JP2006328228A - Water-based covering material - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a water-based covering material which has little bleeding out of a coated film, and is excellent in the weatherability, hot water resistance and cold-crack resistance of a coated film and also is excellent in the mechanical stability and in the dispersing property of a pigment, a resin beads and a silica. <P>SOLUTION: The water-based covering material is characterized by containing (A) an emulsified particle obtained by the emulsion polymerization of a monomer containing (a) 40-93 parts by mass of an ethylenically unsaturated monomer containing none of -COOH, -P(=O)<SB>2</SB>OH, and -SO<SB>4</SB>H, (b) 6-50 parts by mass of an ethylenically unsaturated monomer having a piperidyl group in the molecule, and (c) 1-10 parts by mass of a reactive emulsifier containing an anionic reactive emulsifier having a radically polymerizable unsaturated double bond in the molecule (but, the sum total of (a)+(b)+(c) is 100 parts by mass); and (d) 10-50 parts by mass of an ultraviolet absorber. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an aqueous coating material excellent in weather resistance, and more specifically, as a single film, it has excellent weather resistance such as gloss retention, yellowing resistance, water resistance, solvent resistance, etc. over a long period of time, and a base coating film When applied on top, it can prevent fading of the base, and when used as a resin for various paints, it only exhibits excellent pigment dispersibility, resin beads, silica dispersibility, color development, and storage stability. In addition, the present invention relates to an aqueous coating material capable of simultaneously improving crack resistance at low temperatures. In addition, the present invention drastically improves the weather resistance by adding a small amount to other aqueous resin, without impairing the properties of the other resin, as compared with the resin after adding the same amount of UV stabilizer. It relates to an aqueous coating material that can be used.

  In recent years, in the field of paints used for buildings and civil engineering structures, conversion from solvent-based paints that use organic solvents as solvents to water-based paints that use water as a dispersion medium has been attempted in consideration of the painting work environment. ing. For this reason, the use of water-based paints has been expanded, and accordingly, performance requirements for water-based paints have become high. Among such required performances, it has been pointed out that it is important to improve the appearance, water resistance, weather resistance, etc. of the coating film.

  Patent Document 1 describes that weather resistance is improved by adding an ultraviolet absorber (hereinafter referred to as UVA) and a hindered amine radical scavenger (hereinafter referred to as HALS).

  In Patent Document 2, there is no bleed-out from the coating film at the UV stabilization site by copolymerizing a highly hydrophobic tertiary butyl group-containing polymerizable monomer and a small amount of the UV-stabilizing monomer. There is a description that excellent weather resistance can be obtained over a long period of time.

In Patent Document 3, in a multistage emulsion polymerization method, a silane coupling agent having a hindered amine and a cycloalkyl group is localized in the outermost layer of emulsion particles, so that a homogeneous coating film having excellent compatibility is obtained and long-term weather resistance is obtained. There is a description that an excellent film can be obtained.
Japanese Patent Publication No. 3-46506 Japanese Patent No. 3354906 JP 2004-10805 A

  However, in the method of Patent Document 1, when the additive is blended, it bleeds out from the coating film over time, so it is difficult to maintain the weather resistance for a long period of time. Since it is difficult to dissolve in water, which is the main medium, it is necessary to take a technique such as adding a dispersing agent or the like to disperse the additive in water in advance in order to uniformly disperse it in the paint, and the production method is complicated. There was also a problem in the long-term stability of the manufactured paint. In the method of Patent Document 2, a carboxyl group-containing ethylenically unsaturated monomer must be copolymerized for mechanical stability and pigment dispersibility of particles, and a large amount of polymerizable HALS and UVA are copolymerized. In this case, since the emulsion polymerization system becomes unstable, the polymerization must be performed using a large amount of non-reactive nonionic emulsifier, and the response to the advanced water resistance and warm water resistance was insufficient. . In the method of Patent Document 3, polymerization is performed stably by polymerizing polymerizable HALS in the final stage, but the HALS copolymer layer is the outermost layer, and the layer containing carboxyl groups is the inner layer. However, the mechanical stability and the initial gloss were lowered, and it was insufficient in terms of the response to the advanced design of coatings and the stability of coatings.

  In recent years, in order to satisfy the demand for long-term weather resistance in the market, water-based paints containing silicone-based or fluorine-based resins as components have been developed. In particular, it is known that gloss retention in an accelerated weather resistance test of a fluorine-based resin has a very excellent performance of 5000 hours or more. However, pigment dispersibility, painting workability, and recoatability at the time of renovation in a house are insufficient. Further, as a countermeasure to the above-mentioned problem, a hybrid of an acrylic component and a silicone or fluorine component is also known, but although the gloss retention is good due to the effect of the silicone or fluorine component, the molecular weight of the acrylic moiety is reduced. In comparison with the initial coating film, the strength and adhesion of the coating film are remarkably lowered, so that the long-term weather resistance is still insufficient.

  The present invention has been made in view of the above circumstances, has almost no HALS bleed-out from the coating film, is excellent in weather resistance, fading prevention property, hot water resistance, low temperature cracking property of the coating film, and machine An object is to provide an aqueous coating material excellent in stability, pigment, resin beads, and silica dispersibility.

