Surface-treated steel material

Abstract

Provided is a surface-treated steel material having high corrosion resistance in a processed part. A surface-treated steel material according to the present invention is obtained by arranging a steel material, a Zn-containing plating layer, and a coating, in this order. The coating contains trivalent Cr, an organosilicon compound, and V. The trivalent Cr concentration in the coating is 0.30-15.00 mass%. In the coating, a peak indicating an epoxy group is detected at 930-900 cm-1, as measured by a Fourier transform infrared spectrometer (FT-IR).

Description

Surface-treated steel

[0001] This invention relates to surface-treated steel materials.

[0002] Zinc-based plating layers, formed from zinc or zinc-containing alloys, are known to improve the corrosion resistance of steel materials. To further enhance the corrosion resistance and resistance to blackening of the zinc-based plating layer, an inorganic film may be formed on the surface of the zinc-based plating layer.

[0003] For example, Patent Documents 1 and 2 describe forming a film containing trivalent chromium (Cr) on the surface of a zinc-based plating layer. Patent Documents 1 and 2 also describe that the film containing trivalent Cr improved the corrosion resistance of flat plates and processed parts.

[0004] International Publication No. 2023 / 121175, JP 2024-505793

[0005] Patent documents 1 and 2 describe that the corrosion resistance of steel sheets having a zinc-based plating layer is improved by a coating containing trivalent chromium. However, according to the inventors' findings, the corrosion resistance of steel materials does not always improve even when a coating containing trivalent chromium is used. In particular, the effect of improving corrosion resistance by coating formation tends to be limited in processed areas, so there is a need to improve corrosion resistance in processed areas. Furthermore, when a coating containing trivalent chromium is formed, the sliding coefficient of the coated surface of the steel material sometimes increases.

[0006] In view of these circumstances, the present invention aims to provide a surface-treated steel material that exhibits high corrosion resistance in the processed area and suppresses an increase in the sliding coefficient of the surface on which the coating is formed.

[0007] One aspect of the present invention for solving the above problems relates to the following surface-treated steel materials [1] to

[11] . [1] A surface-treated steel material comprising a steel material, a plating layer containing Zn, and a film arranged in this order, wherein the film contains trivalent Cr, an organosilicon compound, and V, the concentration of trivalent Cr in the film is 0.30% by mass or more and 15.00% by mass or less, and the film has a temperature of 930 to 900 cm² as measured using a Fourier transform infrared spectrophotometer (FT-IR). －１A surface-treated steel material in which a peak indicating an epoxy group is detected. [2] The surface-treated steel material according to [1], wherein the concentration of trivalent Cr in the film is 0.30% by mass or more and 10.00% by mass or less. [3] The surface-treated steel material according to [1] or [2], wherein the peak indicating the epoxy group is a peak derived from the organosilicon compound. [4] The surface-treated steel material according to any one of [1] to [3], wherein the mass concentration ratio (Cr / V) of trivalent Cr to V in the film is 0.02 to 10.00. [5] The surface-treated steel material according to any one of [1] to [4], wherein the film contains Zr. [6] The surface-treated steel material according to [5], wherein the total mass concentration of V and Zr in the film is 0.50% by mass or more and 10.00% by mass or less. [7] The surface-treated steel material according to any one of [1] to [6], wherein the mass concentration ratio (Cr / Si) of the trivalent Cr to the Si derived from the organosilicon compound in the coating is 0.02 or more and 0.85 or less. [8] The surface-treated steel material according to any one of [1] to [7], wherein the coating contains P. [9] The surface-treated steel material according to any one of [1] to [8], wherein the coating contains Co.

[10] The surface-treated steel material according to any one of [1] to [9], wherein the coating has a film thickness of 0.05 μm or more and 1.00 μm or less.

[11] The surface-treated steel material according to any one of [1] to

[10] , wherein the plating layer has an Al content of 1.0% by mass or more and 22.0% by mass or less, an Mg content of 1.5% by mass or more and 10.0% by mass or less, and the remainder consists of Zn and optionally added trace additives.

[0008] According to the present invention, a surface-treated steel material is provided that exhibits high corrosion resistance in the processed area and suppresses an increase in the sliding coefficient of the surface on which the coating is formed.

[0009] An embodiment of the present invention will be described below.

[0010] 1. Surface-treated steel material The surface-treated steel material according to this embodiment has a steel material, a plating layer, and a coating arranged in this order.

[0011] 1-1. The type of steel used as the base material is not particularly limited and may be any type of steel, such as steel plates, steel bars, H-beams, I-beams, wire rods, building hardware, or steel pipes. For example, as steel plates, any type of steel can be used, including hot-rolled mild steel plates and strips as described in JIS G 3131 (2018), hot-rolled steel plates and strips for automobiles as described in JIS G 3113 (2018), cold-rolled steel plates and strips as described in JIS G 3141 (2017), and various types of stainless steel plates (including austenitic, martensitic, ferritic, and ferritic-martensitic duplex types).

[0012] 1-2. Plating Layer The plating layer is a plating layer containing zinc (Zn). Preferably, the plating layer is a plating layer mainly composed of Zn. Note that "mainly composed of Zn" means that the plating layer contains 50% by mass or more of Zn. The plating layer may be a plating layer manufactured by any method such as electroplating, hot-dip plating, or vapor deposition plating. The plating layer may be a Zn plating layer, or it may be a plating layer made of an alloy containing Zn (for example, alloys such as Zn-Al, Zn-Mg, Zn-Ni, Zn-Al-Mg, etc.).

[0013] For example, the plating layer may contain 1.0% by mass or more and 22.0% by mass or less of aluminum (Al). Al acts as a passivator, improving the corrosion resistance of the plating layer and suppressing the generation of dross during manufacturing. By setting the Al content to 1.0% by mass or more, the corrosion resistance of the plating layer can be sufficiently improved and the generation of dross can be sufficiently suppressed. By setting the Al content to 22.0% by mass or less, a decrease in the adhesion of the plating layer can be suppressed and a decrease in the sacrificial corrosion protection effect by Zn can be suppressed. Preferably, the Al content is 12.0% by mass or more and 20.0% by mass or less.

