JPH1180649A - Paint composition with high solid content and top coat forming method therewith - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a novel org. solvent type thermosetting paint composition with high solid content which can form a coating having excellent acid resistance and anti-scratch property at the same time, excellent in low temperature curing, storage stability, and recoating cohesion, and given high enough solid content. SOLUTION: This composition comprises, a compd. contg. carboxyl group (A), at least one epoxide (B) selected from the group consisting of a vinyl polymer (B-1) having an epoxy group, a hydroxyl group, and a hydrolyzing alkoxysilil group in a molecule and having a number average mol.wt. of 1,000-4,000 and a hydroxy group value of 5-100 mgKOH/g, and an epoxy compd. (B-2) having a number average mol.wt. of less than 1,000, a reactive organopolysiloxane (C), a polyol compd. having less than 1,000 mol.wt. and a hydroxy group value of 120-1,000 mgKOH/g(D),and particles of a crosslinking polymer (E), and has a solid content concentration of not lower than 70 wt.%.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel organic solvent type thermosetting high solids coating composition and a method for forming a top coat using the same.

[0002]

2. Description of the Related Art In recent years, in paints for top coats, especially for clear top coats, such as automobile outer panels, etching of paint films and stain-like stains caused by acid rain have become a problem worldwide. Further, with the spread of car wash machines, abrasion caused by the car wash machines has also become a problem. Conventionally, various paints have been proposed as topcoat paints capable of forming a coating film having both acid resistance and abrasion resistance (Japanese Patent Application Laid-Open No. 62-1).
87749, JP-A-6-166741, etc.), any of low-temperature curability, storage stability and recoat adhesion were insufficient.

On the other hand, also in the field of paints, measures to control the use of organic solvents are urgently required due to serious air pollution and demand for resource saving. As one of the measures, there has been a demand for the development of a so-called high solid content paint in which the amount of organic solvent in the paint is reduced to increase the solid content concentration. It is not easy to achieve high solids differentiation of more than weight%.

[0004] The present applicant has previously been able to form a coating film having sufficient acid resistance and abrasion resistance simultaneously,
As a high solid content paint excellent in storage stability and recoat adhesion, a carboxyl group-containing compound, a vinyl polymer having an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group in a molecule, a reactive organopolysiloxane, In addition, a coating composition containing crosslinked polymer fine particles has been proposed (JP-A-9-143421).

However, even in such a coating composition, high solids differentiation is not always sufficient, and it is necessary to further increase solids differentiation from the viewpoint of air pollution prevention and resource saving.

[0006]

SUMMARY OF THE INVENTION An object of the present invention is to form a coating film having excellent acid resistance and scratch resistance at the same time,
In addition, it is an object of the present invention to provide a novel organic solvent type heat-curable high solids coating composition which is excellent in low-temperature curability, storage stability and recoat adhesion, and which is sufficiently solidified.

Another object of the present invention is to provide a method for forming a top coat using the above high solid content paint.

[0008]

Means for Solving the Problems The present inventors have made intensive studies to achieve the above object. As a result, Japanese Patent Application Laid-Open No. 9-143
It has been found that the above object can be achieved by further blending a specific polyol compound in the coating composition of No. 421, and based on this, the present invention has been completed.

That is, the present invention provides (A) a carboxyl group-containing compound, and (B) a compound having an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group in one molecule, and having a number average molecular weight of 1,
000-4,000, hydroxyl value 5-100 mgKOH /
g of the vinyl polymer (B-1) and a number average molecular weight of 1,
At least one epoxide selected from epoxy compounds (B-2) having a molecular weight of less than 000, (C) a reactive organopolysiloxane, (D) a polyol compound having a molecular weight of less than 1,000 and a hydroxyl value of 120 to 1,000 mg KOH / g And (E) an organic solvent-type thermosetting high solids coating composition containing crosslinked polymer fine particles and having a solid content concentration of 70% by weight or more.

The present invention also relates to a method for forming a top coat by sequentially forming a colored base coat and a clear top coat on a material, wherein the paint for forming the clear top coat is the above-mentioned paint composition. The present invention also relates to a method for forming a top coat.

[0011]

BEST MODE FOR CARRYING OUT THE INVENTION Each component of the coating composition of the present invention will be specifically described below.

The compound (A) used in the present invention is a compound having a carboxyl group and usually has an acid value of 50 to 50.
It is 0 mgKOH / g, preferably 80-300 mgKOH / g.

When the acid value of the compound (A) is less than 50 mgKOH / g, the curability of the resulting composition tends to decrease, and the acid resistance and scratch resistance of the coating film tend to decrease. If it exceeds 500 mgKOH / g, the compatibility with the polymer (B) and the reactive organopolysiloxane (C) tends to decrease, and the storage stability tends to be impaired. Examples of the compound (A) include a vinyl polymer (A-1) having a carboxyl group in one molecule and a carboxyl group-containing polyester compound (A-2).

(A-1): a vinyl polymer having a carboxyl group in one molecule. Examples of the polymer include a copolymer of a vinyl monomer having a carboxyl group and another vinyl monomer. Preferred examples include vinyl polymers having a group obtained by half-esterifying an acid anhydride group in one molecule.

Examples of the vinyl monomer having a carboxyl group include acrylic acid, methacrylic acid, crotonic acid, itaconic acid, and maleic acid; and acid anhydrides of vinyl monomers having an acid anhydride group such as maleic anhydride and itaconic anhydride. A vinyl monomer having a group obtained by half-esterifying a group can be used.

Here, the group obtained by half-esterifying an acid anhydride group means a carboxyl group and a carboxylic acid ester group obtained by adding an aliphatic monoalcohol to the acid anhydride group and opening the ring (ie, half-esterifying). And a group consisting of Hereinafter, this group may be simply referred to as a half ester group.

The vinyl polymer having a half ester group in one molecule includes an acid anhydride in a copolymer of a vinyl monomer having an acid anhydride group such as maleic anhydride and itaconic anhydride and another vinyl monomer. Copolymers obtained by half-esterifying groups can be mentioned.

When a half ester group is introduced into the copolymer, the above half esterification may be performed before or after the copolymerization reaction.

The aliphatic monoalcohol used for the half esterification includes low molecular weight monoalcohols such as methanol, ethanol, isopropanol and te.
rt-butanol, isobutanol, methyl cellosolve,
Ethyl cellosolve and the like. The half-esterification reaction can be carried out according to a usual method, usually at a temperature from room temperature to about 80 ° C., using a tertiary amine as a catalyst if necessary.

Other vinyl monomers for obtaining the vinyl copolymer include, for example, vinyl monomers having a hydroxyl group; (meth) acrylates; vinyl ethers and aryl ethers; olefinic compounds and diene compounds; Unsaturated monomer; nitrogen-containing unsaturated monomer.

Examples of the vinyl monomer having a hydroxyl group include:
For example, 2-hydroxyethyl (meth) acrylate,
C2-C8 hydroxyalkyl esters of acrylic acid or methacrylic acid such as 3-hydroxypropyl (meth) acrylate and hydroxybutyl (meth) acrylate; and polyether polyols such as polyethylene glycol, polypropylene glycol, and polybutylene glycol; A) Monoesters with unsaturated carboxylic acids such as acrylic acid; monoethers with polyether polyols such as polyethylene glycol, polypropylene glycol and polybutylene glycol and hydroxyl-containing unsaturated monomers such as 2-hydroxyethyl (meth) acrylate; Monoesterified product of an unsaturated compound containing an acid anhydride group such as maleic acid or itaconic anhydride and a glycol such as ethylene glycol, 1,6-hexanediol, neopentyl glycol, etc. Is a diester product; hydroxyalkyl vinyl ethers such as hydroxyethyl vinyl ether; allyl alcohol and the like; 2-hydroxypropyl (meth) acrylate; α, β-unsaturated carboxylic acid and Cardura E10 (manufactured by Shell Petrochemical Co., Ltd.) Adducts with monoepoxy compounds such as (name) and α-olefin epoxides; adducts of glycidyl (meth) acrylate with monobasic acids such as acetic acid, propionic acid, p-tert-butylbenzoic acid and fatty acids; Adducts of the above hydroxyl group-containing monomer with lactones (eg, ε-caprolactone, γ-valerolactone) and the like can be mentioned.