The aqueous coating material of the present invention comprises 40 to 93 parts by mass of an ethylenically unsaturated monomer (a) that does not contain any of —COOH, —P (═O) ₂ OH, and —SO ₄ H, and the following general formula: 6 to 50 parts by mass of an ethylenically unsaturated monomer (b) having a piperidyl group in the molecule represented by (I) and an anionic reactivity having an unsaturated double bond capable of radical polymerization in the molecule An emulsion obtained by emulsion polymerization of a monomer containing 1 to 10 parts by mass of a reactive emulsifier (c) containing an emulsifier (however, the total of (a), (b) and (c) is 100 parts by mass). Particles (A),
UV absorber (d) 10-50 parts by mass;
It is characterized by containing.

式（Ｉ）中、Ｒ³は水素原子または炭素数１若しくは２のアルキル基、Ｘは酸素原子またはイミノ基、Ｙは水素原子、炭素数１〜２０のアルキル基、またはアルコキシル基、Ｚは水素原子またはシアノ基を示す。

In the formula (I), R ³ is a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, X is an oxygen atom or imino group, Y is a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an alkoxyl group, Z is hydrogen An atom or a cyano group is shown.

  According to the present invention, there is almost no bleed-out from the coating film of the deterioration preventing component, and it has excellent weather resistance, hot water resistance, and low temperature cracking property without containing a carboxyl group that affects the piperidyl group. Therefore, it is possible to provide an aqueous coating material that is excellent in mechanical stability, pigment, resin beads, and silica dispersibility, and can simultaneously improve crack resistance at low temperatures.

The aqueous coating material of the present invention comprises 40 to 93 parts by mass of an ethylenically unsaturated monomer (a) that does not contain any of —COOH, —P (═O) ₂ OH, and —SO ₄ H, and the following general formula: 6 to 50 parts by mass of an ethylenically unsaturated monomer (b) having a piperidyl group in the molecule represented by (I) and an anionic reactivity having an unsaturated double bond capable of radical polymerization in the molecule An emulsion obtained by emulsion polymerization of a monomer containing 1 to 10 parts by mass of a reactive emulsifier (c) containing an emulsifier (however, the total of (a), (b) and (c) is 100 parts by mass). It contains particles (A) and 10 to 50 parts by mass of the ultraviolet absorber (d).

式（Ｉ）中、Ｒ³は水素原子または炭素数１若しくは２のアルキル基、Ｘは酸素原子またはイミノ基、Ｙは水素原子、炭素数１〜２０のアルキル基、またはアルコキシル基、Ｚは水素原子またはシアノ基を示す。

In the formula (I), R ³ is a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, X is an oxygen atom or imino group, Y is a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an alkoxyl group, Z is hydrogen An atom or a cyano group is shown.

Examples of the ethylenically unsaturated monomer (a) include methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, i-propyl (meth) acrylate, and n-butyl (meth) acrylate. , I-butyl (meth) acrylate, sec-butyl (meth) acrylate, t-butyl acrylate, n-amyl (meth) acrylate, i-amyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl ( Alkyl (meth) acrylates such as (meth) acrylate, n-octyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, dodecyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate; Cyclohexyl (me ) Acrylates, cycloalkyl (meth) acrylates such as pt-butylcyclohexyl (meth) acrylate; 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, Hydroxyl group-containing (meth) acrylates such as 4-hydroxybutyl (meth) acrylate and glycerol mono (meth) acrylate; hydroxypolyethylene oxide mono (meth) acrylate, hydroxypolypropyleneoxide mono (meth) acrylate, hydroxy (polyethyleneoxide-polypropylene) Oxide) mono (meth) acrylate, polyalkylene oxide groups such as hydroxy (polyethylene oxide-propylene oxide) mono (meth) acrylate Included (meth) acrylates; lactone-modified hydroxyalkyl (meth) acrylates; 2-aminoethyl (meth) acrylate, 2-dimethylaminoethyl (meth) acrylate, 2-aminopropyl (meth) acrylate, 2-butylaminoethyl Aminoalkyl (meth) acrylates such as (meth) acrylate; amide group-containing ethylenically unsaturated monomers such as (meth) acrylamide; dimethylaminoethyl (meth) acrylate methyl chloride salt, glycidyl (meth) acrylate, (meth ) Other (meth) acrylate monomers such as acrylonitrile, tetrahydrofurfuryl (meth) acrylate, methoxyethyl (meth) acrylate, ethoxyethyl (meth) acrylate; styrene, methylstyrene, chlorostyrene, metho Aromatic ethylenically unsaturated monomers such as xylstyrene; Conjugated diene monomers such as 1,3-butadiene, isoprene and 2-chloro-1,3-butadiene; vinyl acetate, vinyl chloride, ethylene, vinyl propionate However, it is not limited to these as long as they do not contain any of —COOH, —P (═O) ₂ OH, and —SO ₄ H and can be radically polymerized. A monomer (a) can be used individually or in combination of 2 or more types. As the monomer (a), it is preferable to use (meth) acrylates alone or in combination of two or more from the viewpoint of weather resistance, and methacrylates are particularly preferable in order to greatly suppress the decrease in molecular weight. . The expression “(meth) acryl” means acryl or methacryl (the same applies hereinafter). In addition, the monomer classified into the following monomer (b) shall not be contained in the monomer (a).

  The amount of the ethylenically unsaturated monomer (a) represented by the formula (I) is the same as that of the monomer (a) in terms of the weather resistance, water resistance and adhesion required for various coating materials. When the total of the body (b) and the reactive emulsifier (c) is 100 parts by mass, it is necessary that the amount be 40 to 93 parts by mass. A preferable usage amount is 45 to 85 parts by mass.