[0014] Furthermore, the plating layer may contain 1.5% by mass or more and 10.0% by mass or less of magnesium (Mg). Mg uniformly generates dense corrosion products on the surface of the plating layer, preventing erosion by corrosive factors and improving the corrosion resistance of the plating layer. By setting the Mg content to 1.5% by mass or more, sufficient dense and uniform corrosion products can be generated, thereby sufficiently improving the corrosion resistance of the plating layer. By setting the Mg content to 10.0% by mass or less, the reduction in the sacrificial corrosion protection effect by Zn can be suppressed, and the generation of dross can also be suppressed. The Mg content is preferably 2.0% by mass or more and 8.5% by mass or less, and more preferably 4.0% by mass or more and 7.0% by mass or less.

[0015] Furthermore, when the plating layer contains Al, silicon (Si) may be included in a range of 0.005% to 2.0% by mass to improve adhesion between the steel material and the plating layer, thereby suppressing the growth of the Fe-Zn alloy layer and Fe-Al alloy layer at the interface between the steel material and the plating layer. In addition, when the plating layer contains Mg, Zn may be included to avoid adverse effects on appearance and corrosion resistance. １１ Mg ２ To suppress the formation and growth of phases, titanium (Ti), boron (B), Ti-B alloys, Ti-containing compounds, or B-containing compounds may be included. Preferably, the content of these compounds is in the range of 0.001% by mass or more and 0.1% by mass or less for Ti, and in the range of 0.0005% by mass or more and 0.045% by mass or less for B.

[0016] Furthermore, the plating layer may contain trace amounts of additives and unavoidable impurities in addition to Zn. Trace amounts of additives are, for example, elements added to improve the corrosion resistance of the plating layer. Trace amounts of additives can be elements such as Sn, Bi, In, Ca, Y, La, Ce, Si, Cr, Ti, Ni, Co, V, Nb, Cu, Mn, Fe, Sr, Sb, Pb, B, Li, Zr, Mo, W, Ag, and P. The content of these trace amounts can be between the detection limit and 1% by mass.

[0017] The types and amounts of elements contained in the plating layer are measured by inductively coupled plasma analysis (ICP analysis). Specifically, the coating is removed using a known coating remover at a location at least 30 mm away from the edge and towards the inner surface, and at least 30 mm away from the processed area if welding or bending has been performed. After cleaning the exposed surface, the plating layer is dissolved in hydrochloric acid. By performing ICP analysis on the solution in which the plating layer has been dissolved, the types and amounts of elements contained in the plating layer can be identified.

[0018] 1-3. The coating is a film formed by surface treatment on the surface of the plating layer.

[0019] In this embodiment, the coating contains trivalent chromium (Cr), an organosilicon compound, and vanadium (V).

[0020] Organosilicon compounds can be molecules in which an organic functional group and a hydrolyzable functional group are bonded to a silicon molecule. Organic functional groups are organic reactive groups such as amino groups, epoxy groups, (meth)acryloyl groups, vinyl groups, and mercapto groups, while hydrolyzable functional groups are functional groups such as alkoxy groups. The organic functional groups may be bonded to the silicon molecule via alkylene groups, oxyalkylene groups, etc.

[0021] The organosilicon compound forms a cross-linked structure within the film, improving its adhesion to the plating layer. In this embodiment, it is believed that the trivalent chromium dispersed in the film reacts or interacts with the organosilicon compound to form a denser film structure, thereby improving the barrier properties of the film and enhancing the corrosion resistance of the surface-treated steel material. Furthermore, since trivalent chromium has low toxicity, it is not expected to cause any problems such as adverse effects on human health or environmental pollution.

[0022] The concentration of trivalent Cr in the film is 0.30% by mass or more and 15.00% by mass or less. By setting the trivalent Cr concentration to 0.30% by mass or more, the aforementioned dense film structure can be easily formed, and the corrosion resistance of the surface-treated steel material can be improved by enhancing the barrier property. By setting the trivalent Cr concentration to 15.00% by mass or less, an increase in the sliding coefficient caused by the aggregation of trivalent Cr can be suppressed. From the viewpoint of balancing these, the concentration of trivalent Cr in the film is preferably 0.50% by mass or more and 10.00% by mass or less, more preferably 0.50% by mass or more and 8.00% by mass or less, and still more preferably 1.00% by mass or more and 3.50% by mass or less.

[0023] In the film, a peak indicating an epoxy group is detected at 930 to 900 cm －１ by FT-IR measurement. The epoxy group improves the adhesion of the film to the plating layer, and particularly improves the adhesion of the film in processed portions.

[0024] The peak indicating the epoxy group can be, for example, a peak derived from an organosilicon compound containing an epoxy group. In this case, it is preferable to use a silane coupling agent containing one or more epoxy groups as the organosilicon compound.

[0025] In a film containing the organosilicon compound, a peak is confirmed at 1100 to 1000 cm －１ (Si-O (siloxane bond)) using a Fourier transform infrared spectrophotometer (FT-IR). For the peak area ratio of the peak area of the peak detected at 930 to 900 cm －１ (peak derived from epoxy group) to the peak area of the peak detected at 1100 to 1000 cm －１ (peak derived from siloxane bond), the peak area ratio (peak derived from epoxy group / peak derived from siloxane bond) is preferably 0.030 or more and 0.600 or less, and more preferably 0.100 or more and 0.400 or less. Setting the peak area ratio to 0.100 or more results in a dense film structure. Setting the peak area ratio to 0.400 or less can suppress a decrease in corrosion resistance caused by an excess of highly hydrophilic epoxy groups.

[0026] The concentration of Si derived from the organosilicon compound is preferably 2.00% by mass or more and 30.00% by mass or less. By setting the Si concentration to 2.00% by mass or more, a siloxane bond network is formed throughout the entire coating film. Further, the Si concentration is more preferably 10.00% by mass or more and 20.00% by mass or less. The higher the concentration of Si derived from the organosilicon compound, the higher the fingerprint resistance of the surface-treated steel material can be improved. On the other hand, when the Si concentration is 30.00% by mass or less, preferably 20.00% by mass or less, the coating film can be made appropriately flexible, and the workability (bendability) of the surface-treated steel material can be improved.

