WO2014155944A1 - 溶融Al-Zn系めっき鋼板及びその製造方法 - Google Patents
溶融Al-Zn系めっき鋼板及びその製造方法 Download PDFInfo
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- WO2014155944A1 WO2014155944A1 PCT/JP2014/000801 JP2014000801W WO2014155944A1 WO 2014155944 A1 WO2014155944 A1 WO 2014155944A1 JP 2014000801 W JP2014000801 W JP 2014000801W WO 2014155944 A1 WO2014155944 A1 WO 2014155944A1
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- 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
- C23C2/12—Aluminium or alloys based thereon
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- 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
- B32B15/012—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 aluminium or an aluminium alloy
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- C22C21/00—Alloys based on aluminium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- C22C21/00—Alloys based on aluminium
- C22C21/10—Alloys based on aluminium with zinc as the next major constituent
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- 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
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
- C23C2/28—Thermal after-treatment, e.g. treatment in oil bath
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- 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
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- 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
- C23C2/405—Plates of specific length
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- 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
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
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- 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
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
- C23C30/005—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/1275—Next to Group VIII or IB metal-base component
- Y10T428/12757—Fe
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
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- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12785—Group IIB metal-base component
- Y10T428/12792—Zn-base component
- Y10T428/12799—Next to Fe-base component [e.g., galvanized]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12972—Containing 0.01-1.7% carbon [i.e., steel]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12972—Containing 0.01-1.7% carbon [i.e., steel]
- Y10T428/12979—Containing more than 10% nonferrous elements [e.g., high alloy, stainless]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12993—Surface feature [e.g., rough, mirror]
Definitions
- the present invention relates to a molten Al—Zn plated steel sheet having excellent post-painting corrosion resistance and a method for producing the same.
- a molten Al—Zn-based plated steel sheet for example, a molten Al—Zn-based plated steel sheet containing 25 to 90% by mass of Al in a zinc-based plated layer exhibits excellent corrosion resistance as compared with a hot-dip galvanized steel sheet.
- this hot-dip Al-Zn-based plated steel sheet uses a thin steel sheet obtained by hot rolling or cold rolling a steel slab as a base steel sheet, and the base steel sheet is recrystallized and annealed in an annealing furnace of a continuous hot-dip coating line. And a hot dipping process.
- the formed Al—Zn-based plating layer includes an alloy layer present at the interface with the base steel plate and an upper layer present thereon.
- the upper layer mainly comprises Zn in a supersaturated portion and Al is dendrite solidified ( ⁇ -Al phase) and the remaining dendritic gap (Zn rich phase).
- the dendrite solidified portion is in the thickness direction of the plating layer.
- This characteristic film structure of the upper layer complicates the corrosion progress path from the surface and makes it difficult for the corrosion to easily reach the base steel plate.
- the hot-dip Al—Zn-based plated steel sheet can have excellent corrosion resistance as compared with a hot-dip galvanized steel sheet having the same plating layer thickness.
- the plating bath contains inevitable impurities, Fe eluted from the steel plate, equipment in the plating bath, and the like, and Si is usually added to suppress excessive alloy layer growth.
- This Si is present in the form of an intermetallic compound in the alloy layer, or in the form of an intermetallic compound, solid solution or simple substance in the upper layer.
- This Si action suppresses the growth of the alloy layer at the interface of the molten Al—Zn-based plated steel sheet, and the alloy layer thickness is about 1 to 5 ⁇ m. If the plating layer thickness is the same, the thinner the alloy layer, the thicker the upper layer that is effective for improving the corrosion resistance. Therefore, suppressing the growth of the alloy layer contributes to the improvement of the corrosion resistance.
- the alloy layer is harder than the upper layer and acts as a starting point of cracks during processing, the suppression of the growth of the alloy layer also reduces the occurrence of cracks and brings about the effect of improving bending workability. And since the base steel plate is exposed and the generated crack portion is inferior in corrosion resistance, suppressing the growth of the alloy layer and suppressing the generation of cracks also improves the corrosion resistance of the bent portion.
- the plated steel sheet When using hot-dip Al-Zn-based plated steel sheet as an automobile outer panel, the plated steel sheet is supplied to automobile manufacturers, etc. in a state where it has been subjected to plating in a continuous hot-dip plating facility, and after it is processed into a panel part shape, it is converted into a chemical. In general, three-coat coating for automobiles such as electrodeposition coating, intermediate coating, and top coating is applied. However, the outer panel using the hot-dip Al-Zn plated steel sheet is caused by the plating layer with a unique phase structure consisting of the two phases of ⁇ -Al phase and Zn-rich phase when the coating film is damaged.