  In formula (I), Y is preferably an alkyl group having 1 to 20 carbon atoms or an alkoxy group, and more preferably an alkyl group having 1 to 13 carbon atoms or an alkoxy group. Y may be linear or branched and may form a cyclic structure.

As the ethylenically unsaturated monomer (b) represented by the formula (II), those mainly having an ultraviolet stabilizing function can be used. For example, 4- (meth) acryloyloxy-2,2 , 6,6-tetramethylpiperidine, 4- (meth) acryloylamino-2,2,6,6-tetramethylpiperidine, 4- (meth) acryloyloxy-1,2,2,6,6-pentamethylpiperidine 4- (meth) acryloylamino-1,2,2,6,6-pentamethylpiperidine, 4-cyano-4- (meth) acryloyloxy-2,2,6,6-tetramethylpiperidine and the like. . A monomer (b) can be used individually or in combination of 2 or more types. From the viewpoint of weather resistance, it is particularly preferable to use methacrylates in which R ³ = CH ₃ alone or in combination of two or more as the monomer (b).

  The amount of the ethylenically unsaturated monomer (b) represented by the formula (II) is different from that of the monomer (a) from the viewpoint of the weather resistance of the coating film and the dispersibility of the pigment, resin beads and silica. When the total of the monomer (b) and the reactive emulsifier (c) is 100 parts by mass, it is necessary to set the amount to 6 to 50 parts by mass. By setting the monomer (b) to 5 parts by mass or more, the pigment dispersibility is improved, so that the resin beads can be easily dispersed and good color developability can be exhibited even in various pigment systems. In addition, the weather resistance and recoatability of the paint film are improved. Moreover, by setting it as 50 mass parts or less, the weather resistance of a coating film can further be improved, without reducing superposition | polymerization stability. From the viewpoint of high pigment dispersibility and weather resistance, the preferred use amount is 10 to 50 parts by mass.

  As the anionic reactive emulsifier having an unsaturated double bond capable of radical polymerization in the molecule, for example, a reactive emulsifier having an allyl group in the molecule as a reaction site can be used. Specifically, Asahi Denka Co., Ltd. Adekaria Soap SR-10, SE-10 (above trade name), Dai-ichi Kogyo Seiyaku Aqualon KH-05, KH-10, HS-10 (above trade name) etc. Can be mentioned. Anionic reactive emulsifiers can be used alone or in combination of two or more.

  As the reactive emulsifier (c), only an anionic reactive emulsifier may be used, but in applications where high mechanical stability is required, a nonionic reactive emulsifier having an unsaturated double bond capable of radical polymerization in the molecule. It is preferable to use together. As a nonionic reactive emulsifier, Adeka Soap NE-10, ER-10, NE-20, ER-20, NE-30, ER-30, NE-40, ER-40 (trade name) manufactured by Asahi Denka Co., Ltd. ), Aqualon RN-10, RN-20, RN-30, RN-50 (above trade names) manufactured by Daiichi Kogyo Seiyaku Co., Ltd., and the like. It is particularly preferred that the anionic reactive emulsifier: nonionic reactive emulsifier is 8: 2 to 2: 8 (mass ratio).

  The amount of the reactive emulsifier (c) used is the monomer (a) and the monomer (b) from the viewpoints of polymerization stability, mechanical stability and water resistance, warm water resistance, and weather resistance of the aqueous coating material. When the total of the reactive emulsifier (c) is 100 parts by mass, it is necessary to make it 1 to 10 parts by mass. By setting the reactive emulsifier (c) to 1 part by mass or more, polymerization stability and mechanical stability are improved. Moreover, by setting it as 10 mass parts or less, the weather resistance of a coating film can further be improved, without reducing the water resistance of an aqueous coating material. A more preferable usage amount is 1 to 8 parts by mass.

  As the monomer used when synthesizing the emulsion particles (A) constituting the aqueous coating material of the present invention, only the above monomer (a), monomer (b) and reactive emulsifier (c) are used. However, other monomers having an unsaturated double bond capable of radical polymerization can be used in combination.

  When adjusting the molecular weight of the emulsion polymer forming the emulsion particles (A), n-dodecyl mercaptan, t-dodecyl mercaptan, n-octyl mercaptan, n-tetradecyl mercaptan, n-hexyl mercaptan are used as molecular weight modifiers. It can be adjusted by using a known chain transfer agent such as a mercaptan such as carbon tetrachloride or ethylene bromide, or α-methylstyrene dimer. In order not to lower the weather resistance, the amount of the chain transfer agent used is preferably 1% by mass or less based on the entire monomer.

  In addition, in the case where control of the particle size and mechanical stability at a particularly high level are required, it is possible to use a non-reactive surfactant in addition to the reactive emulsifier (c). Examples of the surfactant include various conventionally known anionic or nonionic surfactants and polymer emulsifiers. In that case, it is preferable that it is 5 mass% or less with respect to the whole monomer from the point of water resistance. By setting the non-reactive surfactant to 5% by mass or less, the mechanical stability and temporal stability of the emulsion particles (A) can be further improved without impairing water resistance.