[0027] Further, the mass concentration ratio (Cr / Si) of trivalent Cr in the coating film to Si derived from the organosilicon compound is preferably 0.02 or more and 0.85 or less. The larger Cr / Si is, the more easily the barrier property is improved due to the dense coating structure. The smaller Cr / Si is, the smaller the amount of Cr is, and aggregates of Cr are less likely to be formed in the coating film. When Cr aggregates are formed, local hard protrusions are formed on the surface and inside the coating film, which increases microscopic unevenness and reduces the slidability of the coating film. Therefore, the smaller Cr / Si is, the less likely Cr is unevenly distributed in the coating film, and the higher the slidability of the coating film becomes. In addition, the smaller Cr / Si is, the relatively larger the amount of the organosilicon compound can be, so that the fingerprint resistance of the surface-treated steel material can be improved. From the viewpoint of balancing these factors, Cr / Si is more preferably 0.10 or more and 0.65 or less.

[0028] V functions as an inhibitor to form a precipitate film or a passive film, and further improves the corrosion resistance of the surface-treated steel material. In addition, V forms dense corrosion products in the processed portion, thereby improving the corrosion resistance of the processed portion. In the present embodiment, it is considered that the corrosion resistance in the processed portion is remarkably enhanced due to the improvement of adhesion of the coating film to the plating layer by epoxy groups and the formation of corrosion products by V. In addition, V can further densify the coating structure to make it difficult for the coating film to peel off due to water.

[0029] The amount of V in the coating is preferably 0.10% by mass or more and 9.50% by mass or less, and more preferably 1.0% by mass or more and 7.0% by mass or less, relative to the total mass of the coating. By setting it within the above range, the corrosion resistance of the surface-treated steel material can be further improved.

[0030] The mass concentration ratio (Cr / V) of trivalent Cr to V in the coating is preferably 0.02 to 10.00, and more preferably 0.50 to 7.00. A higher Cr / V ratio is more likely to result in improved barrier properties due to a denser coating structure. A lower Cr / V ratio results in a smaller amount of Cr, making it less likely for Cr aggregates to form in the coating. This makes it less likely for Cr to be unevenly distributed in the coating, improving the sliding properties of the coating.

[0031] The coating preferably contains zirconium (Zr). Zr forms a cross-linked structure within the coating, improving its adhesion to the plating layer and making the coating structure denser, thereby improving its barrier properties and further enhancing the corrosion resistance of the surface-treated steel material. In this embodiment, the combined use of trivalent Cr and zirconium significantly enhances the corrosion resistance improvement effect of zirconium. This is thought to be because both trivalent Cr and zirconium are incorporated into the bonding of the organosilicon compound, making the coating structure very dense. Zr also makes it less likely for the coating to peel off due to water.

[0032] The amount of Zr in the coating is preferably 0.10% by mass or more and 20.00% by mass or less, and more preferably 1.00% by mass or more and 10.00% by mass or less, relative to the total mass of the coating. By setting it within the above range, the adhesion between the plating layer and the coating can be further improved, and the corrosion resistance of the surface-treated steel material can be further enhanced.

[0033] Furthermore, the mass concentration ratio (Cr / Zr) of trivalent Cr to Zr in the coating is preferably 0.50 or more and 7.00 or less, and more preferably 1.50 or more and 7.00 or less. The higher the Cr / Zr ratio, the more likely it is that a denser coating structure will result in improved barrier properties. The lower the Cr / Zr ratio, the less Cr is present, and the less likely Cr aggregates are to form in the coating. This makes it less likely for Cr to be unevenly distributed in the coating, improving the sliding properties of the coating.

[0034] Furthermore, the total mass concentration of V and Zr in the film (V + Zr) is preferably 0.50% by mass or more and 10.00% by mass or less, and more preferably 1.50% by mass or more and 7.00% by mass or less. The greater the V + Zr, the easier it is to improve barrier properties due to a dense film structure. This tends to improve corrosion resistance not only on flat surfaces but also on processed areas. The smaller the V + Zr, the less Cr is present, and the less likely Cr aggregates are to form in the film. This makes it less likely for Cr to be unevenly distributed in the film, improving the sliding properties of the film.

[0035] Furthermore, it is preferable that the coating contains phosphorus (P). P enhances the adhesion of the coating to the plating layer, thereby improving the corrosion resistance of the surface-treated steel material.

[0036] P is typically included in the film as phosphoric acid or a salt thereof. Examples of phosphoric acid or salts thereof include phosphoric acids or salts thereof such as orthophosphate, metaphosphate, pyrophosphate, triphosphate, and tetraphosphate (for example, ammonium salts such as triammonium phosphate and diammonium hydrogen phosphate), phosphonic acids or salts thereof such as aminotri(methylenephosphonic acid), 1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetra(methylenephosphonic acid), and diethylenetriaminepenta(methylenephosphonic acid), as well as organic phosphoric acids or salts thereof such as phytic acid. In addition to ammonium salts, metal salts with Na, Mg, Al, K, Ca, Mn, Ni, Zn, and Fe may also be used. These phosphoric acids or salts thereof may be used individually or in combination of two or more.

[0037] The amount of phosphorus (P) in the coating is preferably 0.10% by mass or more and 25.00% by mass or less, and more preferably 1.00% by mass or more and 15.00% by mass or less, relative to the total mass of the coating. By setting the amount within the above range, the adhesion between the plating layer and the coating can be further improved, and the corrosion resistance of the surface-treated steel material can be further enhanced.

[0038] Furthermore, the coating preferably contains cobalt (Co).

[0039] The content of Co in the film is preferably 0.01% by mass or more and 10.00% by mass or less, and more preferably 0.10% by mass or more and 5.00% by mass or less, based on the total mass of the film. By setting the content within the above range, the blackening resistance of the surface-treated steel material can be effectively improved.

[0040] The film may contain elements such as titanium (Ti), niobium (Nb), tantalum (Ta), and tungsten (W). The film may also contain silica particles, fluoride, or the like. The content of these elements or added components in the film is preferably 0.01% by mass or more and 3.00% by mass or less, and more preferably 0.01% by mass or more and 2.00% by mass or less, based on the total mass of the film.

