JP2020158845A - Surface treatment liquid for hot-dip galvanized steel sheet, galvanized steel sheet and method for manufacturing the same - Google Patents

Abstract

To provide a chromium free surface treatment liquid excellent in scratch corrosion resistance and even excellent in plane part corrosion resistance, bending part corrosion resistance, solvent resistance, coatability after alkaline degreasing, blackening resistance and storage stability and capable of obtaining a chromate free treatment steel sheet suitable for household appliances, building materials and motor vehicles, etc.SOLUTION: The surface treatment liquid is obtained by mixing a resin compound having a specific bisphenol skeleton, cationic urethane resin emulsion, a silane coupling agent, an organic titanium chelate compound, a tetravalent vanadyl compound, a molybdic acid compound, a tripolyphosphate dihydrogen aluminum rust preventive pigment and water at a predetermined ratio.SELECTED DRAWING: None

Description

The present invention relates to a galvanized steel sheet most suitable for automobiles, home appliances, and building material applications, and in particular, relates to an environment-adaptive galvanized steel sheet containing no chromium during manufacturing and manufacturing, and a manufacturing method thereof. ..
The present invention also relates to a surface treatment liquid useful for improving the corrosion resistance of scratches on galvanized steel sheets.

Galvanized steel sheets are widely used in fields such as home appliances, automobiles, and building materials. For the purpose of improving corrosion resistance (white rust resistance, red rust resistance), conventionally, steel sheets in which the surface of galvanized steel sheets are chromate-treated with a treatment liquid containing chromic acid, dichromic acid or salts thereof as a main component are widely used. Has been used. However, due to recent global environmental problems, there is an increasing demand for the use of non-polluting surface-treated steel sheets that are not chromate-treated, so-called chromate-free treated steel sheets, and various chromate-free treated zinc-based steel sheets (hereinafter referred to as "chromate-free treated zinc-based steel sheets"). Chromate-free treated steel sheet) has been developed and put into practical use. In the chromate-free treated steel sheet, the base steel sheet is exposed at the cut part, the processed part such as bending and welding, and the scratched part that enters during transportation and use, and corrosion is particularly likely to proceed.

In particular, since corrosion of scratches has a large effect on the appearance, a chromate-free treated steel sheet having excellent corrosion resistance of scratches is required. Furthermore, considering that chromate-free treated steel sheets are used in various applications such as home appliances, automobiles, and building materials, in addition to the corrosion resistance of scratched parts, the corrosion resistance of flat parts, the corrosion resistance of bent parts, the solvent resistance, and the paintability after alkaline degreasing, It is also required to have excellent blackening resistance and storage stability, and a chromate-free treated steel sheet that satisfies all of them is required.

In Patent Document 1, a surface treatment having galvanized layers on both sides of a plate and a two-layer film composed of a specific acidic inorganic coating layer and a specific alkaline organic-inorganic composite coating layer on the surface of the galvanized layer. Galvanized steel sheets are disclosed.

In Patent Document 2, a surface treatment liquid containing a phenol resin containing a specific skeleton, a cationic urethane resin, a silane coupling agent, an organic titanium compound, and a vanadium compound in a specific ratio is used on the surface. A technique for forming a treated film and imparting excellent corrosion resistance to a zinc-based plated steel sheet is disclosed. Further, Patent Document 3 further includes a molybdic acid compound, and Patent Document 4 discloses a technique using a surface treatment liquid further containing a molybdic acid compound and a fluorine compound.

In Patent Document 5, a solvent-based organic resin (A) and one or more organic metal compounds (B) selected from an organic titanium compound, an organic zirconium compound, and an organic aluminum compound are formed on the surface of a zinc-based plated steel plate. An organic composite coating having a film thickness of 0.1 to 3 μm formed by applying a surface treatment composition containing a non-chromium-based rust preventive additive (C) and drying the composition. Steel plates are disclosed.

Patent Document 6 states that at least one selected from primary aluminum phosphate and / or primary magnesium phosphate, hexafluorotitanate and / or hexafluorotitanate, chelating agent, magnesium hydroxide, magnesium oxide and magnesium carbonate. A technique using a surface treatment agent characterized by containing one or more magnesium compounds has been disclosed.

Japanese Patent No. 5457611 Japanese Unexamined Patent Publication No. 2010-236074 Japanese Unexamined Patent Publication No. 2011-179057 Japanese Unexamined Patent Publication No. 2012-067369 Japanese Unexamined Patent Publication No. 2016-017187 Japanese Unexamined Patent Publication No. 2011-225942

Although Patent Documents 1, 5 and 6 have an object of improving the corrosion resistance of a scratched portion together with an end portion, the level thereof cannot be said to be sufficient. In particular, Patent Documents 5 and 6 have problems in terms of blackening resistance, solvent resistance, and the like, because performance other than scratch resistance is not sufficiently considered.

Patent Documents 2, 3 and 4 are excellent in flat surface corrosion resistance, processed portion corrosion resistance, solvent resistance, coating property after alkaline degreasing, blackening resistance, and storage stability corrosion resistance. However, the corrosion resistance of the wound is not considered and the level is not sufficient.

An object of the present invention is to solve the above problems, to have excellent corrosion resistance for scratches, corrosion resistance for flat surfaces, corrosion resistance for bent parts, solvent resistance, coating property after alkaline degreasing, blackening resistance, and storage stability. The purpose of the present invention is to provide chromate-free treated steel sheets suitable for home appliances, building materials, automobiles, and the like.

As a result of diligent studies by the present inventors in order to solve the above problems, a urethane resin emulsion having a specific resin compound and a specific cationic functional group, a silane coupling agent having a specific functional group, and a specific organic substance are used. Treating the surface of a zinc-based plated steel sheet with a surface treatment solution containing a Ti chelate compound, a tetravalent vanadium compound, a molybdic acid compound, and a specific ratio of an aluminum dihydrogen dihydrogen phosphate rust preventive pigment. As a result, it is possible to form a film having excellent corrosion resistance, blackening resistance, coating property, lubricity, and solvent resistance, as well as corrosion resistance to scratches, and further deterioration of the film characteristics even after storage. It was newly found that The present invention has been completed based on such findings, and its gist structure is as follows.

