WO2009057819A1 - 溶融亜鉛めっき鋼板の製造設備 - Google Patents
溶融亜鉛めっき鋼板の製造設備 Download PDFInfo
- Publication number
- WO2009057819A1 WO2009057819A1 PCT/JP2008/070246 JP2008070246W WO2009057819A1 WO 2009057819 A1 WO2009057819 A1 WO 2009057819A1 JP 2008070246 W JP2008070246 W JP 2008070246W WO 2009057819 A1 WO2009057819 A1 WO 2009057819A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dip galvanized
- hot
- steel sheet
- galvanized steel
- steel plate
- Prior art date
Links
- 229910001335 Galvanized steel Inorganic materials 0.000 title claims abstract description 48
- 239000008397 galvanized steel Substances 0.000 title claims abstract description 48
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 81
- 239000010959 steel Substances 0.000 claims abstract description 81
- 239000003929 acidic solution Substances 0.000 claims abstract description 54
- 238000004140 cleaning Methods 0.000 claims abstract description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000005096 rolling process Methods 0.000 claims abstract description 16
- 238000005246 galvanizing Methods 0.000 claims abstract description 13
- 238000007747 plating Methods 0.000 claims description 33
- 238000004519 manufacturing process Methods 0.000 claims description 26
- 239000011701 zinc Substances 0.000 claims description 24
- 238000007664 blowing Methods 0.000 claims description 21
- 239000000243 solution Substances 0.000 claims description 13
- 238000005275 alloying Methods 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 239000007921 spray Substances 0.000 abstract description 5
- 238000005507 spraying Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 23
- 239000010410 layer Substances 0.000 description 23
- 230000001276 controlling effect Effects 0.000 description 15
- 239000007788 liquid Substances 0.000 description 13
- 239000002253 acid Substances 0.000 description 10
- 230000007423 decrease Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 239000002344 surface layer Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000010306 acid treatment Methods 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000010960 cold rolled steel Substances 0.000 description 3
- 238000007791 dehumidification Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000682 scanning probe acoustic microscopy Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 102100040853 PRKC apoptosis WT1 regulator protein Human genes 0.000 description 2
- 101710162991 PRKC apoptosis WT1 regulator protein Proteins 0.000 description 2
- 229910001297 Zn alloy Inorganic materials 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- 101000993059 Homo sapiens Hereditary hemochromatosis protein Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- -1 etc. can be used Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910052720 vanadium Inorganic materials 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
- C23C2/50—Controlling or regulating the coating processes
- C23C2/51—Computer-controlled implementation
-
- 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
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/54—Furnaces for treating strips or wire
- C21D9/56—Continuous furnaces for strip or wire
- C21D9/561—Continuous furnaces for strip or wire with a controlled atmosphere or vacuum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C11/00—Component parts, details or accessories not specifically provided for in groups B05C1/00 - B05C9/00
- B05C11/10—Storage, supply or control of liquid or other fluent material; Recovery of excess liquid or other fluent material
- B05C11/1002—Means for controlling supply, i.e. flow or pressure, of liquid or other fluent material to the applying apparatus, e.g. valves
- B05C11/1015—Means for controlling supply, i.e. flow or pressure, of liquid or other fluent material to the applying apparatus, e.g. valves responsive to a conditions of ambient medium or target, e.g. humidity, temperature ; responsive to position or movement of the coating head relative to the target
-
- 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
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/1601—Process or apparatus
- C23C18/1633—Process of electroless plating
- C23C18/1689—After-treatment
- C23C18/1692—Heat-treatment
- C23C18/1696—Control of atmosphere
-
- 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
- C23C2/003—Apparatus
-
- 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
- C23C2/26—After-treatment
-
- 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
-
- 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
- C23C2/50—Controlling or regulating the coating processes
- C23C2/52—Controlling or regulating the coating processes with means for measuring or sensing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C3/00—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material
- B05C3/02—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material the work being immersed in the liquid or other fluent material
- B05C3/12—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material the work being immersed in the liquid or other fluent material for treating work of indefinite length
- B05C3/125—Apparatus in which the work is brought into contact with a bulk quantity of liquid or other fluent material the work being immersed in the liquid or other fluent material for treating work of indefinite length the work being a web, band, strip or the like
Definitions
- the present invention relates to equipment for stably producing a hot dip galvanized steel sheet.
- Hot-dip galvanized steel sheets are widely used in a wide range of fields, especially for automobile body applications, due to their excellent weldability and paintability. Hot-dip galvanized steel sheets for such applications are used after being pressed.
