WO2023181427A1 - 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 PDF

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WO2023181427A1
WO2023181427A1 PCT/JP2022/017434 JP2022017434W WO2023181427A1 WO 2023181427 A1 WO2023181427 A1 WO 2023181427A1 JP 2022017434 W JP2022017434 W JP 2022017434W WO 2023181427 A1 WO2023181427 A1 WO 2023181427A1
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steel sheet
plating film
hot
dip
mass
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PCT/JP2022/017434
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English (en)
French (fr)
Japanese (ja)
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利彦 大居
一郎 芦刈
英嗣 藤沢
洋一 飛山
修 進
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Ｊｆｅ鋼板株式会社
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Publication of WO2023181427A1 publication Critical patent/WO2023181427A1/ja

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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
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C21/00—Alloys based on aluminium
    • C22C21/10—Alloys based on aluminium with zinc as the next major constituent
    • 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
    • C23C2/04—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
    • 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

Definitions

  • the present invention relates to a hot-dip Al-Zn plated steel sheet with excellent bending workability and corrosion resistance of the bent portion, and a method for manufacturing the same.
  • Hot-dip Al-Zn coated steel sheets are known to exhibit high corrosion resistance among hot-dip galvanized steel sheets because they have both the sacrificial corrosion protection of Zn and the high corrosion resistance of Al. Therefore, hot-dip Al-Zn plated steel sheets are often used in the field of building materials such as roofs and walls that are exposed to the outdoors for long periods of time, and in the field of civil engineering and construction such as guardrails, wiring piping, and soundproof walls.
  • the demand for materials with excellent corrosion resistance and maintenance-free materials is increasing in harsher usage environments, such as acid rain caused by air pollution, the spraying of snow-melting agents to prevent roads from freezing in snow-covered areas, and coastal area development.
  • demand for hot-dip Al-Zn coated steel sheets has increased in recent years.
  • the plating film of the hot-dip Al-Zn plated steel sheet consists of a main layer and an interfacial alloy layer existing at the interface between the base steel sheet and the main layer, and the main layer mainly contains Zn in a supersaturated state and Al solidifies into dendrites.
  • the ⁇ -Al phase has a structure in which multiple layers are stacked in the thickness direction of the plating film. There is. This characteristic film structure complicates the corrosion progression path from the surface, making it difficult for corrosion to easily reach the underlying steel sheet. Superior corrosion resistance can be achieved compared to hot-dip galvanized steel sheets.
  • hot-dip Al-Zn-based plated steel sheets have excellent corrosion resistance, they have a problem in that the coating film is harder than hot-dip galvanized steel sheets, and their bending workability is inferior. Therefore, when a steel plate is bent, cracks are likely to occur in the plating film at the tip of the bent portion. These cracks will of course damage the appearance, but if the cracks reach halfway through the plating film, the plating cover thickness in that area will become thinner, or the cracks will penetrate through the plating film and expose the underlying steel sheet. , etc., which caused the excellent corrosion resistance inherent in hot-dip Al-Zn coated steel sheets to deteriorate significantly in bent parts.
  • Patent No. 3654521 Japanese Patent Application Publication No. 2013-245355
  • the present inventors have developed a molten Al-Zn-based plating having a plating film containing 45 to 65% by mass of Al and 1.0 to 3.0% by mass of Si, with the remainder consisting of Zn, Fe, and unavoidable impurities.
  • the plating film has dendrites mainly composed of Al primary crystals and dendrite gaps containing Al-Zn eutectic.
  • fine Zn precipitates of 100 nm or less in size dotted within the ⁇ -Al phase matrix affect the hardening of dendrites, and by keeping the Zn content in the matrix low.
  • Al-Zn eutectic has a structure in which Al parts and Zn parts are arranged alternately in stripes (hereinafter referred to as "stripe structure"), and when the period is 2 ⁇ m or less, molten Al-Zn Focusing on reducing the bending workability of plated steel sheets, we have also found that by eliminating the striped structure, it is possible to achieve excellent bending workability and corrosion resistance of the processed parts. In addition, they discovered that bending workability can be further improved by keeping the thickness of the interfacial alloy layer, which has a high hardness, to 1 ⁇ m or less.
  • excellent bending workability as used in the present invention refers to bending workability that is practically sufficient, and when evaluating by "T bending", at least “6T no crack", preferably “4T no crack”. "Crack” level is required.
