JP2006045483A - Antifouling property imparting composition, coating composition and coating film obtained from the composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an antifouling property imparting composition that is capable of exhibiting high gloss and of imparting a good antifouling property, to provide an aqueous coating system to exhibit a good antifouling property and to provide a coating film to exhibit a good antifouling property. <P>SOLUTION: The antifluling property imparting composition is formulated by adding a mixture of an organosilicate compound (A), a water-soluble and/or water-dispersible curing agent (B) having a reactive functional group and a hydrophilic group, a compound (C) to accelerate the hydrolysis/condensation of an alkoxysilane compound and optionally an organic solvent (D) and a dehydrating agent (E) to the aqueous coating. The antifouling property is enhanced by components (A) and (C). The coating film formed from the mixture enhances the hydrophilic property of the coating film and exhibits the good antifouling property. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

The present invention relates to a stain resistance imparting composition that exhibits stain resistance when added to a paint, a paint composition using the composition, and a coating film obtained from the composition.

In recent years, in the field of paints, from the viewpoint of pollution control or resource saving, attempts have been made to switch from using organic solvents to water-soluble or water-dispersed resins. However, water-based paints tended to be inferior in coating film performance compared to solvent-based paints. Under such circumstances, water-based paints are also required to have the same coating film properties as solvent-based paints, and in particular, are required to have high performance such as stain resistance.

As a method for imparting stain resistance to a paint, a method of blending an organosilicate in the paint is known (for example, see Patent Document 1). By this method, the hydrophilicity of the formed coating film is improved, and it is effective in preventing the adhesion of oily contaminants, and the adhered contaminants can be washed away with water droplets such as rain. However, when the above method is applied to an aqueous paint, there is a problem that the miscibility of the organosilicate into the aqueous paint is poor and the surface gloss is lowered.

On the other hand, a method of adding a mixture of an organosilicate and an emulsifier is disclosed as a method for improving the miscibility of an organosilicate in an aqueous paint (see, for example, Patent Document 2). By this method, the miscibility with water-based paints was improved, and the extreme reduction in surface gloss was solved. However, since the emulsifier is water-soluble, it has a drawback of reducing the water resistance and weather resistance of the obtained coating film. Moreover, since the compound which accelerates | stimulates hydrolysis and condensation of an alkoxysilane compound is not used substantially, the expression effect of stain resistance was not enough.

WO94 / 06870 Publication (Table 4) Japanese Patent Laid-Open No. 10-17850 (Gazette 6, page 6, left column, lines 28-43)

The problem to be solved by the present invention is to provide a stain resistance imparting agent and a water-based paint that expresses good stain resistance immediately after coating and forms a highly glossy coating film.

Promotes hydrolysis / condensation of organosilicate compounds, water-soluble and / or water-dispersible curing agents having reactive functional groups and hydrophilic groups (hereinafter water-soluble and / or water-dispersible curing agents), and alkoxysilane compounds The present inventors have found a method of adding a uniform mixture in which a compound (hereinafter referred to as a curing catalyst) is combined to an aqueous paint. By putting the organosilicate and the curing catalyst together in the water-based paint, the hydrolysis reaction of the organosilicate begins simultaneously with the contact of water.
The present invention relates to a stain resistance imparting composition in which the hydrophilicity of an organosilicate is increased and the miscibility with an aqueous paint is good, a paint composition using the composition, and a coating film obtained from the composition.

That is, (A) an organosilicate compound, (B) a water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule, and (C) promoting hydrolysis / condensation of the alkoxysilane compound. A composition for imparting stain resistance to a paint containing a compound (claim 1).

The antifouling composition according to claim 1, wherein the organosilicate as the component (A) is a compound represented by the general formula (1) or a partial hydrolysis condensate thereof (claim 2).

（式中、Ｒは同じかまたは異なり炭素数１〜４のアルキル基）
（Ｂ）成分の反応性官能基が（ブロック）イソシアネート基、エポキシ基、カルボジイ
ミド基、アルコキシシリル基、オキサゾリン基、ヒドラジド基から選ばれる１種または２
種以上であることを特徴とする請求項１又は２いずれか１項に記載の耐汚染性付与組成物
（請求項３）。

(Wherein R is the same or different and has 1 to 4 carbon atoms)
One or two (B) component reactive functional groups selected from (block) isocyanate group, epoxy group, carbodiimide group, alkoxysilyl group, oxazoline group, hydrazide group
It is a seed | species or more, The contamination-resistance imparting composition of any one of Claim 1 or 2 (Claim 3).

(C) Component is a tin compound, The antifouling property composition of any one of Claims 1-3 (Claim 4).

(C) Component contains the organotin compound shown by General formula (2), The stain resistance imparting composition of the coating material of any one of Claims 1-4 characterized by the above-mentioned (Claim 5).

（式中、Ｒ₁、Ｒ₂は同じかまたは異なり炭素数２〜８のアルキル基、Ｒ₃、Ｒ₄は直鎖ある
いは分岐した炭素数１〜２０のアルキル基、アルケン基などの炭化水素基である）
（Ｃ）成分がリン酸エステル単独またはリン酸エステル／アミンの反応物であることを
特徴とする請求項１〜３いずれか１項に記載の耐汚染性付与組成物（請求項６）。

(In the formula, R ₁ and R ₂ are the same or different, and an alkyl group having 2 to 8 carbon atoms, R ₃ and R ₄ are linear or branched hydrocarbon groups such as an alkyl group having 1 to 20 carbon atoms and an alkene group. Is)
The (C) component is a phosphate ester alone or a phosphate ester / amine reaction product, and the stain resistance-imparting composition according to any one of claims 1 to 3 (claim 6).

The organic solvent (D) and the dehydrating agent (E) are contained, The stain resistance imparting composition according to any one of claims 1 to 6, wherein the composition is a stain resistant composition (claim 7).

(B) 1 part or all of the hydrophilic group of a component contains a polyoxypropylene group
The contamination-resistance imparting composition according to any one of? 7. (Claim 8)
A paint composition comprising the stain resistance-imparting composition according to any one of claims 1 to 8 and a binder component (claim 9).

The coating composition according to claim 9, wherein the binder is an emulsion of a synthetic resin (claim 10).

11. The coating composition according to claim 10, wherein the synthetic resin emulsion is an emulsion of an alkoxysilyl group-containing polymer.

The coating composition according to any one of claims 10 to 11, wherein the synthetic resin emulsion is a polyoxyalkylene group-containing polymer emulsion (claim 12).

  The coating film obtained from the coating composition of any one of Claims 9-12 (Claim 13).

  That's all.

The stain resistance-imparting composition of the present invention can be produced at a low cost with a simple operation. In addition, by adding the stain resistance-imparting composition of the present invention to an aqueous coating material, a coating film having high gloss, high stain resistance, and good coating film characteristics due to wet and cold repetition is formed. Moreover, the water resistance, weather resistance, and adhesion of the formed coating film are improved.

Hereinafter, the present invention will be described in detail based on an embodiment thereof.
(Organosilicate)
The organosilicate compound (A) that can be used in the present invention is a compound containing a hydrolyzable silicon group, and is a compound represented by the general formula (1) or a partial decomposition condensate thereof.

（式中Ｒは同じか又は異なり炭素数１〜４のアルキル基）
具体的化合物としては、テトラメトキシシラン、テトラエトキシシラン、テトラ−ｎ−プ
ロポキシシラン、テトラ−ｉ−プロポキシシラン、テトラ−ｎ−ブトキシシラン、テトラ
−ｉ−ブトキシシラン、テトラ−ｔ−ブトキシシラン及びそれらの部分加水分解・縮合物
が例示できる。中でもエチルシリケート４０、エチルシリケート４８が望ましい。

(Wherein R is the same or different and has 1 to 4 carbon atoms)
Specific compounds include tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetra-i-propoxysilane, tetra-n-butoxysilane, tetra-i-butoxysilane, tetra-t-butoxysilane and the like The partial hydrolysis-condensation product can be illustrated. Of these, ethyl silicate 40 and ethyl silicate 48 are preferable.

The said compound may be single 1 type, and may use 2 or more types together. Organosilicates containing different alkoxysilyl groups in the same molecule can also be used. For example, methyl ethyl silicate, methyl propyl silicate, methyl butyl silicate, ethyl propyl silicate, propyl butyl silicate and the like. The ratio of these substituents is 0-10.
It can be arbitrarily changed between 0%. Moreover, although it described that the partial hydrolysis and condensate of these silicates can also be used, about 1-20 are preferable for a condensation degree. A more preferable range of the condensation degree is 3-15.

In the organosilicate compound, compounds having 1 to 4 carbon atoms in the alkoxysilyl group are exemplified, but it is generally known that the reactivity improves as the carbon number decreases.
When added to a water-based paint, an organosilicate having a small number of carbon atoms, such as methyl silicate, is highly reactive, and the time until gelation of the paint, that is, the pot life is shortened. On the other hand, when butyl silicate having a large number of carbon atoms is used, the stain resistance imparting rate is lowered and the pot life is lengthened. Considering the balance between contamination resistance and pot life,
When the alkyl moiety of the alkoxysilyl group has 1 carbon atom and 2, 3 or 4 carbon atoms, it is preferable that 2 carbon atoms and 3 or 4 carbon atoms exist, and the carbon Number 1
. 5-2.8 is preferable. That is, an equimolar mixture of methyl silicate and ethyl silicate or a silicate having the same number of methyl groups and ethyl groups in the same molecule can be said to be the alkyl part 1.5.