Examples of (meth) acrylates include methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, hexyl acrylate 2-ethylhexyl acrylate, n-octyl acrylate, decyl acrylate, stearyl acrylate, lauryl acrylate, cyclohexyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, n methacrylate -Butyl, isobutyl methacrylate, tert-butyl methacrylate, hexyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, decyl methacrylate, lauryl methacrylate,
C1-24 alkyl or cycloalkyl esters of acrylic acid or methacrylic acid such as stearyl methacrylate and cyclohexyl methacrylate; methoxybutyl acrylate, methoxybutyl methacrylate, methoxyethyl acrylate, methoxyethyl methacrylate,
Examples thereof include alkoxyalkyl esters of acrylic acid or methacrylic acid having 2 to 18 carbon atoms, such as ethoxybutyl acrylate and ethoxybutyl methacrylate.

Examples of vinyl ethers and aryl ethers include linear alkyl vinyl ethers such as ethyl vinyl ether, n-propyl vinyl ether, isopropyl vinyl ether, butyl vinyl ether, tert-butyl vinyl ether, pentyl vinyl ether, hexyl vinyl ether and octyl vinyl ether; cyclopentyl vinyl ether; Cycloalkyl vinyl ethers such as cyclohexyl vinyl ether; aryl vinyl ethers such as phenyl vinyl ether and trivinyl ether; aralkyl vinyl ethers such as benzyl vinyl ether and phenethyl vinyl ether; allyl ethers such as allyl glycidyl ether and allyl ethyl ether.

Examples of the olefinic compound and the diene compound include ethylene, propylene, butylene, vinyl chloride, butadiene, isoprene, chloroprene and the like.

Examples of the unsaturated monomer having a hydrocarbon ring include styrene, α-methylstyrene, phenyl (meth) acrylate, phenylethyl (meth) acrylate, phenylpropyl (meth) acrylate, benzyl (meth) acrylate, Phenoxyethyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-
Acryloyloxyethyl hydrogen phthalate, 2
-Acryloyloxypropyl hydrogen phthalate, 2-acryloyloxypropyl hexahydrohydrogen phthalate, 2-acryloyloxypropyl tetrahydrohydrogen phthalate, esterified product of p-tert-butyl-benzoic acid and hydroxyethyl (meth) acrylate, dicyclopentenyl (Meth) acrylate and the like.

Examples of the nitrogen-containing unsaturated monomer include, for example,
N, N-dimethylaminoethyl (meth) acrylate,
N, N-diethylaminoethyl (meth) acrylate,
Nitrogen-containing alkyl (meth) acrylates such as Nt-butylaminoethyl (meth) acrylate; acrylamodo, methacrylamide, N-methyl (meth) acrylamide, N-ethyl (meth) acrylamide, N, N-dimethyl (meth) Polymerizable amides such as acrylamide, N, N-dimethylaminopropyl (meth) acrylamide, N, N-dimethylaminoethyl (meth) acrylamide; 2-vinylpyridine, 1-vinyl-2-pyrrolidone, 4-vinylpyridine and the like Aromatic nitrogen-containing monomers; polymerizable nitriles such as acrylonitrile and methacrylonitrile; allylamine.

As the copolymerization method, a general polymerization method of a vinyl monomer can be used, but a solution-type radical polymerization method in an organic solvent is most suitable in consideration of versatility and cost. That is, aromatic solvents such as xylene and toluene; ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone; ester solvents such as ethyl acetate, butyl acetate, isobutyl acetate and 3-methoxybutyl acetate; n-butanol and isopropyl alcohol By performing a copolymerization reaction in the range of about 60 to 150 ° C. in the presence of a polymerization initiator such as azobisisobutyronitrile and benzoyl peroxide in a solvent such as an alcohol solvent, the desired polymer can be easily obtained. Can be obtained.

The copolymerization amount of each of a vinyl monomer having a carboxyl group, a half ester group or an acid anhydride group and other vinyl monomers is usually
The following ratio is appropriate. That is, a vinyl monomer having a carboxyl group, a half ester group, or an acid anhydride group is 5 to 40 from the viewpoint of curability and storage stability.
%, Preferably 10 to 30% by weight. It is appropriate that the other vinyl monomer accounts for about 60 to 95% by weight, preferably 70 to 90% by weight. The amount of styrene used among the other vinyl monomers is suitably up to about 20% by weight from the viewpoint of the weather resistance of the cured coating film. When a vinyl monomer having an acid anhydride group is used, half-esterification is performed after polymerization as described above.

The compound (A-1) has a number average molecular weight in view of the weather resistance of the coating film and the compatibility with the epoxide (Component (B)) and the reactive organopolysiloxane (Component (C)). An acrylic polymer having a molecular weight of 2,000 to 10,000 is preferred.

(A-2): Carboxyl group-containing polyester compound. Examples of the compound include a carboxyl group-containing polyester polymer, a polyol and 1,2
-Low molecular weight half esters (hereinafter sometimes referred to as "low molecular weight half esters") having a number average molecular weight of less than 1,000 generated by an addition reaction with an acid anhydride. Preferred examples include low molecular weight half esters.

The carboxyl group-containing polyester polymer includes ethylene glycol, butylene glycol,
1,6-hexanediol, trimethylolpropane,
It can be easily obtained by a condensation reaction between a polyhydric alcohol such as pentaerythritol and a polycarboxylic acid such as adipic acid, terephthalic acid, isophthalic acid, phthalic anhydride and hexahydrophthalic anhydride. For example, a carboxyl group-containing polyester polymer can be obtained by a one-step reaction under the compounding condition of polycarboxylic acid with excess carboxyl group. After synthesizing the polyester polymer of the above, a carboxyl group-containing polyester polymer can also be obtained by post-adding an acid anhydride group-containing compound such as phthalic anhydride, hexahydrophthalic anhydride and succinic anhydride.

The carboxyl group-containing polyester polymer obtained has a number average molecular weight of usually 1,000 or more, preferably about 1,100 to 2,000.

The low-molecular-weight half ester is obtained by reacting a polyol with a 1,2-acid anhydride under conditions sufficient for a ring-opening reaction of the acid anhydride to occur and for substantially no polyesterification reaction to occur. Is obtained by Such reaction products have a low molecular weight and a narrow molecular weight distribution. They also exhibit a low volatile organic content in the composition and impart excellent properties in the resulting coating.

The number average molecular weight of the low molecular weight half ester is usually less than 1,000, preferably from 400 to 900.

The low-molecular-weight half ester is prepared by subjecting a polyol and a 1,2-acid anhydride to an inert atmosphere, for example, a nitrogen atmosphere, in the presence of a solvent. Examples of suitable solvents include ketones such as, for example, methyl amyl ketone, diisobutyl ketone, methyl isobutyl ketone; toluene,
Aromatic hydrocarbons such as xylene; or other organic solvents such as dimethylformamide and N-methylpyrrolidone.

The reaction temperature is preferably as low as about 150 ° C. or less. Specifically, it is usually preferably about 70 to 150C, more preferably about 90 to 120C. 150 ° C
If the temperature exceeds, the polyesterification reaction occurs, which is not desirable. If the temperature is lower than 70 ° C., a sufficient reaction rate cannot be obtained, which is not preferable.

The reaction time basically varies somewhat depending on the reaction temperature, but is usually about 10 minutes to 24 hours.

The equivalent ratio of 1,2-anhydride: polyol is about 0.8: 1, calculated as the monofunctional acid anhydride.
The desired half ester can be obtained to the maximum within the range of １．２1.2: 1.

The acid anhydride used for preparing the low molecular weight half ester has about 4 to 32 carbon atoms. Examples of such include aliphatic, cycloaliphatic, olefinic and cyclic olefinic anhydrides and aromatic anhydrides. Substituted aliphatic and substituted aromatic anhydrides, as long as their substituents do not adversely affect the reactivity of the anhydride or the properties of the resulting half ester,
Included in the aliphatic and aromatic anhydrides. Examples of substituents include chloro, alkyl and alkoxy groups. Examples of acid anhydrides include succinic anhydride, methyl succinic anhydride, dodecenyl succinic anhydride, octadecenyl succinic anhydride, phthalic anhydride, tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, hexa Hydrophthalic anhydride, alkylhexahydrophthalic anhydride (eg, methylhexahydrophthalic anhydride), tetrafluorophthalic anhydride, endomethylenetetrahydrophthalic anhydride, chlorendic anhydride, itaconic anhydride, citracone Acid anhydrides and maleic anhydride.

