US20100193081A1 - Process for manufacturing a galvannealed steel sheet by dff regulation - Google Patents

Process for manufacturing a galvannealed steel sheet by dff regulation Download PDF

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Publication number
US20100193081A1
US20100193081A1 US12/666,702 US66670208A US2010193081A1 US 20100193081 A1 US20100193081 A1 US 20100193081A1 US 66670208 A US66670208 A US 66670208A US 2010193081 A1 US2010193081 A1 US 2010193081A1
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Prior art keywords
steel sheet
oxide
temperature
process according
zinc
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Abandoned
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US12/666,702
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English (en)
Inventor
Jean-Michel Mataigne
Florence Bertrand
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ArcelorMittal France SA
Nippon Steel Corp
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ArcelorMittal France SA
Nippon Steel Corp
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Application filed by ArcelorMittal France SA, Nippon Steel Corp filed Critical ArcelorMittal France SA
Assigned to NIPPON STEEL CORPORATION, ARCELORMITTAL FRANCE reassignment NIPPON STEEL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BERTRAND, FLORENCE, Mataigne, Jean-Michel
Publication of US20100193081A1 publication Critical patent/US20100193081A1/en
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Assigned to NIPPON STEEL CORPORATION reassignment NIPPON STEEL CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: NIPPON STEEL & SUMITOMO METAL CORPORATION
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/34Methods of heating
    • C21D1/52Methods of heating with flames
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/52Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
    • C21D9/54Furnaces for treating strips or wire
    • C21D9/56Continuous furnaces for strip or wire
    • C21D9/561Continuous furnaces for strip or wire with a controlled atmosphere or vacuum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/11Making amorphous alloys
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/022Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
    • C23C2/0222Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating in a reactive atmosphere, e.g. oxidising or reducing atmosphere
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/022Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
    • C23C2/0224Two or more thermal pretreatments
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • C23C2/261After-treatment in a gas atmosphere, e.g. inert or reducing atmosphere
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • C23C2/28Thermal after-treatment, e.g. treatment in oil bath
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
    • C23C2/36Elongated material
    • C23C2/40Plates; Strips

