持時間(s) T :退火溫度(°〇 當退火溫度未滿750°C時、或保持(退火)時間未滿15s時, 退火時的沃斯田鐵生成會嫌不足,導致無法確保經退火冷卻 後所必要量的低溫變態相。反之,若退火溫度超過9〇〇t:, 則退火時的沃斯田鐵會明顯增加,導致無法確保經退火冷卻 後所必要量的肥粒鐵。又,若保持時間超過 47.6xl01G/exp(-27016/(T+273))秒,則退火時 Μη 對沃斯田 鐵相的濃化會過度進行,導致頗難就最終組織將肥粒鐵相中 的Μη濃度、與第二相中的Μη濃度比設為0.70以上。 退火後冷卻,在450〜550°C溫度域中保持10〜200s。 當保持溫度超過55CTC時、或保持時間未滿1〇s時,因為 並不會促進變韌鐵變態,幾乎無法獲得變韌肥粒鐵,因而無 法獲得所需的擴孔性。又,當保持溫度未滿45〇ΐ、或保持 時間超過20Gs時’第二相的大半部分會變成因變勃鐵變態 促進而生成的HI 4¼ 1較多之沃斯田鐵與變勃肥粒鐵,導致 無法獲得所㈣珠__率’且硬㈣讀鐵面積率會增 加,導致無法獲得良好的擴孔性與材質安定性。 100102078 16 201137130 在施行上述保持之後,便於實際使用時的防銹能力提升目 的下’對表面施行熔融鍍鋅處理。 為能確保沖壓性、點熔接性及塗料密接性,大多使用在鍍 敷後把行熱處理,俾使鋼板的j?e擴散於鑛敷層中的合金化 熔融鍍鋅鋼板。在製造合金化熔融鍍鋅鋼板時,於熔融鍍鋅 後’更進一步依下述條件施行合金化處理。 [合金化處理條件] 在500〜60(TC溫度域中,Tave :平均保持溫度(。〇、比: 保持時間(s),依滿足下式: 0.45 Sexp[200/(400-Tave)]xln(th)$ 1‘〇 的條件施行鍍敷層之合金化處理。 另外’ exp(X)、1η(χ)分別係表示X的指數函數、自然對 數。 鍍敷層的合金化處理係為能在鍍敷層中獲得適當的 Fe%,便設為500〜600°C範圍。 當 exp[200/(400-Tave)]xln(th)未滿 0.45 時,因為最終組織 中會有較多的麻田散鐵存在,導致上述硬質麻田散鐵鄰接於 軟質肥粒鐵,造成異相間出現較大的硬度差,致使擴孔性降 低。當 exp[200/(400-Tave)]xln(th)超過 1.0 時,未變態沃斯 田鐵幾乎均會變態為碳化鐵體或珠粒鐵,結果導致無法獲得 所需的強度與軋延性均衡。 另外,本發明之製造方法的一連串熱處理中,若在上述溫Sb: 0.002-0.2% When the same is true for Sn, the decarburization of the surface layer 1 (10) from the surface of the steel sheet caused by the nitriding of the steel sheet is suppressed. By suppressing such nitriding, oxidation, good workability and aging resistance, and suppressing nitriding and oxidation, when Sb is added, its content is low, because if it exceeds _, it will lead to a secret drop. It is good to set the content below G.2%. 100102078 12 201137130 Next, the steel structure will be explained. Area ratio of ferrite grain iron phase: 75% or more For the month t to ensure good rolling ductility, the ferrite-iron phase ratio must be more than 75%. The area ratio of the tough ferrite grain iron phase: 1〇/. The above is to ensure good hole expansion for the month b, that is, to alleviate the hardness difference between the soft ferrite iron and the hard Ma Tianzheng iron, and the area ratio of the toughened ferrite iron phase must be more than 1%. Area ratio of the bead iron phase: 1% or more and 1% by mass or less In order to ensure good hole expandability, the area ratio of the bead iron phase is set to be 1% or more. If the area ratio of the bead iron phase exceeds 10%, the rolling ductility (TSXEL) will decrease. Therefore, the area ratio of the bead iron phase is set to be 1% or more and 10% or less. Area ratio of the iron phase of Ma Tian: 10% or less The area ratio of the loose iron phase of the right Ma Tian is more than 10%. The decrease in stretch flangeability tends to be obvious. Therefore, the area ratio of the granulated iron phase is set to be 10% or less. The area ratio of the loose iron in Ma Tian / (the area ratio of the iron toughened ferrite + the area ratio of the bead iron) S0.6 'The difference in strength between the Ma Tian scattered iron system and the ferrite iron is large, which will reduce the stretch flangeability. By coexisting with the toughened ferrite iron and the bead iron, and setting the area ratio of the granulated iron / (the toughened ferrite iron area ratio + the bead iron area ratio) S 0.6, it is possible to suppress the cause of the field The resulting hole expansion is reduced. Therefore, it is set as the area ratio of the granulated iron area / (the area ratio of the toughened ferrite grain to the area of the iron of the bead iron) of $0.6. 100102078 13 201137130 In addition, in addition to ferrite iron, tough ferrite iron, bead iron, and Ma Tian loose iron, there are still cases of carbides such as residual Worth iron, tempered granulated iron, and carbon carbide. 'But if the above-mentioned area ratio of ferrite iron, granule iron, bead iron, and 麻田政铁 is satisfied, the object of the present invention can be achieved. Further, in the present invention, the "area ratio of ferrite iron, tough ferrite iron, bead iron, and 麻田政铁" means the ratio of the area of each phase in the observed area. The microstructure is applied to 1/4 of the thickness of the steel sheet in the rolling direction section, and then etched using 3% Nital, and then observed using a scanning electron microscope at a magnification of 5000 times, and using Media cybemedcs. Image-Pro finds the area ratio of each phase. At this time, since the distinction between the Ma Tian loose iron and the residual Worth iron is difficult, the obtained hot-dip galvanized steel sheet is subjected to tempering treatment for 20 hours (rc), and then, according to the above method, the rolling direction of the steel