WO2014068889A1 - 溶融亜鉛めっき鋼板 - Google Patents
溶融亜鉛めっき鋼板 Download PDFInfo
- Publication number
- WO2014068889A1 WO2014068889A1 PCT/JP2013/006202 JP2013006202W WO2014068889A1 WO 2014068889 A1 WO2014068889 A1 WO 2014068889A1 JP 2013006202 W JP2013006202 W JP 2013006202W WO 2014068889 A1 WO2014068889 A1 WO 2014068889A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dip galvanized
- less
- steel sheet
- hot
- hot dip
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C18/00—Alloys based on zinc
- C22C18/04—Alloys based on zinc with aluminium as the next major constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/01—Layered products comprising a layer of metal all layers being exclusively metallic
- B32B15/013—Layered products comprising a layer of metal all layers being exclusively metallic one layer being formed of an iron alloy or steel, another layer being formed of a metal other than iron or aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C18/00—Alloys based on zinc
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
-
- 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
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
-
- 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
- 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
- C23C2/34—Hot-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
- C23C2/36—Elongated material
- C23C2/40—Plates; Strips
Definitions
- the present invention relates to a hot dip galvanized steel sheet that can be suitably used for an outer plate and an inner plate of an automobile.
- Patent Document 1 discloses a method for producing a hot-dip galvanized steel sheet having excellent slidability at the time of press work, which regulates the amount of Al in the plating layer and the amount of Al at the plating / steel sheet interface.
- Patent Document 1 does not sufficiently consider the durability of the product such as plating adhesion of a processed portion after press working and corrosion resistance after press working. Therefore, it cannot be said that these problems are completely absent.
- the hot dip galvanized steel sheet is used in the fields of automobiles, home appliances, building materials, etc., it is also required to have an excellent appearance after painting.
- the present invention has been made in view of such circumstances, and provides a hot-dip galvanized steel sheet having excellent plating adhesion after press working, excellent post-paint corrosion resistance after press working, and excellent post-paint appearance. For the purpose.
- the hot dip galvanizing process that controls the structure of the hot dip galvanized layer and forms intermetallic compounds between the steel sheet and the hot dip galvanized layer with predetermined properties, rather than simply performing the hot dip galvanized process as in the prior art.
- a hot dip galvanizing process for controlling the solidified structure and surface texture of the hot dip galvanized layer is performed.
- the hot-dip galvanized steel sheet of the present invention is, in mass%, C: 0.001% to 0.005%, Si: 0.10% or less, Mn: 0.70% to 1.50%, P: 0 0.05% or more and 0.100% or less, S: 0.01% or less, N: 0.005% or less, Al: 0.10% or less, B: 0.0015% or less, and Ti: 0 .01% or more and 0.05% or less and Nb: 0.01% or more and 0.05% or less, at least one selected from the group consisting of Fe and inevitable impurities, and substantially ferrite
- the surface roughness Ra of the surface of the hot dip galvanized layer is 0.8 ⁇ m or more and 1.6 ⁇ m or less, and the glossiness (G value) of the surface of the hot dip galvanized layer is 550.
- Zinc basal plane orientation ratio (Zn) which is the ratio of the crystal orientation of the (002) plane of Zn crystal to the crystal orientation of the (004) plane of Zn crystal on the surface of the hot dip galvanized layer. (002) / (004)) is preferably 60 or more and 90 or less.
- the hot dip galvanized steel sheet of the present invention has excellent plating adhesion after press working, excellent post-paint corrosion resistance after press working, and excellent post-paint appearance.
- the hot dip galvanized steel sheet of the present invention has a steel sheet, a hot dip galvanized layer formed on at least a part of the surface of the steel sheet, and a metal compound existing between the steel sheet and the hot dip galvanized layer.
- the steel plate used in the present invention is in mass%, C: 0.001% to 0.005%, Si: 0.10% or less, Mn: 0.70% to 1.50%, P: 0.050. %: 0.100% or less, S: 0.010% or less, N: 0.005% or less, Al: 0.10% or less, B: 0.0015% or less, and Ti: 0.01 % Or more and 0.05% or less and Nb: 0.01% or more and 0.05% or less, and the balance consists of Fe and inevitable impurities.
- the component composition will be described.
- “%” in the component composition means “% by mass” unless otherwise specified.
- C 0.001% or more and 0.005% or less
- the upper limit of the C content is specified to be 0.005%.
- the content of C is less than 0.001%, the crystal grains become coarse, and the surface of the steel sheet is likely to be rough when formed.
- the lower limit of the C content is specified to be 0.001%.
- Si 0.10% or less
- surface defects due to scale are likely to occur.
- content of Si becomes excess, formation of the intermetallic compound mentioned later may be inhibited.
- the Si content is excessive, the generation of Si nuclei is suppressed, and each crystal in the steel sheet structure becomes coarse, resulting in a problem that the plating adhesion after press working deteriorates.
- a preferable Si content is 0.02% or less.
- Mn 0.70% or more and 1.50% or less If the Mn content is less than 0.70%, a steel sheet having sufficient strength cannot be obtained. By containing a large amount of Mn in the steel sheet, the steel sheet can be strengthened, but when Mn is contained excessively, the deep drawability is lowered. Moreover, when Mn is contained excessively, formation of the intermetallic compound mentioned later is inhibited. Moreover, when Mn is contained excessively, the nucleation of Si is suppressed, and each crystal in the steel sheet structure becomes coarse, and the plating adhesion after press working deteriorates. For this reason, the upper limit of the Mn content is 1.50%. A preferable Mn content is 0.75% or more and 1.2% or less.
- S 0.010% or less
- the toughness of the welded portion deteriorates as in the case where the content of P is large.
- the upper limit of the S content is 0.010%.
- a preferable S content is 0.007% or less.
