JP5689210B1 - Paint composition - Google Patents

Abstract

Disclosed is a coating composition that has good storage stability, can maintain stain resistance when exposed outdoors, and can form a coating film with good coating film hardness and processability. The present invention relates to a hydroxyl group-containing resin (a), a crosslinking agent (b), an anionic surfactant (c) containing a sulfonic acid group or a sulfonate group, a specific copolymer resin (d), and a specific organo A coating composition containing a silicate and / or a condensate thereof (e), the sulfonic acid group or the sulfonate group based on 100 parts by mass in total of the solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b) 1 to 20 parts by mass of the anionic surfactant (c) containing 0.1 to 20 parts by mass of the copolymer resin (d), and 0.1 to 10 parts of the organosilicate and / or its condensate (e). The coating composition containing 1-10 mass parts is included.

Description

[Cross-reference of related applications]
This application claims priority based on Japanese Patent Application No. 2013-124861 filed on June 13, 2013, the entire disclosure of which is incorporated herein by reference. To do.

  The present invention relates to a coating composition that has good storage stability, can maintain stain resistance over a long period of time when exposed outdoors, and can form a coating film with good coating film hardness and processability.

Conventionally, outdoor base materials (for example, buildings, display objects, guard fences, appliances, machines, etc.) have been coated with an outdoor paint excellent in weather resistance for the purpose of decoration or protection. Examples of paints used outdoors include polyurethane resin paints, fluororesin paints, silicone resin paints, acrylic resin paints, polyester paints, etc., but these paints are exposed outdoors. As a result, there is a drawback that the surface of the coating is easily soiled due to the influence of soot, sand dust, iron powder, rain (acid rain), sunlight, etc., and the stain resistance is lowered.

  Conventionally, a coating composition for a pre-coated steel sheet comprising (A) a polyol resin, (B) an amino resin, (C) an alkoxysilane compound, and (D) a curing catalyst and having excellent resistance to contamination against rainwater and workability is disclosed. (Patent Document 1).

  Also, it contains organosilicate and / or its condensate, boric acid compound, untreated silica fine particles, and colored pigments with respect to 100 parts by mass of the hydroxyl group-containing coating film-forming resin and amino resin crosslinking agent. On the other hand, the coating composition which can form the coating film excellent in stain resistance is disclosed (patent document 2).

  However, the coating films obtained by applying the coating compositions described in Patent Document 1 and Patent Document 2 are insufficient in the durability of stain resistance, and are particularly semi-added with a matting agent such as silica. In the gloss coating, the contamination resistance was significantly reduced by outdoor exposure.

JP-A-10-67945 JP 2008-81719 A

  The problem to be solved by the present invention is a coating composition that has good storage stability, can maintain stain resistance over a long period of time when exposed outdoors, and can form a coating film with good coating film hardness and workability. Is to provide.

  As a result of intensive studies, the present inventors have found that a hydroxyl group-containing resin (a), a crosslinking agent (b), an anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group, a specific copolymer resin ( d), and a specific organosilicate and / or a condensate thereof (e), a coating composition comprising 100 parts by mass of the total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b), 1-20 parts by mass of an anionic surfactant (c) containing a sulfonic acid group or a sulfonate group, 0.1-20 parts by mass of the copolymer resin (d), the organosilicate and / or its condensation It has been found that the problem can be achieved by a coating composition containing 0.1 to 10 parts by mass of the product (e).

That is, the present invention
1. Hydroxyl group-containing resin (a), crosslinking agent (b), anionic surfactant (c) containing sulfonic acid group or sulfonate group, copolymer resin (d), organosilicate and / or condensate thereof ( e) a coating composition comprising:
1 to 20 parts by mass of an anionic surfactant (c) containing a sulfonic acid group or a sulfonate group with respect to a total solid content of 100 parts by mass of the hydroxyl group-containing resin (a) and the crosslinking agent (b), 0.1 to 20 parts by mass of copolymer resin (d), 0.1 to 10 parts by mass of the organosilicate and / or its condensate (e),
Polymeric unsaturated having an amino group or a quaternary ammonium base-containing polymerizable unsaturated monomer (d11) and a nitrogen atom-containing heterocyclic ring with respect to the total amount of all monomers constituting the copolymer resin (d). 20 to 70% by mass of at least one polymerizable unsaturated monomer (d1) selected from the monomer (d12) and the N-substituted (meth) acrylamide compound (d13), and other polymerizable unsaturated compounds It is a copolymer resin of a monomer mixture with monomer (d2) 30 to 80% by mass,
The organosilicate and / or its condensate (e) is represented by the following formula (1), a coating composition,
Equation _{^{(1): (R 1)}} n -Si- (OR 2) 4-n
(In the formula (1), R ¹ is an alkyl group or a phenyl group having 1 to 18 carbon atoms which may be substituted with an epoxy group or a mercapto group, R ² is an alkyl group having 1 to 6 carbon atoms , N is 0 or 1)
2. 60-95 parts by mass of the hydroxyl group-containing resin (a) and 5-40 parts by mass of the crosslinking agent (b) with respect to 100 parts by mass of the total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b). The coating composition according to 1, which is contained in
3. The coating composition according to item 1 or 2, wherein the anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group is an alkylsulfosuccinic acid-based anionic surfactant,
4). The copolymer resin (d) has an amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11) 1 to 30% by mass and a nitrogen atom-containing heterocycle with respect to the total amount of all monomers constituting the copolymer resin (d). Polymerizable unsaturated monomers (d12) 5 to 60% by mass, N-substituted (meth) acrylamide compound (d13) 0 to 20% by mass and other polymerizable unsaturated monomers (d2) 30 to 80 2. The coating composition according to 1, which is a copolymer resin of a monomer mixture of mass%.
5. The coating composition according to 1, wherein the urea resin particles (f) are contained in an amount of 1 to 50 parts by mass with respect to a total of 100 parts by mass of the solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b).
6). A primer coating film is formed on one side or both sides of a metal plate, and a coating film is formed from the coating composition according to any one of 1 to 5 on at least one side of the primer coating film. A method of forming a coating film,
It is related with the coating metal plate obtained by the coating-film formation method of 7.6.

  The present invention is a coating composition having good storage stability, and the coating film obtained by applying the coating composition can maintain stain resistance over a long period of time when exposed outdoors, and further, the coating film hardness Excellent workability.

Coating composition of the present invention The coating composition of the present invention comprises a hydroxyl group-containing resin (a), a crosslinking agent (b), an anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group base, and a copolymer. It is a coating composition containing resin (d), organosilicate and / or its condensate (e), and, if necessary, urea resin particles (f). Details will be described below.

Hydroxyl-containing resin (a)
The hydroxyl group-containing resin (a) is a resin having two or more hydroxyl groups in one molecule, and may have a carboxyl group as necessary. Specific examples of the hydroxyl group-containing resin (a) include acrylic resins, polyester resins, epoxy resins, polyurethane resins, and the like. From the viewpoint of improving stain resistance, coating film hardness, and processability, hydroxyl group-containing acrylic resins, hydroxyl groups -Containing polyester resins and the like are preferable, and hydroxyl group-containing polyester resins are particularly preferable. The hydroxyl group-containing resin (a) is different from the copolymer resin (d) described later. Accordingly, in the present invention, the hydroxyl group-containing resin (a) means a resin having two or more hydroxyl groups in one molecule (excluding a copolymer resin (d) described later).

  The above-mentioned hydroxyl group-containing acrylic resin is a copolymer resin obtained by copolymerizing a hydroxyl group-containing acrylic monomer and other monomers. The hydroxyl group-containing acrylic resin is different from the copolymer resin (d) described later. Accordingly, in the present invention, the hydroxyl group-containing acrylic resin means an acrylic resin having two or more hydroxyl groups in one molecule (except for the copolymer resin (d) described later). The hydroxyl group-containing monomer is a compound having at least one hydroxyl group and one polymerizable unsaturated bond in one molecule.

  Examples of the hydroxyl group-containing monomer include glycols having 2 to 20 carbon atoms such as hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate, hydroxyicosyl (meth) acrylate, and (meth) acrylic. Examples include monoesterified products with acids.

  Examples of other monomers other than the hydroxyl group-containing monomer include, for example, alkyl esters of 1 to 22 carbon atoms of (meth) acrylic acid, alkoxyalkyl esters of 2 to 18 carbon atoms of (meth) acrylic acid, epoxy group-containing monomers, carboxyl A group-containing monomer, a monomer having an isocyanate group and a polymerizable unsaturated group in one molecule, styrene, α-methylstyrene, vinyl toluene, acrylonitrile, vinyl acetate, vinyl chloride and the like can be used.