式（Ｉ）中、ベンゼン環に結合しているY₁およびY₂は、それぞれ互いに独立に水素原子、あるいは次の一般式（ＩＩ）または（ＩＩＩ）により表されるZ基であり、1ベンゼン環当たりのZ基の置換数の平均値は0.2〜1.0である。nは2〜50の整数を表す。

式（ＩＩ）および（ＩＩＩ）中、R₁、R₂、R₃、R₄及びR₅はそれぞれ互いに独立な水素原子、炭素数1〜10のアルキル基または炭素数1〜10のヒドロキシアルキル基を表し、A−は水酸イオンまたは酸イオンを表す。 The means for solving the above problems are as follows.
1. 1. On the surface of the zinc-based plated steel sheet, a resin compound (A) having a bisphenol skeleton represented by the following general formula (I) and at least one cation selected from the 1st to 3rd amino groups and the quaternary ammonium base A cationic urethane resin emulsion (B) having a sex functional group and one or more silane coupling agents having at least one reactive functional group selected from an active hydrogen-containing amino group, an epoxy group, a mercapto group and a methacryloxy group. (C), organic titanium chelate compound (D), tetravalent vanadium compound (E), molybdic acid compound (F), aluminum dihydrogen dihydrogen tripolyphosphate rust preventive pigment (G), and water. A surface treatment liquid for zinc-based plated steel sheets containing the following conditions (1) to (6) within a range that satisfies the conditions.
(1) Cationicity with respect to the total solid content {(As) + (Bs) + (Cs)} of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C). The solid content (Bs) of the urethane resin emulsion (B) is 0.10 to 0.30 in mass ratio [(Bs) / {(As) + (Bs) + (Cs)}].
(2) Silane coupling with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)} The solid content (Cs) of the agent (C) is 0.60 to 0.85 in mass ratio [(Cs) / {(As) + (Bs) + (Cs)}].
(3) The solid content (Cs) of the silane coupling agent (C) with respect to the titanium equivalent amount (D _Ti ) of the organic titanium chelate compound (D) is 50 by mass ratio {(Cs) / (D _Ti )}. ~ 70
(4) The organic titanium chelate compounds of titanium equivalent amount of (D) relative to (D _Ti), the tetravalent vanadium compound Vanadium amount of (E) (E _V) is the weight ratio {(E _V) / (D _Ti )} from 0.30 to 0.50
(5) The molybdic acid with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)}. The molybdenum equivalent amount (F _Mo ) of compound (F) is 0.003 to 0.030 in mass ratio [(F _Mo ) / {(As) + (Bs) + (Cs)}].
(6) The tetravalent vanadium compound Vanadium amount of (E) solid content of the tripolyphosphate aluminum dihydrogen anticorrosive pigment to (E _V) (G) (Gs) is the weight ratio {(Gs) / ( in E _V)} 3~300

In formula (I), Y ₁ and Y ₂ bonded to the benzene ring are hydrogen atoms independently of each other, or Z groups represented by the following general formulas (II) or (III), and 1benzene. The average number of Z-group substitutions per ring is 0.2-1.0. n represents an integer from 2 to 50.

In formulas (II) and (III), R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independent hydrogen atoms, alkyl groups having 1 to 10 carbon atoms or hydroxyalkyl groups having 1 to 10 carbon atoms, respectively. , And A- represents a hydroxide ion or an acid ion.

2. 2. The aluminum tripolyphosphate dihydrogen rust preventive pigment (G) contains at least one additive element selected from Zn, Mg, Si, and Ca in addition to aluminum dihydrogen tripolyphosphate, and the additive element. mass (G _E) is the mass ratio to phosphorus mass in dihydrogen tripolyphosphate aluminum-based anticorrosive pigment _{(G) (G P) {} (G E) / (G P)} by from 0.1 to 10 The surface treatment liquid for zinc-based plated steel sheets according to 1 above.

3. 3. The surface treatment liquid further contains an acid component (H), and the mass (Hg) of the acid component (H) is the resin compound (A), the cationic urethane resin emulsion (B), and the silane coupling agent (C). The mass ratio [(Hg) / {(As) + (Bs) + (Cs)}] to the total solid content of {(As) + (Bs) + (Cs)} is 0.10 or less. The surface treatment liquid for a galvanized steel sheet according to 1 or 2 above.

4. The surface treatment liquid further contains wax (W), and the solid content (Ws) of the wax (W) is the total solid content of the resin compound (A) and the cationic urethane resin emulsion (B) {(As). The zinc-based plated steel sheet according to any one of 1 to 3 above, wherein the mass ratio [(Ws) / {(As) + (Bs)}] to + (Bs)} is in the range of 0.2 to 0.6. Surface treatment liquid for.

5. The surface treatment liquid according to any one of 1 to 4 above is applied to the surface of the galvanized steel sheet in a range where the amount of adhesion after drying is 0.2 to 1.8 g / m ² per side, and then the reached plate temperature: A method for producing a galvanized steel sheet, which is characterized by drying at 50 to 180 ° C.

6. A galvanized steel sheet having a surface treatment film having an adhesion amount of 0.2 to 1.8 g / m ² per side on the surface, and the surface treatment film is the surface treatment solution according to any one of 1 to 4 above. A galvanized steel sheet, which is obtained by applying it to the surface of a steel sheet and drying it at a temperature of 50 to 180 ° C.

According to the present invention, a chromate-free treatment having excellent corrosion resistance on scratches, corrosion resistance on flat surfaces, corrosion resistance on bent parts, solvent resistance, coating property after alkaline degreasing, blackening resistance, lubricity and storage stability. It becomes possible to provide a steel plate.

Hereinafter, the present invention will be specifically described.
The steel sheet on which the chromate-free treated steel sheet of the present invention is based is a galvanized steel sheet based on a cold-rolled steel sheet for home appliances, building materials, and automobile parts. As the zinc-based plated steel sheet, electric Zn plated steel sheet, hot-dip Zn plated steel sheet, Zn-Al plated steel sheet, Zn-Al-Mg plated steel sheet, Zn-Mg plated steel sheet, Zn-Fe plated steel sheet, Zn-Ni plated steel sheet, etc. are used. Can be done (either electroplating or hot-dip plating can be used).

Further, in the above-mentioned zinc-based plated steel sheet, for the purpose of improving the blackening resistance of the zinc-based plated steel sheet, a small amount of Ni or Co is added to the plating, or an acid or alkaline aqueous solution containing Ni, Co, Fe is used. , These metals may be deposited on the surface of a galvanized steel sheet.