- a hot-dip plated steel sheet is generally provided to a construction company or the like in a state where a base coat or top coat is applied, and is used after being sheared to a required size. For this reason, the end surface of the steel plate which is not necessarily coated is exposed, and the swelling of the coating film called edge creep may occur from this point.
- Patent Document 1 Mg or Sn is further added to the plating composition, and Mg compounds such as Mg 2 Si, MgZn 2 and Mg 2 Sn are formed in the plating layer.
- Mg compounds such as Mg 2 Si, MgZn 2 and Mg 2 Sn are formed in the plating layer.
- a molten Al—Zn-based plated steel sheet that has improved the occurrence of red rust from the end face of the steel sheet is disclosed.
- the corrosion resistance corrosion resistance after painting
- the molten Al—Zn-based plated steel sheet may be used without being coated in the building materials and home appliance fields. Especially, when it is used for a wall material, a back plate of home appliances, and the like, the surface of the plated steel sheet is exposed to the human eye, so a high appearance quality is required.
- the appearance quality mainly means that there is no unevenness in the pattern and color tone in addition to the presence or absence of foreign matter adhesion, non-plating, scratches, and the like. The latter pattern and color tone are more strongly required when the molten Al—Zn-based plated steel sheet is used without coating.
- the surface after plating may gradually turn black (blackening) depending on the component composition of plating. For example, blackening may occur even in a hot-dip Al—Zn-based steel sheet to which Sn is added as disclosed in Patent Document 1. As described above, there is a problem that it is impossible to apply all the molten Al—Zn-based plated steel sheets to applications that are used without coating.
- the present invention has been made in view of such circumstances, and an object of the present invention is to provide a molten Al—Zn plated steel sheet having excellent post-coating corrosion resistance, and a method for producing the same.
- the inventors of the present invention have made extensive studies to solve the above problems. As a result, it has been found that by adding any component of Sn, In and Bi in addition to Al to the plating layer, excellent post-coating corrosion resistance that has not been achieved in the past can be obtained. Further, it was found that the plating layer can be softened by improving the Vickers hardness of the plating layer within a specific range as necessary, and the corrosion resistance of the processed part can be improved with good workability.
- a hot-dip Al—Zn-based plated steel sheet comprising a plated layer containing at least one selected from the group consisting of:
- the plating layer is selected from the group consisting of Sn: 0.01 to 1.0 mass%, In: 0.01 to 1.0 mass%, and Bi: 0.01 to 1.0 mass%.
- the plating bath is selected from the group consisting of Sn: 0.01 to 1.0%, In: 0.01 to 1.0%, and Bi: 0.01 to 1.0% by mass.
- a molten Al—Zn-based plated steel sheet having excellent corrosion resistance, particularly post-coating corrosion resistance can be obtained. Further, by making the molten Al—Zn-based plated steel sheet of the present invention a high-strength steel sheet, it is possible to achieve both weight reduction and excellent corrosion resistance in the automobile field. In addition, the life of the building can be extended by using it as a roofing material or wall material in the building material field.
- the hot-dip Al—Zn-based plated steel sheet of the present invention includes Sn: 0.01 to 2.0%, In: 0.01 to 10%, and Bi: 0.01 to 2 in addition to Al in the plating layer.
- Sn 0.01 to 2.0%
- In 0.01 to 10%
- Bi 0.01 to 2
- the coated steel sheet using the conventional Al-Zn-based plated steel sheet as the base material causes selective corrosion of the Zn-rich phase at the coating film / plating interface starting from the scratch when the coating film is damaged. Proceeds deep into the well-painted area and causes large film swelling. Thereby, corrosion resistance after painting is inferior.
- the Sn, In, and Bi contents in the plating layer were Sn: 0.01 to 2.0%, In: 0.01 to 10%, and Bi: 0.01 to 2.0%, respectively. Because of the reason. When Sn, Bi, and In are less than 0.01%, the Al oxide film that can suppress the selective corrosion of the Zn-rich phase does not occur, so that it is not possible to improve the corrosion resistance after painting. On the contrary, when Sn and Bi each exceed 2.0% or In exceeds 10%, the Al oxide film is severely broken, and the solubility of the entire plating layer is excessively increased.
- Sn: In and Bi are respectively Sn: 0.01 to 2.0%, In: 0.01 to 10%, Bi: 0.01 to It is necessary to contain in the range of 2.0%.
- the Sn, In and Bi contents in the plating layer are preferably in the range of 0.01 to 1.0%, respectively 0.01% More preferably, the content is in the range of ⁇ 0.10%.