  Examples of the alkyl ester having 1 to 22 carbon atoms of the (meth) acrylic acid include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, Examples include octyl (meth) acrylate, lauryl (meth) acrylate, 2-ethylhexyl (meth) acrylate, cyclohexyl (meth) acrylate, and isobornyl (meth) acrylate. Examples of the alkoxyalkyl ester having 2 to 18 carbon atoms of (meth) acrylic acid include methoxybutyl (meth) acrylate and methoxyethyl (meth) acrylate. Examples of the epoxy group-containing monomer include glycidyl acrylate and glycidyl methacrylate. Examples of the carboxyl group-containing monomer include acrylic acid, methacrylic acid, maleic acid, itaconic acid, fumaric acid, mesaconic acid, and anhydrides and half-esterified products thereof. Other monomers other than the hydroxyl group-containing monomer can be used alone or in combination of two or more.

  The number average molecular weight of the hydroxyl group-containing acrylic resin is preferably about 1,000 to 50,000, and more preferably about 2,000 to 20,000. The hydroxyl value of the resin is preferably about 20 to 200 mgKOH / g, and more preferably about 50 to 150 mgKOH / g.

  The hydroxyl group-containing polyester resin can be usually produced by an esterification reaction or a transesterification reaction with the polybasic acid component (a1) and the alcohol component (a2).

  The said polybasic acid component (a1) can use the compound normally used as a polybasic acid component at the time of manufacture of a polyester resin. As a polybasic acid component (a1), an alicyclic polybasic acid, an aliphatic polybasic acid, an aromatic polybasic acid etc. can be used, for example.

  Generally, an alicyclic polybasic acid is a compound having one or more alicyclic structures (mainly 4 to 6-membered rings) and two or more carboxyl groups in one molecule, an acid anhydride of the compound, and the compound. The esterified product. Examples of the alicyclic polybasic acid include 1,2-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-cyclohexene-1,2-dicarboxylic acid, and 3-methyl. -1,2-cyclohexanedicarboxylic acid, 4-methyl-1,2-cyclohexanedicarboxylic acid, 1,2,4-cyclohexanetricarboxylic acid, alicyclic polyvalent carboxylic acid such as 1,3,5-cyclohexanetricarboxylic acid; Examples thereof include anhydrides of these alicyclic polyvalent carboxylic acids; lower alkyl esterified products of these alicyclic polyvalent carboxylic acids. An alicyclic polybasic acid can be used individually or in combination of 2 or more types.

  As the alicyclic polybasic acid, in particular, 1,2-cyclohexanedicarboxylic acid, 1,2-cyclohexanedicarboxylic anhydride, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-cyclohexene-1 , 2-dicarboxylic acid, 4-cyclohexene-1,2-dicarboxylic anhydride can be preferably used. Among the above, 1,2-cyclohexanedicarboxylic acid and 1,2-cyclohexanedicarboxylic anhydride can be particularly preferably used from the viewpoint of hydrolysis resistance.

  The aliphatic polybasic acid is generally an aliphatic compound having two or more carboxyl groups in one molecule, an acid anhydride of the aliphatic compound, and an esterified product of the aliphatic compound, for example, succinic acid, Aliphatic polycarboxylic acids such as glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, brassylic acid, octadecanedioic acid, citric acid; Acid anhydrides; and lower alkyl esterified products of these aliphatic polyvalent carboxylic acids. An aliphatic polybasic acid can be used individually or in combination of 2 or more types.

  As the aliphatic polybasic acid, it is preferable to use a dicarboxylic acid having an alkyl chain having 4 to 18 carbon atoms. Examples of the dicarboxylic acid having an alkyl chain having 4 to 18 carbon atoms include adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, brassic acid, and octadecanedioic acid. Among them, adipic acid can be preferably used.

  The aromatic polybasic acid is generally an aromatic compound having two or more carboxyl groups in one molecule, an acid anhydride of the aromatic compound and an esterified product of the aromatic compound, for example, phthalic acid, Aromatic polycarboxylic acids such as isophthalic acid, terephthalic acid, naphthalenedicarboxylic acid, 4,4′-biphenyldicarboxylic acid, trimellitic acid, pyromellitic acid; anhydrides of these aromatic polycarboxylic acids; And lower alkyl esterified products of monovalent carboxylic acids. Aromatic polybasic acids can be used alone or in combination of two or more.

  As the alcohol component (a2), a polyhydric alcohol having two or more hydroxyl groups in one molecule can be preferably used. As said polyhydric alcohol, an alicyclic diol, an aliphatic diol, an aromatic diol etc. can be mentioned, for example.

  The alicyclic diol is generally a compound having one or more alicyclic structures (mainly 4 to 6-membered rings) and two hydroxyl groups in one molecule. Examples of the alicyclic diol include dihydric alcohols such as 1,4-cyclohexanedimethanol, tricyclodecane dimethanol, hydrogenated bisphenol A, and hydrogenated bisphenol F; ε-caprolactone and the like in these dihydric alcohols. Examples include polylactone diol to which a lactone compound is added, and these can be used alone or in combination of two or more.

  The aliphatic diol is generally an aliphatic compound having two hydroxyl groups in one molecule. Examples of the aliphatic diol include ethylene glycol, propylene glycol, diethylene glycol, trimethylene glycol, tetraethylene glycol, triethylene glycol, dipropylene glycol, 1,4-butanediol, 1,3-butanediol, 2,3 -Butanediol, 1,2-butanediol, 3-methyl-1,2-butanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,2-pentanediol, 1,5-pentanediol 1,4-pentanediol, 2,4-pentanediol, 2,3-dimethyltrimethylene glycol, tetramethylene glycol, 3-methyl-1,5-pentanediol, 2,2,4-trimethyl-1,3 -Pentanediol, 1,6-hexanediol, 1, -Hexanediol, 1,4-hexanediol, 2,5-hexanediol, 1,9-nonanediol, 1,10-decanediol, 1,12-dodecanediol, neopentyl glycol, etc. Or in combination of two or more.

  The aromatic diol is generally an aromatic compound having two hydroxyl groups in one molecule. Examples of the aromatic diol include ester diol compounds such as bis (hydroxyethyl) terephthalate; alkylene oxide adducts of bisphenol A and the like, and these can be used alone or in combination of two or more.

  Examples of the polyhydric alcohol other than the alicyclic diol, aliphatic diol and aromatic diol include polyether diol compounds such as polyethylene glycol, polypropylene glycol and polybutylene glycol; glycerin, trimethylol ethane, trimethylol propane, Trivalent or higher alcohols such as glycerin, triglycerin, 1,2,6-hexanetriol, pentaerythritol, dipentaerythritol, tris (2-hydroxyethyl) isocyanurate, sorbitol, mannitol; these trivalent or higher alcohols And a polylactone polyol compound in which a lactone compound such as ε-caprolactone is added.

  Among the above, trivalent or higher alcohols can be suitably used from the viewpoint of increasing the molecular weight and improving the reactivity of the modification reaction with the fatty acid when using the fatty acid. Examples of the trihydric or higher polyhydric alcohol include glycerin, trimethylolethane, trimethylolpropane, diglycerin, triglycerin, 1,2,6-hexanetriol, pentaerythritol, dipentaerythritol, sorbitol, mannitol and the like. A trilactone (2-hydroxyethyl) isocyanurate, tris (2-hydroxypropyl) isocyanurate; a trilactone (2-hydroxyethyl) isocyanurate; a trilactone (2-hydroxypropyl) isocyanurate; And tris (hydroxyalkyl) isocyanurate such as tris (2-hydroxybutyl) isocyanurate. Of these, trimethylolpropane is particularly preferable.

  Examples of the alcohol component (a2) other than the polyhydric alcohol include monoalcohols such as methanol, ethanol, propyl alcohol, butyl alcohol, stearyl alcohol, and 2-phenoxyethanol; propylene oxide, butylene oxide, and synthetic highly branched saturated fatty acids. Alcohol compounds obtained by reacting a monoepoxy compound such as glycidyl ester (trade name “Cardura E10” manufactured by HEXION Specialty Chemicals) and an acid can be used as necessary.

  The production of the hydroxyl group-containing polyester resin is not particularly limited, and can be performed according to an ordinary method. For example, it is produced by reacting an acid component having the polybasic acid component as an essential component and an alcohol component at 150 to 250 ° C. for 5 to 10 hours in a nitrogen stream and performing an esterification reaction or a transesterification reaction. Can do.

  In the esterification reaction or transesterification reaction, the acid component and alcohol component may be added at once, or may be added in several portions. Moreover, after synthesize | combining a carboxyl group-containing polyester resin first, you may esterify some carboxyl groups in this carboxyl group-containing polyester resin using the said alcohol component. Furthermore, after first synthesizing the hydroxyl group-containing polyester resin, the acid anhydride may be reacted to half-esterify the hydroxyl group-containing polyester resin.