(Water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule)
As a function of the water-soluble and / or water-dispersible curing agent, the reactive functional group in the molecule reacts with the binder component and / or other compounding agent blended in the water-based paint, and further with the curing agent itself. Thus, the water resistance, weather resistance and adhesion of the obtained coating film can be improved.
Further, the water-soluble and / or water-dispersible curing agent has a hydrophilic group in the molecule, and in water, the hydrophilic group is present on the outer side, and a large amount of organosilicate is present in the inner hydrophobic part. This contributes to uniform dispersion in the water-based paint.

This curing catalyst promotes the hydrolysis reaction of the organosilicate when it is introduced into the water-based paint, and develops a high degree of stain resistance immediately after the coating, thereby uniformly dispersing the organosilicate compound (A) in the water-based paint. Contribute. This leads to a high gloss value and excellent stain resistance of the coating film formed from the aqueous paint to which the stain resistance imparting composition is added.

The water-soluble and / or water-dispersible curing agent that is an essential component of the present invention may be a compound having at least one hydrophilic group and one reactive functional group in the same molecule. Also, a copolymer of a hydrophilic group-containing vinyl monomer and a reactive functional group-containing monomer may be used.

Specific examples of the hydrophilic group include a polyoxyalkylene group (for example, a polyoxyethylene group, a polyoxypropylene group, a polyoxyalkylene group in which an oxyethylene group and an oxypropylene group are blocked or randomly bonded, the polyoxyethylene group, a polyoxyethylene group, Oxypropylene groups, polyoxyalkylene groups, and groups in which an oxyoxybutylene group is contained in a block or random bond), amino groups, carboxyl groups, hydroxy groups, alkoxy groups, sulfonic acid (salt) groups, etc. It is done. Of these, a polyalkylene oxide group is preferable, and a polyoxypropylene group is particularly preferable.

Those having a polyoxypropylene group have good compatibility with the organosilicate, and a uniform solution can be obtained without using the organic solvent (D). This greatly contributes to the reduction of the volatile solvent (VOC) in the final paint.

Specific examples of the reactive functional group include (block) isocyanate group, epoxy group, carbodiimide group, alkoxysilyl group, oxazoline group, hydrazide group and the like.

Examples of the water-soluble and / or water-dispersible curing agent having a (block) isocyanate group include 2,4-tolylene diisocyanate (2,4-TDI) and 2,6-tolylene diisocyanate (2,6-TDI). ), 4,4'-diphenylmethane diisocyanate (M
DI), xylylene diisocyanate (XDI), isophorone diisocyanate (IPD)
I), methylcyclohexyl diisocyanate (H6TDI), 4,4'-dicyclohexylmethane diisocyanate (H12MDI), 1,3-bis (isocyanatomethyl) cyclohexane (H6XDI), tetramethylxylylene diisocyanate (TMXDI)
2,2,4-trimethylhexamethylene diisocyanate (TMHDI), hexamethylene diisocyanate (HDI), norbornene diisocyanate (NBDI), 2,4
, 6-Triisopropylphenyl diisocyanate (TIDI), 1,12-diisocyanate dodecane (DDI), 2,4, -bis- (8-isocyanate octyl) -1,3
-Dioctylcyclobutane (OCDI), n-pentane-1,4-diisocyanate and their isocyanurate-modified products, adduct-modified products, burette-modified products, allophanate-modified products, and polymers having one or more isocyanate groups Is modified with a polyalkylene oxide group, a carboxyl group or the like to make it water-soluble and / or water-dispersible. Further, these isocyanate groups may be masked with a blocking agent (phenol, ε-caprolactam, etc.). Among these, those using a non-yellowing or hardly yellowing isocyanate are preferable from the viewpoint of weather resistance.

These include, for example, Bihijoule 3100, Bihijoule 2336, Bihijoule LS2150 / 1, Bihijoule BL116, Bihijoule BL5140, Bihijoule BL5235, Bihijoule TPLS2186, manufactured by Sumika Bayer Urethane Co., Ltd.
, Bihydrol TPLS 2153, Takenate WD-220 manufactured by Mitsui Takeda Chemical Co., Ltd.
Takenate WD-240, Takenate WD-720, Takenate WD-725, Takenate WD-726, Takenate WD-730, Takenate WB-700, Takenate WB
-720, Takenate WB-730, Takenate WB-920, Nippon Polyurethane Industry (
Co., Ltd. Aquanate 100, Aquanate 110, Aquanate 200, Aquanate 2
10, Aquanate 120, Duranate WB40-100 manufactured by Asahi Kasei Corporation, Duranate WB40-80D, Duranate WT20-100, Duranate WT30-100, and the like.

Further, a vinyl monomer having a (block) isocyanate group, a hydrophilic group-containing vinyl monomer, and a copolymer with other vinyl monomers may be used.
Examples of the vinyl monomer having a (block) isocyanate group include 2-methacryloyloxyethyl isocyanate, methacrylic acid-2- (O- [1′-methylpropylideneamino] carboxyamino) ethyl, and m-iso. And propenyl-α and α-dimethylbenzyl isocyanate.

Examples of the hydrophilic group-containing vinyl monomer include α, β-ethylenically unsaturated carboxylic acid, styrene sulfonic acid, vinyl sulfonic acid, sodium styrene sulfonate, sodium 2-sulfoethyl (meth) acrylate, (meth) acrylamide, N-methylol (meth) acrylamide, dialkylaminoalkyl (meth) acrylate, dialkylaminoalkyl (meth) acrylate hydrochloride, 2-aminoethyl (meth) acrylate hydrochloride, vinyl monomer having a polyoxyalkylene chain, etc. can give.

Examples of the α, β-ethylenically unsaturated carboxylic acid include (meth) acrylic acid, itaconic acid, maleic acid, crotonic acid, phthalic acid, citraconic acid and the like.
Examples of the dialkylaminoalkyl (meth) acrylate and dialkylaminoalkyl (meth) acrylate hydrochloride include dimethylaminoethyl (meth) acrylate, diethylamineethyl (meth) acrylate, dimethylaminopropyl (meth) acrylate, and hydrochloride thereof.

The vinyl monomer having a polyoxyalkylene chain is not particularly limited, but an acrylic acid ester or a methacrylic acid ester having a polyoxyalkylene chain is preferred, and specific examples include Bremer PE-90 manufactured by NOF Corporation. PE-200, PE-350, AE-
90, AE-200, AE-350, PP-500, PP-800, PP-1000, A
P-400, AP-550, AP-800, 700PEP-350B, 10PEP-55
0B, 55PET-400, 30PET-800, 55PET-800, 30PPT-8
00, 50PPT-800, 70PPT-800, PME-100, PME-200, P
ME-400, PME-1000, PME-4000, AME-400, 50POEP-
800B, 50AOEP-800B, AEP, AET, APT, PLE, ALE, PSE
, ASE, PKE, AKE, PNE, ANE, PNP, ANP, PNEP-600, Kyoeisha Chemical Co., Ltd. light ester 130MA, 041MA, MTG, light acrylate E
C-A, MTG-A, 130A, DPM-A, P-200A, NP-4EA, NP-8E
A, EHDG-A, MA-30, MA-50, MA-100, MA- manufactured by Nippon Emulsifier Co., Ltd.
150, RMA-1120, RMA-564, RMA-568, RMA-506, MPG
130-MA, Antox MS-60, MPG-130MA, RMA-150M, RM
A-300M, RMA-450M, RA-1020, RA-1120, RA-1820,
Shin-Nakamura Chemical Co., Ltd. NK-ESTER M-20G, M-40G, M-90G, M-
230G, AMP-10G, AMP-20G, AMP-60G, AM-90G, LA, Sanyo Chemical Co., Ltd. Eleminol RS-30, etc. are mentioned.

Examples of the water-soluble and / or water-dispersible curing agent having an epoxy group include Denacol EX-611, EX-612, EX-614, and EX-614 manufactured by Nagase Chemtech Co., Ltd.
B, EX-622, EX-512, EX-521, EX-411, EX-421, EX-
301, EX-313, EX-314, EX-321, EX-211, EX-810, E
X-811, EX-851, EX-821, EX-830, EX-832, EX-841
, EX-861, EX-911, EX-941, EX-920, EX-921, EX-9
31, EX-145, EX-171, EX-701, Kyoeisha Chemical Co., Ltd. Epolite 40
E, Epolite 100E, Epolite 200E, Epolite 400E, Epolite 70P
Epolite 200P, Epolite 400P, Epolite 1500NP, Epolite 80
MF, Epolite 100MF, Sakamoto Pharmaceutical Co., Ltd. SR-NPG, SR-16H, SR
-TMP, SR-TPG, SR-4PG, SR-2EG, SR-8EG, SR-8EGS
, SR-GLG, SR-DGE, SR-4GL, SR-4GLS, Epiol BE-200, G-100, E-100, E-400, E-1000, P-200 manufactured by NOF Corporation
, NPG-100, TMP-100, epiol OH and the like.

Moreover, the copolymer with the vinyl monomer which has an epoxy group, a hydrophilic group containing vinyl monomer, and another vinyl monomer may be sufficient.
Examples of the vinyl monomer having an epoxy group include glycidyl (meth) acrylate, M-GMA manufactured by Daicel Chemical Industries, Ltd., Cycler M-100, and Cyclom.
er A-200, Cycler M-101, Celoxide 2000 and the like.