- the hot dip galvanized steel sheet has the disadvantage that the press formability is inferior to that of the cold rolled steel sheet. This is because the sliding resistance of the hot-dip galvanized steel sheet in the press die is larger than that of the cold-rolled steel sheet. In other words, the hot-dip galvanized steel sheet is less likely to flow into the press mold at the part where the sliding resistance between the mold and the bead is large, and the steel sheet tends to break.
- an alloyed hot-dip galvanized steel sheet is subjected to heat treatment after galvanizing the steel sheet, and Fe in the steel sheet and Zn in the galvanized layer diffuse to cause an alloying reaction.
- a Zn alloy phase is formed, but this Fe-Zn alloy phase is usually a film composed of a ⁇ phase, a ⁇ i phase, and a ⁇ phase, and as the Fe concentration decreases, that is, a ⁇ phase phase ⁇
- the melting point tends to decrease as the hardness increases. For this reason, from the viewpoint of slidability, it is effective to use a coating film with high hardness and high melting point that has a high melting point and is less likely to cause adhesion. Manufactured to increase the average Fe concentration in the film.
- a coating with a high Fe concentration has a problem that a hard and brittle ⁇ phase is easily formed at the interface between the plated steel sheet and the phenomenon of peeling from the interface during processing, so-called powdering.
- the flat portion on the surface of the galvannealed steel plate exists as a convex portion as compared with the surroundings.
- the flat part is the main component that actually contacts the press mold during press molding. Therefore, if the sliding resistance at the flat part is reduced, the press formability can be improved.
- it is effective to prevent adhesion between the plating layer and the mold. To that end, a hard and high melting point film must be formed on the surface of the plating layer. Is effective.
- An object of the present invention is to propose a facility for manufacturing a hot-dip galvanized steel sheet that is easy to put into practical use and can stably form a necessary oxide film without impairing the appearance of the steel sheet surface. Disclosure of the invention
- the gist of the present invention is as follows.
- a hot-dip galvanized steel plate manufacturing facility comprising a hot-dip galvanizing device, a temper rolling mill, an acidic solution contact device, and a cleaning device, the acidic solution contact device and the cleaning device
- the apparatus is disposed with a space between the acidic solution contact apparatus and the cleaning apparatus.
- a facility for producing hot-dip galvanized steel sheets comprising a hot-dip zinc plating device, an alloying heating furnace, a cooling device, a temper rolling mill, an acidic solution contact device, and a cleaning device.
- the acidic solution contact device and the cleaning device are arranged with a space therebetween, and means for controlling absolute humidity is provided between the acidic solution contact device and the cleaning device.
- Manufacturing equipment for hot-dip galvanized steel sheets comprising a hot-dip zinc plating device, an alloying heating furnace, a cooling device, a temper rolling mill, an acidic solution contact device, and a cleaning device.
- the means for controlling the absolute humidity covers the upper and lower surfaces of the steel plate, and a force par that allows the steel plate to penetrate
- An apparatus for producing a hot-dip galvanized steel sheet comprising: blowing means for blowing water vapor or dry air; and measuring means for measuring temperature, relative humidity, or dew point.
- FIG. 1 is a diagram showing an outline of a method for producing a hot dip galvanized steel sheet.
- FIG. 2 is a diagram showing the formation mechanism of the oxide film.
- Fig. 3 is a schematic diagram summarizing the factors affecting the amount of change in the liquid film.
- FIG. 4 is a diagram showing an embodiment of a production facility for hot-dip galvanized steel sheets according to the present invention.
- Figure 5 shows the relationship between absolute humidity and oxide film thickness.
- FIG. 6 is a schematic explanatory view showing another embodiment of the production facility for hot dip galvanized steel sheet according to the present invention.
- FIG. 7 is a schematic explanatory view showing another embodiment of the production facility for hot dip galvanized steel sheet according to the present invention.
- the hot dip galvanized steel sheet in the present invention covers both hot dip galvanized steel sheets that are not subjected to alloying treatment and galvannealed steel sheets that are subjected to alloying treatment after plating.
- steel sheets subjected to hot dip galvanization or subsequently alloyed by heat treatment and subjected to temper rolling are brought into contact with an acidic solution, and after contact is completed, 1 to: 120 seconds. Then, by washing with water, the present invention relates to an improved facility for manufacturing an alloyed hot dip galvanized steel sheet that forms a Zn-based oxide layer of 10 nm or more on the surface of the galvanized steel sheet, that is, an oxide film.
- the manufacturing equipment for the hot dip galvanized steel sheet comprises a hot dip galvanizing device, a temper rolling mill, an acidic solution contact device, and a cleaning device, and the acidic solution contact device and the cleaning device.