  As the polymerization initiator for carrying out emulsion polymerization, those generally used for radical polymerization can be used. Specific examples thereof include persulfates such as potassium persulfate, sodium persulfate and ammonium persulfate; azobisiso Butyronitrile, 2,2′-azobis (2-methylbutyronitrile), 2,2′-azobis (2,4-dimethylvaleronitrile), 2,2′-azobis (4-methoxy-2,4- Oil-soluble azo compounds such as dimethylvaleronitrile) and 2-phenylazo-4-methoxy-2,4-dimethylvaleronitrile; 2,2′-azobis {2-methyl-N- [1,1-bis (hydroxymethyl) ) -2-hydroxyethyl] propionamide}, 2,2′-azobis {2-methyl-N- [2- (1-hydroxyethyl)] propionamide}, 2,2 -Azobis {2-methyl-N- [2- (1-hydroxybutyl)] propionamide}, 2,2'-azobis [2- (5-methyl-2-imidazolin-2-yl) propane] and salts thereof 2,2′-azobis [2- (2-imidazolin-2-yl) propane] and salts thereof, 2,2′-azobis [2- (3,4,5,6-tetrahydropyrimidin-2-yl) Propane] and its salts, 2,2′-azobis {2- [1- (2-hydroxyethyl) -2-imidazolin-2-yl] propane} and its salts, 2,2′-azobis (2-methylpropion) Amidine) and its salts 2,2′-azobis (2-methylpropyneamidine) and its salts, 2,2′-azobis [N- (2-carboxyethyl) -2-methylpropiona Zin] and water-soluble azo compounds such as salts thereof; benzoyl peroxide, cumene hydroperoxide, t-butyl hydroperoxide, t-butyl peroxy-2-ethylhexanoate, t-butyl peroxyisobutyrate, etc. Organic peroxides; and the like. A polymerization initiator can be used individually or in combination of 2 or more types. Further, when acceleration of the polymerization rate and low temperature polymerization at 70 ° C. or lower are desired, it is advantageous to use a reducing agent such as sodium bisulfite, ferrous sulfate, ascorbate in combination with the radical polymerization catalyst. .

  The amount of the polymerization initiator used is preferably in the range of 0.01 to 10% by mass with respect to the whole monomer, but 0.05 to 5% by mass considering the progress of polymerization and reaction control. % Is more preferable.

  The emulsion particles (A) constituting the aqueous coating material of the present invention use, for example, a monomer (a), a monomer (b), and an emulsifier (c) in an aqueous medium, and a radical polymerization initiator. It can produce by carrying out emulsion polymerization. Moreover, emulsion polymerization can also be performed using a pre-emulsion with an ultraviolet absorber (d) described later. The emulsion particles (A) may have a single-layer structure or a multilayer structure, but in the case of a multilayer structure, the emulsion particles (A) preferably have a three-layer structure or less from the viewpoint of production efficiency.

  In the present invention, the glass transition temperature (hereinafter referred to as Tg) of the emulsion particles (A) is not particularly limited, but is preferably 100 ° C. or less, particularly preferably film-forming properties, from the viewpoint of the flexibility of the coating film. It is 70 degrees C or less from a point. Moreover, it is preferably −30 ° C. or higher from the viewpoint of contamination.

In addition, as said Tg, the calculated glass transition temperature calculated | required by the formula of Fox is used. The Fox equation is a relational expression between a glass transition temperature (° C.) of a copolymer and a glass transition temperature (° C.) of a homopolymer obtained by homopolymerizing each of the copolymer monomers, as shown below. (273 + Tg) = Σ (W _i / (273 + Tg _i ))
[Wherein W _i represents the mass fraction of monomer i, and Tg _i represents the Tg (° C.) of the homopolymer of monomer i. ]
As the Tg of the homopolymer, specifically, the values described in “Polymer Handbook 3rd Edition” (A WILEY-INTERSCIENCE PUBLICATION, 1989) can be used.

  It is preferable that a weight average particle diameter is 30 nm-200 nm. If it is less than 30 nm, agglomerates are likely to occur during the polymerization, and a large amount of an emulsifier is required in order not to produce agglomerates, which may reduce the water resistance of the coating film. On the other hand, if it is larger than 200 nm, particle fusion tends to be difficult, and the water resistance may deteriorate. In order to exhibit high water resistance and weather resistance, the weight average particle diameter is particularly preferably 50 nm to 150 nm.

  The aqueous coating material of the present invention contains an ultraviolet absorber (d) in addition to the emulsion particles (A). Examples of the ultraviolet absorber (d) include benzophenone series such as 2,2-dihydroxy-4,4-dimethoxybenzophenone and 2,2 ′, 4,4′-tetrahydroxybenzophenone; 2-ethylhexyl-2-cyano- Cyanoacrylates such as 3,3-diphenyl acrylate; 2- (2-hydroxyphenyl) benzotriazole, 2- (2-hydroxy-5-tertiarybutylphenyl) -2H-benzotriazole, α- [3- [3 -(2H-benzotriazol-2-yl) -5- (1,1-dimethylethyl) -4-hydroxyphenyl] -1-oxopropyl] -ω-hydroxypoly (oxo-1,2-ethanediyl) Triazole type; 2- [4-[(2-hydroxy-3-dodecyloxypropyl) oxy] -2-hi Droxyphenyl] -4,6-bis (2,4-dimethylphenyl) -1,3,5-triazine, 2- [4-[(2-hydroxy-3-tridecyloxypropyl) oxy] -2- Hydroxyphenyl] -4,6-bis (2,4-dimethylphenyl) -1,3,5-triazine, 2,4-bis (2,4-dimethylphenyl) -6- (2-hydroxy-4-iso Hydroxyphenyl triazines such as octyloxyphenyl) -s-triazine, etc. The ultraviolet absorber (d) can be used alone or in combination of two or more.