Polyols that can be used are those having about 2 to 20 carbon atoms.
It has. Preferably, diols, triols and mixtures thereof are used. Examples of such include polyols having 2 to 10 carbon atoms. Examples of suitable are aliphatic polyols,
For example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, glycerol,
2,3-butanetriol, 1,6-hexanediol, neopentyl glycol, diethylene glycol,
Dipropylene glycol, 1,4-cyclohexanedimethanol, 3-methyl-1,5-pentanediol, trimethylolpropane, 2,2,4-trimethylpentane-1,3-diol, pentaerythritol and 1,
2,3,4-butanetetraol is exemplified. Aromatic polyols such as bisphenol A and bis (hydroxymethyl) xylene may be used.

Epoxide (B) in the composition of the present invention
Has an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group in one molecule, and has a number average molecular weight of 1,000 to 4,
And at least one epoxide selected from a vinyl polymer (B-1) having a hydroxyl value of 5 to 100 mgKOH / g and an epoxy compound (B-2) having a number average molecular weight of less than 1,000.

The vinyl polymer (B-1) is obtained by combining the vinyl monomer having an epoxy group, the vinyl monomer having a hydroxyl group, the vinyl monomer having a hydrolyzable alkoxysilyl group and other vinyl monomers with the compound (A-
It can be easily obtained by copolymerization in the same manner as in 1).

Examples of the vinyl monomer having an epoxy group include glycidyl (meth) acrylate and allyl glycidyl ether. Examples of the vinyl monomer having a hydrolyzable alkoxysilyl group include vinyltrimethoxysilane, vinylmethyldimethoxysilane, vinyltriethoxysilane, vinylmethyldiethoxysilane, vinyltris (2-methoxyethoxy) silane, and γ- (meth) silane. Acryloyloxypropyltrimethoxysilane, γ- (meth) acryloyloxypropylmethyldimethoxysilane, vinyltriacetoxysilane, β- (meth) acryloyloxyethyltrimethoxysilane, γ- (meth) acryloyloxypropyltriethoxysilane, γ- (Meth) acryloyloxypropylmethyldiethoxysilane and the like. Among these, from the viewpoint of low-temperature curability and storage stability, the hydrolyzable alkoxysilyl group is a methoxysilyl group or ethoxy. Those which are xylyl groups are preferred. The vinyl monomer having a hydroxyl group and other vinyl monomers are the same as those described above.

The copolymerization amount of each of the vinyl monomer having an epoxy group, the vinyl monomer having a hydroxyl group, the vinyl monomer having a hydrolyzable alkoxysilyl group and other vinyl monomers is usually the following among all monomers. The ratio is appropriate. That is, the amount of the vinyl monomer having an epoxy group is about 5 to 60% by weight, preferably 10 to 40% by weight, from the viewpoints of curability, storage stability, acid resistance and scratch resistance of the coating film. The vinyl monomer having a hydroxyl group is 3 to 50 from the viewpoints of curability, storage stability, acid resistance of coating film, scratch resistance, and water resistance.
%, Preferably about 5 to 30% by weight. The amount of the vinyl monomer having a hydrolyzable alkoxysilyl group is about 3 to 40% by weight, and preferably 5 to 20% by weight, from the viewpoints of curability, acid resistance of the coating film, abrasion resistance, and cost. Further, the amount of other vinyl monomer is suitably about 10 to 80% by weight, preferably 20 to 50% by weight. The amount of styrene used among the other vinyl monomers is suitably up to about 20% by weight from the viewpoint of the weather resistance of the cured coating film.

The polymer (B-1) obtained by polymerization in the above-mentioned copolymerization amount usually has an epoxy group content of 0.5 to 5.0 mmol / g, preferably 0.8.
２．５2.5 mmol / g, the content of the hydrolyzable alkoxysilyl group is 0.3-5.0 mmol / g, preferably 1.
It will be 0-3.0 mmol / g.

The polymer (B-1) has a hydroxyl value of 5
~ 100mgKOH / g, 10 ~ 80mgKO
It is preferably H / g. If the hydroxyl value is less than 5 mgKOH / g, the curability tends to decrease and the abrasion resistance tends to deteriorate, while if it exceeds 100 mgKOH / g, the viscosity of the composition increases and it becomes difficult to obtain a high solid content paint. Both tend to be undesirable.

Further, the polymer (B-1) needs to have a number average molecular weight of 1,000 to 4,000. If the number average molecular weight is less than 1,000, the curability and the weather resistance of the cured coating film tend to decrease, and if it exceeds 4,000, the compound (A), the reactive organopolysiloxane (C) and the polyol compound (D) )) And the viscosity tends to increase.

Further, the polymer (B-1) is preferably an acrylic polymer.

In the present invention, as the epoxide (B), only the epoxy compound (B-2) is used in place of the vinyl polymer (B-1), or the vinyl polymer (B
-1) and the epoxy compound (B-2) can be used in combination, whereby the coating composition can be further solidified. The vinyl polymer (B-1) and the epoxy compound (B-
The combination ratio when 2) is used in combination is not particularly limited, but is usually 90:10 to 50: 5 in terms of solid content of the former: latter.
It is preferably about 0.

The epoxy compound (B-2) includes
Any epoxy compound having a number average molecular weight of less than 1,000 can be used without particular limitation. When the number average molecular weight of the epoxy compound (B-2) is 1,000 or more, the viscosity becomes high and it becomes difficult to obtain a high solid content paint. The epoxy compound (B-2) usually does not have a hydrolyzable alkoxysilyl group in the molecule. Epoxy compound (B-
As 2), the number average molecular weight is preferably about 160 to 800, and the epoxy equivalent is preferably about 80 to 400.

Representative examples of the epoxy compound (B-2) include ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, tripropylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, 1,4 -Butanediol diglycidyl ether, neopentyl glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, glycerin diglycidyl ether, diglycerin tetraglycidyl ether, trimethylolpropane triglycidyl ether, 2,6-diglycidylphenyl ether , Sorbitol triglycidyl ether, triglycidyl isocyanurate, diglycidylamine, diglycidyl benzyl Amine, diglycidyl phthalate, bisphenol A diglycidyl ether, butadiene dioxide, dicyclopentadiene dioxide, diester of 3,4-epoxycyclohexene carboxylic acid with ethylene glycol, 3,4-epoxycyclohexylmethyl-3,4 -Epoxycyclohexanecarboxylate, 3,4-epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methylcyclohexanecarboxylate, bis (3,4-epoxycyclohexylmethyl) adipate, dicyclopentadiene epoxide glycidyl ether , Dipentenedionoxide, an adduct of bisphenol A type epoxy resin and ethylene oxide, Eporide GT300 (manufactured by Daicel Chemical Industries, Ltd., trifunctional alicyclic) Epoxy compound), Epolead GT400 (Daicel Chemical Industries, Ltd.
Epode GT3
01, the same GT302 and the same GT303 (all of which are manufactured by Daicel Chemical Industries, Ltd., trifunctional alicyclic epoxy compound having a ring-opened ε-caprolactone chain); Epolide GT40
1, GT402 and GT403 (all of which are manufactured by Daicel Chemical Industries, Ltd., tetrafunctional alicyclic epoxy compounds having a ring-opened ε-caprolactone chain); Epicoat 828, 834, and 1001 (all of which are described above). Yuko Shell Epoxy Co., Ltd., bisphenol A type epoxy resin); Epicoat 154 (Yuoka Shell Epoxy Co., Ltd., cresol novolak type epoxy resin), celloxides 2081, 2082 represented by the following formula (1): Id 2083
(All of the above are manufactured by Daicel Chemical Industries, Ltd .;
1 and n ′ = 2 are celloxide 2082 and n ′ = 3
Is a celloxide 2083); and Denacol EX-411 (manufactured by Nagase Kasei Co., Ltd.) represented by the following formula (2).

[0052]

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(In the formula (1), n ′ represents an integer of 1 to 3.)

The reactive organopolysiloxane (C) used in the present invention is a compound having a reactive functional group and an organo group on the side chain, the terminal or both of the polysiloxane chain. The reactive organopolysiloxane is a component used to impart high acid resistance and abrasion resistance to the coating film, and is a component which is compatible with the compound (A) and the polymer (B). It can be used without particular limitation.