sheet is observed. The area ratio of the parallel plate thickness profile and the gas obtained by the above method is regarded as the "area ratio of the granulated iron phase of the Matian". The steel plate is polished to a quarter surface in the thickness direction, and the diffraction ray intensity of the 1/4 surface of the plate thickness can be obtained. At this time, the incident X-ray system uses a CoKa line and is directed to the residual Worthfield. The {111}, {200}, {220}, {311} planes of the iron phase are combined with the peak intensity of the {11〇}, {200}, and {211} planes of the ferrite phase to obtain the intensity ratio. And the average value of these is regarded as "the content of the residual Worthite iron phase", and the content is regarded as the "area ratio of the residual Worthite iron." 100102078 】4 201137130 Μη concentration, Μη concentration ratio in the second phase (Mn concentration in the ferrite phase iron phase / Μη concentration in the second phase) is 0.70 or more By forming the Μη distribution in the steel evenly, even if there is no strain introduced by the press working, the absorption energy in the low strain range up to 5% is still large, and the collision resistance property can be improved by the ferrite grain in the iron phase. This effect can be obtained by setting the concentration of Μη and the concentration of Μη in the second phase to 〇.7〇 or more. Therefore, the ratio of Μη in the ferrite phase and the Μn concentration in the second phase are set to The steel material adjusted to the above-mentioned component composition is melted by a converter or the like, and a flat embryo is formed by a continuous casting method or the like. The steel blank is hot rolled to form a hot rolled steel sheet. The hot-rolled steel sheet is subjected to pickling or further cold rolling to form a cold-rolled steel sheet. The acid-washed hot-rolled steel sheet or cold-rolled steel sheet is continuously annealed, and then subjected to hot-dip galvanizing treatment or further Zinc-plated alloying treatment. The reasons for limitation of each step will be described. [Hot-rolling conditions] Coiling temperature: 300 ° C or more and 570. (: The following coiling temperature after hot rolling exceeds 570. (:, in After the roll, it will be promoted The division of Mn into the second phase causes the final tissue to be more difficult to set the concentration of the ferrite in the ferrite phase to the concentration of the niobium in the second phase to be more than 〇.7〇. Also, if the coiling temperature is not When the temperature is 30 (TC, the shape of the hot-rolled sheet is deteriorated, or the strength of the hot-rolled sheet is excessively increased), it is difficult to perform cold rolling. & The coiling temperature is set to 100102078 15 201137130 300 ° C or more and 570 ° C or less. [Continuous Annealing Conditions] 乂 is annealed in the temperature range of 750 to 900 ° C according to the conditions of the following formula: 15 ^ t ^ 47.6x 1 〇-10/exp(-27016/(T+273)) t : Time (s) T : Annealing temperature (° When the annealing temperature is less than 750 ° C, or the holding (annealing) time is less than 15 s, the formation of Worth iron during annealing is insufficient, resulting in failure to ensure annealing cooling The necessary amount of low temperature metamorphic phase. On the other hand, if the annealing temperature exceeds 9 〇〇t:, the Worth iron in the annealing will increase remarkably, and the amount of ferrite iron which is necessary after annealing and cooling cannot be ensured. Moreover, if the holding time exceeds 47.6xl01G/exp(-27016/(T+273)) seconds, the concentration of Μη on the iron phase of the Vostian will be excessively performed during annealing, which makes it difficult to finally form the ferrite phase. The Μη concentration in the middle and the Μη concentration ratio in the second phase are set to 0.70 or more. After annealing, it is cooled and kept at a temperature of 450 to 550 ° C for 10 to 200 s. When the temperature is maintained above 55 CTC, or the holding time is less than 1 〇s, since the toughened iron metamorphosis is not promoted, the toughened ferrite iron is hardly obtained, and thus the desired hole expandability cannot be obtained. In addition, when the temperature is less than 45 〇ΐ, or the holding time exceeds 20 Gs, the majority of the second phase will become HI 41⁄4 1 which is produced by the change of the metamorphosis of the ferrocene. Iron, which leads to the inability to obtain the (four) bead __ rate' and the hard (four) read iron area ratio will increase, resulting in poor hole expandability and material stability. 