  The content of the ultraviolet absorber (d) in the aqueous coating material of the present invention is a single amount that forms the emulsion particles (A) from the viewpoint of weather resistance of the coating film, prevention of fading of the base, dispersibility of the resin beads and silica. When the total of the body (a), the monomer (b), and the reactive emulsifier (c) is 100 parts by mass, it needs to be 10 to 50 parts by mass. By setting the content of the ultraviolet absorber (d) to 10 parts by mass or more, the dispersibility of pigments, resin beads, and silica can be improved, and aggregation during coloring with various pigments can be avoided. The weather resistance of the film and the ability to prevent fading of the base are improved, and the crack resistance at low temperatures can be improved. Moreover, by setting it as 50 mass parts or less, the weather resistance of a coating film and the fading prevention ability can further be improved, without reducing superposition | polymerization stability.

  The ultraviolet absorber (d) may be added after pre-emulsification at the time of emulsion polymerization, or may be added after the emulsion polymerization. From the standpoint of uniform dispersion in the film, it is preferable to pre-emulsify and add during polymerization.

  The emulsion obtained by the emulsion polymerization method can increase the stability of the system after the polymerization by adjusting the pH of the system to be weakly alkaline, that is, in the range of about pH 7.5 to 10.0 by adding a basic compound. . Examples of the basic compound include ammonia, triethylamine, propylamine, dibutylamine, amylamine, 1-aminooctane, 2-dimethylaminoethanol, ethylaminoethanol, 2-diethylaminoethanol, 1-amino-2-propanol, 2 -Amino-1-propanol, 2-amino-2-methyl-1-propanol, 3-amino-1-propanol, 1-dimethylamino-2-propanol, 3-dimethylamino-1-propanol, 2-propylaminoethanol , Ethoxypropylamine, aminobenzyl alcohol, morpholine, sodium hydroxide, potassium hydroxide and the like. In the case of interior use where it is desired not to include VOC, it is preferable to use an inorganic base compound. Furthermore, when it is desired that there is no slight odor, it is preferable to use a non-volatile inorganic base compound such as sodium hydroxide or potassium hydroxide.

  The aqueous coating material of the present invention can be used as it is in the obtained emulsion, but is usually used by appropriately adjusting the solid content to a range of 20 to 80% by mass. In addition, various pigments, antifoaming agents, pigment dispersants, leveling agents, anti-sagging agents, matting agents, UV absorbers, antioxidants, heat resistance improvers, slips are used to develop high performance coating materials. Agents and preservatives may be included. Furthermore, you may mix and use hardening agents, such as another emulsion resin, water-soluble resin, a viscosity control agent, and melamines.

  In order to form a coating film on the surface of various materials using the aqueous coating material of the present invention, for example, spray coating method, roller coating method, bar coating method, air knife coating method, brush coating method, dipping method, etc. The coating method may be selected as appropriate. Moreover, the aqueous coating material of this invention can obtain the coating film which formed the film sufficiently in room temperature drying by adding the film-forming auxiliary of the independent or required amount.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited at all by these. In the following description, “part” is based on mass. About the test as a coating material, the coating material was prepared with the following compounding composition, and the test was implemented according to the following method.

<Production of matte clear paint>
Add CS-12 (trade name, manufactured by Chisso Co., Ltd., film-forming aid) to 100 g of aqueous coating material until the minimum film-forming temperature reaches 5 ° C., and SP Seal H (trade name, manufactured by Kaleido Co., Ltd.). , 10 g of silica-based matting agent, 0.5 g of RHEOLATE 350 (trade name, manufactured by RHEOX Co., Ltd., thickener), Surfynol DF-58 (trade name, manufactured by Air Products Co., Ltd., defoaming agent) 0 .5 g was added, and the mixture was sufficiently stirred and filtered using a 100 mesh nylon bag to obtain a matte clear paint for evaluation.

<Preparation of white enamel paint>
TYPEQUE CR-97 (trade name, manufactured by Ishihara Sangyo Co., Ltd., chlorinated titanium oxide) 707 g, Adeka Coal W-193 (trade name, manufactured by Asahi Denka Kogyo Co., Ltd., pigment dispersant), Surfynol DF-58 ( Product name, Air Products Co., Ltd., defoaming agent) 25 g, deionized water 256 g are mixed well, glass beads are added, and pigment dispersion is performed for 30 minutes with a high-speed disperser, and then glass beads are 300 mesh The product was filtered with a nylon basket to obtain an evaluation mill base (solid content: 71% by mass).

  Next, with respect to 100 g of aqueous coating material (based on solid content of 50% by mass), CS-12 (trade name, manufactured by Chisso Corporation, film-forming aid) is added until the minimum film-forming temperature is 5 ° C., and 47g of mill base for evaluation and 0.5g of RHEOLATE350 (trade name, manufactured by RHEOX Co., Ltd., thickener) were added in order, stirred well, and deionized water with Ford Cup # 4 for about 30 seconds. And adjusted. Thereafter, filtration was again performed using a 300-mesh nylon bag to obtain a white enamel paint for evaluation with PWC = 40%.