The reactive organopolysiloxane (C)
May have any structure such as a linear shape, a branched shape, a net shape, and a ring shape.

The above-mentioned organo group (organic group) includes an alkyl group (methyl group, ethyl group, propyl group, butyl group, hexyl group, etc.), an alkenyl group, an aryl group,
Examples include an allyl group and a phenyl group. Among them, those having a methyl group, a vinyl group, a phenyl group or the like as an organo group are practically advantageous from the viewpoint of cost and the like.

Examples of the reactive functional group include a silanol group, an alkoxysilyl group, an alcoholic hydroxyl group, a glycidyl group, an amino group, a mercapto group, a carboxyl group, an amide group, a vinyl group, and a (meth) acryloxy group. Among them, an alkoxysilyl group, an alcoholic hydroxyl group and a glycidyl group are preferred.

The molecular weight of the component (C) can be appropriately selected within a range compatible with the components (A) and (B), and cannot be unequivocally determined. However, the number average molecular weight is usually about 100 to 10,000. , Preferably 300-5000
The degree is appropriate. As the molecular weight increases beyond this range, the compatibility tends to decrease.

The number of silicon atoms contained in one molecule is preferably 2 to 300, and more preferably 2 to 300.
100 are more preferable, and 3 to 50 are particularly preferable.

The component (C) is known, and specific examples thereof include, for example, JP-A-5-43696 and JP-A-7-
No. 70509 is disclosed.

The following are typical examples.

[0062]

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[0063]

Embedded image

(In the formulas (9) to (12), Ph represents a phenyl group, R represents a phenyl group, an alkyl group having 1 to 4 carbon atoms or a hydroxyl group. M and n represent 1 to 50, respectively.) Indicates an integer.).

[0065]

Embedded image

(In the equations (13) and (14), k is 2
Represents an integer of up to 20. Ph represents a phenyl group. k ′ and m ′ each represent an integer of 1 to 10. ).

As the component (C), one type may be used alone, or two or more types may be used in combination.

The polyol compound (D) in the composition of the present invention has two or more, preferably three, hydroxyl groups in one molecule.
And a molecular weight of less than 1,000, preferably 200
９００900 and hydroxyl value of 120-1,000 mg KO
H / g, preferably 150-800 mg KOH / g. In the compound (D), when the number of hydroxyl groups in one molecule is less than 2, the curability of the composition becomes insufficient, and when the molecular weight is 1,000 or more, the viscosity of the composition increases, so that high solid differentiation of the paint is caused. It is difficult to achieve. The compound (D) has a hydroxyl value of 120 mgKOH
/ G, the curability of the composition decreases, while
If it exceeds 00 mg KOH / g, the viscosity of the composition increases due to hydrogen bonding between hydroxyl groups, making it difficult to achieve high solid differentiation of the paint.

When the polyol compound (D) is cured by heating, the hydrolyzable alkoxysilyl group or epoxy group in the epoxide (B), the reactive organopolysiloxane (C)
It reacts with reactive groups such as silanol group, alkoxysilyl group, and glycidyl group in it to contribute to curing. Further, the compound (D) has a low molecular weight and can contribute to lowering the viscosity of the coating.

The polyol compound (D) can be used without particular limitation as long as it satisfies the above conditions.

Preferred polyol compounds (D) include, for example, those represented by the following general formula

[0072]

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Wherein R ¹ is a (p + r) -valent hydrocarbon group having 2 to 10 carbon atoms.
An integer of 3, p is an integer of 0 to 2, r is an integer of 1 to 3, and (p + r) is an integer of 2 to 4, respectively. And acryl oligomers.

The number of carbon atoms represented by R ¹ is 2 to 10
Examples of the (p + r) -valent hydrocarbon group having

[0075]

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And the like.

The crosslinked polymer fine particles (E) used in the present invention
Is not compatible with the components and the solvent of the carboxyl group-containing compound (A), the epoxide (B), the reactive organopolysiloxane (C) and the polyol compound (D). It is a crosslinked particulate polymer that can be stably dispersed. The component (E) is added to the mixture of (A), (B), (C) and (D) constituting the paint for the purpose of imparting thixotropic properties.

That is, since the above-mentioned mixture shows substantially Newtonian flow characteristics, for example, when the coating operation is performed with the substrate vertical, or when the temperature rises during baking performed after the coating, sagging, Various coating defects such as repelling and the like appear. However, when the crosslinked polymer fine particles (E) are added to the above mixture, the apparent viscosity at the time of standing still increases, but when a high shear stress is applied as at the time of spraying or the like,
The viscosity becomes sufficiently low, so that spraying can be easily performed without sagging, and thixotropic properties have already been developed a few seconds or minutes after application to the base material. However, the effect of preventing coating film defects works sufficiently such that coating film defects such as repelling do not occur.

As specific examples of the crosslinked polymer fine particles (E), there can be used an aqueous emulsion or a known intramolecularly crosslinked fine particle polymer obtained by an aqueous suspension polymerization method or a non-aqueous dispersion polymerization method. . Among them, the aqueous emulsion or the fine particle polymer having an intramolecular crosslinked structure obtained by the aqueous suspension polymerization method is prepared by physical or chemical means such as evaporation or azeotropic distillation of water or precipitation or aggregation of the polymer (particle). , Can be separated in the form of a solid, or when subjected to such physical or chemical means, the medium of the intended crosslinked polymer fine particles can be directly separated from water with another resin or organic solvent, etc. Can be replaced by

In the present invention, as a crosslinked polymer fine particle (E), a polymerizable monomer having at least two radically polymerizable unsaturated groups in a molecule as disclosed in JP-A-3-66770 is used. Crosslinked polymer fine particles obtained by subjecting another radical polymerizable unsaturated monomer to emulsion polymerization in the presence of a reactive emulsifier having an allyl group in the molecule can be suitably used. In this case, the polymer fine particles are internally cross-linked by a polymerizable monomer having at least two unsaturated groups capable of radical polymerization in the molecule.

As the crosslinked polymer fine particles (E), a polymer containing an alkoxysilyl group-containing vinyl monomer as an essential monomer component, as disclosed in JP-A-1-95116, is dispersed and stabilized. A non-aqueous dispersion of a particulate polymer insoluble in the organic liquid obtained by polymerizing a radically polymerizable unsaturated monomer in an organic liquid in the presence of the resin is also preferably used. In this case, the alkoxysilyl groups based on the alkoxysilyl group-containing vinyl monomer in the dispersion stabilizer resin, or the alkoxysilyl groups and the functional groups such as hydroxyl groups in the polymer fine particles are reacted and crosslinked. . Further, as the radical polymerizable unsaturated monomer forming the fine particle polymer, a polymerizable monomer having at least two radically polymerizable unsaturated groups in a molecule, an alkoxysilyl group-containing vinyl monomer or a complementary functional group The polymer fine particles may be further internally cross-linked using two types of monomers that are a combination of groups, and preferably internally cross-linked.

As the combination of the above complementary functional groups,
Examples include a combination of an isocyanate group and a hydroxyl group, and a combination of a carboxyl group and an epoxy group. Examples of the isocyanate group-containing vinyl monomer used in this case include isocyanate ethyl (meth) acrylate, m-isopropenyl-α, α-
Dimethylbenzyl isocyanate and the like can be mentioned. Examples of the hydroxyl group-containing vinyl monomer include those described above, and among them, 2-hydroxyethyl (meth) acrylate can be preferably used. Examples of the carboxyl group-containing vinyl monomer include (meth) acrylic acid and the like. As the epoxy group-containing vinyl monomer,
For example, glycidyl (meth) acrylate, methyl glycidyl (meth) acrylate and the like can be mentioned.

The crosslinked polymer fine particles have a high crosslink density and are substantially non-swellable even in a solvent having a high polymer dissolving power such as toluene or ethyl acetate.
In addition, when added to a binder resin solution or dispersion containing a solvent having a high dissolving power and being non-fusible, the resin content is high without increasing the viscosity of the solution (dispersion). That is, it is possible to obtain a solution (dispersion liquid) having a high solid content. Further, in the composition containing such crosslinked polymer fine particles, after drying, the fine particles and the binder resin together form a cured coating film.