  In the esterification or transesterification reaction, a catalyst may be used to promote the reaction. As the catalyst, known catalysts such as dibutyltin oxide, antimony trioxide, zinc acetate, manganese acetate, cobalt acetate, calcium acetate, lead acetate, tetrabutyl titanate, and tetraisopropyl titanate can be used.

  Further, the hydroxyl group-containing polyester resin can be modified with a fatty acid, an oil or fat, a monoepoxy compound, a polyisocyanate compound or the like during the preparation of the resin, or after the esterification reaction or after the transesterification reaction. A hydroxyl group-containing polyester resin modified with a fatty acid or oil is referred to as an alkyd resin.

  Examples of the fatty acid include coconut oil fatty acid, cottonseed oil fatty acid, hemp seed oil fatty acid, rice bran oil fatty acid, fish oil fatty acid, tall oil fatty acid, soybean oil fatty acid, linseed oil fatty acid, tung oil fatty acid, rapeseed oil fatty acid, castor oil fatty acid, dehydrated castor oil Examples include fatty acids such as fatty acids and safflower oil fatty acids; lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and the like. Examples of the fat include coconut oil, cottonseed oil, hemp seed oil, rice bran oil, fish oil, tall oil, soybean oil, linseed oil, tung oil, rapeseed oil, castor oil, dehydrated castor oil, safflower oil and the like.

  Examples of the polyisocyanate compound used for the modification include aliphatic diisocyanate compounds such as lysine diisocyanate, hexamethylene diisocyanate, and trimethylhexane diisocyanate; hydrogenated xylylene diisocyanate, isophorone diisocyanate, methylcyclohexane-2,4-diisocyanate, methylcyclohexane. -Aliphatic diisocyanate compounds such as 2,6-diisocyanate, 4,4'-methylenebis (cyclohexyl isocyanate), 1,3- (isocyanatomethyl) cyclohexane; aromatics such as tolylene diisocyanate, xylylene diisocyanate, diphenylmethane diisocyanate Diisocyanate compounds; organic polymers such as lysine triisocyanate Isocyanate itself, or an adduct of each of these organic polyisocyanates with polyhydric alcohol, low molecular weight polyester resin or water, or a cyclized polymer of each of the above organic diisocyanates (for example, isocyanurate), biuret type addition And the like. These can be used alone or in combination of two or more.

  The number average molecular weight of the hydroxyl group-containing polyester resin is preferably 2,000 to 30,000, particularly within the range of 3,000 to 25,000, from the viewpoints of coating film hardness, workability, and finish of the resulting coating film. It is preferred to have a number average molecular weight.

  In this specification, the number average molecular weight and the weight average molecular weight are values obtained by converting the number average molecular weight and the weight average molecular weight measured using a gel permeation chromatograph (GPC) based on the molecular weight of standard polystyrene. is there. Specifically, “HLC8120GPC” (trade name, manufactured by Tosoh Corporation) is used as a gel permeation chromatograph, and “TSKgel G-4000HXL”, “TSKgel G-3000HXL”, “TSKgel G-2500HXL” are used as columns. ”And“ TSKgel G-2000HXL ”(trade names, all manufactured by Tosoh Corporation), and can be measured under the conditions of mobile phase tetrahydrofuran, measurement temperature 40 ° C., flow rate 1 mL / min, and detector RI. it can.

  The hydroxyl value of the hydroxyl group-containing polyester resin is preferably from 5 to 250 mgKOH / g, particularly preferably from 10 to 200 mgKOH / g, from the viewpoint of the curability of the resulting coating film. The acid value of the hydroxyl group-containing polyester resin is preferably in the range of 30 mgKOH / g or less, more preferably 20 mgKOH / g or less, from the viewpoint of processability and water resistance.

Crosslinking agent (b)
The crosslinking agent (b) in the coating composition of the present invention can be used without particular limitation as long as it can react with the hydroxyl group of the hydroxyl group-containing resin (a) by heating and can be cured. Examples include benzoguanamine resin, urea resin, and blocked polyisocyanate.

  As said melamine resin, a part or all of methylol group of methylolation melamine is C1-C8 monohydric alcohol, for example, methyl alcohol, ethyl alcohol, n-propyl alcohol, i-propyl alcohol, n-butyl alcohol , Partially etherified or fully etherified melamine resins etherified with i-butyl alcohol, 2-ethylbutanol, 2-ethylhexanol and the like.

  Examples of commercially available melamine resins include Cymel 202, Cymel 232, Cymel 235, Cymel 238, Cymel 254, Cymel 266, Cymel 267, Cymel 272, Cymel 285, Cymel 301, Cymel 303, Cymel 325, Cymel 327, and Cymel 350. , Cymel 370, Cymel 701, Cymel 703, Cymel 1141 (manufactured by Nippon Cytec Industries, Inc.), Uban 20SE60 (manufactured by Mitsui Cytec Co., Ltd.), and the like.

  Examples of the benzoguanamine resin include methylolated benzoguanamine resins obtained by reaction of benzoguanamine and aldehyde. Examples of the aldehyde include formaldehyde, paraformaldehyde, acetaldehyde, benzaldehyde and the like. In addition, those obtained by etherifying this methylolated benzoguanamine resin with one or more alcohols are also included in the benzoguanamine resin. Examples of the alcohol used for etherification include monohydric alcohols such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, isobutyl alcohol, 2-ethylbutanol, and 2-ethylhexanol. . Among these, a benzoguanamine resin obtained by etherifying at least a part of the methylol group of the methylolated benzoguanamine resin with a monohydric alcohol having 1 to 4 carbon atoms is preferable.

  Specific examples of the benzoguanamine resin include, for example, My Coat 102, My Coat 105, My Coat 106 [all of which are manufactured by Mitsui Cytec Co., Ltd.], Nicarak SB-201, Nicarac SB-203, Nicarac SB-301, Nicarac SB. -303, Nicalac SB-401 [above, both are manufactured by Sanwa Chemical Co., Ltd.] and other methyl etherified benzoguanamine resins; Cymel 1123 [above, manufactured by Mitsui Cytec Co., Ltd.], etc. Mixed etherified benzoguanamine resins of methyl ether and ethyl ether, etc. Methyl ether and butyl ether such as My Coat 136 [above, manufactured by Mitsui Cytec Co., Ltd.], Nicarak SB-255, Nicarac SB-355, Nicarac BX-37, Nicarac BX-4000 [over all, manufactured by Sanwa Chemical Co., Ltd.] Etherified benzoguanamine resins; Mycoat 1128 [above, Mitsui Cytec] and the like butyl etherified benzoguanamine resins such as.

  The urea resin is obtained by a condensation reaction of urea and formaldehyde, and can be dissolved or dispersed in a solvent or water. The polyisocyanate compound is a compound having two or more isocyanate groups in one molecule. For example, aromatic diisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, xylylene diisocyanate, naphthalene diisocyanate; tetramethylene diisocyanate, hexamethylene diisocyanate, Aliphatic diisocyanates such as dimer acid diisocyanate and lysine diisocyanate; alicyclic diisocyanates such as methylene bis (cyclohexyl isocyanate), isophorone diisocyanate, methylcyclohexane diisocyanate, cyclohexane diisocyanate and cyclopentane diisocyanate; Ring type adduct These polyisocyanates with low molecular weight or high molecular weight polyol compound (e.g., acrylic polyols, polyester polyols, polyether polyols, etc.) and an isocyanate group excess obtained by reacting the free isocyanate group-containing prepolymer can be mentioned a. Furthermore, the free isocyanate groups of these polyisocyanate compounds are converted into phenolic compounds, oxime compounds, active methylene compounds, lactam compounds, alcohol compounds, mercaptan compounds, acid amide compounds, imide compounds, amine compounds, imidazole compounds, urea systems. A blocked polyisocyanate blocked with a blocking agent such as a compound, a carbamic acid compound, and an imine compound can also be used.

  As a mixing ratio of the hydroxyl group-containing resin (a) and the crosslinking agent (b), the hydroxyl group-containing resin (a) is 60 to 95 parts by mass, preferably 70 to 90 based on the total solid content of both. It is suitable from the point of the adhesiveness with a base material, and sclerosis | hardenability that it is 5-40 mass parts, Preferably it is 10-30 mass parts, a crosslinking agent (b).

  The total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b) is usually 20 to 95 mass%, more preferably 35 to 85 mass%, based on the total solid content of the coating composition of the present invention. %.

Anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group
The coating composition of the present invention contains an anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group. The presence of the anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group in the coating film by the coating composition of the present invention can improve the cleaning property of the contaminants adhered to the coating film surface. it can.