- the devices are spaced apart.
- an alloying heating furnace and a cooling device are provided between the hot-dip zinc plating device and the temper rolling mill.
- means for controlling the absolute humidity between the acidic solution contact device and the cleaning device for example, blowing air containing moisture opens and closes the valve, and automatically or manually adjusts the opening of the flow rate adjusting valve.
- the number of air inlets can be changed arbitrarily, and the amount of water in the air can be changed arbitrarily using a moisture absorbent material or steam.
- the means for controlling the absolute humidity covers the upper and lower surfaces and both side surfaces of the steel plate, and a cover through which the steel plate can penetrate, and a blow in which steam or dry air is blown into the cover in parallel with the steel plate traveling direction.
- Measuring means for example, a thermometer and a hygrometer, a dew point meter, a device for measuring the dew point and absolute humidity from the temperature and humidity, etc.
- a means for controlling the absolute humidity between the acidic solution contact device and the cleaning device preferably providing a cover, a blowing means, and a measuring means is a feature of the present invention and is an important feature. It is matter.
- the reaction process region Zn-based oxides are formed on the steel plate surface, and an acid film is formed on the plated surface of the steel sheet. Is formed.
- the reaction process region By providing means for controlling the absolute humidity between the acidic solution contact device and the cleaning device, which are such reaction process regions, it becomes possible to stably form an oxide film on the plated surface of the steel sheet.
- the cover, the blowing means and the measuring means the atmosphere in the reaction process area can be controlled more strictly, and as a result, a more stable oxide film can be obtained. be able to.
- FIG. 1 is a diagram showing an outline of a method for manufacturing a hot-dip galvanized steel sheet in which an oxide film is formed by applying an acidic solution to the surface of the hot-dip galvanized steel sheet and allowing it to stand for a certain period of time.
- the region between the acid solution contact step and the cleaning step is a reaction process region where an oxide film is formed. In this reaction process region, how stably an acid film is formed on the surface. Is important.
- Figure 2 shows the formation mechanism of the oxide film. According to Fig. 2, while the amount of liquid film is sufficient, the pH in the liquid film increases as the reaction proceeds, but when the amount of liquid film decreases, the reaction proceeds because the concentration of zinc ions increases. It can be seen that the oxidation reaction stops completely when the liquid film is completely dried.
- Fig. 3 is a schematic diagram summarizing the factors affecting the amount of change in the liquid film.
- the amount of change in the liquid film can be divided into two, the decrease Q1 due to drying and the decrease Q2 due to the acid-acid reaction.
- the decrease Q1 due to drying is a decrease in the ambient temperature and humidity during the reaction process. It can be seen that acid treatment increases with increasing liquid temperature and line speed. From Fig. 3, the amount of oxide film generated is considered to be correlated with the volume change of the liquid film, and the following relational expression is estimated.
- Oxide film thickness F (T, P, Ts, V, Q2)
- the liquid film reduction amount Q1 can be reduced and the oxide film amount can be stabilized.
- a stable oxide film can be obtained by providing a humidifier that can control the (dew point) and controlling the humidity.
- a means for controlling the absolute humidity is provided between the acidic solution contact device, which is the reaction process region, and the cleaning device.
- the absolute temperature indicates the amount of water contained in the atmosphere and is the product of saturated vapor pressure and relative humidity.
- FIG. 4 is a diagram showing an embodiment of the present invention.
- the hot dip galvanizing device 7 for plating the steel plate surface, the temper rolling machine 8 for adjusting the roughness of the plating surface, and the temper rolling after the plating treatment is applied to the surface.
- An acidic solution contact device 1 for applying an acidic solution to a steel plate and a cleaning device 2 for cleaning an excess acidic solution after forming an acid film on the plating surface are connected in series.
- the acidic solution contact device 1 and the cleaning device 2 are arranged with a space therebetween.
- a cover 3 between the acidic solution contact device 1 and the cleaning device 2 covers the upper and lower surfaces and both side surfaces of the steel plate as means for controlling the absolute humidity, and allows the steel plate to penetrate therethrough.
- a blowing means 5 for blowing water vapor into the cover, and a measuring means 6 for measuring temperature and relative humidity or dew point are provided.
- the following shows an example of a method for forming an oxide film on the plating surface using this device shown in Fig. 4.
- the steel sheet S is annealed in a continuous annealing furnace 11 provided in front of the hot dip galvanizing equipment, and is struck by a hot dip galvanizing apparatus 7.