- N 0.005% or less
- Al 0.10% or less
- Al (sol. Al) and N do not impair the effects of the present invention as long as they are contained in a normal steel sheet.
- N combines with Ti to form TiN, or N combines with Al to form AlN. Therefore, the Al content is specified to be 0.10% or less, and the N content is specified to be 0.005% or less. If the Al content exceeds 0.10%, formation of an intermetallic compound described later is inhibited. On the other hand, if the Al content exceeds 0.10%, the generation of Si nuclei is suppressed, and each crystal in the steel sheet structure is coarsened, and the plating adhesion during processing deteriorates.
- the N content exceeds 0.005%, the nitride is dispersed in the ferrite grains, and the work hardening rate is lowered.
- the preferable Al content is 0.04% or less, and the preferable N content is 0.002 or less.
- B 0.0015% or less
- B is an element that contributes to strengthening of grain boundaries cleaned by forming carbides.
- the lower limit of the B content is preferably 0.0003%.
- the upper limit of the B content is 0.0015%.
- preferable content of B is 0.0003% or more and 0.0010% or less.
- Ti and Nb form carbides (TiC, NbC) in the ferrite grains.
- the work hardening rate of a steel plate is improved.
- the content of Ti or Nb is less than 0.01%, the amount of carbide of Ti or the amount of carbide of Nb is small, the dislocation motion cannot be controlled, and a sufficient work hardening rate cannot be expected.
- the Nb or Ti content exceeds 0.05%, coarse carbides are precipitated and the work hardening rate is lowered.
- the Nb or Ti content exceeds 0.05%, the grain boundaries in the steel sheet structure are cleaned, and the intermetallic compound grows excessively during the hot dip galvanizing process, resulting in poor plating adhesion.
- at least one of the Ti content and the Nb content is 0.01% or more and 0.05% or less.
- a preferable Ti content is 0.015% or more and 0.04% or less, and a preferable Nb content is 0.01% or more and 0.03% or less.
- both Ti and Nb are included, if one content is outside the above range, it is outside the scope of the present invention.
- Fe and unavoidable impurities The balance other than the above components is Fe and unavoidable impurities.
- the unavoidable impurity is, for example, O (oxygen).
- O is a typical inevitable impurity inevitably mixed.
- the content of inevitable impurities is not particularly limited, and the allowable content of inevitable impurities depends on the type of inevitable impurities. In the case of O, there is no problem if the content is 0.005% or less.
- the steel sheet structure is substantially a ferrite single phase. Since the steel sheet structure is substantially composed of a ferrite single phase, the hot dip galvanized steel sheet is excellent in workability.
- the ferrite single phase substantially includes not only the case where the entire steel sheet structure is the ferrite phase but also the case where 95% or more of the steel sheet structure is the ferrite phase. However, it is normally considered that no phase other than ferrite is generated. Note that the fact that it is substantially a ferrite single phase is confirmed by observing a cross section of the etched sample with an optical microscope.
- the hot dip galvanized layer is a hot dip galvanized layer formed by a normal hot dip galvanizing process.
- the hot-dip galvanized layer contains Al in an amount of 0.3% to 0.6% by mass.
- the hot dip galvanized layer may contain components other than Zn and Al as long as the effects of the present invention are not impaired. Examples of components other than Zn and Al include Fe, Al, Mg, and Cr.
- the Al content is less than 0.3%, it is necessary to reduce the Al concentration in the plating bath.
- the Al concentration is lowered, Fe is eluted, so that dross is deposited and appearance is deteriorated, or hard dross is dispersed in the hot dip galvanized layer.
- the workability of the hot dip galvanized steel sheet deteriorates. If the Al content exceeds 0.6%, a large amount of an oxide film of Al is formed on the surface of the hot dip galvanized layer, and the spot weldability of the hot dip galvanized steel sheet deteriorates.
- the hot-dip galvanized layer preferably has a surface roughness Ra of 0.8 to 1.6 ⁇ m. If the surface roughness Ra is less than 0.8, the oil may not be retained on the surface of the hot dip galvanized layer during pressing of the hot dip galvanized steel sheet, and workability may be poor. If the surface roughness Ra exceeds 1.6 ⁇ m, the sharpness after coating may be inferior and an excellent appearance may not be imparted to the hot-dip galvanized steel sheet after coating.
- the said surface roughness Ra means surface roughness Ra measured by the method as described in an Example.
- the glossiness (G value) of the surface of the hot dip galvanized layer is preferably 550 or more and 750 or less. If the glossiness (G value) is less than 550, the sharpness after coating may be inferior, and an excellent appearance may not be imparted to the hot-dip galvanized steel sheet after coating. If the glossiness (G value) is 750 or more, it may be too smooth, and oil may not be retained on the surface of the hot dip galvanized layer when the hot dip galvanized steel sheet is pressed, resulting in poor formability.
- the said glossiness (G value) means the glossiness (G value) measured by the method as described in an Example.
- Zinc basal plane orientation ratio (Zn (002) / (004)), which is the ratio of the crystal orientation of the (002) plane of Zn crystal to the crystal orientation of the (004) plane of Zn crystal on the surface of the hot dip galvanized layer. ) Is preferably 60 or more and 90 or less. If the orientation ratio of the bottom surface of the zinc base is less than 60, the orientation of the zinc crystals is relatively random, and the crystal size when the zinc solidifies immediately after plating becomes fine. May be inferior in moldability without being held on the surface. If the orientation ratio of the basal plane of the zinc base is more than 90, the orientation of the basal plane of the Zn crystal is too high and the crystal grains are likely to grow. As a result, the dendritic arm develops. The appearance of the steel sheet may deteriorate. Moreover, if the zinc base bottom surface orientation ratio exceeds 90, the corrosion resistance may be deteriorated.
- the zinc base bottom surface orientation ratio can be defined by the following formula.