- the molten Al—Zn-based plated steel sheet of the present invention is a molten Al—Zn-based plated steel sheet containing 25 to 90% of Al in the plating layer. Further, from the balance between corrosion resistance and operation, the preferable range of the Al content in the plating layer is 45 to 70%, and the more preferable range is 50 to 60%. When the Al content in the plating layer is 25% or more, the above-described dendritic solidification of Al occurs in the upper layer existing on the alloy layer existing at the interface with the base steel plate.
- the upper layer is mainly composed of Zn in a supersaturated state
- Al is composed of a dendrite solidified part and the remaining dendrite gap part
- the dendrite solidified part is laminated in the film thickness direction of the plating layer, and has a structure with excellent corrosion resistance.
- Al is preferably made 45% or more.
- Al exceeds 90% the amount of Zn having a sacrificial anticorrosive action for Fe is small, so that the corrosion resistance deteriorates when the steel substrate is exposed. In general, the smaller the amount of plating, the easier the steel substrate is exposed.
- Al is preferably made 70% or less. Further, in Al—Zn-based hot dipping, as the Al content increases, the temperature of the plating bath (hereinafter referred to as “bath temperature”) increases, so there are concerns about operational problems. If it is a content, the bath temperature is moderate and there is no problem.
- base steel plate used in the hot-dip Al—Zn plated steel sheet of the present invention there is no particular limitation on the type of base steel plate used in the hot-dip Al—Zn plated steel sheet of the present invention.
- a hot-rolled steel plate or steel strip that has been pickled and descaled, or a cold-rolled steel plate or steel strip obtained by cold rolling them can be used.
- the plated steel sheet of the present invention preferably contains 10% or more of Zn in the plating layer, more preferably 10 to 75%, more preferably 30 to 55%, and more preferably 40 to 50%. It is particularly preferable to contain it. Since Zn is 10% or more and the plating exhibits a sufficient sacrificial anticorrosive action for Fe, corrosion resistance is sufficiently obtained when the steel substrate is exposed. On the other hand, by making it 75% or less, excessive sacrificial anticorrosive action is prevented, and deterioration of corrosion resistance due to promotion of dissolution of the plating layer is prevented.
- the plated steel sheet of the present invention preferably contains 0.1 to 10% of Si in the plating layer.
- Si is added to the plating bath for the purpose of suppressing the growth of the interfacial alloy layer formed at the interface with the base steel plate and improving the corrosion resistance and workability, and is contained in the plating layer.
- the steel sheet is immersed in the plating bath and at the same time Fe on the steel sheet surface and Al in the bath Si undergoes an alloying reaction to form Fe-Al and / or Fe-Al-Si compounds.
- the formation of the Fe—Al—Si interface alloy layer suppresses the growth of the interface alloy layer.
- the Si content in the plating bath 0.1% or more, it is possible to sufficiently suppress the growth of the interface alloy layer.
- the Si content in the plating bath is 10% or less, it becomes difficult to precipitate as a Si phase that becomes a propagation path of cracks in the manufactured plating layer and deteriorates workability. Therefore, the preferable range of the Si content in the plating bath is 0.1 to 10%.
- the composition of the plating layer is almost equivalent to the composition of the plating bath, so the Si content in the plating layer is equivalent to the preferred range of the Si content in the plating bath and is 0.1 to 10 % Is preferred.
- the plating layer contains 0.01 to 10% in total of one or more elements selected from the group consisting of Mn, V, Cr, Mo, Ti, Ni, Co, Sb, Zr and B It is preferable to do. This is because the stability of the corrosion product can be improved and the effect of delaying the progress of corrosion can be exhibited.
- the component composition of the plating layer can be confirmed by, for example, immersing and dissolving the plating layer in an aqueous solution such as hydrochloric acid and performing the ICP emission spectroscopic analysis or atomic absorption analysis.
- This method is merely an example, and any method may be used as long as the component composition of the plating layer can be accurately quantified, and the method is not particularly limited.
- the plating layer preferably has an average Vickers hardness of 50 to 100 Hv. This is because by setting the Vickers hardness within the above range, excellent post-processing corrosion resistance can be realized. Specifically, by making the Vickers hardness of the plating layer as soft as 100 Hv or less on average, when processing such as bending is performed, the plating layer follows the base steel plate, and generation of cracks can be suppressed. As a result, the same degree of corrosion resistance as that of the flat plate portion can be secured in the bent portion. Further, by setting the lower limit of the Vickers hardness to 50 Hv, it is possible to prevent the plating layer from adhering to a mold or the like during the molding process.
