阅读说明：本技术 三异氰酸酯组合物、水系涂料组合物以及涂膜 (Triisocyanate composition, water-based coating composition, and coating film ) 是由 山内理计 三轮祐一 于 2018-06-12 设计创作，主要内容包括：一种三异氰酸酯组合物,其包含：1种以上的下述通式(I)(式中,存在多个的Y<Sup>1</Sup>各自独立地表示单键、或者任选包含选自由酯结构和醚结构组成的组中的1种以上的碳数1～20的二价烃基；R<Sup>1</Sup>为氢原子或碳数1～12的一价烃基。)所示的三异氰酸酯、以及能与选自由羧基和羟基组成的组中的1种以上进行交联的交联剂,该三异氰酸酯组合物可以得到预干燥后的耐粘连性优异且耐水性、耐溶剂性以及与基底的密合性优异的涂膜,并且水分散性、涂液配混后的适用期良好。<Image he="265" wi="700" file="DDA0002341092560000011.GIF" imgContent="drawing" imgFormat="GIF" orientation="portrait" inline="no"></Image>(A triisocyanate composition comprising: 1 or more species of the following general formula (I) (wherein plural Y's are present) 1 Each independently represents a single bond, or a divalent hydrocarbon group having 1 to 20 carbon atoms, which optionally contains 1 or more kinds selected from the group consisting of an ester structure and an ether structure; r 1 Is a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms.) The triisocyanate composition can give a coating film excellent in blocking resistance after predrying and excellent in water resistance, solvent resistance and adhesion to a substrate, and has good water dispersibility and pot life after blending a coating liquid.)

1. A triisocyanate composition comprising: 1 or more triisocyanates represented by the following general formula (I) and a crosslinking agent capable of crosslinking with 1 or more selected from the group consisting of a carboxyl group and a hydroxyl group,

in the general formula (I), there are plural Y' s¹Each independently represents a single bond, or optionally contains 1 or more divalent hydrocarbon groups having 1 to 20 carbon atoms selected from the group consisting of ester structures and ether structures, and Y is present in plural¹Optionally identical to or different from each other, R¹Is a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms.

2. The triisocyanate composition according to claim 1, wherein there are a plurality of Y's in the triisocyanate¹One or more of which comprise an ester structure.

3. The triisocyanate composition according to claim 1 or 2, wherein the crosslinking agent is 1 or more selected from the group consisting of a carbodiimide group-containing compound, an oxazoline group-containing compound, and a melamine compound.

4. The triisocyanate composition according to any one of claims 1 to 3, wherein a mixing mass ratio (A)/(B) of triisocyanate (A) to 1 or more crosslinking agents (B) capable of crosslinking with a carboxyl group and a hydroxyl group is 10/90 to 90/10.

5. A water-based coating composition comprising the triisocyanate composition according to any one of claims 1 to 4 and a hydroxyl group-and/or carboxyl group-containing resin.

6. A coating film obtained by curing the water-based coating composition according to claim 5.

Technical Field

The present invention relates to a triisocyanate composition, an aqueous coating composition and a coating film.

This application claims priority based on Japanese application No. 2017-130297, 7/3/2017, the contents of which are incorporated herein by reference.

Background

A coating film obtained by curing a coating composition containing a polyisocyanate obtained from an aliphatic diisocyanate or an alicyclic diisocyanate as a curing agent has been widely used as a coating material, an ink, an adhesive, and the like because the coating film exhibits excellent properties in weather resistance, chemical resistance, abrasion resistance, and the like. In recent years, with the growing awareness of environmental issues, there has been an increasing demand for coating compositions to have a low VOC (volatile organic compounds) and a water-based coating composition. Among them, the polyisocyanate is required to have improved dispersibility in an aqueous solvent.

Patent document 1 discloses a polyisocyanate composition having water dispersibility, which is obtained by mixing an allophanate group-containing polyisocyanate with an adduct of an isocyanurate group-containing polyisocyanate and an alkylene oxide of a monool.