- the zinc base bottom orientation ratio (Zn (002) / (004)) represents ⁇ (002) plane Zn crystal orientation ⁇ / ⁇ (004) plane Zn crystal orientation ⁇ .
- (I (xyz) is the Zn intensity measured by X-ray on the (xyz) plane of the sample
- I std (xyz) is the Zn intensity measured by X-ray on the (xyz) plane of the standard sample (pure Zn powder).
- the degree of orientation of the solidified structure affects the gloss, crystal size, and surface roughness (surface roughness). For this reason, it is important to control the press workability in addition to controlling the surface orientation of the hot-dip galvanized steel sheet in order to accurately control the zinc base orientation ratio.
- the zinc base bottom surface orientation ratio is in the above range, the gloss and the surface roughness Ra satisfy the above preferable range.
- the hot dip galvanized layer may be formed on at least a part of the steel plate surface. Since the hot dip galvanized layer is formed on the surface of the steel plate by a method of immersing the steel plate in a plating bath, the hot dip galvanized layer is usually formed on the entire surface of the steel plate.
- the thickness of the hot dip galvanized layer is not particularly limited.
- the thickness of the hot dip galvanized layer can be adjusted by controlling the amount of plating applied during the hot dip galvanizing process.
- Intermetallic compound is composed of an intermetallic compound consisting of at least one of an average particle diameter of 1 ⁇ m or less of Fe 2 Al 5 or FeAl 3, present in the steel sheet and hot-dip galvanizing layer. Further, the intermetallic compound contains 0.12 gm ⁇ 2 or more and 0.22 gm ⁇ 2 or less of Al. The presence of the intermetallic compound can suppress the formation of the FeZn alloy phase and ensure good plating adhesion. This effect cannot be obtained in cases other than an intermetallic compound composed of at least one of Fe 2 Al 5 or FeAl 3 . Other than these, a hard and brittle FeZn intermetallic compound may be formed, and in this case, the plating adhesion deteriorates. The presence of the intermetallic compound can be confirmed by a method of analyzing and detecting the vicinity of the interface with the steel plate in the cross section of the hot dip galvanized layer by electron beam diffraction in a transmission electron microscope.
- the average particle diameter of Fe 2 Al 5 or FeAl 3 exceeds 1 ⁇ m, the hard intermetallic compound is excessively grown, and the impact resistance characteristics of the hot dip galvanized steel sheet deteriorate. For this reason, the upper limit of the average particle diameter is 1 ⁇ m.
- the Al content in the intermetallic compound is less than 0.12 gm ⁇ 2, it is necessary to set the Al concentration in the molten zinc bath of the plating low. If the Al concentration is set low, dross precipitates and the molten zinc The appearance and workability of the plated steel sheet deteriorate. If the Al content in the intermetallic compound exceeds 0.22 gm -2 , the Al concentration in the plating bath needs to be set high. If the Al concentration is set high, an Al oxide film is formed on the surface of the hot dip galvanized layer. A large amount is formed and spot weldability deteriorates.
- the hot dip galvanized steel sheet of the present invention is excellent in plating adhesion after press working and excellent in corrosion resistance after painting of a processed part after press working. And the hot-dip galvanized steel sheet of the present invention has an excellent appearance after coating. For this reason, the hot dip galvanized steel sheet of the present invention can be applied to products having very severe processing parts such as a back door and a hood.
- the hot dip galvanized steel sheet of the present invention has a yield stress (YS) of 220 MPa or more and 320 MPa or less. If the yield stress is in the above range, the hot-dip galvanized steel sheet can be preferably applied to applications that require severe processing such as outer plates and that must ensure shape freezeability.
- a hot-dip galvanized steel sheet can be manufactured by the following method. First, steel having the above component composition is made into a slab by continuous casting, the slab is heated, and scale removal and rough rolling are performed. Next, after cooling, finish rolling, cooling, winding, pickling, and cold rolling are performed. Next, the steel sheet is annealed and hot-dip galvanized in a continuous hot-dip galvanizing facility. Next, an alloying treatment is performed as necessary.
- the heating time, heating temperature, rough rolling conditions, cooling conditions, finish rolling conditions, winding conditions, etc. when heating the slab can be appropriately set based on common technical knowledge.
- the annealing conditions of the steel sheet affect the yield stress of the hot dip galvanized steel sheet.
- the heating temperature during annealing in order to set the yield stress in the above range, it is preferable to set the heating temperature during annealing to 780 ° C. or more and 820 ° C. or less.
- the hot dip galvanizing treatment condition in order to control the Al content of the hot dip galvanized layer and allow an intermetallic compound to exist between the steel plate and the hot dip galvanized layer, the hot dip galvanizing treatment condition needs to be a specific condition. is there. Moreover, in order to make the surface state (surface roughness Ra, glossiness (G value), zinc base bottom orientation ratio) of a hot dip galvanized layer into a desired state, it is necessary to adjust the conditions of the hot dip galvanizing treatment. . Hereinafter, conditions for the hot dip galvanizing process will be described.
- the intrusion plate temperature which is the temperature of the steel plate when the annealed steel plate enters the plating bath, is not particularly limited.
- the temperature of the immersion plate is preferably a temperature of the plating bath (bath temperature) of ⁇ 20 ° C. or higher and a bath temperature of + 20 ° C. or lower. If the infiltration plate temperature is in the above range, the change in bath temperature is small, and it is easy to perform desired hot dip galvanization continuously.
- the composition of the plating bath into which the annealed steel sheet enters is not limited as long as it contains Al in addition to Zn, and may contain other components as necessary.
- the concentration of Al in the plating bath is not particularly limited. In the present invention, the Al concentration is preferably 0.16% by mass or more and 0.25% by mass or less. If the concentration of Al is 0.16% by mass or more and 0.25% by mass or less, an FeAl alloy phase is formed and formation of an FeZn alloy phase is suppressed, which is preferable.