- the hot dip galvanizing device 7 for example, the steel sheet S heated to the vicinity of the galvanizing bath temperature is continuously guided to the galvanizing bath, and after being drawn out of the plating bath, the amount of plating adhered is reduced by gas wiping. It is controlled in to 120 g / m 2.
- the steel sheets that have been hot-dip galvanized in this way are further guided to an alloying furnace (not shown) and subjected to thermal diffusion. An alloyed hot-dip galvanized steel sheet containing about 6 to 15% by mass of Fe in the plating layer is obtained.
- the heating method is not limited, but it is advantageous to use a high frequency induction heating furnace. This is because the steel plate itself can be heated instantaneously by using the high frequency induction heating method. Uniform alloying is possible, and there is little variation in the width direction and length direction of the steel sheet.
- the steel sheet S that has been subjected to hot dip galvanizing and further subjected to alloying treatment has a high temperature. Therefore, it is preferable to cool the steel sheet S to about room temperature by a cooling device using a blower or the like.
- the plated steel sheet s is guided to a temper rolling machine 8 in order to control the material and adjust the roughness of the plating surface.
- the unevenness of plating is relaxed, and a flat portion is formed on the plating surface. Since the slidability of the hot-dip galvanized steel sheet is improved by the relief of the unevenness, it is important to have a flat part on the plating surface.
- the part that is not flattened (recessed part) retains the lubricating oil and prevents oil shortage during press molding, so the presence of a recessed part is also important. From this point of view, it is effective that the area ratio of the flat part of the plating surface is in the range of 20 to 80%, and the reduction ratio during temper rolling should be adjusted so as to be the area ratio of the flat part ' Is preferred.
- the tempered rolled steel sheet S after the temper rolling is guided to the acidic solution contact device 1 and subjected to a treatment for forming a Zn-based oxide on the plated surface flat portion.
- a treatment for forming a Zn-based oxide on the plated surface flat portion is because when the acidic solution is brought into contact with the plated steel sheet S, the plating component Zn dissolves, and the pH of the solution rises due to the hydrogen generation reaction that accompanies this, so that the Zn hydroxide precipitates on the plating surface.
- it is thought that this is because a Zn-based oxide is formed.
- simply contacting with an acidic solution only causes dissolution of Zn, and no Zn-based oxide is formed.
- the region 3 between the acidic solution contact device 1 and the cleaning device 2 is set as a reaction process region, and the region 3 is left for a certain period of time.
- the plated steel sheet S and the acidic solution are brought into contact with each other.
- a device that performs immersion treatment in the acidic solution, a spray device for the acidic solution, a device that applies the acidic solution using a roll, etc. Can be given. It is desirable that it is finally a thin liquid film and exists on the steel sheet surface. This is because when the amount of acidic solution present on the steel plate surface is large, The pH of the solution does not increase even if it occurs, and only the dissolution of zinc occurs one after another. Not only does it take a long time to form the oxide layer, but the plating layer is severely damaged. This is because it is considered that the role as a fender is also lost. From this viewpoint, it is preferable and effective to adjust the amount of the acidic solution film formed on the steel sheet surface to 50 g / m 2 or less. The amount of the solution film can be adjusted with a squeeze roll or air wiping.
- the pH needs to be controlled to about 1.0 to 0.
- hydrochloric acid, sulfuric acid, nitric acid, etc. can be used, and solutions containing compounds such as salt, sulfate, nitrate, etc. may be used. .
- the temperature of the acidic solution is preferably in the range of 20 to 70 ° C. If it is less than 20 ° C, the production reaction of the oxide layer takes a long time, and the productivity may be reduced. On the other hand, when the temperature is high, the reaction proceeds relatively quickly S, and on the other hand, unevenness of processing tends to occur on the surface of the steel sheet.
- the oxide film is formed by leaving the hot-dip galvanized steel plate for a certain period of time. Therefore, in the present invention, as described above, a means for controlling the absolute humidity is provided on this region 3.
- the blowing means 5 and the measuring means 6 as the means for controlling the absolute humidity, the atmosphere in the reaction process region where the Zn-based oxyhydride is formed is controlled. It is possible to do.
- the temperature and relative humidity, or dew point is measured every predetermined time or constantly by the measuring means 6. Then, based on the result of the measuring means 6, the amount of water vapor in the reaction process region (in the power par) is reduced by blowing water vapor from the blowing means 5 into the cover 4 so that the oxide film is formed more stably. adjust. As a result, the oxide film can be formed more stably. Note that it is not necessary to directly apply water vapor to the steel sheet, and it is preferable to blow it substantially parallel to the direction of travel of the steel sheet. As described above, the absolute humidity control means in the present invention has a function of adjusting the absolute degree according to the atmosphere in the reaction process region so that the oxide film formation reaction proceeds stably and surely.