Next, the surface treatment liquid of the present invention will be described.
The surface treatment liquid of the present invention contains a resin compound (A) represented by the following general formula (I), a cationic urethane resin emulsion (B), an active hydrogen-containing amino group, an epoxy group, a mercapto group and a methacryloxy group. One or more silane coupling agents (C) having at least one reactive functional group selected from, an organic titanium chelate compound (D), a tetravalent vanadium compound (E), and a molybdic acid compound ( It is characterized by containing F), an aluminum dihydrogen dihydrogen phosphate rust preventive pigment (G), and water.
Here, (1) cationicity with respect to the total solid content {(As) + (Bs) + (Cs)} of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C). The solid content (Bs) of the urethane resin emulsion (B) is 0.10 to 0.30 in mass ratio [(Bs) / {(As) + (Bs) + (Cs)}].
(2) The silane coupling agent (2) with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)}. The solid content (Cs) of C) is 0.60 to 0.85 in mass ratio [(Cs) / {(As) + (Bs) + (Cs)}].
(3) The solid content (Cs) of the silane coupling agent (C) with respect to the titanium equivalent amount (D _Ti ) of the organic titanium chelate compound (D) is 50 to 50 by mass ratio {(Cs) / (D _Ti )}. It is 70.
(4) an organic titanium chelate compound of titanium equivalent amount of (D) relative to (D _Ti), 4-valent vanadium compounds Vanadium amount of (E) (E _V), the weight ratio ((E _V) / (D _Ti) ) Is 0.30 to 0.50.
(5) The molybdic acid compound (F) with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)}. The molybdenum conversion amount (F _Mo ) of) is 0.003 to 0.03 in terms of mass ratio [(F _Mo ) / {(As) + (Bs) + (Cs)}].
(6) a tetravalent vanadium compound of vanadium equivalent amount of (E) solid content of dihydrogen tripolyphosphate aluminum-based anticorrosive pigment (G) for (E _V) (Gs) is the weight ratio {(Gs) / (E _V )} Is 3 to 300.

In the above formula (I), Y ₁ and Y ₂ bonded to the benzene ring are hydrogen atoms independently of each other, or Z groups represented by the following general formulas (II) or (III). The average number of Z group substitutions per benzene ring is 0.2 to 1.0. n represents an integer from 2 to 50. Here, the average value of the number of substitutions of Z groups is a value obtained by dividing the total number of Z groups introduced by the total number of benzene rings (that is, 2n). In the present invention, when Z groups are selected as Y ₁ and Y ₂ , the first to third amino groups and the first to third amino groups in which the average value of the number of Z group substitutions in the resin compound (A) is in the range of 0.2 to 1.0. By having a cationic functional group of a quaternary ammonium base, it can be more stably dissolved in the surface treatment liquid and storage stability can be obtained. Further, in the present invention, the average degree of polymerization n is 2 or more and 50 or less. If n is less than 2, the effect of imparting corrosion resistance is insufficient. On the other hand, if it exceeds 50, the stability in the treatment liquid is lowered due to the decrease in water solubility, thickening, etc., and the storage stability is insufficient. Preferably, n = 2-8.

In the above formulas (II) and (III), R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independent hydrogen atoms, alkyl groups having 1 to 10 carbon atoms or hydroxyalkyl groups having 1 to 10 carbon atoms, respectively. Represents a group. If the number of carbon atoms of the alkyl group or the hydroxyalkyl group exceeds 10, the resin compound (A) cannot be sufficiently solubilized and becomes unstable in the treatment liquid, so that it cannot be applied. Specific examples of R ₁ , R ₂ , R ₃ , R ₄ and R ₅ include methyl, ethyl, propyl, butyl, hydroxyethyl, 2-hydroxypropyl, hydroxyisobutyl and the like. A ⁻ represents hydroxide ion or acid ion. Specific examples of the acid ion include acetate ion, phosphate ion, formic acid ion and the like.

The resin compound (A) represented by the general formula (I) is a bisphenol-formalin condensate, and the synthesis method thereof is not limited. For example, formalin and amine are acted on bisphenol A in the presence of an alkali catalyst. It can be obtained by letting it.

The cationic urethane resin emulsion (B) in the surface treatment liquid in the present invention has at least one cationic functional group selected from the 1st to 3rd amino groups and the quaternary ammonium base as the cationic functional group. If there is, the polyol, isocyanate component, and polymerization method, which are constituent monomer components, are not particularly limited. Examples of the cationic functional group include an amino group, a methylamino group, an ethylamino group, a dimethylamino group, a diethylamino group, a trimethylamino group, a triethylamino group and the like, and the first to third amino groups or the fourth There is no particular limitation as long as it is a primary ammonium base.

The silane coupling agent (C) in the surface treatment liquid in the present invention has at least one reactive functional group selected from an active hydrogen-containing amino group, an epoxy group, a mercapto group and a methacryloxy group, and one or more of these reactive functional groups. The silane coupling agent is not particularly limited. Particularly, a trialkoxysilane having three alkoxy groups is preferable. Specific examples include N- (2-aminoethyl) 3-aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 3-Methylmethacryloxypropyltrimethoxysilane, 2- (3,4 epoxycyclohexyl) ethyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, etc. can be used.

Examples of the organic titanium chelate compound (D) in the surface treatment liquid in the present invention include titanium acetylacetonate, titanium octylene glycolate, titanium tetraacetylacetonate, and titanium ethylacetate acetate. Inorganic salts such as titanium nitrate, titanium sulfate, titanium acetate, titanium phosphate, and titanium carbonate are not preferable because they cannot be stably dissolved in the treatment liquid of the present invention or do not exhibit the effect of improving corrosion resistance. When the organic titanium chelate compound is dissolved in water and used, titanium is dissolved as a chelate complex, so it is preferable not to add a highly polar water-soluble solvent or peroxide that affects this complex. ..

The tetravalent vanadium compound (E) used in the surface treatment liquid of the present invention is not particularly limited, but specifically, vanadyl sulfate, vanadyl dichloride, vanadyl phosphate, vanadyl oxalate, and vanadyl acetyl. Examples include acetylaceate. The tetravalent vanadium compound has an effect of improving the corrosion resistance of the flat surface portion by its own addition and an effect of improving the corrosion resistance of the scratched portion by adding it together with the aluminum dihydrogen dihydrogen rust preventive pigment described later. As the tetravalent vanadium compound used in the surface treatment liquid of the present invention, a vanadium compound that produces VO ²⁺ (vanadyl) ions is most effective in improving the corrosion resistance of flat surfaces and the corrosion resistance of scratches, and is preferable. A pentavalent vanadium compound (for example, ammonium metavanadate) is not used in the present invention because it is too water-soluble and the corrosion resistance of the flat surface portion is significantly deteriorated.

The type of molybdate compound (F) used in the surface treatment liquid in the present invention is not particularly limited, but specifically, molybdate, ammonium molybdate, sodium molybdate, potassium molybdate, molybdate. Examples thereof include magnesium and zinc molybdate, and examples thereof include phosphomolybdic acid, ammonium phosphomolybdate, and sodium molybdate. In the present invention, it is preferable to use one or more selected from these.