[0041] The content of these elements in the film is measured by inductively coupled plasma analysis (ICP analysis). Specifically, the film is scraped off by a scrubber at a position 30 mm or more inward from the edge, and when processing such as welding or bending has been performed, at a position 30 mm or more away from the processed part. The area for scraping the film can be, for example, 3 cm in width and 3 cm in length, but when the film is thin, the area may be enlarged to obtain a sufficient sample amount. By performing ICP analysis on the scraped film, the types and amounts of elements contained in the film can be identified.

[0042] The valence of Cr is measured by X-ray photoelectron spectroscopy (XPS) on a film collected from the same area. In XPS measurement, mono-Al Kα (hν: 1486.6 eV) is used as the X-ray source. When the detected peak top position is 576 to 578 eV, it is determined as trivalent Cr, and when it is 579 to 580 eV, it is determined as hexavalent Cr.

[0043] For Si, with a Fourier transform infrared spectrophotometer (FT-IR) by the total reflection method (ATR), 1100 to 1000 cm －１ (siloxane bond), 1500 to 1300 cm －１ (C-H bond, Si-CH ３ bending vibration of bond), 900 to 800 cm －１ (Si-CH ３Confirm that absorption peaks are detected in all of the bond stretching vibrations. Furthermore, confirm that this Si originates from an organosilicon compound and not silica or silicone resin. Specifically, for samples obtained by scraping the film with a scrubber, ２９ Solid-state nuclear magnetic resonance measurements targeting Si show a peak (T peak) at -40 to -80 ppm indicating a silanol group (Tn structure) with a Si-C bond, and SiO ４ The peak (Q peak) in the -90 to -120 ppm range, which indicates a (Qn structure), and the peak area ratio (T peak / Q peak) are measured. When this peak area ratio is 6 / 4 to 9 / 1, that is, when the T peak has a larger peak area than the Q peak, which is characteristic of silica or silicone resin, it is determined that there is almost no silica or silicone resin in the film, and the detected Si is derived from an organosilicon compound.

[0044] In this embodiment, the total internal reflection (ATR) method is performed under the following measurement conditions: • ATR crystal: Diamond (or Ge) • Measurement mode: ATR single reflection • Measurement wavenumber range: 4000-650 cm －１ ・Resolution: 4cm －１ • Number of cumulative measurements: 32 • Background: Atmospheric background acquired immediately before measurement • Light source: Mid-infrared light source (Glover) • Detector: DTGS • Sample contact: Measurement performed with constant pressure using an ATR head • Measurement position: Any point at least 30 mm away from the edge of the test piece

[0045] Furthermore, the peak area ratio in this embodiment is measured using the obtained spectrum under the following conditions: • Baseline processing: Linear baseline method • Area calculation method: Wavenumber integral (930-900 cm²) －１ / 1100-1000cm －１ ) ・Analysis software: FT-IR bundled analysis software (e.g., OMNIC, OPUS, etc.)

[0046] The coating may contain resin, but it is preferable to omit resin to reduce manufacturing costs. The presence or absence of resin is confirmed by both thermogravimetric analysis (TGA) showing no significant weight loss due to thermal decomposition in the 300°C to 500°C range, and time-of-flight secondary ion mass spectrometry (ToF-SIMS) showing no detection of polymer fragment ions specific to resin. Specifically, first, the weight change of the coating upon heating is measured by TGA. Generally, organic resins show significant weight loss due to thermal decomposition in the temperature range of approximately 300°C to 500°C. On the other hand, the inorganic skeleton portion of the components derived from the silane coupling agent does not decompose even when heated up to approximately 900°C. Note that the organic groups contained in the silane coupling agent can decompose in the 300°C to 500°C range, but the weight loss is smaller than that of the resin. Therefore, if no significant weight loss due to thermal decomposition is observed in the TGA measurement in the range of 300°C to 500°C, it can be initially determined that the film substantially does not contain resin components. Furthermore, secondary ions emitted from the film surface are analyzed by ToF-SIMS. If resin components are present, C ｘ H ｙ O ｚ － High molecular weight fragment ions such as those listed above are detected. On the other hand, while silane coupling agents also contain organic components, only fragments of low molecular weight origin are detected. Therefore, by confirming that resin-specific high molecular weight fragment ions are not detected in ToF-SIMS analysis, it is possible to confirm that the film does not contain resin components.

[0047] Furthermore, for organosilicon compounds containing epoxy groups, the total internal reflection (ATR) method under the above conditions was measured using a Fourier transform infrared spectrophotometer (FT-IR) at 930–900 cm⁻¹. －１ When an absorption peak is detected, it is determined that the film contains epoxy groups derived from organosilicon compounds.

[0048] The film thickness is preferably 0.05 μm or more and 1.50 μm or less. The thinner the film thickness, the less likely the film is to peel off during processing, thereby improving the corrosion resistance of the processed area. From the above viewpoint, the film thickness is preferably 0.05 μm or more and 1.00 μm or less, and more preferably 0.10 μm or more and 0.80 μm or less.

[0049] The film thickness is measured by cutting a 40 μm × 10 μm test piece from the surface-treated steel material using the cryo-FIB method, cutting it in the thickness direction of the steel material (perpendicular to the surface of the steel plate) in a plan view. When cutting the test piece, it should be cut at a location at least 30 mm away from bends and welds. The cut cross section is observed using a transmission electron microscope (TEM) at a magnification (100,000 to 1,000,000x) where the entire film and a portion of the plating layer are visible in the field of view. The acceleration voltage for this observation is 200 kV. The film observed at the topmost outer edge of the plating layer when observed with FE-TEM is identified as the film formed as described above. The boundary between the film and the plating layer can be easily identified from the observation image by a person skilled in the art. In this way, the distance from the boundary between the film and the plating layer to the surface of the film is measured as the film thickness. The film thickness is measured at three points parallel to the steel surface, with measurement intervals varying by 10 μm, and the average value is taken as the film thickness.

[0050] 2. Method for manufacturing surface-treated steel The surface-treated steel described above can be manufactured by applying a treatment solution containing a trivalent chromium compound, an organosilicon compound containing one or more epoxy groups, and a V compound to the surface of the plating layer of a plated steel having the steel material and the plating layer, and then drying the applied treatment solution.

[0051] The solvent in the treatment solution is preferably an aqueous medium from the viewpoint of explosion prevention during the manufacturing of surface-treated steel materials. The aqueous medium is a liquid medium mainly composed of water, such as water or a mixture of water and a water-soluble organic solvent. The content of the liquid medium can be appropriately determined within a range of solid content concentrations suitable for application of the treatment solution.