- the average Vickers hardness of the plated layer for example, after polishing the plated layer cross section of the molten Al—Zn-based plated steel sheet, a cross section of an arbitrary portion on the upper layer side of the plated layer using a micro Vickers hardness meter It is obtained by measuring several points with low load from the direction and calculating the average.
- the upper and lower limits of the number of measurement points are not particularly defined, but 10 or more are preferable from the viewpoint of measurement accuracy, and the more is more preferable. This method is merely an example, and any method may be used as long as it can accurately quantify the average Vickers hardness of the plating layer, and is not particularly limited.
- the upper and lower limits of the low load are not particularly defined, but if the load is larger than an appropriate load, the indentation becomes large, so that it is easily affected by the hardness of the base steel plate. Therefore, 50 gf or less is preferable from the viewpoint of avoiding the influence of the base steel sheet, and 10 gf or less is more preferable.
- the coating amount of the plated layer of the hot-dip Al—Zn plated steel sheet of the present invention is preferably 35 to 150 g / m 2 per side. If it is 35 g / m 2 or more, excellent corrosion resistance is obtained, and if it is 150 g / m 2 or less, excellent workability is obtained. Further, from the viewpoint of obtaining better corrosion resistance and workability, the adhesion amount is preferably 40 to 110 g / m 2, and more preferably 40 to 80 g / m 2 .
- the hot-dip Al—Zn-based plated steel sheet of the present invention is manufactured in a continuous hot-dip plating facility, and all can be performed by a conventional method except for the composition management of the plating bath.
- the Al content in the plating bath is 25 to 90% by mass, and in addition, Sn: 0.01 to 2.0%, In: 0.01 to 10%, and Bi: 0.01 to 2.0%
- Sn 0.01 to 2.0%
- Bi 0.01 to 2.0%
- some elements such as Mn, V, Cr, Mo, Ti, Ni, Co, Sb, Zr, and B are added to the plating bath. This is possible as long as the effects of the present invention are not impaired.
- the inclusion of 0.01 to 10% of one or more elements selected from Mn, V, Cr, Mo, Ti, Ni, Co, Sb, Zr and B in the plating bath As described above, it is preferable because the corrosion resistance of the manufactured molten Al—Zn-based plated steel sheet can be improved.
- the cooled steel sheet is held at a temperature of 250 to 375 ° C. for 5 to 60 seconds. Is preferred. In this case, it is possible to manufacture an Al—Zn-based plated steel sheet more efficiently than the case where the batch-type heating equipment is further combined with the hot dipping equipment.
- the reason why the steel sheet is held at a temperature of 250 to 375 ° C. for 5 to 60 seconds (temperature holding step) is that the plating layer is not solidified in a non-equilibrium state by rapid cooling and is introduced into the plating layer. Since the strain is released and the two-phase separation of the Al-rich phase and the Zn-rich phase is promoted in Al—Zn-based plating, the plating layer can be softened. As a result, the workability of the steel sheet can be improved. In addition, the softened plating layer can improve the corrosion resistance of the processed portion by reducing the number and width of cracks generated during processing as compared with the conventional hard plating layer.
- the holding temperature is 250 ° C. or higher and the holding time is 5 seconds or longer, the hot dip coating layer does not cure too quickly, and the strain is sufficiently released and the Al-rich phase and Zn-rich phase are separated. Therefore, desired workability can be obtained.
- the holding temperature is 375 ° C. or lower, the cooling before the temperature holding step is sufficient, and the plating is performed when the steel strip after plating carried out from the hot dipping bath in the continuous hot dipping equipment comes into contact with the roll. Is preferable because it does not adhere to the roll and a metal pickup in which a part of the plating layer is peeled off does not occur.
- the holding time is 60 seconds or less, the holding time is not too long and is suitable for production in a continuous hot dip plating facility.
- the holding temperature of the plated steel sheet in the temperature holding step is preferably 300 to 375 ° C, and more preferably 350 to 375 ° C.
- the holding time of the plated steel sheet is preferably 5 to 30 seconds, and more preferably 5 to 20 seconds.
- a molten Al-Zn-based plated steel sheet having excellent post-coating corrosion resistance and excellent workability due to good workability It can be efficiently manufactured with continuous hot dipping equipment.
- Example 1 Samples 1 to 31
- a cold-rolled steel sheet with a thickness of 0.8 mm produced by a conventional method was used as the base steel sheet, and the bath temperature of the plating bath was 600 ° C by a continuous hot-dip plating facility.
- the amount of plating was 50 g / m 2 per side, that is, 100 g / m 2 on both sides.
- the samples 21 to 28 were subjected to the temperature holding treatment shown in Example 2 to be described later.