  • T-bending is a 180° bending test conducted with the thickness of the steel plate sandwiched between them. For example, in the case of "6T bending", six plates of the same thickness are sandwiched inside the target material. Make a 180° bend. At this time, "no cracks” refers to a state in which no cracks are observed when the outer tip of the bent portion is observed at 10x magnification using a magnifying glass, for example.
  • the bending test is based on the plating adhesion test described in JIS G 3321 (2019). Incidentally, the bending workability of a normal hot-dip Al-Zn plated steel sheet is ⁇ 12T no crack'' or better, although it depends on the conditions of the plating film, and even ⁇ 10T bending'' often does not result in ⁇ no crack.''
  • the present invention has been made based on the above findings, and the gist thereof is as follows. 1. Formed on the interface side between a plating film containing 45 to 65 mass% Al and 1.0 to 3.0 mass% Si, with the remainder consisting of Zn, Fe, and unavoidable impurities, and the underlying steel sheet of the plating film.
  • a hot-dip Al-Zn based plated steel sheet comprising an interfacial alloy layer containing Fe, Al, Si, Zn and inevitable impurities,
  • the plating film has dendrites mainly consisting of Al primary crystals and dendrite gaps containing Al-Zn eutectic,
  • the Al primary crystal includes an ⁇ -Al phase matrix and Zn precipitates, and the Zn content in the matrix is 30% by mass or less
  • a hot-dip Al-Zn based plated steel sheet characterized in that the thickness of the interfacial alloy layer is 1 ⁇ m or less.
  • the present invention it is possible to provide a hot-dip Al-Zn-based plated steel sheet that is stable and has excellent bending workability and corrosion resistance of the bent portion, and a method for producing the same.
  • the hot-dip Al-Zn plated steel sheet of the present invention has a plating film on the surface of the steel sheet.
  • the plating film contains 45 to 65% by mass of Al and 1.0 to 3.0% by mass of Si, with the remainder essentially consisting of Zn, Fe, and inevitable impurities.
  • the plating film of the hot-dip plated steel sheet has the above-mentioned composition, good corrosion resistance can be achieved.
  • the plating film consists of an interfacial alloy layer existing on the interface side with the base steel plate and a main layer existing on the interfacial alloy layer.
  • the Al content in the plating film is 45 to 65% by mass, preferably 50 to 60% by mass, in view of the balance between corrosion resistance and operational aspects.
  • the Al content in the plating film is at least 45% by mass, dendrite solidification of Al primary crystals occurs, and a structure in which dendrite solidification structures are stacked in the thickness direction of the plating film can be obtained.
  • the corrosion progression path of the plating film becomes complicated, and corrosion resistance can be improved.
  • the more dendrites are stacked the more complicated the corrosion progression path becomes, making it difficult for corrosion to easily reach the base steel plate, and improving corrosion resistance.
  • Si in the plating film is added for the purpose of suppressing the growth of an interfacial alloy layer generated at the interface with the base steel sheet and not deteriorating the adhesion between the plating film and the base steel sheet.
  • the hot-dip Al-Zn coated steel sheet of the present invention when the steel sheet is immersed in an Al-Zn plating bath containing Si, Fe on the surface of the steel sheet and Al and Si in the plating bath undergo an alloying reaction, resulting in Fe -Al-based and/or Fe-Al-Si-based intermetallic compounds are formed in a layered manner at the interface between the base steel sheet and the plating film (an interfacial alloy layer is formed); -The growth rate is slower than that of the Al-based alloy, so the higher the proportion of the Fe-Al-Si-based alloy, the more suppressed the growth of the entire alloy phase can be.
  • the Si content in the plating film needs to be 1.0% by mass or more.
  • the surplus Si that was not consumed during the formation of the interfacial alloy layer is precipitated in the plating film as a Si phase, but the Si phase is electrochemically more noble than the Al primary crystal or Al-Zn eutectic. Since it acts as a cathode, it has the effect of promoting corrosion of the plating film and reducing its corrosion resistance.
  • the Si content in the plating film exceeds 3.0% by mass, not only the aforementioned effect of suppressing the growth of the alloy phase is saturated, but also the amount of the Si phase increases and corrosion is accelerated.
  • the Si content shall be 3.0% by mass or less. From the same viewpoint, the Si content in the plating film is more preferably 2.5% by mass or less.
  • the plating film contains Zn, Fe, and inevitable impurities.