[0052] Examples of trivalent chromium compounds include chromium nitrate, chromium sulfate, chromium phosphate, chromium fluoride, chromium acetate, chromium oxalate, and chromium chloride. These trivalent chromium compounds may be used individually or in combination of two or more.

[0053] The amount of trivalent chromium compound in the treatment solution is preferably 0.30% by mass or more and 15.00% by mass or less, based on the total mass of the solids in the treatment solution (components constituting the film, excluding solvent components), and more preferably 0.30% by mass or more and 7.50% by mass or less, and more preferably 0.30% by mass or more and 3.50% by mass or less, based on the amount of trivalent Cr element.

[0054] Examples of organosilicon compounds containing one or more epoxy groups include 2-(3,4-epoxycyclohexylethyltrimethoxy)silane, 3-glycidyloxypropyltrimethoxysilane, 3-glycidyloxypropyltriethoxysilane, and 3-glycidyloxypropylmethyldimethoxysilane.

[0055] The treatment solution may also contain other organosilicon compounds. Examples of other organosilicon compounds include methyltriethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, trimethylmethoxysilane, dimethyldiethoxysilane, trimethylethoxysilane, 3-aminopropyltrimethoxysilane, n-methyl-3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-aminopropyltris(2-methoxyethoxy)silane, n-aminoethyl-3-aminopropyltrimethoxysilane, n-aminoethyl-3-aminopropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-acryloxypropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, and 3-mercaptopropyl These include pyrmethyldimethoxysilane, vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris(2-methoxyethoxy)silane, vinyltriacetoxysilane, γ-aminopropyltriethoxysilane, N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, 3-chloropropyltrimethoxysilane, 3-anilidopropyltrimethoxysilane, 3-(4,5-dihydroimidazolepropyltriethoxy)silane, n-phenyl-3-aminopropyltrimethoxysilane, heptadecafluorodecyltrimethoxysilane, tridecafluorooctyltrimethoxysilane, trifluoropropyltrimethoxysilane, 3-isocyanatetopropyltriethoxysilane, and p-styryltrimethoxysilane. These organosilicon compounds may be used individually or in combination of two or more.

[0056] The amount of organosilicon compounds (total of organosilicon compounds having one or more epoxy groups and other organosilicon compounds) in the treatment solution is preferably 2.00% by mass or more and 30.00% by mass or less, and more preferably 10.00% by mass or more and 20.00% by mass or less, based on the total mass of solids in the treatment solution, in terms of Si element.

[0057] Furthermore, the concentration ratio of trivalent chromium compounds and organosilicon compounds in the treatment solution is preferably 0.020 to 0.850 in terms of the concentration ratio of trivalent Cr to Si element (Cr / Si), and more preferably 0.100 to 0.650.

[0058] Furthermore, when the treatment solution contains other organosilicon compounds in addition to organosilicon compounds having one or more epoxy groups, the total amount of these organosilicon compounds is preferably 2.00% by mass or more and 30.00% by mass or less, and more preferably 10.00% by mass or more and 20.00% by mass or less, relative to the total mass of solids in the treatment solution, in terms of Si element. In addition, the concentration ratio of these combined organosilicon compounds is preferably 0.020 or more and 0.850 or less, and more preferably 0.100 or more and 0.650 or less, relative to the concentration ratio of trivalent Cr to Si element (Cr / Si).

[0059] Examples of V compounds include V compounds obtained by reducing pentavalent vanadium compounds such as vanadium pentoxide, metavanadic acid, ammonium metavanadate, sodium metavanadate, and vanadium oxytrichloride to divalent to tetravalent compounds with a reducing agent, as well as divalent to tetravalent V compounds such as vanadium trioxide, vanadium dioxide, vanadium oxysulfate, vanadium oxyoxalate, vanadium oxyacetylacetonate, vanadium acetylacetonate, vanadium trichloride, phosphovanadomolybdic acid, vanadium sulfate, vanadium dichloride, and vanadium oxide. These V compounds may be used individually or in combination of two or more.

[0060] The amount of V compound in the treatment solution is preferably 0.10% by mass or more and 20.00% by mass or less, and more preferably 1.00% by mass or more and 10.00% by mass or less, based on the total mass of solids in the treatment solution, in terms of element V.

[0061] Furthermore, the concentration ratio of the trivalent chromium compound and the V compound in the treatment solution is preferably 0.02 or more and 10.00 or less in terms of the concentration ratio of trivalent Cr to element V (Cr / V), and more preferably 0.50 or more and 7.00 or less.

[0062] The treatment solution may contain a Zr compound.

[0063] Examples of Zr compounds include zirconium n-propylate, zirconium n-butyrate, zirconium tetraacetylacetonate, zirconium monoacetylacetonate, zirconium bisacetylacetonate, zirconium monoethylacetoacetate, zirconium acetylacetonate bisethylacetoacetate, zirconium acetate, zirconium monostearate, zirconic acid fluoride, zirconium carbonate, ammonium zirconium carbonate, potassium zirconium carbonate, and sodium zirconium carbonate. These Zr compounds may be used individually or in combination of two or more.

[0064] The amount of Zr compound in the treatment solution is preferably 0.10% by mass or more and 20.00% by mass or less, and more preferably 1.0% by mass or more and 10.00% by mass or less, based on the total mass of solids in the treatment solution, in terms of Zr element.

[0065] Furthermore, the concentration ratio of trivalent chromium compounds and Zr compounds in the treatment solution is preferably 0.50 or more and 7.00 or less in terms of the concentration ratio of trivalent Cr to Zr elements (Cr / Zr), and more preferably 1.50 or more and 7.00 or less.

[0066] Furthermore, the total mass concentration of the V compound and the Zr compound in the processing solution is preferably 0.50% by mass or more and 10.00% by mass or less, and more preferably 1.50% by mass or more and 7.00% by mass or less, based on the sum of the V and Zr elements (V + Zr).

[0067] The treatment solution may contain phosphoric acid.