Examples of the water-soluble and / or water-dispersible curing agent having a carbodiimide group include water-soluble or self-emulsifying carbodiimide compounds described in JP-A-8-59303.

These are 2,4-tolylene diisocyanate (2,4-TDI), 2,6-tolylene diisocyanate (2,6-TDI), 4,4'-diphenylmethane diisocyanate (
MDI), xylylene diisocyanate (XDI), isophorone diisocyanate (IP
DI), methylcyclohexyl diisocyanate (H6TDI), 4,4'-dicyclohexylmethane diisocyanate (H12MDI), 1,3-bis (isocyanatomethyl)
Cyclohexane (H6XDI), tetramethylxylylene diisocyanate (TMXDI)
), 2,2,4-trimethylhexamethylene diisocyanate (TMHDI), hexamethylene diisocyanate (HDI), norbornene diisocyanate (NBDI), 2,
4,6-triisopropylphenyl diisocyanate (TIDI), 1,12-diisocyanate dodecane (DDI), 2,4, -bis- (8-isocyanate octyl) -1,
One or more polyfunctional isocyanates such as 3-dioctylcyclobutane (OCDI) and n-pentane-1,4-diisocyanate are carbodiimidized by decarbonization condensation reaction, and the residual isocyanate group at the end is made hydrophilic. It is sealed with a sex group.

Examples of the hydrophilic group to be sealed include a residue of an alkyl sulfonate, a quaternary salt of a residue of a dialkylamino alcohol, a residue of a polyoxyalkylene whose end is blocked with an alkoxy group.

These are, for example, Nisshinbo Carbodilite V-02, V-04, V-06, V
-02-L2, E-01, E-02, E-03, E-04, E-05 and the like.

In addition, V-02B, V-04B, Elastostab H0
1 etc.

In the stain resistance-imparting composition of the present invention, it is preferable not to contain water in order to allow the reactive functional group and the organosilicate to coexist. When water is contained, these are used after dehydration or water. It is desirable to use those that do not contain.

Examples of the water-soluble and / or water-dispersible curing agent having an alkoxysilyl group include A-1230, MAC-2101, and MAC-2301 manufactured by Nippon Unicar Co., Ltd.

It can also be obtained by reacting an isocyanate-based silane coupling agent with the terminal hydroxy group of polyoxyalkylene.

The polyoxyalkylene is not particularly limited as long as it has one or more hydroxy groups at the terminal.

As an isocyanate type silane coupling agent, for example, Nippon Unicar Co., Ltd. A-1
310, Y-5187, KBE-9007 manufactured by Shin-Etsu Chemical Co., Ltd. and the like.

It can also be obtained by reacting the water-soluble and / or water-dispersible curing agent having an epoxy group with an amino silane coupling agent.

Examples of the amino silane coupling agent include γ-aminopropyltriethoxysilane, γ-aminopropyltrimethoxysilane, N- (β-aminoethyl) -γ-aminopropyltrimethoxysilane, N- (β-amino). Ethyl) -γ-aminopropyltriethoxysilane, N- (β-aminoethyl) -γ-aminopropylmethyldimethoxysilane,
γ-Phenylaminopropyltrimethoxysilane, Shin-Etsu Chemical Co., Ltd. KBE-910
3, KBM-575, KBM-6123, Nippon Unicar Co., Ltd. A-1102, A-11
22, A-1170, and the like.

Furthermore, it may be a copolymer with an alkoxysilyl group-containing vinyl monomer, a hydrophilic group-containing vinyl monomer, and other vinyl monomers.

Specific examples of vinyl monomers containing alkoxysilyl groups include vinyltrimethoxysilane, vinylmethyldimethoxysilane, vinyltriethoxysilane, vinylmethyldiethoxysilane, vinyltris (2-methoxyethoxy) silane, vinyltrimethyl. Isopropoxysilane, γ- (meth) acryloyloxypropyltrimethoxysilane, γ- (
(Meth) acryloyloxypropylmethyldimethoxysilane, γ- (meth) acryloyloxypropyltriethoxysilane, γ- (meth) acryloyloxypropylmethyldiethoxysilane, γ- (meth) acryloyloxypropyltri-n-propoxysilane, γ -(Meth) acryloyloxypropyltriisopropoxysilane, vinyltriacetoxysilane, β- (meth) acryloyloxyethyltrimethoxysilane and the like.

A water-soluble and / or water-dispersible curing agent having an oxazoline group is commercially available as an aqueous crosslinking agent. For example, Epocros WS-500, K-2010E manufactured by Nippon Curing Catalysts Co., Ltd.
, K-2020E, K-2030E, K-1010E, K-1020E, K-1030E
Etc. Since these are commercially available as aqueous solutions or emulsions, it is desirable to use them after dehydration.

Examples of the water-soluble and / or water-dispersible curing agent having a hydrazide group include carbohydrazide, adipic acid dihydrazide, sebacic acid dihydrazide, dodecanediohydrazide, aminopolyacrylamide, and the like.

The water-soluble and / or water-dispersible curing agent is used in an amount of organosilicate compound (A
) 5 to 300 parts per 100 parts by weight. If it is less than 5 parts by weight, the stain resistance imparting composition is not uniformly dispersed in the water-based paint, and the gloss value of the formed coating film is lowered. Moreover, when 300 weight part or more is used, the hardness of the formed coating film falls. More preferably, it is 20-200 parts.

(Compound that promotes hydrolysis and condensation of alkoxysilane compounds)
As the compound that promotes hydrolysis / condensation of the alkoxysilane compound (C) in the present invention, an organic tin compound, a phosphate ester compound alone or a phosphate ester / amine reaction product, an organoaluminum compound, an organotitanium compound, Examples include organic zirconium compounds. From the viewpoint of imparting stain resistance to the coating film, an organotin compound, a phosphate ester, or a reaction product of a phosphate ester and an amine is particularly preferable.

Examples of organic tin compounds include dibutyltin dilaurate, dibutyltin dimaleate, dibutyltin dioleylmalate, dioctyltin dilaurate, dibutyltin diacetate, dibutyltin dimethoxide, dibutyltin thioglycolate, dibutyltin bisisononyl 3-mercaptopropionate, Dibutyltin bisisooctyl thioglycolate, dibutyltin bis-2-
Ethylhexyl thioglycolate, dimethyltin bisdosyl mercaptide, dimethyltin bisdodecylmercaptide, dibutyltin bisdodecylmercaptide, dioctyltin bisdodecylmercaptide, dimethyltin bis (octylthioglycolate) salt, tin octylate Etc.

Among them, dibutyltin thioglycolate, dibutyltin bisisononyl 3-mercaptopropionate, dibutyltin bisisooctylthioglycolate, dibutyltin bis-2-ethylhexylthioglycol are preferred from the viewpoints of stability in water and stain resistance. Preferred are mercaptides such as lactic acid, dimethyltin bisdodecyl mercaptide, dibutyltin bisdodecyl mercaptide, dioctyltin bisdodecyl mercaptide, dimethyltin bis (octylthioglycolate) salt, particularly dibutyltin bisdodecyl. Organotin compounds represented by the general formula (2) such as mercaptide and dioctyltin bisdodecyl mercaptide are more preferable in that the contact angle is lowered even when a paint after pot life is used.

Examples of phosphoric acid ester compounds include propyl acid phosphate, dibutyl phosphate, 2-ethylhexyl acid phosphate, di-2-ethylhexyl phosphate,
Examples include monoisodecyl acid phosphate, diisodecyl phosphate, lauryl acid phosphate, stearyl acid phosphate and the like. Examples of amine compounds to be reacted with these phosphate ester compounds include triethylamine, n-butylamine, hexylamine, triethanolamine, and diazabicycloundecene. Of these, di-2-ethylhexyl phosphate and diisodecyl phosphate are preferable because the contact angle of the coating film after being immersed in water tends to decrease.

(C) It is preferable to mix | blend 1-50 weight part with respect to 100 weight part of organosilicate. If it is less than 1 part by weight, the effect of imparting stain resistance is low, and if it exceeds 50 parts by weight, the stability of the composition is lowered. When added to a water-based paint, the amount of (C) present increases, and the weather resistance of the coating film decreases. The amount of component (C) is more preferably 3 to 30 parts by weight.

(Organic solvent)
Examples of organic solvents that can be blended include esters, ethers, ketones, hydrocarbons, and alcohols. These organic solvents may be used individually by 1 type, and may use 2 or more types together. By blending these organic solvents in the stain resistance imparting composition, there is an effect of improving the uniformity of the composition. In addition, when the stain resistance imparting composition is added to the water-based paint,
The dispersibility can be improved.

Esters include ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol monobutyl ether acetate, diethylene glycol monomethyl ether acetate, diethylene glycol monomethyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol diacetate, ethyl acetate, butyl acetate. , 2,2,4-trimethylpentadiol-1,3-monoisobutyrate (manufactured by Chisso Corporation, CS-12), etc., ethers such as ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, triethylene glycol dimethyl ether, diethylene glycol ether Methyl ether, diethylene glycol dibutyl ether, dipropylene glycol Methyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether,
Diethylene glycol monoethyl ether, propylene glycol monomethyl ether,
Propylene glycol monoethyl ether, ethyl ether, butyl ether, dioxane, THF, and other hydrocarbons include benzene, toluene, xylene, dodecane,
Examples of ketones include acetone and methyl ethyl ketone, and examples of alcohols include methanol, ethanol, n-propanol, isopropanol, butanol, octanol, ethylene glycol, and propylene glycol.