Patent document 2 discloses the following technique: the amount of isocyanate groups is maintained at a low viscosity without adding a hydrophilic group, thereby enabling water dispersion and improving the durability of the resulting coating film.

On the other hand, patent document 3 discloses a technique for improving physical properties such as water resistance of a coating film obtained from a water-based coating material. Specifically, disclosed is a coating composition using a carbodiimide group-containing compound, an oxazoline group-containing compound, and a melamine compound as crosslinking agents.

Disclosure of Invention

Problems to be solved by the invention

However, depending on the evaluation conditions, the polyisocyanate composition described in patent document 1 may have insufficient water resistance of the coating film and insufficient substrate adhesion during the cleaning coating, while depending on the evaluation conditions, the polyisocyanate composition described in patent document 2 may have insufficient pot life after the coating liquid is mixed, insufficient water resistance of the coating film, and the like.

The coating composition disclosed in patent document 3 has good results in terms of coating film properties such as water resistance, but has a technical problem in blocking resistance after pre-drying in a coating line for automobiles, precoated metals, and the like.

The present invention has been made in view of the above circumstances, and provides a triisocyanate composition which is excellent in water dispersibility and pot life after mixing of a coating liquid, and which can give a coating film excellent in blocking resistance after predrying and excellent in water resistance, solvent resistance and adhesion to a substrate. Further, a water-based coating composition comprising the triisocyanate composition is provided. Also disclosed is a coating film which is obtained by curing the aqueous coating composition and has excellent blocking resistance after predrying, water resistance, solvent resistance and adhesion to a substrate.

Means for solving the problems

That is, the present invention includes the following aspects.

[1] A triisocyanate composition comprising: 1 or more triisocyanates represented by the following general formula (I), and a crosslinking agent capable of crosslinking with 1 or more selected from the group consisting of a carboxyl group and a hydroxyl group.

[ in the general formula (I), a plurality of Y's are present¹Each independently represents a single bond, or a divalent hydrocarbon group having 1 to 20 carbon atoms, which optionally contains 1 or more kinds selected from the group consisting of an ester structure and an ether structure. Y in plural¹Optionally identical to or different from each other. R¹Is a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms.]

[2]According to [1]The triisocyanate composition, wherein Y is present in plural of the triisocyanates¹One or more of which comprise an ester structure.

[3] The triisocyanate composition according to [1] or [2], wherein the crosslinking agent is 1 or more selected from the group consisting of a carbodiimide group-containing compound, an oxazoline group-containing compound, and a melamine compound.

[4] The triisocyanate composition according to any one of [1] to [3], wherein a mixing mass ratio (A)/(B) of the triisocyanate (A) to a crosslinking agent (B) capable of crosslinking with 1 or more selected from the group consisting of a carboxyl group and a hydroxyl group is 10/90 to 90/10.

[5] An aqueous coating composition comprising the triisocyanate composition according to any one of the above [1] to [4] and a hydroxyl group-and/or carboxyl group-containing resin.

[6] A coating film obtained by curing the aqueous coating composition according to [5 ].

ADVANTAGEOUS EFFECTS OF INVENTION

According to the above aspect, a triisocyanate composition can be provided which is excellent in water dispersibility and pot life after mixing of a coating liquid, and which can give a coating film excellent in blocking resistance after predrying and excellent in water resistance, solvent resistance, and adhesion to a substrate. In addition, a water-based coating composition comprising the triisocyanate composition may be provided. Further, a coating film which is obtained by curing the aqueous coating composition and has excellent blocking resistance after predrying and excellent water resistance, solvent resistance and adhesion to a substrate can be provided.

Detailed Description

Hereinafter, a mode for carrying out the present invention (hereinafter, simply referred to as "the present embodiment") will be described in detail. The following embodiments are examples for illustrating the present invention, and are not intended to limit the present invention to the following. The present invention can be appropriately modified and implemented within a range not departing from the gist thereof.