As the crosslinked polymer fine particles (E),
The average particle diameter is about 0.01 to 2 μm, preferably 0.0
Suitably, it is about 5 to 0.5 μm. If the average particle size is smaller than this range, the sagging prevention effect tends to decrease, and if the average particle size is larger than this range, the finished appearance tends to decrease.

The compounding ratio of the carboxyl group-containing compound (A), the epoxide (B), the reactive organopolysiloxane (C), the polyol compound (D) and the crosslinked polymer fine particles (E) which are essential components in the composition of the present invention. Means that the compounding ratio of the compound (A) to the epoxide (B) is 1: 0.
The mixing ratio of the reactive organopolysiloxane (C) is 3 to 50 parts by weight based on 100 parts by weight of the total amount of the compound (A) and the epoxide (B). Wherein the compounding ratio of the compound (D) is
To the total amount of 100 parts by weight of
To 50 parts by weight, and the mixing ratio of the crosslinked polymer fine particles (E) is 10 in total of the compound (A), the epoxide (B), the reactive organopolysiloxane (C) and the compound (D).
The ratio is preferably 1 to 20 parts by weight with respect to 0 parts by weight. If the mixing ratio is outside the above range, the curability tends to decrease, and the acid resistance and abrasion resistance of the coating film tend to decrease.

More preferably, the compounding ratio of the compound (A) to the epoxide (B) is 1: 0.6 to 0.6 in the equivalent ratio of the former carboxyl group to the latter epoxy group.
And the mixing ratio of the reactive organopolysiloxane (C) is 5 to 30 parts by weight based on 100 parts by weight of the total amount of the compound (A) and the epoxide (B).
The compounding ratio of the compound (D) is 5 to 30 parts by weight based on 100 parts by weight of the total amount of the compound (A) and the epoxide (B), and the compounding ratio of the crosslinked fine particle polymer (E) is compound (A). ), Epoxide (B), reactive organopolysiloxane (C) and compound (D) in a proportion of 1 to 10 parts by weight with respect to 100 parts by weight in total.

The curable coating composition of the present invention may optionally contain a curing catalyst. As a curing catalyst that can be used, a catalyst effective for a crosslinking reaction between a carboxyl group and an epoxy group includes tetraethylammonium bromide, tetrabutylammonium bromide, tetraethylammonium chloride, tetrabutylphosphonium bromide, triphenylbenzylphosphonium chloride, and the like. Quaternary salt catalyst; triethylamine,
Examples thereof include amines such as tributylamine. Of these, quaternary salt catalysts are preferred. Further, the quaternary salt mixed with a phosphoric acid compound such as monobutyl phosphoric acid or dibutyl phosphoric acid, which is almost equivalent to the quaternary salt, can improve the storage stability of the coating without impairing the above-mentioned catalytic action and improve the electric power of the coating. This is preferable because a decrease in the suitability for spray coating due to a decrease in resistance can be prevented.

As a catalyst effective for a crosslinking reaction of a hydrolyzable alkoxysilyl group, dibutyltin dilaurate,
Tin catalysts such as dibutyltin diacetate; titanium catalysts such as tetrabutyl titanate; amines such as triethylamine and tributylamine;

The above-mentioned curing catalysts can be used alone or in combination. However, those having different catalytic activities from the viewpoints of curability, scratch resistance, storage stability and the like are used in combination. It is desirable.

In the coating composition of the present invention, if necessary, a so-called dehydrating agent such as trimethyl orthoacetate may be used in order to suppress the deterioration of the coating due to a solvent contained and moisture present in the air. is there.

The coating composition of the present invention may contain, if necessary, known general pigments such as coloring pigments, extender pigments and rust preventive pigments.

Examples of the coloring pigment include quinacridone-based pigments such as quinacridone red, azo-based pigments such as pigment red, phthalocyanine blue, phthalocyanine green, and the like.
Organic pigments such as phthalocyanine based pigments such as perylene red; inorganic pigments such as titanium oxide and carbon black; metallic pigments such as aluminum flakes, nickel flakes, copper flakes, brass flakes, chrome flakes, pearl mica, and colored pearl mica. be able to.

[0093] Various resins such as polyester resin, alkyd resin, silicone resin and fluororesin can be added to the coating composition of the present invention, if necessary. It is also possible to use a small amount of a crosslinking agent such as a melamine resin or a blocked isocyanate. Furthermore, if necessary, general paint additives such as an ultraviolet absorber, an antioxidant, a surface conditioner and an antifoaming agent can be blended.

The coating composition of the present invention is used as an organic solvent type high solid content coating composition. As the solvent, various organic solvents for coatings, for example, aromatic or aliphatic hydrocarbon solvents; alcohol solvents; ester solvents; ketone solvents; ether solvents can be used. As the organic solvent to be used, the one used at the time of preparing the polymer to be blended may be used as it is, or may be added as appropriate. The solid content of the composition can be as high as 70% by weight or more. A preferred solid content concentration is about 70 to 90% by weight.

The coating composition of the present invention is applied to various materials to be coated by an ordinary method, and is usually cured sufficiently at a temperature of about 100 to 180 ° C. for about 10 to 60 minutes to obtain an acid-resistant material. It forms a coating film with excellent properties and scratch resistance.

The method for forming a top coat according to the present invention is the method for forming a top coat in which a colored base coat and a clear top coat are sequentially formed on a material. Is used.

As the material for forming the overcoat film, specifically, a material obtained by electrodepositing a primer on a chemically treated steel sheet and, if necessary, applying an intermediate paint, or various plastic materials (necessary) Surface treatment, primer coating, intermediate coating, etc.), and composite members in which these are combined.

In the method for forming a top coat according to the present invention,
The coating composition of the present invention may be used as a clear top coat coating composition without blending a coloring pigment,
If necessary, a coloring pigment can be blended to such an extent that the colored base coat is not completely concealed.

The method for forming a coating film of the present invention is particularly suitable as a method for forming a top coating film for an automobile outer panel or the like. As the forming method, a coating system known in the automobile industry, for example, a method of forming a colored base coat / clear top coat by a two-coat one-bake method or a two-coat two-bake method;
A method of forming a colored base coat / clear top coat / clear top coat by a three-coat one-bake method or a three-coat two-bake method can be applied.

The most preferred method for forming a topcoat film of the present invention is to apply a coating material for forming a colored base coat to a material, apply a coating material for forming a clear top coat on the coated surface without curing, and then apply This is a two-coat one-bake method in which both coating films are cured by heating.

Next, two coats 1 using the clear top coat coating composition, which is the curable coating composition of the present invention, were prepared.
The coating method using the bake method will be described.

In the two-coat one-bake method, a coating composition for a colored base coat is first applied on the material by a conventional method such as spray coating.

The coating composition for a colored base coat includes:
The coating composition of the present invention containing a coloring pigment may be used, or a coating composition for a colored base coat known per se, which has been conventionally used in a method for forming a top coat, may be used.

Examples of known coating compositions for a colored base coat include acrylic resin / amino resin (melamine resin, etc., the same applies hereinafter), alkyd resin / amino resin, polyester resin / amino resin, acrylic resin / Examples of the coating composition include a polyisocyanate-based resin, an alkyd resin / polyisocyanate-based resin, and a polyester resin / polyisocyanate-based resin as a curable resin component. The form of these known colored base coat paint compositions is not particularly limited,
Any form such as an organic solvent type, a non-aqueous dispersion type, an aqueous solution type, an aqueous dispersion type, and a high solid content type can be used.

[0105] Examples of the coating machine used for spray coating include ordinary air spray guns, airless spray guns, air spray electrostatic coating machines, airless spray electrostatic coating machines, and rotary atomizing electrostatic coating machines. Etc. can be used.

The thickness of the coating composition for the colored base coat is preferably in the range of about 10 to 30 μm (after curing). After applying the coating composition for a colored base coat, leave it at room temperature for several minutes, or force-dry it for several minutes at a temperature in the range of about 50 to 80 ° C., and then paint the clear top coat of the present invention. Paint the composition.

The coating method and coating machine for the clear top coat coating composition can be the same as those used for the colored base coat coating composition.

The thickness of the clear top coat coating composition is preferably in the range of about 20 to 80 μm (after curing).

Next, both the colored base coat coating film and the clear top coat coating film are simultaneously cured by heating. The heating conditions in this case are about 100 to 18
The temperature is preferably 0 ° C. for about 10 to 60 minutes.