  • some Fe is unavoidably contained when the steel plate or equipment in the bath is eluted into the plating bath, and some is supplied by diffusion from the underlying steel plate during the formation of the interfacial alloy layer. This is a component that is inevitably included in the plating film.
  • Fe in the plating film it is not possible to distinguish and quantify Fe incorporated from the base steel sheet and that eluted from the plating bath.
  • the Fe content in the plating film is usually about 0.3 to 2.0% by mass.
  • examples of unavoidable impurities other than Fe include Cr, Ni, Cu, and the like.
  • the total content of the Fe and unavoidable impurities is not particularly limited, but if excessively contained, it may affect various properties of the plated steel sheet, so the total content should be 5.0% by mass or less. is preferable, and more preferably 3.0% by mass or less.
  • the plating film has a total mass of 0.01 to 10%, since it can improve the stability of corrosion products and delay the progress of corrosion. % of one or more selected from Mg, Cr, Mn, V, Mo, Ti, Ca, Ni, Co, Sb and B. The reason why the total content of the above-mentioned components is set to 0.01 to 10% by mass is that a sufficient corrosion retarding effect can be obtained and the effect will not become saturated.
  • the amount of the plating film deposited is preferably 45 to 120 g/m 2 per side from the viewpoint of satisfying various properties.
  • the coating weight of the plating film is 45 g/m 2 or more, sufficient corrosion resistance can be obtained even for applications that require long-term corrosion resistance such as building materials; This is because when it is less than m 2 , excellent corrosion resistance can be achieved while suppressing the occurrence of plating cracking during processing.
  • the amount of the plating film deposited is more preferably 45 to 100 g/m 2 .
  • the adhesion amount of the plating film is calculated, for example, by dissolving and peeling the plating film in a specific area with a mixture of hydrochloric acid and hexamethylenetetramine as shown in JIS H 0401: 2013, and calculating from the difference in weight of the steel plate before and after peeling. It can be derived using the following method. In order to obtain the amount of plating on one side using this method, the above-described dissolution can be performed after sealing with tape so that the plating surface on the non-target side is not exposed.
  • the component composition of the plating film can be confirmed, for example, by immersing the plating film in hydrochloric acid or the like to dissolve it, and then subjecting the solution to ICP emission spectrometry, atomic absorption spectrometry, or the like.
  • This method is just an example, and any method may be used as long as it can accurately quantify the component composition of the plating film, and is not particularly limited.
  • the plating film of the hot-dip Al-Zn-based plated steel sheet obtained by the present invention has approximately the same composition as the plating bath as a whole. Therefore, the composition of the plating film can be precisely controlled by controlling the plating bath composition.
  • the interfacial alloy layer in the plating film is a layer of the plating film that exists at the interface with the base steel sheet, and is a layered interfacial alloy layer containing Fe, Al, Si, Zn, and inevitable impurities. be.
  • the interfacial alloy layer is inevitably formed by an alloying reaction between Fe on the surface of the base steel sheet and Al or Si in the plating bath. This interfacial alloy layer is hard and brittle, and if it grows too thick, it becomes a starting point for cracks during processing, so it needs to be made as thin as possible.
  • the thickness of the interfacial alloy layer is required to be 1 ⁇ m or less, and preferably 0.8 ⁇ m or less. If the thickness of the interfacial alloy layer exceeds 1 ⁇ m, bending workability will be reduced.
  • the interfacial alloy layer is determined by the measured value of the average thickness of the interfacial alloy layer present in each field of view when the cross section of the plating film is observed using a scanning electron microscope (SEM) or the like. This is the average value. Furthermore, there are no particular limitations on the method for reducing the thickness of the interfacial alloy layer. Examples include a method of adjusting the Si content in the plating film, as described above, and a method of adjusting the cooling time when applying a thermal history after forming the plating film, as described later.
  • the plating film has dendrites mainly composed of primary Al crystals and dendrite gaps containing Al-Zn eutectic crystals.
  • the Al primary crystal has Zn precipitates in the ⁇ -Al phase matrix, and the Zn content in the matrix is 30% by mass or less. It is characterized by
  • Zn solidifies as a supersaturated solid solution in the ⁇ -Al phase matrix (Zn content exceeds 30% by mass), hardness increases due to solid solution strengthening of Zn, and elongation decreases. However, bending workability deteriorates. Therefore, in the present invention, by limiting the Zn content in the matrix to 30% by mass or less, solid solution strengthening of the Al primary crystals is suppressed, and the bending workability of the hot-dip Al-Zn plated steel sheet is improved. Improves corrosion resistance. In addition, since the decrease in bending workability due to precipitation strengthening tends to become more pronounced as the Zn precipitates become finer, it is possible to reduce the Zn content in the matrix of the ⁇ -Al phase to 30% by mass or less.