- the glossiness can be adjusted by the Al concentration in the plating bath. When the Al concentration in the plating bath becomes low, FeZn crystals rather than FeAl are formed slightly at the interface between the steel sheet and the hot dip galvanized layer.
- a more preferable Al concentration is 0.19% by mass or more and 0.22% by mass or less.
- the temperature of the plating bath is not particularly limited.
- the bath temperature is preferably 440 ° C. or higher and 480 ° C. or lower.
- a bath temperature of 440 ° C. or higher and 480 ° C. or lower is preferable because an appropriate bath temperature can be stably secured and Zn does not solidify even if the bath temperature distribution is deteriorated.
- the solubility of the FeAl alloy phase decreases as the bath temperature decreases, the amount of FeAl alloy phase generated tends to increase.
- a more preferable range of the bath temperature is 450 ° C. or higher and 460 ° C. or lower.
- the immersion time when the steel sheet is immersed in the plating bath is not particularly limited.
- the immersion time is preferably 0.5 seconds or more and 3 seconds or less.
- the immersion time is in the above range, a desired hot dip galvanized layer is easily formed on the surface of the steel plate.
- the amount of plating adhesion is adjusted by gas jet wiping or the like.
- the plating adhesion amount is not particularly limited.
- the plating adhesion amount is preferably in the range of 20 g / m 2 or more and 120 g / m 2 or less. If the plating adhesion amount is less than 20 g / m 2 , it may be difficult to ensure corrosion resistance. On the other hand, when the plating adhesion amount exceeds 120 g / m 2 , the plating peel resistance may deteriorate.
- temper rolling is performed.
- the type of roll used for the SK treatment is not particularly limited, and an Electro-Discharge Texture roll (EDT roll), an Electron Beam Texture roll (EBT roll), a shotdal roll, a topochrome roll, or the like can be used.
- the rolling reduction rate during SK treatment is not particularly limited.
- the SK pressure ratio is preferably 0.7 to 0.9%. If the SK rolling reduction is in the above range, the surface roughness can be easily adjusted to the above preferable range. Further, if the SK rolling reduction is outside the above range, the dullness that holds the rolling oil may not be obtained, and the formability may be reduced, and the yield strength may be reduced.
- the cooling rate ( ⁇ (cooling end temperature) ⁇ (cooling start temperature) ⁇ / cooling time) after the steel sheet is pulled up from the plating bath is preferably ⁇ 5 ° C./second or more and ⁇ 30 ° C./second or less. If the cooling rate is ⁇ 5 ° C./second or less, spangles may become coarse, which is not preferable. If the cooling rate is ⁇ 30 ° C./second or more, rapid cooling is required to secure the cooling rate, resulting in a deterioration in economy. It is not preferable. On the other hand, if the cooling rate is slow, the FeAl alloy phase is decomposed and the amount of FeAl alloy phase produced is reduced.
- a more preferable range of the cooling rate is ⁇ 7 ° C./second or more and ⁇ 22 ° C./second or less.
- the cooling rate refers to an average cooling rate when the temperature is lowered from 420 ° C. to 400 ° C.
- the hot dip galvanized steel sheet of the present invention has been described.
- the use of the hot dip galvanized steel sheet of the present invention will be described.
- the hot dip galvanized steel sheet of the present invention is preferably used for applications in which a coating film is formed on the surface of the hot dip galvanized layer because it has excellent post-coating corrosion resistance after press working. Moreover, the hot-dip galvanized steel sheet of the present invention is excellent in plating adhesion even when applied to applications requiring strict workability, and does not significantly reduce corrosion resistance and mechanical properties. Examples of applications in which strict processability is required and a coating film is formed include automotive steel plates such as automobile outer plates and inner plates. The method for forming the coating film is not particularly limited. In the present invention, it is preferable that a chemical conversion treatment is performed on the surface of the hot dip galvanized layer to form a chemical conversion film, and then a coating film is formed on the chemical conversion film.
- Either a coating type or a reaction type can be used as the chemical conversion treatment liquid.
- the component contained in a chemical conversion liquid is not specifically limited, either a chromate processing liquid may be used and a chromium free chemical conversion liquid may be used.
- the chemical conversion film may be a single layer or a multilayer.
- the coating method for forming the coating film is not particularly limited. Examples of the coating method include electrodeposition coating, roll coater coating, curtain flow coating, and spray coating. Moreover, in order to dry a coating material, means, such as hot air drying, infrared heating, induction superheating, can be used.
- the black scale of the hot-rolled steel sheet having the steel composition shown in Table 1 is removed by pickling and cold-rolled at a reduction rate of 75%, and then the surface is on the entry side of the CGL (continuous hot dip galvanizing line).
- annealing was performed at an annealing temperature shown in Table 2 in an annealing furnace, and hot dip galvanizing treatment was performed under the conditions shown in Table 2.
- the average cooling rate from 420 to 400 ° C. after plating and wiping was also measured. The cooling rate is also shown in Table 2.
- SK treatment was performed under the conditions shown in Table 2 before cooling.
- the structure of the steel sheet was composed of a ferrite single phase.
- a test piece was collected from the steel plate, the cross section in the rolling direction (L cross section) was polished, etched with a nital solution, and the structure was observed and imaged using an optical microscope (magnification: 50 to 400 times). And the kind of tissue and the fraction (area%) were measured using the image analysis apparatus. All the steel plates were steel plates substantially composed of a ferrite single phase.
- the intermetallic compound composition was identified by the X-ray diffraction method after removing the zinc plating layer with fuming nitric acid. Regarding the amount, the surface of the intermetallic compound on the sample surface prepared in the same manner was dissolved in dilute hydrochloric acid and quantified by ICP. Similarly, the amount of Al in the plating layer was dissolved in dilute hydrochloric acid and determined by ICP.