In the present specification, the "polyisocyanate" refers to a polymer in which a plurality of monomers having 1 or more isocyanate groups (-NCO) are bonded.

In the present specification, the term "polyol" refers to a compound having 2 or more hydroxyl groups (-OH).

Triisocyanate composition

One embodiment of the present invention relates to a triisocyanate composition comprising: 1 or more triisocyanates represented by the following general formula (I) (hereinafter, sometimes referred to as "triisocyanates (I)"), and a crosslinking agent capable of crosslinking with 1 or more selected from the group consisting of carboxyl groups and hydroxyl groups.

[ in the general formula (I), a plurality of Y's are present¹Each independently represents a single bond, or a divalent hydrocarbon group having 1 to 20 carbon atoms, which optionally contains 1 or more kinds selected from the group consisting of an ester structure and an ether structure. Y in plural¹Optionally identical to or different from each other. R¹Is a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms.]

The triisocyanate composition of the present embodiment has excellent water dispersibility, and is therefore suitably used for an aqueous coating composition. Furthermore, a coating film obtained from an aqueous coating composition containing the triisocyanate composition is excellent in blocking resistance after predrying, and is excellent in water resistance, solvent resistance, and adhesion to a substrate.

The constituent components of the triisocyanate composition of the present embodiment are described in detail below.

< triisocyanate (I) >)

The triisocyanate contained in the triisocyanate composition of the present embodiment is a compound represented by the above general formula (I).

[Y¹]

In the general formula (I), there are plural Y' s¹Each independently represents a single bond, or a divalent hydrocarbon group having 1 to 20 carbon atoms, which optionally contains 1 or more kinds selected from the group consisting of an ester structure and an ether structure. Y in plural¹Optionally identical to or different from each other.

The divalent hydrocarbon group having 1 to 20 carbon atoms may be an aliphatic group or an aromatic group. The aliphatic group may be linear, branched or cyclic.

Examples of the linear or branched aliphatic group include: alkanediyl (alkylene), alkylidene, and the like.

Examples of the cyclic aliphatic group include a cycloalkylene group and the like.

Examples of the aromatic group include arylene groups such as phenylene groups.

In addition, as Y¹The divalent hydrocarbon group having 1 to 20 carbon atoms, which may contain 1 or more species selected from the group consisting of ester structures and ether structures, includes, for example, a group represented by the following general formula (II) (hereinafter, may be referred to as "group (II)").

＊¹-(CH₂)_n1-X-(CH₂)_n2-＊²(II)

In the group (II), ＊¹Represents a bond with carbon (C) in the above general formula (I), ＊²Represents a bond to NCO in the above general formula (I). In addition, the integer is 1. ltoreq. n1+ n 2. ltoreq.20. That is, both n1 and n2 are not 0 at the same time, and n2 on the side bonded to NCO is preferably 1 or more.

Wherein n1 and n2 are each independently an integer of 0 to 20, preferably 0 to 4, and more preferably 0 to 2.

As a combination of n1 and n2, for example, a combination of n1 ═ 0 and n2 ═ 2, and a combination of n1 ═ 2 and n2 ═ 2 are preferable.

In the group (II), X is an ester structure or an ether structure. Among them, X is preferably an ester structure in terms of increasing the reaction rate.

In addition, when there are plural Y' s¹When 1 or more of these compounds contain an ester structure, the reactivity of the isocyanate group when the triisocyanate composition of the present embodiment is used as a curing agent for an aqueous coating composition can be further improved. In addition, the blocking resistance of a coating film obtained from the aqueous coating composition containing the triisocyanate composition of the present embodiment after predrying can be further improved.

[R¹]

R¹Is a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms. As R¹The hydrocarbon group in (1) is not particularly limited, and examples thereof include an alkyl group, an alkenyl group, and an alkynyl group. Wherein, as R¹Preferably a hydrogen atom.