  • the Zn content in the matrix is the content of Zn contained in the matrix, and does not include the content of precipitated and separated Zn (Zn precipitate). From the same viewpoint, the Zn content in the matrix is preferably 25% by mass or less, more preferably 20% by mass or less.
  • the above-mentioned Zn precipitates are granular precipitates containing Zn as a main component. Since the spatial resolution of a low-acceleration SEM (referred to as "low-acceleration SEM") is approximately 30 nm, and Zn precipitates smaller than this cannot be observed, those having a diameter of 30 nm or more are considered to be Zn precipitates.
  • low-acceleration SEM a low-acceleration SEM
  • the average maximum diameter of the Zn precipitates in the Al primary crystal is 100 nm or more.
  • the average maximum diameter of the Zn precipitates is, for example, the average diameter of the Zn precipitates that exist in each field of view when Al primary crystals are observed in three or more fields of view using an extremely low acceleration SEM (acceleration voltage of 3 kV, magnification of 20,000 times or more).
  • the long axis of the precipitate mainly composed of Zn was measured at 10 points in ascending order, and the measured values were averaged.
  • the plating film has dendrite gaps containing Al-Zn eutectic.
  • the dendrite gap may contain an elemental Si phase in addition to the Al-Zn eutectic.
  • the Al-Zn eutectic forming the dendrite gap consists of an Al part and a Zn part. When the Al-Zn eutectic is heated to 277° C. or higher, the solid solubility of Zn in the Al portion increases and the Zn portion becomes almost solidly dissolved, resulting in an Al portion containing Zn in a more supersaturated state.
  • the Al-Zn eutectic when the Al-Zn eutectic is cooled, it changes to the Al-Zn eutectic again at a temperature below 277°C, but at this time, the Al-Zn eutectic has a striped pattern in which Al parts and Zn parts alternate. It has a stripe-like structure arranged in.
  • this Al-Zn eutectic striped structure reduces the bending workability of hot-dip Al-Zn plated steel sheets. It was found that when the period of the stripes in the microstructure was as small as 2 ⁇ m or less, the bending workability deteriorated significantly. Therefore, from the viewpoint of further enhancing the bending workability and corrosion resistance of the processed part of the hot-dip Al-Zn coated steel sheet of the present invention, there is no striped structure with a period of 2 ⁇ m or less in the Al-Zn eutectic in the dendrite gap. It is preferable. Note that there is no particular limitation on the lower limit of the stripe period of the striped structure. However, due to the performance of the measuring device described below, it is difficult to confirm the existence of striped structures with a period of less than 30 nm. It is considered to be a striped tissue.
  • the above-mentioned striped structure of the Al-Zn eutectic can be measured by ultra-low acceleration SEM (acceleration voltage 3 kV) like the Zn precipitates in the Al primary crystal.
  • SEM ultra-low acceleration SEM
  • a SEM with a high accelerating voltage for example, an accelerating voltage of 15 kV or more
  • By observing using an accelerated SEM it is possible to confirm the presence or absence of the substance.
  • the Zn precipitates and the Al-Zn eutectic striped structures are both finer than those generated when thermal history is applied, so when observed at an accelerating voltage of 15 kV, for example, No consideration was given to whether or not these existed.
  • the above-mentioned method for controlling the Zn content in the matrix, the maximum diameter of Zn precipitates, and the presence or absence of a striped structure with a period of 2 ⁇ m or less is not particularly limited, and may be controlled by optimizing manufacturing conditions, etc. , can be controlled as appropriate. For example, as described below, by determining the composition of the plating bath and optimizing the thermal history conditions after the formation of the plating film, the Zn content in the matrix and the maximum diameter and period of Zn precipitates can be adjusted. The presence or absence of a striped structure of 2 ⁇ m or less can be controlled.
  • a coating film can be formed on the plating film directly or via an intermediate layer.
  • the type of the coating film and the method of forming the coating film are not particularly limited, and can be appropriately selected depending on the required performance. Examples include forming methods such as roll coater painting, curtain flow painting, and spray painting. After applying a paint containing an organic resin, it is possible to form a coating film by heating and drying using means such as hot air drying, infrared heating, and induction heating.