<Test method>
(1) Weather resistance test Spray coating was performed on the zinc phosphate-treated steel plate (bonderite # 100-treated steel plate, thickness 0.8 mm, 70 mm × 150 mm) so that the dry film thickness was 50 μm. Thereafter, the plate was left to stand at room temperature for 1 hour and forcibly dried at 80 ° C. for 1 hour to obtain a coated plate for weather resistance evaluation. This coated plate is cut into a size of 70 mm × 50 mm, and this test plate is put into a die plastic metal weather KU-R4-W type (trade name, manufactured by Daipura Wintes Co., Ltd.). Test cycle: irradiation 4 hours / condensation 4 Time, UV intensity: 85 mW / cm ² , Black panel temperature: 63 ° C. during irradiation / 30 ° C. during condensation, Humidity: 50% RH during irradiation / 96% RH during condensation 60 ° gloss after 3000 hours The retention rate was used as an indicator of weather resistance, and the determination was made according to the following criteria.

The 60 ° gloss was measured using a polarization gloss meter VG-2000 type (trade name) manufactured by Nippon Denshoku Industries Co., Ltd.
“◎”: 90% or more.
“◯”: 75% or more and less than 90%.
“◯ △”: 60% or more and less than 75%.
“△”: 40% or more and less than 60%.
"X": Less than 40%.

(2) Base fading prevention test As a colored base on zinc phosphate-treated steel plate (bonderite # 100-treated steel plate, thickness 0.8 mm, 70 mm x 150 mm), there is an odorless big 10 gloss made by Asahi Pen Co., Ltd. for outdoor use The blue paint was spray-coated so that the dry film thickness was 50 μm, then left at room temperature for 1 hour, and forcedly dried at 80 ° C. for 1 hour. Subsequently, the matte clear paint was spray-coated so as to have a dry film thickness of 30 μm, then allowed to stand at room temperature for 1 hour, and forcedly dried at 80 ° C. for 1 hour to obtain a coating plate for a base fading prevention test. This coated plate is cut into a size of 70 mm × 50 mm, and this test plate is put into a die plastic metal weather KU-R4-W type (trade name, manufactured by Daipura Wintes Co., Ltd.). Test cycle: irradiation 4 hours / condensation 4 Time, UV intensity: 85 mW / cm ² , Black panel temperature: 63 ° C. during irradiation / 30 ° C. during condensation, Humidity: 50% RH during irradiation / 96% RH during condensation Prevention of ΔE after 3000 hours As an indicator of performance, the following criteria were used.

ΔE was measured using a spectrocolor meter SE-2000 (trade name) manufactured by Nippon Denshoku Industries Co., Ltd.
“◎”: Less than 1.
“◯”: 1 or more and less than 3.
“△”: 3 or more and less than 5.
“×”: 5 or more.

(3) Pigment dispersibility: A zinc phosphate-treated steel plate (bonderite # 100-treated steel plate, thickness 0.8 mm, 70 mm × 150 mm) was spray-coated with a white enamel paint for evaluation so that the dry film thickness was 50 μm, Thereafter, the plate was left to stand at room temperature for 1 hour and forcibly dried at 80 ° C. for 1 hour to obtain a coating plate for pigment dispersibility evaluation. The 60 ° gloss value of this test plate was used as an index of pigment dispersibility, and the determination was made according to the following criteria.

The 60 ° gloss was measured using a polarization gloss meter VG-2000 type (trade name) manufactured by Nippon Denshoku Industries Co., Ltd.
“◎”: 85 or more.
“◯”: 80 or more and less than 85.
“Δ”: 70 or more and less than 80.
"X": Less than 70.

(4) Silica dispersibility test Spray coating was applied to a zinc phosphate-treated steel plate (bonderite # 100-treated steel plate, plate thickness 0.8 mm, 70 mm × 150 mm) so that the dry film thickness was 30 μm. Then, the plate was left for 1 hour at room temperature and forcibly dried at 80 ° C. for 1 hour to obtain a coated plate for silica dispersibility evaluation. The test plate was used as an index of the value of 20 ° gloss, and judged according to the following criteria.

The 20 ° gloss was measured using a polarization gloss meter VG-2000 type (trade name) manufactured by Nippon Denshoku Industries Co., Ltd.
“◯”: Less than 2.
“△”: 2 or more and less than 5.
“×”: 5 or more.

(5) Warm water resistance test A clear paint was applied on a glass plate using an 8MIL applicator, then dried at room temperature for 1 hour, and then forcibly dried at 80 ° C for 1 hour. A coated plate was used. The evaluation coated plate was immersed in water at 50 ° C. for 1 week. The whitening and swelling of the coating film immediately after removal and the occurrence of blisters were confirmed and judged according to the following criteria.
“◎”: No change is observed.
“◯”: Slightly bluish but no swelling or peeling.
“△”: Whitening is observed, but swelling and peeling are not observed.
"X": Remarkable whitening or swelling / peeling is observed.

(6) Low temperature crack test A white enamel paint for evaluation was applied to a slate plate (bonderite # 100 treated steel plate, plate thickness 3 mm, 70 mm × 150 mm) with a brush so that the dry film thickness was 100 μm, and then at room temperature for 1 hour. What was left to stand and forcibly dried at 80 ° C. for 1 hour was used as a coated plate for a low temperature crack test. This test plate is immersed in tap water at 25 ° C. ± 3 ° C. for 18 hours, immediately after being drawn out, cooled in a low temperature layer of −20 ° C. ± 3 ° C. for 3 hours, and immediately taken out and heated in a high temperature bath at 50 ° C. did. The above operation was performed as one cycle for 20 cycles, and the determination was made according to the following criteria.
“O”: No abnormality.
“Δ”: At the end of 20 cycles, there is a slight crack in the thick film portion.
"X": There is a crack on the front surface at the end of 20 cycles.