- Electrodeposition coating Electrodeposition coating made by Kansai Paint Co., Ltd .: GT-100 was used, and the electrodeposition coating was applied so that the film thickness was 15 ⁇ m.
- Intermediate coating Spray coating was performed using TP-65-P, an intermediate coating made by Kansai Paint Co., Ltd. so that the film thickness was 30 ⁇ m.
- Top coating Spray coating was performed using an intermediate coating paint: Neo6000 manufactured by Kansai Paint Co., Ltd. so that the film thickness was 30 ⁇ m. Thereafter, as shown in FIG.
- the sample of the present invention sample unlike the sample of the comparative example, had a maximum coating swell width of 1.5 mm or less, so that a molten Al—Zn-based plated steel sheet having excellent corrosion resistance after coating was obtained.
- Example 2 Among the samples of the present invention produced in Example 1, the hot-dip Al—Zn-based plated steel sheets of Samples 21 to 28 of the present invention were subjected to the above-described hot dipping treatment and cooled to 370 ° C. The temperature holding treatment was performed under the conditions shown in 2. Thereafter, the following evaluation was performed on samples 3 to 5, 10 to 12, 17, 18, and 21 to 31.
- the sample that was kept at a temperature of 250 to 375 ° C. for 5 seconds or more after plating had a softer Vickers hardness of 100 Hv or less than the sample that was not kept at temperature. It turns out that it is excellent in post-processing corrosion resistance which is an effect.
- the molten Al—Zn plated steel sheet of the present invention has excellent post-painting corrosion resistance and can be applied in a wide range of fields such as automobiles, home appliances, and building materials.
- the automobile field when applied to a high-strength steel sheet, it can be used as a surface-treated steel sheet that achieves weight reduction and high corrosion resistance of the automobile.
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Abstract
Description
一般的に、この溶融Al-Zn系めっき鋼板は、鋼スラブを熱間圧延若しくは冷間圧延した薄鋼板を下地鋼板として用い、該下地鋼板を連続式溶融めっきラインの焼鈍炉にて再結晶焼鈍及び溶融めっき処理を行うことによって製造される。この形成されたAl-Zn系めっき層は、下地鋼板との界面に存在する合金層と、その上に存在する上層とを備えている。さらに、上層は、主としてZnを過飽和に含有しAlがデンドライト凝固した部分(α-Al相)と、残りのデンドライト間隙の部分(Znリッチ相)からなり、デンドライト凝固部分はめっき層の膜厚方向に積層している。この上層の特徴的な皮膜構造により、表面からの腐食進行経路が複雑になり腐食が容易に下地鋼板に到達しにくくなる。この結果、溶融Al-Zn系めっき鋼板は、めっき層の厚みが同一の溶融亜鉛めっき鋼板に比べ優れた耐食性を有することが可能である。
しかしながら、特許文献1に開示される溶融Al-Zn系めっき鋼板に塗装を施した場合、後に塗膜に損傷が生じたときの耐食性(塗装後耐食性)は、依然として解消されていなかった。