The present invention is characterized in that an aluminum dihydrogen trihydrophosphate rust preventive pigment (G) is added to the surface treatment liquid as a component for improving the corrosion resistance component of scratches. By adding the aluminum dihydrogen tripolyphosphate rust preventive pigment, the corrosion resistance of the scratched part is significantly improved. The aluminum trihydrophosphate rust preventive pigment (G) used in the surface treatment liquid of the present invention may be pure aluminum dihydrogen tripolyphosphate, but for the purpose of further improving the corrosion resistance of scratches, aluminum dihydrogen tripolyphosphate is used. in addition to, Zn, Mg, Si, comprising at least one kind of additive elements selected from among Ca, and the mass of the additive element (G _E) is, dihydrogen tripolyphosphate aluminum-based anticorrosive pigment (G) mass ratio to phosphorus mass (G _P) in _{{(G E) / (G} P)} more preferably used dihydrogen tripolyphosphate aluminum-based anticorrosive pigments 0.1 to 10.

In the surface treatment liquid of the present invention, with respect to the total solid content {(As) + (Bs) + (Cs)} of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C). The solid content (Bs) of the cationic urethane resin emulsion (B) needs to be 0.10 to 0.30 in terms of mass ratio [(Bs) / {(As) + (Bs) + (Cs)}]. If the mass ratio is less than 0.10, the proportion of urethane resin is too small, and the corrosion resistance of the bent portion and the storage stability of the surface treatment liquid deteriorate. On the other hand, if the mass ratio exceeds 0.30, the solvent resistance is inferior. More preferably, it is 0.12 to 0.28.

Further, in the surface treatment liquid of the present invention, the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs). }, The solid content (Cs) of the silane coupling agent (C) needs to be 0.60 to 0.85 in terms of mass ratio [(Cs) / {(As) + (Bs) + (Cs)}]. If the mass ratio is less than 0.60, the solvent resistance is inferior, and if it is more than 0.85, the corrosion resistance of the bent portion and the storage stability of the surface treatment liquid are lowered. More preferably, it is 0.65 to 0.80.

In the surface treatment liquid of the present invention, the solid content (Cs) of the silane coupling agent (C) with respect to the titanium equivalent amount (D _Ti ) of the organic titanium chelate compound (D) is the mass ratio {(Cs) / (D _Ti ). )} Is 50 to 70. If the mass ratio is less than 50, the corrosion resistance and storage stability of the flat surface portion and the processed portion are deteriorated, and if it is 70 or more, the coatability after alkaline degreasing is deteriorated. More preferably, it is 55 to 65.

In calculating the mass ratio of the present invention, the solid content (Cs) of the silane coupling agent (C) is hydrolyzed by alkoxysilane (R-Si (-OR ₁ ) ₃ ) and silanol ( The mass is R-Si (-OH) ₃ ). Most of this is hydrolyzed when the silane coupling agent is dissolved in water, and the alcohol generated by the hydrolysis volatilizes when the treatment solution of the present invention is applied and dried to form a film, and does not act as an active ingredient. Because.

In the surface treating solution of the present invention, the vanadium equivalent amount of the titanium equivalent amount of the organic titanium chelate compound (D) 4-valent vanadium compounds for (D _Ti) (E) a (E _V), the mass ratio (E _V / D _Ti ) is 0.30 to 0.50. If the mass ratio is less than 0.30, the corrosion resistance of the flat surface portion is lowered. If it exceeds 0.50, the paintability after alkaline degreasing deteriorates. More preferably, it is 0.35 to 0.48.

In the surface treatment liquid of the present invention, with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)}. The molybdenum equivalent amount (F _Mo ) of the molybdic acid compound (F) is 0.003 to 0.030 in terms of mass ratio [(F _Mo ) / {(As) + (Bs) + (Cs)}]. If the mass ratio is less than 0.003, the blackening resistance is inferior, and if it exceeds 0.030, the storage stability of the surface treatment liquid cannot be obtained. In order to obtain a higher degree of blackening resistance, 0.006 or more is preferable.

In the surface treating solution of the present invention, tetravalent vanadium compound of vanadium equivalent amount of (E) solid dihydrogen tripolyphosphate aluminum-based anticorrosive pigment (G) minutes for (E _V) (Gs), the weight ratio {( gs) / (a 3 to 300 in E _V)}. Within this range, the effect of improving the corrosion resistance of the scratched portion can be obtained. If the mass ratio is less than 3, the corrosion resistance of the scratched portion deteriorates. A more preferable range is 20 or more. If it exceeds 300, the corrosion resistance of the flat surface deteriorates. A more preferable range is 200 or less.

The water used in the present invention contains each component of a resin compound (A), a cationic urethane resin emulsion (B), a silane coupling agent (C), an organic titanium chelate compound (D), and an acid component used for pH adjustment. It is preferable that the compound has little influence on the alkali component. When Na, Cl, etc. contained as impurities in water remain in the film, they may reduce the corrosion resistance or the coating adhesion. Therefore, the water used is preferably one having few impurities, and for example, its electric conductivity is preferably less than 100 μS / cm. It is more preferably 50 μS / cm or less, still more preferably 10 μS / cm or less.

The solid content concentration of the surface treatment liquid in the present invention is preferably 4 to 20% by mass as the solid content concentration when dried at 110 ° C. for 2 hours. This is because when the solid content concentration is in the range of 4 to 20% by mass, it becomes easy to secure the amount of adhesion of the surface treatment film described later, and the storage stability of the surface treatment liquid is also excellent.

The basic components of the surface treatment liquid of the present invention have been described above, but in the present invention, the following components can be further contained if necessary.
An acid component (H) can also be added to the surface treatment liquid in the present invention for the purpose of further improving the corrosion resistance of the film. The acid component (H) improves the corrosion resistance, particularly the corrosion resistance of the bent portion, by etching the plating surface and inactivating it. As the acid component (H), phosphoric acid, acetic acid, formic acid, hydrofluoric acid, fluoride and the like are preferable, and it is particularly preferable to use orthophosphoric acid because the effect of improving corrosion resistance is high. On the other hand, strong acids such as sulfuric acid and nitric acid are not preferable. When sulfuric acid or nitric acid is used, cation phenol or cation urethane tends to become a gel in the surface treatment liquid due to pH shock (local and rapid pH change) at the time of addition, and is formed accordingly. This is because the elution of salt is high and the corrosion resistance is lowered.