- the particle size of the intermetallic compound was measured by the following method. A test piece was collected from the steel plate, and the metal structure of a cross section parallel to the rolling direction was observed with a scanning electron microscope (SEM) at a magnification of 5000 to measure the average particle size of the intermetallic compound. The measurement results are shown in Table 2.
- the surface roughness Ra of the hot dip galvanized layer was measured by the following method. In accordance with the provisions of JIS B 0601, the arithmetic average roughness Ra was measured using a stylus type surface roughness meter. The measurement results are shown in Table 2.
- the zinc base bottom surface orientation ratio is shown in Table 2.
- the resulting hot-dip galvanized steel sheet is subjected to chemical conversion treatment, electrodeposition coating, intermediate coating, and top coating to produce a hot-dip galvanized steel sheet on which a coating film has been formed and visually evaluated after coating. did. When there was no appearance defect due to plating unevenness or the like, it was evaluated as good, and when it was present, it was evaluated as defective. The evaluation results are shown in Table 1.
- the punch with a frustum diameter of 5/8 inch is heightened at 1843 g for the part subjected to frustoconical overmolding (molding equivalent to press molding) under the condition of a plate thickness reduction rate of 10%.
- An impact resistance test of dropping from 1 m was performed, and evaluation was performed by a method of peeling cellophane tape. Those with peeling were considered poor adhesion (x), and those without peeling were good adhesion ( ⁇ ). The evaluation results are shown in Table 2.
- ⁇ Cone overhang molding part was subjected to chemical treatment, electrodeposition coating, intermediate coating, and top coating, and the corrosion resistance after coating was evaluated by the following method.
- a salt spray test based on JIS Z 2371 (2000) was conducted for 10 days, and the presence or absence of swelling of the processed part after press working was evaluated. Those with blisters were judged as bad (x), and those without blisters were judged as good ( ⁇ ). The evaluation results are shown in Table 2.
- a JIS No. 5 tensile test piece is taken from the hot dip galvanized steel sheet in the direction of 90 ° with respect to the rolling direction, and a tensile test is performed under the condition that the crosshead speed is 10 mm / min (constant) in accordance with the provisions of JIS Z 2241. It was. A YS of 220 to 320 MPa was considered good. The evaluation results are shown in Table 2.
- the hot-dip galvanized steel sheet of the present invention has extremely good characteristics and does not undergo plating peeling despite being pressed. Corrosion resistance is also good.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coating With Molten Metal (AREA)
Abstract
Description
本発明で用いる鋼板は、質量%で、C:0.001%以上0.005%以下、Si:0.10%以下、Mn:0.70%以上1.50%以下、P:0.050%以上0.100%以下、S:0.010%以下、N:0.005%以下、Al:0.10%以下、B:0.0015%以下を含有し、かつ、Ti:0.01%以上0.05%以下及びNb:0.01%以上0.05%以下のうちから選択される少なくとも一種を含有し、残部がFe及び不可避的不純物からなる。以下、上記成分組成について説明する。なお、なお、本明細書において、成分組成における「%」表示は、特に断らない限り「質量%」を意味する。
Cの含有量が増えると、深絞り性や延性が劣化し自動車外板用や内板用の鋼板に求められる成形性を鋼板に付与することが困難となる。このためCの含有量の上限は0.005%に規定する。一方、Cの含有量が0.001%未満では結晶粒が粗大化して、成形した際に鋼板表面に肌荒れが生じやすくなる。このため、Cの含有量の下限は0.001%に規定する。本発明で用いる鋼板の成分組成におけるCの含有量が上記範囲にあることで、鋼板組織は加工性に優れた実質的にフェライト単相となる。また、好ましいCの含有量は、0.001%以上0.004%以下である。