Specific examples of the triisocyanate contained in the triisocyanate composition of the present embodiment include: 4-isocyanatomethyl-1, 8-octamethylenediisocyanate (hereinafter sometimes referred to as "NTI") (molecular weight 251) disclosed in International publication No. 1996/17881 (reference 1), 1,3, 6-hexamethylene triisocyanate (hereinafter sometimes referred to as "HTI") (molecular weight 209) disclosed in Japanese patent application laid-open No. 57-198760 (reference 2), bis (2-isocyanatoethyl) 2-isocyanatoglutarate (hereinafter sometimes referred to as "GTI") (molecular weight 311) disclosed in Japanese patent publication No. 4-1033 (reference 3), lysine triisocyanate (hereinafter sometimes referred to as "LTI") (molecular weight 267) disclosed in Japanese patent application laid-open No. 53-135931 (reference 4), and the like.

Wherein there are plural Y' s¹1 or more of them contain an ester structure, and are therefore preferably GTI or LTI. By containing these triisocyanates, the reactivity of isocyanate groups when the triisocyanate composition of the present embodiment is used as a curing agent for an aqueous coating composition can be further improved. In addition, the composition can further contain triisocyanogen of the present embodimentThe anti-blocking property of a coating film obtained from the aqueous coating composition of the acid ester composition after pre-drying.

(method for producing triisocyanate (I))

In the present embodiment, the triisocyanate (I) contained in the triisocyanate composition can be obtained by isocyanating an amino acid derivative, an ether amine, an amine such as an alkyl triamine, or the like, for example.

Examples of the amino acid derivative include: 2, 5-diaminopentanoic acid, 2, 6-diaminohexanoic acid, aspartic acid, glutamic acid, and the like. Since these amino acid derivatives are diamine monocarboxylic acids or monoamine dicarboxylic acids, triamines having an ester group can be produced by esterifying a carboxyl group with an alkanolamine such as ethanolamine, for example. The triamine having the ester group obtained can be converted into a triisocyanate having an ester structure by phosgenation of an amine or the like.

Examples of the ether amine include MITSUI FINE CHEMICALS, a trade name of inc, and "D403" as polyoxyalkylene triamine. These ether amines are triamines, and triisocyanates having an ether structure can be produced by phosgenation of amines, etc.

Examples of the alkyltriamine include triisocyanatononane (4-aminomethyl-1, 8-octanediamine). These alkyltriamines are triamines, and triisocyanates containing only hydrocarbons can be produced by phosgenation of amines, etc.

< crosslinking agent >

The crosslinking agent contained in the triisocyanate composition of the present embodiment may be any agent that can crosslink with 1 or more species selected from the group consisting of a carboxyl group and a hydroxyl group.

Examples of the crosslinking agent capable of crosslinking with a carboxyl group include a carbodiimide group-containing compound, an oxazoline group-containing compound, and an epoxy group-containing compound.

Examples of the crosslinking agent capable of crosslinking with a hydroxyl group include melamine compounds, blocked polyisocyanates, and the like.

The triisocyanate composition of the present embodiment may contain these crosslinking agents alone, or may contain 2 or more kinds in combination.

Among them, in a coating film obtained from an aqueous coating composition containing a crosslinking agent, a carbodiimide group-containing compound, an oxazoline group-containing compound, or a melamine compound is preferable as the crosslinking agent from the viewpoints of excellent water resistance and adhesion to a substrate, and easy availability of raw materials.

The carbodiimide group-containing compound can be obtained, for example, by decarbonylation of isocyanate groups of a polyisocyanate compound.

Examples of commercially available products of carbodiimide group-containing compounds include: CARBODILITE V-02, CARBODILITE V-02-L2, CARBODILITE V-04, CARBODILITE E-01, and CARBODILITE E-02 (both trade names, manufactured by Nisshinbo Co., Ltd.), etc.