  • the intermediate layer is not particularly limited as long as it is a layer formed between the plating film of the hot-dip plated steel sheet and the coating film.
  • examples include primers such as chemical conversion coatings and adhesive layers.
  • the chemical conversion film is formed by, for example, chromate treatment or chromium-free chemical conversion treatment in which a chromate treatment liquid or a chromium-free chemical conversion treatment liquid is applied, and a drying treatment is performed at a steel plate temperature of 80 to 300°C without washing with water. Is possible.
  • These chemical conversion coatings may be a single layer or a multilayer, and in the case of a multilayer, a plurality of chemical conversion treatments may be sequentially performed.
  • the method for producing a hot-dip Al-Zn-based plated steel sheet of the present invention includes a step of forming a plating film on a base steel sheet, and a step of imparting a thermal history to the steel sheet after forming the plating film.
  • the method of forming the plating film on the base steel sheet is not particularly limited.
  • it can be manufactured by cleaning, heating, and immersing the base steel sheet in a plating bath in a continuous hot-dip plating facility.
  • recrystallization annealing is performed to control the structure of the base steel plate itself, and a nitrogen-hydrogen atmosphere is applied to prevent oxidation of the steel plate and reduce a trace amount of oxide film existing on the surface.
  • Heating in a reducing atmosphere such as
  • base steel sheet or the components in the steel and cold-rolled steel sheets, hot-rolled steel sheets, etc. can be used as appropriate depending on the required performance and standards.
  • C 0.01 to 0.10% by mass can be used.
  • the present invention does not exclude steel sheets containing less than 0.01% C.
  • trace addition elements include N, S, O, B, V, Nb, Ti, Cu, Mo, Cr, Co, Ni, Ca, Sr, In, Steel plates containing Sn, Sb, etc. are also within the scope of the present invention.
  • the method for obtaining the base steel plate there are no particular limitations on the method for obtaining the base steel plate.
  • the hot-rolled steel plate one that has undergone a hot rolling process and a pickling process can be used, and in the case of the cold-rolled steel plate, it can be manufactured by further adding a cold rolling process. Furthermore, in order to obtain the characteristics of the steel sheet, it is also possible to undergo a recrystallization annealing process or the like before the hot-dip plating process.
  • the composition of the plating film as a whole is almost the same as the composition of the plating bath, Al: 45 to 65% by mass and Si: A composition containing 1.0 to 3.0% by mass, with the remainder consisting essentially of Zn, Fe, and unavoidable impurities is used.
  • the bath temperature of the plating bath is not particularly limited, but is preferably in the temperature range of (melting point + 20°C) to 650°C.
  • the reason why the lower limit of the bath temperature of the plating bath is set to +20°C above the melting point is that in order to perform the hot-dip plating process, the bath temperature needs to be above the freezing point, and by setting the lower limit to the melting point +20°C, This is to prevent coagulation due to a local decrease in bath temperature of the plating bath.
  • the upper limit of the bath temperature was set at 650°C because if it exceeds 650°C, rapid cooling of the plating film becomes difficult and the interfacial alloy layer formed at the interface between the plating film and the base steel sheet becomes thick. This is because there is a risk.
  • the temperature of the base steel sheet entering the plating bath (entering sheet temperature).
  • entering sheet temperature it is preferable to control the temperature of the plating bath within ⁇ 20°C.
  • the time for immersing the base steel sheet in the plating bath is preferably 0.5 seconds or more. This is because if the immersion time is less than 0.5 seconds, a sufficient plating film may not be formed on the surface of the base steel sheet.
  • the upper limit of the immersion time is not particularly limited, but if the immersion time is increased, the interfacial alloy layer formed between the plating film and the steel sheet may become thicker, so it is preferably within 8 seconds. .
  • the maximum temperature reached is 150°C or more and 277°C or less
  • the cooling time from the maximum temperature to 150°C is The cooling time from 150°C to room temperature is 3 hours or more.
  • the maximum temperature when applying the thermal history is set to 150°C or more and 277°C or less is because when the maximum temperature is less than 150°C, Zn diffusion slows down, and solid solution strengthening and precipitation strengthening occur in the Al primary crystals. cannot be sufficiently eliminated, and the striped structure in the Al-Zn eutectic also remains, making it impossible to obtain sufficient bending workability of the hot-dip Al-Zn plated steel sheet.