In the method for forming a top coat according to the present invention, the paint for forming the colored base coat is an aqueous paint or the solid content concentration during spray coating is usually about 15 to 65% by weight (typically about 10 to 55% by volume). ) Organic solvent type paint, wherein the paint forming the clear top coat has a solid content concentration of about 70 to 90% by weight (usually corresponding to about 64 to 88% by volume) at the time of spray coating. It is preferred that

The article coated by the method of forming a coating film of the present invention has a coating film having excellent acid resistance and abrasion resistance, and is particularly suitable for outer panels of automobiles.

[0112]

EXAMPLES Hereinafter, Production Examples, Examples and Comparative Examples will be given,
The present invention will be described more specifically. The parts and percentages in each example are based on weight.

Production Example 1 Half ester (a-1) formed by addition reaction between polyol and 1,2-acid anhydride
In a 5 liter glass flask equipped with a stirrer, thermometer and condenser, 236 parts of 3-methyl-1,5-pentanediol, 134 parts of trimethylolpropane, 1078 parts of hexahydrophthalic anhydride and 780 parts of xylene And heated to 120 ° C. in a nitrogen atmosphere to cause a reaction.
The reaction mixture was kept at this temperature for 4 hours and then cooled, solid content 65%, Gardner viscosity (25 ° C.) R, acid value 271 mg
A solution of KOH / g half ester (a-1) was obtained.

Production Example 2 Production of Acrylic Polymer having Carboxyl Group (a-2) 553 parts of xylene and 276 parts of 3-methoxybutyl acetate were placed in a 5-liter glass flask equipped with a stirrer, thermometer and condenser. Parts, 125 with electric heating mantle
° C, and at that temperature, a mixture of the following monomer compositions was evenly dropped over 4 hours. Incidentally, p-tert-butylperoxy-2-ethylhexanoate is a polymerization initiator.

N-butyl methacrylate 432 parts isobutyl methacrylate 346 parts lauryl methacrylate 360 parts styrene 72 parts methacrylic acid 86 parts acrylic acid 144 parts p-tert-butylperoxy-2-ethylhexanoate 72 parts Next, aging was performed for 30 minutes. Further, 277 parts of 3-methoxybutyl acetate and p-tert-butylperoxy-
A mixture of 14.4 parts of 2-ethylhexanoate was added dropwise over 2 hours, and then aged for 2 hours to obtain a solution of a carboxyl group-containing acrylic polymer (a-2).

The polymer liquid obtained has a resin solid content of 70%,
The Gardner viscosity (25 ° C.) was V. The number average molecular weight of this polymer was 3,000. The acid value of this polymer was 117 mgKOH / g.

Production Example 3 A vinyl polymer having an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group (b-
Production of 1) 410 parts of xylene and n-butanol 7 were placed in a 5-liter glass flask equipped with a stirrer, a thermometer, and a condenser.
After charging 7 parts, the mixture was heated to 125 ° C. with an electric heating mantle, and at that temperature, a mixture of the following monomer compositions was evenly dropped over 4 hours. Incidentally, azobisisobutyronitrile is a polymerization initiator.

Glycidyl methacrylate 504 parts 4-hydroxy n-butyl acrylate 72 parts γ-methacryloxypropyltriethoxysilane 216 parts n-butyl acrylate 360 parts styrene 288 parts Azobisisobutyronitrile 72 parts Next, the mixture was aged for 30 minutes. And 90 parts of xylene,
A mixture of 40 parts of n-butanol and 14.4 parts of azobisisobutyronitrile was added dropwise over 2 hours, and then aged for 2 hours to obtain a solution of acrylic polymer (b-1).

The resin solid content of the obtained polymer liquid is 70%,
The Gardner viscosity (25 ° C.) was T. The number average molecular weight of this polymer was 2,000. The epoxy group content of this polymer was 2.12 mmol / g, the hydroxyl value was 20 mgKOH / g, and the ethoxysilyl group content was 1.55 mmol / g.

Production Example 4 A vinyl polymer having an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group (b-
Production of 2) 410 parts of xylene and n-butanol 7 were placed in a 5-liter glass flask equipped with a stirrer, thermometer and cooling tube.
After charging 7 parts, the mixture was heated to 125 ° C. with an electric heating mantle, and at that temperature, a mixture of the following monomer compositions was evenly dropped over 4 hours. Incidentally, azobisisobutyronitrile is a polymerization initiator.

Glycidyl methacrylate 504 parts 4-hydroxy n-butyl acrylate 216 parts γ-methacryloxypropyltriethoxysilane 216 parts n-butyl acrylate 216 parts Styrene 288 parts Azobisisobutyronitrile 72 parts Next, aging was performed for 30 minutes. And 90 parts of xylene,
A mixture of 40 parts of n-butanol and 14.4 parts of azobisisobutyronitrile was added dropwise over 2 hours, and then aged for 2 hours to obtain a solution of an acrylic polymer (b-2).

The polymer liquid obtained had a resin solid content of 70%,
The Gardner viscosity (25 ° C.) was V. The number average molecular weight of this polymer was 2,000. The epoxy group content of this polymer was 2.12 mmol / g, the hydroxyl value was 58 mgKOH / g, and the ethoxysilyl group content was 1.55 mmol / g.

Production Example 5 Production of a vinyl polymer (b-4) having an epoxy group and a hydrolyzable alkoxysilyl group (for comparison) A 5-liter glass flask equipped with a stirrer, a thermometer and a condenser was used. , Xylene 410 parts and n-butanol 7
After charging 7 parts, the mixture was heated to 125 ° C. with an electric heating mantle, and at that temperature, a mixture of the following monomer compositions was evenly dropped over 4 hours. Incidentally, azobisisobutyronitrile is a polymerization initiator.

Glycidyl methacrylate 504 parts γ-methacryloxypropyltriethoxysilane 216 parts n-butyl acrylate 432 parts Styrene 288 parts Azobisisobutyronitrile 72 parts Then, after aging for 30 minutes, further 90 parts of xylene,
A mixture of 40 parts of n-butanol and 14.4 parts of azobisisobutyronitrile was added dropwise over 2 hours and then aged for 2 hours to obtain a solution of acrylic polymer (b-4).

The polymer liquid obtained had a resin solid content of 70%,
The Gardner viscosity (25 ° C.) was S. The number average molecular weight of this polymer was 2,000. The epoxy group content of this polymer was 2.12 mmol / g, the hydroxyl value was 0 mgKOH / g, and the ethoxysilyl group content was 1.55 mmol / g.

Production Example 6 Production of Crosslinked Polymer Fine Particles (e-1) 1 equipped with a stirrer, thermometer, cooling pipe and heating mantle
In a liter flask, 3547.5 parts of deionized water and 5
20 parts of 0% “Latemul S-120A” (trade name, manufactured by Kao Corporation, trade name, sulfosuccinic allyl group-containing anionic reactive emulsifier) was charged, and the temperature was raised to 90 ° C. while stirring. In addition, “VA”, a water-soluble azoamide polymerization initiator,
-086 "(manufactured by Wako Pure Chemical Industries, Ltd., trade name: 2,2 '
-Azobis [2-methyl-N- (2-hydroxyethyl) -propionamide]) in deionized water 5
20% of the aqueous solution dissolved in 00 parts was added. After 15 minutes, 150 parts of styrene, 550 parts of methyl methacrylate, n
5% of a monomer mixture consisting of 150 parts of -butyl acrylate, 50 parts of 2-hydroxyethyl acrylate and 100 parts of 1,6-hexanediol diacrylate were added. Then, after further stirring for 30 minutes, the dropping of the remaining monomer mixture and polymerization initiator was started. The monomer mixture was added dropwise for 3 hours, and the polymerization initiator was added dropwise for 3.5 hours, during which the polymerization temperature was kept at 90 ° C. After completion of the dropwise addition of the polymerization initiator aqueous solution, the mixture was heated at 30 ° C. for 30 minutes, cooled to room temperature, taken out using a filter cloth, and an aqueous dispersion of aqueous crosslinked polymer fine particles having a solid content of 20% was obtained.