Examples of the oxazoline group-containing compound include a polymer compound having at least 2 oxazoline groups in a side chain, a monomer compound having at least 2 oxazoline groups in one molecule, and the like.

As a commercially available product of the oxazoline group-containing compound, for example, EPOCROS WS-500(Nippon Shokubai Co., Ltd., trade name) and the like are exemplified.

The epoxy group-containing compound may be a resin having 2 or more epoxy groups in one molecule. Specific examples of the epoxy group-containing compound include: bisphenol type epoxy group-containing compounds obtained by adding epichlorohydrin to bisphenol, phenol type epoxy group-containing compounds obtained by adding epichlorohydrin to novolak resins, polyethylene glycol diglycidyl ether, and the like. The epoxy group-containing compound may be in a water-dispersed state as necessary.

Examples of the melamine compound include a partially or completely methylolated melamine resin obtained by a reaction of melamine and an aldehyde.

Examples of the aldehyde include formaldehyde and paraformaldehyde.

In addition, the methylol groups of the methylolated melamine resin may also be partially or completely etherified by an alcohol. Examples of alcohols used for etherification include: methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, 2-ethylbutanol, 2-ethylhexanol, and the like.

Commercially available products of melamine compounds include, for example: CYMEL 303, CYMEL323, CYMEL325, CYMEL327, CYMEL 350, CYMEL 370, CYMEL 380, CYMEL 385, CYMEL 212, CYMEL 251, CYMEL 254, and MYCOAT 776 (all trade names, manufactured by ALLNEX Co., Ltd.).

The blocked polyisocyanate composition may be, for example, a polyisocyanate (hereinafter, sometimes referred to as "blocked polyisocyanate") obtained by blocking the polyisocyanate composition with 1 or more kinds of blocking agents selected from the group consisting of known active methylene-based blocking agents, known oxime-based blocking agents, known amine-based blocking agents and known pyrazole-based blocking agents.

< ratio of triisocyanate to crosslinking agent >

The mixing mass ratio (a)/(B) of the triisocyanate (a) and the crosslinking agent (B) contained in the triisocyanate composition of the present embodiment is not particularly limited, and is preferably 5/95 or more and 95/5 or less, and more preferably 10/90 or more and 90/10 or less, in terms of the mass ratio of the active ingredients.

From the viewpoint of further maintaining the pot life of the water-based coating composition containing the triisocyanate composition of the present embodiment for a long time, the mixing mass ratio (a)/(B) is more preferably 20/80 or more and 85/15 or less, still more preferably 30/70 or more and 80/20 or less, still more preferably 55/45 or more and 80/20 or less.

From the viewpoint of further improving the solvent resistance and the adhesion to the substrate of the coating film obtained from the aqueous coating composition containing the triisocyanate composition of the present embodiment, the mixing mass ratio (a)/(B) is more preferably from 70/30 to 90/10, and still more preferably from 75/25 to 90/10.

< method for producing triisocyanate composition >

The triisocyanate composition of the present embodiment can be produced by mixing the triisocyanate and the crosslinking agent by a known method. More specifically, the triisocyanate and the crosslinking agent are mixed at room temperature using a stirring apparatus or the like, for example, to obtain the triisocyanate composition of the present embodiment. For producing the water-based coating composition, it is preferable to mix the triisocyanate and the crosslinking agent in advance before mixing water with the hydroxyl group-and/or carboxyl group-containing resin or the like because the pot life can be further maintained for a long time.

Water-based paint composition

An aqueous coating composition according to an embodiment of the present invention includes the triisocyanate composition and a hydroxyl group-and/or carboxyl group-containing resin.

The mass ratio of the resin component of the triisocyanate composition is preferably 1 to 25 mass%, more preferably 2 to 20 mass%, and most preferably 4 to 15 mass% with respect to the total mass of the water-based coating composition. By setting the above range, the solvent resistance and pot life of the coating film can be further improved. Here, the resin component mass ratio of the triisocyanate composition means the total mass of the triisocyanate and the crosslinking agent.