さらに、溶融Al-Zn系めっき鋼板の場合、めっきの成分組成によって、めっき後の表面が徐々に黒色に変化(黒変)することがあった。例えば、特許文献1に示されたSnを添加した溶融Al-Zn系めっき鋼板でも、黒変が発生する場合がある。このように、無塗装で使用する用途に全ての溶融Al-Zn系めっき鋼板を適用することができないという問題があった。
さらに、必要に応じて、めっき層のビッカース硬度を特定の範囲にすることで、めっき層を軟質化し、良好な加工性により加工部耐食性を向上できることを見出した。
[1]質量%で、Al:25~90%を含有し、さらに、Sn:0.01~2.0%、In:0.01~10%、及びBi:0.01~2.0%からなる群より選択される一種以上を含有しためっき層を有することを特徴とする溶融Al-Zn系めっき鋼板。
本発明の溶融Al-Zn系めっき鋼板は、めっき層中に、Alに加えて、Sn:0.01~2.0%、In:0.01~10%、及びBi:0.01~2.0%からなる群より選択される一種以上を含有する。めっき層中にSn、In及びBiのうちの少なくとも一種の元素を含有することで、本発明で課題とする塗装後耐食性の改善が可能となる。
前記めっき層中のSn、In、Bi含有量をそれぞれ、Sn:0.01~2.0%、In:0.01~10%、Bi:0.01~2.0%としたのは次の理由からである。それぞれ、Sn、Bi、Inが0.01%未満では、上記したZnリッチ相の選択腐食を抑制可能とするAl酸化膜の破壊が起こらないため、塗装後耐食性の向上は望めない。逆に、Sn、Biがそれぞれ2.0%超え、又はInが10%超えの場合には、Al酸化膜の破壊が激しく起こり、めっき層全体の溶解性が過度に上昇する。その結果、めっき層を均一腐食させても、その溶解速度が大きくなるため、塗装に大きな膨れを生じ、塗装後耐食性が劣化する。よって、優れた塗装後耐食性を安定的に得るためには、Sn、In、Biをそれぞれ、Sn:0.01~2.0%、In:0.01~10%、Bi:0.01~2.0%の範囲で含有する必要がある。
さらに、それぞれ1.0%以下とすることで、塗装を施さず使用する場合でも表面外観が問題となることがない。そのため、塗装後耐食性及びめっき外観を両立するためには、めっき層中のSn、In及びBi含有量を、それぞれ0.01~1.0%の範囲とすることが好ましく、それぞれ0.01%~0.10%の範囲とすることがより好ましい。
具体的には、前記めっき層のビッカース硬度を平均で100Hv以下と軟質にすることで、曲げなどの加工を行った際、めっき層が下地鋼板に追従し、クラックの発生を抑制できる。その結果、曲げ加工部においても平板部と同程度の耐食性を確保できる。また、前記ビッカース硬度の下限を50Hvとすることで、成形加工時にめっき層が金型等に凝着するのを防止することができる。
測定点数の上下限については特に定めないが、測定の精度の観点から10点以上が好ましく、より多いほど好ましい。この方法はあくまでも一例であり、めっき層の平均ビッカース硬度を正確に定量できる方法であればどのような方法でも良く、特に限定するものではない。
また、低荷重の上下限については特に定めないが、適正な荷重よりも大きいと圧痕が大きくなることで下地鋼板の硬さの影響を受けやすくなる。よって下地鋼板の影響を避ける観点から50gf以下が好ましく、10gf以下がより好ましい。
本発明の溶融Al-Zn系めっき鋼板は、連続式溶融めっき設備で製造され、めっき浴の組成管理以外は、全て常用の方法で行うことができる。
また、より優れた加工性を実現する点からは、前記温度保持工程におけるめっき鋼板の保持温度は、300~375℃であることが好ましく、350~375℃であることがより好ましい。さらに、連続式溶融めっき設備における製造性(温度保持工程にかかるコスト)を考慮すると、めっき鋼板の保持時間は、5~30秒であることが好ましく、5~20秒であることがより好ましい。
上記のように、めっき浴の組成管理とめっき後の温度保持工程を組み合わせることで、塗装後耐食性に優れるとともに、良好な加工性により加工部耐食性にも優れた溶融Al-Zn系めっき鋼板を、連続的な溶融めっき設備で効率的に製造することができる。
(実施例1:サンプル1~31)
サンプルとなる全ての溶融Al-Zn系めっき鋼板について、常法で製造した板厚0.8mmの冷延鋼板を下地鋼板として用い、連続式溶融めっき設備によって、めっき浴の浴温を600℃、めっき付着量を片面あたり50g/m2、すなわち両面で100g/m2の条件で製造した。
なお、サンプル21~28の溶融Al-Zn系めっき鋼板については、後述の実施例2に示す温度保持処理を施した。
サンプルとなる溶融Al-Zn系めっき鋼板を、それぞれ100mmΦに打ち抜き、35%の塩酸水溶液に浸漬してめっき層を溶解させた後、溶解液の組成をICP発光分光分析で定量化することで確認した。各サンプルの組成を表1に示す。
サンプルとなる溶融Al-Zn系めっき鋼板をそれぞれ90mm×70mmのサイズに剪断後、自動車外板用塗装処理と同様に、化成処理としてリン酸亜鉛処理を行った後、電着塗装、中塗り、及び上塗り塗装を施した。ここで、リン酸亜鉛処理、電着塗装、中塗り塗装及び上塗り塗装は以下に示す条件で行った。
○リン酸亜鉛処理:日本パーカライジング社製の脱脂剤:FC-E2001、表面調整剤:PL-X、および化成処理剤:PB-AX35M(温度:35℃)を用いて、化成処理液のフリーフッ素濃度を200質量ppm、化成処理液の浸漬時間を120秒の条件で化成処理を施した。
○電着塗装:関西ペイント社製の電着塗料:GT-100を用いて、膜厚が15μmとなるように電着塗装を施した。