Definitions

  • the present invention relates to a process for manufacturing a hot-dip galvannealed steel sheet having a TRIP microstructure.
  • galvanized steel sheets are often submitted to an annealing which promotes the alloying of the zinc coating with the iron of the steel (so-called galvannealing).
  • This kind of coating made of a zinc-iron alloy offers a better weldability than a zinc coating.
  • TRIP steel sheets are obtained by adding a large amount of silicon to steel. Silicon stabilizes the ferrite and the austenite at room temperature, and prevents residual austenite from decomposing to form carbide.
  • TRIP steel sheets containing more than 0.2% by weight of silicon are galvanized with difficulty, because silicon oxides are formed on the surface of the steel sheet during the annealing taking place just before the coating. These silicon oxides show a poor wettability toward the molten zinc, and deteriorate the plating performance of the steel sheet.
  • TRIP steel having low silicon content (less than 0.2% by weight).
  • this has a major drawback: a high level of tensile strength, that is to say about 800 MPa, can be achieved only if the content of carbon is increased. But, this has the effect to lower the mechanical resistance of the welded points.
  • the TRIP effect is observed when the TRIP steel sheet is being deformed, as the residual austenite is transformed into martensite under the effect of the deformation, and the strength of the TRIP steel sheet increases.
  • the purpose of the present invention is therefore to remedy the aforementioned drawbacks and to propose a process for hot-dip galvannealing a steel sheet having a high silicon content (more than 0.5% by weight) and a TRIP microstructure showing high mechanical characteristics, that guarantees a good wettability of the surface steel sheet and no non-coated portions, and thus guarantees a good adhesion and a nice surface appearance of the zinc alloy coating on the steel sheet, and that preserves the TRIP effect.
  • the first subject of the invention is a process for manufacturing a hot-dip galvannealed steel sheet having a TRIP microstructure comprising ferrite, residual austenite and optionally martensite and/or bainite, said process comprising the steps consisting in:
  • the balance of the composition consists of iron and other elements that are usually expected to be found and impurities resulting from the smelting of the steel, in proportions that have no influence on the desired properties.
  • the steel sheet having the above composition is first subjected to an oxidation followed by a reduction, before being hot-dip galvanized in a bath of molten zinc and heat-treated to form said galvannealed steel sheet.
  • the aim is to form an oxidized steel sheet having an outer layer of iron oxide with a controlled thickness which will protect the steel from the selective outer oxidation of silicon, manganese and aluminum, while the steel sheet is annealed before the hot-dip galvanization.
  • Said oxidation of the steel sheet is performed under conditions that allow the formation, on the surface of the steel sheet, of a layer of iron oxide containing no superficial oxides selected from the group consisting of silicon oxide, manganese oxide, aluminum oxide, complex oxide comprising silicon and/or manganese and/or aluminum.
  • a layer of iron oxide containing no superficial oxides selected from the group consisting of silicon oxide, manganese oxide, aluminum oxide, complex oxide comprising silicon and/or manganese and/or aluminum.
  • a layer of an internal oxide of at least one type of oxide selected from the group consisting of silicon oxide, manganese oxide, aluminum oxide, complex oxide comprising Si and Mn, complex oxide comprising Si and Al, complex oxide comprising Mn and Al and complex oxide comprising Si, Mn and Al is thus formed.
  • the oxidation is preferably performed by heating said steel sheet from ambient temperature to a heating temperature T1 which is between 680 and 800° C., in a direct flame furnace where the atmosphere comprises air and fuel, with a ratio air-to-fuel preferably between 1 and 1.2.
  • the iron oxide layer formed on the surface of the steel sheet will contain manganese coming from the steel, and the wettability will be impaired. If the temperature T1 is below 680° C., the internal oxidation of silicon, manganese and aluminum will not be favoured, and the galvanizability of the steel sheet will be insufficient.
  • An atmosphere having a ratio air-to-fuel less than 1 leads to the formation of superficial oxidation of silicon, manganese and aluminum, and thus a superficial layer of oxides selected from the group consisting of silicon oxide, manganese oxide, aluminum oxide, and complex oxide comprising silicon and/or manganese and/or aluminum, possibly in combination with iron oxide is formed, and the wettability is impaired.
  • a ratio air-to-fuel above 1.2 the layer of iron oxide is too thick, and will not be completely reduced. Thus, the wettability will also be impaired.
  • the oxidized steel sheet When leaving the direct flame furnace, the oxidized steel sheet is reduced in conditions permitting the achievement of the complete reduction of the iron oxide into iron.
  • This reduction step can be performed in a radiant tube furnace or in a resistance furnace.
  • Said oxidized steel sheet is thus heat treated in an atmosphere comprising preferably more than 15% by volume of hydrogen, the balance being nitrogen and unavoidable impurities. Indeed, if the content of hydrogen in the atmosphere is less than 15% by volume, the layer of iron oxide can be insufficiently reduced and the wettability is impaired.
  • Said oxidized steel sheet is heated from the heating temperature T1 to a soaking temperature T2, then it is soaked at said soaking temperature T2 for a soaking time t2, and is finally cooled from said soaking temperature T2 to a cooling temperature T3.