This aqueous dispersion was placed on a stainless steel vat for 60 minutes.
It dried in the electric hot air type dryer of ° C, and was taken out as a solid resin. Thereafter, xylene heated to 60 ° C / n-
Dispersed in a mixed solvent of butyl alcohol = 50/50 (weight ratio) to form a crosslinked polymer fine particle (e
-1) A dispersion was obtained.

The resulting dispersion had a Gardner viscosity (25
C) A2, the average particle diameter of the polymer fine particles was 70 nm (measured by "Nanosizer N-4" manufactured by Coulter Inc.).

Production Example 7 Production of Crosslinked Polymer Fine Particles (e-2) (1) Production of Dispersion Stabilizer Resin 100 parts of xylene was heated to 120 ° C., and the following monomers and a polymerization initiator were added dropwise over 3 hours. After dropping, aging was performed for 2 hours.

Γ-methacryloxypropyltrimethoxysilane 5 parts Styrene 10 parts n-butyl methacrylate 35 parts 2-ethylhexyl methacrylate 25 parts Lauryl methacrylate 25 parts 2,2′-azobisisobutyronitrile 4 parts The obtained acrylic resin (Dispersion stabilizer resin) The varnish had a nonvolatile content of 50%, Gardner viscosity (25 ° C.) B, and a weight average molecular weight of the resin of about 10,000.

(2) Production of Non-Aqueous Dispersion of Crosslinked Polymer Fine Particles Heptane 100 parts The above dispersion stabilizer resin varnish 83 parts was charged in a flask, heated and refluxed, and the following monomers and polymerization initiator were added over 3 hours. The mixture was dropped and aged for 2 hours to obtain a dispersion of crosslinked polymer fine particles (e-2) having a solid content of 50%.

Γ-methacryloxypropyltrimethoxysilane 20 parts Styrene 15 parts Acrylonitrile 15 parts Methyl methacrylate 50 parts 2,2′-azobisisobutyronitrile 2 parts The resulting dispersion has a Gardner viscosity (25 ° C.) A1 The average particle diameter of the polymer fine particles was 300 nm (measured by “Nanosizer N-4” manufactured by Coulter Corporation).

Production Example 8 Production of Paint Composition (M-1) for Aqueous Colored Base Coat (1) Preparation of Acrylic Resin Aqueous Dispersion (W-1) In a reaction vessel, 140 parts of deionized water, 30% "Newcol" 7
07SF ”(Nippon Emulsifier Co., Ltd., trade name, surfactant)
2.5 parts and 80 parts of the following monomer mixture (1) were added,
The mixture was stirred and mixed in a nitrogen stream, and a monomer emulsion composed of 4 parts of 3% ammonium persulfate and 42 parts of deionized water was added to the reaction vessel at 60 ° C. over 4 hours using a metering pump. After completion of the addition, aging was performed for 1 hour.

Monomer mixture (1) Methyl methacrylate 55 parts Styrene 10 parts n-butyl acrylate 9 parts 2-hydroxyethyl acrylate 5 parts Methacrylic acid 1 part Next, at 80 ° C., the following monomer mixture (2) 20 0.5 parts and 4 parts of 3% ammonium persulfate were simultaneously dropped into the reaction vessel in parallel over 1.5 hours. After completion of addition, aged for 1 hour, 3
Filtered at 0 ° C. with a 200 mesh nylon cloth. Deionized water was further added to the mixture, and the pH was adjusted to 7.5 with dimethylaminoethanol.
g (glass transition temperature) 46 ° C., and an aqueous acrylic resin dispersion W-1 having a nonvolatile content of 20% was obtained.

Monomer mixture (2) Methyl methacrylate 5 parts n-butyl acrylate 7 parts 2-ethylhexyl acrylate 5 parts Methacrylic acid 3 parts 30% “Newcol 707SF” 0.5 part (2) Acrylic resin aqueous solution (W-2) Preparation of) 60 parts of butyl cellosolve and 15 parts of isobutyl alcohol were added to a reaction vessel, and heated to 115 ° C. in a nitrogen stream. After reaching 115 ° C., n-butyl acrylate 2
6 parts, methyl methacrylate 47 parts, styrene 10 parts,
A mixture of 10 parts of 2-hydroxyethyl methacrylate, 6 parts of acrylic acid and 1 part of azobisisobutyronitrile was added over 3 hours. After completion of the addition, the mixture was aged at 115 ° C. for 30 minutes, a mixture of 1 part of azobisisobutyronitrile and 115 parts of butyl cellosolve was added over 1 hour, and the mixture was aged for 30 minutes and filtered at 50 ° C. with a 200 mesh nylon cloth. The resulting reaction product has an acid value of 48 and a viscosity of Z4.
(Gardner foam viscometer), nonvolatile content 55%, Tg 45 ° C
Met. This was neutralized with dimethylaminoethanol in an equivalent amount, and deionized water was added to obtain an acrylic resin aqueous solution (W-2) having a nonvolatile content of 50%.

(3) Preparation of coating composition (M-1) for aqueous coloring base coat Acrylic resin aqueous dispersion (W-1) 275 parts Acrylic resin aqueous solution (W-2) 40 parts "Symel 350" (Mitsui Toatsu) 25 parts of “Aluminum Paste AW-500B” (trade name, metallic pigment, manufactured by Asahi Kasei Metals Co., Ltd.) 20 parts Butyl cellosolve 20 parts Deionized water 253 parts (Manufactured by Kyoeisha Yushi Kagaku Kogyo Co., Ltd., trade name, thickener), and adjusted the viscosity to 3,000 cps with a B-type viscometer (rotor rotation speed 6 rpm) to reduce the nonvolatile content to about 19%. A metallic water-based paint (M-1) was obtained.

EXAMPLES 1 TO 8 AND COMPARATIVE EXAMPLES 1 TO 7 After preparing a resin mixed solution with the composition shown in Table 1 (indicated by the solid content), 2 parts of an equimolar composition of tetrabutylammonium bromide and monobutyl phosphoric acid were added. Tinuvin 900 "
1 part of (trade name, manufactured by Ciba Geigy, ultraviolet absorber) and 0.1 part of "BYK-300" (trade name, manufactured by Big Chemie, surface conditioner) are added, and "Swazol 1000" (manufactured by Cosmo Oil Co., Ltd.) is added. (Trade name, hydrocarbon solvent), and adjusted to a viscosity of 30 seconds (Ford cup # 4/20 ° C.) to prepare a coating composition of the present invention and a comparative coating composition. Table 1 also shows the results of measuring the nonvolatile content at the time of coating.

Further, the storage stability of each of the obtained compositions was tested by the following method.

Storage stability: 150 g of a composition having a viscosity of 30 seconds
Was placed in a sealed glass bottle, and the viscosity (Ford cup # 4/20 ° C.) after storage at 30 ° C. for 2 weeks was measured to determine the degree of thickening. The evaluation criteria are as follows.

A has good storage stability with a viscosity of less than 40 seconds,
B indicates that the storage stability is slightly inferior when the viscosity is 40 seconds or more and less than 50 seconds, and C indicates that the storage stability is inferior when the viscosity is 50 seconds or more.

The test results are shown in Table 1.

[0142]

[Table 1]

In Table 1, (b-3) used as the epoxide (B) is represented by the formula

[0144]

Embedded image

3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate “X41-1067” (trade name, manufactured by Shin-Etsu Chemical Co., Ltd.) used as the reactive organopolysiloxane (C) is a glycidyl group- and methoxysilyl group-containing organopolysiloxane having a molecular weight of 740, and has the formula

[0146]

Embedded image

Is represented by Further, (d-1) used as the polyol compound (D) has the formula

[0148]

Embedded image

Is represented by

Examples 9 to 16 and Comparative Examples 8 to 14 Each of the coating compositions obtained in Examples 1 to 8 and Comparative Examples 1 to 7 was used as a clear top coat coating composition.
A top coat by coating 1 bake was formed as follows.

0.8m thick with zinc phosphate chemical conversion treatment
m on a dull steel plate, electrodeposited an epoxy-based cationic electrodeposition paint so as to have a dry film thickness of about 20 μm.
After baking for a minute, sharpen with # 400 sandpaper,
After degreased by wiping with petroleum benzine, air spray coating was applied to an automotive intermediate coating surfacer to a dry film thickness of about 25 μm and baked at 140 ° C. for 30 minutes.
The material was sanded with 400 sandpaper, dried with water, dried and then degreased by wiping with petroleum benzene to obtain a test material.