Examples of the anionic surfactant (c) containing a sulfonic acid group or a sulfonic acid group include monoalkyl sulfosuccinic acid ester salts, dialkyl sulfosuccinic acid ester salts, sulfosuccinic acid alkyl disalts, and polyoxyethylene alkyl sulfosuccinic acid disalts. , Sodium alkylamine oxide bistridecyl sulfosuccinate, sodium dioctyl sulfosuccinate, sodium dihexyl sulfosuccinate, sodium dicyclohexyl sulfosuccinate, sodium diamyl sulfosuccinate, sodium diisobutyl sulfosuccinate, disodium isodecyl sulfosuccinate, N-octadecyl sulfosuccinamide Sodium, N- (1,2-dicarboxyethyl) -N-octadecylsulfosuccinamide tetrasodium Succinic acid type anionic surfactants; for example, alkylbenzene sulfonic acid type anionic surfactants such as sodium dodecylbenzene sulfonate; alkyl diphenyl ether disulfonic acid type anionic surfactants such as sodium dodecyl diphenyl ether disulfonate; poly Anionic surfactants based on ammonium sulfate ester having a polyoxyalkylene group, such as ammonium oxyethylene alkyl ether sulfate, polyoxyethylene alkyl phenyl ether ammonium sulfate, polyoxyethylene polycyclic phenyl ether ammonium sulfate; mono- or didodecyl diphenyl Sodium oxide disulfonate, sodium diisopropyl naphthalene sulfonate, sodium naphthalene sulfonate formalin condensate, Kirusuruho acetate, alpha-olefin sulfonate, and the like.
Only 1 type may be used for the anionic surfactant (c) containing these sulfonic acid groups or sulfonate groups, and 2 or more types may be used together.

  Among the anionic surfactants (c) containing the sulfonic acid group or sulfonic acid group, sulfosuccinic acid-based anionic surfactants, particularly dialkylsulfosuccinic acids having the structural formula represented by the following formula (2) Sodium salts are particularly preferred for improving stain resistance.

(R ³ and R ^{4 in} formula (2) are the same or different and each represents an alkyl group having 1 to 15 carbon atoms)

  Commercially available sulfosuccinic acid-based anionic surfactants include “Perex OT-P”, “Perex TR”, “Perex CS” and “Perex TA” manufactured by Kao Corporation; "Call 290-A", "New Call 290-M", "New Call 291-M", "New Call 291-PG", "New Call 291-GL", "New Call 292-PG", "New Call 293 "Neocoal SW-C", "Neocoal YSK", and "Neocoal P" manufactured by Daiichi Kogyo Seiyaku Co., Ltd. may be mentioned.

  In addition, the compounding quantity of the anionic surfactant (c) containing a sulfonic acid group or a sulfonate group is sulfone with respect to 100 mass parts of total solid content of a hydroxyl-containing resin (a) and a crosslinking agent (b). 1-20 parts by weight, preferably 2-10 parts by weight of the anionic surfactant (c) containing an acid group or a sulfonate group is excellent in stain resistance, coating film hardness, and workability This is preferable because a coating film can be obtained.

Copolymer resin (d)
By containing the copolymer resin (d) in the coating composition of the present invention, the effect of retaining the anionic surfactant (c) in the obtained coating film is obtained, and the stain resistance is maintained. Can be secured.

  The copolymer resin (d) is an amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11), a polymerizable unsaturated monomer having a nitrogen atom-containing heterocyclic ring (d12), and N-substituted. It can be obtained by copolymerizing a monomer mixture of at least one polymerizable unsaturated monomer (d1) selected from the (meth) acrylamide compound (d13) and other polymerizable unsaturated monomer (d2). Further, the copolymer resin (d) can be used after neutralization.

  Hereinafter, an amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11), a polymerizable unsaturated monomer having a nitrogen atom-containing heterocyclic ring (d12), and an N-substituted (meth) acrylamide compound ( At least one polymerizable unsaturated monomer (d1) selected from d13) may be referred to as “polymerizable unsaturated monomer (d1)”.

  Examples of the amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11) include aminoethyl (meth) acrylate, Nt-butylaminoethyl (meth) acrylate, and N, N-dimethylaminoethyl (meth). Acrylate, N, N-diethylaminoethyl (meth) acrylate, N, N-dipropylaminoethyl (meth) acrylate, N, N-dibutylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylate, N, N-dimethylaminobutyl (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylamide, N, N-dimethylaminopropyl (meth) acrylamide, N, N-diethylaminoethyl (meth) acrylamide, N, N -Dipropylaminoethyl (meth) Quaternary ammonium bases such as amino group-containing aminoalkyl (meth) acrylate monomers such as amino group-containing (meth) acrylamide compounds such as chloramide, methacryloyloxyethyltrimethylammonium chloride (acrylic ester DMC, trade name, manufactured by Mitsubishi Rayon Co., Ltd.) Examples thereof include unsaturated monomers.

  Examples of the polymerizable unsaturated monomer (d12) having a nitrogen atom-containing heterocyclic ring include (1) vinylpyropidone compounds such as 1-vinyl-2-pyrrolidone and 1-vinyl-3-pyrrolidone, (2) For example, vinyl pyridine compounds such as 2-vinyl pyridine, 4-vinyl pyridine, 5-methyl-2-vinyl pyridine, 5-ethyl-2-vinyl pyridine, etc. (3), for example, 1-vinyl imidazole, 1-vinyl-2 -Vinyl imidazole compounds such as methyl imidazole, (4) vinyl quinoline compounds such as 2-vinyl quinoline, (5) vinyl piperidine compounds such as 3-vinyl piperidine, N-methyl-3-vinyl piperidine, (6 ) For example, morpholine compound of acryloyl morpholine, methacryloyl morpholine, etc. That. Among these polymerizable unsaturated monomers (d12) having a nitrogen atom-containing heterocyclic ring, (1) a vinylpyrrolidone compound (preferably 1-vinyl-2-pyrrolidone etc.), (3) a vinylimidazole compound, (6) A morpholine compound or the like is preferable, and (1) a vinylpyrrolidone compound and (6) a morpholine compound are more preferable.

  Examples of the N-substituted (meth) acrylamide compound (d13) include acrylamide, methacrylamide, N-methyl acrylamide, N-methyl methacrylamide, N-methylol acrylamide butyl ether, N-methylol methacrylamide butyl ether, N-ethylacrylamide, N-ethylmethacrylamide, Nn-propylacrylamide, Nn-propylmethacrylamide, N-isopropylacrylamide, N-isopropylmethacrylamide, N-cyclopropylacrylamide, N-cyclopropylmethacrylamide, Diacetone acrylamide, diacetone methacrylamide, N-hydroxymethyl acrylamide, N-hydroxymethyl methacrylamide, N-hydroxyethyl Kurylamide, N-hydroxyethyl methacrylamide, N, N-dimethylacrylamide, N, N-dimethylmethacrylamide, N, N-diethylacrylamide, N, N-diethylmethacrylamide, N-methyl, N-ethylacrylamide, N- Methyl, N-ethyl methacrylamide, N-methylol acrylamide methyl ether, N-methylol methacrylamide methyl ether, N-methylol acrylamide ethyl ether, N-methylol methacrylamide ethyl ether, N-methylol acrylamide propyl ether, N-methylol methacrylamide Examples thereof include propyl ether, N-methylol acrylamide butyl ether, N-methylol methacrylamide butyl ether and the like. In addition, the (meth) acrylamide compound (d13) which may be N-substituted is a monomer having no amino group. These monomers can be used alone or in combination of two or more.

  Examples of other polymerizable unsaturated monomer (d2) include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, and 4-hydroxybutyl (meth) acrylate. C2-C8 hydroxyalkyl ester of acrylic acid or methacrylic acid, monoesterified product of polyhydric alcohol such as polyethylene glycol mono (meth) acrylate and acrylic acid or methacrylic acid, polyether polyol such as polybutylene glycol Monoether of a hydroxyl group-containing polymerizable unsaturated monomer such as 2-hydroxyethyl (meth) acrylate; ε-caprolactone-modified vinyl obtained by ring-opening polymerization of ε-caprolactone to 2-hydroxyethyl (meth) acrylate Nil monomer (for example, “Placcel FA-1”, “Placcel FA-2”, “Placcel FA-3”, “Placcel FA-4”, “Placcel FA-5”, “Placcel FM-1”, “Placcel FM-” Hydroxyl group-containing polymerizable unsaturated monomers such as “2”, “Placcel FM-3”, “Placcel FM-4”, “Placcel FM-5” (all of which are trade names, manufactured by Daicel Chemical Co., Ltd.); , Methyl (meth) acrylate, ethyl (meth) acrylate, isopropyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, n -Octyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, decyl (meth) acryl Rate, undecyl (meth) acrylate, dodecyl (meth) acrylate, tridecyl (meth) acrylate, stearyl (meth) acrylate, isostearyl (meth) acrylate “Osaka Organic Chemical Co., Ltd.”, cyclohexyl (meth) acrylate, isobornyl (meth) An acrylic ester compound or a methacrylic ester compound which may contain a ring structure having 1 to 24 carbon atoms such as acrylate, dicyclopentanyl (meth) acrylate, dicyclopentenyl (meth) acrylate, benzyl (meth) acrylate; Aromatic ring-containing vinyl compounds such as styrene, vinyl toluene and α-methylstyrene; vinyl ester compounds such as vinyl propionate and vinyl acetate; nitrile compounds of acrylonitrile and methacrylonitrile; glycidyl Epoxy group-containing vinyl compounds such as (meth) acrylate, 3,4-epoxycyclohexylmethyl (meth) acrylate, vinylcyclohexene monoepoxide, N-glycidylacrylamide, and allylglycidyl ether; acrylic acid, methacrylic acid, maleic acid, fumaric acid, itacone Examples thereof include carboxyl group-containing vinyl compounds such as acids; acid anhydride group-containing vinyl compounds such as maleic anhydride, itaconic anhydride, and hymic anhydride. These can be used alone or in combination of two or more.