  • Said soaking temperature T2 is preferably between 770 and 850° C.
  • T2 When the steel sheet is at the temperature T2, a dual phase microstructure composed of ferrite and austenite is formed.
  • T2 When T2 is above 850° C., the volume ratio of austenite grows too much, and external selective oxidation occurs on the steel surface. But when T2 is below 770° C., the time required to form a sufficient volume ratio of austenite is too high.
  • sufficient austenite must be formed during the soaking step, so that sufficient residual austenite is s maintained during the cooling step.
  • the soaking is performed for a time t2, which is preferably between 20 and 180 s. If the time t2 is longer than 180 s, the austenite grains coarsen and the yield strength R e of the steel after forming will be limited. Furthermore, the hardenability of the steel is low. However, if the steel sheet is soaked for a time t2 less than 20 s, the proportion of austenite formed will be insufficient and sufficient residual austenite and bainite will not form when cooling.
  • the reduced steel sheet is finally cooled at a cooling temperature T3 near the temperature of the bath of molten zinc, in order to avoid the cooling or the re-heating of said bath.
  • T3 is thus preferably between 460 and 510° C. Therefore, a zinc-based coating having a homogenous microstructure can be obtained.
  • the steel sheet When the steel sheet is cooled, it is hot dipped in the bath of molten zinc whose temperature is preferably between 450 and 500° C.
  • This bath can contain 0.08 to 0.135% by weight of dissolved aluminium, the balance being zinc and unavoidable impurities.
  • Aluminum is added in the bath in order to deoxidize the molten zinc, and to make it easier to control the thickness of the zinc-based coating. In that condition, precipitation of delta phase (FeZn 7 ) is induced at the interface of the steel and of the zinc-based coating.
  • the steel sheet When leaving the bath, the steel sheet is wiped by projection of a gas, in order to adjust the thickness of the zinc-based coating. This thickness, which is generally between 3 and 10 ⁇ m, is determined according to the required resistance to corrosion.
  • the hot-dip galvanized steel sheet is finally heat-treated so that a coating made of a zinc-iron alloy is obtained, by diffusion of the iron from steel to the zinc of the coating.
  • This alloying treatment can be performed by maintaining said steel sheet at a temperature T4 between 460 and 510° C. for a soaking time t4 between 10 and 30 s. Thanks to the absence of external selective oxidation of silicon, manganese and aluminum, this temperature T4 is lower than the conventional alloying temperatures. For that reason, large quantities of molybdenum to the steel are not required, and the content of molybdenum in the steel can be limited to less than 0.01% by weight. If the temperature T4 is below 460° C., the alloying of iron and zinc is not possible.
  • the time t4 is adjusted so that the average iron content in the alloy is between 8 and 12% by weight, which is a good compromise for improving the weldability of the coating and limiting the powdering while shaping.
  • Samples A and B are pre-heated from ambient temperature (20° C.) to 750° C., in a direct flame furnace. They are subsequently and continuously annealed in a radiant tube furnace, where they are heated from 750° to 800° C., then they are soaked at 800° C. for 60 s, and finally they are cooled to 460° C.
  • the atmosphere in the radiant tube furnace comprises 30% by volume of hydrogen, the balance being nitrogen and unavoidable impurities.
  • samples A and B are hot dip galvanized in a molten zinc-based bath comprising 0.12% by weight of aluminium, the balance being zinc and unavoidable impurities.
  • the temperature of said bath is 460° C.
  • the thickness of the zinc-based coating is 7 ⁇ m.
  • the aim is to compare the wettability and the adherence of these samples, when the air-to-fuel ratio in the direct flame furnace fluctuates.
  • the air-to-fuel ratio is 0.90 for sample A, and 1.05 according to the invention for sample B.
  • the results are shown in table II.
  • the wettability is visually controlled by an operator.
  • the adherence of the coating is also visually controlled after a 180° bending test of samples.
  • FIG. 1 is a photography of sample A after the pre-heating step and before the annealing step
  • FIG. 2 is a photography of sample B after the pre-heating step and before the annealing step.
  • the aim is to show the effect of the internal selective oxidation of silicon and manganese on the temperature of alloying.
  • the temperature of alloying treatment applied to sample B in order to obtain a galvannealed steel sheet according to the invention is compared with the temperature of alloying of sample A.
  • Sample B which has been hot dip galvanized is then subjected to an alloying treatment by heating it to 480° C., and by maintaining it at this temperature for 19 s.
  • the inventors have checked that the TRIP microstructure of the obtained hot dip galvannealed steel sheet according to the invention was not lost by this alloying treatment.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Coating With Molten Metal (AREA)
  • Heat Treatment Of Sheet Steel (AREA)
US12/666,702 2007-06-29 2008-06-06 Process for manufacturing a galvannealed steel sheet by dff regulation Abandoned US20100193081A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP07290816.3 2007-06-29
EP07290816A EP2009129A1 (en) 2007-06-29 2007-06-29 Process for manufacturing a galvannealed steel sheet by DFF regulation
PCT/IB2008/001462 WO2009004425A1 (en) 2007-06-29 2008-06-06 Process for manufacturing a galvannealed steel sheet by dff regulation