The mass ratio of the hydroxyl group-and/or carboxyl group-containing resin to the total mass of the water-based coating composition is preferably 10 to 70 mass%, more preferably 15 to 60 mass%, and most preferably 20 to 50 mass%. By setting the above range, the paint viscosity can be adjusted to a more suitable level.

The water-based coating composition of the present embodiment can promote the formation of a crosslinked structure from the triisocyanate and the hydroxyl group-and/or carboxyl group-containing resin by including a crosslinking agent. Therefore, a coating film obtained from the aqueous coating composition is excellent in blocking resistance after preliminary drying, and is excellent in water resistance, solvent resistance, and adhesion to a substrate.

In the present specification, the term "water-based coating composition" refers to a composition containing 50% by mass or more of water based on the total mass of liquid components constituting the coating composition.

The water content is 50 mass% or more, preferably 60 mass% or more, more preferably 70 mass% or more, further preferably 80 mass% or more, particularly preferably 90 mass% or more, and most preferably 95 mass% or more, based on the total mass of the liquid components constituting the water-based coating composition of the present embodiment.

On the other hand, the upper limit of the water content may be 98% by mass relative to the total mass of the liquid components constituting the water-based coating composition of the present embodiment.

The triisocyanate composition contained in the water-based coating composition of the present embodiment includes the same ones as described above.

The hydroxyl group-and/or carboxyl group-containing resin contained in the water-based coating composition of the present embodiment is described in detail below.

< resin containing hydroxyl group and/or carboxyl group >

Examples of the hydroxyl group-and/or carboxyl group-containing resin (resin having at least one group selected from the group consisting of a hydroxyl group and a carboxyl group) contained in the water-based coating composition of the present embodiment include a polyester resin, an acrylic resin, a polyurethane resin, a polyolefin resin, and a fluorine-based resin. The water-based coating composition of the present embodiment may contain these resins alone, or may contain 2 or more kinds in combination.

Among these, the hydroxyl group-and/or carboxyl group-containing resin is preferably a polyester resin, an acrylic resin, or a polyurethane resin, and the acrylic resin or the polyurethane resin is preferably used in order to improve the water resistance, solvent resistance, and adhesion to the substrate of the coating film obtained from the aqueous coating composition of the present embodiment.

In the water-based coating composition of the present embodiment, the solvent is mainly composed of water from the viewpoint of environmental problems, and therefore the component constituting the hydroxyl group-and/or carboxyl group-containing resin is preferably water-dispersible, and preferably has a hydroxyl group.

[ polyester resin ]

The polyester resin can be obtained, for example, by condensation reaction of a single dibasic acid or a mixture of 2 or more types with a single polyhydric alcohol or a mixture of 2 or more types.

Examples of the dibasic acid include carboxylic acids such as succinic acid, adipic acid, sebacic acid, dimer acid, maleic anhydride, phthalic anhydride, isophthalic acid, and terephthalic acid.

Examples of the polyhydric alcohol include polyhydric alcohols selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol, neopentyl glycol, trimethylolpropane, glycerol, and the like.

Alternatively, for example, polycaprolactone obtained by ring-opening polymerization of epsilon caprolactone using a polyol can be used.

When a carboxylic acid component such as the dibasic acid or the epsilon-caprolactone is reacted with a polyol component, it is preferable that the hydroxyl group of the polyol is reacted so as to be more excessive than the carboxyl group of the carboxylic acid component, and the hydroxyl group is left in the finally obtained polyester resin.

When the polyester resin is dispersed in water, a polyester resin having a hydrophilic functional group is generally used. Examples of the hydrophilic functional group include a carbonyl group and a sulfonyl group. Among these, a carbonyl group is preferable as the hydrophilic functional group because the adhesion between the coating film obtained from the water-based coating composition of the present embodiment and the substrate becomes better.