(7) Mechanical stability test For the emulsions of Examples 1 to 8 and Comparative Examples 1 to 5, 100 g of each was tested with a Malone tester over a 15 kg share for 10 minutes, and filtered through a 100 mesh nylon basket. The amount of the residue was measured and evaluated according to the following criteria.
“◎”: The amount of the residue is less than 0.01 g or hardly seen.
“◯”: The amount of the residue is 0.01 g or more and less than 0.1 g.
“Δ”: The amount of the residue is 0.1 or more and less than 0.5 g.
“X”: The amount of the residue is 0.5 g or more, or gels during the test.

(8) Storage stability About the emulsion of Examples 1-8 and Comparative Examples 1-5, each 200g was put into mayonnaise bottle, and it put into the 50 degreeC thermostat for one week. Thereafter, the product was taken out, the presence / absence of a solidified product and the viscosity were confirmed, and evaluation was performed according to the following criteria.
“◯”: There is no coagulum, and the rate of change in viscosity is less than ± 20%.
“◯ Δ”: There is no coagulum, and the rate of change in viscosity is ± 20% or more and less than ± 30%.
“Δ”: There is no coagulum, and the rate of change in viscosity is ± 30% or more.
"X": A coagulum is seen.

(9) Polymerization stability In Examples 1 to 8 and Comparative Examples 1 to 5, the cullet at the time of polymerization was collected by filtration with a 100-mesh nylon basket, dried in a drying furnace at 50 ° C. for 24 hours, and its weight was measured. The evaluation was based on the following criteria.
“◎”: The amount of cullet in the dry state is less than 100 ppm.
“◯”: The amount of cullet in the dry state is 100 ppm or more and less than 1000 ppm.
“Δ”: The amount of cullet in the dry state is 1000 ppm or more, but polymerization is possible.
“×”: Polymerization is impossible due to instability.

<Example>
Example 1
A flask equipped with a stirrer, a reflux condenser, a temperature controller, a dropping pump, and a nitrogen introduction tube was reacted with 45 parts of deionized water and 5% by mass of the pre-emulsified product of Emulsion A blended in the proportions shown in Table 1. Charge into the vessel, heat up to 75 ° C while replacing the inside of the reaction vessel with nitrogen, and then add seed solution of 0.1 part ammonium persulfate (polymerization initiator) in 1 part water to form seed particles did. After measuring the temperature of the solution with a thermometer and confirming an exothermic peak, an initiator solution in which 0.2 part of ammonium persulfate (polymerization initiator) was dissolved in 3 parts of water and the rest of the emulsion A were treated at an internal temperature of 75. The mixture was added dropwise at 4 ° C. over 4 hours, and further aged for 2 hours at an internal temperature of 75 ° C., whereby the monomer of the emulsion A was polymerized to form emulsion particles (A).

  Thereafter, cooling was performed, and neutralization was performed with 0.2 part of a 28% by mass aqueous ammonia solution at a temperature of 60 ° C. or lower to obtain an aqueous coating material.

(Examples 2 to 8)
In the same manner as in Example 1, an aqueous coating material using the emulsion A blended at the ratio shown in Table 1 was prepared.

(Comparative Examples 1-5)
In the same manner as in Example 1, an aqueous coating material using the emulsion A blended at the ratio shown in Table 1 was prepared. In Comparative Example 3, polymerization was stopped because a solidified product was formed 10 minutes after the start of the dropping of the polymerization and stirring became difficult.

  In Examples 1-8 and Comparative Examples 1-5, the calculated Tg of emulsion particles (A), the minimum film-forming temperature (the temperature at which film formation is possible without causing cracks in the film), and the solid content of the resulting aqueous coating material Table 1 shows the results for (NV), viscosity, pH, and weight average particle diameter of the emulsion particles (A). As the solid content, a value obtained by drying the aqueous coating material at 105 ° C. for 2 hours and obtaining the weight before and after drying was used. As the viscosity, the value measured with an R-100 type viscometer (trade name) manufactured by Toki Sangyo Co., Ltd. was used, with the temperature of the aqueous coating material being 25 ° C. As the weight average particle diameter, a value obtained by measuring a sample adjusted to a concentration of 1% at 25 ° C. using a concentrated analyzer FPAR-1000 (trade name) manufactured by Otsuka Electronics Co., Ltd. was used.

  In addition, the aqueous coating materials obtained in Examples 1 to 8 and Comparative Examples 1 to 5 were subjected to polymerization stability evaluation, mechanical stability test, storage stability test, and white prepared using the aqueous coating material. Using an enamel paint, a weather resistance test, a pigment dispersibility test, and a low temperature crack property were conducted, and using a clear paint, a fading prevention property, a silica dispersibility, and a hot water resistance test were conducted. The results are shown in Table 2 below.