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US20100193081A1 true US20100193081A1 (en) 2010-08-05

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US (1) US20100193081A1 (pt)
EP (2) EP2009129A1 (pt)
JP (2) JP5713673B2 (pt)
KR (1) KR101273308B1 (pt)
CN (1) CN101809182B (pt)
AR (1) AR067339A1 (pt)
AT (1) ATE521726T1 (pt)
BR (1) BRPI0813687B1 (pt)
CA (1) CA2701091C (pt)
ES (1) ES2371985T3 (pt)
PL (1) PL2171116T3 (pt)
RU (1) RU2451107C2 (pt)
WO (1) WO2009004425A1 (pt)

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US9068255B2 (en) 2009-12-29 2015-06-30 Posco Zinc-plated steel sheet for hot pressing having outstanding surface characteristics, hot-pressed moulded parts obtained using the same, and a production method for the same
US9909194B2 (en) 2012-09-06 2018-03-06 ArcelorMittal Investigación y Desarrollo, S.L. Process for manufacturing press-hardened coated steel parts and precoated sheets allowing these parts to be manufactured
US10570472B2 (en) 2013-12-10 2020-02-25 Arcelormittal Method of annealing steel sheets
CN111315911A (zh) * 2017-11-08 2020-06-19 安赛乐米塔尔公司 一种镀锌退火钢板
US11319610B2 (en) 2015-07-09 2022-05-03 Arcelormittal Steel for press hardening and press hardened part manufactured from such steel
US11649522B2 (en) 2017-06-20 2023-05-16 Arcelormittal Zinc-coated steel sheet with high resistance spot weldability

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TWI504757B (zh) * 2011-09-30 2015-10-21 Nippon Steel & Sumitomo Metal Corp High strength molten galvanized steel sheet and its manufacturing method
KR20130076589A (ko) * 2011-12-28 2013-07-08 주식회사 포스코 도금표면 품질 및 도금밀착성이 우수한 고강도 용융아연도금강판 및 그 제조방법
WO2013157146A1 (ja) * 2012-04-17 2013-10-24 Jfeスチール株式会社 めっき密着性および摺動特性に優れた合金化溶融亜鉛めっき鋼板の製造方法
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JP5920249B2 (ja) * 2013-03-05 2016-05-18 Jfeスチール株式会社 めっき密着性に優れた高強度溶融亜鉛めっき鋼板およびその製造方法
WO2014135753A1 (fr) 2013-03-06 2014-09-12 Arcelormittal Investigacion Y Desarrollo, S.L. Procédé de réalisation d'une tôle à revêtement znal avec un essorage optimisé, tôle, pièce et véhicule correspondants
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JP5799996B2 (ja) 2013-09-12 2015-10-28 Jfeスチール株式会社 外観性とめっき密着性に優れる溶融亜鉛めっき鋼板および合金化溶融亜鉛めっき鋼板ならびにそれらの製造方法
CN110088322B (zh) * 2017-01-25 2021-06-15 日本制铁株式会社 钢板
CN108165892A (zh) * 2017-11-23 2018-06-15 南阳汉冶特钢有限公司 一种低温压力容器用35-50mm厚Q420R高强钢及其生产方法
CN113969336B (zh) 2020-07-23 2023-03-28 宝山钢铁股份有限公司 一种热镀锌钢板的制造方法、钢板及车用构件

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US3925579A (en) * 1974-05-24 1975-12-09 Armco Steel Corp Method of coating low alloy steels
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US9945020B2 (en) 2009-12-29 2018-04-17 Posco Zinc-plated steel sheet for hot pressing having outstanding surface characteristics, hot-pressed moulded parts obtained using the same, and a production method for the same
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