The acid component (H) in the surface treatment liquid of the present invention is the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) +. Mix so that the mass (Hg) of the acid component (H) with respect to (Bs) + (Cs)} is 0.10 or less in the mass ratio [(Hg) / {(As) + (Bs) + (Cs)}]. .. This is because if the mass ratio exceeds 0.10, the storage stability deteriorates. The mass (Hg) of the acid component (H) in the present invention is the mass of the pure acid component (H). When an acid component (H) diluted with water or the like is used, the mass (Hg) of the acid component (H) is the specific gravity of the acid component solution (g / mL) x 1,000 (mL) x purity of the acid component solution. It is calculated by (w / w%). The lower limit of the mass ratio is not particularly limited, but is preferably about 0.05 in order to obtain better corrosion resistance.

Further, in the present invention, wax (W) can be contained in the surface treatment liquid for the purpose of ensuring the lubricity of the film. In the wax (W), the solid content (Ws) of the wax (W) is the mass ratio of the solid content of the resin compound (A) and the cationic urethane resin emulsion (B) to the total solid content {(As) + (Bs)}. It is preferable to mix [(Ws) / {(As) + (Bs)}] so as to be 0.2 to 0.6. When the above content is 0.2 or more, desired lubricity can be obtained, while when it is 0.6 or less, lubricity can be effectively ensured, which is economically advantageous and does not further reduce corrosion resistance, which is preferable. .. The range of 0.3 to 0.6 is more preferable.

As the wax (W) used in the present invention, it is preferable to use at least one selected from those having a melting point: 70 to 120 ° C., and specific examples thereof include polyethylene wax, polyethylene oxide wax, polypropylene wax, and microcrystalline wax. Wax and the like can be mentioned. Lubricity can be obtained when the melting point is 70 ° C or higher, and lubricity can be obtained without being too hard when the melting point is 120 ° C or lower.

The wax (W) is preferably an emulsion that is stably dispersed in water with an emulsifier, and preferably has a particle size of 0.08 to 0.3 μm. When the particle size is 0.08 μm or more, the desired lubricity effect can be obtained, and since the amount of emulsifier used does not increase, the alkali resistance and coatability do not deteriorate. On the other hand, when the particle size is 0.3 μm or less, floating separation in the treatment liquid does not occur due to a decrease in the specific gravity of the wax (W), and storage stability is excellent, which is preferable.

Further, a defoaming agent or a wettability improving agent may be added to the surface treatment liquid of the present invention, if necessary. The type of defoaming agent is not particularly limited, and for example, a silicone-based or fatty acid-based emulsion type can be used. The wettability improver lowers the surface tension of the surface treatment liquid, improves the wettability of the galvanized steel sheet, and improves the appearance uniformity. Examples of the wettability improving agent include, but are not limited to, water-soluble solvents such as ethanol, T-butanol, and butyl cellosolve. In addition, a wettability improver containing acetylene is suitable because it also has a defoaming effect. Nitrate such as nickel nitrate and ammonium nitrate may be added to the surface treatment liquid of the present invention for the purpose of further improving the blackening resistance. As mentioned above, nitric acid gives a pH shock, but nitrate does not give a pH shock.

Next, a method for producing a plated steel sheet using the above surface treatment liquid and a plated steel sheet obtained by the method, that is, a chromate-free treated steel sheet of the present invention will be described.
When a surface treatment film is formed on a plated steel sheet using the surface treatment liquid of the present invention, the surface treatment liquid is applied to the plated steel sheet, dried at a reaching plate temperature of 50 to 180 ° C., and the surface of the steel sheet is exposed to one side. It is necessary to form a surface treatment film with an adhesion amount of 0.2 to 1.8 g / m ² . At this time, if the adhesion amount per side of the surface treatment film is less than 0.2 g / m ² , sufficient corrosion resistance cannot be obtained, while if it exceeds 1.8 g / m ² , the effect of the adhesion amount is saturated and economically. Not only is it disadvantageous, but it also reduces paintability. Therefore, the amount of adhesion per side is 0.2 to 1.8 g / m ² . Incidentally, such a coating weight is preferably ^{0.3~1.6g / m 2, 0.4~1.4g / m} 2 is more preferable.

As a method of applying the surface treatment liquid of the present invention to a galvanized steel sheet, any conventionally known method such as a roll coater (3-roll method, 2-roll method, etc.) squeeze coater, die coater, bar coater, etc. may be used. It is also possible to adjust the coating amount, make the appearance uniform, and make the film thickness uniform by the air knife method or the roll drawing method after the coating treatment with a squeeze coater or the like, the dipping treatment, and the spray treatment.

After coating (coating) the surface treatment liquid of the present invention on a galvanized steel sheet, heat drying is preferably performed without washing with water. As the drying means, a dryer, a hot air furnace, a high frequency induction heating furnace, an infrared furnace and the like can be used. As described above, the drying is performed in the range of 50 to 180 ° C. at the temperature of the plated steel sheet itself. If the reaching plate temperature is lower than 50 ° C., a large amount of water remains in the film, resulting in insufficient corrosion resistance. On the other hand, when the reaching plate temperature exceeds 180 ° C., not only is it uneconomical, but the film becomes hard and brittle, and the corrosion resistance of the processed portion is lowered.

The plated steel sheet (chromate-free treated steel sheet) of the present invention having a surface-treated film formed by the above-mentioned method can be further coated with a resin film on the surface to obtain a higher degree of corrosion resistance. The surface treatment film formed by the surface treatment liquid of the present invention may be applied to either one side or both sides of the plated steel sheet.

Next, the action of the present invention will be described. It is presumed that each component has the following actions in the surface treatment liquid of the present invention, but the present invention is not limited by these speculations.

The surface treatment liquid of the present invention contains a resin compound (A), a cationic urethane resin emulsion (B), and a silane coupling agent (C) as main components, and the skeleton of the film is formed by these main components. By having a cationic functional group (the above-mentioned general formula (II) or (III)), the resin compound (A) becomes insoluble in an alkaline solution and becomes an alkali-resistant film. Further, by selecting bisphenol as the skeleton of the phenol of the resin compound (A), it becomes difficult to dissolve in a polar solvent (imparting solvent resistance), and adhesion and corrosion resistance are improved.
However, the resin compound (A) tends to be yellowish by heating (decrease in heat-resistant yellowing) and tends to form a hard film. Therefore, in the present invention, by blending the cationic urethane resin emulsion (B), the hardness of the phenol resin is softened and the corrosion resistance of the processed portion is ensured.

While the cationic urethane resin emulsion (B) has the above-mentioned effect, it makes it easy to peel off the film against a polar solvent. Therefore, in the present invention, a silane coupling agent (C) is blended for the purpose of ensuring solvent resistance to polar solvents and yellowing resistance. Since the alkoxy group at the end of the silane coupling agent (C) is hydrolyzed to generate an active silanol group (Si-OH), it contributes to the improvement of adhesion to the material (zinc-based plating layer) and the topcoat film. Furthermore, a part of the silane coupling agent (C) is dehydrated and condensed to form a siloxane bond (Si-O-Si), which is continuously polymerized (polysiloxane formation: -Si-O-Si-O-". Si-). As a result, the structure becomes extremely stable, and it is possible to impart excellent corrosion resistance and solvent resistance to the flat surface portion of the film.