- a means having a humidifying function and a means having a dehumidifying function can be fisted.
- a control method for example, temperature and relative humidity or dew point are measured, and humidification and dehumidification are performed based on the results.
- the size, material, and the like of the cover 4 are not particularly limited as long as the cover 4 covers the upper and lower surfaces and both side surfaces of the steel plate and can penetrate the steel plate.
- the cross-sectional shape of the force par 4 in the traveling direction of the steel plate is not particularly limited, and may be circular or rectangular.
- the blowing means 5 is for blowing water vapor or dry air into the force par 4.
- a steam pipe is installed for each predetermined section in the traveling direction of the steel sheet, and a plurality of outlets are arranged in the steam pipe. You can also In this case, the pipe length, the number of outlets, and the like are appropriately set according to the equipment length of the cover 4. Note that the steam or dry air is preferably blown in substantially parallel to the traveling direction of the steel sheet.
- It can be installed on either or both of the front and back sides of the steel plate. Furthermore, it is preferable to install it at a distance of 500 mm or more in the vertical direction from the steel plate surface so that water vapor or the like does not directly hit the steel plate. It can also be installed on the bottom of the facility.
- Delivery direction of the steam or dry air is preferably a steel sheet traveling direction and substantially parallel to steam nozzle conditions, as a guide for the diffusion in the cover 4 is sufficiently performed, be carried out by the following vapor pressure 0. 5kg f / cm 2 Is preferred. By carrying out under such conditions, the blown out water vapor is sufficiently diffused into the cover 4.
- the measuring means 6 is for measuring temperature and relative humidity, or dew point. More specifically, it is a thermometer, hygrometer, or dew point meter, etc. It is preferable to install in the range. In addition, it is preferable to install it at a distance of lm or more from the air outlet so as not to be affected by water vapor or dry air. Furthermore, the measuring means is preferably attached to the side opposite to the air outlet.
- Figure 5 shows that the oxide film thickness increases with increasing absolute humidity.
- the line speed reaction time
- the line speed is taken into account, for example, 2000 mass ppm or more is required to secure the required film thickness.
- absolute humidity is required. Therefore, in order to prevent drying of the acidic solution on the steel sheet surface layer and to secure an oxide film thickness that is greater than the required film thickness, the water vapor amount is 2000 masses using the cover 7, blowing means 8 and measuring means 6 in FIG. It will be kept above ppm (dew point: 12.7 ° C or higher).
- the absolute humidity is too high, the oxide film thickness becomes too thick, which adversely affects the paintability. Therefore, the upper limit of absolute humidity should be determined according to the required paintability.
- the steel sheet that has passed through the reaction process region is subjected to a washing process 2 in which the acidic solution component remaining on the surface is washed away. If this ⁇ purification treatment is inadequate, the acidic solution component remains on the plating surface, which may promote corrosion when it becomes an actual product. For this reason, it is also effective to neutralize the acidic solution component remaining on the plating surface by introducing it to a neutralization treatment device instead of washing the steel plate with water.
- the solution used for the neutralization treatment is not particularly limited as long as it is an alkaline solution, and an aqueous solution such as sodium hydroxide or sodium phosphate can be used.
- the Zn-based oxide layer in the present invention is a layer made of an oxide containing Z as an essential component and Z or hydroxide.
- the average thickness of the oxide layer containing Zn as an essential component is 10 nm or more in the pressure-regulating portion surface layer and the unregulated portion surface layer. It is necessary. If the average thickness of the oxide layer is reduced to less than lOnm in the pressure-regulating part and the non-pressure-regulating part, the effect of reducing the sliding resistance becomes insufficient. On the other hand, when the average thickness of the oxide layer containing Zn as an essential component exceeds lOOnm in the pressure-regulating part and the non-pressure-adjusting part, the film breaks down during press molding, and the sliding resistance increases. In addition, the weldability tends to decrease, which is not preferable.
- the additive element components other than A1 are not particularly limited. That is, even if Pb, Sb, Si, Sn, Mg, Mn, Ni, Ti, Li, Cu or the like is contained or added in addition to A1, the effect of the present invention is not impaired.
- FIG. 6 is a schematic explanatory view showing another embodiment of the production facility for hot dip galvanized steel sheet according to the present invention.
- the same components as those in FIG. 4 are denoted by the same reference numerals, and detailed description thereof is omitted.
- a humidifying device 9 for controlling the atmosphere in the reaction process region.