100102078 16 201137130 After the above holding is carried out, it is easy to carry out the rust-preventing ability in actual use, and the surface is subjected to hot-dip galvanizing treatment. In order to ensure the punchability, the spot weldability, and the adhesion of the coating, an alloyed hot-dip galvanized steel sheet which is heat-treated after plating and which causes the steel sheet to diffuse into the ore layer is often used. In the production of the alloyed hot-dip galvanized steel sheet, after the hot-dip galvanizing, the alloying treatment was carried out under the following conditions. [Alloying treatment conditions] In 500 to 60 (TC temperature range, Tave: average holding temperature (.〇, ratio: holding time (s), according to the following formula: 0.45 Sexp [200/(400-Tave)] xln (th) The condition of $1'〇 is applied to the alloying of the plating layer. In addition, 'exp(X) and 1η(χ) respectively represent the exponential function of X and the natural logarithm. The alloying treatment of the plating layer is When the appropriate Fe% is obtained in the plating layer, it is set in the range of 500 to 600 ° C. When exp[200/(400-Tave)]xln(th) is less than 0.45, there will be more in the final structure. The existence of loose iron in Ma Tian causes the above-mentioned hard ram field loose iron to be adjacent to the soft ferrite iron, resulting in a large hardness difference between the heterophases, resulting in a decrease in hole expandability. When exp[200/(400-Tave)]xln(th) exceeds At 1.0, the untransformed Worthite iron is almost always metamorphosed into carbon carbide or bead iron, and as a result, the required strength and rolling ductility are not obtained. Further, in the series of heat treatments of the manufacturing method of the present invention, temperature
S 100102078 17 201137130 度範圍内,則保持溫度並無必要為一定,若在所規定範圍内 便不會損及本發明主旨。又,若連熱經歷(heat history)亦能 滿足,則鋼板依任何設備施行熱處理均無妨。除此之外,在 熱處理後為施行形狀端正’而對本發明鋼板施行調質軋延之 事’亦涵蓋於本發明範圍内。另外,本發明係假設鋼素材經 由通常的製鋼、鑄造、熱軋等各步驟而進行製造之情況,但 亦可例如利用薄板鑄造等並省略部分或全部熱軋步驟而進 行製造的情況。 其他之製造方法並無特別的限定,相關較佳一例係如下 ✓ 1、 ° [鑄造條件] 所使用的鋼胚係為防止成分的巨觀偏析,最好依連續鑄造 法進行製造,但亦可依造塊法、薄胚鑄造法進行製造。又, 除在製造鋼胚後,暫時先冷卻至室溫,然後再度施行加熱的 習知方法之外,未冷卻至室溫,而依熱片的狀態插入於加熱 爐中,或者在稍施行保熱後便馬上施行軋延的直送軋延•直 接軋延等省能源製程,亦均毫無問題地可適用。 [熱軋條件] 扁胚加熱溫度:1100°c以上 扁胚加熱溫度係就能量而言,最好為低溫加熱,但若加熱 溫度未滿ll〇〇°C ’便會有碳化物無法充分固溶、或因軋延 荷重增加導致熱軋時發生故障的危險性增大等問題發生。另 100102078 18 201137130 外’因為隨氧化量增力口會造成錄皮損失(scalel〇ss)增加等, 因而爲胚加熱溫度最好設為以下。 另外,就從即便降低扁胚加熱溫度,仍可防止熱軋時故障 的觀點,亦可活用將片料以加熱之所則條加熱器。 精軋溫度:Ar3變態點以上 若精乳結束溫度未滿_變態點,在札延中會生成〇與^ 導致鋼板中容易生成帶狀組織’該帶狀組織在冷軋後與退火 後仍會殘留’會有成為使材料特性發生非等向性、或使加工 性降低之原因的情況發生。因而’精軋溫度最好設為A 悲點以上。 另外’本發明的熱軋步驟中,為減輕熱軋時的軋延荷重, 亦可將精軋其中-部分或全料為潤滑軋延。施行潤滑札延 之事’係就從鋼板形狀均勻化、材f均勻化的觀點,亦屬有 效。另外,施行潤滑軋延時的摩擦係數最好設為Q25〜㈣ 祀圍内。又’最好設為將相前後的片條彼此間施行接合,並 連續施行精軋的連續軋延製程。採用連續軋延製程之^,就 從熱軋的作業安定性觀點,亦屬較佳。 厅 [冷軋條件] 接著,當施行冷乳時’較佳係將熱軋鋼板表面的氧化鐵垢 利用酸洗料除去後,再提供給冷軋㈣成既定板厚的冷乳 鋼板。此處就酸洗條件與冷軋條件並無特別的限制,只魏 照常法便可。冷軋的軋縮率較佳係設為4〇%以上。 乂 100102078 ,Λ 201137130 [熔融鍍鋅條件] 敷處理係利用〇.〇8〜0.18%溶解A1量的鍍浴,依浴溫 440〜500°C的鍍浴使鋼板浸入於鍍浴中而實施,再利用氣刷 法等進行附著量的調整。另外,經熔融鍍鋅處理後的鋼板, 為形狀矯正、表面粗度等的調整,亦可施行調質軋延。又, 即便施行諸如樹脂或油脂塗敷、各種塗裝等處理,亦不會有 任何不良情況。 [實施例] 將具有表1所示成分組成,其餘為Fe及不可避免的雜質 (表1中,N係不可避免的雜質)構成的鋼,利用轉爐進行熔 製,並利用連續鑄造法形成鑄片。 100102078 20 201137130S 100102078 17 In the range of 201137130, it is not necessary to maintain the temperature. If it is within the specified range, the gist of the present invention will not be impaired. Moreover, if the heat history can be satisfied, the steel plate may be subjected to heat treatment according to any equipment. In addition to this, it is also within the scope of the present invention to perform the temper rolling of the steel sheet of the present invention after the heat treatment to perform the shape of the shape. Further, the present invention is a case where the steel material is manufactured by various steps such as ordinary steel making, casting, hot rolling, etc., but it may be manufactured by, for example, thin-plate casting or the like, and some or all of the hot rolling steps are omitted. The other production method is not particularly limited, and a preferred example is as follows: ✓1, ° [Casting conditions] The steel germ system used is a macroscopic segregation of the component, and it is preferably produced by a continuous casting method. Manufactured by the block method and the thin blank casting method. In addition, in addition to the conventional