As described above, it is considered that various performances can be obtained in a well-balanced manner by using the resin compound (A), the cationic urethane resin emulsion (B), and the silane coupling agent (C) in an appropriate ratio. Be done. However, it cannot be said that the corrosion resistance is sufficient only with the above-mentioned main components. Therefore, in the surface treatment liquid of the present invention, the organic titanium chelate compound (D) is an essential component in addition to the above main components. The organic titanium chelate compound (D) is presumed to act as a catalyst for promoting polysiloxane formation when the surface treatment liquid is dried to form a film. As a result, the barrier property of the film is dramatically improved, the corrosion resistance of the flat surface portion and the corrosion resistance after alkaline degreasing are improved, and the solvent resistance and the coating property are also improved.

In order to obtain the above effect, as described above, a predetermined amount of the organic titanium chelate compound (D) determined according to the amount of the silane coupling agent (C) is required. If the amount is small, the desired effect cannot be obtained, and if the amount is excessive, the amount of polysiloxane increases too much to form a hard and brittle film, and the corrosion resistance of the processed portion is lowered. In addition, it is ideal that polysiloxane formation by the organic titanium chelate compound (D) is promoted at the time of film formation, but since polysiloxane formation is promoted even during storage of the surface treatment liquid, when the content is excessive. In addition, thickening and gelation progress, and a stable surface treatment liquid cannot be obtained.

The surface treatment liquid of the present invention also contains a tetravalent vanadium compound (E) as an essential component. In the present invention, the tetravalent vanadium compound (E) (1) acts as a corrosion inhibitor (for example, passivation of zinc) to improve the corrosion resistance of the flat surface, and (2) dipolypolyphosphate in a corrosive environment. It is presumed that there are two actions to improve the corrosion resistance of the scratched part by eluting with the aluminum hydrogen hydrogen rust preventive pigment and covering the exposed part of the base iron of the scratched part. The tetravalent vanadium compound (E), especially vanadyl ion [VO ²⁺ ] having one oxygen, is basically difficult to elute in a moist environment and exerts an inhibitory effect while staying in the film. As a result, excellent flat surface corrosion resistance can be obtained. On the other hand, since it is difficult to elute, the effect of tetravalent vanadium compound (E) alone on the corrosion resistance of the wound is small.

Therefore, in the present invention, an aluminum dihydrogen trihydrophosphate rust preventive pigment (G) is added in order to improve the corrosion resistance of the scratched portion. The aluminum dihydrogen phosphate rust preventive pigment easily elutes in a moist environment, and after elution from the film, it has an action of forming a phosphate precipitate on the exposed portion of the ground iron of the wounded portion. This aluminum dihydrogen tripolyphosphate rust preventive pigment (G) is compounded with a part of the tetravalent vanadium compound (E) by compound addition with the tetravalent vanadium compound (E) and eluted together, resulting in scratches. A vanadium-containing phosphate precipitate is formed on the exposed portion of the base iron. The vanadium-containing phosphate precipitated in the exposed portion of the base iron greatly improves the corrosion resistance of the scratched portion due to its high corrosion suppressing effect.
Further, as the aluminum dihydrogen trihydrophosphate rust preventive pigment (G), in addition to aluminum dihydrogen tripolyphosphate, at least one additive element selected from Zn, Mg, Si and Ca is contained, and the above addition element mass (G _E), when 0.1 to 10 by mass ratio of phosphorus amount in dihydrogen tripolyphosphate aluminum-based anticorrosive pigment _{(G) (G P) {} (G E) / (G P)} By incorporating Zn, Mg, Si, and Ca into the vanadium-containing phosphate precipitate that precipitates on the exposed portion of the base iron, a protective film having a higher barrier property is formed, and the corrosion resistance of the scratched portion is further improved.

However, if the amount of the aluminum dihydrogen trihydrogen rust preventive pigment (G) is too large with respect to the tetravalent vanadium compound (E), the elution amount of the tetravalent vanadium compound (E) becomes too large and the flat surface corrosion resistance. Deteriorates. On the other hand, if the amount of the aluminum dihydrogen trihydrogen rust preventive pigment (G) is too small with respect to the tetravalent vanadium compound (E), the amount of vanadium-containing phosphate precipitated in the exposed portion of the base metal decreases, resulting in scratches. The corrosion resistance of the part deteriorates.

Further, the molybdic acid compound (F) is also an essential component in the surface treatment liquid of the present invention. This is because, in the present invention, excellent blackening resistance can be obtained by adding the molybdic acid compound (F). Blackening of zinc-based plating occurs regardless of the type of plating (electricity, melting), and in particular, hot-dip galvanizing is used to improve corrosion resistance or the adhesion between zinc plating and the material (iron plate). Mg and Al are added, and these are concentrated on the plating interface of galvanized plating and the surface layer of plating to promote blackening and become blacker. Further, it is known that the blackening resistance is lowered by performing a surface treatment for improving the white rust resistance of zinc-based plating.

The cause of the phenomenon that zinc-based plating turns black under high temperature and high humidity conditions is not yet clear, but zinc oxide generated on the outermost surface of zinc-based plating is deprived of oxygen and becomes oxygen-deficient zinc oxide. It is said that zinc oxide becomes oxygen-deficient type due to insufficient oxygen supply in the process of conversion or corrosion (oxidation) of zinc, and this appears black.

In the present invention, excellent blackening resistance can be obtained by introducing a molybdic acid compound into the surface treatment film. Molybdenum is a transition metal, the oxygen combines with molybdenum oxide (MoO _2, MoO ₃₎ and molybdate (MoO ₄ ^2-) is produced. In the present invention, in some high temperature and high humidity or corrosive environment of molybdate (MoO ₄ ^2-), by changing the oxide of molybdenum (MoO _2, MoO _3), moderately oxygen galvanized surface Since it is supplied, it is considered that oxygen-deficient zinc oxide is less likely to be formed. The inventors presume that a surface-treated film that suppresses blackening was obtained by such a mechanism.