- blowing means 5 and measuring means 6 for measuring temperature and relative humidity or dew point. Details of each facility are as follows.
- the area that seems to be the most dry 3 depends on the temperature, relative humidity, and plate-feeding speed during the reaction process. Within 14m immediately after contact device 1. Therefore, it is preferable to install the humidifying equipment 9 at this position, and in FIG. 6, it is installed at 1 m immediately after the acidic solution contact apparatus 1.
- the cross-sectional shape in the traveling direction of the steel plate was a square, and the material used was chlor chloride.
- the distance between the acidic solution contact device 1 and the cleaning device 2 is 30 m.
- the humidification range in the humidification equipment 9 is preferably 6 m or more, and in FIG.
- the time for the steel sheet to pass through the humidification equipment 9 was set to 2 seconds.
- Delivery direction of the steam is substantially parallel to the steel sheet travel direction, the steam nozzle conditions, as a guide for the diffusion of the humidifying equipment 9 is performed sufficiently, and less vapor pressure 0. 5kgf / C m 2.
- a dehumidifier 10 is installed instead of the humidifier 9 in Fig. 6 (Fig. 7).
- the dehumidifying equipment 10 was dehumidified by blowing dry air in place of the water vapor blowing of the humidifying means 9.
- the absolute humidity of the dry air can be selected according to the required humidity conditions.
- the inlet position, conditions, etc. are the same as for the humidifier 9.
- a measuring means is attached in the vicinity of the plate surface on the side opposite to the air outlet. In Fig. 6, the dew point was measured by the measuring means.
- the hot dip galvanized steel sheet was manufactured using the hot dip galvanized manufacturing equipment shown in Fig. 6 or Fig. 7 above.
- an alloyed hot-dip galvanized film was formed on a cold-rolled steel sheet with a thickness of 0.8 mm by a conventional method, and further subjected to temper rolling. Thereafter, 50 ° C, is led into P H2.
- Acid solution contacting device 1 filled with sulfuric acid solution of 0, plated steel sheet S immersed in acidic solution, the coated steel sheet S in Rukoto be advanced over area 3 1 After contact with the atmosphere for 3 seconds, washing with the washing device 2 and removing water with a drying device (not shown), a hot-dip galvanized steel sheet with an oxide film formed on the plating surface was obtained. Finally, a simple fouling oil was applied and coiled into a product.
- the line speed was 100 mpm.
- the dew point in the humidifying equipment 9 or the dehumidifying equipment 10 is measured by the measuring means 6 when the steel sheet S passes through the humidifying equipment 9 or the dehumidifying equipment 10, and the humidifying equipment is used by the blowing means 5 based on this result. Steam or dry air was blown so that the dew point in 9 or dehumidification facility 10 was -12. 7 ° C or higher and below the dew point upper limit value set from the upper limit value of the oxide film thickness.
- the film thickness of the oxide layer of the pressure regulation part of a plating surface layer and the non-pressure regulation part was measured with the following method. As a result, it was confirmed that an oxide film sufficient to improve the slidability was formed in the pressure adjusting part and the non-pressure adjusting part.
- the content (at.%) Of each element was measured for the pressure-adjusted and unadjusted parts of the surface layer by Auger electron spectroscopy (AES), and subsequently Ar-sputtered to a predetermined depth, and then measured by AES.
- AES Auger electron spectroscopy
- the composition distribution of each element in the depth direction was measured.
- the depth that is 1/2 of the sum of the maximum value and the constant value is the thickness of the oxide, 2 parts of oxide each against the yopi unregulated part
- the thickness was measured, and the average value of these values was defined as the oxide thickness of the pressure-regulating part and the non-pressure-regulating part, respectively.
- Ar contamination was performed for 30 seconds to remove the contamination layer on the specimen surface.
- the necessary acid-oxide film can be reliably formed on the plated steel sheet surface without impairing the appearance of the steel sheet surface. Then, for example, without blowing steam directly, such as the amount of water vapor in the reaction step can be adjusted to more than 2000 mass ppm, an easy equipment commercialized q
- the necessary oxide film can be stably formed without impairing the appearance of the steel sheet surface, so that it can be applied in a wide range of fields, mainly for automobile body applications.