method of cooling to room temperature and then heating again after manufacturing the steel embryo, it is not cooled to room temperature, but is inserted into the heating furnace according to the state of the hot sheet, or is slightly protected. After the heat is applied, the direct rolling and rolling, direct rolling and other energy-saving processes can be applied without any problem. [Hot rolling conditions] Flat embryo heating temperature: 1100 °c or more Flat embryo heating temperature is preferably low temperature heating in terms of energy, but if the heating temperature is less than 〇〇 ° ° C, there will be insufficient carbide solidification. Solubility, or increased risk of failure during hot rolling due to an increase in rolling load, occurs. In addition, since the increase in the skin loss (scalel 〇ss) is caused by the increase in the amount of oxidation, the heating temperature for the embryo is preferably set to the following. Further, from the viewpoint of preventing the failure at the time of hot rolling even if the heating temperature of the slab is lowered, it is also possible to use a heater which heats the sheet material. Finishing temperature: If the finishing temperature of Ar3 is above the metamorphic point, if the end temperature of the fine milk is not full _ metamorphic point, 〇 and ^ will be formed in the Zhayan, resulting in the formation of banded structure in the steel plate. The banded structure will still be after cold rolling and after annealing. Residues may occur as a cause of anisotropy in material properties or a decrease in workability. Therefore, the finishing temperature is preferably set to be above A stagnation point. Further, in the hot rolling step of the present invention, in order to reduce the rolling load during hot rolling, it is also possible to carry out the rolling rolling of the part or the whole of the finish rolling. It is also effective from the viewpoint of uniformizing the shape of the steel sheet and homogenizing the material f. In addition, it is preferable to set the friction coefficient of the lubrication rolling delay to be within the range of Q25 to (4). Further, it is preferable to perform a continuous rolling process in which the preceding and succeeding strips are joined to each other and the finish rolling is continuously performed. It is also preferable from the viewpoint of the stability of the hot rolling operation by using the continuous rolling process. Hall [Cold Rolling Condition] Next, when cold milk is applied, it is preferable to remove the iron oxide scale on the surface of the hot-rolled steel sheet by the pickling material, and then supply it to the cold-rolled steel sheet having a predetermined thickness. Here, there are no particular restrictions on the pickling conditions and the cold rolling conditions, and only the usual method can be used. The cold rolling reduction ratio is preferably set to 4% by weight or more.乂100102078,Λ201137130 [Metal galvanizing conditions] The coating treatment is carried out by immersing the steel sheet in a plating bath at a bath temperature of 440 to 500 ° C using a plating bath in which 8 to 0.18% of A1 is dissolved. The amount of adhesion is adjusted by an air brush method or the like. Further, the steel sheet subjected to the hot-dip galvanizing treatment may be subjected to adjustment of shape correction, surface roughness, or the like, and may be subjected to temper rolling. Moreover, there is no problem even if a treatment such as resin or grease coating or various coatings is applied. [Examples] Steel having the composition shown in Table 1 and having Fe and unavoidable impurities (N, unavoidable impurities in Table 1) was melted in a converter and cast by a continuous casting method. sheet. 100102078 20 201137130
備註 發明鋼 發明鋼 發明鋼 發明鋼 |發明鋼| 發明鋼 發明鋼 發明鋼 發明鋼 |發明鋼| 1發明鋼I 比較鋼 |比較鋼| 丨比較鋼I |比較鋼| |比較鋼| 發明鋼 發明鋼 發明鋼 發明鋼 化學成分(mass%) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Sb : 0.007 Ta,Sn 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Ta : 0.005 Sn : 0.007 Ta : 0.008 1 Ca,REM 1 1 1 1 1 1 1 1 1 Ca : 0.002 REM : 0.002 1 1 1 1 1 1 1 1 1 Ti,Nb,B,Ni,Cu 1 1 1 1 Ti : 0.04 Nb : 0.03 Ti : 0.015,B : 0.0010 m 〇 Cu : 0.4,Ni : 0.2 1 1 1 1 1 1 1 Nb : 0.02 Nb : 0.04 1 1 Cr,V,Mo 1 Cr : 0.2 Y : 0.05 CN 〇 〇 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0.0025 0.0042 0.0033 0.0045 〇·〇_ 0.0041 | 0.0029 | | 0.0039 | 0.0042 | | 0.0020 I 1 0.0035 1 | 0.0036 1 0.0040 0.0025 0.0038 0.0031 0.0035 0.0042 0.0028 0.0031 0.03 