Next, the metallic base coat paint (M-1) obtained in Production Example 8 was applied on this material so as to have a cured film thickness of 20 μm, and was forcibly dried at 80 ° C. for 10 minutes. The above clear top coat coating composition was applied to a cured film thickness of 40 μm at 140 ° C.
For 30 minutes to cure both coating films to form an overcoating film.

[0153] A coating workability test was conducted as follows.

Critical film thickness: The critical film thickness (μm) at which no curling occurs when the film is applied to a stationary vertical surface.

Critical film thickness of sagging: The critical film thickness (μm) at which no sagging occurs when a stationary vertical surface is applied.

Further, a performance test of the obtained top coat was carried out as follows.

Coating appearance: The smoothness of the coating was visually evaluated. The evaluation criteria are as follows.

A is excellent in smoothness without any abnormality in the coating film;
Indicates that the skin is slightly worn out or that considerable unevenness is observed and the smoothness is poor.

Acid resistance: A test coated plate was diluted 1/40 with a 40% sulfuric acid solution.
After immersion for 2 hours and left at 50 ° C. for 5 hours, it was washed with water and the coated surface was observed. The evaluation criteria are as follows.

A shows that there is no change, B shows that there is no abnormality in the coated surface, but shows a slight step difference at the boundary between the immersed portion and the non-immersed portion, and C shows that the coated surface is whitened.

Scratch resistance: After the automobile coated with the test coated plate on the roof was washed 15 times with a car washer, the coated surface of the coated plate was observed. The car washer was manufactured by Yasui Sangyo
0FWRC "was used. The evaluation criteria are as follows.

A shows almost no damage by visual observation, B shows a little abrasion, but the degree is very slight.
C shows that scratches are noticeable by visual observation.

Impact resistance: Using a Dupont impact tester, the test was performed with a radius of a tip of a bombardment of 1/2 inch and a falling weight of 500 g. The evaluation was made based on the maximum height (in 5 cm increments) at which no cracks entered the coated surface. If there is no crack on the coated surface even at 50 cm, it is described as 50 <.

Water resistance: After being immersed in warm water of 40 ° C. for 240 hours, it was washed with water and the coated surface was observed. The evaluation criteria are as follows.

A shows no change, B shows a slight gloss, and C shows a whitened coating surface.

Recoat adhesion: 30 minutes at 140 ° C.
After baking for a minute, the same top coat (base coat /
Clear coat) was similarly applied, baked at 120 ° C. for 30 minutes, 100 cross cuts were inserted at 1 mm intervals, and the adhesion between the first and second coats when peeled off with cellophane tape was examined. The evaluation criteria are as follows.

A shows no peeling at all, B shows slight peeling, and C shows significant peeling.

Table 2 shows the test results.

[0169]

[Table 2]

[0170]

[Table 3]

As shown in Table 2 above, when the coating composition of the present invention is used as a clear coating composition, the solid content of the coating composition of the present invention is higher than that of the comparative coating composition. Regardless, it is clear that various performances equivalent to those using the comparative coating composition are exhibited.

[0172]

According to the present invention, an organic solvent type thermosetting high solids coating composition having a solid content concentration of 70% by weight or more by having a specific compounding component, and a method for forming a top coat using the same. The composition or the method has a remarkable effect of being able to form a coating film having excellent acid resistance and abrasion resistance, and having excellent low-temperature curability, storage stability and recoat adhesion. You.

──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. ⁶ Identification code FI C09D 167/02 C09D 167/02 183/06 183/06 (72) Inventor ▲ Yabu ▼ Tadashi Motoshi 4-Higashi-Hachiman, Hiratsuka-shi, Kanagawa Prefecture 17-1 Kansai Paint Co., Ltd. (72) Inventor Yasumasa Okumura 4-1-1 Higashi-Hachiman, Hiratsuka-shi, Kanagawa Prefecture Kansai Paint Co., Ltd.

Claims (13)

[Claims] 1. A carboxyl group-containing compound (A), (B)
One molecule has an epoxy group, a hydroxyl group and a hydrolyzable alkoxysilyl group, and has a number average molecular weight of 1,000 to 4,000.
0, at least one epoxide selected from a vinyl polymer (B-1) having a hydroxyl value of 5 to 100 mg KOH / g, and an epoxy compound (B-2) having a number average molecular weight of less than 1,000, and (C) reactivity. Organopolysiloxane,
(D) a molecular weight of less than 1,000 and a hydroxyl value of 120 to
It contains 1,000 mg KOH / g of a polyol compound and (E) crosslinked polymer fine particles, and has a solid content of 7%.
Organic solvent type thermosetting high solid content coating composition characterized by being at least 0% by weight. 2. The compound (A) has an acid value of 50 to 500 mg.
The composition of claim 1 wherein the composition is KOH / g. 3. The compound (A) is produced by an addition reaction of a vinyl polymer and / or a polyol having a half esterified acid anhydride group in one molecule with a 1,2-acid anhydride. The composition according to claim 1, which is a half ester having a number average molecular weight of less than 1,000. 4. The epoxide (B) is an epoxy compound (B
The composition according to claim 1, wherein the composition is a mixture of -2) alone or a combination of the vinyl polymer (B-1) and the epoxy compound (B-2). 5. The vinyl polymer (B-1) which is an epoxide (B) has an epoxy group content of 0.5 to 5.0 mmol / g, a hydroxyl value of 10 to 80 mg KOH / g, and a hydrolyzable alkoxysilyl. Group content 0.3-5.0 mmol /
The composition according to claim 1, wherein the composition is g of an acrylic polymer. 6. The composition according to claim 1, wherein the reactive functional group of the reactive organopolysiloxane (C) is one or more selected from an alkoxysilyl group, an alcoholic hydroxyl group and a glycidyl group. 7. The polyol compound (D) has a general formula: (Wherein R ¹ has 2 to 10 carbon atoms (p +
and r) a valent hydrocarbon group. q is an integer of 1 to 3, p is an integer of 0 to 2, r is an integer of 1 to 3, and (p + r) is 2
The integers of 4 are shown. The composition according to claim 1, which is a compound represented by the formula: 8. A crosslinked polymer fine particle (E) comprising a polymerizable monomer having at least two radically polymerizable unsaturated groups and another radically polymerizable unsaturated monomer in the molecule, and an allyl group in the molecule. Crosslinked polymer fine particles obtained by emulsion polymerization in the presence of a reactive emulsifier contained therein, and / or
Alternatively, a polymer containing an alkoxysilyl group-containing vinyl monomer as an essential monomer component is used as a dispersion stabilizer resin, and a radical polymerizable unsaturated monomer is used in an organic liquid in the presence of the dispersion stabilizer resin. The composition according to claim 1, which is a crosslinked polymer fine particle obtained by polymerization. 9. The compounding ratio of the compound (A) to the epoxide (B) is such that the equivalent ratio of the former carboxyl group to the latter epoxy group is 1: 0.5 to 0.5: 1. The compounding ratio of the reactive organopolysiloxane (C) is 3 to 50 parts by weight based on 100 parts by weight of the total amount of the compound (A) and the epoxide (B), and the compounding ratio of the compound (D) is: Total amount of compound (A) and epoxide (B) 100
The mixing ratio of the crosslinked polymer fine particles (E) is 3 to 50 parts by weight based on the weight of the compound (A), the epoxide (B), the reactive organopolysiloxane (C) and the compound (D). The composition according to claim 1, wherein the amount is 1 to 20 parts by weight based on 100 parts by weight in total. 10. A method of forming a top coat by sequentially forming a colored base coat and a clear top coat on a material, wherein the paint for forming the clear top coat is the coating composition according to claim 1. Top coating film formation method. 11. A method of applying a paint for forming a colored base coat to a material, applying a paint for forming a clear top coat on an uncured colored base coat, and then heating and curing both paint films. 11. The method for forming a top coat according to claim 10, wherein the two coats and the bake system are used. 12. The paint for forming the colored base coat is a water-based paint or an organic solvent type paint having a solid content of 15 to 65% by weight at the time of spray coating, and the paint for forming the clear top coat is at the time of spray coating. The method for forming a top coat according to claim 10, which is an organic solvent type paint having a solid content of 70% by weight or more. 13. An article on which a coating film is formed by the coating film forming method according to claim 10.