Siの含有量が0.10%を超えるとスケールに起因した表面欠陥が発生しやすくなる。また、Siの含有量が過剰になると、後述する金属間化合物の形成を阻害する場合がある。また、Siの含有量が過剰になると、Siの核発生が抑制され鋼板組織中の1つ1つの結晶が粗大化し、プレス加工後のめっき密着性が劣化する問題が生じる。好ましいSiの含有量は0.02%以下である。
Mnの含有量が0.70%未満では充分な強度を有する鋼板が得られない。Mnを鋼板に多量に含有させることで、鋼板を高強度化できるが、Mnを過剰に含有させると深絞り性が低下する。また、Mnを過剰に含有させると、後述する金属間化合物の形成が阻害される。また、Mnを過剰に含有させると、Siの核発生が抑制され鋼板組織中の1つ1つの結晶が粗大化し、プレス加工後のめっき密着性が劣化する。このため、Mnの含有量の上限は1.50%とする。また、好ましいMnの含有量は0.75%以上1.2%以下である。
Pの含有量が0.050%未満では、鋼板の加工性が良好にならず、また、降伏応力(YS)等の機械特性が所望の水準を満たさない。Pの含有量が0.100%を超えると溶接部の靱性が劣化したり、延性が劣化したりする。好ましいPの含有量は0.050%以上0.085%以下である。
Sの含有量が多いと、Pの含有量が多い場合と同様に溶接部の靭性が劣化する。このためSの含有量の上限は0.010%とする。好ましいSの含有量は0.007%以下である。
Al(sol.Al)とNは、通常の鋼板が含有する量であれば本発明の効果を損なわない。また、Nは、Tiと結合してTiNを形成したり、Alと結合してAlNを形成したりする。そこで、Alの含有量を0.10%以下、Nの含有量を0.005%以下に規定する。Alの含有量が0.10%を超えると、後述する金属間化合物の形成が阻害される。また、Alの含有量が0.10%を超えると、Siの核発生が抑制され鋼板組織中の1つ1つの結晶が粗大化し、加工時のめっき密着性が劣化する。また、Nの含有量が0.005%を超えると窒化物がフェライト粒内に分散して加工硬化率が低下する。好ましいAlの含有量は0.04%以下であり、好ましいNの含有量は0.002以下である。
Bは、炭化物を形成して清浄化された粒界の強化に寄与する元素である。この効果を得る観点からは、Bの含有量の下限は0.0003%であることが好ましい。しかしながら、B含有量が0.0015%を超えると、固溶強化により加工硬化率が低下する。また、Bは再結晶焼鈍時における表面の選択酸化を促進する。そのため、Bの含有量の上限は0.0015%とする。また、好ましいBの含有量は0.0003%以上0.0010%以下である。
TiやNbは、フェライト粒内で炭化物(TiC、NbC)を形成することにより、鋼板の加工硬化率を向上させる。ただし、TiやNbの含有量が0.01%未満では、Tiの炭化物量やNbの炭化物量が少なく、転位運動の制御ができず、十分な加工硬化率の上昇を望めない。一方、NbやTi含有量が0.05%を超えると、粗大な炭化物が析出し、加工硬化率が低下する。また、NbやTi含有量が0.05%を超えると、鋼板組織中の粒界が清浄化されて溶融亜鉛めっき処理時に金属間化合物が過剰に成長してめっき密着性が劣化する。このため、Ti及びNbの併用又は単独使用に関わらず、Tiの含有量、Nbの含有量は少なくとも一方が0.01%以上0.05%以下とする。好ましいTiの含有量は0.015%以上0.04%以下であり、好ましいNbの含有量は0.01%以上0.03%以下である。なお、TiとNbの両方を含む場合に、一方の含有量が上記範囲外であれば、本発明の範囲外である。
上記した成分以外の残部は、Fe及び不可避的不純物である。ここで不可避的不純物とは、例えばO(酸素)である。Oは不可避的に混入する代表的な不可避的不純物である。不可避的不純物の含有量は特に限定されず、許容される不可避的不純物の含有量は不可避的不純物の種類にもよる。Oの場合には含有量が0.005%以下であれば問題が無い。
鋼板組織は実質的にフェライト単相である。鋼板組織が実質的にフェライト単相から構成されることで、溶融亜鉛めっき鋼板は加工性に優れる。ここで、実質的にフェライト単相には、鋼板組織の全てがフェライト相である場合の他、鋼板組織の95%以上がフェライト相である場合も含まれる。ただし、通常はフェライト以外の相が生成しないと考えられる。なお、実質的にフェライト単相であることは、光学顕微鏡でエッチングした試料断面を観察して確認する。
溶融亜鉛めっき層とは、通常の溶融亜鉛めっき処理によって形成される溶融亜鉛めっき層である。また、溶融亜鉛めっき層は、Alを質量%で0.3%以上0.6%以下含む。本発明においては、溶融亜鉛めっき層にZn、Al以外の成分を、本発明の効果を害さない範囲で含んでもよい。Zn、Al以外の成分としてはFe、Al、Mg、Cr等が挙げられる。
上記のようにして亜鉛基底面配向率を規定すれば、Znはhcp構造をとり通常は基底面に配向し易く、どの程度結晶がランダムに配向したかが分かる。この凝固組織の配向程度は、光沢、結晶サイズ、表面での粗度(表面粗さ)に影響する。このため、亜鉛基底配向率を正確に制御することは、溶融亜鉛めっき鋼板の表面性状を調整する際に重要であることに加えて、プレス加工性を制御する際にも重要である。なお、亜鉛基底面配向率が上記範囲にあれば、光沢や表面粗さRaは上記好ましい範囲を満たす。
金属間化合物は、平均粒径1μm以下のFe2Al5もしくはFeAl3の少なくとも一種からなる金属間化合物から構成され、鋼板と溶融亜鉛めっき層間に存在する。また、金属間化合物は、0.12gm-2以上0.22gm-2以下のAlを含む。上記金属間化合物が存在することでFeZn合金相の形成を抑制して良好なめっき密着性が確保できる。この効果はFe2Al5もしくはFeAl3の少なくとも一種からなる金属間化合物以外の場合には得られない。これら以外では、硬くて脆いFeZn金属間化合物が生成する場合があり、この場合めっき密着性が劣化する。なお、金属間化合物が存在していることの確認は、溶融亜鉛めっき層の断面における鋼板との界面付近を透過電子顕微鏡中で、電子線回折によって解析して検出する方法で行うことができる。
本発明の溶融亜鉛めっき鋼板は、プレス加工後のめっき密着性に優れ、プレス加工後における加工部の塗装後耐食性に優れる。そして、本発明の溶融亜鉛めっき鋼板は、優れた塗装後外観を有する。このため、本発明の溶融亜鉛めっき鋼板は、バックドアやフードなどの非常に厳しい加工部位を有する製品にも適用可能である。
続いて、溶融亜鉛めっき鋼板の製造方法について説明する。例えば、以下の方法で溶融亜鉛めっき鋼板を製造可能である。先ず、上記のような成分組成を有する鋼を連続鋳造によりスラブとし、該スラブを加熱し、スケール除去および粗圧延を施す。次いで、冷却した後、仕上げ圧延し、冷却し、巻取り、次いで、酸洗、冷間圧延を行う。次いで、連続式溶融亜鉛めっき設備において、鋼板の焼鈍および溶融亜鉛めっき処理を行う。次いで、必要に応じて合金化処理を行う。
Claims (2)
- 質量%で、C:0.001%以上0.005%以下、Si:0.10%以下、Mn:0.70%以上1.50%以下、P:0.050%以上0.100%以下、S:0.010%以下、N:0.005%以下、Al:0.10%以下、B:0.0015%以下を含有し、かつ、Ti:0.01%以上0.05%以下及びNb:0.01%以上0.05%以下のうちから選択される少なくとも一種を含有し、残部がFe及び不可避的不純物の組成からなり、実質的にフェライト単相から構成される鋼板と、
前記鋼板の表面の少なくとも一部に形成された、Alを質量%で0.3%以上0.6%以下含む溶融亜鉛めっき層と、
前記鋼板と前記溶融亜鉛めっき層間に存在する、0.12gm-2以上0.22gm-2以下のAlを含み、かつ平均粒径1μm以下のFe2Al5もしくはFeAl3の少なくとも一種からなる金属間化合物と、を有し、
降伏応力(YS)が220MPa以上320MPa以下である溶融亜鉛めっき鋼板。 - 前記溶融亜鉛めっき層の表面の表面粗さRaが0.8μm以上1.6μm以下であり、
前記溶融亜鉛めっき層の表面の光沢度(G値)が550以上750以下であり、
前記溶融亜鉛めっき層の表面における、Zn結晶の(002)面の結晶配向性とZn結晶の(004)面の結晶配向性との比である亜鉛基底面配向率(Zn(002)/(004))が60以上90以下であることを特徴とする請求項1に記載の溶融亜鉛めっき鋼板。