These organic solvents may be used alone or in combination of two or more. Among these,
There is no particular limitation as long as it does not have a functional group that reacts with the reactive group of the water-soluble and / or water-dispersible curing agent.
These organic solvents are preferably not used from the viewpoint of environmental problems, but the amount added is preferably about 5 to 300 parts by weight with respect to 100 parts by weight of the organosilicate.
Note that it is preferable to use a water-soluble and / or water-dispersed curing agent having a poly (propylene oxide) group as a hydrophilic group because the organic solvent can be eliminated or reduced.

(Dehydrating agent)
Since organosilicate has a dehydrating action, dehydrating agent (E) is usually used in a stain-imparting composition.
However, it is preferable to add a dehydrating agent (E) when an organosilicate having high reactivity with water or a water-soluble and / or water-dispersed curing agent is used.

Examples of the dehydrating agent (E) include trialkyl orthoformate such as trimethyl orthoformate, triethyl orthoformate or tributyl orthoformate; trialkyl orthoacetate such as trimethyl orthoacetate, triethyl orthoacetate or tributyl orthoacetate; or trimethyl orthoborate. Orthocarboxylic acid esters such as trialkyl orthoborate such as triethyl orthoborate and tributyl orthoborate.

Further, there are isocyanates such as benzenesulfonyl isocyanate, tosyl isocyanate, phenyl isocyanate, p-chlorophenyl isocyanate, 2,4-toluene diisocyanate, metaxylylene diisocyanate or hexamethylene diisocyanate, preferably benzenesulfonyl isocyanate, tosyl isocyanate, Such as phenyl isocyanate or p-chlorophenyl isocyanate,
And various monoisocyanates.

When alcohols are used as the organic solvent (D), they react with isocyanates. Therefore, it is preferable to avoid the use of isocyanates when alcohols are used as the organic solvent.

(Preparation method of stain resistance imparting composition)
As a method for producing the stain resistance-imparting composition of the present invention, the above components (A) to (C), and in some cases (D) and (E) can be obtained by simply mixing and stirring. is there. Further, as another method, it is possible to cope with heating to such an extent that physical properties are not affected.

When the temperature is higher than 100 ° C. or when moisture is mixed, the condensation reaction of the component (A) and / or self-crosslinking of the component (B) occurs, and the antifouling composition itself is thickened. There is also a possibility of gelation. In addition, even if it does not gel, it may be deteriorated in functions such as a decrease in stain resistance and a decrease in gloss of the coating film formed by adding to the water-based paint.

(Emulsion of synthetic resin)
Examples of synthetic resin emulsions that can be used in the present invention include, but are not limited to, acrylic resin emulsions, urethane resin emulsions, fluorine resin emulsions, epoxy resin emulsions, polyester resin emulsions, alkyd resin emulsions, and melamine resin emulsions. I don't mean. These may be used alone or in combination of two or more. Among these, acrylic resin emulsion is advantageous because of its high cost and high degree of freedom in resin design.
As the acrylic resin emulsion, those obtained by radical copolymerization of an acrylic monomer and a monomer copolymerizable with the acrylic monomer can be used.

The monomer that can be used is not particularly limited, but specific examples include methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl acrylate, iso-butyl acrylate, tert-butyl acrylate, and benzyl. (Meth) acrylate, cyclohexyl acrylate, n-butyl methacrylate, iso-butyl methacrylate,
(Meth) acrylate monomers such as tert-butyl methacrylate, 2-ethylhexyl methacrylate, isodecyl methacrylate, lauryl methacrylate, tridecyl methacrylate, stearyl methacrylate, cyclohexyl methacrylate, isobornyl methacrylate; styrene, α-methylstyrene, chlorostyrene Aromatic vinyl monomers such as 4-hydroxystyrene and vinyltoluene; vinyl esters and allyl compounds such as vinyl acetate, vinyl propionate and diallyl phthalate; nitrile group-containing vinyl monomers such as (meth) acrylonitrile Body; epoxy group-containing vinyl monomer such as glycidyl (meth) acrylate; 2-hydroxypropyl (meth) acrylate, 2-
Hydroxypropyl (meth) acrylate, 2-hydroxyethyl vinyl ether, hydroxystyrene, Aronics 5700 (manufactured by Toagosei Co., Ltd.), placelFA-
1, pixelFA-4, placeFM-1, placeFM-4 (above, manufactured by Daicel Chemical Industries, Ltd.), HE-10, HE-20, HP-10, HP-20 (above made by Nippon Curing Catalysts, Inc.) , Blemmer PEP series, Blemmer NKH-5050,
Bremermer GLM (manufactured by Nippon Oil & Fats Co., Ltd.), hydroxyl group-containing vinyl monomers such as hydroxyl group-containing vinyl-modified hydroxyalkyl vinyl monomers; AS-6 and AN- which are macromonomers manufactured by Toagosei 6, compounds such as AA-6, AB-6, and AK-5, vinyl methyl ether, propylene, butadiene, and the like.

Furthermore, a hydrophilic vinyl monomer capable of improving the stability of the emulsion can also be used. Examples of the vinyl monomer having a hydrophilic group that can be used include sodium styrenesulfonate, sodium 2-sulfoethyl methacrylate, 2-sulfoethyl methacrylate ammonium, and vinyl monomers having a polyoxyalkylene chain. Although there is no limitation in the vinyl-type monomer which has a polyoxyalkylene chain, the acrylic acid ester or methacrylic acid ester which has a polyoxyalkylene chain is preferable.

Specific examples include Blemmer PE-90, PE-200, and PE-350 manufactured by NOF Corporation.
AE-90, AE-200, AE-350, PP-500, PP-800, PP-10
00, AP-400, AP-550, AP-800, 700PEP-350B, 10PE
P-550B, 55PET-400, 30PET-800, 55PET-800, 30P
PT-800, 50PPT-800, 70PPT-800, PME-100, PME-2
00, PME-400, PME-1000, PME-4000, AME-400, 50P
OEP-800B, 50AOEP-800B, AEP, AET, APT, PLE, ALE
, PSE, ASE, PKE, AKE, PNE, ANE, PNP, ANP, PNEP-60
0, Kyoeisha Chemical Co., Ltd. light ester 130MA, 041MA, MTG, light acrylate EC-A, MTG-A, 130A, DPM-A, P-200A, NP-4EA, N
P-8EA, EHDG-A, Nippon Emulsifier Co., Ltd. MA-30, MA-50, MA-100
MA-150, RMA-1120, RMA-564, RMA-568, RMA-506
, MPG130-MA, Antox MS-60, MPG-130MA, RMA-150
M, RMA-300M, RMA-450M, RA-1020, RA-1120, RA-1
820, Shin-Nakamura Chemical Co., Ltd. NK-ESTER M-20G, M-40G, M-90
G, M-230G, AMP-10G, AMP-20G, AMP-60G, AM-90G,
LA, Sanyo Chemical Co., Ltd. Eleminol RS-30, etc. are mentioned.

It is also possible to use a monomer having two or more polymerizable unsaturated bonds such as polyethylene glycol di (meth) acrylate, ethylene glycol di (meth) acrylate, triallyl cyanurate, allyl (meth) acrylate and divinylbenzene. Is possible. In this case, the generated particles have a structure having cross-linking, and the water resistance of the formed coating film is improved.

Moreover, trifluoro (meth) acrylate, pentafluoro (meth) acrylate, perfluorocyclohexyl (meth) acrylate, 2,2,3,3-tetrafluoropropyl methacrylate, β- (perfluorooctyl) ethyl (meth) acrylate, etc. A fluorine-containing acrylic resin emulsion having a high level of water and oil repellency can be produced by using a fluorine-containing vinyl monomer.

Further, a carbonyl group-containing vinyl monomer is copolymerized with the above monomer, and hydrazine and / or
Alternatively, a cross-linked acrylic resin emulsion containing a compound containing a hydrazide group can also be produced. The water resistance of the coating film obtained from such a crosslinked acrylic resin emulsion is:
Very good.

Furthermore, an acrylic resin emulsion containing a hydrolyzable silyl group can be prepared by copolymerizing the monomer and a monomer having a hydrolyzable silyl group.

As the monomer containing a hydrolyzable silyl group, an alkoxysilyl group-containing vinyl monomer is preferable from the viewpoint of ease of handling, cost, and the difficulty of producing a reaction byproduct. Specific examples of vinyl monomers containing an alkoxysilyl group include vinyl trimethoxysilane,
Vinylmethyldimethoxysilane, vinyltriethoxysilane, vinylmethyldiethoxysilane, vinyltris (2-methoxyethoxy) silane, vinyltriisopropoxysilane, γ- (meth) acryloyloxypropyltrimethoxysilane, γ- (meth) acryloyloxy Propylmethyldimethoxysilane, γ- (meth) acryloyloxypropyltriethoxysilane, γ- (meth) acryloyloxypropylmethyldiethoxysilane, γ- (meth) acryloyloxypropyltri-n-propoxysilane, γ- (meth)
Acryloyloxypropyltriisopropoxysilane, vinyltriacetoxysilane,
β- (meth) acryloyloxyethyltrimethoxysilane and the like can be mentioned.

These hydrolyzable silyl group-containing vinyl monomers may be used alone or in combination of two or more.