<Preparation of surface treatment liquid>
The resin compound (A) shown in Table 1 (Table 1a and Table 1b), the cationic urethane resin emulsion (B) shown in Table 2, the silane coupling agent (C) shown in Table 3, and the titanium compound (D) shown in Table 4. ), The vanadium compound (E) shown in Table 5, the molybdic acid compound (F) shown in Table 6, the aluminum dihydrogen dihydrogen rust preventive pigment (G) shown in Table 7, the acid component (H) shown in Table 8, and The wax (W) emulsions shown in Table 9 were mixed at the compounding ratios shown in Tables 11 to 13 and prepared with deionized water so that the solid content concentration when dried at 110 ° C. for 2 hours was 10% by mass. As the above-mentioned deionized water, ion-exchanged water having an electric conductivity of 10 μS / cm was used. The hot-dip galvanized steel sheet shown in Table 10 was used as the treated original plate.

The surface of the plated steel sheet shown in Table 10 is subjected to alkaline degreasing treatment, washed and dried with water, and then the surface treatment liquid shown in Tables 11 to 13 is applied to one side by a bar coater, and Tables 11-2 to 13-2 are not washed with water. A plated steel sheet having a surface-treated film was produced by heating and drying so that each drying temperature shown in (1) reached the reached plate temperature. The amount of adhesion of the surface treatment film per side was adjusted according to the coating conditions (bar count, etc.). The amount of adhesion is shown in Tables 11-2 to 13-2. The amount of adhesion was determined by quantifying the Si of the blended silane coupling agent (C) with a fluorescent X-ray analyzer and converting the amount of Si adhesion to the amount of film adhesion.

Quality of surface treatment liquid and manufactured galvanized steel sheet (corrosion resistance of scratched part, corrosion resistance of flat part, corrosion resistance of bent part (simply referred to as bent part in the table), after alkaline degreasing (simply described as after degreasing in the table) Corrosion resistance, blackening resistance, paintability (indicated as it is in the table), coating property after alkaline degreasing (simply described as after degreasing in the table), solvent resistance, storage stability and lubricity) are as follows. Evaluated by conditions. The results are shown in Table 14. Here, the evaluations Δ and × were rejected due to insufficient performance.

(1) Scratch corrosion resistance Each sample was cross-cut with an NT cutter (A300 type manufactured by NT Co., Ltd.) and then subjected to a salt spray test (JIS-Z-2371-2000), and after 120 hours had passed. The maximum rust width on one side was evaluated. The evaluation criteria are as follows.
◎: Rust width less than 1 mm ○ +: Rust width 1 mm or more and less than 3 mm ○: Rust width 3 mm or more and less than 5 mm Δ: Rust width 5 mm or more and less than 10 mm ×: Rust width 10 mm or more

(2) Corrosion resistance on flat surface A salt spray test (JIS-Z-2371-2000) was performed on each sample, and the width of white rust after 240 hours was evaluated. The evaluation criteria are as follows.
◎: White rust generation area rate 0%
○ +: White rust occurrence area rate less than 5% ○: White rust occurrence area rate 5% or more and less than 10% ○ −: White rust occurrence area rate 10% or more, less than 20% Δ: White rust occurrence area rate 20% or more , Less than 40% ×: White rust occurrence area rate 40% or more

(3) Corrosion resistance of the bent portion Each sample was bent 180 ° so as to be sandwiched between rods (made of stainless steel) having a diameter of 2 mm, and narrowed down using a vise. A salt spray test (JIS-Z-2371-2000) was performed on this bent sample, and the area ratio of white rust on the outside (front) side of the bent part after 72 hours was evaluated. The evaluation criteria are as follows.
◎: Area ratio of white rust generated in the bent part is 0%
○ +: White rust generation area ratio of the bending part is less than 5% ○: White rust generation area ratio of the bending part is 5% or more and less than 10% ○ −: White rust generation area ratio of the bending part is 10% or more, 40 % Δ: White rust generation area ratio of bending part 40% or more, less than 80% ×: White rust generation area ratio of bending part 80% or more

(4) Corrosion resistance after alkaline degreasing The alkaline degreasing agent CL-N364S (manufactured by Nihon Parkerizing Co., Ltd.) was dissolved in pure water at a concentration of 20 g / L and heated to 60 ° C. Each sample was immersed in this alkaline solution for 2 minutes, removed, washed with water and dried. A salt spray test (JIS-Z-2371-2000) was performed on each sample, and the area ratio of white rust after 72 hours was evaluated. The evaluation criteria are as shown in the evaluation described in (2) above.

(5) Blackening resistance Changes in brightness (L value) when each sample is allowed to stand in a constant temperature and humidity chamber controlled to an atmosphere of temperature: 80 ° C. and relative humidity: 95% for 24 hours (ΔL = after test) It was calculated by (L value-L value before the test). The evaluation criteria are as follows. The L value was measured in SCI mode (including specular reflection light) using SR2000 manufactured by Nippon Denshoku Kogyo Co., Ltd.
⊚: -6 ≦ △ L
◯: -10 ≦ ΔL <-6
Δ: −14 ≦ ΔL <-10
X: ΔL <-14

(6) Paintability Each sample is coated with Delicon (registered trademark) # 700 (manufactured by Dainippon Paint Co., Ltd.), which is a melamine alkyd paint, and baked at 130 ° C for 30 minutes to form a coating film with a film thickness of 30 μm. After that, it was immersed in boiling water for 2 hours, and immediately, a cut was made to reach the steel base of the grid (10 x 10 pieces, 1 mm interval). Further, a 5 mm extrusion process was performed using an Eriksen extrusion machine so that the cut portion was on the outer (front) side, and the coating film was attached and peeled off with an adhesive tape, and the peeled area of the coating film was measured. The evaluation criteria are as follows. The Eriksen extrusion conditions were based on JIS Z-2247-2006, with a punch diameter of 20 mm, a die diameter of 27 mm, and a drawing width of 27 mm.
◎: No peeling ○ +: Peeling area less than 3% ○: Peeling area 3% or more and less than 10% ○ −: Peeling area 10% or more and less than 20% Δ: Peeling area 20% or more and less than 50% ×: Peeling area 50% or more

(7) Coating property after alkaline degreasing Alkaline degreasing was performed in the same manner as described in (4) above, and the same coating property test as described in (6) above was performed on the sample. The evaluation criteria are the same as those described in (6) above.

(8) Solvent resistance A gauze impregnated with ethanol on the surface of each sample was pressed under a load of 4.90 N (500 gf) and rubbed so as to reciprocate 10 times with the load. The rubbing marks were visually evaluated. The evaluation criteria are as follows.
◎: No trace.
○ +: No trace can be seen when viewed from above, but slightly visible when viewed from an angle.
○: No trace can be seen when viewed from above, but it is clearly visible when viewed from an angle.
○-: Slight traces can be seen when viewed from above.
Δ: Traces are clearly visible when viewed from above.
X: The film is peeled off.