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201380056703.XA CN104755647B (zh) | 2012-10-31 | 2013-10-21 | 热镀锌钢板 |
| MX2015005403A MX348834B (es) | 2012-10-31 | 2013-10-21 | Lámina de acero galvanizada. |
| KR1020157010673A KR101718469B1 (ko) | 2012-10-31 | 2013-10-21 | 용융 아연 도금 강판 |
| IN2531DEN2015 IN2015DN02531A (ja) | 2012-10-31 | 2013-10-21 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012239974A JP5825244B2 (ja) | 2012-10-31 | 2012-10-31 | 溶融亜鉛めっき鋼板 |
| JP2012-239974 | 2012-10-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2014068889A1 true WO2014068889A1 (ja) | 2014-05-08 |
Family
ID=50626841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2013/006202 Ceased WO2014068889A1 (ja) | 2012-10-31 | 2013-10-21 | 溶融亜鉛めっき鋼板 |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JP5825244B2 (ja) |
| KR (1) | KR101718469B1 (ja) |
| CN (1) | CN104755647B (ja) |
| IN (1) | IN2015DN02531A (ja) |
| MX (1) | MX348834B (ja) |
| TW (1) | TWI511875B (ja) |
| WO (1) | WO2014068889A1 (ja) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104195434A (zh) * | 2014-09-22 | 2014-12-10 | 武汉钢铁(集团)公司 | 抗拉强度390MPa级轿车内部结构件用热镀锌高强钢及其生产方法 |
| WO2016030171A1 (de) * | 2014-08-25 | 2016-03-03 | Voestalpine Stahl Gmbh | Mikrolegierter stahl und zusammengesetzte platinen aus mikrolegiertem stahl und pressgehärtetem stahl |
| WO2016059741A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
| WO2016059743A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 溶融亜鉛めっき鋼板 |
| WO2016059742A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5678951B2 (ja) * | 2012-12-27 | 2015-03-04 | Jfeスチール株式会社 | 溶融亜鉛めっき鋼板 |
| CN106521522B (zh) * | 2016-11-11 | 2018-12-28 | 攀钢集团攀枝花钢钒有限公司 | 一种生产具有均匀锌花尺寸热镀铝锌钢板的方法 |
| CN106319416B (zh) * | 2016-11-11 | 2018-11-23 | 攀钢集团攀枝花钢钒有限公司 | 一种热镀铝锌钢板锌花尺寸的控制方法 |
| CN110199056A (zh) * | 2017-01-26 | 2019-09-03 | 日本制铁株式会社 | 镀覆钢丝、钢丝帘线及橡胶-镀覆钢丝复合体 |
| JP6772930B2 (ja) * | 2017-03-30 | 2020-10-21 | Jfeスチール株式会社 | 溶融亜鉛めっき鋼板および溶融亜鉛めっき鋼板の製造方法 |
| TWI628310B (zh) * | 2017-08-08 | 2018-07-01 | 中國鋼鐵股份有限公司 | High-strength lubricating galvanized steel sheet and manufacturing method thereof |
| CN110629000A (zh) * | 2018-06-25 | 2019-12-31 | 上海梅山钢铁股份有限公司 | 屈服强度280MPa级冷轧热镀锌钢板及其制造方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002173754A (ja) * | 2000-09-29 | 2002-06-21 | Kawasaki Steel Corp | 溶融亜鉛めっき鋼板およびその製造方法 |
| WO2011161833A1 (ja) * | 2010-06-21 | 2011-12-29 | 新日本製鐵株式会社 | 耐加熱黒変性に優れた溶融a1めっき鋼板及びその製造方法 |
| WO2013047812A1 (ja) * | 2011-09-30 | 2013-04-04 | 新日鐵住金株式会社 | 高強度溶融亜鉛めっき鋼板 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6372296B2 (en) * | 1999-05-21 | 2002-04-16 | University Of Cincinnati | High aluminum galvanized steel |
| JP3646685B2 (ja) * | 2000-09-29 | 2005-05-11 | Jfeスチール株式会社 | スポット溶接性に優れた溶融亜鉛めっき鋼板およびその製造方法 |
| JP4934946B2 (ja) * | 2003-03-28 | 2012-05-23 | Jfeスチール株式会社 | スポット溶接性及びプレス加工時の摺動性に優れた自動車用溶融亜鉛めっき鋼板の製造方法 |
| EP2009127A1 (en) * | 2007-06-29 | 2008-12-31 | ArcelorMittal France | Process for manufacturing a galvanized or a galvannealed steel sheet by DFF regulation |
| US20110256420A1 (en) | 2008-07-30 | 2011-10-20 | Pangang Group Steel Vanadium & Titanium Co., Ltd. | Hot-dip galvanized steel plate and production method thereof |
| CN100591794C (zh) * | 2008-07-31 | 2010-02-24 | 攀钢集团研究院有限公司 | 热镀锌钢板的镀锌方法 |
| KR20100034118A (ko) * | 2008-09-23 | 2010-04-01 | 포항공과대학교 산학협력단 | 마르텐사이트 조직을 가진 초고강도 용융아연도금 강판 및 그 제조 방법 |
-
2012
- 2012-10-31 JP JP2012239974A patent/JP5825244B2/ja active Active
-
2013
- 2013-10-21 IN IN2531DEN2015 patent/IN2015DN02531A/en unknown