Γ- (meth) acryloyloxypropylmethyldimethoxysilane, γ- (meth) acryloyloxypropyltriethoxysilane, from the viewpoint of storage stability when a water-based paint is used,
γ- (Meth) acryloyloxypropylmethyldiethoxysilane, γ- (meth) acryloyloxypropyltri-n-propoxysilane, and γ- (meth) acryloyloxypropyltriisopropoxysilane are particularly preferred.

The hydrolyzable silyl group-containing monomer is desirably copolymerized using 0.1 to 50 parts by weight in 100 parts by weight of all monomers. If it is less than 0.1 part by weight, the water resistance and durability are lowered, and if it exceeds 50 parts by weight, the emulsion becomes unstable. More preferably, it is 0.5 to 20 parts by weight.

When the alkoxysilyl group-containing acrylic emulsion obtained as described above is mixed with the compound (C) that promotes hydrolysis and condensation of the alkoxysilane compound of the present invention,
The crosslinking reaction proceeds, and the coating film has good water resistance and weather resistance.
Further, by copolymerizing a vinyl monomer containing a functional group capable of reacting with the reactive functional group of the water-soluble and / or water-dispersible curing agent (B) of the present invention, Weather resistance, water resistance, adhesion, etc. are improved.

Examples of the functional group capable of reacting with a water-soluble and / or water-dispersible curing agent having a (block) isocyanate group include a hydroxyl group, an amino group, and a carboxyl group.
Examples of the functional group capable of reacting with a water-soluble and / or water-dispersible curing agent having a carbodiimide group include a carboxyl group, an amino group, and a hydroxyl group.

As the functional group capable of reacting with a water-soluble and / or water-dispersible curing agent having an epoxy group,
Examples thereof include a carboxyl group, an amino group, a hydroxyl group, and a glycidyl group.
Examples of the functional group capable of reacting with the water-soluble and / or water-dispersible curing agent having an alkoxysilyl group include an alkoxysilyl group and a hydroxyl group.

Examples of the functional group capable of reacting with a water-soluble and / or water-dispersible curing agent having an oxazoline group include a carboxyl group.
As the functional group capable of reacting with a water-soluble and / or water-dispersible curing agent having a hydrazide group,
Examples thereof include a carbonyl group.

The acrylic resin emulsion that can be used in the present invention can be obtained by adopting a usual method, but an emulsion polymerization method is preferred in consideration of the particle size and stability of the emulsion.

The emulsion polymerization method is not particularly limited, and can be appropriately selected from various emulsion polymerization methods such as a batch polymerization method, a monomer dropping polymerization method, and an emulsion monomer dropping polymerization method. In particular, in order to ensure the stability of the emulsion at the time of production, a monomer dropping polymerization method and an emulsion monomer dropping polymerization method are preferred.

In emulsion polymerization, commonly used ionic or nonionic surfactants can be used.

Examples of the ionic surfactant include an anionic surfactant having a polyoxyethylene chain such as polyoxyethylene nonylphenyl ether sulfate, polyoxyethylene allyl ether sulfate, octylphenoxyethoxyethyl sulfonate, polyoxyethylene tridecyl ether sulfate, and the like. Sulfonic acid salts such as sodium lauryl sulfonate, sodium dodecylbenzene sulfonate and sodium isooctylbenzene sulfonate; ammonium salts such as imidazoline laurate and ammonium hydroxide are typical examples. An anionic surfactant having an oxyethylene chain is preferred.

Examples of the nonionic surfactant include polyethylene glycol nonylphenyl ether; polyoxyethylenes such as polyoxyethylene nonylphenyl ether and polyoxyethylene lauryl ether; L-77, L-720, L-5410, L -76
Typical examples include nonionic surfactants containing silicone such as 02, L-7607 (manufactured by Union Carbide).

In the present invention, it is preferable to use a reactive surfactant having a polymerizable double bond in one molecule as the surfactant in terms of water resistance and weather resistance. In particular, when a reactive surfactant having a polyoxyalkylene group in the molecule is used, the mechanical stability can be improved.

Specific examples of such reactive surfactants include, for example, Adeka Soap ER-10, ER-20, ER-30, ER-40, SR-10, SR-20, SR manufactured by Asahi Denka Kogyo Co., Ltd.
-1025, NE-10, NE-20, NE-30, NE-40, SE-10N), Nippon Emulsifier Co., Ltd. Antox-MS-60, RMA-1120, RMA-564, RMA-
568, RMA-506, Aqualon KH-05, KH-10, R, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.
N-20, RN-30, RN-50, RN-2025, HS-10, HS-20, HS-
1025, BC05, BC10, BC0515, BC1025, Sanyo Kasei Kogyo Co., Ltd. Eleminol JS-2, Eleminol RS-30, Kao Co., Ltd. Latemul S-180, S-
180A, PD-104, PD-420, PD-430 and the like.

  Of these, non-alkylphenol-based ones are desirable in consideration of the environment.

The surfactants can be used alone or in admixture of two or more, and the amount used is
It is 10 parts by weight or less, preferably 0.5 to 8 parts by weight with respect to 100 parts by weight of the total amount of monomers.

Although there is no limitation in particular as a polymerization initiator, In order to perform superposition | polymerization more stably, it is desirable to use a redox system as a polymerization initiator. In addition, the stability of the liquid mixture during polymerization is maintained,
In order to carry out the polymerization stably, the temperature is 70 ° C. or lower, preferably 40 to 65 ° C., pH
Is preferably adjusted to 5-9.

Examples of the initiator used in the redox system include potassium persulfate, ammonium persulfate, hydrogen peroxide, t-butyl hydroperoxide, benzoyl peroxide, cumene hydroperoxide, and the like. Sodium acid sulfite, Rongalite, Bruggolite FF-6 (Bruggama
nn Chemical US), thiourea dioxide, L-ascorbic acid and the like. In particular, a combination of an organic peroxide such as t-butyl hydroperoxide, benzoyl peroxide, cumene hydroperoxide and the like and Rongalite, Bruggolite FF-6 or thiourea dioxide is preferable.

Note that the reducing agent is Brugolite, which does not generate formaldehyde due to environmental considerations.
FF-6 and thiourea dioxide are particularly preferred.

The amount of the polymerization initiator used is 0.01 to 10 parts, preferably 0.05 to 5 parts by weight based on 100 parts by weight of the total amount of monomers. When the amount of the polymerization initiator used is less than 0.01 parts by weight, the polymerization may be difficult to proceed. When the amount exceeds 10 parts by weight, the molecular weight of the produced polymer tends to decrease. is there.

In order to stably impart the catalytic activity of the polymerization initiator, a compound containing a divalent iron ion such as iron sulfate and a chelating agent such as disodium ethylenediaminetetraacetate may be used. The amount of the chelating agent used is 0.0001 to 1 part by weight, preferably 0.001 to 0.5 part by weight, based on 100 parts by weight of the total amount of monomers.

Chain transfer agents can be added to control the molecular weight of the polymer. Known chain transfer agents such as n-dodecyl mercaptan, tert-dodecyl mercaptan, n
-Mercaptan compounds such as butyl mercaptan, γ-mercaptopropyltrimethoxysilane, γ-mercaptopropyltriethoxysilane, γ-mercaptopropylmethyldimethoxysilane, γ-mercaptopropylmethyldiethoxysilane, organics such as chloroform and carbon tetrachloride Halide, sulfide benzene, isopropyl benzene, ferric chloride and the like.

The resin solid content concentration in the acrylic resin emulsion is preferably 20 to 70% by weight, and more preferably 30 to 60% by weight. When the resin solid content concentration exceeds 70% by weight, the concentration of the system increases remarkably, making it difficult to remove the heat generated by the polymerization reaction or taking a long time to remove from the polymerization vessel. There is a tendency to become necessary.
Further, when the resin solid content concentration is less than 20% by weight, there is no problem in terms of polymerization operation, but the amount of resin produced by one polymerization operation is small, which is disadvantageous in terms of economy.

The acrylic resin emulsion used in the present invention has an average particle size of 0.02-1.
About 0 μm is preferable. The average particle size can be adjusted by the amount of the emulsifier charged in the initial stage of polymerization.

These acrylic resin emulsions are commercially available from companies such as Dainippon Ink & Chemicals Co., Ltd. Boncoat, Watersol, Nippon Shokubai Co., Ltd. Acre Reset, Udouble, Showa Polymer Co., Ltd. Polysol, Japan NS Co., Ltd. Yodosol, Kanebinol, Asahi Kasei Kogyo Co., Ltd. Polytron, Polydurex, Chuo Rika Kogyo Co., Ltd., Rikabond, Nippon Acrylic Co., Ltd. Primal, BASF Dispersion Co., Ltd. Examples include Movinyl manufactured by Kaneka Chemical Industry Co., Ltd., Kanekazemulac, Kanebilak, etc.

Urethane resin emulsions include those in which urethane resin is dispersed in water, and those in which urethane resin is given a hydrophilic group and made self-dispersing, and those in which hydrophobic urethane resin is forcibly emulsified with an emulsifier, etc. Any of them can be used.