  • the maximum temperature reached when imparting the thermal history is preferably 170°C or more and 250°C or less, more preferably 190°C or more and 230°C or less.
  • the cooling time from the maximum temperature to 150°C is set to less than 2 hours to suppress the growth of the interfacial alloy layer and thereby improve bending workability.
  • the cooling time from the maximum temperature to 150° C. is preferably 1 hour or less.
  • the cooling time from 150°C to room temperature is set to 3 hours or more to ensure the temperature and time for Zn to diffuse in the Al primary crystals, and to ensure that the Zn in the matrix This is to ensure that the content is 30% by mass or less and the average maximum diameter of the Zn precipitates is 100 nm or more to sufficiently eliminate solid solution strengthening and precipitation strengthening in Al primary crystals.
  • the above-mentioned "normal temperature” means room temperature, and is assumed to be around 25°C.
  • the cooling time from 150° C. to room temperature is preferably within 10 hours from the viewpoint of manufacturing efficiency.
  • FIG. 1 shows an equilibrium phase diagram of the Al-Zn binary system.
  • cooling after plating is rapid, so Zn is not discharged from the dendrite in time during solidification, and the matrix solidifies with Zn supersaturated (more than 30% by mass) in solid solution. Therefore, solid solution strengthening occurs due to the supersaturated solid solution of Zn in the ⁇ -Al phase (matrix) of Al primary crystals, which increases hardness, reduces elongation, and lowers bending workability.
  • the Al-Zn eutectic consists of an Al part and a Zn part, and when it is heated above 277°C, the Zn solid solubility in the Al part increases and the Zn part becomes almost a solid solution, containing more supersaturated Zn. This becomes the Al part.
  • Al-Zn eutectic again at 277°C or below, but this Al-Zn eutectic may form a striped structure in which Al parts and Zn parts are arranged in alternating stripes. Recognize.
  • the method further includes the step of forming a coating film directly or via an intermediate layer on the hot-dip Al-Zn plated steel sheet obtained by the above-described method for producing a hot-dip Al-Zn plated steel sheet of the present invention. You can also do that.
  • the method for forming the coating film is not particularly limited, and can be appropriately selected depending on the required performance. Examples include forming methods such as roll coater painting, curtain flow painting, and spray painting. After applying a paint containing an organic resin, it is possible to form a coating film by heating and drying using means such as hot air drying, infrared heating, and induction heating.
  • the intermediate layer is not particularly limited as long as it is a layer formed between the plating film of the hot-dip plated steel sheet and the coating film.
  • the type and formation method of the intermediate layer are the same as those explained in the hot-dip Al-Zn plated steel sheet of the present invention.
  • Examples 1 to 30> Manufacture of hot-dip Al-Zn coated steel sheets A cold-rolled steel sheet with a thickness of 0.35 mm manufactured by a conventional method was used as a base steel sheet, and annealing and plating were performed in a continuous hot-dip coating facility. Hot-dip Al-Zn-based plated steel sheets A to C having the coating film composition and coating weight shown below were prepared.
  • the composition of the plating bath used in the production of hot-dip galvanized steel sheets is Al: 55% by mass, Si: 1.6% by mass, Fe: 0.4% by mass, and the remainder is essentially Zn and unavoidable impurities (plating A).
  • a composition was used in which the content of each component was changed (plating B, plating C).
  • the bath temperature of the plating bath was 590° C. in each case, and the temperature was controlled so that the plate temperature of the underlying steel sheet was the same as the plating bath temperature.
  • the amount of plating film deposited was controlled to be 85 ⁇ 10 g/m 2 on each side.
  • the solid content was dried and incinerated in a heating furnace at 650°C, and then melted by adding sodium carbonate and sodium tetraborate.
  • insoluble Si was quantified by dissolving the melt with hydrochloric acid and subjecting the solution to ICP emission spectroscopy.
  • the Si concentration in the plating film is the sum of the soluble Si concentration obtained by filtrate analysis and the insoluble Si concentration obtained by solid content analysis.
  • the compositions and coating amounts of the resulting plating films A to C are shown in Table 1.
  • Plating film conditions For each sample of hot-dip Al-Zn coated steel sheet, the cross section of the plating film was observed using ultra-low acceleration SEM and analyzed using energy dispersive X-ray spectroscopy (hereinafter referred to as "EDX"). went.