- 2013-10-21 WO PCT/JP2013/006202 patent/WO2014068889A1/ja not_active Ceased
- 2013-10-21 MX MX2015005403A patent/MX348834B/es active IP Right Grant
- 2013-10-21 CN CN201380056703.XA patent/CN104755647B/zh active Active
- 2013-10-21 KR KR1020157010673A patent/KR101718469B1/ko active Active
- 2013-10-28 TW TW102138903A patent/TWI511875B/zh not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002173754A (ja) * | 2000-09-29 | 2002-06-21 | Kawasaki Steel Corp | 溶融亜鉛めっき鋼板およびその製造方法 |
| WO2011161833A1 (ja) * | 2010-06-21 | 2011-12-29 | 新日本製鐵株式会社 | 耐加熱黒変性に優れた溶融a1めっき鋼板及びその製造方法 |
| WO2013047812A1 (ja) * | 2011-09-30 | 2013-04-04 | 新日鐵住金株式会社 | 高強度溶融亜鉛めっき鋼板 |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016030171A1 (de) * | 2014-08-25 | 2016-03-03 | Voestalpine Stahl Gmbh | Mikrolegierter stahl und zusammengesetzte platinen aus mikrolegiertem stahl und pressgehärtetem stahl |
| CN104195434A (zh) * | 2014-09-22 | 2014-12-10 | 武汉钢铁(集团)公司 | 抗拉强度390MPa级轿车内部结构件用热镀锌高强钢及其生产方法 |
| KR20170054512A (ko) * | 2014-10-17 | 2017-05-17 | 제이에프이 스틸 가부시키가이샤 | 고강도 용융 아연 도금 강판 |
| CN106795612A (zh) * | 2014-10-17 | 2017-05-31 | 杰富意钢铁株式会社 | 高强度热浸镀锌钢板 |
| WO2016059742A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
| JP5907323B1 (ja) * | 2014-10-17 | 2016-04-26 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
| JP5907324B1 (ja) * | 2014-10-17 | 2016-04-26 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
| JP6037056B2 (ja) * | 2014-10-17 | 2016-11-30 | Jfeスチール株式会社 | 溶融亜鉛めっき鋼板 |
| WO2016059741A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 高強度溶融亜鉛めっき鋼板 |
| WO2016059743A1 (ja) * | 2014-10-17 | 2016-04-21 | Jfeスチール株式会社 | 溶融亜鉛めっき鋼板 |
| EP3178960A4 (en) * | 2014-10-17 | 2017-08-02 | JFE Steel Corporation | High-strength hot-dip-galvanized steel sheet |
| EP3178961A4 (en) * | 2014-10-17 | 2017-09-13 | JFE Steel Corporation | High-strength hot-dip-galvanized steel sheet |
| US9963771B2 (en) | 2014-10-17 | 2018-05-08 | Jfe Steel Corporation | High-strength galvanized steel sheet |
| US9994939B2 (en) | 2014-10-17 | 2018-06-12 | Jfe Steel Corporation | High-strength galvanized steel sheet |
| KR101897054B1 (ko) | 2014-10-17 | 2018-09-10 | 제이에프이 스틸 가부시키가이샤 | 고강도 용융 아연 도금 강판 |
| CN106795612B (zh) * | 2014-10-17 | 2019-06-04 | 杰富意钢铁株式会社 | 高强度热浸镀锌钢板 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20150060904A (ko) | 2015-06-03 |
| CN104755647A (zh) | 2015-07-01 |
| JP2014088605A (ja) | 2014-05-15 |
| JP5825244B2 (ja) | 2015-12-02 |
| MX2015005403A (es) | 2015-08-05 |
| TWI511875B (zh) | 2015-12-11 |
| TW201434617A (zh) | 2014-09-16 |
| IN2015DN02531A (ja) | 2015-09-11 |
| CN104755647B (zh) | 2016-10-26 |
| MX348834B (es) | 2017-06-30 |
| KR101718469B1 (ko) | 2017-03-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5825244B2 (ja) | 溶融亜鉛めっき鋼板 | |
| JP5678951B2 (ja) | 溶融亜鉛めっき鋼板 | |
| KR101721483B1 (ko) | 프레스 가공용 용융 아연 도금 강판 | |
| CN104040001B (zh) | 合金化热镀锌钢板 | |
| CN105283573A (zh) | 热冲压成形体及热冲压成形体的制造方法 | |
| JP5907324B1 (ja) | 高強度溶融亜鉛めっき鋼板 | |
| JP5907323B1 (ja) | 高強度溶融亜鉛めっき鋼板 | |
| TWI521092B (zh) | 熔融Al-Zn系鍍覆鋼板及其製造方法 | |
| JP6037056B2 (ja) | 溶融亜鉛めっき鋼板 | |
| JP4720618B2 (ja) | 合金化溶融亜鉛めっき鋼板及びその製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13851581 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 20157010673 Country of ref document: KR Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: MX/A/2015/005403 Country of ref document: MX |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: IDP00201503154 Country of ref document: ID |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 13851581 Country of ref document: EP Kind code of ref document: A1 |