ＭＭＡ：メチルメタクリレート
ｔ−ＢＭＡ：ターシャリーブチルメタクリレート
ＣＨＭＡ：シクロヘキシルメタクリレート
ｎ−ＢＭＡ：ノルマルブチルメタクリレート
ｎ−ＢＡ：ノルマルブチルアクリレート
２−ＥＨＡ：２−エチルヘキシルアクリレート
２−ＨＥＭＡ：２−ヒドロキシエチルメタクリレート
ＭＭＡ：メチルメタクリレート
ＡＡ：アクリル酸
４−ＭＯ−ＴＭＰ：４−メタクリロイルオキシ−２，２，６，６−テトラメチルピペリジン
４−ＭＯ−ＰＭＰ：４−メタクリロイルオキシ−１，２，２，６，６−ペンタメチルピペリジン
４−ＭＡ−ＴＭＰ：４−メタクリロイルアミノ−２，２，６，６−テトラメチルピペリジン
アデカリアソープＳＲ−１０：反応型アニオン性界面活性剤（商品名、旭電化（株）製）
アクアロンＨＳ−１０：反応型アニオン性界面活性剤（商品名、第一工業製薬（株）製）
アデカリアソープＮＥ−２０：反応型ノニオン性界面活性剤（商品名、旭電化（株）製）
アデカリアソープＥＲ−３０：反応型ノニオン性界面活性剤（商品名、旭電化（株）製）
アデカリアソープＥＲ−４０：反応型ノニオン性界面活性剤（商品名、旭電化（株）製）
Ｔｉｎｕｖｉｎ１１３０：紫外線吸収剤（商品名、チバ・スペシャルティ・ケミカルズ社製）
Ｔｉｎｕｖｉｎ４００：紫外線吸収剤（商品名、チバ・スペシャルティ・ケミカルズ社製）
リボノックスＮＣ−３００：非反応型ノニオン性界面活性剤（商品名、ライオン（株）製）
ラテムルＥ−１１８Ｂ：非反応型アニオン性界面活性剤（商品名、花王（株）製）

MMA: methyl methacrylate t-BMA: tertiary butyl methacrylate CHMA: cyclohexyl methacrylate n-BMA: normal butyl methacrylate n-BA: normal butyl acrylate 2-EHA: 2-ethylhexyl acrylate 2-HEMA: 2-hydroxyethyl methacrylate MMA: methyl Methacrylate AA: Acrylic acid 4-MO-TMP: 4-Methacryloyloxy-2,2,6,6-tetramethylpiperidine 4-MO-PMP: 4-methacryloyloxy-1,2,2,6,6-pentamethyl Piperidine 4-MA-TMP: 4-methacryloylamino-2,2,6,6-tetramethylpiperidine adecalia soap SR-10: reactive anionic surfactant (trade name, manufactured by Asahi Denka Co., Ltd.)
Aqualon HS-10: reactive anionic surfactant (trade name, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
Adekaria soap NE-20: reactive nonionic surfactant (trade name, manufactured by Asahi Denka Co., Ltd.)
ADEKA rear soap ER-30: reactive nonionic surfactant (trade name, manufactured by Asahi Denka Co., Ltd.)
ADEKA rear soap ER-40: reactive nonionic surfactant (trade name, manufactured by Asahi Denka Co., Ltd.)
Tinuvin 1130: UV absorber (trade name, manufactured by Ciba Specialty Chemicals)
Tinuvin400: UV absorber (trade name, manufactured by Ciba Specialty Chemicals)
Ribonox NC-300: Non-reactive nonionic surfactant (trade name, manufactured by Lion Corporation)
Latemul E-118B: non-reactive anionic surfactant (trade name, manufactured by Kao Corporation)

表２から明らかなように、本発明の水性被覆材は、耐候性、耐温水性、退色防止性、低温クラック性に優れると共に顔料分散性、シリカ分散性、機械安定性、貯蔵安定性、重合安定性に優れている。これに対して、比較例のように、特定の組成範囲に入っていないものは、重合安定性が劣っていたり、重合可能であったとしても耐候性、耐温水性等の性能が不足している。以上の説明から明らかなように、本発明によれば、重合安定性が良く、塗装皮膜からのブリードアウトが無い、すぐれた耐候性を有する水性被覆材を提供することが可能である。

As is apparent from Table 2, the water-based coating material of the present invention is excellent in weather resistance, hot water resistance, anti-fading property, and low-temperature cracking property, as well as pigment dispersibility, silica dispersibility, mechanical stability, storage stability, and polymerization. Excellent stability. On the other hand, as in the comparative example, those that are not in a specific composition range are inferior in the stability of the polymerization, such as weather resistance, hot water resistance, etc. Yes. As is apparent from the above description, according to the present invention, it is possible to provide an aqueous coating material having excellent weather resistance and good polymerization stability and no bleed-out from the coating film.

  The aqueous coating material of the present invention is made of various materials such as cement mortar, slate board, gypsum board, extruded board, foamable concrete, metal, glass, porcelain tile, asphalt, wood, waterproof rubber material, plastic, calcium silicate base material, etc. It can be used for the surface finishing of steel and is extremely useful in industry.

Claims (1)

40-93 parts by mass of ethylenically unsaturated monomer (a) not containing any of —COOH, —P (═O) ₂ OH, and —SO ₄ H, and represented by the following general formula (I), Reactive emulsifier (c) containing 6-50 parts by mass of ethylenically unsaturated monomer (b) having a piperidyl group in the molecule and an anionic reactive emulsifier having an unsaturated double bond capable of radical polymerization in the molecule ) 1 to 10 parts by mass (provided that the total of (a), (b), and (c) is 100 parts by mass), and emulsion particles (A) obtained by emulsion polymerization of monomers,
UV absorber (d) 10-50 parts by mass;
A water-based coating material comprising:

In the formula (I), R ³ is a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, X is an oxygen atom or imino group, Y is a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an alkoxyl group, Z is hydrogen An atom or a cyano group is shown.