0.04 0.03 0.04 0.03 0.03 0.04 「0.05 「0.03 0.02 「0.031 「0.03 Γ〇.03 「0.03 「0.03 0.04 0.03 「0.04 0.04 (0.03 0.0030 0.0025 0.0040 0.0028 0.0014 0.0012 0.0008 0.0035 1 0.0020 | | 0.0031 I 1 0.0028 | 0.0015 | 0.0015 0.0015 0.0009 0.0012 0.0021 0.0024 0.0015 0.0009 0.010 0.010 0.009 0.008 0.012 0.012 0.009 0.011 0.008 | | 0.012 I 1 0.014 | o.oio 0.010 0.012 0.008 0.008 0.009 0.007 0.010 0.009 Mn vq r"H 00 vq H 00 CN rn v〇 in 00 VO v〇 c> ΓΠ cs VO 寸· <N 00 cs f-H r·^ oo 1-H o (N <N y—4 O) t-H CN CN iTi CO ITi 〇 cs oo f-H υ 0.06 0.10 0.08 0.05 0.07 0.10 0.12 0.08 |0.0』 0別 0.07 0.03 0.15 0.07 0.07 0.09 0.08 0.10 0.07 0.09 < m U Q o HH o CL, a Pi OO H -SZOSIOOI 15 201137130 2及表3所示條件,純為板厚 鋼板,並— 23mm λλ^α 又,其中一部分係將熱軋為板厚 .、.4鋼板,再經酸洗後便直接提供施行退火。 耆,對該等冷軋鋼板物L鋼板,利用連魏融麟生 著==2及表3所示條件施行退火與鍍敷處理。鍍敷附 .者里係§又為每單面35〜45g/m2。 =對所獲得她的微觀_、拉伸特性、㈣凸緣性及耐 衝擊特性進行調查,結果如表4及表5所示。 、另外,微觀組織係針對鋼板軋延方向剖面的板厚Μ部 分’使用掃描式電子顯微鏡依倍率5〇〇〇倍的視野進行觀 察,並依照上述方法求取各相之面積率。 肥粒鐵相與第二相十的Μη濃度係利用ΕΡΜΑ依〇.ιμιη 間隔,施行Μη的線分析而進行測定。將各粒子的Μη濃度 平均值視為該粒子的Μη濃度,並針對肥粒鐵相與第二相各 10粒子進行測定,且將其平均值視為肥粒鐵相及第二相的 Μη濃度。 加工性係就軋延性、擴孔性(拉伸凸緣性)進行評估。 軋延性係使用從無加工鋼板的軋延方向之直角方向所採 取的JIS5號試驗片,依應變速度i〇-3/s施行拉伸試驗,並 測定TS(拉伸強度)、EL(總伸長率),將TSxELg 19000MPa·% 的情況判定為「良好」。 100102078 22 201137130 拉伸凸緣性係根據日本鋼鐵聯盟規格JFST1〇〇i實施。將 所獲得鋼板切斷為l〇〇mmx100mm後,針對板厚2 以 上係依間隙12%±1%、而板厚未滿2Gmm係依間隙 12%±2%,衝孔直徑10mm孔之後,再使用内捏75誦的模 具,在依皺摺壓住力9ton進行按押的狀態下,將6〇。圓錐 衝頭壓入孔中,測定龜裂發生極限的孔直徑,從下式求取極 限擴孔率λ(%),並從該極限擴孔率的數值進行拉伸凸緣性 評估。 極限擴孔率 λ(%)={(ϋ「D〇)/D〇}xl〇0 其中’ Df係龜裂發生時的孔徑(mm),D〇係初期孔徑(mm)。 本發明中’將λ^70(%)的情況判定屬良好。 衝擊吸收特性係從無加工鋼板軋延方向的直角方向所採 取到平行部之寬5mm、長度7mm的試驗片,求取直到依應 變速度2000/s施行拉伸試驗時之應變量的吸收能量(參照鐵 與鋼、Vol.83(1997)、p.748),依所求得吸收能量與靜態TS 的比(AE/TS)評估衝擊吸收特性。另外,吸收能量係藉由將 應力-真應變曲線依應變量0〜5%的範圍進行積分而求得。 100102078 23Remarks invention steel invention steel invention steel invention steel | invention steel | invention steel invention steel invention steel invention steel | invention steel | 1 invention steel I comparative steel | comparative steel | 丨 comparative steel I | comparative steel | | comparative steel | Steel invented steel Invented steel chemical composition (mass%) 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Sb : 0.007 Ta,Sn 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Ta : 0.005 Sn : 0.007 Ta : 0.008 1 Ca, REM 1 1 1 1 1 1 1 1 1 Ca : 0.002 REM : 0.002 1 1 1 1 1 1 1 1 1 Ti, Nb, B, Ni, Cu 1 1 1 1 Ti : 0.04 Nb : 0.03 Ti : 0.015, B : 0.0010 m 〇Cu : 0.4, Ni : 0.2 1 1 1 1 1 1 1 Nb : 0.02 Nb : 0.04 1 1 Cr, V, Mo 1 Cr : 0.2 Y : 0.05 CN 〇〇1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0.0025 0.0042 0.0033 0.0045 〇·〇_ 0.0041 | 0.0029 | | 0.0039 | 0.0042 | | 0.0020 I 1 0.0035 1 | 0.0036 1 0.0040 0.0025 0.0038 0.0031 0.0035 0.0042 0.0028 0.0031 0.03 0.04 0.03 0.04 0.03 0.03 0.04 "0.05 "0.03 0.02 "0.031 "0.03 Γ〇.03 "0.03 "0.03 0.04 0.03 "0.04 0.04 (0.03 0.0030 0.0025 0.0040 0.0 028 0.0014 0.0012 0.0008 0.0035 1 0.0020 | | 0.0031 I 1 0.0028 | 0.0015 | 0.0015 0.0015 0.0009 0.0012 0.0021 0.0024 0.0015 0.0010 0.010 0.010 0.010 0.009 0.008 0.012 0.012 0.009 0.011 0.008 | | 0.012 I 1 0.014 | o.oio 0.010 0.012 0.008 0.008 0.009 0.007 0.010 Mn vq r"H 00 vq H 00 CN rn v〇in 00 VO v〇c> ΓΠ cs VO inch · <N 00 cs fH r·^ oo 1-H o (N <N y—4 O) tH CN CN iTi CO ITi 〇cs oo fH υ 0.06 0.10 0.08 0.05 0.07 0.10 0.12 0.08 |0.0』 0 别 0.07 0.03 0.15 0.07 0.07 0.09 0.08 0.10 0.07 0.09 < m UQ o HH o CL, a Pi OO H -SZOSIOOI 15 The conditions shown in 201137130 2 and Table 3 are purely plate-thick steel plates, and - 23mm λλ^α, some of which are hot-rolled into plate thicknesses, .4 steel plates, and then directly subjected to acid annealing to provide annealing.耆, the cold-rolled steel sheet L-steel was subjected to annealing and plating treatment using conditions of the combination of Wei Ronglin and ==2 and Table 3. In the plating, the § is 35~45g/m2 per side. = Investigation was made on the microscopic_, tensile properties, (f) flangeability and impact resistance properties obtained. The results are shown in Tables 4 and 5. Further, the microstructure is observed with respect to the thickness of the steel sheet in the section of the rolling direction of the steel sheet by using a scanning electron microscope at a magnification of 5 times the magnification, and the area ratio of each phase is obtained by the above method. The ferrogranular iron phase and the second phase ten Μη concentration were measured by line analysis of Μη by using ΕΡΜΑμ.