These include, for example, Superflex 90, 107M, 11 manufactured by Daiichi Kogyo Seiyaku Co., Ltd.
0, 126, 130, 150, 150HS, 160, 300, 361, 370, 410,
420, 460, 460S, 500, 600, E-2000, E-2500, E-400
0, E-4500, E-4700, R-5000, Elastron BN-08, BN-11
, BN-50D, NeoRez R-960, R-972, R-9 manufactured by Avecia KK
637, R-9679, AX-311, R-966, R-967, R-9603, R-6
00, R-9320, R-9617, R-9621, NeoPac R-9000, R-
9699, Takelac W-615, W-6010, W-602 manufactured by Mitsui Takeda Chemical Co., Ltd.
0, W-6061, W-511, W-405, W-7004, W-605, W-512A
6, W-635, W-635C, WS-7000, WS-5000, WS-5070X,
WS-4000, XW-75-X35, Adekabon titer HUX- manufactured by Asahi Denka Kogyo Co., Ltd.
290H, HUX-290K, HUK-290N, HUX-395D, HUX-394,
HUX-232, HUX-240, HUX-320, HUX-350, HUX-380,
HUX-381, HUX-388, HUX-380A, HUX-386, HUX-401
, HUX-750, HUX-670, HUX-680, HUX-575, HUX-580
, Etc. The urethane resin emulsion can be used alone or in a mixed system with other resin emulsions. In particular, a mixed system with an acrylic resin emulsion is useful in terms of ease of coating design and cost.

As the fluororesin emulsion, a dispersion of a fluoroolefin polymer and / or a copolymer of a monomer copolymerizable with the fluoroolefin in water can be used.

Examples of the fluoroolefin include vinylidene fluoride, trifluoroethylene, chlorotrifluoroethylene, tetrafluoroethylene, pentafluoropropylene, hexafluoropropylene and the like.

Monomers that can be copolymerized with fluoroolefins include olefins such as ethylene and propylene, vinyl ethers such as ethyl vinyl ether, propyl vinyl ether, butyl vinyl ether, and cyclohexyl vinyl ether, butyl vinyl ester, octyl vinyl ester, vinyl acetate, and versatic acid. Vinyl esters such as vinyl (Japan Epoxy Resin Co., Ltd. Veova 10, Veova 9, Veova 11), aromatic vinyl compounds such as styrene and vinyl toluene, allyl ethers such as ethyl allyl ether, and allyl such as butyl allyl ester Examples thereof include compounds and (meth) acrylic acid esters.

These are commercially available from various companies, such as Lumiflon manufactured by Asahi Glass Co., Ltd., Zeffle manufactured by Daikin Industries, Ltd., Cefral Coat manufactured by Central Glass Co., Ltd., Dainippon Ink and Chemicals, Inc.
Fluoronate manufactured by Co., Ltd.

If necessary, pigments that are usually used in paints (white pigments such as titanium dioxide, calcium carbonate, barium carbonate, kaolin, and colored pigments such as carbon, bengara, and cyanine blue) are used in the synthetic resin emulsion that can be used in the invention. Can be used. Titanium dioxide is the most used and important among the pigments. Gloss and weather resistance are improved by using titanium dioxide surface-treated with alumina or zirconia. Also for ordinary coatings such as film-forming aids, colloidal silica, plasticizers, solvents, dispersants, thickeners, antifoaming agents, antiseptics, fungicides, algaeproofing agents, ultraviolet absorbers, light stabilizers, etc. Additives used as ingredients can also be blended.

(Addition of antifouling composition to water-based paint)
As a method for mixing the stain resistance-imparting composition and the aqueous paint in the present invention, the stain-resistance imparting composition may be added directly to the aqueous paint. It is possible to add a stain resistance-imparting composition to a synthetic resin emulsion in advance and add a paint compounding agent to make a water-based paint. A method of adding a stain resistance-imparting composition can be mentioned.
This method is preferable because there is little change in physical properties of the coating film when the coating is applied. With this method, it is possible to stably form a coating film having excellent stain resistance and high gloss. It is also possible to use both the above methods in combination. That is, this is a method of further adding a stain resistance imparting composition to a water-based paint obtained by adding a stain resistance imparting composition to a synthetic resin emulsion before coating.

The mixing ratio of the water-based paint and the stain resistance-imparting composition is such that the organosilicate compound (A) is 2 to 40 parts by weight with respect to 100 parts by weight of the resin solid content in the water-based paint. It is preferable to do. If the component (A) is less than 2 parts by weight, the stain resistance performance is not sufficiently exhibited, and if it exceeds 40 parts by weight, the compatibility between the resin in the aqueous paint and the organosilicate compound decreases. There is a tendency to decrease gloss. Furthermore, the usage-amount of a preferable organosilicate compound (A) is 5-20 weight part.
Further, when the stain resistance imparting composition is used in a paint having an alkoxysilyl group-containing resin as a binder component, the water solubility in the stain resistance imparting composition and 100 parts by weight of the resin solid content in the aqueous paint and It is preferable to add 3 to 20 parts by weight of the water-dispersible curing agent (B).

By adding in this way, the coating film can be provided with appropriate flexibility, and the brittleness peculiar to the alkoxysilyl group-containing resin coating film can be improved. As a result, it is possible to apply to soft bases that have been difficult to apply up to now, such as elastic coating materials and waterproofing materials.

The water-based paint imparted with stain resistance of the present invention is, for example, for interior and exterior of buildings, for automobiles such as metallic base or clear on metallic base, for direct coating of metal such as aluminum and stainless steel, slate, concrete, roof tile, mortar, Gypsum board, asbestos slate, asbestos board, precast concrete, lightweight cellular concrete, calcium oxalate board,
It is used as a paint or top treatment for ceramics such as tiles and bricks, for direct coating of glass, for glass, natural marble, granite and the like. In addition to direct coating, water-based or solvent-based primer, acrylic rubber, multi-layer finish top coat, flexible top finish coat, water-based inorganic base materials such as concrete Alternatively, it can be used for coating on a solvent-based permeable water absorption preventing material.

Hereinafter, the present invention will be described based on examples, but the present invention is not limited thereto.

(Synthesis example of alkoxysilyl group-containing water-soluble and / or water-dispersed curing agent)
In a reaction vessel equipped with a stirrer, a reflux condenser, a nitrogen gas inlet tube and a dropping funnel, 100 parts by weight of Pluronic L-34 (Asahi Denka Kogyo Co., Ltd., orioxyethylene-polyoxypropylene condensate) and dibutyl First, 0.01 parts by weight of tin bisisooctylthioglycolate was charged, and 29 parts by weight of A-1310 (manufactured by Nippon Unicar Co., Ltd., γ-isocyanatopropyltriethoxysilane) was slowly added while stirring well under a nitrogen atmosphere. Stirring was continued for 30 minutes. Thereafter, the temperature was raised to 70 ° C. with stirring, and the reaction was advanced to obtain an alkoxysilyl group-containing water-soluble and / or water-dispersed curing agent (B-1). Determination of the end of the reaction is infrared absorption (
It was confirmed by the disappearance of the absorption of the isocyanate group having a wavelength of 2200 to 2300 cm @ -1 by IR measurement.

(Manufacturing method of stain resistance imparting composition: Production Examples 1 to 36)
Stir the components shown in Tables 1 to 4 in the order of (D), (C), (E), (A), and (B) in a container equipped with a stirrer, reflux condenser, nitrogen gas inlet tube, and dropping funnel. While throwing in. After completion of the addition, the mixture was stirred for 30 minutes to obtain the stain resistance imparting compositions of Production Examples 1 to 36. The obtained stain resistance-imparting composition was put in a transparent container and visually checked for separation / sedimentation.

メチルシリケート５１：メチルシリケート部分加水分解縮合物（シリカ残量比率５１％）
エチルシリケート４０：エチルシリケート部分加水分解縮合物（シリカ残量比率４０％）
メチルブチルシリケート：同一分子中にメチル基８５％、ブチル基１５％を含有するシリ
ケート（シリカ残量比率５１％）
エチルイソプロピルシリケート：同一分子中にエチル基７５％、イソプロピル基２５％を
含有するシリケート（シリカ残量比率４２％）
バイヒジュール２３３６（住化バイエルウレタン（株）製）：水分散型ポリイソシアネー
ト
タケネートＷＤ−７２０（三井武田ケミカル（株）製）：水分散型ポリイソシアネート
バイヒジュールＴＰＬＳ ２１５０／ｌ（住化バイエルウレタン（株）製）：水分散型ポ
リイソシアネート
カルボジライトＶ−０４Ｂ（日清紡製）：水溶性ポリカルボジイミド
デナコールＥＸ−１７１（ナガセケムテックス（株）製）：ラウリルポリオキシエチレン
グリシジルエーテル
デナコールＥＸ−８３２（ナガセケムテックス（株）製）：ポリエチレングリコールジグ
リシジルエーテル
エポライト２００Ｐ（共栄社（株）製）：トリプロピレングリコールジグリシジルエーテ
ル
Ａ−１２３０（日本ユニカー（株）製）：ポリエーテル変性シランカップリング剤
アディティブＴＩ（住化バイエルウレタン（株）製）：トシルイソシアネート
ＳＲ−ＴＰＧ：（阪本薬品工業（株）製）トリプロピレングリコールジグリシジルエーテ
ル
デナコールＥＸ−９２０（ナガセケムテックス（株）製）：トリプロピレングリコールジ
グリシジルエーテル
（オルガノシリケート乳化剤混合物の比較製造例）
ニューコール５６０ＳＦＣ（日本乳化剤（株）製、ポリオキシエチレンノニルフェノー
ルエーテル硫酸アンモニウム）７部、ニューコール５０４（日本乳化剤（株）製、ポリオ
キシエチレンノニルフェニルエーテル）３部とをよく混合し、ついでエチルシリケート４
０（エチルシリケート部分加水分解縮合物：シリカ残量比率４０％）１００重量部、イソ
プロピルアルコール１００部を加え、良く混合することによって、オルガノシリケートと
乳化剤の混合物を調整した（Ｓ−１）。