  The blending amount of the polymerizable unsaturated monomer (d1) and the other polymerizable unsaturated monomer (d2) at the time of producing the copolymer resin (d) is that of all the monomer components constituting the copolymer resin (d). Polymerizable unsaturated monomer (d1): 20 to 70% by mass, preferably 30 to 65% by mass, other polymerizable unsaturated monomer (d2): 30 to 80% by mass, preferably 35% to the total amount It is desirable for it to exist in the range of 70 mass% for the coating-film performance improvement.

  In particular, the amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11) is 1 to 30% by mass, preferably 5 to 25% by mass, based on the total amount of all monomers constituting the copolymer resin (d). %, A polymerizable unsaturated monomer having a nitrogen atom-containing heterocyclic ring (d12) 5 to 60% by mass, preferably 10 to 55% by mass, an N-substituted (meth) acrylamide compound (d13) 0 to 20 % By weight, preferably 0-15% by weight ("0% by weight" means not blended), and other polymerizable unsaturated monomer (d2) 30-80% by weight, preferably 35-70% by weight. It is preferable that it is within the range from the viewpoint of the durability of stain resistance in the coating film, the hardness of the coating film, and the workability.

  As a method for obtaining a copolymer resin (d) by copolymerizing a monomer mixture comprising the above polymerizable unsaturated monomer (d1) and other polymerizable unsaturated monomer (d2), a radical polymerization method known per se is available. A bulk polymerization method, a solution polymerization method, a bulk-suspension two-stage polymerization method in which suspension polymerization is performed after the bulk polymerization can be preferably used.

  In the production of the copolymer resin (d), as the polymerization initiator, a polymerization initiator generally used in a production method of an acrylic polymer or the like is used, and the amount thereof is usually a polymerizable unsaturated monomer (d1). And it is in the range of 0.1-20 mass% with respect to the total amount of other polymerizable unsaturated monomer (d2).

  Examples of the polymerization initiator include azo polymerization initiators such as 2,2′-azobisisobutylnitrile, azobis-2-methylbutyronitrile, azobisdivaleronitrile; t-butylperoxyisobutyrate, t -Butylperoxy-2-ethylhexanoate, t-amylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyisopropyl carbonate, 2,2-bis (4,4-di-t-butyl Peroxycyclohexyl) propane and other organic peroxide polymerization initiators.

  As a method for obtaining the copolymer resin (d), any known method can be used, and the solution polymerization method is particularly preferable. Examples of the method by the solution polymerization method include a method in which the monomer mixture is dissolved or decomposed in an organic solvent and heated in the presence of a polymerization initiator with stirring at a temperature of usually about 80 ° C to 200 ° C. . The reaction time is usually preferably 1 to 10 hours.

  Examples of the organic solvent include hydrocarbon solvents such as heptane, toluene, xylene, octane and mineral spirit; ester solvents such as ethyl acetate, n-butyl acetate, isobutyl acetate, ethylene glycol monomethyl ether acetate, and diethylene glycol monobutyl ether acetate; Ketone solvents such as methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone; alcohol solvents such as methanol, ethanol, isopropanol, n-butanol, sec-butanol, isobutanol; n-butyl ether, dioxane, ethylene glycol monomethyl ether, ethylene Ether solvents such as glycol monoethyl ether; SWAZOL 310, SWAZOL 1000, SWAZOL 1500 manufactured by Cosmo Oil Co., Ltd. Aromatic petroleum solvents such as

  These organic solvents can be used alone or in combination of two or more. At the time of copolymerization, the organic solvent is usually used in a range of 400% by mass or less based on the total amount of the polymerizable unsaturated monomer (d1) and the other polymerizable unsaturated monomer (d2).

  In the copolymerization reaction for obtaining the copolymer resin (d), the method for adding the monomer component and the polymerization initiator is not particularly limited, but the polymerization initiator is used from the initial stage of polymerization to the late stage of polymerization rather than being charged all at the initial stage of polymerization. It is preferable to divide and drop over the range from the viewpoint of suppressing the formation of defective cross-linked products.

  The copolymer resin (d) obtainable by the above copolymerization reaction has a weight average molecular weight of 5,000 to 30,000, more preferably 8,000 to 20,000. It is suitable from the viewpoint of easy handling (resin viscosity not very high), coating film hardness, and workability.

  It is preferable that the amine value is 5 to 90 mgKOH / g, preferably 10 to 60 mgKOH / g, and the hydroxyl value is 5 to 70 mgKOH / g, preferably 10 to 60 mgKOH / g from the viewpoint of processability. From the point of view, it is preferable.

  The blending amount of such copolymer resin (d) is 0.1 to 20 parts by mass, preferably 2 with respect to 100 parts by mass in total of the solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b). It is preferable that the content is ˜16 parts by mass, more preferably 3 to 10 parts by mass because a coating film excellent in contamination resistance, coating film hardness, and workability can be obtained.

Organosilicate and / or condensate thereof (e)
The coating composition of this invention contains the organosilicate represented by following formula (1), and / or its condensate (e).
Formula (1): (R _< ¹ _> ) _n- Si- (OR _< ² _> ) _4-n
(In the formula (1), R ¹ is an alkyl group or a phenyl group having 1 to 18 carbon atoms which may be substituted with an epoxy group or a mercapto group, R ² is an alkyl group having 1 to 6 carbon atoms , N is 0 or 1)

  The organosilicate and / or its condensate (e) is used for efficiently maintaining the stain resistance on the surface of the substrate after coating. From the viewpoint of this effect, the condensate of the organosilicate is used. More preferred.

  In addition, the coating film obtained by applying the coating composition of the present invention comprises an anionic surfactant (c) containing the sulfonic acid group or sulfonate group, an organosilicate and / or a condensate thereof (e). By coexisting with this, long-term contamination resistance is excellent.

Specific examples of R ¹ in the above general formula include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, pentyl, hexyl, heptyl, n-octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, Tetradecyl, hexadecyl, octadecyl, glycidyl, methylglycidyl (2-methylglycidyl)-, mercaptomethyl, 2-mercaptoethyl, 2-mercaptopropyl, 3-mercaptopropyl, 4-mercaptobutyl, phenyl, p-mercaptophenyl groups, etc. Can be mentioned.

  Specific examples of the organosilicate of the organosilicate and / or its condensate (e) include tetrafunctional silanes such as tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetraisopropoxysilane, tetrabutoxysilane, tetraisobutoxysilane and the like. Methyltrimethoxysilane, methyltriethoxysilane, methyltripropoxysilane, methyltriisopropoxysilane, methyltrin-butoxysilane, methyltriisobutoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltripropoxysilane, phenyl Triisopropoxysilane, phenyltri-n-butoxysilane, phenyltriisobutoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, lauryl Trifunctional silanes such as methoxysilane, lauryltriethoxysilane, mercaptomethyltrimethoxysilane, mercaptoethyltrimethoxysilane, mercaptomethyltriethoxysilane, mercaptoethyltriethoxysilane, mercaptopropyltrimethoxysilane, mercaptopropyltriethoxysilane It is done.

  Examples of the condensate of the organosilicate include a condensate of one or a combination of two or more of these tetrafunctional or trifunctional silanes.

  Organosilicate condensates can be produced by conventional methods, and examples of commercially available organosilicate condensates include MKC silicate MS51, MKC silicate MS56, MKC silicate MS57, MKC silicate MS56S, and MKC silicate MS56SB5. MKC silicate MS58B15, MKC silicate MS58B30, MKC silicate ES40, MKC silicate EMS31, MKC silicate BTS (all are trade names, manufactured by Mitsubishi Chemical Corporation), methyl silicate 51, ethyl silicate 40, ethyl silicate 40T, ethyl silicate 40T 48 (all of which are manufactured by Colcoat Co., Ltd., trade names), KR500, KR9218, X-41-1805, X-41-1810, X-41-1818, X-4 -1053, X-41-1056 (or more, both Shin-Etsu Chemical Co., Ltd., trade name) and the like can be given.