[0068] Examples of phosphoric acids include phosphoric acids such as orthophosphate, metaphosphate, pyrophosphate, triphosphate, and tetraphosphate, or their salts (e.g., ammonium salts such as triammonium phosphate and diammonium hydrogen phosphate), phosphonic acids such as aminotri(methylenephosphonic acid), 1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetra(methylenephosphonic acid), and diethylenetriaminepenta(methylenephosphonic acid), or their salts, as well as organic phosphoric acids such as phytic acid, or their salts. In addition to ammonium salts, metal salts with Na, Mg, Al, K, Ca, Mn, Ni, Zn, and Fe may also be used. These phosphoric acids or their salts may be used individually or in combination of two or more.

[0069] The amount of phosphoric acid in the treatment solution is preferably 0.10% by mass or more and 25.00% by mass or less, and more preferably 1.00% by mass or more and 15.00% by mass or less, based on the total mass of solids in the treatment solution, in terms of element P.

[0070] The treatment solution may contain Co compounds.

[0071] Examples of Co compounds include Cobalt salts such as cobalt nitrate, cobalt sulfate, and cobalt carbonate.

[0072] The amount of Co compound in the treatment solution is preferably 0.01% by mass or more and 10.00% by mass or less, and more preferably 0.10% by mass or more and 5.00% by mass or less, based on the total mass of solids in the treatment solution, in terms of Co element.

[0073] The treatment solution may contain an etching agent. The etching agent activates the surface of the Zn-based plating layer and contributes to improving the adhesion of the chemical conversion treatment film to the Zn-based plating layer. Examples of etching agents include fluorides. The fluoride may be included in the treatment solution as a fluoride of Zr (such as zirconate fluoride) or as another fluoride.

[0074] Furthermore, the treatment solution may contain rheology control agents or other inorganic compounds.

[0075] The treatment solution is preferably applied to the surface of the plating layer by methods such as roll coating, bar coating, and spraying.

[0076] The drying (baking) of the treatment solution applied to the surface of the plating layer is preferably carried out at a temperature higher than 50°C but lower than 250°C, more preferably at a temperature between 70°C and 150°C, and even more preferably at a temperature higher than 100°C but lower than 140°C. Raising the drying temperature above 50°C allows for sufficient volatilization of the solvent. Lowering the drying temperature below 250°C can suppress the decomposition of film components (especially organic chains).

[0077] 3. Applications The above-mentioned surface-treated steel is useful in a variety of applications, such as exterior and interior building materials. For example, the above-mentioned surface-treated steel can be suitably used in a variety of applications, such as roofing materials and exterior materials for buildings, steel pipes, structural steel, supports, and beams for greenhouses or agricultural greenhouses, transport components, sound barriers, soundproof walls, sound-absorbing walls, snow barriers, guardrails, railings, protective fences, supports, components for railway vehicles, components for overhead lines, components for electrical equipment, components for safety and environmental applications, structural components, solar panel mounting frames, and air conditioner outdoor units.

[0078] Furthermore, the above-mentioned surface-treated steel material can be effectively used in applications where surface-treated steel material has traditionally been used, such as sound barriers, windbreaks, and enclosures for power distribution panels.

[0079] The present invention will be described in detail below with reference to examples, but the present invention is not limited to these examples.

[0080] 1. Preparation of materials 1-1. Plated steel sheets Three types of plated steel sheets, A1 to A3 below, were prepared by plating 1.2 mm thick steel sheets with zinc-based plating baths of different compositions. The basis weight of the plating layer was 150 g / m² per side for all of them. ２ The following were determined: • A1: Hot-dip Zn-0.5 mass%Al-1 mass%Mg plated steel sheet • A2: Hot-dip Zn-11 mass%Al-3 mass%Mg-0.2 mass%Si plated steel sheet • A3: Hot-dip Zn-19 mass%Al-6 mass%Mg-0.2 mass%Si plated steel sheet

[0081] 1-2. Surface Treatment Solution A surface treatment solution was prepared by mixing the following materials in the ratios shown in Table 1. In order to suppress the gelation caused by the rapid reaction of the organosilicon compounds, a beaker containing pure water and chromium nitrate nonahydrate was placed in a bath containing ice, and then the organosilicon compounds were added dropwise while stirring to prepare the treatment solution. The trivalent chromium compound and cobalt compound were in hydrate form, and the amount of each hydrate used is shown in Table 1. • Trivalent chromium compounds: Chromium nitrate notahydrate (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) • Organosilicon compounds: (Type B1) 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (manufactured by Tokyo Chemical Industries, Ltd.) (Type B2) Ethyltriethoxysilane (manufactured by Tokyo Chemical Industries, Ltd.) • Vanadium compounds: Vanadium pentoxide (manufactured by Tokyo Chemical Industries, Ltd.) • Zirconium compounds: Zirconate fluoride (manufactured by Sigma-Aldrich) • Phosphorus compounds: Phosphoric acid (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) • Cobalt compounds: Cobalt nitrate hexahydrate (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.)

[0082]

[0083] 2. Surface Treatment: A silicate-based alkaline degreasing agent (Fine Cleaner 4336, manufactured by Nippon Parkerizing Co., Ltd.) was sprayed onto the surface of each plated steel sheet at a concentration of 20 g / L and a temperature of 60°C for 2 minutes. After rinsing with pure water for 30 seconds and drying, the surface of each plated steel sheet was degreased.

[0084] Each surface treatment solution was applied to the surface of a degreased plated steel sheet using a bar coater to achieve the desired film thickness. After standing for 3 seconds, the sheet was baked to form a film using the treatment solution. The baking process involved placing the test piece in a 120°C oven for 30 seconds. During baking, the pure water contained in the surface treatment solution, as well as the water in the trivalent chromium compound hydrate and cobalt compound hydrate, evaporates, forming the film.

[0085] 3. Measurement 3-1. A 40 μm × 10 μm test piece was cut from a steel sheet (surface-treated steel sheet) with a thick film formed on it using the cryo-FIB method, in the thickness direction of the steel sheet (perpendicular to the surface of the steel sheet) in a plan view. Next, the cross-section was observed with a transmission electron microscope (TEM) at a magnification (100,000 to 1,000,000 times) in which the entire film and a portion of the plating layer were visible in the field of view. The acceleration voltage during this observation was 200 kV. The film observed at the topmost outside of the plating layer when observed with FE-TEM was identified as the film formed as described above. The boundary between the film and the plating layer can be easily identified from the observation image by a person skilled in the art. In this way, the distance from the boundary between the film and the plating layer to the surface of the film was measured as the film thickness. The film thickness was measured at three points parallel to the steel surface, with measurement intervals changed by 10 μm each, and the average value was taken as the film thickness.