Methyl silicate 51: methyl silicate partial hydrolysis condensate (silica residual ratio 51%)
Ethyl silicate 40: ethyl silicate partial hydrolysis condensate (silica residual ratio 40%)
Methylbutyl silicate: Silicate containing 85% methyl group and 15% butyl group in the same molecule (silica residual ratio 51%)
Ethyl isopropyl silicate: Silicate containing 75% ethyl group and 25% isopropyl group in the same molecule (silica residual ratio 42%)
Bihijoule 2336 (manufactured by Sumika Bayer Urethane Co., Ltd.): Water-dispersed polyisocyanate takenate WD-720 (manufactured by Mitsui Takeda Chemical Co., Ltd.): Water-dispersed polyisocyanate bihijoule TPLS 2150 / l (Suika Bayer Urethane) (Manufactured by Co., Ltd.): water-dispersed polyisocyanate carbodilite V-04B (manufactured by Nisshinbo): water-soluble polycarbodiimide denacol EX-171 (manufactured by Nagase ChemteX Corporation): lauryl polyoxyethylene glycidyl ether denacol EX -832 (manufactured by Nagase ChemteX Corporation): Polyethylene glycol diglycidyl ether Epolite 200P (manufactured by Kyoeisha Co., Ltd.): tripropylene glycol diglycidyl ether A-1230 (manufactured by Nippon Unicar Co., Ltd.): polyether-modified silane Coupling agent Additive TI (manufactured by Sumika Bayer Urethane Co., Ltd.): Tosyl isocyanate SR-TPG: (manufactured by Sakamoto Yakuhin Kogyo Co., Ltd.) tripropylene glycol diglycidyl ether Denacol EX-920 (manufactured by Nagase ChemteX Corporation): Tri Propylene glycol diglycidyl ether (Comparative production example of organosilicate emulsifier mixture)
7 parts of New Coal 560 SFC (manufactured by Nippon Emulsifier Co., Ltd., polyoxyethylene nonylphenol ether ammonium sulfate) and 3 parts of New Coal 504 (manufactured by Japan Emulsifier Co., Ltd., polyoxyethylene nonylphenyl ether) are mixed well, and then ethyl silicate. 4
A mixture of an organosilicate and an emulsifier was prepared by adding 100 parts by weight of 0 (ethyl silicate partial hydrolysis condensate: 40% silica remaining ratio) and 100 parts of isopropyl alcohol and mixing well (S-1).

(Synthesis Example 1 of alkoxysilyl group-containing acrylic emulsion)
In a reaction vessel equipped with a stirrer, reflux condenser, nitrogen gas inlet tube and dropping funnel, 200 parts by weight of deionized water, Newcol-707SF (manufactured by Nippon Emulsifier Co., Ltd .: active ingredient 30%) 0
. 16 parts by weight and 0.05 parts by weight of sodium hydrogen carbonate were charged, and 50 nitrogen was introduced while introducing nitrogen gas.
The temperature was raised to ° C. After raising the temperature, 12 parts by weight of the monomer mixture shown in the core part of Table 5 (E-1), 0.14 parts by weight of t-butyl hydroperoxide, and 0.4 parts by weight of Rongalite were added, and the initial period was 30 minutes. Polymerization was performed. 268 parts by weight of Aqualon BC0515 (Daiichi Kogyo Seiyaku Co., Ltd .: active ingredient 15%) 9.7 parts by weight, Aqualon RN
2.7 parts by weight of 2025 (Daiichi Kogyo Seiyaku Co., Ltd .: active ingredient 20%)
A monomer emulsion obtained by adding parts by weight and emulsified monomer and 0.20 parts by weight of t-butyl hydroperoxide were added at a constant rate over 145 minutes. Polymerization was performed after 1 hour after the addition was completed.

Furthermore, Aqualon B was added to 120 parts by weight of the monomer mixture shown in the shell part of Table 5 (E-1).
C0515 6.0 parts by weight, Aqualon RN2025 1.6 parts by weight and deionized water 2
A monomer emulsion emulsified by adding 7 parts by weight and 0.15 parts by weight of t-butyl hydroperoxide were added at a constant rate over 65 minutes. Polymerization was performed after 1 hour after the addition was completed. After adding 2.0 parts of sodium hydrogencarbonate to the obtained synthetic resin emulsion, the solid part was adjusted to 50% with deionized water (E-1).

(Synthesis example 2 of alkoxysilyl group-containing acrylic emulsion)
In a reaction vessel equipped with a stirrer, reflux condenser, nitrogen gas inlet tube and dropping funnel, 200 parts by weight of deionized water, 1.0 part by weight of Newcol-707SF (manufactured by Nippon Emulsifier Co., Ltd.), 0. 05 parts by weight were charged, and the temperature was raised to 50 ° C. while introducing nitrogen gas. After the temperature rise, 20 parts by weight of the monomer mixture shown in the core part of Table 5 (E-2), 0.14 parts by weight of t-butyl hydroperoxide, 0.5 parts by weight of Bruggolite FF-6 were added, Initial polymerization was performed for 30 minutes. The remaining 180 parts by weight of the monomer mixture is 3 parts by weight of Adeka Soap SR-10 (Asahi Denka Kogyo Co., Ltd .: active ingredient 100%), Adeka Soap ER-20 (Asahi Denka Kogyo Co., Ltd .: active ingredient) 75%) a monomer emulsion obtained by adding 1.9 parts by weight and 64 parts by weight of deionized water and emulsifying, and t-butyl hydroperoxide 0.1
4 parts by weight was added at a constant speed over 100 minutes. Polymerization was performed after 1 hour after the addition was completed.

Furthermore, 200 parts by weight of the monomer mixture shown in the shell part of Table 5 (E-2), 3.0 parts by weight of ADEKA rear soap SR-10, 1.9 parts by weight of ADEKA rear soap ER-20, and 64 parts by weight of deionized water A monomer emulsion obtained by adding a part and emulsified monomer and 0.21 part by weight of t-butyl hydroperoxide were added at a constant rate over 110 minutes. Polymerization was performed after 1 hour after the addition was completed.
After adding 1.0 part of sodium hydrogencarbonate to the obtained synthetic resin emulsion, the solid part was adjusted to 50% with deionized water (E-2).

(Synthesis example of hydroxyl-containing acrylic emulsion)
Polymerization was performed in the same manner as in Production Example 2 except that Table 5 (E-3) was used as the monomer (E-3).
).
(Synthesis example of cross-linked acrylic emulsion)
Polymerization was performed in the same manner as in Synthesis Example 2 except that Table 5 (E-4) was used as the monomer. further,
Thus obtained, 6.2 parts of adipic acid dihydrazide was added to the synthetic resin emulsion to obtain a crosslinked acrylic emulsion (E-4).

(Synthesis example 5 of polyoxyalkylene chain-containing acrylic emulsion)
Polymerization was performed in the same manner as in Synthesis Example 2 except that Table 5 (E-5) was used as the monomer (E-5).
).

(Synthesis example of carboxyl group-containing acrylic emulsion)
Polymerization was conducted in the same manner as in Synthesis Example 2 except that Table 4 (E-6) was used as the monomer (E-6).
).

合成した樹脂エマルジョンおよび、市販の樹脂エマルジョンを用い、表６の顔料ペースを
用いて、表７に示す配合処方で塗料を作成した。
（アルコキシシリル基含有アクリル樹脂塗料）（ＡＳ−１〜２）。
（水酸基含有アクリル樹脂塗料）（ＡＵ−１）。
（架橋型アクリル樹脂塗料）（ＣＡ−１）。
（ウレタン変性アクリル樹脂塗料）（ＡＵ−２）。
（ポリオキシアルキレン鎖含有アクリル樹脂塗料）（Ａ−１）。
（カルボキシル基含有アクリル樹脂塗料）（Ａ−２）。
（スチレン−アクリル樹脂塗料）（ＳＡ−１）。
（ふっ素樹脂塗料）（Ｆ−１）。

Using the synthesized resin emulsion and a commercially available resin emulsion, a paint was prepared with the formulation shown in Table 7 using the pigment pace shown in Table 6.
(Alkoxysilyl group-containing acrylic resin paint) (AS-1 to 2).
(Hydroxyl-containing acrylic resin paint) (AU-1).
(Crosslinked acrylic resin paint) (CA-1).
(Urethane-modified acrylic resin paint) (AU-2).
(Polyoxyalkylene chain-containing acrylic resin paint) (A-1).
(Carboxyl group-containing acrylic resin paint) (A-2).
(Styrene-acrylic resin paint) (SA-1).
(Fluororesin paint) (F-1).

（物性評価）
・塗料の増粘
作製した水性塗料に本発明の耐汚染性付与組成物を添加し１分間攪拌後、すぐに粘度を
測定した。さらに、２３℃の恒温槽中に２時間放置後、粘度を測定し、２時間後の増粘率
を算出した。粘度はＢＭ型粘度計を用い、２３℃の恒温で測定した。Ｎｏ．４ローターを
用い、６ｒｐｍの速度で測定を実施した。増粘率の評価は基準を以下に示す。

(Evaluation of the physical properties)
-Thickening of paint The stain resistance-imparting composition of the present invention was added to the prepared aqueous paint and stirred for 1 minute, and the viscosity was measured immediately. Further, after being left in a thermostat at 23 ° C. for 2 hours, the viscosity was measured, and the thickening rate after 2 hours was calculated. The viscosity was measured at a constant temperature of 23 ° C. using a BM viscometer. No. Measurement was carried out at a speed of 6 rpm using 4 rotors. The standard for the evaluation of the thickening rate is shown below.