In the coating composition of the present invention, the organosilicate and / or its condensate (e) may be used alone or in combination of two or more. In the organosilicate represented by the general formula and / or the condensate thereof (e), the OR ² group has a methoxy group and an alkoxy group having 2 to 6 carbon atoms, and has a methoxy group / 2 to 6 carbon atoms. The ratio of the number of alkoxy groups is preferably in the range of 95/5 to 30/70 from the viewpoint of storage stability.

  In the coating composition of the present invention, the amount of the organosilicate and / or its condensate (e) is the organosilicate based on the total solid content of 100 parts by mass of the hydroxyl group-containing resin (a) and the crosslinking agent (b). And / or its condensate (e) is 0.1 to 10 parts by weight, preferably 0.2 to 8 parts by weight, more preferably 0.3 to 5 parts by weight, storage stability and stain resistance. It is preferable because a coating film excellent in coating film hardness and workability can be obtained.

Urea resin particles (f)
The coating composition of the present invention can reduce the gloss of the coating film by blending the urea resin particles (f). For example, the 60-degree specular gloss is 1 to 65, preferably the 60-degree specular gloss. A matte coating film of 5 to 55 can be obtained.

  The urea resin particles (f) are in the form of powder obtained by pulverizing a resin obtained by condensation reaction of urea and an aldehyde component, and those having an average particle diameter of 1 to 10 μm, preferably 2 to 8 μm are suitable. . The average particle diameter is a median diameter (d50) value of a volume-based particle size distribution measured by a laser diffraction scattering method using a Microtrac particle size distribution measuring device (trade name “MT3300”, manufactured by Nikkiso Co., Ltd.).

  As the aldehyde component, formaldehyde, acetaldehyde, crotonaldehyde, benzaldehyde or the like can be used. Among these, when formaldehyde is used, the condensation reaction is easy to proceed, which is convenient.

  Examples of commercially available urea resin particles (f) include Pergo Pack M3, Pergo Pack M4, Pergo Pack M5 (manufactured by Lonza Japan, trade name), SOOFINE JJ POWDER (trade name, produced by Hangzhou Seika Kogyo Co., Ltd.), and the like.

  The urea resin particles (f) blended into the coating composition of the present invention as necessary are blended according to the degree of the desired matting coating film, when the matting coating film is formed, Usually, the amount of urea resin particles (f) is 1 to 50 parts by weight, preferably 2 to 30 parts by weight, more preferably 3 to 15 parts by weight, based on 100 parts by weight of the total solid content of a) and the crosslinking agent (b). It is desirable from the viewpoint of obtaining coating stability and a matte coating film.

  Further, the coating composition of the present invention includes, as necessary, pigments such as a lubricity imparting agent, coloring pigments and extender pigments, curing catalysts, pigment dispersants, ultraviolet absorbers, ultraviolet stabilizers, antifoaming agents, surface Conditioning agents, coating additives such as surfactants different from the above anionic surfactant (c), other matting agents such as silica fine powder and dehydrating agents, organic solvents, and other resins, conventionally used in coatings Known materials used can also be used.

  The coating composition of the present invention has good storage stability, but the storage stability can be further improved by adding a dehydrating agent. Examples of the dehydrating agent include methyl orthoacetate and methyl orthoformate.

  In the present invention, when a dehydrating agent is blended, the blending ratio of the dehydrating agent is 1 to 20 parts by mass, preferably 100 parts by mass of the total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b). Is preferably 2 to 15 parts by mass, more preferably 3 to 10 parts by mass from the viewpoint of improving storage stability.

  As the above-mentioned lubricity-imparting agent, conventionally known lubricants in the paint field can be used as long as they can impart slipperiness to the coating surface without deteriorating the appearance of the coating surface. Examples include polyolefin waxes such as polyethylene wax; polyether-modified silicone oil, higher fatty acid ester-modified silicone oil, modified silicone oil such as higher alkoxy-modified silicone oil; paraffin wax such as microcrystalline wax; montan wax, lanolin wax, carna Examples thereof include fatty acid ester waxes such as uba wax, beeswax and whale wax, and fluorine waxes such as ethylene tetrafluoride.

  Specific examples of the pigment include white pigments such as titanium white and zinc white; blue pigments such as cyanine blue and indanthrene blue; green pigments such as cyanine green and patina; organic red pigments such as azo and quinacridone. Red pigments such as Bengala, Bengala; organic yellow pigments such as benzimidazolone, isoindolinone, isoindoline, and quinophthalone; yellow pigments such as titanium yellow, yellow lead, and yellow iron oxide; carbon black, graphite, Examples thereof include coloring pigments such as black pigments such as pine smoke; extender pigments such as clay, talc, barita and calcium carbonate; rust preventive pigments such as aluminum tripolyphosphate, zinc molybdate and vanadium pentoxide; The pigment is usually 10 to 300 parts by mass, preferably 20 to 150 parts by mass (total solids of the coating composition) with respect to 100 parts by mass of the total solids of the hydroxyl group-containing resin (a) and the crosslinking agent (b). 3 to 70% by mass, preferably 8 to 50% by mass) with respect to the amount.

  For example, the curing catalyst is blended as necessary to promote the reaction between the hydroxyl group-containing resin (a) and the crosslinking agent (b), and when the crosslinking agent (b) is an amino resin. A sulfonic acid compound or an amine neutralized product of a sulfonic acid compound is preferably used.

  Representative examples of the sulfonic acid compound include p-toluenesulfonic acid, dodecylbenzenesulfonic acid, dinonylnaphthalenesulfonic acid, dinonylnaphthalenedisulfonic acid, and the like. The amine in the amine neutralized product of the sulfonic acid compound may be any of primary amine, secondary amine, and tertiary amine. Among these, the amine neutralized product of p-toluenesulfonic acid and / or the amine neutralized product of dodecylbenzenesulfonic acid is preferable from the viewpoints of coating stability, reaction promoting effect, and obtained coating film properties.

  When the crosslinking agent (b) is a blocked polyisocyanate compound, examples of the curing catalyst include tin octylate, dibutyltin di (2-ethylhexanoate), dioctyltin di (2-ethylhexanote), Mention may be made of organometallic compounds such as dioctyltin diacetate, dibutyltin dilaurate, dibutyltin oxide, monobutyltin trioctate, lead 2-ethylhexinate and zinc octylate. The curing catalyst is 0.1 to 5.0 parts by weight, preferably 0.2 to 1.5 parts by weight, based on 100 parts by weight of the total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b). Is suitable.

  The coating composition of the present invention comprises a hydroxyl group-containing resin (a), a crosslinking agent (b), a sulfonic acid group or sulfonate group-containing anionic surfactant (c), a copolymer resin (d), and an organosilicate. And / or its condensate (e), if necessary, urea resin particles (f), and the above-mentioned other components can be obtained by uniformly mixing.

Coating method of the present invention For coating the coating composition of the present invention, Ford Cup No. It is preferable to adjust the solid content concentration within a range of 20 to 60% by mass so that a viscosity within a range of 10 to 100 seconds is obtained at 4 (20 ° C.).

  The coating film forming method using the coating composition of the present invention forms a primer coating film on one or both surfaces of a metal plate, and forms a top coating film by the coating composition on at least one surface of the primer coating film. It is characterized by doing.

  Specifically, the metal plate that is the object to be coated is a cold-rolled steel plate, hot-dip galvanized steel plate, electrogalvanized steel plate, alloy galvanized steel plate (galvanized steel plate such as iron-zinc, aluminum-zinc, nickel-zinc). , Aluminum plate, stainless steel plate, copper plate, copper plated steel plate, tin plated steel plate and the like.

  When painting on a metal plate, the metal surface, which is the material to be coated, may be painted as it is if it is not contaminated with oil or other pollutants, but it is well known for improving adhesion and corrosion resistance with the coating film. It is desirable to apply a metal surface treatment. These known surface treatment methods include phosphate surface treatment, chromate surface treatment, zirconium surface treatment and the like.

  As a primer for forming a primer coating film on a metal plate, a known primer used in the colored color steel sheet coating field, the industrial machine coating field, the metal part coating field, or the like can be applied. From the viewpoint of environmental protection, it is preferable to use a chromium-free primer coating that does not contain a chromium-based rust preventive component.

  The chrome-free primer coating is appropriately selected depending on the type of material to be coated and the type of metal surface treatment. Epoxy-based and polyester-based primer coatings and their modified primer coatings are particularly suitable, and workability is particularly required. In this case, a polyester primer paint is suitable. The primer coating is applied by a known coating method such as roll coating or spray coating so that the primer coating thickness is 1 to 30 μm, preferably 2 to 20 μm, and it is usually at an ambient temperature of 80 to 300 ° C. for 5 seconds. When coil coating is applied for about 1 hour, it is preferably cured by heating for 15 seconds to 120 seconds under the condition that the maximum material reaching temperature is 140 to 250 ° C.