○中塗り塗装:関西ペイント社製の中塗り塗料:TP-65-Pを用いて、膜厚が30μmとなるようにスプレー塗装を施した。
○上塗り塗装:関西ペイント社製の中塗り塗料:Neo6000を用いて、膜厚が30μmとなるようにスプレー塗装を施した。
その後、図1に示すとおり、評価面の端部5mm、及び非評価面(背面)をテープでシール処理を行った後、評価面の中央にカッターナイフでめっき鋼板の地鉄に到達する深さまで、長さ60mm、中心角90°のクロスカット傷を加えたものを塗装後耐食性の評価用サンプルとした。
上記評価用サンプルを用いて図2に示すサイクルで腐食促進試験を実施した。腐食促進試験を湿潤からスタートし、60サイクル後まで行った後、傷部からの塗膜膨れが最大である部分の塗膜膨れ幅(最大塗膜膨れ幅:傷部を中央にした片側の最大塗膜膨れ幅)を測定し、塗装後耐食性を下記の基準で評価した。評価結果を表1に示す。
○:最大塗膜膨れ幅≦1.5mm
×:最大塗膜膨れ幅>1.5mm
サンプルとなる溶融Al-Zn系めっき鋼板について、めっき処理を施した後1時間以内に、雰囲気:大気、温度:20℃、相対湿度:50%に調節した恒温恒湿槽内に入れた。以後、90日間放置した後、サンプルを取り出しめっき表面の目視観察を行い、下記の基準で外観品位を評価した。評価結果を表1に示す。
○:黒変が認められない
△:黒変は認められるが、塗装を施さない用途で特に問題にならない
×:黒変が塗装を施さない用途で問題になる
また、本発明例のサンプルの中において、めっき層中のSn含有量、又はIn含有量、又はBi含有量をそれぞれ適切な範囲に制御することで、優れた外観品位と塗装後耐食性との両立が可能な溶融Al-Zn系めっき鋼板が得られることがわかる。
実施例1で製造された本発明例のサンプルのうち、本発明例のサンプル21~28の溶融Al-Zn系めっき鋼板については、上述した溶融めっき処理を施し、370℃まで冷却した後、表2に示す条件で温度保持処理を施した。
その後、サンプル3~5、10~12、17、18及び21~31について、以下の評価を行った。
上述した溶融Al-Zn系めっき鋼板の各サンプルについて、めっき層断面を研磨した後、マイクロビッカース硬度計を用いて、めっき層の上層側の任意の箇所を断面方向から荷重5gfで各20点ずつビッカース硬度を測定した。測定した20点の平均値をめっき層の硬度として算出した。算出結果を表2に示す。
上述した溶融Al-Zn系めっき鋼板の各サンプルについて、同板厚の板を内側に4枚挟んで180°曲げの加工(4T曲げ)を施した後、曲げの外側にJIS Z 2371-2000に準拠した塩水噴霧試験を行った。各サンプルの赤錆が発生するまでの時間を測定し、以下の基準により評価した。評価結果を表2に示す。
○:赤錆発生時間≧4000時間
×:赤錆発生時間<4000時間
Claims (12)
- 質量%で、Al:25~90%を含有し、さらにSn:0.01~2.0%、In:0.01~10%、及びBi:0.01~2.0%からなる群より選択される一種以上を含有しためっき層を有することを特徴とする溶融Al-Zn系めっき鋼板。
- 前記めっき層が、質量%で、さらにZnを10%以上含有することを特徴とする請求項1に記載の溶融Al-Zn系めっき鋼板。
- 前記めっき層が、質量%で、さらにSiを0.1~10%を含有することを特徴とする請求項1又は2に記載の溶融Al-Zn系めっき鋼板。
- 前記めっき層のAl含有量が45~70質量%であることを特徴とする請求項1~3のいずれか一項に記載の溶融Al-Zn系めっき鋼板。
- 前記めっき層は、Sn:0.01~1.0質量%、In:0.01~1.0質量%及びBi:0.01~1.0質量%からなる群より選択される一種以上を含有することを特徴とする請求項1~4のいずれか一項に記載の溶融Al-Zn系めっき鋼板。
- 前記めっき層のビッカース硬度が、平均で50~100Hvであることを特徴とする請求項1~5のいずれか一項に記載の溶融Al-Zn系めっき鋼板。
- 連続式の溶融めっき設備において、質量%で、Al:25~90%を含有し、さらに、Sn:0.01~2.0%、In:0.01~10%、及びBi:0.01~2.0%からなる群より選択される一種以上を含有し、残部がZn及び不可避的不純物からなるめっき浴中に、下地鋼板を浸漬させて溶融めっきを施すことを特徴とする溶融Al-Zn系めっき鋼板の製造方法。
- 前記めっき浴が、質量%で、Znを10%以上含有することを特徴とする請求項7に記載の溶融Al-Zn系めっき鋼板の製造方法。
- 前記めっき浴が、質量%で、Siを0.1~10%を含有することを特徴とする請求項7又は8に記載の溶融Al-Zn系めっき鋼板の製造方法。
- 前記めっき浴が、質量%で、Sn:0.01~1.0%、In:0.01~1.0%及びBi:0.01~1.0質量%からなる群より選択される一種以上を含有することを特徴とする請求項7~9のいずれか一項に記載の溶融Al-Zn系めっき鋼板の製造方法。
- 前記溶融めっき後の鋼板を250~375℃の温度で5~60秒間保持することを特徴とする請求項7~10のいずれか1項に記載の溶融Al-Zn系めっき鋼板の製造方法。
- 前記溶融めっき後の鋼板を300~375℃で5~60秒間保持することを特徴とする請求項11に記載の溶融Al-Zn系めっき鋼板の製造方法。
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KR1020157024573A KR101736737B1 (ko) | 2013-03-28 | 2014-02-17 | 용융 Al-Zn계 도금 강판 및 그의 제조 방법 |