ιμιη intervals. The average value of the Μη concentration of each particle is regarded as the Μη concentration of the particle, and the iron particle phase and the second phase of each of the 10 particles are measured, and the average value thereof is regarded as the ferrogranular iron phase and the Μη concentration of the second phase. . The workability is evaluated in terms of rolling ductility and hole expandability (stretch flangeability). For the rolling property, the JIS No. 5 test piece taken from the direction perpendicular to the rolling direction of the unprocessed steel sheet was subjected to a tensile test at a strain rate i 〇 -3 / s, and TS (tensile strength) and EL (total elongation) were measured. Rate), the case of TSxELg 19000 MPa·% was judged as "good". 100102078 22 201137130 The stretch flangeability is implemented according to the Japan Iron and Steel Federation specification JFST1〇〇i. After the obtained steel sheet is cut into l〇〇mmx100mm, the thickness of the plate is 2% or more depending on the gap of 12%±1%, and the thickness of the plate is less than 2Gmm according to the gap of 12%±2%, and the punching hole is 10mm hole, and then Using a mold that is kneaded in a 75-inch state, 6 〇 is placed in a state where the crease is pressed by a force of 9 ton. The conical punch was pressed into the hole, and the diameter of the hole at which the crack occurred was determined. The ultimate hole expansion ratio λ (%) was obtained from the following formula, and the tensile flangeability evaluation was performed from the value of the ultimate hole expansion ratio. The ultimate hole expansion ratio λ(%)={(ϋ"D〇)/D〇}xl〇0 where 'Df is the hole diameter (mm) at which the crack occurs, and the initial diameter (mm) of the D〇 system. In the present invention The case where λ^70 (%) was judged to be good. The impact absorption characteristic was obtained from a direction perpendicular to the rolling direction of the unprocessed steel sheet to a test piece having a width of 5 mm and a length of 7 mm in the parallel portion, and was obtained until the strain rate was 2000/ s The absorbed energy of the strain in the tensile test (see Iron and Steel, Vol. 83 (1997), p. 748), and the impact absorption characteristics are evaluated according to the ratio of absorbed energy to static TS (AE/TS). In addition, the absorbed energy is obtained by integrating the stress-true strain curve according to the range of 0 to 5% of the variable. 100102078 23
—sso- 201137130 【s 備註 發明例 發明例 發明例 發明例 發明例 發明例 發明例 發明例 發明例 發明例 發明例 $ f 合金化 exp[200/(400- Tavs)]xln(th) 0.79 0.73 0.92 0.82 0.71 0.64 0.82 1 0.73 0.64 0.79 0.85 保持時間 th(s) un (N 〇 (Ν 平均保持;跋 Tave〇C) 550 Ο VO κη Ο 芝 沄 Ο m ο 〇 m to Ο 冷卻後直到鍍浴 浸潰前的保持時間 ⑻ 〇 ο ο ο ο § 安 g Ο 1 冷卻後直到鍵浴浸潰 前的平均保持溫度 CC) 480 〇 ο 沄 ο Ο o 寸 ο Ο 〇 s Ο 47.6x10'10/exp (-27016/(T+273)) 258 m ro νο 00 00 1086 g Μ Μ Ό Ό 1—^ Ό ν〇 保持時間 ⑻ 〇 ο 沄 〇 ο g § 1退火溫度 ΓΟ 820 〇 ο οο ο 00 ο 00 o ο 00 ο 〇 Ο ΟΟ Ο οο 冷軋有無 杯 杷 杯 4sp 杯 杯 枇 杯 熱軋條件 1 I捲取溫度 CC) 丨 430 | 〇 ο ο ο ο ο 00 m 〇 00 C^i ο ο ο ο 〇 ο CN ο 1 :精軋溫度 CC) 910 | 〇 5; ο Os 00 ο Ον 00 ο CM Os 〇\ g 00 g 00 in ο ΓΊ Qs ο m Ον 加熱溫度 CC) 1250 1250 1250 1250 Γ 1250 \ 1250 1 1 1250 1 1250 | 1250 1 1250 1 1250 \Ά1 〇 ζΛ Η < 02 U 鋼板 ν〇 00 m o 5 3 5 4 SAOSlool s 20 一寸硌一 no p— I»r· l?\ 寸 c> d 空 r〇 m c? d Ϊ i i S ir> c> o h 備註1 i >fe i[ aJ s i 錄 λ3 if ? ±i a a £ i 落 空 i 兰 ¥ Λ3 Λ3 λ3 彰 Jj £ lT> m 〇 d 兰 錄 jD id .»» 〇 c> —— CS 00 <〇 in o d ir> <〇 O d o d <〇 in 〇 c5 〇 〇 d K o o si m CO S 〇〇 l〇 P jtj p ο ο κ> ο ο ο rS o — —— jr; Ο Ο 0.063 I § O d S o d oo η d s o o m m o d § 〇 σ\ s ο m ο ο Ο ο ο ci o o 寸 3 C> d t 〇 d < ΦΊ ^7 式ω 倒 ο ν〇 cn O 〇〇 (N [ΤΙ m cs -I - OO r〇 o i— cn ΚΠ m o〇 ?; P; Ρ; 00 Ρ; _ (Ν Ρ; t: 寸 寸 o (N m Os Ό 1/Ί r〇 — oo m r〇 v〇 〇〇 r〇 m 1 ir> 00 vn … m m r-H OO 泛 ΓΛ OO 5 1 ir> v£> in m 1 寸 ^ rt Nw/ ΓΛ OS ψ· Η Γ〇 Ον ? CN σ> «—H οο ο ο 宕 ο 00 f—Η μ CN ΟΟ σ^ v〇 宕 oo d Oj r*H m CN oc 00 O Ό (N v〇 s 卜 rs s S 00 f—1 00 jn <—· 〇 <〇 卜 卜 J s CN 寸 S 00 r~H CN ΟΟ 2 \ο ο 卜 卜 m 落 s tN m oo 1-H m d〇 <〇 1-H O CTN ί s ON _ ro 寸 CN δ ι—Η 异 (Ν ΓΛ Ο Γ〇 Ο | s (N r〇 m 宕 v£> 汔 s1 n s 00 1 . 1 1 1 cs oo 异 r-l r-i o CS On jr; 00 ON i cs vn σΝ CN v〇 ΓΟ Γ〇 Γ〇 ΓΟ 〇 S (Ν \η S (Ν m 〇ι in r3 ο l/Ί cn g in (N ΓΛ r·^ »/") ON iTi ro 寸 S r^ cn s f〇 o s m 〇s CO Ό m 00 U-> o PO s Ό m ΓΛ cs ΓΟ SS m ΓΛ oc s m (N o v> fn f~H Ό ΓΛ 00 δ m cs CO v£> Pi o m 茎 s m m rn v〇 IT) uo σ\ IT) CN 〇 戚 Μ \\^ Si 00 卜 c> S c5 JTJ Ο I 窆 ο d 1 c5 0.84 I d d 〇> o Os d o^ o 0.82 CN 00 c5 (Ν 00 c5 〇〇 〇 s o 1 0.82 <〇 v〇 d 〇 s 〇 ir> m Ό Ο rO 〇 o OO o in oo o in r- o f—H OO o 茎 O p o 其他相; I 1 I 雜 (φΚ! 