[0086] 3-2. Amount of elements in the coating For all samples, the coating was scraped off with a scrubber in a 3 cm wide and 3 cm long area at a distance of 30 mm or more from the edge of the plated steel sheet. The concentrations of Cr, Si, P, V, Zr, Co, Zn, Al, Mg, and O were calculated from the scraped coating by ICP analysis. The Cr / Si ratio was calculated by converting the ICP results to a mass ratio.

[0087] Furthermore, the Cr content in the coating was investigated using X-ray photoelectron spectroscopy (XPS) on coatings collected from the same area. For the XPS measurements, a mono-Al Kα (hν: 1486.6 eV) X-ray source was used. If the detected peak top position was between 576 and 578 eV, it was determined to be trivalent Cr; if it was between 579 and 580 eV, it was determined to be hexavalent Cr.

[0088] Furthermore, the Si contained in the coating was confirmed to originate from organosilicon compounds using a Fourier transform infrared spectrophotometer (FT-IR). Total internal reflection (ATR) was used at 1100–1000 cm⁻¹. －１ (Siloxane bond), 1500–1300 cm －１ (C-H bond, Si-CH ３ (Bending vibration of the coupling), 900-800 cm (Si-CH ３Since absorption peaks were detected in all of the bond stretching vibrations, it was determined that the Si originated from an organosilicon compound. The surface-treated steel plate 5 was 1100-1000 cm －１ (Siloxane bond) and 900-800 cm －１ (Si-CH ３ No absorption peaks (for coupling stretching vibrations) were detected.

[0089] Furthermore, the types of organosilicon compounds contained in the coating were confirmed using a Fourier transform infrared spectrophotometer (FT-IR). Organosilicon compound B1 was detected by total internal reflection (ATR) at 930–900 cm⁻¹. －１ When the absorption peak was detected, it was determined that epoxy groups derived from organosilicon compound B1 were present in the coating. Surface-treated steel plates 5 and 6 were 930-900 cm². －１ No absorption peak was detected. The peak area ratio for epoxy group / siloxane bond was 930–900 cm². －１ Area of ​​absorption peak / 1100-1000 cm² －１ It was calculated from the area of ​​the absorption peak.

[0090] The Total Internal Reflection (ATR) method was performed under the following measurement conditions: • ATR crystal: Diamond (or Ge) • Measurement mode: ATR single reflection • Measurement wavenumber range: 4000–650 cm －１ ・Resolution: 4cm －１ • Number of cumulative measurements: 32 • Background: Atmospheric background acquired immediately before measurement • Light source: Mid-infrared light source (Glover) • Detector: DTGS • Sample contact: Measurement performed with constant pressure using an ATR head • Measurement position: Any point at least 30 mm away from the edge of the test piece

[0091] Furthermore, the peak area ratio was measured using the obtained spectrum under the following conditions: • Baseline processing: Linear baseline method • Area calculation method: Wavenumber integral (930–900 cm²) －１ / 1100-1000cm －１ )

[0092] Table 2 shows the type of plated steel sheet, the type of treatment solution, the amount of each element, the concentration of trivalent Cr and Si in the film, the mass ratio of Cr / Si, and the film thickness for surface-treated steel sheets coated with each treatment solution. Note that the concentration of trivalent Cr and Si in the film is the concentration in the film formed with anhydrous materials.

[0093]

[0094] 4. Evaluation 4-1. Planar Corrosion Resistance The corrosion resistance of the planar surfaces of the surface-treated steel sheets was evaluated. More specifically, test pieces (70 mm wide x 150 mm long) cut from each surface-treated steel sheet were sealed at the end face, and then subjected to a salt spray process, a drying process, and a wetting process for one cycle (totaling 8 hours). This cycle was repeated until the area rate of white rust occurrence reached 10%.

[0095] In the salt spray process, a 5% NaCl aqueous solution at 35°C was sprayed onto the test specimens for 2 hours. In the drying process, the test specimens were left for 4 hours in an environment with a temperature of 60°C and a relative humidity of 30%. In the wetting process, the test specimens were left for 2 hours in an environment with a temperature of 50°C and a relative humidity of 95%. The test specimens were evaluated according to the following criteria based on the number of cycles until the area rate of white rust reached 10%. Scores from SS to A were considered acceptable.

[0096] <Evaluation Criteria> Score SS: Over 330 cycles S: Over 280 cycles and 330 cycles or less A: Over 160 cycles and 280 cycles or less B+: Over 120 cycles and 160 cycles or less B: 120 cycles or less

[0097] 4-2. Corrosion Resistance of Processed Areas The corrosion resistance of the processed areas of the surface-treated steel sheets was evaluated. More specifically, test pieces (50 mm wide x 50 mm long) cut from each surface-treated steel sheet were extruded to a thickness of 7 mm using an Erichsen extrusion apparatus. The same test as the evaluation of planar corrosion resistance described above was performed on the obtained extruded samples, and the test pieces were evaluated according to the following criteria based on the number of cycles until the area rate of white rust reached 10%. Scores of S and A were considered acceptable.

[0098] <Evaluation Criteria> Score: More than 21 cycles A: More than 15 cycles and 21 cycles or less B+: More than 10 cycles and 15 cycles or less B: 10 cycles or less

[0099] 4-3. Fingerprint Resistance The fingerprint resistance of the surface-treated steel sheets was evaluated. More specifically, the increase or decrease in L value (ΔL) before and after the application of petroleum jelly was measured using a colorimeter on test pieces (50 mm wide x 50 mm long) cut from each surface-treated steel sheet. Both S and A scores were considered acceptable.