(9) Storage stability Each surface treatment solution shown in Tables 11 to 13 was stored in a constant temperature bath at 40 ° C. for 30 days. After taking out and stirring, the appearance of each surface treatment liquid was visually inspected and evaluated. The evaluation criteria are as follows.
⊚: No change ○: A very small amount of precipitate was observed Δ: A small amount of precipitation was observed or the viscosity became slightly high ×: A large amount of precipitation was observed or gelled.

(10) Lubrication A disk-shaped test piece having a diameter of 100 mm was cut out from each sample and molded into a cup shape under the conditions of a punch diameter: 50 mm, a die diameter: 51.91 mm, and a wrinkle pressing force: 1 ton. The appearance of the drawn surface (outside the side surface of the cup) of the molded product was visually inspected, and the degree of damage and the degree of blackening were evaluated. The evaluation criteria are as follows.
◎: Almost no change over the entire surface, the appearance is uniform ○ +: Very slight blackening occurs, but the appearance is uniform ○: Scratches and blackening occur a little, and the appearance is clearly uneven ○-: Local The appearance is clearly uneven due to scratches and blackening. Δ: Severe scratches and blackening occur mainly at the corners ×: Cracked without being able to be molded

As shown in Table 14, all of the test steel sheets produced by using the surface treatment liquid of the present invention have excellent scratch corrosion resistance, and the flat surface, the bent portion, the corrosion resistance after degreasing, the blackening resistance, and the coating. It also shows excellent results in properties (without and after degreasing), solvent resistance, storage stability and lubricity. On the other hand, in the comparative example in which any of the requirements deviates from the appropriate range of the present invention, any of the above characteristics cannot be sufficiently obtained. In particular, for Comparative Examples 1,2,3,6,7,8,11,12, since the type of the resin compound (A) or the urethane resin emulsion (B) is out of the scope of the present invention, the surface treatment is performed. At the time of preparation of the liquid, a large amount of precipitate was formed, and the test could not be carried out.

Claims (6)

On the surface of the zinc-based plated steel sheet, a resin compound (A) having a bisphenol skeleton represented by the following general formula (I) and at least one cation selected from the 1st to 3rd amino groups and the quaternary ammonium base A cationic urethane resin emulsion (B) having a sex functional group and one or more silane coupling agents having at least one reactive functional group selected from an active hydrogen-containing amino group, an epoxy group, a mercapto group and a methacryloxy group. (C), organic titanium chelate compound (D), tetravalent vanadium compound (E), molybdic acid compound (F), aluminum dihydrogen dihydrogen tripolyphosphate rust preventive pigment (G), and water. A surface treatment liquid for zinc-based plated steel sheets containing the following conditions (1) to (6) within a range that satisfies the conditions.
(1) Cationicity with respect to the total solid content {(As) + (Bs) + (Cs)} of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C). The solid content (Bs) of the urethane resin emulsion (B) is 0.10 to 0.30 in mass ratio [(Bs) / {(As) + (Bs) + (Cs)}].
(2) Silane coupling with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)} The solid content (Cs) of the agent (C) is 0.60 to 0.85 in mass ratio [(Cs) / {(As) + (Bs) + (Cs)}].
(3) The solid content (Cs) of the silane coupling agent (C) with respect to the titanium equivalent amount (D _Ti ) of the organic titanium chelate compound (D) is 50 by mass ratio {(Cs) / (D _Ti )}. ~ 70
(4) The organic titanium chelate compounds of titanium equivalent amount of (D) relative to (D _Ti), the tetravalent vanadium compound Vanadium amount of (E) (E _V) is the weight ratio {(E _V) / (D _Ti )} from 0.30 to 0.50
(5) The molybdic acid with respect to the total solid content of the resin compound (A), the cationic urethane resin emulsion (B) and the silane coupling agent (C) {(As) + (Bs) + (Cs)}. The molybdenum equivalent amount (F _Mo ) of compound (F) is 0.003 to 0.030 in mass ratio [(F _Mo ) / {(As) + (Bs) + (Cs)}].
(6) The tetravalent vanadium compound Vanadium amount of (E) solid content of the tripolyphosphate aluminum dihydrogen anticorrosive pigment to (E _V) (G) (Gs) is the weight ratio {(Gs) / ( in E _V)} 3~300

In formula (I), Y ₁ and Y ₂ bonded to the benzene ring are hydrogen atoms independently of each other, or Z groups represented by the following general formulas (II) or (III), and 1benzene. The average number of Z-group substitutions per ring is 0.2-1.0. n represents an integer from 2 to 50.

In formulas (II) and (III), R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independent hydrogen atoms, alkyl groups having 1 to 10 carbon atoms or hydroxyalkyl groups having 1 to 10 carbon atoms, respectively. , And A ⁻ represents a hydroxide ion or an acid ion. The aluminum tripolyphosphate dihydrogen rust preventive pigment (G) contains at least one additive element selected from Zn, Mg, Si, and Ca in addition to aluminum dihydrogen tripolyphosphate, and the additive element. mass (G _E) is the mass ratio to phosphorus mass in dihydrogen tripolyphosphate aluminum-based anticorrosive pigment _{(G) (G P) {} (G E) / (G P)} by from 0.1 to 10 The surface treatment liquid for zinc-based plated steel sheets according to claim 1, wherein the surface treatment liquid is characterized by. The surface treatment liquid further contains an acid component (H), and the mass (Hg) of the acid component (H) is the resin compound (A), the cationic urethane resin emulsion (B), and the silane coupling agent. The mass ratio [(Hg) / {(As) + (Bs) + (Cs)}] to the total solid content of (C) {(As) + (Bs) + (Cs)} is 0.10 or less. The surface treatment liquid for a galvanized steel sheet according to claim 1 or 2, which is characterized. The surface treatment liquid further contains a wax (W), and the solid content (Ws) of the wax (W) is the total solid content of the resin compound (A) and the cationic urethane resin emulsion (B) {( The invention according to any one of claims 1 to 3, wherein the mass ratio [(Ws) / {(As) + (Bs)}] to As) + (Bs)} is in the range of 0.2 to 0.6. Surface treatment liquid for galvanized steel sheets. The surface treatment liquid according to any one of claims 1 to 4 is applied to the surface of a galvanized steel sheet in a range in which the amount of adhesion after drying is 0.2 to 1.8 g / m ² per side, and then reaches. Plate temperature: A method for producing a galvanized steel sheet, which is characterized by drying at 50 to 180 ° C. A galvanized steel sheet having a surface-treated film having an adhesion amount of 0.2 to 1.8 g / m ² per side on the surface, wherein the surface-treated film is the surface according to any one of claims 1 to 4. A galvanized steel sheet characterized by being obtained by applying a treatment liquid to the surface of a steel sheet and drying it at a plate temperature of 50 to 180 ° C.