  • the conditions for observation and analysis of the above-mentioned plating film were to use Zeiss's ULTRA55 (ultra-low acceleration SEM) and Oxford Instruments' Ultim Extreme (EDX), with an acceleration voltage of 3kV, observation magnification of 3000x and 20000x, and a specified location. Point analysis.
  • the average maximum diameter of the precipitates mainly composed of Zn present in the primary crystals of Al was determined by observing 3 fields of view at a magnification of 20,000 times, and 10 precipitates mainly composed of Zn were observed from the primary crystals of Al in each field in descending order of size. It was obtained by extracting it, measuring its major axis, and calculating the average.
  • the minimum period of the striped structure was determined by observing three fields of view at 20,000 times magnification, measuring the stripe period of the existing striped structure, and taking the smallest one among them as the minimum period.
  • FIG. 2 shows photographs of precipitates mainly consisting of Zn present in Al primary crystals for the hot-dip Al-Zn-based plated steel sheets of Samples 1 and 14.
  • FIG. 3 shows photographs of the striped Al-Zn eutectic structures of the hot-dip Al-Zn plated steel sheets of Sample 1, Sample 14, and Sample 22.
  • no cracks when observed refers to a state in which no cracks are observed when the outer tip of the bent portion is observed at 10x magnification with a magnifying glass.
  • the "limit of bending T” refers to the smallest T among the T-bending that resulted in no cracks. For example, if no cracks are observed in 6T bending, but cracks are observed in 4T bending, the bending T limit is "6T".
  • each sample of the present invention example is excellent in both bending workability and corrosion resistance of the processed part in a well-balanced manner compared to each sample of the comparative example.
  • the present invention it is possible to provide a hot-dip Al-Zn-based plated steel sheet that is stable and has excellent bending workability and corrosion resistance of the bent portion, and a method for producing the same.

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PCT/JP2022/017434 2022-03-24 2022-04-08 溶融Ａｌ－Ｚｎ系めっき鋼板及びその製造方法 WO2023181427A1 (ja)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02274851A (ja) * 1989-04-14 1990-11-09 Nisso Kinzoku Kagaku Kk 溶融めっき用亜鉛合金
JPH11343554A (ja) * 1998-05-28 1999-12-14 Nkk Corp 耐食性に優れた溶融Ａｌ−Ｚｎ系合金めっき鋼板
JPH11343559A (ja) * 1998-05-30 1999-12-14 Nkk Corp 耐クラック性及び耐食性に優れた溶融Ａｌ−Ｚｎ系合金めっき鋼板
JP2003268518A (ja) * 2002-03-18 2003-09-25 Nisshin Steel Co Ltd 加工性に優れた塗装原板
JP2005098923A (ja) * 2003-09-26 2005-04-14 Jfe Steel Kk 薄膜の厚さ及び厚さ分布の評価方法
JP2013007071A (ja) * 2011-06-22 2013-01-10 Yodogawa Steel Works Ltd Ａｌ−Ｚｎ合金めっき鋼板とその製造方法および製造装置

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6368730B2 (ja) * 2015-03-02 2018-08-01 Ｊｆｅ鋼板株式会社 溶融Ａｌ−Ｚｎ−Ｍｇ−Ｓｉめっき鋼板とその製造方法
KR20210133266A (ko) * 2019-03-01 2021-11-05 제이에프이 코우반 가부시키가이샤 용융 Al-Zn-Mg-Si-Sr 도금 강판 및 그 제조 방법

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02274851A (ja) * 1989-04-14 1990-11-09 Nisso Kinzoku Kagaku Kk 溶融めっき用亜鉛合金
JPH11343554A (ja) * 1998-05-28 1999-12-14 Nkk Corp 耐食性に優れた溶融Ａｌ−Ｚｎ系合金めっき鋼板
JPH11343559A (ja) * 1998-05-30 1999-12-14 Nkk Corp 耐クラック性及び耐食性に優れた溶融Ａｌ−Ｚｎ系合金めっき鋼板
JP2003268518A (ja) * 2002-03-18 2003-09-25 Nisshin Steel Co Ltd 加工性に優れた塗装原板
JP2005098923A (ja) * 2003-09-26 2005-04-14 Jfe Steel Kk 薄膜の厚さ及び厚さ分布の評価方法
JP2013007071A (ja) * 2011-06-22 2013-01-10 Yodogawa Steel Works Ltd Ａｌ−Ｚｎ合金めっき鋼板とその製造方法および製造装置

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