寒 j 5 1 1 i 翁 5 1 1 1 1 1 1 1 挪 额 1 1 1 卜 SB 1 1 1 I 1 1 1 1 1 1 1 c- 挪 ? έ <〇 m d o o Ο CS ο 1 卜 d 〇 1 〇 0.20 o 1.00 1 0.55 | 〇 o CN 0.25 1 in d Ο 〇 d 寸 τ—Η ο ro ΓΛ d 沄 o 〇 d ri ο 〇 沄 c5 o o c> o o o ^T) 宕 c5 s o 敏^ ie uo 卜 ο σ\ v〇 Ο r- o O VO CN 二 iT> m ro 寸 寸 <〇 寸 寸 m 寸 CN cs CN ^1 Ol W5 甘 甘 ··— ο o Ο o (N o VO o rn Ό Ο 寸 <Ν 寸 寸 m \r\ 寸 i〇 CN 卜 OO CN 二 1 m <〇 變微鐵1 m 00 yn v〇 〇〇 J 卜 ο CN 00 Ο o r-^ VO o. VO m \T) m VO <〇 in 寸 00 r^ IT) 必 O ν〇 m CN <η <N m r«H r-H Ol o r—' Mt <Ν 00 »〇 〇\ VD 00 On m CO OO 00 00 00 7Γ m 00 m 00 ro 00 oo m 00 S τ $ -) 00 ~a (N 00 _ oo 00 — m 00 -M m 00 卜 m 00 > ss 飞 U^i 00 1 l m s a 1 3 Ξ B 綦 -c f-H -— i 二 Γ〇 PQ 寸 ^O U 卜 oo Ov U o 叫 EJ rj W r〇 »-H 寸 □ Ό 卜 Ι-Η V. 00 r-' J ON CN CN <N r〇 CN CN CM r*H m P? m r〇 (釙無喵镣怼诞+釙您洄黎一^設踩鉍)/济弊喵辕赛田瘩:(d+g)/w 9Z; ssslool 201137130 備註 發明例 發明例 發明例 1發明例I 發明例 發明例 發明例 1發明例I 發明例 發明例 I發明例I ±i AE/TS 0.058 0.053 ! 0.055 0.059 0.055 0.053 0.057 0.061 0.056 0.058 0.055 直到5%的吸收 能量 AE(MJ/m3) Ο m <N m OS m ο m m m m /—S 's—✓ 〇〇 (N OO § 00 oo oo m oo g 00 so TSxEL (MPa · %) 20670 21248 19648 19734 21630 | \ 21744 | 19068 19740 1 19520 I 20064 | 20825 | wg (N cn <N m cn CO m 00 CN (N CO cn cn in CO h| 〇\ 00 寸 oo os oo S OO v〇 OO VO 〇 00 〇 微觀組織 Ί ^ 城:铡 绿1 0.80 1_ 0.74 0.78 0.80 0.75 0.72 0.78 0.82 0.80 0.78 0.77 其他相 1 1 1 I殘留γ I 1 1 1 I殘留γ 1 1 1 1 M/(B+P) 0.25 1 | 0.25 | | 0.13 I 1 0.29 1 | 0.44 | | 0.50 [0.40 I [0.40 1 Γ 〇.33| [0.30 o 珠粒鐵 P(°/〇) 寸 卜 CM <N ^T) VO 麻田散鐵 M(%) m (N CN <N 寸 寸 CN cn 變韌肥粒鐵 B(%) 〇〇 in Os 寸 ro 寸 m 寸 cn 肥粒鐵F(%) oo (N OO OO 00 00 ON OO 00 00 g 1 α Pi X/l H < CQ U 鋼板 m \〇 P: 00 Os m 〇 寸 rn (铢樂《黎為#+铢嬤《瓌4嬰蕊翱)/跻無《恝^田燧:(<1+9)/2 LZ ssslos s 201137130 本發明例,TS達590MPa以上,軋延性、拉伸凸緣性均 優異’且依應變速度2000/s直到應變量5%為止的吸收能量 與靜態TS的比(AE/TS)係達0.050以上,可獲得在高應變速 度下的小應變域加工,具有高耐衝擊特性的高強度合金化熔 融鍍鋅鋼板。相對於此,比較例因為上述AE/TS未滿0.050, 因而高應變速度下的小應變域加工之高耐衝擊特性差,或者 軋延性、拉伸凸緣性中至少任一特性較差。 (產業上之可利用性) 本發明的高強度熔融鍍鋅鋼板係加工性優異,並具有優異 ==性。本發明的高強度炫融鑛辞鋼板不僅;適用二 ==撞部位的鋼板’亦可適用為侧面碰撞鋼 极且亦可利用為彎曲加工等加 綱 板。 里較小部位所使用的鋼 100102078 28—sso- 201137130 [s] Remarks Inventive Example of Invention Invention Example of Invention Invention Example Invention Example Invention Example Invention Example Invention Example Invention Example $ f Alloying exp[200/(400-Tavs)]xln(th) 0.79 0.73 0.92 0.82 0.71 0.64 0.82 1 0.73 0.64 0.79 0.85 Retention time th(s) un (N 〇 (Ν average hold; 跋Tave〇C) 550 Ο VO κη 沄Ο 沄Ο 沄Ο m ο 〇m to Ο After cooling until the plating bath is immersed Pre-hold time (8) 〇ο ο ο ο § Ang Ο 1 After cooling until the average holding temperature before the key bath is dipped CC) 480 〇ο 沄ο Ο o inch ο Ο 〇s Ο 47.6x10'10/exp (- 27016/(T+273)) 258 m ro νο 00 00 1086 g Μ Ό Ό Ό 1—^ Ό ν〇 Hold time (8) 〇ο 沄〇ο g § 1 Annealing temperature 820 820 〇ο οο ο 00 ο 00 o ο 00 ο 〇Ο ΟΟ Ο οο Cold rolled with or without cups, cups, cups, cups, cups, cups, cups, hot rolling conditions, 1 I coiling temperature, CC) 丨 430 | 〇ο ο ο ο ο ο 00 m 〇00 C^i ο ο ο ο 〇 ο CN ο 1 : Finishing temperature CC) 910 | 〇5; ο Os 00 ο Ον 00 ο CM Os 〇\ g 00 g 00 in ο Γ Qs ο m Ον heating temperature CC) 1250 1250 1250 1250 Γ 1250 \ 1250 1 1 1250 1 1250 | 1250 1 1250 1 1250 \Ά1 〇ζΛ Η < 02 U steel plate ν〇00 mo 5 3 5 4 SAOSlool s 20 one inch 硌a no p—I»r· l?\ inch c> d empty r〇mc? d Ϊ ii S ir>c> oh Remark 1 i >fe i[ aJ si recorded λ3 if ? ±iaa £ i lost i blue ¥ Λ3 Λ3 λ3 彰 Jj £ lT> m 〇d lankan jD id .»» 〇c> —— CS 00 <〇in od ir><〇O dod <〇in 〇c5 〇〇d K oo si m S 〇 〇 j j j j j 63 Inch 3 C> dt 〇d < ΦΊ ^7 ω 倒 ο ν〇cn O 〇〇 (N [ΤΙ m cs -I - OO r〇oi— cn ΚΠ mo〇?; P; Ρ; 00 Ρ; _ (Ν Ρ; t: inch inch o (N m Os Ό 1/Ί r〇— oo mr〇v〇〇〇r〇m 1 ir> 00 vn ... mm rH OO ΓΛ OO 5 1 ir>v£> in m 1 inch^ rt Nw/ ΓΛ OS ψ· Η Γ〇 ν ? CN σ> «—H οο ο ο 宕ο 00 f—Η μ CN ΟΟ σ^ v〇宕oo d Oj r*H m CN oc 00 O Ό (N v〇s 卜 s S 00 f-1 00 jn <—· 〇<〇卜卜J s CN inch S 00 r~H CN ΟΟ 2 \ο ο 卜卜m s tN m oo 1-H md〇<〇1-HO CTN ί s ON _ ro 寸 CN δ ι—Η 异(Ν ΓΛ Ο Γ〇Ο | s (N r〇m 宕v£> 汔s1 ns 00 1 . 1 1 1 cs oo different rl ri o CS On jr; 00 ON i Cs vn σΝ CN v〇ΓΟ Γ〇Γ〇ΓΟ 〇S (Ν \η S (Ν m 〇ι in r3 ο l/Ί cn g in (N ΓΛ r·^ »/") ON iTi ro inch S r ^ cn sf〇osm 〇s CO Ό m 00 U-> o PO s Ό m ΓΛ cs ΓΟ SS m ΓΛ oc sm (N o v> fn f~H Ό ΓΛ 00 δ m cs CO v£> Pi om Stem smm rn v〇IT) uo σ\ IT) CN 〇戚Μ \\^ Si 00 卜 c> S c5 JTJ Ο I 窆ο d 1 c5 0.84 I dd 〇> o Os do^ o 0.82 CN 00 c5 ( 00 00 c5 〇〇〇so 1 0.82 <〇v〇d 〇s 〇ir> m Ό Ο rO 〇o OO o in oo o in r-of-H OO o Stem O po Other phases; I 1 I ΚΚ! 