  The primer coating film may be a single layer or two layers in which a second primer coating film (intermediate coating film) is formed on the first primer coating film. When the primer film has two layers, the first primer film has an anticorrosion function, and the second primer film (intermediate film) has processability and chipping resistance. The primer coating can also have different functions.

  The present coating composition in the coating film forming method of the present invention is coated on at least one surface of the primer coating film. Examples of the coating method include curtain coating, roll coater coating, dip coating, and spray coating. Usually, the coating thickness after drying is 5 to 50 μm, preferably 8 to 25 μm. Is done.

  When the coating composition of the present invention is applied by coil coating, the coating method is not limited, but curtain coating and roll coater coating are recommended in view of the economics of coil coating. When roll coater coating is applied, the bottom feed method (so-called reverse coating or natural coating) using a normal two-roll system is practically performed, but the uniformity of the coating surface is best. Therefore, a top feed or bottom feed method using three rolls can be performed.

  The method for forming a coating film according to the present invention may include a step of curing the coating film of the coating composition of the present invention obtained in the above step. The conditions for curing the coating film with the coating composition of the present invention are usually about 15 to 30 minutes at a material maximum temperature of 120 to 260 ° C. In the field of pre-coating, which is applied by coil coating or the like, it is usually carried out at a raw material maximum temperature of 160 to 260 ° C. for a baking time of 15 to 90 seconds.

  Further, the matte coating film by the coating composition in which the urea resin particles (f) are added to the composition of the present invention is difficult for the contaminants to adhere, and the antifouling property can be improved even in the matte coating film. It is a thing.

  Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples. The present invention is not limited in any way by the following examples. Hereinafter, both “parts” and “%” are based on mass.

Production and production example 1 of hydroxyl group-containing polyester resin (a) Production of polyester resin solution (a1 component)
A reactor equipped with a thermometer, a stirrer, a heating device and a rectifying tower was charged with 1079 parts of isophthalic acid, 407 parts of adipic acid, 466 parts of neopentyl glycol and 802 parts of trimethylolpropane, and the temperature was raised to 160 ° C. The temperature was gradually raised from 160 ° C. to 230 ° C. over 3 hours.

  Next, after continuing the reaction at 230 ° C. for 30 minutes, the rectifying column was replaced with a water separator, and 124 parts of xylene was added to the contents, and xylene was also added to the water separator to azeotrope water and xylene. The condensed water was removed, the reaction was continued until the acid value reached 10 mgKOH / g, the mixture was cooled, and 855 parts of cyclohexanone was added to the reaction product to obtain a polyester resin solution having a solid content of 55%. The obtained resin had a hydroxyl value of 184 mgKOH / g and a number average molecular weight of 3,400.

Production Example 2 Production of acrylic resin solution (a2 component)
Into a reaction vessel equipped with a thermometer, thermostat, stirrer, reflux condenser and dropping device, 480 parts of butyl acetate was charged and heated to 130 ° C. while blowing nitrogen gas, and then the styrene was removed from the dropping device while maintaining the temperature. A mixed solution of 200 parts, 290 parts of methyl methacrylate, 250 parts of cyclohexyl methacrylate, 260 parts of 2-hydroxyethyl methacrylate and 2,2′-azobis (50 parts of 2-methylbutyronitrile) was added dropwise over 3 hours.

  After completion of dropping, the reaction product was aged at 130 ° C. for 1 hour, and the solid content was adjusted with cyclohexanone to obtain an acrylic resin solution having a resin solid content of 55%. The obtained resin had a hydroxyl value of 107 mgKOH / g and a number average molecular weight of 8,000.

Production Example of Copolymer Resin (d) Production Example 3 Copolymer Resin (d) No. 1 Preparation of solution To a 4 liter flask equipped with a thermometer, reflux condenser and stirrer, 28 parts of Swazol 1000 (Cosmo Oil Co., Ltd., aromatic hydrocarbon organic solvent) and 85 parts of toluene were added. A mixture of 12 parts N, N-dimethylaminoethyl methacrylate, 52 parts 1-vinyl-2-pyrrolidone, 13 parts 2-hydroxyethyl methacrylate, 23 parts 2-ethylhexyl methacrylate and 4 parts azobismethylbutyronitrile, The reaction was carried out at 110 ° C. under nitrogen gas.

  Next, the solid content was adjusted with toluene, and copolymer resin (d) No. 5 having a solid content of 55% by mass was obtained. One solution was obtained. Copolymer resin (d) No. The resin solid content of No. 1 was an amine value of 42 mgKOH / g, a hydroxyl value of 56 mgKOH / g, and a weight average molecular weight of 10,000.

Production Examples 4 to 14 Copolymer resin (d) No. 2-No. Production of 12 solution In the same manner as in Production Example 3 except that a monomer mixture having the composition shown in Table 1 was used, copolymer resin (d) No. 1 was prepared. 2-No. 12 solutions were obtained.

(Note 1) Acryester DMC78: Mitsubishi Rayon Co., Ltd., trade name, methacryloyloxyethyltrimethylammonium chloride, quaternary ammonium base-containing polymerizable saturated monomer (Note 2) Plaxel FM-3: Daicel Chemical Industries, Ltd., product Name, ε-caprolactone modified vinyl monomer of 2-hydroxyethyl methacrylate

Example 1 Coating composition no. Production of 1 80 parts (solid content) of the polyester resin solution obtained in Production Example 1, 20 parts (Solid content) of Cymel 303 (Note 4), 5 parts of New Coal 291-GL (Note 6), obtained in Production Example 3 Copolymer resin no. 1 part 5 parts (solid content), SMKC silicate MS56S (Note 9) 2.5 parts (solid content), and Taipei CR-95 (Note 14) 120 parts, dodecylbenzenesulfonic acid 0.5 part, organic solvent ( Cyclohexanone / Swazole 1500 = 40/60 (mass ratio) mixed solvent) and diluted to obtain a coating composition No. having a viscosity of 80 seconds (Ford Cup # 4, 25 ° C.). 1 was obtained.

Examples 2 to 30 Coating composition No. 2-No. 30 manufacturing
A coating composition No. 1 was prepared in the same manner as in Example 1 except that the contents shown in Tables 2 and 3 were used. 2-No. 30 was obtained.

(Note 3) Byron KS-1430V: manufactured by Toyobo Co., Ltd., polyester resin, number average molecular weight 12,000, hydroxyl value 11 mgKOH / g, glass transition point 1 ° C.
(Note 4) Cymel 303: Nippon Cytec Industries, Ltd., trade name, methyl etherified melamine resin (Note 5) Block polyisocyanate compound A: oxime blocked product of hexamethylene diisocyanate trimer, solid content 37% by mass, NCO 3.6% content
(Note 6) New Coal 291-GL: trade name, Nippon Emulsifier Co., Ltd., dialkylsulfosuccinic acid sodium salt having the structural formula represented by the above formula (2) (Note 7) New Coal 292-PG: trade name, Japan Emulsifier Stock Company, dialkylsulfosuccinic acid sodium salt of the structural formula represented by the above formula (2) (Note 8) New Coal 293: trade name, Nippon Emulsifier Co., Ltd., monoalkylsulfosuccinic acid of the structural formula represented by the following formula (3) Disodium salt

(R ⁵ in the formula represents an alkyl group having 1 to 15 carbon atoms)
(Note 9) MKC silicate MS56S: manufactured by Mitsubishi Chemical Corporation, trade name, methyl esterified silicate which is a condensate of tetramethoxysilane.
(Note 10) MKC silicate MS58B30: manufactured by Mitsubishi Chemical Corporation, trade name, methyl / butyl mixed esterified silicate which is a condensate of tetraalkoxysilane, the ratio of methyl / butyl number is 70/30.
(Note 11) X-41-1805: manufactured by Shin-Etsu Chemical Co., Ltd., trade name, condensate of mercaptoalkyl group-containing trialkoxysilane, mercaptoalkyl group has 18 or less carbon atoms, alkoxy group has 6 or less carbon atoms It is.
(Note 12) SOOFINE JJ POWDER: trade name, urea resin particles, average particle size 2.5 μm, manufactured by Hangzhou Seika Co., Ltd.
(Note 13) Silicia 445: manufactured by Fuji Silysia Chemical Co., Ltd., trade name, silica fine powder, matting agent (Note 14) Type CR-95: trade name, titanium white, manufactured by Ishihara Sangyo Co., Ltd.