[ acrylic resin ]

The acrylic resin may be an acrylic resin having a hydroxyl group obtained by copolymerizing a single substance or a mixture of monomers having an ethylenically unsaturated bond and a single substance or a mixture of the monomers having an ethylenically unsaturated bond. Further, as the carboxyl group-containing acrylic resin, there can be mentioned an acrylic resin obtained by copolymerizing a single substance or a mixture of carboxylic acids containing an ethylenically unsaturated bond.

Examples of the ethylenically unsaturated bond-containing monomer include the following monomers. These monomers may be used alone, or 2 or more of them may be used in combination.

(i) Acrylic esters such as methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, n-hexyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, benzyl acrylate, and phenyl acrylate.

(ii) Methacrylic acid esters such as methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, n-hexyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate, benzyl methacrylate and phenyl methacrylate.

(iii) Unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid, and itaconic acid.

Unsaturated amides such as acrylamide, methacrylamide, N-methylenebisacrylamide, diacetone acrylamide, diacetone methacrylamide, maleimide and maleimide.

(iv) Vinyl monomers such as glycidyl methacrylate, styrene, vinyl toluene, vinyl acetate, acrylonitrile, and dibutyl fumarate.

(v) Vinyl monomers having a hydrolyzable silyl group such as vinyltrimethoxysilane, vinylmethyldimethoxysilane and γ - (meth) acryloyloxypropyltrimethoxysilane.

Examples of the ethylenically unsaturated bond-containing monomer having a hydroxyl group include: hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxybutyl acrylate, hydroxyethyl methacrylate, hydroxypropyl methacrylate, hydroxybutyl methacrylate, and the like. Among them, as the ethylenically unsaturated bond-containing monomer having a hydroxyl group, hydroxyethyl acrylate or hydroxyethyl methacrylate is preferable.

[ polyurethane resin ]

The polyurethane resin can be produced by a conventional method, specifically, for example, by reacting a polyol having no carboxyl group with a polyisocyanate.

Examples of the polyol not containing the carboxyl group include: low molecular weight polyols such as ethylene glycol and propylene glycol; and high molecular weight polyols such as acrylic polyols, polyester polyols, and polyether polyols.

When a polyol having no carboxyl group is reacted with a polyisocyanate, it is preferable that the hydroxyl group of the polyol is reacted so as to be more excessive than the isocyanate group of the polyisocyanate, and the hydroxyl group remains in the finally obtained polyurethane resin.

[ hydroxyl value and acid value of hydroxyl group-and/or carboxyl group-containing resin ]

The hydroxyl value of the hydroxyl group-and carboxyl group-containing resin is not particularly limited, and is preferably 10mgKOH/g to 200mgKOH/g, more preferably 20mgKOH/g to 200mgKOH/g, still more preferably 30mgKOH/g to 200mgKOH/g, particularly preferably 40mgKOH/g to 200mgKOH/g, and most preferably 50mgKOH/g to 200 mgKOH/g.

The acid value of the hydroxyl group-and carboxyl group-containing resin is not particularly limited, but is preferably 5mgKOH/g to 50mgKOH/g, more preferably 8mgKOH/g to 45mgKOH/g, still more preferably 10mgKOH/g to 40mgKOH/g, particularly preferably 12mgKOH/g to 35mgKOH/g, and most preferably 15mgKOH/g to 30 mgKOH/g.

The hydroxyl value and acid value of the hydroxyl-and carboxyl-containing resin composition can be measured according to JIS K1557.

< molar equivalent ratio of isocyanate group to hydroxyl group (NCO/OH) >)

In the water-based coating composition of the present embodiment, the molar equivalent ratio (NCO/OH) of the isocyanate group of the triisocyanate to the hydroxyl group of the hydroxyl group-and carboxyl group-containing resin is preferably 0.2 or more and 5.0 or less, more preferably 0.4 or more and 3.0 or less, further preferably 0.6 or more and 2.5 or less, particularly preferably 0.8 or more and 2.0 or less, and most preferably 1.0 or more and 2.0 or less.