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Abstract
Description
Claims
Priority Applications (6)
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KR1020127029746A KR20120135436A (ko) | 2007-10-31 | 2008-10-30 | 용융 아연 도금 강판의 제조 설비 |
CN200880114216A CN101842510A (zh) | 2007-10-31 | 2008-10-30 | 热镀锌钢板的制造设备 |
CA2701060A CA2701060C (en) | 2007-10-31 | 2008-10-30 | Apparatus for manufacturing molten zinc coated steel sheet |
EP08844330.4A EP2204464B1 (en) | 2007-10-31 | 2008-10-30 | Equipment for producing hot dip galvanized steel plate |
KR1020107008699A KR101237318B1 (ko) | 2007-10-31 | 2008-10-30 | 용융 아연 도금 강판의 제조 설비 |
US12/738,647 US9222146B2 (en) | 2007-10-31 | 2008-10-30 | Apparatus for manufacturing molten zinc coated steel sheet |
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JP2007282805A JP5211642B2 (ja) | 2007-10-31 | 2007-10-31 | 溶融亜鉛めっき鋼板の製造設備及び溶融亜鉛めっき鋼板の製造方法 |
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US (1) | US9222146B2 (ja) |
EP (1) | EP2204464B1 (ja) |
JP (1) | JP5211642B2 (ja) |
KR (2) | KR101237318B1 (ja) |
CN (1) | CN101842510A (ja) |
CA (1) | CA2701060C (ja) |
TW (1) | TWI449805B (ja) |
WO (1) | WO2009057819A1 (ja) |
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EP2835432B1 (en) * | 2012-04-06 | 2016-11-02 | JFE Steel Corporation | Continuous hot-dip zinc plating facility |
JP5962168B2 (ja) * | 2012-04-20 | 2016-08-03 | Jfeスチール株式会社 | 外観性に優れた高潤滑溶融亜鉛めっき鋼板の製造方法 |
JP5335159B1 (ja) * | 2012-04-25 | 2013-11-06 | 日新製鋼株式会社 | 黒色めっき鋼板の製造方法および黒色めっき鋼板の成形体の製造方法 |
JP6137089B2 (ja) * | 2014-09-02 | 2017-05-31 | Jfeスチール株式会社 | 冷延鋼板の製造方法および冷延鋼板の製造設備 |
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 |
JP6269547B2 (ja) * | 2015-03-23 | 2018-01-31 | Jfeスチール株式会社 | 連続溶融亜鉛めっき装置及び溶融亜鉛めっき鋼板の製造方法 |
CN105861970B (zh) * | 2016-05-30 | 2018-08-03 | 浙江慧钢技术发展有限公司 | 一种高效的热浸镀锌生产线 |
CN111676434A (zh) * | 2020-06-09 | 2020-09-18 | 首钢集团有限公司 | 一种耐黑变锌铝镁镀层钢板及其制备方法 |
KR20230090142A (ko) * | 2021-12-14 | 2023-06-21 | 주식회사 엘지에너지솔루션 | 절대 습도 산출 장치 및 그것의 동작 방법 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0681166A (ja) * | 1991-10-14 | 1994-03-22 | Toyota Motor Corp | 鉄鋼材の表面処理方法 |
JP2003306781A (ja) | 2002-04-18 | 2003-10-31 | Jfe Steel Kk | 合金化溶融亜鉛めっき鋼板の製造方法 |
JP3608519B2 (ja) | 2001-03-05 | 2005-01-12 | Jfeスチール株式会社 | 合金化溶融亜鉛めっき鋼板の製造方法および合金化溶融亜鉛めっき鋼板 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2656284A (en) * | 1949-09-07 | 1953-10-20 | Ohio Commw Eng Co | Method of plating rolled sheet metal |
US3857362A (en) * | 1972-05-23 | 1974-12-31 | D Brooks | Metal powder coating apparatus |
JPH01108358A (ja) | 1987-10-21 | 1989-04-25 | Nippon Steel Corp | 溶融合金化亜鉛メッキ鋼板のメッキ層表面酸化物生成方法 |
JPH02190460A (ja) | 1989-01-18 | 1990-07-26 | Nippon Steel Corp | スポット溶接性に優れた合金化亜鉛めっき鋼板の製造方法 |
JPH1043652A (ja) * | 1996-08-07 | 1998-02-17 | Fuji Xerox Co Ltd | 浸漬塗布方法および浸漬塗布装置 |
JP3397150B2 (ja) * | 1998-11-25 | 2003-04-14 | 住友金属工業株式会社 | 溶融亜鉛系めっき鋼板 |
US7238430B2 (en) * | 1999-10-07 | 2007-07-03 | Isg Technologies Inc. | Composition for controlling spangle size, a coated steel product, and a coating method |
KR100495443B1 (ko) * | 1999-10-07 | 2005-06-14 | 아이에스쥐 테크놀로지 인코포레이티드 | 강 제품 코팅 조성물, 코팅된 강 제품 및 강 제품 코팅방법 |