Comparative Example 1 Paint composition No. 31 production
80 parts (solid content) of the polyester resin solution obtained in Production Example 1, 20 parts (solid content) of Cymel 303 (Note 4), copolymer resin No. 1 obtained in Production Example 3. 1 part 5 parts (solid content), SMKC silicate MS56S (Note 9) 2.5 parts (solid content), and Taipei CR-95 (Note 14) 120 parts, dodecylbenzenesulfonic acid 0.5 part, organic solvent ( A mixed solvent of cyclohexanone / swazol 1500, 40/60) and diluted to a coating composition No. having a viscosity of 80 seconds (Ford Cup # 4, 25 ° C.). 31 was obtained.

Comparative Examples 2 to 14 Coating composition No. 32-No. 44 manufacture
A coating composition No. 1 was prepared in the same manner as in Comparative Example 1 except that the contents shown in Table 4 were used. 32-No. 44 was obtained.

Preparation of test plate On a zinc-aluminum alloy plated steel plate (GL material, plate thickness 0.35 mm) on which a primer coating film having a dry film thickness of 3 m was formed, using a roll coater, the following examples and comparative examples were used. The obtained coating composition No. 1-No. No. 44 was coated to a dry film thickness of 18 μm and baked for 40 seconds under the condition that the maximum material arrival temperature was 220 ° C. to obtain a test plate. Tables 2 to 4 show the results of testing using each test plate according to the test conditions described below.

(Note 15) Storage stability:
Each coating composition was hermetically stored in a constant temperature room at 40 ° C., and the state after storage for 60 days was evaluated according to the following criteria.
When S is stirred, the coating composition immediately returns to the state before storage, and there is no problem. A, the coating composition settles and a cake layer is observed, but stirring for less than 10 minutes (using a stirring blade with a diameter of 3 cm is 500 rpm ), It returns to the state before storage without aggregation.
In B, the coating composition settles and a cake layer is observed, but returns to the state before storage of the cohesives by stirring for 10 to 60 minutes (500 rpm using a stirring blade having a diameter of 3 cm).
As for C, the coating composition settles and a cake layer is observed, and even if stirring is performed for more than 60 minutes (500 rpm using a stirring blade having a diameter of 3 cm), cohesive spots remain.

(Note 16) Initial appearance of painted surface:
In the case of A, no abnormality in the paint surface such as repellency, dents, or cloudiness is observed on the paint surface.
In B, no coating surface abnormality such as repelling or dents is observed, but clouding is observed on the coating surface.
In C, abnormal paint surfaces such as repellency and dents are observed on the paint surface.

  (Note 17) Pencil hardness: A pencil scratch test specified in JIS K 5600-5-4 (1999) was performed on the coating film of the test plate, and evaluation was performed by tearing the coating film. Higher hardness is preferred.

(Note 18) Outdoor exposure test: An outdoor exposure test piece (100 x 300 mm) is attached to an installation table that models the eaves at an angle of 4 degrees from the vertical so that the coating faces the north side. An exposure test was conducted on the rooftop of Kansai Paint Co., Ltd. in Ota-ku, Tokyo. The color difference (△ E) from the initial coating plate was “based on JIS Z8370” in “2 months after the start of exposure” and “12 months after the start of exposure”. Then, measurement was performed using a multi-light source spectrocolorimeter MSC-5N manufactured by Suga Test Instruments Co., Ltd., and evaluation was performed according to the following criteria.
S is △ E is less than 1 A is △ E is 1 or more and less than 2 B is △ E is 2 or more and less than 5,
For C, ΔE is 5 or more.

(Note 19) Workability: In a room at 20 ° C., the test plate was folded 180 degrees with a vise with the coating surface facing outside, and the T number at which no crack occurred at the bent portion was displayed. The T number is 0T when bending 180 degrees without anything inside the bent part, 1T, 2 when a sheet of the same thickness as the test plate is folded. In the case of a sheet, 2T,... (The same applies hereinafter)... The results were determined by:
S is not cracked in 2T folding process A is cracked in 2T folding process, but crack is not recognized in 4T folding process B is cracked in 4T folding process However, cracks are not recognized in the 6T folding process. C is cracked in the 6T folding process.

(Note 20) 60 degree specular gloss:
The 60-degree specular reflectance was measured according to the 60-degree specular gloss specified in JIS Z 8741 (1997).

Comprehensive evaluation In the field of paints to which the present invention belongs, a coating composition having good storage stability of the coating composition, maintaining stain resistance when exposed outdoors, high coating film hardness, and good workability. It is desirable that it can be formed.
Therefore, a comprehensive evaluation was performed based on the following criteria:
A Storage stability, outdoor exposure test (2 months after the start of exposure), outdoor exposure test (12 months after the start of exposure) and processability are all S or A, and the pencil hardness is 3H or more. B Storage stability , Outdoor exposure test (2 months after the start of exposure), outdoor exposure test (12 months after the start of exposure) and processability are all S, A or B, and at least one of these 4 items is B C Storage stability, outdoor exposure test (2 months after the start of exposure), outdoor exposure test (12 months after the start of exposure), and processability are all S, A, B or C. Of these 4 items , At least one is C

  It is possible to provide a coating composition that has good storage stability, can maintain stain resistance when exposed outdoors, and can form a coating film with good coating film hardness and processability.

Claims (6)

Hydroxyl group-containing resin (a), crosslinking agent (b), anionic surfactant (c) containing sulfonic acid group or sulfonate group, copolymer resin (d), organosilicate and / or condensate thereof ( e) a coating composition comprising:
The hydroxyl group-containing resin (a) comprises a hydroxyl group-containing acrylic resin, a hydroxyl group-containing polyester resin, or a combination of a hydroxyl group-containing acrylic resin and a hydroxyl group-containing polyester resin;
The anionic surfactant (c) containing the sulfonic acid group or sulfonate group is
Or a dialkylsulfosuccinic acid sodium salt having the structural formula represented by the following formula (2):
(R ³ and R ^{4 in} formula (2) are the same or different and each represents an alkyl group having 1 to 15 carbon atoms)
A monoalkylsulfosuccinic acid sodium salt having a structural formula represented by the following formula (3):
(R ⁵ in the formula represents an alkyl group having 1 to 15 carbon atoms)
The copolymer resin (d) is different from the hydroxyl group-containing resin (a) ,
1 to 20 parts by mass of an anionic surfactant (c) containing a sulfonic acid group or a sulfonate group with respect to a total solid content of 100 parts by mass of the hydroxyl group-containing resin (a) and the crosslinking agent (b), 0.1 to 20 parts by mass of copolymer resin (d), 0.1 to 10 parts by mass of the organosilicate and / or its condensate (e),
The copolymer resin (d) is a polymerizable unsaturated monomer having an amino group or a quaternary ammonium base-containing polymerizable unsaturated monomer (d11) and a nitrogen atom-containing heterocyclic ring, based on the total amount of all monomers constituting the copolymer resin (d). 20 to 70% by mass of at least one polymerizable unsaturated monomer (d1) selected from the monomer (d12) and the N-substituted (meth) acrylamide compound (d13), and other polymerizable unsaturated monomers (D2) a copolymer resin of a monomer mixture of 30 to 80% by mass,
The said organosilicate and / or its condensate (e) are coating compositions represented by following formula (1).
Equation ^{(1): (R 1)} n -Si- (OR 2) 4-n
(In the formula (1), R ¹ is an alkyl group or a phenyl group having 1 to 18 carbon atoms which may be substituted with an epoxy group or a mercapto group, R ² is an alkyl group having 1 to 6 carbon atoms , N is 0 or 1)   60-95 parts by mass of the hydroxyl group-containing resin (a) and 5-40 parts by mass of the crosslinking agent (b) with respect to 100 parts by mass of the total solid content of the hydroxyl group-containing resin (a) and the crosslinking agent (b). The coating composition according to claim 1, which is contained in The copolymer resin (d) has an amino group or quaternary ammonium base-containing polymerizable unsaturated monomer (d11) 1 to 30% by mass and a nitrogen atom-containing heterocycle with respect to the total amount of all monomers constituting the copolymer resin (d). Polymerizable unsaturated monomer (d12) 5 to 60% by mass, N-substituted (meth) acrylamide compound (d13) 0 to 20% by mass and other polymerizable unsaturated monomer (d2) 30 to 80% by mass coating composition according to claim 1 or 2 is a copolymer resin% of the monomer mixture.   The coating composition of Claim 1 which contains 1-50 mass parts of urea resin particles (f) with respect to a solid content total of 100 mass parts of hydroxyl-containing resin (a) and a crosslinking agent (b). A primer coating film is formed on one surface or both surfaces of a metal plate, and a coating film is formed from the coating composition according to any one of claims 1 to 4 on at least one surface of the primer coating film. A method of forming a coating film characterized by A coated metal plate obtained by the coating film forming method according to claim 5 .