When the NCO/OH ratio is not less than the lower limit, the solvent resistance of the coating film obtained from the aqueous coating composition of the present embodiment after preliminary drying can be further improved. When the NCO/OH ratio is not more than the above upper limit, the solvent resistance of the coating film obtained from the water-based coating composition of the present embodiment can be further improved.

< other constituent Components >

The water-based coating composition of the present embodiment may contain the following constituent components in addition to the triisocyanate and the hydroxyl-and/or carboxyl-group-containing resin.

[ organic solvent ]

The water-based coating composition of the present embodiment may contain an organic solvent in order to disperse the triisocyanate.

Examples of the organic solvent include: 1-methylpyrrolidone, butylene glycol acetate, ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, propylene glycol monomethyl ether, methyl ethyl ketone, acetone, methyl isobutyl ketone, propylene glycol monomethyl ether acetate, ethanol, methanol, isopropanol, 1-propanol, isobutanol, 1-butanol, 2-ethylhexanol, cyclohexanol, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 1, 4-butanediol, 1, 3-butanediol, 2-n-butoxyethyl acetate, ethyl acetate, isopropyl acetate, butyl acetate, toluene, xylene, pentane, isopentane, hexane, isohexane, cyclohexane, solvent naphtha, mineral spirits, and the like. These organic solvents may be contained alone or in combination of 2 or more.

Among these, as the organic solvent, those having a solubility in water of 5 mass% or more are preferable from the viewpoint of stable dispersion of triisocyanate in water. In addition, the organic solvent is preferably one having a boiling point of 100 ℃ or higher, from the viewpoint that the surface appearance of the coating film obtained from the aqueous coating composition of the present embodiment can be further improved. Specifically, butanediol acetate and the like are preferable.

[ other constituent Components ]

The water-based coating composition of the present embodiment may contain various additives used in the art, such as a catalyst, a pigment, a leveling agent, an antioxidant, an ultraviolet absorber, a light stabilizer, a plasticizer, and a surfactant, depending on the purpose and use thereof, within a range not to impair the effects of the present embodiment.

As the catalyst, any catalyst may be used as long as it can accelerate curing of the water-based coating composition of the present embodiment, and examples thereof include: metal salts such as dibutyltin dilaurate, tin 2-ethylhexanoate, zinc 2-ethylhexanoate, and cobalt salts; tertiary amines such as triethylamine, pyridine, picoline, benzyldimethylamine, N-dimethylcyclohexylamine, N-methylpiperidine, pentamethyldiethylenetriamine, N '-ethylenepiperazine, and N, N' -dimethylpiperazine.

< use >)

The water-based coating composition of the present embodiment can be used as a coating material for roll coating, curtain coating, spray coating, bell jar coating, electrostatic coating, and the like.

The water-based coating composition of the present embodiment is useful as a primer, a surface coating and/or an intermediate coating for a material such as a metal (e.g., a steel sheet, a surface-treated steel sheet), a plastic, a wood, a film, an inorganic material, and the like.

The water-based coating composition of the present embodiment is also useful as a coating material for imparting decorativeness, weather resistance, acid resistance, rust resistance, chipping resistance, and the like to precoated metals including rust-proof steel sheets, coated parts of automobiles, and the like.

The water-based coating composition of the present embodiment is also useful as a urethane material for adhesives, pressure-sensitive adhesives, elastomers, foams, surface-treating agents, and the like.

(film coating)

A coating film according to an embodiment of the present invention is obtained by curing the above-described aqueous coating composition.

The coating film of the present embodiment is obtained by coating the above-mentioned aqueous coating composition by a known method such as roll coating, curtain coating, spray coating, bell jar coating, electrostatic coating, or the like, and curing the coating film.

The coating film of the present embodiment has excellent blocking resistance after preliminary drying, and is excellent in water resistance, solvent resistance, and adhesion to a substrate.