[0100] <Evaluation Criteria> Score S: ΔL is less than 0.5 A: ΔL is 0.5 or more and less than 1.0

[0101] 4-4. Sliding Properties The sliding properties of the surface-treated steel sheets were evaluated. More specifically, test pieces (17 mm wide x 300 mm long) cut from each surface-treated steel sheet were subjected to a drawbead testing machine with a pressing load of 2.0 to 5.5 kN and a pulling speed of 500 mm / min, sliding for 200 mm. The load when sliding at each pressing load was measured as the pulling load, and the slope of the line plotted with the pressing load on the x-axis and the pulling load on the y-axis was calculated as the sliding coefficient. The sliding properties were evaluated according to the following sliding coefficient criteria. A score of A was considered a passing grade.

[0102] <Evaluation Criteria> Score S: Sliding coefficient less than 0.5 A: Sliding coefficient of 0.5 or more and less than 0.7 B: Sliding coefficient of 0.7 or more

[0103] 4-5. The blackening resistance of the surface-treated steel sheets obtained was evaluated. More specifically, test pieces (50 mm wide x 50 mm long) cut from each surface-treated steel sheet were placed in a constant temperature chamber at 70°C and 80% humidity for 144 hours, and the lightness (L* value) of the test pieces was measured before and after the test. Lightness was measured using a colorimeter (Konica Minolta, Inc., CR-400) with a diffuse illumination vertical receiving method including specular reflection light in accordance with JIS Z8722:2009. The illumination diameter during measurement was 11 mmφ, and the measurement diameter was 8 mmφ. Based on the change in lightness (ΔL* value) before and after the test, the blackening resistance was evaluated according to the following criteria. Both a score of S and a score of A were considered acceptable.

[0104] <Evaluation Criteria> Score S: ΔL* value is 0 or greater and less than 10 A: ΔL* value is 10 or greater and less than 15

[0105] The evaluation results for each surface-treated steel sheet are shown in Table 3.

[0106]

[0107] As shown in Tables 1 to 3, the coating contains trivalent Cr, an organosilicon compound, and V, with a trivalent Cr concentration of 0.30% by mass or more and 15.0% by mass or less in the coating, and measurements using a Fourier transform infrared spectrophotometer (FT-IR) of the coating show a temperature of 930 to 900 cm⁻¹. －１ Surface-treated steel materials in which peaks indicating epoxy groups were detected exhibited high corrosion resistance in the processed area and a low coefficient of friction.

[0108] Furthermore, in the surface-treated steel sheet 4, which does not contain trivalent Cr or Zr, the area rate of white rust reached 10% after 106 cycles in the planar corrosion resistance test, and after 8 cycles in the processed surface corrosion resistance test. In contrast, in the surface-treated steel sheet 18, which does not contain trivalent Cr but contains Zr, the area rate of white rust reached 10% after 131 cycles in the planar corrosion resistance test, and after 12 cycles in the processed surface corrosion resistance test. Thus, Zr alone can improve the corrosion resistance of surface-treated steel sheets.

[0109] Furthermore, in the surface-treated steel sheet 1 containing trivalent Cr but not Zr, the area rate of white rust reached 10% after 194 cycles in the planar corrosion resistance test, and after 18 cycles in the processed surface corrosion resistance test. In contrast, in the surface-treated steel sheet 9 containing both trivalent Cr and Zr, the area rate of white rust reached 10% after 303 cycles in the planar corrosion resistance test, and after 28 cycles in the processed surface corrosion resistance test.

[0110] These results show that the degree of improvement in corrosion resistance due to Zr when trivalent Cr is included (comparison between surface-treated steel sheet 1 and surface-treated steel sheet 18) is significantly higher than the degree of improvement due to Zr when trivalent Cr is not included (comparison between surface-treated steel sheet 4 and surface-treated steel sheet 18).

[0111] On the other hand, surface-treated steel sheet 2, with a trivalent Cr concentration of less than 0.30 mass%, exhibited lower corrosion resistance on its flat surface and processed areas compared to other surface-treated steel sheets. This is thought to be because a dense film structure was not formed by trivalent Cr, resulting in insufficient barrier properties. Furthermore, surface-treated steel sheet 3, with a trivalent Cr concentration exceeding 15.00 mass%, had a higher coefficient of friction than other surface-treated steel sheets. This is thought to be due to the aggregation and uneven distribution of trivalent Cr.

[0112] This application claims priority to Japanese Patent Application No. 2025-057070, filed on 28 March 2025. The matters set forth in the original specifications and claims of these applications are incorporated herein by reference.

[0113] The surface-treated steel materials described above exhibit high corrosion resistance in processed areas. Therefore, they are useful in various applications where such properties are required.

Claims

1. A surface-treated steel material comprising a steel material, a plating layer containing Zn, and a coating, arranged in this order, wherein the coating contains trivalent Cr, an organosilicon compound, and V, the concentration of trivalent Cr in the coating is 0.30% by mass or more and 15.00% by mass or less, and the coating has a density of 930 to 900 cm² as measured using a Fourier transform infrared spectrophotometer (FT-IR). －１ Surface-treated steel material in which peaks indicating epoxy groups are detected.

2. The surface-treated steel material according to claim 1, wherein the concentration of trivalent Cr in the coating is 0.30% by mass or more and 10.00% by mass or less.

3. The surface-treated steel material according to claim 1, wherein the peak indicating the epoxy group is a peak derived from the organosilicon compound.

4. The surface-treated steel material according to claim 1, wherein the mass concentration ratio (Cr / V) of the trivalent Cr to the V in the coating is 0.02 or more and 10.00 or less.

5. The surface-treated steel material according to claim 1, wherein the coating contains Zr.

6. The surface-treated steel material according to claim 5, wherein the total mass concentration of V and Zr in the coating is 0.50% by mass or more and 10.00% by mass or less.

7. The surface-treated steel material according to claim 1, wherein the mass concentration ratio (Cr / Si) of the trivalent Cr to the Si derived from the organosilicon compound in the coating is 0.02 or more and 0.85 or less.

8. The surface-treated steel material according to claim 1, wherein the coating contains P.

9. The surface-treated steel material according to claim 1, wherein the coating contains Co.

10. The surface-treated steel material according to claim 1, wherein the coating has a thickness of 0.05 μm or more and 1.00 μm or less.

11. The surface-treated steel material according to any one of claims 1 to 10, wherein the plating layer has an Al content of 1.0% by mass or more and 22.0% by mass or less, an Mg content of 1.5% by mass or more and 10.0% by mass or less, and the remainder consists of Zn and optionally added trace additives.

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