US6428851B1 (en) * | 2000-03-01 | 2002-08-06 | Bethlehem Steel Corporation | Method for continuous thermal deposition of a coating on a substrate |
JP2001355078A (ja) * | 2000-04-11 | 2001-12-25 | Toshiba Tec Corp | ニッケルメッキ方法及びその装置並びに被メッキ物 |
WO2002018065A2 (en) * | 2000-09-01 | 2002-03-07 | Bethlehem Steel Corporation | Process for applying a coating to a continuous steel sheet and a coated steel sheet product therefrom |
JP2003137512A (ja) * | 2001-11-02 | 2003-05-14 | Rigaku Corp | 金属酸化物の製造方法,半導体装置及び金属酸化物製造装置 |
KR100704692B1 (ko) * | 2002-09-13 | 2007-04-10 | 제이에프이 스틸 가부시키가이샤 | 용융도금 금속대의 제조방법 및 제조장치 |
DE10255994A1 (de) * | 2002-11-30 | 2004-06-09 | Sms Demag Ag | Verfahren und Vorrichtung zur Schmelztauchbeschichtung eines Metallstranges |
FR2876710B1 (fr) * | 2004-10-19 | 2014-12-26 | Kappa Thermline | Procede et dispositif de limitation de la vibration de bandes d'acier ou d'aluminium dans des zones de refroidissement par soufflage de gaz ou d'air |
JP2007010267A (ja) | 2005-07-01 | 2007-01-18 | Daikin Ind Ltd | 空気調和装置 |
JP4650128B2 (ja) * | 2005-07-06 | 2011-03-16 | Jfeスチール株式会社 | 合金化溶融亜鉛めっき鋼板の製造方法および合金化溶融亜鉛めっき鋼板 |
JP4692120B2 (ja) | 2005-07-19 | 2011-06-01 | Jfeスチール株式会社 | 合金化溶融亜鉛めっき鋼板の製造方法 |
US8025835B2 (en) * | 2007-07-31 | 2011-09-27 | ArcelorMittal Investigación y Desarrollo, S.L. | Furnace configured for use in both the galvannealing and galvanizing of a metal strip |
EP2835432B1 (en) * | 2012-04-06 | 2016-11-02 | JFE Steel Corporation | Continuous hot-dip zinc plating facility |
-
2007
- 2007-10-31 JP JP2007282805A patent/JP5211642B2/ja active Active
-
2008
- 2008-10-30 EP EP08844330.4A patent/EP2204464B1/en active Active
- 2008-10-30 KR KR1020107008699A patent/KR101237318B1/ko active IP Right Grant
- 2008-10-30 US US12/738,647 patent/US9222146B2/en active Active
- 2008-10-30 KR KR1020127029746A patent/KR20120135436A/ko not_active Application Discontinuation
- 2008-10-30 WO PCT/JP2008/070246 patent/WO2009057819A1/ja active Application Filing
- 2008-10-30 CA CA2701060A patent/CA2701060C/en active Active
- 2008-10-30 CN CN200880114216A patent/CN101842510A/zh active Pending
- 2008-10-31 TW TW097141989A patent/TWI449805B/zh not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0681166A (ja) * | 1991-10-14 | 1994-03-22 | Toyota Motor Corp | 鉄鋼材の表面処理方法 |
JP3608519B2 (ja) | 2001-03-05 | 2005-01-12 | Jfeスチール株式会社 | 合金化溶融亜鉛めっき鋼板の製造方法および合金化溶融亜鉛めっき鋼板 |
JP2003306781A (ja) | 2002-04-18 | 2003-10-31 | Jfe Steel Kk | 合金化溶融亜鉛めっき鋼板の製造方法 |
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Publication number | Publication date |
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CA2701060C (en) | 2012-09-11 |
KR101237318B1 (ko) | 2013-02-28 |
KR20100057908A (ko) | 2010-06-01 |
EP2204464A1 (en) | 2010-07-07 |
CN101842510A (zh) | 2010-09-22 |
TW200932949A (en) | 2009-08-01 |
CA2701060A1 (en) | 2009-05-07 |
US9222146B2 (en) | 2015-12-29 |
JP2009108377A (ja) | 2009-05-21 |
US20100212590A1 (en) | 2010-08-26 |
TWI449805B (zh) | 2014-08-21 |
KR20120135436A (ko) | 2012-12-13 |
JP5211642B2 (ja) | 2013-06-12 |
EP2204464A4 (en) | 2010-10-27 |
EP2204464B1 (en) | 2013-10-30 |
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