寒j 5 1 1 i 翁5 1 1 1 1 1 1 1 Move 1 1 1 Bu SB 1 1 1 I 1 1 1 1 1 1 1 c- Move? έ <〇mdoo Ο CS ο 1 卜d 〇1 〇0.20 o 1.00 1 0.55 | 〇o CN 0.25 1 in d Ο 〇d inch τ—Η ο ro ΓΛ d 沄o 〇d ri ο 〇沄c5 oo c> ooo ^T) 宕c5 so 敏^ ie uo οο σ\ v〇Ο r- o O VO CN II iT> ; m ro inch inch < inch inch inch m inch CN cs CN ^1 Ol W5 Gangan··— ο o Ο o (N o VO o rn Ό Ο inch <Ν inch inch m \r\ inch i〇CN 卜 OO CN 11 m <〇变微铁1 m 00 yn v〇〇〇J 卜ο CN 00 Ο o r-^ VO o. VO m \T) m VO <〇in inch 00 r^ IT) must O ν 〇m CN <η <N mr«H rH Ol or—' Mt <Ν 00 »〇〇\ VD 00 On m CO OO 00 00 00 7Γ m 00 m 00 ro 00 oo m 00 S τ $ -) 00 ~a (N 00 _ oo 00 — m 00 -M m 00 卜 m 00 > ss fly U^i 00 1 lmsa 1 3 Ξ B 綦-c fH -— i two Γ〇 PQ inch ^ OU oo Ov U o is called EJ rj W r〇»-H inch □ Ι Ι Ι-Η V. 00 r-' J ON CN CN <N r〇CN CN CM r*H m P? mr〇(钋无喵镣怼Birthday + 钋 洄 洄 洄^ 铋 铋 / / / / 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 喵辕 37 37 37 37 37 37 37 37 37 37 37 37 37 Example I Inventive Example I ±i AE/TS 0.058 0.053 ! 0.055 0.059 0.055 0.053 0.057 0.061 0.056 0.058 0.055 up to 5% absorption energy AE(MJ/m3) Ο m <N m OS m ο mmmm /−S 's— ✓ 〇〇 (N OO § 00 oo oo m oo g 00 so TSxEL (MPa · %) 20670 21248 19648 19734 21630 | \ 21744 | 19068 19740 1 19520 I 20064 | 20825 | wg (N cn <N m cn CO m 00 CN (N CO cn cn in CO h| 〇 00 00 oo os oo S OO v〇OO VO 〇 00 〇 Microstructure Ί ^ City: 铡 Green 1 0.80 1_ 0.74 0.78 0.80 0.75 0.72 0.78 0.82 0.80 0.78 0.77 Other phases 1 1 1 I residual γ I 1 1 1 I residual γ 1 1 1 1 M/(B+P) 0.25 1 | 0.25 | | 0.13 I 1 0.29 1 | 0.44 | | 0.50 [0.40 I [0.40 1 Γ 〇.33 [0.30 o Bead iron P(°/〇) Inch CM <N ^T) VO Ma Tian loose iron M (%) m (N CN <N inch inch CN cn Toughened ferrite iron B (%) 〇 〇in Os inch ro inch m inch cn fertilizer Iron F (%) oo (N OO OO 00 00 ON OO 00 00 g 1 α Pi X/l H < CQ U steel plate m \〇P: 00 Os m 〇 inch rn (铢乐《黎为#+铢嬷"瓌4 翱 翱 翱 跻 跻 翱 跻 ( ( ( ( ( ( ( ( ( ( ( ( 2011 2011 2011 2011 2011 2011 2011 2011 2011 2011 2011 2011 37 2011 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 37 According to the strain rate of 2000/s until the strain 5%, the ratio of absorbed energy to static TS (AE/TS) is 0.050 or more, and small strain range processing at high strain speed can be obtained, which has high impact resistance. Strength alloyed hot-dip galvanized steel sheet. On the other hand, in the comparative example, since the AE/TS is less than 0.050, the high strain resistance of the small strain range processing at a high strain rate is inferior, and at least one of the rolling property and the stretch flangeability is inferior. (Industrial Applicability) The high-strength hot-dip galvanized steel sheet according to the present invention is excellent in workability and excellent in ==. The high-strength smelting ore plate of the present invention is not only applicable to the steel plate of the second == collision portion but also to the side impact steel electrode and can also be used as an additional plate for bending. Steel used in smaller parts 100102078 28
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JP4998756B2 (en) * | 2009-02-25 | 2012-08-15 | Jfeスチール株式会社 | High-strength hot-dip galvanized steel sheet excellent in workability and manufacturing method thereof |
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2010
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2011
- 2011-01-18 WO PCT/JP2011/051150 patent/WO2011090179A1/en active Application Filing
- 2011-01-18 KR KR1020127019654A patent/KR101464844B1/en active IP Right Grant
- 2011-01-18 CN CN201180006862.XA patent/CN102712977B/en active Active
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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TWI612151B (en) * | 2011-11-17 | 2018-01-21 | 杰富意鋼鐵股份有限公司 | Hot strip for high strength galvanized steel sheet and high strength galvannealed steel sheet, and method for manufacturing thereof |
US10253387B2 (en) | 2013-12-27 | 2019-04-09 | Nippon Steel & Sumitomo Metal Corporation | Hot-pressed steel sheet member, method of manufacturing the same, and steel sheet for hot pressing |
US10711322B2 (en) | 2013-12-27 | 2020-07-14 | Nippon Steel Corporation | Hot-pressed steel sheet member, method of manufacturing the same, and steel sheet for hot pressing |
TWI513829B (en) * | 2014-01-03 | 2015-12-21 | Nippon Steel & Sumitomo Metal Corp | A hot-pressed steel sheet member, a method for manufacturing the same, and a steel sheet for hot pressing |
Also Published As
Publication number | Publication date |
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CN102712977A (en) | 2012-10-03 |
WO2011090179A1 (en) | 2011-07-28 |
TWI429759B (en) | 2014-03-11 |
JP2011168876A (en) | 2011-09-01 |
CN102712977B (en) | 2014-11-26 |
JP5786316B2 (en) | 2015-09-30 |
KR101464844B1 (en) | 2014-11-25 |
KR20120099505A (en) | 2012-09-10 |
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