AU2014240655A AU2014240655B2 (en) | 2013-03-28 | 2014-02-17 | Hot-dip Al-Zn alloy coated steel sheet and method for producing same |
MX2015013517A MX2015013517A (es) | 2013-03-28 | 2014-02-17 | Lamina de acero recubierta de aleacion de ai-zn por inmersion en caliente y metodo para la produccion de la misma. |
CN201480016958.8A CN105051239B (zh) | 2013-03-28 | 2014-02-17 | 热浸镀Al-Zn系钢板及其制造方法 |
MYPI2015702509A MY177462A (en) | 2013-03-28 | 2014-02-17 | Hot-dip al-zn alloy coated steel sheet and method for producing same |
US14/763,913 US9758853B2 (en) | 2013-03-28 | 2014-02-17 | Hot-dip Al—Zn alloy coated steel sheet and method for producing same |
EP14775425.3A EP2980261B1 (en) | 2013-03-28 | 2014-02-17 | Molten-al-zn-plated steel sheet and method for manufacturing same |
JP2014527419A JP5994856B2 (ja) | 2013-03-28 | 2014-02-17 | 溶融Al−Zn系めっき鋼板及びその製造方法 |
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WO2018169085A1 (ja) | 2017-03-17 | 2018-09-20 | 新日鐵住金株式会社 | めっき鋼板 |
WO2018169084A1 (ja) | 2017-03-17 | 2018-09-20 | 新日鐵住金株式会社 | めっき鋼板 |
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JP2016060946A (ja) * | 2014-09-18 | 2016-04-25 | Jfeスチール株式会社 | 溶融Al系めっき鋼板 |
JP6337711B2 (ja) * | 2014-09-18 | 2018-06-06 | Jfeスチール株式会社 | 溶融Al系めっき鋼板 |
CN105483590B (zh) * | 2015-12-20 | 2018-06-15 | 安徽伟宏钢结构集团股份有限公司 | 一种钢构件热浸镀锌工艺 |
CN107641781B (zh) * | 2017-09-15 | 2019-04-23 | 中国矿业大学 | 一种清洁的热浸镀锌合金方法 |
CN108315684B (zh) * | 2018-04-24 | 2020-11-24 | 中国科学院力学研究所 | 一种圆环链的渗铝方法 |
CN108977695B (zh) * | 2018-09-30 | 2020-12-01 | 济南大学 | 一种含钛和锑的热浸镀锌铝镁合金及其制备方法 |
DE102020107278A1 (de) * | 2020-03-17 | 2021-09-23 | Airbus Defence and Space GmbH | Korrosionsschützende Beschichtung und mit einer korrosionsschützenden Beschichtung beschichteter Gegenstand insbesondere für die Verwendung an einem Flugzeug |
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KR20150119063A (ko) | 2015-10-23 |
KR101736737B1 (ko) | 2017-05-17 |
JP5994856B2 (ja) | 2016-09-21 |
AU2014240655B2 (en) | 2016-08-18 |
CN105051239A (zh) | 2015-11-11 |
MY177462A (en) | 2020-09-16 |
AU2014240655A1 (en) | 2015-08-27 |
JPWO2014155944A1 (ja) | 2017-02-16 |
CN105051239B (zh) | 2018-09-18 |
EP2980261B1 (en) | 2019-07-31 |
WO2014155944A8 (ja) | 2015-07-23 |
EP2980261A4 (en) | 2016-04-13 |
MX2015013517A (es) | 2016-02-05 |
US9758853B2 (en) | 2017-09-12 |
EP2980261A1 (en) | 2016-02-03 |
US20150361538A1 (en) | 2015-12-17 |
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