○: Thickening rate of 110% or less Δ: Thickening rate of 200% or less ×: Impossible to measure due to gelation.

-Gloss The stain resistance-imparting composition of the present invention was added to the produced water-based paint, and it was applied to a glass plate with a 6 mil applicator and cured at room temperature for 7 days. After curing, gloss value Mu of incident angle 60 °
It was measured by lti-Gloss 268 (Minolta Co., Ltd.). For the gloss value, the average value of the values measured three times was calculated.

-Evaluation of contamination resistance The SK # 1000 primer (manufactured by SK Kaken Co., Ltd., epoxy primer) was applied to the bending exposed plate (aluminum plate), and after curing at room temperature for 1 day, each paint was spray-coated. The state of dirt on the 45 degree surface and the vertical surface of this test plate was confirmed. Contamination was measured with a color difference meter (Minolta Co., Ltd .: CR300) by measuring the absolute value (ΔL value) of the difference in brightness before and after exposure for 3 months in Northeastern Settsu, Osaka. A scale. A smaller ΔL value indicates less contamination.

A: ΔL value is 3 or less ○: ΔL value is 3-5
Δ: ΔL value is 5-8
X: ΔL value is 8 or more.

-Preparation of water contact angle measurement sample SK # 1000 primer was applied on an aluminum flat plate, cured at room temperature for 1 day, sprayed with each paint, and cured at room temperature for 14 days.

・ Measurement of water contact angle of coating film Water contact angle of coating film, which is an index of contamination resistance, is measured using a contact angle measuring machine (Kyowa Interface Science Co., Ltd .: CA-
S150 type) and measured. The evaluation was performed after the prepared sample was immersed in water for 1 day and after outdoor exposure evaluation.

In addition, in the evaluation of the coating film contact angle and the stain resistance in Table 14, the initial period and after the pot life use the coated plate coated with the paint within 30 minutes in the initial stage, and the paint after the pot life. A coated plate prepared by painting and coating after standing for 6 hours at room temperature is used. In the other tables, in the results of the coating film contact angle, the resistance to wet / cold heat resistance and the contamination resistance, those not described as initial and after pot life are the results under the conditions corresponding to the initial in Table 14.

・ Wet and cold-heat repeatability Ares rubber wall (Kansai Paint Co., Ltd., acrylic rubber waterproofing material) is applied on the mortar with Ares rubber tile sealer (Kansai Paint Co., Ltd., salt rubber base coat). Cured and spray-painted each paint. Using this test body, a wet and cold repeated test according to JIS A 6909 was performed, and the presence or absence of cracking and blistering of the coating film after 10 and 20 cycles was confirmed.
A: No cracks or blisters are observed even after 20 cycles.
○: No cracks or blisters are observed after the end of 10 cycles, but they are observed after the end of 20 cycles.
X: Cracks or blisters are observed after 10 cycles.

Table 8, Table 9, Table 10, Table 11, Table 12, Table 13, and Table 14 show the physical property evaluation results when a stain resistance imparting agent is added to the water-based paints produced.

（実施例１〜１２）
分子中に反応性官能基と親水性基を有する水溶性および／または水分散性硬化剤の種類
を変化させたが、何れも高い光沢および良好な耐汚染性を示した。また、温冷繰り返し試
験において、ふくれ、割れは見られなかった。

(Examples 1-12)
Although the type of water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule was changed, all showed high gloss and good stain resistance. Further, no blistering or cracking was observed in the repeated heating and cooling test.

(Examples 13 to 20)
Although the kind of organosilicate was changed, all showed good stain resistance. Further, no blistering or cracking was observed in the repeated heating and cooling test.

(Examples 21 to 25)
Although the kind and amount of the compound that promotes hydrolysis / condensation of the alkoxysilane compound were changed, all showed good stain resistance. Further, no blistering or cracking was observed in the repeated heating and cooling test. In Examples 23 and 24 using mercaptide tin, the viscosity increase rate after mixing the stain resistance-imparting composition was low, and particularly good stain resistance was exhibited.

(Examples 26 to 30)
Although the addition amount of the organosilicate and the water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule was changed, all showed good stain resistance. Those having a large amount of the water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule have good crack resistance in the hot and cold repeated test.

(Examples 31-41)
The type of water-based paint was changed, but all showed good stain resistance. Further, no blistering or cracking was observed in the repeated heating and cooling test. Examples 31 to 38 using a resin having a polyoxyalkylene chain as a binder component showed particularly good contamination resistance. Especially, Examples 31-32 which used resin which has an alkoxy silyl group for a binder component showed the further favorable stain | pollution resistance.

(Examples 42 to 47)
The compound (C) that promotes hydrolysis and condensation of the alkoxysilane compound is represented by the general formula (2).
), The contact angle and antifouling effects were good even after pot life, as shown in Table 14.

(Comparative Example 1)
When the stain resistance imparting composition was not added, the stain resistance was not exhibited. Moreover, since the compound which accelerates | stimulates hydrolysis and condensation of an alkoxysilane compound was not added, water resistance fell and the blistering was seen by the hot and cold repeated test.

(Comparative Example 2)
Ethyl silicate 40 alone was added to the aqueous paint, but ethyl silicate 40 was slightly separated. Although it was painted as it was, a significant decrease in gloss occurred. Moreover, since the compound which accelerates | stimulates hydrolysis and condensation of an alkoxysilane compound was not added, stain resistance was not expressed.

(Comparative Example 3)
Ethyl silicate 40 was diluted with a solvent and added to the aqueous paint, but no significant improvement in gloss was observed. Moreover, since the compound which accelerates | stimulates hydrolysis and condensation of an alkoxysilane compound was not added, stain resistance was not expressed.

(Comparative Example 4)
When ethyl silicate 40 was added to an aqueous coating material together with a compound and a solvent for promoting hydrolysis / condensation of the alkoxysilane compound, the gloss reduction was improved, but it was insufficient.

(Comparative Example 5)
When added to a water-based paint together with a dispersible curing agent and a solvent, the gloss reduction was improved, but it was insufficient. Moreover, since the compound which accelerates | stimulates hydrolysis and condensation of an alkoxysilane compound was not added, stain resistance was not expressed.

(Comparative Example 6)
When a mixture of a water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule, a solvent and a compound that accelerates hydrolysis / condensation of an alkoxysilane compound is added to an aqueous paint, the gloss decreases. Was not observed, but did not exhibit stain resistance.

(Comparative Examples 7-8)
When a mixture of an organosilicate and an emulsifier was added instead of the stain resistance-imparting composition, no reduction in gloss was observed, but no compound that promotes hydrolysis / condensation of the alkoxysilane compound was added, so no contamination was observed. Sex did not develop.

The stain resistance-imparting composition of the present invention can be produced at a low cost with a simple operation. In addition, by adding the stain resistance-imparting composition of the present invention to an aqueous coating material, a coating film having high gloss, high stain resistance, and good coating film characteristics due to wet and cold repetition is formed. Moreover, the water resistance, weather resistance, and adhesion of the formed coating film can be improved.

Claims (13)

(A) an organosilicate compound, (B) a water-soluble and / or water-dispersible curing agent having a reactive functional group and a hydrophilic group in the molecule, and (C) a compound that promotes hydrolysis / condensation of the alkoxysilane compound. A composition for imparting stain resistance to a paint to be contained. The composition for imparting stain resistance according to claim 1, wherein the organosilicate as the component (A) is a compound represented by the general formula (1) or a partial hydrolysis condensate thereof.

(Wherein R is the same or different and has 1 to 4 carbon atoms) The reactive functional group of component (B) is one or more selected from (block) isocyanate groups, epoxy groups, carbodiimide groups, alkoxysilyl groups, oxazoline groups, and hydrazide groups. Or the contamination-resistance imparting composition of any one of 2. (C) Component is a tin compound, The antifouling property composition of any one of Claims 1-3 characterized by the above-mentioned. The component (C) contains an organotin compound represented by the general formula (2).
The stain resistance imparting composition for a paint according to any one of -4.

Wherein R ₁ and R 2 are the same or different and are alkyl groups having 2 to 8 carbon atoms, R ₃ and R ₄ are linear or branched hydrocarbon groups having 1 to 20 carbon atoms, alkene groups, and the like. ) The component (C) is a phosphoric acid ester alone or a phosphoric acid ester / amine reaction product. An organic solvent (D) and a dehydrating agent (E) are contained, The any one of Claims 1-6 characterized by the above-mentioned.
The composition for imparting stain resistance according to Item. (B) 1 part or all of the hydrophilic group of component contains a polyoxypropylene group
7. The composition for imparting stain resistance according to any one of 7 above. A coating composition containing the stain resistance-imparting composition according to any one of claims 1 to 8 and a binder component. The coating composition according to claim 9, wherein the binder is an emulsion of a synthetic resin. 11. The coating composition according to claim 10, wherein the emulsion of the synthetic resin is an emulsion of an alkoxysilyl group-containing polymer. The coating composition according to any one of claims 10 to 11, wherein the emulsion of the synthetic resin is an emulsion of a polyoxyalkylene group-containing polymer. The coating film obtained from the coating composition of any one of Claims 9-12.